Adsorption of acetone vapor by activated carbon at low temperatures

1967 ◽  
Vol 3 (4) ◽  
pp. 241-245
Author(s):  
V. N. Kir'yakov ◽  
I. P. Usyukin ◽  
V. M. Shleinikov
2012 ◽  
Vol 51 (36) ◽  
pp. 11667-11673 ◽  
Author(s):  
Yanli Wang ◽  
ChuanZhang Ge ◽  
Liang Zhan ◽  
Cui Li ◽  
Wenming Qiao ◽  
...  

2019 ◽  
Vol 211 ◽  
pp. 421-429 ◽  
Author(s):  
Junyeong Kim ◽  
Jeong Yeon Do ◽  
Keepyung Nahm ◽  
No-Kuk Park ◽  
Junhwa Chi ◽  
...  

2019 ◽  
Vol 44 (26) ◽  
pp. 13523-13537 ◽  
Author(s):  
Kaijie Liu ◽  
Qingbo Yu ◽  
Baolan Wang ◽  
Huaqing Xie ◽  
Wenjun Duan ◽  
...  

1991 ◽  
Vol 6 (5) ◽  
pp. 1040-1047 ◽  
Author(s):  
K. Kuriyama ◽  
M.S. Dresselhaus

The conductivity and photoconductivity are measured on a high-surface-area disordered carbon material, i.e., activated carbon fibers, to investigate their electronic properties. This material is a highly disordered carbon derived from a phenolic precursor, having a huge specific surface area of 1000–2000 m2/g. Our preliminary thermopower measurements show that the dominant carriers are holes at room temperature. The x-ray diffraction pattern reveals that the microstructure is amorphous-like with Lc ≃ 10 Å. The intrinsic electrical conductivity, on the order of 20 S/cm at room temperature, increases by a factor of several with increasing temperature in the range 30–290 K. In contrast, the photoconductivity in vacuum decreases with increasing temperature. The magnitude of the photoconductive signal was reduced by a factor of ten when the sample was exposed to air. The recombination kinetics changes from a monomolecular process at room temperature to a bimolecular process at low temperatures, indicative of an increase in the photocarrier density at low temperatures. The high density of localized states, which limits the motion of carriers and results in a slow recombination process, is responsible for the observed photoconductivity.


2017 ◽  
Vol 62 (7) ◽  
pp. 1973-1982 ◽  
Author(s):  
Florian Birkmann ◽  
Christoph Pasel ◽  
Michael Luckas ◽  
Dieter Bathen

2015 ◽  
Vol 23 ◽  
pp. 16-20 ◽  
Author(s):  
Young-Chul Lee ◽  
Sang Moon Lee ◽  
Won G. Hong ◽  
Yun Suk Huh ◽  
So Young Park ◽  
...  

2014 ◽  
Vol 56 ◽  
pp. 23-26 ◽  
Author(s):  
Wen Jing ◽  
Qianqian Guo ◽  
Yaqin Hou ◽  
Guoqiang Ma ◽  
Xiaojin Han ◽  
...  

2020 ◽  
Vol 65 (2) ◽  
pp. 706-716
Author(s):  
Sonja Schmittmann ◽  
Christoph Pasel ◽  
Michael Luckas ◽  
Dieter Bathen

1929 ◽  
Vol 2 (3) ◽  
pp. 421-430
Author(s):  
H. P. Stevens ◽  
W. H. Stevens

Abstract (1) At low temperatures by means of accelerators it is possible to produce vulcanites containing “combined sulfur” considerably in excess of that required for the formula C5H8S. Such vulcanites may be obtained by vulcanizing at 100° with a variety of ultra-accelerators with and without zinc oxide as an activator. If zinc oxide or a zinc salt is used the excess coefficient cannot be explained by the presence of the zinc sulfide in the vulcanite. (2) The amount of sulfur combined with the rubber, given sufficient heating and presence of accelerator, is mainly dependent on the excess of sulfur present. (3) Extraction of the vulcanite with hydrochloric acid-ether mixture removes a part of the “combined” sulfur. A considerable amount is removed when the amount of combined sulfur is very large, but even then the amount of sulfur remaining is considerably in excess of that required by the formula C5H8S. (4) Vulcanization at low temperatures in solution in accordance with Whitby's procedure with the aid of accelerators also yields vulcanites with coefficients in excess of that required for the formula C5H8S. (5) The result of vulcanization at low temperatures is approximately the same, whether the rubber contains all the protein and serum ingredients, the usual proportion, or very little. (6) Extraction of sulfur from vulcanite with hot acetone vapor is not complete after 1210 hrs. (7) Having regard to the hydrogen sulfide and other volatile sulfur compounds evolved in appreciable quantities during vulcanization, it is evident that part of the combined sulfur results from substitution of hydrogen by sulfur. This substituted product is decomposed by the hydrochloric acid-ether mixture. It may not be possible to decompose the whole in this manner. Consequently, any “combined” sulfur in excess of that required by the formula C5H8S may result from substitution in the molecule.


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