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The inhibitory effect of graphene oxide on photocatalytic hydrogenation from organic fatty acids

机译:石墨烯氧化的抑制作用从有机光催化氢化脂肪酸

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摘要

Two catalysts, carbon doped TiO2 (C-TiO2) and C-TiO2 conjugated with reduced graphene oxide (rGO)-C-TiO2/rGO were synthesized and compared with respect to the photocatalytic hydrogen (H-2) production using three organic fatty acids (OFAs) as electron donors under visible light irradiation. Our results show that the hybridization between C-TiO2 and rGO did not subtaintially improve the production of H-2 but instead elicited inhibitory effects compared to C-TiO2. For instance, the specific H-2 production on C-TiO2 was 214 and 336 mu mol.h(-1).g(-1) for acetic and propionic acids, respectively, whereas C-TiO2/rGO only achieved 155 and 161 mu mol.h(-1).g(-1), respectively. With butyric and lactic acids as electron donors, C-TiO2 and C-TiO2/rGO led to almost the same H-2 production rates (233 and 155 mu mol.h(-1).g(-1), respectively). The inhibitory effect of rGO on photocatalytic activity could be due to the potential deposition of OFAs on graphene sheets that may reduce the mobility and accessibility of OFAs toward catalytic reactions with C-TiO2. The electron spin resonance spectrometry (ESR) tests revealed that O-2(center dot-) and CH3 center dot were the major radicals responsible for OFA degradation. Moreover, the produced concentration of CH3 center dot was consistently higher in C-TiO2 suspension than that in C-TiO2/rGO suspension. The estimated aqueous/solid mass transfer rate constant (s(-1)) was lower on the catalyst surface of C-TiO2/rGO than C-TiO2. Consequently, the decoration of rGO sheets on C-TiO2 may not always promote photocatalytic H-2 production especially when using OFAs as electron donors. The results demonstrated hereby aim to provide new evidence on potential drawbacks of graphene-based photocatalysis. (c) 2018 American Institute of Chemical Engineers Environ Prog, 38: 410-416, 2019
机译:两个催化剂,碳掺杂二氧化钛(C-TiO2)和与石墨烯氧化物减少C-TiO2共轭(rGO) -C-TiO2 / rGO合成和比较关于光催化氢气(h2)生产使用三个有机脂肪酸(所谓)作为电子给体下可见光辐照。杂交C-TiO2和rGO之间没有subtaintially提高2的生产而引起的抑制效果相比C-TiO2。C-TiO2是214和336亩mol.h (1) .g (1)乙酸和丙酸,分别,而C-TiO2 / rGO只达到155和161亩mol.h (1) .g(分别为1)。乳酸酸作为电子给体,C-TiO2和C-TiO2 / rGO导致2生产几乎相同率(233和155亩mol.h (1) .g (1),分别)。光催化活性可能是由于潜在的,所谓沉积在石墨烯表这可能减少的流动性和可访问性所谓对与C-TiO2催化反应。电子自旋共振谱(ESR)测试显示0 2点(中心)和CH3中心点的自由基主要负责吗退化。甲基中心圆点一直较高比C-TiO2 C-TiO2暂停/ rGO悬架。传输速率常数(s(1))是较低的催化剂的表面比C-TiO2 C-TiO2 / rGO。因此,rGO表上的装饰C-TiO2可能并不总是促进光催化2尤其是当使用,所谓电子生产捐助者。提供新证据的潜在缺陷石墨烯光催化。化学工程师学会环境掠夺,38:410-416, 2019

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