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Characterization of alkali treated and untreated Abutilon indicum FIBERS

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... It is deemed that the low thickness of the fiber is owing to the structure of the inkberry plant fiber. Because the fiber contains a large amount of cellulose, its high density can be explained [71]. Inkberry fiber density is determined as higher than some original cellulosic fibers, such as Abutilon indicum (1170 kg/m 3 ) [71], Streblus asper (1388 kg/m 3 ) [72], Spinifex littoreus (780 kg/m 3 ) [73], and Himalayacalamus falconeri culms (1300 kg/m 3 ) [74] and lower than Hibiscus canescens (1425 kg/m 3 ) [75]. ...
... Because the fiber contains a large amount of cellulose, its high density can be explained [71]. Inkberry fiber density is determined as higher than some original cellulosic fibers, such as Abutilon indicum (1170 kg/m 3 ) [71], Streblus asper (1388 kg/m 3 ) [72], Spinifex littoreus (780 kg/m 3 ) [73], and Himalayacalamus falconeri culms (1300 kg/m 3 ) [74] and lower than Hibiscus canescens (1425 kg/m 3 ) [75]. ...
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In this study, a novel cellulosic plant-based fiber was extracted from Phytolacca americana (inkberry) as a sustainable substitute natural fiber for synthetic fibers. For this purpose, an extended characterization of inkberry fibers was carried out. The elemental composition was determined as 58.27% carbon and 41.70% oxygen. Moreover, an image processing approach was presented and used for computing the average thickness of cellulosic inkberry stem fiber. Fiber diameter was estimated from the scanning electron microscope micrographs with image processing as 480.56 µm. The scanning electron microscope image indicated that inkberry fiber has a smooth surface with a channel structure. X-ray diffraction analysis revealed that the fiber has a 4 nm crystalline size with a 51.4% crystalline index. Fiber functional groups were characterized with Fourier transform infrared analysis. The mechanical behaviors of inkberry fiber were tested with a single fiber tensile test device, and tensile strength was determined as 146.5 MPa, Young’s modulus was found as 24.8 GPa, and elongation at break of fiber was obtained as 2.37%, respectively. Furthermore, the fiber was thermally stabilized up to 435.37 °C with thermogravimetric analysis. These physico-chemical behaviors confirm that inkberry fiber may be recognized as a promising reinforcement fiber in polymer matrix composites for many non-structural applications, which are interior body panels in yachts, automobiles, partition boards in buildings, and barriers. Graphical Abstract
... Natural fiber composites exhibit several limitations, including high moisture absorption [15], poor thermal stability [16], and reduced durability, which hinder their broader industrial applications. Surface modification, especially with silane treatment, offers a solution by improving fiber-matrix bonding through the formation of chemical bridges [17]. ...
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... Natural fiber composites exhibit several limitations, including high moisture absorption [15], poor thermal stability [16], and reduced durability, which hinder their broader industrial applications. Surface modification, especially with silane treatment, offers a solution by improving fiber-matrix bonding through the formation of chemical bridges [17]. ...
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In this work, the effects of alkali treatment on the chemical composition and thermal decomposition of Acacia planifrons fibers were investigated. The fibers originating from the bark of an Acacia planifrons tree were alkali treated with various concentrations (2% and 5% w/v) for 30 min. The treatment was found to diminish the amorphous contents, improve the crystallinity index and thermal stability of the fiber. The crystallinity index of the untreated, 2% alkali-treated and 5% alkali-treated fibers was estimated to be 65.38%, 69.94% and 74.76%, respectively. The thermal stability of the alkali-treated fiber was quite higher than that of the untreated fiber. The results revealed that 5% alkali-treated Acacia planifrons fibers are suitable to be used as reinforcement in polymer composites.
Article
The aim of this study is to investigate natural cellulosic fibers extracted from Tridax procumbens plants. The obtained fibers were alkali treated for their effective usage as reinforcement in composites. The physical, chemical, crystallinity, thermal, wettability and surface characteristics were analyzed for raw, and alkali treated Tridax procumbens fibers (TPFs). The test results conclude that there was an increase in cellulose content with a reduction in hemicellulose, lignin, and wax upon alkali treatment. This enhanced the thermal stability, tensile strength, crystallinity, and surface roughness characteristics. The contact angle was also lesser for treated TPFs which prove its better wettability with the liquid phase. The Weibull distribution analysis was adopted for the analysis of the fiber diameter and tensile properties. Thus the considerable improvement in the properties of alkali treated TPFs would be worth for developing high-performance polymer composites.
