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Synthesis, characterization, and stability of iron (III) complex ions possessing phenanthroline-based ligands
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作者 Shawnt Tosonian Charles J. Ruiz +2 位作者 Andrew Rios Elma Frias Jack F. Eichler 《Open Journal of Inorganic Chemistry》 2013年第1期7-13,共7页
It has previously been demonstrated that phenanthroline-based ligands used to make gold metallotherapuetics have the ability to exhibit cytotoxicity when not coordinated to the metal center. In an effort to help asses... It has previously been demonstrated that phenanthroline-based ligands used to make gold metallotherapuetics have the ability to exhibit cytotoxicity when not coordinated to the metal center. In an effort to help assess the mechanism by which these ligands may cause tumor cell death, iron binding and removal experiments have been considered. The close linkage between cell proliferation and intracellular iron concentrations suggest that iron deprivation strategies may be a mechanism involved in inhibiting tumor cell growth. With the creation of iron (III) phen complexes, the iron binding abilities of three polypyridal ligands [1,10-phenanthroline (phen), 2,9-dimethyl-1, 10-phenanthroline (methylphen), and 2,9-di-sec-butyl-1, 10-phenanthroline (sec-butylphen)] can be tested via a competition reaction with a known iron chelator. Therefore, iron (III) complexes possessing all three ligands were synthesized. Initial mass spectrometric and infrared absorption data indicate that iron (III) tetrachloride complex ions with protonated phen ligands (RphenH+) were formed: [phenH][FeCl4], [methylphenH][FeCl4], [sec-butylphenH][FeCl4]. UV-vis spectroscopy was used to monitor the stability of the complex ions, and it was found that the sec-butylpheniron complex was more stable than the phen and methylphen analogues. This was based on the observation that free ligand was observed immediately upon the addition of EDTA to the [phenH][FeCl4] and [methylphenH] [FeCl4] complex ions. 展开更多
关键词 POLYPYRIDYL LIGANDS PHENANTHROLINE IRON (iii) COMPLEX ionS
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The Electrode for Potentiometric Determinаtion of Chromium (III, VI) in Wаter Solutions
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作者 Shаmshiyа Аmerkhаnovа Dana Belgibayeva +1 位作者 Rustаm Shlyаpov Аitolkyn Uаli 《Journal of Materials Science and Chemical Engineering》 2014年第1期52-56,共5页
The possibility of determining of chromium (III, VI) ions was investigated in this paper. It is shown that the electrode on а basis of heаzlewoodite has high selectivity to chromium (III) ions. Also the stability co... The possibility of determining of chromium (III, VI) ions was investigated in this paper. It is shown that the electrode on а basis of heаzlewoodite has high selectivity to chromium (III) ions. Also the stability constants of complexes, forming in system “Cr3+-Mohr’s salt-Ca(OH)2-PVA ÷ PAA” were determined by potentiometric titration with ion-selective electrode. 展开更多
