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Silica Gel Supported Solid Amine Sorbents for CO_(2) Capture
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作者 Baljeet Singh Zahra Eshaghi Gorji +2 位作者 Rustam Singh Vikas Sharma Timo Repo 《Energy & Environmental Materials》 2025年第1期273-291,共19页
Point source CO_(2) capture(PSCC)is crucial for decarbonizing various industrial sectors,while direct air capture(DAC)holds promise for removing CO_(2) directly from the air.Sorbents play a critical role in both techn... Point source CO_(2) capture(PSCC)is crucial for decarbonizing various industrial sectors,while direct air capture(DAC)holds promise for removing CO_(2) directly from the air.Sorbents play a critical role in both technologies,with their performances,efficiency,cost,etc.,largely depending on which type is used(physical or chemical).Solid amine sorbents(SAS)employed in the chemical adsorption of CO_(2) are suitable for both PSCC and DAC.SAS offer significant advantages over liquid amines such as monoethanolamine(MEA),due to their ability to perform cyclic adsorption–desorption with much lower energy requirement.The environmental concern associated with MEA can be mitigated by SAS.Support materials have a significantly important role in stabilizing amine and enhancing stability and kinetics;varieties of support materials have been screened at a laboratory scale.One promising support material is a silica gel(SG),which is commercially available and attractive for designing cost-effective sorbents for large-scale CO_(2) capture.Various impregnation methods such as physical adsorption and covalent functionalization have been employed to functionalize silica surfaces with amines.This review provided a comprehensive critical analysis of SG-based SAS for CO_(2) capture.We discussed and evaluated them in terms of their adsorption capacity,adsorption,and desorption conditions,and the kinetics involved in these processes.Finally,we proposed a few recommendations for further development of low-cost,lower carbon footprint SAS for large-scale deployment of CO_(2) capture technology. 展开更多
关键词 direct air capture point source CO_(2)capture silica gel solid amine sorbent
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High-temperature H_2S Removal with Calcium-based Sorbent
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作者 Chen Jilu(Scientific and Educational Bureau, State Power Corporation) 《Electricity》 1998年第3期23-26,共4页
The H2S removal characteristics of Taxada lime tinder the high temperature of 600-900℃ have been investigated. The test results indicated that this kind of sorbent almost was inert to H2S When temperature lowered dow... The H2S removal characteristics of Taxada lime tinder the high temperature of 600-900℃ have been investigated. The test results indicated that this kind of sorbent almost was inert to H2S When temperature lowered down to 600℃,while its reactivity increased with increased temperature and the equilibrium conversion reached up to over 60% at temperatLlre of 900℃.However, side reactions of H2S in conjunction with high-temperature decomposition and mineral catalysis to elemental sulfur and sulfur dioxide were testified. 展开更多
关键词 CA FIGURE High-temperature H2S Removal with calcium-based sorbent
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Synthesis of highly reactive sorbent from industrial wastes and its CO_2 capture capacity 被引量:1
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作者 孙荣岳 李英杰 《Journal of Southeast University(English Edition)》 EI CAS 2015年第2期209-214,共6页