Article
This study aims to examine the effect of sodium hydroxide (NaOH) treatment on the physico-chemical properties, structure, thermal, tensile and surface topography of Carica papaya fibers (CPFs). The surface of raw CPFs was modified by soaking with 5% NaOH solution for 15, 30, 45, 60, 75 and 90 min. The results of thermo-gravimetric analysis revealed that the optimum treatment time for alkali treatment was 60 min. It was found that the alkali treatment improved the properties of the CPFs. The results of TGA, FT-IR, XRD and AFM suggest that the treated CPF is a suitable alternative as reinforcement in polymer composites.
Article
The physical, chemical, tensile, crystalline, thermal, and surface morphological properties of raw and alkali treated Coccinia Grandis.L Fibers (CGFs) were characterized for the first time in this work. The results of the chemical analysis indicate that, after alkali treatment, the cellulose content of CGFs increased whereas hemicelluloses, lignin and wax contents decreased. This directly influenced the tensile strength, crystallinity index, thermal stability and the roughness of alkali-treated CGFs. The thermal stability and activation energy of the CGFs improved from 213.4 °C to 220.6 °C and 67.02 kJ/mol to 73.43 kJ/mol, respectively, due to alkali treatment. The statistical approach, Weibull distribution was adopted to analyze the tensile properties. The improved properties of the alkali treated CGF indicate that it could be an appropriate material for reinforcement in polymer composites.
Article
Increasing environmental concerns, along with the potential declination of the crude worldwide reserves, have made the human beings to utilize more regenerable resources to substitute for the design and development of more new products. This has made us to use the synthetic and natural fibers to develop innovative products. However, more eco-friendly properties of natural fibers have made them to be preferable over the synthetic fibers. To make efficient use of these fibers, it is essential to know the behavioral characteristics of these fibers. So, in this review II paper, an effort has been made to discuss the various characterization analysis studies, like Fourier transform-infrared spectra spectral analysis, X-ray and thermogravimetric methods carried out by various researchers.
Article
The world is in need of more eco-friendly material, therefore researchers around the globe focus on developing new materials that would improve the environmental quality of products. This need for new green materials has led to the utilization of composites made from raw natural fibers and polymer matrices, and this has become one of the most widely investigated research topics in recent times. Natural fiber composites are an alternative for replacing environmentally harmful synthetic materials and help control pollution problems. In addition, they are low cost, have better mechanical properties and require low production energy consumption. Also, using such materials in construction works, it is possible to improve the sustainability by eliminating construction wastes. Keeping in view all the benefits of natural fiber reinforced polymer composites, this paper first discusses various fabrication techniques employed for the production of these composites and then presents a detailed review of the research devoted to the analysis of their structure and properties by a variety of characterization techniques.
Article
The natural fiber Epipremnum aureum was extracted from its plant. E. aureum fibers (EAFs) were investigated by chemical analysis, Fourier transform infrared spectroscopy (FTIR), X-ray diffraction, thermogravimetric analysis, scanning electron microscopy, and single fiber tensile test. Chemical analysis, FTIR, and X-ray analysis evidenced that these fibers has 66.34% cellulose content with crystallinity index of 49.33%. The thermogravimetric analysis reveals that EAFs can thermally withstand temperatures until 328.9°C. The morphology of the EAFs was observed by scanning electron microscope. It was established that the fiber can be utilized as reinforcement in polymer composites.
Article
The aim of this study is to examine the use of new natural fibers, which are extracted from the Saharan aloe vera cactus plant leaves as reinforcement in polymer composites. The physicochemical, mechanical and thermal properties of the Saharan Aloe Vera Cactus Leaves (SACL) fibers are investigated, through the effect of alkali treatment. The contents of α-cellulose, hemicellulose, wax and moisture present in SACL fibers were characterized by standard test methods The mechanical properties of SACL fibers were measured through single fiber tensile test. The interfacial strength between the fiber and matrix was estimated by the fiber pull-out test. These results ensure that the chemical and mechanical properties of the fibers are improved after the alkali treatment. FT-IR spectroscopic analysis confirms that the alkali treatment process has removed certain amount of amorphous materials from the fibers. XRD analysis results show that the alkali treatment has enhanced the Crystallinity Index and Crystalline Size of the fibers. Thermal behavior of the fibers was analyzed by using TGA. The thermal stability and the thermal degradation temperature increases after the alkali treatment of fibers. The morphologies of fibers were analyzed by SEM and prove that the fiber surfaces become rough after alkali treatment.
