济南泰星精细化工有限公司

环保阻燃剂系列：（HT-101）聚烯烃专用环保阻燃剂、（HT-102）工程塑料专用环保阻燃剂，（HT-103）PVC专用环保阻燃剂、（HT-104）溴化环氧树脂、（HT-105）环保三氧化二锑、（HT-106）十溴二苯乙烷、（HT-107）六溴环十二烷、（HT-208）四溴双酚A、（HT-109）ABS专用环保阻燃剂     

济南泰星精细化工有限公司

环保阻燃剂系列：（HT-101）聚烯烃专用环保阻燃剂、（HT-102）-V程塑料专用环保阻燃剂、（HT-103）PVC专用环保阻燃剂、（HT-104）溴化环氧树脂、（HT-105）环保三氧化二锑、（HT-106）十溴二苯乙烷、（HT-107）六溴环十二烷、（HT-108）四溴双酚A、（HT-109）ABS专用环保阻燃剂、（HT-110）溴化聚苯乙烯     

济南泰星精细化工有限公司

阻燃剂系列环保阻燃剂系列:(HT-101)聚烯烃专用环保阻燃剂、(HT-102)工程塑料专用环保阻燃剂、(HT-103)PVC专用环保阻燃剂、(HT-104)溴化环氧树脂、(HT-105)环保三氧化二锑、(HT-106)十溴二苯乙烷、(HT-107)六溴环十二烷、(HT-108)四溴双酚A、(HT-109)ABS专用环保阻燃剂、(HT-110)溴化聚苯乙烯     

发射药塑料包装箱的阻燃性能研究

目的为提高发射药塑料包装箱的阻燃性能,设计一种新型阻燃改性HDPE塑料箱。方法利用燃烧和相容性实验研究了十溴二苯醚和三氧化二锑2种阻燃剂含量、比例对HDPE塑料阻燃性能和相容性的影响,并通过理论分析探讨了2种阻燃剂对HDPE塑料的阻燃机理。结果实验结果表明,未经阻燃改性的HDPE塑料阻燃效果较差,随着阻燃剂含量的增加,阻燃性能得到提高,相容性变差。结论阻燃剂中十溴二苯醚和三氧化二锑的质量比为2∶1时,阻燃效果最佳,阻燃剂含量(质量分数)低于11%时,可以满足相容性要求。     

双酚A型环氧树脂(E-51)改性二氧化双环戊二烯(CDR-0122)的性能研究

采用双酚A型环氧树脂(E-51)对耐高温环氧树脂体系二氧化双环戊二烯(CDR-0122)进行了改性处理。分析了E-51改性前后的物理特性,考察了改性前后浇铸体的冲击性能、弯曲性能和玻璃化转变温度,以及树脂基玻纤复合材料的基本力学性能。实验结果表明,E-51与CDR-0122有良好的相容性,且CDR-0122和E-51/CDR-0122树脂体系都应密封保存。添加E-51后浇铸体的冲击强度和弯曲强度分别提高了141.48%和52.38%,玻璃化转变温度下降了2.73%;E-51改性后的树脂基玻纤复合材料的弯曲强度和拉伸强度分别提高了20.5%和19.1%。     

F-48环氧树脂改性双酚A型氰酸酯树脂的研究

采用FT-IR与DSC研究了F-48酚醛型环氧改性双酚A型氰酸酯树脂的固化行为及固化工艺,通过DMA、TGA、介电性能和冲击强度测试对F-48酚醛型环氧改性双酚A型氰酸酯树脂的热性能、介电性能和韧性进行了研究。结果表明,随着F-48环氧树脂含量的增加,改性氰酸酯的Tg总体呈升高趋势,最高达到255℃;改性后的氰酸酯树脂热分解温度逐渐降低;F-48环氧树脂加入量为氰酸酯质量的25%时,改性氰酸酯树脂具有较低的介电常数和介电损耗;改性氰酸酯的冲击强度较纯氰酸酯树脂提高25%。     

与液氧相容聚合物基体材料

为改善环氧树脂与液氧的相容性,研究了环氧／溴环氧／氰酸酯树脂三元共固化体系,并探讨了2-乙基-4-甲基咪唑 ( 2E4MZ ) 对于共固化体系的促进作用。实验发现,2E4MZ可以显著降低共固化体系在不同温度下的凝胶时间。采用傅立叶红外光谱跟踪固化过程,结果表明,无论在环氧基团过量还是氰酸酯基团过量情况下,2E4MZ均能够明显加快固化反应速度,同时增大固化产物中共聚产物的比例,提高反应的选择性。热分析、闪点和氧指数以及液氧冲击试验结果表明,2E4MZ促进的较低氰酸酯含量的共固化体系具有较好的抗氧化和阻燃性能,与液氧的相容性也得到较大幅度改善。采用咪唑促进这种相对简单有效的改性途径,可得到与液氧相容性较好的、综合性能理想、成本合理的环氧树脂体系。      

