FORMATION OF NANO STRUCTURES IN RESULT OF HOMOGENOUS NUCLEATION OF CARBON OBTAINED IN THERMAL PLASMA UNDER ATMOSPHERIC PRESSURE

IF 0.6 Q4 CHEMISTRY, MULTIDISCIPLINARY
M. Shavelkina, R. Amirov, T. Borodina, V. Kiselev, T. Shatalova, K. Rabadanov
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引用次数: 0

Abstract

Thermal plasma processing of carbon sources using a plasma jet with high heat capacity is one of the most promising methods for the synthesis of new materials. This paper describes the low-temperature deposition of carbon nanomaterials by remote plasma-enhanced chemical vapor deposition (PECVD) in the absence of catalysts. The remote PECVD process differs from conventional and direct PECVD process in two ways: (a) only a subset of the process reactants and/or diluents are directly plasma excited; and (b) thin film deposition takes place on a substrate that is outside of the plasma glow region. In conventional CVD methods, carbon is produced from the decomposition of carbon sources such as hydrocarbons, carbon monoxide, alcohols, and so on, over a metal catalyst. The unavoidable metal species remaining in carbon nanomaterials would lead to obvious disadvantages for property characterization and application exploration. Despite sustained efforts, it is still an intractable problem to remove metal catalysts completely from carbon nanomaterials samples without introducing defects and contaminations. Good reactor design allowed to overcome problems of chemical and structural purity, and poor process robustness in terms of phase composition of product from run to run. For the synthesis of graphene materials, carbon black, carbon nanotubes, nanowires we used the thermal plasma generator which is a high current divergent anode-channel DC plasma torch. The experiment involved a simultaneous input of hydrocarbons (methane, propane, butane, acetylene) with the plasma forming gas (helium, argon, nitrogen) into the plasma torch, wherein heating and decompositions occurred in the plasma jet and in the region of the arc discharge, followed by condensation of the synthesis product on metallic surfaces. The deposition rate was varied with distance from the plasma. Consumption of carbon source, plasma forming gas and plasma torch power were changed independently from each other. For the experimental conditions the electric power of plasma torch was set up to 40 kW. Regularities of formation of carbon thread-like nanostructures and graphene in the course of hydrocarbons pyrolysis in thermal plasma without participation of catalytic particles were studied by means of electron microscopy, X-ray diffraction, IR-spectrometry and thermogravimetry. Depending on the pyrolytic synthesis parameters, different proportions of crystal carbon and soot may be obtained. It has been demonstrated that the phase composition is varied by hydrocarbons flow rate, plasma forming gas pressure and dc plasma torch power. It has been established through the experiments that carbon nucleation is volumetric and proceeds according to the model of explosive soot formation.
在大气压力下,在热等离子体中获得的碳均匀成核的结果形成纳米结构
利用高热容量等离子体射流对碳源进行热等离子体处理是合成新材料最有前途的方法之一。本文介绍了在无催化剂的情况下,远距离等离子体增强化学气相沉积(PECVD)技术在低温下沉积碳纳米材料。远程PECVD工艺与常规PECVD工艺和直接PECVD工艺在两个方面不同:(a)只有一部分工艺反应物和/或稀释剂被直接等离子体激发;(b)薄膜沉积发生在等离子体发光区域外的衬底上。在传统的CVD方法中,碳是由碳源(如碳氢化合物、一氧化碳、醇等)在金属催化剂上分解产生的。碳纳米材料中不可避免的金属残留对其性能表征和应用开发造成了明显的不利。尽管经过了持续的努力,但如何在不引入缺陷和污染的情况下完全去除碳纳米材料样品中的金属催化剂仍然是一个棘手的问题。良好的反应器设计可以克服化学和结构纯度的问题,以及从运行到运行的产品相组成方面较差的过程稳健性。对于石墨烯材料、炭黑、碳纳米管、纳米线的合成,我们使用了热等离子体发生器,它是一种大电流发散阳极通道直流等离子体炬。实验将碳氢化合物(甲烷、丙烷、丁烷、乙炔)与等离子体形成气体(氦气、氩气、氮气)同时输入等离子体炬,在等离子体射流和电弧放电区域发生加热和分解,随后合成产物在金属表面冷凝。沉积速率随距离等离子体的远近而变化。碳源消耗量、等离子体成形气体消耗量和等离子体炬功率的变化相互独立。在实验条件下,等离子炬的功率设置为40 kW。采用电子显微镜、x射线衍射、红外光谱和热重等方法研究了无催化颗粒参与的热等离子体热解过程中碳线状纳米结构和石墨烯的形成规律。根据热解合成参数的不同,可以得到不同比例的结晶碳和烟灰。结果表明,相组成随烃类流量、等离子体成形气体压力和直流等离子体炬功率的变化而变化。通过实验确定了碳成核是体积成核的,是按照爆炸烟灰形成模型进行的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.40
自引率
44.40%
发文量
83
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