检索结果-南通市图书馆

Unveiling the secondary pollution in the catalytic elimination of chlorinated organics: The formation of dioxins

Chinese Chemical Letters 2020年第6期31卷 1410-1414页

作者： Jiajia Liu Xiaoxia Dai Zhongbiao Wu Xiaole Weng Key Laboratory of Environment Remediation and Ecological Health Ministry of EducationCollege of Environmental and Resource SciencesZhejiang Universityand Zhejiang Provincial Engineering Research Center of Industrial Boiler&Furnace Flue Gas Pollution ControlHangzhou 310058China

Since the discovery of polychlorinated dibenzo-p-dioxins and dibenzofurans(PCDD/Fs)in the process of municipal solid waste incineration(MSWI),a large number of researches have been conducted to reveal their formation mechanisms and emission characteristics.As one of national priority control pollutants,chlorinated organics are inclined to transfer into PCDD/Fs in the heterogeneously catalyzed process,which has been considered to be one of great challenges in environmental catalysis.However,so far direct evidences to support such a conversion process are insufficient,and the reaction mechanisms are lack of exploration.This study investigated the catalytic elimination of chlorobenzene(CBz)over a range of industrially applied active species including Pt,Ru,V,Ce and Mn oxides,and explored their reaction byproducts,chlorine adsorption/desorption behaviors and PCDD/F formations.We found that all of these species could generate the PCDD/Fs,amongst which,Mn species were the most active for PCDD/F formation.Approximately 140 ng I-TEQg-1 PCDD/Fs were detected on the Mn-CNT surface after ageing at250℃for 30 h.Even using the dichloromethane(DCM)as a precursor,significant PCDD/Fs were still detected.The Ru and V species were shown to generate much less polychlorinated byproducts and PCDD/Fs,owning to their sufficiently high abilities in Cl desorption,which were through the semi-Deacon and Br(?)nsted H reactions,respectively.

关键词： VOCs oxidation chlorinated organics Secondary pollution Dioxin Electrophilic chlorination Environmental catalysis

来源：

维普期刊数据库

同方期刊数据库评论

在线全文

学校读者我要写书评

暂无评论

Catalytic destruction of chlorobenzene over K-OMS-2: Inhibition of high toxic byproducts via phosphate modification

引用

Journal of Environmental Sciences 2023年第5期127卷 844-854页

作者： Yunpeng Long Jiajia Liu Meiling Chen Renna Li Xiaole Weng Zhongbiao Wu Key Laboratory of Environment Remediation and Ecological Health Ministry of EducationCollege of Environmental and Resource SciencesZhejiang UniversityHangzhou 310058China Zhejiang Provincial Engineering Research Center of Industrial Boiler and Furnace Flue Gas Pollution Control Zhejiang University-Hangzhou Global Scientific and Technological Innovation CenterHangzhou 311200China

In the process of catalytic destruction of chlorinated volatile organic compounds(CVOCs),the catalyst is prone to chlorine poisoning and produce polychlorinated byproducts with high toxicity and persistence,bringing great risk to atmospheric environment and human health.To solve these problems,this work applied phosphate to modify K-OMS-2 catalysts.The physicochemical properties of catalysts were determined by using X-ray powder diffraction(XRD),scanning electron microscope(SEM),X-ray photoelectron spectroscopy(XPS),hydrogen temperature programmed reduction(H_(2)-TPR),pyridine adsorption Fouriertransform infrared(Py-IR)and water temperature programmed desorption(H_(2)O-TPD),and chlorobenzene was selected as a model pollutant to explore the catalytic performance and byproduct inhibition function of phosphating.Experimental results revealed that 1 wt.%phosphate modification yielded the best catalytic activity for chlorobenzene destruction,with the 90%conversion(T90)at approximately 247℃.The phosphating significantly decreased the types and yields of polychlorinated byproducts in effluent.After phosphating,we observed significant hydroxyl groups on catalyst surface,and the active centerwas transformed into Mn(IV)-O…H,which promoted the formation of HCl,and enhanced the dechlorination process.Furthermore,the enriched Lewis acid sites by phosphating profoundly enhanced the deep oxidation ability of the catalyst,which promoted a rapid oxidation of reaction intermediates,so as to reduce byproducts generation.This study provided an effective strategy for inhibiting the toxic byproducts for the catalytic destruction of chlorinated organics.

关键词： Catalytic destruction chlorinated organics Phosphoric modification K-OMS-2 Secondary pollution

来源：

维普期刊数据库

同方期刊数据库评论

在线全文

学校读者我要写书评

暂无评论

Unveiling the importance of reactant mass transfer in environmental catalysis:Taking catalytic chlorobenzene oxidation as an example

引用

Chinese Chemical Letters 2021年第3期32卷 1206-1209页

作者： Kexin Cao Xiaoxia Dai Zhongbiao Wu Xiaole Weng Key Laboratory of Environment Remediation and Ecological Health Ministry of EducationCollege of Environmental and Resource SciencesZhejiang UniversityHangzhou 310058China Zhejiang Provincial Engineering Research Center of Industrial Boiler&Furnace Flue Gas Pollution Control Hangzhou 310058China

To date,investigations onto the regulation of reactants mass transfer has been paid much less attention in environmental catalysis.Herein,we demonstrated that by rationally designing the adsorption sites of multi-reactants,the pollutant destruction efficiency,product selectivity,reaction stability and secondary pollution have been all affected in the catalytic chlorobenzene oxidation(CBCO).Experimental results revealed that the co-adsorption of chlo robenzene(CB)and gaseous O_(2)at the oxygen vacancies of CeO_(2)led to remarkably high CO_(2)generation,owning to their short mass transfer distance on the catalyst surface,while their separated adsorptions at Bronsted HZSM-5 and CeO_(2)vacancies resulted in a much lower CO_(2)generation,and produced significant polychlorinated byproducts in the off-gas.Howeve r,this separated adsorption model yielded superior long-term stability for the CeO_(2)/HZSM-5 catalyst,owning to the protection of CeO_(2)oxygen vacancies from Cl poisoning by the preferential adsorption of CB on the Bronsted acidic sites.This work unveils that design of environmental catalysts needs to consider both of the catalyst intrinsic property and reactant mass transfer;investigations of the latter could pave a new way for the development of highly efficient catalysts towards environmental pollution control.

关键词： VOCs oxidation chlorinated organics Reactant mass transfer Secondary pollution Catalyst design Environmental catalysis

来源：

维普期刊数据库

同方期刊数据库评论

在线全文

学校读者我要写书评

暂无评论

欢迎您,

建议与咨询留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

时间限定

文献类型

馆藏选择

核心期刊

语言

文献类型

帮助

文字说明：

检索规则说明：

检索范例：

分类表

所选分类

限定检索结果

文献类型

馆藏范围

日期分布

学科分类号

主题

机构

作者

语言

在线全文

在线全文

在线全文

请选择保存的检索档案：

请选择收藏分类：

通借通还

欢迎您,

建议与咨询 留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

时间限定

文献类型

馆藏选择

核心期刊

语言

文献类型

帮助

文字说明：

检索规则说明：

检索范例：

分类表

所选分类

限定检索结果

文献类型

馆藏范围

日期分布

学科分类号

主题

机构

作者

语言

在线全文

在线全文

在线全文

请选择保存的检索档案： 新增检索档案 确定 取消

请选择收藏分类： 新增自定义分类 确定 取消

通借通还

建议与咨询留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

请选择保存的检索档案：

请选择收藏分类：