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Biocatalytic enhancement of laccase immobilized on ZnFe_(2)O_(4) nanoparticles and its application for degradation of textile dyes
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作者 Yuhang Wei Qingpeng Zhu +3 位作者 Weiwei Xie Xinyue Wang Song Li Zhiming Chen 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2024年第4期216-223,共8页
Efficient and convenient treatment of industrial dyeing wastewater is of great significance to guarantee human and animal health.This work presented the enhanced catalytic activity at pH 3.0 of laccase immobilized on ... Efficient and convenient treatment of industrial dyeing wastewater is of great significance to guarantee human and animal health.This work presented the enhanced catalytic activity at pH 3.0 of laccase immobilized on amino-functionalized ZnFe_(2)O_(4) nanoparticles(ZnFe_(2)O_(4)-laccase)and its application for the degradation of textile dyes.Due to the existence of a large number of oxygen vacancies on the surface of the ZnFe_(2)O_(4) nanoparticles,negative ions accumulated on the magnetic carriers,which resulted in a harsh optimal pH value of the ZnFe_(2)O_(4)-laccase.Laccase activity assays revealed that the ZnFe_(2)O_(4)-laccase possessed superior pH and thermal stabilities,excellent reusability,and noticeable organic solvent tolerance.Meanwhile,the ZnFe_(2)O_(4) laccase presented efficient and sustainable degradation of high concentrations of textile dyes.The initial decoloration efficiencies of malachite green(MG),brilliant green(BG),azophloxine,crystal violet(CV),reactive blue 19(RB19),and procion red MX-5B were approximately 99.1%,95.0%,93.3%,87.4%,86.1%,and 85.3%,respectively.After 10 consecutive reuses,the degradation rates of the textile dyes still maintained about 98.2%,92.5%,83.2%,81.5%,79.8%and 65.9%,respectively.The excellent dye degradation properties indicate that the ZnFe_(2)O_(4)-laccase has a technical application in high concentrations of dyestuff treatment. 展开更多
关键词 ZnFe_(2)O_(4)-laccase catalytic activity Stability and reusability degradation of textile dye
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Photocatalytic Degradation of Water-Soluble Dyes by LaCoO_3 被引量:9
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作者 傅希贤 杨秋华 +2 位作者 王俊珍 白树林 桑丽霞 《Journal of Rare Earths》 SCIE EI CAS CSCD 2003年第4期424-426,共3页
Perovskite type oxides LaCoO 3 was prepared by citrate method in granula of 20~30 nm. Using a fluorescent Hg lamp or sunlight as irradiator, the degradation experiments of various water soluble dyes were carried o... Perovskite type oxides LaCoO 3 was prepared by citrate method in granula of 20~30 nm. Using a fluorescent Hg lamp or sunlight as irradiator, the degradation experiments of various water soluble dyes were carried out in the suspension system of LaCoO 3. The results show that the perovskite type oxide LaCoO 3 has good photocatalytic activity. With the study of X ray photoelectron spectroscopy and photoacoustic spectra, its photocatalytic activity is mainly related with the factors such as the d electron structure of ion Co 3+ , Co O binding energy and adsorbed oxygen on the surface etc. 展开更多
关键词 catalytic chemistry water soluble dye perovskite type LaCoO 3 photocatalytic degradation rare earths
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Catalytic degradation of methylene blue by Fenton like system: model to the environmental reaction 被引量:4
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作者 Sanjay R Thakare 《Journal of Environmental Sciences》 SCIE EI CAS CSCD 2004年第2期285-287,共3页
To develop more efficient chemical methods for the demineralization of organic pollutants from water bodies, which one was also mimic to the nature, a degradation of methylene blue by Fe(Ⅲ) and H 2O 2 in the absenc... To develop more efficient chemical methods for the demineralization of organic pollutants from water bodies, which one was also mimic to the nature, a degradation of methylene blue by Fe(Ⅲ) and H 2O 2 in the absence of light instead of Fe(Ⅱ) and H 2O 2 was studied. Results showed that use of Fe (Ⅲ) is more promising than Fe(Ⅱ). The present study reflects that Fenton reaction is more efficient, in the presence of a small amount of salicylic acid is added which is a one of the priority pollutant. 展开更多
