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离子色谱法测定复方聚乙二醇电解质散(Ⅲ)中氯离子、硫酸根和碳酸氢根的含量
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作者 张先华 赵钰馨 +5 位作者 周海燕 朱晓璐 赖登燕 朱姣 彭涛 叶世春 《中国药房》 CAS 北大核心 2024年第22期2769-2772,共4页
目的建立同时测定复方聚乙二醇电解质散(Ⅲ)中氯离子、硫酸根和碳酸氢根含量的离子色谱法。方法色谱柱为Dionex Ionpac^(TM) AS11-HC阴离子分析柱,保护柱为Dionex IonPac^(TM) AG11-HC,以10 mmol/L氢氧化钾为淋洗液进行等度洗脱,流速为1... 目的建立同时测定复方聚乙二醇电解质散(Ⅲ)中氯离子、硫酸根和碳酸氢根含量的离子色谱法。方法色谱柱为Dionex Ionpac^(TM) AS11-HC阴离子分析柱,保护柱为Dionex IonPac^(TM) AG11-HC,以10 mmol/L氢氧化钾为淋洗液进行等度洗脱,流速为1.2 mL/min,检测器为电导检测器,抑制器为Dionex AERS,抑制电流为30 mA,柱温为30℃,进样体积为10μL;按外标法计算氯离子和硫酸根的含量,按双对数拟合的标准曲线法计算碳酸氢根的含量。结果该色谱条件下,氯离子、硫酸根、碳酸氢根能有效分离,其线性范围分别为0.055~0.219 mg/mL(r为0.9999)、0.155~0.618 mg/mL(r为1.0000)、0.065~0.121 mg/mL(r为0.9999);回收率分别为98.06%~101.34%、97.37%~101.25%、97.16%~99.81%,RSD分别为1.1%、1.3%、1.0%(n=9);精密度、准确度、稳定性、耐用性考察的RSD均小于2%。结论建立的离子色谱法简单快速,准确度、精密度和耐用性良好,可同时测定复方聚乙二醇电解质散(Ⅲ)中氯离子、硫酸根、碳酸氢根的含量,适用于该药品的质量控制。 展开更多
关键词 离子色谱法 复方聚乙二醇电解质散() 氯离子 硫酸根 碳酸氢根
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Effect of cerium ion(Ⅲ) on corrosion resistance of organic-inorganic hybrid coating on surface of aluminum-tube used in refrigeration equipment
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作者 肖围 缪畅 +1 位作者 黄雄 满瑞林 《Transactions of Nonferrous Metals Society of China》 SCIE EI CAS CSCD 2015年第11期3847-3854,共8页
Organic?inorganic hybrid coating on the surface of aluminum-tube used in refrigeration equipment using cerium ion (III) as the additive was fabricated by sol?gel method, and the structure of the coating was confirmed ... Organic?inorganic hybrid coating on the surface of aluminum-tube used in refrigeration equipment using cerium ion (III) as the additive was fabricated by sol?gel method, and the structure of the coating was confirmed by FT-IR. The results of the characterization show that the corrosion resistance of the coating with 1.5 mmol/L cerium ion (III) gains significant improvement, in which the colour retention time of CuSO4 extends to 500 s, the anti-acid and alkali corrosion rates reduce by 67% and 70% compared with the blank one, respectively, and the salt spray tests also show good corrosion resistance. The electrochemical tests demonstrate that the self-corrosion current density and potential of the sample with hybrid coating are about 2.877×10?7 A/cm2 and?0.550 V, respectively. The metallographic and SEM images show that the hybrid coating is uniform and dense, and the EDS analysis confirms that the coating is mainly composed of Al, Si and Ce elements. 展开更多
关键词 aluminum-tube organic-inorganic hybrid coating corrosion resistance cerium ion() refrigeration equipment
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Cr(Ⅲ)离子印迹聚合物的制备及性能研究 被引量:1
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作者 付冬雪 汪鑫 +3 位作者 王贵芳 洪玉文 杨保民 成会玲 《云南大学学报(自然科学版)》 CAS CSCD 北大核心 2023年第6期1304-1313,共10页
