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H2SO4
Kinds of H2SO4 Terms modified by H2SO4 Selected AbstractsElectrocatalytic Reduction and Determination of Iodate and Periodate at Silicomolybdate-Incorporated-Glutaraldehyde- Cross-Linked Poly- L -lysine Film ElectrodesELECTROANALYSIS, Issue 10 2010Yu-Ching Pan Abstract The present work describes reduction of iodate (IO3,), and periodate (IO4,) at silicomolybdate-doped-glutaraldehyde-cross-linked poly- L -lysine (PLL-GA-SiMo) film coated glassy carbon electrode in 0.1,M H2SO4. In our previous study, we were able to prepare the PLL-GA-SiMo film modified electrode by means of electrostatically trapping SiMo12O404, mediator in the cationic film of PLL-GA, and the voltammetric investigation in pure supporting indicated that the charge transport through the film was fast. Here, the electrocatalytic activity of PLL-GA-SiMo film electrode towards iodate and periodate was tested and subsequently used for analytical determination of these analytes by amperometry. The two electron reduced species of SiMo12O404, anion was responsible for the electrocatalytic reduction of IO3, at PLL-GA-SiMo film electrode while two and six electron reduced species were showed electrocatalytic activity towards IO4, reduction. Under optimized experimental conditions of amperometry, the linear concentration range and sensitivity are 2.5×10,6 to 1.1×10,2,M and 18.47,,A mM,1 for iodate, and 5×10,6 to 1.43×10,4,M and 1014.7,,A mM,1 for periodate, respectively. [source] Effect of Platinum and Ruthenium Incorporation on Voltammetric Behavior of Nitrogen Doped Diamond-Like Carbon Thin FilmsELECTROANALYSIS, Issue 23 2009W. Khun Abstract Nitrogen doped diamond-like carbon thin films with or without platinum and ruthenium incorporation (N-DLC or PtRuN-DLC) were deposited on highly conductive p-Si substrates by DC magnetron sputtering to study the effect of Pt and Ru doping on the voltammetric performance of the N-DLC films. The potential windows of these film electrodes were measured in different electrolytic solutions, such as H2SO4, HCl and KCl. The cyclic voltammograms obtained from the N-DLC film electrodes in these solutions showed wide potential windows while the introduction of Pt and Ru into the film electrodes apparently narrowed down the potential windows due to their catalytic activities. [source] Performance of Impedimetric Biosensors Based on Anodically Formed Ti/TiO2 ElectrodesELECTROANALYSIS, Issue 20 2005Aikaterini Abstract The advantages and limitations of impedimetric sensors based on Ti/TiO2 architectures are described. Titanium dioxide (titania) was potentiostatically formed onto titanium electrodes of 2,mm diameter, at 10 and 30,V in 1,M H2SO4. The thickness of the titania layers was ellipsometrically determined to be 30 and 86,nm respectively and they are highly insulating with charge-transfer resistances in the M, range, as they were measured with electrochemical impedance spectroscopy under specific experimental conditions. Low voltage anodization (<10,V) results to amorphous TiO2, whereas at higher applied voltages (>25,V), anatase is the predominant form. SEM images are indicative of quite smooth, compact coatings without any severe cracks. [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] Variations of nitrate and sulfate in the atmosphere on days of high and low particulate mattersENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 4 2005Chung-Yih Kuo Abstract Particulate matters with aerodynamicdiameter less than 10 ,m (PM10) were collected with high-volume samplers for four periods of consecutive samplings. Each period included a high PM10 (defined as PM10 ,110 ,g/m3) episode. The concentrations of all ionic species of high PM10 day (HPD) samples were higher than those of low PM10 (defined as PM10 < 110,g/m3) d (LPD) samples. Using the ionic concentrations of HPD samples at each station divided by those of LPD samples at respective stations, the results showed thatNO increased most from LPD to HPD among the eight ionic species examined. A high mean value (3.15) of NO/elemental carbon (EC) ratio of HPD divided by that of LPD indicates that concentration variations due to chemical formation and nonchemical factors apparently were higher than those of the concentration variations due to nonchemical factors alone. The NO/SO ratio of HPD divided by that of LPD ranged from 1.62 to 3.92 for the four periods. The results indicate that more nitrate than sulfate had formed