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将三(2-羟乙基)异氰脲酸酯(THEIC)与丙烯酸(AA)在适当条件下进行酯化反应,合成了含三嗪环的多官能度丙烯酸酯单体.考察了催化剂种类和用量、原料配比、带水荆用量以及反应温度和时间等因素对酯化反应的影响,获得了较佳的反应条件:THEIC与AA以及甲苯与环己烷的质量比均为1:2,以对甲笨磺酸为催化剂,其用量为THEI...  相似文献   

3.
用PERKIN—ELMER公司的DSC—7仪器测定了改性双马来酰亚胺树脂体系的固化反应。根据DSC测试原理和Arrhenius公式建立的固化反应动力学方程,借助DSC—7动力学软件,求出该树脂体系的固化反应动力学参数—Ea、n、z。利用已得到的动力学参数,进一步预测其固化反应程度(a)、固化反应温度(T)和固化反应时间(t)三者之间的关系。并求出该体系的凝胶化温度(Tgel)、固化温度(Tcure)和后处理温度(Ttreat)的近似数值。  相似文献   

4.
《化工中间体》2007,(12):29-30
桐油酸酐(TOA)的综合性能较好,而TOA-环氧树脂固化物更具有优良的机械力学性能和电性能。三(2-羟乙基)异氰尿酸酯(THEIC)中含有稳定的刚性六元碳氮杂环结构,因而具有优异的化学及热稳定性,且分子中具有3个活泼的羟基。若利用羟基的反应活性将它引入到高分子主链上,则能提高材料的强度、耐热性和耐候性。  相似文献   

5.
用差示扫描量热仪(DSC)、傅立叶交换红外光谱(FT-IR)对不同配比的低溴环氧/氰酸酯树脂的共固化反应机理以及固化物的结构特征进行了研究,同时测定和讨论了其层压板的耐热性和介电性能等。研究结果表明,在低溴环氧/氰酸酯树脂的固化体系中,氰酸酯和环氧树脂通过两种途径反应最终生成噁唑烷酮结构:固化反应温度与体系的组成有关,体系中低溴环氧树脂减少固化反应温度降低:加入催化剂能明显促进体系共固化反应,同时也降低了层压板的耐热性和介电性能。在性能方面,低溴环氧树脂中加入氰酸酯使共固化物耐热性增加、Tg升高,但氰酸酯用量增加到一定范围后,低溴环氧树脂/氰酸酯配比对Tg影响不大;低溴环氧树脂/氰酸酯层压板的耐热性和介电性能在一定实验范围内随着氰酸酯用量的增加明显提高。  相似文献   

6.
A novel novolac curing agent containing both naphthalene and dicyclopentadiene (DCPD) moieties was prepared to produce a highly heat-resistant cured polymer network. The chemical structure was characterized using Fourier transform infrared spectroscopy, nuclear magnetic resonance, mass spectrometry, and gel permeation chromatography analyses. The thermal properties of the resulting polymer from diglycidyl ether of bisphenol A epoxy resin cured with the novel curing agent were evaluated using dynamic mechanical thermal analysis and thermogravimetric analysis. Compared with the conventional curing agent, the resulting polymer cured with naphthalene/DCPD navolac shows considerable improvement in heat resistant properties such as higher glass transition temperature (Tg) and thermal stability. The result also shows better moisture resistance because of the hydrophobic nature of naphthalene/DCPD structure.  相似文献   

7.
用 PE DSC-7仪器测定了 N,N,N′,N′—四烯丙基二苯甲烷二胺改性双马来酰亚胺树脂的比热容,并借助DSC-7动力学软件得到该树脂的固化反应级数n=1.39±0.10、反应活化能E_a=138±7.77kJ/mol和表观频率因子InZ=28.6±1.921/sec;还预测了树脂的固化反应程度(d),固化反应温度(T)和固化反应时间 (t)三者间相互关系,并计算了凝胶化温度(Tgel)、固化温度(Tcure)和后处理温度(Ttreat)。  相似文献   

8.
介绍了双马来酰亚胺/氰酸酯(BMI/CE)树脂的固化机制及其应用范围,特别综述了BMI/CE树脂的改性研究(如新型结构树脂单体改性、环氧树脂改性、烯丙基化合物改性和聚苯醚改性等)。最后对BMI/CE树脂今后的研究与发展方向进行了展望。  相似文献   

9.
咪唑盐的合成、固化反应及性能研究   总被引:1,自引:1,他引:1  
本文合成了三种咪唑盐,并就其固化反应特点及对固化物性能的影响作了初步探讨。  相似文献   

10.
双马来酸亚胶树脂基体耐热性好,具有优异的使用性能;但固化温度往往高于200℃。引发剂可有效地降低固化温度,但所得树脂基体脆性很大。本文在二元胺扩链、烯丙基双酚A共聚后的双马来酰亚胺树脂锄中加入引发剂,制得一种软化点低、韧性适中、耐热性好、贮存稳定的低温固化双马来酰亚胺树脂BDDD体系。为今后该树脂在复合材料构件上的应用奠定了良好的基础。  相似文献   

11.
A series of bismaleimide monomers with amide groups were prepared and characterized. Structurally different bismaleimides (with amide units) were synthesized by a reaction between 4‐maleimidobenzoyl chloride and various diamines. The monomers were characterized by infrared spectroscopy, proton nuclear magnetic resonance spectroscopy, and elemental analysis. The thermal characterization of the bismaleimides was accomplished with differential scanning calorimetry and dynamic thermogravimetric analysis. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 567–572, 2006  相似文献   