环三磷腈衍生物的合成及其阻燃环氧树脂应用研究

合成了六(4-甲氧基苯氧基)环三磷腈(HMPCP)和六(4-羟基苯氧基)环三磷腈(HHPCP)。将HMPCP和HHPCP应用于TDE-85环氧树脂中,研究添加两者后环氧树脂的阻燃性能,结果表明HHPCP阻燃效果优异,添加8%(wt,质量分数,下同)HHPCP的环氧树脂氧指数从18.2%提高至23.7%,450℃时残炭率高达12%;HHPCP阻燃机理为膨胀阻燃机理。     

真空辅助成型(VARI)用低黏度环氧树脂研究进展

综述了以环氧树脂为主的国内外真空辅助成型技术(VARI)用低黏度树脂基体的研发现状,以及双酚F及改性双酚F环氧树脂研究现状,分析了双酚F及改性双酚F环氧树脂应用于真空辅助成型技术(VARI)的潜力.     

双酚A型环氧树脂（E-51）改性二氧化双环戊二烯（CDR-0122）的性能研究

采用双酚A型环氧树脂（E-51）对耐高温环氧树脂体系二氧化双环戊二烯（CDR一0122）进行了改性处理。分析了E-51改性前后的物理特性，考察了改性前后浇铸体的冲击性能、弯曲性能和玻璃化转变温度，以及树脂基玻纤复合材料的基本力学性能。实验结果表明，E-51与CDR-0122有良好的相容性，且CDR-0122和E-51／...     

液晶环氧树脂增韧改性E-51树脂体系性能研究

目的研究液晶环氧树脂含量对E-51树脂体系固化性能和力学性能的影响。方法采用动态DSC法,研究了液晶环氧树脂对固化反应性的影响;采用力学性能测试和扫描电镜的方法,研究了液晶环氧树脂对固化物力学性能的影响,及其增韧机理。结果液晶环氧树脂含量越高,树脂体系固化反应越快。液晶环氧树脂的加入使冲击强度、弯曲强度和拉伸强度均得到提高。结论液晶环氧树脂质量分数为7%的配方,冲击强度和弯曲强度最高;质量分数为10%的配方拉伸强度最高。     

海因环氧树脂/HHPA体系的制备与性能

合成了海因环氧树脂,采用红外光谱和核磁共振进行了表征,以六氢苯酐(HHPA)为固化剂,制备了海因环氧树脂/HHPA体系,研究了海因环氧树脂/HHPA体系的固化反应性及其固化物的性能。结果表明:树脂体系在升温速率为10℃/min的条件下,在90～210℃有一放热峰,峰值温度为152.5℃;100℃下的凝胶时间大于42min,在140℃下为8min;树脂浇铸体的氧指数为23,抗弯强度为122MPa,弯曲模量为2.7GPa,冲击强度为14.9kJ/m2。     

海因环氧树脂/DDS体系的制备与性能

合成了海因环氧树脂,采用红外光谱和核磁共振进行了表征,制备了海因环氧树脂/二氨基二苯砜(DDS)体系,研究了海因环氧树脂/DDS体系的固化反应特性及固化物的性能。结果表明,树脂体系在100℃~296℃有一放热峰,峰值温度为197℃,140℃的凝胶时间长于42 min,在180℃下仅8 min;树脂浇铸体的氧指数为26.6,弯曲强度为111MPa,弯曲模量为4.14 GPa,冲击强度为14.8 kJ/m2。     

Hyperbranched polymers as modifiers of epoxy adhesives

A novel hyperbranched poly(amide-ester)s (HBP) has been synthesized through the AB₂ approach in one-step polycondensation without solvents. The synthesized HBP has been characterized and used as filler for epoxy resin with the aim obtain materials which exhibit improved toughness. Composites containing 6% and 12% wt/wt of HBP in diglycidylether of bisphenol A (DGEBA) were produced and characterized. Results obtained from DMA tests showed that HBP has good compatibility with the epoxy resin. Impact tests proved that composites containing 12% HBP showed an improvement of about 25% on impact strength with respect to neat DGEBA. Moreover, adhesive properties were evaluated in terms of the lap-shear strength value of composite joints bonded using the investigated blend. Results showed an improvement of shear strength value of DGEBA added with 12% HBP with respect to neat DGEBA. The water uptake behavior was also evaluated.     

