煅烧温度对用过的烹调油与生物燃料发生热裂解反应时硅助镍铜坩埚性能的影响

Figosstar Hartono, Ahmad Suseno, Yayuk Astuti, D. S. Widodo
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引用次数: 0

摘要

加氢裂化反应是一种将植物油中的碳氢化合物键断裂成较短碳氢化合物的反应,以便将其用作生物燃料。镍和铜金属在这一反应中非常常用,其中镍金属在反应中起到活性催化剂的作用,而铜金属则在加氢裂化反应中起到增加镍金属稳定性的作用,防止焦炭的形成。介孔二氧化硅具有高稳定性和孔隙率,因此被用作镍和铜金属的载体。煅烧是合成介孔二氧化硅的过程之一,其目的是去除二氧化硅中的模板,并在二氧化硅结晶度和孔隙率的形成过程中发挥作用。煅烧温度的变化会影响二氧化硅的孔隙率和结晶度,从而导致镍和铜金属分布的差异。Ni 和 Cu 金属分布的差异会影响活性位点的表面积,从而影响催化剂在加氢裂化反应中的活性和选择性。本研究旨在合成一种 Ni-Cu/Silica 催化剂,用于将废食用油加氢裂化反应转化为生物燃料。采用水热法合成介孔二氧化硅。然后,通过在介孔二氧化硅中浸渍和还原镍和铜金属,合成出 Ni-Cu/Silica 催化剂。然后将 Ni-Cu/Silica 催化剂用于废食用油加氢裂化反应,以测试其活性和选择性。傅立叶变换红外光谱的表征结果表明,Ni-Cu/二氧化硅催化剂具有一个振动峰,表明存在硅醇(Si-O-Si)和硅氧烷(Si-OH)基团。根据酸度测试,SM-400、SM-500 和 SM-600 催化剂的傅立叶变换红外吸收峰上检测到路易斯酸位点和布朗斯泰德酸位点,其中 SM-500 的酸度最高。XRD 结果表明,Ni-Cu/二氧化硅催化剂为无定形结晶,XRD 衍射图中检测到 Ni 和 Cu 金属位点。GSA 结果表明,SM-400、SM-500 和 SM-600 催化剂的主要孔隙尺寸位于介孔区。气相色谱-质谱(GC-MS)结果表明,与不使用催化剂的加氢裂化相比,使用催化剂的加氢裂化产生更多的产品,与其他催化剂相比,SM-500 催化剂具有最高的活性和选择性。
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EFFECT OF CALCINATION TEMPERATURE ON THE PROPERTIES OF SILICA-SUPPORTED Ni-Cu CATALYST FOR THE HYDROCRACKING REACTION OF USED COOKING OIL TO BIOFUEL
The hydrocracking reaction is a reaction that breaks hydrocarbon bonds from vegetable oil into shorter hydrocarbons so that they can be used as biofuel. Ni and Cu metals are quite commonly used in this reaction, where Ni metal functions as an active catalyst in the reaction, and Cu metal plays a role in increasing the stability of Ni metal from coke formation during the hydrocracking reaction. Mesoporous silica is used as a carrier for Ni and Cu metals because it has high stability and porosity. Calcination is one of the processes in the synthesis of mesoporous silica which aims to remove the template from the silica and plays a role in the formation of silica crystallinity and porosity. Changes in calcination temperature will affect the porosity and crystallinity of silica which causes differences in the distribution of Ni and Cu metals. The difference in the distribution of Ni and Cu metals affects the surface area of the active site which can influence the activity and selectivity of the catalyst in the hydrocracking reaction. This research aims to synthesize a Ni-Cu/Silica catalyst for the hydrocracking reaction of used cooking oil into biofuel. Mesoporous silica is synthesized by the hydrothermal method. Then, the Ni-Cu/Silica catalyst was synthesized by impregnating and reducing Ni and Cu metal into mesoporous silica. The Ni-Cu/Silica catalyst was then applied to the used cooking oil hydrocracking reaction to test its activity and selectivity. The results of characterization using FTIR show that the Ni-Cu/Silica catalyst has a vibration peak which indicates the presence of silanol (Si-O-Si) and siloxane (Si-OH) groups. Based on the acidity test, the SM-400, SM-500, and SM-600 catalysts have Lewis acid sites and Brondsted acid sites detected on the FTIR absorption peak with SM-500 having the highest acidity level. The XRD results show that the Ni-Cu/Silica catalyst has amorphous crystallinity and has Ni and Cu metal sites detected in the XRD diffractogram. The GSA results show that the SM-400, SM-500, and SM-600 catalysts have dominant pore sizes in the mesoporous region. The GC-MS results show that hydrocracking using a catalyst produces more product compared to hydrocracking without a catalyst and the SM-500 catalyst has the highest activity and selectivity compared to other variations of catalyst.
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