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Iranian Polymer Journal
17 (6), 2008, 451-477
hydrogel;
superabsorbent;
swelling;
water;
polymerization.
(*) To whom correspondence to be addressed.
E-mail: m.zohuriaan@ippi.ac.ir
ABSTRACT
Key Words:
Superabsorbent Polymer Materials:
A Review
Mohammad J. Zohuriaan-Mehr*and Kourosh Kabiri
Iran Polymer and Petrochemical Institute, P.O. Box: 14965-115, Tehran, Iran
Received 24 February 2008; accepted 21 June 2008
Superabsorbent polymer (SAP) materials are hydrophilic networks that can
absorb and retain huge amounts of water or aqueous solutions. They can uptake
water as high as 100,000%. Common SAPs are generally white sugar-like
hygroscopic materials, which are mainly used in disposable diapers and other applica-
tions including agricultural use. This article reviews the SAP literature, background,
types and chemical structures, physical and chemical properties, testing methods,
uses, and applied research works. Due to variability of the possible monomers and
macromolecular structure, many SAP types can be made. SAPs are originally divided
into two main classes; i.e., synthetic (petrochemical-based) and natural (e.g., polysac-
charide- and polypeptide-based). Most of the current superabsorbents, however, are
frequently produced from acrylic acid (AA), its salts, and acrylamide (AM) via solution
or inverse-suspension polymerization techniques. The main synthetic (internal) and
environmental (external) factors affecting the acrylic anionic SAP characteristics are
described briefly. The methods for quantifying the SAP practical features, i.e., absorp-
tion capacity (both load-free and under load), swelling rate, swollen gel strength, wick-
ing capacity, sol fraction, residual monomer, and ionic sensitivity were discussed. The
SAP applications and the related research works, particularly the hygienic and agricul-
tural areas are reviewed. Meanwhile, the research findings on the effects of SAP in soil
and agricultural achievements in Iran, as an arid country are treated as well. Finally, the
safety and environmental issues concerning SAP practical applications are discussed
as well.
CONTENTS
Available online at: http://journal.ippi.ac.ir
Introduction .......................................................................................................................... 452
Absorbing versus Superabsorbing Materials .................................................................... 452
History and Market .......................................................................................................... 453
Literature Review.............................................................................................................. 454
SAPs Types and Preparation ................................................................................................. 455
Classification ................................................................................................................... 455
Main Starting Materials ................................................................................................... 455
Synthetic SAPs ................................................................................................................ 456
Polysaccharide-based SAPs ............................................................................................. 457
Poly (amino acid)-based SAPs ......................................................................................... 458
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Saps Properties Determination Factors .................................... 459
SAP Technical Features ....................................................... 459
Reaction Variables ............................................................... 460
Effect of “Synthetic Factors” on Properties .................... 460
Effect of “Environmental Factors” on Properties .............. 460
Production Processes: ASnap Shot .......................................... 460
Solution Polymerization ...................................................... 461
Inverse-suspension Polymerization .................................... 461
Analytical Evaluation .............................................................. 462
Free-absorbency Capacity ................................................... 462
Tea-bag Method .............................................................. 462
Centrifuge Method ......................................................... 462
Sieve Method .................................................................. 462
Absorbency under Load (AUL) ........................................... 463
Wicking Rate and Capacity ................................................. 463
Swelling Rate ...................................................................... 464
Vortex Method ................................................................ 464
Swelling-time Profile ..................................................... 464
Swollen Gel Strength .......................................................... 464
Soluble Fraction .................................................................. 465
Residual Monomer .............................................................. 465
Ionic Sensitivity .................................................................. 465
Uses and Applied Research Works .......................................... 466
Hygienic and Bio-related Areas .......................................... 466
Agricultural Areas ............................................................... 466
Other Areas ......................................................................... 468
Safety and Environmental Issues ............................................. 469
Conclusion and Outlook .......................................................... 469
References ............................................................................... 470
INTRODUCTION
Hydrophilic gels that are usually referred to as hydro-
gels are networks of polymer chains that are some-
times found as colloidal gels in which water is the dis-
persion medium [1]. In another word, they are water
absorbing natural or synthetic polymers (they may
contain over 99% water). Hydrogels have been
defined as polymeric materials which exhibit the abil-
ity of swelling in water and retaining a significant
fraction (>20%) of water within their structure, with-
out dissolving in water [2-4]. They possess also a
degree of flexibility very similar to natural tissue due
to their large water content.
The applications of hydrogels are grown exten-
sively [3-6]. They are currently used as scaffolds in
tissue engineering where they may contain human
cells in order to repair tissue. Environmental sensitive
hydrogels have the ability to sense environmental
stimuli, such as changes of pH, temperature, or the
concentration of metabolite and then release their load
as a result of such a change. Hydrogels that are
responsive to specific molecules, such as glucose or
antigens can be used as biosensors as well as in drug
delivery systems (DDS). These kinds of hydrogels are
also used as controlled-release delivery devices for
bio-active agents and agrochemicals. Contact lenses
are also based on hydrogels.
Special hydrogels as superabsorbent materials are
widely employed in hygienic uses particularly dispos-
able diapers and female napkins where they can cap-
ture secreted fluids, e.g., urine, blood, etc.
Agricultural grade of such hydrogels are used as gran-
ules for holding soil moisture in arid areas.
Absorbing versus Superabsorbing Materials
The hygroscopic materials are usually categorized
into two main classes based on the major mechanism
of water absorption, i.e., chemical and physical
absorptions. Chemical absorbers (e.g., metal
hydrides) catch water via chemical reaction convert-
ing their entire nature. Physical absorbers imbibe
water via four main mechanisms [8]; (i) reversible
changes of their crystal structure (e.g., silica gel and
anhydrous inorganic salts); (ii) physical entrapment of
water via capillary forces in their macro-porous struc-
ture (e.g., soft polyurethane sponge); (iii) a combina-
tion of the mechanism (ii) and hydration of function-
al groups (e.g., tissue paper); (iv) the mechanism
which may be anticipated by combination of mecha-
nisms of (ii) and (iii) and essentially dissolution and
thermodynamically favoured expansion of the macro-
molecular chains limited by cross-linkages.
Superabsorbent polymer (SAP) materials fit in the lat-
ter category, yet, they are organic materials with enor-
mous capability of water absorption.
SAPs as hydrogels, relative to their own mass can
absorb and retain extraordinary large amounts of
water or aqueous solution [2,3]. These ultrahigh
absorbing materials can imbibe deionized water as
high as 1,000-100,000% (10-1000 g/g) whereas the
absorption capacity of common hydrogels is not more
than 100% (1 g/g). Visual and schematic illustrations
of an acrylic-based anionic superabsorbent hydrogel
in the dry and water-swollen states [7] are given in
Figure 1.
Commercial SAP hydrogels are generally sugar-
Superabsorbent Polymer Materials: A Review Zohuriaan-Mehr MJ et al.
Iranian Polymer Journal / Volume 17 Number 6 (2008)
452
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like hygroscopic materials with white-light yellow
colour. The SAP particle shape (granule, fibre, film,
etc.) has to be basically preserved after water absorp-
Table 1. Water absorbency of some common absorbent
materials [2] in comparison with a typical commercial SAP
sample.
(a) Agricultural SAP produced by Rahab Resin Co., Ltd., Iran [9].
tion and swelling, i.e., the swollen gel strength should
be high enough to prevent a loosening, mushy, or
slimy state. This is a major practical feature that dis-
criminates SAPs from other hydrogels.
Traditional absorbent materials (such as tissue
papers and polyurethane foams) unlike SAPs, will lost
most of their absorbed water when they are squeezed.
Table 1 compares water absorptiveness of some com-
mon absorbent materials [2] with a typical sample of
a commercially available SAP [9].
History and Market
The synthesis of the first water-absorbent polymer
goes back to 1938 when acrylic acid (AA) and
divinylbenzene were thermally polymerized in an
aqueous medium [2]. In the late 1950s, the first gen-
eration of hydrogels was appeared. These hydrogels
453
Iranian Polymer Journal / Volume 17 Number 6 (2008)
Superabsorbent Polymer Materials: A Review
Zohuriaan-Mehr MJ et al.
Figure 1. Illustration of a typical acrylic-based anionic SAP material: (a) A visual comparison of the
SAP single particle in dry (right) and swollen state (left). The sample is a bead prepared from the
inverse-suspension polymerization technique. (b) A schematic presentation of the SAP swelling.
(b)
Absorbent Material Water Absorbency (wt%)
Whatman No. 3 filter paper
Facial tissue paper
Soft polyurethane sponge
Wood pulp fluff
Cotton ball
Superab A-200a
180
400
1050
1200
1890
20200
(a)
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were mainly based on hydroxyalkyl methacrylate and
related monomers with swelling capacity up to 40-
50%. They were used in developing contact lenses
which have make a revolution in ophthalmology [10].
The first commercial SAP was produced through
alkaline hydrolysis of starch-graft-polyacrylonitrile
(SPAN). The hydrolyzed product (HSPAN) was
developed in the 1970s at the Northern Regional
Research Laboratory of the US Department of
Agriculture [6]. Expenses and inherent structural dis-
advantage (lack of sufficient gel strength) of this
product are taken as the major factors of its early
market defeat.
Commercial production of SAP began in Japan in
1978 for use in feminine napkins. Further develop-
ments lead to SAP materials being employing in baby
diapers in Germany and France in 1980. In 1983,
low-fluff diapers (contained 4-5 g SAP) were market-
ed in Japan. This was followed shortly by the intro-
duction of thinner superbasorbent diapers in other
Asian countries, US and Europe. Because of the
effectiveness of SAPs, nappies became thinner, as the
polymer mainly replaced the bulkier cellulose fluff
that could not retain much liquid under pressure [3].
As a result, SAP caused a huge revolution in the per-
sonal health care industries in just over ten years.
In late 1990, the world production of the SAP
resins was more than one million tons. The greatest
SAP manufacturers are the Amcol (Chemdal),
Stockhausen, Hoechst, Sumitomo, Sanyo, Colon,
Nalco, and SNF Floerger Companies [8]. According
Figure 2. World SAP producer capacities estimated for
2005 according to the last data from EDANA [11].
to European Disposables and Nonwovens
Association (EDANA) [11], the total production in
2005 approached to around 1,483,000 tons; 623,000
tons in Asia (mostly by Nippon Shokubai, San-Dia
Polymers and Sumitomo Seika Chemicals), 490,000
tons in the North America (by Degussa, BASF, Dow
and Nippon Shokubai), and 370,000 tons in Europe
(mostly by Degussa and BASF). Specialty markets
for SAPs have also been developed in agriculture,
sealants, air-fresheners, toys, etc. Figure 2 shows the
worldwide SAP production distribution.
In the Middle East, SAP production was started
around 2004 by Rahab Resin Co., an Iranian private
sector company, under the license of Iran Polymer
and Petrochemical Institute (IPPI) [9].
Literature Review
Several papers have been published to review SAP
hydrogel materials, each with own individual out-
look. As a general framework, synthetic methods and
properties of hydrogel networks were reviewed [12].
Synthetic, semi-synthetic and biopolymeric hydro-
gels were also briefly reviewed [13]. Chemistry and
physics of agricultural hydrogels were reviewed by
Kazanskii and Dubrovskii [14]. Bouranis et al. have
reviewed the synthetic polymers as soil conditioners
[15].
Superabsorbents obtained from shellfish waste
have also been reviewed [16]. Ichikawa and
Nakajima have reviewed the superabsorptive materi-
als based on the polysaccharides and proteins [17]. A
review profile of water absorbing resins based on
graft copolymers of acrylic acid and gelatinized
starch was presented by Athawale et al. [18].
Buchholz has elaborated the uses of superab-
sorbents based on cross-linked, partially neutralized
poly(acrylic acid) and graft copolymers of starch and
acrylic acid [19]. In another review, the synthesis of
cross-linked acrylic acid-co-sodium/potassium acry-
late has been described. The solution and suspension
polymerization techniques used for preparing the
acrylate superabsorbents have been discussed in
detail [10].
In a unique article published in 1994, Ricardo Po
[5] critically surveyed the water-absorbent polymers
in accordance with the patent literature. Within an
industrial production viewpoint, a useful profile has
Iranian Polymer Journal / Volume 17 Number 6 (2008)
454
Superabsorbent Polymer Materials: A Review Zohuriaan-Mehr MJ et al.
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been published about acrylic SAPs by the Stanford
Research Institute, SRI [20].
Two valuable books on the synthetic SAP materi-
als were published in 1990-1998 [2,3] and the funda-
mental phenomena dealing with the synthetic hydro-
gels were reflected very clearly [3]. In 2002, another
valuable book was published, focused mainly on the
fibres and textiles with high water absorbency charac-
teristics [21].
