期刊文献+
共找到65篇文章
< 1 2 4 >
每页显示 20 50 100
Graphene-loaded nickel−vanadium bimetal oxides as hydrogen pumps to boost solid-state hydrogen storage kinetic performance of magnesium hydride
1
作者 Dong-qiang GAO Fu-ying WU +4 位作者 Zhi ZHANG Zi-chuan LU Ren ZHOU Hu ZHAO Liu-ting ZHANG 《Transactions of Nonferrous Metals Society of China》 SCIE EI CAS CSCD 2024年第8期2645-2657,共13页
To modify the thermodynamics and kinetic performance of magnesium hydride(MgH_(2))for solid-state hydrogen storage,Ni_(3)V_(2)O_(8)-rGO(rGO represents reduced graphene oxide)and Ni_(3)V_(2)O_(8)nanocomposites were pre... To modify the thermodynamics and kinetic performance of magnesium hydride(MgH_(2))for solid-state hydrogen storage,Ni_(3)V_(2)O_(8)-rGO(rGO represents reduced graphene oxide)and Ni_(3)V_(2)O_(8)nanocomposites were prepared by hydrothermal and subsequent heat treatment.The beginning hydrogen desorption temperature of 7 wt.%Ni_(3)V_(2)O_(8)-rGO modified MgH_(2)was reduced to 208℃,while the additive-free MgH_(2)and 7 wt.%Ni_(3)V_(2)O_(8)doped MgH_(2)appeared to discharge hydrogen at 340 and 226℃,respectively.A charging capacity of about 4.7 wt.%H_(2)for MgH_(2)+7 wt.%Ni_(3)V_(2)O_(8)-rGO was achieved at 125℃ in 10 min,while the dehydrogenated MgH_(2)took 60 min to absorb only 4.6 wt.%H_(2)at 215℃.The microstructure analysis confirmed that the in-situ generated Mg_(2)Ni/Mg_(2)N_(i)H_(4) and metallic V contributed significantly to the enhanced performance of MgH_(2).In addition,the presence of rGO in the MgH_(2)+7 wt.%Ni_(3)V_(2)O_(8)-rGO composite reduced particle aggregation tendency of Mg/MgH_(2),leading to improving the cyclic stability of MgH_(2)during 20 cycles. 展开更多
关键词 hydrogen storage properties MgH_(2) graphene-loaded Ni−V bimetal oxides catalytic mechanism
下载PDF
Advances in Noble Metal-Decorated Metal Oxide Nanomaterials for Chemiresistive Gas Sensors:Overview 被引量:5
2
作者 Li‑Yuan Zhu Lang‑Xi Ou +3 位作者 Li‑Wen Mao Xue‑Yan Wu Yi‑Ping Liu Hong‑Liang Lu 《Nano-Micro Letters》 SCIE EI CAS CSCD 2023年第6期353-427,共75页
Highly sensitive gas sensors with remarkably low detection limits are attractive for diverse practical application fields including real-time environmental monitoring,exhaled breath diagnosis,and food freshness analys... Highly sensitive gas sensors with remarkably low detection limits are attractive for diverse practical application fields including real-time environmental monitoring,exhaled breath diagnosis,and food freshness analysis.Among various chemiresistive sensing materials,noble metal-decorated semiconducting metal oxides(SMOs)have currently aroused extensive attention by virtue of the unique electronic and catalytic properties of noble metals.This review highlights the research progress on the designs and applications