A kind of industrial solid waste, i.e., carbide slag, was used as CaO precursor to synthesize CO2 sorbent. The highly reactive synthetic sorbent was prepared from carbide slag, aluminum nitrate hydrate and glycerol wa... A kind of industrial solid waste, i.e., carbide slag, was used as CaO precursor to synthesize CO2 sorbent. The highly reactive synthetic sorbent was prepared from carbide slag, aluminum nitrate hydrate and glycerol water solution by the combustion synthesis method. The results show that the synthetic sorbent exhibits a much higher CO2 capture capacity compared with carbide slag. The CO2 capture capacity and the carbonation conversion of the synthetic sorbent are 0. 38 g/g and 0. 70 after 50 cycles, which are 1.8 and 2. 1 times those of carbide slag. The average carbonation conversion and the CO2 capture efficiency of the synthetic sorbent are higher than those of carbide slag with the same sorbent flow ratios. The required sorbent flow ratios are lower for synthetic sorbent to achieve the same CO2 capture efficiency compared with carbide slag. With the same sorbent flow ratio and CO2 capture efficiency, the energy requirement in calciner for the synthetic sorbent is less than that for carbide slag. 展开更多
关键词 carbide slag synthetic co2 sorbent co2 capture
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利用钢渣制备钙基CO_(2)循环吸附材料 被引量:1
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作者 刘军 李宇蒙 +3 位作者 曹志众 刘玉峰 陶梦洁 赵青 《钢铁研究学报》 北大核心 2025年第2期258-268,共11页
“碳中和2060”背景下研究钢渣碳捕集应用的意义不言而喻。为提高钢渣资源的综合利用,减少钢铁冶炼过程排放的CO_(2),采用湿法浸出技术提取了钢渣中的Ca、Mg组元,针对获得的Ca-Mg-Si-Al体系,开展了利用化学共沉淀法、溶胶-凝胶法和水热... “碳中和2060”背景下研究钢渣碳捕集应用的意义不言而喻。为提高钢渣资源的综合利用,减少钢铁冶炼过程排放的CO_(2),采用湿法浸出技术提取了钢渣中的Ca、Mg组元,针对获得的Ca-Mg-Si-Al体系,开展了利用化学共沉淀法、溶胶-凝胶法和水热合成法3种方式制备CO_(2)吸附剂的实验研究,通过XRF、XRD、SEM、BET等检测手段对吸附剂的物化特性及循环吸附性能进行了表征分析。结果表明,与其他2种方法相比,化学共沉淀法在50℃、pH=10和陈化时间2 h条件下制备的吸附剂具有较高的初次吸附容量,为0.258 g/g。制备方式不同,CO_(2)吸附剂循环吸附性能表现出不同规律。化学共沉淀法制备的CO_(2)吸附剂吸附容量随循环次数增加呈下降趋势,水热合成法制备的CO_(2)吸附剂,呈先增高后降低的趋势。 展开更多
关键词 钢渣 CO_(2)吸附剂 化学共沉淀法 溶胶-凝胶法 水热合成法
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1000 MW燃煤机组钙循环烟气CO_(2)捕集系统模拟研究
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作者 王长清 谭煜幺 +4 位作者 徐瑞昌 周子健 刘文强 胡勇 徐明厚 《动力工程学报》 北大核心 2025年第5期738-746,共9页
基于Aspen Plus软件建立了高温钙基吸附剂碳捕集的系统模型,开展了1 000 MW燃煤机组烟气CO_(2)捕集工艺流程模拟研究。针对煅烧炉煤富氧燃烧供能存在的高能耗与污染物排放问题,提出采用外部电加热供能方式为煅烧炉提供热量。详细考察了... 基于Aspen Plus软件建立了高温钙基吸附剂碳捕集的系统模型,开展了1 000 MW燃煤机组烟气CO_(2)捕集工艺流程模拟研究。针对煅烧炉煤富氧燃烧供能存在的高能耗与污染物排放问题,提出采用外部电加热供能方式为煅烧炉提供热量。详细考察了烟气进入碳捕集系统后,系统关键性能参数的变化;在此基础上分析了系统的能量和物质守恒情况,以及不同操作参数对系统性能的影响。结果表明:当1 000 MW燃煤发电机组增加碳捕集系统后,发电热效率将下降26.11%;碳化炉温度稳定在645℃时,CO_(2)捕集效率可达92.13%;煅烧炉温度设定在900℃时,CaCO3会分解得更彻底;碳酸化炉温度的提升会减少煅烧能耗并提高发电热效率,而煅烧温度的升高会增加能耗并降低发电热效率;钙碳摩尔比的增加导致钙基碳捕集系统的固体循环量增加,而钙基吸附剂的平均碳转化率则呈现出负相关性。 展开更多
关键词 CO_(2)捕集 钙基吸附剂 燃煤烟气 Aspen Plus
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高温钙基固体吸附CO_(2)捕集技术研究进展
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作者 杜振 张立麒 +4 位作者 张杨 刘博 朱文韬 罗聪 喻江 《洁净煤技术》 北大核心 2025年第6期36-52,共17页
在全球气候变化和“双碳”目标的推动下,碳捕集、利用与封存(CCUS)技术成为工业领域实现温室气体减排的关键。高温钙基固体吸附CO_(2)捕集技术因成本低、吸附容量高而备受关注,然而CaO吸附剂在循环过程中易烧结、磨损,致使性能衰减,限... 在全球气候变化和“双碳”目标的推动下,碳捕集、利用与封存(CCUS)技术成为工业领域实现温室气体减排的关键。高温钙基固体吸附CO_(2)捕集技术因成本低、吸附容量高而备受关注,然而CaO吸附剂在循环过程中易烧结、磨损,致使性能衰减,限制了其规模化应用。综述了近年来CaO吸附剂的改性方法、规模化制备工艺、反应器设计以及钙循环中试装置的研究进展。在改性方法上,有机酸、碱金属盐、生物质衍生材料、金属氧化物及固体废弃物等均可用于改性CaO吸附剂,例如,丙酸改性的石灰石在100次循环后CO_(2)捕集能力为未处理样品的4倍。吸附剂颗粒制备技术包括挤压法、滚圆法、挤压–滚圆法、浇铸法、核壳法等,不同方法制备的颗粒在机械强度、CO_(2)捕集能力等方面各有差异。例如,挤压−滚圆法结合喷雾干燥技术制备的吸附剂微球,25次循环后CO_(2)吸附量较高且抗磨损能力强,旋转3000次后的失重率低于0.8%。在反应器方面,流化床反应器应用最为广泛,但存在颗粒磨损的问题;移动床反应器可缩小反应器尺寸,但存在阻力的问题。另外,多个国家和地区的中试装置验证了钙循环CO_(2)捕集技术的可行性,如德国斯图加特的200 kWh平台、西班牙La Pereda的1.7 MWh平台等,可实现约90%的CO_(2)捕集效率。最后,指出未来需突破低成本规模化制备工艺,解决现有成型技术原材料成本高、成品率低等问题;优化反应器传热传质性能;推进构建余热梯级利用的能量集成系统,降低捕集能耗,从而推动CaO吸附剂CO_(2)捕集技术从工程验证迈向工业化应用的关键跨越。 展开更多