during high PM10 episodes. Multiple linear regression analysis showed that the percentage of NH associated with nitrate and sulfate decreased and the percentage that could be explained by Ca2+ and Na+ increased on HPD. The reactions of HNO3 and H2SO4 with sea salt particles and with aqueous carbonates on soil particles during HPD were considered the main causes leading to these variations. [source] An Efficient Approach for the Synthesis of N-1 Substituted HydantoinsEUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Issue 11 2008Vinod Kumar Abstract An efficient three-step route for the synthesis of N - 1 alkyl/aryl-substituted hydantoins was developed from inexpensive commercially available substrates. The reaction of amines with cyanogen bromide takes place to give monoalkyl/aryl cyanamides. This on treatment with methyl bromoacetate in the presence of sodium hydride in tetrahydrofuran affords methyl N -cyano- N -alkyl/arylaminoacetate, which undergoes hydrolysis and cyclization in the presence of 50,% H2SO4 to afford N - 1 substituted hydantoins in very good-to-excellent yields. Wide varieties of final products having primary, secondary, tertiary, and aryl substituents at the N - 1 position were successfully synthesized by this method. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008) [source] Evaluation of RuxWySez Catalyst as a Cathode Electrode in a Polymer Electrolyte Membrane Fuel CellFUEL CELLS, Issue 1 2010K. Suárez-Alcántara Abstract The oxygen reduction reaction (ORR) on RuxWySez is of great importance in the development of a novel cathode electrode in a polymer electrolyte membrane fuel cell (PEMFC) technology. The RuxWySez electrocatalyst was synthesised in an organic solvent for 3,h. The powder was characterised by transmission electron microscopy (TEM), and powder X-ray diffraction (XRD). The electrocatalyst consisted of agglomerates of nanometric size (,50,150,nm) particles. In the electrochemical studies, rotating disc electrode (RDE) and rotating ring-disc electrode (RRDE) techniques were used to determine the oxygen reduction kinetics in 0.5,M H2SO4. The kinetic studies include the determination of Tafel slope (112,mV,dec,1), exchange current density at 25,°C (1.48,×,10,4,mA,cm,2) and the apparent activation energy of the oxygen reaction (52.1,,,0.4,kJ,mol,1). Analysis of the data shows a multi-electron charge transfer process to water formation, with 2% H2O2 production. A single PEMFC with the RuxWySez cathode catalysts generated a power density of 180,mW,cm,2. Performance achieved with a loading of 1.4,mg,cm,2 of a 40,wt% RuxWySez and 60,wt% carbon Vulcan (i.e. 0.56,mg,cm,2 of pure RuxWySez). Single PEMFC working was obtained with hydrogen and oxygen at 80,°C with 30,psi. [source] Nitrogen-Enriched Nonporous Carbon Electrodes with Extraordinary SupercapacitanceADVANCED FUNCTIONAL MATERIALS, Issue 11 2009Denisa Hulicova-Jurcakova Abstract Nitrogen-enriched nonporous carbon materials derived from melamine,mica composites are subjected to ammonia treatment to further increase the nitrogen content. For samples preoxidized prior to the ammonia treatment, the nitrogen content is doubled and is mainly incorporated in pyrrol-like groups. The materials are tested as electrodes for supercapacitors, and in acidic or basic electrolytes, the gravimetric capacitance of treated samples is three times higher than that of untreated samples. This represents a tenfold increase of the capacitance per surface area (3300,µF,cm,2) in basic electrolyte. Due to the small volume of the carbon materials, high volumetric capacitances are achieved in various electrolytic systems: 280,F,cm,3 in KOH, 152,F,cm,3 in H2SO4, and 92,F,cm,3 in tetraethylammonium tetrafluoroborate/propylene carbonate. [source] Syntheses and structures of sulfilimine, sulfone diimine, and sulfoximine derivatives of a monocyclic thiophene, 3,4-di- tert -butylthiopheneHETEROATOM CHEMISTRY, Issue 5 2001Juzo Nakayama The reaction of 3,4-di-tert-butylthiophene (6a) with N-[(p-tolylsulfonyl)imino]-phenyliodinane (TsN=IPh) in the presence of Cu(MeCN)4PF6 in MeCN at room temperature provided 3,4-di-tert-butyl-1-[(p-tolylsulfonyl)imino]-1,1-dihydrothiophene (3b),3,4-di-tert-butyl-1,1-bis[(p-tolylsulfonyl)imino]-1,1-dihydrothiophene (5a), and 1-(p-tolylsulfonyl)-3,4-di-tert-butylpyrrole (7a) as the principal products. The use of 20 molar amounts of 6a gave 3b in an increased yield of 61%. Treatment of 3,4-di-tert-butylthiophene 1-oxide (1a) with (CF3CO)2O or (CF3SO2)2O, followed by reactions with RSO2NH2, ROC(=O)NH2, or RCONH2, furnished a series of S-imino derivatives (3b,c,e,h) of 6a, which carry an electron-withdrawing substituent on the imino nitrogen atom. Treatment of the S-imino derivative 3f (substituent on the nitrogen atom = COBu) with CF3CO2H gave an aminosulfonium salt (13), whose deprotonation led to the parent N-unsubstituted 1-imide derivative (3n). Treatment of 2,4-di-tert-butylthiophene 1-oxide (1b) with TsN=IPh in the presence of Cu(MeCN)4PF6 in MeCN at room temperature provided 2,4-di-tert-butyl-1-[(p-toluenesulfonyl)imino]-1,1-dihydrothiophene 1-oxide (4e) in 81% yield. Hydrolysis of 4e by concentrated H2SO4 at room temperature furnished 2,4-di-tert-butyl-1-imino-1,1-dihydrothiophene 1-oxide (4f) in 89% yield. A pair of enantiomers of 4f were separated by high-performance liquid chromatography (HPLC) on a chiral column, and their absolute configurations were determined by an X-ray crystallographic analysis. Structures of sulfilimine, sulfone diimine, and sulfoximine derivatives of monocyclic thiophenes, obtained in these ways, are discussed based on spectroscopies (IR and 1H and 13C NMR) and X-ray crystallographic analyses. © 2001 John Wiley & Sons, Inc. Heteroatom Chem 12:333,348, 2001 [source] Effect of surfactant micelles on the kinetics of oxidation of D -fructose by cerium(IV) in sulfuric acid mediumINTERNATIONAL JOURNAL OF CHEMICAL KINETICS, Issue 1 2006Kabir-ud-Din Kinetics of the oxidation of D -fructose by cerium(IV) has been investigated both in the absence and presence of surfactants (cetyltrimethylammonium bromide, CTAB, and sodium dodecyl sulfate, SDS) in sulfuric acid medium. The reaction exhibits first-order kinetics each in [cerium(IV)] and [D -fructose] and inverse first order in [H2SO4]. The Arrhenius equation is found to be valid for the reaction between 30,50°C. A detailed mechanism with the associated reaction kinetics is presented and discussed. While SDS has no effect, CTAB increases the reaction rate with the same kinetic behavior in its presence. The catalytic role of CTAB micelles is discussed in terms of the pseudophase model proposed by Menger and Portnoy. The association constant Ks that equals to 286 mol,1 dm3 is found for the association of cerium(IV) with the positive head group of CTAB micelles. The effect of inorganic electrolytes (Na2SO4, NaNO3, NaCl) has also been studied and discussed. © 2005 Wiley Periodicals, Inc. Int J Chem Kinet 38: 18,25, 2006 [source] Isolation and identification of Alicyclobacillus acidocaldarius by 16S rDNA from mango juice and concentrateINTERNATIONAL JOURNAL OF FOOD SCIENCE & TECHNOLOGY, Issue 7 2005Pieter A. Gouws Summary In this study we investigate the spoilage of ultra high temperature UHT mango juice as well as a carbonated fruit juice blend to identify organisms contributing to the spoilage. The mango concentrate, the final product, as well as the other ingredients used during manufacturing, were tested for the presence of Alicyclobacillus by polymerase chain reaction (PCR) and sequencing analyses. Microbiological examination of the mango pureé and spoiled fruit juices, using YSG agar [yeast extract 2 g, glucose 1 g, soluble starch 2 g, pH 3.7 (adjust with 2N H2SO4), H2O 1000 mL, bacto agar 15 g] incubated at 55 °C, detected sporeforming, acid dependent and thermotolerant bacteria. The hyper variable region of the 16S rDNA was amplified. The nucleotide sequence of the PCR fragments was determined using the ABI Prism 310 automated DNA sequencer and the collected sequencing data were analysed and compared with the non-redundant database using NCBI-BLAST. Alicyclobacillus acidocaldarius were isolated and identified by 16S rDNA gene sequences analyses. The results indicated that the mango purèe, as well as the final product of mango juice and the fruit juice blend, were positive for Alicyclobacillus. The preventative measures of low pH, pasteurization of mango juice and the subsequent use of aseptic packaging were not regarded as sufficient to prevent the outgrowth of Alicyclobacillus spoilage organisms. [source] Synthesis and properties of homopolyamide and copolyamides fibers based on 2,6-bis(p -aminophenyl)benzo[1,2-d;5,4- d,]bisoxazoleJOURNAL OF APPLIED POLYMER SCIENCE, Issue 3 2008Xiangqun Chen Abstract A novel aromatic homopolyamide with benzobisoxazole units in the main chain was synthesized with 2,6-bis(p -aminophenyl)benzo[1,2- d;5,4- d,]bisoxazole and terephthaloyl