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Preparation and characterization of water-absorbent poly(acrylamide-co-acrylic acid salt)'s.

机译:吸水性聚(丙烯酰胺-丙烯酸盐)的制备与表征。

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摘要

Poly(acrylamide-co-acrylic acid salt) gel beads prepared by inverse suspension polymerization were used as model polymers for studying the swelling mechanism of water-absorbent polymers and the effects of polymerization parameters on swelling properties. It was found that the free swelling of single beads in water could be described as anomalous diffusion. However, the transport of fluid through a polymer bead bed (defined as penetration absorption) is a combination of diffusion absorption and capillary transport. Capillary transport was found to be the rate-controlling step and was defined as the controlling mechanism for the penetration absorption. The particle size of the beads and the nature of the liquid and the polymer matrix, are the three major parameters determining the swelling properties.; The kinetics of the penetration absorption, i.e., the water uptake (Q{dollar}sb{lcub}rm t{rcub}{dollar}) at time t, can be described by two parameters: the equilibrium water uptake (Q{dollar}sb{lcub}infty{rcub}{dollar}) and a characteristic time constant ({dollar}tausb{lcub}rm d{rcub}{dollar}). High values of Q{dollar}sb{lcub}infty{rcub}{dollar} and low values of {dollar}tausb{lcub}rm d{rcub}{dollar} are required to achieve a high rate of water absorption. Both values are primarily dependent on the chemical structure of the polymer matrix. In addition, {dollar}tausb{lcub}rm d{rcub}{dollar} is also affected by the capillary transport.; The effects of the polymerization parameters on the water-absorbing properties (i.e., Q{dollar}sb{lcub}infty{rcub}{dollar} and Q{dollar}sb{lcub}rm t{rcub}{dollar}) were examined by varying the polymerization stabilizer, crosslinking monomer and initiator concentrations, the feed monomer ratio and the type of base used to neutralize the acrylic acid. The values of Q{dollar}sb{lcub}rm t{rcub}{dollar} decreased with increasing stabilizer concentration owing to the decrease in particle size. Other polymerization parameters led to changes in chemical structure. The values of Q{dollar}sb{lcub}infty{rcub}{dollar} increased with decreasing crosslink density of the gel beads. While the crosslinking monomer formed crosslinks between the polymer chains through their multifunctional groups, the initiator and the feed monomer ratio affected the degree of crosslinking caused by chain transfer to polymer (defined as the self-crosslinking). The degree of crosslinking was enhanced by increasing the crosslinking monomer and initiator concentration. The highest degree of self-crosslinking was observed at the 50:50 molar ratio of acrylamide to acrylic acid salt.; The value of {dollar}tausb{lcub}rm d{rcub}{dollar} can be reduced by optimizing the crosslinking monomer concentration, increasing the initiator concentration and decreasing the interactions between polyions and counterions. To improve the kinetics of water absorption, the following are suggested: (1) prepare polymer beads with a narrow size distribution in the size range of 200 {dollar}mu{dollar}m; (2) prevent the formation of water-soluble polymers; (3) decrease the crosslinking monomer concentration as much as possible; and (4) increase the initiator concentration as much as possible.
机译:以反相悬浮聚合法制备的聚丙烯酰胺-丙烯酸盐凝胶珠为模型聚合物,研究吸水聚合物的溶胀机理及聚合参数对溶胀性能的影响。发现单个珠在水中的自由溶胀可被描述为异常扩散。但是,通过聚合物珠床的流体传输(定义为渗透吸收)是扩散吸收和毛细管传输的结合。发现毛细管传输是速率控制步骤,并且被定义为渗透吸收的控制机制。珠粒的粒度以及液体和聚合物基质的性质是决定溶胀性能的三个主要参数。渗透吸收的动力学,即在时间t的吸水量(Q {dollar} sb {lcub} rm t {rcub} {dollar})可以用两个参数来描述:平衡吸水量(Q {dollar} sb {lcub} infty {rcub} {dollar})和特征时间常数({dollar} tausb {lcub} rm d {rcub} {dollar})。为了获得高的吸水率,需要较高的Q {dollar} sb {lcub} infty {rcub} {dollar}和较低的{dollartausb {lcub} rm d {rcub} {dollar}。这两个值主要取决于聚合物基质的化学结构。此外,毛细血管运输也会影响{auusb {lcub} rm d {rcub} {dollar}。考察了聚合参数对吸水性能的影响(即Q {dollar} sb {lcub} infty {rcub} {dollar和Q {dollar} sb {lcub} rm t {rcub} {dollar})。通过改变聚合稳定剂,交联单体和引发剂的浓度,进料单体的比例和中和丙烯酸的碱类型。由于颗粒尺寸的减小,随着稳定剂浓度的增加,Q {dollar} sb {lcub} rm t {rcub} {dollar}的值减小。其他聚合参数导致化学结构的变化。 Q {dollar} sb {lcub} infty {rcub} {dollar}的值随着凝胶珠的交联密度的降低而增加。尽管交联单体通过它们的多官能团在聚合物链之间形成交联,但引发剂和进料单体的比例影响了由链转移至聚合物引起的交联度(定义为自交联)。通过增加交联单体和引发剂浓度可以提高交联度。在丙烯酰胺与丙烯酸盐的摩尔比为50:50时观察到最高的自交联度。可以通过优化交联单体的浓度,增加引发剂的浓度以及减少聚离子与抗衡离子之间的相互作用来降低tausb {lcub} rm d {rcub} {dollar}的值。为了改善吸水动力学,提出以下建议:(1)制备在200 {μm范围内具有窄粒度分布的聚合物珠粒; (2)防止水溶性聚合物的形成; (3)尽可能降低交联单体的浓度; (4)尽可能提高引发剂浓度。

著录项

  • 作者

    Chang, Yin-Shen.;

  • 作者单位

    Lehigh University.;

  • 授予单位 Lehigh University.;
  • 学科 Chemistry Polymer.
  • 学位 Ph.D.
  • 年度 1991
  • 页码 200 p.
  • 总页数 200
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 高分子化学(高聚物);
  • 关键词

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