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pH. Copyright (ph + copyright)
Selected AbstractsEffect of changes of pH on the anaerobic/aerobic transformations of biological phosphorus removal in wastewater fed with a mixture of propionic and acetic acidsJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 6 2006Yinguang Chen Abstract Most studies on the transformation of enhanced biological phosphorus removal have used acetic acid as the carbon source and focused on the anaerobic phase. In this paper the anaerobic and aerobic transformations of phosphorus removal microorganisms at various pH values were investigated with wastewater containing 3.14 mM C propionic acid and 1.56 mM C acetic acid. It was observed that the influence of acidic pH on the concentrations of mixed-liquor suspended solids and biomass was stronger than that of basic pH, and the maximal cell growth appeared at pH 7.6. The observed uptake rate of propionic acid was much faster than that of acetic acid at all pH values investigated, and both were affected by pH. The anaerobic transformations of polyhydroxyalkanoates and glycogen linearly decreased with increasing pH from 6.6 to 8.6, and a greater glycogen transformation correlated to greater polyhydroxyalkanoate transformation in both anaerobic and aerobic stages. Further studies revealed that at pH 6.6 and 8.6 the overall phosphorus release and uptake was low and there was no net phosphorus removal, although the initial phosphorus release was high. However, when the pH was controlled at pH 7.1 and 7.6, a phosphorus removal efficiency of 97.03% and 96.43% was achieved, respectively, which was greater than that of 87.46% at uncontrolled pH. Copyright © 2006 Society of Chemical Industry [source] Ammonia exchange on clinoptilolite from mineral deposits located in MexicoJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 6 2004Roberto Leyva-Ramos Abstract This work investigated the ion exchange of ammonia on clinoptilolite obtained from mineral deposits located in San Luis Potosi and Sonora, Mexico. Experimental ion exchange isotherm data were obtained in a batch adsorber. The effects of temperature and solution pH on the ion exchange capacity were studied and it was found that the exchange capacity was slightly increased by augmenting the temperature and by decreasing the pH from 6 to 3. The ion exchange capacity was independent of the diameter of the zeolite particles. The reversibility of ion exchange was analyzed by desorbing the ammonia exchanged on the zeolite. The ion exchange was reversible when 1% NaCl solution was used as the desorbing solution, but more ammonia was desorbed using 1% KCl solution in the desorption step. It was concluded that a considerable amount of ammonia was exchanged on the clinoptilolite and that the exchange capacity was slightly dependent on the temperature and pH. Copyright © 2004 Society of Chemical Industry [source] Factor analysis of spectroelectrochemical reduction of FAD reveals the pKa of the reduced state and the reduction pathwayJOURNAL OF CHEMOMETRICS, Issue 12 2007Edmund R. Malinowski Abstract The free flavin adenine dinucleotide (FAD) cofactor is known to exhibit a pH-dependent midpoint potential involving a simultaneous two-electron transfer step (n,=,2). Uv-vis spectroelectrochemical reductions of FAD at constant pH, ranging from 5 to 9, were recorded and analyzed by factor analysis. Principal factor analysis was used to determine the number of species present at each pH. The results indicate that only two composite forms of FAD are present: the oxidized and the reduced forms. Window factor analysis was used to extract the concentration profiles of the controlling species. The oxidized form was found to be a single pH-independent species, whereas the reduced form consists of two species. The pH-dependent spectroscopic changes of reduced FAD were best modeled by a single proton transfer step involving two different ionization states with an apparent pKa,=,6.3. This value compares favorably with those obtained from NMR and from midpoint potential measurements. At pH 6, the reduction of FAD was found to be first order, whereas at pH 9 the reduction is zero order; these observations are explained in terms of the reaction pathway involving xanthine oxidase, its substrate, and the pH. Copyright © 2007 John Wiley & Sons, Ltd. [source] Kinetics and mechanism of oxidation of apple pectin by CrVI in aqueous acid medium,JOURNAL OF PHYSICAL ORGANIC CHEMISTRY, Issue 12 2008Sebastián E. Bellú Abstract Selective oxidation of galacturonic acid residues of apple pectin by CrVI affords CO2/HCO2H, oxidized pectin, and CrIII as final redox products. The reaction shows first-order kinetics in [pectin], [CrVI], and [H+], at fixed ionic strength and temperature. Kinetic studies show that the redox reaction proceeds through a mechanism combining CrVI,,,CrIV,,,CrII and CrVI,,,CrIV,,,CrIII pathways. The mechanism is