chloride by low temperature solution polycondensation, the inherent viscosity of which was 1.98 dL/g. The diamine and p -phenylendiamine with terephthaloyl chloride were used to synthesize the copolyamides. The structures of homopolyamide and copolyamides were characterized by IR spectra, elemental analysis, and wide-angle X-ray diffraction. Wide-angle X-ray diffraction measurements showed that homopolyamide and copolyamides were predominantly crystallinity. The results of thermal analysis indicated that the thermal stabilities of the copolymer increased with an increase of the molar fraction of benzobisoxazole in the copolymers. The thermal stability of the copolyamides with decomposition temperatures (at 10% weight loss) above 570°C was better than that of poly(p -phenylene terephthalamide) (PPTA). Fibers of homopolyamide and copolyterephthalamides were spun from lyotropic liquid crystal dope in 100% H2SO4. When compared with PPTA fibers prepared under the same conditions, the tensile strengths of copolyamides fibers improved by 20,33% with tensile strengths of 1.81 GPa, tensile moduli of 76 GPa, and elongations at break of 3.8,4.1%, which indicated that copolyamides fibers had outstanding mechanical properties. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Supercapacitor studies of electrochemically deposited PEDOT on stainless steel substrateJOURNAL OF APPLIED POLYMER SCIENCE, Issue 2 2007S. Patra Abstract There has been increasing interest on various properties and applications of electronically conducting polymers. Polyethylenedioxythiophene (PEDOT) is an interesting polymer of this type as it exhibits very high ionic conductivity. In the present study, PEDOT has been electrochemically deposited on stainless steel (SS) substrate for supercapacitor studies. PEDOT/SS electrodes prepared in 0.1M H2SO4 in presence of a surfactant, sodium dodecylsulphate (SDS), have been found to yield higher specific capacitance (SC) than the electrodes prepared from neutral aqueous electrolyte. The effects of concentration of H2SO4, concentration of SDS, potential of deposition, and nature of supporting electrolytes used for capacitor studies on SC of the PEDOT/SS electrodes have been studied. SC values as high as 250 F/g in 1M oxalic acid have been obtained during the initial stages of cycling. However, there is a rapid decrease in SC on repeated charge-discharge cycling. Spectroscopic data reflect structural changes in PEDOT on extended cycling. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007 [source] Polyethylene glycol and polyvinyl alcohol as corrosion inhibitors for aluminium in acidic mediumJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2007S. A. Umoren Abstract The corrosion inhibition of aluminum in H2SO4 in the presence of polyethylene glycol (PEG) and polyvinyl alcohol (PVA) as inhibitors at 30,60 °C was studied using gravimetric, gasometric, and thermometric techniques. The inhibition efficiency (%I) increased with increase in concentration of the inhibitors. Increase in temperature increased the corrosion rate in the absence and presence of inhibitors but decreased the inhibition efficiency. Both PEG and PVA were found to obey Temkin adsorption isotherm at all concentrations and temperatures studied. Phenomenon of physical adsorption is proposed from the activation parameters obtained. Thermodynamic parameters reveal that the adsorption process is spontaneous. PEG was found to be a better inhibitor than PVA. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007 [source] Biodiesel production by direct methanolysis of oleaginous microbial biomassJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 8 2007Bo Liu Abstract Biodiesel is a renewable fuel conventionally prepared by transesterification of pre-extracted vegetable oils and animal fats of all resources with methanol, catalyzed by strong acids or bases. This paper reports on a novel biodiesel production method that features acid-promoted direct methanolysis of cellular biomass of oleaginous yeasts and filamentous fungi. The process was optimized for tuning operation parameters, such as methanol dosage, catalyst concentration, reaction temperature and time. Up to 98% yield was reached with reaction conditions of 70 °C, under ambient pressure for 20 h and a dried biomass to methanol ratio 1:20 (w/v) catalyzed by either 0.2 mol L,1 H2SO4 or 0.4 mol L,1 HCl. Cetane numbers for these products were estimated to range from 56 to 59. This integrated