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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 178 (1977), S. 1215-1219 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 2
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Isotactic and syndiotactic poly(alkyl methacrylate)s (R = CH3, C2H5, isoC3H7, n-C4H9 and t-C4H9) were prepared by anionic mechanism and the spin-lattice relaxation times T1 of individual carbons and protons were measured mainly in toluene-d8 by the inversion-recovery Fourier transform (IRFT) method. The T1's of the carbons in the isotactic polymers were consistently longer than those of the comparable carbons in the syndiotactic polymers. The ratios of 13C-T1's for syndiotactic and isotactic polymers were always in the range of ca. 0,4-0,6 for all types of carbons. The 13C-T1's decreased with an increase in the bulkiness of the ester group in both polymers. From the measurements of the nuclear Overhauser enhancement (NOE) it was found that the spin-lattice relaxations of carbons in polymethacrylates are dominated by 13C-1H dipolar interactions and that the extreme narrowing condition is satisfied at least above 70°C. The effect of solvent on 13C-T1 was also studied. The results of the measurements of 1H-T1's were parallel to those in the carbons' case. It was concluded that the dependence of T1 upon the configuration of the polymer is mainly caused by the configurational dependence of the segmental mobility of the polymer.
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  • 3
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 5 Tab.
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  • 4
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 43 (1997), S. 3105-3110 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: To determine the behavior of hydrogen in tetralin, the reaction of tetralin with tritiated gaseous hydrogen was studied in a flow reactor at 400-450°C, 2.5-9.8 MPa for various residence times. The amount of hydrogen exchange between tetralin and tritiated hydrogen was estimated from the balance of hydrogen and tritium. Although yields of methylindan and naphthalene, and the hydrogen-exchange ratio (HER) of tetralin increased monotonously with residence time, these values were scarcely influenced by the reaction pressure at every temperature. It was thought that the formation of tetralyl radicals in this system would be the rate-determining step for both the conversions of tetralin into methylindan and naphthalene, and the hydrogen exchange of tetralin. Conversions of tetralin into methylindan and naphthalene, and the hydrogen-exchange reaction using the autoclave were very close to those using the flow reactor.
    Additional Material: 5 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 18 (1979), S. 25-34 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The complex dielectric constant of collagen in aqueous solutions (polymer concentration, Cp = 0.02-0.2%) was measured at 10°C in the frequency range from 3 Hz to 30 kHz. The loss peak for Cp = 0.02% is located at 90 Hz and the dielectric relaxation time τD is estimated to be 1.8 ± 0.3 msec. The τD agrees well with the rotational relaxation time estimated from the reduced viscosity, and the relaxation is ascribed to the end-over-end rotation of the molecule. The Cp dependence of τD and the dielectric increment Δε are interpreted in terms of the aggregation of molecules. The dipole moment of a molecule, obtained from Δε at Cp = 0.02% and pH 6.5, is (5.2 ± 0.2) × 104D, which is explained by the asymmetrical distribution of the ionized side chains of the molecule.
    Additional Material: 9 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 19 (1985), S. 1031-1041 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: This study was conducted to examine if an aminoglycoside (dibekacin sulfate, DKB) incorporated into a coating layer on outer and inner surface of indwelling catheters would be released into urine both in vitro and in clinical cases on a sustained basis and if the released DKB would have any efficacy on delaying lower urinary tract infections. Released amounts of DKB from the catheter silicone rubber (SR) catheter were periodically measured both in vitro and in clinical applications. During the clinical applications, the catheters were indwelled in 14 patients. Organism counts in the patients' urine were determined and organisms were isolated from bacteriuria (defined as ≧104 CFU/mL) and MICs to DKB were measured. Observations on several combined symptoms frequently associated with indwelling catherization were performed. Results showed that sustained release of DKB continued for more than 25 days and 13 days in vitro and in clinical cases, respectively. Clinical studies suggested that 8 days of sterile urine after catherization might be expected in patients without systemic administration of antibiotics and more than 2 weeks if combined with it. No particular problems in its use and associated symptoms were recognized.
