生物炭
催化作用
草酸
热解
生物量(生态学)
化学
水溶液
污染物
降级(电信)
化学工程
碳纤维
活性炭
人口
核化学
环境化学
材料科学
无机化学
有机化学
吸附
复合材料
工程类
电信
海洋学
人口学
社会学
复合数
计算机科学
地质学
作者
Anton López‐Francés,Belén Ferrer,Herme G. Baldoví,Amarajothi Dhakshinamoorthy,Sergio Navalón
标识
DOI:10.1002/adsu.202500108
摘要
Abstract Valorization of biomass wastes into carbon‐based catalysts for water treatment is a clear paradigm of sustainability.Herein, we investigate an unprecedented transformation of pine needle waste biomass into activated biochars (PNCs) as ozonation catalysts for aqueous oxalic acid degradation. The physico‐chemical and textural properties of PNCs are tailored by combining pyrolysis temperatures up to 1200 °C and the use or not of KOH or K 2 CO 3 as activating agents. The physico‐chemical and structural properties of these carbocatalysts are correlated with their catalytic activities. The PNC catalyst pyrolized at 1200 °C for 4 h using K 2 CO 3 (PNC1200‐4K 2 CO 3 ) provides a complete pollutant degradation after 150 min, while PNC catalyst pyrolized at 1200 °C for 4 h without activation requires 300 min. PNC1200‐4K 2 CO 3 performance compares favorably with previous reports. The superior catalytic activity of this reusable catalyst is attributed to its highest population of π‐extended aromatic domains as active sites together with high porosity. The catalytic formation of 1 O 2 , HO . and HOO . radicals are supported by electron paramagnetic resonance measurements and selective quenching experiments. Unlike most of the previous analogous reports, herein, we demonstrate that 1 O 2 in the presence of PNC1200‐4K 2 CO 3 can degrade oxalic acid even in the presence of common radical scavengers.
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