盐浓度对交联聚合物线团形态的影响

用核孔膜过滤法 (过滤体积对过滤时间作图 )、动态光散射法 (DLS)和扫描电镜法 (SEM )研究了交联反应前后盐 (NaCl)浓度变化对低浓度HPAM与AlCit形成的交联聚合物溶液 (LPS)中交联聚合物线团 (LPC)形态的影响。所用HPAM相对分子质量 1.1× 10 7～ 1.4× 10 7,LPS中HPAM与Al的质量比 2 0∶1,HPAM浓度 0 .1或 0 .2 g/L ,交联反应温度 40℃ ,时间 7天。实验结果表明 :①LPC的平均水力半径Rh(DLS测定值 )随交联反应时盐浓度的增大先减小后增大 ,盐浓度由 0 .5 g/L增加到 2 g/L时Rh 由 45 0nm迅速减小到 2 5 0nm ,盐浓度增加到 2 0 g/L时Rh达到最小值 16 0nm ,此后随盐浓度的继续增加Rh 有所增大 ;盐浓度 0 .5和 2 .0 g/L时Rh 的SEM测定值分别为45 0和 2 5 0nm ,与DLS结果一致。②交联反应完成后改变LPS的盐浓度 ,也可改变LPC的Rh 值 ,但改变幅度较小 ;盐浓度 0 .5 g/L时形成的LPS ,当盐浓度增加至 2 g/L时 ,Rh 值由 45 0nm减小至 35 9nm ,大于盐浓度 2 g/L时形成的LPS的Rh 值 (2 46nm) ;盐浓度 2 g/L时形成的LPS ,当盐浓度减少至 0 .5 g/L时 ,Rh 值由 2 46nm增大至32 6nm ,小于盐浓度 0 .5g/L时形成的LPS的Rh 值 (4 5 0nm)。用盐浓度改变引起LPC水化层厚度改变 ,线团收缩或舒张解释盐浓度改变时Rh 测定值的     

聚酯亚胺漆包线漆适度交联结构与性能研究

利用酯交换后亚胺化法合成180级聚酯亚胺漆包线漆。根据适度交联理论,探讨了配方中赛克含量和亚胺基含量对漆性能的影响,利用FTIR、GPC等对所制备的漆包线漆进行了分析与表征,并对所涂制的漆包线性能进行了分析检测。结果表明:合成的聚酯亚胺漆包线漆具有表面流平性好、击穿电压高、热冲击性能优越和软化击穿温度高等特点。     

聚氯乙烯化学交联方法的研究进展

综述了应用化学方法交联聚氯乙烯(PVC)的研究进展,着重介绍了过氧化物交联、硅烷交联、三嗪类化合物交联、化学微交联、共混交联等交联方法。并指出了这些交联方法中存在的问题和发展方向。     

Grafting maleic anhydride onto EVA and effect on the physical and rheological properties of PETG/EVA-g-MAH blends

Maleic anhydride (MAH) was grafted onto ethylene vinyl acetate copolymer (EVA) in the internal mixer in the presence of dicumyl peroxide (DCP), and a prepared reactive compatibilizer, MAH-g-EVA, was blended with Poly (ethylene glycol-co-cyclohexane-1,4-dimethanol terephthalate) (PETG). The gel content determination and element analysis (EA) was performed to confirm the grafting reaction. It was found that grafting reaction of MAH on to EVA could compete with crosslinking reaction of DCP during the modification process. In addition, the introduction of small amount of MAH showed a great effect on reducing gel content by decreasing crosslink reaction. As MAH content increased, grafted MAH concentration increased, whereas the grafting yield decreased. It was also confirmed that MAH-g-EVA acted as a reactive compatibilizer in the blend with PETG, and enhanced compatibility by reacting with the hydroxyl end groups, OH, of PETG. Addition of EVA in the blend leads a plastic deformation of PETG, and MAH had a great effect on enhancing interfacial adhesion resulting in significant increasing of % strain; however, improved compatibility could not be changed much in low strain tensile strength and Young's modulus. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Cholesteric monomer and elastomers containing menthyl groups: Synthesis and phase behavior

