首页 > 最新文献

Kataliz v promyshlennosti最新文献

英文 中文
Comprehensive comparison of high productivity cobalt catalysts for Fischer – Tropsch synthesis with different types of heat-conductive frames 不同类型导热骨架的高生产率钴费托合成催化剂的综合比较
Pub Date : 2022-07-19 DOI: 10.18412/1816-0387-2022-4-6-21
K. Gryaznov, L. V. Sineva, E. Asalieva, V. Mordkovich
The results of physicochemical comparative study of Fischer – Tropsch industrial cobalt zeolite-containing catalysts are presented. The catalysts are based on heat-conductive additive (aluminum flakes or exfoliated graphite) and were tested in one tube industrial scale reactor (length – 6000 mm, inner diameter – 12 mm). For comparison purposes, the testing results of catalyst without heat-conductive additive are presented. It’s shown that exfoliated graphite-based catalyst is more suitable for industrial scale application in high syngas gas hour space velocities due to higher thermal stability and higher hydrocarbon productivity.
介绍了含钴沸石Fischer - Tropsch工业催化剂的理化对比研究结果。催化剂基于导热添加剂(铝片或剥离石墨),并在一管工业规模反应器(长- 6000毫米,内径- 12毫米)中进行了测试。为了比较,给出了不含导热添加剂的催化剂的测试结果。结果表明,石墨基脱片状催化剂具有较高的热稳定性和较高的产油率,更适合在高合成气气时空速条件下的工业规模应用。
{"title":"Comprehensive comparison of high productivity cobalt catalysts for Fischer – Tropsch synthesis with different types of heat-conductive frames","authors":"K. Gryaznov, L. V. Sineva, E. Asalieva, V. Mordkovich","doi":"10.18412/1816-0387-2022-4-6-21","DOIUrl":"https://doi.org/10.18412/1816-0387-2022-4-6-21","url":null,"abstract":"The results of physicochemical comparative study of Fischer – Tropsch industrial cobalt zeolite-containing catalysts are presented. The catalysts are based on heat-conductive additive (aluminum flakes or exfoliated graphite) and were tested in one tube industrial scale reactor (length – 6000 mm, inner diameter – 12 mm). For comparison purposes, the testing results of catalyst without heat-conductive additive are presented. It’s shown that exfoliated graphite-based catalyst is more suitable for industrial scale application in high syngas gas hour space velocities due to higher thermal stability and higher hydrocarbon productivity.","PeriodicalId":17783,"journal":{"name":"Kataliz v promyshlennosti","volume":"24 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-07-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73035876","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Sorption-catalytic steam conversion of CO on a mechanical mixture of Pt/Ce0.75Zr0.25O2 catalyst and NaNO3/MgO sorbent Pt/Ce0.75Zr0.25O2催化剂和NaNO3/MgO吸附剂的机械混合吸附-催化蒸汽转化CO
Pub Date : 2022-07-19 DOI: 10.18412/1816-0387-2022-4-28-35
A. Gorlova, I. E. Karmadonova, V. S. Derevshchikov, V. Rogozhnikov, P. Snytnikov, D. Potemkin
The sorption-catalytic steam conversion of CO using a mechanical mixture of 5 wt.% Pt/Ce0.75Zr0.25O2 catalyst grains and 10 mol.% NaNO3/MgO sorbent was studied. It was shown under the model conditions that initially MgO adsorbs СО2 only slightly, whereas its promotion with NaNO3 leads to a considerable growth of the adsorption dynamic capacity in the temperature range of 300–350 °С with a maximum at 320 °С. High activity and selectivity of the catalyst in steam conversion of CO were demonstrated for a model mixture with the composition (vol.%) 11.6 CO, 61 H2 and 27.4 H2O: the concentration of СО at the reactor outlet did not exceed 1 vol.% in the temperature range of 220– 400 °С (the minimum value of 0.3 vol.% was observed at 240 °С), and СН4 – at temperatures below 320 °С (0.61 vol.% at this point). The use of the sorbent in a mixture with the catalyst in the sorption-catalytic steam conversion of CO at 320 °С led to a considerable decrease in its sorption capacity; this may be related to the conversion of all NaNO3 into Na2CO3, which decomposed incompletely during regeneration. Nevertheless, this made it possible to decrease twofold the outlet concentrations of СО and СН4 as compared to the values observed at the indicated temperature in the experiment without a sorbent: particularly, in the middle of the first adsorption cycle they were equal to 6.1·10–4 and 8.2·10–2 vol.%, respectively, on a dry gas basis. Thus, the indicated approach to the sorption-catalytic conversion of CO was shown to be promising; further studies are needed to increase the capacity and stability of the presented type of sorbents.