In spite of the foresaid reviewing sources, to the
best of our knowledge, there is no other published
review with a comprehensive perspective on SAP
hydrogels. The present article represents a different
outlook; it gives an account of all types of SAP mate-
rials with a practical viewpoint from structure to
usage, based on either the current literature or our
long experience on these materials. The main target is
appraisal the SAPs to be useful for either academies
or industries. Meanwhile, a very beneficial section
related to the practical methods of the SAP testing and
evaluation has also been included in the analytical
evaluation section.
SAPs TYPES AND PREPARATION
Classification
Resembling the hydrogel family, the SAPs can also be
classified based upon different aspects. SAPs may be
categorized to four groups on the basis of presence or
absence of electrical charge located in the cross-
linked chains [8]:
1- non-ionic
2- ionic (including anionic and cationic)
3- amphoteric electrolyte (ampholytic) containing
both acidic and basic groups
4- zwitterionic (polybetaines) containing both
anionic and cationic groups in each structural repeat-
ing unit
For example, the majority of commercial SAP
hydrogels are anionic. SAPs are also classified based
on the type of monomeric unit used in their chemical
structure, thus the most conventional SAPs are held in
one of the following categories [5, 8]:
(a) cross-linked polyacrylates and polyacry-
lamides
(b) hydrolyzed cellulose-polyacrylonitrile (PAN)
or starch-PAN graft copolymers
(c) cross-linked copolymers of maleic anhydride
However, according to original sources, SAPs are
often divided into two main classes; i.e., synthetic
(petrochemical-based) and natural. The latter can be
divided into two main groups, i.e., the hydrogels
based on polysaccharides and others based on
polypeptides (proteins). The natural-based SAPs are
usually prepared through addition of some synthetic
parts onto the natural substrates, e.g., graft copoly-
merization of vinyl monomers on polysaccharides.
It should be pointed out when the term “superab-
sorbent” is used without specifying its type, it actual-
ly implies the most conventional type of SAPs, i.e.,
the anionic acrylic that comprises a copolymeric net-
work based on the partially neutralized acrylic acid
(AA) or acrylamide (AM).
Main Starting Materials
Variety of monomers, mostly acrylics, is employed to
prepare SAPs. Acrylic acid (AA) and its sodium or
potassium salts, and acrylamide (AM) are most often
used in the industrial production of SAPs (discussed
later).
The AA monomer is inhibited by methoxyhydro-
quinone (MHC) to prevent spontaneous polymeriza-
tion during storage. In industrial production, the
inhibitor is not usually removed due to some technical
reasons [2]. Meanwhile, AA is converted to an unde-
sired dimer that must be removed or minimized.
The minimization of acrylic acid dimer (DAA) in
the monomer is important due to its indirect adverse
effects on the final product specifications, typically
soluble fraction and the residual monomer. As soon as
AA is produced, diacrylic acid (β-acryloxypropionic
acid) is formed spontaneously in the bulk of AA via a
sluggish Michael-addition reaction [2]. Since temper-
ature, water content, and pH have impact on the rate
of DAA formation, the rate can be minimized by con-
trolling the temperature of stored monomer and
excluding the moisture [22]. Increasing water concen-
tration has a relatively small impact on the DAA for-
mation rate. Nevertheless, the rate roughly doubles
for every 5ºC increase in temperature. For example, in
an AA sample having 0.5% water, the dimerization
rate is 76 and 1672 ppm/day at 20ºC and 40ºC, respec-
tively. DAA, however, can be hydrolyzed in alkaline
Superabsorbent Polymer Materials: A Review
Zohuriaan-Mehr MJ et al.
Iranian Polymer Journal / Volume 17 Number 6 (2008) 455
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media to produce AA and β-hydroxypropionic acid
(HPA). Since the latter is unable to be polymerized, it
remains as part of the SAP soluble fraction.
Fortunately, alkaline media used conventionally for
AA neutralization with NaOH favours this hydrolytic
reaction. For instance, in an 80% neutralized AA, the
dimerization rate at 23ºC and 40ºC has been deter-
mined to be 125 and 770 ppm/day, respectively [2].
DAA can also be polymerized to go into the SAP
network. It may be then thermally cleaved through a
retro-Michael reaction in the course of heating in the
drying step of the final product. As a result, free AA
will be released and causes the enhancement of the
level of residual monomer.
On laboratory scales, however, number of
monomers such as methacrylic acid (MAA),
methacrylamide (MAM), acrylonitrile (AN), 2-
hydroxyethylmethacrylate (HEMA), 2-acrylamido-2-
methylpropane sulphonic acid (APMS), N-vinyl
pyrrolidone (NVP), vinyl sulphonic acid (VSA) and
vinyl acetate (VAc) are also used.
In the modified natural-based SAPs (i.e., hybrid
superabsorbents) trunk biopolymers such as cellulose,
starch, chitosan, gelatin and some of their possible
derivatives e.g., carboxymethyl cellulose (CMC) are
also used as the modifying substrate (polysaccharide-
based SAPs section).
The bifuntional compound N,N’-methylene
bisacrylamide (MBA) is most often used as a water
soluble cross-linking agent. Ethyleneglycole
dimethacrylate (EGDMA), 1,1,1-trimethylolpropane
triacrylate (TMPTA), and tetraalyloxy ethane (TAOE)
are known examples of two-, three- and four-func-
tional cross-linkers, respectively.
Potassium persulphate (KPS) and ammonium per-
sulphate (APS) are water soluble thermal initiators
used frequently in both solution and inverse-suspen-
sion methods of polymerization (discussed in the snap
shot section of production processes). Redox pair ini-
tiators such as Fe2+-H2O2(Fenton reagent) and APS-
sodium sulphite are also employed particularly in the
solution method.
Synthetic SAPs
The greatest volume of SAPs comprises full synthetic
or of petrochemical origin. They are produced from
the acrylic monomers, most frequently acrylic acid
(AA), its salts and acrylamide (AM). Figure 3 shows
Superabsorbent Polymer Materials: A Review Zohuriaan-Mehr MJ et al.
456 Iranian Polymer Journal / Volume 17 Number 6 (2008)
O
HO
O
H2N
O
M+O-
++
Hydrophilic monomers
O
X
R
X
O(a)
Init iat o r
Init iat o r O
H2NM+O-
COOH
O
Water-soluble
prepolymer chain
XH
R
XH
(b)
Wa ter - s w e llab le p o lyme r ne tw o rk
OCOO- M+
X
R
O
H2N
O
H2N
O
XR
X
H2N
O
COO- M+
OCOOH
COO- M+O
H2NX
R
O
X
H2N
O
H2N
O
H2N
O
COO- M+
COOH
COO-M+
Figure 3. Chemical structures of the reactants and general pathways to prepare an acrylic SAP network: (a) Cross-linking
polymerization by a polyvinylic cross-linker, (b) Cross-linking of a water-soluble prepolymer by a polyfunctional cross-linker.
R is often CH2or another aliphatic group. M stands for the sodium or potassium cations [7]. X= O, NH.
(a) (b)
Water-swellable polymer network
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two general pathways to prepare acrylic SAP net-
works, i.e., simultaneous polymerization and
crosslinking by a polyvinylic cross-linker, and cross-
linking of a water-soluble prepolymer by a polyfunc-
tional cross-linker. More discussions on the synthetic
SAPs are provided in the related sections.
Polysaccharide-based SAPs
Although the majority of the superabsorbents are
nowadays manufactured from synthetic polymers
(essentially acrylics) due to their superior price-to-
efficiency balance [2,5,9], the worlds firm decision
for environmental protection potentially support the
ideas of partially/totally replacing the synthetics by
"greener" alternatives [17].
Carbohydrate polymers (polysaccharides) are the
cheapest and most abundant, available, and renewable
organic materials. Chitin, cellulose, starch, and natu-
ral gums (such as xanthan, guar and alginates) are
some of the most important polysaccharides.
Generally, the reported reactions for preparing the
polysaccharide-based SAPs are held in two main
groups; (a) graft copolymerization of suitable vinyl
monomer(s) on polysaccharide in the presence of a
cross-linker, and (b) direct cross-linking of polysac-
charide.
In graft copolymerization, generally a polysaccha-
ride enters reaction with initiator by either of two sep-
arate ways. First, the neighbouring OHs on the sac-
charide units and the initiator (commonly Ce4+) inter-
act to form redox pair-based complexes. These com-
plexes are subsequently dissociated to produce carbon
radicals on the polysaccharide substrate via homoge-
neous cleavage of the saccharide C-C bonds. These
free radicals initiate the graft polymerization of the
vinyl monomers and cross-linker on the substrate.
In the second way of initiation, an initiator such as
persulphate may abstract hydrogen radicals from the
OHs of the polysaccharide to produce the initiating
radicals on the polysaccharide backbone. Due to
employing a thermal initiator, this reaction is more
affected by temperature compared to previous
method.
The earliest commercial SAPs were produced
from starch and AN monomer by the first mentioned
method without employing a cross-linker. The starch-
g-PAN copolymer (SPAN) was then treated in
Figure 4. The mechanism of in-situ cross-linking during the
alkaline hydrolysis of polysacchride-g-PAN copolymer to
yield superabsorbing hybrid material.
alkaline medium to produce a hybrid SAP, hydrolyzed
SPAN (H-SPAN) while an in-situ cross-linking
Superabsorbent Polymer Materials: A Review
Zohuriaan-Mehr MJ et al.
Iranian Polymer Journal / Volume 17 Number 6 (2008) 457
CN CN
C
N
C
N
C
N
H O
(Sacc haride unit
of TG)
OH
(T G backbone)
CN CN C
N
C
N
C
N
Conjugated imine intermediate
(deep re d)
(TG backbone)
(TG backbone)
CONH 2N
NNN
NN
COO
COO COO
OH
(TG backbone)
OH
NNN
H
COO COO
OH
..
(Adjacent s imilar
acrylic chain)
(- NH
3
)
OH
(TG backbone)
OO O
CONH 2
COOCOO
COO
NH (Adjacent s imilar
acrylic chain)
(TG bac kbone)
(Another
TG chain)
Lightly crosslinke d
TG-g-poly(sodium acrylate-co-acrylamide)
(light yellow)
H2O
H2O
(- NH
3 )
TG-g-polyacrylonitrile
(light yellow)
OH
H2O
Polysaccharide-g-PAN
Polysaccharide
backbone
Polysaccharide
backbone
Polysaccharide backbone
Backbone
Conjugated imine intermediate Backbone
(deep red)
Backbone
Backbone
Polysaccharide
backbone
Lightly crosslinked
Polysaccharide-g-poly(AANa-co-AM);
A SAP hybrid hydrogel
Lightly cross-linked
Polysaccharide-g-poly(AANa-co-AM)
A SAP hybrid hydrogel
Polysaccharide-g-PAN
Conjugated imine intermediate
(deep red)
-NH3
-NH3
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Figure 5. Typical cellulose-based SAP prepared via direct
cross-linking of sodium carboxymethyl cellulose (CMC; R=
H, COO-Na+) or hydroxyethyl cellulose (HEC; R= H,
CH2CH2OH) [24].
occurred simultaneously. This fascinating approach
(Figure 4) has been employed to convert various
polysaccharides into SAP hydrogel hybrids [23].
In the method direct cross-linking of polysaccha-
rides, polyvinylic compounds (e.g., divinyl sulphone,
DVS) or polyfunctional compounds (e.g., glycerol,
epichlorohydrine and glyoxal) are often employed
[13,23]. POCl3is also used for the cross-linking.
Figure 5 exhibits the structure of valuable CMC- and
hydroxyethyl cellulose (HEC)-based SAPs prepared
by Saninno et al. [24]. Most recently, they have also
synthesized fully natural SAP hydrogels via cross-
linking of the cellulosics by citric acid [25].
Poly(amino acid)-based SAPs
Dissimilar to polysaccharide-based hydrogels, rela-
tively fewer works have been reported on the natural-
based SAP hydrogels comprising polypeptides as the
main or part of their structure. Proteins from soybean,
fish, and collagen-based proteins are the most fre-
quently used hetero-polypeptides for preparation of
proteinaceous super-swelling hydrogels.
The most important research programme of the
protein-based SAPs has been conducted by
Damodaran et al. [26-35] working in the Department
of Food Science, University of Wisconsin, Madison,
USA. They converted soy and fish proteins to SAP
through modification by ethylenediamine tetraacetic
dianhydride (EDTAD) in the first stage. EDTAD has
low toxicity because the only reactive group intro-
duced into the network is the carboxyl group, and
lysyl residues of the protein that can be modified with
EDTAD in a relatively fast reaction. They often used
the soy protein isolate (SPI) for the modification. The
modified product was prepared by extraction of defat-
ted soy flour with water at pH 8 at a meat-to-water
ratio of 1:10 [26].
In the second stage, the remaining amino groups
of the hydrophilized protein are lightly cross-linked
by glutaraldehyde to yield a hydrogel network with
superabsorbing properties. The SAP was capable of
imbibing 80-300 g of deionized-water/g of dry gel
after centrifugating at 214 g, depending on the extent
of modification, protein structure, cross-link density,
protein concentration during the second step, gel par-
ticle size, and environmental conditions such as pH,
ionic strength, and temperature [26].
