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81.
Sequential injection lab-on-valve (LOV) was first proposed for analyzing ultra-trace amounts of Pb using differential pulse anodic stripping voltammetry (DPASV) with a miniaturized electrochemical flow cell fabricated in the LOV unit. Deposition and stripping processes took place between the renewable mercury film carbon paste electrode and sample solution, the peak current was employed as the basis of quantification. The mercury film displayed a long-term stability and reproducibility for at least 50 cycles before next renewal, the properties of integrated miniature LOV unit not only enhanced the automation of the analysis procedure but also declined sample/reagent consumption. Potential factors that affect the present procedure were investigated in detail, i.e., deposition potential, deposition time, electrode renewable procedure and the volume of sample solution. The practical applicability of the present procedure was demonstrated by determination of Pb in environmental water samples. 相似文献
82.
83.
Conductivities of some tetraalkylammonium halides, viz. tetrabutylammonium bromide (Bu4NBr), tetrapentylammonium bromide (Pen4NBr), tetrahexylammonium bromide (Hex4NBr) and tetraheptylammonium bromide (Hep4NBr) were measured at 298.15 K in THF + C6H6 mixtures with 10, 20, 30 and 40 mass% of C6H6. A minimum in the conductance values was observed as concentration increases, which dependent both on the salt and the solvent. The observed molar conductivities were explained by the formation of ion-pairs (M+ + X− ↔ MX, KP) and triple-ions (2 M+ + X− ↔ M2X+; M+ + 2X− ↔ MX2−, KT). A linear relationship between the triple-ion formation constants [log(KT/KP)] and the salt concentrations at the minimum conductivity (log Cmin) was given for all salts in C6H6 + THF mixtures. The formation of triple-ions might be attributed to the ion sizes in solutions in which coulombic interactions and covalent bonding forces act as the main forces between the ions (R4N+ X−). 相似文献
84.
Harald Brand Dr. Jörn Martens Peter Mayer Dr. Axel Schulz Prof. Dr. Markus Seibald Thomas Soller 《化学:亚洲杂志》2009,4(10):1588-1603
The synthesis, structure, and bonding of alkali salts of resonance stabilized amides, such as diformylamide (dfa), formylcyanoamide (fca), nitrocyanoamide (nca), and for comparision, the well‐known dicyanoamide (dca), are discussed on the basis of experimental and theoretical data. The first structural reports of K(18‐crown‐6)+dfa?, K(18‐crown‐6)+fca?, Na+nca?, and Li(TMEDA)+dca? are presented. Examination of the X‐ray data reveals almost planar anions with strong cation–anion interactions resulting in network‐like structures in the solid state. For comparison, the X‐ray structures of covalently bound phenyldicyanoamide and diformamide are also discussed. The thermal behavior of the alkali salts of these amides is studied by thermoanalytical experiments. Moreover, several novel ionic liquids based on resonance stabilized amides have been prepared and were fully characterized, namely the dfa, fca, and nca salts of EMIM (1‐ethyl‐3‐methyl‐imidazolium), BMIM (1‐butyl‐3‐methyl‐imidazolium), and HMIM (1‐hexyl‐3‐methyl‐imidazolium). Most of them are liquid at room temperature, except BMIM+fca? that melts at 32 °C. These ionic liquids are neither heat nor shock sensitive, are thermally stable up to over 200 °C, and can be prepared easily in large quantities. 相似文献
85.
James Courmarcel Gildas Le Gland Loic Toupet Fr d ric Paul Claude Lapinte 《Journal of organometallic chemistry》2003,670(1-2):108-122
The synthesis of the new (η2-dppe)(η5-C5Me5)Fe---CC---1,3-(C6H4X) (m-2a/2b; X=F/Br) and (η2-dppe)(η5-C5Me5)Fe---CC---1,4-(C6H4I) (2c) complexes, as well as the solid-state structure of the known (η2-dppe)(η5-C5Me5)Fe---CC---1,4-(C6H4F) (2a) complex are described. The catalytic coupling reactions of the bromo complexes with various alkynes were next investigated. Starting from the known (η2-dppe)(η5-C5Me5)Fe---CC---1,4-(C6H4Br) complex (2b), the synthesis of the (η2-dppe)(η5-C5Me5)Fe---CC---1,4-(C6H4)---CC---H complex (6d) and of the corresponding silyl-protected precursors (η2-dppe)(η5-C5Me5)Fe---CC---1,4-(C6H4)CC---SiR3 (6b/6c; R=iPr/Me) are reported. By use of lithium---bromine exchange reactions on 2b, the silyl- (7a; E=Si; R=Me) and tin- (7b–7d; E=Sn; R=Me, Bu, Ph) substituted analogues (η2-dppe)(η5-C5Me5)Fe---CC---1,4-(C6H4)ER3 are also isolated. The spectroscopic and electrochemical characterisations of all these new Fe(II)/Fe(III) redox-active building blocks are presented and the electronic substituent parameters for the “(η2-dppe)(η5-C5Me5)Fe---CC” group are determined by means of 19F-NMR. 相似文献
86.