关键词 Heаzlewoodite CHROMIUM (iii VI) ionS POTENTIOMETRIC Method
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Determination of Apparent Formation Constants of Eu(III) with Humic Substances by Ion Selective Liquid Membrane Electrode
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作者 Takayuki Sasaki Hatsumi Yoshida +2 位作者 Taishi Kobayashi Ikuji Takagi Hirotake Moriyama 《American Journal of Analytical Chemistry》 2012年第7期462-469,共8页
This is the novel measurement of the apparent formation constants of trivalent lanthanide with humic substances by potentiometric titration using an ion selective electrode (ISE) consisting of bis(diphenylphosphoryl)m... This is the novel measurement of the apparent formation constants of trivalent lanthanide with humic substances by potentiometric titration using an ion selective electrode (ISE) consisting of bis(diphenylphosphoryl)methane as an ionophore. The ISE prepared exhibited a Nernstian response to the Eu3+ concentration in the test solutions in the presence of humic acid and fulvic acid. The effect of the solution conditions, including the pH, initial metal and humic substance concentrations, and ionic strength, on the formation constants was examined. The present formation constants were compared with the reported data using solvent extraction method. 展开更多
关键词 APPARENT Formation Constant HUMIC Substance EU(iii) ion SELECTIVE ELECTRODE Titration
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Removal of Chromium(III) from the Waste Solution of an Indian Tannery by Amberlite IR 120 Resin
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作者 Pratima Meshram Sushanta Kumar Sahu +2 位作者 Banshi Dhar Pandey Vinay Kumar Tilak Raj Mankhand 《International Journal of Nonferrous Metallurgy》 2012年第3期32-41,共10页
The extraction of chromium(III) from a model waste solution and also from a waste solution of an Indian tannery with Amberlite IR 120 resin is described, and the performance of this resin is compared with other simila... The extraction of chromium(III) from a model waste solution and also from a waste solution of an Indian tannery with Amberlite IR 120 resin is described, and the performance of this resin is compared with other similar resins. The parameters that were optimized include effect of mixing time, pH, loading and elution behaviours of chromium(III) for this resin. Sorption of chromium(III) on Amberlite IR 120 followed Freundlich isotherm and Langmuir isotherm model, and the maximum