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M NaOH (m + naoh)
Terms modified by M NaOH Selected AbstractsInfluence of Metal Nanoparticles on the Electrocatalytic Oxidation of Glucose by Poly(NiIIteta) Modified ElectrodesELECTROANALYSIS, Issue 5 2010Pratap Azad Abstract Conductive polymeric [NiII(teta)]2+ (teta=C-meso-5,5,7,12,12,14-hexamethyl-1,4,8,11-tetra-azacyclotetradecane) films (poly(Ni)) have been deposited on the surface of glassy carbon (GC), Nafion (Nf) modified GC (GC/Nf) and Nf stabilized Ag and Au nanoparticles (NPs) modified GC (GC/Ag-Nf and GC/Au-Nf) electrodes. The cyclic voltammogram of the resulting electrodes, show a well defined redox peak due to oxidation and reduction of poly(Ni) system in 0.1,M NaOH. They show electrocatalytic activity towards the oxidation of glucose. AFM studies reveal the formation of poly(Ni) film on the modified electrodes. Presence of metal NPs increases electron transfer rate and electrocatalytic oxidation current by improving the communication within the Nf and poly(Ni) films. In the presence of metal NPs, 4 fold increase in current for glucose oxidation was observed. [source] Catalytic Effect on Silver Electrodeposition of Gold Deposited on Carbon ElectrodesELECTROANALYSIS, Issue 19 2004Alfredo de, Escosura-Muñiz Abstract A new methodology, based on silver electrocatalytic deposition and designed to quantify gold deposited onto carbon paste electrode (CPE) and glassy carbon electrode (GCE), has been developed in this work. Silver (prepared in 1.0,M NH3) electrodeposition at ,0.13,V occurs only when gold is previously deposited at an adequate potential on the electrode surface for a fixed period of time. When a CPE is used as working electrode, an adequate oxidation of gold is necessary. This oxidation is carried out in both 0.1,M NaOH and 0.1,M H2SO4 at oxidation potentials. When a GCE is used as working electrode, the oxidation steps are not necessary. Moreover, a cleaning step in KCN, which removes gold from electrode surface, is included. To obtain reproducibility in the analytical signal, the surface of the electrodes must be suitably pretreated; this electrodic pretreatment depends on the kind of electrode used as working electrode. Low detection limits (5.0×10,10,M) for short gold deposition times (10,min for CPE and 5,min for GCE) were achieved with this novel methodology. Finally, sodium aurothiomalate can be quantified using silver electrocatalytic deposition and GCE as working electrode. Good linear relationship between silver anodic stripping peak and aurothiomalate concentration was found from 5.0×10,10,M to 1.0×10,8,M. [source] Electrochemical Overoxidation of Polyindole and Its Cation-Permselective BehaviorELECTROANALYSIS, Issue 12 2004Mihaela Ghita Abstract Polyindole films prepared by potentiostatic growth in dichloromethane solution were subjected to overoxidation studies in aqueous media. Overoxidation at potentials greater than 1.1,V (vs. SCE) in 0.1,M KNO3 or 0.1,M H2SO4 was possible. Overoxidation in 0.1,M NaOH resulted in mechanically unstable films which were not adherent to the electrode surface. The overoxidation process in 0.1,M KNO3 involved removal of one electron per four indole monomer moieties in the polymer film. Nucleophilic attack led to introduction of carboxylate functionality and to cation permselective behavior, as tested by cyclic voltammetry and hydrodynamic voltammetry of hexamminoruthenium(III) and hexacyanoferrate(III). Such films may be useful in various electrochemical sensor applications. [source] Multiple-point electrochemical detection for a dual-channel hybrid PDMS-glass microchip electrophoresis deviceELECTROPHORESIS, Issue 19 2009Mario Castaño-Álvarez Abstract A new PDMS-based dual-channel MCE with multiple-point amperometric detection has been evaluated. Electrophoresis has been optimised in a single-channel device. Pretreatment with 0.1,M NaOH is very important for increasing and stabilising the EOF. The precision is adequate for a day's work in terms of both peak current and migration time. The RSD of the peak current for five successive signals was 1.9, 2.4 and 3.1% for dopamine, p- aminophenol and hydroquinone. RSD for the migration time was always less than 1.3%, which demonstrates the stability of the EOF and the possibility of running multiple experiments in the same microchip. The adequate inter-microchip