关键词 advanced oxidation technology Fenton reaction iron(Ⅲ) catalytic degradation environmental application
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Science Letters:Structure relationship of nitrochlorobenzene catalytic degradation process in water over palladium-iron bimetallic catalyst 被引量:1
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作者 NIU Shao-feng ZHOU Hong-yi +2 位作者 AO Xu-ping XU Xin-hua LOU Zhang-hua 《Journal of Zhejiang University-Science B(Biomedicine & Biotechnology)》 SCIE CAS CSCD 2006年第7期548-552,共5页
Two isomers of nitrochlorobenzene (o-, and p-NCB) were treated by a Pd/Fe catalyst in aqueous solutions through catalytic amination and dechlorination. Nitrochlorobenzenes are rapidly converted to form chloroanilines ... Two isomers of nitrochlorobenzene (o-, and p-NCB) were treated by a Pd/Fe catalyst in aqueous solutions through catalytic amination and dechlorination. Nitrochlorobenzenes are rapidly converted to form chloroanilines (CAN) first through an amination process, and then rapidly dechlorinated to become aniline (AN) and Cl?, without the involvement of any other inter-mediate reaction products. The amination and dechlorination reaction are believed to take place predominantly on the surface site of the Pd/Fe catalysts. The dechlorination rate of the reductive degradation of the two isomers of nitrochlorobenzene (o-, and p-NCB) in the presence of Pd/Fe as a catalyst was measured experimentally. In all cases, the reaction rate constants were found to increase with the decrease in the Gibbs free energy (correlation with the activation energy) of NCBs formation; the activation energy of each dechlorination reaction was measured to be 95.83 and 77.05 kJ/mol, respectively for o- and p-NCB. The results demonstrated that p-NCBs were reduced more easily than o-NCBs. 展开更多
关键词 催化解聚 NCBs 结构 Pd/Fe催化剂 硝基氯苯
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A New Property of Conjugated Polymer PFP: Catalytic Degradation of Methylene Blue Aqueous Solution
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作者 Bi Tao SU Shi Xiong SHE Shi Xiong MIN Zhan Ying MA 《Chinese Chemical Letters》 SCIE CAS CSCD 2005年第10期1361-1363,共3页
A new property of conjugated polymer poly(furancarbinol-co-phenol)(PFP) was studied. The target copolymer was used as a catalyst after proper heating treatment. And dye methylene blue (MB) could be fully degrade... A new property of conjugated polymer poly(furancarbinol-co-phenol)(PFP) was studied. The target copolymer was used as a catalyst after proper heating treatment. And dye methylene blue (MB) could be fully degraded and largely mineralized on PFP, under natural light or even in dark, in a few minutes. Furthermore, the catalytic activity could be preserved after several runs and the catalyst was readily separated. The effect of calcination temperature was also observed. 展开更多
关键词 PFP catalytic property MB degradation mineralization.
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MESOPOROUS ACID SOLID AS A CARRIER FOR METALLOCENE CATALYST IN ETHYLENE POLYMERIZATION AND A CATALYST IN CATALYTIC DEGRADATION OF POLYETHYLENE
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作者 Wen-xi Cheng Li-ya Shi +2 位作者 Shi-yun Li Hui Chen Tao Tang 《Chinese Journal of Polymer Science》 SCIE CAS CSCD 2007年第2期187-195,共9页
The possibility of mesoporous acid solid as a carder for metallocene catalyst in ethylene polymerization and catalyst for polyethylene (PE) catalytic degradation was investigated. Here, HMCM-41 and AIMCM-41, and mes... The possibility of mesoporous acid solid as a carder for metallocene catalyst in ethylene polymerization and catalyst for polyethylene (PE) catalytic degradation was investigated. Here, HMCM-41 and AIMCM-41, and mesoporous silicoaluminophosphate molecular sieves (SAPO1 and SAPO2) were synthesized and used as acid solid. Much more gases were produced during catalytic degradation in PE/acid solid mixtures via in situ polymerization than those via physical mixing. The particle size distribution results exhibited that the particle size of SAPO1 in the PE/SAPOI mixture via in situ polymerization was about 1/14 times of that of the original SAPO1 or SAPO1-supported metallocene catalyst. This work shows a novel technology for chemical recycling of polyolefin. 展开更多
关键词 catalytic degradation Acid solids Supported metallocene catalysts Polyethylene.