以Cr(Ⅲ)为模板离子,采用表面印迹法,将氨基化多壁碳纳米管改性为乙烯化多壁碳纳米管作为固体基质,通过印迹体系的优化,制备了一系列Cr(Ⅲ)离子印迹聚合物[Cr(Ⅲ)-IIPs]及相应的非印迹聚合物[Cr(Ⅲ)-NIPs].在较优实验条件下制备的Cr(Ⅲ)... 以Cr(Ⅲ)为模板离子,采用表面印迹法,将氨基化多壁碳纳米管改性为乙烯化多壁碳纳米管作为固体基质,通过印迹体系的优化,制备了一系列Cr(Ⅲ)离子印迹聚合物[Cr(Ⅲ)-IIPs]及相应的非印迹聚合物[Cr(Ⅲ)-NIPs].在较优实验条件下制备的Cr(Ⅲ)-IIP1,吸附量为3.82 mmol·g^(−1),印迹因子为1.65.通过扫描电子显微镜(SEM)、氮气吸附/脱附(BET)、红外光谱(FIR)、热重分析(TG)等对Cr(Ⅲ)-IIP1及相应的Cr(Ⅲ)-NIP1,进行结构表征和性能评价.研究结果表明,Cr(Ⅲ)-IIP1属于热稳定性良好的吸附材料,吸附行为符合准二级动力学模型和Freundlich等温吸附模型,以化学吸附和多分子层吸附为主;在“竞争离子”Co(Ⅱ)、Ni(Ⅱ)和Pb(Ⅱ)共存条件下,对Cr(Ⅲ)离子具有较强的吸附能力和良好的选择性.说明在较优实验条件下制备的Cr(Ⅲ)-IIP1,有望作为一种新型的Cr(Ⅲ)离子吸附材料,去除和回收废水中的Cr(Ⅲ)离子. 展开更多
关键词 铬离子Cr() 离子印迹聚合物 表面印迹聚合法 碳纳米管
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Effect of fluoride addition on electrochemical behaviors of V(Ⅲ) in molten LiCl-KCl 被引量:1
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作者 Rui YUAN Cheng LÜ +4 位作者 He-li WAN Shao-long LI Yu-si CHE Ji-lin HE Jian-xun SONG 《Transactions of Nonferrous Metals Society of China》 SCIE EI CAS CSCD 2022年第8期2736-2745,共10页
X-ray photoelectron spectroscopy(XPS)and Raman spectroscopy were used to analyze the complexes in LiCl−KCl eutectic salt containing VCl_(3) and KF.The additional fluoride ions would replace chloride ions and combine w... X-ray photoelectron spectroscopy(XPS)and Raman spectroscopy were used to analyze the complexes in LiCl−KCl eutectic salt containing VCl_(3) and KF.The additional fluoride ions would replace chloride ions and combine with V(Ⅲ)to form VF_(6)^(3-).The electrochemical behavior of V(Ⅲ)was evaluated under condition of the molar concentration ratio of F−to Vn+(α)equal to 0:1,1:1,2:1,5:1,20:1 and 50:1,respectively.The results showed that a new reduction step appeared:VF_(6)^(3-)→V^(2+),and the reduction mechanism of vanadium ions became more complicated.The metallic vanadium was deposited on the tungsten electrode at−2.90 V in the LiCl−KCl melts for 6 h,and the products were characterized by SEM−EDS.It was indicated that the particle size of the product decreased with adding fluoride ions for the forming of the coordination compound VF_(6)^(3-). 展开更多
关键词 V() ion molten salt electrochemical behavior reduction mechanism complex
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Effect of Fe(Ⅲ) on the bromate reduction by humic substances in aqueous solution 被引量:4
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作者 XIE Li SHANG Chii ZHOU Qi 《Journal of Environmental Sciences》 SCIE EI CAS CSCD 2008年第3期257-261,共5页
