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  • 1
    Publication Date: 2012-03-06
    Description: Author(s): K. Y. Ma (马克岩), J. B. Lu (陆景彬), D. Yang (杨东), H. D. Wang (王辉东), Y. Z. Liu (刘运祚), X. G. Wu (吴晓光), Y. Zheng (郑云), and C. Y. He (贺创业) The candidate chiral doublet bands in 128 La have been searched for through the 118 Sn( 14 N, 4n) 128 La reaction at a beam energy of 69 MeV. A positive-parity sideband with the same configuration as that of the yrast band has been identified. The positive-parity and spins of the sideband have been assign... [Phys. Rev. C 85, 037301] Published Mon Mar 05, 2012
    Keywords: Nuclear Structure
    Print ISSN: 0556-2813
    Electronic ISSN: 1089-490X
    Topics: Physics
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  • 2
    Publication Date: 2012-08-02
    Description: Author(s): K. Y. Ma (马克岩), J. B. Lu (陆景彬), D. Yang (杨东), H. D. Wang (王辉东), Y. Z. Liu (刘运祚), X. G. Wu (吴晓光), Y. Zheng (郑云), and C. Y. He (贺创业) Previous to the present study, three isolated rotational bands with tentative spin assignments had been reported in the literature and the authors estimated that, to meet the predicted alignments, the spin of these bands has to be increased by 4 ℏ to 5 ℏ . Based on the linking transitions observed in t... [Phys. Rev. C 86, 027301] Published Wed Aug 01, 2012
    Keywords: Nuclear Structure
    Print ISSN: 0556-2813
    Electronic ISSN: 1089-490X
    Topics: Physics
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  • 3
    Publication Date: 2013-11-15
    Description: Author(s): K. Y. Ma (马克岩), J. B. Lu (陆景彬), S. P. Ruan (阮圣平), D. Yang (杨东), J. Li (李剑), Y. Z. Liu (刘运祚), Y. J. Ma (马英君), X. G. Wu (吴晓光), Y. Zheng (郑云), and C. Y. He (贺创业) High-spin states of 126 La have been populated using the 116 Sn( 14 N, 4 n ) 126 La reaction at a beam energy of 77 MeV. A side band linking to the known yrast π h 11/2 ⊗ ν h 11/2 band is observed. B ( M 1)/ B ( E 2) ratios and alignments of the side band and DCO ratios of linking transitions between the side band and t... [Phys. Rev. C 88, 057302] Published Thu Nov 14, 2013
    Keywords: Nuclear Structure
    Print ISSN: 0556-2813
    Electronic ISSN: 1089-490X
    Topics: Physics
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  • 4
    Publication Date: 2018-01-13
    Description: Author(s): K. Y. Ma (马克岩), J. B. Lu (陆景彬), Z. Zhang (张哲), J. Q. Liu (刘佳强), D. Yang (杨东), Y. M. Liu (刘玉敏), X. Xu (许旭), X. Y. Li (李潇祎), Y. Z. Liu (刘运祚), X. G. Wu (吴晓光), Y. Zheng (郑云), and C. B. Li (李聪博) High-spin states of Pm 138 have been populated using the Te 124 ( F 19 , 5 n ) Pm 138 reaction at a beam energy of 105 MeV. A new positive-parity side band with the same π h 11 / 2 ⊗ ν h 11 / 2 configuration as that of the yrast band is observed in Pm 138 . The properties of the two positive-parity bands show general agre... [Phys. Rev. C 97, 014305] Published Fri Jan 12, 2018
    Keywords: Nuclear Structure
    Print ISSN: 0556-2813
    Electronic ISSN: 1089-490X
    Topics: Physics
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 27 (1989), S. 819-835 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The rheological behavior of the thermotropic liquid crystal copolyesters composed of p-hydroxybenzoic acid and 2-hydroxy-6-naphthoic acid (indicated as HBA/HNA) is investigated for three different compositions: 75:25, 58:42, 30:70 (in mol%). The inherent viscosities are 9.2, 5.1, and 7.8 dl/g, respectively. Yield stress is observed for all three samples. This indicates the existence of crystallites in the melt which may be related to the shear thinning viscosity at low shear stress. Melt fracture, and a die swell ratio which increases with shear rate, are also observed at higher temperatures and at low shear stress for the two copolyesters having compositions 75:25 and 30:70. We have also estimated for 30HBA/70HNA at 335°C the entrance pressure loss, Δpent, and ΔPent/δw, where δw is the shear stress at the capillary wall. The large value of ΔPent/δw suggest that HBA/HNA is a highly elastic polymeric material. It is found that both ΔPent and ΔPent/δw increase with shear rate. However, the high elasticity does not account for the disappearance of melt fracture and contraction of die swell at high shear stress. This abnormal phenomenon is ascribed to the formation of a network of crystallites caused by blocky regions in the copolymer.
