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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 39 (1992), S. 20-26 
    ISSN: 0006-3592
    Keywords: reversed micelle ; extraction ; solubilizing water ; AOT ; protein ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The extraction of protein using reversed micelles was investigated in relation to the amount of solubilizing water in the reversed micellar organic phase. The minimal concentration of amphiphilic molecule di-2-ethylhexyl sodium sulfosuccinate (C20H37O7Na) (AOT) required for 100% cytochrome c extraction was recognized. This critical AOT concentration increased with protein concentration in the aqueous phase. On this minimal AOT condition, the molar ratio of solubilizing water to extracted protein was found to be a constant of 3500 under CKCI = 1.0 × 102 mol · m-3 in this system. This ratio means the hydrophillic surroundings required for extracting one protein molecule into the micellar organic phase under the suitable pH and salt concentration for the forward extraction. In this regard, AOT molecules seemed to take the part of water solubilizing agent in the reversed micellar extraction. This role of AOT is important to extract protein under the suitable pH and salt concentration. The amount of solubilizing water in the protein-containing system was larger than in the protein-free system. This difference shows that the water molecules accompany the extracted protein into the reversed micellar organic phase at constant ratio 2200 under CKCI = 1.0 × 102 mol · m-3, i.e., accompanying water molecules per one extracted protein. The minimal AOT concentration increased with ionic strength. On this minimal AOT condition, the molar ratio of solubilizing water to extracted protein also increased with ionic strength, so that in higher ionic strength, more solubilizing water was required. Then more AOT was required to provide the hydrophillic surroundings for protein. The pH affected the minimal AOT concentration required for 100% protein extraction.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 42 (1993), S. 854-858 
    ISSN: 0006-3592
    Keywords: phenol ; tyrosinase ; immobilization ; chitosan ; immobilized enzyme ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: An enzymatic method for removal of phenols from industrial wastewater was investigated. Phenols in an aqueous solution were removed after treatment with mushroom tyrosinase. The reduction order of substituted phenols is catechol 〉 p-cresol 〉 p-chlorophenol 〉 phenol 〉 p-methoxyphenol. In the treatment of tyrosinase alone, no precipitate was formed but a color change from colorless to dark-brown was observed. The colored products were removed by chitin and chitosan which are available abundantly as shellfish waste. In addition, the reduction rate of phenols was observed to be accelerated in the presence of chitosan. Tyrosinase, immobilized by using amino groups in the enzyme on cation exchange resins, can be used repeatedly. By treatment with immobilized tyrosinase, 100% of phenol was removed after 2 h, and the activity was reduced very little even after 10 repeat treatments. © 1993 John Wiley & Sons, Inc.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 5 (1991), S. 67-69 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: 6- and 8-prenylated flavanones were distinguishable from each other by means of their fast-atom bombardment (FAB) spectral patterns, while the corresponding electron ionization spectral patterns were very similar to each other. It was suggested that 6- and 8-prenylated flavonoids can, in general, be distinguished by means of FAB.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 8 (1994), S. 215-221 
    ISSN: 0268-2605
    Keywords: Gallium arsenide ; arsenic compounds ; heme biosynthesis ; oral and intratracheal administration ; rat ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The acute influences of arsenic compounds on the metabolism of porphyrins and heme in various organs of rats after oral or intratracheal administration of disodium arsenate (Na2HAsO4) and gallium arsenide (GaAs) were examined and compared.For the oral administration experiments, 21 or 84 mg of Na2HAsO4, or 2 or 4 g of GaAs, per cm3 saline per kg body weight of each animal was administered to Jcl: Wistar male rats and the organs were removed after exsanguination from the vein of the right axilla under anesthesia with ether, 16 h after administration. In the case of intratracheal administration, rats given 8.2 or 16.4 mg of Na2HAsO4, or 0.2 or 0.4 g GaAs per cm3 saline per kg body weight were examined under the same experimental conditions as for the administration route.Increase in the body weight of rats was suppressed after intratracheal administration of the two arsenic compounds. In these rats the hematocrit value increased significantly. These changes were not shown by the orally administered rats. Elevation in δ-aminolevulinate synthase (ALA-S, EC 2.3.1.37) activity in erythroblasts by Na2HAsO4 was much higher after intratracheal administration than after oral administration. Suppression in the activities of δ-aminolevulinate dehydratase (ALA-D, EC 4.2.1.24) and porphobilinogen deaminase (PBG-D, EC 4.3.1.8) in peripheral erythrocytes by Na2HAsO4 and GaAs were stronger by intratracheal administration than by the oral route. Influences of GaAs on the activity of PBG-D in rat liver were shown to be more effective by oral administration than by the intratracheal route. Oral administration of Na2HAsO4 and GaAs had a stronger suppression effect on the activities of ALA-D and PBG-D in rat kidney.It seems from these results that the different extents of the influence of arsenic compounds might depend on the routes of intake.
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 1185-1196 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The role of radical species in the degradation of poly(methyl methacrylate) (PMMA) induced by γ-irradiation has been studied by means of electron spin resonance and electron spin echo spectroscopy. The major radical species generated initially at 77 K are assigned to main chain — CH — and side chain — COOCH2 radicals, and — COOCH3- anion radical. Only the — COOCH2 radical converts to the scission-type — CH2 — C(CH3)COOCH3 radical on warming the sample of 〉180 K. A part of the — CH — radical disappears on warming the sample of 〉265 K. It is concluded that the scission of PMMA main chain occurs by the intramolecular process from the — COOCH2 radical as the precursor state.