precision as well as the rapid and simple manufacturing procedure indicates the disposable nature of the PDMS microchips. A dual-channel device with very simple multiple-point amperometric detection is proposed here. Elasticity of the PDMS allows removing the polymer slightly and aligning gold wires working electrodes. Injection can be performed from each of the sample reservoirs or from both simultaneously. The distance between the separation channels is critical for obtaining adequate signals as well as the introduction of a high-voltage electrode in the buffer reservoir. Simultaneous measurement of the same analytes in both channels is possible by applying the same potential. Moreover, since no cross-separation is produced, different analytes or samples can be simultaneously measured. [source] High-efficiency protein extraction from polyacrylamide gels for molecular mass measurement by matrix-assisted laser desorption/ionization-time of flight-mass spectrometryELECTROPHORESIS, Issue 6 2005Ya Jin Abstract A simple and fast method of protein extraction from Coomassie Brilliant Blue (CBB)-stained polyacrylamide gels suited for molecular mass measurement of proteins by matrix-assisted laser desorption/ionization-time of flight-mass spectrometry (MALDI-TOF-MS) is reported. Proteins in CBB-stained gel pieces were extracted by a 10-min soaking in 0.1,M NaOH at 25°C. The recovery of this one-step extraction method was 34,73% for proteins <67,kDa. CBB adduction to proteins during mass spectrometric analysis was avoided by a destaining step before the alkaline extraction. The molecular mass values of the extracted proteins coincided with those of purified proteins within ±0.01,0.10% deviation for all the proteins <36,kDa. Because of the high extraction recovery, mass measurement was possible for the proteins extracted from CBB-stained gels with loaded protein quantities as little as 34,ng for cytochrome,c, ,-lactalbumin, myoglobin, ,-lactoglobulin, trypsinogen, and carbonic anhydrase (12.4,29.0,kDa), 340,ng for glyceraldehyde-3-phosphate dehydrogenase (35.6,kDa) and albumin (66.3,kDa). This method provides a highly efficient approach to utilize CBB-stained one- or two-dimensional gels for whole protein analysis using MALDI-TOF-MS. [source] Apatite Deposition on NaOH-Treated PEEK and UHMWPE Films for Sclera Materials in Artificial Cornea Implants,ADVANCED ENGINEERING MATERIALS, Issue 7 2010Monica Pino Abstract Cornea implants consist of a clear optic portion with a surrounding ring known as the skirt, which needs to integrate with the sclera. However, currently used skirt materials lead to poor tissue integration. Improvements in this respect may be achieved by using a bioactive skirt material that adapts to the metabolic activity of the cornea. Polyether etherketone (PEEK) and ultra-high molecular weight polyethylene (UHMWPE) might provide interesting alternatives, if they can be rendered bioactive. We, therefore, investigated the potential of surface-modifying PEEK and UHMWPE films through the use of a two-step treatment. This process involved a suitable chemical surface modification (via immersion in NaOH), with subsequent formation of apatite layers on the polymers' surfaces through exposure to supersaturated simulated body fluid (1.5 SBF). In the present work the effect of 5 and 10,M NaOH on formation of the apatite layer has been investigated with regard to wettability and topography features. In addition, the chemical stability of the apatite layer formed has been analyzed. Our data demonstrate that with an increase in NaOH concentration the wettability of the polymer increased, whilst some changes to the polymer film topography (increase/decrease in roughness) were observed. Most beneficially, the apatite layer that subsequently was grown on pre-treated PEEK and UHMWPE films through immersion in 1.5 SBF contained phosphate and carbonate ions, in similar ratios to those found in the apatite in dentine, thus, promising good in vivo bioactivity of these polymer films,a necessity if they are to be integrated into artificial cornea. [source] Deprotonation of Indole Derivatives in Aqueous Cationic SurfactantsEUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Issue 5 2004Nicoletta Spreti Abstract Deprotonations of 5-nitroindole, 1a, and its 2-carboxylate ion, 2a, have been monitored in 0.01, 0.1, and 0.5 M NaOH in micellar solutions of cetyl trialkylammonium bromide, alkyl = Me, Et, nPr, nBu, CTABr, CTEABr, CTPABr, CTBABr. Extents of deprotonation (% f) have been fitted using the pseudophase model of micellar effects with interionic competition described by ion exchange or by independent association constants. Both treatments indicate that base dissociation constants in dilute OH, are lower than in water by factors of ca. 3,11, and decrease with increasing bulk of the head groups, and that these factors increase modestly as the OH, concentration increases to 0.5 M. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004) [source] Electrochemical Reduction of Oxygen on Carbon Supported Pt and Pt/Ru Fuel Cell Electrodes in Alkaline SolutionsFUEL CELLS, Issue 4 2003E.H. Yu Abstract A study of O2 reduction in 1 M NaOH solution at gas diffusion electrodes made from carbon supported Pt and Pt/Ru catalysts is reported. Two Tafel regions were observed for both the Pt and Pt/Ru electrodes. Although the same mechanism was suggested for oxygen reduction on both Pt and Pt/Ru catalysts, the O2 reduction activity was lower on Ru. Electrochemical Impedance Spectroscopy (EIS) analysis was carried out at different potentials and showed the significant contribution of diffusion on the reaction process and kinetics. The effect of methanol on O2 reduction was investigated in solutions containing various concentrations of methanol. The electrode performance deteriorated with increasing methanol concentration because of a mixed cathode potential. The methanol tolerance, i. e., the methanol concentration which polarises the O2 reduction reaction for O2 reduction, at the Pt/C electrode with a Pt loading of 1.2 mg cm,2 is 0.2 M methanol in 1 M NaOH. [source] Kinetics and mechanism of alkaline hydrolysis of 4-nitrophthalimide in the absence and presence of cationic micellesINTERNATIONAL JOURNAL OF CHEMICAL KINETICS, Issue 7 2001M. Niyaz Khan Pseudo-first-order rate constants (kobs) for alkaline hydrolysis of 4-nitrophthalimide (NPTH) decreased by nearly 8- and 6-fold with the increase in the total concentration of cetyltrimethyl-ammonium bromide ([CTABr]T) from 0 to 0.02 M at 0.01 and 0.05 M NaOH, respectively. These observations are explained in terms of the pseudophase model and pseudophase ion-exchange model of micelle. The increase in the contents of CH3CN from 1 to 70% v/v and CH3OH from 0 to 80% v/v in mixed aqueous solvents decreases kobs by nearly 12- and 11-fold, respectively. The values of kobs increase by nearly 27% with the increase in the ionic strength from 0.03 to 3.0 M. The mechanism of alkaline hydrolysis of NPTH involves the reactions between HO, and nonionized NPTH as well as between HO, and ionized NPTH. The micellar inhibition of the rate of alkaline hydrolysis of NPTH is attributed to medium polarity effect. © 2001 John Wiley & Sons, Inc. Int J Chem Kinet 33: 407,414, 2001 [source] Chitin production by Lactobacillus fermentation of shrimp biowaste in a drum reactor and its chemical conversion to chitosanJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 9 2005Mukku Shrinivas Rao Abstract Chitin was produced by fermenting shrimp heads and shells with Lactobacillus plantarum 541 in a drum reactor with an internal volume of 3 dm3. The crude chitin yield from heads and shells was 4.5 and 13% respectively, comparable to the values obtained by the chemical method. For shrimp heads 83% deproteination and 88% demineralisation and for shrimp shells 66% deproteination and 63% demineralisation were achieved. The liquor obtained in both cases was of good sensory quality with a high content of essential amino acids and therefore with potential to produce protein powder for human consumption. The crude chitin was refined and converted to chitosan using 12.5 M NaOH. The chitosan obtained had a residual ash and protein content below 1%, a solubility of more than 98%, a viscosity in the range 50,400 cP and a degree of deacetylation of 81,84%. The molecular weight was in the range (0.8,1.4) × 106 Da. IR analysis indicated that the chitosan obtained through fermentation was similar to that obtained by the chemical method. Copyright © 2005 Society of Chemical Industry [source] Instrumental and Consumer Evaluation of Beef Patties Extended with Extrusion-Textured Whey ProteinsJOURNAL OF FOOD SCIENCE, Issue 3 2002A. B. Hale ABSTRACT: : We