    Additional Material: 18 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 24 (1996), S. 803-810 
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: The mercaptoesters have been recognized as an effective coupling agent for bonding metals using acrylate and epoxy adhesives with enhanced bonding strength and improved durability. Here, we report the results of our investigation of the interaction of thioester coupling agents with a gold surface using a grazing angle FTIR (GA/FTIR) spectroscopic technique. We investigated the interaction of alkyl functional thioesters (octylthioglycolate, dodecyl-thioglycolate and stearylthioglycolate) coupling agents with the metal at the interface region. The formation of strong chemical bonding is proven to be the key feature of this application rather than wetting or hydrogen bonding for conventional adhesive applications. Based on our results we have concluded that the deposited layers exist as thioester bonded to the gold surface through the sulfur-metal bond and that the polarization results indicate that only those thioesters containing C12 and C18 hydrocarbon tail chains self-assemble readily and close pack on the surface. For dodecyl thioglycolate, the C12 alkyl chains are densely packed and oriented perpendicular to the substrate surface. For the stearyl thioglycolate, the C18 alkyl tail chains are also closely packed and oriented, but the chains appear to tilt from the normal surface. However, the carbonyl group of the C18 thioester appears to be parallel to the surface. For short-chain mercaptoesters, such as octyl thioglycolate, the alkyl chains do not self-assemble or orient on the gold surface. The molecular orientation of the coupling agent at the interface region has also been shown to play an important role in determining the interaction of the adhesive with the coupling agent layers. Results of the interfacial shear strength promotion on mild steel by the mercaptoester coupling agents are also reported.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 20 (1993), S. 407-415 
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Tertiary alkylamines of different chain lengths have been used as primers for adhesive bonding strength promotion for polyolefinic surfaces with cyanoacrylate (CA) adhesives. A combination of the construction of model polyolefin surfaces and advanced molecular-sensitive analysis tools has been employed for understanding the promoter/polyolefin interaction at the interface. Characterization of primer structure and interfacial properties has been carried out using grazing angle reflection-absorption Fourier transform infrared spectroscopy (GA/FTIR), ellipsometry, x-ray photoelectron spectroscopy (XPS) and contact angle titration using different pH probe liquids. Our work has focused on the design and construction of a model polyolefin surface using a new in situ polyethylene (PE) polymerization technique to form a controllable thickness (〈400 Å) of PE film on a reflective metal surface. The new technique of in situ PE polymerization is based on diazomethane chemistry. Both protonated and deuterated PE films have been successfully prepared. The results of spectroscopic investigations of these model deuterated and non-deuterated PE surfaces are disclosed. Molecular parameters that affect adhesion promotion have been studied. The parameters studied include molecular structure and alkyl chain length of tertiary alkylamines.
