Search results for "Plastics"
showing 10 items of 2724 documents
Kinetic treatment of slow initiation in living carbocationic polymerization and investigation of benzyl halides as initiators for the polymerization …
1998
In contrast to earlier conclusions it is demonstrated that kinetic analysis of incremental monomer addition (IMA) experiments for living carbocationic polymerizations with slow initiation leads only to the ratio of apparent rate constants of initiation and propagation. The apparent rate constants depend on the true (bimolecular) rate constants and on the positions of the equilibria between dormant and active states of initiator and polymer chain ends, respectively. The same considerations are true for other living processes involving dormant species, e.g., group transfer polymerization or controlled radical polymerization. Slow initiation of living carbocationic polymerization of isobutylen…
Synthesis of linear and three-arm star tert-chlorine-telechelic polyisobutylenes by a two-step conventional laboratory process
1997
A two-step conventional laboratory process was developed for the synthesis of mono- and difunctional linear and three-arm star tert-chlorine-telechelic polyisobutylenes (PIB) with desired molecular weights (MW) and narrow molecular weight distribution (MWD) by living carbocationic polymerization (LCCP). This polymerization method applies easy to handle operations and chemicals. LCCP of isobutylene (IB), was carried out in CH2Cl2 as solvent and with BCl3 as coinitiator in the first step to obtain soluble low MW PIB prepolymer with narrow MWD. This was followed by addition of hexane, TiCl4 and additional monomer in the second step to prepare PIBs with desired MW and narrow MWD in practically …
Endfunctional Polymers by Functionalization of Living Cationic Chain Ends with 1,1-Diphenylethylene
1995
Abstract A new functionalization method has been developed for the synthesis of 2,2-diphenylvinyl(DPV)-telechelic polyisobutylene (PIB). First, living carbocationic polymerization (LCCP) of isobutylene (IB) is quantitatively end-quenched with a nonpolymerizable olefin, 1,1-diphenylethylene (DPE). This process yields a mixture of diphenyl substituted vinyl and tertiary chlorine endgroups. Treatment of the resulting polymer with potassium-tert-butoxide (tBuOK) leads to the quantitative formation of DPV-telechelic PIB which is a potential macroinitiator precursor for living anionic polymerizations.
Bioadhesive Matrix Tablets Loaded with Lipophilic Nanoparticles as Vehicles for Drugs for Periodontitis Treatment: Development and Characterization
2019
Periodontitis treatment is usually focused on the reduction or eradication of periodontal pathogens using antibiotics against anaerobic bacteria, such as metronidazole (MTR). Moreover, recently the correlation between periodontal diseases and overexpression of reactive oxygen species (ROS) led to the introduction of antioxidant biomolecules in therapy. In this work, bioadhesive buccal tablets, consisting of a hydrophilic matrix loaded with metronidazole and lipophilic nanoparticles as a vehicle of curcumin, were developed. Curcumin (CUR)-loaded nanostructured lipid carriers (NLC) were prepared using glycyrrhetic acid, hexadecanol, isopropyl palmitate and Tween®
Binding of Short Alkyl Chain Surfactants to the (Ethylene oxide)13−(Propylene oxide)30−(Ethylene oxide)13and (Ethylene oxide)75−(Propylene oxide)30−(…
2002
The enthalpy of transfer (ΔHt) of neutral copolymers, at a fixed and low concentration ca. 10-3 mol kg-1, from water to the aqueous surfactant solutions as a function of the surfactant concentration (fSmS) was determined at 25 °C. The surfactants studied are sodium octanoate, sodium decanoate, N-octylpyridinium chloride (OPC), and N,N-dimethyloctylamine-N-oxide (ODAO). The copolymers are (ethylene oxide)13−(propylene oxide)30−(ethylene oxide)13 (L64) and (ethylene oxide)75−(propylene oxide)30−(ethylene oxide)75 (F68). The two copolymers show different hydrophilic−hydrophobic ratios, the larger being for F68. As a general feature, the shape of the ΔHt vs fSmS curve depends on the nature of t…
Studies of host-guest thin films of corona-poled betaine-type polar molecules by kelvin probe technique and atomic force microscopy
2004
In this work betaine-type molecules were investigated. As a result of the asymmetry of charge distribution, molecules possess in the ground state a considerable permanent dipole moment. The decay of surface potential of poled polymer films is dependent at least on two relaxation processes. The influence of glass transition of PMMA on thermal dependence of the surface potential is shown. The transition temperature, where no changes of the surface potential appeared, is related to glass transition temperature of the host-guest system. The topography of the film surface was obtained by AFM.
Hydrophilic and Hydrophobic Polymeric Derivatives of Anti-Inflammatory Agents Such as Alclofenac, Ketoprofen, and Ibuprofen
1991
Macromolecular prodrugs of a hydrophilic polymer [α,β-poly( N- hydroxyethyl)-DL-aspartamide (PHEA)] was used as a drug carrier. Three poly- (HEA)-NSAID adducts were studied: poly(HEA)-Alclofenac, poly(HEA)-Keto profen, and poly(HEA)-Ibuprofen. Prodrugs with different drug content were synthesized both as water-soluble and water-insoluble agents. Hydrolysis of water-soluble adducts in a simulated gastric juice was studied.
Polymerization reactions and modifications of polymers by ionizing radiation
2020
International audience; Ionizing radiation has become the most effective way to modify natural and synthetic polymers through crosslinking, degradation, and graft polymerization. This review will include an in-depth analysis of radiation chemistry mechanisms and the kinetics of the radiation-induced C-centered free radical, anion, and cation polymerization, and grafting. It also presents sections on radiation modifications of synthetic and natural polymers. For decades, low linear energy transfer (LLET) ionizing radiation, such as gamma rays, X-rays, and up to 10 MeV electron beams, has been the primary tool to produce many products through polymerization reactions. Photons and electrons in…
What Limits the Molecular Weight and Controlled Synthesis of Poly(3-alkyltellurophene)s?
2016
Polytellurophenes are an emerging class of conjugated polymers; however, their controlled polymerization leading to high molecular weight materials has been a major challenge. Here we present a systematic investigation of the synthesis of poly(3-alkyltellurophene)s using the catalyst transfer polycondensation methodology. Learning that previous syntheses were limited by both polymerization reaction kinetics and polymer solubility, we design new tellurophene monomers to overcome these limitations. Controlled polymerization behavior up to Mn = 25 kDa, chain extension, block copolymerization, external initiation, and well-defined end groups are demonstrated for poly(3-alkyltellurophene)s with …
Branched and Functionalized Polybutadienes by a Facile Two-Step Synthesis
2008
Anionic polymerization was used to prepare silane-endfunctionalized polybutadiene macromonomers with different molecular weights ranging from 9 000 to 34000 g .mol- 1 . These were polymerized by a hydrosilylation reaction in bulk to obtain branched polymers, using Karstedt's catalyst. Surprisingly, the addition of monofunctional silanes during the polymerization showed only a minimal effect concerning the degree of polymerization. Furthermore, it was possible to introduce a variety of functional silanes without increasing the overall number of reaction steps by a convenient AB 2 + A type "pseudocopolymerization" method. All branched polymers were analyzed by SEC, SEC-MALLS, SEC-viscosimetry…