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Charge Neutralization (charge + neutralization)
Selected AbstractsElectrostatic Charge Measurement and Charge Neutralization of Fine Aerosol Particles during the Generation ProcessPARTICLE & PARTICLE SYSTEMS CHARACTERIZATION, Issue 5 2005Chuen-Jinn Tsai Abstract An aerosol charge analyzer has been constructed to measure the charge distribution of NaCl particles generated in the laboratory. A radioactive electrostatic charge neutralizer utilizing Po-210 was used to neutralize the electrostatic charge of the particles. The atomization technique was used to generate NaCl particles with diameters of 0.2 to 0.8 ,m, while the evaporation and condensation method was adopted to generate particles of 0.01 to 0.2 ,m in diameter. The experimental data demonstrates that the absolute average particle charge depends on the particle diameter, and is higher than that calculated by the Boltzmann charge equilibrium for particles within the range of 0.2 to 0.8 ,m. The charge increases with decreasing NaCl concentration. When these particles are neutralized using the Po-210 neutralizer, it is found that the electrostatic charge reaches the Boltzmann charge equilibrium. For 0.01 to 0.2 ,m NaCl particles generated using the evaporation and condensation method, test results show that the absolute average particle charge is higher than that calculated by the Boltzmann charge equilibrium for particles larger than 0.03 to 0.05 ,m in diameter, while it is lower than that predicted by the Fuchs theory [1], for particles smaller than 0.03 to 0.05 ,m. However, after charge neutralization, particles with diameter above 0.05 ,m reach the Boltzmann charge equilibrium condition, and the charges for particles with diameters of 0.010 to 0.05 ,m, agree well with Fuchs' theory. [source] Role of the surface charges D72 and K8 in the function and structural stability of the cytochrome c6 from Nostoc sp.FEBS JOURNAL, Issue 13 2005PCC 711 We investigated the role of electrostatic charges at positions D72 and K8 in the function and structural stability of cytochrome c6 from Nostoc sp. PCC 7119 (cyt c6). A series of mutant forms was generated to span the possible combinations of charge neutralization (by mutation to alanine) and charge inversion (by mutation to lysine and aspartate, respectively) in these positions. All forms of cyt c6 were functionally characterized by laser flash absorption spectroscopy, and their stability was probed by urea-induced folding equilibrium relaxation experiments and differential scanning calorimetry. Neutralization or inversion of the positive charge at position K8 reduced the efficiency of electron transfer to photosystem I. This effect could not be reversed by compensating for the change in global charge that had been introduced by the mutation, indicating a specific role for K8 in the formation of the electron transfer complex between cyt c6 and photosystem I. Replacement of D72 by asparagine or lysine increased the efficiency of electron transfer to photosystem I, but destabilized the protein. D72 apparently participates in electrostatic interactions that stabilize the structure of cyt c6. The destabilizing effect was reduced when aspartate was replaced by the small amino acid alanine. Complementing the mutation D72A with a charge neutralization or inversion at position K8 led to mutant forms of cyt c6 that were more stable than the wild-type under all tested conditions. [source] Flocculated decolorization of vinylsulfone reactive dye solutions with a ,-cyclodextrin-based copolymerJOURNAL OF APPLIED POLYMER SCIENCE, Issue 1 2010Xiuzhi Tian Abstract A ,-cyclodextrin (,-CD)-based copolymer (,-CD,maleic anhydride,N -trimethylaminoethylmethacrylate chloride) with good thermal stability was designed and synthesized for flocculated decolorization of Reactive Brilliant Blue KN-R solutions. Jar tests indicated that with the optimal stirring mode as 120 rpm for 5 min and then 40 rpm for 5 min with a flocculant-to-dye ratio of 2 : 5 (w/w), a pH of 8,10, and a temperature of 20°C, the maximum color removal reached. It is reported first in this article that, in addition to the polymer bridge and charge neutralization, the covalent bond of the reactive dye to the target flocculant molecules, which had a similar chemical structure to that of cellulose, contributed to the mechanism of flocculated decolorization. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source] Substituent effects in reductions of heteroaromatic cationsJOURNAL OF PHYSICAL ORGANIC CHEMISTRY, Issue 10 2002David Heyes Abstract A set of 11 each of 2,4,6-triphenylpyrylium, -thiopyrylium and - N -methylpyridinium tetrafluoroborates carrying a range of substituents in the phenyl rings were prepared. First and second wave reduction potentials were determined. For the thiopyrylium series there are linear correlations between scaled potentials (E°/0.05915) and summed Hammett constants for substituents in the pendant phenyl groups (,,=,2.29 and 3.38 for first and second waves respectively). For the pyrylium series, a good linear relationship (,,=,2.79) is obtained for all substituent patterns for the first wave reduction potentials, but for the second wave there are separate correlations for salts carrying substituents in the 4-phenyl and for those carrying substituents in 2- and 6-phenyls. For the pyridinium series, the first wave potentials show separate correlations for salts carrying substituents in the 4-phenyl and for those carrying substituents in 2-and 6-phenyls, but a single linear relationship for the second wave potentials. These are related to particular structural features in the cations, radicals and anions in each series. Rates and products were determined for reductions of the pyrylium and thiopyrylium cations by sodium cyanoborohydride and of all cations by sodium borohydride in acetonitrile solution. Reactions are first order in reducing agent and cation. Primary kinetic isotope effects were determined for borohydride reduction of the least reactive of each of the series of cations. Plots of logarithms of second-order rate constants against summed Hammett constants for substituents in the pendant phenyl groups are linear for all combinations of reagent