Humic substances are ubiquitous redox-active organic compounds of environment. In this study, experiments were conducted to determine the reduction capacity of humic acid in the man-ix of bromate and Fe(Ⅲ) solution... Humic substances are ubiquitous redox-active organic compounds of environment. In this study, experiments were conducted to determine the reduction capacity of humic acid in the man-ix of bromate and Fe(Ⅲ) solutions and the role of Fe(Ⅲ) in this redox process. The results showed that the humic acid regenerated Fe(Ⅱ) and reduced bromate abiotically. The addition of Fe(Ⅲ) could accelerate the bromate reduction rate by forming humic acid-Fe(Ⅲ) complexes. Iron species acts as electron mediator and catalyst for the bromate reduction by humic acid, in which humic acid transfers electrons to the complexed Fe(Ⅲ) to form Fe(Ⅱ), and the regenerated Fe(Ⅱ) donate the electrons to bromate. The kinetics study on bromate reduction further indicated that bromate reduction by humic acid-Fe(Ⅲ) complexes is pH dependent. The rate decreased by 2-fold with the increase in solution pH by one unit. The reduction capacity of Aldrich humic acid was observed to be lower than that of humic acid or natural organic matter of Suwanne River, indicating that such redox process is expected to occur in the environment. 展开更多
关键词 humic acid Fe( ion bromate reduction electron mediator
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聚合物改性膨润土对钢渣渗滤液及其Cr(Ⅲ)离子的阻隔与吸附特性研究 被引量:1
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作者 姜璐莎 陈晓雄 +2 位作者 蒲诃夫 董晓强 谢世平 《太原理工大学学报》 CAS 北大核心 2023年第4期577-584,共8页
【目的】针对传统膨润土防渗衬垫在侵蚀性环境中防渗性能会大幅劣化的难题,自主研发了一种聚合物改性膨润土。【方法】通过渗透实验研究了聚合物改性膨润土对高盐溶液、强碱溶液和实际钢渣渗滤液的渗透系数,并采用Batch吸附实验探究了... 【目的】针对传统膨润土防渗衬垫在侵蚀性环境中防渗性能会大幅劣化的难题,自主研发了一种聚合物改性膨润土。【方法】通过渗透实验研究了聚合物改性膨润土对高盐溶液、强碱溶液和实际钢渣渗滤液的渗透系数,并采用Batch吸附实验探究了吸附时间、溶液pH值和溶液浓度对聚合物改性膨润土吸附钢渣渗滤液中Cr(Ⅲ)离子的影响。【结果】实验结果表明:未改性的钠化钙基膨润土对侵蚀性溶液的刚性壁渗透系数高达1×10^(-8)m/s,而聚合物改性膨润土对高盐、强碱和钢渣渗滤液的柔性壁渗透系数均小于1×10^(-11)m/s,且刚性壁渗透系数约为3×10^(-11)m/s,在高盐、强碱等侵蚀性环境中表现出更优越的防渗性能。【结论】聚合物改性膨润土对Cr(Ⅲ)的吸附量随着吸附时间、溶液pH值和溶液浓度的增加而增加。钠化钙基膨润土和聚合物改性膨润土对Cr(Ⅲ)吸附符合准二阶吸附动力学模型;Langmuir等温吸附模型更好地描述了钠化钙基膨润土和聚合物改性膨润土对Cr(Ⅲ)的吸附特性。 展开更多
关键词 膨润土 聚合物 渗透性 吸附性能 铬离子 钢渣渗滤液
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Kinetics and Mechanism of Iridium(Ⅲ)-Catalyzed Oxidation of Ethanol Amine by Cerium(Ⅳ) in Sulfuric Acid Media 被引量:1
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作者 ZHAI Yong-qing LIU Hong-mei YANG Lin YANG Guo-zhong SONG Wen-yu LIU Yu-kai 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2007年第3期333-338,共6页
In this study, the kinetics and mechanism of the iridium( Ⅲ ) -catalyzed oxidation of ethanol amine(EAN) by cerium(Ⅳ) in a sulfuric acid medium was investigated using titrimetric technique of redox in a temper... In this study, the kinetics and mechanism of the iridium( Ⅲ ) -catalyzed oxidation of ethanol amine(EAN) by cerium(Ⅳ) in a sulfuric acid medium was investigated using titrimetric technique of redox in a temperature range of 298--313 K. It was found that the reaction is of first order with respect to Ce( Ⅳ ) and