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Facile Preparation of PVA-AA/TiO2 Composite Gel Particles and Their Tunable Photo-catalytic Property for the Degradation of Methyl Orange
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作者 方艳红 SU Xiaoying +1 位作者 QUAN Zhilong 萧聪明 《Journal of Wuhan University of Technology(Materials Science)》 SCIE EI CAS 2019年第6期1479-1483,共5页
In the presence of titanium dioxide powder, cross-linking reaction between commercial polyvinyl alcohol(PVA)-based macromonomer and acrylic acid(AA) was initiated with potassium persulfate in an emulsifying system. As... In the presence of titanium dioxide powder, cross-linking reaction between commercial polyvinyl alcohol(PVA)-based macromonomer and acrylic acid(AA) was initiated with potassium persulfate in an emulsifying system. As a result, PVA-AA/TiO2 composite gel particles were obtained. The morphology and composition of the particles were analyzed with scanning electron microscopy(SEM), energy scattering x-ray spectroscopy(EDS), Fourier infrared spectroscopy(FTIR), and thermogravimetric analysis(TGA). The analysis results confirmed that the particles were the expected ones. TiO2 was dispersed homogeneously within the spheroidal particles. Compared to the control gel, the composite gel particles not only contained Ti element but also showed higher thermal stability. In addition, the photo-catalytic behavior of the particles for the degradation of methyl orange contained in aqueous solution was examined. The particles exhibited photocatalytic characteristic for the degradation of the model dye, which could be modulated by simply varying the amount of cross-linking agent or TiO2. The photo-catalytic degradation percentage of methyl orange maintained at 91%-96% after using the particles three times, which indicated that TiO2 could played its role repeatedly via being fixated within polyvinyl alcohol-based gel. 展开更多
关键词 titanium dioxide composite gel particles controlled preparation photo-catalytic degradation
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Dual-functional MnS_(2)/MnO_(2) heterostructure catalyst for efficient acidic hydrogen evolution reaction and assisted degradation of organic wastewater
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作者 Wen Kang Zhao Zi Qiang Ma +6 位作者 Jia Yu Zheng Chang Bao Han Kai Ling Zhou Ming Yang Hao De Cai Fang Yi Xia Hui Yan 《Journal of Energy Chemistry》 SCIE EI CSCD 2023年第12期215-224,I0007,共11页