of different noble metal-decorated SMOs with diverse nanostructures(e.g.,nanoparticles,nanowires,nanorods,nanosheets,nanoflowers,and microspheres)for high-performance gas sensors with higher response,faster response/recovery speed,lower operating temperature,and ultra-low detection limits.The key topics include Pt,Pd,Au,other noble metals(e.g.,Ag,Ru,and Rh.),and bimetals-decorated SMOs containing ZnO,SnO_(2),WO_(3),other SMOs(e.g.,In_(2)O_(3),Fe_(2)O_(3),and CuO),and heterostructured SMOs.In addition to conventional devices,the innovative applications like photo-assisted room temperature gas sensors and mechanically flexible smart wearable devices are also discussed.Moreover,the relevant mechanisms for the sensing performance improvement caused by noble metal decoration,including the electronic sensitization effect and the chemical sensitization effect,have also been summarized in detail.Finally,major challenges and future perspectives towards noble metal-decorated SMOs-based chemiresistive gas sensors are proposed. 展开更多
关键词 Noble metal bimetal Semiconducting metal oxide Chemiresistive gas sensor Electronic sensitization Chemical sensitization
下载PDF
Pt–Pd bimetallic nanoparticles anchored on uniform mesoporous MnO_(2) sphere as an advanced nanocatalyst for highly efficient toluene oxidation 被引量:2
3
作者 Jiaqin He Dongyun Chen +4 位作者 Najun Li Qingfeng Xu Hua Li Jinghui He Jianmei Lu 《Green Energy & Environment》 SCIE EI CSCD 2022年第6期1349-1360,共12页
Improving catalytic performance is a yet still challenge in thermal catalytic oxidation.Herein,uniform mesoporous MnO_(2) nanospheresupported bimetallic Pt–Pd nanoparticles were successfully fabricated via a SiO_(2) ... Improving catalytic performance is a yet still challenge in thermal catalytic oxidation.Herein,uniform mesoporous MnO_(2) nanospheresupported bimetallic Pt–Pd nanoparticles were successfully fabricated via a SiO_(2) template strategy for the total catalytic degradation of volatile organic compounds at low temperature.The introduction of mesopores into the MnO_(2) support induces a large specific surface area and pore size,thus providing numerous accessible active sites and enhanced diffusion properties.Moreover,the addition of a secondary noble metal can adjust the O_(ads)/O_(latt) molar ratios,resulting in high catalytic activity.Among them,the catalyst having a Pt/Pd molar ratio of 7:3 exhibits optimized catalytic activity at a weight hourly space velocity of 36,000 mL g^(-1) h^(-1),reaching 100%toluene oxidation at 175℃ with a lower activation energy(57.0 kJ mol^(-1))than the corresponding monometallic Pt or non-Pt-based catalysts(93.8 kJ mol^(-1) and 214.2 kJ mol^(-1)).Our findings demonstrate that the uniform mesoporous MnO_(2) nanosphere-supported bimetallic Pt–Pd nanoparticles catalyst is an effective candidate for application in elimination of toluene. 展开更多