It( Ⅲ ), and a positive fractional order with respect to EAN. It was also found that the pseudo-first-order ( [EAN ] 〉〉 [ Ce ( Ⅳ) ] ) rate constant koba decreases with the increase of [ H^+ ] and [ HSO^-4 ]. Under the protection of nitrogen gas, the reaction system can initiate the polymerization of acrylonitrile, indicating the generation of free radicals. On the basis of the experimental results, a suitable mechanism was proposed. From the dependence of koba on the concentration of hydrogen sulfate, Ce(SO4)2 was found to be the kinetically active species. The rate constants of the rote-determining step together with the activation parameters were evaluated. 展开更多
关键词 Iridium( ion Cerium(Ⅳ) ion Ethanol amine Catalytic oxidization Kinetics and mechanism
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Adsorption of Rare Earth Ion La(Ⅲ) on Yunnan Bowl Tea Surface from Aqueous Solution
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作者 木冠南 周俊 +1 位作者 唐丽斌 赵天培 《Journal of Rare Earths》 SCIE EI CAS CSCD 2003年第S1期23-27,共5页
The adsorption characteristics of rare earth ion La(Ⅲ) on Yunnan bowl tea surface from aqueous solution and effects of various surfactants on the adsorption were studied. It was found that Yunnan bowl tea can adsorb ... The adsorption characteristics of rare earth ion La(Ⅲ) on Yunnan bowl tea surface from aqueous solution and effects of various surfactants on the adsorption were studied. It was found that Yunnan bowl tea can adsorb strongly La(Ⅲ) and pH may affect drastically the adsorption amount of La(Ⅲ). The adsorption law of La(Ⅲ) on Yunnan bowl tea surface follows the Langmuir equation. The maximum adsorption amount of La(Ⅲ) can reach 15 mg·g (-1). A comprehensive adsorption model is suggested according to the experimental results. 展开更多
关键词 Yunnan bowl tea ADSORPTion lanthanum() ion surfactant rare earths
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Electroreduction of Co(Ⅱ) and La(Ⅲ)in UreaMelt
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作者 杨绮琴 丘开容 潘仕健 《Rare Metals》 SCIE EI CAS CSCD 1995年第1期13-17,共5页
Electroreduction of Co(Ⅱ)to metallic cohalt in urea melt is irrevsible in one step.The transfer coeffi-cient of electrode reaction of Co(Ⅱ)+2e=Co(O)and the diffusion coefficient of Co(Ⅱ)were determined.The lanthanu... Electroreduction of Co(Ⅱ)to metallic cohalt in urea melt is irrevsible in one step.The transfer coeffi-cient of electrode reaction of Co(Ⅱ)+2e=Co(O)and the diffusion coefficient of Co(Ⅱ)were determined.The lanthanum can be inductively codeposited with cobalt. The contents of lanthanum in cobalt-lanthanum de-posts increase with the shift of electrode potential to the negative direction and the raise of La(Ⅲ)/Co(Ⅱ)mo-lar ratio in the melt. The cyclic voltammetry,open circuit potential-time curve after potentiostatic electrolysisand electron probe analyas were used. 展开更多
