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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 28 (1995), S. 5225-5229 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 28 (1995), S. 8381-8387 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Review of Scientific Instruments 69 (1998), S. 1955-1960 
    ISSN: 1089-7623
    Source: AIP Digital Archive
    Topics: Physics , Electrical Engineering, Measurement and Control Technology
    Notes: A high-pressure fiber-optic light-scattering spectrometer has been constructed for in situ observation of molecular dissolution/association as well as the polymerization process in supercritical fluids. Single (or multiple) fiber-optic probes, each comprised of a single optical fiber (or multiple optical fibers) and a graded index microlens, are used to transmit the incident laser beam and to receive the scattered light as well as the transmitted light from the high pressure cell. The direct immersion in the scattering medium of the fiber-optic probes makes the spectrometer more compact and more flexible with an easier alignment process. With the miniaturization and flexibility, our high-pressure light-scattering cell can be transported and adapted in combination with other physical techniques, such as synchrotron small angle x-ray scattering which requires a different set of windows (e.g., made of diamond) suitable for x-ray transmissions. This spectrometer has been successfully used for the in situ study of the molecular association behavior of a diblock copolymer of 1,1-dihydroperfluorooctylacrylate and vinyl acetate in supercritical carbon dioxide under pressures up to 552 bar. © 1998 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Review of Scientific Instruments 72 (2001), S. 2679-2685 
    ISSN: 1089-7623
    Source: AIP Digital Archive
    Topics: Physics , Electrical Engineering, Measurement and Control Technology
    Notes: A cell for in situ observation of self-assembled nanostructured materials in high-pressure fluids, including supercritical carbon dioxide, has been constructed and tested. The compact cell can be used for simultaneous small-angle x-ray scattering, laser light scattering, visual observation, and some other types of spectroscopic measurements. The light scattering plane is normal to the x-ray scattering plane with the optical axis and the x-ray axis being perpendicular to each other. The scattering is detected at the intersection of the light and x-ray beams, and thus one effectively probes the same scattering volume. Some preliminary experimental results for the micellar self-assembly of a fluorinated block copolymer in supercritical carbon dioxide are presented. © 2001 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Catalysis letters 20 (1993), S. 179-183 
    ISSN: 1572-879X
    Keywords: Methane oxidative coupling ; barium-titanium oxides ; oxyfluorides
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The addition of F− to Ba-Ti mixed oxide catalysts significantly improves the catalytic performances for the oxidative coupling of methane (MOC), which can achieve high C2 yields at wide feed composition range and high GHSV. The effect is particularly marked for the BaF2− TiO2 catalysts containing more than 50 mol% BaF2. The C2 yield of 17% and the C2 selectivity of 〉 60% were achieved over these catalysts at 700 ° C. After being on stream for 31 h, the ≥ 50 mol% BaF2-TiO2 catalysts showed only a 1–1.5% decrease in the C2 yields. Results obtained by XRD show that various Ba-Ti oxyfluoride phases were formed due to the substitution of F− to O2−.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 240 (1996), S. 123-136 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The volume phase transition of poly(N-isopropylacrylamide) (PNIPAM) spherical microgel particles was studied by static and dynamic laser light scattering (LLS). The results were compared with the coil-to-globule transition of individual long linear PNIPAM chains. The microgel particles have a higher transition temperature, but a less sharp phase transition, in comparison with that of long linear chains. This difference has been attributed to both the short length and the broad length distribution of the subchains inside the microgels. A combination of static and dynamic LLS results revealed that even in a highly collapsed state the microgel particles retained ∼70% of water and the density of the microgel networks increased from 0.021 g/cm3 to ∼0.30 g/cm3 during the phase transition. The temperature-dependence of the NMR spin-lattice relaxation times T1 of PNIPAM indicate an association between water and the CH proton on the N-isopropyl group. Our results also showed that the transition was strongly influenced by the presence of surfactant. Addition of anionic surfactant, such as sodium dodecyl sulfate (SDS), promotes the swelling of the particles and shifts the transition to a higher temperature, while the addition of a cationic surfactant, such as dodecyl pyridine bromide (DPB), has less effects on the swelling and phase transition, which has been attributed to the electron-rich amide group in PNIPAM. Moreover, a two-step phase transition was observed for the first time in the presence of SDS. The dynamic LLS results demonstrates that SDS is expelled gradually from the microgel in the first-step volume phase transition.