Progress in Organic Coatings Journal Impact Factor & Information

Publisher: Elsevier

Current impact factor: 2.36

Impact Factor Rankings

2015 Impact Factor Available summer 2016
2011 Impact Factor 1.977

Additional details

5-year impact 2.43
Cited half-life 6.80
Immediacy index 0.34
Eigenfactor 0.01
Article influence 0.54
Other titles Progress in organic coatings
ISSN 0033-0655
OCLC 1585841
Material type Periodical, Internet resource
Document type Journal / Magazine / Newspaper, Internet Resource

Publisher details


  • Pre-print
    • Author can archive a pre-print version
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    • Author can archive a post-print version
  • Conditions
    • Authors pre-print on any website, including arXiv and RePEC
    • Author's post-print on author's personal website immediately
    • Author's post-print on open access repository after an embargo period of between 12 months and 48 months
    • Permitted deposit due to Funding Body, Institutional and Governmental policy or mandate, may be required to comply with embargo periods of 12 months to 48 months
    • Author's post-print may be used to update arXiv and RepEC
    • Publisher's version/PDF cannot be used
    • Must link to publisher version with DOI
    • Author's post-print must be released with a Creative Commons Attribution Non-Commercial No Derivatives License
    • Publisher last reviewed on 03/06/2015
  • Classification

Publications in this journal

  • [Show abstract] [Hide abstract]
    ABSTRACT: Iron oxide nanoparticles with fiber-like and polygon morphologies were synthesized in the presence of triethanolamine and urea surfactants. The synthesized particles were then treated by 3-amino propyl trimethoxy silane (APTMS). Then, the nanocomposites were prepared through incorporation of 1 wt.% unmodified and surface modified nanopigments into the epoxy resin. The phase composition and morphology of the nanoparticles were characterized by X-ray diffraction (XRD) and field-emission scanning electron microscope (FE-SEM), respectively. The chemical grafting of silane chains on the surface of nanoparticles was studied by Fourier transform infrared spectroscopy (FT-IR). The mechanical properties and fracture morphology of the nanocomposites were investigated by tensile test. SEM and XRD analyses revealed that surfactants significantly affected the size and morphology of the nanopigments. FT-IR analysis confirmed chemical functionalization of APTMS chains on the surface of nanopigments. It was found that surface treatment of nanoparticles by APTMS effectively improved the compatibility and dispersion of particles in the epoxy matrix. The nanoparticle synthesized in the presence of urea increased the fracture toughness and tensile strength of the composite greater than the nanopigment synthesized in the presence of triethanolamine. Results obtained from tensile test revealed the noticeable improvement of the interfacial interactions between Fe3O4/APTMS particle and epoxy matrix. Inclusion of surface modified nanopigments into the epoxy coating resulted in higher tensile strength and fracture toughness compared to the coating filled with unmodified nanopigments. It was found that the morphology and surface chemistry of the nanopigment significantly affected the mechanical properties of the epoxy coating.
    Progress in Organic Coatings 01/2016; 90:10-20. DOI:10.1016/j.porgcoat.2015.09.018
  • [Show abstract] [Hide abstract]
    ABSTRACT: Hydrazones are present in many of the bioactive heterocyclic compounds that are of wide interest due to their biological applications. This article focuses on the synthesis of the hydrazone ligand and its metal complexes and their potential application as anti-microbial, antifouling and flame retardant additives in epoxy formulations for surface coating application. Selected divalent (CoII) and trivalent (CrIII and FeIII) metal complexes of arylhydrazones, namely o-hydroxyacetophenone benzoylhydrazone (HBH) have been isolated and characterized by a combination of elemental analysis, FTIR, 1HNMR and mass spectra. The ligand and its metal complexes were physically added to an epoxy resin. Experimental coatings were produced on a laboratory scale, and then applied using a brush onto both wood and steel panels. Results obtained from an oxygen index value indicated that the epoxy resin containing the ligand (HBH) and its metal complexes as additives, exhibit a very good flame retardancy effect. The results of the biological activity indicated that the HBH ligand and its metal complexes exhibit a very good antimicrobial and antifouling effect, with the metal complexes showing better results than the ligand. Both physical and mechanical resistance properties were also studied, to evaluate any drawbacks due to the inclusion of the additives. The additives did not affect the flexibility, hardness and adhesion of the epoxy resin formula. The gloss was increased due to the incorporation of the aromatic ring, and the impact strength was also increased due to the incorporation of metal into the epoxy resin formulation.
    Progress in Organic Coatings 12/2015; 89(89):106–113. DOI:10.1016/j.porgcoat.2015.08.001

