Hristea Gabriela, Iordoc Mihai, Culcea Andreea
Environment, Energy & Climate Change Department, National Institute for Research and Development in Electrical Engineering ICPE-CA, Splaiul Unirii 313, 030138 Bucharest, Romania.
Materials (Basel). 2021 Aug 30;14(17):4932. doi: 10.3390/ma14174932.
The relative performance of different porous solids in different applications is highly dependent on the internal pore structure of each material. Highly porous carbon materials can be prepared by evaporative drying and the pyrolysis of resorcinol-formaldehyde gels. By determining the correct synthesis parameters, the pore system of such materials can be reshaped. Depending on some important processing factors such as the dilution ratio or the initial pH of the precursor solution, various porous or non-porous carbon materials can be synthesized. This paper addresses carbon xerogels (CX) designed as a material electrode in capacitive deionization (CDI) systems for water desalination. In this work CX materials were synthesized via poly-condensation reactions of resorcinol with formaldehyde (RF) on a carbon felt sheet followed by pyrolysis. The resulting sheets were used as electrodes to develop a CDI experimental multi-cell laboratory system. The initial pH of the RF solution and the dilution ratio effect on the resulting carbon surface area and structure were analyzed. Surface area measurements using the BET method and an electrochemical capacitance evaluation of the obtained xerogels through electrochemical impedance spectroscopy were also performed. Finally, using our experimental CDI multi-cell laboratory system based on the obtained CX, we discuss the experimental data for the desalination rate as a function of the voltage and salt concentration. As a result, the developed model's efficiency is demonstrated. The main goal of this work was to develop an efficient electrode-based novel carbon that could be commercially competitive, as well as to create guidelines for future desalination research using CX electrode materials.
不同多孔固体在不同应用中的相对性能高度依赖于每种材料的内部孔隙结构。高孔隙率碳材料可通过间苯二酚-甲醛凝胶的蒸发干燥和热解来制备。通过确定正确的合成参数,可以重塑此类材料的孔隙系统。根据一些重要的加工因素,如稀释比或前驱体溶液的初始pH值,可以合成各种多孔或无孔碳材料。本文探讨了设计用于电容去离子(CDI)系统中海水淡化的碳干凝胶(CX)作为材料电极的情况。在这项工作中,CX材料是通过间苯二酚与甲醛(RF)在碳毡片上的缩聚反应,然后进行热解来合成的。所得的片材用作电极,以开发一个CDI实验多单元实验室系统。分析了RF溶液的初始pH值和稀释比对所得碳表面积和结构的影响。还使用BET方法进行了表面积测量,并通过电化学阻抗谱对所得干凝胶进行了电化学电容评估。最后,使用基于所获得的CX的实验性CDI多单元实验室系统,我们讨论了脱盐率作为电压和盐浓度函数的实验数据。结果,证明了所开发模型的效率。这项工作的主要目标是开发一种高效的基于电极的新型碳材料,使其具有商业竞争力,并为未来使用CX电极材料的海水淡化研究制定指导方针。