The synthesis of a new cholesteric monomer ( M_LC) containing menthyl groups and a series of cholesteric elastomers ( LCE₁−LCE₄ ) is described. Their chemical structures and purity were characterized by FTIR, ¹H-NMR, and elemental analyses. The phase behavior and thermal stability were investigated by differential scanning calorimetry, polarizing optical microscopy, X-ray diffraction, and thermogravimetric analysis. By inserting a flexible spacer between the mesogenic core and the terminal menthyl groups, mesomorphism of M _LC was realized. LCE₁−LCE₄ with low content of crosslinking unit exhibited cholesteric phase because of the introduction of the nematic crosslinking unit. This indicates that low levels of chemical crosslinking do not significantly affect the phase behavior and mesomorphism of the elastomers, and reversible mesophase transitions can be observed. In addition, with increasing the content of crosslinking unit, the corresponding T_g decreased for LCE₁−LCE₄ , whereas their T_i did not remarkable change. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Leachability of degradation products from hard chairside reline resins in artificial saliva: Effect of water‐bath post‐polymerization treatment

The effect of a post‐polymerization treatment on the leaching of methacrylic acid (MA) and benzoic acid (BA) from the reline resins [Kooliner (K), New Truliner (N), Ufi Gel hard (U), and Tokuso Rebase Fast (T)] was evaluated. Specimens of each material were divided into two groups: Group C (control) – left untreated; Group WB (water‐bath) – immersion in water at 55 ± 1°C for 10 min. Specimens were placed in artificial saliva at 37 ± 1°C and, after 1‐, 3‐, 5‐, 24‐h and 3‐, 7‐, 14‐, and 30‐day intervals, aliquots were removed and analyzed using high performance liquid chromatography. Data were analyzed by using Wilcoxon, Mann–Whitney or Kruskal–Wallis tests (α = 0.05). At 1 h, the concentration of MA released from U control specimens was higher than those of the other ones, and decreased after 3 h. WB specimens released lower amounts of MA than control specimens only for material U, at the 1‐ and 3‐h periods. For all control specimens, concentrations of leached BA progressively decreased within 5 h and from 24 h to the end. WB specimens released significantly lower amounts of BA than did the control groups. The highest concentration of MA was leached from control specimens of Ufi Gel hard. Water‐bath post‐polymerization treatment caused a significant reduction in elution of BA. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Characteristics of hemicelluloses obtained from sweet sorghum based on successive extractions

Hemicelluloses were successively extracted from sweet sorghum by hot water, dioxane, DMSO, and different concentrations of NaOH between 0.5% and 6.0%. The yields of the seven fractions together accounted for 88.6% of the original hemicelluloses. The obtained hemicellulosic subfractions were comprehensively investigated by both destructive methods such as alkaline nitrobenzene oxidation and acid hydrolysis and nondestructive techniques such as gel permeation chromatography, Fourier‐transform infrared, ¹³C‐nuclear magnetic resonance, and 2D‐heteronuclear singular quantum correlation. Sugar composition studies showed that the water‐soluble polysaccharides consisted mainly of glucose, while xylose, arabinose, and glucuronic acid were the major sugars in other hemicellulosic fractions. It was found that the hemicelluloses from sweet sorghum were l‐ arabino‐(4‐O‐methyl‐d‐ glucurono)‐xylans. Comparison with the hemicellulosic fractions dissolved by the alkali treatment, the hemicellulosic fraction extracted by DMSO had lower molecular weight. In addition, it was also found that the hemicelluloses prepared by dioxane and DMSO were more branched since that they had higher nonxylose/xylose ratios than those extracted by the alkali treatment, which were more linear and contained higher amounts xylose. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42790.     

Smart carboxymethylchitosan hydrogels that have thermo‐ and pH‐responsive properties

Thermo‐responsive poly(N‐isopropylacrylamide) (poly(NIPAAm)) and pH‐responsive poly(N,N′‐diethylaminoethyl methacrylate) (poly(DEAEMA)) polymers were grafted to carboxymethylchitosan (CMC) via radical polymerization to form highly water swellable hydrogels with dual responsive properties. Ratios of CMC, NIPAAm to DEAEMA used in the reactions were finely adjusted such that the thermo and pH responsiveness of the hydrogels was retained. Scanning electron microscopy (SEM) indicated the formation of an internal porous structure for the swollen CMC hydrogels upon incorporation of poly(NIPAAm) and poly(DEAEMA). Effect of temperature and pH changes on water swelling properties of the hydrogels was investigated. It was found that the water swelling of the hydrogels was enhanced when the solution pH was under basic conditions (pH 11) or the temperature was below its lower critical solution temperature (LCST). These responsive properties can be used to regulate releasing rate of an entrapped drug from the hydrogels, a model drug, indomethacin was used to demonstrate the release. These smart and nontoxic CMC‐based hydrogels show great potential for use in controlled drug release applications with controllable on‐off switch properties. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41505.