关键词 Molten salt Co(Ⅱ) ion to() ion Electrede process Elec-trolytic codeposition
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PREPARATION AND CHARACTERIZATION OF NOVEL CHITOSAN DERIVATIVES:ADSORPTION EQUILIBRIUM OF IRON(Ⅲ) ION
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作者 Ke-long Huang Ping Ding +2 位作者 Su-qin Liu Gui-yin Li Yan-fei Liu 《Chinese Journal of Polymer Science》 SCIE CAS CSCD 2008年第1期1-11,共11页
The adsorption of Fe(Ⅲ)ions from aqueous solution by chitosan alpha-ketoglutaric acid(KCTS)and hydroxamated chitosan alpha-ketoglutaric acid(HKCTS)was studied in a batch adsorption system.Experiments were carried out... The adsorption of Fe(Ⅲ)ions from aqueous solution by chitosan alpha-ketoglutaric acid(KCTS)and hydroxamated chitosan alpha-ketoglutaric acid(HKCTS)was studied in a batch adsorption system.Experiments were carried out as function of pH,temperature,agitation rate and concentration of Fe(Ⅲ)ions.The Langmuir and Freundlich adsorption models were applied to describe the equilibrium isotherms and isotherm constants were determined.The Langmuir model agrees very well with experimental data.The pseudo-first-order a... 展开更多
关键词 Chitosan derivatives Fe()ion Adsorption kinetics
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Fe(Ⅲ)表面印迹硅胶聚合物的制备及其吸附性能研究
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作者 何红星 张炜业 +2 位作者 邓秀君 甘强 冯长根 《安全与环境学报》 CAS CSCD 北大核心 2023年第3期899-910,共12页
选用硅胶为基质材料、乙烯基膦酸为功能单体、Fe^(3+)为模板离子、乙二醇双甲基丙烯酸酯为交联剂,通过表面印迹技术制备了一种新型膦酸功能化的Fe(Ⅲ)印迹硅胶聚合物。对印迹吸附材料的吸附条件、吸附选择性和重复利用率进行了研究。通... 选用硅胶为基质材料、乙烯基膦酸为功能单体、Fe^(3+)为模板离子、乙二醇双甲基丙烯酸酯为交联剂,通过表面印迹技术制备了一种新型膦酸功能化的Fe(Ⅲ)印迹硅胶聚合物。对印迹吸附材料的吸附条件、吸附选择性和重复利用率进行了研究。通过FT-IR、SEM、EDX、TG和N_(2)吸附/脱附分析对印迹材料进行了表征,分析了印迹吸附剂对Fe^(3+)的吸附机理。结果表明:印迹吸附剂在8 min可达吸附平衡,最大吸附量达16.12 mg/g,吸附行为符合准二级动力学方程和Langmuir吸附等温式,印迹吸附剂展现出较高的选择性识别能力,与Cr^(3+)、Mn^(2+)和Zn^(2+)相比,对Fe^(3+)的选择性系数k分别为8.9、10.75和12.37。经过6次吸附-解吸试验,印迹材料吸附Fe^(3+)的能力仅下降了5.9%,证明其具有很好的可重复使用性能。 展开更多
关键词 环境工程学 表面印迹技术 印迹硅胶聚合物 Fe()离子 吸附选择性
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Complexity of Gold(Ⅲ)Ion With Cefotaxime and Cefepime Drugs:Spectroscopic,Antimicrobial and Antitumor Discussions
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作者 Lamia A Albedair Samar O Aljazzar +1 位作者 Mohamed I Kobeasy Moamen S Refat 《光谱学与光谱分析》 SCIE EI CAS CSCD 北大核心 2020年第10期3315-3320,共6页
