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首页> 外文期刊>Fullerenes, nanotubes, and carbon nanostructures >The role of carbon nanostructures in the ozonization of different carbon black grades, together with graphite and rubber crumb in an IR gas cell
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The role of carbon nanostructures in the ozonization of different carbon black grades, together with graphite and rubber crumb in an IR gas cell

机译:碳纳米结构与红外气室中的石墨和橡胶屑一起在不同炭黑等级的臭氧化中的作用

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Four carbon black grades (namely N234, N375, N660, and N991) having surface area of 120, 90, 36, and 8 m(2)/g have been studied together with a micronized synthetic graphite and a rubber crumb in their reaction with ozone. The study was conducted at room temperature in heterogeneous and static conditions inside an infrared gas cell. Using gas-phase infrared spectroscopy it has been followed the evolution Of CO2 formed by the O-3 attack directed toward the carbon surface and the consumption of ozone admitted into the cell using the ozone absorption band at 1056 cm(-1). The pseudofirst kinetic rate constant k derived from the ozone consumption in presence of carbon materials was determined for all the carbon materials studied. The reaction between ozone and carbon blacks essentially involves two stages: the gasification of the surface to CO2 and its functionalization with oxygenated chemical groups, mainly under the form of COOH but also many other groups. The pseudorfirst order kinetics appears adequate to describe the heterogeneous reaction between ozone and the selected carbon materials. Graphite reacts with O-3 in the conditions selected in this work with evolution of CO2. Graphite is less reactive with ozone than carbon blacks but its reactivity is comparable to that shown by powdered solid C-60 and C-70 fullerenes. Rubber crumb can be considered a carbon material in fact it reacts with ozone releasing CO2 at least at the early stages of exposure. This fact is really surprising and a mechanism involving free carbon black on the crumb surface has been advocated to justify this result. The discussion of the results has been focused on the role played by carbon nanostructures, in particular by the fullerene-like structures present in the graphene sheets to explain the phenomena of gasification and surface functionalization.
机译:研究了表面积分别为120、90、36和8 m(2)/ g的四种炭黑等级(即N234,N375,N660和N991)以及微粉化的合成石墨和橡胶屑,它们与臭氧。该研究是在室温下在红外气体池内的非均质和静态条件下进行的。使用气相红外光谱法,已经观察到由O-3攻击向碳表面定向而形成的CO2的释放,以及使用1056 cm(-1)的臭氧吸收带吸收进入电池的臭氧的消耗量。对于所有研究的碳材料,确定了从碳材料存在下的臭氧消耗量得出的拟一级动力学速率常数k。臭氧与炭黑之间的反应主要涉及两个阶段:将表面气化为CO2以及用含氧化学基团(主要为COOH形式)以及许多其他基团进行官能化。拟一级动力学似乎足以描述臭氧与所选碳材料之间的异质反应。在此工作中选择的条件下,石墨会与O-3反应,并释放出CO2。石墨与臭氧的反应性不如炭黑,但其反应性可与粉状固体C-60和C-70富勒烯所显示的反应性相媲美。橡胶屑可以被认为是一种碳材料,实际上,它至少在接触初期会与臭氧发生反应,释放出二氧化碳。这个事实确实令人惊讶,并且已经提出了一种在屑屑表面使用游离炭黑的机制来证明这一结果的合理性。结果的讨论集中在碳纳米结构,特别是石墨烯片中存在的富勒烯样结构所起的作用上,以解释气化和表面功能化现象。

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