关键词 MnO_(2)nanospheres Mesoporous structure Pt-Pd bimetal VOCs oxidation
下载PDF
Origin of the synergistic effects of bimetallic nanoparticles coupled with a metal oxide heterostructure for accelerating catalytic performance
4
作者 Wail Al Zoubi Abdullah Al Mahmud +4 位作者 Farah Hazmatulhaq Mohammad R.Thalji Stefano Leoni Jee-Hyun Kang Young Gun Ko 《SusMat》 SCIE EI 2024年第3期227-239,共13页
Precisely tuning bicomponent intimacy during reactions by traditional methods remains a formidable challenge in the fabrication of highly active and stable catalysts because of the difficulty in constructing well-defi... Precisely tuning bicomponent intimacy during reactions by traditional methods remains a formidable challenge in the fabrication of highly active and stable catalysts because of the difficulty in constructing well-defined catalytic systems and the occurrence of agglomeration during assembly.To overcome these limitations,a PtRuPNiO@TiO_(x)catalyst on a Ti plate was prepared by ultrasound-assisted low-voltage plasma electrolysis.This method involves the oxidation of pure Ti metal and co-reduction of strong metals at 3000◦C,followed by sonochemical ultrasonication under ambient conditions in an aqueous solution.The intimacy of the bimetals in PtRuPNiO@TiOx is tuned,and the metal nanoparticles are uniformly distributed on the porous titania coating via strong metal-support interactions by leveraging the instantaneous high-energy input from the plasma discharge and ultrasonic irradiation.The intimacy of PtRuPNiO@TiO_(x)increases the electron density on the Pt surface.Consequently,the paired sites exhibit a high hydrogen evolution reaction activity(an overpotential of 220 mV at a current density of 10 mA cm^(−2)and Tafel slope of 186 mV dec^(−1)),excellent activity in the hydrogenation of 4-nitrophenol with a robust stability for up to 20 cycles,and the ability to contrast stated catalysts without ultrasonication and plasma electrolysis.This study facilitates industrially important reactions through synergistic chemical interactions. 展开更多
关键词 bimetalS nanoparticles oxideS HETEROSTRUCTURES HYDROGENATION
原文传递
Pt-Re/rGO bimetallic catalyst for highly selective hydrogenation of cinnamaldehyde to cinnamylalcohol 被引量:3
5
作者 Zuojun Wei Xinmiao Zhu +4 位作者 Xiaoshuang Liu Haiqin Xu Xinghua Li Yaxin Hou Yingxin Liu 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2019年第2期369-378,共10页