sorption capacity was determined to be 142.86 mg Cr(III)/g of the resin. Higher Freundlich constant (Kf) values (6.30 and 13.46 for aqueous feed of 500 and 1000 ppm Cr(III)) indicated strong chemical interaction through ion exchange mechanism of the metal ion with the resin. The kinetic data showed good fit to the Lagergren first order model for extraction of chromium(III). Desorption of chromium(III) from the loaded resin increased with the increase in concentration of eluent (5-20% H2SO4). With 20% (v/v) sulphuric acid solution 94% chromium(III) was eluted in three stages. Elution of the Cr(III) in the column experiments was however, found to be lower (82%) than that of the shake flask data. In case of Indian tannery’s waste solution, it was observed that almost total chromium was extracted in four stages with Amberlite IR 120. 展开更多
关键词 Chromium(iii) ion exchange Amberlite IR 120 TANNERY WASTE SOLUTion
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Adsorption of Cr(III) from an Aqueous Solution by Chitosan Beads Modified with Sodium Dodecyl Sulfate (SDS)
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作者 Munkhpurev Bat-Amgalan Zoltuya Khashbaatar +5 位作者 David Eva Vanessa Anak Muhammad Nabil Md Sari Naoto Miyamoto Naoki Kano Hee-Joon Kim Ganchimeg Yunden 《Journal of Environmental Protection》 2021年第11期939-960,共22页
This study is to prepare chitosan beads modified with sodium dodecyl sulfate (SDS) to effectively remove Cr(III) from an aqueous solution. The characterizations of SDS-chitosan by scanning electron microscopy-energy d... This study is to prepare chitosan beads modified with sodium dodecyl sulfate (SDS) to effectively remove Cr(III) from an aqueous solution. The characterizations of SDS-chitosan by scanning electron microscopy-energy dispersive X-ray spectroscopy (SEM-EDS), Fourier transform-infrared spectroscopy (FT-IR) and X-ray photoelectron spectroscopy (XPS) proved the successful synthesis of the adsorbent. The adsorption of Cr(III) on the SDS material was investigated by varying experimental conditions such as pH, contact time and adsorbent dosage. The maximum adsorption capacity of SDS-chitosan for Cr(III) was estimated to be 3.42 mg?g<sup>-1</sup>. The results of adsorption kinetics and isothermal models show that the adsorption process conforms to the pseudo-second-order and Langmuir isotherm models, indicating that the adsorption is single-layer chemical adsorption. Thermodynamic analyses indicate that the adsorption of Cr(III) is an endothermic reaction. These results show that the new adsorbent has obvious application prospect to eliminate Cr(III). 展开更多
关键词 Chitosan Beads Sodium Dodecyl Sulfate (SDS) Trivalent Chromium ions (Cr(iii)) ADSORPTion Adsorption Isotherms Adsorption Kinetics