The availability of chemical and biological data presented in this paper is the basis for understanding not only the current state of anti-cancer drugs based on gold(Ⅲ),but also the rationale for strategies for futur... The availability of chemical and biological data presented in this paper is the basis for understanding not only the current state of anti-cancer drugs based on gold(Ⅲ),but also the rationale for strategies for future drug design.New Au(Ⅲ)nanosized complexes of cefotaxime(ceph-3)and cefepime(ceph-4)ligands as a 3rd and 4th of cephalosporin generation drugs were synthesized.Gold(Ⅲ)complexes were discussed based on the elemental,molar conductance,thermal and magnetic moment measurements as well as spectral(FTIR,1HNMR,UV-Vis,and XRD)techniques.FT-IR spectra revealed that the ceph-3 and ceph-4 ligands reacted as a bidentate ligands through carboxylate oxygen andβ-lactam oxygen groups.The analytical analysis confirm that the molar ratio is 1∶1(Au 3+/ceph)with general formula[Au(L)(Cl)2]where L=ceph-3 or ceph-4.The structures of Au(Ⅲ)complexes were presence as a square planar geometry.X-ray diffraction patterns referred to a crystalline nature for all synthesized complexes.TEM analyses confirmed that the synthetic gold(Ⅲ)complexes have a nanosized particles.In vitro antimicrobial activities of Au(Ⅲ)complexes were evaluated towards two types of bacteria(G+&G-).The antitumor activities of gold(Ⅲ)complexes are appraised against breast(MCF-7)and colorectal adenocarcinoma(Caco-2)cell lines,which means that the two complexes may consider promising anticancer drugs. 展开更多
关键词 Cefotaxime sodium Cefepime hydrochloride COMPLEXITY Gold()ions Nanoscale Structure ANTICANCER
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Separation of indium(Ⅲ), gallium(Ⅲ), and zinc(Ⅱ) with Levextrel resin containing di(2-ethylhexyl) phosphoric acid (CL-P204): Part Ⅱ. Mechanism and kinetics of adsorbing indium(Ⅲ)
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作者 LIUJunshen ZHOUBaoxue +2 位作者 CAIChunguang CAIJun CAIWeimin 《Rare Metals》 SCIE EI CAS CSCD 2004年第1期1-5,共5页
The mechanism of adsorbing indium(Ⅲ) from sulfate solutions with CL-P204Levextrel resin containing di(-2-ethylhexyl) phosphoric acid was examined by batch operation andinfrared spectra. The results showed that the P2... The mechanism of adsorbing indium(Ⅲ) from sulfate solutions with CL-P204Levextrel resin containing di(-2-ethylhexyl) phosphoric acid was examined by batch operation andinfrared spectra. The results showed that the P204 adsorbed on the resin behaved in the similar wayto solvent extraction except that it was as a monomer in resin adsorbing but in dimeric form insolvent extraction. Three factors including temperature, indium(Ⅲ) concentration of solution, andthe size of resin particles which influence the In^(3+)/H^+ exchange on CL-P204 Levextrel resin wereinvestigated by the modified limited batch technique in order to determine the kinetics ofIn^(3+)/H^+ exchange. It was found that the rate of ion exchange increased with the temperature andthe concentration of solution increasing and with the size of the resin particles decreasing.According to the expression developed by Boyd et al., the controlling factor of In^(3+)/H^+ exchangeon CL-P204 Levextrel resin was the diffusion through the resin particles. The effective diffusioncoefficient, activation energy, and entropy of activation in the particle-diffusion were determinedas 1.57 x 10^(-10) m^2/s, 11.9 kJ/mol, -84.1 J/(mol·K), respectively. 展开更多
