溶聚丁苯橡胶聚合溶液粘度的研究

研究了（乙二醇二甲醚、二乙二醇二甲醚）－正丁基锂－抽余油体系地溶聚乙苯橡胶不同聚合时间聚合溶液粘度的变化，发现聚合溶粘度与活性种的活性有关，高温严重破坏活性种的活性，计节剂量是杀死活性种活性的另一因素。同时考察了不同苯乙烯／丁二烯（S／B）体系，正丁基锂引发剂用量对聚合粘影响规律，发现S／B越大，聚合粘度越小，S／B越小，聚合粘度越大，引发剂用量减少，聚合液粘度增大。     

Synthesis and characterization of radiation grafted copolymer for removal of nonionic organic contaminants

Nonionic organic contaminants such as phenol, benzene, and toluene from contaminated wastewater on laboratory scale can be effectively sorbed by cellulosic wood pulp sheet incorporated with three polar functional groups. The synthesis was carried out by graft copolymerization reaction of N,N‐dimethylaminoethylmethacrylate with methacrylic acid onto wood pulp. The preparation conditions at which the grafting process proceeds homogeneously are determined. Characterization and some selected properties of the original and grafted wood pulp were evaluated using FTIR and scanning electron microscope, also, the removal of phenol, benzene, and toluene on laboratory scale was investigated by using gas chromatography. It was found that phenol shows the highest removal percent than that of benzene and toluene. The efficiency of removal of the nonionic contaminants is found to be 97%, which shows a great promise for its applicability in the removal of organic contaminates from wastewater. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 3589–3595, 2006     

Role of mixing parameters in the preparation of poly(ethylene vinyl acetate) nanocomposites by melt blending

Polymer/layered‐silicate nanocomposites have gathered momentum as cost‐effective and versatile materials since the middle of the 20th century. Many publications discuss the chemistry of organomodification and properties of nanocomposites, but relatively few deal with the significance of processing conditions. This article takes into account three mixing parameters and discusses the contribution of each toward nanocomposite formation. Organomodified natural sodium‐type bentonite clay was used in this study. The nanocomposites formed were characterized by X‐ray diffraction and mechanical property tests. Response surface regression was used to optimize the tensile modulus. The analysis shows that nanocomposite formation is promoted by a diffusion mechanism and that the interactions of parameters are as important as individual parameters. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 2652–2658, 2006     

Effect of polymerization conditions on o‐phenylenediamine and o‐phenetidine oxidative copolymers

A series of new o‐phenylenediamine (OPD)/o‐phenetidine (PHT) copolymers with partly phenazine‐like structures has been successfully synthesized at three polymerization temperatures by chemically oxidative polymerization in four different polymerization media. The molecular structures and properties of the resulting OPD/PHT polymers were investigated by IR, UV–vis and high‐resolution ¹H NMR spectroscopies, and DSC, in order to ascertain the effect of reaction temperature, comonomer ratio and acid medium. The copolymerization mechanism of OPD with PHT monomers has been proposed. It is found that the statistical OPD/PHT copolymer obtained at a temperature of 118 °C has a higher degree of polymerization than that obtained at 12–17 °C. The OPD content in the copolymers calculated from NMR spectroscopic analysis is higher than that in the feed OPD content, whereas the OPD content calculated from element analysis is slightly lower than the feed OPD content. It can be predicted that denitrogenation takes place in the OPD units during the polymerization process at OPD/PHT molar ratios of 90/10 and 100/0. These OPD/PHT copolymers exhibit a much better solubility than the OPD homopolymer, hence suggesting an incorporation of PHT units into the phenazine structure of the homopolymer. The thermal behavior of the copolymers was also studied. Copyright © 2004 Society of Chemical Industry     

Entanglement network and relaxation temperature dependence of single‐site catalyzed ethylene/1‐hexene copolymers

In this work, we investigate the linear viscoelastic response of high molecular weight ethylene/1‐hexene copolymers, characterized by a narrow molecular weight distribution and comonomer content in the range from 0 to 10 mol %. A variation in the entanglement plateau modulus has been found in agreement with the recently developed packing length model. The packing model applied to viscoelastic data suggests decreased values of the characteristic ratio, accordingly with recent computer simulation results. The flow activation energy increases as the side chain content increases. This feature is thought to be related to the mobility of the molecules. The presence of side branches due to the comonomer hinders the mobility of the molecules, and increases the thermal barrier for the segmental motion. Then in the comonomer content range studied, the increase of the flow activation energy goes parallel with a decrease in the characteristic ratio. This result suggests that more parameters than only the stiffness of the chain modulate the thermal dependence of viscoelastic properties. A more refined study is necessary combining experiments with computer simulations in order to elucidate these aspects. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Furan–thiophene copolymers: Electrosynthesis and electrochemical behavior

The electrochemical copolymerization of furan and thiophene was performed at a constant electrode potential in a binary solvent system consisting of boron trifluoride/ethyl ether and an additional amount of ethyl ether (molar ratio = 1 : 2). The obtained homopolymers and copolymers were characterized with cyclic voltammetry and infrared spectroscopy. The influence of the applied electropolymerization potential and the monomer feed ratio of furan and thiophene on the copolymers was investigated. The furan–thiophene copolymers showed good stability of the redox activity in an acetonitrile‐based electrolyte solution. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2008     

Preparation of branched polyacrylonitrile through self‐condensing vinyl copolymerization

Branched polyacrylonitrile (PAN) was prepared through a self‐condensing vinyl copolymerization of acrylonitrile and 2‐(2‐bromopropionyloxy)ethyl acrylate (BPEA). The branched architecture of the product was confirmed by NMR spectra and the average degree of branching (DB ) was estimated. Through a comparison of the intrinsic viscosity of the product with that of its linear analogue, the contraction factor g′ was calculated. It was found that the viscosity of the branched PAN was obviously lower that that of linear PAN. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

NMR studies of poly(2-hydroxy ethyl methacrylate-co-2-vinyl pyridine)

Copolymers of 2-hydroxy ethyl methacrylate-2-vinyl pyridine (H/V) of different composition were synthesized by free radical bulk polymerization using azobisisobutyronitrile (AIBN) as an initiator under nitrogen atmosphere. The copolymer compositions were calculated from ¹H NMR spectra. The reactivity ratios for H/V copolymers obtained from a linear Kelen-Tudos method (KT) and nonlinear error-in-variables method (EVM) are r_H = 0.50 ± 0.10, r_V = 1.04 ± 0.08 and r_H = 0.55, r_V = 1.06 respectively. The complete spectral assignment of methine, methylene, methyl, carbonyl, and aromatic carbon regions in term of compositional and configurational sequences of H/V copolymers were done with the help of ¹³C{¹H} NMR, distortionless enhancement by polarization transfer (DEPT), two-dimensional heteronuclear single quantum coherence (HSQC) along with total correlated spectroscopy (TOCSY). © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008