The design and synthesis of non-precious metal dual-functional electrocatalysts through the modulation of electronic structure are important for the development of renewable hydrogen energy.Herein,MnS_(2)/MnO_(2)-CC h... The design and synthesis of non-precious metal dual-functional electrocatalysts through the modulation of electronic structure are important for the development of renewable hydrogen energy.Herein,MnS_(2)/MnO_(2)-CC heterostructure dual-functional catalysts with ultrathin nanosheets were prepared by a twostep electrodeposition method for efficient acidic hydrogen evolution reaction(HER) and degradation of organic wastewater(such as methylene blue(MB)).The electronic structure of Mn atoms at the MnS_(2)/MnO_(2)-CC heterostructure interface is reconfigured under the joint action of S and O atoms.Theoretical calculations show that the Mn d-band electron distribution in MnS_(2)/MnO_(2)-CC catalyst has higher occupied states near the Fermi level compared to the MnO_(2) and MnS_(2) catalysts,which indicates that MnS_(2)/MnO_(2)-CC catalyst has better electron transfer capability and catalytic activity.The MnS_(2)/MnO_(2)-CC catalysts require overpotential of only 66 and 116 mV to reach current density of 10 and 100 mA cm^(-2)in MB/H_(2)SO_(4) media.The MnS_(2)/MnO_(2)-CC catalyst also has a low Tafel slope(26.72 mV dec^(-1)) and excellent stability(the performance does not decay after 20 h of testing).In addition,the MB removal efficiency of the MnS_(2)/MnO_(2)-CC catalyst with a better kinetic rate(0.0226) can reach 97.76%,which is much higher than that of the MnO_(x)-CC catalyst(72.10%).This strategy provides a new way to develop efficient and stable non-precious metal dual-functional electrocatalysts for HER and organic wastewater degradation. 展开更多
关键词 Hydrogen evolution reaction(HER) Dual-functional electrocatalysts HETEROSTRUCTURE catalytic activity degradation of organic wastewater
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Iron–doped bismuth oxybromides as visible-light-responsive Fenton catalysts for the degradation of atrazine in aqueous phases
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作者 Yong-Li Cai Yu-Hang Xu +4 位作者 Ji-Zun Xiang Zhi-Qiang Zhang Qiu-Xiang He Ya-Feng Li Jian Lü 《Journal of Environmental Sciences》 SCIE EI CAS CSCD 2024年第3期321-332,共12页
Pesticides and its degradation products,being well–known residues in soil,have recently been detected in many water bodies as pollutants of emerging concerns,and thus there is a contemporary demand to develop viable ... Pesticides and its degradation products,being well–known residues in soil,have recently been detected in many water bodies as pollutants of emerging concerns,and thus there is a contemporary demand to develop viable and cost–effective techniques for the removal of related organic pollutants in aqueous phases.Herein,a visible-light-responsive Fenton system was constructed with iron–doped bismuth oxybromides(Fe–BiOBr)as the catalysts.Taking the advantage of sustainable Fe(Ⅲ)/Fe(Ⅱ)conversion and optimized H_(2)O_(2)utilization,the optimal Fe–BiOBr–2 catalyst showed an excellent atrazine removal efficiency of 97.61%in 120 min,which is superior than the traditional homogeneous Fenton and the majority of heterogeneous processes documented in the literature.In this