共查询到17条相似文献,搜索用时 62 毫秒
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用甲基丙烯酸甲酯(MMA)作油相,反相胶束微乳液作为模板,制备了纳米氯化银(AgCl)粒子,再进行原位聚合制备了纳米氯化银/聚甲基丙烯酸甲酯(AgCl/PMMA)复合材料.透射电镜(TEM)分析表明,纳米AgCl的尺寸为20~80 nm.扫描电镜(SEM)测试表明纳米AgCl粒子均匀地存在于PMMA基材中.红外分析证明,胶束中水和表面活性剂AOT的羰基在MMA聚合后微观环境发生变化,纳米粒子同聚合物之间有吸附行为.动态力学(DMTA)分析复合材料,发现纳米AgCl粒子与聚合物之间存在强烈相互作用,形成了中间相层(interphase layer),改变了聚合物的动态力学性能. 相似文献
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通过将烯丙基溴/高氯酸银引发体系引发四氢呋喃活性正离子开环聚合与"grafting onto"合成方法相结合,原位制备了不同接枝密度和接枝链长度的新型聚醋酸乙烯酯-g-聚四氢呋喃接枝共聚物(PVAc-g-PTHF)及其与纳米银(Ag)的复合材料.采用傅里叶变换红外光谱(FTIR)、核磁共振波谱(1H-NMR)和多角度激光光散射-黏度-凝胶渗透色谱仪(MALLS-VIS-GPC)分别表征了该接枝共聚物的化学结构、共聚组成、分子量、分子量分布、接枝支链数目及支化度,采用原子力显微镜(AFM)、示差扫描量热分析(DSC)、偏光显微镜(POM)研究了接枝共聚物中接枝支链数目及支链长度对其微观形态、单端受限链段结晶行为的影响,并探讨了该纳米复合材料的抗菌性能.结果表明:所制备的不同支链数目和支链长度的PVAc-g-PTHF/Ag纳米复合材料,均表现出良好的抗菌性能;接枝共聚物PVAc-g-PTHF的重均分子量可达4.52×10~5,分子分子量较窄(M_w/M_n~1.8),支化因子可达0.19.接枝共聚物PVAc-g-PTHF可形成明显的相分离结构,其微观形态与接枝支链数目有关;相比相同分子量的双端不受限的PTHF链,PVAc-g-PTHF接枝共聚物中单端受限PTHF支链的结晶速率明显降低;在确定接枝支链数目的情况下,随着支链中PTHF链段长度增加,其结晶逐渐增强,结晶熔融温度及熔融焓均稍有增加. 相似文献
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利用聚合物乳液合成聚甲基丙烯酸甲酯/二氧化硅纳米杂化材料 总被引:10,自引:0,他引:10
通过正硅酸乙酯分别在聚甲基丙烯酸甲酯乳液和四氢呋喃溶液中的溶胶-凝胶反应制备出不同的聚甲基丙烯酸甲酯/二氧化硅复合材料。利用扫描电镜、透镜电镜、差热分析和热失重对试样进行了分析。结果表明,利用聚合物乳液可以获得纳米分散的聚甲基丙烯酸甲酯/二氧化硅复合材料,并且在某种程度上其分散尺度小于利用聚合物溶液获得的复合材料。同时,利用聚合物乳液来制备聚甲基丙烯酸甲酯/二氧化硅杂化材料更有利于凝胶过程中二氧化硅网络的形成。 相似文献
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SiO2交联剂交联MMA聚合制备PMMA/SiO2纳米复合材料 总被引:3,自引:0,他引:3
用SiO2交联剂(SiO2HPA)交联甲基丙烯酸甲酯(MMA)自由基聚合制备PMMA SiO2纳米复合材料。采用两步法将可聚合乙烯基单体以化学键的形式键接到SiO2表面合成SiO2交联剂,首先利用过量的甲苯2,4二异氰酸酯(TDI)对SiO2纳米粒子表面进行化学修饰合成出表面带有高反应活性NCO基团的功能化SiO2粒子(SiO2TDI),SiO2TDI与丙烯酸羟丙酯(HPA)反应合成SiO2交联剂。系统研究了MMA单体与SiO2交联剂投料比及聚合时间对聚合反应的影响。此外,利用红外光谱(FT IR)、DSC、TGA、可见光光谱仪等实验手段对纳米复合材料进行了表征分析。结果表明,纳米SiO2粒子在复合材料中起着物理交联点和化学交联点作用,复合材料玻璃化转变温度(Tg)明显地高于其纯PMMA的玻璃化转变温度,随着纳米SiO2粒子含量的增加,复合材料玻璃化温度升高,而透明度明显降低。 相似文献
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SiO2/PVAc无机-有机复合微球的合成及其膜性能研究 总被引:1,自引:0,他引:1
以纳米二氧化硅粒子(SiO2)为稳定剂,在少量反应型阴离子乳化剂——烯丙氧基羟丙磺酸钠(HAPS)作助稳定剂的情况下,制备了具有草莓型结构的二氧化硅/聚醋酸乙烯酯(SiO2/PVAc)无机-有机纳米复合微球.研究表明,纳米SiO2与PVAc的氢键作用是形成这种单分散草莓型SiO2/PVAc无机-有机纳米复合微球的关键.透射电镜(TEM)观察显示,纳米SiO2吸附在PVAc表面,形成草莓型结构.讨论了纳米二氧化硅溶胶的种类和用量、乳化剂种类对复合微球形态及其膜性能的影响,并讨论了复合微球的形成机理. 相似文献
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采用高压剪切分散(HPSH)的方法先将纳米SiO2分散在合成聚氨酯原料中,再应用原位聚合的方法制备了纳米SiO2/聚氨酯复合树脂。 用热重分析、动态机械热分析(DMTA)和扫描电子显微镜等测试技术研究了纳米SiO2的用量及其分散方法对聚氨酯树脂的热稳定和力学性能的影响。 结果表明,二苯甲基二异氰酸酯(MDI)中的-NCO和纳米SiO2表面的-OH发生了化学反应,SiO2表面的包覆率约为7%;通过高压剪切分散的方法能够使纳米SiO2在聚氨酯基体中均匀的分散开来,粒径为30~40 nm,而超声处理的纳米SiO2会聚集约为200 nm聚集体。 当SiO2的添加质量分数为3%时复合树脂(HPSH处理SiO2)的拉伸强度和断裂伸长率均达到最大值,分别为84.3 MPa和438.7%。 此外,与纯树脂相比,复合树脂(4%纳米SiO2)的Tg、Td和T-50%分别增加了17.2、9和21 ℃。 相似文献
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以氯金酸为前驱体,十二烷基硫醇和硼氢化钠分别作为稳定剂和还原剂,采用相转移法制备了单分散的金纳米粒子.将金纳米粒子通过乳液聚合的方法制备了纳米金/聚苯乙烯复合粒子.通过紫外-可见吸收光谱(UV-Vis)研究了纳米金和纳米金/聚苯乙烯复合粒子的光吸收特性,使用傅立叶变换红外光谱(FT-IR)、X射线衍射(XRD)、透射电子显微镜(TEM)和动态光散射(DLS)对产物的组成、晶体结构、形貌、以及粒径进行了表征.结果表明,复合粒子为粒径分布较窄的球形,其中的金纳米粒子为面心立方结构.热失重分析(TGA)说明制备的纳米金/聚苯乙烯复合粒子具有很好的热稳定性. 相似文献
