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  • 1
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 67 (1995), S. 1573-1575 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Optical properties of ordered Ga0.5In0.5P epitaxial layers grown by metalorganic vapor phase epitaxy are investigated by photoluminescence (PL) in a temperature range of 10–200 K using excitation power densities between 0.35 W/cm2 and 20 W/cm2. It is found that the intensity of the highest-energy PL peak of the ordered Ga0.5In0.5P epilayer decreases first, then increases and finally goes down again with increasing temperature. A model of ordered Ga0.5In0.5P epitaxial layers is proposed, in which the ordered Ga0.5In0.5P epilayer is regarded as a type-II quantum well structure with band-tail states, and the dependence of PL spectra on the temperature and excitation intensity is reasonably explained. © 1995 American Institute of Physics.
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 103 (1995), S. 3289-3292 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We have examined both the absorption and resonance Raman spectra of mass-selected Ta tetramers. The tetramers are produced in a sputtering source and mass filtered with a Wien filter, then neutralized and deposited in an Ar matrix at low temperatures. The absorption spectrum indicates two broad transitions, one in the red at 768 nm and another to the blue at 532 nm. Raman resonances could be excited in both regions giving three distinct fundamental frequencies at 270.2(1) cm−1, 185.1(1) cm−1, and 130.6(2) cm−1. The lowest vibration shows a long progression (up to seven overtones) with alternating separations of 135 cm−1 and 126 cm−1, indicative of a weak Jahn–Teller effect in the tetramer ground state. This, along with the observation that the fundamental frequency ratios are close to 2:(square root of)2:1 indicate that the molecule has a tetrahedral ground state geometry with an electronic E state symmetry. The appearance of three fundamentals in the resonance Raman spectrum indicates that both excited states corresponding to the observed absorption bands arise from severely distorted T electronic states. © 1995 American Institute of Physics.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of intelligent manufacturing 7 (1996), S. 243-250 
    ISSN: 1572-8145
    Keywords: Job-shop scheduling ; real-time dispatching ; simulation ; neural networks
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: To schedule a job shop, the first task is to select an appropriate scheduling algorithm or rule. Because of the complexity of scheduling problems, no general algorithm sufficient for solving all scheduling problems has yet been developed. Most job-shop scheduling systems offer alternative algorithms for different situations, and experienced human schedulers are needed to select the best dispatching rule in these systems. This paper proposes a new algorithm for job-shop scheduling problems. This algorithm consists of three stages. First, computer simulation techniques are used to evaluate the efficiency of heuristic rules in different scheduling situations. Second, the simulation results are used to train a neural network in order to capture the knowledge which can be used to select the most efficient heuristic rule for each scheduling situation. Finally, the trained neural network is used as a dispatching rule selector in the real-time scheduling process. Research results have shown great potential in using a neural network to replace human schedulers in selecting an appropriate approach for real-time scheduling. This research is part of an ongoing project of developing a real-time planning and scheduling system.
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 643-650 
    ISSN: 0887-624X
    Keywords: photopolymerization of N-substituted phenyl maleimides ; N,N-dimethyl-4-Toluidine ; exciplex ; radical intermediate ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Several N-phenyl maleimides with different p-substituents have been synthesized from the maleic anhydride and relevant aromatic amine. In the presence of N,N-dimethyl-4-toluidine (DMT), the N-substituted phenyl maleimide (4-XPhMIs) could be polymerized under UV irradiation. It was observed that a new absorption appeared on the UV-Vis spectrum of the mixture solution of 4-XPhMI and DMT, which reveals the formation of charge-transfer complex in the ground state. It was found that the fluorescence of DMT was quenched by 4-XPhMI and the quenching constant of 4-XPhMI, obtained from the Stern-Volmer plot, increases with the electron-deficiency of ethylene double bond of 4-XPhMI. The dynamic quenching of the fluorescence of DMT by 4-XPhMI suggests the formation of exciplex in excited state between DMT and 4-XPhMI. The radicals formed in the systems have been detected by spin-trapping techniques and electron paramagnetic resonance (EPR) spectrometer. Based on all of these results, it has been proposed that the initiation process of the polymerization involves the formation of exciplex and the initial radicals were produced by proton-transfer in the exciplex from DMT to 4-XPhMI. © 1997 John Wiley & Sons, Inc.
