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Surface chemistry driven dynamic rheology, microstructure of fumed and colloidal silica particles in nematic liquid crystals

机译:方形化学驱动动态流变学,烟雾液晶中的微观结构和胶体晶体晶体中的微观结构

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We investigate the influence of surface chemistry of silica particles on the dynamic rheology and underlying microstructure of silica in nematic liquid crystal (NW), 4-cyano-4-pentylbiphenyl (5CB) suspensions. The hydrophilic fumed silica (Aerosil 200), synthesized (uncoated) and N-methyl-3-aminopropyltrimethoxysilane (MAP) coated colloidal silica particles in 5CB suspensions form gels at a critical particle concentration of 1.5 wt % (phi = 0.007), 15 wt% (phi = 0.075) and 20 wt% (phi = 0.103) respectively. On the other hand hydrophobic fumed silica (Aerosil RX300) and Dimethyl octadecyl [3-(trimethoxysilyl) propyl] ammonium chloride (DMOAP) coated colloidal silica particles in 5CB suspensions form gels at relatively higher particle loading of 3.5 wt% (phi = 0.016) and 50 wt% (phi = 0314) respectively. The storage modulus (G') of the Aerosil 200/5CB, uncoated silica/5CB and MAP coated silica/5CB suspensions follow power-law scaling G' similar to phi(m), where m is 4.74 +/- 0.5 and 5.89 +/- 03 and 628 +/- 05 respectively. In contrast, Aerosil RX300/5CB suspensions have a higher value of m (6.53 +/- 0.4). Dynamic rheology data of solid gel-like Aerosil 200/5CB, uncoated silica/5CB and MAP coated silica/5CB suspensions exhibit signatures of soft glassy materials, exemplified by (a) an almost frequency (omega) independent G' and a minima in loss modulus (G '') and (b) strain overshoot in G '', whereas Aerosil RX300/5CB and DMOAP coated silica/5CB suspensions show signatures of flocculated gels with strong dependence of G' on omega, an absence of minima in G '' and no strain overshoot in G ''. Furthermore, G' of gel-like Aerosil 200/5CB suspension is insensitive to the nematic-isotropic phase transition (T-NI) of 5CB, while the Aerosil RX300/5CB suspension shows a liquid-like behavior (G '' > G') at temperature (T) >T-NI of 5CB. We believe that the observed differences in the dynamic rheology are dictated by the surface anchoring or interactions of 5CB molecules with the -OH groups of hydrophilic silica The microscopy results show that at T < T-N , the 5CB in Aerosil 200/5CB suspensions gets restricted in the network of Aerosil 200 nanoparticles, whereas the flocs of Aerosil RX300 nanoparticles are expelled by the nucleating 5CB domains to form a particulate network in Aerosil RX300/5CB suspensions. Moreover, the uncoated, MAP and DMOAP coated colloidal silica/5CB suspensions do not exhibit the prominent effect of T on rheology except the discontinuity in G' and G '' at T-NI of 5CB. (C) 2020 Elsevier B.V. All rights reserved.
机译:我们研究了二氧化硅颗粒表面化学对甲型液晶(NW),4-氰基-4-戊基苯吡啶基(5CB)悬浮液中二氧化硅动态流变和底层微观结构的影响。亲水性气相二氧化硅(Aerosil 200),合成(未涂覆的)和N-甲基-3-氨基丙基三甲氧基硅烷(MAP)在5CB悬浮液中涂覆的胶体二氧化硅颗粒在临界颗粒浓度为1.5wt%(PHI = 0.007),15重量% %(PHI = 0.075)和20wt%(PHI = 0.103)。另一方面,另一方面,疏水性气相二氧化硅(Aerosil RX300)和二甲基十八烷基[3-(三甲氧基甲硅烷基)丙基氯化铵(DMOAP)涂覆5cb悬浮液中的胶体二氧化硅颗粒在相对较高的颗粒载量为3.5wt%(phi = 0.016)中形成凝胶和50wt%(PHI = 0314)。 AEROSIL 200 / 5CB,未涂覆的二氧化硅/ 5CB和MAP涂层二氧化硅/ 5CB悬浮液的储存模量(G')遵循类似于PHI(M)的Power-Lab缩放G',其中M为4.74 +/- 0.5和5.89 + / - 03和628 +/- 05。相比之下,Aerosil Rx300 / 5CB悬浮液的悬浮液较高的M(6.53 +/- 0.4)。固体凝胶的动态流变数据200 / 5CB,未涂覆二氧化硅/ 5CB和MAP涂层二氧化硅/ 5CB悬浮液表现出软玻璃材料的特征,其例示于(a)几乎频率(ω)独立的G'和最小值模量(g'')和(b)菌株在g''中过冲,而Aerosil Rx300 / 5cb和Dmoap涂覆的二氧化硅/ 5cb悬浮液显示絮凝凝胶的签名,其在ω上的G'依赖于ω,而不是g'不存在最小值'没有菌株在g''中过时。此外,GEL的凝胶状AEROSIL 200 / 5CB悬浮液对5CB的向量 - 各向同性相转变(T-NI)不敏感,而Aerosil RX300 / 5CB悬浮液显示出液体样行为(G''G' )在5cb的温度(t)> t-ni。我们认为,动态流变学的观察到的差异由5CB分子与亲水性二氧化硅的-OH分子的相互作用来决定显微镜结果表明,在T

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