12.
通过接枝反应合成了一系列侧链含联苯类介晶基元的聚醚型树脂,并对合成工艺进行了探讨.各步产物的IR表征结果与预期相符,树脂的接枝率与介晶基元单体的活性有关,一般随产率增大而递增并大于相应的产率.示差扫描量热(DSC)和偏光显微镜(POM)测试结果表明,除对氰基联苯酚与聚环氧氯丙烷的接枝产物(HPCN)在70~130℃表现出典型纹影织构的向列相液晶态外,其余树脂均不具有液晶性,而为半结晶性物质.介晶基元的极性对树脂的热形态有很大影响,含强极性端基(如-CN)的介晶基元有利于液晶相的形成.  相似文献   

13.
ACS树脂的结构与热性能   总被引:1,自引:0,他引:1  
通过相差显微图片和红外光谱分析ACS树脂[丙烯腈(AH)-氯化聚乙烯(CPE)-苯乙烯(S_t)]的结构,利用差热分析(DTA)和热失重(TG)曲线剖析ACS树脂的热性能。结果表明,ACS树脂系CPE、CPE-g-AS和AS以分散的橡胶相(CPE相)与连续的塑料相(AS相)共存的多相抗冲体系。CPE和ACS的热解聚机理均为脱氯化氢,氧化降解。ACS热稳定性明显优于CPE。  相似文献   

14.
高吸水性树脂合成方法与性能   总被引:1,自引:0,他引:1  
系统地介绍了高吸水性树脂的合成方法及其主要性能。  相似文献   

15.
Abstract

Six modified bismaleimide (BMI) resin systems are developed. The modifier is diallyl bisphenol A, diallyl bisphenol A ether. TDE-85 epoxy/MNA anhydride, and styrene. respectively. In view of structure of those cured resins, relationships between structure and dielectric properties have been studied emphatically, while effects of postcure temperature and catalysts on dielectric properties were also shown. Results indicate that dielectric properties lie on structure of cured resin and postcure temperature; catalysts can strikingly improve the heat-resistance of materials, but has little effect on the dielectric properties. In addition, mechanical and thermal properties of neat resins were also shown.  相似文献   

16.
本文利用甲基丙烯酸缩水甘油酯(GMA),丙烯酸丁酯(BA),苯乙烯(St)为原料进行溶液聚合,得到共聚物(PA);再利用PA和不同比例DOPO反应,获得一系列磷含量不同的阻燃树脂。对聚合物的结构、玻璃化温度、以及阻燃性进行测试与表征。结果表明:随着聚合物中DOPO含量的增加,玻璃化温度升高,阻燃效果逐渐变好。  相似文献   

17.
李三梅  赵磊 《广东化工》2012,39(11):31-33
以丙烯酸甲酯和二乙醇胺为原料,制得N,N-二羟乙基-3-胺基丙酸甲酯(DAMP);接着,用DAMP与三羟乙基异氰脲酸酯(THEIC)经酯交换反应,合成出一种超支化聚酯多元醇;再以该多元醇与丙烯酸通过酯化反应,制备了可UV固化的超支化聚酯丙烯酸酯。实验结果表明:以对甲苯磺酸为催化剂,当THEIC与DAMP的物质的量比为1∶9时,可制得二代超支化聚酯多元醇;该聚酯丙烯酸酯的玻璃化温度为53.0℃,与环氧丙烯酸酯(9104)混合组成的组合物,具有固化速度快、固化膜柔韧性佳的特点;附着力可达0级,摆杆硬度为0.751。  相似文献   

18.
We have synthesized a series of epoxy resins containing melamine phosphate (MP) and investigated their thermal and flame retardation properties. MP functions as a hardener and a flame retardant or as an additive of the cured epoxy resin to enhance flame retardation properties of epoxy resins. The reactions of DGEBA cured in the presence of MP were monitored by NMR and FTIR. Our results show that in both reactive and additive modes, MP is effective in increasing limiting oxide index (LOI) and the char yields of epoxy resins at lower phosphorous content. We observed that flame retardation by MP in its reactive mode is better than in its additive mode; the same phenomenon was found also for the glass-transition temperature (T g). Thermogravimetric analysis (TGA) demonstrated that epoxy resins containing MP decompose at relatively lower temperatures than those lacking MP; this decomposition results in a protective layer forming that prevents the epoxy resins from decomposing further by combustion.  相似文献   

19.
The effect of catalyst content on the thermal and mechanical properties of diglycidyl ethers of bisphenol A (DGEBA)/BPH system was investigated at elevated temperatures. The contents of the catalyst, N‐benzylpyrazinium hexafluoroantimonate (BPH), examined were 0.5, 1, and 3 wt.‐% and the elapsed heating time was varied from 0 to 1 024 h. As a result, the thermal‐oxidative resistance and mechanical properties, including flexural strength, elastic modulus in flexure, and impact strength showed a maximum value at 1 wt.‐% BPH. By increasing the elapsed time to 4 h, the thermal and mechanical properties of the specimens were also improved. These results showed that the internal structure of the epoxy system was stabilized and post‐cured as the elapsed time increased, resulting in an improvement of the thermal and mechanical properties of the specimens.

Impact strength of the DGEBA/BPH system as a function of BPH content and elapsed heating time.  相似文献   


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