采用5 wt.% Pt/Ce0.75Zr0.25O2催化剂颗粒和10 mol.% NaNO3/MgO吸附剂的机械混合物,研究了CO的吸附-催化蒸汽转化。结果表明,在模型条件下,MgO最初对СО2的吸附作用较弱,而NaNO3对MgO的促进作用使其在300-350°С温度范围内的吸附动态容量显著增加,在320°С温度范围内达到最大值。该催化剂在CO蒸汽转化过程中具有较高的活性和选择性,其组成为(vol.%) 11.6 CO, 61 H2和27.4 H2O的模型混合物:反应器出口的СО浓度在220 - 400°С温度范围内不超过1 vol.%(最小值为0.3 vol.%),在240°С温度范围内,СН4 -温度低于320°С(此时为0.61 vol.%)。在320°С下CO的吸附-催化蒸汽转化过程中,将吸附剂与催化剂混合使用导致其吸附能力明显下降;这可能与所有的NaNO3都转化为Na2CO3有关,而Na2CO3在再生过程中分解不完全。尽管如此,与没有吸附剂的实验中在指定温度下观察到的值相比,这使得СО和СН4的出口浓度降低了两倍:特别是,在第一个吸附循环的中间,它们在干气基础上分别等于6.1·10-4和8.2·10-2 vol.%。因此,所指出的吸附催化转化CO的方法是有前途的;需要进一步的研究来提高所提出的吸附剂的容量和稳定性。
{"title":"Sorption-catalytic steam conversion of CO on a mechanical mixture of Pt/Ce0.75Zr0.25O2 catalyst and NaNO3/MgO sorbent","authors":"A. Gorlova, I. E. Karmadonova, V. S. Derevshchikov, V. Rogozhnikov, P. Snytnikov, D. Potemkin","doi":"10.18412/1816-0387-2022-4-28-35","DOIUrl":"https://doi.org/10.18412/1816-0387-2022-4-28-35","url":null,"abstract":"The sorption-catalytic steam conversion of CO using a mechanical mixture of 5 wt.% Pt/Ce0.75Zr0.25O2 catalyst grains and 10 mol.% NaNO3/MgO sorbent was studied. It was shown under the model conditions that initially MgO adsorbs СО2 only slightly, whereas its promotion with NaNO3 leads to a considerable growth of the adsorption dynamic capacity in the temperature range of 300–350 °С with a maximum at 320 °С. High activity and selectivity of the catalyst in steam conversion of CO were demonstrated for a model mixture with the composition (vol.%) 11.6 CO, 61 H2 and 27.4 H2O: the concentration of СО at the reactor outlet did not exceed 1 vol.% in the temperature range of 220– 400 °С (the minimum value of 0.3 vol.% was observed at 240 °С), and СН4 – at temperatures below 320 °С (0.61 vol.% at this point). The use of the sorbent in a mixture with the catalyst in the sorption-catalytic steam conversion of CO at 320 °С led to a considerable decrease in its sorption capacity; this may be related to the conversion of all NaNO3 into Na2CO3, which decomposed incompletely during regeneration. Nevertheless, this made it possible to decrease twofold the outlet concentrations of СО and СН4 as compared to the values observed at the indicated temperature in the experiment without a sorbent: particularly, in the middle of the first adsorption cycle they were equal to 6.1·10–4 and 8.2·10–2 vol.%, respectively, on a dry gas basis. Thus, the indicated approach to the sorption-catalytic conversion of CO was shown to be promising; further studies are needed to increase the capacity and stability of the presented type of sorbents.","PeriodicalId":17783,"journal":{"name":"Kataliz v promyshlennosti","volume":"42 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-07-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77252834","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Experimental investigations and kinetics of hydrogen oxidation by oxygen in the media of carbon dioxide under elevated pressure at fiber-glass Pt/Pd catalysts 玻璃纤维Pt/Pd催化剂在二氧化碳介质中高压氧化氢的实验研究和动力学
Pub Date : 2022-07-19 DOI: 10.18412/1816-0387-2022-4-22-27
A. Zagoruiko, S. Lopatin, P. Mikenin, A. Elyshev