photo–Fenton system,hydroxyl(·OH)and superoxide(·O_(2)^(-))radicals were dominant active species contributed to the oxidative degradation of atrazine.Due to the production of various active radicals,five degradation pathways were proposed based on the identification of intermediates and degradation products.Overall,this work not only demonstrates a fundamental insight into creating highly efficient and atom economic photo-Fenton systems,but also provides a complementary strategy for the treatment of organic pollutants in water. 展开更多
关键词 Bismuth oxybromide Photo–Fenton ATRAZINE catalytic degradation
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Degradation analysis of A^2/O combined with AgNO3 + K2FeO4 on coking wastewater 被引量:3
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作者 Pengyu Zhu Kaijin Zhu +1 位作者 Rob Puzey Xiaoli Ren 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2018年第7期1555-1560,共6页
In this work, a coking wastewater was selected and a biochemical A^2/O treatment device for fractional degradation was designed and employed. After each stage of the treatment, the products were analyzed through gas c... In this work, a coking wastewater was selected and a biochemical A^2/O treatment device for fractional degradation was designed and employed. After each stage of the treatment, the products were analyzed through gas chromatography–mass spectroscopy(GC–MS) to determine their composition. Finally, AgNO_3+ K_2 FeO_4 was used as an advanced deep catalytic oxidation treatment. It was concluded from the analysis that cyclic organics could be degraded and the chemical oxygen demand(COD) was controlled within 50 mg·L^(-1), in line with the target value. Meanwhile, the spectra obtained from the GC–MS were in accordance with the conclusions reached based on the COD. The research results showed that all hard-degradable organics in coking wastewater could be eliminated through the A^2/O bio-membrane treatment and the advanced treatment of making use of K_2FeO_4 as an oxidant and Ag+as a catalyst, the catalytic efficiency with Ag+as a catalyst of K+2FeO_4 was very high. Agcould evidently improve the oxidation capacity of K_2FeO_4 to wastewater in its short stability time, and this is an important innovation. 展开更多
关键词 K2FeO4 AGNO3 废水 级分 生物化学 催化剂 氧化处理 GCMS
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Degradation of Residual Formaldehyde in Fabric by Photo-catalysis 被引量:1
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作者 YAO Yadong GUO Xiangli KANG Yunqing LI Xieji CHEN Aizheng YANG Weizhong YIN Guangfu 《Journal of Wuhan University of Technology(Materials Science)》 SCIE EI CAS 2008年第2期147-150,共4页
