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Ionic Group Derivitized Nano Porous Carbon Electrodes for Capacitive Deionization 被引量:4
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作者 Marc Andelman 《Journal of Materials Science and Chemical Engineering》 2014年第3期16-22,共7页
Capacitance for electrostatic adsorption forms primarily within a Debye length of the electrode surface. Capacitive carbon electrodes were derivatized with ionic groups by means of adsorbing a surfactant in order to t... Capacitance for electrostatic adsorption forms primarily within a Debye length of the electrode surface. Capacitive carbon electrodes were derivatized with ionic groups by means of adsorbing a surfactant in order to test the theory that attached ionic groups would exclude co-ions and increase coulombic efficiency without the need for an added charge barrier membrane. It has been discovered that capacitive electrodes surface derivatized with ionic groups become polarized and intrinsically more coulombically efficient. 展开更多
关键词 Capacitive DEIONIZATION Flow Through Capacitor Polarized Electrode NANOPOROUS CARBON derivitized CARBON ELECTRODES DEIONIZATION DESALINATION Water Purification IONIC Groups
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The Fate of Chromium in Weathered Ultramafic Rocks and Their Derivitative Soils in Cuba: Clues from Spectroscopic Studies
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作者 Andrea L.FOSTER 《Acta Geologica Sinica(English Edition)》 SCIE CAS CSCD 2017年第S1期12-,共1页
In its cationic,trivalent form,Chromium(Cr)it is a micronutrient,and exhibits low environmental mobility.In hexavalent form,however,it is a human carcinogen and also highly mobile.Climate is a key environmental factor... In its cationic,trivalent form,Chromium(Cr)it is a micronutrient,and exhibits low environmental mobility.In hexavalent form,however,it is a human carcinogen and also highly mobile.Climate is a key environmental factor controlling weathering rates and stability of primary and secondary Cr-bearing minerals.Knowledge of Cr oxidation state and mineral residence is therefore essential to estimating the risk posed by Cr in serpentinites,chromite mine wastes,and soils developed on these parent materials.X-ray absorption spectroscopy(XAS)is currently the best available technique for determination of the relative abundance of Cr(III)and Cr(VI)in situ(that is,without digestion of solid phases).A brief review of relevant XAS studies of is presented below,focusing on studies in tropical climates1,as they will be most relevant to eastern Cuba’s extensively serpentinized ophiolite belt.Cr(III)-bearing spinels are usually the dominant and most refractory Cr host in ultramafic rocks.Previous XAS studies2 indicate that in tropical climates,Cr-spinels weather rapidly to form Cr(III)-bearing secondary Fe(III)(hydr)oxides(goethite,hematite).Manganese(Mn)is also enriched in ultramafic rocks2;as Mn(IV),it can also co-precipitate with Fe(III)(hydr)oxides,or form its own secondary(hydr)oxides.A previous study found up to 20%Cr(VI)in