The EDTAD-modified soy protein SAPs are
reported to be highly pH sensitive. It also exhibits
reversible swelling-deswelling behaviour when the
swollen gel is alternatively exposed to 0.15 m NaCl,
and deionized water [26,32].
Some patents have also been disclosed, investigat-
ing extensively on the preparation and properties of
the SAPs based on the soy protein isolate [32,33].
The inventors have specified that similar approaches
can be used on other proteins such as leaf (alfalfa)
protein, microbial and animal proteins and those
recovered from food-processing wastes.
Following the introduction of a large number of
hydrophilic groups into fish protein (FP) concentrate
by modification with EDTAD, the proteins are report-
ed to be cross-linked by sulphhydryl-disulphide inter-
change reaction between the endogenous sulphhydryl
groups (-SH) and -S-S- bonds to produce a SAP net-
work [28]. The swelling capacity of a 76% EDTAD-
modified FP is reported to be 540 g/g at 214 g,
assumed to be dependent on pH and ionic strength of
the swelling media, similar to what observed for
EDTAD-modified SPI hydrogels [26,27,32,34].
When glutaraldehyde (GA) was employed as a cross-
linker, the SAP swelling ability was diminished to
150-200 g/g, whereas the gel rigidity was enhanced.
Therefore, these SAPs are preferred to be used for
water absorption under pressure in real applications,
such as diapers.
458 Iranian Polymer Journal / Volume 17 Number 6 (2008)
Superabsorbent Polymer Materials: A Review Zohuriaan-Mehr MJ et al.
O
O
O
ORO
OR
OR
OR
RO
O
RO
OR
OR
RO
O
O
O
O
O
OR
O
S
O
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Proteins can also be modified by either polysac-
charides or synthetics to produce hybrid hydrogels
with super-swelling properties. For instance, the
researchers have studied the water swelling property
of binary polymer networks (frequently as interpene-
trated polymer networks, IPNs) of modified proteins
with some water-soluble, hydrophilic, biodegradable,
and non-toxic polymers, e.g., modified soy protein,
gelatin, sodium carboxymethyl cellulose (CMC),
poly(ethylene glycol) (PEG), poly(vinyl alcohol),
guar gum, chitosan, and carboxymethyl chitosan [30,
35-40].
Collagen-based proteins including gelatin and
hydrolyzed collagen (H-collagen; very low molecular
weight products of collagen hydrolysis) have been
used for preparing SAP materials. For example, gela-
tin-g-poly (NaAA-co-AM) hydrogel has been synthe-
sized through simultaneous cross-linking and graft
polymerization of AA/AM mixtures onto gelatin [41].
The hybrid hydrogels in 0.15 mol salt solutions show
appreciable swelling capacity (e.g., in NaCl 38 g/g,
and in CaCl212 g/g). The SAP hydrogels exhibit high
sensitivity to pH, thus swelling changes may be
observed in a wide range of pH 1-13.
H-collagen was also graft copolymerized with AA
[42] , binary mixtures of AA and AM [43], AM and
AMPS [44], AA and AMPS [45,46], AM and
methacrylic acid (MAA) [47], and AA and hydrox-
yethyl acrylate (HEA) [48] for preparation of SAP
hybrid materials.
Homo-poly(amino acid)s of poly(aspartic acid)s,
poly(L-lysine) and poly(γ-glutamic acid)s have also
been employed to prepare SAP materials. In 1999,
Rohm and Haas Company’s researchers reported
lightly cross-linked high MW sodium polyaspartates
with superabsorbing, pH- and electrolyte-responsive-
ness properties [49]. They used ethylene glycol digly-
cidylether (EGDGE) as a cross-linker. Polyethylene
glycol diglycidylether (PEG-diepoxide) with different
MWs has also been employed to synthesize
biodegradable poly(aspartic acid) hydrogels with
super-swelling behaviour [50]. To enhance the
swelling capacity, several hydrophilic polymers (i.e.,
starch, ethyl cellulose, carrageenan, PAM, β-
cyclodextrin, and CMC) were incorporated into the
hydrogels (after or before the hydrolysis step) to
attain modified SAP composites [51].
Super-swelling hydrogels based on poly(γ-glutam-
ic acid), PGA, has been prepared by cross-linking
reactions via both irradiation [52-54] and chemical
approaches [55-61]. Similar to PGA, highly swollen
hydrogels based on L-lysine homopolymer have been
also prepared simply by γ-irradiation of their aqueous
solutions [52-54,62].
SAPs PROPERTIES DETERMINATION
FACTORS
SAP Technical Features
The functional features of an ideal SAP material can
be listed as follows [8]:
- The highest absorption capacity (maximum equi-
librium swelling) in saline
- Desired rate of absorption (preferred particle size
and porosity) depending on the application require-
ment
- The highest absorbency under load (AUL)
- The lowest soluble content and residual monomer
- The lowest price
- The highest durability and stability in the swelling
environment and during the storage
- The highest biodegradability without formation of
toxic species following the degradation
- pH-neutrality after swelling in water
- Colourlessness, odourlessness, and absolute non-
toxicity
- Photostability
- Re-wetting capability (if required)
The SAP has to be able to give back the imbibed solu-
tion or to maintain it; depending on the application
requirement (e.g., in agricultural or hygienic applica-
tions).
Obviously, it is impossible that a SAP sample
would simultaneously fulfil all the above mentioned
required features. In fact, the synthetic components
for achieving the maximum level of some of these
features will lead to inefficiency of the rest.
Therefore, in practice, the production reaction vari-
ables must be optimized such that an appropriate bal-
ance between the properties is achieved. For example,
a hygienic SAP must possess the highest absorption
rate, the lowest re-wetting and the lowest residual
monomer. In contrary, for an agricultural SAP the
Superabsorbent Polymer Materials: A Review
Zohuriaan-Mehr MJ et al.
Iranian Polymer Journal / Volume 17 Number 6 (2008) 459
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absorption rate is not much necessary; instead it must
acquire higher AUL and lowest sensitivity to salinity.
Reaction Variables
According to the voluminous research on the acrylic
anionic SAP literature [2-6,8,10,14,18,41-48] the
most important reaction variables affecting the final
properties are as follows:
(a) Cross-linker type and concentration
(b) Initiator type and concentration
(c) Monomer(s) type and concentration
(d) Type, size, and amount of inorganic particles
incorporated (if any)
(e) Polymerization method
(f) Polymerization temperature
(g) Amount and type of the surfactant used
(h) Stirrer/reactor geometry and rate of stirring
(i) Porosity generating method or the amount and
type of the porogen (if used)
(j) Drying; its method, temperature, and time
(k) Post-treatments such as surface cross-linking
to enhance the swollen gel strength
Each of the above mentioned variables has its own
individual effects on the SAP properties. However, to
optimize a process, a set of variables having the most
special effects on the desired SAP product should be
taken into consideration.
Effect of “Synthetic Parameters” on Properties
Employing fixed type of reactants, the acrylic SAP
properties are affected by the main synthetic factors
abstracted in Table 2 [8]. Many researchers have
studied the effects of the preparative reaction vari-
ables on the SAP characteristics. These table contents
have been actually extracted from numerous pub-
lished works [2-6, 63-86].
Additionally in recent years, researchers have par-
tially focused on SAP composites [69,78,87-91] and
nanocomposites [92-94] to improve particularly the
mechanical and thermal properties of the hydrogels.
Effect of “Environmental Parameters” on Properties
The SAP particle physical specifications (e.g., size
and porosity) as well as the swelling media also
greatly affect their properties. These physical and
environmental factors, particularly for acrylic anion-
ic SAPs, have been studied widely by many
researchers [2-6, 63-94]. Table 3 summarizes the
results of plenty published works on the convention-
al SAPs properties [8].
PRODUCTION PROCESSES: A SNAP SHOT
Acrylic acid (AA) and its sodium or potassium salts,
and acrylamide (AM) are most frequently used in the
SAP industrial production. AM, a white powder, is
pure enough to be often used without purification.
AA, a colourless liquid with vinegar odour, however,
has a different story due to its ability to convert into
its dimer (sub-section main starting materials). In this
regard, the DAA level must be minimized to prevent
the final product deficiencies, e.g., yield reduction,
loss of soluble fraction, residual monomers, etc. Due
to the potential problems originating from the inher-
ent nature of AA to dimerize over time, manufactur-
Superabsorbent Polymer Materials: A Review Zohuriaan-Mehr MJ et al.
460 Iranian Polymer Journal / Volume 17 Number 6 (2008)
Variation in synthetic
factorb
Absorption
capacity
Absorption
rate
Swollen gel strength
or AUL
Soluble
fraction
Increase in crosslinker concentration
Increase in initator concentration
Increase in monomer concentration
Increase in reaction temperature
Increase in particles porosity
Surface cross-linking
-
+
-
+
×c
-
-
-
+
-
+
-+
+
-
-
-
-
+
-
+
+
+
-+
-+
Table 2. Effect of the main synthetic (internal, structural) factors affecting SAP material properties [8]a.
(a) + = increasing, - = decreasing, +- = varied, depending on the reagents and/or techniques employed. (b) Each factor is
considered under a constant value of the rest factors. (c) Some authors have reported absorption enhancement, however,
no absorption rise has to be logically observed if more accurate methods are employed for swelling measurement, e.g., cen-
trifuge method.
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ers work properly with AA, such as timely order
placement, just-in-time delivery, moisture exclusion,
and temperature-controlled storage (typically 17-
18ºC). In the laboratory scale syntheses, however,
AA is often distilled before use, to purify and remove
the impurities including the inhibitor and DAA.
AA salt solutions are usually produced by slow
addition of appropriate solution of a desired metal
hydroxide (NaOH or KOH) to cooled AA while stir-
ring mild. The temperature of this extremely exother-
mic neutralization reaction must be precisely con-
trolled to prevent undesired polymerization.
As mentioned before, the SAP materials are often
synthesized through free-radically-initiated polymer-
ization of acrylic monomers. The resins are prepared
either in aqueous medium using solution polymeriza-
tion or in a hydrocarbon medium where the
monomers are well-dispersed. These different meth-
ods are briefly discussed in the following sections.
Some additional treatments, such as modified gel
drying methods [2,64,72] and, particularly, surface
cross-linking [2] and porosity generating techniques
[2,64,68,70] are important approaches for altering
and fine-tuning the SAP morphology and physico-
chemical properties.
Solution Polymerization
Free-radical initiated polymerization of AA and its
salts (and AM), with a cross-linker is frequently used
for SAP preparation.
The carboxylic acid groups of the product are par-
tially neutralized before or after the polymerization
step. Initiation is most often carried out chemically
with free-radical azo or peroxide thermal dissociative
species or by reaction of a reducing agent with an
oxidizing agent (redox system) [5,19]. In addition,
radiation is sometimes used for initiating the poly-
merization [2-5].
The solution polymerization of AA and/or its salts
with a water-soluble cross-linker, e.g., MBA in an
aqueous solution is a straight forward process. The
reactants are dissolved in water at desired concentra-
tions, usually about 10-70%. A fast exothermic reac-
tion yields a gel-like elastic product which is dried
and the macro-porous mass is pulverized and sieved
to obtain the required particle size. This preparative
method usually suffers from the necessity to handle a
rubbery/solid reaction product, lack of a sufficient
reaction control, non-exact particle size distribution
[95,96], and increasing the sol content mainly due to
undesired effects of hydrolytic and thermal cleavage
[72]. However, for a general production of a SAP
with acceptable swelling properties, the less expen-
sive and faster technique, i.e., solution method may
often be preferred by the manufacturers.
Inverse-Suspension Polymerization
Dispersion polymerization is an advantageous
method since the products are obtained as powder or
microspheres (beads), and thus grinding is not
Superabsorbent Polymer Materials: A Review
Zohuriaan-Mehr MJ et al.
Iranian Polymer Journal / Volume 17 Number 6 (2008) 461
FactorbAbsorption
capacity
Absorption
rate
Swollen gel strength
or AUL
Soluble
fraction
Increase in Particle size
Increase in Porosity
Increase in Ionic Strength of Medium
Increase in Temperature of Medium
Photo-/Bio-degradation
pH > 7
pH < 7
×c
×c
-
×
+
+
-
-
+
-
+
-
+
-
+
-
-+
×
-
-+
-+
×
×
×
×
+
×
×
Table 3. Effect of physical and environmental (external) factors on behaviour of the conventional anionic SAP
materials [8] a.
(a) += increasing, - =decreasing, ×= non-effective, +- = depending on the other various factors. (b) Each factor is consid-
ered under a constant value of the rest factors. (c) Lower particle size and higher porosity are usually reported as factors
that increase the swelling capacity. However, the capacity should not to be actually influenced by the particle size and poros-
ity, if the absorption capacity is accurately measured by more precise methods, e.g., centrifuge method.
