Water-selective adsorption sites on detonation nanodiamonds

被引:19
作者
Pnia-Salazar, Elda-Zoraida [1 ]
Kukobat, Radovan [2 ]
Futamura, Ryusuke [2 ]
Hayashi, Takuya [3 ]
Toshio, Sakai [4 ]
Osawa, Eiji [5 ]
Kaneko, Katsumi [2 ]
机构
[1] Shinshu Univ, Interdisciplinary Sch Sci & Technol, Nagano 380855, Japan
[2] Shinshu Univ, Ctr Energy & Environm Sci, Nagano 3808553, Japan
[3] Shinshu Univ, Dept Elect Engn, Nagano 3808553, Japan
[4] Shinshu Univ, Fac Engn, Dept Mat Chem, Nagano 3808553, Japan
[5] Nanocarbon Res Inst Ltd, Nagano 3868567, Japan
关键词
ACTIVATED CARBON; MESOPOROUS CARBONS; SURFACE; POWDER; NITROGEN; VAPOR; FTIR; FIELDS; GEL;
D O I
10.1016/j.carbon.2018.07.036
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Nanodiamond particles form aggregates having porosity in the range of micropores to mesopores with an average pore diameter of 4.5 nm. The measured porosity depends on the removal of pre-occupied water and gases from the nanodiamond aggregates, which is sensitive to thermal treatments. We heated hydrogel nanodiamonds at 423-623 K in vacuo in order to understand the relationship between water adsorptivity and pore structure evaluated from nitrogen and argon adsorption isotherms at 77 K and 87 K, respectively. Temperature-programmed evolved gas analysis showed the evolution of water and CO2 on heating nanodiamonds in vacuo up to 700 K. The surface functional groups of nanodiamonds were not affected by the thermal treatments, as shown by FTIR and XPS analyses. However, the water adsorptivity was enhanced by heating at 623 K due to the removal of the pore blocking effect originated from water molecules selectively adsorbed. Water molecules adsorbed on these selective sites should cause the intensive hygroscopic property of nanodiamonds. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:853 / 860
页数:8
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