利用NiCo-LDH@NiC2O4/NF阳极†对褐煤碱溶性衍生物进行电氧化升级清洁生产黄腐酸

IF 9.2 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Green Chemistry Pub Date : 2024-11-22 DOI:10.1039/d4gc04899g
Haiyan Ge , Jining Zhou , Zhicai Wang , Xiaobiao Yan , Chunxiu Pan , Zhiping Lei , Zhanku Li , Jingchong Yan , Weidong Zhang , Shibiao Ren , Shigang Kang , Hengfu Shui
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引用次数: 0

摘要

利用可再生电力和具有成本效益的碳资源促进水电解制氢是一种有前途和有效的能量储存和转换技术。阳极氧化通过选择性氧化可以产生有价值的化学品,提供了一个更清洁的替代化学氧化。为了改善褐煤碱溶性衍生物(ASD),本研究采用连续电化学沉积方法开发了一种新型NiCo-LDH@NiC2O4/NF电极。当电极用作阳极时,在1.0 M KOH溶液中,在1.5 V恒定电位(相对于RHE)下,该电极在1小时内实现了85%的桃酸(MA)转化为苯甲酸,选择性超过95%。同时,75%的ASD成功升级为黄腐酸(FA),选择性超过90%。与NiCo-LDH/NF和NiC2O4/NF电极相比,NiCo-LDH@NiC2O4/NF电极表现出更好的电催化活性和稳定性。NiCo-LDH为主要活性相,而NiC2O4的预沉积显著提高了其催化活性和稳定性。MA的降解涉及由于OH活化导致的ArC(OH) -C键的裂解,而ASD解聚成FA主要归因于芳香核的开环氧化。本工作提供了一种绿色高效的电氧化策略,结合一种新型非贵金属电催化剂,生产煤基芳香羧酸,标志着向更可持续和环境友好的煤基化学制造迈出了重要的一步。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Electro-oxidative upgrading of lignite alkali-soluble derivatives for clean production of fulvic acids using NiCo-LDH@NiC2O4/NF anode†

Electro-oxidative upgrading of lignite alkali-soluble derivatives for clean production of fulvic acids using NiCo-LDH@NiC2O4/NF anode†
Utilizing renewable electricity and cost-effective carbon resources to facilitate water electrolysis for hydrogen production represents a promising and efficient technology for energy storage and conversion. Anode valorization via selective oxidation can produce valuable chemicals, offering a cleaner alternative to chemical oxidation. In this study, to upgrade lignite alkali-soluble derivatives (ASD), a novel NiCo-LDH@NiC2O4/NF electrode was developed using a continuous electrochemical deposition method. When employed as the anode, this electrode achieved an 85% conversion of mandelic acid (MA) to benzoic acid with over 95% selectivity at a constant potential of 1.5 V (vs. RHE) in a 1.0 M KOH solution over 1 h. Concurrently, 75% of ASD was successfully upgraded to fulvic acid (FA) with a selectivity exceeding 90%. Compared to NiCo-LDH/NF and NiC2O4/NF electrodes, the NiCo-LDH@NiC2O4/NF demonstrated superior electro-catalytic activity and stability. NiCo-LDH is the main active phase, while the pre-deposited NiC2O4 significantly enhances both its catalytic activity and stability. The degradation of MA involves the cleavage of the ArC(OH)–C bond due to OH activation, whereas the depolymerization of ASD into FA is primarily attributed to the ring-opening oxidation of aromatic nuclei. The present work provides a green and efficient electro-oxidation strategy, coupled with a novel non-precious metal electrocatalyst, to produce coal-based aromatic carboxylic acids, marking a significant step towards more sustainable and environmentally friendly coal-based chemical manufacturing.
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来源期刊
Green Chemistry
Green Chemistry 化学-化学综合
CiteScore
16.10
自引率
7.10%
发文量
677
审稿时长
1.4 months
期刊介绍: Green Chemistry is a journal that provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998), which defines green chemistry as the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry aims to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. The journal welcomes submissions on all aspects of research relating to this endeavor and publishes original and significant cutting-edge research that is likely to be of wide general appeal. For a work to be published, it must present a significant advance in green chemistry, including a comparison with existing methods and a demonstration of advantages over those methods.
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