All‐aromatic liquid crystalline thermosets with high glass transition temperatures

We have synthesized and characterized a new family of low melting all‐aromatic ester‐based liquid crystal oligomers end‐capped with reactive phenylethynyl end groups. In a consecutive, high‐temperature step, the reactive end groups were thermally activated and polymerization was initiated. This reactive oligomer approach allows us to synthesize liquid crystal thermosets with outstanding mechanical and thermal properties, which are superior to well‐known high‐performance polymers such as PPS and PEEK. We have modified an intractable LC formulation based on hydroquinone and terephthalic acid, with M_n = 1000, 5000, and 9000 g mol^?1, and varied the backbone composition using isophthalic acid, resorcinol, 4‐hydroxy‐benzoic acid, 6‐hydroxy‐2‐naphthoic acid, and chlorohydroquinone. All fully cured polymers showed glass transition temperatures in the range of 164–275 °C, and high storage moduli at room temperature (～ 5 GPa) and elevated temperature (～ 2 GPa at 200 °C). All oligomers display nematic mesophases and in most cases, the nematic order is maintained after cure. Rheology experiments showed that the phenylethynyl end group undergoes predominantly chain extension below 340 °C and crosslinking above this temperature. Highly aligned fibers could be spun from the nematic melt, and we found that the order parameter 〈P₂〉 was not affected by the chain extension and crosslink chemistry. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 1368–1380, 2009     

Calcul fonctionnel a plusieurs variables pour des operateurs pseudodifferentiels dansR n

We study aC ^∞ functional calculus with several variables forv pseudodifferential operatorsP ₁, …,P _v inR ⁿ . Whenf is a function belonging to the classS _1.0 ^r (R ^v ) of Hörmander, we prove that, under some conditions,f(P ₁,…,P _v) is a pseudodifferential operator, and we give an asymptotic formula for its symbol.     

Neutron scattering in polymer gels at the theta temperature

Small angle elastic neutron scattering was performed on three polystyrene networks swollen to equilibrium in cyclohexane at the theta temperature. Comparison of the SANS spectra with similar measurements in uncross-linked solutions reveals that in the intermediate Q region the gels behave like solutions of lower concentration than the equivalent solutions. We assume that the gel spectra are composed of a static component plus a dynamic, or solution-like part. By a suitable fitting procedure, the former can be estimated, yielding the mean square static concentration fluctuation <Δφ²> generated by cross-linking contraints in the gel. Independent measurement of the swelling pressure of these gels permits an estimate to be made of the scattering intensity I(Q=0) of the dynamic part of the spectrum. Plausible agreement is found between the macroscopic and microscopic estimations of the osmotic compressibility if allowance is made for the concentration polydispersity in the gels.     

Inhomogeneous biopolymer gels

The microstructure and rheological behaviour of inhomogeneous biopolymer gels was studied using a model system of β-lactoglobulin. It can form both fine-stranded and particulate gels which can be homogeneous or inhomogeneous depending on pH and heating rate. The dense and loose regions of the fine-stranded gels had different relaxation times which significantly influenced the mechanical spectrum. The particulate gels showed coarser inhomogeneities influencing the fracture properties of the gels.     

Hexamethylhydrazinocyclotriphosphazene N3P3(NMeNH2)6: Starting reagent for the synthesis of multifunctionalized species,macrocycles, and small dendrimers

Hexamethylhydrazinocyclotriphosphazene N₃P₃ (NMe-NH₂)₆ 1 is a useful precursor for the synthesis of functionalized hexahydrazones ( 3a-f ), multicyclic ( 5 ) and multimacrocyclic ( 7 ) species, and small dendrimers ( 8 and 10 ). © 1996 John Wiley & Sons, Inc.     

Quasi-elastic neutron scattering in gels and solutions

Measurements of swelling pressure, neutron spin-echo scattering, and dynamic light scattering were made in an end-linked poly(dimethylsiloxane) (PDMS) gel swollen to equilibrium in a good solvent (toluene) and also in the equivalent solution. The macroscopic osmotic modulus is depressed in the gel. Neutron spin echo observations at intermediate and high values of the scattering vector Q reveal that the mobility of the monomers is unaffected by cross-linking. Elastic neutron scattering at small Q detects non-uniformities in the polymer concentration distribution, which are absent from the solution. These non-uniformities play a major role in the dynamic response of the system at lower Q, and and appear to be the cause of the observed reduction in osmotic pressure.     

Calcium induced volume transition in polyelectrolyte gels

The osmotic properties and the small angle neutron scattering (SANS) behaviour of fully neutralized sodium polyacrylate gels are investigated in the presence of calcium ions. Analysis of the SANS response displays three characteristic length scales, two of which are of thermodynamic origin, while the third, associated with the frozen-in structural inhomogeneities, is static. The SANS results are consistent with direct osmotic observations which indicate that the thermodynamic properties cannot be adequately described by a single correlation length. The concentration dependence of the osmotic pressure displays a power law behaviour with an exponent that decreases with increasing calcium concentration.     

Ion condensation in a polyelectrolyte gel

Anomalous small angle X-ray scattering is used to determine the distribution of divalent ions in a neutralized polyelectrolyte gel of sodium polyacrylate in the vicinity of the volume transition. At the five different energies of the incident beam used to vary the contrast, the scattering curves have similar shapes, and are separated only by constant multiplying factors. This result, in conjunction with SANS results from the same sample, indicates that the divalent ion (strontium) is confined on the polymer backbone.