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首页> 外文期刊>Iranian polymer journal >Effect of ionomer/multiplet formation on mechanical properties and ascorbic acid release behavior of PNIPAAm hydrogels copolymerized by DMAEMA, DMAPMAAm and MAPTAC
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Effect of ionomer/multiplet formation on mechanical properties and ascorbic acid release behavior of PNIPAAm hydrogels copolymerized by DMAEMA, DMAPMAAm and MAPTAC

机译:离聚物/多重形成对DMAEMA,DMAPMAAm和MAPTAC共聚的PNIPAAm水凝胶的力学性能和抗坏血酸释放行为的影响

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摘要

Poly(N-isopropylacrylamide) (PNIPAAm) hydrogels containing N-[3-(N,N-dimethylamino)propyl]methacrylamide (DMAPMAAm), 2-(N,N-dimethylamino)ethyl methacrylate (DMAEMA) and [3-(methacryloylamino)propyl]trimethylammonium chloride (MAPTAC) as cationic monomers were cross-linked with N,N'-methylenebisacrylamide (BIS) and tetraallylammonium bromide (TAB). The swelling degrees, uniaxial compression moduli and L-ascorbic acid (L-AA) releases of these cationic PNIPAAm hydrogels synthesized in 1,4-dioxane were compared with the one prepared in distilled-deionized water (DDW) and in aqueous sodium hydroxide solution (0.1 N NaOH). P(NIPAAm-co-MAPTAC)/BIS and P(NIPAAm-co-DMAEMA)/BIS hydrogels at 37 degrees C in DDW and at 37 degrees C/pH 4 exhibited higher gel strengths and compressive moduli than all the others cross-linked and copolymerized with TAB and DMAPMAAm, respectively. All the observations indicated that the physical cross-linking points created by ionomer pairs of MAPTA(+)Cl(-) units and the hydrophobic contributions of ester groups in the DMAEMA units might be a reason of their improved mechanical properties in DDW at 37 degrees C. Further, the charge screening effect of chloride ions in the swelling medium at pH 4 also resulted in the improved compressive moduli compared to the ones in DDW. The water diffusion into/from all the copolymeric PNIPAAm hydrogels during the swelling/deswelling processes at 25 degrees C/37 degrees C in DDW and their L-AA releases at 37 degrees C in DDW also revealed the importance of these ionic and hydrophobic effects. Water transport through the ones cross-linked with TAB was controlled by non-Fickian process due to the repulsive forces between the quaternized ammonium groups on the chemical cross-links while in the case of P(NIPAAm-co-MAPTAC)/BIS, water transport followed Fickian diffusion because the multiplet formations behaved as additional cross-links. Furthermore, P(NIPAAm-co-MAPTAC)/BIS hydrogel due to the ionomer-multiplet transitions at 37 degrees C in DDW has exhibited less-Fick diffusion that resulted in a lower diffusion coefficient during the release of L-AA as compared to the others.
机译:含有N- [3-(N,N-二甲基氨基)丙基]甲基丙烯酰胺(DMAPMAAm),甲基丙烯酸2-(N,N-二甲基氨基)乙基酯(DMAEMA)和[3-(甲基丙烯酰氨基)N-(N-异丙基丙烯酰胺)(PNIPAAm)水凝胶阳离子单体])丙基]三甲基氯化铵(MAPTAC)与N,N'-亚甲基双丙烯酰胺(BIS)和溴化四烯丙基铵(TAB)交联。将这些在1,4-二恶烷中合成的阳离子PNIPAAm水凝胶的溶胀度,单轴压缩模量和L-抗坏血酸(L-AA)释放与在蒸馏去离子水(DDW)和氢氧化钠水溶液中制备的一种进行比较(0.1 N NaOH)。 P(NIPAAm-co-MAPTAC)/ BIS和P(NIPAAm-co-DMAEMA)/ BIS水凝胶在DDW中在37摄氏度和37摄氏度/ pH 4下显示出比所有其他交联聚合物更高的凝胶强度和压缩模量分别与TAB和DMAPMAAm共聚。所有观察结果均表明,由MAPTA(+)Cl(-)单元的离聚物对产生的物理交联点和DMAEMA单元中酯基团的疏水作用可能是其在DDW中37度时机械性能提高的原因。 C.此外,与DDW相比,在pH 4的溶胀介质中氯离子的电荷屏蔽作用还导致压缩模量提高。在DDW中在25摄氏度/ 37摄氏度的溶胀/溶胀过程中,水扩散到所有共聚PNIPAAm水凝胶中/从其中扩散,以及DDW在37摄氏度的L-AA释放过程中,它们的L-AA释放也揭示了这些离子和疏水作用的重要性。由于P(NIPAAm-co-MAPTAC)/ BIS的化学交联作用下季铵化铵基团之间的排斥力,通过TAB交联的水的传输受非菲克过程控制。迁移遵循菲克扩散,因为多重结构形成了额外的交联。此外,由于DDW中37摄氏度的离聚物-多重跃迁,P(NIPAAm-co-MAPTAC)/ BIS水凝胶的Fick扩散较少,与L-AA释放相比,扩散系数较低。其他。

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