甲基丙烯酸甲酯/丙烯酸丁酯的无皂乳液共聚

以甲基丙烯酸甲酯(MMA)和丙烯酸丁酯(BA)为主要原料,过硫酸铵为引发剂,进行无皂乳液聚合.结果表明:在不添加乳化剂的情况下,当MMA/BA=1:1、引发剂用量为0.24%、反应温度为80℃、反应时间8.0h时,所得乳液最稳定,单体转化率为81.84%,此无皂乳液对牛皮纸的粘接性比常规乳液好.     

无皂乳液聚合制备含氟温敏型微凝胶

在微波辐射下,采用无皂乳液聚合方法,制备了稳定的含氟N-异丙基丙烯酰胺(FA-NIPAAm)温度敏感型微凝胶乳液.利用FT-IR表征了微凝胶的化学组成;采用激光光散射粒度仪(PCS)研究了微凝胶粒径在不同温度的变化,测定了微凝胶的低临界溶解温度(LCST);用透射电子显微镜(TEM)观察了微凝胶的形貌;考察了微凝胶乳液...     

Synthesis and characterization of two new vinyl groups containing alkoxysilanes and their uses in the vinyl acetate/2-ethylhexylacrylate copolymer latexes

The incorporation of alkoxysilanes into latex systems is of major interest in the field of colloidal science. Two novel vinyl-containing alkoxysilanes, 3-(trimethoxysilyl) propylthiomethacrylate (TMSPTM) and methacryloxyethyl triethoxysilylpropylcarbamate (METESPC) were prepared by the condensation reaction of methacryloyl chloride (MC) with (3-mercaptopropyl)-trimethoxysilane (MPTMS) and addition reaction of 2-hydroxyethyl methacrylate (HEMA) with (3-isocyanatopropyl) triethoxysilane (ICPTES), respectively. Then these monomers were copolymerized with vinyl acetate and 2-ethylhexylacrylate (VAc/2-EHA) by seeded emulsion polymerization, and copolymer latexes were obtained. One kind of vinyl-containing alkoxysilane, the triethoxyvinylsilane (TEVS) has been used as coupling reagent for comparison of the effects of alkoxysilane types on the latexes. The structural elucidation of monomers was carried out by FT-IR, ¹H NMR, and ¹³C NMR spectroscopic techniques. The VAc/2-EHA copolymer latexes with TMSPTM or MPTMS were also characterized by FT-IR. The thermal stability of copolymers was respectively studied by thermogravimetric analysis (TGA) and dynamic mechanical thermal analysis (DMTA). The morphologies of the latexes were characterized with scanning electron microscopy (SEM).     

环氧-丙烯酸酯杂化乳液的制备及其涂膜性能的研究

采用一种特制的齿状搅拌头(简称STB搅拌头),在600 r/min的转速下均质化,成功制备了环氧-丙烯酸酯杂化"细乳液".然后用傅里叶红外光谱(FTIR)、激光光散射粒径仪(PCS)及透射电镜(TEM)对乳液的相关性能进行了表征.结果表明:杂化乳液的聚合稳定性和储存稳定性优异,且其涂膜的耐水性、附着力和耐磨性能良好.     

橡胶粒子尺寸对ABS树脂性能的影响

通过乳液聚合制备了橡胶粒子尺寸为64～420 nm的丙烯腈-丁二烯-苯乙烯(ABS)共聚物.然后将其与SAN-T树脂熔融共混制备橡胶质量分数为15%的ABS树脂.研究了橡胶粒子尺寸对ABS树脂力学性能影响和材料内部形态结构.结果表明:随着橡胶粒子尺寸的增加ABS树脂的冲击韧性提高.当橡胶粒子尺寸在320 nm时,拉伸强度达到最大,ABS树脂的综合性能达到最好.粒子尺寸在64～110 nm时,橡胶粒子在基体内部发生团聚,材料发生脆性断裂.当橡胶粒子尺寸在216～420 nm时,材料主要以韧性断裂为主,发生脆韧转变.具有双峰分布ABS-110nm/ABS-275 nm共混物大、小橡胶粒子间发生明显的协同作用.     

Transitional emulsion polymerisation: Zero-one to pseudo-bulk

The transitional behaviours of emulsion polymerisation for styrene and butyl acrylate (BA) monomers from zero-one to pseudo-bulk regime were mechanistically investigated. A dynamic mathematical model, which incorporates cross-over mechanism from zero-one to pseudo-bulk kinetics was developed for emulsion polymerisation and compared with experimental data for conversion, particle size and molar mass. Particles smaller than cross-over size follow zero-one kinetics and particles greater than cross-over size, they follow pseudo-bulk kinetics. In our mechanistic approach, particles nucleated from micelles, grow until the cross-over size is attained, based on zero-one kinetics, and subsequently continue to grow based on pseudo-bulk kinetics. Key findings from our work are that the developed transitional model predictions agree reasonably with experimental data on process and product attributes such as conversion, average molecular weight, molecular weight distribution (MWD), average particle size and particle size distribution (PSD). Optimal strategies for semibatch operation was developed using reaction temperature and monomer feed rate as process variables with specified initial conditions.     