关键词 ion exchange MECHANISM batch test KINETICS indium() CL-P204 levextrelresin
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壳聚糖对铬(Ⅲ)离子吸附作用的研究 被引量:9
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作者 邢巍巍 安悦 李继平 《辽宁师范大学学报(自然科学版)》 CAS 2000年第2期155-157,共3页
研究了壳聚糖对铬 ( )离子的吸附性能 ,测定了吸附等温线和吸附动力学曲线 .实验结果表明壳聚糖对铬 ( )离子有较强的吸附能力 .吸附率受 p H值影响较大 .在此基础上 ,通过 IR、UV、SEM等检测手段证实铬 ( )离子与壳聚糖之间发生了... 研究了壳聚糖对铬 ( )离子的吸附性能 ,测定了吸附等温线和吸附动力学曲线 .实验结果表明壳聚糖对铬 ( )离子有较强的吸附能力 .吸附率受 p H值影响较大 .在此基础上 ,通过 IR、UV、SEM等检测手段证实铬 ( )离子与壳聚糖之间发生了配位作用 . 展开更多
关键词 壳聚糖 吸附 铬离子 铬污染 废水处理
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CdTe量子点的制备及其与Au(Ⅲ)的作用 被引量:7
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作者 张渝阳 董娇 +2 位作者 王娜 高鹏 臧树良 《分析科学学报》 CAS CSCD 北大核心 2009年第2期135-138,共4页
以金属铝作为还原剂,制备(NH4)2Te前体,合成了水溶性荧光CdTe量子点(QDs),该QDs在紫外光照射下有较强的荧光且发射波长可调谐,并可稳定放置。计算了发射峰位置在575nmCdTeQDs的粒径为2.82nm,与TEM图像进行对比,计算了量子产... 以金属铝作为还原剂,制备(NH4)2Te前体,合成了水溶性荧光CdTe量子点(QDs),该QDs在紫外光照射下有较强的荧光且发射波长可调谐,并可稳定放置。计算了发射峰位置在575nmCdTeQDs的粒径为2.82nm,与TEM图像进行对比,计算了量子产率为28%;讨论了在不同的实验条件下,Au(Ⅲ)对CdTeQDs的荧光猝灭,Au(Ⅲ)的浓度在2.1×10^-8~6.0×10^-7mol·L^-1与荧光猝灭值呈线性关系,线性方程为△F=0.0903+1.713c,r=0.9984,检出限为9.4×10^-9mol·L^-1。 展开更多
关键词 CDTE量子点 Au() 荧光猝灭
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一例Eu-MOF材料的构筑及对Fe^(3+)与硝基芳香族爆炸物的荧光检测性能
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作者 冀超 李文 +2 位作者 张丽荣 华佳 刘云凌 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 2024年第2期16-24,共9页
金属阳离子和硝基芳香族爆炸物的大量排放对环境和人体健康造成了严重威胁,对它们的高效检测具有重要的研究意义和挑战性,金属-有机骨架(MOFs)是一类新型的荧光传感检测材料.本文采用溶剂热法合成了一例具有fcu拓扑结构的Eu-MOF材料,[(C... 金属阳离子和硝基芳香族爆炸物的大量排放对环境和人体健康造成了严重威胁,对它们的高效检测具有重要的研究意义和挑战性,金属-有机骨架(MOFs)是一类新型的荧光传感检测材料.本文采用溶剂热法合成了一例具有fcu拓扑结构的Eu-MOF材料,[(CH_(3))_(2)NH_(2)]_(2)[Eu_(6)(μ_(3)-OH)_(8)(EDDC)_(6)]·8DMA·3MeOH·6H_(2)O[JLUMOF128,H_(2)EDDC=(E)-4,4′-(乙烯-1,2-取代基)二苯甲酸],并通过单晶X射线衍射、粉末X射线衍射、X射线光电子能谱、红外光谱、元素分析和热重分析对其结构及组成进行了表征.结果表明,由于荧光配体H_(2)EDDC的引入,JLU-MOF128表现出显著的荧光性能,在DMF溶液中对Fe^(3+)、2,4,6-三硝基苯酚(TNP)和2,4-二硝基苯酚(2,4-DNP)具有较好的检测效果,Ksv值分别为2.09×10^(4),8.49×10^(4)和5.75×10^(4)L/mol,检测限分别为5.99,1.51和1.93μmol/L.在金属阳离子和硝基芳香族爆炸物的检测方面,JLU-MOF128是一种理想的多感应荧光传感材料. 展开更多
关键词 铕-金属-有机骨架 荧光检测 Fe^(3+)离子 硝基芳香族爆炸物
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离子色谱-电感耦合等离子体质谱联用法测定西湖水中的痕量Sb(Ⅴ)和Sb(Ⅲ) 被引量:11
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作者 黄旭 徐子刚 +2 位作者 朱敏 姚琪 朱岩 《分析测试学报》 CAS CSCD 北大核心 2007年第3期420-422,共3页
