用于CO2捕集的新型酒石酸钠交联海藻酸钠膜的制备（英文）

The membrane-based CO2 separation process has an advantage compared to traditional CO2 separation technologies. The membrane is the key of the membrane separation process. In this paper, preparation, characteriza-tion and laboratory testing of the membrane, which was prepared from sodium alginate, hydrogen bond cross-linked with sodium tartrate and used for CO2/N2 separation, were reported. The resistance to SO2 of the membrane was also investigated. The experimental results demonstrate that the membrane possesses a high resistance to SO2. Finally, based on experimental results, the economic feasibility of the membrane used for CO2/N2 separation was evaluated, indicating the two-stage membrane process can compete with the traditional chemical absorption method.     

环戊烷/水乳化液水合法捕获烟道气中CO_2(英文)

Capture of CO2 by hydrate is one of the attractive technologies for reducing greenhouse effect.The primary challenges are the large energy consumption,low hydrate formation rate and separation efficiency.This work presents a new method for capture of CO2 from simulated flue gasCO2(16.60%,by mole) /N2 binary mixture by formation of cyclopentane(CP) hydrates at initial temperature of 8.1°C with the feed pressures from 2.49 to 3.95 MPa.The effect of cyclopentane and cyclopentane/water emulsion on the hydrate formation rate and CO2 separation efficiency was studied in a 1000 ml stirred reactor.The results showed the hydrate formation rate could be increased remarkably with cyclopentane/water emulsion.CO2 could be enriched to 43.97%(by mole) and 35.29%(by mole) from simulated flue gas with cyclopentane and cyclopentane/water(O/W) emulsion,respectively,by one stage hydrate separation under low feed pressure.CO2 separation factor with cyclopentane was 6.18,higher than that with cyclopentane/water emulsion(4.01) ,in the range of the feed pressure.The results demonstrated that cyclopentane/water emulsion is a good additive for efficient hydrate capture of CO2.     

Dynamic modelling and simulation of a post-combustion CO2 capture process for coal-fired power plants

Solvent-based post-combustion capture technologies have great potential for CO₂mitigation in traditional coal-fired power plants.Modelling and simulation provide a low-cost opportunity to evaluate performances and guide flexible operation.Composed by a series of partial differential equations,first-principle post-combustion capture models are computationally expensive,which limits their use in real time process simulation and control.In this study,we propose a first-principle approach to develop the basic structure of a reduced-order model and then the dominant factor is used to fit properties and simplify the chemical and physical process,based on which a universal and hybrid post-combustion capture model is established.Model output at steady state and trend at dynamic state are validated using experimental data obtained from the literature.Then,impacts of liquidto-gas ratio,reboiler power,desorber pressure,tower height and their combination on the absorption and desorption effects are analyzed.Results indicate that tower height should be designed in conjunction with the flue gas flow,and the gas-liquid ratio can be optimized to reduce the reboiler power under a certain capture target.     

Review on current advances,future challenges and consideration issues for post-combustion CO2 capture using amine-based absorbents☆

Among the current technologies for post-combustion CO2 capture, amine-based chemical absorption appears to be the most technologically mature and commercial y viable method. This review highlights the opportunities and challenges in post-combustion CO2 capture using amine-based chemical absorption technologies. In addi-tion, this review provides current types and emerging trends for chemical solvents. The issues and performance of amine solvents are reviewed and addressed in terms of thermodynamics, kinetics, mass transfer, regeneration and solvent management. This review also looks at emerging and future trends in post-combustion CO2 capture using chemical solvents in the near to mid-term.     

Recent developments on catalytic membrane for gas cleaning

Catalytic membrane, a novel membrane separation technology that combines catalysis and separation, exhibits significant potential in gas purification such as formaldehyde, toluene and nitrogen oxides(NO_x). The catalytic membrane can remove solid particles through membrane separation and degrade gaseous pollutants to clean gas via a catalytic reaction to achieve green emissions. In this review, we discussed the recent developments of catalytic membranes from two aspects: preparation of catalytic membrane and its application in gas cleaning.Catalytic membranes are divided into organic catalytic membranes and inorganic catalytic membranes depending on the substrate materials. The organic catalytic membranes which are used for low temperature operation(less than 300 °C) are prepared by modifying the polymers or doping catalytic components into the polymers through coating, grafting, or in situ growth of catalysts on polymeric membrane. Inorganic catalytic membranes are used at higher temperature(higher than 500 °C). The catalyst and inorganic membrane can be integrated through conventional deposition methods, such as chemical(physical) vapor deposition and wet chemical deposition. The application progress of catalytic membrane is focused on purifying indoor air and industrial exhaust to remove formaldehyde, toluene, NO_x and PM2.5, which are also summarized. Perspectives on the future developments of the catalytic membranes are provided in terms of material manufacturing and process optimization.     