In the present work, a series of Pt-based catalysts, alloyed with a second metal, i.e., Re, Sn, Er, La, and Y, and supported on activated carbon, ordered mesoporous carbon, N-doped mesoporous carbon or reduced graphen... In the present work, a series of Pt-based catalysts, alloyed with a second metal, i.e., Re, Sn, Er, La, and Y, and supported on activated carbon, ordered mesoporous carbon, N-doped mesoporous carbon or reduced graphene oxide(rGO), have been developed for selective hydrogenation of cinnamaldehyde to cinnamylalcohol. Re and rGO were proved to be the most favorable metal dopant and catalyst support, respectively. Pt_(50) Re_(50)/rGO showed the highest cinnamylalcohol selectivity of 89% with 94% conversion of cinnamaldehyde at the reaction conditions of 120 °C, 2.0 MPaH_2 and 4 h. 展开更多
关键词 CATALYST HYDROGENATION SELECTIVITY CINNAMALDEHYDE bimetal Reduced Graphene oxide
下载PDF
锰(Mn)钴(Co)双金属负载石墨相氮化碳活化过硫酸盐用于非自由基主导的高级氧化(AOP)降解污染物研究
6
作者 庄立恒 毛辉麾 +3 位作者 范郑洋 王桂灵 葛吕洁 桂豪冠 《现代化工》 CAS CSCD 北大核心 2024年第7期180-185,共6页
采用两步煅烧法成功制备了钴锰双金属氧化物负载的石墨相氮化碳(CMCN)。锰氧化物主要以Mn3O4和MnCO3形式存在,钴氧化物以CoO形式存在。由于g-C_(3)N_(4)的存在,金属Mn和Co都分布均匀没有出现团聚现象。XPS表征结果表明,Co和Mn都具有2个... 采用两步煅烧法成功制备了钴锰双金属氧化物负载的石墨相氮化碳(CMCN)。锰氧化物主要以Mn3O4和MnCO3形式存在,钴氧化物以CoO形式存在。由于g-C_(3)N_(4)的存在,金属Mn和Co都分布均匀没有出现团聚现象。XPS表征结果表明,Co和Mn都具有2个价态存在于CMCN中,并且保持了g-C_(3)N_(4)的结构单元。通过对罗丹明B降解评估催化剂CMCN的催化降解性能。结果表明,在Mn和Co的协同作用下,罗丹明B降解率在1 min可达到99%以上。电子顺磁共振和淬灭试验表明,非自由基氧化(1O2)在罗丹明B降解过程中占主导地位。 展开更多
关键词 双金属氧化物 石墨相氮化碳 过氧单硫酸盐 协同作用 非自由基
下载PDF
MgO–SBA-15 Supported Pd–Pb Catalysts for Oxidative Esterification of Methacrolein with Methanol to Methyl Methacrylate 被引量:4
7
作者 姜丽 刁琰琰 +3 位作者 韩军兴 闫瑞一 张香平 张锁江 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2014年第10期1098-1104,共7页
Novel Mg O–SBA-15 supported catalysts were prepared for oxidative esterification of methacrolein(MAL) with methanol to methyl methacrylate(MMA). The Mg O–SBA-15 supports were synthesized with different magnesia load... Novel Mg O–SBA-15 supported catalysts were prepared for oxidative esterification of methacrolein(MAL) with methanol to methyl methacrylate(MMA). The Mg O–SBA-15 supports were synthesized with different magnesia loadings from different magnesium precursors and hydrochloric acid molar concentrations. The Mg O–SBA-15 supports and Pd–Pb/Mg O–SBA-15 catalysts were characterized by several analysis methods. The results revealed that the addition of Mg O improved the ordered structure of SBA-15 supports and provided surface alkalinity of SBA-15 supports. The average size of the Pd3 Pb particles on magnesia-modified Pd–Pb/Mg O–SBA-15 catalysts was smaller than that on the pure silica-based Pd–Pb/SBA-15 catalysts. The experiments on catalyst performance showed that the magnesia-modified Pd–Pb/Mg O–SBA-15 catalysts had higher activity than pure silica-based Pd–Pb/SBA-15 catalysts, showing the strong dependence of catalytic activity on the average size of active particles. The difference of activity between Pd–Pb/SBA-15 catalysts and Pd–Pb/Mg O–SBA-15 catalysts was due to the discrepant structural properties and surface alkalinity provided by Mg O, which led to the different Pd3 Pb particle sizes and then resulted in the different number of active sites. Besides magnesia loadings, other factors, such as hydrochloric acid molar concentration and magnesium precursors, had considerable influences on the catalytic activity. 展开更多