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 1301-1307 
    ISSN: 0887-624X
    Keywords: 1,4-dioxan-2-one ; trimethylene carbonate ; stannous octoate ; drug delivery system ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Poly(1,4-dioxan-2-one-co-trimethylene carbonate), P(DON-co-TMC), copolymers with different compositions were synthesized by copolymerizations of 1,4-dioxan-2-one (DON) and trimethylene carbonate (TMC) at 120°C in the presence of Sn(Oct)2. Their structures and compositions were determined with FT-IR and 1H-NMR spectroscopies. The intrinsic viscosities of copolymers increased with the increase of the TMC fraction in feed. The DSC results of copolymers showed that the glass transition temperatures (Tgs) of copolymers are lower than those of homopolymers. Most copolymers are amorphous except for one with a high DON composition. The hydrophilicity of the copolymers is in proportion with the DON molar fraction in the copolymers. It was found that the Levonorgestrel (LNG) release rate is dependent of the composition and flexibility of polymer chains. The fastest one is the copolymer with nearly a equivalent fraction of DON to TMC. Among copolymers with other compositions, a higher DON fraction would be favorable to the release of LNG. All measurements demonstrate an almost constant release rate in the period of 1 month. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 1301-1307, 1998
    Additional Material: 8 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 695-702 
    ISSN: 0887-624X
    Keywords: ABA-type block copolymers ; ring-opening polymerization ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ABA-type block copolymers of poly(trimethylene carbonate) with poly(ethylene glycol) (Mn 6820), PTMC-b-PEG-b-PTMC, were synthesized by the ring-opening polymerization of 1,3-dioxan-2-one (trimethylene carbonate) in the presence of poly-(ethylene glycol) with stannous octoate catalyst, and the copolymers with various compositions were obtained. The PTMC-b-PEG-b-PTMC copolymers were characterized with Fourier transform infrared and nuclear magnetic resonance spectroscopies. The intrinsic viscosities of resulting copolymers increased with the increase of 1,3-dioxan-2-one content in feed while the molar ratio of monomer over catalyst kept constant. It has been observed that the glass transition temperature (Tg) of the PTMC segments in copolymers, recorded from differential scanning calorimetry, was dependent on the composition of copolymers. The melting temperature (Tm) of PEG blocks in copolymer was lower than that of PEG polymer, and then disappeared as the length of PTMC blocks increased. The results of dynamic contact angle measurement clearly revealed that the hydrophilicity of resulting copolymers increased greatly with the increase of PEG content in copolymers. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 695-702, 1998
    Additional Material: 6 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 1607-1613 
    ISSN: 0887-624X
    Keywords: sol-gel ; hybrid material ; poly(styrene-co-maleic anhydride) ; tetraethoxysilane ; (3-aminopropyl)triethoxysilane ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Poly(styrene-co-maleic anhydride)/silica hybrid material has been successfully prepared from styrene-maleic anhydride copolymer and tetraethoxysilane (TEOS) in the presence of a coupling agent (3-aminopropyl)triethoxysilane (APTES) by an in situ sol-gel process. It was observed that the gel time of sol-gel solution was dramatically influenced by the amount of APTES. The hybrid material exhibits optical transparency almost as good as both silica gel and the copolymer. The covalent bonds between organic and inorganic phases were introduced by the aminolysis reaction of the amino group with maleic anhydride units of copolymer to form a copolymer bearing trimethoxysilyl groups, which undergo hydrolytic polycondensation with TEOS. The differential scanning calorimetry (DSC) showed that the glass transition temperature of the hybrid materials increases with increasing of SiO2 composition. Photographs of scanning electron microscopy (SEM) and atomic force microscopy (AFM) inferred that the size of the inorganic particles in the hybrid materials was less than 20 nm. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 1607-1613, 1998
    Additional Material: 8 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    IIE transactions 29 (1997), S. 624-625 
    ISSN: 1573-9724
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 230 (1995), S. 143-157 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Inhibition der Imidisierung einer Polyamidsäure (PAA), dem Vorprodukt eines Polyimids, in Gegenwart von Kupfer wurde durch die Zugabe von Cu2+ -Ionen zu PAA-Filmen bestätigt. Die Imidisierung verlief unterhalb 300°C unvollständig, doch bei Temperaturen über 300°C begann die Zersetzung. Die Vorbehandlung einer Kupferoberfläche mit einer Grundierung aus den zwei Komponenten Polybenzimidazol und 2-Mercaptobenzimidazol ermöglicht, die Imidisierung ohne Verzögerung ablaufen zu lassen und die Zersetzung oberhalb 300°C zu verhindern. Durch geeignete Oberflächenbehandlungssysteme kann die Adhäsion zwischen Polyimid und Kupfersubstrat verbessert werden.
    Notes: The inhibition of the imidization of polyamic acid, a precursor of polyimide, in the presence of Cu, was confirmed by the incorporation of Cu2+ ions in polyamic acid films. It was found that the imidization reaction was incomplete below 300°C but decomposition took place when heating above 300°C. Pretreating the Cu surface with a two-component primer solution containing polybenzimidazole and 2-mercaptobenzimidazole can make the imidization proceed without retardation and avoid the decomposition above 300°C. By choosing appropriate surface treatment systems, one can achieve the improvement of adhesion between PI and Cu substrate.
    Additional Material: 9 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 507-515 
    ISSN: 0887-6266
    Keywords: poly(acrylic acid) ; FTIR ; polyelectrolyte ; conformation ; conformers ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Fourier transform infrared (FTIR) spectroscopic measurements have been undertaken to estimate the conformational energies of poly(acrylic acid) (PAA) cast films in the temperature range of 40-130°C. The temperature dependence of the IR spectra in the C=O stretching region has been analyzed to yield the side-chain and backbone conformational energies. The estimated energies are close to those previously obtained by polarized Raman spectroscopic measurements for PAA solutions. Combining the FTIR value of conformational energy with the simplified rotational isomeric state (RIS) model proposed in the Raman analysis provides a persistence length in accordance with earlier SAXS experiments. The data also agree with the Gibbs-DiMarzio predictions, further substantiating the validity of the analysis. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys, 35: 507-515, 1997
    Additional Material: 7 Ill.
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