关键词 CaO吸附剂 CO_(2)捕集 造粒 反应器设计 抗烧结
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The Al_(2)O_(3)and Mn/Al_(2)O_(3)sorbents highly utilized in destructive sorption of NF_(3)
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作者 Yanfei Pan Hejian Li +1 位作者 Li Zheng Xiufeng Xu 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2024年第1期54-62,共9页
NF_(3)is commonly used as an etching and cleaning gas in semiconductor industry,however it is a strongly greenhouse gas.Therefore,the destruction of disposal NF_(3)is an urgent task to migrate the greenhouse effect.Am... NF_(3)is commonly used as an etching and cleaning gas in semiconductor industry,however it is a strongly greenhouse gas.Therefore,the destruction of disposal NF_(3)is an urgent task to migrate the greenhouse effect.Among the technologies for NF_(3)abatement,the destructive sorption of NF_(3)over metal oxides sorbents is an effective way.Thus,the search for a highly reactive and utilized sorbent for NF_(3)destruction is in great demand.In this work,AlOOH supported on carbon-sphere(AlOOH/CS)as precursors were synthesized hydrothermally and heat-treated to prepare the Al_(2)O_(3)sorbents.The influence of AlOOH/CS hydrothermal temperatures on the reactivity of derived Al_(2)O_(3)sorbents for NF_(3)destruction was investigated,and it is shown that the Al2O3 from AlOOH/CS hydro-thermalized at 120℃is superior to others.Subsequently,the optimized Al_(2)O_(3)was covered by Mn(OH)x to prepare Mn/Al_(2)O_(3)sorbents via changing hydrothermal temperatures and Mn loadings.The results show that the Mn/Al_(2)O_(3)sorbents are more utilized than bare Al_(2)O_(3)in NF_(3)destructive sorption due to the promotional effect of Mn_(2)O_(3)as surface layer on the fluorination of Al_(2)O_(3)as substrate,especially the optimal 5%Mn/Al2O3(160℃)exhibits a utilization percentage as high as 90.4%,and remarkably exceeds all the sorbents reported so far.These findings are beneficial to develop more efficient sorbents for the destruction of NF_(3). 展开更多
关键词 Greenhouse gas NF_(3)destructive sorption sorbents Al_(2)O_(3) Mn/Al_(2)O_(3) REACTIVITY
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Modification of CaO-based sorbents prepared from calcium acetate for CO_2 capture at high temperature 被引量:8
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作者 Xiaotong Liu Junfei Shi +2 位作者 Liu He Xiaoxun Ma Shisen Xu 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2017年第5期572-580,共9页
CaO-based sorbent is considered to be a promising candidate for capturing CO_2 at high temperature. However,the adsorption capacity of CaO decreases sharply with the increase of the carbonation/calcination cycles. In ... CaO-based sorbent is considered to be a promising candidate for capturing CO_2 at high temperature. However,the adsorption capacity of CaO decreases sharply with the increase of the carbonation/calcination cycles. In this study, CaO was derived from calcium acetate(CaAc_2), which was doped with different elements(Mg, Al,Ce, Zr and La) to improve the cyclic stability. The carbonation conversion and cyclic stability of sorbents were tested by thermogravimetric analyzer(TGA). The sorbents were characterized by N_2 isothermal adsorption measurements, scanning electron microscopy(SEM) and X-ray diffraction(XRD). The results showed that the cyclic stabilities of all modified sorbents were improved by doping elements, while the carbonation conversions of sorbents in the 1st cycle were not increased by doping different elements. After 22 cycles, the cyclic stabilities of CaO–Al, CaO–Ce and CaO–La were above 96.2%. After 110 cycles, the cyclic stability of CaO–Al was still as high as 87.1%. Furthermore, the carbonation conversion was closely related to the critical time and specific surface area. 展开更多