The study is dedicated to the performance of glass-fiber catalysts (GFCs) in the practically important reaction of hydrogen oxidation by oxygen in the media of carbon dioxide at elevated pressures. The samples of the catalysts were synthesized using Pt and Pd as active metals and thermostable high-silica glass-fiber textiles both unpromoted and promoted by Zr. The used catalyst preparation methods include surface thermal synthesis and leaching/impregnation approaches. All three tested samples showed approximately equal activity, but the preference was given to Pt-based GFC synthesized by means of surface thermal synthesis method because it uses the much cheaper and widely available glass-fiber textile instead of rare and expensive Zr-promoted materials. Resource testing of this catalyst for more than 200 hours demonstrated its high stability. The reaction rate may be described by kinetic equation corresponding to mass-action law with linear dependence upon the reaction pressure. The studied GFC may be arranged into structured cartridges with low pressure drop and highly intensive heat and mass transfer under the commercial process conditions, so its further practical application looks promising.
研究了玻璃纤维催化剂(GFCs)在高压二氧化碳介质中氧氧化氢反应中的性能。以Pt和Pd为活性金属,用Zr促进和未促进的耐热高硅玻璃纤维织物合成催化剂样品。所用的催化剂制备方法包括表面热合成法和浸出/浸渍法。所有三种测试样品的活性大致相同,但优先考虑采用表面热合成方法合成的基于pt的GFC,因为它使用更便宜和广泛使用的玻璃纤维纺织品,而不是稀有和昂贵的zr促进材料。经200小时以上的资源测试表明,该催化剂具有较高的稳定性。反应速率可以用质量作用定律对应的动力学方程来描述,该方程与反应压力呈线性关系。在工业工艺条件下,所研究的GFC可以布置在结构筒体中,具有低压降和高强度的传热传质,具有进一步的实际应用前景。
{"title":"Experimental investigations and kinetics of hydrogen oxidation by oxygen in the media of carbon dioxide under elevated pressure at fiber-glass Pt/Pd catalysts","authors":"A. Zagoruiko, S. Lopatin, P. Mikenin, A. Elyshev","doi":"10.18412/1816-0387-2022-4-22-27","DOIUrl":"https://doi.org/10.18412/1816-0387-2022-4-22-27","url":null,"abstract":"The study is dedicated to the performance of glass-fiber catalysts (GFCs) in the practically important reaction of hydrogen oxidation by oxygen in the media of carbon dioxide at elevated pressures. The samples of the catalysts were synthesized using Pt and Pd as active metals and thermostable high-silica glass-fiber textiles both unpromoted and promoted by Zr. The used catalyst preparation methods include surface thermal synthesis and leaching/impregnation approaches. All three tested samples showed approximately equal activity, but the preference was given to Pt-based GFC synthesized by means of surface thermal synthesis method because it uses the much cheaper and widely available glass-fiber textile instead of rare and expensive Zr-promoted materials. Resource testing of this catalyst for more than 200 hours demonstrated its high stability. The reaction rate may be described by kinetic equation corresponding to mass-action law with linear dependence upon the reaction pressure. The studied GFC may be arranged into structured cartridges with low pressure drop and highly intensive heat and mass transfer under the commercial process conditions, so its further practical application looks promising.","PeriodicalId":17783,"journal":{"name":"Kataliz v promyshlennosti","volume":"27 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-07-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"81150882","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Hydrogenation of 1,3-pentadiene on modified Pd-containing catalysts 1,3-戊二烯在改性含pd催化剂上的加氢反应
Pub Date : 2022-05-26 DOI: 10.18412/1816-0387-2022-3-31-37
