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以烯丙基嵌段聚醚(PAB)为反应型乳化剂,采用全氟烷基乙基丙烯酸酯单体(FEA)对其进行改性,并通过羟甲基丙烯酰胺(HMA)进行自交联,以醋酸乙烯酯(VAc)、丙烯酸丁酯(BA)、甲基丙烯酸(MAA)为主要单体,通过乳液聚合法制备了全氟自交联型聚醋酸乙烯酯乳液。同时考察了全氟单体对乳液的稳定性及涂膜的常规性能及耐水性、耐候性和耐蚀性的影响。研究结果表明,当氟单体含量为4.0%时,涂膜光泽度达84.5%,硬度2H,附着力1级,柔韧性1级,耐冲击性50cm,全氟自交联醋酸乙烯酯共聚物成膜时产生了较大取向作用,含氟基团向空气/聚合物界面伸展,对聚合物内部分子形成了很好的保护作用,故全氟自交联型聚醋酸乙烯酯膜具有良好的耐水性、耐候性和耐蚀性。 相似文献
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以烯丙基聚乙二醇(APEG),甲基丙烯酸(MAA),烯丙基磺酸钠(SAS)为单体,在引发剂过硫酸钾(K2S2O8)、阻聚剂对苯二酚作用下直接聚合得到一系列具不同侧链长度的三元聚醚聚羧酸盐分散剂。通过红外光谱、热重分析、差示扫描量热分析和凝胶渗透色谱等手段对聚合物的结构、热力学性能和相对分子质量及其分布进行了表征和分析。将其作用于彬长煤制浆,考察了浆体的表观黏度、流变性、Zeta电位、最大成浆浓度和稳定性,并测定和煤的接触角。结果表明,侧链长度为SAS/MAA/APEG1000(n=23)的聚羧酸盐分散剂在最佳用量为0.4%时,水煤浆最高制浆浓度可达到72%,Zeta电位由-12.6 mV变化到-53.1 mV,具有良好的润湿效果,对彬长煤具有更好的降粘、分散和稳定作用。 相似文献
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以离子液体氯代1-烯丙基-3-甲基咪唑([AMIM]Cl)为溶剂来纺制纤维素/聚醚砜共混中空纤维膜,考察了聚醚砜含量对中空纤维膜结构与性能的影响。采用扫描电子显微镜(SEM)对膜内、外表面形态结构进行了观察,测试了中空纤维膜的水通量、截留率等渗透性能,最大拉伸强度、断裂伸长率、杨氏模量等力学性能以及透析性能。结果表明:随着聚醚砜含量的增加,中空纤维膜外表面孔洞结构变大,内表面结构变得更加疏松,膜孔隙率与水通量升高,最大拉伸强度、断裂伸长率、杨氏模量等力学性能则逐渐下降;对尿素的清除效率逐渐提升;对溶菌酶和牛血清白蛋白的清除效率逐渐增大,在聚醚砜含量为13%时分别达到最大值24.05%和19.91%。 相似文献
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DMAc / LiCl 体系下纤维素 / 聚醚砜共混膜的制备与表征 总被引:1,自引:1,他引:0
采用 N,N-二甲基乙酰胺(DMAc) / 氯化锂(LiCl)体系作为纤维素溶剂,制备了纤维素 / 聚醚砜共混膜。探讨了共混比对膜的断裂强度、断裂伸长率和纯水通量等膜性能的影响,并确定了纤维素 / 聚醚砜最佳共混比为 1 : 16。 对共混膜进行了 SEM 和 DSC 分析,确认了纤维素 / 聚醚砜共混膜是一个相容的聚合物共混体系。 相似文献
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以全氟聚醚酰氟为原料,水解制成全氟聚醚羧酸,再将全氟聚醚羧酸进一步氨化成全氟聚醚酰胺。利用非离子表面活性剂等将其乳化,制得水性有机氟乳液型脱模剂。通过改变水性乳液中各组分含量提高脱模剂的脱模性能及稳定性能,并进行了红外光谱分析、表面接触角的分析以及剥离试验等表征。结果表明:水性有机氟乳液型脱模剂的含量在3.5%,水性有机氟脱模剂的性能最好,涂覆的膜层能在25℃下28min内快速固化,脱模次数可达到20次以上,并多次脱模后其剥离力低于4.8N/cm。可用于树脂等制品的脱模。制备乳液时,乳化剂采用TO-7和TO-12比值为1∶7复配制备的有机氟乳液亲水亲油平衡(HLB)值达11.5,乳化时温度控制在68℃时制备的乳液最为稳定,放置2月后不会变性。 相似文献
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由聚醚型聚丙二醇二缩水甘油醚和甲基丙烯酸合成了可光固化的聚丙二醇二缩水甘油醚二甲基丙烯酸酯(DMA),再按不同质量配比将此合成物与双酚A型环氧甲基丙烯酸酯(BEMA)混合,经紫外光照射得到复合光固化膜,然后对所得固化膜的耐热性、柔韧性、硬度、光泽度、可见光透过率和微观形貌进行表征.研究结果表明,复合膜兼具DMA和BEM... 相似文献
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多功能基共改性聚甲基三氟丙基硅氧烷的合成表征与膜形貌 总被引:2,自引:0,他引:2
通过聚甲基三氟丙基含氢硅氧烷与端烯丙基聚氧乙烯醚、丙烯酸十八醇酯、烯丙基缩水甘油醚的硅氢化加成反应,制备了一种十八酯基/聚醚/环氧基共改性聚甲基三氟丙基硅氧烷(PSA-PFMS)。用红外光谱(FT-IR)、核磁共振氢谱(1H-NMR)、场发射扫描电镜(FESEM)、原子力显微镜(AFM)等仪器分别对PSA-PFMS的结构、成膜形态及性能进行表征和研究。结果表明,在棉纤维和单晶硅表面,PSA-PFMS均可成膜。在单晶硅表面,可形成粗糙度大(2μm×2μm的扫描范围内,硅膜的均方粗糙度达1.197 nm)、呈微观相分离结构的疏水膜。该膜附着在纤维表面,能使处理后织物表面水的静态接触角达到129.2°。 相似文献