Electrochemical copolymerization of thiophene derivatives; a precursor to photovoltaic devices

This work presents an electrochemical technique for the polymerization and copolymerization of thiophene derivatives like 7,9-dithiophene-2yl-8H-cyclopenta[a]acenaphthalene-8-one and 3-hexylthiophene. The structural characterization of chemically synthesized monomers and electrochemically synthesized polymers was carried out by nuclear magnetic resonance and Fourier transform infrared spectroscopy. Thermal characterizations indicate that copolymer has increased thermal stability than that of homopolymer. Morphological studies of the polymerized films carried out by scanning electron microscopy shows network structure of copolymer. Optical properties of the homopolymers and copolymer were studied by UV–visible spectrometer and it was observed that band gap of copolymer is less than the homopolymers. HOMO and LUMO levels, band gap values of the respective polymers were also calculated from the cyclic voltammetry technique with various scan rates. By the peak current obtained from various scan rates shows that all polymerization reactions are diffusion controlled process. Charge transfer resistances of polymers were determined using Nyquist plots. Conductivity of synthesized polymers shows higher conductivity for copolymer than homopolymers.     

Expression for turbulent power draw of an in-line Silverson high shear mixer

We report the validation of an expression to accurately describe the power draw of an in-line rotor–stator mixer over a range of flow rates and rotor speeds. The expression consists of a term which reflects the power required to rotate the shaft in response to the liquid resistance and a term to reflect the power convected away from the mixing chamber. A specially commissioned high speed (12,000 rpm), instrumented 150/250 MS Silverson mixer has been developed with power draw determined from both torque and calorimetric measurements. Experiments are carried out using water over a range of independently controlled flow rates and rotor speeds with losses for both techniques carefully accounted for. For the torque measurement the value of the constants for the two terms above are Po_z=0.197 and k₁=9.35, respectively. For the calorimetric technique the measured temperature rise was similar to some of the corrections and losses over a significant range of the experimental space but nevertheless with careful experimentation constants similar to those for the torque technique were obtained, Po_z=0.229 and k₁=7.46. Allowing the calibration of the temperature probes to be a fit parameter in the regression routine increased the value of k₁=8.10 but did not affect the value of Po_z. A simple graphical method is also proposed using a dimensionless form of the expression which yielded slightly higher value of Po_z but a slightly lower value of k₁. The accuracy of both measurement techniques improves with rotor speed and the differences between the constants is attributed to the better accuracy of the torque technique at higher flow rates whereas the calorimetric technique is more accurate at low flow rates where the temperature rise is larger. Several repeats of the calorimetric technique with a reduced set of experimental points show good reproducibility. Finally at low flow rates (<10% of the maximum) the power unexpectantly increases and a modification to the expression is proposed by considering the pumping efficiency.     

Dynamic modeling of gas phase propylene homopolymerization in fluidized bed reactors

A new model with comprehensive kinetics for propylene homopolymerization in fluidized bed reactors was developed to investigate the effect of mixing, operating conditions, kinetic and hydrodynamic parameters on the reactor performance as well as polymer properties. Presence of the particles in the bubbles and the excess gas in the emulsion phase was considered to improve the two-phase model, thus, considering the polymerization reaction to take place in both the bubble and emulsion phases. It was shown that in the practical range of superficial gas velocity and catalyst feed rate, the ratio of produced polymer in the bubble phase to the total production rate is roughly between 10% and 13%, which is a substantial amount and cannot be ignored. Simulation studies were carried out to compare the results of the improved two-phase, conventional well-mixed and constant bubble size models. The improved two-phase and well mixed models predicted a narrower and safer window at the same running conditions compared with the constant bubble size model. The improved two-phase model showed close dynamic behavior to the conventional models at the beginning of polymerization, but starts to diverge with the evolution of time.     

聚丙烯装置三元共聚产品生产可行性分析及展望

通过对聚丙烯三元共聚产品、市场现状分析及国内聚丙烯装置三元共聚产品生产现状介绍引出对抚顺石化公司乙烯化工厂聚丙烯装置三元共聚产品生产可行性分析,并提出抚顺聚丙烯装置三元共聚生产改造方案及目前项目进展情况,