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required. Since water-in-oil (W/O) process is chosen
instead of the more common oil-in-water (O/W) the
polymerization is referred to as "inverse-suspen-
sion". In this technique, the monomers and initiator
are dispersed in the hydrocarbon phase as a homoge-
nous mixture. The viscosity of the monomer solution,
agitation speed, rotor design, and dispersant type
mainly govern the resin particle size and shape [2-6].
Some detailed discussions on heterophase poly-
merizations have already been published [97,98].
The dispersion is thermodynamically unstable and
requires both continuous agitation and addition of a
low hydrophilic-lipophilic-balance (HLB) suspend-
ing agent. The inverse-suspension is a highly flexible
and versatile technique to produce SAPs with high
swelling ability and fast absorption kinetics [99]. A
water-soluble initiator shows a better efficiency than
the oil-soluble type. When the initiator dissolves in
the dispersed (aqueous) phase, each particle contains
all the reactive species and therefore behaves like an
isolated micro-batch polymerization reactor [100].
The resulting microspherical particles are easily
removed by filtration or centrifugation from the con-
tinuous organic phase. Upon drying, these particles
or beads will directly provide a free flowing powder.
In addition to the unique flowing properties of these
beads, the inverse-suspension process displays addi-
tional advantages compared to the solution method.
These include a better control of the reaction heat-
removal, ab initio regulation of particle-size distribu-
tion, and further possibilities for adjusting particle
structure or morphology alteration [99].
ANALYTICAL EVALUATION
This section contains the SAP testing methods that
are very useful in a practical point of view for aca-
demic and industrial analysts.
Free-absorbency Capacity
Generally, when the terms swelling or absorbency
are used without specifying its conditions; it implies
uptake of distilled water while the sample is freely
swollen, i.e., no load is put on the testing sample.
There are several simple methods for the free-
absorbency testing which are dependent mainly on
the amount of the available sample, the sample
absorbency level, and the method's precision and
accuracy.
Tea-bag Method
This method is the most conventional, fast, and suit-
able for limited amounts of samples (W0= 0.1-0.3 g)
[63,75-86]. The SAP sample is placed into a tea-bag
(acrylic/polyester gauze with fine meshes) and the
bag is dipped in an excess amount of water or saline
solution for one hour to reach the equilibrium
swelling. Then excess solution is removed by hang-
ing the bag until no liquid is dropped off. The tea bag
is weighed (W1) and the swelling capacity is calcu-
lated by eqn (1). The method's precision has been
determined to be around ±3.5%.
Se= (W1-W0)/W0(1)
Centrifuge Method
The centrifugal data are more accurate than the tea-
bag method and are occasionally reported in patents
and data sheets [2, 4, 6, 101]. Thus, 0.2 g (W1) of
SAP is placed into a bag (60×60 mm) made of non-
woven fabric. The bag is dipped in 100 mL of saline
solution for half an hour at room temperature. It is
taken out, and then excess solution is removed with a
centrifugal separator (3 min at 250 g). Then, weight
of bag (W2) is measured. The same stages are carried
out with an empty bag, and the weight of bag (W0) is
measured. The swelling capacity is calculated by the
eqn (2).
Se= (W2-W0-W1)/W1(2)
Since the inter-particle liquid is noticeably removed
by this method, the measured values are often more
accurate and lower than those obtained from the tea-
bag method values.
Sieve Method
SAP sample (W1, g) is poured into excess amount of
water or a solution and dispersed with mild magnet-
ic stirring to reach equilibrium swelling (0.5-3 h
depending on the sample particle size). The swollen
sample is filtered at desired time through weighed
100-mesh (150 μm) wire gauze (sieve). Then it is
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462 Iranian Polymer Journal / Volume 17 Number 6 (2008)
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dewatered carefully and rapidly using a piece of soft
open-cell polyurethane foam (by repeated rubbing
under the gauze bottom and squeezing the foam) until
the gel no longer slips from the sieve when it is held
vertical [65-71,95,96,100,102]. The quantitative fig-
ures of swelling can be calculated by eqn (3).
St= [(At+ B) – (B+ W1)]/ W1(3)
where, St= swelling at time t; g/g (gram of absorbed
fluid per gram of polymer sample)
At= weight of water-absorbed polymer at time t; g
B = weight of the sieve; g
This method, also called filtering and rubbing
method [7], needs a large amount of sample (1-2 g).
The method's standard deviation has been determined
to be around ±2.1% [102].
Absorbency Under Load (AUL)
The absorbency under load (AUL) data is usually
given in the patent literature and technical data sheets
by industrial SAP manufacturers [101]. When the
term AUL is used without specifying its swelling
media; it implies an uptake of 0.9% NaCl solution
while the testing sample is pressurized by some loads
(often specified to be pressures 0.3, 0.6, or 0.9 psi). A
typical AUL tester is a simple but finely made device
including a macro-porous sintered glass filter plate
(porosity # 0, d=80 mm, h=7 mm) placed in a Petri
dish (d=118 mm, h=12 mm). The weighed dried SAP
sample (0.90±0.01g) is uniformly placed on the sur-
face of polyester gauze located on the sintered glass.
A cylindrical solid load (Teflon, d=60 mm, variable
height) is put on the dry SAP particles while it can be
freely slipped in a glass cylinder (d=60 mm, h=50
mm). Desired load (applied pressure 0.3, 0.6, or 0.9
psi) is placed on the SAP sample (Figure 6).
Saline solution (0.9% NaCl) is then added when
the liquid level is equal the height of the sintered
glass filter. The whole set is covered to prevent sur-
face evaporation and probable change in the saline
concentration. After 60 min, the swollen particles are
weighed again, and AUL is calculated using the fol-
lowing equation [73]:
(4)
Figure 6. A typical AUL tester picture (a) and various parts
(b) [8].
Where, W1and W2denote the weight of dry and
swollen SAP, respectively.
The AUL is taken as a measure of the swollen gel
strength of SAP materials [73,103].
Wicking Capacity and Rate
An originating simple test has been suggested by pio-
neering researchers Fanta and Doane [104] to quanti-
fy the wicking capacity (WC) of SAP materials with
conventional physical appearance, i.e., sugar-like
particle.
Thus, SAP sample (W1= 0.050±0.0005 g) is
added to a folded (fluted) filter paper cone prepared
from an accurately tared circle of 9 cm Whatman 54
paper. The cone was lightly tapped to settle the sam-
ple into the tip, and the tip of the cone is then held for
60 s in a 9 cm Petri dish containing 25 mL of water.
Water wicks up the entire length of the paper in a
minute. Excess water is then allowed to drain from
the paper by contacting the tip for 60 s with a circle
of dry filter paper on a square of absorbent towel. The
Iranian Polymer Journal / Volume 17 Number 6 (2008) 463
Superabsorbent Polymer Materials: A Review
Zohuriaan-Mehr MJ et al.
1
12
)/( W
WW
ggAUL
−
=
(a)
(b)
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weight of wet paper plus swollen polymer is deter-
mined (A), and the absorbency of the sample in g/g is
then calculated after correcting for the weight of dry
paper and the amount of water absorbed under iden-
tical conditions by the paper alone in the absence of
sample (eqn 5). Each test is preferred to be repeated
3-5 times and the results are averaged.
WC = (A-B-W1)/W1(5)
where, B is wet paper without polymer.
Assuming a monotonous absorption for the dura-
tion of 60 s, an estimation of wicking rate (g/g.s) of
the SAP may be obtained by dividing the WC value
by 60.
Swelling Rate
Vortex Method
The vortex method, the most rapid and simple way to
evaluate the SAP swelling rate, is often employed in
R&D and technical laboratories [8]. Water or saline
solution (50.0 g) is poured in a 100 mL beaker and its
temperature is adjusted at 30ºC. It is stirred at 600
rpm using a magnetic stirrer (stirrer bar length 400
mm). Superabsorbent sample (mesh 50-60, W0=
0.50-2.0 g) is added and a stopwatch is started. The
time elapsing from the addition of SAP into the fluid
to the disappearance of vortex (tvd, sec) is measured.
This swelling rate (SR, g/g.s) is calculated by eqn (6).
SR = (50/W0)/tvd (6)
Swelling-time Profile
The profiles of swelling vs. time is obtained via sep-
arating swelling measurements of sample absorbed
desired fluid at consecutive time intervals. Either,
tea-bag, centrifuge, or sieve methods can be used for
the measurements depending on the amount of the
available sample and the desired precision. Typically,
several 2 L Erlenmeyer flasks containing distilled
water or desired solution are labeled and SAP sample
(e.g. 1.0 g, 50-60 mesh) is poured into each flask and
is dispersed with mild stirring. At consecutive time
intervals (e.g., 15, 30, 45, 60, 90, 120, 180, 300, 600,
1800 s), the absorbency of the sample is measured by
sieve method [7]. A typical profile is shown in
Figure 7.
Figure 7. Representative curve for swelling kinetics of a
hybrid SAP sample in distilled water [75].
The swelling kinetics of the SAPs can be studied
by means of a Voigt-based viscoelastic model [105]:
St= Se(1-e-t/r) (7)
where Stis the degree of swelling (g/g) at any
moment, Se, the equilibrium swelling, is swelling at
infinite time or maximum water-holding capacity, t is
the swelling time (s), and r, the rate parameter (s), is
the time required to reach 0.63 of the equilibrium
swelling.
The swelling values obtained from the above
measurements are fitted into eqn (7), using a suitable
software like Easyplot, to find the values of the rate
parameters. According to Kabiri et al. [63], swelling
rate (SR, g/g.s) may be defined as follows (eqn (8)):
SR= St-mr/tmr (8)
Where, St-mr stands for swelling at the time related to
minimum rate parameter tmr (s) obtained from com-
parable SAP samples or SAPs prepared from a set of
similar experiments (Figure 7). Actually, tmr is relat-
ed to the point where departure from maximum
swelling rate takes place.
Most recently, open circuit potential measurement
was reported to be used for tracing the swelling kinet-
ics of super absorbents [106].
Swollen Gel Strength
The mechanical strength or modulus of swollen SAPs
464 Iranian Polymer Journal / Volume 17 Number 6 (2008)
Superabsorbent Polymer Materials: A Review Zohuriaan-Mehr MJ et al.
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is important from a practical viewpoint. The authors
have recently proposed rotational rheometry to quan-
tify the swollen gel strength of SAP materials with
conventional shape, i.e., sugar-like particles [73].
Thus, the rheological measurements are performed
using parallel plate geometry (plate diameter of 25
mm, gap of 3 mm) at 25°C. The strain used are cho-
sen to be in the linear viscoelastic (LVE) range, where
the G' and G" are independent of the strain amplitude.
After a strain sweep test, the test conditions for the
frequency sweeps are selected to ensure that the test is
really carried out in the LVE range.
The G'(γ) function is conventionally taken for the
analysis because G' curve almost falls before another
curve (i.e., G). For determination of LVE, approxi-
mately 100-150 mg of dried SAP with average parti-
cle sizes of 180 μm is dispersed in 200 mL of distilled
water for 30 min to reach maximum swelling. The
excess water is removed and the swollen gel particles
are then placed on the parallel plate of rheometer and
the rheological properties are evaluated. The effect of
shear strain on the measured G' and Gat constant fre-
quency (ω= 1 rad/s) is evaluated. Below 0.2% defor-
mation, G'(ω) is often independent of the applied
strain i.e., LVE behaviour [107]. Therefore, G' is
obtained at constant strain, over a range of frequency.
A typical SAP by this time absorbs saline solution
under 0.3-0.9 psi, for instance, it shows an overall
storage modulus above 1000 Pa at 25ºC. Most recent-
ly, Ramazani et al. [103] have explored linear rela-
tions that are active between the AUL and G' data
over the rubber-elastic plateau.
Soluble Fraction
The soluble fraction (sol) is sum of all water-soluble
species including non-crosslinked oligomers, HPA
and non-reacted starting materials such as residual
monomers. The sol content is simply measured by
extraction of SAP sample in distilled water (this is
why the sol is frequently referred to "extractable").
Therefore, a certain amount of the SAP sample (e.g.,
0.10 g) is poured into excess amount of water and dis-
persed with mild magnetic stirring to reach equilibri-
um swelling (0.5-3 h depending on the sample parti-
cle size). The swollen sample is filtered and oven-
dried. The sample weight loss easily results in the sol-
uble fraction [8]. For a synthesized SAP, the gel con-
tent can also be obtained by the simple eqn (9). The
gel content may be taken as an actual yield of the
cross-linking polymerization.
Sol(%) + Gel(%) = 100 (9)
UV spectrometry technique has been also reported for
the determination of SAP sol content [108].
Residual Monomer
In SAP materials, particularly hygienic SAPs where
the residual monomer content is of very significant
importance, the allowed safe level of the residual
acrylic acid has dropped from over 1000 ppm to less
than 300 ppm throughout the past two decades. High
performance liquid chromatography (HPLC) is often
taken as a preferred method to quantify the residual
monomer. In this method, orthophosphoric acid solu-
tion is usually used as an extractant. During the
extraction, the total residual monomer in form of
either acid or salt are removed from the hydrogel net-
work to be measured in the next step. The acrylic salt
is converted to acrylic acid at the acidic pH of both the
extracting and the eluting media, i.e., mobile phase
(pH<3) [74].
