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聚合物浓度、剪切速率和温度对水凝胶化时间的影响。 Silica-Poly(ethylene-oxide)“摇凝胶”。

The effects of polymer concentration, shear rate and temperature on the gelation time of aqueous Silica-Poly(ethylene-oxide) "Shake-gels".

机构信息

Department of Chemical Engineering, Imperial College London, Prince Consort Road, London SW7 2BB, UK.

Department of Chemical Engineering, Imperial College London, Prince Consort Road, London SW7 2BB, UK.

出版信息

J Colloid Interface Sci. 2018 May 1;517:1-8. doi: 10.1016/j.jcis.2018.01.094. Epub 2018 Jan 31.

Abstract

HYPOTHESIS

Aqueous mixtures of silica and Poly(ethylene-oxide) (PEO) are known as "Shake-gels" due to the formation of reversible gels when subject to an applied force, such as shaking. This shear-thickening effect can be observed using a rheometer, via distinct and abrupt increases in the viscosity of the material. Preliminary experiments qualitatively showed that the time elapsed before this occurs, termed the gelation time, varied depending on the conditions used. This paper reports on a systematic study into the effects of polymer concentration, shear rate and temperature on the gelation time, to quantify any relationships that exist between the variables and develop understanding of the gelation mechanism and kinetics.

EXPERIMENTS

Different constant shear rates were applied to samples at various polymer concentrations and temperatures using a rheometer with concentric cylinder geometry.

FINDINGS

The gelation time varied significantly from several seconds to an hour or more and was exponentially accelerated by shear rate. A peak in gelation time occurred at medium polymer concentrations of 0.35-0.40% (25% silica) and at a temperature about 20 °C. Higher temperatures also exponentially accelerated the gelation time as kinetic effects dominated the thermodynamic and structural resistances to gel formation.

摘要

假设

二氧化硅和聚(氧化乙烯)(PEO)的水混合物由于在施加力(如摇晃)时形成可逆凝胶而被称为“摇凝胶”。这种剪切增稠效应可以使用流变仪观察到,材料的粘度会明显且突然增加。初步实验定性地表明,发生这种情况之前经过的时间,称为凝胶时间,取决于所使用的条件而变化。本文报道了一项系统研究聚合物浓度、剪切速率和温度对凝胶时间的影响,以量化变量之间存在的任何关系,并深入了解凝胶化机制和动力学。

实验

使用具有同心圆筒几何形状的流变仪,在不同的聚合物浓度和温度下向样品施加不同的恒定剪切速率。

发现

凝胶时间变化很大,从几秒钟到一个小时或更长时间不等,并且被剪切速率显著加速。在聚合物浓度为 0.35-0.40%(25%二氧化硅)和温度约 20°C 的中等聚合物浓度下,凝胶时间出现峰值。较高的温度也会使凝胶时间呈指数加速,因为动力学效应主导了对凝胶形成的热力学和结构阻力。

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