关键词 co2 capture CaO-based sorbent Carbonation conversion Cyclic stability Critical time Mesoporous structure
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Supported ionic liquid sorbents for CO_2 capture from simulated flue-gas 被引量:1
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作者 Jiajia Ren Zheng Li +2 位作者 Yifeng Chen Zhuhong Yang Xiaohua Lu 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2018年第11期2377-2384,共8页
Supported ionic liquid(IL) sorbents for CO_2 capture were prepared by impregnating tetramethylammonium glycinate([N1111][Gly]) into four types of porous materials in this study. The CO_2 adsorption behavior was invest... Supported ionic liquid(IL) sorbents for CO_2 capture were prepared by impregnating tetramethylammonium glycinate([N1111][Gly]) into four types of porous materials in this study. The CO_2 adsorption behavior was investigated in a thermogravimetric analyzer(TGA). Among them, poly(methyl methacrylate)(PMMA)-[N1111][Gly]exhibits the best CO_2 adsorption properties in terms of adsorption capacity and rate. The CO_2 adsorption capacity reaches up to 2.14 mmol·g-1 sorbent at 35 °C. The fast CO_2 adsorption rate of PMMA-[N1111][Gly] allows 60 min of adsorption equilibrium time at 35 °C and much shorter time of 4 min is achieved at 75 °C. Further, Avrami's fractional-order kinetic model was used and fitted well with the experiment data, which shows good consistency between experimental results and theoretical model. In addition, PMMA-[N1111][Gly] remained excellent durability in the continuous adsorption–desorption cycling test. Therefore, this stable PMMA-[N1111][Gly] sorbent has great potential to be used for fast CO_2 adsorption from flue-gas. 展开更多
关键词 co2 ADSORPTION AMINO acid IONIC LIQUID Supported IONIC LIQUID sorbent ADSORPTION kinetics
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造粒方法对烟气CO_(2)捕集钙基吸附剂煅烧过程抗硫特性的影响
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作者 殷万儒 《湖北电力》 2025年第1期11-17,共7页
为了缓解全球变暖对气候的不利影响,提出CO_(2)捕集与封存技术来应对碳排放过量的问题。钙循环工艺被认为是最有前景的CO_(2)捕集技术之一。然而,在燃煤电厂实际应用中,钙循环碳捕集技术仍存在粉末样品扬析损失多和原位煅烧再生过程失... 为了缓解全球变暖对气候的不利影响,提出CO_(2)捕集与封存技术来应对碳排放过量的问题。钙循环工艺被认为是最有前景的CO_(2)捕集技术之一。然而,在燃煤电厂实际应用中,钙循环碳捕集技术仍存在粉末样品扬析损失多和原位煅烧再生过程失活机理不明等理论与技术难题。通过采用石墨成型法和挤压-滚圆法制备钙基吸附剂颗粒,并模拟实际钙循环工艺中的煅烧环节,探究成型吸附剂与煤粉混燃对其性能的影响规律。探究不同成型造粒方法制备的钙基吸附剂颗粒与煤粉混合煅烧后的脱碳性能的影响。研究结果表明,在煤粉原位煅烧条件下,挤压滚圆制备的钙基吸附剂颗粒表现出更好的CO_(2)吸附性能,为深入理解成型造粒方法对钙基吸附剂与煤粉原位煅烧条件下的CO_(2)吸附性能的影响机制提供了重要依据,为优化钙基吸附剂的制备工艺,优化钙基吸附剂的抗中毒特性提供了理论支持。 展开更多
关键词 CO_(2)捕集 钙循环 钙基吸附剂颗粒 吸附剂失活 煤原位煅烧
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碳基固体吸附剂的制备及其CO_(2)吸附性能研究
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作者 姚雅珂 胡庚申 《当代化工研究》 2025年第9期185-187,共3页
在水热釜中以硬模板法制备了具有超大孔体积的介孔碳材料CSiO_(2),然后通过浸渍法将四乙烯五胺(TEPA)负载到CSiO_(2)上,制备了一种具有优异CO_(2)吸附性能的固体吸附剂TEPA/CSiO_(2)。通过透射电镜、物理吸附和红外等测试手段对碳基固... 在水热釜中以硬模板法制备了具有超大孔体积的介孔碳材料CSiO_(2),然后通过浸渍法将四乙烯五胺(TEPA)负载到CSiO_(2)上,制备了一种具有优异CO_(2)吸附性能的固体吸附剂TEPA/CSiO_(2)。通过透射电镜、物理吸附和红外等测试手段对碳基固体吸附剂进行了表征,采用穿透曲线法对吸附剂的CO_(2)吸附性能进行了测试。探究了胺负载量、吸附温度对吸附剂吸附性能的影响。研究结果表明,碳基载体CSiO_(2)具有超大的孔体积(3.28cm^(3)/g)和较大的比表面积(554m^(2)/g)。60% TEPA/CSiO2吸附剂在75℃时吸附量达到6.45mmol/g,吸附剂还具有优异的循环稳定性,经过8次循环,吸附性能的保持率达到了91.5%。 展开更多