固体环氧树脂水分散体的制备和性能

用中等分子量的固体双酚A型环氧树脂ER-1和环氧乙烷/环氧丙烷的嵌段共聚物Lutrol F68合成了一种活性非离子型乳化剂F68-E,对乳化剂F68-E的结构以及合成过程进行了分析。用乳化剂F68-E对环氧树脂ER-1进行乳化,探讨了使用相反转法乳化时,乳化剂浓度、乳化温度和溶剂种类对环氧树脂水分散体的粒径和力学稳定性的影响。此外,将环氧树脂水分散体制成中温固化体系,对其干膜固化物进行了吸水率测试和动态热机械分析。结果表明,引入12%的乳化剂F68-E后,固化体系的吸水率由1.38%降至0.97%,玻璃化转变温度由102.5℃降至82.6℃。     

Epoxy resin/liquid natural rubber system: secondary phase separation and its impact on mechanical properties

An investigation was carried out to explore the morphology and mechanical properties of diglycidyl ether of bisphenol A epoxy resin (DGEBA) with liquid natural rubber possessing hydroxyl functionality (HLNR). Though modification of epoxies by synthetic rubber has been extensively studied not much attention has been paid to liquid natural rubber. Photo depolymerisation of natural rubber enables us to synthesise low molecular weight oligomers by varying the experimental parameters. Epoxy resin was cured using nadic methyl anhydride as hardener in presence of N,N-dimethyl benzyl amine accelerator. Hydroxylated natural rubber of different concentrations is used as modifier for epoxy resin. The addition of such chemically modified liquid rubber to an anhydride hardener–epoxy resin mixture has given rise to the formation of a two-phase microstructure in the cured systems, consisting of spherical particles of liquid natural rubber strongly bonded to the surrounding matrix, there by providing the required mechanism for toughness enhancement. Subinclusions of epoxy resin were present in the elastomer domains as secondary particles (particle in particle morphology) as evidenced from the SEM (scanning electron micrograph) photomicrographs. The origin of the so-called secondary phase separation is due to the combined effect of hydrodynamics, viscoelastic effects of rubber phase, diffusion, surface tension, polymerisation reaction and phase separation. In a dynamic asymmetric system, the diffusion of the fast dynamic phase is prevented by the slow dynamic phase, and hence the growth of fast dynamic phase gets retarded due to the slow dynamic phase. In the case of low viscosity blends the growth of fast dynamic phase turns fast and hence diffusion of fast dynamic phase cannot follow geometrical growth and cannot establish local concentration equilibrium and hence double phase separation takes place. The double phase separation is responsible for the enhanced impact and toughness behaviour of the blends. The mechanical behaviour of the liquid rubber-modified epoxy resin was evaluated in terms of tensile and flexural properties.     

有机硅改性双酚F环氧树脂的性能

合成了脂肪族二官能度端环氧基聚二甲基硅氧烷、含酚羟基烷氧基硅烷及3,3′,3″-三羟基苯氧基硅烷三缩水甘油醚,研究了有机硅对环氧树脂力学性能的影响,并用TMA及化学分析方法研究了改性固化物的热性能和树脂/玻璃纤维复合材料的耐酸性。研究结果表明,3,3′,3″-三羟基苯氧基硅烷三缩水甘油醚可使环氧树脂的拉伸强度、弯曲强度分别提高10.4%及53.6%,线胀系数降低18.8%,抗开裂指数提高52.2%,同时保持固化物较高的玻璃化温度,提高耐酸性,是一种理想的环氧树脂新型改性剂。     

聚合物材料与液氧相容性的表征研究

通过研究四种具有结构差异的环氧树脂与氰酸酯的共聚物,分别对其进行液氧冲击实验和热分析测试,发现两种测试方法得到的结果之间存在较好的一致性.在深入探讨液氧冲击敏感性实验机理的基础上,认为热分析可以作为判定聚合物材料与液氧相容性的有效表征手段.     

Structural-mechanical relationship of epoxy compatibilized polyamide 6/polycarbonate blends

Polyamide 6 (PA6)/polycarbonate (PC) blends compatibilized with solid epoxy resin (bisphenol type-A) were prepared by extrusion followed by injection molding. The effects of epoxy resin on the microstructure, tensile, impact and compatibility of the PA6/PC blends were investigated. The results showed that both the tensile modulus and elongation at break of PA6/PC blends were inferior as compared to their parent polymers. This resulted from incompatibility between the PA6 and PC phases. SEM observation revealed that the introduction of 0.5 part per hundred (phr) epoxy resin into the PA6/PC75/25 blend yields a finer dispersion of PC phase in PA6 matrix. The boundaries between the PC domains and PA6 matrix became obscure with the incorporation of 1 phr epoxy resin. Such an improvement in compatibility was suggested to be resulted from the formation of in situ epoxy bridged PA6-PC block copolymer in the blend during compounding. Consequently, the tensile modulus, yield strength and impact strength of the PA6/PC 75/25 blend improved considerably with increasing epoxy content.