L. Kustov, A. L. Tarasov, A. Kustov
Activity and selectivity of alumina-supported palladium catalysts, particularly the sulfurized ones, in the hydrogenation of 1,3-pentadiene to pentenes were investigated. Preliminary sulfurizing of palladium catalysts considerably enhances the selectivity to olefins in a wide range of the H2 /diene molar ratio (from 2.5 to 10). Samples activated in H2 at elevated temperatures demonstrate a higher activity toward diene hydrogenation. Palladium catalysts are more active at low temperatures of the reaction; however, the earlier studied sulfurized Ni catalysts compare well with palladium ones in terms of their selectivity to olefins and productivity, and are more selective in an excess of hydrogen. Modification of palladium with chromium, silver or lithium increases the selectivity to olefins.
研究了铝负载钯催化剂,特别是硫化钯催化剂在1,3-戊二烯加氢制戊烯反应中的活性和选择性。钯催化剂的初步硫化在H2 /二烯摩尔比(2.5 ~ 10)范围内显著提高了对烯烃的选择性。在H2中活化的样品在高温下对二烯加氢表现出更高的活性。钯催化剂在低温下反应更活跃;然而,早期研究的硫化镍催化剂在对烯烃的选择性和生产效率方面与钯催化剂相比要好,并且在过量的氢中更具选择性。用铬、银或锂对钯进行改性,可提高对烯烃的选择性。
{"title":"Hydrogenation of 1,3-pentadiene on modified Pd-containing catalysts","authors":"L. Kustov, A. L. Tarasov, A. Kustov","doi":"10.18412/1816-0387-2022-3-31-37","DOIUrl":"https://doi.org/10.18412/1816-0387-2022-3-31-37","url":null,"abstract":"Activity and selectivity of alumina-supported palladium catalysts, particularly the sulfurized ones, in the hydrogenation of 1,3-pentadiene to pentenes were investigated. Preliminary sulfurizing of palladium catalysts considerably enhances the selectivity to olefins in a wide range of the H2 /diene molar ratio (from 2.5 to 10). Samples activated in H2 at elevated temperatures demonstrate a higher activity toward diene hydrogenation. Palladium catalysts are more active at low temperatures of the reaction; however, the earlier studied sulfurized Ni catalysts compare well with palladium ones in terms of their selectivity to olefins and productivity, and are more selective in an excess of hydrogen. Modification of palladium with chromium, silver or lithium increases the selectivity to olefins.","PeriodicalId":17783,"journal":{"name":"Kataliz v promyshlennosti","volume":"27 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-05-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84302895","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Deactivation of hydrotreating catalysts (A review) 加氢处理催化剂的失活(综述)
Pub Date : 2022-05-26 DOI: 10.18412/1816-0387-2022-3-38-65
S. V. Budukva, D. D. Uvarkina, O. Klimov, A. Noskov
The results of studies on deactivation of hydrotreating catalysts reported in scientific and technical literature are considered and systematized in the review. The effect exerted by the feedstock composition and hydrotreatment conditions on the catalyst coking is revealed. The factorsleading to changes in the morphology of active component and the possibilities to weaken this type of catalyst deactivation during commercial operation are considered. The effect of a pressure drop over the catalyst bed on the run time as well as the action of catalytic poisons and the ways of their penetration into hydrotreatment distillates are shown. This review can be interesting and useful to chemical engineers involved in the study of catalytic systems and to oil industry specialists.
