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Water Ratio (water + ratio)
Selected AbstractsInvestigation of penetratin peptides Part 1.JOURNAL OF PEPTIDE SCIENCE, Issue 4 2002The environment dependent conformational properties of penetratin, two of its derivatives Abstract The homeodomain, the DNA-binding domain of Antennapedia homeoprotein, is composed of three ,-helices and one ,-turn between helices II and III. Its third helix from the N -terminal (helix III) can translocate through the cell membrane into the nucleus and can be used as an intracellular vehicle for the delivery of oligopeptides and oligonucleotides. To the best of our knowledge, this helix III, called penetratin, which consists of 16 amino acids, is internalized by cells in a specific, non-receptor-mediated manner. For a better understanding of the mechanism of the transfer, the structure of penetratin was examined in both extracellular matrix-mimetic and membrane-mimetic environments; 1H-NMR and CD spectroscopic measurements were performed in mixtures of TFE/water with different ratios. The molecular conformations of two analogue peptides [(6,14-Phe)-penetratin and a 12 amino acid penetratin derivative (peptide 3)] were also studied. An atomic level comprehensive analysis of penetratin and its two analogues was performed. In a membrane-mimetic solvent system (TFEd2/water = 9 : 1), on the basis of 553 distance restraints, the 4,12 region of penetratin exhibits a bent, irregular helical structure on NMR examination. Interactions between hydrophobic amino acid residues in conjunction with H-bonds stabilize the secondary structure of the molecule. Thus, both derivatives adopt a helix-like conformation. However, while (6,14-Phe)-penetratin displays both ,-helical and 310 -helical features, the structure of peptide 3 is predominantly a 310 -helix. Of the three peptides, surprisingly (6,14-Phe)-penetratin has the largest helical content. An increase in the polarity of the molecular environment gradually disintegrates these helix-like secondary structures. In a highly aqueous molecular system (TFEd2/water = 1 : 9), the fast exchange of multiple conformers leads to too few distance restraints being extracted, therefore the NMR structures can no longer be determined. The NMR data show that only short-range order can be traced in these peptides. Under these conditions, the molecules adopt nascent helix-like structures. On the other hand, CD spectra could be recorded at any TFE/water ratio and the conformational interconversion could therefore be monitored as a function of the polarity of the molecular environment. The CD data were analysed comprehensively by the quantitative deconvolution method (CCA+). All three penetratin peptides display helical conformational features in a low dielectric medium, with significant differences as a function of their amino acid composition. However, these conformational features are gradually lost during the shift from an apolar to a polar molecular environment. Copyright © 2002 European Peptide Society and John Wiley & Sons, Ltd. [source] The effect of water on particle size, porosity and the rate of drug release from implanted titania reservoirsJOURNAL OF BIOMEDICAL MATERIALS RESEARCH, Issue 2 2010Tessy Lopez Abstract The implantation of controlled drug release devices represents a new strategy in the treatment of neurodegenerative disorders. Sol,gel titania implants filled with valproic acid, have been used for this purpose to treat induced epilepsy in rats. The kinetics of the drug release depend on: (a) porosity, (b) chemical interactions between valproic acid and surface hydroxyl groups of titania, (c) particle size, and (d) particle size agglomerates. The concentration of water used in the hydrolysis reaction is an important variable in the degree of porosity, hydroxylation, and structural defects of the nanostructured titanium oxide reservoir. The titanium n -butoxide/water ratio was systematically varied during the sol,gel synthesis, while maintaining the amount of valproic acid constant. Characterization studies were performed using DTA-TGA, FTIR, Raman, TEM, SEM, BET, and in vitro release kinetic measurements. The particle agglomerate size and porosity were found to depend on the amount of water used in the sol,gel reaction. © 2010 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2010 [source] Effect of clay/water ratio during bentonite clay organophilization on the characteristics of the organobentonites and its polypropylene nanocompositesPOLYMER ENGINEERING & SCIENCE, Issue 9 2009Suédina M.L. Silva A sodium bentonite (montmorillonite-based layered silicate clay) was organically modified with cetyl trimethyl ammonium bromide (cetrimide), using different clay/water ratios,but the same clay/cetrimide ratio,to suspend the bentonite clay and perform its organophilization. Infrared spectroscopy and thermogravimetric analysis indicated the incorporation of organic modifier into the bentonite. Wide-angle X-ray scattering showed that the incorporation of surfactant