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  • 7
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Two kinds of polyetherurethane (PEU), U-3 and U-8, were coated in thin layers on an ethylene-vinylalcohol copolymer (EVAL) film 0.1 mm thick. U-3 is a nonsegmented PEU prepared from 4,4′-diisocyanatodiphenylmethane (MDI) and poly(tetramethylene oxide) of Mn = 1,000 (PTMO 1000), and U-8 is a segmented PEU prepared from MDI, PTMO 1000, and 1,4-butanediol. The coating thicknesses were 0.0068 and 0.022 mm for U-3 and U-8, respectively. These coated films were implanted subcutaneously into rats and retrieved after various weeks. The coatings on the retrieved samples were dissolved in tetrahydrofuran (THF), and the average molecular weight (MW) was determined by injecting the THF solution into a gel permeation chromatograph. In the case of U-3, MW increased after 2 weeks, then decreased over the implantation period. After 10 weeks, U-3 almost disappeared from the base film. In the case of U-8, MW reached the maximum at 4 weeks postimplantation then decreased gradually over the implantation period. The rate and degree of MW change were greater in U-3 than in U-8. Here, we argue that, in the early stage, low molecular weight PTMO/MDI oligomers leached out from the PEUs to the inflammatory exudate to increase MW, and in the later stage macrophage attachment/activation had a role in the degradation of PEUs. The surface morphologic changes observed by scanning electron microscopy are also discussed. © 1994 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
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  • 8
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: In vivo degradation of polyetherurethanes (PEUs) was studied using two kinds of PEUs, U-3 and U-8, coated on a base film of ethylene/vinyl alcohol copolymer (EVAL). U-3 is a nonsegmented PEU prepared from 4,4′-diisocyanato-diphenylmethane (MDI) and poly(tetramethylene oxide) (PTMO 1000). U-8 is a segmented PEU prepared from MDI, PTMO 1000, and 1,4-butanediol. Previous studies of PEUs were conducted using gel permeation chromatography and scanning electron microscopy. In this study, the explanted materials were examined with contact angle measurement, ATR-FTIR, and nuclear magnetic resonance (NMR) spectroscopies. All data obtained by these methodologies indicate that the PTMO/MDI oligomers diffused to the material surface in the early stage of implantation. Then, the lowmolecular-weight fraction of the oligomers leached out from the surface to the exudate. Degradation became dominant after 2-4 weeks. In the case of PU-8, the PTMO fraction decreased approximately 35-40% from the surface at 24 weeks postimplantation. In the case of PU-3, the loss of coating material (U-3) on the base film (EVAL) was observed after 10 weeks. The PTMO fraction of the surface U-3 remained on EVAL at 6 weeks postimplantation, however, it was 64% of the initial material. The molecular weight of the U-3 remaining on EVAL also decreased. Degradation of U-3 occurred more rapidly than that of U-8. The data obtained with our materials were insufficient in determining evidence of oxidative degradation with IR or NMR spectra. © 1995 John Wiley & Sons, Inc.
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  • 9
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 25 (1990), S. 39-43 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Unimolecular reactions of the metastable silicenium ion (CH3)3SiOSi(CH3)2 + generated by dissociative ionization of bexamethyldisiloxane were investigated by mass-analysed ion kinetic energy (PUKE) Spectrometry. The characteristic fragmentations observed were losses of CH4 and (CH3)2Si=O molecules. Complete scrambling of all methyl groups prior to these reactions was found by investigating the MIKE spectra of deuterium labelled analogues (CD3)3SiOSi(CH3)2+ and (CH3)3SiOSi(CD3)3+. The loss of methane was accompanied by a large kinetic energy release (T0.5 = 482 meV). The MIKE spectra of silicenium ions were compared with those of their carbon analogues. The most predominant reaction of metastable (CH3)3COC(CH3)3+ ion was the loss of CH2=C(C H3)2 leading to protonated acetone. Significant differences between the ion fragmention characteristics of silicon and carbon compounds were found.
    Additional Material: 5 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 22 (1991), S. 759-762 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: By combining a high-sensitivity charge-coupled device detector with the total reflection technique, Raman spectra in the CH stretching region were recorded for thin Langmuir-Blodgett (LB) films of dipalmitoylphosphatidylcholine (DPPC) prepared at various surface pressures encompassing the plateau region of its surface pressure-area isotherm. Surface-pressure dependences of the lateral packing and the conformational order are discussed using the peak intensity ratio between the 2880 and 2850 cm-1 bands and that between the 2935 and 2850 cm-1 bands. The results indicate that at higher surface pressures above the plateau, the hydrocarbon chains of DPPC are tightly packed and highly oriented with the all-trans conformation. Below the plateau, however, the chains are disordered because of the increased number of the gauche conformers. The loosely packed hydrocarbon chains observed for the LB films deposited at lower surface pressures are gradually reoriented with time to form stable and highly ordered aggregates.
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