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采用溶胶-凝胶和浸渍-提拉而后煅烧的方法得到了在可见光作用下具有光催化性能的纳米ZnO/聚醋酸乙烯酯(PVAc)复合薄膜.通过正交设计实验,研究了PVAc的浓度、煅烧温度、煅烧时间、复合薄膜层数和附加ZnO膜层数等工艺因素对光催化性能的影响,并通过SEM,XRD和FT-IR对其进行了分析与表征.在室内普通照明用白炽灯作用下,以甲基橙溶液为催化对象,PVAc含量10%的、在250℃煅烧30min所得到的纳米ZnO/PVAe复合薄膜的光催化性能的实验结果表明,复合薄膜对甲基橙降解率达60%,而使用250℃煅烧30min所得到的纳米ZnO 4层薄膜或PVAc 4层薄膜催化的甲基橙溶液的浓度变化很小. 相似文献
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对用(NH4)2S2O8-环己酮NaHSO2加合物新型氧化还原体系引发的醋酸乙烯酯聚合过程进行研究,求得该聚合反应的表观活化能为84.6kJ/mol,并测定了聚合产物的粘均分子量. 相似文献
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Xinjian Cheng Min Chen Shuxue Zhou Limin Wu 《Journal of polymer science. Part A, Polymer chemistry》2006,44(12):3807-3816
A series of SiO2/PMMA composite particles with different morphologies were prepared by conventional emulsion polymerization by the aid of acid–base interaction between the silanol groups of unmodified silica particles and the amino groups of 4‐vinylpyridine. In this approach, no surface treatment for nanosilica particles was required. The morphologies of composite particles, for example, multicore–shell, raspberry‐like, and conventional core–shell, could be controlled by modulating emulsifier content, monomer/silica ratio, silica size, and monomer feed method. The possible particle formation mechanisms were discussed. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 3807–3816, 2006 相似文献
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Preparation of PEG-modified urethane acrylate emulsion and its emulsion polymerization 总被引:5,自引:0,他引:5
In order to improve stability and reduce droplet size, the PEG-modified urethane acrylates were synthesized by the reaction of polyethylene glycol (PEG) with residual isocyanate groups of urethane acrylate to incorporate hydrophilic groups into the molecular ends. The droplet sizes of the PEG-modified urethane acrylate emulsions were much smaller than those of unmodified urethane acrylate emulsions at the same surfactant composition, and the droplet sizes of these emulsions were significantly effected not by surfactant compositions and types, but by the reaction molar ratio of PEG, because the urethane acrylate containing polyoxyethylene groups as terminal groups aided the interfacial activity of surfactant molecules and acted as a polymeric surfactant. The actions of PEG-modified urethane acrylate were confirmed by the investigation of adsorption of urethane acrylate in a water/benzene interface.For polymerization of emulsions, the stability of emulsion in the process of emulsion polymerization was changed by the type of surfactant or initiator. In the case of emulsion polymerization with a water soluble initiator (K2S2O8), the emulsions prepared using TWEEN 60 were broken in the process of polymerization. However, polymerization of these emulsions could be carried out using an oil soluble initiator (AIBN). The conversion of emulsion polymerization changed with the type of urethane acrylates, that is, the reaction molar ratio of PEG to 2-HEMA. 相似文献
