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  • 1
    Electronic Resource
    Electronic Resource
    The extinction of hydrocarbon flames based on the heat-absorption processes which occur in them (1984)
    New York, NY [u.a.] : Wiley-Blackwell
    Fire and Materials 8 (1984), S. 148-156 
    Details
    ISSN: 0308-0501
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Architecture, Civil Engineering, Surveying , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: An empirical relation has been developed which correlates and predicts the fire-suppression effectiveness of a wide variety of gaseous, liquid and solid agents. The flame-extinguishment model is based on the premise that extinction is dominated by heat-absorption processes and that a flame is extinguished when sufficient heat has been removed by the extinguishant to reduce the temperature to a limit value. This limit value. This limit is the minimum temperature at which the effective rate of the combustion reactions is sufficient to maintain flamepropagation, and it depends in a predictable way on the properties of the suppressant and flame system. The heat-balance equation describing this is derived in two stages. In the first, a preliminary equation is obtained by considering only those substances which are thermally stable and act only as heat-capacity sinks. In the second, the equation is generalized by consideration of all endothermic reaction sinks, e.g. vaporization, dissociation and decomposition. The general equation correlates most of the extinction data found in the literature. The results suggest that for most substances the extinguishing capacity is related to heat-extraction data found in the literature. The results suggest that for most substances the extinguishing capacity is related to heat-extraction and that many of the effects previously attributed to chemical mechanisms may be thermodynamic in nature rather than kinetic.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/fam.810080305
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  • 2
    Electronic Resource
    Electronic Resource
    Binary and ternary blends of poly(vinyl chloride), hytrel, and a polyurethane (1981)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 26 (1981), S. 3467-3473 
    Details
    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: Binary blends of poly(vinyl chloride) and a poly(ether urethane) containing 20 and 40 weight percent, respectively, of poly(vinyl chloride) have been prepared by solution blending from tetrahydrofuran and their degree of mixing investigated using dynamic mechanical analysis. In the polyurethane, transitions were found at -19°C and -119°C. The former was attributed to the glass transition and the latter to a Schatzki type of motion of the polyether sequences. This latter transition occurred at a temperature which is higher than the literature value for the low temperature transition in poly(tetrahydrofuran), which is equivalent to the polyether sequence in the polyurethane. This discrepancy is attributed to the influence of neighboring hard segments present because of incomplete segmental phase separation of the polyurethane. For the blends only one very broad transition was observed, indicating that there was substantial mixing of these two polymers. Three ternary blends were prepared, also by solution blending, containing poly(vinyl chloride), Hytrel, and the polyurethane in the ratios 1:1:1, 1:2:1, and 2:1:1, respectively. In the first two blends there was clear evidence of phase separation. It was only in the 2:1:1 blend that an apparently significantly compatible material resulted.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1981.070261025
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  • 3
    Electronic Resource
    Electronic Resource
    Polymeric systems for acoustic damping. III. Blends of poly(vinyl chloride), segmented poly(ether ester), and poly(methyl acrylate) (1981)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 26 (1981), S. 3487-3491 
    Details
    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: A solution blend of poly(vinyl chloride) and a segmented poly(ether ester) and blends containing these two polymers plus poly(methyl acrylate) were investigated by dynamic mechanical analysis and electron microscopy. The binary blend, which contained 75% by weight of the poly(ether ester), showed only one loss peak, but also evidence of some phase separation. It is believed that the polyether sequences of the poly(ether ester) are extensively mixed with poly(vinyl chloride). Poly(methyl acrylate) was added to spread the damping range and produce a material of potential use as an acoustic damper. It is evident from both electron microscopy and dynamic mechanical analysis that poly(methyl acrylate) is substantially incompatible in the other polymers.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1981.070261027
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  • 4
    Electronic Resource
    Electronic Resource
    A study of the PE-PTFE system. II. ESCA measurements (1982)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 20 (1982), S. 1001-1012 
    Details
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Samples of polyethylene and polytetrafluorethylene were sintered at 200°C. The samples were cleaved and cut, and the two types of surfaces were studied by ESCA. The possibility of chemical interaction between the two polymers and the formation of a transitional layer is postulated on the basis of the results. A morphological model of the structure of these samples is given.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1982.180200608
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  • 5
    Electronic Resource
    Electronic Resource
    Carriers for drugs and enzymes based on copolymers of allyl glycidyl ether with acrylamide (1982)
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 183 (1982), S. 781-788 
    Details
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Copolymerization of acrylamide with allyl glycidyl ether yielded water soluble polymers containing an epoxy group; addition of a crosslinking agent, N,N′-methylenebis(acrylamide), to the copolymerization mixtures resulted in the formation of similar though water insoluble polymers. Condensation of a potent beta-adrenergic antagonist Alm—H, which contains a reactive amino group, with a polymer containing an epoxy group yeilded a pharmacologically active polymer. The polymer containing the epoxy group was also converted, by reaction with sodium thiosulfate and subsequent reduction, into a mecapto groups containing polymer which was also water soluble. The latter polymer was converted by condensation with a beta-adrenergic antagonist Alm—COCH2Br, which contains a reactive bromoacetamido group, into a pharmacologically active polymer.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/macp.1982.021830403
