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首页> 外文期刊>Dyes and Pigments >Impact of stabilisers on the thermal catalytic activity of micro-and nano-particulate titanium dioxide in oxidizing condensed mediums
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Impact of stabilisers on the thermal catalytic activity of micro-and nano-particulate titanium dioxide in oxidizing condensed mediums

机译:稳定剂对氧化性介质中微米级和纳米级二氧化钛热催化活性的影响

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This investigation was undertaken to elucidate an interplay between stabilisers and titanium dioxide nano-particles in oxidizing condensed mediums comprising of the initiatied(initiator is 2,2'-azobisisobutyronitrile,AIBN)oxidation of cumene and ethylbezene and an intercompar-ison with the thermal oven ageing of high-density polyethylene(HDPE).As a preliminary study,the catalytic influence of different nano and micro-particle sized anatase and rutile titanium dioxide pigments on the uninitiated oxidation of cumene at moderate temperature(60 °C)has been established.The oxidation rates depend linearly on the square root of the concentration of the titanium dioxides over a sufficiently wide range and thereby follow the mechanism of oxidation with recombination of peroxy radicals.Kinetic measurements of oxidation rates of the model reactions of initiated oxidation of cumene and ethylbenzene in the absence and presence of a hindered piperidine stabiliser,Chimassorb 119 FL,Cyasorb 3529 and sterically hindered Irganox 1010 stabilisers clearly showed that the stabilisers promote over-additional initiating activity of titanium dioxide pigments.This effect was found to be very large,i.e.the values of afforded additional initiation rates are 2-9 times more than those compared with the value of the initial initiation rate induced by titanium dioxides in the system without stabilisers.In the case of hindered amine stabilisers this phenomenon is more pronounced than that for the Irganox phenolic antioxidants.On the basis of susceptibility towards all the examined stabilisers,resulting in a sharp increase of the initial initiating activity,the titanium dioxides can be ordered as nano-rutile untreated > nano-anatase treated hydroxyapatite > nano-anatase untreated >(nano-anatase(75%)+ nano-rutile(25%))untreated > micro-anatase untreated > micro-rutile treated.These additional initiation rates of titanium dioxides which are affected by the stabilisers can be explained in terms of physical absorption of the stabilisers onto the surface of the titanium dioxide particles.The stabilisers being adsorbed onto the surface of titanium dioxides block titania surface-OH groups and thereby prevent the formation of water in the oxidizing system to promote the additional catalytic capacity of the titanium dioxide pigments.Basic amine functionalities of Chimassorb 119 FL and Cyasorb 3529 are energetically more protonated by the titanium dioxides' surface hydroxyls during oxidation than when compared with phenolic hydroxyl and ester groups of Irganox 1010 and thereby the amine functionalities stimulate a relatively higher level of additional initiating activity of the pigments.This explanation is in good accordance with the data of work elsewhere [Allen NS,Edge M,Sandoval G,Ortega A,Liauw CM,Stratton J,et al.Factors affecting the interfacial adsorption of stabilizers on to titanium dioxide particles(flow microcalorimetry,modeling,oxidation and FTIR studies);nano versus pigmentary grades.Dyes Pigments 2006;70(3);192-203].Nano-anatase pigment C is shown to exhibit a sensitizing effect at a concentration of 1 and 2% w/w in the model reaction of cumene initiated oxidation whereas it exhibits a different effect in the thermal sensitizing oxidation at 1% w/w to the stabilising at 2% w/w during thermooxidative ageing in HDPE film.
机译:进行了这项研究以阐明稳定剂与二氧化钛纳米颗粒之间的氧化相互作用,该氧化介质包括异丙苯和乙基苯的引发剂(引发剂为2,2'-偶氮二异丁腈,AIBN)的氧化(引发剂为氧化,引发剂与热炉的比较)作为初步研究,已经建立了不同的纳米和微粒尺寸的锐钛矿型和金红石型二氧化钛颜料在中等温度(60°C)下对异丙苯未引发氧化的催化作用。氧化速率在足够宽的范围内线性依赖于二氧化钛浓度的平方根,从而遵循氧化与过氧自由基重组的机理。异丙苯和乙苯引发氧化的模型反应的氧化速率的动力学测量在不存在和存在受阻哌啶稳定剂的情况下,Chimassorb 119 FL,Cyasorb 3529和s明显受阻的Irganox 1010稳定剂清楚地表明,该稳定剂促进了二氧化钛颜料的过度加成引发活性。发现这种作用非常大,即提供的额外引发速率的值是该值的2-9倍。在没有稳定剂的体系中由二氧化钛引起的初始引发速率的影响。在胺稳定剂受阻的情况下,这种现象比Irganox酚类抗氧化剂的现象更为明显。通过增加初始引发活性,可以订购二氧化钛,其形式为未经处理的纳米金红石>纳米锐钛矿处理的羟基磷灰石>未经处理的纳米锐钛矿>(未经处理的(纳米锐钛矿(75%)+纳米金红石(25%)) -锐钛型酶未处理>微金红石处理。这些受稳定剂影响的二氧化钛的额外引发速率可以用phy来解释稳定剂在二氧化钛颗粒表面上的基本吸收。稳定剂吸附在二氧化钛表面上会阻止二氧化钛表面的OH基团,从而防止氧化体系中水的形成,从而促进钛的额外催化能力与Irganox 1010的酚羟基和酯基相比,氧化期间二氧化钛的表面羟基在能量上使Chimassorb 119 FL和Cyasorb 3529的基本胺官能团质子化程度更高,因此胺官能团可激发相对较高水平的附加颜料的引发活性。这一解释与其他地方的工作数据[Allen NS,Edge M,Sandoval G,Ortega A,Liauw CM,Stratton J等]完全吻合。影响稳定剂在钛上的界面吸附的因素二氧化碳颗粒(流动微量量热法,建模,氧化和FTIR研究);纳米与色素y等级。DyesPigments 2006; 70(3); 192-203]。在异丙苯引发的氧化模型反应中,纳米锐钛矿型颜料C在1和2%w / w的浓度下显示出敏化作用。在HDPE膜的热氧化老化过程中,热敏氧化对1%w / w的稳定化表现出与2%w / w的稳定化作用不同。

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