significantly increased the interlayer spacing in the bentonite for all concentrations studied. It was found that clay/water ratio employed during the modification affects neither the amount of organic salt incorporated nor the interlayer spacing in the organobentonites, but influences its degree of structural disorder. Lower clay/water ratios resulted in a more disorderly structure, as established by the decrease of the areas under the X-ray peaks as the clay/water ratio diminishes. The modified bentonites were melt compounded with maleic anhydride-grafted polypropylene. X-ray diffraction patterns of the hybrids revealed that the more disorderly organobentonites were better dispersed in the polymer matrix, indicating that, in the present system, the structure of polymer nanocomposites obtained were affected by the clay/water ratio used in organobentonite preparation. POLYM. ENG. SCI., 2009. © 2009 Society of Plastics Engineers [source] Snap-off of a liquid drop immersed in another liquid flowing through a constricted capillaryAICHE JOURNAL, Issue 8 2009T. J. Peña Abstract Emulsions are encountered at different stages of oil production processes, often impacting many aspects of oilfield operations. Emulsions may form as oil and water come in contact inside the reservoir rock, valves, pumps, and other equipments. Snap-off is a possible mechanism to explain emulsion formation in two-phase flow in porous media. Quartz capillary tubes with a constriction (pore neck) served to analyze snap-off of long ("infinite") oil droplets as a function of capillary number and oil-water viscosity ratio. The flow of large oil drops through the constriction and the drop break-up process were visualized using an optical microscope. Snap-off occurrence was mapped as a function of flow parameters. High oil viscosity suppresses the breakup process, whereas snap-up was always observed at low dispersed-phase viscosity. At moderate viscosity oil/water ratio, snap-off was observed only at low capillary number. Mechanistic explanations based on competing forces in the liquid phases were proposed. © 2009 American Institute of Chemical Engineers AIChE J, 2009 [source] Enzymatic hydrolysis of Alaska pollack (Theragra chalcogramma) skin and antioxidant activity of the resulting hydrolysateJOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE, Issue 4 2010Jianping Jia Abstract BACKGROUND: Fish skin, a by-product of the food industry, contains a large amount of collagen. However, only a small proportion of fish skin is used in the production of leather materials and animal feedstuffs, most of it being discarded. The aims of this study were to prepare peptides from Alaska pollack (Theragra chalcogramma) skin by enzymatic hydrolysis and to evaluate the antioxidant activity of the resulting hydrolysate. RESULTS: Protamex was the most efficient enzyme for preparing antioxidant peptides from Alaska pollack skin. The optimal hydrolysis conditions were as follows: hydrolysis time 8 h; enzyme/substrate ratio 2:1000; skin/water ratio 1:6; temperature 55 °C; pH 6.0. Under these conditions the highest yield of peptides was 83.44%, with 85.95% of the hydrolysate being mainly composed of oligopeptides with molecular weights ranging from 180 to 1000 Da. The hydrolysate showed 2,2-diphenyl-1-picrylhydrazyl radical-scavenging activity, with an IC50 value of 2.5 mg mL,1, and its reducing power was 0.14 at 1 mg mL,1, 53.8% of that of reduced glutathione at the same concentration. CONCLUSION: This study demonstrated that the hydrolysate of Alaska pollack skin was mainly composed of oligopeptides with two to eight amino acid residues and possessed antioxidant activity. Copyright © 2010 Society of Chemical Industry [source] Nanoparticles of [Fe(NH2 -trz)3]Br2,3,H2O (NH2 -trz=2-Amino-1,2,4-triazole) Prepared by the Reverse Micelle Technique: Influence of Particle and Coherent Domain Sizes on Spin-Crossover PropertiesCHEMISTRY - A EUROPEAN JOURNAL, Issue 25 2009Thibaut Forestier Dr. Abstract By changing the surfactant/water ratio, nanoparticles of the iron(II) spin crossover material, [Fe(NH2 -trz)3]Br2,3,H2O (with NH2 -trz=4-amino-1,2,4-triazole), have been synthesised from 1,,m down to 30,nm (see figure). Magnetic and reflectivity experiments indicate that the critical size for observing a thermal hysteresis in this 1D polymer family is around 50,nm, and powder X-ray diffraction shows that particles of about 30,nm are constituted by about one coherent domain. This paper describes the synthesis of iron(II) spin-crossover nanoparticles prepared by the reverse micelle technique by using the non-ionic surfactant Lauropal (Ifralan D0205) from the polyoxyethylenic family. By changing the surfactant/water ratio, the size of the particles of [Fe(NH2 -trz)3]Br2,3H2O (with NH2trz=4-amino-1,2,4-triazole) can be controlled. On the macroscopic scale this complex exhibits cooperative thermal spin crossovers at 305 and 320,K. We find that when the size is reduced down to 50,nm, the spin transition becomes gradual and no hysteresis can be detected. For