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Synergistic Process for High Nitrogen Content Feedstocks Catalytic Cracking: A Case Study of Controlling the Reactions of Nitrogen Compounds in Situ

机译:协同过程氮含量高原料催化裂化:一个案例研究控制氮的化合物的反应原位

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摘要

There is currently a growing need to process heavier and tougher feedstocks with increased nitrogen content for fluid catalytic cracking (FCC) units. A coker gas oil with high nitrogen content was catalytically cracked in a pilot-scale riser FCC apparatus under different conditions based on different FCC processes. Then the nitrogen balance and the conversion of saturates, aromatics, resins, and asphaltenes (SARA) were calculated, and the acid amounts of coked catalysts were analyzed by the NH3-TPD method. The results show that in the synergistic process the adsorption of nitrogen-containing species on the catalyst was controlled and more acid sites were available, thus more nitrogen-free hydrocarbons, mainly the saturates, could be cracked, while the nitrogen compounds were enriched in the cracked heavy oil. Furthermore, the compositional and structural identification of nitrogen compounds in cracked heavy oils was carried out by electrospray ionization (ESI) Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS). Six nitrogen class species, N1, N2, N1O1, N1O22, N1S1, and N1O1S1, were assigned in the positive-ion spectrum, while only three class species, N1, N1,O1, and N1S1, were assigned in the negative-ion spectrum. The N1 class nitrogen compounds were the dominant species, and the N1O1S1. species were generated during the FCC process. Most of the nitrogen-containing species were 4—5 rings with short alkyl side chains. The MS data also show that the synergistic process not only inhibited the adsorption of nitrogen compounds on the catalyst but also changed their reaction pathways.
机译:目前越来越多的人需要的过程更重和更严格的原料增加流化床催化裂解的含氮量(FCC)单位。内容是催化地裂缝半工业规模下立管FCC装置不同基于不同的FCC过程条件。氮平衡和转换饱和烃、芳烃、树脂和沥青质(SARA)计算,酸量的焦化NH3-TPD催化剂进行了分析方法。氮含量的吸附过程物种催化剂控制等等酸网站可用,因此更多物品的碳氢化合物,主要是饱和烃,可以被破解,而氮的化合物浓缩在了重油。此外,成分和结构含氮化合物在裂缝的识别重油是由电喷射电离(ESI)傅里叶变换离子回旋共振质谱(FT-ICR MS)。氮类物种,N1、N2 N1O1, N1O22,N1S1 N1O1S1,被分配正离子频谱,而只有三个类物种,N1, N1、O1群和N1S1,被分配负离子频谱。化合物的优势种,N1O1S1。的过程。4 - 5环烷基侧链较短。女士的数据还表明,协同过程不仅抑制了氮的吸附化合物在催化剂也改变了他们反应途径。

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