关键词 METHACROLEIN Methyl METHACRYLATE oxidative ESTERIFICATION Pd–Pb bimetal SBA-15
下载PDF
Bimetallic oxide coupled with B-doped graphene as highly efficient electrocatalyst for oxygen evolution reaction 被引量:2
8
作者 Yuanyuan Jiang Kai Dong +4 位作者 Yizhong Lu Jiawei Liu Bo Chen Zhongqian Song Li Niu 《Science China Materials》 SCIE EI CSCD 2020年第7期1247-1256,共10页
Developing electrocatalysts with high performance and low cost for the oxygen evolution reaction(OER)is of great importance for fabricating renewable energy storage and conversion devices.Here,a series of boron-doped ... Developing electrocatalysts with high performance and low cost for the oxygen evolution reaction(OER)is of great importance for fabricating renewable energy storage and conversion devices.Here,a series of boron-doped graphene(BG)-supported bimetallic oxides of Co and Ni were obtained and served as OER electrocatalysts.Surprisingly,the annealed Co-Ni-Ox/BG with a Co/Ni ratio of 1:1 exhibits high performance toward oxygen evolution in alkaline electrolyte.The overpotential is only 310 mV at the current density of 10 mA cm-2,superior to many mono-metallic oxides reported before,and even comparable to the commercial RuO2.The regulation of charge distribution in bimetallic oxides and the strong synergistic coupling effects together contribute to the superior electrocatalytic performance of the Co-Ni-Ox/BG toward OER.This study also offers several effective ways to design high-performance OER electrocatalysts for water splitting. 展开更多
关键词 bimetal oxide B-doped graphene oxygen evolution reaction ELECTROCATALYST hydrogen generation
原文传递
DNA Induced FePt Bimetallic Nanoparticles on Reduced Graphene Oxide for Electrochemical Determination of Dopamine
9
作者 ZHANG Wenyan LIU Yang 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2015年第3期406-411,共6页
FePt bimetallic nanoparticles were formed on reduced graphene oxide(rGO) with the help of double-stranded DNA(dsDNA) via a simple and universal route to obtain a FePt/DNA-rGO composite. The FePt nanoparticles with... FePt bimetallic nanoparticles were formed on reduced graphene oxide(rGO) with the help of double-stranded DNA(dsDNA) via a simple and universal route to obtain a FePt/DNA-rGO composite. The FePt nanoparticles with an average size of about 5 nm were well dispersed on rGO. FePt/DNA-rGO modified glassy carbon electrode(GCE) exhibited excellent electrocatalytic activity for the oxidation of dopamine(DA) with a detec- tion limit of 100 nmol/L(S/N = 3). In addition, the FePt/DNA-rGO based electrochemical sensor showed an excellent selectivity for DA in the presence of ascorbic acid(AA), uric acid(UA) and other interference reagents. The as-prepared electrochemical biosensor shows great promise in the application of clinical diagnostics. 展开更多
