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Initial Concentration (initial + concentration)
Kinds of Initial Concentration Selected AbstractsLong-term stability of biological denitrification process for high strength nitrate removal from wastewater of uranium industryENVIRONMENTAL PROGRESS & SUSTAINABLE ENERGY, Issue 3 2008Prashant M. Biradar Abstract The aim of the present study was to biologically denitrify uranium nitrate raffinate (UNR) from nuclear industry, which is a principle source of high strength nitrate waste. To denitrify the high nitrate waste, a pilot-scale continuous stirred tank reactor was designed with two inbuilt settlers. Acclimatization of mixed culture with synthetic waste was carried out prior to the inoculation of the acclimatized sludge into the reactor. Initial concentration of nitrate in uranium raffinate was 77,000 mg/L NO3. It was diluted and used as a feed to the reactor. Concentration of nitrate in feed was increased gradually from 10,000 mg/L NO3 to 40,000 mg/L NO3 with hydraulic retention time (HRT) maintained at 34.4 h. Complete denitrification of 40,000 mg/L NO3 was achieved in a specified HRT. To facilitate understanding of the treatablity and long-term stability of biological denitrification of UNR, study was carried out for 211 days by periodical perturbation of the system. Furthermore, to find the volume ratio of reactor to settler required for the full-scale design of the denitrification plant, settling of acclimatized sludge was carried out. © 2008 American Institute of Chemical Engineers Environ Prog, 2008 [source] Co-composting of pharmaceutical wastes in soilLETTERS IN APPLIED MICROBIOLOGY, Issue 4 2001T.F. Guerin Aims:,Soils at a commercial facility had become contaminated with the pharmaceutical chemical residues, Probenecid and Methaqualone, and required remediation. Methods and Results:,Soil composting was investigated as an alternative to incineration for treatment. In laboratory trials, a factorial experimental design was used to evaluate organic matter amendment type and concentration, and incubation temperature. In pilot scale trials, Probenecid was reduced from 5100 mg kg,1 to < 10 mg kg,1 within 20 weeks in mesophilic treatments. An 8 tonne pilot scale treatment confirmed that thermophilic composting was effective under field conditions. In the full-scale treatment, 180 tonnes of soil were composted. Initial concentrations of the major contaminants in the full-scale compost treatment were 1160 mg kg,1 and 210 mg kg,1, for Probenecid and Methaqualone, respectively. Probenecid concentration reached the target level of 100 mg kg,1 in 6 weeks, and removal of Methaqualone to < 100 mg kg,1 was achieved after 14 weeks. Conclusions:,Co-composting was effective in reducing soil concentrations of Probenecid and Methaqualone residues to acceptable values. Significance and Impact of the Study:,Co-composting is a technology that has application in the remediation of pharmaceutical contaminants in soil. [source] Temperature gradient focusing in a PDMS/glass hybrid microfluidic chipELECTROPHORESIS, Issue 24 2007Takuya Matsui Abstract This paper reports the application of temperature gradient focusing (TGF) in a PDMS/glass hybrid microfluidic chip. With TGF, by the combination of a temperature gradient along a microchannel, an applied electric field, and a buffer with a temperature-dependent ionic strength, analytes are focused by balancing their electrophoretic velocities against the bulk velocity of the buffer containing the analytes. In this work, Oregon Green 488 carboxylic acid was concentrated approximately 30 times as high as the initial concentration in 45,s at moderate electric strength of 70,V/cm and a temperature gradient of 55°C across the PDMS/glass hybrid microfluidic chip with a 1,cm long capillary. [source] A 3-D dielectrophoretic filter chipELECTROPHORESIS, Issue 7 2007Ciprian Iliescu Dr. Abstract The paper presents a 3-D filter chip employing both mechanical and dielectrophoretic (DEP) filtration, and its corresponding microfabrication techniques. The device structure is similar to a classical capacitor: two planar electrodes, made from a stainless steel mesh, and bonded on both sides of a glass frame filled with round silica beads. The solution with the suspension of particles flows through both the mesh-electrodes and silica beads filter. The top stainless steel mesh (with openings of 60,,m and wires of 30,,m-thickness) provides the first stage of filtration based on mechanical trapping. A second level of filtration is based on DEP by using the nonuniformities of the electric field generated in the capacitor due to the nonuniformities of the dielectric medium. The filter can work also with DC and AC electric fields. The device was tested with yeast cells (Saccharomyces cerevisae) and achieved a maximal trapping efficiency of 75% at an applied AC voltage of 200,V and a flow rate of 0.1,mL/min, from an initial concentration of cells of 5×105 cells/mL. When the applied frequency was varieted in the range between 20 and 200,kHz, a minimal value of capture efficiency (3%) was notticed at 50,kHz, when yeast cells exhibit negative DEP and the cells are repelled in the space between the