Search results for "Condensation"

Hyperbranched Polymers

2012

Life is branched! Statistically branched (=hyperbranched) polymers have become an important class of materials in modern chemistry. Not only due to straightforward synthetic approaches which were developed in the last decade but also due to the vast amount of available monomers, hyperbranched polymers have replaced perfect dendrimers in many areas and they will have an even higher impact in future. This chapter highlights classic and modern syntheses of hyperbranched polymers and their unique properties and presents their versatility in the macromolecular toolbox for the design of complex nonlinear architectures.

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.…

1994

Polymer blends can undergo, during processing, degradation phenomena because of the presence of both temperature and mechanical stresses. With respect to pure homogeneous polymers, the degradation of polymer blends shows distinct features because of the possible interaction between the different chemical species. These interaction can give rise to both a faster degradation or to the formation of copolymers which act as stabilizing agents. This latter phenomena is particularly important in the processing of condensation polymers

Composite membranes of aromatic-polyamide for desalination: Membrane preparation and characterization.

1987

A new reverse osmosis composite membrane composed of the following aromatic polymer was estudied. Composite membranes were successfully prepared from PTDS by the conventional phase-inversion method. A typical example of the basic membrane performances is as follows; water flux, 440 1/m2 day and salt rejection, 97.7% determined under the pressure of 40 atm., using 0.1% NaCl solution at 25 °C. The PTDS membrane was characterized by its excellent chemical and thermal resistances, especially against acid, alkali and oxidative atmospheres. These features suggest that the PTDS membrane is a promising candidate for water desalination.

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…