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  • Articles  (13)
  • oxidation
  • Springer  (13)
  • American Chemical Society
  • 1995-1999  (13)
  • Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition  (8)
  • Technology  (5)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Cellulose 5 (1998), S. 153-164 
    ISSN: 1572-882X
    Keywords: cellulose ; TEMPO ; polyglucuronic acid ; degree of polymerization ; oxidation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract Various cellulose samples were oxidized by 2,2,6,6,-tetramethylpipelidine-1-oxyl radical (TEMPO)-NaBr-NaClO systems, and the effects of oxidation conditions on chemical structures and degrees of polymerization of the products obtained were studied. In the case of regenerated and mercerized celluloses, almost all C6 primary alcohol groups were selectively oxidized to carboxyl groups, and water-soluble polyglucuronic acid (cellouronic acid) sodium salts were obtained almost quantitatively; the degrees of polymerization were influenced greatly by the amount of TEMPO added, and the oxidation time and temperatures. Cellouronic acids prepared from mercerized linter and kraft pulps had size exclusion chromatograms with two separate peaks due to higher and lower molecular weight fractions. On the other hand, only small amounts of carboxyl groups were introduced into native cellulose samples. Since polyglucuronic acids prepared from cellulose by the TEMPO–NaBr– NaClO systems regularly consist of the glucuronic acid repeating unit, differing from the conventional water-soluble cellulose derivatives, they may open new fields of cellulose utilization.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Cellulose 2 (1995), S. 265-272 
    ISSN: 1572-882X
    Keywords: Hydrogen peroxide ; oxycellulose ; bleaching ; oxidation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract Peroxides are important bleaching agents, industrially, for cellulosic products. They are also used in detergents. Peroxides can degrade cellulose as well as decolorize it and remove stains. Both free radicals and perhydroxyl anions have been suggested as the intermediates in the reactions occurring between cellulosic products and hydrogen peroxide. The proposed mechanisms are reviewed with emphasis primarily on cotton cellulose. Further work is required to establish unequivocally the mechanism of degradation and decolorization of cellulose products.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    European journal of nutrition 36 (1997), S. 336-339 
    ISSN: 1436-6215
    Keywords: Amino acids ; protein ; metabolism ; meal feeding ; oxidation ; breath test ; Aminosäuren ; Protein ; Stoffwechsel ; Fütterung ; Oxidation ; Atemtest
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Medicine
    Description / Table of Contents: Zusammenfassung Die aktuellen Mengen an freien Aminosäuren im Blut reichen nur aus, um die Ganzkörper-Proteinsynthese für einige Minuten aufrecht zu erhalten. Das zeigt, daß die freien Aminosäurenkonzentrationen in der Zirkulation klein und konstant gehalten werden im Vergleich zu den Mengen der Aminosäuren, die täglich aufgenommen und über die Körperproteine umgesetzt werden. Das Verschwinden der Aminosäuren exogenen oder endogenen Ursprungs aus dem freien Aminosäuren-Pool, findet hauptsächlich durch die Proteinsynthese und den Aminosäurenabbau statt. Die Partitionierung der Nahrungs-Aminosäuren zwischen diesen beiden Prozessen im Kurzzeitbereich werden als bedeutsam für die Ökonomie der Ganzkörper-Aminosäuren angesehen. Eine Verbesserung der Aminosäurenökonomie könnte durch solche nutritiven Maßnahmen erreicht werden, welche die Clearance der Nahrungsaminosäuren durch die Proteinsynthese anstelle des Aminosäurenabbaus begünstigen. Diese nutritiven Maßnahmen sollten sich an den „Schwellenwerten“ des Abbaus der individuellen Aminosäuren orientieren.
    Notes: Summary Actual amounts of free amino acids in the blood are sufficient to support whole body protein synthesis for some minutes only. This indicates that the levels of free amino acids in the circulation are kept small and constant relative to the amounts of amino acids supplied by daily intake and turnover of body proteins. The clearance of the amino acids originating from either endogenous or exogenous sources is mainly due to protein synthesis and metabolic degradation. The partitioning of dietary amino acids between these processes, on the short term, is supposed to play an important role in whole body amino acid economy. Therefore whole body amino acid economy could be improved by nutritional measures that favour the clearance of dietary amino acids by protein synthesis instead of by metabolic degradation. These nutritional measures should to be focused on threshold values for metabolic degradation of individual amino acids.