Feng X Lu JY Hao Y Banic C Schroeder WH 《Analytical and bioanalytical chemistry》2003,376(7):1137-1140
In this study, a diffusion-type device for generating gaseous mercuric chloride (HgCl2) was systematically evaluated and applied to validate the annular denuder method for sampling gaseous HgCl2 species in a synthetic gas stream. The results show that it takes at least 48 h for the system to reach a steady-state condition after the diffusion cell reaches the temperature set-point and the carrier gas is activated. The primary Hg species from the source was proven to be HgCl2. In the temperature range from –5.00 to 11.80 °C, the Hg emission rates from the source vary from 1.8 to 14.2 pg min–1. It is shown that, under the experimental conditions examined, KCl-coated annular quartz denuders designed for ambient reactive gaseous mercury (RGM) collection could quantitatively collect HgCl2. It is also demonstrated that the impactors used to remove coarse airborne particulate matter could lead to a loss of up to one third of the HgCl2 in the gas stream. 相似文献
87.
铜锌超氧化物歧化酶(Cu2Zn2SOD)在汞电极上的吸附研究 总被引:8,自引:0,他引:8
金属氧化还原蛋白质的电化学行为作为生物电化学领域中一个重要的研究内容,受到了广泛的关注犤1~3犦,生物体系一些重要的反应均与基本电荷运动有关,如生物催化、神经传导、光合作用以及呼吸作用等均涉及到一些重要氧化还原蛋白质的氧化还原过程。利用电化学的基本原理和实验方法,不但能在生命体系和有机组织的整体水平上,更主要是能在分子和细胞水平上研究氧化还原蛋白质体系中的电子转移以及氧化态转化的化学本质和规律。铜锌超氧化物歧化酶(Cu2Zn2SOD)是一个二聚体,由两个等同的亚单位组成,每一个亚单位含有咪唑桥联的铜?和锌?离子,催… 相似文献
88.
中国居民的头发铅、镉、砷、汞正常值上限 总被引:13,自引:0,他引:13
秦俊法 《广东微量元素科学》2004,11(4):29-37
根据普适性和实用性的原则,采用标准实验室测定的已有数据进行统计处理,并参照国内文献值及国际临床实验室资料作适当修正,提出了适用于中国居民的头发铅、镉、砷、汞正常值上限,供流行病学调查或疾病筛选时参考。 相似文献
89.
冷原子荧光法测定鲨鱼肝脏中的痕量汞 总被引:1,自引:0,他引:1
研究了冷原子荧光法测定鲨鱼肝脏中痕量汞的工作条件。样品风干后在2mol/L HNO3-4mol/L HCI体系中以V2O5为催化剂消解1h,上清液中的汞被SnCl2还原后于253.7nm用冷原子荧光法测定,在以10%SnCl2为还原剂时,线性范围0~0.2ng/mL,r=0.9997,检出限为0.05ng/mL,相对标准偏差2.5%,平均回收率94.0%~109.5%,该法简便、快速、准确。 相似文献
90.
亚临界水条件下煤中汞的脱除 总被引:1,自引:5,他引:1
运用半连续反应装置对山西吴家坪煤中汞在亚临界水中的脱除规律进行了研究。考察了反应温度为290 ℃、320 ℃ 、350 ℃、 380 ℃,反应压力为5 MPa、10 MPa、15 MPa,萃取时间为10 min、30 min、60 min、100 min时对汞脱除率的影响。结果表明,在290 ℃~380 ℃,随着温度升高,汞脱除率明显增加;在5 MPa~15 MPa,压力越大,汞的脱除率也越大;在10 min~100 min,随着萃取时间的延长,汞脱除率增加;在380 ℃, 15 MPa, 1 h,汞的脱除率最大可达96%以上。 相似文献