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In Situ Measurement Methods for the CO

机译:原位测量方法为CO

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摘要

This work presents two novel methods to investigate in situ the carbon dioxide (CO2)-induced gelation of biopolymer-based solutions. The CO2-induced gelation is performed in a viewing cell at room temperature under CO2 pressure (20 to 60 bar), whereby calcium precursors are used as cross-linkers. The novel methods allow the in situ optical observation and evaluation of the gelation process via the change in turbidity due to dissolution of dispersed calcium carbonate (CaCO3) particles and in situ pH measurements. The combination of both methods enables the determination of the gelation direction, gelation rate, and the pH value in spatial and temporal resolution. The optical gelation front and pH front both propagate equally from top to bottom through the sample solutions, indicating a direct link between a decrease in the pH value and the dissolution of the CaCO3 particles. Close-to-vertical movement of both gelation front and pH front suggests almost one dimensional diffusion of CO2 from the contact surface (gel–CO2) to the bottom of the sample. The gelation rate increases with the increase in CO2 pressure. However, the increase in solution viscosity and the formation of a gel layer result in a strong decrease in the gelation rate due to a hindrance of CO2 diffusion. Released carbonate ions from CaCO3 dissolution directly influence the reaction equilibrium between CO2 and water and therefore the change in pH value of the solution. Increasing the CaCO3 concentrations up to the solubility results in lower gelation rates.
机译:本作品呈现了两种新方法来研究原位二氧化碳(CO2) - 诱导基于生物聚合物的溶液的凝胶化。 CO2诱导的凝胶化在CO 2压力(20至60巴)下的室温下在观察细胞中进行,由此钙前体用作交联剂。新方法允许通过浊度导致的分散碳酸钙(CaCO 3)颗粒的溶解和原位pH测量的浊度变化,允许原位光学观察和评估凝胶化过程。两种方法的组合能够确定空间和时间分辨率的凝胶化方向,凝胶率和pH值。光凝胶化前面和pH正面都通过样品溶液从上到下传播,表明在pH值的降低和CaCO 3颗粒的溶解之间的直接链路。两个凝胶化前面和pH正面的近侧垂直运动表明CO2的几乎一维扩散来自接触表面(凝胶-CO2)到样品的底部。随着二氧化碳压力的增加,凝胶化速率增加。然而,由于CO 2扩散的阻断,溶液粘度的增加和凝胶层的形成导致凝胶化速率的强烈降低。从CaCO 3溶解中释放的碳酸盐离子直接影响CO 2和水之间的反应平衡,因此溶液的pH值变化。将CaCO 3浓度增加到溶解度导致较低的凝胶化速率。

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