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甲基纤维素与表面活性剂相互作用的微量量热法和流变学研究

Micro-DSC and rheological studies of interactions between methylcellulose and surfactants.

作者信息

Li Lin, Liu Erjia, Lim Chun Hoong

机构信息

School of Mechanical and Aerospace Engineering, Nanyang Technological University, 50 Nanyang Avenue, 639798 Singapore.

出版信息

J Phys Chem B. 2007 Jun 14;111(23):6410-6. doi: 10.1021/jp0712957. Epub 2007 May 22.

Abstract

The effects of a cationic surfactant, cetyltrimethylammonium bromide (CTAB), on the gelation of methylcellulose (MC) in aqueous solutions have been investigated by micro differential scanning calorimetry (micro DSC) and rheology. Methylcellulose had a weight average molecular weight of 310,000 and a degree of substitution of 1.8. The concentration of MC was kept at 0.5 wt % (0.016 mM) and 1 wt % (0.032 mM), and the concentration of CTAB in the MC solutions was varied from 0 to 0.6 wt % (16.5 mM). Upon heating, a single endothermic peak, which is due to the hydrophobic association and gelation of MC, shifts to lower temperatures with increasing CTAB for CTAB < or = CMC (0.93 mM or 0.034 wt %), and then it shifts to higher temperatures lineally with CTAB for CTAB > CMC. At the same time, the endothermic enthalpy decreases with increasing CTAB concentration. Even though CTAB shows a significant "salt-in" effect on the gelation of MC, it does not affect the pattern of the sol-gel transition as well as the gel strength of MC. At the highest concentration of CTAB, 0.60 wt %, MC is still able to form a gel. At a given ratio of CTAB/MC, the effect of CTAB on MC becomes stronger when the MC concentration is lower. The results for the MC-CTAB system are compared with an ionic surfactant, SDS and the significant differences in affecting the gelation of MC between two surfactants are recognized.

摘要

通过微量差示扫描量热法(微量DSC)和流变学研究了阳离子表面活性剂十六烷基三甲基溴化铵(CTAB)对甲基纤维素(MC)在水溶液中凝胶化的影响。甲基纤维素的重均分子量为310,000,取代度为1.8。MC的浓度保持在0.5 wt%(0.016 mM)和1 wt%(0.032 mM),MC溶液中CTAB的浓度在0至0.6 wt%(16.5 mM)之间变化。加热时,由于MC的疏水缔合和凝胶化产生的单个吸热峰,对于CTAB≤临界胶束浓度(CMC,0.93 mM或0.034 wt%),随着CTAB浓度增加向较低温度移动,然后对于CTAB>CMC,它随CTAB线性地向较高温度移动。同时,吸热焓随着CTAB浓度增加而降低。尽管CTAB对MC的凝胶化表现出显著的“盐溶”效应,但它不影响MC的溶胶-凝胶转变模式以及凝胶强度。在CTAB的最高浓度0.60 wt%时,MC仍然能够形成凝胶。在给定的CTAB/MC比例下,当MC浓度较低时,CTAB对MC的影响更强。将MC-CTAB体系的结果与离子型表面活性剂十二烷基硫酸钠(SDS)进行了比较,认识到两种表面活性剂在影响MC凝胶化方面的显著差异。

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