关键词 CO_(2)吸附剂 介孔碳 超大孔体积 TEPA
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O_2/CO_2气氛下燃煤的钙基脱硫规律的实验研究 被引量:10
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作者 张礼知 王宏 +2 位作者 张庆丰 邱建荣 郑楚光 《燃料化学学报》 EI CAS CSCD 北大核心 2000年第6期508-512,共5页
对含硫量较高的煤种在不同气氛和工况条件下 ,SO2 的排放和吸收过程 ,开展了较为系统的实验和分析工作。实验结果表明 :较之空气气氛 ,高CO2 浓度对煤燃烧过程中SO2 的排放有重要影响 ,并可显著提高钙基脱硫剂的高温脱硫效率。这些结果... 对含硫量较高的煤种在不同气氛和工况条件下 ,SO2 的排放和吸收过程 ,开展了较为系统的实验和分析工作。实验结果表明 :较之空气气氛 ,高CO2 浓度对煤燃烧过程中SO2 的排放有重要影响 ,并可显著提高钙基脱硫剂的高温脱硫效率。这些结果为利用新型O2 CO2 循环燃烧方式下污染排放的综合治理技术奠定了基础。 展开更多
关键词 O2/二氧化碳气氛 燃煤 钙基脱硫剂 脱硫 燃烧
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Effect of sulfation during carbonation on CO_2 capture in calcium looping cycle 被引量:1
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作者 王春波 刘洪才 +2 位作者 陈亮 Lufei Jia Yewen Tan 《Journal of Southeast University(English Edition)》 EI CAS 2015年第2期215-219,共5页
Abstract: Two Canadian limestones with different properties were tested to determine the effect of SO2 during the carbonation of sorbent on the CO2 capture performance in Ca- looping. When the reaction gas is mixed w... Abstract: Two Canadian limestones with different properties were tested to determine the effect of SO2 during the carbonation of sorbent on the CO2 capture performance in Ca- looping. When the reaction gas is mixed with SO2, the carbonation ratio of the sorbent is always lower than that without SO2 for each cycle under the same conditions, and the sulfation ratio increases almost linearly with the increase in the cycle times. At 650 ℃, there is little difference in the carbonation ratio of the sorbent during the first four cycles for the two carbonation time, 5 and 10 rain at 0. 18% SO2. The indirect sulfation reaction that occurs simultaneously with the carbonation of CaO is responsible for the degradation of the sorbent for CO2 capture, and the carbonation duration is not the main factor that affects the ability of the sorbent. 680℃ is the best carbonation temperature among the three tested temperatures and the highest carbonation ratio can be obtained. Also, the sulfation ratio is the highest. The probable cause is the different effects of temperature on the carbonation rate and sulfation rate. A higher SO2 concentration will decrease the carbonation ratio clearly, but the decrease in the carbonation capability of the sorbent is not proportional to the increase of the SO2 concentration in flue gases. 展开更多
关键词 Ca-based sorbent CARBONATION SULFATION LOOPING co2 capture
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失活石灰石自活化增强循环捕集CO_(2)特性 被引量:1
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作者 孙荣岳 胡天骄 +3 位作者 尹鹏祥 申昊 陶成飞 吕勋 《洁净煤技术》 CAS CSCD 北大核心 2024年第2期340-346,共7页
钙循环工艺是一种低成本高效率捕集CO_(2)技术,运行过程需不断补充新鲜吸收剂并排出失活吸收剂,实现失活钙基吸收剂原位资源化利用具有重要意义。为研究颗粒状石灰石失活后自活化特性,运用双固定床反应器制备了失活石灰石,分析了自活化... 钙循环工艺是一种低成本高效率捕集CO_(2)技术,运行过程需不断补充新鲜吸收剂并排出失活吸收剂,实现失活钙基吸收剂原位资源化利用具有重要意义。为研究颗粒状石灰石失活后自活化特性,运用双固定床反应器制备了失活石灰石,分析了自活化后石灰石碳酸化转化率随循环次数的变化规律,采用XRD、SEM、N_(2)吸附等分析测试手段探究了自活化提高失活石灰石循环捕集CO_(2)性能机理。结果表明,失活石灰石置于环境中可吸收空气中水分生成Ca(OH)_(2),吸水率φ达100%后,继续吸水生成氢氧化钙水合物,极限吸水率为130%。不同程度自活化后的石灰石循环捕集CO_(2)性能均有不同程度提高,随吸水率变化呈线性升高趋势。与分析纯CaCO3相比,失活石灰石对吸水率变化更敏感,随吸水率升高其循环捕集CO_(2)性能提高更快。吸水率为130%时,自活化后石灰石循环捕集CO_(2)性能甚至优于新鲜石灰石。微观结构分析结果显示:新鲜石灰石因高温烧结而失活过程中,CaO晶粒尺寸由41.9 nm长大至72.2 nm,孔隙结构发生坍塌阻塞,比孔容和比表面积显著降低。经过自活化,煅烧后的石灰石中CaO晶粒尺寸降低,原本密实的表面重新生成孔隙结构;吸水率为130%时,晶粒尺寸降至35.1 nm,比孔容和比表面积分别恢复至新鲜石灰石的70.5%和107.6%,特别是10~100 nm孔隙得以再生,因此失活石灰石循环捕集CO_(2)性能恢复。虽然自活化过程会加剧失活石灰石颗粒磨损速率,但吸水率100%的自活化石灰石磨损导致直径每小时减小量仅为颗粒直径的0.55%。综上所述,自活化后的失活石灰石完全可替代新鲜石灰石,作为补充钙基吸收剂用于钙循环捕集CO_(2)。 展开更多
