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Functionalized graphene oxide as an efficient adsorbent for CO2 capture and support for heterogeneous catalysis

机译:功能化的氧化石墨烯可有效捕获CO2,并支持多相催化

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We have designed new imine-functionalized graphene oxide (IFGO) through post synthetic modifications involving co-condensation of 3-aminopropyltriethoxysilane with graphene oxide basal plane containing hydroxyl and epoxy functional groups, followed by Schiff base condensation reaction with 2,6-diformyl-4-methylphenol and impregnation of copper(II) to it through covalent attachment (Cu-IFGO). Powder Xray diffraction, N-2 sorption analysis, FT-IR, HR-TEM, FE-SEM and TGA/DTA analysis are employed to characterize the materials. The IFGO material exhibits good CO2 storage capacity of 8.10 mmol g(-1) (35.64 wt%) and 2.10 mmol g(-1) (9.24 wt%) at 273 K and 298 K temperature, respectively, up to 3 bar pressure, suggesting its potential application in environmental clean-up. Also, Cu-IFGO showed high catalytic activity in microwave-assisted one-pot three-component C-S coupling reactions for a diverse range of aryl halides with thiourea and benzyl bromide in aqueous medium to obtain aryl thioether products (maximum yield 86%), which are derivatives of natural products. Moreover, having imine and hydroxyl groups in functionalized graphene oxide, the grafted Cu(II) chelated at the graphene oxide surface so strongly that it could not be leached out from the material during the course of the coupling reaction. Thus, it displayed very small decrease in product yield up to the sixth reaction cycle suggesting a sustainable future of this Cu(II)-grafted catalyst.
机译:我们通过后合成修饰设计了新的亚胺官能化氧化石墨烯(IFGO),该合成涉及将3-氨基丙基三乙氧基硅烷与含有羟基和环氧基官能团的氧化石墨烯基面共缩合,然后通过席夫碱与2,6-二甲酰基-4缩合反应-甲基苯酚和通过共价键合(Cu-IFGO)将铜(II)浸入其中。用粉末X射线衍射,N-2吸附分析,FT-IR,HR-TEM,FE-SEM和TGA / DTA分析来表征材料。 IFGO材料在273 K和298 K的温度下(最高3 bar压力)分别具有8.10 mmol g(-1)(35.64 wt%)和2.10 mmol g(-1)(9.24 wt%)的良好CO2储存能力,说明其在环境清洁中的潜在应用。同样,Cu-IFGO在微波辅助的一锅三组分CS偶联反应中表现出高催化活性,该反应是在水性介质中对各种范围的芳基卤化物与硫脲和苄基溴的反应,以获得芳基硫醚产物(最大收率86%),是天然产物的衍生物。此外,由于官能化的氧化石墨烯中具有亚胺和羟基,接枝的Cu(II)在氧化石墨烯表面上强烈螯合,以致在偶联反应过程中不能从材料中浸出。因此,它显示出直至第六反应循环的产物收率的非常小的降低,表明该Cu(II)接枝的催化剂的可持续未来。

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