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41.
Thermodynamics of the dissociation of 2-aminopyridinium ion in synthetic seawater and a standard for pH in marine systems 总被引:1,自引:0,他引:1
Buffer solutions composed of 2-aminopyridinium chloride and 2-aminopyridine in synthetic seawater are useful as a supplement to buffers of Tris (pH 8.2) and Bis (pH 8.8) in standardizing measurements of hydrogen ion concentration (pm
H
or pH(SWS)) in oceanography. The dissociation constant of 2-amino-pyridinium ion over the range of salinities (S) from 30 to 40 has now been determined from the emf of cells without liquid junction at eight temperatures (T) from 278.15 to 313.15 K. The results fit the equation pK=2498.31/T–15.3274+2.4050 lnT+S(0.012928–2.9417×10–5T) with a standard deviation of 0.0023. Thermodynamic constants for the dissociation process and standard reference values of pm
H
and pH(SWS) were derived from the data. The pm
H
of the buffer consisting of 2-aminopyridinium chloride and 2-aminopyridine (each 0.04 molal) in synthetic seawater of salinity 35 varies from 7.356 at 278.15 K to 6.601 at 313.15 K. 相似文献
42.
Yoshiharu Yamane Yozo Nakamura Hiroyuki Okamoto Hiroshi Ooshima Jyoji Kato 《Applied biochemistry and biotechnology》1995,50(3):317-322
Effects of pH and dissolved oxygen concentration on batchwise riboflavin production by a 5-fluorouracil (5-FU)-resistant mutant
ofArthrobacter sp. were investigated. The reaction was carried out in a jar fermentor. The optimal pH of culture medium was around 7.3.
Dissolved oxygen concentration was almost constant during fermentation at 600 rpm of agitation rate. Production of riboflavin
reached a maximum of 160 mg/L after 70 h fermentation under the agitation rate of 600 rpm, aeration rate of 1.0 L/min, and
pH 7.0. 相似文献
43.
M. Durga Prasad 《Theoretical chemistry accounts》1994,88(5):383-388
Summary Finite order expressions are derived for expectation values and transition matrix elements within the framework of the coupled cluster method. 相似文献
44.
本文对微型管状离子选择电极在流动条件下的电化学特征进行了研究,并设计了新的集成微管路离子选择以电极功能块。用此微型装置测定了土壤、血清、水和药物中的K~+、Na~+、pH、Cl~-、F~-、阿托品、东茛菪碱,并和各种标准方法作了比较,获得满意分析结果。 相似文献
45.
Single-molecule studies that allow to compute pKa values, proton affinities (gas-phase acidity/basicity) and the electrostatic energy of solvation have been performed for a heterogeneous set of 26 organic compounds. Quantum mechanical density functional theory (DFT) using the Becke-half&half and B3LYP functionals on optimized molecular geometries have been carried out to investigate the energetics of gas-phase protonation. The electrostatic contribution to the solvation energies of protonated and deprotonated compounds were calculated by solving the Poisson equation using atomic charges generated by fitting the electrostatic potential derived from the molecular wave functions in vacuum. The combination of gas-phase and electrostatic solvation energies by means of the thermodynamic cycle enabled us to compute pKa values for the 26 compounds, which cover six distinct chemical groups (carboxylic acids, benzoic acids, phenols, imides, pyridines and imidazoles). The computational procedure for determining pKa values is accurate and transferable with a root-mean-square deviation of 0.53 and 0.57 pKa units and a maximum error of 1.0 pKa and 1.3 pKa units for Becke-half&half and B3LYP DFT functionals, respectively. 相似文献
46.
The enantiomers of some amino acids have been separated on commercial chiral TLC plates in reversed-phase mode. The effect
of the pH* of the aqueous-organic mobile phase on the retention and mobility of the enantiomers and on selectivity was investigated.
It was shown that for most of the amino acids investigated the highest enantioselectivity was obtained at pH* 3–4 or 6–7.
The drift and disturbance of the baseline on the chromatograms were also much smaller at pH* 3–4 and 6–7. 相似文献
47.
Published thermodynamic data measured in aqueous mixtures of sodium or potassium dihydrogen phosphate with hydrogen phosphate
and chloride at 25°C were used to test recently developed methods for calculation of the pH of phosphate buffer solutions.