method is thus effective and technically attractive, as dried microbial biomass as feedstocks omits otherwise tedious and time-consuming oil extraction processes. Copyright © 2007 Society of Chemical Industry [source] Utilization of spent petrochemical sulfuric acid in the production of wet-process phosphoric acidJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 12 2005Andrzej Chojnacki Abstract The possibility of the application of spent sulfuric acid from the petrochemical industry in wet-process phosphoric acid technology was investigated. The effect of organic impurities in sulfuric acid from benzol acidic refining on the solubility of calcium sulfate hydrates is discussed. Solubility isotherms and regression equations for CaSO4,H3PO4,H2SO4,H2O (pure and containing impurities) systems are presented. Phase transition temperatures between dihydrate and hemihydrate calcium sulfate were determined. The difference between pure and polluted sulfuric acid systems observed is negligible over the range of typical wet-process phosphoric acid technology parameters. It is concluded that the application of spent sulfuric acid from benzol acidic refining does not have a negative influence on the crystallization process of dihydrate calcium sulfate and therefore can be applied in wet-process phosphoric acid technology. Copyright © 2005 Society of Chemical Industry [source] Pretreatment of barley husk for bioethanol productionJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 1 2005Beatriz Palmarola-Adrados Abstract This paper reports on the optimization of steam pretreatment of barley husk for high pentose and hexose recovery in the subsequent enzymatic hydrolysis step, as well as high ethanol yield, following simultaneous saccharification and fermentation. The parameters optimized in the steam pretreatment step were residence time (5,15 min), temperature (190,215 °C), and concentration of the acid catalyst (0 or 0.5% H2SO4). A microwave oven was employed for screening of the optimal conditions to obtain the highest sugar yield following combined pretreatment and enzymatic hydrolysis. The final optimization of the pretreatment prior to enzymatic hydrolysis was performed on a larger scale, in a steam pretreatment unit. Simultaneous saccharification and fermentation was carried out following steam pretreatment on 5 and 10% dry matter steam-pretreated slurries. Fermentability tests were performed to determine the effect of by-products (ie furfural and 5-hydroxymethyl furfural) in the bioconversion of glucose to ethanol by baker's yeast. The maximum glucose yield, 88% of the theoretical, was obtained following steam pretreatment with 0.5% H2SO4 at 200 °C for 10 min. Under these conditions, a sugar to ethanol conversion of 81% was attained in simultaneous saccharification and fermentation. Copyright © 2004 Society of Chemical Industry [source] Separation of cobalt and nickel from acidic sulfate solutions using mixtures of di(2-ethylhexyl)phosphoric acid (DP-8R) and hydroxyoxime (ACORGA M5640)JOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 5 2004Arisbel Cerpa Abstract DP-8R and ACORGA M5640 extractants diluted in Exxsol D100 were used to co-extract cobalt and nickel from aqueous acidic sulfate media. The influences of equilibration time, temperature, equilibrium pH and reagent concentrations on the extraction of both metals have been studied. It was observed that both cobalt and nickel extraction are slightly sensitive to temperature but are pH dependent. Metal extraction equilibria are reached within about 5 min contact time. In addition, cobalt extraction depends on the extractant concentration in the organic phase. For a solution containing 0.5 g dm,3 each of cobalt and nickel and an initial pH of 4.1, conditions were established for the co-extraction of both metals and selective stripping (with H2SO4) of cobalt and nickel. Using the appropriate reagent concentrations the yield (extraction stage) for both metals exceeded 90%, and stripping of cobalt and nickel was almost quantitative. Copyright © 2004 Society of Chemical Industry [source] Direct filtration of Procion dye bath wastewaters by nanofiltration membranes: flux and removal characteristicsJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 12 2003Ismail Koyuncu Abstract The treatment and reuse of industrial wastewaters by membrane processes has become more attractive in the last few years due to constraints on water usage. The aim of this study was to