supported by the observation of free radicals, CrO (the formation of which implies involvement of CrII and CrIV) and CrV (formed in monoelectronic redox processes) as reaction intermediates. The reduction of CrIV and CrV by pectin was independently studied and found to occur more than 103 times faster than pectin,+,CrVI reaction, in acid medium. At pH 3,5, apple pectin,+,CrVI redox reaction is slow, oxo-chromate(V),pectin species stabilize and remain in solution during several hours. The present results show that these abundant and ubiquitous components of the cell walls of all land plants are able to reduce CrIV,VI or stabilize high-valent chromium depending on pH. Copyright © 2008 John Wiley & Sons, Ltd. [source] Control of polyaniline conductivity and contact angles by partial protonationPOLYMER INTERNATIONAL, Issue 1 2008Natalia V Blinova Abstract Many studies require a specific value of conductivity when investigating conducting polymers. The conductivity of polyaniline can efficiently be controlled by partial protonation of the polyaniline base. Although this is a simple task in principle, practical guidelines are missing. In the present study, the changes in the conductivity of polyaniline base after immersion in aqueous solutions of various acids are reported. Polyaniline base has been reprotonated in aqueous solutions of picric, camphorsulfonic and phosphoric acids. The conductivity of partially reprotonated polyaniline varied between 10,9 and 100 S cm,1. The relation between the pH of a phosphoric acid solution, which was in equilibrium with polyaniline, and the conductivity , is pH = 0.77 , 0.64 log(, [S cm,1]). The wettability, i.e. water contact angles, can similarly be set by partial protonation to between 78° for polyaniline base and 44° for polyaniline reprotonated in 1 mol L,1 phosphoric acid. In solutions of picric acid, the transition from the non-conducting to the conducting state occurs over a narrow range of acid concentrations, and the tuning of conductivity is consequently difficult. Phosphoric acid is well suited for the control of conductivity of polyaniline because of the moderate dependence of the conductivity on the acid concentration or pH. Copyright © 2007 Society of Chemical Industry [source] Hydrophobically modified polyelectrolytes II: synthesis and characterization of poly(acrylic acid-co-alkyl acrylate)POLYMERS FOR ADVANCED TECHNOLOGIES, Issue 11-12 2001Dong-qing Zhuang Abstract A series of hydrophobically modified poly(acrylic acid)(RH -PAA) were synthesized by solution copolymerization of acrylic acid with a small amount of alkyl acrylate (alkyl chain with a length of 8, 12, 14, 16, 18) and their solution properties were also systematically studied. It was found that the random distribution of alkyl acrylate along the polymeric backbone imparts these new materials pronounced associating ability in aqueous solution and the associating abilities vary with the chain length of the hydrophobic groups. In dilute solution, intramolecular association is observed from the intrinsic viscosity and the dependence of the intrinsic viscosity on chain length and ionic strength is also discussed. In semiconcentration solution, the modified polymers exhibit viscosities of several orders of magnitude higher than the unmodified poly(sodium acrylate) due to the strong intermolecular hydrophobic association. And the viscosifying effects become more significant with the increasing length of the alkyl chain. The copolymer solutions are highly pseudoplastic. Evidences for the hydrophobically associating interaction between hydrocarbon groups are provided by the dependence of the Brookfield viscosity on concentration, temperature, shear rate, ionic strength and pH. Copyright © 2001 John Wiley & Sons, Ltd. [source] Use of capillary electrophoresis in drug quality assessment of synthetic porcine secretinBIOMEDICAL CHROMATOGRAPHY, Issue 1 2005Baile A. Moumakwa Abstract The purity pro,le for porcine secretin attributable to contamination by equilibrium products such as aspartoyl3 secretin has been shown to be dependent on the pH of the analytical system. Capillary zone electrophoresis (CZE) methods have been developed for the ef,cient separation of synthetic porcine secretin, its equilibrium products and other impurities in aqueous solutions at both acidic and alkaline pH. These conditions are more representative of those used for the reconstitution and administration of porcine secretin, and good results cannot be achieved using HPLC due to poor peak shape above pH 5.8. The in,uence of various CZE operational parameters was systematically examined. The methods were validated for accuracy, precision, linearity, LOD and LOQ. A comparative evaluation of the stability of test solutions was determined using CZE and HPLC over a range of pH values. HPLC and CZE methods produced similar results at low pH. Copyright © 2004 John Wiley & Sons, Ltd. [source] | |||||||||||||