Equations for ionic activity coefficients are used in these methods. It is shown that all data used in the tests up to an
ionic strength of about 0.5 mol-kg-1 can be accurately predicted by the two methods recommended. In one of these methods, equations of the Hückel type are used
for ionic activity coefficients and in the other equations of the Pitzer type. Several sets of phosphate buffer solutions
are recommended,e.g., for calibrations of glass electrode cells. In the recommended sets, the pH of the buffer solutions can be calculated either
by the Hückel or Pitzer method, and the pH predictions of these methods agree in most cases within 0.005 at least up to ionic
strengths of about 0.2 mol-kg-1. The pH values of the two primary pH standards endorsed by IUPAC based on aqueous mixtures of KH2PO4 and Na2HPO4,i.e., pH values of 6.865 and 7.413, can also be accurately predicted by the equations recommended in this study. 相似文献
48.
Niu CG Gui XQ Zeng GM Guan AL Gao PF Qin PZ 《Analytical and bioanalytical chemistry》2005,383(2):349-357
A fluorescence ratiometric sensor for pH determination is described in this paper. The sensor incorporated the pH-sensitive
dye meso-5,10,15,20-tetra-(4-allyloxyphenyl)porphyrin (TAPP) as an indicator and a pH-insensitive dye N-(2-methacryloxyethyl)benzo[k,l]thioxanthene-3,4-dicarboximide (MBTD), a benzothioxanthene derivative, as a reference for fluorescence ratiometric measurement.
To prevent leakage of the dyes, both were photocopolymerized with acrylamide, hydroxyethyl methacrylate, and triethylene glycol
dimethacrylate on the silanized glass surface. The reproducibility and response time of the prepared sensor were sufficient.
Most common coexisting inorganic ions and organic compounds did not interfere with pH sensing. In the acidic pH range from
1.5 to 5.0 the fluorescence intensity ratio of the two dyes varied linearly as a function of pH. The sensing membrane was
found to have a lifetime of at least one month. The sensor was applied to the analysis of waste water and artificial samples. 相似文献
49.
Jia-you Shu Mo Zhu Yi Shu Qi-jun Liu Tong Li 《高分子科学》2006,(4):395-401
The new chelate resins, abbreviated as PNBMZs and PBBMZs based on epoxide polymer, were synthesized by polycondensation of N,N-diglycidyl-4-glycidyloxyaniline or 1,4-bis(2,3-epoxypropyl)benzene with the primary amine group of 1,3-bis(benzimidazol-2yl)propylamine (BBPAH). The ion exchangers contain 2.71-3.23 mmol of the ligand contents per gram of the resin. Batch extraction capacities were determined for the metal chloride salts in buffer solutions in the pH range from -1 to 6.0. The chelate resins were very selective for Cu^2+, Zn^2+, Cd^2+ in the presence of other divalent transition metal ions. The maximum uptake capacities of PNBMZ (synthetic molar ratio = 1:1.5) under non-competitive condition were found to be 0.94 mmol/g for Cu^2+ at pH = 2, 1.3 mmol/g for Cd^2+ at pH = 1 and 1.75 mmol/g for Zn^2+ at pH = -1 respectively. While in the case of PBBMZ, it was 1.39 mmol/g for Cd〉 at pH = 1. The metal-uptake behaviors for both of them showed strong pH dependence, and their extraction capacities increase with decreasing pH. The uptake of Cu^2+ by the resin PNBMZs at pH = 1 was found to be rather fast with t1/2 = 18 min. Metal-uptake experiments under competitive conditions also confirm that the chelate resins have a high selectivity for Cu^2+, Zn^2+, Cd^2+ and the contrary pH dependence. 相似文献
50.
Tsutomu Oishi Kensoh Kagawa Minoru Fujimoto 《Journal of polymer science. Part A, Polymer chemistry》1995,33(8):1341-1352
Two types of optically active N-[N′-(α-methylbenzyl)amino/carbonyl-n-alkyl]maleimides (MBAC) were synthesized from maleic anhydride, 6-amino-n-caproic acid (or 12-amino-n-dodecanoic acid), and (R)-(+)-α-methylbenzylamine. Radical homopolymerizations of MBAC were performed in several solvents at 60 and 110°C for 24 h to give optically active polymers. Radical copolymerizations of MBAC were performed with styrene (ST) and methyl methacrylate (MMA) in dioxane at 60°C. The monomer reactivity ratios and the Alfrey-Price Q-e values were determined. Chiroptical properties of the polymers and copolymers were investigated. © 1995 John Wiley & Sons, Inc. 相似文献