本平台为互联网非涉密平台,严禁处理、传输国家秘密或工作秘密

活性炭结构对卷烟主流烟气化学成分吸附效率的影响

Effects of Activated Carbon Structure on its Efficiency for Adsorbing Chemical Components in Mainstream Cigarette Smoke

  • 摘要: 为考察活性炭表面结构特性对卷烟主流烟气化学成分吸附效率的影响,分析了5种结构特性不同的活性炭对卷烟主流烟气中挥发性羰基物、酚类化合物、5种挥发性有机化合物(1,3-丁二烯、异戊二烯、丙烯腈、苯、甲苯)和香味成分的吸附效率。结果表明:①吸附效率主要与活性炭的比表面积有关,在用量一定的情况下,烟气成分的吸附效率随活性炭比表面积的增加而增大;②微孔(r<2 nm)含量高的活性炭滞留小分子的能力强,对乙醛、1,3-丁二烯和异戊二烯等小分子化合物的吸附效率较高;同时微孔含量高的活性炭传质阻力大,对酚类的吸附较少,适当增加中孔会增加大分子化合物的吸附效率。③吸附效率与化合物的分子量和沸点有关:挥发性羰基物和5种挥发性有机化合物的吸附效率随化合物分子量和沸点的升高呈升高趋势;酚类化合物的吸附效率明显低于挥发性羰基物和5种挥发性有机化合物的吸附效率,且二元酚的吸附效率低于一元酚的吸附效率;同类香味成分的吸附效率随化合物分子量和沸点的升高呈下降趋势。

     

    Abstract: In order to investigate the effects of surface structure of activated carbon on its efficiency for adsorbing chemical components in mainstream cigarette smoke (MCS), the efficiencies of 5 activated carbons of different structure for adsorbing four kinds of components, including carbonyls,5 volatile organic compounds (1, 3-butadiene, isoprene, acrylonitrile, benzene and toluene), phenols and aroma components in MCS were analyzed. The results showed that: 1) Adsorption efficiency mainly depended on the specific surface area of activated carbon; when carbon amount was fixed, adsorption efficiency raised with the increase of specific surface area. 2) The activated carbon containing more micropores (r < 2 nm) presented stronger ability for retaining compounds of small molecular, such as acetaldehyde, 1,3-butadiene, isoprene among others; however, its higher resistance to mass transfer was adverse to phenols adsorption. Increasing mesopores would enhance macromolecular compound adsorption. 3) Adsorption efficiency was also related to the molecular weight and boiling point of compound. For volatile carbonyls and 5 volatile organic compounds, adsorption efficiency increased with the increase of molecular weight and boiling point, while it was on the contrary for aroma components of the same kind. Adsorption efficiency for phenols was significantly lower than that for volatile carbonyls and 5 volatile organic compounds, and that for dihydric phenol was lower than that for monohydric phenol.

     

/

返回文章
返回