Polyesterpolyolacrylate/bentonite nanocomposites, capable of in situ photo polymerization, were synthesized and characterized. The organically modified bentonite clay was prepared by an ion exchange process, in which sodium ions were replaced by alkyl ammonium ions. Organo modification of bentonite was confirmed from X-ray diffraction and fourier transform-infrared data. Microstructures were characterized by XRD data and transmission electron microscopy (TEM). Both XRD data and TEM images of polyester polyol acrylate/organo modified bentonite nanocomposites indicated that most of silicate layers were intercalated into the acrylate matrix. The resulting nanocomposites were characterized by gel content, water equilibrium swell, tensile strength, and in vitro degradation. The results showed that water equilibrium swell and in vitro degradation of these nanocomposites decreased with increase in the clay content. The tensile strength of these nanocomposites also increased with increase in the clay content. Release of two model drugs namely sulfamethoxazole and diclofenac sodium (DS) from these nanocomposites was studied in phosphate buffer saline pH = 7.4 at 37 degrees C. The drug release studies showed that sulfamethoxazole released slower than DS from polyester polyol acrylate nanocomposites. Therefore, these materials may be useful for mucoadhesive drug carriers and other biomedical applications.
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http://dx.doi.org/10.1002/jbm.b.31496 | DOI Listing |
Polymers (Basel)
December 2024
CNBM Zhongyan Technology Co., Ltd., Beijing 100024, China.
This study aims to develop castable polyurethane suitable for applications on wet substrates or underwater construction. Polyurethanes were synthesized using various polyols with similar hydroxyl values, including poly(tetrahydrofuran) polyol, polyester polyol, castor oil-modified polyol, soybean oil-modified polyol, and cashew nut shell oil-modified polyol. The corresponding polyurethane curing products were evaluated for their underwater curing characteristics by volume expansion ratios and adhesion strength on dry and wet substrates, combined with analyses of reaction exothermic behavior, wetting properties on dry and wet substrates, interfacial tension, and microstructure characterization from the perspectives of reaction activity and water solubility.
View Article and Find Full Text PDFPolymers (Basel)
December 2024
C & S Partner, Hanam Technovalley U1 Center, Hanam-si 12982, Republic of Korea.
A fully bio-based polyester polyol based on isosorbide (ISB) and dimer fatty acid (DA) was synthesized through esterification. An ISB-based polyester polyol (DIS) was developed to synthesize a bio-based polyurethane elastomer (PUE) with enhanced mechanical and self-healing properties. The rigid bicyclic structure of ISB improved tensile properties, while the urethane bonds formed between the hydroxyl groups in ISB and isocyanate exhibited reversible characteristics at elevated temperatures, significantly enhancing the self-healing performance of DIS-based PUE compared to the control PUE (self-healing efficiency: 98% for DIS-based PUE vs.
View Article and Find Full Text PDFPolymers (Basel)
November 2024
INESCOP Footwear Technology Centre, Alemania 102, 03600 Elda, Alicante, Spain.
This study aimed to enhance the initial adhesion performance of reactive polyurethane hot-melt adhesives by using a bio-based polycarbonate polyol instead of traditional polyester or polyether polyols and by incorporating thermoplastic polyurethane (TPU) in varied proportions. Adhesives synthesized from bio-based polycarbonate polyols and polypropylene glycol with MDI as the isocyanate were characterized chemically, thermally, and mechanically (FTIR, DSC, plate-plate rheology, DMA, and T-peel strength test). Adding 10-15 wt.
View Article and Find Full Text PDFACS Omega
November 2024
Center for Sustainable Polymers, Mindanao State University - Iligan Institute of Technology, Iligan City 9200, Philippines.
Polymers (Basel)
October 2024
Adhesion and Adhesives Laboratory, University of Alicante, 03080 Alicante, Spain.
Polyurethanes (PUs) synthesized with blends of polycarbonate and polyester polyols (CD+PEs) showed intrinsic self-healing at 20 °C. The decrease in the polycarbonate soft segments content increased the self-healing time and reduced the kinetics of self-healing of the PUs. The percentage of C-O species decreased and the ones of C-N and C=O species increased by increasing the polyester soft segments in the PUs, due to higher micro-phase separation.
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