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Nutrient cycling in agroecosystems 49 (1997), S. 91-95 
    ISSN: 1573-0867
    Keywords: greenhouse effect ; land use ; methane ; oxidation ; soils
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Intact core samples from soils with different textures and land use were tested for their capacity to oxidise methane. The soil cores were taken from arable land, grassland and forest. It was found that coarse textured soils (6.74–16.38 µg CH4 m-2 h-1) showed a higher methane uptake rate than fine textured soils (4.66–5.34 µg CH4 m-2 h-1). Increasing soil tortuosity was thought to reduce the methane oxidation rate in fine textured soils. The oxidation rate of forest soils (16.32–16.38 µg CH4 m-2 h-1), even with a pH below 4.5, was very pronounced and higher than arable land (11.40–14.47 µg CH4 m-2 h-1) and grassland (6.74–9.30 µg CH4 m-2 h-1). Within the same textural class arable land showed a faster methane uptake rate than grassland. In grassland with a fine texture, even methane production was observed. Nitrogen availability and turnover in these land use systems were thought to cause the different oxidation rates. Decreasing the moisture content slowed down the oxidation rate in all soils. This could be caused by an increased N turnover and a starvation of the methanotrophic bacteria.
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  • 5
    Electronic Resource
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    Springer
    Nutrient cycling in agroecosystems 49 (1997), S. 59-70 
    ISSN: 1573-0867
    Keywords: land use ; methane ; nitrogen fertilizer ; oxidation ; soil
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Aerobic soils are an important sink for methane (CH4) contributing up to 15% of annual global CH4 destruction. However, the sink strength is significantly affected by land management, nitrogen (N) fertilizers and acidity. We tested these effects on samples taken from the Broadbalk Continuous Wheat, Park Grass permanent grassland and Broadbalk and Geescroft Wilderness experiments at Rothamsted. The rates of uptake from the atmosphere of both enhanced (10 ppmv) and ambient (2 ppmv) concentrations of CH4 were measured in laboratory incubations of soil cores under controlled conditions. The most rapid rates of uptake were measured in soil from deciduous woodland at pH 7 (measured in water); acidic (pH 4) woodland soil showed no net CH4 oxidation. While disturbance of the cores used in the experiments did not affect the rate of CH4 uptake, extended (150 years) cultivation of land for arable crops reduced uptake rate by 85% compared to that in the soil under calcareous woodland. The long-term application of ammonium- (NH4) based fertilizer, but not nitrate- (NO3) based fertilizer, completely inhibited CH4 uptake, but the application for the same period of farmyard manure that contained more N than the fertilizer had no inhibitory effect. Although the effects of agricultural practice on the oxidation of CH4 in soil are significant, the differences in oxidation rates between land use types are even greater. The likely effects of forest clearance, agricultural intensification and anthropogenic emissions of CH4 over the last 2500 years have been estimated for the United Kingdom. The calculations indicate that 54% of the current CH4 uptake by UK soils is the result of increased CH4 mixing ratio. They also indicate that land use change has decreased the potential sink strength by 62% or 37 kt CH4 g-1. In countries with much larger land areas than the UK, such as China, aerobic soil is likely to be a more significant factor in calculating net fluxes of CH4. It is important that the impacts of different agricultural managements and land use systems are understood and quantified so that the best possible estimate of CH4 sinks is calculated for comparison with sources.
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  • 6
    ISSN: 1572-8986
    Keywords: RF SiCl4 discharge ; mass spectrometry ; kinetics ; decomposition ; oxidation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Technology
    Notes: Abstract Time-resolved mass spectrometry was used for analysis of the plasma reactions in radio frequency (RF) SiCl 4 and SiCl 4 −O 2 discharges as functions of starting partial pressure and electrical power. Molecular concentrations of the reactants and products from SiCl 4 alone and with O 2 were obtained from the mass spectra and used for plotting the kinetic curves. The SiCl 4 and O 2 consumption rates were calculated from the kinetic curves and compared with results of theoretical simulation of the reaction. Direct electron impact decomposition was found to be the main pathway for pure SiCl 4 conversion. On the contrary, the consumption of SiCl 4 in the SiCl 4 +O 2 mixtures was largely chemical. The experimental macrokinetics are in agreement with a model in which oxidation is caused by the atomic oxygen.
