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Bound Water (bound + water)
Terms modified by Bound Water Selected AbstractsGas permeation related to the moisture sorption in films of glassy hydrophilic polymersJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2010F.L. Laksmana Abstract The purpose of this article is to elucidate the effect of integral sorption of moisture on gas permeation in glassy hydrophilic polymers. The oxygen and the simultaneous moisture sorption into various hydroxypropyl methylcellulose (HPMC) films were measured under a wide range of relative humidities using sorption analyzer equipment. Correspondingly, the oxygen permeability at different ambient conditions was measured using an oxygen detector. The solubility of oxygen in the HPMC film was found to be affected by the amount of water and therefore by the water state. At low moisture content, the water molecules are present as bound water, which promotes the sorption of oxygen in the HPMC films. At moisture content higher than 5%, water clusters are rapidly formed, which increase the affinity of HPMC polymer towards water rather than towards oxygen molecules, resulting in a decrease of oxygen solubility in the polymer. This was found to be the governing factor for the reduction in the oxygen permeability in glassy HPMC films at high water activity. This proposes a specific interaction between moisture sorption and oxygen transport in coating films like HPMC, which is of important aspect in the coating design and formulation. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source] Thermal analysis of polymer,water interactions and their relation to gas hydrate inhibitionJOURNAL OF APPLIED POLYMER SCIENCE, Issue 4 2007Manika Varma-Nair Abstract Gas hydrates formed in oil production pipelines are crystalline solids where hydrocarbon gas molecules such as methane, propane, and their mixtures are trapped in a cagelike structure by hydrogen-bonded water molecules to form undesirable plugs. Methanol and glycol are currently used to prevent these plugs via thermodynamic inhibition. Small amounts of water-soluble polymers may provide an alternate approach for preventing gas hydrates. In this study, we expand the fundamental understanding of water,polymer systems with differential scanning calorimetry. Nonfreezable bound water was used to quantify polymer,water interactions and relate them to the chemical structure for a series of polymers, including acrylamides, cyclic lactams, and n -vinyl amides. For good interactions, the water structure needs to be stabilized through hydrophobic interactions. An increased hydrophobicity of the pendant group also appears to favor polymer performance as a gas hydrate inhibitor. Good inhibitors, such as poly(diethyl acrylamide) and poly(N -vinyl caprolactam), also show higher heat capacities, which indicate higher hydrophobicity, than poor performers such as polyzwitterions, in which hydrophilicity dominated. The phase behavior and thermodynamic properties of dilute polymer solutions were also evaluated through measurements of the heat of demixing and lower critical solution temperature. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 2642,2653, 2007 [source] Esterification of n -butyric acid with n -butyl alcohol and transesterification of (R,,S)-phenylethanol by lipase immobilized on cellulose acetate,TiO2 gel fibreJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 1 2002Yuko Ikeda Abstract Lipase (EC 3.1.1.3) was immobilized on cellulose acetate,TiO2 gel fibre by the sol,gel method. The immobilized lipases were used for esterification of n -butyric acid with n -butyl alcohol and enantioselective acylation of (R, S)-phenylethanol using vinyl acetate as an acyl donor. Compared with native lipase, the activity of the immobilized lipase was stable and relatively unaffected by the water content of the solvent and the substrate concentration. The data indicate that the lipases are immobilized on the fibre surface and that enzyme activity is influenced by bound water. However, the thermal reactivity and enantioselectivity of the immobilized lipase were less than those of native lipase. This may not reflect thermal inactivation of the enzyme but rather significant thermal contraction of the gel fibre by cellulose crystallization, resulting in liberation of bound water and a decrease in the amount of enzyme which is available for the reaction. Copyright © 2001 Society of Chemical Industry [source] RING CHARACTERIZATION OF QUALITY INDICES IN BUTTERHEAD LETTUCE CULTIVATED UNDER MULCH AND BARE SOILJOURNAL OF FOOD QUALITY, Issue 4 2010MARÍA G. GOÑI ABSTRACT Butterhead lettuce was characterized by physical, microbiological and nutritional quality indices as a function of plant zoning and soil management (bare soil and mulch). Quality indices were measured in all the rings from the external toward the internal ratio. Assayed indices were: relative water content, water content, free and bound water, and the ratio between free water and total water, leaf area and color, total microbial counts (TMC) and ascorbic acid content (AA). The lettuce characterization