    Additional Material: 10 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 23 (1995), S. 276-288 
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: We have observed that methacrylic acid (MA) is far more corrosive than acrylic acid (AA) on copper surfaces when copper was exposed to the vapor of these two acids at ambient temperature and environment. With the aid of modern surface-sensitive instrumentation, which included grazing angle Fourier transform infrared (FTIR), XPS, x-ray-induced Auger electron and SEM/energy-dispersive spectroscopies and white light stereo and metallurgical microscopy, we are reporting our results of an extensive study of the roles that MA and AA have in this unusual phenomenon of copper corrosion.By grazing angle FTIR analysis we demonstrated that copper carboxylate salt formation is very rapid upon short contact with the vapor of both acids, and the acids showed no evidence of polymerization. We have also demonstrated by XPS and x-ray-induced Auger electron spectroscopy that copper surfaces exposed to the MA vapor contains mainly Cu(II) species. However, the oxidation state of the copper exposed to AA vapor will depend on exposure time and environment. With limited exposure to the air, the copper surface remained shiny for up to 12 months test time. The spectrum obtained from the shiny area of the AA/Cu surface shows that it contains mainly Cu(I) mixed with some copper (II). When the spectrum was taken from a dull area of AA/Cu surfaces, the Cu(II) state was found to be predominant. These results strongly indicate that when the shiny AA/Cu surface changed to a dull color, the oxidation state of the copper also changed from +1 to +2. The molecular structure of the Cu(II)-AA salt is also believed to be altered.Both stereo microscopic and SEM/energy-dispersive spectroscopy techniques were also used to perform the visual and microanalysis of the surface texture and elemental compositions of the corroded surfaces, respectively. The presence of oxygen was also found to play an important role in the overall corrosion processes. The differences in molecular structure of copper carboxylate salts of different oxidation states are discussed and are believed to be responsible for this unusual phenomenon. We believe that this finding will provide a good explanation for the cause of drastic differences of copper corrosion by acrylic and methacrylic acids.
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Acta Polymerica 47 (1996), S. 285-289 
    ISSN: 0323-7648
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Epitaxial crystallization behavior of HDPE/iPP double layers under quenching and annealing conditions has been studied by means of transmission electron microscopy (TEM). The results obtained from bright field TEM observations indicate that in the as-quenched state the HDPE that is in direct contact with the surface of the oriented iPP substrate recrystallizes in the form of oriented crystallites dispersed on the iPP substrate. The electron diffraction results show that besides the two normally observed epitaxial orientations between HDPE and iPP, there is also a special orientation with [001]HDPE ‖ [001]iPP. The HDPE which is in contact with the clean surface of a glass slide crystallizes in small lamellae with random orientation. In the boundary region, the epitaxially crystallized HDPE small lamellae stop right on the boundary of the oriented iPP film. If the quenched samples are annealed at 128°C (below Tm of HDPE) for 2 h, the small HDPE crystals grow to thick lamellae in both areas. But only the epitaxial orientation of HDPE with [001]HDPE ‖ [101]iPP has been observed.
    Additional Material: 8 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 30 (1985), S. 1035-1047 
    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: Sorption isotherms and diffusion coefficients of water in a 0.3-mil Kapton polyimide film at 30, 45, and 60°C are reported. The data are well described by the dual mode sorption and transport models at low activities. At high penetrant activities, clustering of water is suggested by a Zimm-Lundberg analysis of the sorption data and the fact that the diffusion coefficient for water decreases with increasing external vapor activity. The effect of temperature on the diffusion coefficients at infinite dilution and the dual mode sorption parameters kD, b, and CH′ are presented and discussed. The magnitude of the activation energy of the diffusion coefficient at infinite dilution, 5.4 kcal/mol, is smaller than the corresponding activation energy in more flexible chain polymers, perhaps suggesting that rather small backbone motions are associated with diffusion of water through the Kapton matrix. The predictions for the isosteric enthalpy of sorption from the dual mode model are presented and compared with the values determined from graphical analysis of the sorption isotherms performed independently without reference to the dual mode sorption model.
    Additional Material: 7 Ill.
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