beads. [source] Bioreductive deposition of palladium (0) nanoparticles on Shewanella oneidensis with catalytic activity towards reductive dechlorination of polychlorinated biphenylsENVIRONMENTAL MICROBIOLOGY, Issue 3 2005Wim De Windt Summary Microbial reduction of soluble Pd(II) by cells of Shewanella oneidensis MR-1 and of an autoaggregating mutant (COAG) resulted in precipitation of palladium Pd(0) nanoparticles on the cell wall and inside the periplasmic space (bioPd). As a result of biosorption and subsequent bioreduction of Pd(II) with H2, formate, lactate, pyruvate or ethanol as electron donors, recoveries higher than 90% of Pd associated with biomass could be obtained. The bioPd(0) nanoparticles thus obtained had the ability to reductively dehalogenate polychlorinated biphenyl (PCB) congeners in aqueous and sediment matrices. Bioreduction was observed in assays with concentrations up to 1000 mg Pd(II) l,1 with depletion of soluble Pd(II) of 77.4% and higher. More than 90% decrease of PCB 21 (2,3,4-chloro biphenyl) coupled to formation of its dechlorination products PCB 5 (2,3-chloro biphenyl) and PCB 1 (2-chloro biphenyl) was obtained at a concentration of 1 mg l,1 within 5 h at 28°C. Bioreductive precipitation of bioPd by S. oneidensis cells mixed with sediment samples contaminated with a mixture of PCB congeners, resulted in dechlorination of both highly and lightly chlorinated PCB congeners adsorbed to the contaminated sediment matrix within 48 h at 28°C. Fifty milligrams per litre of bioPd resulted in a catalytic activity that was comparable to 500 mg l,1 commercial Pd(0) powder. The high reactivity of 50 mg l,1 bioPd in the soil suspension was reflected in the reduction of the sum of seven most toxic PCBs to 27% of their initial concentration. [source] Reduction of perchlorate in river sedimentENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 4 2006Rupert Simon Abstract The transformation of perchlorate was investigated in river sediment during laboratory batch and column studies to determine if reduction of perchlorate is a viable pathway in natural sediment without previous exposure to perchlorate. Perchlorate at an initial concentration of 10 ,M was reduced quantitatively to chloride in 3 d after a lag phase of 2 d in sediment slurries amended with lactate. Raising the initial concentration of perchlorate to 1,000 ,M increased the lag phase to 20 d before reduction occurred. At perchlorate concentrations greater than 1,000 ,M, the reduction of perchlorate was not observed within 40 d. We speculate that the high concentration of perchlorate specifically was problematic to the microbes mediating the reduction of perchlorate. High levels of nitrate inhibited the reduction of perchlorate as well. In sediment slurries amended with 870 ,M sodium nitrate, the reduction of perchlorate at an initial concentration of 100 ,M did not occur before day 15 of the experiment, but complete removal of nitrate had occurred by day four. Sediment column studies further demonstrated the dependence of perchlorate reduction on endogenous nitrate levels. [source] Dissipation kinetics and mobility of chlortetracycline, tylosin, and monensin in an agricultural soil in Northumberland County, Ontario, CanadaENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 1 2006Jules C. Carlson Abstract A robust high-throughput method was refined to extract three growth-promoting antibiotics, tylosin (TYL), chlortetracycline (CTC), and monensin (MON), from soil. Analysis was performed by electrospray liquid chromatography tandem mass spectrometry. Soil dissipation rate studies were performed in a farm field soil for antibiotics applied with and without manure. Tylosin, CTC, and MON followed first-order dissipation kinetics with half-lives of 4.5, 24, and 3.3 d, respectively, with the addition of manure and 6.1, 21, and 3.8 d, respectively, without manure. Manure application significantly increased TYL dissipation rate, perhaps because of the introduced microbial flora, but had no significant effect on CTC or MON. Monensin dissipation half-life was found to be much shorter in the field study than in a controlled laboratory study, perhaps because of differences in microbial communities. The antimicrobials were not highly mobile. Chlortetracycline was the only antibiotic detected at 25 to 35 cm depth and only up to 2% of the initial concentration in a sandy loam soil. These antibiotics are therefore expected to degrade primarily in agricultural soils before moving to greater depths or to groundwater in significant concentrations in most agricultural systems. [source] Toxicity and fate of two munitions constituents in spiked sediment exposures with the marine amphipod Eohaustorius estuariusENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 11 2005Gunther Rosen Abstract The lethal toxicity of the explosive compounds 14C-labeled 2,4,6-trinitrotoluene (TNT) and nonradiolabeled hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) to the estuarine amphipod Eohaustorius estuarius was investigated in 10-d spiked sediment exposures. The 10-d median lethal concentration (LC50) was determined using the sum molar initial concentration of TNT, ami-nodinitrotoluenes (ADNTs), and diaminonitrotoluenes (DANTs), as determined by high-performance liquid chromatography (HPLC), and collectively referred to as HPLC-TNT*. Despite expectations of higher toxicity in sandy sediment (Yaquina Bay [YB], OR, USA) compared to relatively fine-grained sediment (San Diego Bay [SDB], CA, USA), LC50 values were similar: 159 and 125 ,mol/kg, for YB and SDB sediments, respectively. When expressed as the sum of TNT and all its degradation products (14C-TNT*), LC50s were approximately two times the corresponding LC50s determined by HPLC. The HPLC-TNT* fraction likely corresponds to the most bioavailable and toxic transformation products. The concentrations of 14C-TNT* in tissues were substantially higher than those for HPLC-TNT*, suggesting that compounds other than TNT and its major aminated transformation products were prevalent. Critical body residues were similar for exposures to SDB (11.7 ,mol/kg) and YB sediments (39.4 ,mol/kg), despite marked differences in the nature of compounds available for uptake in the exposure media. The critical body residues for E. estuarius are lower than those reported for other aquatic invertebrates (83,172 ,mol/kg). Unlike observations for TNT, RDX was only loosely associated with SDB sediment, with near complete recovery of the parent compound by chemical analysis. Exposure to RDX did not result in significant mortality even at the highest measured sediment concentration of 10,800 ,mol/kg dry weight, nor tissue concentrations as high as 96 ,mol/kg wet weight. The lack of RDX lethal effects in this study is consistent with results reported for other invertebrate species. [source] Sorption and leaching behaviour of polar aromatic acids in agricultural soils by batch and column leaching testsEUROPEAN JOURNAL OF SOIL SCIENCE, Issue 3 2005R. Celis Summary Aromatic acids can reach the soil from direct anthropogenic activities or, indirectly, from the degradation of many aromatic compounds, such as pesticides or polycyclic aromatic hydrocarbons. Because of the anionic character of aromatic acids at the pH of most soil and sediment environments, they are expected to move rapidly through the soil profile and to pose a great risk of ground water contamination. We designed batch and column leaching tests to characterize the behaviour of three aromatic acids differing in their chemical structures, picloram (4-amino-3,5,6-trichloropicolinic acid), phthalic acid (2,2-benzenedicarboxylic acid), and salicylic acid (2-hydroxybenzoic acid), in four European soils with different physicochemical characteristics. Batch experiments revealed that the persistence of the three acids in soil:water suspensions decreased in the order: picloram , phthalic acid > salicylic acid, and their dissipation curves were relatively independent of soil type. Sorption by the soils, their clay-size fractions and model sorbents indicated much greater affinity of soil constituents for salicylic acid than for picloram or phthalic acid, most likely due to the ability of salicylic acid to form bidentate complexes with positively charged soil components. The extent of leaching of the aromatic acids in hand-packed soil columns decreased in the order: picloram (90,96%) > phthalic acid (25,90%) > salicylic acid (0,37%), which was consistent with the sorption and persistence results of the batch tests. The organic C content, the amount of small-size pores, and the initial concentration of aromatic acid in soil appeared to be important factors influencing the leaching patterns of phthalic acid and salicylic acid in the soils studied, but did not greatly influence the leaching pattern of picloram. Sorption and leaching of polar aromatic acids in soil can therefore vary considerably depending on the structural characteristics of the aromatic acid or soil type. [source] Biotransformation in vitro of the 22R and 22S epimers of budesonide by human liver, bronchus, colonic mucosa and skinFUNDAMENTAL & CLINICAL PHARMACOLOGY, Issue 1 2001Julio Cortijo The pharmacological effects of glucocorticoids are greatly influenced by their pharmacokinetic properties. In the present report, the in vitro biotransformation of the 22R and 22S epimers of the topical steroid budesonide was studied in the S-9 fraction of human liver, bronchus, skin and colonic mucosa. The disappearance of unchanged epimers of budesonide was measured during 90 min of incubation by high performance liquid chromatography. The rate of disappearance was high in human liver while little biotransformation occurred in bronchial tissue and colonic mucosa, and none was detected in the skin. A marked decay of the initial concentration of unchanged budesonide epimers was noticed after 2 h incubation in cultured human hepatocytes, while only a small decrease was observed after 24 h incubation in cultured human airway smooth muscle cells and BEAS-2B cells. The 22R epimer of budesonide suffered greater in vitro biotransformation than the 22S epimer in human hepatic, bronchial and colonic tissues. These findings extend those of other studies, and confirm that the high therapeutic ratio of budesonide is due to negligible local biotransformation combined with high level of liver metabolism for locally absorbed