New process development and process evaluation for capturing CO2 in flue gas from power plants using ionic liquid [emim][Tf2N]

Using the ionic liquid [emim][Tf_2N] as a physical solvent, it was found by Aspen Plus simulation that it was possible to attempt to capture CO_2 from the flue gas discharged from the coal-fired unit of the power plant.Using the combination of model calculation and experimental determination, the density, isostatic heat capacity,viscosity, vapor pressure, thermal conductivity, surface tension and solubility of [emim][Tf_2N] were obtained.Based on the NRTL model, the Henry coefficient and NRTL binary interaction parameters of CO_2 dissolved in[emim][Tf_2N] were obtained by correlating [emim][Tf_2N] with the gas–liquid equilibrium data of CO_2. Firstly,the calculated relevant data is imported into Aspen Plus, and the whole process model of the ionic liquid absorption process is established. Then the absorption process is optimized according to the temperature distribution in the absorption tower to obtain a new absorption process. Finally, the density, constant pressure heat capacity,surface tension, thermal conductivity, and viscosity of [emim][Tf_2N] were changed to investigate the effect of ionic liquid properties on process energy consumption, solvent circulation and heat exchanger design. The results showed that based on the composition of the inlet gas stream to the absorbers, CO_2 with a capture rate of 90% and a mass purity higher than 99.5% was captured. These results indicate that the [emim][Tf_2N] could be used as a physical solvent for CO_2 capture from coal-fired units. In addition, the results will provide a theoretical basis for the design of new ionic liquids for CO_2 capture.     

Preparation of Palladium-Silica Conjugated Membrane for Selective Hydrogen Permeation

Palladium membranes were prepared on an a-alumina support by metal-organic compound chemical vapor deposition (MOCVD) method from palladium(Ⅱ) acetate precursor. Permeation properties of hydrogen and helium gas were studied as a function of the number of times of deposition of palladium on the peeling off phenomenon of palladium, which is common in electroless plated membrane, was observed. Silica was introduced into the pores to prevent the palladium grain from peeling off. The palladium-silica conjugated membrane does not show the peeling off phenomenon and can withstand the high temperature up to 800CCCC which is the upper limit of our apparatus. The separation factor for hydrogen gas over carbon dioxide gas was improved with the increase of number of times of silica coating by sacrificing the H2 permeation and finally increased to four times. The improvement on the separation of hydrogen gas over carbon dioxide for palladium-silica conjugated membrane was evaluated and a model of permeation pattern     

Experimental study on SO2 recovery using a sodium-zinc sorbent based flue gas desulfurization technology

A sodium–zinc sorbent based flue gas desulfurization technology (Na–Zn-FGD) was proposed based on the experiments and analyses of the thermal decomposition characteristics of CaSO3 and ZnSO3·2.5H2O, the waste products of calcium-based semi-dry and zinc-based flue gas desulfurization (Ca–SD-FGD and Zn–SD-FGD) tech-nologies, respectively. It was found that ZnSO3·2.5H2O first lost crystal H2O at 100 °C and then decomposed into SO2 and solid ZnO at 260 °C in the air, while CaSO3 is oxidized at 450 °C before it decomposed in the air. The ex-perimental results confirm that Zn–SD-FGD technology is good for SO2 removal and recycling, but with problem in clogging and high operational cost. The proposed Na–Zn-FGD is clogging proof, and more cost-effective. In the new process, Na2CO3 is used to generate Na2SO3 for SO2 absorption, and the intermediate product NaHSO3 reacts with ZnO powders, producing ZnSO3·2.5H2O precipitate and Na2SO3 solution. The Na2SO3 solution is clogging proof, which is re-used for SO2 absorption. By thermal decomposition of ZnSO3·2.5H2O, ZnO is re-generated and SO2 with high purity is co-produced as well. The cycle consumes some amount of raw material Na2CO3 and a small amount of ZnO only. The newly proposed FGD technology could be a substitute of the traditional semi-dry FGD technologies.     

Pd-SiO2复合膜的氢气选择渗透特性

Palladium membranes were prepared on an a-alumina support by metal-organic compound chemical vapor deposition (MOCVD) method from palladium(Ⅲ) acetate precursor. Permeation properties of hydrogen and helium gas were studied as a function of the number of times of deposition of palladium on the peeling off phenomenon of palladium, which is common in electroless plated membrane, was observed. Silica was introduced into the pores to prevent the palladium grain from peeling off. The palladium-silica conjugated membrane does not show the peeling off phenomenon and can withstand the high temperature up to 800℃ which is the upper limit of our apparatus.The separation factor for hydrogen gas over carbon dioxide gas was improved with the increase of number of times of silica coating by sacrificing the H2 permeation and finally increased to four times. The improvement on the separation of hydrogen gas over carbon dioxide for pulladium-silica conjugated membrane was evaluated and a model of permeation pattern (palladium and silica) was proposed. This model suggests that the separation factor for hydrogen over carbon dioxide could be improved by introducing silica layer because the silica layer fills the pores and reduces the gas permeation without sacrificing the hydrogen permeation through the palladium region. These results indicate that the introduction of silica into the palladium grain is a promising means to improve the hydrogen separation performance of palladium based composite membranes.     