  • Progress in Organic Coatings 11/2015; DOI:10.1016/porgcoat.2015.11.011

  • Progress in Organic Coatings 11/2015;

  • Progress in Organic Coatings 11/2015; 90. DOI:10.1016/j.porgcoat.2015.11.001

  • Progress in Organic Coatings 11/2015; DOI:10.1016/j.porgcoat.2015.07.006
  • [Show abstract] [Hide abstract]
    ABSTRACT: Staudinger-Vilarrasa reaction is an efficient pathway to make amide bound starting with azide and carboxylic acid. That fast reaction is a key tool for synthesis of wild range of monomers for electrodeposition. In this work, we report the first use of Staudinger-Vilarrasa reaction in order to prepare monomers for hydrophobic and superhydrophobic surface by electrodeposition. This work includes the synthesis of different monomers with various hydrophobic chains, study of the surface properties and morphologies depending on the hydrophobic chain and the number of deposition scans.
    Progress in Organic Coatings 10/2015; DOI:10.1016/j.porgcoat.2015.10.022
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    ABSTRACT: A new method named two-step emulsification process was developed to synthesize high solid content waterborne polyurethanes by strict control of the bimodal particle size distribution. In the first step, a series of 40% solid content polyester-based (WPU-1) with low content of hydrophilic group and large particle size were firstly synthesized. In the second step, polyether-based prepolymers (WPU-2 prepolymers) with high content of hydrophilic group were firstly prepared and WPU-1 emulsions were used to emulsify WPU-2 prepolymers to obtain the final emulsions with high solid content (WPU-3). The particle size of WPU-3 present bimodal distribution and the diameter ratio and volume percentage of large particles to small particles in WPU-3 were able to be strictly controlled by this method. The viscosity of WPU-3 with 55% solid content was only 489.1 mPa s−1 when the diameter ratio of large particles to small particles was 9.2 and the volume percentage of large particles was 74%.
    Progress in Organic Coatings 09/2015; 86. DOI:10.1016/j.porgcoat.2015.03.013
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    ABSTRACT: Optically anisotropic films by shear coating of a lyotropic chromonic liquid crystal (LCLC) aqueous solution were developed on a triacetyl cellulose (TAC) film instead of a glass substrate. The TAC film surface was treated using a sodium hydroxide (NaOH) solution to increase its surface energy for wetting ability. Although the desired surface energy, which is competitive with glass, was achieved, the TAC film surface became rougher during NaOH hydrolysis, which aggravated the alignment of LCLC aggregates, especially for those with a small length-to-width ratio. To alleviate the surface roughness without compensating the surface energy, further treatment of the NaOH-hydrolyzed TAC film was performed using atmospheric pressure Ar/O2 plasma. After optimization of the treatment conditions, the combined method could enhance the polarization efficiency (Peff) of the anisotropic film on the TAC substrate from 91.2% to 95.9%, which was nearly equal to that on a glass substrate.
    Progress in Organic Coatings 08/2015; 85. DOI:10.1016/j.porgcoat.2015.03.001
  • [Show abstract] [Hide abstract]
    ABSTRACT: Polymerized solid-type urushiol (YPUOH) with high thermal stability and excellent antimicrobial properties was prepared and incorporated into low-density polyethylene (LDPE) via melt-compounding and subsequent melt-extrusion processes. To investigate the feasibility of as-prepared LDPE/YPUOH composite films for use in packaging applications, the films were characterized as a function of YPUOH using Fourier-transform infrared spectroscopy (FT-IR), X-ray diffraction (WAXD), scanning electron microscopy (SEM), thermogravimetric analysis (TGA), contact angle, and antimicrobial activity assays. The physical properties and antimicrobial activities were found to be strongly dependent upon