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低阶煤原位制备ZnO基活性炭脱硫剂
引用本文:演康,杨颂,刘守军,杨超,樊惠玲,上官炬. 低阶煤原位制备ZnO基活性炭脱硫剂[J]. 化工学报, 2021, 72(9): 4921-4930. DOI: 10.11949/0438-1157.20210041
作者姓名:演康  杨颂  刘守军  杨超  樊惠玲  上官炬
作者单位:太原理工大学化学化工学院,山西太原030024;山西省民用洁净燃料工程研究中心,山西太原030024;太原理工大学化学化工学院,山西太原030024;太原理工大学,煤科学与技术教育部和山西省重点实验室,山西太原030024;山西省民用洁净燃料工程研究中心,山西太原030024;太原理工大学,煤科学与技术教育部和山西省重点实验室,山西太原030024;太原理工大学,煤科学与技术教育部和山西省重点实验室,山西太原030024;山西省民用洁净燃料工程研究中心,山西太原030024
基金项目:国家自然科学基金项目(22078223);山西省高等学校科技创新项目(2019L0313);山西省专利推广实施资助计划(20200719)
摘    要:将金属氧化物活性组分通过浸渍负载的方式分散到多孔载体上,是制备高活性金属氧化物脱硫剂的常用方法。然而,由于活性组分的负载易使载体孔隙率下降,导致活性组分的脱硫能力不能充分发挥。本文直接以廉价的低阶煤为原料,经过预处理后在煤中加入硝酸锌,通过物理-化学活化法一步制备ZnO基活性炭常温脱硫剂,即将活性炭的制备与活性组分的负载一步完成。研究了硝酸锌加入量、活化温度和活化时间对脱硫剂脱硫性能的影响。结果表明:当硝酸锌加入量为20%(质量),活化温度为850℃,活化时间为1 h时,脱硫剂的穿透时间为210 min,其对应的穿透硫容为71.4 mg/g,其脱硫性能是同等实验条件下商业活性炭负载ZnO脱硫剂的5.3倍,较高的脱硫性能主要归因于其发达的介孔孔隙,不仅有利于传质,而且有利于硫化产物的存储。

关 键 词:原位制备  活性炭  脱硫剂  吸附  H2S
收稿时间:2021-01-08

In-situ preparation of ZnO-based activated carbon desulfurizer from low-rank coal
Kang YAN,Song YANG,Shoujun LIU,Chao YANG,Huiling FAN,Ju SHANGGUAN. In-situ preparation of ZnO-based activated carbon desulfurizer from low-rank coal[J]. Journal of Chemical Industry and Engineering(China), 2021, 72(9): 4921-4930. DOI: 10.11949/0438-1157.20210041
Authors:Kang YAN  Song YANG  Shoujun LIU  Chao YANG  Huiling FAN  Ju SHANGGUAN
Affiliation:1.College of Chemistry and Chemical Engineering, Taiyuan University of Technology, Taiyuan 030024, Shanxi, China;2.Key Laboratory of Coal Science and Technology of Ministry of Education and Shanxi Province, Taiyuan University of Technology, Taiyuan 030024, Shanxi, China;3.Shanxi Engineering Center of Civil Clean Fuel, Taiyuan University of Technology, Taiyuan 030024, Shanxi, China
Abstract:Dispersing the metal oxide active component on the porous carrier by impregnation and loading is a common method for preparing highly active metal oxide desulfurizers. However, due to the decrease of porosity of the carrier due to the loading of active components, the desulfurization capacity of active components cannot be fully utilized. In this study, cheap low-rank coal was directly used as raw material. After pretreatment, zinc nitrate was added into the coal to prepare ZnO based activated carbon desulfurizer at room temperature in one step through physical-chemical activation method. The preparation of activated carbon and the loading of active components were completed in one step. The effects of zinc nitrate immersion amount, activation temperature and activation time on desulfurization performance of desulfurizer were studied. The results showed that when the immersion amount was 20%(mass), the activation temperature was 850℃, and the activation time was 1 h, the breakthrough time of desulfurizer was 210 min, and its sulfur capacity was 71.4 mg/g. Its desulfurization performance was 5.3 times that of commercial activated carbon supported ZnO desulfurizer under the same experimental conditions. The high desulfurization performance is mainly attributed to its developed mesoporous pores, which is not only conducive to mass transfer, but also beneficial to the storage of sulfide products.
Keywords:in-situ preparation  activated carbon  desulfurizer  adsorption  hydrogen sulfide  
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