Search results for "Mola"
showing 10 items of 1216 documents
Relative strength of H-bonding groups on biodegradable polymer-based blends in solution
2006
The intermolecular hydrogen bonding interactions between poly(3-hydroxybutyrate) and poly(styrene-co-vinyl phenol) copolymers with mutual solvent epichlorohydrin were thoroughly investigated by steady-state fluorescence and viscosity techniques. Fluorescence spectroscopy along with viscosity technique was used to asses the intermolecular hydrogen bonding between poly-(3-hydroxybutyrate) and its blends with five copolymer samples of styrene–vinyl phenol, containing different proportions of vinyl phenol but similar average molecular weight and polydispersity index. In the case of very low OH contents (2–4 mol %), as expected, both components of poly(3-hydroxybutyrate) and poly(styrene-co-4-vi…
Specialty and advanced polymers by carbocationic macromolecular engineering
1993
This study briefly surveys a variety of new advanced polymeric materials and controlled synthetic processes available by carbocationic macromolecular engineering techniques and having potential commercial interest. These recent developments, mainly by living carbocationic polymerization, have led to new opportunities in polymerization process control, and in designing microstructure, functionality, molecular weight and molecular weight distribution (MWD) and thus properties of a wide variety of unique polymer systems. The fundamentals of these new emerging technologies and the novel materials offered by them, such as macromonomers, telechelics, polymers with pendant functional groups (liqui…
Polydispersity and Molecular Weight Distribution of Hyperbranched Graft Copolymers via “Hypergrafting” of ABm Monomers from Polydisperse Macroinitiat…
2013
The hypergrafting strategy designates the synthesis of hyperbranched graft copolymers (HGCs) in a grafting-from approach, using ABm monomers, from multifunctional, polydisperse macroinitiator cores by slow monomer addition. Hypergrafting leads to complex polymer topologies with defined molecular weight, degree of branching (DB), and polydispersity (PD). By a generating function formalism, a generally applicable equation for the PD of HGCs (PD = PDf + (m – 1)/f) is derived, where PDf is the polydispersity of the core and f its average functionality. In addition, the complete molecular weight distribution function has been calculated for varied m and f as well as for a given distribution of i…
Time-resolved rheology as a tool to monitor the progress of polymer degradation in the melt state - Part I: Thermal and thermo-oxidative degradation …
2015
Abstract Thermal and thermo-oxidative degradation of polyamide 11 (PA11) in the melt state (T = 215 °C) are studied by resorting to time-resolved mechanical spectroscopy. Such an approach allows to elude the changes in the rheological properties occurring while testing, thus enabling the rigorous study of polymer degradation in the melt state. Different concurrent degradation reactions in oxidative (air) and non-oxidative (N2) environment are promptly guessed by studying the time evolutions of rheological functions. In particular, changes in the zero-frequency complex viscosity reflects changes in the average molecular weight, while the appearance of a yield stress in the complex viscosity …
Melt Strength and Extensibility of High-Density Polyethylene
1984
The extensional flow of polymer melts has been extensively studied because of its importance in many technological processing operations and, from a more fundamental point of view, because the tensile properties of the polymer melts cannot be correlated directly with shear viscosity behavior.1–5
Die Bestimmung der Molekulargewichtsverteilung von nichtkristallisierenden Polymeren mit dem Elektronenmikroskop, 6. Fehlerkorrektur der experimentel…
1977
A mathematical treatment is described, by means of which the effect of the measuring errors on the number molecular weight distribution of polymers, as obtained with an electron microscope (EM), can be eliminated. It is shown, that the difference in the nonuniformities of the measured and the corrected distribution would be negligible only in the case of samples with high average degrees of polymerization and sufficiently broad distributions. Otherwise differences of 10% or more can be found, depending on the size of the actual measuring error. This is shown by means of four practical examples. For a practical application the measuring error may not exceed some critical value, which, though…
Physicochemical Properties of Copper(II) Bis(2-ethylhexyl) Sulfosuccinate Reversed Micelles
1998
Abstract Measurements of some physicochemical properties (density, viscosity, conductance, UV–vis spectra, IR spectra) of the water/copper(II) bis(2-ethylhexyl) sulfosuccinate (Cu(DEHSS) 2 )/CCl 4 microemulsions, at a fixed surfactant molal concentration ([Cu (DEHSS) 2 ] = 0.05003 mol kg −1 ), as function of the molar ratio R ( R = [water]/[DEHSS − ]) have been performed at 25°C. Information on some structural and dynamical properties of the water-containing Cu(DEHSS) 2 reversed micelles and of their evolution with R are derived from the experimental results. The comparison with the same properties of water-containing sodium bis(2-ethylhexyl) sulfosuccinate reversed micelles allows to evide…
Volumes and heat capacities of the aqueous sodium dodecanoate/sodium perfluorooctanoate mixtures in the presence of β-cyclodextrin
2003
Apparent molar volumes (VΦ) and heat capacities (CΦ) of the sodium dodecanoate (NaL)/sodium perfluorooctanoate (NaPFO) mixtures in the water/β-cyclodextrin (β-CD) solvent as functions of the surfactant total molality (mt) were determined at 25°C. For a given surfactant mixture, VΦ decreases with mt to ca. 0.05 mol kg−1 thereafter it increases tending to a constant value. CΦ displays a behaviour opposite to VΦ. The mt values where the apparent molar properties exhibit extrema are nearly coincident with the critical micellar concentrations determined by conductivity. An equation correlating VΦ to mt was derived by assuming that the equilibria for the 1∶1 surfactant/cyclodextrin complex format…
FT-IR and nuclear overhauser enhancement study of the state of urea confined in AOT-reversed micelles
2003
Abstract The system urea/sodium-bis(2-ethylhexyl)sulfosuccinate (AOT) dispersed in CCl 4 and benzene-d6 was investigated by viscosimetry, FT-IR and high-resolution 1 H NMR spectroscopy, as a function of urea/AOT molar ratio ( R urea ) at fixed AOT molal concentration (0.3467 mol kg −1 ) and as a function of AOT concentration at fixed R urea (0.5) at 25 °C. The experimental data are consistent with the hypothesis that urea is encapsulated as small-size hydrogen-bonded cluster in the hydrophilic micellar core of the AOT-reversed micelles and that this structure is maintained well above the volume fraction of the dispersed phase, where a percolative transition occurs. Intermolecular nuclear ov…
Polyelectrolytes in dilute solution: viscometric access to coil dimensions and salt effects
2015
Copolymers of acrylamide (AM) and diallyldimethylammonium chloride (DADMAC), differing in molar masses M (52.3 to 227 kDa) and degrees of charging y (0.2 to 0.6), were studied with respect to their viscometric behavior in dilute aqueous solutions containing variable amounts of NaCl. Complementary measurements were performed on a Brookhaven 90 plus particle size analyzer. M dominates the intrinsic viscosities [η]. For the viscometric interaction parameters B this is only true for large concentrations of extra salt. [η] and B as a function of solvent salinity follow Boltzmann laws. Coil dimensions, determined either via dynamic light scattering or viscometry, agree well. For low salt contents…