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1.
低温甲醇洗净煤气硫含量超标浅析   总被引:1,自引:0,他引:1  
低温甲醇洗是一种节能型的酸性气体净化工艺。本文介绍了低温甲醇洗净化流程、基本原理。利用甲醇的选择性吸收特性,在高压、低温条件下,甲醇对CO2、H2S进行选择性吸收。重点讨论了影响因素如甲醇浓度、甲醇循环量、温度、压力等对净煤气总硫含量的影响及相应的调整措施。  相似文献   

2.
通过优化固化工艺、有机蒙脱土含量及树脂组分改善环氧涂层的耐热性,制备应用于高温H2S/CO2腐蚀环境中的环氧耐热防腐涂层,采用高温高压釜试验测试了涂层的耐热防腐效果。结果表明:适当的高温处理能显著提高基体树脂的玻璃化转变温度;环氧树脂在80℃机械搅拌条件下插入有机蒙脱土的层间,质量分数为3%的有机蒙脱土在基体中分散均一,为插层/剥离混合型复合结构,兼顾材料的热机械性能和阻隔性能;清漆涂层的玻璃化转变温度为153.7℃,其防腐涂层在150℃以下含H2S/CO2的油气环境中的防腐效果良好,说明玻璃化转变温度作为防腐涂层的使用上限温度是可行的。  相似文献   

3.
模拟含H2S/CO2高温高压井下腐蚀环境,研究温度对80SS油管钢腐蚀行为的影响.结果表明:随着温度升高,80SS油管钢的腐蚀速率呈现先增大后减小的趋势,在100℃时腐蚀速率达到最大(6.13 mm/a);150℃时腐蚀速率下降到4.14mm/a.随着温度升高,材料表面形成的腐蚀产物膜由致密、覆盖均匀逐渐变得颗粒粗大且疏松,当温度超过100℃时,腐蚀产物膜又变得颗粒较小且致密;膜的厚度也呈现先增加后减小的趋势;80SS油管钢的腐蚀形态为均匀腐蚀;在温度低于100℃时腐蚀产物膜主要由FeCO3和FeS0.9组成;高温(150℃)时,腐蚀中夹杂了Fe的氧化,产物膜主要由FeO(OH)、FeCO3和FeS0.9组成.  相似文献   

4.
为掌握CO变换制氢过程中催化剂中毒机理,采用热力学非均相反应体系中G ibbs自由能最小原理,分析了铜基低温变换催化剂在463.15—523.15 K内H2S中毒过程中可能发生的化学反应及其产物,并结合文献实验结果综合讨论了铜基低温变换催化剂的H2S中毒机理。结果表明:催化剂的H2S中毒过程中,硫酸盐和积碳会造成催化剂的暂时性中毒,生成Cu2S和CuS化合物造成永久性中毒;O2的存在会加快催化剂的中毒反应;铜基低温变换催化剂不适合用于含高体积分数CO原料气的变换反应过程。  相似文献   

5.
CO2/H2S对油气管材的腐蚀规律   总被引:1,自引:0,他引:1  
焦卫东  张耀宗  张清 《化工机械》2003,30(4):250-253
综述了CO2 、H2 S对油气管材的腐蚀机理及影响因素 ,提出了开发经济型油管的设想。  相似文献   

6.
Mixed solvents are a combination of chemical and physical solvents and have some advantages over traditional treating solvents for the removal of acid gases from gas streams. The solubility of H2S and CO2in a mixed solvent consisting of AMP (2-amino-2-methyl-l-propanol), sulfolane, and water has been measured at 40 and 100°C at partial pressures of the acid gas to 6000 kPa. The solubility in the mixed solvent was compared with the solubility in an aqueous solution of equivalent amine concentration. At solution loadings less than 1 mol acid gas/mol amine, the solubility of the acid gas is lower in the mixed solvent than in the corresponding amine solvent. At higher loadings, the trend is reversed and the solubility is greater in the mixed solvent. The results are rationalized in terms of the effect of the physical solvent component on the chemical reaction and physical vapor-liquid equilibria. The solubility model of Deshmukh and Mather was used to correlate the data.  相似文献   

7.
    