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 32 (1994), S. 2487-2492 
    ISSN: 0887-624X
    Keywords: PMMA ; radiolysis ; temperature effect ; degradation ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Effect of irradiation temperature on the main-chain scission of poly (methyl methacrylate) (PMMA) caused by γ-irradiation was studied by means of gel permeation chromatography and ESR spectroscopy. Although no temperature dependency was observed on the scission efficiency for purified PMMA, the efficiency for crude or monomer-doped purified PMMA was decreased by decreasing the temperature below ca. 200 K. Above 200 K the efficiency was constant and did not depend on the purity of PMMA. ESR study of the irradiated PMMA revealed that the suppression of the scission below 200 K is induced by the addition of methyl methacrylate monomer to primary radical species, which otherwise cause the main-chain scission by warming the polymer above 200 K. The primary radical generated above 200 K immediately converts to the scission-type — CH2 — Ċ(CH3) COOCH3 radical through the β-scission of the polymer main chain, so that the efficiency of the scission does not depend on both the impurity and the irradiation temperature. © 1994 John Wiley & Sons, Inc.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 54 (1994), S. 105-112 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: To investigate the application of supersorbing materials in the food industry, the water sorption of polyion complex films, prepared by solvent-casting from poly(∊-lysine) (PEL) and carboxymethyl cellulose (CMC), were examined and some physical properties of the hydrogels were studied. Three CMC samples having various degrees of substitution (DS) and molecular weights (MW) were applied to show a variety of water-sorption behavior and physical properties. The ratio of PEL/CMC was changed from 10/90 to 50/50. Good film swelling in water was achieved when the complex was made from PEL and CMC with a low DS and an appropriate molecular weight, and when the PEL/CMC ratio was low. This indicated that the carboxyl groups in the CMC are not readily dissociated, and that the strength of cationic and anionic interactions affects the film swelling. In line with this view, the addition of electrolytes markedly lowered the film swelling. Nonelectrolytes such as sucrose or urea had no effect. IR and NMR spectra showed that a fraction of the ionic groups in the polyelectrolytes interact. Tensile moduli of complex dry films decreased linearly as the PEL content increased. Compressive moduli of swollen films were affected by neither the degree of swelling nor the molecular weights of CMC. The lower the DS values of CMC, the higher the compressive moduli were. We also examined the relation between the rigidity of polymer component and the ratio of nonfreezable bound water in complex films. On swelling in acetone-water or ethanol-water mixed solvent, expansion-shrinkage transition of the polymer gels occurred at about 20 mol % acetone or ethanol concentrations for every complex film. The overall characterstics of PEL/CMC consisting of a linear polyanionic polypeptide and a chain of cationic rings are reminiscent of polycationic chitosan and polyanionic polyglutamic acid. © 1994 John Wiley & Sons, Inc.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 54 (1994), S. 1321-1327 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Polyurethane-urea microcapsules were prepared by an interfacial polymerization method. Dynamic mechanical measurements were carried out on the polyurethane-urea microcapsules coated on a paper substrate. The glass transition temperatures (Tg) of capsule wall were observed in the temperature scan data. Tg as the temperatures of tan δ peaks were decreased with increasing amounts of core materials. The apparent activation energies of the glass transition were estimated at about 100 kcal/mol. Master curves were obtained by shifting the tan δ spectra along the frequency axis, and the glass transition regions were unaffected by core materials studied. The shift factors were found to depend on the core/wall ratio and discussed in terms of a morphological change of microcapsules. © 1994 John Wiley & Sons, Inc.
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  • 9
    ISSN: 0884-3996
    Keywords: Chemiluminescence ; Cypridina luciferin analogue ; horseradish peroxidase ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: The chemiluminescence of the Cypridina luciferin analogue, 2-methyl-6-(p-methoxyphenyl)-3,7-dihydroimidazo[1,2-a]pyrazin-3-one (MCLA) was observed at 462nm in the presence of horseradish peroxidase (HRP) and the total spectrum of light emitted was found to depend linearly on HRP concentration. Methods for the determination of HRP concentration using the chemiluminescence was investigated. HRP could be detected in the range from 100 pmol/L to 100nmol/L under the optimum condition, H2O2 (10mmol/L) and MCLA (10μmol/L) at pH 5.8.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 23 (1991), S. 971-987 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Decomposition of hydrogen peroxide in high-purity water has been measured at temperatures ranging 100 to 280°C in a laboratory test loop. A first-order decomposition kinetics has been observed in all cases, but the decomposition rates were found to vary widely, depending on the material used in the reaction chamber. In a 4 mm ID stainless steel tubing, the decomposition rate constant is determined to be k = 2 × 105 exp(-14800/RT). This decomposition rate is approximately 100 times faster than that observed in a Teflon tubing.The variation of decomposition rate in different reaction chambers is attributed to the heterogeneous catalytic effects. There is no evidence of reaction between H2 and H2O2 in the highpurity water at temperatures up to 280°C.
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