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  • 7
    Electronic Resource
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    Springer
    Plasma chemistry and plasma processing 19 (1999), S. 131-151 
    ISSN: 1572-8986
    Keywords: Styrene ; oxidation ; silent discharge ; plasma ; dielectric barrier
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Technology
    Notes: Abstract A silent discharge plasma reactor has been developed to study the oxidation of styrene vapor in argon/oxygen mixtures. A number of analytical techniques were employed to determine the destruction efficiency and to characterize the intermediate products. The destruction efficiency was measured as a function of initial styrene concentration, temperature, and energy density of the plasma. The formation of solid products was observed in most experiments. At low temperature (100°C), the solid deposit was polymeric in nature, while at high temperature (300°C) the solid appeared to be amorphous carbon. A combination of high temperature and high energy density resulted in high destruction efficiency and minimal production of solid films. The destruction efficiency vs. energy density is shown to be more complex than a simple model predicting exponential behavior. Several reasons for the discrepancy are suggested. The “e-folding” energy density for the destruction of styrene is compared to literature values for other organic compounds, measured using similar types of plasma reactors.
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Plasma chemistry and plasma processing 19 (1999), S. 383-394 
    ISSN: 1572-8986
    Keywords: Nonthermal plasma ; benzene ; Al2O3 ; BaTiO3 ; oxidation ; absorption ; atmospheric pressure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Technology
    Notes: Abstract The combination of plasma discharge and adsorption was examined for oxidation of dilute benzene in air in a plasma reactor packed with a mixture of BaTiO 3 pellets and porous Al 2 O 3 pellets (i.e., an alumina hybrid reactor). The oxidative decomposition of benzene was enhanced by the benzene concentrating on the Al 2 O 3 pellets. Furthermore, there was a higher selectivity to CO 2 in the products from the hybrid than from a plasma reactor packed with BaTiO 3 pellets alone. The presence of the Al 2 O 3 pellets suppressed the formation of N 2 O.
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  • 9
    Electronic Resource
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    Plasma chemistry and plasma processing 19 (1999), S. 421-443 
    ISSN: 1572-8986
    Keywords: Streamer corona ; NO x removal ; nonthermal plasma ; oxidation ; reduction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Technology
    Notes: Abstract In this paper, the NO-to-NO 2 conversion in various gaseous mixtures is experimentally investigated. Streamer coronas are produced with a dc-superimposed high-frequency ac power supply (10–60 kHz). According to NO x removal experiments in N 2 +NO x and N 2 +O 2 +NO x gaseous mixtures, it is supposed that the reverse reaction NO 2 +O→NO+O 2 may not only limit NO 2 production in N 2 +NO x mixtures, but also increase the energy cost for NO removal. Oxygen could significantly suppress reduction reactions and enhance oxidation processes. The reduction reactions, such as N+NO→N 2 +O, induce negligible NO removal provided the O 2 concentration is larger than 3.6%. With adding H 2 O into the reactor, the produced NO 2 per unit removed NO can be significantly reduced due to NO 2 oxidation. NH 3 injection could also significantly decrease the produced NO 2 via NH and NH 2 - related reduction reactions. Almost 100% of NO 2 can be removed in gaseous mixtures of N 2 +O 2 +H 2 O+NO 2 with negligible NO production.
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  • 10
    ISSN: 1572-8978
    Keywords: Plasma polymers ; oxidation ; XPS ; photoelectron binding energy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Technology
    Notes: Abstract The incorporation of oxygen into nitrogen-containing plasma deposited polymers was studied by X-ray Photoelectron Spectroscopy (XPS). As the oxygen content of the plasma polymer increased, the binding energy of the N 1s photoelectrons increased. Conversely, the binding energy of the O 1s photoelectrons was inversely proportional to the nitrogen content of the plasma polymer. The data from a large number of samples all obeyed the same “universal” correlations of photoelectron binding energy versus chemical composition. The data were described by the same curve regardless of whether the oxygen was incorporated rapidly into the thin film during plasma deposition or whether the oxygen was added slowly during spontaneous oxidation of the film in air. This implies that the same thermodynamic principles of radical reactions governed the addition of oxygen to the plasma polymer. The shift in the O 1s and N 1s photoelectron binding energies as a function of chemical composition was used to monitor the proximity of nitrogen and oxygen. By contrasting the experimental data with a simple binomial model which described the random addition of oxygen to a lattice containing carbon and nitrogen, we were able to show that oxygen was preferentially added near nitrogen-containing groups in plasma polymers.
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  • 11
    Electronic Resource
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    Springer
    Plant and soil 173 (1995), S. 329-335 
    ISSN: 1573-5036
    Keywords: calcium sulfite ; flue gas desulfurization residue ; oxidation ; sulfur dioxide ; toxicity ; Triticum aestivum L.