关键词 CO_(2)捕集 钙循环 钙基吸收剂 烧结 自活化 磨损特性
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CeO_2掺杂对CaO基吸收剂CO_2捕获性能的影响 被引量:3
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作者 杨彬 余钟亮 +5 位作者 李春玉 周兴 郭帅 李光 赵建涛 房倚天 《燃料化学学报》 EI CAS CSCD 北大核心 2019年第3期344-351,I0006,共9页
以P123作为软模板剂,通过均相沉淀法制备了CeO_2掺杂的CaO基吸收剂,研究了CeO_2掺杂对CO_2捕获的影响。结果表明,CeO_2掺杂可促进表面氧物种的生成,从而促进CaO与CO_2的碳酸化反应。CaO-CeO_2的相互作用一方面促进了从Ca到表面氧物种的... 以P123作为软模板剂,通过均相沉淀法制备了CeO_2掺杂的CaO基吸收剂,研究了CeO_2掺杂对CO_2捕获的影响。结果表明,CeO_2掺杂可促进表面氧物种的生成,从而促进CaO与CO_2的碳酸化反应。CaO-CeO_2的相互作用一方面促进了从Ca到表面氧物种的电子转移;另一方面,由于部分Ca离子对晶格中Ce离子的取代,晶格的电中性被打破,有利于CeO_2中晶格氧的逸出,以及氧空位和O^(2-)的生成。本实验制备的纯CaO吸收剂的碳酸化反应活化能为28.1 kJ/mol,而掺杂CeO_2后活化能显著降低,且当Ce/Ca(物质的量比)为0.25时达到最低值10.2 kJ/mol。另外,CeO_2的掺杂有利于CaO的分散,进而减缓CaO烧结。CeO_2掺杂的吸收剂在碳酸化/煅烧循环中表现出良好的CO_2捕获性能和循环稳定性。 展开更多
关键词 CaO基吸收剂 co2 捕获 CeO2掺杂 碳酸化
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Recent progress of amine modified sorbents for capturing CO2 from flue gas 被引量:6
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作者 Xinglei Zhao Qian Cui +5 位作者 BaodengWang Xueliang Yan Surinder Singh Feng Zhang Xing Gao Yonglong Li 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2018年第11期2292-2302,共11页
Under the Paris agreement, China has committed to reducing CO_2 emissions by 60%–65% per unit of GDP by 2030.Since CO_2 emissions from coal-fired power plants currently account for over 30% of the total carbon emissi... Under the Paris agreement, China has committed to reducing CO_2 emissions by 60%–65% per unit of GDP by 2030.Since CO_2 emissions from coal-fired power plants currently account for over 30% of the total carbon emissions in China, it will be necessary to mitigate at least some of these emissions to achieve this goal. Studies by the International Energy Agency(IEA) indicate CCS technology has the potential to contribute 14% of global emission reductions, followed by 40% of higher energy efficiency and 35% of renewable energy, which is considered as the most promising technology to significantly reduce carbon emissions for current coal-fired power plants.Moreover, the announcement of a Chinese national carbon trading market in late 2017 signals an opportunity for the commercial deployment of CO_2 capture technologies.Currently, the only commercially demonstrated technology for post-combustion CO_2 capture technology from power plants is solvent-based absorption. While commercially viable, the costs of deploying this technology are high. This has motivated efforts to develop more affordable alternatives, including advanced solvents, membranes,and sorbent capture systems. Of these approaches, advanced solvents have received the most attention in terms of research and demonstration. In contrast, sorbent capture technology has less attention, despite its potential for much lower energy consumption due to the absence of water in the sorbent. This paper reviews recent progress in the development of sorbent materials modified by amine functionalities with an emphasis on material characterization methods and the effects of operating conditions on performance. The main problems and challenges that need to be overcome to improve the competitiveness of sorbent-based capture technologies are discussed. 展开更多
关键词 co2 sorbent AMINE FLUE gas co2 adsorption co2 REGENERATION
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Study on Zn_2SiO_4 Formation Kinetics and Activity Stability of Desulfurization Sorbent 被引量:4
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作者 Zou Kang Lin Wei +3 位作者 Tian Huiping Xu Guangtong Wang Lei Xu Hua 《China Petroleum Processing & Petrochemical Technology》 SCIE CAS 2015年第1期6-15,共10页