本文对科技文献中关于加氢处理催化剂失活的研究结果进行了综合和整理。揭示了原料组成和加氢处理条件对催化剂结焦的影响。考虑了导致活性组分形态变化的因素以及在商业操作中削弱这种催化剂失活的可能性。介绍了催化剂床上压降对加氢反应运行时间的影响,以及催化毒物的作用及其渗透加氢馏出物的途径。这篇综述对于从事催化系统研究的化学工程师和石油工业专家来说是有趣和有用的。
{"title":"Deactivation of hydrotreating catalysts (A review)","authors":"S. V. Budukva, D. D. Uvarkina, O. Klimov, A. Noskov","doi":"10.18412/1816-0387-2022-3-38-65","DOIUrl":"https://doi.org/10.18412/1816-0387-2022-3-38-65","url":null,"abstract":"The results of studies on deactivation of hydrotreating catalysts reported in scientific and technical literature are considered and systematized in the review. The effect exerted by the feedstock composition and hydrotreatment conditions on the catalyst coking is revealed. The factorsleading to changes in the morphology of active component and the possibilities to weaken this type of catalyst deactivation during commercial operation are considered. The effect of a pressure drop over the catalyst bed on the run time as well as the action of catalytic poisons and the ways of their penetration into hydrotreatment distillates are shown. This review can be interesting and useful to chemical engineers involved in the study of catalytic systems and to oil industry specialists.","PeriodicalId":17783,"journal":{"name":"Kataliz v promyshlennosti","volume":"3 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-05-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76927456","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
The use of microalgae biomass for the production of marketable products. Part 1. Approaches to the production of microalgae biomass 利用微藻生物量生产适销产品。第1部分。微藻生物量生产的途径
Pub Date : 2022-05-26 DOI: 10.18412/1816-0387-2022-3-66-85
K. N. Sorokina, Y. V. Samoylova, V. Parmon
The literature review is devoted to recent studies on the production of microalgae biomass and its processing using chemical and bioengineering approaches into marketable substances: biofuel, ethanol, butanol, hydrogen and others. The review consists of three parts: approaches to the production of microalgae biomass (part 1), the synthesis of biofuel from microalgae (part 2), and the production of marketable substances by bioengineering (part 3). The first part of the review considers the promising strains of microalgae that produce lipids and serve to obtain biofuel complying with ASTM D6751 and EN 14214 standards. Factors affecting the accumulation and composition of microalgae lipids (the composition of nutritional medium, illumination, temperature, and salinity of the medium) are also discussed. Approaches to the production of microalgae biomass, particularly with the use of flue gases and sewage, are analyzed.
