绘制受硫控制的 FCCVD 合成过程中的碳纳米管长宽比、浓度和纺丝图

IF 3.1 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY
Miguel Vazquez-Pufleau , Raul Fernandez Torres , Luis Arevalo , Nabil Abomailek , Juan J. Vilatela
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引用次数: 0

摘要

浮动催化剂化学气相沉积(FCCVD)可超快合成 CNT 和其他一维纳米粒子,并将其直接组装成宏观固体。FCCVD 中的铬化生长促进剂可产生高纵横比的 CNT,这些 CNT 可在气相中聚集并形成气凝胶,气凝胶可被连续纺成宏观纤维或薄片。我们研究了硫在控制 CNT 形状和聚集方面的作用,方法是在各种 S/C 比(0.001 至 5 wt.%)下合成 CNT,并确定其直径和长度分布、数量浓度和聚集形式。在此范围内提高 S/C 比率可将 CNT 壁的平均数量从 1 个增加到 8 个,将平均长度从 34 微米减少到 6 微米,但 CNT 数量浓度大致保持在 8 × 108#/cm3 不变。假设碳纳米管在反应器的前 3 厘米内生长,则不同形态的碳纳米管的纵向生长速度为 1.5-6.5 微米/秒,但质量吞吐量相似,均为 700 微克/催化剂。这表明,无论催化剂中硫的含量如何,到达催化剂并固化为碳纳米管的碳量始终保持不变,这说明限制速率的过程并不在催化剂/促进剂界面,而是在碳质活性前体向催化剂的传输过程中,这可能是由于它们在气相中的扩散或分解动力学所致。生成的碳纳米管既有容易捆绑并形成气凝胶的聚合物状,也有不容易捆绑并形成气凝胶的棒状。我们提供了不同 CNT 浓度、长宽比和 CNT 弯曲刚度下的气凝胶 "相图"。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Mapping carbon nanotube aspect ratio, concentration and spinning in FCCVD synthesis controlled by sulphur

Mapping carbon nanotube aspect ratio, concentration and spinning in FCCVD synthesis controlled by sulphur

Floating catalyst chemical vapor deposition (FCCVD) enables ultrafast synthesis of CNTs and other 1D nanoparticles and their direct assembly as macroscopic solids. The chalcogen growth promotor in FCCVD produces high aspect ratio CNTs that can aggregate in the gas phase and form an aerogel which can be continuously spun as macroscopic fibres or sheets. We study the role of sulphur in controlling CNT morphology and aggregation by synthesising CNTs under a wide range of S/C ratios (0.001 to 5 wt.%) and determining their diameter and length distributions, number concentration and form of aggregation. Increasing S/C ratio in this range increases mean number of CNT walls from 1 to 8, decreases mean length from 34 to 6 µm, but CNT number concentration remains approximately constant at 8 × 108#/cm3. Assuming growth within the first 3 cm of the reactor, longitudinal growth rate spans 1.5- 6.5 µm/s for the different CNT morphologies, but with similar mass throughput of 700 attogram/catalyst. This indicates the amount of carbon reaching the catalyst and solidifying as CNT remains constant regardless of the sulphur available in the catalyst, suggesting the rate limiting process is not at the catalyst/promoter interface but instead in the transport of carbonaceous active precursors to the catalyst, either due to their diffusion in the gas phase or decomposition kinetics. The CNTs produced range from polymer-like, which readily bundle and form aerogels, to rod-like that do not. We include aerogelation “phase diagrams” for different CNT concentrations, aspect ratios and CNT bending stiffness.

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来源期刊
Carbon Trends
Carbon Trends Materials Science-Materials Science (miscellaneous)
CiteScore
4.60
自引率
0.00%
发文量
88
审稿时长
77 days
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