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采用含有相变单元的单体缩聚法合成了侧链含有聚乙二醇单甲醚(MPEG)的新型固-固相变储能复合材料(相变共聚物缩写名称为(MGPM)/蛋白石(opal)),通过广角X射线衍射(WAXD)、差热扫描量热仪(DSC)和热台偏光显微镜(POM)、热重(TG)等测试手段对其结晶结构、结晶行为、结晶形态和热稳定性进行了研究,结果表... 相似文献
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Xianfeng Li 《Materials Letters》2007,61(2):421-426
By using the interaction between the sulfonated groups and silver ions, nanosilver particles were successfully introduced into S-PEEK nanostructures (nanospheres and nanofibers) by electrospinning. The nanoparticles were characterized by scanning electron microscope (SEM), transmission electron microscope (TEM), X-ray photoelectron spectra (XPS), UV/vis, etc. The size of the spheres increases with the weight concentration of silver exchanged sulfonated poly(ether ether ketone) (S-PEEK-Ag) increasing. The size of the silver particles can be controlled by adjusting the sulfonated degree (number of sulfonate groups per repeating unit) of sulfonated poly(ether ether ketone) (S-PEEK) and the weight ratio of the S-PEEK solutions. This paper provides a new method for the preparation of nanometal particles into nanostructures. 相似文献
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耐高温聚酰亚胺导电复合材料的性能 总被引:1,自引:0,他引:1
采用涂膜法制备了以碳纳米管(CNTs)、乙炔黑和石墨粉为导电填料的聚酰亚胺(PI)导电复合材料,研究了其电学性能、力学性能和粘接性能。结果显示,PI/CNTs导电复合材料有较好的综合性能。 相似文献
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采用环氧树脂为碳源制备出碳芯结构LiFePO4/C复合材料.利用X射线衍射、扫描电镜、透射电镜和X光电子能谱等分别对复合材料的晶体结构、表面形貌及表面成分进行表征,采用恒电流充放电和电化学阻抗方法研究试样的电化学性能.实验结果表明:碳芯结构复合材料是由无定形碳线和纳米LiFePO4颗粒组成.碳芯结构LiFePO4/C复合材料在15mA/g的电流密度下,首次放电容量达到166mAh/g,当电流密度增加到750mA/g,放电容量高达131mAh/g,经过50次循环后,容量保持率高达99.2%. 相似文献
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New poly(ether–amide)/layered silicate nanocomposites (PEAN) containing dibenzalacetone and cinnamoyl moieties were prepared via solution intercalation technique from poly(ether–amide) 6 and organo-MMT in a solution of N,N-dimethylacetamide (DMAc). New dicarboxylic acid 4 was synthesis from two step reactions. At first 4,4′-bis(1,4-diphenoxybutane) dialdehyde 3 was synthesized from 1,4-dibromobutane and 4-hydroxybenzaldehyde, then solvent free reaction using to synthesis 4,4′-bis(1,4-diphenoxybutane) diacrylic acid from dialdehyde 3 and malonic acid. Poly(ether–amide) (PEA) chains were synthesized from 4,4′-bis(1,4-diphenoxybutane)diacrylic acid 4 and 2,5-bis(4-aminobenzylidene)cyclopentanone 5 via a direct