budesonide. [source] Ignition and oxidation of 1-hexene/toluene mixtures in a shock tube and a jet-stirred reactor: Experimental and kinetic modeling studyINTERNATIONAL JOURNAL OF CHEMICAL KINETICS, Issue 9 2007M. Yahyaoui The oxidation of several binary mixtures 1-hexene/toluene has been investigated both in a shock tube and in a jet-stirred reactor (JSR). The self-ignition behavior of binary mixtures was compared to that of neat hydrocarbons studied under the same conditions. Furthermore, molecular species concentration profiles were measured by probe-sampling and GC/MS, FID, TCD analyses for the oxidation of the mixtures in a JSR. Experiments were carried out over the temperature range 750,1860 K. Mixtures were examined under two pressures 0.2 and 1 MPa, with 0.1% initial concentration of fuel. The equivalence ratio was varied from 0.5 to 1.5. The experiments were modeled using a detailed chemical kinetic reaction mechanism. The modeling study showed that interactions between hydrocarbons submechanisms were not limited to small reactive radicals. Other types of interactions involving hydrocarbon fragments derived from the oxidation of the fuel components must be considered. These interactions mainly consist of hydrogen abstraction reactions. For example, benzyl radical that is the major radical produced from the oxidation of toluene at high temperature can abstract hydrogen from 1-hexene and their products such as hexenyl radicals. Similarly, propyl, allyl, and hexenyl radicals that are the major radicals produced during 1-hexene oxidation at high temperature can abstract hydrogen from toluene. Improved modeling was achieved when such interaction reactions were included in the model. Good agreement between experimental and calculated data was obtained using the proposed detailed chemical kinetic scheme. © 2007 Wiley Periodicals, Inc. Int J Chem Kinet 39: 518,538, 2007 [source] Kinetics and mechanism of esterification of epoxy resin in presence of triphenylphosphineINTERNATIONAL JOURNAL OF CHEMICAL KINETICS, Issue 5 2004Neelam Pal The kinetics of esterification of bisphenol-A based epoxy resin with acrylic acid in presence of triphenylphosphine has been studied. The reaction exhibits a first-order rate dependence with respect to [Epoxy] and [Catalyst]. A first-order dependence of rate with respect to [Acid] has been observed during a particular kinetic run. However, a retarding effect of [Acid] on the rate has been observed by increasing the initial concentration of acid. A suitable mechanism consistent with the kinetic data is proposed and discussed. © 2004 Wiley Periodicals, Inc. Int J Chem Kinet 36: 280,285, 2004 [source] Uncatalyzed and ruthenium(III)-catalyzed reaction of acidic chlorite with methylene violetINTERNATIONAL JOURNAL OF CHEMICAL KINETICS, Issue 7 2003S. B. Jonnalagadda The kinetics and mechanism of the uncatalyzed and Ru(III)-catalyzed oxidation of methylene violet (3-amino-7-diethylamino-5-phenyl phenazinium chloride) (MV+) by acidic chlorite is reported. With excess concentrations of other reactants, both uncatalyzed and catalyzed reactions had pseudo-first-order kinetics with respect to MV+. The uncatalyzed reaction had first-order dependence on chlorite and H+ concentrations, but the catalyzed reaction had first-order dependence on both chlorite and catalyst, and a fractional order with respect to [H+]. The rate coefficient of the uncatalyzed reaction is (5.72 ± 0.19) M,2 s,1, while the catalytic constant for the catalyzed reaction is (22.4 ± 0.3) × 103 M,1 s,1. The basic stoichiometric equation is as follows: 2MV+ + 7ClO2, + 2H+ = 2P + CH3COOH + 4ClO2 + 3Cl,, where P+ = 3-amino-7-ethylamino-5-phenyl phenazinium-10-N-oxide. Stoichiometry is dependent on the initial concentration of chlorite present. Consistent with the experimental results, pertinent mechanisms are proposed. The proposed 15-step mechanism is simulated using literature; experimental and estimated rate coefficients and the simulated plots agreed well with the experimental curves. © 2003 Wiley Periodicals, Inc. Int J Chem Kinet 35: 294,303, 2003 [source] Experimental study on sulfur trioxide decomposition in a volumetric solar receiver,reactorINTERNATIONAL JOURNAL OF ENERGY RESEARCH, Issue 9 2009Adam Noglik Abstract Process conditions for the direct solar decomposition of sulfur trioxide have been investigated and optimized by using a receiver,reactor in a solar furnace. This decomposition reaction is a key step to couple concentrated solar radiation or solar high-temperature heat into promising sulfur-based thermochemical cycles for solar production of hydrogen from water. After proof-of-principle a modified design of the reactor was applied. A separated chamber for the evaporation of the sulfuric acid, which is the precursor of sulfur trioxide in the mentioned thermochemical cycles, a higher mass flow of reactants, an independent control and optimization of the decomposition reactor were possible. Higher mass flows of the reactants improve the reactor efficiency because energy losses are almost independent of the mass flow due to the predominant contribution of re-radiation losses. The influence of absorber temperature, mass flow, reactant initial