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用于热解α-纤维素加氢裂化的、在SBA-15内外表面均匀分散的镍纳米颗粒。

Well-dispersed nickel nanoparticles on the external and internal surfaces of SBA-15 for hydrocracking of pyrolyzed α-cellulose.

作者信息

Trisunaryanti Wega, Suarsih Endah, Falah Iip Izul

机构信息

Department of Chemistry, Universitas Gadjah Mada Indonesia

出版信息

RSC Adv. 2019 Jan 9;9(3):1230-1237. doi: 10.1039/c8ra09034c.

DOI:10.1039/c8ra09034c
PMID:35518034
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9059615/
Abstract

Catalysts comprising nickel supported on SBA-15 were prepared by wet impregnation and co-impregnation methods. Wet impregnation was performed by directly dispersing an Ni(NO)·6HO aqueous solution into SBA-15, whereas in co-impregnation, ethylene glycol (EG) was added to nickel nitrate aqueous solution prior to dispersion into SBA-15. After drying and calcination, NiO/SBA-15w and NiO/SBA-15c were produced. Later, after the reduction process, Ni/SBA-15w and Ni/SBA-15c were obtained. The prepared catalysts were evaluated for the hydrocracking of pyrolyzed α-cellulose. The TEM images revealed that the catalysts prepared by wet impregnation showed inhomogeneous distribution of nickel loading, whereas catalysts prepared by co-impregnation using EG exhibited homogeneous distribution and formed no nickel aggregates. During hydrocracking of pyrolyzed α-cellulose, Ni/SBA-15c with total acidity, nickel loading, particle size, and specific surface area of 7.27 m mol g, 5.20 wt%, 3.17 nm, and 310.0 m g, respectively, exhibited the best catalytic performance compared to other prepared catalysts with 67.35 wt% conversion of liquid product with maximum selectivity in producing 13.09 wt% of 3-methyl-pentane. Moreover, Ni/SBA-15w with total acidity, nickel loading, particle size, and specific surface area of 10.87 m mol g, 8.15 wt%, 7.01 nm, and 628.0 m g, respectively, produced 69.89 wt% liquid product without hydrocarbons. Study of selectivity towards the formation of liquid hydrocarbons was carried out double step hydrocracking using Ni/SBA-15w, and 18.55 wt% of -hexane was produced in the liquid product.

摘要

采用湿浸渍法和共浸渍法制备了负载在SBA - 15上的镍基催化剂。湿浸渍法是将硝酸镍六水合物(Ni(NO₃)·6H₂O)水溶液直接分散到SBA - 15中,而共浸渍法则是在将硝酸镍水溶液分散到SBA - 15之前先加入乙二醇(EG)。干燥和煅烧后,得到了NiO/SBA - 15w和NiO/SBA - 15c。随后,经过还原过程,得到了Ni/SBA - 15w和Ni/SBA - 15c。对制备的催化剂进行了热解α - 纤维素加氢裂化性能评价。透射电子显微镜(TEM)图像显示,湿浸渍法制备的催化剂镍负载分布不均匀,而采用EG共浸渍法制备的催化剂镍负载分布均匀且未形成镍聚集体。在热解α - 纤维素加氢裂化过程中,总酸度、镍负载量、粒径和比表面积分别为7.27 mmol/g、5.20 wt%、3.17 nm和310.0 m²/g的Ni/SBA - 15c与其他制备的催化剂相比表现出最佳的催化性能,液体产物转化率为67.35 wt%,生成3 - 甲基戊烷的最大选择性为13.09 wt%。此外,总酸度、镍负载量、粒径和比表面积分别为10.87 mmol/g、8.15 wt%、7.01 nm和628.0 m²/g的Ni/SBA - 15w产生了69.89 wt%不含烃类的液体产物。使用Ni/SBA - 15w对液态烃形成的选择性进行了两步加氢裂化研究,液体产物中生成了18.55 wt%的正己烷。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa65/9059615/3e174d120761/c8ra09034c-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa65/9059615/7251b141b7ed/c8ra09034c-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa65/9059615/17379b281b80/c8ra09034c-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa65/9059615/be45f4693cbc/c8ra09034c-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa65/9059615/59691a30c7a5/c8ra09034c-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa65/9059615/23e768fc385d/c8ra09034c-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa65/9059615/3e174d120761/c8ra09034c-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa65/9059615/7251b141b7ed/c8ra09034c-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa65/9059615/17379b281b80/c8ra09034c-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa65/9059615/be45f4693cbc/c8ra09034c-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa65/9059615/59691a30c7a5/c8ra09034c-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa65/9059615/23e768fc385d/c8ra09034c-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa65/9059615/3e174d120761/c8ra09034c-f6.jpg

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本文引用的文献

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