Synthesis,characterization and properties of functionalized styrene–maleimide copolymers

New functionalized styrene–maleimide copolymers were prepared by free radical copolymerization of styrene (St) and N‐4‐carboxybutylmaleimide (NBMI) in chloroform, using 2,2′‐azobisisobutyronitrile (AIBN) as initiator. Monomer and copolymer characterization was carried out by ¹H‐ and ¹³C‐NMR. Copolymer composition was determined by elemental analysis and Fourier‐transform infrared (FTIR) spectroscopy. The glass transition temperature (from DSC) and the thermogravimetric analysis (TGA) of the copolymers were consistent with the thermal behavior and stability observed for alternating St–maleimide copolymers. St–NBMI copolymers crosslinked with divinylbenzene (DVB) were also synthesized and their cation exchange properties evaluated in order to assess the capacity of the new copolymers to bind metallic ions. Copyright © 2005 Society of Chemical Industry     

PAA-PSF交联复合膜的制备及对低浓度有机醇水溶液反渗透分离性能研究

进行了ＰＡＡ（ＰｏｌｙａｃｒｙｌｉｃＡｃｉｄ）－ＰＳＦ（Ｐｏｌｙｓｕｌｆｏｎｅ）交联复合膜的制备，研究了交联剂、添加剂对膜性能的影响，并通过扫描电镜观察了膜的断面结构．研究了ＰＡＡ－ＰＳＦ交联复合膜对低浓度有机醇类水溶液反渗透分离性能．发现对于１０００×１０－６乙醇水溶液截留率达到６６．２％，透过流束可达０．９×１０－６（ｍ３·ｍ－２·ｓ－１）．随醇的分子量的增加，截留率不断上升，对戊醇的截留率达９４．３％，而透过流束则保持相对稳定．对不同结构醇类的分离性能研究表明，截留率存在有：ｔｅｒｔ－＞ｓｅｃ－＞ｉｓｏ－＞ｎ－的规律．     

Calorimetric determination of the enthalpy change for the binding of methyl orange to poly(vinylpyrrolidone) in aqueous solution

Thermodynamic parameters have been determined for the interaction of methyl orange and poly(vinylpyrrolidone) in aqueous solutions containing tris, tris and hydrochloric acid, or water only. Enthalpy changes were determined by use of a flow microcalorimeter. Free energy changes were calculated from the results of equilbrium dialysis studies. The results are interpreted in terms of the behaviour of poly(vinylpyrrolidone) in these systems. Analysis of data shows that the hydrophobic interactions in the systems are in the order: tris > wateronly > tris-HC1.     

Surface tailoring of an ethylene propylene diene elastomeric terpolymer via plasma‐polymerized coating of tetramethyldisiloxane

In the research presented here, we explore the use of a low‐energy plasma to deposit thin silicone polymer films using tetramethyldisiloxane (TMDSO) (H(CH₃)₂? Si? O? Si? (CH₃)₂H) on the surface of an ethylene propylene diene elastomeric terpolymer (EPDM) in order to enhance the surface hydrophobicity, lower the surface energy and improve the degradation/wear characteristics. The processing conditions were varied over a wide range of treatment times and discharge powers to control the physical characteristics, thickness, morphology and chemical structure of the plasma polymer films. Scanning electron microscopy (SEM) shows that pore‐free homogeneous plasma polymer thin films of granular microstructure composed of small grains are formed and that the morphology of the granular structure depends on the plasma processing conditions, such as plasma power and time of deposition. The thicknesses of the coatings were determined using SEM, which confirmed that the thicknesses of the deposited plasma‐polymer films could be precisely controlled by the plasma parameters. The kinetics of plasma‐polymer film deposition were also evaluated. Contact angle measurements of different solvent droplets on the coatings were used to calculate the surface energies of the coatings. These coatings appeared to be hydrophobic and had low surface energies. X‐ray photoelectron spectroscopy (XPS) and photoacoustic Fourier‐transform infrared (PA‐FT‐IR) spectroscopy were used to investigate the detailed chemical structures of the deposited films. The optimum plasma processing conditions to achieve the desired thin plasma polymer coatings are discussed in the light of the chemistry that takes place at the interfaces. Copyright © 2004 Society of Chemical Industry     

吸水膨胀型膨润土/交联聚丙烯酰胺颗粒堵剂

使丙烯酰胺、少量N，N-亚甲基双丙烯酰胺在钙膨润土存在下进行水溶液引发接枝共聚合，聚合产物经造粒、粉碎、筛分，得到粒径0．5～1．0mm的颗粒堵剂。根据颗粒堵剂吸水量大小确定丙烯酰胺与膨润土最佳质量比为7：1，引发剂最佳用量为500g／t，交联剂最佳用量为300g／t，吸水量与这3个参数之间的关系曲线都经过最大值，颗粒堵剂在去离子水中的吸水量为560～650mL/g。该堵剂已大规模生产，在胜利、中原油田许多采油厂已用于调剖、堵水和调驱施工，在青海、江苏、大港、冀东等油田也已开始使用。在胜利东辛采油厂的一个井组，连续3个月在3口井注入该堵剂共27t，使井口压力上升3MPa，产油量大幅度增加。表l参l。     

F2.4微孔膜的制备及在膜蒸馏过程中应用的初步研究

采用相转化法制备了F2 4的疏水微孔膜 ,并对F2 4和PVDF微孔膜的机械性能以及疏水性等方面进行了对比 .结果表明 ,F2 4微孔膜在拉伸时的应变以及断裂伸长率约为PVDF微孔膜的 6～ 9倍 ;其接触角 (77 4°)也大于PVDF膜的接触角 (6 6 7°) .尽管膜蒸馏的数据显示F2 4微孔膜的蒸馏通量尚不及PVDF膜 ,但通过调节各项制膜参数 ,F2 4可能具有良好的应用前景     

Dyestuff—fibre interactions

The strength and nature of dye–fibre interactions vary according to fibre type and dye type. In the case of acid dyes for polyamide fibres, cationic dyes for acrylic fibres, disperse dyes for hydrophobic fibres, and direct dyes for cellulosic fibres, these interactions may be classified as non-covalent, a classification which includes van der Waals (VDW), electrostatic, induction, solvophobic and charge-transfer interactions.
Reactive dyes are a notable exception to the above, since the interaction which is responsible for their excellent wet fastness is the dye–fibre covalent bond, however, these dyes are increasingly viewed as environmentally unfriendly due to high salt usage and residual unfixed colour. This situation may be improved by either incorporating amine sites in the cellulose or by reversing the system to incorporate reactive residues in the fibre and nucleophilic sites in the dye.
Nonionic disperse dyes are valuable for hydrophobic fibres such as polyester but have made little impact on hydrophilic fibres such as silk, wool and cotton. Experiments to develop simple treatments to render the latter fibres disperse dyeable are described and the combined role of solvophobic and – interactions discussed.     

动态交联热塑性弹性体增韧聚丙烯合金

用动态交联方法制备聚烯烃热塑性弹性体（ＴＰＯ）增韧聚丙烯，制备了具有低温冲击性能良好、综合力学性能比较均衡的聚丙烯合金。同时，研究了ＴＰＯ组成、工艺及基体组成与ＴＰＯ增韧聚丙烯共混物力学性能的关系。并通过差热扫描量热计和扫描电镜考察了共混物的形态结构。