多苯基三联苯有机硅化合物的合成及其对聚合物耐热性影响的研究

本文通过Diels-Alder反应合成了1,4-双(2′,3′,6′-三苯基,4′-四甲基乙烯基二硅氧基苯基)苯(简称Ⅰ)和1,4-双(2′,3′,6′-三苯基,4′-三乙氧基硅基苯基)苯(Si称Ⅱ)两种新的多苯基三联苯有机硅单体,产率均为80％左右,并作了下列耐热性研究,其结果:(1)把化合物(Ⅰ)作为硅橡胶的热稳定剂,所得硅弹性体在300℃×150小时老化后,具有较好的耐热性和机械性能;(2)化合物(Ⅱ)可以做室温胶的交联剂,所得胶片在300℃×48小时老化,仍保持好的弹性。     

The improvement of thermal stability and adhesion of silicone rubber composites modified by phenolic epoxy resin

The phenolic epoxy resin (F51) was siliconized by KH550 and the product was named as FKS. A hydroxyl-terminated polydimethylsiloxane (HTPDMS) which was modified with FKS was prepared. The siliconization reaction ensured a segment of siloxane on the side chain of F51. FT-IR and ¹H-NMR were employed to confirm the chemical structure of FKS. Morphology observations revealed that the enhancement of mechanical properties of the silicone rubber systems can be attributed to good compatibility between FKS and silicone rubber matrix. Thermogravimetric analysis showed that the residual yield at 800?°C of silicone rubber composites increased significantly when compared with that of neat HTPDMS. The mechanical properties demonstrated that tensile strength and elongation at break of silicone rubber system increased distinctly after modification, especially when 30 phr siliconized F51 were added to the silicone rubber. Shear strength was improved gradually with the addition of FKS. These above observations emphasize the vital effect of FKS on the behavior of modified HTPDMS.     

多苯基芳基类硅化合物作为硅聚合物热稳定剂的研究

本文通过Diels-Alder反应合成了四苯(基)苯基三乙氧基硅烷及四苯(基)苄基三乙氧基硅烷,产率均为96％左右。并作了下列耐热性研究:(1)把两种化合物分别作为硅橡胶混炼时的热稳定剂,所得硅弹性体其热老化稳定性及机械强度均较好。(2)把两种化合物分别作为室温硫化硅橡胶固化时的交联剂,所制得的胶片在350℃老化10小时仍保持弹性。(3)两种化合物分别与H_3BO_3反应,制得耐热性硅硼树脂,是一种优良的耐高温涂料。     

硅氢加成型室温固化硅橡胶胶粘剂的研究

<正> 我们研制了一种硅氢加成型室温固化硅橡胶,这种橡胶不但有较好的力学性能,而且与各类材料如金属、塑料、陶瓷、玻璃等都有很好的粘结力,是一种具有弹性的胶粘剂。该胶粘剂是利用一种含乙烯基聚硅氧烷、含氢聚硅氧烷以及二氧化硅补强剂在铂催化剂     

剥离型硅橡胶/黏土纳米复合材料研究

利用层状硅酸盐制备有机 无机纳米复合材料是当前人们研究的热点[1,2 ] ,这类材料具有较常规聚合物 无机填料复合材料无法比拟的优点 ,可以明显改善高分子材料的物理机械性能、热稳定性、气体阻隔性、阻燃性、导电性、光学性等 .一般来说 ,聚合物 层状硅酸盐 (Ｐｏｌｙｍｅｒｌａｙｅｒｅｄｓｉｌｉｃａｔｅ ,ＰＬＳ)纳米复合材料可分为插层型和剥离型两种类型 .插层型纳米复合材料即聚合物插入到硅酸盐层中 ,硅酸盐在近程仍保持原有的有序晶体结构 ,在远程则是无序的 .对弹性体而言 ,硅酸盐含量在插层型杂化材料中的含量比较高 ,力学性能…     

Novel poly(vinyl chloride) based thermoplastic elastomers incorporating vinyl-functionalized silicone rubber

ABSTRACT

Novel poly(vinyl chloride) (PVC) based thermoplastic elastomers were developed by blending with different proportions of vinyl-functionalized silicone rubber. Scanning electron microscopy (SEM) confirmed good compatibility between PVC and silicone rubber which allowed enhancement of the stress-strain behavior. On the contrary to neat PVC, exposure to heat or UV radiation was found not to cause any considerable deterioration to the stress-strain behavior. Fourier Transform Infrared (FTIR) revealed a possible chemical interaction between the blend components involving the vinyl groups from the silicone rubber, which is thought to be the reason for maintaining the mechanical properties unaltered. Further investigation with ultraviolet-visible (UV-Vis.) spectroscopy signified absence of intensive dehydrochlorination usually encountered for PVC after exposure to heat or UV radiation, which indicates a potential stabilizing effect for the silicone rubber and build up of a network structure comprising both hard and soft segments.     