The separation is usually performed in isocratic
mode at a 1.8 mL/min flow rate and ambient temper-
ature on an analytical column (e.g., 250 ×4.6 mm, 5
μm). The mobile phase is an aqueous 0.01%
orthophosphoric acid [109]. The UV-vis absorbance
over the 190-400 nm range is registered and the wave-
length used for quantification is 200 nm.
The HPLC technique can also be employed for
quantifying the residual AM in SAPs [110].
Ionic Sensitivity
To achieve a comparative measure of sensitivity of
the SAP materials towards the kind of aqueous fluid,
a dimensionless swelling factor, f, is defined as fol-
lows (eqn 10) [85]:
f = 1-(Absorption in a given fluid/Absorption in
distilled water) (10)
Larger fvalue means the higher absorbency-loss of
the sample swollen in salt solutions. Therefore, SAPs
with lower fare usually preferred. Negative values of
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Zohuriaan-Mehr MJ et al.
Iranian Polymer Journal / Volume 17 Number 6 (2008) 465
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freveal that the absorbency is not decreased, but, it is
increased in salt solutions. The SAP hydrogels with
betaine structures exhibit such surprising behaviour
[63].
USES AND APPLIED RESEARCH WORKS
Hygienic and Bio-related Areas
The most volume of SAP produced all over the world
is used in disposable diapers. Therefore, most
research works have been focused on hygienic grades
which are usually used with fluff in diapers. As shown
in Figure 8, the AUL has increased to about 30 g/g
while free-absorbency has dropped to around 50 g
(saline)/g (polymer) over past two decades. Because
of the market requests for a thinner diaper, more SAP
and less fluff is being incorporated into the diapers.
This approach limits the maximum amount of SAP in
a diaper to about 10 g/piece, and this is required for
the AUL to be enhanced. A target for AUL of 35-40 is
achievable using current technology, but it is desir-
able to have AUL as high as 45-50 g/g to obtain a
much thinner diaper [6].
In addition to the absorbency parameters, the level
of residual acrylic acid (RM, ppm) has dropped over
1000 to less than 30 ppm in 2000s. The extractable
fraction (sol content) of the SAP has also decreased
from ~13 to around 4% over time (Figure 8).
Figure 8. Trends of improvements of hygienic SAP materi-
al characteristics, i.e., free absorbency in saline, saline-
absorbency under load (AUL), residual monomer (RM), and
soluble fraction (sol) [6].
The efforts of manufacturers have been stressed on
improving the production and engineering SAPs with
higher performance, i.e., higher AUL, lower levels of
RM, sol fraction and fine particles (<50 μm). Some
enzymes and additives may be incorporated to pre-
vent infection and unpleasant smell. Other hygienic
applications comprise more or less similar require-
ments of the diaper uses.
Recently, a new generation of hygienic superab-
sorbent named Safe and Natural Absorbent Polymer
(SNAP) has been introduced to the market [111].
SNAPs are totally natural with no residual monomer
therefore they are rapidly biodegraded in the environ-
ment. However, they possess lower absorbency and
higher price than the full-synthetic counterparts.
Most recently, using superabsorbent fibre and vis-
cous fibre, a method of preparing absorbent core for
ultra-thin high-absorbent sanitary napkins has been
presented [112].
SAPs are one of the members of the family of
smart hydrogels, hence they can be potentially
employed in separation science and technology, par-
ticularly bioseparation. Due to large changes in the
swelling ratio, the hydrogels have been used widely in
the separation of various molecules including proteins
[113]. In medicine, SAPs may be used for elimination
of body water during surgery, e.g., treatment of edema
[24].
In the field of pharmaceutics, some superab-
sorbents called super-porous hydrogels (SPHs)
invented by Kinam Park et al. [114] have also been
developed for gastric retention applications. They are
different from SAPs since SPHs swell fast, within
minutes, to the equilibrium swollen state regardless of
their size. The very fast swelling property is based on
water absorption through open porous structure by
capillary force. SPHs have been designed for con-
trolled delivery of drugs to stomach or intestine. The
poor mechanical strength of SPHs was overcome by
developing the second-generation SPH composites
and the third-generation SPH hybrids [115].
Agricultural Areas
The presence of water in soil is essential to vegeta-
tion. Liquid water ensures the feeding of plants with
nutritive elements, which makes it possible for the
plants to obtain a better growth rate. It seems to be
Superabsorbent Polymer Materials: A Review Zohuriaan-Mehr MJ et al.
466 Iranian Polymer Journal / Volume 17 Number 6 (2008)
www.SID.ir
Archive of SID
interesting to exploit the existing water potential by
reducing the losses of water and also ensuring better
living conditions for vegetation. Taking into account
the water imbibing characteristics of SAP materials,
the possibilities of its application in the agricultural
field has increasingly been investigated to alleviate
certain agricultural problems.
SAPs have been successfully used as soil amend-
ments in the horticulture industry to improve the
physical properties of soil in view of increasing their
water-holding capacity and/or nutrient retention of
sandy soils to be comparable to silty clay or loam.
SAP hydrogels potentially influence soil permeabili-
ty, density, structure, texture, evaporation, and infil-
tration rates of water through the soils. Particularly,
the hydrogels reduce irrigation frequency and com-
paction tendency, stop erosion and water run off, and
increase the soil aeration and microbial activity [116].
In arid areas, the use of SAP in the sandy soil
(macroporous medium), to increase its water-holding
capacity seems to be one of the most significant
means to improve the quality of plants [117]. The
SAP particles may be taken as "miniature water reser-
voirs" in soil. Water will be removed from these reser-
voirs upon the root demand through osmotic pressure
difference.
The hydrogels also act as a controlled release sys-
tem by favouring the uptake of some nutrient ele-
ments, holding them tightly, and delaying their disso-
lution. Consequently, the plant can still access some
of the fertilizers, resulting in improved growth and
performance rates [118-121].
On the other hand, SAPs in agriculture can be used
as retaining materials in the form of seed additives (to
aid in germination and seedling establishment), seed
coatings, root dips, and for immobilizing plant growth
regulator or protecting agents for controlled release
[116].
The SAPs used in the agriculture are polyelec-
trolyte gels often composed of acrylamide (AM), AA,
and potassium acrylate. Therefore, they swell much
less in the presence of monovalent salt and can col-
lapse in the presence of multivalent ions [119] (Figure
9). These ions can be naturally provided in the soil or
introduced by the use of fertilizers and pesticides
[118]. In saline media, however, the uptake capacity
is yet as high as 30-60 g/g (i.e., 3000-6000%).
Figure 9. Representative absorbency behaviours of typical
samples of agricultural SAPs (S1 and S2) swollen in deion-
ized water and irrigative water with various salinities and
electrical conductivities (ECs) [119].
There are numerous examples for the SAP assess-
ment in the agricultural field, e.g., Abedi-Koupai et al.
have experienced the SAP effect on both soil water
retention and on plant indices [122]. They have eval-
uated the effect of superabsorbents on water retention
and potentialities of three types of soils to confirm
certain positive effects of the SAP on water retention
of the soils.
A distinctive instance for the agricultural applica-
tion of SAP has been recently practiced. Thus, the
SAP effect on the growth indices of an ornamental
plant (Cupressus arizonica) under reduced irrigation
regimes in the field and on the soil water retention
curve in a laboratory was investigated [123]. There
Figure 10. Number of days to reach PWP due to applica-
tion of 4 and 6 g/kg Superab A200 [123].
Superabsorbent Polymer Materials: A Review
Zohuriaan-Mehr MJ et al.
Iranian Polymer Journal / Volume 17 Number 6 (2008) 467
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Figure 11. Effects of various amounts of SAP on the sport
turf characteristics: (a) colour and wilting, and (b) coverage
and density based on the NTEP standard [124].
were marked responses in the number of days to per-
manent wilting point (PWP) as a result of polymer
application and increases in polymer concentration
(Figure 10). Samples containing 6 g/kg polymer had
the maximum period to reach PWP (22 days) com-
pared to the control samples (12 days).
Additional interesting instance is a research
recently conducted on the effect of SAP materials on
the characteristics of sport turf. Turf is of significant
importance as an inseparable part of all kinds of green
spaces. Irrigation water consumption of turf is very
huge, especially in the hot and dry climates due to sur-
face evaporation and infiltration. In the research con-
ducted by Mousavinia et al. [124] encouraging results
were obtained. Briefly, as exhibited in Figure 11,
based on the NTEP standard (The National Turfgrass
Evaluation Program), the turf density, colour intensi-
ty and coverage percentage is increased, while its
wilting level is substantially decreased when SAP is
used [8].
The effect of levels of SAP and different drought
stress levels on growth and yield of olive plants [125,
126] and forage corn [126] have been investigated.
Effect of SAP on the efficiency of clay mulch and bio-
logical fixation of sand dunes has been also studied
[127]. Asadzadeh et al. have investigated the food ele-
ment-enriched SAP in low-water treated hydroponic
substrates [128]. SAP materials have shown excellent
influence on decreasing damages (up to 30%) in the
productive process of the olive sapling [129].
Meanwhile, non-cross-linked anionic polyacry-
lamides (PAM, containing <0.05% AM) having very
high molecular weight (12–15×106g.mol-1), have
also been used to reduce irrigation-induced erosion
and enhance infiltration. Its soil stabilizing and floc-
culating properties improve runoff water quality by
reducing sediments, N-dissolved reactive phosphorus
(DRP) and total P, chemical oxygen demand (COD),
pesticides, weed seeds, and microorganisms in runoff.
In a series of field studies, PAM eliminated 80-99%
(94% avg.) of sediment in runoff from furrow irriga-
tion, with a 15-50% infiltration increase compared to
controls on medium to fine-textured soils [130].
Other Areas
Various applications and active fields of applied
research works on SAPs are well-reviewed by Po [5].
In addition to the hygienic and agricultural areas, SAP
materials are (or can potentially be) used in many
other fields, e.g, artificial snow, ornamental
(coloured) products, entertaining/educational toys and
tools, building internal decoration, fire extinguish-
ing/retarding gels, cryogenic gels, food/meat packag-
ing, etc. [5]. Concrete strengthening [131], reduction
of the ground-resistance in the electrical industry
[132] and controlled release of pesticides and agro-
chemicals [119-121, 133-141], are other instances for
the SAP applied research. In the field of food process-
ing, for instance, yogurt dewatering was recently
investigated using permeable membrane and acrylic
SAP [142].
Superabsorbent Polymer Materials: A Review Zohuriaan-Mehr MJ et al.
468 Iranian Polymer Journal / Volume 17 Number 6 (2008)
(a)
(b)
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Most recently, photochromic SAPs with excellent
water absorption (2800 g/g) were synthesized using
an azobenzene surface cross-linker [143]. Under irra-
diation at 350 nm, water expulsion from the SAP is
observed. The SAP preparation and characterization
has been investigated in details [143,144]. These
photo-active hydrogels may be candidates to design
new photochemically controlled systems for pharma-
ceutical, biomedical or optical switching applications.
A surprising application of SAP materials was
examined by Peter Cordani for modifying the weath-
er condition [145]. Thus, a hurricane was seeded with
almost 30,000 lbs of a SAP by means of a transport
plane flying through the leading edge of the storm.
Within 20 seconds, the SAP obtained over 70% of its
absorption capacity or nearly 300 times its weight.
The winds of the storm would continue to disperse the
materials causing a form of internal flocculation dis-
rupting the feeding nature of the storm. When seeded
close to land, the storm did not have sufficient time to
reform to its previous destructive strength.
SAFETY AND ENVIRONMENTAL ISSUES
Alike each man-made material, some common mat-
ters are also primarily questioned about the SAP mate-
rials: (a) the toxicity and safety, and (b) the environ-
mental fate.
SAP materials cannot return to their starting
monomers, i.e., they are scientifically irreversible to
toxic initiating materials. Here, like so many poly-
mers, the starting toxic monomers are converted
chemically to totally non-toxic product via polymer-
ization reaction [2-6]. SAPs are organic materials with
well-known general structure. For instance, the agri-
cultural SAP with the name of “cross-linked acry-
lamide/potassium acrylate copolymer” has been
recorded in the most valid data centre of chemicals,
i.e. the Chemical Abstracts, with CAS No. 31212-13-
2. In the material safety data sheet (MSDS) of the
superabsorbent manufacturers, they are called as
“Safe and Non-toxic Material” [146-149].
The conventional SAP materials are neutral and
inert. They are moderately bio-degraded in the soil by
the ionic and microbial media to convert finally to
water, carbon dioxide and organic matter [146-151].
Therefore, SAPs do not contaminate the soil and envi-
ronment. They do not exhibit systemic toxicity (oral
LD50 for rate ~5000 mg/kg). In addition, their safety
in the soil has been approved by the Agriculture
Ministry of France (APV No 8410030) [146].