The residual formaldehyde (HCHO) in fabric was degraded using photo-catalysis assisted by the compound catalyst of nano-TiO2 and nano-ZnO. The effects of several factors on the degradation, such as the composing of ... The residual formaldehyde (HCHO) in fabric was degraded using photo-catalysis assisted by the compound catalyst of nano-TiO2 and nano-ZnO. The effects of several factors on the degradation, such as the composing of catalyst, irradiation time, pH value and the H2CHO concentration of the immersed solution were investigated. Results showed that H2CHO of the immersed solution had degraded 93% after 5 h irradiation, and the degradation ratio of formaldehyde could be improved and the aging of the fabric can be avoided with the addition of ZnO nanoparticles and pH value of the immersed-fibric solution. The fabric with residual formaldehyde about 1 800 μg/g can be efficiently treated to satisfy the China National Standard (GB/2912.1-1998) with the photo-catalytic degradation. 展开更多
关键词 photo-catalytic degradation FABRIC FORMALDEHYDE
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Oil Pollutants Degradation of Nano-MgO in Micro-Polluted Water
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作者 Meng-Fu Zhu Cheng Deng +4 位作者 Hong-Bo Su Xiu-Dong You Lu Zhu Ping Chen Ying-Hai Yuan 《Computational Water, Energy, and Environmental Engineering》 2013年第3期12-15,共4页
The removal of oil pollutants from water and purifying process of oil-polluted water are studied through catalytic degradation method with nano-MgO. The results indicated that catalytic degradation effect of nano-MgO ... The removal of oil pollutants from water and purifying process of oil-polluted water are studied through catalytic degradation method with nano-MgO. The results indicated that catalytic degradation effect of nano-MgO on the oil pollutants was associated with dosage of nano-MgO, pH and water temperature. When oil content was 1.8 mg/L, 0.17 g nano-MgO was used and the removal rate of oil was 93.92%. Furthermore, nano-Mgo was a non-photosensitive catalyst. GC/MS analysis showed that the amount of petroleum-based pollutants in water was reduced 73.77% from the previous 61 kinds to 16 kinds, and the total peak area was reduced 96.05% after catalytic degradation of nano-MgO. Therefore, nano-MgO has an excellent effect on the catalytic degradation of oil pollutants and can be applied in the treatment of oil wastewaters. 展开更多
关键词 Nano-MgO OIL POLLUTANTS catalytic degradation MICRO-POLLUTED WATER WATER Treatment
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Effects of Cu(Ⅱ) or Zn(Ⅱ) on photodegradation of some toxic organic compounds in wastewater by using TiO_2 as catalyst
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作者 丁敦煌 宋强 +2 位作者 刘德全 Wolfram Thiemann 杨松青 《中国有色金属学会会刊:英文版》 EI CSCD 2002年第5期1011-1014,共4页