PREPARATION OF HIGH-TEMPERATURE VULCANIZED SILICONE RUBBER OF EXCELLENT MECHANICAL AND OPTICAL PROPERTIES USING HYDROPHOBIC NANO SILICA SOL AS REINFORCEMENT

Hydrophobic nano silica sol(HNSS)was incorporated into polyvinylmethylsiloxane to prepare reinforced high- temperature vulcanized(HTV)silicone rubber.HTV silicone rubber filled with 40 phr HNSS showed excellent mechanical and optical properties:the tensile strength reached 11.7 MPa and the optical transmittance was higher than 90%.Possible reasons for reinforcement and transparency were discussed on the basis of the bound rubber percentage,total crosslink density,and SEM analysis.Our work suggests that H...     

Design and preparation of poly(lactic acid) hydroxyapatite nanocomposites reinforced with phosphorus‐based organic additive: Thermal,combustion, and mechanical properties studies

A new phosphorus‐based organic additive (PDA) was designed and successfully synthesized using a three‐component reaction for improvement of the thermal and combustion resistance of polylactic acid (PLA). For compensate for mechanical properties of PLA, hydroxyapatite nanoparticles was modified via in situ surface modification with PDA and was used for preparation of PLA nanocomposites. The structure and morphology as well as thermal, combustion, and mechanical properties of the all PLA systems were investigated. The X‐ray diffraction (XRD) and field‐emission scanning electron microscopy (FE‐SEM) results indicated that the presence of PDA as surface modifier has been necessary for a desirable dispersion of hydroxyapatite (HA) nanoparticles in the PLA matrix. The thermal, combustion, and mechanical properties of the PLA system films were investigated using thermogravimetric analysis (TGA), microscale combustion calorimeter (MCC), and tensile test, respectively. The initial decomposition temperature and char residue of PLA containing 6 mass% of PDA along with 2 mass% HA nanoparticles were increased 20°C and 12% respectively, compared with that of the neat PLA. The peak of heat release rate was decreased from 566 W/g for the neat PLA to 412 W/g for PLA containing 2 mass% of PDA along with 6 mass% HA nanoparticles. By incorporation of only 2 mass% HA nanoparticles and 6 mass% of PDA, the tensile strength was obtained 51 MPa higher than that of the neat PLA.     

PLA Electrospun Fibers Reinforced with Organic and Inorganic Nanoparticles: A Comparative Study

In this work, different poly (lactic acid) (PLA)-based nanocomposite electrospun fibers, reinforced with both organic and inorganic nanoparticles, were obtained. As organic fibers, cellulose nanocrystals, CNC, both neat and functionalized by “grafting from” reaction, chitosan and graphene were used; meanwhile, hydroxyapatite and silver nanoparticles were used as inorganic fibers. All of the nanoparticles were added at 1 wt% with respect to the PLA matrix in order to be able to compare their effect. The main aim of this work was to study the morphological, thermal and mechanical properties of the different systems, looking for differences between the effects of the addition of organic or inorganic nanoparticles. No differences were found in either the glass transition temperature or the melting temperature between the different electrospun systems. However, systems reinforced with both neat and functionalized CNC exhibited an enhanced degree of crystallinity of the electrospun fibers, by up to 12.3%. From a mechanical point of view, both organic and inorganic nanoparticles exhibited a decreased elastic modulus and tensile strength in comparison to neat electrospun PLA fibers, improving their elongation at break. Furthermore, all of the organic and inorganic reinforced systems disintegrated under composting conditions after 35 days.     

An investigation of dynamic mechanical, thermal, and electrical properties of housing materials for outdoor polymeric insulators

The present paper reports the results about a study of mechanical, thermal, dynamic mechanical and electrical properties of housing (weather shed) materials for outdoor polymeric insulators. Silicone rubber, ethylene-propylene-diene monomer (EPDM) and alloys of silicon-EPDM are known polymers for use as housing in high voltage insulators. The result of dynamical mechanical measurement shows that the storage modulus of blends enhances with increase EPDM in formulation. It can be seen from the result of TGA measurement that initial thermal degradation of silicone rubber improves by the effect of EPDM in blends. The blends of silicone-EPDM show good breakdown voltage strength compared to silicone rubber. Surface and volume resistance of silicone rubber improve by EPDM content. The mechanical properties of EPDM such as strength, modulus and elongation at break improve by silicone.     