关键词 Reduced graphene oxide FePt bimetal nanoparticle DNA ELECTROANALYSIS DOPAMINE
原文传递
过渡金属活化过硫酸盐降解双酚A的研究进展 被引量:4
10
作者 张伟 李梅 +3 位作者 许文 丁超民 王文海 白毛毛 《应用化工》 CAS CSCD 北大核心 2023年第3期939-944,954,共7页
综述了过渡金属离子、零价金属和双金属等不同类型金属催化剂活化PMS/PDS降解双酚A(BPA)的研究现状;探讨了双金属催化剂活化过硫酸盐去除BPA的降解机理、双金属之间的协同作用以及氧空位与表面羟基的重要作用;分析了活化过程的影响因素... 综述了过渡金属离子、零价金属和双金属等不同类型金属催化剂活化PMS/PDS降解双酚A(BPA)的研究现状;探讨了双金属催化剂活化过硫酸盐去除BPA的降解机理、双金属之间的协同作用以及氧空位与表面羟基的重要作用;分析了活化过程的影响因素、水基质条件,催化剂的可重复使用性与稳定性;对金属催化剂降解BPA研究方向进行了展望。 展开更多
关键词 双金属催化剂 过一硫酸盐 过二硫酸盐 高级氧化技术(AOPs) 双酚A(BPA)
下载PDF
ZrO_(2)基双金属氧化物催化CO加氢行为的研究 被引量:1
11
作者 刘竞舸 闫国春 +2 位作者 李艺 卢卫民 张成华 《煤炭转化》 CAS CSCD 北大核心 2023年第1期72-80,共9页
以UiO-66(一种以Zr为金属中心,以苯二甲酸为有机配体的刚性金属有机框架材料)为前驱物制备得到一系列杂元素修饰的ZrO_(2)基双金属氧化物(杂元素分别有Zn,Cu,Ce,Mn和In),将其作为双功能催化剂中的加氢组分,考察杂元素的引入对ZrO_(2)催... 以UiO-66(一种以Zr为金属中心,以苯二甲酸为有机配体的刚性金属有机框架材料)为前驱物制备得到一系列杂元素修饰的ZrO_(2)基双金属氧化物(杂元素分别有Zn,Cu,Ce,Mn和In),将其作为双功能催化剂中的加氢组分,考察杂元素的引入对ZrO_(2)催化性能的影响。通过X射线衍射(XRD)、透射电子显微镜(TEM)和N_(2)-物理吸脱附等手段对样品的形貌结构进行表征,发现杂元素的引入并不影响前驱物UiO-66的形成,焙烧后得到的催化剂普遍具有较高的比表面积,且杂元素均匀分布在ZrO_(2)表面;采用吡啶-红外(Py-IR)、NH_(3)-程序升温吸脱附(NH_(3)-TPD)、X射线光电子能谱(XPS)和电子顺磁谱(EPR)等手段对样品表面结构进行分析,发现杂元素的引入降低了ZrO_(2)表面的酸性位、氧空位数量。由于杂元素的引入对ZrO_(2)的理化性质造成显著影响,从而导致样品间催化性能的不同,单独对ZrO_(2)基双金属氧化物进行评价,其中Cu-ZrO_(2),Mn-ZrO_(2),In-ZrO_(2)具有较高的CO转化率,产物以CH4为主;相较而言,Zn-ZrO_(2)和Ce-ZrO_(2)上CO转化率较低,产物中含有大量的CH_(3)OH。 展开更多
关键词 双功能催化剂 合成气 芳烃 UiO-66 双金属氧化物
下载PDF
纤维状CuO/Co_(3)O_(4)的制备及其催化水解氨硼烷的研究 被引量:1
12
作者 高春园 宋亚坤 +3 位作者 陈濛濛 王豪 刘军辉 刘振 《化工新型材料》 CAS CSCD 北大核心 2023年第3期215-220,233,共7页
采用静电纺丝技术制备了一种纤维状钴铜双金属氧化物催化剂,并考察了催化剂中不同金属比例、不同催化剂制备方法、催化剂加入量、氨硼烷加入量以及水解温度对氨硼烷水解释氢的影响。结果表明:由于钴和铜之间存在强的协同效应,从而提高... 采用静电纺丝技术制备了一种纤维状钴铜双金属氧化物催化剂,并考察了催化剂中不同金属比例、不同催化剂制备方法、催化剂加入量、氨硼烷加入量以及水解温度对氨硼烷水解释氢的影响。结果表明:由于钴和铜之间存在强的协同效应,从而提高了催化剂的催化性能。当钴和铜的摩尔比为8∶1时,所制备的催化剂Co_(8)Cu_(1)O_(x)-NF性能最优,催化氨硼烷水解的活化能为38.41kJ/mol,反应转化频率(TOF)为2443.52mL/(min·g_(metal)),经过5次循环使用仍能保持较高的催化活性,该催化剂对氨硼烷水解具有良好的催化活性和循环稳定性。 展开更多
关键词 水解释氢 氨硼烷 静电纺丝 催化剂 双金属氧化物
下载PDF
聚合物负载铁-锰双金属氧化物去除水中锑的研究 被引量:1
13
作者 贾祥苓 闵奇 +1 位作者 白仁碧 杨晶晶 《化工新型材料》 CAS CSCD 北大核心 2023年第4期231-237,共7页
针对载铁壳聚糖醋酸纤维素吸附剂(CS/CA-FeO_(x))易受pH影响问题,选择向制备液中引入Mn^(2+)制备复合吸附剂CS/CA-FeMnO_(x),并研究其对水溶液中Sb(Ⅲ)和Sb(Ⅴ)的去除特性及吸附机理。结果表明:在pH=4.0条件下CS/CA-FeMnO_(x)对初始浓度... 针对载铁壳聚糖醋酸纤维素吸附剂(CS/CA-FeO_(x))易受pH影响问题,选择向制备液中引入Mn^(2+)制备复合吸附剂CS/CA-FeMnO_(x),并研究其对水溶液中Sb(Ⅲ)和Sb(Ⅴ)的去除特性及吸附机理。结果表明:在pH=4.0条件下CS/CA-FeMnO_(x)对初始浓度为5mg/L的Sb(Ⅲ)和Sb(Ⅴ)吸附的最佳投量均为1.2g/L,最大吸附容量为44.42mg/g和56.73mg/g;pH从4.0升高至7.0,对Sb(Ⅲ)的去除率影响不大,但是对Sb(Ⅴ)的去除率影响显著降低,去除率下降25.3%;准二级速率反应方程更能准确地描述吸附剂CS/CA-FeMnO_(x)对Sb(Ⅲ)和Sb(Ⅴ)的吸附过程,说明对二者的吸附均是物理吸附与化学吸附相结合的过程;Freundlich模型能更好地描述CS/CA-FeMnO_(x)对两种不同形态锑的吸附;X射线衍射结果未显示锰氧化物的峰,可能是复合吸附剂中锰含量较少或者锰以无定形存在。X射线光电子能谱和分峰结果显示,水中锑与复合吸附剂上的金属发生结合,且Sb(Ⅴ)的结合强度高于Sb(Ⅲ)。综上,少量锰的添加能够显著削弱pH对去除Sb(Ⅴ)的影响,为构建静电富集、化学吸附的除锑体系提供技术依据。 展开更多