Article
This research study was aimed at examining newly identified natural fiber from the bark of Azadirachta indica (AI). The various properties were analyzed and compared with other available bark fibers. The chemical composition of Azadirachta indica fibers (AIFs), high cellulose (68.42 wt.%) content, and low lignin (13.58 wt.%) were discovered. The lower density of 740 kg/m3, and crystallinity index of 65.04% properties were identified. The maximum peak temperature obtained was 321.2 °C in Differential thermogravimetry (DTG) curve. Taken together, all the properties of AIFs indicated that they could be suitable to make green composites for various types of applications.
Article
The aim of this paper is to investigate the effect of an alkali treatment on physical, chemical, mechanical, and morphological properties of Phoenix Sp. fibers. The use of natural fibers as reinforcement in polymer composites requires a deep investigation to understand their behavior and which treatment is more appropriate to improve the quality of the untreated material. For this reason, fibers were extracted from the petioles of the Phoenix Sp. plant and they were treated with NaOH solution in different weight concentrations (5%, 10%, and 15%). The mechanical behavior was investigated through tensile test on single fiber at different gauge length (20 mm, 30 mm, 40 mm, 50 mm, and 60 mm). Chemical and physical analysis were performed to define the material properties. In particular, density analysis of untreated and treated fibers, optical analysis to measure the diameter of the fibers, moisture content evaluation, and a chemical composition analysis were carried out through standard methods. The modification of the surface morphology due to the alkali treatment was analyzed through scanning electron microscope analysis.
Article
With growing inclination towards the eco-friendly technology, natural fiber based polymer composite materials have been gaining a lot of momentum nowadays. The present review discusses the much research that has been carried out in the area of the epoxy-based composites reinforced with natural fibers. Influence of the various factors like the fiber content, fiber geometry, fiber size, surface treatment technique, and coupling agent on different properties like mechanical, thermal, behavior towards water absorption and others have been presented. It can be inferred that there is a need and scope for improvement of the surface properties of natural fiber using various methods like physical and chemical treatments, addition of coupling agents, etc. for the manufacturing of the composites having desired properties. These techniques not only modify surface morphology, but also improve other processing parameters like the hydrophilic character of fiber (which is desirable to be low), and hence improve several characteristics such as mechanical properties, thermal stability, water absorption and other considerations of the composites.
Article
Characterization of new natural fiber is rising due to its excellent properties and drives the investigators to create high performance composites. This present investigation was designed to study the physico-chemical properties of fibers obtained from the leaf of theArtistida hystrix(AH). The Artistida hystrix fibers (AHFs) had crystallinity index (44.85%), cellulose (59.54 wt.%), hemicellulose (11.35 wt.%), lignin (8.42 wt.%) and density (540 kg/m3). The tensile strength of AHFs was 440 ± 13.4 MPa with an average strain rate of 1.57 ± 0.04%. Further calculated microfibril angle of AHFs was 12.64° ± 0.45° which influenced the mechanical properties.
Article
Cellulose samples are routinely analyzed by X-ray diffraction to determine their crystal type (polymorph) and crystallinity. However, the connection is seldom made between those efforts and the crystal structures of cellulose that have been proposed with synchrotron X-radiation and neutron diffraction over the past decade or so. In part, this desirable connection is thwarted by the use of different conventions for description of the unit cells of the crystal structures. In the present work, powder diffraction patterns from cellulose Iα, Iβ, II, IIII, and IIIII were calculated based on the published atomic coordinates and unit cell dimensions contained in modified “crystal information files” (.cif) that are supplied in the Supplementary Information. The calculations used peak widths at half maximum height of both 0.1 and 1.5° 2, providing both highly resolved indications of the contributions of each contributing reflection to the observable diffraction peaks as well as intensity profiles that more closely resemble those from practical cellulose samples. Miller indices are shown for each contributing peak that conform to the convention with c as the fiber axis, a right-handed relationship among the axes and the length of a b. Adoption of this convention, already used for crystal structure determinations, is also urged for routine studies of polymorph and crystallinity. The calculated patterns are shown with and without preferred orientation along the fiber axis. Diffraction intensities, output by the Mercury program from the Cambridge Crystallographic Data Centre, have several uses including comparisons with experimental data. Calculated intensities from different polymorphs can be added in varying proportions using a spreadsheet program to simulate patterns such as those from partially mercerized cellulose or various composites.