The effects of Cu (Ⅱ) or Zn (Ⅱ) on the photo-catalytic degradation of some organic chemicals in water, such as acetone, phenol, dyes, and tea saponin were studied. Dyes in wastewater from a textile factory can be ef... The effects of Cu (Ⅱ) or Zn (Ⅱ) on the photo-catalytic degradation of some organic chemicals in water, such as acetone, phenol, dyes, and tea saponin were studied. Dyes in wastewater from a textile factory can be effectively degraded by photo-catalysis with TiO 2 and ultraviolet light or sunshine, but the reaction rate could be slowed down if copper or zinc salt exists in the solution. 展开更多
关键词 二氧化钛 染料废水 丙酮 苯酚 茶叶皂苷 光降解
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对苯二甲酸乙二醇酯降解机理密度泛函的理论研究 被引量:1
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作者 周梅 李思佳 +3 位作者 徐玮峰 黄金保 罗小松 吴雷 《原子与分子物理学报》 北大核心 2024年第4期43-50,共8页
采用密度泛函理论方法B3P86/6-31++G(d, p),对对苯二甲酸乙二醇酯一聚体降解反应机理进行了理论研究.设计了对苯二甲酸乙二醇酯一聚体纯热解、水解和醇解、水或醇作为催化剂降解过程的各种可能反应路径,对参与反应的各种中间体、过渡态... 采用密度泛函理论方法B3P86/6-31++G(d, p),对对苯二甲酸乙二醇酯一聚体降解反应机理进行了理论研究.设计了对苯二甲酸乙二醇酯一聚体纯热解、水解和醇解、水或醇作为催化剂降解过程的各种可能反应路径,对参与反应的各种中间体、过渡态及产物进行了几何结构优化和频率计算以获得热力学与动力学参数值.计算结果表明:当水或甲醇作为对苯二甲酸乙二醇酯热降解过程中的催化剂时,利用水或甲醇O-H中H提供到对苯二甲酸乙二醇酯一聚体主链酯键中O原子上形成对苯二甲酸,而乙烷基脱掉的H原子与水中羟基(-OH)或醇中甲氧基(-OCH3)结合形成新的水或者甲醇,从而降低对苯二甲酸乙二醇酯热解过程中的反应能垒(251.4 kJ/mol→181.1 kJ/mol(甲醇)和187.5 kJ/mol(水));当水或甲醇作为对苯二甲酸乙二醇酯热降解过程中的反应物参与反应时,利用水或甲醇O-H中H提供到对苯二甲酸乙二醇酯一聚体主链乙烷基旁O原子上形成乙二醇,而水中羟基(-OH)或醇中甲氧基(-OCH3)结合对苯二甲酸乙二醇酯一聚体主链羰基中C原子上形成对苯二甲酸或对苯二甲酸单甲酯,进而达到降低对苯二甲酸乙二醇酯热解过程中的反应能垒(156.4 kJ/mol(醇解)和170.1 kJ/mol(水解)).在反应过程中,无论是水/甲醇催化或是水/甲醇参与反应都能在一定程度上降低对苯二甲酸乙二醇酯一聚体主要基元反应步的反应能垒,使反应更易于进行. 展开更多
关键词 对苯二甲酸乙二醇酯 密度泛函理论 热解 水解 醇解 催化降解 反应机理
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焦化污泥炭重金属风险及其处理焦化废水研究
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作者 余丽 宇晓虹 +4 位作者 朱嘉讯 药钰 王莉 赵颖 卫皇曌 《中国环境科学》 EI CAS CSCD 北大核心 2024年第6期3189-3196,共8页
以焦化污泥制备焦化污泥炭,研究在炭化和硝酸改性过程中重金属形态变化和风险评价,并探索改性焦化污泥炭用于焦化废水处理的效能.焦化污泥(CWS)中Cr和Ni重金属含量远高于其他几种重金属,通过炭化得到焦化污泥炭(CWS-C),再活化后得到改... 以焦化污泥制备焦化污泥炭,研究在炭化和硝酸改性过程中重金属形态变化和风险评价,并探索改性焦化污泥炭用于焦化废水处理的效能.焦化污泥(CWS)中Cr和Ni重金属含量远高于其他几种重金属,通过炭化得到焦化污泥炭(CWS-C),再活化后得到改性焦化污泥炭(CWS-N),生态风险因子(RI)从122.79(CWS)降低至33.70(CWS-N),说明CWS-N重金属污染风险很低.与CWS-C相比,CWS-N具有多种铁物相(FeO、Fe_(2)Al_(2)O_(4)、Fe_(3)O_(4)和Fe_(0.95)C_(0.005)),有利于Fe(II)/Fe(III)循环,能有效催化H_(2)O_(2)产生•OH,对焦化废水TOC的去除率高达66.3%.CWS-N上的活性组分铁的流失率低于0.5%,具有良好的催化稳定性.焦化废水中溶解性有机物主要为木质素类、脂质类和稠环化合物类,含N、S化合物占81.1%,经CWS-N催化降解后可去除大部分有机物. 展开更多
关键词 焦化废水 污泥炭 重金属 催化降解
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磷掺杂碳量子点的制备及活化过一硫酸盐降解亚甲基蓝
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作者 张利洁 李德刚 +3 位作者 韩文渊 徐会君 张维民 郁宸 《无机盐工业》 CAS CSCD 北大核心 2024年第1期126-133,共8页
报道了一种磷掺杂碳量子点(P-CQDs)的方法,用红外光谱(FT-IR)、X射线光电子能谱仪(XPS)、透射电子显微镜(TEM)等对P-CQDs进行了详细表征,结果证实磷成功接入了CQDs。引入磷可以减少CQDs的禁带宽度,从而提高对光的吸收和促进光生电子转... 报道了一种磷掺杂碳量子点(P-CQDs)的方法,用红外光谱(FT-IR)、X射线光电子能谱仪(XPS)、透射电子显微镜(TEM)等对P-CQDs进行了详细表征,结果证实磷成功接入了CQDs。引入磷可以减少CQDs的禁带宽度,从而提高对光的吸收和促进光生电子转移。在可见光照射下,P-CQDs的用量为0.5 g/L、过一硫酸盐(PMS)的浓度为0.4 mmol/L时,10 min内亚甲基蓝(MB)的降解率为99%。考察了P-CQDs用量、PMS浓度和MB浓度等因素对体系降解MB效率的影响。同时,用自由基淬灭实验考察了P-CQDs光催化活化PMS降解MB的机理,结果表明超氧自由基(O_(2)^(·-))是主要的活性物质。 展开更多
关键词 碳量子点 过一硫酸盐 催化降解 亚甲基蓝
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铁-三联吡啶配合物活化高碘酸盐体系构建及其对染色废水的催化降解机制
