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作 者:李国强[1] 田福海[1] 张永发[1] 丁佳丽[1] 付亚利[1] 王影[1] 张国杰[1]
机构地区:[1]太原理工大学煤科学与技术教育部与山西省重点实验室,山西太原030024
出 处:《新型炭材料》2014年第6期486-492,共7页New Carbon Materials
基 金:山西省自然科学基金(2010011014-1);国家科技支撑计划(2012BAA04B03);国家自然科学基金(51274147)~~
摘 要:以竹炭与褐煤混合料压块制备出柱状母料,500℃炭化30min后,经0-21.91%氨水气化,850℃活化2h,获得胺化竹村褐煤活性炭。采用BET和XPS研究竹木/褐煤活性炭的孔结构和表面化学,在100℃下考察活性炭对模拟烟气(0.1439%SO2、8.02%O2和10.11%水蒸气)中SO2的脱除性能。结果表明,氨水活化与水蒸气活化形成的竹木/褐煤活性炭孔径分布类似,主要分布于1~2.5nm,2.42%氨水活化制备的活性炭硫容是水蒸气活化的1.52倍;两种活性炭表面有相同种类的含碳基团,氨水活化后活性炭表面出现了类吡啶或类腈基团和胺、酰胺、酰亚胺及类吡咯基团;竹木/褐煤活性炭的脱硫性能主要与类吡啶基团有关。A columnarbamboo/lignite material was prepared by briquetting a mixture of bamboo carbon and lignite. Activated car- bons were obtained by carbonizing the material at 500 ℃ for 30 min, followed by activation at 850℃ for 2 h using either steam or a gaseous mixture of ammonia in water with an ammonia concentration of 2.42 mass%. The ammonia-activated carbon was soaked in 21.91% ammonia water for 5 h and dried at 200℃ to modify its surface chemical properties. The pore structure and surface chemical states of the activated carbons were investigated by physical adsorption and XPS. Their desulfurization performance was e- valuated in a simulated flue gas (SO2 0.1439%, 02 8.02% and water vapor 10.11% ) at 100 ℃. Results show that the activated carbons produced with and without ammonia have similar pore size distributions in the range 1-2.5 nm. Sulfur adsorption capacity of the ammonia-activated one ( 106.1 mg/g) is significantly higher than those of the steam-activated one (69.8 mg/g). Surface modi- fication of the ammonia-activated carbon further improves its sulfur adsorption capacity to 155.9 mg/g. The surfaces of the two kinds of activated carbons contain the same type of carbon groups. The ammonia-activated carbon and its surface modified derivative have similar nitrogen contents with a similar proportion of pyridine or nitrile groups ( 398.3-398.9 eV), amine, amide, imide and pyrrole class groups (400.2-400.8 eV).
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