by rings showed a remarkable plant zoning as a function of leaf age and development; also, some initial indices were affected by the soil management employed. Plastic mulches affect the microclimate around the plant, resulting in better plant water status. However, the use of black plastic covers could absorb sunlight therefore increasing soil temperature and causing lower AA and higher TMC in lettuce tissue. PRACTICAL APPLICATIONS During lettuce development, each leaf had a different level of exposure to environmental conditions, such as light, humidity, nutrients absorption and temperature affecting the quality indices of the raw material and introducing a source of variability in the physico-chemical, biochemical, nutritional and microbiological indices within the plant. In this way, the location of the leaf within the whole plant is an important factor to be considered. Moreover, during lettuce heads trading, it is a common practice to remove the external leaves as storage advances. These leaves are more perishable than middle and internal ones because of their direct exposure to environmental conditions. Understanding the way in which physical, microbiological and nutritional indices were distributed in the whole lettuce plant could be of interest, to know the value of the losses of regular green grocers' practices, from a nutritional and a safety point of view. [source] Magnetic resonance imaging of spatially resolved acrylamide photopolymerizationMAGNETIC RESONANCE IN CHEMISTRY, Issue 4 2003Tom J. Lees Abstract Magnetic resonance imaging was employed to examine spatially and temporally resolved photopolymerization of acrylamide gels. Fast exchange between free and bound water results in single exponential T2 decay, where 1/T2 scales linearly with polymer concentration. Measured T2s are sensitive to the experimental conditions; however, the 1/T2 relationship to polymer concentration allows a straightforward interpretation of image contrast changes during photopolymerization. The polymer appears to form at a nearly constant rate until the monomer concentration is significantly depleted. Conventional spin-echo images and quantitative CPMG-weighted spin-echo images were acquired. Photopolymerization of a partially masked sample produced a sharp transition (1 mm width) between polymer and monomer regions of the sample. The image intensity is uniform throughout the illuminated region of the sample, indicating uniform polymer formation. Interrupting the illumination quenches polymer formation. Copyright © 2003 John Wiley & Sons, Ltd. [source] Identification of bound waters in the solution structure of ribonuclease T1 using the double pulsed field gradient spin-echo NMR technique for selective water excitationMAGNETIC RESONANCE IN CHEMISTRY, Issue 9 2002Mitsuru Tashiro Abstract Novel pulse sequences incorporating the double pulsed field gradient spin-echo technique are presented that have particular use in identifying macromolecular bound water. The use of these sequences is illustrated using ribonuclease T1. Five amide protons cross-relaxing with bound water protons were observed. Examination of the crystal structure revealed that all of these amide protons donate hydrogen bonds or are in close proximity to water molecules with very low temperature factors, indicating that these amide protons are highly correlated with the bound water molecules. This method rapidly provides reliable information for characterizing macromolecular bound water molecules. Copyright © 2002 John Wiley & Sons, Ltd. [source] Comparative 1H NMR studies of saturation transfer in copolymer gels and mouse lensesNMR IN BIOMEDICINE, Issue 6 2010Koji Nakamura Abstract Saturation transfer in cross-linked copolymer gels and excised intact and perforating trauma-induced cataract mouse lenses (4- or 8-week-old) were studied using intermolecular cross-relaxation rates (1/TIS(H2O); 1/TIS), monitored with f2 -irradiation at ,8.79, ,4.00, and 7.13,ppm (,H2/2,,,,69,Hz). [1] The 1/TIS(7.13,ppm) vs dry weight [W (%)] profiles for hydrophilic copolymer gels were far steeper than those for hydrophobic copolymer gels, indicating the participation of an amount of bound water and a number of copolymer hydroxyl groups in the saturation transfer process. In contrast, the 1/TIS(,8.79,ppm) vs W (%) profiles exhibited little difference between the hydrophilic and hydrophobic copolymer gels, indicating the major participation of molecular rigidity, i.e. W (%) in the saturation transfer process. [2] The 1/TIS(7.13,ppm) values for cataractous mouse lenses were larger than those for intact lenses, indicating the formation of large, immobile lens protein associates or aggregates containing a sufficient amount of bound water for the saturation transfer. [3] The 1/TIS(7.13,ppm) vs W (%) profiles for the hydrophilic copolymer gels exhibited similar characteristics to the intact and cataractous mouse lenses with regard to the saturation transfer process. Copyright © 2010 John Wiley & Sons, Ltd. [source] Synthesis and Characterization of Nanostructured Manganese Dioxide Used as Positive Electrode Material for Electrochemical Capacitor