Article
The X-ray diffraction-based Segal Crystallinity Index (CI) was calculated for simulated different sizes of crystallites for cellulose Iβ and II. The Mercury software was used, and different crystallite sizes were based on different input peak widths at half of the maximum peak intensity (pwhm). The two cellulose polymorphs, Iβ and II, gave different CIs despite having the same pwhm values and perfect periodicity. The higher CIs for cellulose II were attributed to a greater distance between the major peaks that are closest to the recommended 2-θ value for assessing the amorphous content. That results in less peak overlap at the recommended 2-θ value. Patterns calculated with simulated preferred orientation had somewhat higher CIs for cellulose Iβ, whereas there was very little effect on the CIs for cellulose II.
Article
The crystal and molecular structure together with the hydrogen-bonding system in cellulose Ibeta has been determined using synchrotron and neutron diffraction data recorded from oriented fibrous samples prepared by aligning cellulose microcrystals from tunicin. These samples diffracted both synchrotron X-rays and neutrons to better than 1 Angstrom resolution (>300 unique reflections; P2(1)). The X-ray data were used to determine the C and 0 atom positions, The resulting structure consisted of two parallel chains having slightly different conformations and organized in sheets packed in a "parallel-up" fashion, with all hydroxymethyl groups adopting the tg conformation. The positions of hydrogen atoms involved in hydrogen-bonding were determined from a Fourier-difference analysis using neutron diffraction data collected from hydrogenated and deuterated samples. The hydrogen atoms involved in the intramolecular O3...O5 hydrogen bonds have well-defined positions, whereas those corresponding to 02 and 06 covered a wider volume, indicative of multiple geometry with partial occupation. The observation of this disorder substantiates a recent infrared analysis and indicates that, despite their high crystallinity, crystals of cellulose Ibeta have an inherent disorganization of the intermolecular H-bond network that maintains the cellulose chains in sheets.
Article
Quantitative x‐ray diffraction methods have been used to study the orientation of the cellulose chains and lateral ordering around the long chain axes in various commercial and experimental rayons. Lateral order can vary independently of orientation in cellulose, as is the case with other linear polymers such as the polyamides. The degree of lateral order obtainable by aqueous annealing of regenerated cellulose appears to be restricted by the structure originally set up. As noted by Sisson, the well‐known relations between yarn tenacity and orientation and elongation to break and orientation are not unique. At a given orientation, a range of tenacities and elongations are possible, depending upon the influence of other variables. Study of a series of yarns prepared under constant mechanical conditions showed that elongation to break increased with lateral disordering of the cellulose chains at constant orientation. The data support Baker's proposal that local chain disordering in any linear polymer favors higher extensibility. Some yarns of essentially the same orientation and lateral order have shown different properties indicating that other as yet undefined structural variables also have an important effect on physical properties.
Article
The crystal and molecular structure, together with the hydrogen-bonding system in cellulose I(alpha), has been determined using atomic-resolution synchrotron and neutron diffraction data recorded from oriented fibrous samples prepared by aligning cellulose microcrystals from the cell wall of the freshwater alga Glaucocystis nostochinearum. The X-ray data were used to determine the C and O atom positions. The resulting structure is a one-chain triclinic unit cell with all glucosyl linkages and hydroxymethyl groups (tg) identical. However, adjacent sugar rings alternate in conformation giving the chain a cellobiosyl repeat. The chains organize in sheets packed in a "parallel-up" fashion. The positions of hydrogen atoms involved in hydrogen-bonding were determined from a Fourier-difference analysis using neutron diffraction data collected from hydrogenated and deuterated samples. The differences between the structure and hydrogen-bonding reported here for cellulose I(alpha) and previously for cellulose I(beta) provide potential explanations for the solid-state conversion of I(alpha) --> I(beta) and for the occurrence of two crystal phases in naturally occurring cellulose.
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