화학공학소재연구정보센터
Fuel Processing Technology, Vol.90, No.2, 196-203, 2009
A thermal investigation on coals from Assam (India)
A thermal characterization of two coal samples from Ledo and Tikak collieries of Makum coalfield, Assam, India using XRD, FT-IR, and TGA was reported in this paper. The coal samples were heated for 20, 40 and 60 min in a 1000-watt heater (temperature similar to 250 degrees C) in presence of air and characterized by XRD and FT-IR spectroscopy. Both the coals contain amorphous and crystalline phases. The raw coals also contain very small peaks due to quartz, calcite, gypsum, pyrite, and chlorite. The XRD patterns were found to change upon heating. In the coals heated for 20 and 40 min, it was observed that both amorphous and crystalline parts are common in them; crystalline part being the major one in the 40 min heated samples. The XRD patterns of the samples heated for 60 min indicate the presence of major quantities of alpha-quartz, hematite, and chlorite in them. They also show some new peaks, which are assigned to be kaolinite, illite, magnetite and very small in comparison to the amorphous portion in raw coals. a-quartz was found to be most stable crystalline phase of silica in the coals. The crystallinity % (X-ray) of the coals heat-treated for different times was determined and found to be increasing with time of heating. The FT-IR spectra of raw and heat-treated coal samples at 250 degrees C were also recorded and compared. The spectra were observed to be almost similar and it was observed that few functional groups disappear on heating at 250 degrees C. The same coal samples were also characterized by thermogravimetric analysis (TGA) and differential thermal analysis (DTA) techniques. On heat treatment in air atmosphere up to 800 degrees C, 20-27% weight loss occurs due to removal of various volatile materials. DTA results indicate the chemical reactivity of the coal sample initially at 80-110 degrees C due to loss of water, and two other major reactions at around 420 and 530 degrees C due to primary and secondary volatization. (C) 2008 Elsevier B.V. All rights reserved,