our data it seems that the critical size, for which the existence of a thermal hysteresis can be detected, is around 50,nm. Interestingly, the change of the particle size induces almost no change in the temperature of the thermal spin transition. A systematic determination of coherent domain size carried out on the nanoparticles by powder X-ray diffraction indicates that at approximately 30,nm individual particles consist of one coherent domain. [source] Effect of water composition on phosphorus concentration in runoff and water-soluble phosphate in two grassland soilsEUROPEAN JOURNAL OF SOIL SCIENCE, Issue 2 2006M. Schärer Summary Many irrigation experiments determine phosphorus (P) losses from soil. Often, these studies cannot be compared, because the irrigation water was not characterized. We used calcium-rich tap water and deionized water to investigate the influence of water composition on P concentrations in induced runoff. We irrigated two grassland sites: one acid and one calcareous. Less P was measured in runoff from tap water irrigation than from deionized water, especially for the acid soil. Batch experiments confirmed the findings of the field experiments. Tap water decreased water-soluble phosphate and increased calcium in the solid phase. This interaction increased with decreasing soil:water ratio. Water of low ionic strength gave results comparable to rainwater. Our findings demonstrate that solution chemistry and the soil:water ratio can strongly influence the availability of P for transport. We recommend that P tests or irrigation experiments should use water resembling that of the system of interest. Irrigation experiments aiming to simulate P losses by surface runoff should be carried out with water having a composition comparable to rainwater. [source] The application of response surface methodology to the production of phenolic extracts of lemon grass, galangal, holy basil and rosemaryINTERNATIONAL JOURNAL OF FOOD SCIENCE & TECHNOLOGY, Issue 2 2006T. Juntachote Summary The effects of independent variables (ethanol:water ratio, temperature and time) on the extraction yield and antioxidant properties of phenolic extracts from lemon grass, galangal, holy basil and rosemary were studied. The extraction solvent ratio of ethanol to water was found to have a significant (P < 0.05) influence on extraction yield, reducing power and total phenolic content, but not on the antioxidant activity of all herb and spice samples, while extraction temperature had only minor effects. Extraction time had a significant (P < 0.05) effect only on the reducing power of holy basil extracts. The optimum extraction conditions, i.e. extraction solvent ratio of ethanol to water, extraction temperature and extraction time for maximum total phenolic content, were 3:1 at 25 °C for 30 min for lemon grass, 3:1 at 75 °C for 90 min for galangal and holy basil and 3:1 at 75 °C for 30 min for rosemary. [source] Performance of the hydrolyzation film bed and biological aerated filter (HFB,BAF) combined system for the treatment of low-concentration domestic sewage in south ChinaJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 2 2006Xiao Ling Abstract The performance of the hydrolyzation film bed and biological aerated filter (HFB,BAF) combined system in pilot scale (with a daily treatment quantity of 600,1300 m3 d,1), operated for 234 days, for low-strength domestic sewage was assessed using different amounts of aeration, reflux ratios and hydraulic loading rates (HLR). In steady state it was found that the average removal efficiency of chemical oxygen demand (COD) and biological oxygen demand at 5 days (BOD5) were 82.0% and 82.2% and the average effluent concentrations were 15.8 mg L,1 and 9.4 mg L,1 respectively as the HFB was running at an HLR of 1.25,1.77 m3 m,2 h,1 and the BAF was running at an HLR of 1.56,2.21 m3 m,2 h,1. In general, the removal efficiency of total nitrogen (TN) fluctuated with the HLR, gas,water ratio and reflux ratio, so the ratio of gas to water should be controlled from 2:1 to 3:1 and the reflux ratio should be as high as possible. The effluent concentration of TN was 10.4 mg L,1 and the TN removal averaged 34.3% when the gas,water ratio was greater than 3:1 and the reflux ratio was 0.5. The effluent concentration and removal efficiency of NH4+ -N averaged respectively 2.3 mg L,1 and 78.5%. The overall reduction of total phosphorus (TP) was 30% and the average effluent concentration was 0.95 mg L,1. The removal efficiency of linear alkylbenzene sulfonates (LAS) reached 83.8% and the average effluent concentration was almost 0.9 mg L,1. The effluent concentration and removal efficiency of polychlorinated biphenyls (PCBs) were 0.0654 µ g L,1 and 37.05% respectively when the influent concentration was 0.1039 µ g L,1. The excess sludge containing water (volume 15 m3) was discharged once every 3 months. The power consumption of aeration was 0.06,0.09 kWh of sewage treated. The results show that the HFB,BAF combined technology is suitable for the treatment of low-concentration