Electronic Waste-to-Catalyst Upcycling: Selective Lignin C–O Bond Hydrogenolysis and RCF over a Cu–Iron Oxide/P-Doped Carbon Catalyst

IF 6.3 Q1 ENGINEERING, ENVIRONMENTAL
ACS ES&T engineering Pub Date : 2026-09-11 Epub Date: 2026-07-21 DOI:10.1021/acsestengg.6c00534
Arzoo Chauhan, Sonu Bhandari, Rajat Ghalta, Rajaram Bal, Rajendra Srivastava
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引用次数: 0

Abstract

The development of sustainable catalysts from secondary waste resources provides an attractive strategy for addressing both electronic-waste management and biomass valorization challenges. In this work, a multifunctional heterogeneous catalyst (ML@ATP1/CP2-60) was constructed by integrating copper recovered from a discarded motherboard, toner powder-derived iron oxide, and phosphorus-doped carbon derived from chitosan as a heteroatom-engineered support. Comprehensive structural and surface characterization using XRD, Raman spectroscopy, XPS, HR-TEM, EPR, and temperature-programmed desorption analyses confirmed the formation of mixed-valence Cu species anchored on a defect-rich spinel iron oxide framework with interfacial acidic sites associated with iron oxide and P–O functionalities. The catalyst exhibited excellent activity and selectivity for the hydrogenolysis of benzyl phenyl ether, achieving complete conversion with exclusive formation of phenol and toluene via selective cleavage of the benzylic C(sp3)–O bond without aromatic ring hydrogenation. Mechanistic investigations, including selective poisoning experiments, revealed a cooperative dual-site pathway involving Cu-mediated hydrogen activation and adjacent acidic centers responsible for ether bond polarization. Importantly, the catalyst demonstrated effective performance in the reductive catalytic fractionation of wheat straw, affording aromatic monomers with molecular-weight distributions comparable to those obtained using conventional 5 wt % Ru/C while suppressing deep aromatic hydrogenation. CHEM21 green metrics analysis confirms the near-ideal intrinsic reaction efficiency of the protocol (AE ≈ 100%, RME = 97.6%), with solvent usage identified as the primary contributor to process-level mass intensity. These results highlight a strategy for transforming multiple waste streams into efficient catalytic platforms for selective lignin valorization.

电子废弃物到催化剂的升级回收:选择木质素C-O键氢解和在铜铁氧化物/ p掺杂碳催化剂上的RCF
从二次废物资源中开发可持续催化剂为解决电子废物管理和生物质增值挑战提供了一种有吸引力的策略。在这项工作中,通过整合从废弃主板中回收的铜,碳粉衍生的氧化铁和壳聚糖衍生的磷掺杂碳作为杂原子工程载体,构建了多功能异相催化剂(ML@ATP1/CP2-60)。利用XRD、拉曼光谱、XPS、HR-TEM、EPR和程序升温解吸分析等综合结构和表面表征证实,在富含缺陷的尖晶石氧化铁框架上形成了混合价铜,其界面酸性位点与氧化铁和P-O官能团相关。该催化剂对苯基苯醚的氢解反应表现出良好的活性和选择性,通过选择性裂解苯基C(sp3) -O键,实现了苯酚和甲苯的完全转化,而没有芳环加氢。机械研究,包括选择性中毒实验,揭示了cu介导的氢活化和相邻的酸性中心负责醚键极化的合作双位点途径。重要的是,该催化剂在麦秆的还原催化分馏中表现出了有效的性能,提供了与使用常规5 wt % Ru/C获得的分子量分布相当的芳香单体,同时抑制了深层芳香族氢化。CHEM21绿色指标分析证实了该方案接近理想的固有反应效率(AE≈100%,RME = 97.6%),溶剂使用量被确定为工艺级质量强度的主要贡献者。这些结果强调了将多种废物流转化为有效的选择性木质素化催化平台的策略。
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来源期刊
ACS ES&T engineering
ACS ES&T engineering ENGINEERING, ENVIRONMENTAL-
CiteScore
8.50
自引率
0.00%
发文量
0
期刊介绍: ACS ES&T Engineering publishes impactful research and review articles across all realms of environmental technology and engineering, employing a rigorous peer-review process. As a specialized journal, it aims to provide an international platform for research and innovation, inviting contributions on materials technologies, processes, data analytics, and engineering systems that can effectively manage, protect, and remediate air, water, and soil quality, as well as treat wastes and recover resources. The journal encourages research that supports informed decision-making within complex engineered systems and is grounded in mechanistic science and analytics, describing intricate environmental engineering systems. It considers papers presenting novel advancements, spanning from laboratory discovery to field-based application. However, case or demonstration studies lacking significant scientific advancements and technological innovations are not within its scope. Contributions containing experimental and/or theoretical methods, rooted in engineering principles and integrated with knowledge from other disciplines, are welcomed.
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