in a tropical,serpentine soil that contained substantial Mn,and a strong correlation between the*amounts of Cr(VI)and Mn(IV)in the soil profile2.Theresults of several XAS studies suggest that a close association of Mn(IV)and Cr(III)in secondary Fe(hydr)oxides is necessary for oxidation of Cr(III)to Cr(VI)via electron transfer reactions with Mn(IV);however,additional XAS studies have shown that organic matter3and Cr-bearing aluminosilicates4 may also be important sources of Cr(III)to the environment under specific conditions.The stability and fate of Cr has not been studied in detail for these two host phase types,to the best of our knowledge.Access to XAS facilities to perform Cr geochemical experiments is limited and will only become more so in the future.We are working to develop and apply(micro)Raman spectroscopy to evaluate Cr oxidation state and mineral residence(in crystalline and amorphous materials).In addition to standard Raman scattering,we are employing resonance Raman(785 nm laser)to enhance signal from Cr(VI)-bearing phases and laser-stimulated photoluminescence to identify Cr(III)associated with Al-rich alteration products 展开更多
关键词 Cr Clues from Spectroscopic Studies The Fate of Chromium in Weathered Ultramafic Rocks and Their derivitative Soils in Cuba
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柱前衍生非水毛细管电泳分离钴、镍和铜 被引量:6
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作者 刘笔锋 刘良斌 程介克 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 1998年第8期1232-1235,共4页
提出柱前衍生非水毛细管电泳分离金属离子的方法.应用新合成的2-(6-甲基-2-苯并噻唑偶氮)-5-二乙胺基酚作为柱前衍生试剂,乙醇和N,N-二甲基甲酰胺为非水溶剂,在6min内实现了钴、镍和铜的分离,灵敏度高,检测限... 提出柱前衍生非水毛细管电泳分离金属离子的方法.应用新合成的2-(6-甲基-2-苯并噻唑偶氮)-5-二乙胺基酚作为柱前衍生试剂,乙醇和N,N-二甲基甲酰胺为非水溶剂,在6min内实现了钴、镍和铜的分离,灵敏度高,检测限分别为9.18×10-8mol/L、2.79×10-7mol/L和4.47×10-7mol/L.考察了柱前衍生条件、非水溶剂配比以及分离参数对分离的影响. 展开更多
关键词 柱前衍生 非水 毛细管电泳 分离
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化妆品及保健品中Cr^(3+)和Cr^(6+)的柱后衍生-离子色谱法测定 被引量:8
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作者 钟志雄 朱炳辉 吴西梅 《分析测试学报》 CAS CSCD 北大核心 2008年第5期546-548,552,共4页
建立了化妆品和保健品中Cr3+、Cr6+的柱后衍生-离子色谱检测法。样品中的铬经柱前络合为2,6-嘧啶二羧酸铬,柱后衍生为1,5二苯碳酰二肼铬,于520 nm波长检测。优化了衍生反应条件,提高了检测灵敏度,Cr3+和Cr6+方法检出限(LODs,3σ)分别为0... 建立了化妆品和保健品中Cr3+、Cr6+的柱后衍生-离子色谱检测法。样品中的铬经柱前络合为2,6-嘧啶二羧酸铬,柱后衍生为1,5二苯碳酰二肼铬,于520 nm波长检测。优化了衍生反应条件,提高了检测灵敏度,Cr3+和Cr6+方法检出限(LODs,3σ)分别为0.12、0.011 mg/kg。样品加标回收率为89%~108%,重复性好。共存离子Fe2+、Fe3+、Pb2+、Cu2+、Al3+、Zn2+、Hg2+等,以及常见有机物均不干扰测定。 展开更多
关键词 柱后衍生 离子色谱法 化妆品 保健品 CR^3+ CR^6+
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反相离子对色谱柱后衍生法测定生物组织中四种生物胺的含量 被引量:4
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作者 杨文军 张丽英 +2 位作者 贺平丽 王宗义 李冰颖 《现代科学仪器》 2007年第3期107-109,共3页
采用反相色谱柱后衍生法测定肌肉组织中的酪胺、亚精胺、腐胺和尸胺含量。样品经0.6mol/L的高氯酸溶液匀浆提取;流动相为10mmol/L的辛烷磺酸钠溶液(pH5.2)与0.1mol/L乙酸钠溶液-乙腈(pH4.5),流速1mL/min;柱后衍生液为0.1%邻苯二甲醛(OPA... 采用反相色谱柱后衍生法测定肌肉组织中的酪胺、亚精胺、腐胺和尸胺含量。样品经0.6mol/L的高氯酸溶液匀浆提取;流动相为10mmol/L的辛烷磺酸钠溶液(pH5.2)与0.1mol/L乙酸钠溶液-乙腈(pH4.5),流速1mL/min;柱后衍生液为0.1%邻苯二甲醛(OPA)溶液(pH10.5~11.0),流速0.5mL/min;Discovery C18分离柱和保护柱;荧光检测器的激发波长和发射波长分别为340nm和450nm;采用62min的梯度洗脱程序;外标法定量测定。该方法在0.2~10μg/mL的浓度范围内具有良好的线性关系,酪胺、亚精胺、腐胺、尸胺的方法回收率在85.2%~103.3%之间,最低检测限为0.2μg/mL。 展开更多