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract CaSO3 is a by-product formed by several of the processes used for scrubbing SO2 from flue gas produced by coal-burning power generators. Using CaSO3 to improve the calcium status of acid soils would be a beneficial alternative to disposal in landfills. CaSO3 has biocidal properties and is used as a disinfectant and food and drink preservative. It is important to evaluate under what conditions application to soils would not harm plant growth. Laboratory experiments confirmed that two transformations of CaSO3 occurred in soil systems: (1) decomposition to produce SO2 gas, and (2) oxidation to calcium sulfate. Conversion to SO2 occurred in solution and soil at low pH, and acid soils treated with CaSO3 were initially toxic to seedling root growth. The degree of toxicity was time-dependent, with reduction in toxicity occurring as CaSO3 oxidized to calcium sulfate. Soil reaction also influenced toxicity, and at soil pH levels above 6, little seedling toxicity was evident.
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  • 12
    ISSN: 1573-0867
    Keywords: elemental sulphur ; oxidation ; organic S ; mineralization ; immobilization ; S fertilizers ; semiarid soils ; subtropical region
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract The increasing sulphur (S) deficiency in soils of several parts of world has led to the use of fertilizer S, an important factor in enhancing the production and quality of crops. Very limited information is available on the use of elemental sulphur (S0) as a fertilizer, its oxidation into SO42- and transformation into organic S in semiarid subtropical soils. We studied the impact of three temperature regimes on the mineralization of soil organic S, and the oxidation and immobilization of S0 in acidic (pH 4.9), neutral (pH 7.1) and alkaline (pH 10.2) subtropical soils of north-western India. Repacked soil cores were incubated under aerobic conditions (60% water-filled pore space) for 0, 14, 28 and 42 d with and without incorporated S0 (500 μg g-1 soil). Temperature had profound effects on all three soils processes, the rates of mineralization of native soil organic S, oxidation of applied S0 and transformation of S0 into soil organic S being greatest at 36 °C, irrespective of soil pH. Mineralization of native soil organic S (without added S0) resulted in the accumulation of 39, 66 and 47 μg SO42-–S g-1 soil in acidic, neutral and alkaline soil in 42 d period at 36 °C. Of the total mineralization, the majority (62 – 74%) occurred during the first 14 d period. Oxidation rate of added S0 during initial 14 d period at 36 °C was highest in alkaline soil (292 μg S cm-2 d-1), followed by neutral soil ((180 μg S cm-2 d-1) and lowest in acidic soil (125 μg S cm-2 d-1). Of the applied 500 μg S0 g-1 soil, 3.2 – 10.0%, 6.8 – 15.4% and 10.0 – 23.0% oxidized to SO42-, and 13.4 – 28.6%, 16.0 – 29.0% and 14.6 – 29.0% were transformed into organic S in 42 d period in acidic, neutral and alkaline soil, respectively. The results of our study suggest that in order to synchronize the availability of S with plant need, elemental S may be applied well before the seeding of crops, especially in acidic soil and in regions where temperature remains low. Substantial mineralization of native soil organic S in the absence of applied S0 and immobilization of applied S0 into organic S suggest that the role of soil biomass as source and sink could be exploited in long term S management.
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  • 13
    ISSN: 1572-9729
    Keywords: Diphenyl ether ; ligninolytic enzymes ; metabolites ; oxidation ; Trametes versicolor ; white-rot fungi
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Energy, Environment Protection, Nuclear Power Engineering , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract The white-rot fungi Trametes versicolor SBUG 1050, DSM 11269 and DSM 11309 are able to oxidize diphenyl ether and its halogenated derivatives 4-bromo- and 4-chlorodiphenyl ether. The products formed from diphenyl ether were 2- and 4-hydroxydiphenyl ether. Both 4-bromo- and 4-chlorodiphenyl ether were transformed to the corresponding products hydroxylated at the non-halogenated ring. Additionally, ring-cleavage products were detected by high perfomance liquid chromatography and characterized by gas chromatography/mass spectrometry and proton nuclear magnetic resonance spectroscopy. Unhalogenated diphenyl ether was degraded to 2-hydroxy-4-phenoxymuconic acid and 6-carboxy-4-phenoxy-2-pyrone. Brominated derivatives of both these compounds were formed from 4-bromodiphenyl ether, and 4-chlorodiphenyl ether was transformed in the same way to the analogous chlorinated ring cleavage products. Additionally, 4-bromo- and 4-chlorophenol were detected as intermediates from 4-bromo- and 4-chlorodiphenyl ether, respectively. In the presence of the cytochrome-P450 inhibitor 1-aminobenzotriazole, no metabolites were formed by cells of Trametes versicolor from the diphenyl ethers investigated. Cell-free supernatants of whole cultures with high laccase and manganese peroxidase activities were not able to transform the unhydroxylated diphenyl ethers used.
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