municipal sewage in south China. Copyright © 2005 Society of Chemical Industry [source] Size distributions and stability of toluene diluted heavy oil emulsionsAICHE JOURNAL, Issue 3 2006Chandra W. Angle Abstract The sizes and stability of oil droplets created from various concentrations of heavy oil-in-toluene at a fixed oil:water ratio were investigated during turbulent flow in model process water. The Reynolds number (Re) ranged from 17,000 to 34,500 and was obtained by stirred tank mixing with a Rushton turbine. The droplet sizes were monitored using laser light scattering. Results showed that at high Re and low oil concentrations (that is, low drop-surface coverage), breakage of the droplets was the dominant process, but as Re was reduced, coalescence was dominant. Droplets were less prone to breakage as the oil concentrations in toluene increased, and droplet sizes approached a steady state quickly during mixing. Their size distributions broadened and stability increased as heavy oil in toluene increased. Stability was attributed to a surface coverage by asphaltenes and the consequent interfacial elasticity that provided resilience to breakage. Equilibrium interfacial tension ,E was determined by fitting a diffusion-limited kinetic mathematical model to the data. The Gibbs adsorption model gave a monolayer surface coverage of 3 nm2/mol asphaltenes, consistent with other published results. High zeta potential of the droplets also hindered coalescence. © 2005 American Institute of Chemical Engineers AIChE J, 2006 [source] New method of predicting dry weight using bioelectrical impedance analysis in haemodialysis patientsNEPHROLOGY, Issue 8 2009SEOUNG WOO LEE SUMMARY: Aim: There were significant differences in the slopes of the ultrafiltration (UF) amount removed during haemodialysis (HD) sessions versus the percentage change in the extracellular fluid/total body water ratio for the right lower extremity (ECF/TBWright leg) plot in normohydrated (NH) and overhydrated states. The purpose of this study was to develop and validate a method for predicting dry weight (DW) using these results. Methods: It was hypothesized that for patients to become NH, the slope of the UF amount versus the percentage changes in ECF/TBWright leg plot should be same as that of NH patients and a method for predicting DW was developed. To validate the accuracy of this method, the ECF/TBWright leg was measured by eight-point tactile-electrode bioelectrical impedance analysis before and after HD in 17 newly enrolled NH patients. Using the current DW (cDW) of subjects as a reference, we compared the accuracies of pDW1 (our devised method) and pDW2 (the normovolaemia/hypervolaemia slope method). Results: The mean cDW, pDW1 and pDW2 values were 56.8 ± 7.9, 56.4 ± 7.7 and 56.3 ± 8.0 kg, respectively. No significant differences existed between cDW, pDW1 and pDW2. pDW1 had a lower root mean square error than pDW2 (1.12 vs 1.69). On the Bland,Altman plot, differences between pDW1 and cDW were closer to zero than between pDW2 and cDW. Conclusion: A new method was developed of predicting the DW using the relationship between the UF amount and the percentage change in the ECF/TBW ratio of the lower extremities after HD. The devised method appears to be as accurate as the normovolaemia/hypervolaemia slope method. [source] Water Resource Implications of 18O and 2H Distributions in a Basalt Aquifer SystemGROUND WATER, Issue 6 2000Kathryn R. Larson Ongoing decline of water levels in the confined basalt aquifers of the Pullman-Moscow Basin of Washington and Idaho has prompted study of the timing, amount and distribution of recharge to the system. Previous radiocarbon ages indicate residence times on the order of 103 years and greater and suggest a low rate of recharge to the lower basalt aquifer since the end of Pleistocene time. By contrast, more recent hydrodynamic flow modeling studies invoke a larger Holocene recharge rate through the unconfined loess unit to the upper and lower basalt aquifers, which implies relatively short residence times (102 years). Stable isotopes were used to independently assess contrasting recharge models by comparing 18O/16O and D/H ratios of late-Holocene shallow ground water and deep ground water. Linear regression of local precipitation ratios yields ,D = 6.9 ,18O ,18.5. There is no evidence of fractionation of ground water ratios by recharge processes or water-rock interactions. Deep basalt ground water ,18O values are depleted by 0.4 to 4.9 per mil relative to shallow, recently recharged ground waters and have ,18O values statistically distinct from waters sampled from other stratigraphic units. These findings suggest that the deep waters in the basin were not precipitated under current climate conditions and that aquifer recharge rates to the deep basalt aquifer are substantially lower than have been recently estimated. This in turn suggests that a sustainable ground water exploitation scheme must reduce reliance on the deep ground water resource. [source] Evidence for seasonal