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Cu(Ⅱ)催化NaOCl氧化碘帕醇的效果和过程解析
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作者 魏红 滕锐杰 +3 位作者 郑佳欣 高美娟 钮金芬 蔡谦 《中国环境科学》 EI CAS CSCD 北大核心 2024年第6期3167-3178,共12页
本文研究Cu(Ⅱ)催化NaOCl氧化非离子型碘代X射线造影剂—碘帕醇(IPM),对IPM降解过程中Cu的回收和形态进行解析,考察Cu(Ⅱ)、NaOCl浓度和卤素离子对IPM降解效果及碘代消毒副产物-碘仿的生成影响;采用XRD、XPS分析Cu(Ⅱ)反应后的产物晶型... 本文研究Cu(Ⅱ)催化NaOCl氧化非离子型碘代X射线造影剂—碘帕醇(IPM),对IPM降解过程中Cu的回收和形态进行解析,考察Cu(Ⅱ)、NaOCl浓度和卤素离子对IPM降解效果及碘代消毒副产物-碘仿的生成影响;采用XRD、XPS分析Cu(Ⅱ)反应后的产物晶型和形态变化,结合循环伏安曲线和计时电流表征Cu(Ⅲ)的生成,推测Cu(Ⅱ)催化NaOCl氧化IPM的机理.利用HPLC/MS/MS分析中间产物,推测IPM的降解路径.结果表明,与Co(Ⅱ)、Fe(Ⅱ)、Mn(Ⅱ)相比,Cu(Ⅱ)显著提高了NaOCl的分解率和IPM的氧化效果,25℃、pH=6.71,500r/min,NaOCl和Cu(Ⅱ)浓度分别为0.5和0.05mmol/L,60min,8.0mg/L IPM的降解率达到77.51%;HO·、活性氯自由基和Cu(Ⅲ)都有助于Cu(Ⅱ)/NaOCl氧化IPM,且Cu(Ⅲ)的贡献随pH值升高而增大.NaOCl浓度在0.1~2.5mmol/L范围增加,IPM降解率增加;Cu(Ⅱ)浓度在0.005~0.5mmol/L存在适宜值.HPLC/MS/MS共检测出13种产物,IPM的降解途径主要包括:侧链酰胺键水解和氧化,碘取代、羟基加成.Cl^(−)、Br^(−)和I^(−)(1~5mmol/L)在影响IPM氧化效果的同时,Br^(-)显著促进了CHI_(3)的生成,生成量达到48.28μg/L. 展开更多
关键词 碘帕醇 Cu(Ⅱ)/NaOCl Cu(Ⅲ) 碘仿
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铱(III)离子催化铈(IV)离子氧化四氢糠醇的动力学及机理 被引量:1
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作者 宋文玉 赵荣慧 降青梅 《物理化学学报》 SCIE CAS CSCD 北大核心 2005年第8期929-933,共5页
在酸性介质中用氧化还原滴定法研究了铈(IV)离子在痕量铱(III)离子催化作用下,于298 ̄313K区间氧化四氢糠醇(THFA)的反应动力学.结果表明,反应对铈(IV)离子为一级,对铱(III)离子也为一级,对四氢糠醇的表观反应级数为正分数.准一级速率常... 在酸性介质中用氧化还原滴定法研究了铈(IV)离子在痕量铱(III)离子催化作用下,于298 ̄313K区间氧化四氢糠醇(THFA)的反应动力学.结果表明,反应对铈(IV)离子为一级,对铱(III)离子也为一级,对四氢糠醇的表观反应级数为正分数.准一级速率常数kobs随[H+]增加而增大,而随[HSO-4]增加而减小.在氮气保护下,反应能引发丙烯腈聚合,说明在反应中有自由基产生.通过kobs与[HSO4-]的依赖关系,找到本反应体系的动力学活性物种是Ce(SO4)2,并计算出平衡常数,速控步骤的速率常数及相应的活化参数. 展开更多
关键词 铱(Ⅲ)离子 铈(Ⅳ)离子 四氢糠醇 催化剂 动力学 机理
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铬(III)离子催化铈(IV)离子氧化四氢糠醇的反应动力学及机理 被引量:1
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作者 宋文玉 降青梅 《化学学报》 SCIE CAS CSCD 北大核心 2005年第2期109-113,共5页
在酸性介质中用氧化还原滴定法研究了铈(IV)离子在铬(III)离子催化作用下,于25~40℃区间氧化四氢糠醇的反应动力学.结果表明反应对铈(IV)和四氢糠醇均为一级.准一级速率常数kobs随催化剂[Cr(III)]增加而增大,亦随[H+]增加而增大,而随[H... 在酸性介质中用氧化还原滴定法研究了铈(IV)离子在铬(III)离子催化作用下,于25~40℃区间氧化四氢糠醇的反应动力学.结果表明反应对铈(IV)和四氢糠醇均为一级.准一级速率常数kobs随催化剂[Cr(III)]增加而增大,亦随[H+]增加而增大,而随[HSO-4]增加而减小.在氮气保护下,反应不能引发丙烯酰胺聚合,说明在反应中没有自由基产生.提出了催化剂、底物和氧化剂间生成双核加合物的反应机理.通过kobs与HSO-4的依赖关系,并结合Ce(IV)在溶液中的平衡,找到了本反应体系的动力学活性物种是Ce(SO4)2.还计算出一些速率常数及相应的活化参数. 展开更多
关键词 四氢糠醇 催化剂 氧化 反应动力学 加合物 聚合 铬(Ⅲ) 速率常数 双核 离子
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An ion-imprinted polymer supported by attapulgite with a chitosan incorporated sol-gel process for selective separation of Ce(Ⅲ) 被引量:6
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作者 Chun Xiang Li Jian Ming Pan Jie Gao Yong Sheng Yan Gan Qing Zhao 《Chinese Chemical Letters》 SCIE CAS CSCD 2009年第8期985-989,共5页