with Lithium Hydroxide ElectrolyteCHINESE JOURNAL OF CHEMISTRY, Issue 1 2008An-Bao YUAN Abstract A nanostructured manganese dioxide electrode material was prepared using a solid-reaction route starting with MnCl2·4H2O and NH4HCO3, and its electrochemical performance as a positive electrode for MnO2/activated carbon hybrid supercapacitor with 1 mol·L,1 LiOH electrolyte was reported. The material was proved to be a mixture of nanostructured , -MnO2 and , -MnO2 containing some bound water in the structure, which was characterized by X-ray diffraction analysis, infrared spectrum analysis, and transmission electron microscope observation. Electrochemical properties of the MnO2 electrode and the MnO2/AC capacitor were investigated by cyclic voltammetry, ac impedance and galvanostatic charge/discharge methods. Experimental results showed that the MnO2 electrode exhibited faradaic pseudocapacitance behavior and higher specific capacitance in 1 mol·L,1 LiOH electrolyte. The MnO2/AC hybrid capacitor with 1 mol·L,1 LiOH electrolyte presented excellent rate charge/discharge ability and cyclic stability. [source] Practical aspects of ROESY experiments for identification of bound waters in the cyclic tetrasaccharideMAGNETIC RESONANCE IN CHEMISTRY, Issue 12 2005Kazuo Furihata Abstract ROESY pulse sequences are presented and evaluated to identify bound waters in the cyclic tetrasaccharide. The first experiment incorporated the double-pulsed field gradient spin-echo (DPFGSE) for selective water excitation at the initial portion of the pulse sequence. Although long, shaped pulses were used in DPFGSE to achieve the highly selective excitation of water resonance that is very close to resonances of the cyclic tetrasaccharide, the approach was not effective because of the loss of sensitivity. Concomitant use of long delays and moderate length of shaped pulses in the portion of DPFGSE gained more sensitivity. A simple approach incorporating spin-echo with long delays instead of DPFGSE also afforded a sensitive spectrum. Practical aspects of these ROESY experiments are illustrated using the cyclic tetrasaccharide cyclo -{,6}-,- D -Glcp -(1,3)-,- D -Glcp -(1,6)-,- D -Glcp -(1,3)-,- D -Glcp -(1,). Copyright © 2005 John Wiley & Sons, Ltd. [source] Identification of bound waters in the solution structure of ribonuclease T1 using the double pulsed field gradient spin-echo NMR technique for selective water excitationMAGNETIC RESONANCE IN CHEMISTRY, Issue 9 2002Mitsuru Tashiro Abstract Novel pulse sequences incorporating the double pulsed field gradient spin-echo technique are presented that have particular use in identifying macromolecular bound water. The use of these sequences is illustrated using ribonuclease T1. Five amide protons cross-relaxing with bound water protons were observed. Examination of the crystal structure revealed that all of these amide protons donate hydrogen bonds or are in close proximity to water molecules with very low temperature factors, indicating that these amide protons are highly correlated with the bound water molecules. This method rapidly provides reliable information for characterizing macromolecular bound water molecules. Copyright © 2002 John Wiley & Sons, Ltd. [source] Apocrustacyanin C1 crystals grown in space and on earth using vapour-diffusion geometry: protein structure refinements and electron-density map comparisonsACTA CRYSTALLOGRAPHICA SECTION D, Issue 7 2003Jarjis Habash Models of apocrustacyanin C1 were refined against X-ray data recorded on Bending Magnet 14 at the ESRF to resolutions of 1.85 and 2,Å from a space-grown and an earth-grown crystal, respectively, both using vapour-diffusion crystal-growth geometry. The space crystals were grown in the APCF on the NASA Space Shuttle. The microgravity crystal growth showed a cyclic nature attributed to Marangoni convection, thus reducing the benefits of the microgravity environment, as reported previously [Chayen et al. (1996), Q. Rev. Biophys.29, 227,278]. A subsequent mosaicity evaluation, also reported previously, showed only a partial improvement in the space-grown crystals over the earth-grown crystals [Snell et al. (1997), Acta Cryst. D53, 231,239], contrary to the case for lysozyme crystals grown in space with liquid,liquid diffusion, i.e. without any major motion during growth [Snell et al. (1995), Acta Cryst. D52, 1099,1102]. In this paper, apocrustacyanin C1 electron-density maps from the two refined models are now compared. It is concluded that the electron-density maps of the protein and the bound waters are found to be better overall for the structures of apocrustacyanin C1 studied from the space-grown crystal compared with those from the earth-grown crystal, even though both crystals were grown using vapour-diffusion crystal-growth geometry. The improved residues are on the surface of the protein, with two involved in or nearby crystal lattice-forming interactions, thus linking an improved crystal-growth mechanism to the molecular level. The structural comparison procedures developed should themselves be valuable for evaluating crystal-growth procedures in the future. [source] | ||||||||||