Catalytic membrane reactors based on oxygen-permeable membranes are recently studied for hydrogen separation because their hydrogen separation rates and separation factors are comparable to those of Pd-based membranes. New membrane materials with high performance and good tolerance to CO2 and H2S impurities are highly desired. In this work, a new membrane material Ce0.85Sm0.15O1.925–Sr2Fe1.5Mo0.5O6-δ (SDC–SFM) was prepared for hydrogen separation. It exhibits high conductivities at low oxygen partial pressures, which is benefit to electron transfer and ion diffusion. A high hydrogen separation rate of 6.6 mL cm−2 min−1 was obtained on a 0.5-mm-thick membrane coated with Ni/SDC catalyst at 900°C. The membrane reactor was operated steadily for 532 h under atmospheres containing CO2 and H2S impurities. Various characterizations reveal that SDC–SFM has good stability in the membrane reactor for hydrogen separation. All facts confirm that SDC–SFM is promising for hydrogen separation in practical applications. © 2018 American Institute of Chemical Engineers AIChE J, 65: 1088–1096, 2019  相似文献   

8.
福海创石油化工有限公司一套凝析油分离装置直馏液化气管线直管段局部腐蚀破裂,通过对工艺、物料、设备、腐蚀产物进行分析,判断腐蚀机理,确定该管线的腐蚀成因及合理应对措施。  相似文献   

9.
SIMULTANEOUS ABSORPTION OF H2S AND CO2 INTO A SOLUTION OF SODIUM CARBONATE   总被引:1,自引:0,他引:1  
The simultaneous absorption of H2S and CO2 has been studied both experimentally and theoretically. A model has been developed which predicts the absorption rates of H2S and CO2 into a sodium carbonate solution. The absorption rates are calculated according to the two-film theory. In the liquid film, the finite rate of the CO2 reaction was considered. Otherwise, in the liquid film as well as in the liquid bulk, equilibrium conditions for all reactions were assumed. Absorption experiments were performed on a packed column using a counter-flow strategy. In the experiments the influence of the initial carbonate concentration, the gas flow rate and the temperature on the removal efficiencies of H2S and CO2 and the selectivity of H2S were investigated. It is desirable to absorb the H2S but not the CO2. The agreement between the absorption model and the experimental results from the absorber tower was satisfactory. The mass transfer coefficients were determined by fitting the experimental data to the model with respect to the H2S and CO2 content in the outgoing gas. The H2S content was used to determine the gas side mass transfer coefficient and the CO2 content was used to determine the liquid side mass transfer coefficient, The effective contact area of mass transfer was taken from published data. With a constant packing height, both the experiments and the model indicated that high carbonate concentration benefits the removal efficiency of H2S. Higher gas flow rate also benefits the selectivity for H2S. However, the removal efficiency will decrease. At higher temperatures the selectivity and the removal efficiency of H2S decreased. Under the conditions investigated, the absorption of H2S was essentially controlled by gas-side mass transfer and the absorption of CO2 was controlled by liquid-side mass transfer  相似文献   

10.
刘矿伟  续静静  刘硕 《广州化工》2011,39(13):155-157
介绍了河南煤业化工集团义马气化厂30万t/a甲醇项目配套的低温甲醇洗工艺流程,分析了该工艺设计的特点;实践证明低温甲醇洗在实际应用中能够对酸性气体进行有效的脱除,净化气质量稳定,可以满足甲醇工段和城市煤气的生产需求。  相似文献   

11.
An experimental investigation for the simultaneous absorption of CO2 and H2S in 20 wt% hot K2CO3 solution have been conducted in a pilot scale packed absorber-stripper. The effects of liquid circulation rate, gas flow rate, inlet gas composition, steam pressure at bottom of stripper, and DEA promoter concentration, on the individual gas removal % and stripping efficiency were studied. The results showed that the performance of the absorber and stripper influenced one another and so must be considered together.  相似文献   

12.
Information on acid gas solubility in solvents utilized is needed for the design of gas plants. A mathematical model for the prediction of equilibrium solubility of CO2 and H2S in aqueous 2-amino-2-methyl-l-propanol (AMP) solutions is presented. The equilibrium constant, K1 governing the main amine reaction is expressed as a function of not only temperature but also acid gas partial pressure and AMP concentration. Model predictions agree favourably with experimental data.  相似文献   

13.
周明宇  于长海  刘龙 《辽宁化工》2006,35(8):497-500
随着流程模拟技术在炼油化工生产中的不断推广应用,越来越多的装置已经开始通过模拟来优化装置的操作,从而提高企业的经济效益。通过使用HYSYS.Process稳态流程模拟软件平台,建立生产装置部分模型,进行换热结构调整,计算新添加换热器所需的换热面积。  相似文献   

14.
高志博  史桂青  高鲲 《煤化工》2013,41(2):39-42
介绍了国电赤峰化工一期工程52万t/a尿素项目配套的低温甲醇洗工艺流程,分析了该工艺流程的设计特点:采用真空鼓风机抽真空,提高了甲醇半贫液的贫度、CO2产品气的纯度;采用CO2吸收塔,可同时处理来自H2S吸收塔的脱硫气和甲烷转化装置来的转化气;变换气冷却器采用缠绕式换热器,可降低能耗等。生产实践表明,采用低温甲醇洗技术能够有效脱除酸性气体,且净化气质量稳定,可满足合成氨工段和生产尿素的需求。  相似文献   

15.
    