The surface ion-imprinting concept and chitosan incorporated sol-gel process were applied to the synthesis of a new attapulgitesupported polymer for selective separation of Ce(III) from aqueous solution. The imprint... The surface ion-imprinting concept and chitosan incorporated sol-gel process were applied to the synthesis of a new attapulgitesupported polymer for selective separation of Ce(III) from aqueous solution. The imprinting mechanism of prepared ion-imprinted polymer were discussed with the Characteristics of FT-IR and SEM. Results from the experiments of adsorption capacity and selectivity suggested that ion-imprinted polymer offered a fast kinetics for the adsorption of Ce(III) under the optimum conditions. Its maximum adsorption capacity was 38.02 mg/g, and the selective recognition towards Ce(III) was much higher than that of the non-imprinted polymer and attapulgite. The prepared functional polymer was shown to be promising for selective separation and enrichment of trace Ce(III) in environmental samples. ?2009 Yong Sheng Yan. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved. 展开更多
关键词 ATTAPULGITE CHITOSAN Surface ion-imprinted Selective adsorption Ce(iii
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A kinetic study of the electron-transfer in the reaction of tribenzylchlorotin with[CoW_(12)O_(40)]^(5-)
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作者 Fatemeh F.Bamoharram Mohammad M.Heravi +1 位作者 Touran Ardalan Pouran Ardalan 《Chinese Chemical Letters》 SCIE CAS CSCD 2009年第8期1005-1009,共5页
A kinetic study of the electron-transfer in the reaction of tribenzylchlorotin with potassium 12-tungsto cobalt (Ⅲ) ate ion, Ks[CoW12O40], abbreviated as Co(III)W, has been performed in different solvents. The st... A kinetic study of the electron-transfer in the reaction of tribenzylchlorotin with potassium 12-tungsto cobalt (Ⅲ) ate ion, Ks[CoW12O40], abbreviated as Co(III)W, has been performed in different solvents. The studies were carried out in methanol, ethanol, acetonitrile and acetic acid/water. The rate constants, reaction rates and activation parameters were calculated. Our findings show that the rate of disappearance of the Co(Ⅲ) is pseudo-first order. The kinetic data is strongly affected by used solvents. The maximum and minimum rate constants were achieved in the ethanol and acetic acid/water (70/30) as a solvent, respectively. In all of the used solvents, negative value of activation entropies was observed, but negative activation enthalpies are observed in methanol, ethanol and acetonitrile. The reaction rate is increased with increase of Co(Ⅲ) concentration. ?2009 Fatemeh E Bamoharram. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved. 展开更多
关键词 Kinetic study Potassium 12-tungsto cobalt (iii) ate ion Pseudo-first order KEGGIN