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作者 武守营 黄启超 +4 位作者 张开封 张琳萍 钟毅 徐红 毛志平 《纺织学报》 EI CAS CSCD 北大核心 2024年第6期105-112,共8页
为开发新型、高效的染色废水处理方法,通过铁-三联吡啶(Fe^(Ⅲ)(tpy)C_(l3))配合物活化高碘酸盐(PI)构建了Fe^(Ⅲ)(tpy)C_(l3)/PI催化氧化体系。在此基础上,采用酸性红1(AR1)作为染色废水模型污染物测试了该体系的催化降解性能,并通过... 为开发新型、高效的染色废水处理方法,通过铁-三联吡啶(Fe^(Ⅲ)(tpy)C_(l3))配合物活化高碘酸盐(PI)构建了Fe^(Ⅲ)(tpy)C_(l3)/PI催化氧化体系。在此基础上,采用酸性红1(AR1)作为染色废水模型污染物测试了该体系的催化降解性能,并通过捕获和探针实验研究了Fe^(Ⅲ)(tpy)C_(l3)配合物活化PI降解酸性红1的机制。结果表明:Fe^(Ⅲ)(tpy)C_(l3)配合物能够高效活化PI实现酸性红1的快速降解,15 min内对AR1的去除率高达98%;Fe^(Ⅲ)(tpy)C_(l3)/PI体系对酸性红1的降解符合伪一级动力学模型,同时酸性红1的降解速率常数随Fe^(Ⅲ)(tpy)C_(l3)配合物和PI浓度的增加而呈线性增加;在Fe^(Ⅲ)(tpy)C_(l3)/PI体系中包含超氧自由基、单线态氧以及高价铁,这些活性物质共同促进酸性红1的降解;该体系不仅对多种有机物的降解表现出普适性,同时催化降解过程不受溶液pH值以及常见无机盐离子的干扰。 展开更多
关键词 配合物 高碘酸盐 染色废水 降解 催化机制 废水处理 铁-三联吡啶
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Fe-Mn/TiO_(2)的制备及其催化臭氧氧化双酚A的性能研究
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作者 薛代惠美 任宏洋 +3 位作者 商佳俭 李冰睿 陶建 王兵 《现代化工》 CAS CSCD 北大核心 2024年第6期150-155,共6页
采用浸渍法制备Fe-Mn/TiO_(2)双金属催化材料,以双酚A(BPA)为目标降解物,探究了Fe-Mn/TiO_(2)对其的降解效果及降解机制。结果表明,Fe-Mn/TiO_(2)催化臭氧氧化降解BPA的去除率相较于单独TiO_(2)处理提升了83.4%;Fe、Mn成功负载且催化剂... 采用浸渍法制备Fe-Mn/TiO_(2)双金属催化材料,以双酚A(BPA)为目标降解物,探究了Fe-Mn/TiO_(2)对其的降解效果及降解机制。结果表明,Fe-Mn/TiO_(2)催化臭氧氧化降解BPA的去除率相较于单独TiO_(2)处理提升了83.4%;Fe、Mn成功负载且催化剂孔洞较丰富;相较于TiO_(2),Fe-Mn/TiO_(2)中锐钛矿质量分数增加能产生更多的羟基自由基。同时,Fe、Mn在TiO_(2)表面能发生价态转化,可作为活性位点促进臭氧分解为·OH等活性物质,增强催化反应活性。 展开更多
关键词 Fe/Mn双金属 催化臭氧氧化 非均相 锐钛矿相TiO_(2) 降解机理
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Au/γ-Al_(2)O_(3)催化剂的绿色制备及其催化降解亚甲基蓝性能
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作者 肖伽励 金党琴 +3 位作者 周慧 周龙生 王升文 郑炳云 《化学研究与应用》 CAS 北大核心 2024年第3期634-639,共6页
利用侧柏叶提取液为还原剂制备了纳米金负载型Au/γ-Al_(2)O_(3)催化剂,研究了负载条件对金颗粒物理状态及催化剂比表面积的影响。利用XRD、BET、SEM、TEM对催化剂的晶型、孔结构和形貌进行表征,以亚甲基蓝作为目标污染物探究了Au/γ-Al... 利用侧柏叶提取液为还原剂制备了纳米金负载型Au/γ-Al_(2)O_(3)催化剂,研究了负载条件对金颗粒物理状态及催化剂比表面积的影响。利用XRD、BET、SEM、TEM对催化剂的晶型、孔结构和形貌进行表征,以亚甲基蓝作为目标污染物探究了Au/γ-Al_(2)O_(3)的催化降解能力。结果显示,最佳金负载率为1.00%,最佳煅烧温度为300℃。当Au/γ-Al_(2)O_(3)投加量为0.7 g·L^(-1)时,15 mL 0.5 g·L^(-1) NaBH_(4)能在10 min内降解97.67%的亚甲基蓝,且循环利用5次后单位质量催化剂的亚甲基蓝降解率不下降,说明Au/γ-Al_(2)O_(3)催化剂有良好的催化活性和稳定性。 展开更多
关键词 绿色制备 Au/γ-Al_(2)O_(3) 催化降解能力
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金属有机框架/聚丙烯纤维基复合材料对化学战剂模拟物的快速降解
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作者 张诗雨 姚依婷 +5 位作者 董晨珊 张如全 杨红军 顾绍金 黄菁菁 杜杰毫 《纺织学报》 EI CAS CSCD 北大核心 2024年第6期134-141,共8页
为将金属有机框架(MOFs)均匀且稳固地固定在纤维材料表面,创造出柔软且具备自净化防护面料,采用单宁酸-3-氨丙基三乙氧基硅烷(TA-APTES)涂层改性的聚丙烯(PP)非织造布作为载体,通过原位生长法制备高MOFs负载量的纤维基复合材料。借助扫... 为将金属有机框架(MOFs)均匀且稳固地固定在纤维材料表面,创造出柔软且具备自净化防护面料,采用单宁酸-3-氨丙基三乙氧基硅烷(TA-APTES)涂层改性的聚丙烯(PP)非织造布作为载体,通过原位生长法制备高MOFs负载量的纤维基复合材料。借助扫描电子显微镜、红外光谱仪、X-射线衍射仪、X-射线光电子能谱仪等手段对复合材料的表面形貌、组成和化学结构进行表征,并对复合材料的MOFs负载量和表面浸润性进行了分析。结果表明:TA-APTES涂层能够显著提高复合材料中MOFs的负载量,可达20.96%;并且有效提高复合材料的表面湿润性,从而提高其在水溶液中的催化降解效率,实现快速降解化学战剂模拟物4-硝基苯磷酸二甲酯(DMNP),在30 min左右即可实现100%的转化率,其降解半衰期短(4.8 min)。 展开更多
关键词 金属有机框架 化学战剂 催化降解 原位生长法 涂层改性 聚丙烯非织造布
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