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Carbon Materials from Lignin and Sodium Lignosulfonate via Diisocyanate Cross-Linking and Subsequent Carbonization

机译:木质素和木质素磺酸钠通过二异氰酸酯交联和后续碳化得到的碳材料

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Applications for lignin and lignosulfonates are limited today due to the undefined structure and varying properties of the substance. However, lignin, as the second most abundant bio-resource besides cellulose and the bio-resource with one of the highest natural carbon contents, has the potential to act as a precursor for carbon materials. In this study we have applied a Kraft lignin and a sodium lignosulfonate with the cross-linker toluene-2,4-diisocyanate. The reaction mixture was molded to form small cylindrical shaped paddings. Cross-linked lignin-polyurethane and lignosulfonate-polyurethane networks were analyzed via elemental analysis and thermogravimetric analysis and finally carbonized. The carbon material was analyzed for its BET surface area and its surface structure via scanning electron microscopy. Surface areas between 70 and 80 m²·g−1 could be reached. Moreover, the material was tested for its adsorption potential of crude oil from water and could take up to twice its own weight. For better understanding of the core chemistry of the cross-linking reaction, we have studied the reaction with model substances to define the reactive groups and the influence of sulfonate groups in the cross-linking reaction of lignin and lignosulfonates with toluene-2,4-diisocyanate.
机译:由于木质素和木质素磺酸盐的不确定结构和变化的特性,今天的应用受到限制。然而,木质素作为除了纤维素和自然碳含量最高的生物资源之外的第二大生物资源,具有作为碳材料前体的潜力。在这项研究中,我们应用了硫酸盐木质素和木质素磺酸钠以及交联剂甲苯-2,4-二异氰酸酯。将反应混合物模制成小的圆柱形填料。通过元素分析和热重分析对交联的木质素-聚氨酯和木质素磺酸盐-聚氨酯网络进行分析,最后碳化。通过扫描电子显微镜分析碳材料的BET表面积和表面结构。表面积可达到70至80m²·g -1 。此外,还对该材料进行了对原油从水中的吸附潜力的测试,该材料最多可吸收其自身重量的两倍。为了更好地理解交联反应的核心化学过程,我们研究了与模型物质的反应,以确定木质素和木质素磺酸盐与甲苯-2,4-的交联反应中的反应性基团和磺酸盐基团的影响。二异氰酸酯。

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