关键词 生物胺 肌肉组织 反相色谱柱后衍生法
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HPLC在线二阶微分光谱法检测人表皮生长因子的C-端肽
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作者 张丽华 屠红 +2 位作者 吴高德 徐来根 夏其昌 《高技术通讯》 CAS CSCD 1995年第5期7-10,共4页
Trp(色氨酸)与Tyr(酪氨酸)二阶微分光谱能被用来在线检测RP-HPLC(反相高效液相色谱)中含芳香族氨基酸的肽段,这些特征光谱是通过二极管矩阵检测器(DAD)得到的,用这种方法分析人表皮生长因子(hEGF)的胰... Trp(色氨酸)与Tyr(酪氨酸)二阶微分光谱能被用来在线检测RP-HPLC(反相高效液相色谱)中含芳香族氨基酸的肽段,这些特征光谱是通过二极管矩阵检测器(DAD)得到的,用这种方法分析人表皮生长因子(hEGF)的胰蛋白酶酶解图谱,能鉴别出含Trp的C-端肽。 展开更多
关键词 二阶微分光谱 C-端肽序列分析 人表皮生长因子
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衍生化法测定水果中还原型谷胱甘肽(GSH)和总巯基含量 被引量:5
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作者 朴玉莲 沈丽 +1 位作者 韩玲 崔胜云 《食品工业科技》 CAS CSCD 北大核心 2012年第20期60-64,共5页
用衍生化试剂5,5-二硫硝基苯甲酸(DTNB)对巯基化合物的衍生化反应和邻苯二甲醛(OPA)与GSH的荧光衍生化反应,分别采用UV—vis分光光度法和荧光光度法测定了猕猴桃、大枣、酸浆中总巯基含量和GSH的含量。被测样品中GSH和总巯基相对... 用衍生化试剂5,5-二硫硝基苯甲酸(DTNB)对巯基化合物的衍生化反应和邻苯二甲醛(OPA)与GSH的荧光衍生化反应,分别采用UV—vis分光光度法和荧光光度法测定了猕猴桃、大枣、酸浆中总巯基含量和GSH的含量。被测样品中GSH和总巯基相对含量分布有较大的差异,其中猕猴桃和大枣中含有相对较高的GSH浓度分布,分别达0.7092、0.8374mol/g,酸浆中含有较高的总巯基含量分布,达1.4173mol/g。本测定方法的回收率达95.38%-101.9%,满足测定准确度的要求,总巯基含量和GSH含量测定最低检测限分别为9.6×10^-7,2.69×10^-7mol/L。 展开更多
关键词 谷胱甘肽 巯基化合物 衍生化 5 5-二硫双-2-硝基苯甲酸 邻苯二甲醛
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Microanalysis and preliminary pharmacokinetic studies of a sulfated polysaccharide from Laminariajaponica 被引量:4
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作者 张文静 孙德林 +3 位作者 赵峡 金维华 王晶 张全斌 《Chinese Journal of Oceanology and Limnology》 SCIE CAS CSCD 2016年第1期177-185,共9页
A rapid, sensitive and reproducible high performance liquid chromatography (HPLC) method with post-column fluorescence derivatization has been developed to determine the amount of low-molecular- weight sulfated poly... A rapid, sensitive and reproducible high performance liquid chromatography (HPLC) method with post-column fluorescence derivatization has been developed to determine the amount of low-molecular- weight sulfated polysaccharide (GFS) in vivo. The metabolism of GFS has been shown to fit a two component model following its administration by intravenous injection, and its pharmacokinetic parameters were determined to be as follows: half-time of distribution phase (t1/2α)=11.2±2.93 min, half-time of elimination phase (tl/2α)=98.20±25.78 min, maximum concentration (Cmax)=110.53 gg/mL and peak time (Tmax)=5 min. The pharmacokinetic behavior of GFS was also investigated following intragastric administration. However, the concentration of GFS found in serum was too low for detection, and GFS could only be detected for up to 2 h after intragastric administration (200 mg/kg body weight). Thus, the bioavailability of GFS was low following intragastric administration because of the metabolism of GFS. In conclusion, HPLC with post-column derivatization could be used for quantitative microanalysis and pharmacokinetic studies to determine the presence of polysaccharides in the serum following intravenous injection. 展开更多
关键词 sulfated polysaccharide HPLC post-column derivatization MICROANALYSIS PHARMACOKINETICS