The high fractional free volume (FFV) endowed polymers of intrinsic microporosity (PIMs) with high gas permeability but low selectivity. Herein, an intermediate temperature range was deliberately utilized to tune PIM-1 membrane microstructure in nitrogen atmosphere to enhance gas separation performance. During intermediate thermal manipulation, the synergistic effects of thermal-induced cross-linking and decomposition on PIM-1 membranes have optimized the micropores for significantly increasing membrane molecular-sieving ability with the boosted selectivity of 350 (H2/N2), 1,472 (H2/CH4), 3,774 (H2/C3H8), and 197 (CO2/CH4) respectively, with the H2 permeability of 234 Barrer, correspondingly, surpassing the “Robeson's Upper Bound”. The facile strategy simultaneously utilizing the thermal-induced cross-linking and decomposition, might provide a new platform to develop the high-performance membranes for highly-efficient hydrogen purification and CO2 separations.  相似文献   

16.
    
Novel polymeric membranes are to be developed for hot H2/CO2 separation. In this work, network polyimide (PI) membranes are prepared via a simple interfacial polymerization method using low-cost melamine and pyromellitic dianhydride monomers. The membrane performance surpasses the upper bound of H2/CO2 separation. Moreover, the membranes exhibit a H2/CO2 separation factor of 18.7 at 623 K and a robust performance after treatment with steam and H2S.  相似文献   

17.
国内油气资源分散、单井产量小,边远地区的油气资源较丰富,可以利用小型液化天然气装置制成LNG后外输,同时小型天然气膨胀液化工艺又是我国LNG研究工作的重点。利用Aspen Hysys软件对N2-CH4膨胀制冷液化流程进行模拟、研究和分析,得出影响该流程的主要参数:制冷剂高压压力、主换热器出口温度、制冷剂氮气含量、天然气进料压力和LNG储存压力对液化率和比功耗的影响。  相似文献   

18.
    
A new method is introduced to predict reliable estimation of heats of detonation of aromatic energetic compounds. At first step, this procedure assumes that the heat of detonation of an explosive compound of composition CaHbNcOd can be approximated as the difference between the heat of formation of all H2O CO2 arbitrary (H2O, CO2, N2) detonation products and that of the explosive, divided by the formula weight of the explosive. Overestimated results based on (H2O CO2 arbitrary) can be corrected in the next step. Predicted heats of detonation of pure energetic compounds with the product H2O in the liquid state for 31 aromatic energetic compounds have a root mean square (rms) deviation of 2.08 and 0.34 kJ g−1 from experiment for (H2O CO2 arbitrary) and new method, respectively. The new method also gives good results as compared to the second sets of decomposition products, which consider H2, N2, H2O, CO, and CO2 as major gaseous products. It is shown here how the predicted heats of detonation by the new method can be used to obtain reliable estimation of detonation velocity over a wide range of loading densities.  相似文献   

19.
管道用酚醛环氧树脂内涂层失效分析   总被引:1,自引:0,他引:1  
周斌葛  何毅  王雅诗  周林 《广东化工》2012,39(7):7-8,32
使用电化学工作站中的交流阻抗实验、结合高温高压釜实验以及端口扫描电镜(SEM)分析技术,研究了酚醛环氧树脂管道内涂层在含饱和H2S/CO2的3.5%NaCl(质量分数)水溶液中不同温度下的失效规律。结果表明,在电化学交流阻抗测试中,随着温度(50℃、70℃、90℃)的升高,涂层失效减缓:在高温高压釜16h实验后,涂层表观正常(未出现起泡、开裂、表面颜色无明显变化)、附着力良好:结合端口扫描电镜(SEM)技术,进一步证明温度升商会导致涂层在含H2S/CO2的3.5%NaCl溶液中失效减缓。  相似文献   

20.
The feasibility of using a cobalt-molybdenum (Co-Mo) sulfide catalyst that was prepared from a commercial Co-Mo oxide catalyst for the production of elemental sulfur from hydrogen sulfide (H2S) and carbon dioxide (CO2) in a packed bed catalytic reactor was studied. It was demonstrated that the desired sulfide catalyst could be prepared by first reducing, then sulphiding the corresponding oxide. The results showed that the prepared catalyst was capable of producing elemental sulfur from the thermal decomposition of H2S in the presence of CO2 over a temperature range of 465-700°C and at atmospheric pressure. A specific rate coefficient was calculated as well as the Arrhenius parameters for the non-equilibrated reaction. The H2S decomposition reaction was found to be a second order reaction and have an activation energy of 114.4kJ/mol(27.3kcal/mol).  相似文献   

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