concentration, acid concentration, and residence time on sulfur trioxide conversion and reactor efficiency has been investigated systematically. The experimental investigation was accompanied by energy balancing of the reactor for typical operational points. The absorber temperature turned out to be the most important parameter with respect to both conversion and efficiency. When the reactor was applied for solar sulfur trioxide decomposition only, reactor efficiencies of up to 40% were achieved at average absorber temperature well below 1000°C. High conversions almost up to the maximum achievable conversion determined by thermodynamic equilibrium were achieved. As the re-radiation of the absorber is the main contribution to energy losses of the reactor, a cavity design is predicted to be the preferable way to further raise the efficiency. Copyright © 2009 John Wiley & Sons, Ltd. [source] Controlled Growth of Se Nanoparticles on Ag Nanoparticles in Different Ratios,ADVANCED MATERIALS, Issue 4 2005X. Gao The integration of multiple nano- particles (NPs) with different physical properties into a multifunctional hybrid NP is a challenge. Here, a new wet chemical synthesis is used to generate hybrid NPs by the heterogeneous growth of one NP onto another equivalent-sized NP (see Figure). The hybrid NPs consist of Ag-NPs and Se-NPs in controlled nanoparticle ratios of 1:1, 1:2, and 1:3, respectively. The Se-NPs were grown on the Ag-NP, and the number of Se-NPs was controlled by the initial concentration of Se ions. [source] Changes in total carotenoid content at different stages of traditional processing of yellow-fleshed cassava genotypesINTERNATIONAL JOURNAL OF FOOD SCIENCE & TECHNOLOGY, Issue 12 2009Busie Maziya-Dixon Abstract The changes in content of total carotenoid at each stage of processing cassava storage roots were investigated with three improved yellow-fleshed cassava varieties (TMS 94/0006, TMS 01/1235 and TMS 01/1371) grown in 2005/2006 in a randomised complete block design with two replications at Ibadan, Nigeria. When the cassava roots were grated to a mash, results obtained indicate that there was a significant reduction in total carotenoid content for all the genotypes. The reduction was highest for TMS 01/1235 (1.20 ,g g,1), intermediate for TMS 01/1371 (0.78 ,g g,1) and least for TMS 94/0006 (0.35 ,g g,1). In most cases, we observed higher total carotenoid concentration, especially when the intermediate step involved pressing to remove excess water, and during roasting compared with the initial concentration in the raw cassava storage roots. In conclusion, grating, drying and cooking to a paste resulted in reduction of total carotenoid content, while roasting and pressing resulted in higher carotenoid concentration. A change in total carotenoid content during processing depends on variety, processing method, especially unit operation and the initial total carotenoid content of the variety. [source] Effect of initial concentration of bacterial suspensions on their inactivation by high hydrostatic pressureINTERNATIONAL JOURNAL OF FOOD SCIENCE & TECHNOLOGY, Issue 5 2002S. Furukawa The effects of initial concentration [104,109 colony forming units (CFU) mL,1] on the inactivation of vegetative cell suspensions (Escherichia coli) and spore suspensions (Bacillus subtilis) by hydrostatic pressure treatment were investigated. The inactivation rates of E. coli and B. subtilis decreased as the initial concentration of cell and spore suspensions increased. In the practical application of hydrostatic pressure treatment, it was considered that the initial concentration of the bacteria suspensions should be as low as possible. [source] TLM for diffusion: consistent first time step.INTERNATIONAL JOURNAL OF NUMERICAL MODELLING: ELECTRONIC NETWORKS, DEVICES AND FIELDS, Issue 3 2002Two-dimensional case Abstract In initializing a transmission line matrix (TLM) diffusion model it is necessary to consider both initial concentration (temperature) and initial flow. As usual, only one of them is given; an auxiliary formula is necessary to calculate the distribution for the first time step. It has been shown that the standard formula may introduce additional numerical errors (International Journal of Numerical Modelling: Electronic Networks, Devices and Fields 1993; 6:135; International Journal of Numerical Modelling: Electronic Networks, Devices and Fields 1993; 6:161) and that these errors can persist over many time steps. In this paper, we show how an initial modification to the normal TLM algorithm can remove such errors, and we demonstrate the method by applying it to a two-dimensional TLM heat diffusion model for a copper plate. Copyright © 2002 John Wiley & Sons, Ltd. [source] Adsorption of Cd(II), Pb(II), and Ag(I) in aqueous solution on hollow chitosan microspheresJOURNAL OF APPLIED POLYMER SCIENCE, Issue 2 2010Shan Wang Abstract Cross-linked chitosans synthesized by the inverse emulsion cross-link method were used to investigate adsorption of three metal ions [Cd(II), Pb(II), and Ag(I)] in an aqueous solution. The chitosan microsphere, was characterized by FTIR and SEM, and adsorption of Cd(II), Pb(II), and Ag(I) ions onto a cross-linked chitosan was examined through analysis of pH, agitation time, temperature, and initial concentration of the metal. The order of adsorption capacity for the three metal ions was Cd2+ > Pb2+ > Ag+. This method showed that adsorption of the three metal ions in an aqueous solution followed the monolayer coverage of the adsorbents through physical adsorption phenomena and coordination because the amino (NH2) and/or hydroxy (OH) groups on chitosan chains serve as coordination sites. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source] Adsorption of Hg2+ on a novel chelating fiber prepared by preirradiation grafting and aminationJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2009Ying Yang Abstract A novel chelating fiber was prepared by the irradiation-induced grafting copolymerization of glycidyl methacrylate on polypropylene fiber and consequent amination with diethylenetriamine. The effects of the reaction conditions, such as reaction time, temperature, and monomer concentration, on the degree of grafting were investigated. The optimal conditions for grafting were found to be 3 h, 100°C, and a 50% (v/v) glycidyl methacrylate concentration in tetrahydrofuran solution. This fiber showed good adsorption performance at different concentrations of Hg2+, in particular for trace Hg2+. Under the adsorption conditions of pH = 4, initial concentration = 1000 mg/L, and time = 20 h, the adsorption capacity of the chelating fiber for Hg2+ reached 785.28 mg/g. It completely adsorbed the Hg2+ ions in solution within a short contact time, showing a very high adsorption rate for Hg2+. Furthermore, the chelating fiber also had a high selectivity for mercury, whereas Cu2+ coexisted in different concentrations. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009 [source] Synthesis of morphologically different, metal absorbing aniline-formaldehyde polymers including micron-sized sphere using simple alcohols as morphology modifierJOURNAL OF APPLIED POLYMER SCIENCE, Issue 2 2008Rik Rani Koner Abstract Aniline-formaldehyde condensate (AFC) is an amine functional group containing polymer. The sticky resinous nature of the polymer limits its usefulness. Synthesis of AFC in presence of methanol, isopropanol, t -butanol, n -octanol or glycerine formed solid cakes instead of resinous material. The scanning electron microscopic (SEM) picture of the polymer synthesized in presence of t -butanol shows the formation of micron sized spheroids while the presence of methanol, isopropanol, n -octanol and glycerine leads to amorphous polymer. The polymers were characterized with IR, MALDI-TOF mass and Energy Dispersive X-ray (EDAX) analysis. To probe the accessibility of the amine functional groups by external reagents and as an application, metal removal property of the polymers were tested using aqueous Cr(VI) solution. All the polymers remove Cr(VI) efficiently at pH 3 with extent of metal removal depends on their morphology. Polymer synthesized in presence of isopropanol removes , 66% Cr(VI) removal from an initial concentration of 9 mg/L. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Preparation and adsorption properties of chitosan,poly(acrylic acid) nanoparticles for the removal of nickel ionsJOURNAL OF APPLIED POLYMER SCIENCE, Issue 4 2008Jian-Wen Wang Abstract Chitosan (CS) nanoparticles with different mean sizes ranging from 100 to 195 nm were prepared by ionic gelation of CS and poly(acrylic acid) (PAA). Variations in the final solution pH value and CS : PAA volume ratio were examined systematically for their effects on nanoparticle size, intensity of surface charge, and tendency toward particle aggregation. The sorption capacity and sorption isotherms of the CS,PAA nanoparticles for nickel ions were evaluated. The parameters for the adsorption of nickel ions by the CS,PAA nanoparticles were also investigated. The CS,PAA nanoparticles could sorb nickel ions effectively. The sorption rate for nickel ions was affected significantly by the initial concentration of the solution, sorbent amount, particle size, and pH value of the solution. The samples of nanoparticles were well correlated with Langmuir's isotherm model, and the adsorption kinetics of nickel correlated well with the pseudo-second-order model. The maximum capacity for nickel sorption deduced from the use of the Langmuir isotherm equation was 435 mg/g, which was significantly higher than that of the micrometer-sized CS. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2008 [source] Photocatalytic degradation of methyl tert -butyl ether (MTBE) in contaminated water by ZnO nanoparticlesJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 11 2008Akbar Eslami Abstract BACKGROUND: Over the past several decades methyl tert -butyl ether (MTBE) as additive to gasoline, intended to either boost ratings of fuel or to reduce air pollution, has been accepted worldwide. Since MTBE has high water solubility, the occurrence of fuel spills or leaks from underground storage tanks or transferring pipeline has led to the contamination of natural waters. In this study the degradation of aqueous MTBE at relatively high concentrations was investigated by a UV-visible/ZnO/H2O2 photocatalytic process. The effects of important