首页> 外文会议>ACS National Meeting Exhibition >EFFECT OF l,2-CYCLOHEXANEDIAMINE-N,N, N', N'-TETRAACETIC ACID AS COMPLEXING AGENT IN A HYDRODESULFURIZATION NIWS/AL2O3 CATALYST
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EFFECT OF l,2-CYCLOHEXANEDIAMINE-N,N, N', N'-TETRAACETIC ACID AS COMPLEXING AGENT IN A HYDRODESULFURIZATION NIWS/AL2O3 CATALYST

机译:L,2-环己二胺-N,N,N',N'-四乙酸作为络合剂在加氢脱硫NiWs / Al2O3催化剂中的影响

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The NiW catalyst has demonstrated higher hydrogenating (HYD) capacity than typical hydrotreating (HDT) catalysts, NiMo and CoMo, therefore it possess potential for deep hydrodesulfurization (HDS) processes. Similar to Mo-based catalysts, NiW/Al2O3 solids exhibit surface phenomena that are detrimental to the formation of active phase, the so-called "Ni-W-S" phase. However, the concentration of Ni in the Ni-W-S phase has still not been optimized because NiS_x segregation and nickel migration occur. Furthermore, the dispersion and sulfidation of active phase components should be improved [1]. In this sense, addition of complexing agents has shown to be beneficial on the catalytic activity in sulfide HDT catalysts [2]. Firstly, the effect of 1, 2-cyclohexanediamine-N, N, N', N'-tetraacetic acid (CyDTA) incorporation in the synthesis of NiMo and CoMo catalysts has been studied, displaying significant increases in the promotion of MoS2 and consequently, obtaining improvements in HDS activity [2-4]. Meanwhile, Kishan et al [5] studied NiW/SiO2 catalyst prepared with CyDTA and observed similar improvements, which were associated with a delay in the sulfidation of nickel entities, simultaneous sulfidation with tungsten and resulting in close contacts that favored the promotion of WS2 edges. Recently, Suarez-Toriello et al [6] showed that control of pH of the nickel-citric acid solution had an important role over the modulation of metal-support interactions, achieving favorable conditions for the formation of the sulfide phase and reaching important increases in catalytic activity in the HDS of 4,6-dimethyldibenzothiophene (46DMDBT).
机译:NiW催化剂已经表现出比典型的加氢处理(HDT)催化剂,NiMO和COMO更高的氢化(HYP)容量,因此它具有深加氢脱硫(HDS)方法具有潜力。与基于Mo的催化剂类似,NiW / Al 2 O 3固体表现出对形成活性相的不利的表面现象,所谓的“Ni-W-S”相。然而,由于NIS_X偏析和镍迁移,仍未得到优化Ni-W-S相中Ni的浓度。此外,应改善活性相组分的分散和硫化[1]。从这个意义上讲,添加络合剂已经显示有利于硫化物HDT催化剂中的催化活性[2]。首先,研究了1,2-环己二胺-N,N,N',N'-四乙酸(CYDTA)在合成NiMO和COMO催化剂中的作用,在促进MOS2的情况下显示显着增加,获得HDS活动的改进[2-4]。同时,吉山等[5]研究了用CyDTA制备的NiW / SiO 2催化剂,并观察到类似的改进,其与镍实体硫化的延迟相关,与钨的同时硫化并导致接近触点,这些接触是有利于促进WS2边缘的密切触点。最近,Suarez-Toriello等[6]显示,对金属支持相互作用的调节,对镍 - 柠檬酸溶液的pH的控制具有重要作用,实现了形成硫化物相的有利条件,并达到重要增加在4,6-二甲基二苯甲酸苯甲乙烯(46dmdbt)的HDS中的催化活性。

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