含磷有机硅杂化环氧树脂固化体系性能研究

通过磷酸与γ-环氧丙氧基三甲氧基硅烷反应得到含磷有机硅氧烷,并加入到环氧树脂/4,4'-二氨基二苯基甲烷体系中混合,通过溶胶-凝胶的方法制备了含磷有机硅杂化环氧树脂固化物.对固化体系进行了玻璃化转变温度、热失重、阻燃、拉伸强度、冲击强度测试分析.结果表明,该固化体系的阻燃性得到提高,极限氧指数在25.8～29.3,玻璃化转变温度得到提高,在161～179℃;虽然初始分解温度比纯环氧树脂固化物低,但800℃残炭率可以达到26.5%,提高了36%;拉伸强度得到提高,在71～94 MPa,冲击强度可以达到14.36 kJ/m2,提高了14%.该固化体系具有较好的阻燃性能和热性能,同时具有较好的力学性能.     

双马来酰亚胺在改进硅橡胶热稳定性中的作用

双马来酰亚胺能改进硅橡胶在空气或氧气中的热稳定性。热老化试验和热降解动力学分析表明,其机理可能是双马来酰亚胺能优先与氧作用,避免了硅橡胶链上侧甲基被氧化,减轻了交联密度的提高,从而提高了硅橡胶的热稳定性。     

双马来酰亚胺在改进硅橡胶热稳定性中的作用

 双马来酰亚胺能改进硅橡胶在空气或氧气中的热稳定性。热老化试验和热降解动力学分析表明,其机理可能是双马来酰亚胺能优先与氧作用,避免了硅橡胶链上侧甲基被氧化,减轻了交联密度的提高,从而提高了硅橡胶的热稳定性。     

硅橡胶/氟橡胶并用胶的制备及力学性能

硅橡胶和氟橡胶作为国防、航天等重要领域的耐热材料一直被人们青睐,但其有着各自地优缺点且价格昂贵,本文尝试将这两种橡胶制成并用胶以解决氟橡胶不耐低温和加工性差的问题,以期增大其使用温度范围。采用机械共混法制备硅橡胶/氟橡胶并用胶,研究了硅橡胶和氟橡胶的混炼工艺、并用比、共硫化体系和硫化条件对并用胶力学性能的影响。结果表明,当硅橡胶/氟橡胶的质量比为10∶90,共硫化体系为3~#硫化剂/过氧化二异丙苯(DCP),一段硫化温度为170℃、硫化压力为10MPa、硫化时间为30min,二段硫化温度为200℃、硫化时间为6h时,并用胶的力学性能达到最好。     

Preparation and Performance of HGM/PPENK-based High Temperature-resistant Thermal Insulating Coatings

Novel high temperature-resistant coatings with high mechanical strength and thermal-insulating performance were prepared with poly(ether nitrile ketone)(PPENK) resin as matrix and hollow glass microspheres(HGMs) as thermal-insulating filler. The corresponding mechanical and thermal-insulating study indicated that the mechanical properties of the coatings decreased with the increase of HGM content,and were improved after surface modification of HGM by KH570 resulting in enhancement of interaction between HGM and PPENK resin. The thermal conductivity of HGM/PPENK thermal-insulating coating decreased with the increase of HGM content and coating thickness, along with the decrease of the true density. It also showed slight increase trend due to HGMs surface modification. The HGM/PPENK coating filled with modified HGMs showed better thermal resistance than that of unmodified HGM/PPENK coating. The thermal decomposition temperature at 5%weight loss of the coating containing modified HGMs was 10 °C lower than that of pure PPENK, and 40 °C higher than that of neat HGM/PPENK coating. The coating exhibited commendable appearance after 400 °C for 30 min. The merits of HGM/PPENK-based thermal coatings obviously demonstrated promising prospect in thermal protection fields.     

The influence of nano silica particles on gamma-irradiation ageing of elastomers based on chlorosulphonated polyethylene and acrylonitrile butadiene rubber

The goal of this work was to study gamma irradiation ageing of rubber blends based on acrylonitrile butadiene rubber (NBR) and chlorosulphonated polyethylene rubber (CSM) reinforced by silica nano particles. The NBR/CSM compounds (50: 50, w/w) filled with different content of filler (0–100 phr) were crosslinked by sulfur. The vulcanization characteristics were assessed using the rheometer with an oscillating disk. The vulcanizates were prepared in a hydraulic press. The obtained materials were exposed to the different irradiation doses (100, 200, 300 and 400 kGy). The mechanical properties (hardness, modulus at 100% elongation, tensile strength and elongation at break) and swelling numbers were assessed before and after gamma irradiation ageing.     

