In order to improve the drying efficiency of lignite and restrain the moisture re-adsorption of dewatered coal, the drying characteristics of typical Chinese lignite, the re-adsorption performances of dewatered samples and the change in pore structure throughout the entire processes were investigated in this study. Lignite samples with four different particle size fractions were dried in a fixed-bed reactor in the temperature range 60-160 C. The re-adsorbing moisture behaviors of dewatered coal samples containing different water contents were investigated at temperatures of 20-40 C and humidities of 55-95%. The changes in the pore structure of raw coal and different dried samples were measured by mercury intrusion porosimetry (MIP) and the relations between their re-adsorption performance and change in pore structure were explored. The moisture removal yields of lignite increased with an increase in drying time and temperature and was close to 100% above 120 C and over 100% after holding 40 and 15 min at temperatures of 140 and 160 C due to the release of CO 2 from the decomposing carboxyl group in the coal matrix. The re-adsorbed moisture content in dewatered coal was influenced by drying temperature and coal particle size through varying pore structure. The temperature and relative humidity in the re-adsorbing process were the main factors that influenced the moisture re-adsorption capacity of dewatered lignite, in which the re-adsorbing temperature mainly operated by varying the bonding ability of water on the surface of dewatered coal, and the relative humidity was connected with the pore structure as well. The mesopore was the main factor that influenced the re-adsorption of dewatered coal and the re-adsorption of moisture in dewatered coal at 100 C was highest due to the narrow range of the pore radius and because the relative volume ratio of 5 to 50 nm mesopore (above 91%) was high. The water loss yield of lignite with smaller particle size was higher due to its larger pore volume and surface area, but its re-adsorption capacity was lower because of lower volume ratio of 5 to 50 nm mesopore volume in dewatered coal obtained from the smaller size lignite. INTRODUCTIONCoal will continue to play an important role in China to maintain the steady development of China's economic society and improve the people's living standards. Inferior coals with relatively abundant in resource reserves, especially lignite, have attracted increasing attention in supplying primary energy with the rapid consumption of high-quality coal. However, the high moisture content of lignite and re-adsorption properties of dewatered coal, which result in a lower calorific value, higher power consumption, lower efficiency, greater spontaneous combustion risk, and higher storage and transportation cost, critically restrict the exploitation and utilization range of lignite. [1,2] Therefore, it is important to efficiently reduce its moisture content and restrain the re-adsorption capacity of dewatered coal.Removing moisture by drying enables ...

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Bamboo, with its advantages of fast growth, short renovation, easy propagation and rich in cellulose and hemicellulose, is a potential feedstock for bioethanol or other biofuels production. The objective of this study was to examine the feasibility of microwave assistant KOH pretreatments to enhance enzymatic hydrolysis of bamboo. Pretreatment was carried out by immersing the bamboo in KOH (12% and 8% w/w bamboo) solutions and exposing the slurry to microwave radiation power of 400 W for 30min. Chemical composition of the pretreated substrates and spent liquor was analyzed. Pretreated substrates were enzymatic hydrolyzed, and glucose and xylose in the hydrolysate were analyzed. The results showed that the pretreated substrate with microwave assisted KOH had significantly higher sugar yield than the untreated samples. The fermentation inhibitors formic acid, furfural, HMF and levulinic acid were much lower than acid pretreatment reported.

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Hydrogen bonding patterns and halogen⋯halogen interactions, C/N–H⋯Cl hydrogen bonding in a series of multi-component molecular structures constructed by tetrachlorophthalic acid with N-heterocycles were discussed.