三种木质纤维素生物质材料(大麦壳、玉米芯、龙舌兰叶)作为活性炭前体的评价

Q4 Computer Science
F. Prieto García, R. A. Canales-Flores, Judith PRIEO-MÉNDEZ, Otilio A. Acevedo-Sandoval, E. Otazo-Sánchez
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引用次数: 4

摘要

木质纤维素生物质是一种很有前途的替代能源和可再生能源,可以转化为其他增值产品,如活性炭。目的是评价大麦壳(Hordeum vulgare L.),玉米芯(Zea Mays L.)和龙舌兰叶(agave salmiana)作为活性炭的潜在前体。这些前体是从墨西哥伊达尔戈州的Almoloya和Apan获得的。原料经蒸馏水洗涤,在105℃烘箱中干燥72 h,在叶片磨机中研磨,得到0.3-1.0 mm的粒度,最后通过18和45的筛网过筛。湿度根据ASTM D3173 (ASTM, 1996)测定,灰分根据ASTM D3174 (ASTM, 2000)测定,挥发物根据ASTM D3175 (ASTM, 1997)测定,固定碳根据ASTM D3172 (ASTM, 1997)测定,总糖和脂肪根据TAPPI T204 (TAPPI, 1997)测定,木质素根据TAPPI T222 (TAPPI, 1998)测定,全纤维素根据(Wise et al., 1946)描述的方法测定,纤维素根据TAPPI T203 (TAPPI 1999)测定。结果表明:测定的总纤维素含量为82% ~ 83%,纤维素含量为52% ~ 79%,木质素含量为15% ~ 26%。元素分析表明其含碳量高,为42 ~ 45%。粒径在390.9 ~ 610.7 mm之间。热重分析显示了类似的热分解曲线,纤维素为主要阶段,峰值在300°C左右。在表面形貌上,木质纤维素残基呈纤维状和多孔结构。从这些发现可以确定所分析的前体可以被认为是活性炭的潜在前体。本文提出的结果可能有助于改善这种木质纤维素残留物的热解和活化区域。实验结果表明:炭化温度为400℃,炭化时间为30 min,前驱体质量为2 ~ 10 g, N2流量为150 cc/min。在这些条件下产生的生物碳进行了物理和化学表征。玉米芯(CCB)、大麦皮(BHB)和龙舌兰叶(ALB)的生物炭产率分别为19.75%、32.88%和31.14%。得到了以大孔结构为主、无定形结构、大量氧官能团、阴离子表面和中等灰分含量的生物碳。研究结果表明,大麦壳、玉米芯和龙舌兰叶具有良好的染料吸附能力,可能是生产生物炭的前体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
EVALUATION OF THREE LIGNOCELLULOSE BIOMASS MATERIALS (BARLEY HUSK, CORN COBS, AGAVE LEAVES) AS PRECURSORS OF ACTIVATED CARBON
Lignocellulosic biomass is a promising alternative and renewable energy source that can be transformed into other value-added products such as activated carbon. The objective was to evaluate the barley husk (Hordeum vulgare L.), the corn cobs (Zea Mays L.) and the agave leaves (Agave salmiana) as potential precursors of activated carbon. These precursors were obtained from Almoloya and Apan in the State of Hidalgo, Mexico. The raw materials were washed with distilled water, dried at 105 ºC for 72 h in an oven, ground in a blade mill to obtain a particle size of 0.3-1.0 mm and finally sieved through mesh sieves of 18 and 45. Humidity was determined according to ASTM D3173 (ASTM, 1996), ash according to ASTM D3174 (ASTM, 2000), volatile matter according to ASTM D3175 (ASTM, 1997), fixed carbon according to ASTM D3172 (ASTM, 1997), total sugars and fats according to TAPPI T204 (TAPPI, 1997), Klason Lignin according to TAPPI T222 (TAPPI,   1998), holocellulose according to the method described by (Wise et al., 1946), and (, ( and ( cellulose according to TAPPI T203 (TAPPI 1999). The results show that contents from 82 to 83% for holocellulose, from 52 to 79% for cellulose, and from 15 to 26% for lignin, were determined. Elemental analysis showed high carbon contents with values of 42-45%. Particle sizes between 390.9 mm and 610.7 mm were found. Thermogravimetric analysis showed similar profiles of thermal decomposition, being cellulose the main stage, with peaks around 300 °C. Regarding the surface morphology, the lignocellulosic residues showed fibrous and porous structure. From these findings, it is established that the precursors analyzed can be considered as potential precursors of activated carbons. The results presented here may facilitate improvements in the pyrolysis and activation areas of this lignocellulosic residues. The conditions for an acceptable yield of biochar were tested, these were: carbonization temperature of 400 °C, carbonization time of 30 min, precursor mass of 2-10 g and N2 flow rate of 150 cc/min. The biocarbons produced under these conditions were physically and chemically characterized. Biochar yields of 19.75% were obtained for corn cob (CCB), 32.88% for barley husk (BHB) and 31.14% for Agave salmiana leaves (ALB). Biocarbons with a predominantly macroporous structure, amorphous structure, numerous oxygen functional groups, anionic surface and moderate ash content were obtained. The results of this investigation show that barley husk, corn cob, and agave leaves are likely precursors for biochar production with good dye adsorption capacities.
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