文献综述致力于微藻生物量的生产及其使用化学和生物工程方法加工成可销售物质的最新研究:生物燃料、乙醇、丁醇、氢和其他。本综述由三部分组成:微藻生物质的生产方法(第一部分),微藻合成生物燃料(第二部分),以及生物工程生产可销售物质(第三部分)。第一部分综述考虑了有前途的微藻菌株,这些菌株生产脂质并用于获得符合ASTM D6751和EN 14214标准的生物燃料。还讨论了影响微藻脂质积累和组成的因素(营养培养基的组成、光照、温度和培养基的盐度)。分析了生产微藻生物量的方法,特别是利用烟道气和污水的方法。
{"title":"The use of microalgae biomass for the production of marketable products. Part 1. Approaches to the production of microalgae biomass","authors":"K. N. Sorokina, Y. V. Samoylova, V. Parmon","doi":"10.18412/1816-0387-2022-3-66-85","DOIUrl":"https://doi.org/10.18412/1816-0387-2022-3-66-85","url":null,"abstract":"The literature review is devoted to recent studies on the production of microalgae biomass and its processing using chemical and bioengineering approaches into marketable substances: biofuel, ethanol, butanol, hydrogen and others. The review consists of three parts: approaches to the production of microalgae biomass (part 1), the synthesis of biofuel from microalgae (part 2), and the production of marketable substances by bioengineering (part 3). The first part of the review considers the promising strains of microalgae that produce lipids and serve to obtain biofuel complying with ASTM D6751 and EN 14214 standards. Factors affecting the accumulation and composition of microalgae lipids (the composition of nutritional medium, illumination, temperature, and salinity of the medium) are also discussed. Approaches to the production of microalgae biomass, particularly with the use of flue gases and sewage, are analyzed.","PeriodicalId":17783,"journal":{"name":"Kataliz v promyshlennosti","volume":"54 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-05-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78084458","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
The production of monomers by dehydrogenation at PJSC «Nizhnekamskneftekhim» 在PJSC«Nizhnekamskneftekhim»脱氢生产单体
Pub Date : 2022-05-26 DOI: 10.18412/1816-0387-2022-3-21-30
I. R. Nabiullin, A. Boretskaya, M. V. Berezkina, R. Gilmullin, A. M. Busygina, A. Z. Kurbangaleeva, S. Egorova
The paper describes the production of base monomers by dehydrogenation at PJSC «Nizhnekamskneftekhim». Special emphasis is made on the development of advanced domestic catalysts in cooperation with Kazan Federal University. Drawbacks of the existing catalytic systems and possible variants of their improvement are described.
本文介绍了在Nizhnekamskneftekhim PJSC脱氢生产碱单体的情况。特别强调与喀山联邦大学合作开发先进的国产催化剂。描述了现有催化系统的缺点及其改进的可能变体。
{"title":"The production of monomers by dehydrogenation at PJSC «Nizhnekamskneftekhim»","authors":"I. R. Nabiullin, A. Boretskaya, M. V. Berezkina, R. Gilmullin, A. M. Busygina, A. Z. Kurbangaleeva, S. Egorova","doi":"10.18412/1816-0387-2022-3-21-30","DOIUrl":"https://doi.org/10.18412/1816-0387-2022-3-21-30","url":null,"abstract":"The paper describes the production of base monomers by dehydrogenation at PJSC «Nizhnekamskneftekhim». Special emphasis is made on the development of advanced domestic catalysts in cooperation with Kazan Federal University. Drawbacks of the existing catalytic systems and possible variants of their improvement are described.","PeriodicalId":17783,"journal":{"name":"Kataliz v promyshlennosti","volume":"31 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-05-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80968217","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Supported and polyfunctional hybrid cobalt catalysts for selective Fischer – Tropsch synthesis (A review) 选择性Fischer - Tropsch合成的负载型和多能杂化钴催化剂(综述)
Pub Date : 2022-05-26 DOI: 10.18412/1816-0387-2022-3-5-20
R. Yakovenko, V. G. Bakun, S. Sulima, G. B. Narochnyi, S. Mitchenko, I. Zubkov, A. Savost’yanov
The review considers modern approaches to the development of a technology for producing cobalt catalysts that are applied in the majority of known processes aimed to synthesize hydrocarbons from СО and Н2 by the Fischer – Tropsch method. The development of efficient catalysts makes it possible to replace the fuel produced from fossil oil by an alternative ultrapure fuel, thus reducing the detrimental effect on the environment. The results of R&D studies, particularly those obtained recently by the authors, were analyzed to reveal topical trends in the development of high-performance catalysts for the synthesis of hydrocarbons by the Fischer – Tropsch method within the classical and integrated GTL technology, including the creation of polyfunctional systems of new types. The review provides information mainly on the catalytic characteristics of the supported cobalt catalysts synthesized by impregnation and the related polyfunctional hybrid catalysts for the selective synthesis of fuel fraction hydrocarbons. The control of selectivity and productivity as well as changes in activity and physicochemical properties of the catalysts during a long-term operation are considered.