Research has shown little or no consistent adverse
effect on soil microbial populations [152]. The envi-
ronmental fate of SAPs and their microbial degrada-
tion was investigated by many researchers [152-157].
The researchers at the University of California, Los
Angles (UCLA) found that no toxic species were
remained in soil after several-year SAP consuming
[158].
CONCLUSION AND OUTLOOK
During more than one decade research on SAP mate-
rials, we have realized that everybody is impressed by
observing the surprising behaviour of swelling of SAP
particles poured in a glass of water. It is really fantas-
tic, however, beyond the “glass-of-water presenta-
tion”, SAPs have been applicable increasingly in
many uses ranged from personal care products to agri-
culture.
SAPs are commonly made from petrochemical
starting materials, i.e., acrylic monomers. However,
bio-modified or natural-based SAPs are being inter-
ested due to the world steadfast decision towards the
environmental protection. The biopolymer-contained
SAPs, however, possess typically higher cost and less
performance than their fully synthetic counterparts.
Besides various applications, the most volume of SAP
world production (106tons/year) is yet consumed in
hygienic uses, i.e., disposable diapers (as baby or
adult diapers, feminine napkins, etc.).
SAPs have created a very attractive area in the
viewpoint of super-swelling behaviour, chemistry, and
designing the variety of final applications. When
working in this field, we always deal with water,
aqueous media and bio-related systems. Thus, we
increasingly walk in a green area becoming greener
via replacing the synthetics with the bio-based mate-
rials, e.g., polysaccharides and polypeptides. This,
however, is a long-term perspective. More or less, the
acrylic kingdom will extend its domination in the
future markets.
Superabsorbent Polymer Materials: A Review
Zohuriaan-Mehr MJ et al.
Iranian Polymer Journal / Volume 17 Number 6 (2008) 469
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Archive of SID
In spite of the SAP attractiveness, there are some
drawbacks seeming to be worth noting. First of all,
the researchers do not use a unified standard for
swelling measurement in their works, a problem that
makes the comparison of hydrogels more or less
impossible.
Another drawback in this field in general is an
absence of sol fraction data in nearly all reports
involving the SAP synthesis. Considering this fact
that hygiene occupies the largest market for SAP and
diapers making up 83% of the worldwide market
applications for superabsorbing hydrogels, the neces-
sity of producing new kind of SAPs with high gel
content (minimum extractable or soluble fraction)
seems more tenable. Thus, there is now a need to
develop new hydrogels with minimized sol fraction
and residual monomer; characteristics that usually are
neglected by the academic researchers. Another point
to note is that, unlike the SAPs manufacturers, the
academic researchers do not usually report saline-
absorbency under load (AUL) values in the case of
newly synthesized hydrogels. It should be empha-
sized that load-free absorbency (free-swelling) that
are usually reported in research articles, is not an
important factor from the practical or industrial point
of view. Thus, measurement and reporting the men-
tioned practical data will be extremely beneficial.
Finally, considering high-cost and increasing
prices of crude oil, the necessity of preparing natural-
based SAPs seems more obvious. This paves the way
to further developments in this area in the mid and far
future ahead.
REFERENCES
1. Gel, Wikipedia, The free encyclopedia, http://
en.wikipedia.org/wiki/gel, available in 28 May
2008.
2. Buchholz FL, Graham AT, Modern
Superabsorbent Polymer Technology, Wiley-
VCH, New York, Ch 1-7, 1998.
3. Brannon-Peppas L, Harland RS, Absorbent
Polymer Technology, Elsevier, Amsterdam, Ch 1-
4, 1990.
4. Andrade JD, Hydrogels for medical and related
applications, ACS Symp. Series, 31, American
Chemical Society, Washington DC, 1, 1976.
5. Po R, Water-absorbent polymers: A patent survey,
J Macromol. Sci-Rev Macromol Chem Phys, C34,
607-662, 1994.
6. Buchholz FL, Peppas NA, Superabsorbent
Polymers Science and Technology, ACS
Symposium Series, 573, American Chemical soci-
ety, Washington, DC, Ch 2, 7, 8, 9, 1994.
7. Omidian H, Zohuriaan-Mehr MJ, Kabiri K, Shah
K, Polymer chemistry attractiveness: Synthesis
and swelling studies of gluttonous hydrogels in the
advanced academic laboratory, J Polym Mater, 21,
281-292, 2004.
8. Zohuriaan-Mehr MJ, Super-Absorbents (in
Persian), Iran Polymer Society, Tehran, 2-4, 2006.
9. Superabsorbent hydrogels, Website of the leading
Iranian manufacturer of superabsorbent polymers;
Rahab Resin Co., Ltd.; www.rahabresin.com,
available in 10 September 2007.
10. Dayal U, Mehta SK, Choudhari MS, Jain R,
Synthesis of acrylic superabsorbents, J Macromol
Sci-Rev Macromol Chem Phys, C39, 507-525,
1999.
11. Superabsorbents, Website of the European
Disposables and Nonwovens Association
(EDANA); www.edana.org, available in 28 May
2008.
12. Mathur AM, Moorjani SK, Scranton AB,
Methods for synthesis of hydrogel networks: A
review, J Macromol Sci-Rev Macromol Chem
Phys, C36, 405-430, 1996.
13. Kulicke W-M, Nottelmann H, Structure and
swelling of some synthetic, semisynthetic, and
biopolymer hydrogels, Adv Chem Ser, 223, 15-44,
1989.
14. Kazanskii KS, Dubrovskii SA, Chemistry and
physics of “agricultural” hydrogels, Adv Polym
Sci, 104, 97-140, 1992.
15. Bouranis DL, Theodoropoulos AG, Drossopoulos
JB, Designing synthetic polymers as soil condi-
tioners, Commun Soil Sci Plant Anal, 26, 1455-
1480, 1995.
16. Dutkiewicz JK, Superabsorbent materials from
shellfish waste-A review, J Biomed Mater Res
(Appl Biomater), 63, 373-381, 2002.
17. Ichikawa T, Nakajima T, Superabsorptive
Polymers (from natural polysaceharides and
Superabsorbent Polymer Materials: A Review Zohuriaan-Mehr MJ et al.
470 Iranian Polymer Journal / Volume 17 Number 6 (2008)
www.SID.ir
Archive of SID
polypeptides), In: Polymeric Materials
Encyclopedia, Salamone (Ed), CRC, Boca Raton
(Florida), 8051-8059, 1996.
18. Athawale VD, Lele V, Recent trends in hydrogels
based on starch-graft-acrylic acid: A review,
Starch/Starke, 3, 7-13, 2001.
19. Buchholz FL, Recent advances in superabsorbent
polyacrylates, Trend Polym Sci, 2, 277-281, 1994.
20. Chin Y-R, Al-Dayel A, Acrylic acid based super-
absorbent polymer, Process Economics Program
Review No. 85-1-2, Stanford Research Institute,
SRI International, Dec. 1985.
21. Chatterjee PK, Gupta BS (Eds), Absorbent
Technology, Elsevier, Amsterdam, ch 1-2, 2002.
22. Wampler FM, Formation of diacrylic acid during
acrylic acid storage, Plant/Operation Prog, 7(3),
183-189, 1988.
23. Zohuriaan-Mehr MJ, Pourjavadi A, Kurdtabar M,
Salimi H, Polysaccharide-based superabsorbent
hydrogels: A Review, Carbohydr Polym, submit-
ted, 2008.
24. Sannino A., Esposito A., De Rosa A., Cozzolino
A., Ambrosio L., Nicolais L., Biomedical applica-
tion of a superabsorbent hydrogel for body water
elimination in the treatment of edemas, J Biomed
Mater Res, 67A, 1016-1024, 2003.
25. Demitri C, Delsole R, Scalera F, Sannino A,
Vasapollo G, Maffezzoli A, Nicolais L, Novel
superabsorbent cellulose-based hydrogels cross-
linked with citric acid, J Appl Polym Sci, 2008,
(in press).
26. Hwang D-C, Damodaran S. Equilibrium swelling
properties of a novel ethylenediamine tetraacetic
dianhydride (EDTAD)-modified soy protein
hydrogel. J Appl Polym Sci, 62, 1285-1293, 1996.
27. Hwang D-C, Damodaran S, Chemical modifica-
tion strategies for synthesis of protein-based
hydrogelm, J Agric Food Chem, 44, 751-758,
1996.
28. Hwang D-C, Damodaran S, Synthesis and proper-
ties of Fish protein-based hydrogel. J Am Oil
Chem Soc, 74, 1165-1171, 1997.
29. Rathna GVN, Damodaran S, Swelling behavior of
protein-based superabsorbent hydrogels treated
with ethanol, J Appl Polym Sci, 81, 2190-2196,
2001.
30. Rathna GVN, Damodaran S, Effect of nonprotein
polymers on water-uptake properties of fish pro-
tein-based hydrogel, J Appl Polym Sci, 85, 45-51,
2002.
31. Hwang D-C, Damodaran S, Metal-chelating prop-
erties and biodegradability of an ethylenediamine
tetraacetic acid dianhydride modified soy protein
hydrogel, J Appl Polym Sci, 64, 891-901, 1997.
32. Damodaran S, Hwang D-C, Carboxyl-modified
superabsorbent protein hydrogel, US Patents
5,847,089, 1998.
33. Stern T, Lamas MC, Benita S, Design and charac-
terization of protein-based microcapsules as a
novel catamenial absorbent system, Int J Pharm,
242, 185-190, 2002.
34. Damodaran S, Carboxyl-modified superabsorbent
protein hydrogel, US Patents 6,310,105 B1, 2001.
35. Damodaran S, Protein-polysaccharide hybrid
hydrogels, US Patents 6,821,331 B2, 2004.
36. Chatterji PR, Kaur H, Interpenetrating hydrogel
network. 3. Properties of the gelatin-sodium car-
boxymethylcellulose system, Polymer, 33, 2388-
2391, 1992.
37. Yao KD, Yin YJ, Xu MX, Wang YF, Investigation
of pH-sensitive drug delivery system of chi-
tosan/gelatin hybrid polymer network, Polym Int,
38, 77-82, 1995.
38. Fang Y-E, Cheng Q, Lu X-B, Kinetics of in-vitro
release from chitosan/gelatin hybrid membranes,
J Appl Polym Sci, 68, 1751-1758, 1998.
39. Yao KD, Liu WG, Lin Z, Qiu XH, In situ atomic
force microscopy measurement of the dynamic
variation in the elastic modulus of swollen chi-
tosan/gelatin hybrid polymer network gels in
media of different pH, Polym Int, 48, 794-798,
1999.
40. Chen L, Du Y, Huang R. Novel pH, ion sensitive
polyampholyte gels based on carboxymethyl chi-
tosan and gelatin, Polym Int, 52, 56-61, 2003.
41. Pourjavadi A, Sadeghi M, Mahmodi Hashemi M,
Hosseinzadeh H, Synthesis and absorbency of
gelatin-graft-poly(sodium acrylate-co-acry-
lamide) superabsorbent hydrogel with salt- and
pH-responsiveness properties. e-Polymers, No.
057:1-15 2006 (http://www.e-polymers.org).
42. Pourjavadi A, Kurdtabar M, Mahdavinia GR,
Hosseinzadeh H, Synthesis and super-swelling
behavior of a novel protein-based superabsorbent
Superabsorbent Polymer Materials: A Review
Zohuriaan-Mehr MJ et al.
Iranian Polymer Journal / Volume 17 Number 6 (2008) 471
www.SID.ir
Archive of SID
hydrogel, Polym Bull, 57, 813-824, 2006.
43. Pourjavadi A, Kurdtabar M, Collagen-based
highly porous hydrogel without any porogen:
synthesis and characteristics, Eur Polym J, 43,
877-889, 2007.
44. Pourjavadi A., Salimi H., Kurdtabar M,
Hydrolyzed collagen-based hydrogel with salt
and pH-responsiveness properties, J Appl Polym
Sci, 106, 2371-2379, 2007.
45. Pourjavadi A, Kurdtabar M, Ghasamzadeh H,
Salt- and pH-resisting collagen-based highly
porous hydrogel, Polym J, 40, 94-103, 2008.
46. Seidi Ghalehgah F, Optimization of novel gela-
tin-based superabsorbent hydrogels using
Taguchi method and investigation of their
swelling behavior in various conditions, M.Sc.
dissertation, Chem Dept, Sharif Univ Tech, 2006.
47. Bagheri Marandi G, Biranvand F, Babapour M,
Esfandiari K, Sadeh S, Kurdtabar M. Synthesis
and swelling behavior of hydrolyzed collagen-g-
poly(methacrylic acid-co-acrylamide) hydrogel.
J Appl Polym Sci, 2007 (submitted).
48. Pourjavadi A, Salimi H, A new protein-based
hydrogel with superabsorbing properties: Effect
of monomer ratio on swelling behavior and kinet-
ics, Ind Eng Chem Res, 2008, submitted.