extruded a dry mix of 2 parts whey protein concentrate (80% protein) and 1 part cornstarch using water, 0.1 N HCl, or 0.2 M NaOH as the liquid, or adding calcium (1.69% w/w) to the dry mix with water as the liquid. The functionality and acceptability of textured whey protein (TWP) extrudates was determined. Ground beef patties containing up to 40% (w/w) of hydrated TWP extrudates made with base (TWPbase) were as acceptable to a consumer panel as all beef patties. Additionally, patties containing 40% (w/w) TWPbase incurred less cook loss and less diameter reduction after cooking, but were less cohesive than all beef patties. [source] Hydrothermal conversion of carbohydrate biomass to lactic acidAICHE JOURNAL, Issue 10 2010Xiuyi Yan Abstract We investigated the hydrothermal conversion of the carbohydrates including glucose, cellulose, and starch to lactic acid using NaOH and Ca(OH)2 as alkaline catalysts. Both catalysts significantly promoted the lactic acid formation. The highest yield of lactic acid from glucose was 27% with 2.5 M NaOH and 20% with 0.32 M Ca(OH)2 at 300°C for 60 s. The lactic acid yields from cellulose and starch were comparable with the yield from glucose with 0.32 M Ca(OH)2 at 300°C, but the reaction time in the case of cellulose was 90 s. The mechanism of lactic acid formation from glucose was discussed by identifying the intermediate products. Lactic acid may be formed via the formation of aldoses of two to four carbons including aldose of three carbons, which are all formed by reverse aldol condensation and double bond rule of hexose. This implies that carbon,carbon cleavage occurs at not only C3C4 but also at C2C3. © 2010 American Institute of Chemical Engineers AIChE J, 2010 [source] Effects of non-ionic and mixed non-ionic,cationic micelles on the rate of aqueous cleavages of phenyl benzoate and phenyl salicylate in alkaline mediumJOURNAL OF PHYSICAL ORGANIC CHEMISTRY, Issue 5 2004M. Niyaz Khan Abstract Pseudo-first-order rate constants (kobs) for the hydrolysis of phenyl salicylate (PSH) and phenyl benzoate (PB) in the alkaline medium show a monotonic decrease with the increase in [C16E20]T (total concentration of Brij 58) at constant [CH3CN] and [NaOH]. This micellar effect is explained in terms of the pseudophase model of micelles. These results show a characteristic difference between the effects of [C16E20]T and previously published effects of [C12E23]T (total concentration of Brij 35) on the rates of aqueous cleavage of PSH and PB at [CnEm]T/[NaOH],,3. The values of kobs, obtained at different [C16E20]T in the presence of a constant amount of CTABr, follow the empirical relationship kobs=(k0+,K[C16E20]T)/(1+K[C16E20]T), where , and K are empirical parameters. The values of , are not affected whereas the values of K decrease with increase in [CTABr]T in a mixed C16E20,CTABr micellar system. The values of , at different [CTABr]T show that ,>k0 for hydrolysis of PSH and , Effects of non-ionic and mixed cationic,non-ionic micelles on the rate of alkaline hydrolysis of phthalimideJOURNAL OF PHYSICAL ORGANIC CHEMISTRY, Issue 7 2002M. Niyaz Khan Abstract Pseudo-first-order rate constants (kobs) for the alkaline hydrolysis of phthalimide (PTH) show a monotonic decrease with the increase in [C16E20]T (total concentration of Brij 58) at constant [CH3CN] and [NaOH]. This micellar effect is explained in terms of the pseudophase model of micelles. The rate of hydrolysis of PTH in C16E20 micellar pseudophase appears to be negligible compared with that in the aqueous pseudophase. The values of kobs for C12E23 (Brij 35) show a sharp decrease at very low values of [C12E23]T followed by a very slow decrease with increase in [C12E23]T at relatively higher values of the latter. The rate of hydrolysis becomes too slow to monitor at [C12E23]T ,0.04,M in the absence of cetyltrimethylammonium bromide (CTABr) and at [C12E23]T ,0.05,M in the presence of 0.006,0.02,M CTABr at 0.02,M NaOH whereas such characteristic behavior is kinetically absent with C16E20. The values of kobs, obtained at different [NIS]T (where NIS represents C16E20 and C12E23) in the presence of a constant amount of CTABr, follow the empirical relationship kobs,=,(k0,+,kK[NIS]T)/(1,+,K[NIS]T) where k and K are empirical parameters. The values of k are only slightly affected whereas the values of K decrease with increase in [CTABr]T for the