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Performance Evaluation of the Fe-IR-120(Na)-DEHPA Impregnated Resin in the Removal Process of As(V) from Aqueous Solution
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作者 Mihaela Ciopec Adina Negrea +3 位作者 Lavinia Lupa Comeliu Davidescu Petru Negrea Paula Sfarloaga 《材料科学与工程(中英文B版)》 2011年第4期421-432,共12页
关键词 DEHPA 浸渍树脂 水溶液 LANGMUIR模型 IR NA 搬运过程 绩效评价
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Silicon and III-V Solar Cells: From Modus Vivendi to Modus Operandi
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作者 Alexander Buzynin Yury Buzynin +5 位作者 Vladimir Shengurov Vladimir Voronkov Ansgar Menke Albert Luk’yanov Vitaly Panov Nickolay Baidus 《Green and Sustainable Chemistry》 2017年第3期217-233,共17页
In the present paper, some novel opportunities for the development of high-efficient Si and III-V-based solar cells are considered: energy-saving environment friendly low-temperature technology of forming p-n junction... In the present paper, some novel opportunities for the development of high-efficient Si and III-V-based solar cells are considered: energy-saving environment friendly low-temperature technology of forming p-n junctions in Si (1), elaboration of structurally perfect GaAs/Ge/Si epitaxial substrates (2) and application of protective antireflecting coatings based on cubic zirconia (3). As a result: 1) New technique of forming p-n junctions in silicon has been elaborated. The technique provided easy and comparatively cheap process of production of semiconductor devices such as solar cells. The essence of the technique under the study is comprised in formation p-n junctions in silicon by a change of conductivity in the bulk of the sample occurring as a result of redistribution of the impurities, which already exists in the sample before its processing by ions. It differs from the techniques of diffusion and ion doping where change of conductivity and formation of p-n junction in the sample occur as a result of introduction of atoms of the other dopants from the outside;2) The conditions for synthesis of GaAs/Ge/Si epitaxial substrates with a thin (200 nm) Ge buffer layer featured with (1 - 2) × 105 cm-2 density of the threading dislocation in the GaAs layer. Ge buffer was obtained by chemical vapor deposition with a hot wire and GaAs layer of 1 μm thick was grown by the metal organic chemical vapor deposition. Root mean square surface roughness of GaAs layers of the less than 1 nm and good photoluminescence properties along with their high uniformity were obtained;3) The conditions ensuring the synthesis of uniform functional (buffer, insulating and protective) fianite layers on Si and GaAs substrates by means of magnetron and electron-beam sputtering have been determined. Fianite films have been shown to be suitable for the use as an ideal anti-reflecting material with high protective and anticorrosive properties. 展开更多