A new industrial S Zorb sorbent(Ni/Zn O-P) was prepared by using the spray drying technique. The other two traditional sorbents(Ni/Zn O-M and Ni/Zn O-H) were prepared in exactly the same way except the use of differen... A new industrial S Zorb sorbent(Ni/Zn O-P) was prepared by using the spray drying technique. The other two traditional sorbents(Ni/Zn O-M and Ni/Zn O-H) were prepared in exactly the same way except the use of different silica-alumina binder matrices. The XRD, Rietveld quantitative phase analysis, BET, and laser particle size analysis were employed to characterize their physico-chemical properties. The deactivation mechanism and desulfurization kinetics of sorbent was investigated on a water vapor aging treatment device. It was shown that both the water vapor pressure and reaction temperature significantly could influence the formation rate of inactive Zn2 Si O4, which could decrease the sulfur storage capacity of sorbents. The Zn2 Si O4 content profiles could be fitted into the zero order equation, from which the apparent rate constant k and the activation energy E a were calculated. The matrix P greatly raised the E a of Zn2 Si O4 formation due to the less bridged hydroxyl silanol groups on its surface, which accounted for the high stability of Ni/Zn O-P. The desulfurization performance of the fresh and aged sorbents showed that the overall average sulfur conversion of Ni/Zn O-P(aged) was 92%, which was close to that of fresh sorbents(95%), and was higher than that of Ni/Zn O-M(aged)(86%) and Ni/Zn O-H(aged)(90%). Based on these findings, the application of Ni/Zn O-P can greatly improve the long-term running stability of the industrial unit. 展开更多
关键词 kinetics Zn2SiO4 DESULFURIZATION activity sorbent high STABILITY
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CO2 capture over molecular basket sorbents:Effects of SiO2 supports and PEG additive 被引量:4
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作者 Lin Zhang Xiaoxing Wang +2 位作者 Mamoru Fujii Linjun Yang Chunshan Song 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2017年第5期1030-1038,共9页
The objective of this work is to study the influences of silica supports and PEG additive on the sorption performance of molecular basket sorbent(MBS) for COcapture consisting of polyethylenimine and one of the foll... The objective of this work is to study the influences of silica supports and PEG additive on the sorption performance of molecular basket sorbent(MBS) for COcapture consisting of polyethylenimine and one of the following supports: SBA-15(2-D structure), TUD-1(3-D sponge-like structure) and fumed silica HS-5(3-D disordered structure). Effects of the supports regarding pore structures and pore properties, the PEI loading amount as well as the sorption temperature were examined. Furthermore, polyethylene glycol(PEG) was introduced as an additive into the sorbents and its effect was investigated at different PEI loadings and sorption temperatures. The results suggest that the pore properties of MBS(after PEI loading) play a more important role in the COsorption capacity, rather than those of the supports alone.MBS with 3D pore structure exhibits higher COsorption capacity and amine efficiency than those with 2D-structured support. Among the sorbents studied, fumed silica(HS-5) based MBS showed the highest COsorption capacity in the temperature range of 30-95 °C, probably due to its unique interstitial pores formed by the aggregation of polymer-loaded SiOparticles. It was found that the temperature dependence is directly related to the PEI surface coverage layers. The more PEI surface coverage layers, the higher diffusion barrier for COand the stronger temperature dependence of COcapacity. 