polycondensation reaction. The synthesized PEA was characterized by Fourier transform infrared spectra (FTIR), nuclear magnetic resonance (1H NMR), gel permeation chromatography (GPC) and UV–Vis spectroscopy. The distribution of organoclay and nanostructure of the nanocomposites were investigated by X-ray diffraction (XRD) and transmission electron microscopy (TEM) analyses. The thermal properties and flammability of the nanocomposites were investigated by thermogravimetric analysis (TGA), differential scanning calorimetric (DSC) and microscale combustion calorimeter (MCC). In the presence of organoclay shows a good effect on improving the flame retardancy of the PEA, reflecting the decrease in heat release rate (HRR) and the total heat release (THR) of the nanocomposites, while the thermal stability of nanocomposites only changed slightly compared to the neat polymer. With the increase of the loading of organoclay, the nanocomposites showed improved flame retardancy and higher char residues. 相似文献
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以酸处理的多壁碳纳米管(MWCNTs)为载体,采用水热合成法制备了InVO4/MWCNTs光催化剂.利用场发射扫描电镜、X射线粉末衍射、BET-N2吸附、傅里叶红外光谱和紫外-可见漫反射吸收光谱等技术对样品的形貌、晶相组成、比表面积和吸光性能等物理性质进行了表征,并以气相的苯作为模型污染物,研究催化剂样品在可见光(λ>420 nm)照射下的光催化氧化能力.结果表明,InVO4颗粒均匀附着于MWCNTs,表面粒径约100 nm.与纯InVO4相比,InVO4/MWCNTs的比表面积和可见光吸收性能显著提高.在可见光照射下,InVO4/MWCNTs具有良好的光催化活性,反应4 h光催化降解苯的转化率和矿化率分别为41.0%和43.4%,其转化率分别是InVO4的1.5倍和掺氮TiO2的3倍,InVO4/MWCNTs光催化活性的提高与载体MWCNTs良好的电子传输特性有关. 相似文献
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Allyl phenyl thiophene ether as novel potential dielectric materials for organic thin film transistors have been synthesized by coupling 2-bromothiophene with 4-bromo allyl phenyl ether and was systematically characterized by elemental analysis and NMR. 4-bromo allyl phenyl ether was synthesized by the reaction between 4-bromophenol and allyl bromide. Self assembled mono-layers of these materials have been covalently grafted onto (111) hydrogenated silicon surfaces through thermal hydrosilation with the alkene end by Si-C bonding mechanism. Monolayer formation was carried out using solutions of the alkene in the high boiling point solvent 1,3,5-triethylbenzene and was characterized by X-ray photoelectron spectroscopy (XPS), contact angle, Atomic Force Microscopy(AFM) and Scanning Tunneling Microscopy (STM). We anticipate these monolayers as potential dielectric materials for organic electronics 相似文献