关键词 双金属氧化物 原位改性 吸附
下载PDF
Ce-La双金属氧化物同步去除酸性废水中磷酸盐和氟的性能与机理
14
作者 李含 赵雨 +5 位作者 陈嘉超 许海民 朱雅娴 陈志辉 申萌萌 杨文澜 《中国环境科学》 EI CAS CSCD 北大核心 2023年第10期5248-5256,共9页
采用共沉淀法制备出能同步吸附磷酸盐和氟的Ce-La双金属氧化物纳米吸附剂(CLBOs).结果表明,CLBOs主要以粒径20~50nm的纳米颗粒或纳米团簇的形式存在,比表面积为117.9m^(2)/g.CLBOs在pH为4~12的范围内具有良好的稳定性,且酸性条件有利于C... 采用共沉淀法制备出能同步吸附磷酸盐和氟的Ce-La双金属氧化物纳米吸附剂(CLBOs).结果表明,CLBOs主要以粒径20~50nm的纳米颗粒或纳米团簇的形式存在,比表面积为117.9m^(2)/g.CLBOs在pH为4~12的范围内具有良好的稳定性,且酸性条件有利于CLBOs的除磷除氟;在pH=4.0、磷酸盐和氟初始浓度为30、10mg/L的条件下,CLBOs最大磷、氟吸附量分别可达59.14,19.25mg/g.得益于静电吸引、配体交换和内配位络合的综合作用,CLBOs表现出优异的同步除磷除氟性能,且在高浓度竞争离子体系中能实现磷酸盐和氟的选择性吸附.CLBOs除磷除氟过程符合准二级动力学,且对氟的吸附速率显著快于磷酸盐,其中磷酸盐的吸附平衡时间约为240min,氟达到吸附平衡仅需100min.吸附饱和的CLBOs具有较好的再生性能,可长期重复使用,在含磷、氟酸性废水的深度处理领域具备良好的应用潜力. 展开更多
关键词 Ce-La双金属氧化物 酸性废水 磷酸盐 同步去除
下载PDF
铁-铜双金属负载催化剂应用于非均相芬顿水处理研究发展
15
作者 侯玉玮 高徐奕 +2 位作者 蒿琳静 张杰 蒋苏毓 《应用化工》 CAS CSCD 北大核心 2023年第8期2370-2376,共7页
综述了近年来非均相芬顿工艺中负载型Fe-Cu双金属催化剂的研究进展,概述了在非均相芬顿水处理中适用于Fe-Cu双金属的各种载体材料(如氧化物或介孔材料、大分子物质和其他材料),并对Fe-Cu双金属催化剂对污染物的降解性能进行了批判性评... 综述了近年来非均相芬顿工艺中负载型Fe-Cu双金属催化剂的研究进展,概述了在非均相芬顿水处理中适用于Fe-Cu双金属的各种载体材料(如氧化物或介孔材料、大分子物质和其他材料),并对Fe-Cu双金属催化剂对污染物的降解性能进行了批判性评价。分析表明,相比于单独的Fe、Cu金属负载催化剂,Fe-Cu双金属负载催化剂对于污染物的降解能够表现出更好的性能。基于金属催化剂在芬顿工艺反应机理,为进一步开发催化剂向更有效的非均相芬顿反应及其在实际水处理中的应用提出了研究前景。 展开更多
关键词 芬顿反应 铁铜双金属 水处理 高级氧化
下载PDF
复合Fe-Ag/rGO催化剂的制备及其电催化氮还原性能研究
16
作者 杨江蕊 王迪 +2 位作者 佟磊 王怀正 张亲亲 《山东化工》 CAS 2023年第5期19-22,25,共5页
氨是重要的无机化工产品和清洁能源载体。合成氨的工业方法—哈伯工艺存在能耗高且释放大量CO 2温室气体等问题。电催化氮还原合成氨因反应条件温和、能耗低、绿色环保而得到广泛关注,该过程急需开发兼具成本低廉、高导电性、高活性、... 氨是重要的无机化工产品和清洁能源载体。合成氨的工业方法—哈伯工艺存在能耗高且释放大量CO 2温室气体等问题。电催化氮还原合成氨因反应条件温和、能耗低、绿色环保而得到广泛关注,该过程急需开发兼具成本低廉、高导电性、高活性、高选择性等特点的复合催化剂。本文首先制备了氧化石墨烯(GO),然后采用一步化学还原法制备了以还原氧化石墨烯(rGO)为载体的Fe-Ag/rGO复合双金属催化剂以及Fe/rGO、Ag/rGO两种单金属催化剂,采用SEM、EDS和XRD对其微观形貌、元素组成以及晶相结构进行了表征,最后,对比了Fe-Ag/rGO复合双金属催化剂以及Fe/rGO、Ag/rGO两种单金属催化剂的电催化氮还原合成氨性能。 展开更多
关键词 电催化 氮还原 双金属 复合催化剂 还原氧化石墨烯
下载PDF
Strong metal-support interaction between AuPd nanoparticles and oxygen-rich defect ZrO_(2) for enhanced catalytic 5-hydroxymethylfurfural oxidation
17
作者 Yunlei Zhang Yiran Liu +3 位作者 Wen Guan Mengxue Cao Yao Chen Pengwei Huo 《Chinese Chemical Letters》 SCIE CAS CSCD 2024年第2期507-511,共5页
