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Preparation and Swelling Properties of Semi-IPN Hydrogels Based on Chitosan-g-Poly(acrylic acid) and Phosphorylated Polyvinyl Alcohol

机译:壳聚糖-g-聚(丙烯酸)和磷酸化聚乙烯醇的半IPN水凝胶的制备及溶胀性能

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The phosphorylated poly(vinyl alcohol) (PPVA) samples with various substitution degrees were prepared through the esterification reaction of PVA and phosphoric acid. By using chitosan (CTS), acrylic acid (AA) and P-PVA as raw materials, ammonium persulphate (APS) as an initiator and N,N-methylenebisacrylamide as a crosslinker, the CTS-,g-PAA/P-PVA semi-interpenetrated polymer network (IPN) ssuperabsorbent hydrogel was prepared in aqueous solution by the graft copolymerization of CTS and AA and followed by an interpenetrating and crosslinking of P-PVA chains. The hydrogel was characterized by Fourier transform infrared (FTIR), scanning electron microscopy (SEM), and differential scanning calorimetry (DSC) techniques, and the influence of reaction variables, such as the substitution degree and content of P-PVA on water absorbency were also investigated. FTIR and DSC results confirmed that PAA had been grafted onto CTS backbone and revealed the existence of phase separation and the formation of semi-IPN network structure. SEM observations indicate that the incorporation of P-PVA induced highly porous structure, and P-PVA was uniformly dispersed in the polymeric network. Swelling results showed that CTS-g-PAA/P-PVA semi-IPN superabsorbent hydrogel exhibited improved swelling capability (421 g-g(-1) in distilled water and 55 g-g-1 in 0.9 wt % NaCl solution) and swelling rate compared with CTS-g-PAA/PVA hydrogel (301. g.g(-1) in distilled water and 47 g-g-1 in 0.9 wt %, NaCl solution) due to the phosphorylation of PVA.
机译:通过PVA与磷酸的酯化反应,制备了具有不同取代度的磷酸化聚乙烯醇(PPVA)样品。以壳聚糖(CTS),丙烯酸(AA)和P-PVA为原料,过硫酸铵(APS)为引发剂,N,N-亚甲基双丙烯酰胺为交联剂,CTS-,g-PAA / P-PVA半通过CTS和AA的接枝共聚反应,然后将P-PVA链相互渗透和交联,在水溶液中制备高互穿聚合物网络(IPN)超吸收水凝胶。通过傅里叶变换红外光谱(FTIR),扫描电子显微镜(SEM)和差示扫描量热法(DSC)技术表征了水凝胶,并考察了反应变量(如取代度和P-PVA的含量)对吸水率的影响。还进行了调查。 FTIR和DSC结果证实PAA已接枝到CTS骨架上,并揭示了相分离的存在和半IPN网络结构的形成。 SEM观察表明,P-PVA的引入引起高度多孔的结构,并且P-PVA均匀地分散在聚合物网络中。溶胀结果表明,与CTS相比,CTS-g-PAA / P-PVA半IPN超吸收水凝胶显示出改善的溶胀能力(在蒸馏水中为421 gg(-1),在0.9 wt%NaCl溶液中为55 gg-1)。 -g-PAA / PVA水凝胶(在蒸馏水中为301. gg(-1),在0.9 wt%的NaCl溶液中为47 gg-1)是由于PVA的磷酸化作用。

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