operational parameters such as pH, amount of H2O2, catalyst loading and irradiation time were also investigated. Concentration of MTBE and intermediates such as tert -butyl formate and tert -butyl alcohol were measured. RESULTS: Time required for complete degradation increased from 20 to 150 min when the initial concentration was increased from 10 to 500 mg L,1. The first-order rate constants for degradation of MTBE were estimated to be 0.183,0.022 min,1 as the concentration increased from 10 to 500 mg L,1. Study of the overall mineralization monitored by total organic carbon analysis showed that at an initial concentration of 100 mg L,1 MTBE complete mineralization was obtained after 100 min under UV-visible/ZnO/H2O2 photocatalysis. CONCLUSION: The data presented in this paper clearly indicated that UV-visible/ZnO/O2 as an advanced oxidation process provides an efficient treatment alternative for the remediation of MTBE-contaminated waters. Copyright © 2008 Society of Chemical Industry [source] The effect of solids on the electrochemical treatment of olive mill effluentsJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 5 2007Efi Kotta Abstract The electrochemical oxidation of an olive mill effluent over Ti,Pt anodes was studied. The effluent had an average total chemical oxygen demand (COD) value of 234 g L,1, soluble COD of 61 g L,1, soluble phenolic content 3.4 g L,1, total solids of 80 g L,1 and pH = 5.1. Experiments were conducted in a 10 L vessel with the effluent recirculating at 1 L s,1. The applied current was varied between 5 and 20 A, the salinity between 1 and 4% NaCl, and experiments were performed with the effluent diluted with water to achieve the desired initial concentration. Emphasis was given to the effect of the presence of solids as well as of varying operating conditions on process performance as assessed in terms of COD, color and phenols removal. In general, degradation of phenols occurred relatively fast with conversion increasing with increasing applied current and decreasing initial organic loading and this was accompanied by low COD removal levels and moderate decolorization. The presence of solids had practically no effect on phenols removal, which, in most cases, was complete in less than about 180 min of reaction. However, oxidation in the presence of solids resulted in a substantial solid fraction being dissolved and this consequently increased sample color and the soluble COD content. The solid content typically found in olive mill effluents may partially impede its treatment by electrochemical oxidation, thus requiring more severe operating conditions and greater energy consumption. Copyright © 2007 Society of Chemical Industry [source] Enhanced photodegradation of bisphenol A in the presence of ,-cyclodextrin under UV lightJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 5 2006Guanghui Wang Abstract Enhancement of the photodegradation of bisphenol A (BPA) by ,-cyclodextrin (,-CD) was investigated under a 30 W UV disinfection lamp (,max = 254 nm). The photodegradation rate of BPA in aqueous solutions with ,-CD was faster than that in aqueous solutions without ,-CD; for example, after 50 min of UV irradiation, ,-CD had increased the photodegradation efficiency by about 46.5% for 10 mg dm,3 BPA. The photodegradation of 2.5,20 mg dm,3 BPA in aqueous solutions was found to follow pseudo-first-order kinetics. The first-order rate constant showed a 12-fold increase in the presence of ,-CD. Factors such as ,-CD concentration, pH, BPA initial concentration and organic solvent influencing the photodegradation of BPA were studied and are described in detail. Variations in the pH and electrical conductivity of solutions were observed during the photodegradation process. The enhancement of photodegradation of BPA results mainly from the lower bond energy between some atoms in the BPA molecule after inclusion interaction with ,-CD. Copyright © 2006 Society of Chemical Industry [source] Advanced oxidation processes for destruction of cyanide from thermoelectric power station waste watersJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 2 2004José M Monteagudo Abstract Several advanced oxidation processes for the destruction of cyanide contained in waste waters from thermoelectric power stations of combined-cycle were studied. Thus, oxidation processes involving ozonation at basic pH, ozone/hydrogen peroxide, ozone/ultraviolet radiation and ozone/hydrogen peroxide/ultraviolet radiation have been carried out in a semi-batch reactor. All these methods showed that total cyanide can be successfully degraded but with different reaction rates, and the decrease in the total cyanide concentration can be described by pseudo-first order kinetics. The influence of pH and initial concentration of hydrogen peroxide was studied to find the optimal conditions of the oxidation process. Experimental results of the single ozone treatment indicated that total cyanide is destroyed more rapidly at higher pH (12), while ozonation combined with H2O2 and/or UV is faster at pH 9.5. The optimum concentration of H2O2 was 20.58 × 10,2M because an excess of peroxide decreases the reaction rate, acting as a radical scavenger. The total cyanide