the changes in chemical and morphological structures originating from different compositions of the composite films. The thermal stability of the composite films was effectively improved with YPUOH addition. Incorporating YPUOH caused the water vapor transmission rate (WVTR) to decrease from 10.3 to 6.5 g/m2·day, suggesting that the barrier properties of LDPE, which are relatively good per se, were further improved. Furthermore, the LDPE/YPUOH composite films exhibited good antimicrobial activities against both Gram-negative and Gram-positive micro-organisms. However, the dispersion of YPUOH in the LDPE matrix was not satisfactory due to a weak interaction between LDPE and YPUOH, which may adversely affect the thermal and barrier properties at higher contents of YPUOH. Further studies are required to increase the compatibility and dispersion of YPUOH in the LDPE matrix in order to optimize its performance and expand its applications.
    Progress in Organic Coatings 08/2015; 85. DOI:10.1016/j.porgcoat.2015.03.012
  • [Show abstract] [Hide abstract]
    ABSTRACT: To enhance the thermal stability and barrier properties of pure poly(vinyl alcohol) (PVA), five different cross-linked poly(vinyl alcohol)/boric acid (PVA/BA) hybrid films were prepared via a solution blending method, and their properties including barrier properties, thermal stability, transparency, and mechanical properties were investigated as a function of the BA content. The physical properties of the PVA/BA hybrid films were strongly dependent upon the chemical structure and morphology of the films originating from the amount of BA and change in degree of cross-linking. With increasing BA content, the size and amount of PVA crystallites decreased, whereas the cross-linking density increased, resulting in more compact packing of the molecules and lower free volume in the amorphous regions. The glass transition temperature and thermal stability were highly enhanced with increasing BA content. The oxygen transmission rate (OTR) of pure PVA decreased from 5.96 to 0.15 cc/m2 day with increasing BA content and were greatly suppressed by 22.8% for 1% BA, 7.7% for 3% BA, and 2.5% for 3% BA, respectively, relative to pure PVA film. With increasing BA content, their water-resistant pressure and tensile strength increased with BA loading. All the hybrid films showed good transparency. These properties of the cross-linked PVA/BA hybrid films make them potential candidates for versatile applications as coatings, films, and packaging materials.
    Progress in Organic Coatings 08/2015; 85. DOI:10.1016/j.porgcoat.2015.03.005
  • [Show abstract] [Hide abstract]
    ABSTRACT: The present investigation reports the preparation and characterization of the thermally stable poly(vinyl alcohol)/(poly(amide-imide)-SiO2) nanocomposite (PVA/PAI-SiO2 NC) films. For this reason, the surface of SiO2 nanoparticles (NPs) was modified with N-trimellitylimido-l-methionine and subsequently, 5 wt.% of modified SiO2 NPs were dispersed in the PAI matrix via sonochemical reaction. The resulting NC was studied by different techniques. Finally, the PAI-SiO2 NC was employed as nanofiller and was incorporated into the PVA matrix for the enhancement of its mechanical and thermal properties. The synthesized NCs were studied by Fourier transform infrared and X-ray diffraction spectroscopy analysis. The surface topography and morphology of the NCs were studied by atomic force microscopy techniques, field emission scanning electron microscopy and transmission electron microscopy. The micrographs demonstrated that the nanofillers were homogeneously dispersed in the PVA matrix. The thermo gravimetric analysis curves indicated that the thermal decomposition of the PVA/PAI-SiO2 NC films shifted toward higher temperature in comparison with the pure PVA. The effect of nanofiller on the mechanical properties of NC films was also explored.
    Progress in Organic Coatings 08/2015; 85. DOI:10.1016/j.porgcoat.2015.03.003