mixed C16E20,CTABr micellar system. The rate of hydrolysis of PTH at ,0.01,M C12E23 and ,0.01,M CTABr reveals the formation of phthalic anhydride whereas this was not observed in the mixed C16E20,CTABr micellar system under similar experimental conditions. Copyright © 2002 John Wiley & Sons, Ltd. [source] Benzene polycarboxylic acids,A ubiquitous class of compounds in soilsJOURNAL OF PLANT NUTRITION AND SOIL SCIENCE, Issue 5 2010Ludwig Haumaier Abstract Black carbon (BC) occurs ubiquitously in the environment. Its oxidation in the laboratory yields a suite of benzene polycarboxylic acids (BPCAs), suggesting similar oxidation products in soils. Since only for a few soils the occurrence of BPCAs in the free form has been documented, screening for them in a broad range of contrasting soils was conducted. They were extracted from soil samples with 0.5 M NaOH and quantified using gas chromatography,mass spectrometry. As expected, BPCAs turned out to be as ubiquitous as BC. They were detected not only in every soil sample investigated so far, but also in samples from drill cores up to a depth of 10 m and in recently deposited calcareous tufa. The concentrations covered a range similar to that of some phenolic acids. The range exceeded those reported for low-molecular-weight aliphatic acids or simple sugars in soils. The distribution of BPCAs in soil profiles indicated a considerable potential of translocation within, and export from, soil, in particular of benzene hexacarboxylic (mellitic) acid. Mellitic acid may therefore be present in almost any geochemical sample affected by seepage water from soils. Its high water solubility and strong metal-complexing ability suggest it may be involved in metal-transport processes, at least on geological timescales. [source] FTIR-spectroscopic characterization of humic acids and humin fractions obtained by advanced NaOH, Na4P2O7, and Na2CO3 extraction proceduresJOURNAL OF PLANT NUTRITION AND SOIL SCIENCE, Issue 4 2007Michael Tatzber Abstract Aim of our study was the development of the methodological basis for the characterization of humic fractions of a long-term field experiment. Humic acids (HAs) were extracted from three layers of a nontilled soil using three different extractants (1 M NaOH, 0.1 M Na4P2O7, 1 M Na2CO3), and the humin fraction was enriched. NaOH as extractant for FTIR analysis of humic substances yields higher resolved IR spectra, especially in the important regions of stretching vibrations including aromatic and aliphatic groups and in the fingerprint area including amides, aliphats, and aromats than the other extractants. The NaOH extraction has lower extraction yields as compared to Na4P2O7 and Na2CO3 and represents a different part of the soil organic matter (SOM). This is reflected by lower C : N ratios and higher E4 : E6 and fulvic acid,to,humic acid ratios as compared to the other extractants. The FTIR band areas of HA fraction obtained by NaOH showed an increase of the aromatic and carbonyl groups and a decrease of amide groups with increasing soil depth. Aliphatic groups showed contradicting results: The bands of the stretching vibrations increased, and the band of the bending vibrations decreased. We assume that band interactions in the bending vibrations were responsible for that phenomenon under the assumption of an increase of aliphatic groups with increasing soil depth. The IR bands of the enriched humin fraction showed a decreasing trend in case of both aliphatic bands deriving from stretching vibrations and an increase of aromatic characteristics with depth. Our study led to the conclusion that HA fractions obtained by 1 M NaOH represent a small and dynamic fraction indicated by the measured yields in combination with values of Nt, C : N, E4 : E6 ratios, and ratios of fulvic acids (FA) to HA. The humin fraction has a high contribution to the total organic C and represents a more stabilized fraction of SOM which still shows changes in its aromatic and aliphatic characteristics with soil depth. [source] Influence of Tithonia diversifolia and triple superphosphate on dissolution and effectiveness of phosphate rock in acidic soilJOURNAL OF PLANT NUTRITION AND SOIL SCIENCE, Issue 5 2006Isaac Savini Abstract An incubation and a pot experiment were conducted to evaluate the dissolution and agronomic effectiveness of a less reactive phosphate rock, Busumbu