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Duk Ki Kim Kyung Wha Oh Seong Hun Kim 《Journal of Polymer Science.Polymer Physics》2008,46(20):2255-2266
The composite of polyaniline (PANI) and multiwall carbon nanotube carboxylated through acid treatment (c‐MWCNT) was synthesized by chemical oxidative polymerization in an inverse emulsion system. The resultant composites were compared with products from aqueous emulsion polymerization to observe the improvements in electrical conductivity, structural properties, and thermal stability obtained by this synthetic method. Prior to the inverse emulsion polymerization, MWCNT was treated with a strong acid mixture to be functionalized with carboxylic acid groups. Carboxylic acid groups on surfaces induced selective dispersibility between polar and nonpolar solvents because of the increase of hydrophilicity. As the content of c‐MWCNT was increased, the electrical conductivity was increased by a charge transport function from the intrinsic electrical conductivity of MWCNT and the formation of a highly ordered dense structure of PANI molecules on the surface of c‐MWCNT. The images observed with electron spectroscopy showed the capping of c‐MWCNT with PANI. The growth of additional ordered structures of PANI/c‐MWCNT composite, which was observed through wide‐angle X‐ray diffraction patterns, supported the capping by PANI. It was observed that the doping of the composite had a significant relationship with the concentration of dodecylbenzenesulfonic acid (DBSA). The thermal stability of PANI composite was improved by the addition of c‐MWCNT; this was thought to be related with structure ordering by inverse emulsion polymerization. © 2008 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 46: 2255–2266, 2008 相似文献
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Su Chen Jianjun Sui Li Chen John A. Pojman 《Journal of polymer science. Part A, Polymer chemistry》2005,43(8):1670-1680
Polyurethane–nanosilica hybrids were synthesized with frontal polymerization. Structurally well‐dispersed and stable hybrids were obtained via a two‐step functionalization process: First, the silica was encapsulated with 3‐aminopropyltriethoxysilane (APTS). Second, poly(propylene oxide) glycol, toluene 2,4‐diisocyanate, 1,4‐butanediol, and a catalyst (stannous caprylate) were dissolved in dimethylbenzene and mixed together at room temperature along with the modified nanosilica. A constant‐velocity propagating front was initiated via the heating of the end of the tubular reactor. For the complete encapsulation of the silica with APTS, different weight ratios of APTS to silica were investigated. The polyurethane hybrids were characterized with Fourier transform infrared, differential scanning calorimetry, and transmission electron microscopy. The polyurethane hybrids produced by frontal polymerization had the same properties as those produced by batch polymerization with stirring, but the frontal polymerization method required significantly less time and lower energy input than the batch polymerization method. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 1670–1680, 2005 相似文献
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Zheming Gu Chunzhong Li Gengchao Wang Ling Zhang Xiaohui Li Wendong Wang Shilei Jin 《Journal of Polymer Science.Polymer Physics》2010,48(12):1329-1335
This work demonstrates a feasible route to synthesize the layered polypyrrole/graphite oxide (PPy/GO) composite by in situ emulsion polymerization in the presence of cationic surfactant cetyltrimethylammonium bromide (CTAB) as emulsifier. AFM and XRD results reveal that the GO can be delaminated into nanosheets and well dispersed in aqueous solution in the presence of CTAB. The PPy nanowires are formed due to the presence of the lamellar mesostructured (CTA)2S2O8 as a template. The results of the PPy/GO composite indicate the PPy insert successfully into GO interlayers, and the nanofiber‐like PPy are deposited onto the GO surface. Owing to π–π electron stacking effect between the pyrrole ring of PPy and the unoxided domain of GO sheets, the electrical conductivity of PPy/GO composite (5 S/cm) significantly improves in comparison with pure PPy nanowires (0.94 S/cm) and pristine GO (1 × 10?6 S/cm). © 2010 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 48: 1329–1335, 2010 相似文献
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M. B. Urquiola V. L. Dimonie E. D. Sudol M. S. El-Aasser 《Journal of polymer science. Part A, Polymer chemistry》1992,30(12):2619-2629
A polymerizable surfactant, sodium dodecyl allyl sulfosuccinate (TREM LF-40; Henkel) and its nonpolymerizable counterpart were used in comparative studies of the emulsion polymerization of vinyl acetate. The conversion-time behavior differed for the two surfactants; the TREM LF-40 showed a decrease in the polymerization rate with increasing concentration while its hydrogenated derivative showed the opposite behavior, the rate increasing with increasing surfactant. Particle size analysis revealed a decreasing particle size with increasing surfactant concentration for both series of reactions. An explanation for the seemingly ambiguous results obtained for the polymerizable surfactant was sought by examining the reactivity of its vinyl group in copolymerization with vinyl acetate and its allylic group in a chain transfer reaction. The results suggest that both the copolymerization and chain transfer reactions can lead to the observed reduction in polymerization rate with increasing TREM LF-40 concentration. © 1992 John Wiley & Sons, Inc. 相似文献