Enhancement of a magnetorheological PDMS elastomer with carbonyl iron particles

A magnetorheological elastomer based on silicone rubber with carbonyl iron micro-particles was developed. The influence of the different amount of iron particles was experimentally studied by means of XRD, SEM, FTIR, EDS, XPS, uniaxial tension and rheological and cyclic tests. Different contents of carbonyl iron particles (10–40 wt%) were used to obtain the ratio of magnetic particles/silicone rubber that could provide the best mechanical properties on the MRE material. It was found that the composite material can have an increase of about 95% in its tensile strength when adding 20% of carbonyl iron particles to the raw rubber material. SEM analysis indicates a good dispersion of the magnetic particles on the rubber matrix, and the FTIR and XPS techniques confirm, as expected, that there is no chemical interaction between the iron from the carbonyl iron particles and the silicone rubber matrix due to a proper coating of the particles with silicone oil used as coupling agent. The TGA results evidenced that the addition of coated carbonyl iron particles had an impact on the thermal stability of the MRE and on the formation of cross-linked structures. The viscoelastic behavior of the magnetorheological elastomer is described by running experimental test on a rheometer device. Furthermore, cyclic testing were performed on the material sample to characterize the Mullin's effect.     

Enhancement of thermal conductivity and tensile strength of liquid silicone rubber by three-dimensional alumina network

ABSTRACT

Rapidly increasing demands for higher integration density and stability of electronic devices embrace higher requirements for thermally conductive silicone rubber, which is promisingly used in ultra-thin components. In this work, alumina whiskers (AWs) and alumina flakes (AFs) are used to modify liquid silicone rubber (LSR) by fabricating binary (AFs/LSR) or ternary (AWs/AFs/LSR) composites. The thermal conductivity and mechanical strength of the binary and ternary composites were investigated. Thermal conductivity of the binary AFs/LSR composite (25AFs/LSR) was 0.1990 W m^?1 K^?1, while the thermal conductivity of the ternary AFs/AWs/LSR composite (20AFs/5AWs/LSR) was 0.2655 W m^?1 K^?1. Furthermore, the tensile strength of the ternary AWs/AFs/LSR composites increased by 180.9% as compared with the binary system, increased to 7.81 MPa from 2.78 MPa due to the introduction of 1 wt% AWs. As a reason, a significant synergistic effect of AWs and AFs in the enhancement of both thermal and mechanical properties of the LSR was proved. Furthermore, the dielectric property measurements demonstrated that the ternary composites exhibited a lower dielectric constant and dielectric loss, indicating that the AWs/AFs/LSR composites were qualified to be applied in the field of electronic devices.     

Theoretical investigation of polymer molecular structure influence on dielectric properties and mechanical properties

Triboelectric nanogenerator (TENG) technologies have explosive development in the field of energy harvesting and self-powered sensing. As the key element of triboelectric devices, dielectric polymers have obtained much attention in recent years. The dielectric properties of polymer determine the output performance of TENG. In this paper, we take silicone rubber as an example of dielectric polymers, to study the properties of molecular structure influence on the dielectric properties and mechanical properties by the molecular dynamics simulation method. The free volume fraction, dielectric constant, and mechanical properties of silicone rubbers with different branch chains were calculated. The dielectric constant is highly related to the free volume distribution and the dipole moments of silicone rubbers with different amounts of branch chains. For fewer branch chains silicone rubber, the free volume distribution contributes most to the dielectric constant; for more branch chains silicone rubber, the dipole moment dominates the dielectric constant. Therefore, the silicone rubber ratio has a great influence on the dielectric constant of silicone rubber. With the increase of temperature, the dielectric constant of 2-chain silicone rubber increases at first and then decreases, and the maximum value is obtained near 300 K. Therefore, it is necessary to control the temperature when silicone rubber is used as a dielectric material. This work can be a guide for improving the dielectric properties of silicone rubber, and it provides a new approach to the optimal design of high-performance triboelectric nanogenerators.     

Preparation and Characterization of Polyhydroxyurethane/Attapulgite Nanocomposites Via In-Situ Surface-Initiated Polymerization

The polyhydroxyurethane/attapulgite nanocomposites (PHU/ATP) were prepared by in-situ surface-initiated polymerization of a five-membered cyclic carbonate, 2, 2-bis [p-(1, 3-dioxolan-2-one-4-yl-methoxy) phenyl] propane (B5CC) and hexamethylene diamine, from the surface of the aminopropyl attapulgite nanoparticles (APATP) for the first time. The chemical grafting of the polymer on the surface of ATP was confirmed by FTIR and the morphology of the attapulgite nanoparticles in the nanocomposites was examined by TEM. The thermal stabilities of the polyhydroxyurethane (PHU) and the polyhydroxyurethane/attapulgite nanocomposites (PHU/ATP) were compared with thermogravimetric analysis (TGA).The %G of the attapulgite nanoparticles was also calculated from the results of TGA after the free polyhydroxyurethane was washed off.