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81.
82.
流动注射电位滴定研究:氟化物沉淀滴定测锂 总被引:4,自引:0,他引:4
设计制作了一种简便的梯度混合室,并考察了其性能,试验结果证实了此混合室的合理性和有效性.用此混合室建立了流动注射电位滴定测锂的新方法,载流为1×10~(-5)~1×10~(-4)mol·L~(-1)的F~乙醇-水(9 1)溶液,流速4.2ml·min~(-1),混合室体积400μl,进样体积120μl,分析速度60样·h~(-1),检出范围取决于载流中滴定剂的浓度,方法用于卤水中锂的测定,结果令人满意. 相似文献
83.
Mokoena Emma M. Datye Abhaya K. Coville Neil J. 《Journal of Sol-Gel Science and Technology》2003,28(3):307-317
DL-tartaric acid was used as a template for the formation of silica nanotubes and spheres by the sol-gel method from tetraethylorthosilicate (TEOS) as silica source. The reactions were carried out in ethanol/water mixtures in the presence of aqueous ammonia, between 0°C and 75°C, using both stirred and non-stirred conditions. TEM and SEM images show that the yield and microstructure of the silica is influenced by the synthetic conditions (temperature, ammonia (aq) concentration, gelation time, solvent mixture). It was observed that the chiral form of the tartaric acid used and the diffusion of TEOS to the template determines the eventual silica structure. 相似文献
84.
磷肥中有效磷的示波滴定 总被引:2,自引:0,他引:2
根据Pb2+能与PO_4 ̄(3-)定量形成沉淀,过量的Pb2+在NaClO3-六次甲基四胺底液示波图上有敏锐切口的性质,报告了磷肥中有效磷含量测定的示波滴定新方法。该法与通用方法相比较,具有操作简便、测定快速、终点直观的优点。 相似文献
85.
倒数示波计时电位滴定新技术 总被引:2,自引:1,他引:2
倒数交流示波极谱具有抑制充电电流、突出电解电流的优点,利用(dE/dt)~(-1)-E曲线上去极剂峰的突然消失或出现指示滴定终点的方法称作倒数示波计时电位滴定法.由运算放大器组装的模拟电子线路可以对(dE/dt)~(-1)-E曲线进行反馈、反对数及微分处理,从而获得各种类型的倒数示波计时电位曲线(图1),以进一步提高滴定的灵敏度。 相似文献
86.
1 INTRODUCTION The crystal structures of several tetrahalogeno-mercurates (II) have been reported with a wide va-riety of stereochemical arrangements[1, . These stu- 2]dies have shown that the Hg atom… 相似文献
87.
The activity of enzyme I (EI), the first protein in the bacterial PEP:sugar phosphotransferase system, is regulated by a monomer–dimer equilibrium where a Mg2+-dependent autophosphorylation by PEP requires the homodimer. Using inactive EI(H189A), in which alanine is substituted for the active-site His189, substrate binding effects can be separated from those of phosphorylation. Whereas 1 mM PEP (with 2 mM Mg2+) strongly promotes dimerization of EI(H189A) at pH 7.5 and 20 °C, 5 mM pyruvate (with 2 mM Mg2+) has the opposite effect. A correlation between the coupling of N- and C-terminal domain unfolding, measured by differential scanning calorimetry, and the dimerization constant for EI, determined by sedimentation equilibrium, is observed. That is, when the coupling between N- and C-terminal domain unfolding produced by 0.2 or 1.0 mM PEP and 2 mM Mg2+ is inhibited by 5 mM pyruvate, the dimerization constant for EI(H189A) decreases from >108 to <5 × 105 or 3 × 107 M−1, respectively. With 2 mM Mg2+ at 15–25 °C and pH 7.5, PEP has been found to bind to one site/monomer of EI(H189A) with KA′106 M−1 (ΔG′=−33.7±0.2 kJ mol−1 and ΔH=+16.3 kJ mol−1 at 20 °C with ΔCp=−1.4 kJ K−1 mol−1). The binding of PEP to EI(H189A) is synergistic with that of Mg2+. Thus, physiological concentrations of PEP and Mg2+ increase, whereas pyruvate and Mg2+ decrease the amount of dimeric, active, dephospho-enzyme I. 相似文献
88.
用^13C HPDEC MAS NMR与热分析方法表征了在四氢呋喃(THF)-Na2O-SiO2- Al2O3-H2O体系中水热合成的高硅Na-THF-FER沸石、酸交换后的H-THF-FER沸石以及 吸附于Na-FER和H-FER沸石中的THF。结果证明,模板剂分子THF位于Na-THF-FER沸 石骨架的FER笼内,平衡骨架阳离子Na^+主要存在于十元环孔道;而吸附子FER沸石 中的THF仅处于十元环孔道中,合成样品中THF的化学位移与液态THF相比,向低场 移动,谱线明显变宽,表明THF分子与FER笼之间存在很强的相互作用。 相似文献
89.
C. Y. Zhu R. M. Izatt J. S. Bradshaw N. K. Dalley 《Journal of inclusion phenomena and macrocyclic chemistry》1992,13(1):17-27
Equilibrium constant (K), enthalpy change (H), and entropy change (S) values have been determined calorimetrically at 25°C in 90%MeOH 10%H2O (v/v) for the interactions of pyridino-18-crown-6 (P18C6) and diketopyridino-18-crown-6 (K2P18C6) with perchlorate salts of ammonium, benzylammonium,-phenylethylammonium,-phenylethylammonium, and-(1-naphthyl)ethyl-ammonium cations. The crystal structure of the complex of P18C6 with benzylammonium perchlorate was determined by X-ray crystallography. The1H 1D and 2D NMR spectra of some of these complexes were used to elucidate their structural features in solution. The logK values for the interaction of the ammonium cations with P18C6 are larger than those with K2P18C6, probably due to the higher degree of structural flexibility of P18C6. Ligand K2P18C6 displays appreciable - interaction with the-(1-naphthyl)ethylammonium cation, but not with the-phenylethylammonium cation.- interaction between ligand and cationSupplementary Data relating to this article are deposited with the British Library as Supplementary Publication No SUP 00000 (22 pages) 相似文献
90.
This paper describes the use of a thin-layered dual-band electrochemical cell operating at flow conditions to determine dipyrone (sodium salt of 1-phenil-2,3-dimethyl-4-methylaminomethanesulfonate-5-pyrazolone) by reaction with electrogenerated iodine. The electrolytic cell consisted of two closely spaced gold electrodes, the upper stream electrode serving as the generator electrode and the downstream electrode working as the collector electrode. A linear dynamic range from 2 to 15 μmol l−1 dipyrone was obtained by using a sample volume of 100 μl, with a detection limit of 1.1 μmol l−1. Standard deviation (S.D.) of 3.4% for 20 repetitive injections of a 40 μmol l−1 dipyrone solution and sampling frequency of 90 h−1 were achieved. The results obtained with the thin-layered dual-band electrochemical cell for dipyrone determination in three different pharmaceutical samples compared well with those found by iodimetry with coulometrically generated iodine. 相似文献