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Construction of Post-column Micro-membrane Reactor for Protein Analysis in Capillary Electrophoresis with Laser Induced Fluorescence Detection
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作者 LIU Fan ZHANG Ling-yi QIAN Jun-hong GAO Fang-yuan REN Jun ZHANG Wei-bing 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2013年第5期828-830,共3页
Proteomics is becoming more and more mature, but the detection of low abundance proteins is still a difficult task. Laser-induced fluorescence(LIF) detection is one of the most sensitive detection methods in a capil... Proteomics is becoming more and more mature, but the detection of low abundance proteins is still a difficult task. Laser-induced fluorescence(LIF) detection is one of the most sensitive detection methods in a capillary electrophoresis(CE) system. However, most proteins do not exhibit favourable native fluorescence, a derivatization procedure is necessary for LIF detection of proteins. Since the derivatization reaction between protein and fluorescent reagent takes place after the separation of protein, the separation cannot be compromised by multiple derivatization products, the post-column derivatization becomes an attractive method for derivatization in CE-LIF system. 展开更多
关键词 post-column micro-membrane reactor Capillary electrophoresis Laser induced fluorescence detection
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含腙类结构化合物生物活性研究进展 被引量:6
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作者 康圣鸿 胡德禹 +1 位作者 吴剑 宋宝安 《农药》 CAS 北大核心 2012年第4期238-242,245,共6页
含腙类结构的化合物具有杀虫、杀菌、除草等广泛生物活性,在新农药创制中占有重要地位。根据农药用途进行分类,对其生物活性进行了介绍,并对其发展前景作进一步展望。
关键词 腙类衍生物 杀虫活性 杀菌活性 除草活性 进展
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含腙类化合物的设计、合成与生物活性
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作者 吴峤 王秀丽 +1 位作者 杨吉春 宋玉泉 《农药》 CAS CSCD 北大核心 2014年第9期631-632,646,共3页
[目的]含腙类结构的化合物具有杀虫、杀菌、除草等生物活性,在新农药创制中占有重要地位。发现具有更好生物活性的新化合物。[方法]利用新颖中间体合成含腙类化合物5个。并利用1H NMR等分析手段确定化合物的结构。[结果]生测活性测定表... [目的]含腙类结构的化合物具有杀虫、杀菌、除草等生物活性,在新农药创制中占有重要地位。发现具有更好生物活性的新化合物。[方法]利用新颖中间体合成含腙类化合物5个。并利用1H NMR等分析手段确定化合物的结构。[结果]生测活性测定表明某些化合物在600 mg/L下对小菜蛾显示出较好防效。该类化合物可作为先导化合物进行进一步优化研究。 展开更多
关键词 含腙类化合物 合成 生物活性
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金边土鳖HPLC指纹图谱及氨基酸含量测定 被引量:7
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作者 刘梦云 毕晓黎 +2 位作者 陈伟韬 李养学 江洁仪 《中国实验方剂学杂志》 CAS CSCD 北大核心 2018年第14期63-68,共6页
目的:建立金边土鳖氨基酸HPLC指纹图谱分析方法,并同时定量分析了6种氨基酸成分,为制订金边土鳖的质量标准提供参考。方法:采用异硫氰酸苯酯(PITC)-高效液相色谱(HPLC)柱前衍生化法,以Waters XBridge C18(4.6 mm×250 mm,5μ... 目的:建立金边土鳖氨基酸HPLC指纹图谱分析方法,并同时定量分析了6种氨基酸成分,为制订金边土鳖的质量标准提供参考。方法:采用异硫氰酸苯酯(PITC)-高效液相色谱(HPLC)柱前衍生化法,以Waters XBridge C18(4.6 mm×250 mm,5μm)为色谱柱;流动相A为0.1 mol·L^-1乙酸钠(p H 6.5)-乙腈(95∶5),B为乙腈-水(4∶1);检测波长254 nm;流速0.8 m L·min^-1梯度洗脱;柱温40℃。采用"中药色谱指纹图谱相似度评价系统(2004A版)"和SPSS 22.0软件分别对其进行相似度评价和聚类分析。结果:初步建立了金边土鳖游离氨基酸HPLC指纹图谱共有模式,确定了21个共有峰,并指认了13种氨基酸成分;综合14批金边土鳖相似度分析、聚类分析和定量分析,结果显示相似度分析和聚类分析基本一致,且发现精氨酸含量的高低可能与产地有一定的关系。结论:建立了金边土鳖HPLC指纹图谱分析方法,可较全面反映该药材中氨基酸成分的信息,为金边土鳖药材鉴定和质量标准的制订提供参考。 展开更多
关键词 金边土鳖 氨基酸 指纹图谱 含量测定 柱前衍生化 高效液相色谱
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