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 35 (1995), S. 385-392 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The solution behavior of four chitosans (91% deacetylated chitin) with different molecular weights in 0.2M CH3COOH/0.1M CH3COONa aqueous solution was investigated at 25°C by dynamic laser light scattering (LLS). The Laplace inversion of the precisely measured intensity-intensity lime correlation function leads us to an estimate of the line-width distribution G(Γ), which could be further reduced too translational diffusion coefficient distributions G(D). By using a combination of static and dynamic LLS results, i.e., Mw and G (D), we were able to establish a calibration of D = kDM-αD with kD = (3.14 ± 0.20) × 10-4 and αD = 0.655 ± 0.015. By using this calibration, we successfully converted G(D) into a molecular weight distribution fw(M). The larger αD value confirms that the chitosan chain is slightly extended in aqueous solution even in the presence of salts. This is mainly due to its backbone and polyelectrolytes nature. As a very sensitive technique, our dynamic LLS results also revealed that even in dilute solution chitosan still forms a small amount of larger sized aggregates that have been overlooked in previous studies. The calibration obtained in this study will provide another way to characterize the molecular weight distribution of chitosan in aqueous solution at room temperature. © 1995 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 1597-1604 
    ISSN: 0887-6266
    Keywords: poly(N-isopropylacrylamide) ; phase transition ; surfactant effects ; laser light scattering ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The effects of both anionic (sodium dodecyl sulfate, SDS) and cationic (dodecylpyridine bromide, DPB) surfactants on the phase transition of narrowly distributed poly(N-isopropylacrylamide) (PNIPAM) microgel particles were investigated by laser light scattering. The addition of SDS swells the particles and increases the phase transition temperature, while DPB has a much smaller effect. This difference cannot be due to an association between the surfactant hydrophobic tail and PNIPAM because DPB and SDS have an identical hydrophobic tail. The amide groups in PNIPAM are slightly protonized in deionized water (pH ∼ 5.5). Our results contradict a previous prediction that oppositely charged surfactants will collapse a polyelectrolyte gel. After adding SDS, a two-step phase transition of the PNIPAM gel is observed. This suggests that SDS forms micelles inside the microgel with the help of the immobilized counter ions on the gel network. The SDS micelles are broken into individual SDS molecules in the first step of phase transition, while in the second step individual SDS molecules are gradually expelled. Surfactant effects on the microgel particles are compared with those of individual PNIPAM chains. © 1996 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 889-900 
    ISSN: 0887-6266
    Keywords: Pluronic P103 ; micellar formation and structure ; supramolecular structure ; laser light scattering ; small-angle X-ray scattering ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Both laser light scattering (LLS) and small-angle X-ray scattering (SAXS) were used to study the water-induced formation and structure of micelles and supramolecules of Pluronic P103 [(EO)17(PO)60(EO)17] in o-xylene, a selective solvent for the long middle block. In pure o-xylene, P103 molecules exist as unimer coils with an equivalent hard-sphere radius of 1.6 nm even at fairly high concentrations. Micelles with a PEO/water core and a PPO dominated corona were formed in the presence of water when the P103 concentration ≥0.046 g/mL. The size and structure of micelles have been studied as a function of solubilized water content Z (the molar ratio of water to EO units) in micelles. The micelles change from a somewhat open structure with some EO units either dangling out of the micellar core or being incorporated into neighboring micellar cores at low Z values to a flower-like structure with relatively sharp interface at high Z values. At low Z values (〈 about 2.9), micelles tend to have a structure with part of the poorly solvated PEO blocks present in the corona. With more water added to the core, the PEO blocks in the corona gradually entered into the core, and the PPO blocks backfolded to form loops. With increasing Z, the micellar core radius, Rc, and the hard-sphere volume fraction, φ, of micelles increased; the aggregation number, N, kept nearly a constant; but the hydrodynamic radius, 〈Rh〉0, and the corona thickness, Rs, decreased. At high Z values (〉 about 2.9), micelles have a flower-like structure with the two end PEO blocks belonging to the small micellar core. With increasing Z, the values of Rc, φ, and N increased, while Rs kept nearly a constant. In the concentrated regime (C 〉 0.30 g/mL), a stiff polymer network at a critical φ value of 0.49 was formed. The supramolecular structures with a face-center cubic packing, and a possible hexagonal packing at higher polymer concentrations (i.e. 〉 0.55 g/mL), were observed, respectively. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 889-900, 1998
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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