degradation rate in the O3/H2O2(20.58 × 10,2M) treatment was the highest among all the combinations studied. However, COD reduction, in the processes using UV radiation such as O3/UV or O3/H2O2/UV was about 75%, while in the processes with H2O2 and/or O3/H2O2 was lower than 57% and was insignificant, when using ozone alone. Copyright © 2003 Society of Chemical Industry [source] Wet chemical synthesis of low bulk density aluminium hydroxide powderJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 5 2003JK Pradhan Abstract Fine, low bulk density aluminium hydroxide powdered gel was prepared by the mild base hydrolysis of an aqueous solution of aluminium sulfate with hydrazine hydrate. Parameters such as method of addition of reactant, initial concentration of Al3+, mole ratio, final pH and hydrolysis temperature have a profound effect on the lightness and particle size of the powder. Optimized conditions showed that the final pH, Al3+ concentration and method of addition of reactant have a major contribution on the formation of lighter grade powder. Experiments conducted using other bases also produced lighter particles under similar conditions. Deviation from the optimized conditions led to formation of a higher bulk density product. Copyright © 2003 Society of Chemical Industry [source] Variation of intraparticle diffusion parameter during adsorption of p -chlorophenol onto activated carbon made from apricot stonesJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 5 2003B Koumanova Abstract The adsorption of para -chlorophenol onto an active carbon made from waste apricot stones has been studied. The batch kinetic adsorption processes have been measured for a range of system variables including agitation rate, initial concentration of para -chlorophenol, mass of carbon and particle size of carbon. The extent of adsorption is reported as plots of solid phase concentration against the square root of time. An intraparticle diffusion parameter is used to describe the mass transfer within the adsorbent. This parameter varies with the square root of time and can be related to the type of structure which occurs within an activated carbon. A correlation is proposed relating the process variable with the intraparticle diffusion parameter in each of the three mass transfer regions. Copyright © 2003 Society of Chemical Industry [source] Sorption of tannic acid on zirconium pillared clayJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 1 2002P Vinod Abstract Zirconium pillared clay (PILC) was prepared using montmorillonite as the base clay. Adsorption of tannic acid (tannin) was studied by a batch equilibrium technique, as a function of adsorbate concentration, temperature, pH, agitation speed, particle size of the adsorbent and ionic strength. The process of uptake is governed by diffusion controlled first-order reversible rate kinetics. The higher uptake for the pH range 4.0,6.0 was attributed to external hydrogen bonding between phenolic-OH groups of tannin molecules and the hydrogen bonding sites on the clay. The removal of tannin by adsorption was found to be >99.0% depending on the initial concentration in the pH range of 4.0,6.0. The process involves both film and pore diffusion to different extents. The effects of solute concentration, temperature, agitation speed and particle size on the diffusion rate were investigated. Tannin uptake was found to increase with ionic strength due to the compression of diffuse double layers. The applicability of Langmuir and Freundlich isotherm models has been tested. The maximum adsorption capacity of PILC was found to be 45.8,µmol,g,1 of clay and the affinity constant is 2.9,×,10,2,dm3,µmol,1 at 30,°C. Thermodynamic parameters such as ,G,°,,H,° and ,S,° were calculated to predict the nature of adsorption. The isosteric enthalpies of adsorption were also determined and found to decrease with increasing surface coverage. Regeneration with hot water (60,°C) has been investigated for several cycles with a view to recovering the adsorbed tannin and also restoring the sorbent to its original state. Copyright © 2001 Society of Chemical Industry [source] Computational techniques applied to the study of the oxidation kinetics of iron and molybdenum cyanocomplexes by peroxynitrous acidJOURNAL OF CHEMOMETRICS, Issue 10 2008H. Herrero Abstract The oxidation kinetics of iron and molybdenum cyanocomplexes by peroxynitrous acid were studied by computational techniques. The rate constants of ONOOH decomposition and substrate oxidation were calculated by fitting the experimental data to the solution of the ordinary differential equations mechanism. There is a linear relationship between the rate constants which is solved by varying the initial concentration of one of the reactive species. The rate constants of the steps involved in ONOOH decomposition were also determined following the same procedure and considering a linear relationship between the rate constants. The results are consistent with the values previously found using the conventional method of integration, and they validate the prior steady state assumption. Copyright © 2008 John Wiley & Sons, Ltd. [source] | |||||||||||||||||||||||||||||||||||||||||||