关键词 Solar Cells Green Technologies p-n JUNCTionS Ar ion-IRRADIATion Inversion of Conductivity Silicon iii-V GaAs on Si Ge Buffer YSZ ANTIREFLECTion Coatings
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基于Fe(Ⅲ)和邻苯二胺显色反应快速检测硫化物
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作者 赵灵芝 赵柳 +2 位作者 张小清 罗杰 杨喆 《精细化工》 EI CAS CSCD 北大核心 2023年第6期1319-1324,1392,共7页
比较了不同金属离子(Fe^(2+)、Fe^(3+)、Cu^(2+)、Zn^(2+)、Al^(3+)、Na^(+)、Ca^(2+)、Mg^(2+)、K^(+)、Ag^(+)、Cr^(3+))对邻苯二胺(OPD)的氧化能力,基于Fe^(3+)能直接氧化OPD产生黄色发荧光的产物而构建了Fe^(3+)-OPD显色体系。结合... 比较了不同金属离子(Fe^(2+)、Fe^(3+)、Cu^(2+)、Zn^(2+)、Al^(3+)、Na^(+)、Ca^(2+)、Mg^(2+)、K^(+)、Ag^(+)、Cr^(3+))对邻苯二胺(OPD)的氧化能力,基于Fe^(3+)能直接氧化OPD产生黄色发荧光的产物而构建了Fe^(3+)-OPD显色体系。结合硫化物的还原性以及对金属离子较强的亲和性,开发了一种通过比色法选择性检测硫化物的方法。结果表明,在pH 4.0NaAc-HAc缓冲液中,Fe^(3+)-OPD显色体系的吸光度和荧光强度与NaHS的浓度分别在10~200μmol/L和5~150μmol/L范围内呈线性关系,荧光法的检出限可达0.1μmol/L,体系内其他还原性物质及硫醇对NaHS的检测无干扰。将Fe^(3+)-OPD显色体系结合纸芯片构建的纸基比色体系蓝色分析色道值(B值)与NaHS的浓度在20~150μmol/L范围内呈线性关系,检出限为2μmol/L,并可用于定量检测加标自来水和胎牛血清中的硫化物。 展开更多
关键词 Fe(Ⅲ) 邻苯二胺 硫化物 硫化氢 纸基比色法 功能材料
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康惠尔银离子藻酸盐抗菌敷料治疗Ⅲ级糖尿病足伤口的效果分析
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作者 林惠娟 康鹏飞 邹漳峰 《糖尿病新世界》 2023年第16期175-178,共4页
目的 研讨康惠尔银离子藻酸盐抗菌敷料治疗Ⅲ级糖尿病足伤口的效果。方法 选取2019年1月—2022年1月漳州市第二医院收治的70例Ⅲ级糖尿病足患者为研究对象,按照抽签法将患者分为常规组和研究组,每组35例。常规组接受传统敷料治疗,研究... 目的 研讨康惠尔银离子藻酸盐抗菌敷料治疗Ⅲ级糖尿病足伤口的效果。方法 选取2019年1月—2022年1月漳州市第二医院收治的70例Ⅲ级糖尿病足患者为研究对象,按照抽签法将患者分为常规组和研究组,每组35例。常规组接受传统敷料治疗,研究组接受康惠尔银离子藻酸盐抗菌敷料治疗。对比两组临床治疗效果、创面缩小面积、创面愈合时间。结果 研究组治疗有效率(96.43%)高于常规组(60.71%),差异有统计学意义(χ^(2)=16.606,P<0.05)。研究组创面缩小面积大于常规组,差异有统计学意义(P<0.05)。研究组创面愈合时间短于常规组,差异有统计学意义(P<0.05)。结论 康惠尔银离子藻酸盐抗菌敷料在Ⅲ级糖尿病足伤口治疗中可以发挥显著疗效,加快创面愈合。 展开更多
关键词 康惠尔银离子藻酸盐抗菌敷料 Ⅲ级糖尿病足 溃疡创面治疗
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001×14.5强酸性树脂对铬(Ⅲ)的吸附性能 被引量:6
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作者 杨金杯 韩淑萃 +1 位作者 余美琼 邱挺 《中国有色金属学报》 EI CAS CSCD 北大核心 2012年第6期1791-1797,共7页
采用离子交换树脂法吸附铬(Ⅲ),通过树脂选型确定强酸性阳离子交换树脂001×14.5对铬(Ⅲ)吸附容量最大,用所选的001×14.5树脂研究铬(Ⅲ)的吸附性能。静态吸附实验表明:转速大于120 r/min时,对树脂吸附的影响可忽略,即外扩散基... 采用离子交换树脂法吸附铬(Ⅲ),通过树脂选型确定强酸性阳离子交换树脂001×14.5对铬(Ⅲ)吸附容量最大,用所选的001×14.5树脂研究铬(Ⅲ)的吸附性能。静态吸附实验表明:转速大于120 r/min时,对树脂吸附的影响可忽略,即外扩散基本消除,pH=7.0时,吸附最佳,铬(Ⅲ)吸附率随树脂用量的增加而增大;001×14.5树脂吸附铬(Ⅲ)的过程符合Langmuir等温曲线,且为优惠吸附;吸附过程符合拟二级动力学方程,吸附过程的表观活化能Ea=23.4 kJ/mol,颗粒内扩散为吸附速率的主要控制步骤;用1 mol/L的硫酸对吸附后的饱和树脂进行脱附再生,脱附率可达99%。 展开更多
关键词 离子交换树脂 铬(Ⅲ) 吸附 热力学 动力学
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生物膜载体吸附剂对Cr^(3+)的吸附动力学研究 被引量:6
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作者 张敬 姜斌 +2 位作者 刘瑞轩 孙津生 李鑫钢 《昆明理工大学学报(理工版)》 2005年第2期78-82,共5页