soft ore (BPR), in an Oxisol in Kenya. Resin (anion and anion + cation)-extractable P and sequentially extracted P with 0.5 M NaHCO3, 0.1 M NaOH, and 1 M HCl were analyzed. Dissolution was determined from the increase in anion resin (AER),, NaHCO3 -, and NaOH-extractable P in soil amended with PR compared with the control soil. Where P was applied, resin P significantly increased above the no-P treatment. Busumbu-PR solubility was low and did not increase significantly in 16 weeks. Anion + cation (ACER)-extractable P was generally greater than AER-P. The difference was greater for PR than for triple superphosphate (TSP). The ACER extraction may be a better estimate of plant P availability, particularly when poorly soluble P sources are used. Addition of P fertilizers alone or in combination with Tithonia diversifolia (TSP, BPR, TSP + Tithonia, and BPR + Tithonia) increased the concentration of labile inorganic P pools (NaHCO3 - and NaOH-Pi). Cumulative evolved CO2 was significantly correlated with cumulative N mineralized from Tithonia (r, 0.51, p < 0.05). Decrease in pH caused NH -N accumulation while NO -N remained low where Tithonia was incorporated at all sampling times. However, when pH was increased, NH -N declined with a corresponding rise in NO -N. Tithonia significantly depressed soil exchangeable acidity relative to control with time. A significant increase (p < 0.05) was observed for P uptake but not dry-mass production in maize where BPR was applied. The variations in yield and P uptake due to source and rates of application were statistically significant. At any given P rate, highest yields were obtained with Tithonia alone. Combination of Busumbu PR with TSP or Tithonia did not enhance the effectiveness of the PR. The poor dissolution and plant P uptake of BPR may be related to the high Fe content in the PR material. [source] Evaluation of selective composite cryogel for bromate removal from drinking waterJOURNAL OF SEPARATION SCIENCE, JSS, Issue 12 2010Solmaz Hajizadeh Abstract Bromate, which is a potential carcinogen, should be removed from drinking water to levels of less than 10,,g/L. A chitosan-based molecularly imprinted polymer (MIP) and a sol,gel ion-exchange double hydrous oxide (Fe2O3·Al2O3·xH2O) adsorbent (inorganic adsorbent) were prepared for this purpose. The sorption behavior of each adsorbent including sorption kinetics, isotherms, effect of pH and selective sorption were investigated in detail. Sorption experimental results showed that the MIP adsorbents had better selectivity for bromate, even in the presence of high concentrations of nitrate, as compared to the inorganic adsorbent. It was found that pH does not affect the adsorption of bromate when using the inorganic adsorbent. Additionally, both adsorbents were immobilized in a polymeric cryogel inside plastic carriers to make them more practical for using in larger scale. Regeneration of the cryogels either containing MIP or inorganic adsorbents were carried out by 0.1,M NaOH and 0.1,M NaCl, respectively. It was found that the regenerated MIP and inorganic adsorbents could be used at least three and five times, respectively, without any loss in their sorption capacity. [source] Characterisation of oxazepam degradation products by high-performance liquid chromatography/electrospray ionisation mass spectrometry and electrospray ionisation quadrupole time-of-flight tandem mass spectrometryRAPID COMMUNICATIONS IN MASS SPECTROMETRY, Issue 5 2010Thomas J. P. Smyth Oxazepam has been subjected to controlled degradation at 100°C for 3,h in 0.5,M HCl and 0.5,M NaOH. Following neutralisation of the degradation mixture and removal of salts by solid-phase extraction (SPE), isocratic high-performance liquid chromatography/mass spectrometry (HPLC/MS) using water/methanol (25:75,v/v) as the mobile phase was carried out using a flow diverter to collect fractions prior to their characterisation by electrospray ionisation multi-stage mass spectrometry (ESI-MSn) and proposal of the corresponding fragmentation patterns. The elemental compositions of the degradation products and their MS fragments were evaluated using electrospray ionisation quadrupole time-of-flight tandem mass spectrometry (ESI-QTOF-MS/MS) which was then used to support the proposed fragmentation patterns. Copyright © 2010 John Wiley & Sons, Ltd. [source] Degradation of phenylarsonic