49. Chang CJ, Swift G. Poly(aspartic acid) hydrogel,
J Macromol Sci-Pure Appl Chem, A36, 963-970,
1999.
50. Min SK, Kim J-H, Chung DJ, Swelling behavior
of biodegradable crosslinked gel based on
poly(aspartic acid) and PEG-diepoxide, Korea
Polym J Macromol Res, 9, 143-149, 2001.
51.Yang J, Fang L, Tan T, Synthesis and characteri-
zation of superabsorbent hydrogels composites
based on polysuccinimide, J Appl Polym Sci,
102, 550-557, 2006.
52. Kunioka M, Choi HJ, Hydrolytic degradation
and mechanical properties of hydrogels prepared
from microbial poly(amino acid)s, Polym
Degrad Stab, 59, 33-37, 1998.
53. Choi HJ, Yang R, Kunioka M, Synthesis and
characterization of pH-sensitive and biodegrad-
able hydrogels prepared by γirradiation using
microbial poly(γ-glutamic acid) and poly(ε-
lysine), J Appl Polym Sci,58, 807-814, 1995.
54. Kunioka M, Biodegradable water absorbent syn-
thesized from bacterial poly(amino acid)s,
Macromol Biosci, 4, 324-329, 2004.
55. Gonzales D, Fan K, Sevoian M, Synthesis and
swelling characterizations of a poly(gamma-glu-
tamic acid) hydrogel, J Polym Sci A Polym
Chem, 34, 2019-2027, 1996.
56. Kunioka M, Furusawa K, Poly(γ-glutamic acid)
hydrogel prepared from microbial poly(γ-glutam-
ic acid) and alkanediamine with water-soluble
carbodiimide, J Appl Polym Sci, 65, 1889-1896,
1997.
57. Matsusaki M, Yoshida H, Akashi M, The con-
struction of 3D-engineered tissues composed of
cells and extracellular matrices by hydrogel tem-
plate approach, Biomaterials, 28, 2729-2737,
2007.
58. Shimokuri T, Kaneko T, Akashi M, Specific ther-
mosensitive volume change of biopolymer gels
derived from propylated poly(γ-glutamate)s, J
Polym Sci A Polym Chem, 42, 4492-4501, 2004.
59. Matsusaki M, Serizawa T, Kishida A, Akashi M,
Novel functional biodegradable polymer. III. The
construction of poly(γ-glutamic acid)-sulfonate
hydrogel with fibroblast growth factor-2 activity,
J Biomed Mater Res, 73A, 485-491, 2005.
60. Markland P, Zhang Y, Amidon GL, Yang VC, A
pH- and ionic strength-responsive polypeptide
hydrogel: Synthesis, characterization and prelim-
inary protein release studies, J Biomed Mater
Res, 47, 595-602, 1999.
61. Yang Z, Zhang Y, Markland P, Yang VC,
Poly(glutamic acid) poly(ethylene glycol) hydro-
gels prepared by photoinduced polymerization:
Synthesis, characterization, and preliminary
release studies of protein drugs, J Biomed Mater
Res, 62, 14-21, 2002.
62. Kunioka M, Choi HJ, Properties of biodegrad-
able hydrogels prepared by irradiation of micro-
bial poly(ε-lysine) aqueous solutions, J Appl
Polym Sci, 58, 801-806, 1995.
63. Kabiri K, Faraji-Dana S, Zohuriaan-Mehr MJ,
Novel sulfobetaine-sulfonic acid-contained
superswelling hydrogels, Polym Adv Technol, 16,
659-666, 2005.
64. Kabiri K, Zohuriaan-Mehr MJ, Porous superab-
sorbent hydrogel composites: Synthesis, mor-
phology and swelling rate, Macromol Mater Eng,
Superabsorbent Polymer Materials: A Review Zohuriaan-Mehr MJ et al.
472 Iranian Polymer Journal / Volume 17 Number 6 (2008)
www.SID.ir
Archive of SID
289, 653-661 2004.
65. Kabiri K, Zohuriaan-Mehr MJ, Superabsorbent
hydrogels from concentrated solution terpolymer-
ization, Iran Polym J, 13, 423-430, 2004.
66. Omidian, H; Hashemi, SA, Sammes PG, Meldrum
I, Modified acrylic-based superabsorbent poly-
mers. Effect of temperature and initiator concen-
tration, Polymer, 39, 3459-3466, 1998.
67. Kabiri K, Omidian H, Hashemi SA, Zohuriaan-
Mehr MJ, Concise synthesis of fast-swelling
superabsorbent hydrogels: Effect of initiator con-
centration on porosity and absorption rate, J
Polym Mater, 20, 17-22, 2003.
68.Kabiri K, Omidian H, Hashemi SA, Zohuriaan-
Mehr MJ, Synthesis of fast-swelling superab-
sorbent hydrogels: Effect of crosslinker type and
concentration on porosity and absorption rate, Eur
Polym J, 39, 1341-1348, 2003.
69. Kabiri K, Zohuriaan-Mehr MJ, Superabsorbent
hydrogel composites, Polym Adv Technol, 14,
438-444, 2003.
70. Kabiri K, Omidian H, Zohuriaan-Mehr MJ, Novel
approach to highly porous huperabsorbent hydro-
gels: Synergistic effect of porogens on porosity
and swelling rate, Polym Int, 52, 1158-1164, 2003.
71. Omidian H, Zohuriaan-Mehr MJ, DSC studies on
synthesis of superabsorbent hydrogels, Polymer,
43, 269-277, 2002.
72. Kabiri K, Mirzadeh H, Zohuriaan-Mehr MJ,
Undesired effects of heating on hydrogels, J Appl
Polym Sci, 2008, accepted.
73. Ramazani-Harandi MJ, Zohuriaan-Mehr MJ,
Ershad-Langroudi A, Yousefi AA, Kabiri K,
Rheological determination of the swollen gel
strength of the superabsorbent polymer hydrogels,
Polym Test, 25, 470-474, 2006.
74. Jamshidi A, Ahmad Khan Beigi F, Kabiri K,
Zohuriaan-Mehr MJ, Optimized HPLC determi-
nation of residual monomer in hygienic SAP
hydrogels, Polym Test, 24, 825-828, 2005.
75. Zohuriaan-Mehr MJ, Motazedi Z, Kabiri K,
Ershad-Langroudi A, Allahdadi I, Gum arabic-
acrylic superabsorbing hydrogel hybrids: Studies
on swelling rate and environmental responsive-
ness, J Appl Polym Sci, 102, 5667-5674, 2006.
76. Mahdavinia GR, Pourjavadi A, Zohuriaan-Mehr
MJ, A convenient one-step preparation of chi-
tosan-poly(sodium acrylate-co-acrylamide)
hydrogel hybrids with super-swelling properties, J
Appl Polym Sci, 99, 1615-1619, 2006.
77. Mohamadnia Z, Zohuriaan-Mehr MJ, Kabiri K,
Razavi-Nouri M, Tragacanth gum-graft-polyacry-
lonitrile: Synthesis, characterization and hydroly-
sis, J Polym Res, 15, 173-180, 2008.
78. Pourjavadi A, Hosseinzadeh H, Mahdavinia GR,
Zohuriaan-Mehr MJ, Carrageenan-g-poly(sodium
acrylate)/kaolin superabsorbent hydrogel compos-
ites: Synthesis, characterisation and swelling
behavior, Polym Polym Comp, 15, 43-51, 2007.
79. Pourjavadi A, Ghassempouri N, Zohuriaan-Mehr
MJ, Hosseinzadeh H, Modified CMC. 5.
Synthesis and super-swelling behavior of
hydrolyzed CMC-g-PAN hydrogel, J Appl Polym
Sci, 103, 877-883, 2007.
80. Zohuriaan-Mehr MJ, Motazedi Z, Kabiri K,
Ershad-Langroudi A, New superabsorbing hydro-
gel hybrid from arabic gum and acrylic
monomers, J Macromol Sci-Pure Appl Chem, 42,
1655-1666, 2005.
81. Hosseinzadeh H, Pourjavadi A, Mahdavinia GR,
Zohuriaan-Mehr MJ, Modified carrageenan. 1. H-
CarragPAM, a novel biopolymer-based superab-
sorbent hydrogel, J Bioact Compat Polym, 20,
475-490, 2005.
82. Pourjavadi A, Zohuriaan-Mehr MJ, Mahdavinia
GR, Modified chitosan. III. superabsorbency, salt-
and pH-sensitivity of smart ampholytic hydrogels
from chitosan-g-PAN, Polym Adv Technol, 15,
173-180, 2004.
83. Mahdavinia GR, Pourjavadi A, Hosseinzadeh H,
Zohuriaan MJ, Modified chitosan. 4.
Superabsorbent hydrogels from poly(acrylamide-
co-acrylic acid) grafted chitosan with salt- and
pH-responsiveness properties, Eur Polym, 40,
1399-1407, 2004.
84. Hosseinzadeh H, Pourjavadi A., Zohuriaan-Mehr
MJ, Modified carrageenan. 2. Hydrolyzed
crosslinked kappa-carrageenan-g-PAAm as a
novel smart superabsorbent hydrogel with low salt
sensitivity, J Biomater Sci, Polym Edn, 15, 1499-
1511 2004.
85. Zohuriaan-Mehr MJ, Pourjavadi A,
Superabsorbent hydrogels from starch-g-PAN:
Effect of some reaction variables on swelling
Superabsorbent Polymer Materials: A Review
Zohuriaan-Mehr MJ et al.
Iranian Polymer Journal / Volume 17 Number 6 (2008) 473
www.SID.ir
Archive of SID
behavior, J Polym Mater, 20, 113-120, 2003.
86. Pourjavadi A, Mahdavinia GR, Zohuriaan-Mehr
MJ, Modified chitosan. II. H-ChitoPAN, a novel
pH-responsive superbasorbent hydrogel, J Appl
Polym Sci, 90, 3115-3121, 2003.
87. Zheng Y, Wang A, Study of superabsorbent com-
posites. XVIII. Preparation, characterization and
property evaluation of poly(acrylic acid-co-acry-
lamide)/organomontmorillonite/sodium humate
superabsorbent composites, J Appl Polym Sci,
108, 211-219, 2008.
88. Zheng Y, Gao T, Wang A, Preparation, swelling
and slow-release characteristics of superab-
sorbent composite containing sodium humate,
Ind Eng Chem Res, 47, 1766-1773, 2008.
89. Su X, Zhang G, Xu K, Wang J, Song C, Wang P,
The effect of MMT/modified MMT on the struc-
ture and performance of the superabsorbent com-
posite, Polym Bull, 60, 69-78, 2008.
90. Pourjavadi A, Seidi F, Salimi H, Soleyman R,
Grafted CMC/silica gel superabsorbent compos-
ite: synthesis and investigation of swelling
behavior in various media, J Appl Polym Sci, 108,
3281-3290, 2008.
91. Pourjavadi A, Ayyari M, Amini-Fazl MS,
Taguchi optimized synthesis of collagen-g-
poly(acrylic acid)/kaolin composite superab-
sorbent hydrogel, Eur Polym J, 44, 1209-1216,
2008.
92. Kasgoz H, Durmus A, Kasgoz A, Enhanced
swelling and adsorption properties of AAm-
AMPSNa/clay hydrogel nanocomposites for
heavy metal ion removal, Polym Adv Tech, 19,
213-220, 2008.
93. Al E, Guclu G, Iyim T, Emik S, Ozgumu S,
Synthesis and properties of starch-graft-acrylic
acid/Na-montmorillonite superabsorbent com-
posite hydrogels, J Appl Polym Sci, 109, 16-22,
2008.
94. Qiu H, Yu J, Polyacrylate/(carboxymethylcellu-
lose modified montmorillonite) superabsorbent
nanocomposite: preparation and water absorben-
cy, J Appl Polym Sci, 107, 118-123, 2008.
95. Omidian H, Hashemi SA, Askari F, Nafisi S,
Modifying acrylic-based superabsorbents. I.mod-
ification of crosslinker and comonomer nature, J
Appl Polym Sci, 54, 241-249, 1994.
96. Omidian H, Hashemi SA, Askari F, Nafisi S,
Modifying acrylic-based superabsorbents. II.
Modification of process nature J. Appl Polym Sci,
54, 251-256, 1994.
97. Hunkeler D, Synthesis and characterization of
high molecular weight water-soluble polymers,
Polym Int, 27, 23-33, 1992.
98. Watanabe N, Hosoya Y, Tamura A, Kosuge H,
Characteristics of water-absorbent polymer emul-
sions, Polym Int, 30, 525-531,1993.
99. Trijasson P, Pith T, Lambla M, Hydrophilic poly-
electrolyte gels by inverse suspension, Macromol
Chem Macromol Symp, 35/36, 141-169, 1990.
100. Askari F, Nafisi S, Omidian H, Hashemi SA,
Synthesis and characterization of acrylic-based
superabsorbents J. Appl Polym Sci, 50, 1851-
1855, 1993.
101. Technical Brochure of Superabsorbent Polymer
Research Lab., Nippon Shokubai Co.,
www.shokubai.co.jp, available in 15 August
2005.