subglacial outburst events at a polythermal glacier, Finsterwalderbreen, SvalbardHYDROLOGICAL PROCESSES, Issue 12 2001J. L. Wadham Bulk runoff and meteorological data suggest the occurrence of two meltwater outburst events at Finsterwalderbreen, Svalbard, during the 1995 and 1999 melt seasons. Increased bulk meltwater concentrations of Cl, during the outbursts indicate the release of snowmelt from storage. Bulk meltwater hydrochemical data and suspended sediment concentrations suggest that this snowmelt accessed a chemical weathering environment characterized by high rock:water ratios and long rock,water contact times. This is consistent with a subglacial origin. The trigger for both the 1995 and 1999 outbursts is believed to be high rates of surface meltwater production and the oversupply of meltwater to areas of the glacier bed that were at the pressure melting point, but which were unconnected to the main subglacial drainage network. An increase in subglacial water pressure to above the overburden pressure lead to the forcing of a hydrological connection between the expanding subglacial reservoir and the ice-marginal channelized system. The purging of ice blocks from the glacier during the outbursts may indicate the breach of an ice dam during connection. Although subglacial meltwater issued continually from the glacier terminus via a subglacial upwelling during both melt seasons, field observations showed outburst meltwaters were released solely via an ice-marginal channel. It is possible that outburst events are a seasonal phenomenon at this glacier and reflect the periodic drainage of meltwaters from the same subglacial reservoir from year to year. However, the location of this reservoir is uncertain. A 100 m high bedrock ridge traverses the glacier 6·5 km from its terminus. The overdeepened area up-glacier from this is the most probable site for subglacial meltwater accumulation. Copyright © 2001 John Wiley & Sons, Ltd. [source] Retention of arsenic species on zwitterionic stationary phase in hydrophilic interaction chromatographyJOURNAL OF SEPARATION SCIENCE, JSS, Issue 6-7 2010Dan Xie Abstract Zwitterionic hydrophilic interaction chromatography (ZIC® -HILIC) was used to study the retention of selected organoarsenicals. The retention behavior of nine organic arsenic species on ZIC® -HILIC was investigated to elucidate which is the driving force for their separation, hydrophilic partitioning or adsorption driven by hydrogen bonds with surface H-donor/acceptor groups of the stationary phase. For this, the retention factor of the compounds k was correlated with log PO/W and with the calculated strength of hydrogen bonding of the analytes. By examining aliphatic and phenylic compounds separately, improved correlation was received. This indicates that both phenomena contribute to the separation of these arsenic species on ZIC® -HILIC. The results obtained evidence that considerable electrostatic interactions also occur on ZIC® -HILIC. Retention behavior of arsenic species was investigated by varying the separation conditions, which shows that the composition of the eluent has a strong influence on the retention behavior. It is highly dependent on water/acetonitrile ratio, pH value and salt additives. Dissociation degree and polarity of arsenic species, which are varying with pH, regulate the distribution of arsenic species between stationary and mobile phases in HILIC. Increase in the ammonium acetate concentration leads to shortened or to prolonged retention depending on the structure of the arsenic species. [source] A field study of critical chloride content in reinforced concrete with blended binderMATERIALS AND CORROSION/WERKSTOFFE UND KORROSION, Issue 8 2009L. Tang Abstract This paper presents the results from the investigation of chloride-induced reinforcement corrosion in concrete slabs after over 13 years exposure in the marine environment. In the beginning of 1990s over 40 reinforced concrete slabs with different types of binder and water/binder ratios were exposed in a marine environment at Swedish west coast. In this study a new rapid technique was used for non-destructive measurement of corrosion. Based on the results from the non-destructive measurement, the actual corrosion of steel bars in five concrete slabs was visually examined and the chloride profiles in the penetrating direction as well as at the cover level were measured. The results show that the visible corrosion normally occurred about 10,20 cm under the seawater level, where the oxygen may be sufficiently available for initiating the corrosion. It is also found that chloride may easily penetrate through a poor interface between concrete and mortar spacer and initiate an early corrosion. As a conclusion, although the chloride level 1% by mass of binder may not be the same as the conventionally defined threshold value, it can be taken as the critical level for significant on-going corrosion that is visible by destructive visual examination, despite types of binder. [source] | ||||||||||||||||||||||||||||