建立了离子色谱-电感耦合等离子体质谱联用技术(IC-ICP-MS)测定西湖水中的痕量Sb(Ⅴ)和Sb(Ⅲ)的方法。采用Dionex IonPacAS14(4.6 mm×250 mm id)色谱柱,流速1 mL/min,3 mg/L EDTA和0.2mg/L邻苯二甲酸氢钾(KHP)(pH4.7)混合溶液为淋... 建立了离子色谱-电感耦合等离子体质谱联用技术(IC-ICP-MS)测定西湖水中的痕量Sb(Ⅴ)和Sb(Ⅲ)的方法。采用Dionex IonPacAS14(4.6 mm×250 mm id)色谱柱,流速1 mL/min,3 mg/L EDTA和0.2mg/L邻苯二甲酸氢钾(KHP)(pH4.7)混合溶液为淋洗液。50μL的进样量时,Sb(Ⅴ)的检出限为0.36μg/L,Sb(Ⅲ)的检出限为1.62μg/L。 展开更多
关键词 Sb(Ⅴ) Sb() 离子色谱 电感耦合等离子体质谱
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温度对铽(Ⅲ)-转铁蛋白溶液构象的影响 被引量:4
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作者 杨斌盛 白海静 +1 位作者 刘文 丰九英 《化学学报》 SCIE CAS CSCD 北大核心 2002年第4期737-743,共7页
在pH 7.4,0 .0 1mol/LN 2 羟乙基哌嗪 N′ 2 乙磺酸 (Hepes)条件下 ,铽 (Ⅲ )与N ,N′ 二 (2 羟苄基 )乙二胺 N ,N′ 二乙酸 (HBED)结合并发生交换相互作用使铽 (Ⅲ )荧光增强 10 4 倍 ,通过监测铽 (Ⅲ ) 5 45nm荧光强度的变化测定... 在pH 7.4,0 .0 1mol/LN 2 羟乙基哌嗪 N′ 2 乙磺酸 (Hepes)条件下 ,铽 (Ⅲ )与N ,N′ 二 (2 羟苄基 )乙二胺 N ,N′ 二乙酸 (HBED)结合并发生交换相互作用使铽 (Ⅲ )荧光增强 10 4 倍 ,通过监测铽 (Ⅲ ) 5 45nm荧光强度的变化测定了Tb HBED配合物的条件稳定常数是lgK =14.30± 0 .49;Tb HBED配合物中配体、铽 (Ⅲ )荧光强度均随着温度的升高而降低 .在pH 7.4,0 .0 1mol/LHepes条件下 ,TbN apoTf TbC 配合物中蛋白质的荧光强度随着温度的升高而降低 ,而能量受体铽 (Ⅲ )的荧光强度随着温度的升高而增强 ,主要源于铽 (Ⅲ )与螺旋 5色氨酸残基间的无辐射能量转移 ;当温度由 0℃上升到 5 5℃时 ,平均能量转移效率AE值增加了 2 9%,给体、受体间距离R有约 4.2 %的减小 ,温度变化引起TbN apoTf TbC 配合物大的构象变化 ;铽 (Ⅲ )与人血清脱铁转铁蛋白的结合使蛋白质的变性温度降低 .同样条件下 ,TbN apoOTf TbC 配合物与TbN apoTf TbC 配合物有所不同 ,虽然能量给体的荧光强度随着温度的增加而减小 ,但铽 (Ⅲ )荧光强度没有明显的增强 ;铽 (Ⅲ )对蛋白质的变性温度几乎没有影响 . 展开更多
关键词 温度 铽()离子 转铁蛋白 溶液构象 荧光光谱 荧光强度
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CL-P204萃淋树脂吸萃铟(Ⅲ)的离子交换动力学 被引量:8
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作者 刘军深 何争光 +1 位作者 贾淑华 蔡伟民 《稀有金属》 EI CAS CSCD 北大核心 2003年第1期104-107,共4页
为确定CL P2 0 4萃淋树脂 (内含二 ( 2 乙基己基 )磷酸萃取剂 )在硫酸介质内吸萃铟 (Ⅲ )过程中In3+ H+ 的离子交换动力学 ,以有限浴法考察了影响In3+ H+ 进行离子交换的三个因素 :温度、树脂的粒度和铟 (Ⅲ )离子的浓度。结果表明 ... 为确定CL P2 0 4萃淋树脂 (内含二 ( 2 乙基己基 )磷酸萃取剂 )在硫酸介质内吸萃铟 (Ⅲ )过程中In3+ H+ 的离子交换动力学 ,以有限浴法考察了影响In3+ H+ 进行离子交换的三个因素 :温度、树脂的粒度和铟 (Ⅲ )离子的浓度。结果表明 ,在实验范围内 ,其交换速度随温度的升高、铟 (Ⅲ )离子浓度的增大和树脂粒度的减小而增大。根据Body理论模型可推知 :粒内扩散是CL P2 0 4萃淋树脂在硫酸介质中吸萃铟 (Ⅲ )过程中In3+ H+ 交换的主控步骤。求得了In3+ H+ 离子交换过程中铟 (Ⅲ )离子在树脂上扩散的有效扩散常数、表观扩散活化能和活化熵 ,分别为 1 5 7× 10 - 1 0 m2 ·s- 1 ,11 9kJ·mol- 1 ,-84 1J·(mol·K) - 1 。 展开更多
关键词 动力学 离子交换 CL-P204萃淋树脂
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电气石吸附Cu^(2+),As(Ⅲ),F^-影响因素及机理研究 被引量:14
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作者 李珍 陈文 +1 位作者 王雪琴 杨密纯 《矿物岩石》 CAS CSCD 北大核心 2007年第4期8-12,共5页
以新疆电气石为原料,通过原子荧光光谱仪、原子吸收分光光度研究电气石的不同粒度、用量、吸附时间、热处理温度等对水中Cu2+,As(Ⅲ)吸附的影响;进而探讨分析电气石的吸附机理。研究结果表明:(1)电气石对Cu2+,As(Ⅲ),F-离子的去除率随... 以新疆电气石为原料,通过原子荧光光谱仪、原子吸收分光光度研究电气石的不同粒度、用量、吸附时间、热处理温度等对水中Cu2+,As(Ⅲ)吸附的影响;进而探讨分析电气石的吸附机理。研究结果表明:(1)电气石对Cu2+,As(Ⅲ),F-离子的去除率随着电气石粒径的减小而增加。随着电气石用量的增加,去除率逐渐提高,增至一定值后下降。热处理温度为300℃,500℃时,可提高电气石吸附Cu2+,As(Ⅲ)的效率。加热预处理未改善电气石对F-离子吸附能力。(2)电气石对带电性质不同的阴、阳离子都具有较好的吸附作用。电气石的极性和表面性质使其对离子可能存在络合吸附和静电吸附两种形式。电气石对Cu2+,As(Ⅲ)吸附为表面络合吸附与静电吸附共同作用,吸附效果好。对F-吸附只存在静电吸附,吸附效果差。 展开更多
关键词 电气石 Cu^2+ As() F^-离子 吸附 去除率
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