以F200和Sorbead WS为保护层真空变压吸附捕集CO2（英文）

In order to solve the water issues when 13X zeolite was applied to capture CO 2 from wet flue gas by vacuum swing adsorption process, multi-layered adsorption system was considered regarding activated alumina F200 and silica gel based Sorbead WS as pre-layer materials. LBET (extended Largmuir-BET) model and extended CMMS (cooperative multimolecular sorption) equation were simulated respectively to describe water loading on F200 and Sorbead WS. The two equations can be well added into our in-house simulator to simulate double-layered CO 2 -VSA (vacuum swing adsorption) process. Results indicated that water can be successfully stopped in pre-layers with a good CO 2 capture performance.     

二氧化碳驱伴生气分离技术综述

对CO2驱油田伴生气成分复杂、二氧化碳浓度高等特点进行了分析,详细介绍了几种当前热门的伴生气分离提纯技术,包括化学吸收法、膜分离法、变压吸附法、低温分馏法等,并对各类方法的原理、优缺点进行了深入解析。对伴生气CO2分离技术及复配方法进行了综合对比,得出膜分离+化学吸收法、低温分馏+化学吸收、膜分离+变压吸附更适用于分离CO2驱油田伴生气中的CO2。     

13X-APG沸石真空变压变温耦合工艺吸附捕集烟道气中CO2

采用13X-APG沸石吸附捕集烟道气中CO2,并研发了五步循环真空变压变温(VTSA)耦合吸附捕集工艺. 实验测定了循环吸附/解吸过程中吸附剂再生率、烟道气中CO2回收率、产品气量及产品气中CO2纯度,并与传统的真空变压吸附工艺(VSA)和变温吸附工艺(TSA)比较. 由于VTSA在真空解吸的同时加热吸附剂,减少了真空泵的电耗,可在较温和的真空下(约3′103 Pa)操作,附加的吸附剂再生温度也不高,90~150℃下吸附剂再生率达97%以上,CO2回收率达98%以上. 吸附剂捕集CO2的量可提高到1.8 mol/kg,是VSA工艺产品气量的2倍,且产品气中CO2纯度提高到90%以上.     

膜分离-变压吸附集成工艺脱除天然气中酸性气体

天然气中含有酸性气体,在使用或输送前必须去除。介绍了两种天然气脱除酸性气体的技术:气体膜分离技术和变压吸附技术,单独使用其中任何一种技术都不能达到经济地脱除酸性气体的目的。集成两种技术的优点,开发出膜分离-变压吸附集成工艺,可以在满足天然气酸性气体含量指标的同时,提高了回收率,为天然气工业提供一定的借鉴和参考。     

温室气体CO2的捕集和分离--分离技术面临的挑战与机遇

介绍了采用溶剂吸收、膜分离和变压吸附等方法捕集和分离温室气体CO2的最新进展,并对技术发展动向进行了讨论。     

变压吸附气体分离技术应用及展望窥探

为了深入探究变压吸附气体分离技术,分析了技术工作原理,依据此原理,研究此项技术在H_2、CO_2、C0、氯乙烯精馏尾气的回收与提取中的应用方法,并探究参数指标变化下气体回收与提取纯度的影响。基于变压吸附技术应用现状,气体吸附提取纯度仍有上升空间,具有较高的研发应用前景。     

Analysis of energetics and economics of sub-ambient hybrid post-combustion carbon dioxide capture

Adsorption of CO₂ from post-combustion flue gas is one of the leading candidates for globally impactful carbon capture systems. This work focused on understanding the opportunities and limitations of sub-ambient CO₂ capture processes utilizing a multistage separation process. A hybrid process design using a combination of pressure-driven separation of CO₂ from flue gas (e.g., adsorption- or membrane-based separation) followed by CO₂-rich product liquefaction to produce high-purity (>99%) CO₂ at pipeline conditions is considered. The operating pressure of the separation unit is a key cost parameter and also an important process variable that regulates the available heat removal necessary to reach the sub-ambient operating conditions. The economic viability of applying pressure swing adsorption (PSA) processes using fiber sorbent contactors with internal heat management was found to be most influenced by the productivity of the adsorption system, with productivities as high as 0.015 /kg_sorb⁻¹ sec⁻¹ being required to reduce costs of capture below $60/ton CO₂ captured. This analysis was carried out using a simplified two-bed process, and thus there is opportunity for further cost reduction with exploration of more complex cycle designs. Three exemplar fiber sorbents (MIL-101(Cr), UiO-66, and zeolite 13X) were considered for application in the sub-ambient process of PSA unit. Among the considered sorbents, zeolite 13X fiber composites were found to perform better at ambient temperatures as compared to sub-ambient. MIL-101(Cr) and UiO-66 fiber composites had improved purity, recovery, and productivity at colder temperatures reducing costs of capture as low as $61/ton CO₂. Future economic improvement could be achieved by reducing the required operating pressure of the PSA unit and pushing the Pareto frontier closer to the final pipeline requirement via a combination of PSA cycle design and material selection.     