and cation with 0.91 < , < 1.50 across all substituent patterns. For parent pyrylium and thiopyryliums, kBH4/kCNBH3,=,8.4,×,104 and 1.5,×,104, respectively, and for reductions by borohydride the reactivities of the pyrylium, thiopyrylium and pyridinium, series decrease in the order 1.4,×,105:8.8,×,103:1. Constant selectivities are not observed. Comparison of the correlations for electrochemical reduction and for hydride addition leads to the conclusion that charge neutralization in the hydride addition transition states runs ahead of bonding changes at the originating B,H bond. Copyright © 2002 John Wiley & Sons, Ltd. [source] H4 acetylation does not replace H3 acetylation in chromatin remodelling and transcription activation of Adr1-dependent genesMOLECULAR MICROBIOLOGY, Issue 5 2006Eleonora Agricola Summary Histone acetylation regulates gene expression. Whether this is caused by a general increase in nucleosome fluidity due to charge neutralization or by a more specific code is still matter of debate. By using a set of glucose-repressed Adr1-dependent genes of Saccharomyces cerevisiae, whose transcription was previously shown to require both Gcn5 and Esa1, we asked how changes of histone acetylation patterns at the promoter nucleosomes regulate chromatin remodelling and activation. When the signal of glucose reduction reaches the cells, H4 acetylation is kept constant while an increase of H3 acetylation occurs, in an Adr1- and Gcn5-dependent manner. In cells lacking Gcn5 activity, the H3 acetylation increase does not occur and an unexpected increase of histone H4 acetylation is observed. Nevertheless, chromatin remodelling and transcription activation are impaired, suggesting that acetylation of H3 and H4 histones plays different roles. [source] Size and Structure Characterization of Dye Flocs during Coagulation of Reactive Black 5 DyePARTICLE & PARTICLE SYSTEMS CHARACTERIZATION, Issue 2 2006Marta Janeczko Abstract This paper deals with results from laboratory scale experiments with model dye effluents comprising of the commercially used textile diazo dye, CI "Reactive Black 5", coagulated with ZETAG type primary coagulants. Size and structure analysis of flocs in coagulated dye sludge was undertaken in order to evaluate their separation abilities. The particle size distribution was estimated by use of a Galai CIS-100 particle counting system working on a time-of-transition principle, while their fractal dimension was obtained from laser scattering instrument in LALS mode. An image analysis of the flocculated dye-sludge has also been carried out. In parallel to the flocs characterization, the measurement of surface charge density of coagulated dye sludge was performed with the aim of linking surface charge data with the floc characteristics, and on this basis, to outline the predominant mechanism of color removal. It was found that flocs produced at optimal dosage are characterized by large sizes and a high value of fractal dimension, which is manifested in a very good level of color removal by sedimentation. The evident correlation between the surface charge density progression of coagulated dye flocs and color removal, suggests adsorption and charge neutralization as the predominant mechanism of dye destabilization. [source] Electrostatic Charge Measurement and Charge Neutralization of Fine Aerosol Particles during the Generation ProcessPARTICLE & PARTICLE SYSTEMS CHARACTERIZATION, Issue 5 2005Chuen-Jinn Tsai Abstract An aerosol charge analyzer has been constructed to measure the charge distribution of NaCl particles generated in the laboratory. A radioactive electrostatic charge neutralizer utilizing Po-210 was used to neutralize the electrostatic charge of the particles. The atomization technique was used to generate NaCl particles with diameters of 0.2 to 0.8 ,m, while the evaporation and condensation method was adopted to generate particles of 0.01 to 0.2 ,m in diameter. The experimental data demonstrates that the absolute average particle charge depends on the particle diameter, and is higher than that calculated by the Boltzmann charge equilibrium for particles within the range of 0.2 to 0.8 ,m. The charge increases with decreasing NaCl concentration. When these particles are neutralized using the Po-210 neutralizer, it is found that the electrostatic charge reaches the Boltzmann charge equilibrium. For 0.01 to 0.2 ,m NaCl particles generated using the evaporation and condensation method, test results show that the absolute average particle charge is higher than that calculated by the Boltzmann charge equilibrium for particles larger than 0.03 to 0.05 ,m in diameter, while it is lower than that predicted by the Fuchs theory [1], for particles smaller than 0.03 to 0.05 ,m. However, after charge neutralization, particles with diameter above 0.05 ,m reach the Boltzmann charge equilibrium condition, and the charges for particles with diameters of 0.010 to 0.05 ,m, agree well with Fuchs' theory. [source] The 2.0 Å crystal structure of the ER, ligand-binding domain complexed with lasofoxifenePROTEIN SCIENCE, Issue 5 2007Felix F. Vajdos Abstract Lasofoxifene is a new and potent selective estrogen receptor modulator (SERM). The structural basis of its interaction with the estrogen receptor has been investigated by crystallographic analysis of its complex with the ligand-binding domain of estrogen receptor , at a resolution of 2.0 Å. As with other SERMs, lasofoxifene diverts the receptor from its agonist-bound conformation by displacing the C-terminal AF-2 helix into the site at which the LXXLL motif of coactivator proteins would otherwise be able to bind. Lasofoxifene achieves this effect by occupying the space normally filled by residue Leu 540, as well as by modulating the conformation of residues of helix 11 (His 524, Leu 525). A well-defined salt bridge between lasofoxifene and Asp 351 suggests that charge neutralization in this region of the receptor may explain the some of the antiestrogenic effects of lasofoxifene. The results suggest general features of ER,/SERM recognition, and add a new dimension to efforts to rationalize differences between the biological activity profiles exhibited by these important pharmacological agents. [source] | |||||||||||||