Silioc Christelle, Maleki Atoosa, Zhu Kaizheng, Kjøniksen Anna-Lena, Nyström Bo
Department of Chemistry, University of Oslo, P.O. Box 1033, Blindern, N-0315 Oslo, Norway.
Biomacromolecules. 2007 Feb;8(2):719-28. doi: 10.1021/bm061090o.
Rheological characteristics during chemical gelation with the cross-linker ethylene glycol diglycidyl ether (EGDE) of semidilute aqueous solutions of hydroxyethylcellulose (HEC) and of two hydrophobically modified analogues (HM-1-HEC and HM-2-HEC) are reported. In addition, rheological features of gelling samples (dextran and its hydrophobically modified analogue (HM-dextran)) of a different structure have been examined. Some swelling experiments on these gels in the postgel region are also reported. The gelation time of the hydroxyethylcellulose systems decreased with increasing cross-linker concentration, and incorporation of hydrophobic units of HEC resulted in a slower gelation. The time of gelation for the dextran system was only slightly affected by the incorporation of hydrophobic groups (HM-dextran). At the gel point, a power law frequency dependence of the dynamic storage modulus (G' proportional to omegan') and loss modulus (G'' proportional to omegan'') was observed for all gelling systems with n' = n'' = n. The attachment of hydrophobic moieties on the dextran chains had virtually no impact on the value of n (n = 0.77), and the percolation model describes the incipient dextran gels. By increasing the number of hydrophobic groups of the HEC polymer, the value of n for the corresponding incipient gel drops significantly, and the value of the gel strength parameter increases strongly. Incorporation of hydrophobic units in the HEC chains promotes the formation of stronger incipient gels because of the contribution from the hydrophobic association effect. The frequency dependence of the complex viscosity reveals that all the investigated gels become more solidlike in the postgel domain. Far into the postgel region, the hydrophobicity of HEC plays a minor role for the strength of the gel network, whereas the values of the complex viscosity are significantly higher for HM-dextran than for the corresponding dextran gel. The swelling experiments on HEC, HM-1-HEC, and HM-2-HEC systems disclose that the degree of swelling of the postgels in water is quite different, depending on the relative distance from the gel point at which the cross-linker reaction is quenched. At a given distance from the gel point, the swelling of the HEC gel is less pronounced than for the corresponding hydrophobically modified samples. At this stage, the swelling of the HM-dextran gel is stronger than for the dextran gel.
本文报道了羟乙基纤维素(HEC)及其两种疏水改性类似物(HM-1-HEC和HM-2-HEC)的半稀释水溶液与交联剂乙二醇二缩水甘油醚(EGDE)发生化学凝胶化过程中的流变特性。此外,还研究了不同结构的凝胶化样品(右旋糖酐及其疏水改性类似物(HM-右旋糖酐))的流变特性。同时也报道了这些凝胶在凝胶后区域的一些溶胀实验。羟乙基纤维素体系的凝胶化时间随交联剂浓度的增加而缩短,且引入HEC的疏水单元会导致凝胶化速度减慢。右旋糖酐体系的凝胶化时间仅受疏水基团(HM-右旋糖酐)引入的轻微影响。在凝胶点,所有凝胶化体系的动态储能模量(G'与ω^n'成正比)和损耗模量(G''与ω^n''成正比)均呈现幂律频率依赖性,其中n' = n'' = n。右旋糖酐链上疏水部分的连接对n值(n = 0.77)几乎没有影响,且渗流模型可描述初始的右旋糖酐凝胶。通过增加HEC聚合物的疏水基团数量,相应初始凝胶的n值显著下降,而凝胶强度参数值大幅增加。由于疏水缔合效应的作用,在HEC链中引入疏水单元促进了更强初始凝胶的形成。复数粘度的频率依赖性表明,所有研究的凝胶在凝胶后区域都变得更像固体。在深入凝胶后区域时,HEC的疏水性对凝胶网络强度的作用较小,而HM-右旋糖酐的复数粘度值明显高于相应的右旋糖酐凝胶。对HEC、HM-1-HEC和HM-2-HEC体系的溶胀实验表明,凝胶后在水中的溶胀程度差异很大,这取决于交联剂反应猝灭时距凝胶点的相对距离。在距凝胶点给定距离处,HEC凝胶的溶胀不如相应的疏水改性样品明显。在此阶段,HM-右旋糖酐凝胶的溶胀比右旋糖酐凝胶更强。