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首页> 外文期刊>Journal of the American Chemical Society >M2(ITmIT-dobdc) (M = Mn, Fe, Co, Ni) Metal-Organic Frameworks as Highly Selective, High-Capacity Adsorbents for Olefin/Paraffin Separations
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M2(ITmIT-dobdc) (M = Mn, Fe, Co, Ni) Metal-Organic Frameworks as Highly Selective, High-Capacity Adsorbents for Olefin/Paraffin Separations

机译:M2(ITmIT-dobdc) (M = Mn, Fe, Co, Ni) 金属有机骨架作为烯烃/石蜡分离的高选择性、高容量吸附剂

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摘要

The metal-organic frameworks M-2(m-dobdc) (M = Mn, Fe, Co, Ni; m-dobdc(4-) = 4,6-dioxido-1,3-benzenedicarboxylate) were evaluated as adsorbents for separating olefins from paraffins. Using single-component and multicomponent equilibrium gas adsorption measurements, we show that the coordinatively unsaturated M2+ sites in these materials lead to superior performance for the physisorptive separation of ethylene from ethane and propylene from propane relative to any known adsorbent, including para-functionalized structural isomers of the type M-2(p-dobdc)(p-dobdc(4-) = 2,5-dioxido-1,4-benzenedicarboxylate). Notably, the M-2(m-dobdc) frameworks all exhibit an increased affinity for olefins over paraffins relative to their corresponding structural isomers, with the Fe, Co, and Ni variants showing more than double the selectivity. Among these frameworks, Fe-2(m-dobdc) displays the highest ethylene/ethane (>25 ) and propylene/propane (>55) selectivity under relevant conditions, together with olefin capacities exceeding 7 mmol/g. Differential enthalpy calculations in conjunction with structural characterization of ethylene binding in Co-2(m-dobdc) and Co-2(p-dobdc) via in situ single-crystal X-ray diffraction reveal that the vast improvement in selectivity arises from enhanced metal-olefin interactions induced by increased charge density at the metal site. Moderate olefin binding enthalpies, below 55 and 70 kJ/mol for ethylene and propylene, respectively, indicate that these adsorbents maintain sufficient reversibility under mild regeneration conditions. Additionally, transient adsorption experiments show fast kinetics, with more than 90 of ethylene adsorption occurring within 30 s after dosing. Breakthrough measurements further indicate that Co-2(m-dobdc) can produce high purity olefins without a temperature swing, an important test of process applicability. The excellent olefin/paraffin selectivity, high olefin capacity, rapid adsorption kinetics, and low raw materials c
机译:以金属有机骨架M-2(m-dobdc)(M = Mn, Fe, Co, Ni;m-dobdc(4-) = 4,6-二氧代-1,3-苯二甲酸酯)作为从石蜡中分离烯烃的吸附剂进行了评价。使用单组分和多组分平衡气体吸附测量,我们表明,相对于任何已知的吸附剂,包括M-2(p-dobdc)(p-dobdc(4-) = 2,5-二氧代-1,4-苯二甲酸酯)的对位官能化结构异构体,这些材料中的配位不饱和M2+位点导致乙烯与乙烷和丙烷丙烯的物理吸附分离性能优越。值得注意的是,M-2(m-dobdc)框架相对于其相应的结构异构体,对烯烃的亲和力都高于石蜡,其中Fe、Co和Ni变体的选择性增加了一倍以上。其中,Fe-2(m-dobdc)在相关条件下的乙烯/乙烷(>25)和丙烯/丙烷(>55)选择性最高,烯烃容量超过7 mmol/g。微分焓计算与Co-2(m-dobdc)和Co-2(p-dobdc)中乙烯结合的结构表征相结合,通过原位单晶X射线衍射表明,选择性的巨大提高源于金属位点电荷密度增加引起的金属-烯烃相互作用的增强。中等烯烃结合焓,乙烯和丙烯分别低于55和70 kJ/mol,表明这些吸附剂在温和的再生条件下保持足够的可逆性。此外,瞬态吸附实验显示出快速的动力学,超过90%的乙烯吸附发生在给药后30秒内。突破性的测量进一步表明,Co-2(m-dobdc)可以生产高纯度烯烃而没有温度变化,这是对工艺适用性的重要测试。优异的烯烃/石蜡选择性、高烯烃容量、快速吸附动力学和低原料

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