生物膜载体吸附重金属离子是目前发展起来的一种新型废水处理方法.该文对生物膜吸附Cr3+的行为进行了准一级动力学方程和Elovich模型方程的拟合,对吸附等温线作了测定.结果表明,Cr3+在生物膜载体吸附剂上的吸附过程与Elovich方程有较好... 生物膜载体吸附重金属离子是目前发展起来的一种新型废水处理方法.该文对生物膜吸附Cr3+的行为进行了准一级动力学方程和Elovich模型方程的拟合,对吸附等温线作了测定.结果表明,Cr3+在生物膜载体吸附剂上的吸附过程与Elovich方程有较好的拟合度(R2=0.97466),吸附等温模型与L-F平衡方程吻合较好(R2=0.9845).实验中考察了pH及温度对生物膜吸附Cr3+的影响.结果表明,pH=4~6,在室温20℃去除率可达到87%以上. 展开更多
关键词 生物膜 重金属离子 CR^3+ 吸附动力学
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铱(Ⅲ)离子催化铈(Ⅳ)离子氧化异丁醇的反应动力学及机理 被引量:3
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作者 宋文玉 李红变 刘红梅 《物理化学学报》 SCIE CAS CSCD 北大核心 2004年第8期801-805,共5页
在酸性介质中用氧化还原滴定法研究了铈(IV)离子在痕量铱(III)离子催化作用下,于25~40℃区间氧化异丁醇(BA)的反应动力学.结果表明反应对铈(IV)离子为一级,对异丁醇的表观反应级数为正分数.准一级速率常数kobs随犤H+犦及催化剂犤Ir(Ⅲ... 在酸性介质中用氧化还原滴定法研究了铈(IV)离子在痕量铱(III)离子催化作用下,于25~40℃区间氧化异丁醇(BA)的反应动力学.结果表明反应对铈(IV)离子为一级,对异丁醇的表观反应级数为正分数.准一级速率常数kobs随犤H+犦及催化剂犤Ir(Ⅲ)犦增加而增大,随犤HSO-4犦增加而减小.在氮气保护下,反应不能引发丙烯酰胺聚合,说明在反应中没有自由基产生.提出了催化剂、底物和氧化剂间生成双核加合物的反应机理,通过kobs与HSO-4的依赖关系,找到本反应体系的动力学活性物种是Ce(SO4)2+,并计算出平衡常数、速控步骤的速率常数及相应的活化参数. 展开更多
关键词 铱(Ⅲ)离子 铈(Ⅳ)离子 异丁醇 催化剂 动力学及机理
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高价离子还原菌还原机理及研究进展 被引量:5
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作者 翟思媛 李杰 +2 位作者 王亚娥 冯娟娟 豆宁龙 《环境科学与管理》 CAS 2013年第2期46-51,共6页
高价离子还原菌普遍存在于自然环境中,它们在环境的原位修复中起着非常重要的作用。本文主要介绍了三种典型的高价离子还原菌:异化Fe(III)还原菌(IRB)、硝酸盐还原菌及硫酸盐还原菌(SRB),分别以Fe3+、NO3-和SO24-为电子受体,以有机物作... 高价离子还原菌普遍存在于自然环境中,它们在环境的原位修复中起着非常重要的作用。本文主要介绍了三种典型的高价离子还原菌:异化Fe(III)还原菌(IRB)、硝酸盐还原菌及硫酸盐还原菌(SRB),分别以Fe3+、NO3-和SO24-为电子受体,以有机物作为电子供体,在将高价离子还原的同时,达到对污染环境的修复作用。文章综述了此类细菌的特性、作用机理、影响因素以及在国内外实际中的应用,分析了异化Fe(III)还原菌、硝酸盐还原菌及硫酸盐还原菌的异同点,并对该类细菌在环境污染治理中的发展趋势进行了评述。 展开更多
关键词 Fe(Ⅲ)还原菌 反硝化细菌 硫酸盐还原菌 高价离子还原菌
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镧(Ⅲ)离子诱导的菲律宾蛤仔金属硫蛋白性质研究 被引量:1
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作者 付海防 孟范平 +2 位作者 张毅 赵顺顺 高鹰 《生态毒理学报》 CAS CSCD 2010年第6期817-822,共6页
稀土离子能否诱导海洋生物的金属硫蛋白(MT)合成,将影响到MT对海水重金属的指示作用.以菲律宾蛤仔(Ruditapes philippinarum)为试验动物,采用含镧(Ⅲ)离子(La3+)的人工海水对其进行暴露培养,测定蛤仔鳃部和内脏中MT含量.结果表明,La3+... 稀土离子能否诱导海洋生物的金属硫蛋白(MT)合成,将影响到MT对海水重金属的指示作用.以菲律宾蛤仔(Ruditapes philippinarum)为试验动物,采用含镧(Ⅲ)离子(La3+)的人工海水对其进行暴露培养,测定蛤仔鳃部和内脏中MT含量.结果表明,La3+暴露能够增加蛤仔体内MT含量,其中,10~1×100μg·L-1的La3+对鳃部诱导作用较大;10~1×10000μg·L-1的La3+对内脏MT均有较好诱导;同时,过柱层析洗脱液的光谱扫描及十二烷基的硫酸盐钠-聚丙烯酰胺凝胶电泳法(SDS-PAGE)分析表明,La3+诱导的蛤仔内脏中的MT在258nm处有特征吸收峰,主要以二聚体和三聚体的形式存在,分子量为13.1kD和18.3kD. 展开更多
关键词 镧(Ⅲ)离子(La3+) 金属硫蛋白(MT) 菲律宾蛤仔
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活性炭纤维对水中铁的吸附研究 被引量:4
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作者 王洛秋 《环境科学与管理》 CAS 2006年第8期159-161,共3页
以活性炭纤维(ACF)为溶液中铁离子的吸附剂,考察了吸附时间、吸附温度、ACF比表面积及表面酸碱性对Fe3+吸附行为的影响。通过平衡吸附实验获得的吸附等温线,并不符合Langmu ir与Freund lich经验吸附方程。吸附温度升高与ACF比表面积增加... 以活性炭纤维(ACF)为溶液中铁离子的吸附剂,考察了吸附时间、吸附温度、ACF比表面积及表面酸碱性对Fe3+吸附行为的影响。通过平衡吸附实验获得的吸附等温线,并不符合Langmu ir与Freund lich经验吸附方程。吸附温度升高与ACF比表面积增加,都有利于铁离子的吸附,说明吸附过程同时具备物理和化学吸附行为的双重特征。ACF表面碱性基团是影响铁离子吸附的主要因素。 展开更多
关键词 活性炭纤维 铁离子 吸附
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