investigate the direct filtration of reactive dye house wastewaters by nanofiltration membranes based on permeate flux, and sodium chloride and colour removal. Experiments were performed using both synthetic and industrial dye bath wastewaters with the fluxes of the industrial dye bath wastewaters lower than those of the synthetic solutions. The effects of operating conditions such as pressure and pH were assessed. Studies with DS5 DK type (polysulfone,polyamide) membranes showed that nanofiltration membranes are suitable for direct treatment of wastewaters and the permeate quality was appropriate for reuse in the dyeing process. Pre-treatment and neutralisation were important for recovery of large amounts of salt and water from the permeate stream. Neutralisation of the solution with HCl rather than H2SO4 gave a better permeate from the point of view of the reuse. The highest permeate flux and colour removal and the lowest salt removal were achieved with the HCl neutralisation. Copyright © 2003 Society of Chemical Industry [source] Towards waste minimisation in WWTP: activated carbon from biological sludge and its application in liquid phase adsorptionJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 7 2002Maria J Martin Abstract Surplus sludge produced during the biological treatment of wastewater requires costly disposal procedures. With increasing environmental and legislative constraints, increasing sludge production and more limited disposal options, new recycling alternatives have to be found. The possibility of obtaining activated carbons from surplus biological sludge by chemical activation with H2SO4 has been investigated. Operational parameters such as the amount of H2SO4 added, the temperature, and activation time were modified to ascertain their influence on the quality of the activated carbon obtained. The quality of the sludge-based activated carbons was evaluated by established characterisation parameters for adsorption from solution such as phenol value, iodine number, methylene blue number and tannin value and compared with commercial activated carbons. Activation at 700,°C for 30,min in the presence of 0.5,cm3 H2SO4,g,1 dry solids in the sludge led to an activated carbon with a good capacity for iodine and tannic acid. The sludge-derived activated carbon obtained is mesoporous in nature with a high presence of large macropores. Weak and moderate acidic surface functional groups were detected on the surface, which impart a hydrophilic nature to the solid. When compared with a commercial activated carbon, the sludge-derived activated carbon performed better when removing dyes with a high presence of anionic solubilising groups and heavy metals. The results indicate that COD adsorption from a biologically-treated effluent may also be an area for application. © 2002 Society of Chemical Industry [source] Spectrophotometric determination of leukocytes in bloodJOURNAL OF CLINICAL LABORATORY ANALYSIS, Issue 5 2002Huriye Kuzu-Karsilayan Abstract The determination of leukocyte concentration in human blood depending on the detection of oxidized o-dianisidine in acidic solution is studied. The oxidation of o-dianisidine was carried out by peroxidase enzymes found in leukocytes. The reaction was stopped by the addition of 4N H2SO4 to the solution, and a very stable, colored o-dianisidine derivative was obtained. The calibration graph was plotted with the recorded absorbance values at 400 nm assigned to the y-axis, and leukocyte counts in 1-mL blood samples to the x-axis. The equation of the calibration graph was y=0.0025x+0.0904, with a correlation coefficient of R=0.994. The coefficient of variation and P -value of the method were 4.00% and 0.05%, respectively. J. Clin. Lab. Anal. 16:233,236, 2002. © 2002 Wiley-Liss, Inc. [source] Regioselective unusual formation of spirocyclic 4-{3,-benzo(2,,3,-dihydro)furo}-9-methyl-2,3,9-trihydrothiopyrano [2,3- b]indole by acid-catalyzed reaction of enol ethersJOURNAL OF HETEROCYCLIC CHEMISTRY, Issue 1 2009K. C. Majumdar Spirocyclic 4-{3,-benzo(2,,3,-dihydro)furo}-9-methyl-2,3,9-trihydrothiopyrano[2,3- b]indoles are regioselectively synthesized by treating suitable enol ethers, 4-aryloxymethylene-9-methyl-2,3,9-trihydrothio-pyrano[2,3- b]indoles with H2SO4 in dichloromethane-methanol-water. The substrates for the aforesaid reaction are in turn synthesized by the thio -Claisen rearrangement of 2-(4,-aryloxybut-2,-ynylthio)-1-methylindoles. J. Heterocyclic Chem., 46, 62 (2009). [source] Beckmann rearrangement of cyclohexanone oxime to ,-caprolactam in microreactorsAICHE JOURNAL, Issue 5 2010K. T. Zuidhof Abstract Selectivities are presented of the Beckmann rearrangement of cyclohexanone oxime to ,-caprolactam with oleum for various conditions in three microreactors, viz., Y-junction, interdigital, and split and recombine mixers, followed by a 50-cm long microchannel of 250 ,m internal diameter. Cyclohexanone oxime is dissolved in cyclooctane, which is inert for oleum. The selectivity is measured in the temperature range of 80,132°C. The concentration range of caprolactam in the reaction mixture is 31,41 wt %, in oleum. The total volumetric flow rate is 0.4 ml/min, whereas the flow rate ratio of ,-caprolactam/oleum over cyclohexanone oxime/cyclooctane ranges from 0.3 to 3. The selectivities measured with the three microreactors are: 70,99+%, 93,99+%, and 95,99+%, respectively. High ,-caprolactam concentration (41 wt %), high temperature (110,132°C), and a ratio of free H2SO4 to SO3 of unity have a negative effect on the selectivity. © 2009 American Institute of Chemical Engineers AIChE J, 2010 [source] Liquid,liquid two-phase flow in pore array microstructured devices for scaling-up of nanoparticle preparationAICHE JOURNAL, Issue 12 2009Shaowei Li Abstract Nanoparticles have been produced by a T-junction microchannel device in our previous work (Li et al., Langmuir. 2008;24:4194-4199). As a scaling-up strategy, pore array microstructured devices were designed to prepare nanoparticles in this article. H2SO4 and BaCl2, respectively, in two phases to form BaSO4 nanoparticles was used as a test system. The characteristics of a well controlled liquid,liquid two-phase flow in the pore array microstructured devices were presented. Nanoparticles with small size and good dispersibility were produced through drop or disk flows in the microstructured devices. The influence of mass transfer and chemical reaction on interfacial tension and flow patterns was discussed based on the experiments. Meanwhile, the effect of the two phase flow patterns on the nanoparticle size was discussed. It was found that the increase of the amount of mass transfer and chemical reaction could change the flow patterns from disk flow to drop flow. The droplet diameter could be changed in a wide range. Flow patterns could be distinguished based on the measured interfacial tension in different concentrations. The prepared nanoparticles were ranged from 10 nm to 30 nm. Apparently the particle size was decreased with the increase of the droplet size in both the drop flow region and the disk flow region whereas it had a reverse trend in the transition region. © 2009 American Institute of Chemical Engineers AIChE J, 2009 [source] Development of an electrochemical cell for efficient hydrogen production through the IS processAICHE JOURNAL, Issue 8 2004Mikihiro Nomura Abstract The Bunsen reaction (SO2 + I2 + 2H2O = H2SO4 + 2HI) was examined by an electrochemical cell featuring a cation-exchange membrane as the separator, using sulfuric acid dissolving sulfur dioxide as the anolyte and hydriodic acid dissolving iodine as the catholyte. In galvanostatic electrolysis, the molality of H2SO4 in the anolyte and that of HI in the catholyte were increased up to 17.8 and 14.9 mol kgH2O,1, respectively. These concentrations were far higher than those that were obtained by the Bunsen reaction carried out in the presence of a large amount of iodine (such as I2/HI = 4). I2 concentration after the concentration procedure was at I2/HI = 0.95, which is lower than the reported value. I2 is one of the recycling agents in the IS process. HI and H2SO4 were successfully concentrated under low I2 concentration. The concentration of HI agreed with the calculated value, based on the amount of electricity consumed, indicating high current efficiency. Heat/mass balance using this type of electrochemical cell through the IS process is discussed for evaluation of the reactor. The thermal efficiency to produce hydrogen was calculated at 42.1%, without heat recovery for electricity, by optimizing HI and H2SO4 concentrations after application of the electrochemical cell. © 2004 American Institute of Chemical Engineers AIChE J, 50: 1991,1998, 2004 [source] Chemical synthesis and electric properties of the conducting copolymer of aniline and o -aminophenolJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 23 2007Jing Zhang Abstract A copolymer, poly(aniline- co-o -aminophenol), was prepared chemically by using ammonium peroxydisulfate as an oxidant. The monomer concentration ratio of o -aminophenol to aniline strongly influences the copolymerization rate and properties of the copolymer. The optimum composition of a mixture for the chemical copolymerization consisted of 0.3 M aniline, 0.021 M o -aminophenol, 0.42 M ammonium peroxydisulfate, and 2 M H2SO4. The result of cyclic voltammograms in a potential region of ,0.20 to 0.80 V (vs.SCE) indicates that the electrochemical activity of the copolymer prepared under the optimum condition is similar to that of polyaniline in more acid solutions. However, the copolymer still holds the good electrochemical activity until pH 11.0. Therefore, the pH dependence of the electrochemical property of the copolymer is improved, compared with poly(aniline- co-o -aminophenol) prepared electrochemically, and is much better than that of polyaniline. The spectra of IR and 1H NMR confirm that o -aminophenol units are included in the copolymer chain, which play a key role in extending the usable pH region of the copolymer. The visible spectra of the copolymers show that a high concentration ratio of o -aminophenol to aniline in a mixture inhibits the chain growth. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 5573,5582, 2007 [source] Synthesis of Hydrated Aluminum Sulfate from Kaolin by Microwave ExtractionJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 6 2000Seong Soo Park The feasibility of extracting alumina from kaolin via a microwave extraction process was investigated by comparing reaction times, reaction temperatures, and acid concentrations under microwave treatment with the same factors under conventional thermal extraction. The maximum amount of alumina extracted from kaolin under conventional processing at 90°C for 240 min with 1M H2SO4 was 99.9%; the same amount of alumina was extracted under microwave processing at 90°C for 120 min with 1M H2SO4. [source] Modelling of the hydrolysis of sorghum straw at atmospheric pressureJOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE, Issue 5 2002Simón J Téllez-Luis Abstract Sorghum straw is a renewable, cheap and widespread resource. The acid hydrolysis of sorghum straw to obtain xylose solutions could be a good alternative for this abundant resource. The H2SO4 hydrolysis of sorghum straw at two different temperatures (80 and 100,°C) and three H2SO4 concentrations (2, 4 and 6%) using a solid/liquid ratio of 1:10 (w/w) was studied. Kinetic parameters of mathematical models for predicting the concentrations of xylose, glucose, acetic acid and furfural were determined. The activation energy of the release reaction was 183.3,kJ,mol,1 for xylose and 185.8,kJ mol,1 for glucose. The optimal conditions found were 6% H2SO4 at 100,°C for 60,min, which allow one to obtain a solution with 18.27,g xylose l,1, 6.78,g glucose l,1, 0.7,g furfural l,1 and 1.35,g acetic acid l,1. It is concluded that this process has potential for utilisation of this renewable lignocellulosic resource. © 2002 Society of Chemical Industry [source] Lyotropic Liquid Crystalline Polyamides Containing Aromatic, Heterocyclic Structures: Preparation and PropertiesMACROMOLECULAR CHEMISTRY AND PHYSICS, Issue 17 2006Pengtao Liu Abstract Summary: A series of novel lyotropic liquid crystalline polyamides derived from 1,2-dihydro-2-(4-aminophenyl)-4-[4-(4-(aminophenoxyl)phenyl)]-phthalazinone (DHPZ-DA), p -phenylene diamine (PPD) and terephthaloyl dichloride (TPC) have been successfully synthesized by the low temperature solution polycondensation method. The copolymers obtained with inherent viscosity of ,1.21 to 3.29 dl,·,g,1, determined in NMP (1 wt.-% LiCl) or concentrated H2SO4 at 25,°C, were confirmed to be amorphous by WAXD and differential scanning calorimetry (DSC). Their solubility was improved by the introduction of non-coplanar, twisted phthalazinone moieties and ether linkages into the main chain with the result that they can be soluble in some polar solvents containing a small amount of LiCl. Their Tgs were all above 310,°C and 10% weight loss temperatures in nitrogen above 500,°C. Most of these polyamides can form an anisotropic phase in concentrated H2SO4, NMP (1 wt.-% LiCl) and DMAc (1 wt.-% LiCl) solutions, observed on a polarizing light microscope. Optical micrograph (×40) of polyamide P-4060 at 10 wt.-% in NMP/LiCl (1% w/v) solution at room temperature. [source] | ||||||||||||||||||||||||||||||||||||||||