该综述考虑了生产钴催化剂的技术发展的现代方法,这些催化剂应用于大多数已知工艺,旨在通过Fischer - Tropsch方法从СО和Н2合成碳氢化合物。高效催化剂的发展使得用超纯燃料替代化石燃料成为可能,从而减少了对环境的有害影响。通过对研发研究的结果,特别是作者最近获得的研究结果进行分析,揭示了在经典和集成GTL技术中使用Fischer - Tropsch方法合成碳氢化合物的高性能催化剂的发展趋势,包括新型多功能体系的创建。主要介绍了浸渍法制备的负载型钴催化剂及相关的多官能杂化催化剂在选择性合成燃料馏分烃中的催化性能。考虑了催化剂在长期运行过程中对选择性和产率的控制以及活性和理化性质的变化。
{"title":"Supported and polyfunctional hybrid cobalt catalysts for selective Fischer – Tropsch synthesis (A review)","authors":"R. Yakovenko, V. G. Bakun, S. Sulima, G. B. Narochnyi, S. Mitchenko, I. Zubkov, A. Savost’yanov","doi":"10.18412/1816-0387-2022-3-5-20","DOIUrl":"https://doi.org/10.18412/1816-0387-2022-3-5-20","url":null,"abstract":"The review considers modern approaches to the development of a technology for producing cobalt catalysts that are applied in the majority of known processes aimed to synthesize hydrocarbons from СО and Н2 by the Fischer – Tropsch method. The development of efficient catalysts makes it possible to replace the fuel produced from fossil oil by an alternative ultrapure fuel, thus reducing the detrimental effect on the environment. The results of R&D studies, particularly those obtained recently by the authors, were analyzed to reveal topical trends in the development of high-performance catalysts for the synthesis of hydrocarbons by the Fischer – Tropsch method within the classical and integrated GTL technology, including the creation of polyfunctional systems of new types. The review provides information mainly on the catalytic characteristics of the supported cobalt catalysts synthesized by impregnation and the related polyfunctional hybrid catalysts for the selective synthesis of fuel fraction hydrocarbons. The control of selectivity and productivity as well as changes in activity and physicochemical properties of the catalysts during a long-term operation are considered.","PeriodicalId":17783,"journal":{"name":"Kataliz v promyshlennosti","volume":"108 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-05-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88050287","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Processes for the synthesis of γ-acetopropyl alcohol γ-乙酰丙醇的合成工艺
Pub Date : 2022-03-24 DOI: 10.18412/1816-0387-2022-2-5-17
V. E. Tarabanko, M. Smirnova, E. Zhizhina
The literature on the existing processes for the synthesis of γ-acetopropyl alcohol (acetopropanol, 5-hydroxypentan-2-one, APA) is reviewed. This substance is used to produce vitamin B1, antimalarial drugs and polymers. The promising methods for APA production are the hydrogenation-hydration of sylvan (2-methylfuran), hydrogenation of furfural, and syntheses based on allyl acetate, sodium acetoacetic ether, and γ-butyrolactone.