The unique properties of metal oxide surfaces,crystal surfaces and defects play vital roles in biomass upgrading reactions.In this work,hierarchical porous bowl-shaped ZrO_(2)(HB-ZrO_(2))with mixed crystal phase was d... The unique properties of metal oxide surfaces,crystal surfaces and defects play vital roles in biomass upgrading reactions.In this work,hierarchical porous bowl-shaped ZrO_(2)(HB-ZrO_(2))with mixed crystal phase was designed and employed as the support for loading AuPd bimetal with different proportions to synthesize AuPd/HB-ZrO_(2) catalysts.The effects of surface chemistry,oxygen defects,bimetal interaction and metal-support interaction of AuPd/HB-ZrO_(2) on catalytic performance for the selective oxidation of 5-hydroxymethylfurfural(HMF)to 2,5-furandicarboxylic acid(FDCA)were systematically investigated.The Au 2 Pd1/HB-ZrO_(2) catalyst afforded a satisfactory FDCA yield of 99.9%from HMF oxidation using O_(2) as the oxidant in water,accompanied with an excellent FDCA productivity at 97.6 mmol g^(−1) h^(−1).This work offers fresh insights into rationally designing efficient catalysts with oxygen-rich defects for the catalytic upgrading of biomass platform chemicals. 展开更多
关键词 5-Hydroxymethylfurfural oxidation 2 5-Furandicarboxylic acid Oxygen-rich defect ZrO_(2) AuPd bimetal Bowl-shaped structure
原文传递
砷在金属氧化物/水界面上的吸附机制Ⅰ.金属表面羟基的表征和作用 被引量:18
18
作者 张昱 豆小敏 +3 位作者 杨敏 贺泓 余运波 何士龙 《环境科学学报》 CAS CSCD 北大核心 2006年第10期1586-1591,共6页
利用红外光谱对铁铈氧化物(Fe-Ce)吸附材料中的金属表面羟基(M—OH)进行了表征,并探讨了金属羟基在砷吸附中的作用.透射和原位温度漫反射-傅立叶变换红外光谱(FTIR)表征结果表明,Fe-Ce表面存在丰富的M—OH,但M—OH含量随制备温度升高而... 利用红外光谱对铁铈氧化物(Fe-Ce)吸附材料中的金属表面羟基(M—OH)进行了表征,并探讨了金属羟基在砷吸附中的作用.透射和原位温度漫反射-傅立叶变换红外光谱(FTIR)表征结果表明,Fe-Ce表面存在丰富的M—OH,但M—OH含量随制备温度升高而逐渐减少;Fe-Ce上的M—OH与一般金属氧化物的表面羟基特性存在显著不同,可能是一种特殊类型的结构性羟基.对砷吸附前后的Fe-Ce材料进行透射FTIR表征,发现砷饱和吸附后M—OH的摇摆振动消失,同时生成了新的As—O振动峰,表明M—OH在砷的去除中起着重要的作用;初始吸附pH由9.0降至5.0只引起了吸附剂上As—O键的伸缩振动向高频略微偏移;综合FTIR结果可以推测,M—OH和砷阴离子发生了直接的表面络合,在不同的pH条件下均与砷形成了内层络和物. 展开更多
关键词 吸附机制 表面羟基 双金属氧化物 红外光谱
下载PDF
铁锰复合氧化物的制备及其吸附除砷性能 被引量:64
19
作者 常方方 曲久辉 +4 位作者 刘锐平 刘会娟 雷鹏举 张高生 武荣成 《环境科学学报》 CAS CSCD 北大核心 2006年第11期1769-1774,共6页
采用共沉淀法制备了新型铁锰复合氧化物吸附剂,并对其表面特性及除砷性能进行了初步研究.ξ电位测试表明,铁锰复合氧化物pHzpc在6.0附近,SEM/EDX表征证明吸附剂表面Fe和Mn的相对摩尔比为3∶1;铁锰复合氧化物对As(V)和As(Ⅲ)均表现出很... 采用共沉淀法制备了新型铁锰复合氧化物吸附剂,并对其表面特性及除砷性能进行了初步研究.ξ电位测试表明,铁锰复合氧化物pHzpc在6.0附近,SEM/EDX表征证明吸附剂表面Fe和Mn的相对摩尔比为3∶1;铁锰复合氧化物对As(V)和As(Ⅲ)均表现出很强的吸附能力,并且吸附速度快,在60min内即可达到平衡吸附容量的80%;该吸附剂在天然水环境pH范围内均有良好吸附除砷能力,磷酸根、硅酸根、碳酸根等阴离子对除砷效果有不同程度的影响,其余共存阴、阳离子及天然有机物在中性水环境中对除砷效果影响不大;采用Langmuir吸附等温线能较好地描述铁锰复合氧化物吸附As(V)的过程(R2=0.997),而Freundlich方程能较好地拟合As(Ⅲ)的吸附过程(R2=0.989),对As(V)与As(Ⅲ)的饱和吸附容量分别达到227mg·g-1和312mg·g-1. 展开更多
关键词 铁锰复合氧化物 ξ电位 吸附容量
下载PDF
铁锰复合氧化物处理含铬废水的研究 被引量:11
20
作者 许可 刘军坛 +3 位作者 彭伟功 李见云 王香平 刘蕾 《水处理技术》 CAS CSCD 北大核心 2011年第12期20-23,27,共5页
采用铁锰复合氧化物用于含铬废水的净化,考察了pH、吸附剂用量、反应时间、磷初始质量浓度和反应温度对净化过程的影响。结果表明,铬净化过程适宜的pH范围为5~7,在pH6时净化率达到最大值。随着吸附剂加入量的增加和初始溶液的降低,铬... 采用铁锰复合氧化物用于含铬废水的净化,考察了pH、吸附剂用量、反应时间、磷初始质量浓度和反应温度对净化过程的影响。结果表明,铬净化过程适宜的pH范围为5~7,在pH6时净化率达到最大值。随着吸附剂加入量的增加和初始溶液的降低,铬的净化率逐渐增加。铁锰复合氧化物对水中铬的净化过程速度较快,吸附过程符合假2级模型。在20~60℃温度范围内,温度对铬吸附过程影响不明显。铁锰复合氧化物对铬的吸附等温线符合Freudlich方程,1/n为0.363。 展开更多
关键词 铁锰复合氧化物 净化 吸附
下载PDF
上一页 1 2 4 下一页 到第
使用帮助 返回顶部