用于油田注气的燃煤电站锅炉烟气处理工艺分析

将燃煤电厂锅炉产生的烟气经处理后注入油井既能提高原油采收率,同时还可以实现CO2温室气体的减排,因而具有经济和社会的双重效益。利用电厂燃煤锅炉烟气的关键在于烟气的净化处理工艺,本文针对注入烟道气和CO2气两种情况,对烟气处理技术路线进行了分析。对注入烟道气的情况,推荐采用非选择性催化烟气脱硝除氧 石灰石湿法脱硫 静电或袋式除尘 冷冻或吸附干燥处理工艺流程,同时,烟道气的输送采用高压管道输送方式。对注入CO2气的情况,推荐采用非选择性催化烟气脱硝除氧 石灰石湿法脱硫 静电或袋式除尘 化学溶剂吸收法CO2分离 冷冻或吸附法CO2干燥 氨制冷法CO2液化处理工艺流程,同时,CO2的输送可以采用管道输送或罐车运送方式。     

水合物法分离二氧化碳的研究现状

介绍了利用水合物法从火力发电厂排放的烟气和从整体煤气化联合循环发电系统（IGCC）合成气中分离二氧化碳（CO₂）的研究及发展现状,包括水合物形成促进剂和添加剂的选择,水合物分离捕集工艺以及成本核算。TBAB和THF在研究中证明能有效地提高水合物形成速度、降低反应压力、提高CO₂的分离捕集效率。在此基础上,提出了不同的分离捕集工艺,这些工艺都是以水合物法分离为主,结合化学吸附法或者膜分离法而展开。通过与传统的化学吸附法的成本核算做比较,发现水合物法分离捕集每吨CO₂的成本约为USD 26,比化学吸附法要便宜约31%,并且随着水合物法研究的进一步深入,水合物法分离捕集CO₂的成本还可能进一步降低,显示了未来的工业应用中有光明的前景。     

低分压CO_2回收新技术捕集燃煤电厂烟气CO_2

基于分子模拟和设计,开发了以一乙醇胺(MEA)为主溶剂,优选添加了活性胺、抗氧化剂和缓蚀剂组成了适用于回收低分压CO2的优良复合吸收剂,在华能北京热电厂建立了我国第1套燃煤电站烟气CO2捕集示范装置,并完成了运行测试。结果表明:CO2回收装置出来的CO2纯度为99.5%(体积分数),每tCO2蒸汽消耗为3.5GJ,每tCO2溶液消耗小于1.5kg。该套装置的建成和各项指标试验的进行将为我国大规模推广电站CO2捕集奠定基础。     

Simulations of Membrane Gas Separation: Chemical Solvent Absorption Hybrid Plants for Pre- and Post-Combustion Carbon Capture

Solvent absorption and membrane gas separation are two carbon capture technologies that show great potential for reducing emissions from stationary sources such as power plants. Here, plants combining chemical solvent absorption and membrane gas separation are considered for post-combustion capture as well as pre-combustion capture. In all ASPEN HYSYS simulations the membrane stage initially concentrates CO₂ into either the permeate or the retentate stream, which is then passed to a monoethanolamine (MEA) based solvent absorption process. In particular, post-combustion capture scenarios examined a membrane that is selective for CO₂ against N₂, while for the pre-combustion scenario a H₂-selective membrane was studied. It was found the energy demand of the combined hybrid plant was always more than that of a stand alone MEA solvent process. This was mainly due to the need to generate a pressure driving force upstream of the membrane in the post-combustion scenario or to recompress downstream gas streams in the pre-combustion scenarios. For both scenarios concentrating the CO₂ in the feed to the solvent system reduced the absorber column height and diameter, which could represent a CAPEX saving for the hybrid plant, dependent upon the membrane price. The use of a hydrogen selective membrane downstream of an oxygen fired gasifier was identified as the most prospective scenario, as it led to significant reductions in absorber size, for a relatively small membrane area and energy penalty.