acid and its derivatives into arsenate by hydrothermal treatment and photocatalytic reactionAPPLIED ORGANOMETALLIC CHEMISTRY, Issue 2 2005Tsunenori Nakajima Abstract The degradation of phenylarsonic acid (PA) and its derivatives by hydrothermal treatment (HTT) was examined, especially focusing on the effect of adding H2O2 upon the degradation efficiency. The degradation was assessed by the generation of arsenate resulting from the cleavage of AsC bonds in the PA derivatives. When PA (without substituents) was subjected to an HTT with H2O2 (H2O2 -HTT; 0.5,1% H2O2) at 175,200 °C, PA was almost completely degraded into arsenate, whereas an HTT with NaOH (NaOH-HTT; 3 M NaOH) at the temperatures provided almost no degradation. The H2O2 -HTT also worked well for the degradation of PA derivatives with hydroxy and/or nitro groups on the phenyl ring. However, the degradation of aminophenylarsonic acids was not favorably performed by the H2O2 -HTT. The effect of the structure of PA derivatives upon the degradation susceptibility was discussed. A photocatalytic reaction using TiO2 was also attempted for the degradation of PA derivatives. Copyright © 2005 John Wiley & Sons, Ltd. [source] Development of Cellulose-DNA ImmunoadsorbentARTIFICIAL ORGANS, Issue 2 2002Deling Kong Abstract: The aim of this study was to prepare a DNA immunoadsorbent for the specific, extracorporeal removal of anti-DNA antibodies from the blood of patients with systemic lupus erythematosus (SLE) and rheumatoid arthritis (RA). Two kinds of cellulose beads were applied as a carrier. Calf thymus DNA was covalently coupled to the carrier using the epichlorohydrin method. Efforts were focused on optimization of conditions for activation and coupling, trying to couple as much DNA as possible to a certain amount of carrier. It was found that the activation level increased with the increase of NaOH concentration and the amount of epichlorohydrin used. The mole of epichlorohydrin must be in excess of that of NaOH because excess NaOH could react further with the epoxy groups in the beads resulting in a decrease of activation level. High activation level could be obtained in a medium of 3.0 M NaOH. The DNA coupling was found to be mainly temperature and pH dependent. Using 0.1 M Tris-HCl buffer, pH 8 at a temperature of 50,90°C, more than 3 mg of DNA could be coupled to 1 ml of wet beads. Prolonging the coupling reaction under 50°C to 72 h resulted in the same coupling capacity as that obtained under 90°C. To evaluate the adsorption ability for anti-DNA of this immunoadsorbent, batch and circulation tests were applied using SLE patient plasma. The immunoadsorbents showed excellent adsorption capacity, especially the cellulose with smaller size (200,300 ,m). The incubation of 20 ml of patient's plasma with 1 ml of adsorbent resulted in an 80% decline in the anti-DNA antibody level. In the circulation tests, 30 ml of plasma was circulated through a column containing 3 ml of adsorbent. The maximum decline in anti-DNA level, 80%, was obtained after 60 min. Such high adsorption capacity and high adsorption rate suggest this immunoadsorbent may be used for treatment. For comparison, 1,4-butanediol diglycidyl ether activation method and other DNA sources were tested with the same protocol. [source] Antioxidants in soil organic matter and in associated plant materialsEUROPEAN JOURNAL OF SOIL SCIENCE, Issue 2 2009D. L. Rimmer Summary The presence of antioxidants in soil could have a significant effect on the dynamics of soil organic matter. In this paper we report some preliminary experiments, which demonstrate that antioxidants can be extracted from soils and that the quantities vary from soil to soil. Extraction with 1.0 m NaOH was effective, and this was then used on a range of mineral and organic soils, and the antioxidant capacity of the resulting extracts was measured. The antioxidant capacities obtained were positively correlated with soil carbon contents and with the dissolved organic carbon contents of the extracts. Expressing the data per mass of soil carbon showed that the antioxidants generally decreased with depth in the soil profile, suggesting that they were subject to degradation during humification. In a follow-up study, soil, litter and fresh plant samples were collected from 15 sites with a wide variety of vegetation types and analysed for their