3D MBS exceeds 2D MBS at the same PEI coverage layers due to lower diffusion barrier. Adding PEG can significantly enhance the COsorption capacity and improve amine efficiency of all MBS, most likely by alleviating the diffusion barrier within PEI bulk layers through the inter-molecular interaction between PEI and PEG. 展开更多
关键词 co2 capture Molecular basket sorbents Mesoporous molecular sieve Polyethylenimine(PEI) Polyethylene glycol(PEG)
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CO_(2) capture by double metal modified CaO-based sorbents from pyrolysis gases 被引量:1
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作者 Xiaobin Chen Yuting Tang +3 位作者 Chuncheng Ke Chaoyue Zhang Sichun Ding Xiaoqian Ma 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2022年第3期40-49,共10页
High-temperature pyrolysis technology can effectively solve the problem of municipal solid waste pollution.However,the pyrolysis gas contains a large amount of CO_(2),which would adversely affect the subsequent utiliz... High-temperature pyrolysis technology can effectively solve the problem of municipal solid waste pollution.However,the pyrolysis gas contains a large amount of CO_(2),which would adversely affect the subsequent utilization.To address this problem,a novel method of co-precipitation modification with Ca,Mg and Zr metals was proposed to improve the CO_(2)capture performance.X-ray diffraction(XRD)patterns and energy dispersive X-ray spectroscopy analysis showed that the two inert supports MgO and CaZrO_(3)were uniformly distributed in the modified calcium-based sorbents.In addition,the XRD results indicated that CaZrO_(3)was produced by the reaction of ZrO_(2)and CaO at high temperatures.The effects of doping ratios,adsorption temperature,calcination temperature,CO_(2)concentration and calcination atmosphere on the adsorption capacity and cycle stability of the modified calcium-based sorbent were studied.The modified calcium-based sorbent achieved the best CO_(2)capture performance when the doping ratio was 10:1:1 with carbonation at 700℃ under 20%CO_(2)/80%N_(2)atmosphere and calcination at 900℃ under100%N_(2)atmosphere.After ten cycles,the average carbonation conversion rate of Ca-10 sorbent was 72%.Finally,the modified calcium-based sorbents successfully reduced the CO_(2)concentration of the pyrolysis gas from 37%to 5%. 展开更多
关键词 Pyrolysis gas CO_(2)capture CO-PRECIPITATION CaO-based sorbents Modified sorbents
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弱极性超微孔Sc/In-CPM-66A用于CH_(4)/N_(2)吸附分离性能 被引量:2
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作者 唐宇昊 张迎迎 +4 位作者 赵智伟 鲁梦悦 张飞飞 王小青 杨江峰 《化工学报》 EI CSCD 北大核心 2024年第9期3210-3220,共11页
低浓度煤层气的提质利用对缓解国内天然气不足的现状具有重要意义,然而煤层气中存在的氮气杂质限制了该类资源的进一步应用,进行低浓度煤层气中CH_(4)/N_(2)混合物的分离至关重要。制备了两种具有弱极性超微孔的金属有机框架材料Sc-CPM-... 低浓度煤层气的提质利用对缓解国内天然气不足的现状具有重要意义,然而煤层气中存在的氮气杂质限制了该类资源的进一步应用,进行低浓度煤层气中CH_(4)/N_(2)混合物的分离至关重要。制备了两种具有弱极性超微孔的金属有机框架材料Sc-CPM-66A和In-CPM-66A,研究材料从CH_(4)/N_(2)混合物中富集CH_(4)的性能,利用PXRD、77 K N_(2)吸附、TGA和FTIR光谱对材料的结构进行了表征。IAST选择性计算表明,In-CPM-66A和Sc-CPM-66A的CH_(4)/N_(2)选择性达到6.0。受益于材料表面存在的大量的甲基基团,两种材料对CH_(4)的吸附热低于被报道的大部分材料,材料与甲烷分子之间弱的相互作用有利于吸附剂的脱附再生。穿透实验进一步表明,CPM-66A可以实现动态条件下CH_(4)/N_(2)混合物的分离,循环穿透实验显示该类材料具有良好的可重复性。 展开更多
关键词 天然气 CH_(4)/N_(2) 弱极性 CPM-66A 选择性 吸附剂
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