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Improving polyimide membrane resistance to carbon dioxide plasticization in natural gas separations.

机译:提高天然气分离过程中聚酰亚胺膜对二氧化碳增塑的抵抗力。

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Polyimide membranes have been widely applied for gas separations due to their attractive permeability, selectivity, and processing characteristics. Their use for natural gas and hydrocarbon separations is limited by plasticization-induced selectivity losses in feeds with significant partial pressures of CO 2 and C3+ hydrocarbons. This project focuses on understanding CO2-induced plasticization of polyimide membranes and how it can be controlled by thermal annealing and crosslinking.; Covalent and ionic crosslinking are investigated as approaches for suppressing plasticization, while retaining attractive transport properties. A novel covalent crosslinking protocol has been developed, which offers significant advantages over the traditional post-treatment that was initially used. The two-step crosslinking treatment allows for spectroscopic characterization of the reaction yields in the monoesterification and transesterification reactions. These crosslinking reactions occur at temperatures well below the glass transition and no additives are required in the casting solution, making the approach attractive for the eventual production of asymmetric hollow fibers.; The ionically crosslinked membranes are not as stable against CO 2 plasticization as the covalently crosslinked materials. By varying the ionic crosslinking density, the effects on long-term sorption and permeation at high CO2 pressures were investigated. From STEM images, it does not appear that heterogeneity in the ion distribution is the cause of the membrane plasticization.; With covalent crosslinking, the copolymer composition, crosslinking agent, and thermal treatment are important factors in determining the final membrane transport properties. The crosslinking reaction is accompanied by a heat treatment that can also lead to stabilization of aromatic polyimides. These effects were decoupled by systematic variations in the polymer structure and thermal treatment.; In a plasticized membrane, the sorption, diffusion, and swelling processes are all interdependent. The key to controlling plasticization is to control the membrane swelling, since this is related to the increase in polymer chain segmental mobility facilitated by the CO2 sorption. Mixed gas separations demonstrate the non-ideal factors that must be accounted for when modeling membrane performance over a wide range of pressures. The separation performance at practically relevant feed conditions is intrinsically better and more stable than the commercial polymeric membranes currently used for natural gas separations.
机译:聚酰亚胺膜由于具有吸引力的渗透性,选择性和加工特性而被广泛应用于气体分离。它们在天然气和碳氢化合物分离中的使用受到增塑引起的选择性损失的限制,该损失是在CO 2和C3 +碳氢化合物分压很大的情况下进料的。该项目着重于了解二氧化碳诱导的聚酰亚胺膜的塑化以及如何通过热退火和交联来控制它。研究了共价和离子交联作为抑制塑化的方法,同时保留了吸引人的运输性能。已经开发了一种新颖的共价交联方案,与最初使用的传统后处理相比,它具有明显的优势。两步交联处理可对单酯化和酯交换反应中的反应收率进行光谱表征。这些交联反应在远低于玻璃化转变温度的温度下发生,并且在浇铸溶液中不需要添加剂,使得该方法对于最终生产不对称中空纤维具有吸引力。离子交联的膜对CO 2塑化的稳定性不如共价交联的材料。通过改变离子交联密度,研究了在高CO2压力下对长期吸附和渗透的影响。从STEM图像来看,似乎离子分布中的不均匀性不是膜塑化的原因。对于共价交联,共聚物组成,交联剂和热处理是决定最终膜传输性能的重要因素。交联反应伴随着热处理,该热处理也可以导致芳族聚酰亚胺的稳定化。这些影响通过聚合物结构和热处理的系统变化来消除。在增塑膜中,吸附,扩散和溶胀过程都是相互依赖的。控制增塑的关键是控制膜溶胀,因为这与由CO2吸附促进的聚合物链节段迁移率的增加有关。混合气体分离证明了在较大压力范围内对膜性能进行建模时必须考虑的非理想因素。在实际相关进料条件下的分离性能本质上比目前用于天然气分离的商用聚合物膜更好,更稳定。

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