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  • 6
    Electronic Resource
    Electronic Resource
    Conformations of cyclic peptide/calcium complexes in solution (1982)
    New York : Wiley-Blackwell
    Biopolymers 21 (1982), S. 169-179 
    Details
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthetic cyclic octapeptides of general structure cyclo[Glu(γOBzl)-Sar-Gly-(N-R)Gly]2 (R = n-hexyl and cyclohexyl) transport calcium ions selectively across organic phases and phospholipid membranes. We have now used proton nmr spectroscopy (360 MHz) to study the solution conformation(s) of their calcium complexes. When Ca(ClO4)2 was added to solutions of these peptides in CDCl3, nmr spectra of the resulting calcium complexes were characteristic of a single C2-symmetric conformer. From a Karplus-Bystrov analysis of vicinal coupling constants in both the peptide backbone and Glu side chain (treated as an ABCC′MX spin system), in conjuction with model-building studies, a structure was proposed in which the calcium ion is bound in an octahedral-type complex by the four (coplanar) carbonyl groups of the (all-trans) Glu-Sar and Gly-(N-R)Gly peptide bonds. Occurrence of preferred rotamers about Glu side chain Cα-Cβ bonds indicated that restricted rotation in peptide side chains arises upon calcium binding.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bip.360210114
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  • 7
    Electronic Resource
    Electronic Resource
    Nearest-neighbor and next-nearest-neighbor effects in the proton NMR spectra of the oligoribonucleotides ApGpX and CpApX (1980)
    New York : Wiley-Blackwell
    Biopolymers 19 (1980), S. 557-573 
    Details
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The variable-temperature proton nmr spectra of the oligoribonucleotides in the series CpApX and the series ApGpX, X = A, G, C, U, together with the parent dimers CpA and ApG have been measured. A complete analysis of all the nonexchangeable base proton resonances and ribose H-1′ proton resonances was made. The presence of trends in the shielding abilities of the various bases at both the nearest-neighbor and next-nearest-neighbor positions were identified. The observed shieldings could be used to predict the chemical shifts of protons in related systems. Based on the empirical results from ribodinucleoside monophosphates, the temperature-dependent behavior of the J1′2′ coupling constants of the triribonucleotides suggested that the compounds in the CpApX series stacked from the 5′-end to the 3′-end, while those in the ApGpX series stacked from the 3′-end to the 5′-end.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bip.1980.360190309
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  • 8
    Electronic Resource
    Electronic Resource
    Nearest-neighbor and next-nearest-neighbor effects in the proton NMR spectra of the oligoribonucleotides ApXpG, CpXpG, CpApXpUpG, ApGpXpC, and ApGpXpCpU (1981)
    New York : Wiley-Blackwell
    Biopolymers 20 (1981), S. 1383-1398 
    Details
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The proton nmr spectra of the oligoribonucleotides in the series CpXpG, ApXpG, CpApXpUpG, and ApGpXpC (X = A, G, C, and U), together with the reference compounds CpG, ApG, CpApUpG, and ApGpC, have been measured. A complete analysis of all the nonexchangeable base protons and the ribose H-1′ protons was made. The insertion of a nucleotide X into a oligoribonucleotide led to shift changes at both nearest-neighbor and next-nearest-neighbor positions, which were rationalized in terms of the shielding abilities of the various bases. The derived shielding trends in the ApGpXpC series of compounds were successfully used to predict the chemical shifts of resonances in the related ApGpXpCpU series.
    Additional Material: 13 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bip.1981.360200703
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  • 9
    Electronic Resource
    Electronic Resource
    An experimental and theoretical study of the transmission function of a commercial hemispherical electron energy analyserPaper presented at the International Conference on Quantitative Surface Analysis held at the National Physical Laboratory, Teddington, UK, 24-25 November 1981. (1982)
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 4 (1982), S. 220-226 
    Details
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: The electron energy analyser transmission (peak area/incident current) of a VG Scientific ESCALAB has been measured as a function of kinetic energy, analyser energy and source position for a point source of electrons in the sample plane (produced using a specially designed mini electron gun). Results have been obtained in both CAE (constant analyser energy) and CRR (constant retard ratio) modes. The results are extrapolated to give the energy dependence of the analyser transmission for an extended current source, such as encountered in routine XPS analysis applications. A detailed theoretical study explains the rationale behind this data extrapolation and predicts an analyser transmission in fair agreement with experimental results, possible causes for the discrepancies between theory and experiment are discussed.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/sia.740040509
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  • 10
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    Midlatitude Pi2 pulsations: AFGL and ISEE magnetometer observations correlated (1982)
    In:  CASI
    Details
    Publication Date: 2019-06-28
    Description: The ISEE observations of the pi2 magnetic pulsations occuring substorm onset in the inner magnetosphere are discussed. One of these events which was also detected as a pi2 event by the AFGL midlatitude magnetometers is considered. The event occurred when the foot of the ISEE field line was over North America. The ground and satellite signals are remarkably similar: they start and stop at the same time, have the same period and can be correlated cycle by cycle. The waves are detected in the electric field data from ISEE 1 and in the magnetic field data from both ISEE 1 and ISEE 2. Calculation of the Poynting vector at ISEE 1 shows that the energy flowed mainly westward, but that there was also a component towards the nearer (southern) ionospheric foot of the field line. The phases between the various field components measured by ISEE 1 and 2 indicate that this is a standing hydromagnetic oscillation.
    Keywords: ASTROPHYSICS
    Type: NASA-TM-84763 , NAS 1.15:84763
    Format: application/pdf
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    NASA TECHNICAL REPORTS
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