102. Omidian H, Hashemi SA, Sammes PG,
Meldrum, I. Modified acrylic-based superab-
sorbent polymers (dependence on particle size
and salinity), Polymer, 40, 1753-1761, 1999.
103. Ramazani-Harandi MJ, Zohuriaan-Mehr MJ,
Ershad-Langroudi A, Yousefi AA, Kabiri K, On
the structure-property relation in SAP gels:
Effect of structural variables on AUL and rheo-
logical behavior, Polym Eng Sci, submitted,
2008.
104. Fanta GF, Doane WM, In: Agricultural and
Synthetic Polymers: Biodegradability and
Utilization, Glass JE, Swift G (Eds.), American
Chemical Society, Washington DC, 288-303,
1990.
105. Omidian H, Hashemi, SA, Sammes PG,
Meldrum I, Amodel for the swelling of superab-
sorbent polymers, Polymer, 39, 6697-6704,
1998.
106. Qi X, Liu M, Chen Z, Zhang F, Study of the
swelling kinetics of superabsorbent using open
circuit potential measurement, Eur Polym J, 44,
743-754, 2008.
107. Lu S, Duan M, Lin S, Synthesis of superab-
sorbent starch-graft-poly(potassium acrylate-
co-acrylamide) and its properties, J Appl Polym
Superabsorbent Polymer Materials: A Review Zohuriaan-Mehr MJ et al.
474 Iranian Polymer Journal / Volume 17 Number 6 (2008)
www.SID.ir
Archive of SID
Sci, 88, 1536-1542, 2003.
108. Chervyakova GN, Pomerantseva EG, Klyuzhin
ES, Kruglyachenko MB, Determination of the
gel fraction content of a superabsorbent based
on acrylic acid by UV spectroscopy, Int Polym
Sci Technol, 23, T/87-T/88, 1996.
109. Brown L, High-performance liquid chromato-
graphic determination of acrylic acid monomer
in natural and polluted aqueous environments
and polyacrylates, Analyst, 104, 1165, 1979.
110. Fallahi D, Biocompatibility evaluation of
hydrophilic and hydrophobic silicone rubbers,
M.Sc. dissertation, Department of Biomaterials,
Iran Polymer and Petrochemical Institute, 2000.
111. Natural superabsorbents, Web page for the
introduction of the superabsorbent SNAP made
by Lysac Technologies; www.lysac.com/lysac/
english/about.html, available in 2 February
2008.
112. Das A, Kothari VK, Makhija S, Avyaya K,
Development of high-absorbent light-weight
sanitary napkin, J Appl Polym Sci, 107, 1466-
1470, 2008.
113. Kim JJ, Park K, Smart hydrogels for biosepara-
tion, Bioseparation, 7, 177-184, 1998.
114. Chen J, Park H, Park K, Synthesis of super-
porous hydrogels: hydrogels with fast swelling
and superabsorbent properties, J Biomed Mater
Res, 44, 53-62 1999.
115. Omidian H, Roccaa JG, Park K, Advances in
superporous hydrogels, J Contr Rel, 102, 3-12,
2005.
116. Abd El-Rehim HA, Hegazy ESA, Abd El-
Mohdy HL, Radiation synthesis of hydrogels to
enhance sandy soils water retention and increase
plant performance, J Appl Polym Sci, 93, 1360-
1371, 2004.
117. Bakass M, Mokhlisse A, Lallemant M,
Absorption and desorption of liquid water by a
superabsorbent polymer: Effect of polymer in
the drying of the soil and the quality of certain
plants, J Appl Polym Sci, 83, 234-243, 2002.
118. Liu M, Liang R, Zhan F, Liu Z, Niu A,
Preparation of superabsorbent slow release
nitrogen fertilizer by inverse suspension poly-
merization, Polym Int, 56, 729-737, 2007.
119. Bowman DC, Evans RY, Paul JL, Fertilizer salts
reduce hydration of polyacryamide gels and
affect physical properties of gel-amended con-
tainer media, J Amer Soc Hort Sci, 11 5, 382-
386, 1990.
120. Wu L, Liu M, Liang R, Preparation and proper-
ties of a double-coated slow-release NPK com-
pound fertilizer with superabsorbent and water-
retention, Bioresource Tech, 99, 547-554, 2008.
121. Wu L, Liu M, Preparation and characterization
of cellulose acetate-coated compound fertilizer
with controlled-release and water-retention,
Polym Adv Tech, 2008, in press (DOI:
10.1002/pat.1034).
122. Abedi-Koupai J, Sohrab F, Evaluation the effect
of superabsorbents on water retention and
potential of three soils, J Polym Sci Technol
(Persian), 17, 163-173, 2004.
123. Abedi-Koupai J, Asadkazemi J, Effects of a
Hydrophilic Polymer on the Field Performance
of an Ornamental Plant (Cupressus arizonica)
under Reduced Irrigation Regimes, Iran Polym
J, 15, 715-725, 2006.
124. Mousavinia SM, Atapour A, Investigating the
effect of polymer Superab A-200 on the irriga-
tion water of turf grass, 3rd Specialized Training
Course and Seminar on the Application of
Superabsorbent Hydrogels in Agriculture, Iran
Polymer and Petrochemical Institute, Tehran,
Iran, Nov, 7, 2005.
125. Allahdadi I, Investigation the effect of superab-
sorbent hydrogels on reducing plant dry stress,
2nd Specialized Training Course and Seminar
on the Application of Superabsorbent Hydrogels
in Agriculture, Iran Polymer and Petrochemical
Institute, Tehran, Iran, 2002.
126. Moazen Ghamsari B, Evaluation of levels of
superabsorbent polymer (Superab A-200) and
different levels of drought stress on growth and
yield of forage corn, Faculty of Plant and
Animal Sciences, M.Sc. Dissertation,
University College of Aburaihan, Tehran Univ,
June 2006.
127. Jafarzadeh S, Effect of superabsorbent on the
efficiency of clay mulch and biological fixation
of sand dunes, M.Sc. thesis, Department of
Agriculture, Isfahan University of Technology,
2004.
Superabsorbent Polymer Materials: A Review
Zohuriaan-Mehr MJ et al.
Iranian Polymer Journal / Volume 17 Number 6 (2008) 475
www.SID.ir
Archive of SID
128. Assadzadeh A, Investigation of the effect of
superabsorbent hydrogels and low irrigation on
preserving nutrients in hydroponic systems, 3rd
Specialized Training Course and Seminar on the
Application of Superabsorbent Hydrogels in
Agriculture, Iran Polymer and Petrochemical
Institute, Tehran, Iran, Nov. 7, 2005.
129. A. Mirhejazi, Remarkable reduction of olive
sapling casualty via employing superabsorbent
Superab A-300, 3rd Specialized Training Course
and Seminar on the Application of
Superabsorbent Hydrogels in Agriculture, Iran
Polymer and Petrochemical Institute, Tehran,
Iran, Nov. 7, 2005.
130. Sojka1 RE, Bjorneberg1 DL, Entry1 JA, Lentz
RD, Orts WJ, Polyacrylamide in Agriculture
and Environmental Land Management, Adv
Agronomy, 92 , 75-162, 2007.
131. Gao D, Heimann RB, Alexander SDB, Box-
Behnken design applied to study the strengthen-
ing of aluminate concrete modified by a super-
absorbent polymer/clay composite, Adv Chem
Res, 9, 93-97,1997.
132. Yamane H, Ideguchi T, Tokuda M, Koga H, A
new ground-reducing material based on water-
absorbent polymer, Electronics and
Communications in Japan, Part 1, 77, 68-77,
1994.
133. Kenawy E-R, Recent advances in controlled
release of agrochemicals, J Macromol Sci-Rev
Macromol Chem Phys, C38, 365-390, 1998.
134. Rudzinski WE, Dave AM, Vaishnav UH,
Kumbar SG, Kulkarni AR, Aminabhavi TM,
Hydrogels as conclolled release devices in agri-
culture, Designed Monomers Polym, 5, 39-65,
2002.
135. Guo M, Liu M, Zhan F, Wu L, Preparation and
properties of a slow release membrane-encapsu-
lated urea fertilizer with superabsorbent and
moisture preservation, Ind Eng Chem Res, 44,
4206-4211, 2005.
136. Liu M, Liang R, Zhan F, Liu Z, Niu A, Synthesis
of a slow-release and superabsorbent nitrogen
fertilizer and its properties, Polym Adv Technol,
17, 430-438, 2006.
137. Liang R, Liu M, Wu L, Controlled release NPK
compound fertilizer with the function of water
retention, React Func Polym, 67, 769-779,
2007.
138. Guo M, Liu M, Liang R, Niu A, Granular urea-
formaldehyde slow-release fertilizer with super-
absorbent and moisture preservation, J Appl
Polym Sci, 99, 3230-3235, 2006.
139. Liu M, Liang R, Zhan F, Liu Z, Niu A,
Preparation of superabsorbent slow release
nitrogen fertilizer by inverse suspension poly-
merization, Polym Int, 56, 729-737, 2007.
140. Wu L, Liu M, Preparation and properties of chi-
tosan-coated NPK compound fertilizer with
controlled-release and water-retention,
Carbohydr Polym, 72, 240-247, 2008.
141. Levy R, Nichols MA, Miller TW, Evaluation of
superabsorbent polymer-pesticide formulations
for prolonged insect control, ASTM Special
Technical Publication, No. 1234, 330-339,
Proceedings of the 14th Symposium on
Pesticide Formulations and Application
Systems, Dallas, TX, Oct. 12-13, 1995.
142. Ahmadpour A, Maskoki A, Rezaie M, Iran J
Polym Sci Tech (in Persian), Dewatering of
yogurt using a permeable membrane and acrylic
superabsorbent hydrogel, 20, 551-559, 2007.
143. Mudiyanselage TK, Neckers DC, Photochromic
superabsorbent polymers, Soft Matter, 4, 768-
774, 2008.
144. Mudiyanselage TK, Neckers DC, Highly
absorbing superabsorbent polymer, J Polym Sci
A Polym Chem, 46, 1357-1364, 2008.
145. Cordani P, Method of modifying weather, U.S.
Patents 6,315,213, 2001.
146. Agricultural Section, Web site of SNF Co.,
Agricultural Section, Technical data Sheet of
Superabsorbent; www.snf-
group.com/IMG/pdf/Aquasorb_E. pdf, avail-
able in 28 February 2004.
147. The Trawet Super absorbents Catalogue, The
Trawet Corporation, San Diego, CA, 1993
(Water absorbents, www.terawet.com, available
in 21 June 2003.).
148. Superabsorber, Website of Stockhausen, Inc.,
the manufacturer of the superabsorbent
STOCKOSORB; www.stockhausen-inc.com,
available in 2 April 2006.
149. Material Safty Data Sheet of the commercial
Superabsorbent Polymer Materials: A Review Zohuriaan-Mehr MJ et al.
476 Iranian Polymer Journal / Volume 17 Number 6 (2008)
www.SID.ir
Archive of SID
superabsorbents; www.hydrosource.com/
web_clb/990310/msds0399.htm, available in 20
July 2006.
150. Superabsorbent Super-Hydro-Grow made by
Super Absorbent Co., www.superabsorbent.
com, available in 5 October 2005.
151. Horta-Sorb Superabsorbents, Website of
Horticultural Alliance, Inc., www.hortsorb.com,
available in 7 April 2003.
152. Stahl JD, Cameron MD, Haselbach J, Aust SD,
Biodegradation of superabsorbent polymers in
soil, Environ Sci Pollut Res, 7, 83-88, 2000.
153. Wolter M, Wiesche C, Zadrazil F, Hey S,
Haselbach J, Schnug E, Biological degradabili-
ty of synthetic superabsorbent soil conditioners,
Landbauforschung Volkenrode, 1, 43-52, 2002.
154. Larson RJ, Bookland EA, Williams RT, Yokom
KM, Saucy DA, Freeman MB, Swift G,
Biodegradation of acrylic acid polymers and
oligomers by mixed microbial communities in
activated sludge, J Environment Polym Degrad,
5, 41-48, 1997.
155. Cutie SS, Buzanowski WC, Berdasco JA, Fate
of superabsorbents in the environment (analyti-
cal techniques), J Chromatogr A, 513, 93-105,
1990.
156. Barvenik FW, Polyacrylamide characteristics
related to soil applications, Soil Sci, 158, 235-
243, 1994.
157. Grula MM, Huang M-L, Sewell G, Interactions
of certain polyacrylamides with soil bacteria,
Soil Sci, 158, 291-300, 1994.
158. Wallace A, Wallace GA, Abuzamzam AM,
Effects of a polymer as soil conditioner on
yields and mineral nutrition of plants, Soil Sci,
143, 377-380, 1986.
Superabsorbent Polymer Materials: A Review
Zohuriaan-Mehr MJ et al.
Iranian Polymer Journal / Volume 17 Number 6 (2008) 477
www.SID.ir