Search results for "Plastics"
showing 10 items of 2724 documents
Shear Effects on the Phase Diagrams of Solutions of Highly Incompatible Polymers in a Common Solvent. 2. Experiment and Theory
1997
Cloud point temperatures (Tcp) were measured at different constant shear rates for three representatives of the ternary system cyclohexanone/polystyrene/poly(n-butyl methacrylate) (CHO/PS/PBMA) by means of a newly constructed rheo-optical apparatus that can be operated in the temperature range from 0 to 100 °C up to maximum shear rates of 1440 s-1 and maximum stresses of 384 Pa. In all cases one observes an extension of the homogeneous region as the shear rate γ is raised. With the system CHO/PS 196w/PBMA 2050 (the figures denote the molar masses of the polymers in kilograms/mole) the effects become maximum for high concentrations of PBMA, where the demixing temperatures increase by more th…
Shear Effects on the Phase Diagrams of Solutions of Highly Incompatible Polymers in a Common Solvent. 1. Equilibrium Behavior and Rheological Propert…
1997
Phase diagrams (cloud points, tie lines, critical compositions) and viscosities of homogeneous solutions were determined at temperatures ranging from 20 to 100 °C for three representatives of the ternary system cyclohexanone/polystyrene/poly(n-butyl methacrylate) [CHO/PS/PBMA] in preparation of a study on shear influences. An only moderate increase of the two-phase region observed upon heating (LCST behavior) witnesses little heat effects upon mixing. Tie lines which are nearly parallel to the PS/PBMA edge of the Gibbs phase triangle indicate comparable solvent quality of CHO for both polymers. The quantitative mathematical description of the equilibrium behavior-required for a theoretical …
Ternary Polymer Solutions with Hydrogen Bonds, 2
2007
Experimental ternary phase diagrams for ternary systems CHL/PS-MAA/PVPy with diverse MAA contents have been determined by GPC. The presence of MAA in the copolymers gives rise to specific interactions, by hydrogen bond formation between both polymeric components, so strong that the isotherm for the system with the highest MAA content so far studied, CHL/PS-MAA(8%)/PVPy, is representative of a complex coacervation situation. By applying the theoretical background deduced by coupling the Flory-Huggins lattice model to the AET developed for ternary polymeric systems SPP with specific intermolecular interactions (via hydrogen bonds), free energy surfaces for the CHL/PS-MAA/PVPy systems are cons…
Effect of Processing Conditions on the Degradation and on the Recycling of Polycarbonate
2003
Polycarbonate, like other polycondensation polymers, can be easily recycled without significant loss of properties only with careful drying. Indeed, the presence of humidity strongly decreases the molecular weight of the polymer by hydrolytic chain scission. In this paper, the degradation and the recycling of an extrusion grade polycarbonate sample has been investigated considering mainly the effect of the humidity. Some degradation is observed also for the material reprocessed in dry conditions and due to the thermomechanical stress acting on the melt. The chain scission is strongly reduced if the processing is carried out under nitrogen flow. In these conditions less degradation effects …
(Photo)crosslinkable Smectic LC Main-Chain Polymers
2007
This paper presents the synthetic route to SmA LC main-chain polymers, that can be (photo)-crosslinked without solvent in the bulk phase. They are based on soluble polymalonates, in which higher ordered phases can be suppressed by copolymerization with a laterally brominated biphenyl. Two routes were developed to incorporate the crosslinkable groups into the polyester backbone. The first consists in the incorporation of phenols into the polyester. These phenols are not reactive enough to participate in the transesterification reaction used to build up the polymer, but they can be esterified afterwards with acrylates. Thermally or photochemically created radicals then start the crosslinking.…
Synthesis of Precision Poly(1,3-adamantylene alkylene)s via Acyclic Diene Metathesis Polycondensation
2019
[Image: see text] Fully saturated, aliphatic polymers containing adamantane moieties evenly distributed along the polymer backbone are of great interest due to their exceptional thermal stability, yet more synthetic strategies toward these polymers would be desirable. Herein, we report for the first time the synthesis of poly(1,3-adamantylene alkylene)s based on α,ω-dienes containing bulky 1,3-adamantylene defects precisely located on every 11th, 17th, 19th, and 21st chain carbon via acyclic diene metathesis polycondensation. All saturated polymers revealed excellent thermal stabilities (452–456 °C) that were significantly higher compared to those of structurally similar polyolefins with al…
Long-chain branched ROMP polymers
2009
This article describes the construction of branched ROMP-polymer architectures via polycondensation of ABn-type macromonomers. For this convergent strategy, a polymer was synthesized that carries several hydroxyl-groups along the polymer chain and one carboxylic acid group at the chain end. An esterification reaction between these functional groups yielded long-chain branched polymers. The polymers were analyzed by NMR and SEC to monitor the condensation reaction. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2009
Recycling of dry and wet polyamide 6
2002
Recycling of polycondensation polymers can give rise to secondary materials with good mechanical properties only if a careful drying is carried out before the melt reprocessing operations. The presence of humidity provokes the hydrolytic chain scission of the macromolecules and the consequent decrease of molecular weight and properties. In this work, the drying step was substituted by the addition of an antioxidant that is able to protect the macromolecules because it is the autioxidant is more prone to hydrolysis, thus removing the water from the melt. The mechanical properties of polyamide 6 reprocessed more times in wet conditions and in the presence of this stabilizer are even better th…
Molecular Parameters of Hyperbranched Polymers Made by Self-Condensing Vinyl Polymerization. 2. Degree of Branching
1997
Using a modified definition, the average degree of branching, , the fraction of branchpoints, , as well as the fractions of various structural units are calculated as a function of conversion of double bonds for hyperbranched polymers formed by self-condensing vinyl polymerization (SCVP) of monomers (or “inimers”) with the general structure AB*, where A is a vinyl group and B* is an initiating group. The results are compared to those for the polycondensation of AB2-type monomers. At full conversion, is somewhat smaller for SCVP ( ∞ ≈ 0.465) than for AB2 systems ( ∞ = 0.5). There are two kinds of linear groups in SCVP whereas there is only one kind in AB2 systems. Since there are two differe…
LC Ionomers with Phosphonate Groups and Their Multilayer Build-Up
2002
This paper describes the synthesis of new liquid-crystalline (LC) ionomers (semiflexible LC mainchain polymers with ionic groups as side groups) by polycondensation of substituted malonates with mesogenic diols. Phosphonic acids were used as negative groups, and phosphonium and ammonium ions as positive groups. The presence of these ionic groups leads to gelation (physical crosslinking) of the polymers, which display a rubbery consistency. As expected from the reference polymers without an ionic group, all polymers show smectic phases. These phases are destabilized by bulky side groups (e.g., phosphonium ions or phosphonic acid esters). They are, however, stabilized by phosphonic acid group…