综述了γ-乙酰丙醇(乙酰丙醇,5-羟基戊烷-2- 1,APA)的现有合成工艺。这种物质被用来生产维生素B1、抗疟疾药物和聚合物。目前比较有前途的APA合成方法有:森林(2-甲基呋喃)加氢水化法、糠醛加氢法、醋酸烯丙酯、乙酰乙酸钠和γ-丁内酯合成法。
{"title":"Processes for the synthesis of γ-acetopropyl alcohol","authors":"V. E. Tarabanko, M. Smirnova, E. Zhizhina","doi":"10.18412/1816-0387-2022-2-5-17","DOIUrl":"https://doi.org/10.18412/1816-0387-2022-2-5-17","url":null,"abstract":"The literature on the existing processes for the synthesis of γ-acetopropyl alcohol (acetopropanol, 5-hydroxypentan-2-one, APA) is reviewed. This substance is used to produce vitamin B1, antimalarial drugs and polymers. The promising methods for APA production are the hydrogenation-hydration of sylvan (2-methylfuran), hydrogenation of furfural, and syntheses based on allyl acetate, sodium acetoacetic ether, and γ-butyrolactone.","PeriodicalId":17783,"journal":{"name":"Kataliz v promyshlennosti","volume":"14 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-03-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83875588","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A dust-collecting device for dehydrogenation of paraffin hydrocarbons with a fluidized catalyst bed 一种用流化催化剂床进行石蜡烃脱氢的集尘装置
Pub Date : 2022-03-24 DOI: 10.18412/1816-0387-2022-2-57-64
E. Salakhova, A. V. Dmitriev, V. Zinurov, I. R. Nabiullin, I. Salakhov
The paper considers the problem of collecting solid particles in the production line with dehydrogenation of С4–С5 isoparaffins to isoolefins in a fluidized catalyst bed. The collecting of finely dispersed catalyst particles for dehydrogenation of paraffin hydrocarbons using a standard CN-15 cyclone and a new dust-collecting device (NDD) with arched elements was studied. The results of numerical simulation of CN-15 and NDD are reported. A comparative study revealed that NDD is more efficient than CN-15 in collecting the finely dispersed solid particles with the size below 20 μm. For NDD, determinate variations in the pressure and rate profiles, without any critical deviations, were observed. The gas flow rate through the arched elements of NDD was found to be stable, in distinction to CN-15, where high rates appear at the cyclone edges, thus raising the probability of dust breakthrough into the flow to be purified.
本文研究了在流化床催化剂床上С4 -С5异烷烃脱氢制异烯烃生产线中固体颗粒的收集问题。研究了用标准CN-15旋风分离器和一种新型拱形元素集尘装置(NDD)对石蜡脱氢催化剂颗粒的集尘效果。报道了CN-15和NDD的数值模拟结果。对比研究表明,NDD对粒径小于20 μm的细分散固体颗粒的收集效率高于CN-15。对于NDD,在没有任何临界偏差的情况下,观察到压力和速率曲线的确定变化。通过NDD的拱形元件的气体流速被发现是稳定的,与CN-15不同,CN-15在旋风边缘出现高流速,从而提高了灰尘进入待净化气流的可能性。
{"title":"A dust-collecting device for dehydrogenation of paraffin hydrocarbons with a fluidized catalyst bed","authors":"E. Salakhova, A. V. Dmitriev, V. Zinurov, I. R. Nabiullin, I. Salakhov","doi":"10.18412/1816-0387-2022-2-57-64","DOIUrl":"https://doi.org/10.18412/1816-0387-2022-2-57-64","url":null,"abstract":"The paper considers the problem of collecting solid particles in the production line with dehydrogenation of С4–С5 isoparaffins to isoolefins in a fluidized catalyst bed. The collecting of finely dispersed catalyst particles for dehydrogenation of paraffin hydrocarbons using a standard CN-15 cyclone and a new dust-collecting device (NDD) with arched elements was studied. The results of numerical simulation of CN-15 and NDD are reported. A comparative study revealed that NDD is more efficient than CN-15 in collecting the finely dispersed solid particles with the size below 20 μm. For NDD, determinate variations in the pressure and rate profiles, without any critical deviations, were observed. The gas flow rate through the arched elements of NDD was found to be stable, in distinction to CN-15, where high rates appear at the cyclone edges, thus raising the probability of dust breakthrough into the flow to be purified.","PeriodicalId":17783,"journal":{"name":"Kataliz v promyshlennosti","volume":"27 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-03-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73005657","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
期刊
Kataliz v promyshlennosti
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1