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C9 Petroleum Resin Hydrogenation over a PEG1000-Modified Nickel Catalyst Supported on a Recyclable Fluid Catalytic Cracking Catalyst Residue

机译:C9石油树脂氢化在可再循环流体催化裂解催化剂残留物上的PEG1000改性的镍催化剂上

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A PEG1000-modified nickel-based catalyst (Ni-PEG1000/FC3R) supported on an activated fluid catalytic cracking catalyst residue (FC3R) was synthesized and applied to C9 petroleum resin (C9PR) hydrogenation. The results of the Brunauer–Emmett–Teller method, X-ray diffraction, H_(2) temperature-programmed reduction, and scanning electron microscopy–energy-dispersive X-ray spectroscopy show that the Ni-PEG1000/FC3R catalyst had a smaller crystallite size and higher Ni dispersion than those of a Ni/FC3R catalyst. The prepared Ni-PEG1000/FC3R catalyst was applied in a hydrogenation of C9PR at 270 °C and 6 MPa H_(2) pressure for 3 h. Under these conditions, the bromine value of C9PR was decreased from 46.1 g Br/100 g (Gardner color grade no. 11) to 0.72 g Br/100 g (Gardner color grade no. 1), and the sulfur content was reduced from 25.7 to 1.66 mg kg~(–1). Experimental results show that the Ni-PEG1000/FC3R catalyst exhibited high activity and stability for C9PR hydrogenation.
机译:合成了在活性流体催化裂化催化剂残基(FC3R)上负载的PEG1000改性的镍基催化剂(Ni-PEG1000 / FC3R)并施加到C9石油树脂(C9PR)氢化。 Brunauer-Emmett-exchar方法,X射线衍射,H_(2)的温度减小和扫描电子显微镜 - 能量 - 分散X射线光谱结果表明,Ni-PEG1000 / FC3R催化剂具有较小的微晶尺寸和较高的Ni分散体比Ni / Fc3R催化剂的催化剂。将制备的Ni-PEG1000 / FC3R催化剂在270℃和6MPa H_(2)压力下施加氢化C9PR,3小时。在这些条件下,C9PR的溴值从46.1g BR / 100g(Gardner Color Dea,11)降低至0.72g Br / 100g(Gardner Color级No.1),硫含量从25.7降低1.66 mg kg〜(-1)。实验结果表明,Ni-PEG1000 / FC3R催化剂表现出C9PR氢化的高活性和稳定性。

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