antioxidant capacities. The aim was to show that the antioxidant capacities in the soils were related to the antioxidant capacities of the fresh plant material and/or litter above. The antioxidant capacities of the soil samples were less than those in either fresh material or litter. While there was a significant positive relationship between the antioxidant capacities of fresh material and litter, no relationship existed between the antioxidant capacities of the soils and those of either fresh material or litter. [source] The erosive potential of flavoured sparkling water drinksINTERNATIONAL JOURNAL OF PAEDIATRIC DENTISTRY, Issue 2 2007CATRIONA J. BROWN Objective., The potential role of acidic drinks in the aetiology of dental erosion is well recognized. Whilst the wide-scale consumption of bottled waters is unlikely to contribute significantly to erosion, the role of flavoured sparkling water drinks is unclear. The aim of this study was to determine the pH, titratable acidity and in vitro erosive potential of a selection of these drinks drawn from the UK market to identify what dietary advice would be appropriate in relation to their consumption. Methods., pH was measured using a pH electrode and titratable acidity recorded by titration with 0.1- m NaOH. Erosive potential was assessed using an in vitro dissolution assay with hydroxyapatite powder and electron microscopic examination of surface enamel of extracted human teeth, following exposure to the flavoured sparkling waters for 30 min. Results., All of the flavoured waters tested showed appreciable titratable acidity (0.344,0.663 mmol) and low pH (2.74,3.34). In the hydroxyapatite dissolution assay, all of the waters demonstrated erosive potential (89,143%) similar to or greater than that of pure orange juice, an established erosive drink. Exposure of the extracted teeth to the flavoured waters resulted in surface changes consistent with erosive dissolution. Conclusions., Flavoured sparkling waters should be considered as potentially erosive, and preventive advice on their consumption should recognize them as potentially acidic drinks rather than water with flavouring. [source] Extracellular cross-linking of maize arabinoxylans by oxidation of feruloyl esters to form oligoferuloyl esters and ether-like bondsTHE PLANT JOURNAL, Issue 4 2009Sally J. Burr Summary Primary cell walls of grasses and cereals contain arabinoxylans with esterified ferulate side chains, which are proposed to cross-link the polysaccharides during maturation by undergoing oxidative coupling. However, the mechanisms and control of arabinoxylan cross-linking in vivo are unclear. Non-lignifying maize (Zea mays L.) cell cultures were incubated with l- [1- 3H]arabinose or (E)-[U- 14C]cinnamate (radiolabelling the pentosyl and feruloyl groups of endogenous arabinoxylans, respectively), or with exogenous feruloyl-[3H]arabinoxylans. The cross-linking rate of soluble extracellular arabinoxylans, monitored on Sepharose CL-2B, peaked suddenly and transiently, typically at ,9 days after subculture. This peak was not associated with appreciable changes in peroxidase activity, and was probably governed by fluctuations in H2O2 and/or inhibitors. De-esterified arabinoxylans failed to cross-link, supporting a role for the feruloyl ester groups. The cross-links were stable in vivo. Some of them also withstood mild alkaline conditions, indicating that they were not (only) based on ester bonds; however, most were cleaved by 6 m NaOH, which is a property of p- hydroxybenzyl,sugar ether bonds. Cross-linking of [14C]feruloyl-arabinoxylans also occurred in vitro, in the presence of endogenous peroxidases plus exogenous H2O2. During cross-linking, the feruloyl groups were oxidized, as shown by ultraviolet spectra and thin-layer chromatography. Esterified diferulates were minor oxidation products; major products were: (i) esterified oligoferulates, released by treatment with mild alkali; and (ii) phenolic components attached to polysaccharides via relatively alkali-stable (ether-like) bonds. Thus, feruloyl esters participate in polysaccharide cross-linking, but mainly by oligomerization rather than by dimerization. We propose that, after the oxidative coupling, strong p- hydroxybenzyl,polysaccharide ether bonds are formed via quinone-methide intermediates. [source]
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