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TREATMENT OF WASTEWATER CONTAINING AROMATIC NITRO COMPOUNDS USING THE A2O-MBBR METHOD a20 - mbbr法处理含芳香族硝基化合物废水
IF 0.9 Q4 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2018-10-22 DOI: 10.6060/ivkkt.20186109-10.5541
Vu Duy Nhan, N. V. Tu, N. Nhan, L. Huong, Y. Tsarev, L. Huong
2,4,6-Trinitrotoluene (TNT) is widely used in explosives production. Since it is toxic and mutagenic to humans and animals, decontamination of TNT wastewater is necessary. Wastewater, containing TNT, from four factories in Vietnam producing industrial explosives were collected. The samples had different characteristics and varied widely, especially in terms of TNT concentration, depending on the technology and production management method at each plant. The TNT concentration ranged from 25 to 128 mg/l, chemical oxygen demand (COD) ranged from 128 to 650 mg/l, BOD5 ranged from 28 to 67 mg/l, NH4+ranged from 23 to 325 mg/l, T-P ranged from 0.13 to 0.38, and pH ranged from 6.5 to 8.2. In Vietnam, removal of TNT is carried out using granular activated carbon adsorption and an incineration method. This method is expensive and generates secondary pollution. To overcome these drawbacks, the combination of an anaerobic-anoxic-oxic and moving bed biofilm reactor (A2O-MBBR) for treating TNT wastewater was investigated in this study. Reaction tanks of the A2O-MBBR system were supplemented with activated sludges, from a wastewater treatment station in Chemical and Electrical Engineering Company 15, containing biological preparations of nitrifying and denitrifying bacteria. The results showed that after 30 days under operating conditions of COD of 200-250 mg/l, MSLL of 1800-3000 mg/l, and DO of 5 mg/l, COD removal efficiency reached approximately 70-83%, the TNT concentration decreased by 91-99.7% (to approximately 0.5- 2 mg/l), and the ammonium concentration fell to 15-17 mg/l (reaching 42.8–66% removal efficiency after 24 h of treatment). For citation: Nhan Vu Duy, Tu Nguyen Van, Nhan Nguyen Thi, Huong Le Mai, Tsarev Yu.V., Huong Le Thi Mai Treatment of wastewater containing aromatic nitro compounds using the A2O-MBBR method. Izv. Vyssh. Uchebn. Zaved. Khim. Khim. Tekhnol. 2018. V. 61. N 9-10. P. 113-119
2,4,6-三硝基甲苯(TNT)在炸药生产中应用广泛。由于TNT对人类和动物具有毒性和诱变性,因此有必要对TNT废水进行净化。来自越南四家生产工业炸药的工厂的含有TNT的废水被收集起来。样品具有不同的特性,差异很大,特别是在TNT浓度方面,这取决于每个工厂的技术和生产管理方法。TNT浓度范围为25至128 mg/l,化学需氧量(COD)范围为128至650 mg/l,BOD5范围为28至67 mg/l,NH4+范围为23至325 mg/l,T-P范围为0.13至0.38,pH范围为6.5至8.2。在越南,TNT的去除采用颗粒活性炭吸附和焚烧法。这种方法成本高昂,而且会产生二次污染。为了克服这些缺点,本研究采用厌氧-缺氧-好氧和移动床生物膜反应器(A2O-MBBR)联合处理TNT废水。A2O-MBBR系统的反应槽补充有来自化学和电气工程公司15的废水处理站的活性污泥,其中含有硝化和反硝化细菌的生物制剂。结果表明,在COD为200-250mg/l、MSLL为1800-3000mg/l、DO为5mg/l的操作条件下,30天后,COD去除率达到约70-83%,TNT浓度下降91-99.7%(降至约0.5-2mg/l),铵浓度降至15-17mg/l(处理24小时后去除率达到42.8-66%)。引用:Nhan Vu Duy,Tu Nguyen Van,Nhan Nguyen Thi,Huong Le Mai,Tsarev Yu.V,Hung Le Thi Mai使用A2O-MBBR方法处理含芳香硝基化合物的废水。伊兹夫。维什。Uchebn。扎维德。Khim。Khim。Tekhnol。2018年第61条。N 9-10。第113-119页
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引用次数: 0
THE HISTORY OF DEVELOPMENT AND APPLYING OF ANTIOXIDANT ADDITIVES FOR FUEL AND OIL 燃油抗氧化添加剂的发展与应用历史
IF 0.9 Q4 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2018-10-22 DOI: 10.6060/IVKKT.20186109-10.5848
K. Alexanyan, O. A. Stokolos, E. V. Solodova, Y. N. Zaytceva, S. Salmanov, N. R. Yarullin, A. V. Naletova, E. Mikhailov
The history of development and improvement of antioxidant additives develops and changes as the development of the engineering industry and in petrochemistry. This article describes the importance of additives for fuels and oils. The requirements for the quality of fuel have become much stricter, in connection with both environmental requirements and the requirements for the operation of the car. As a rule, new additives are developed because the technology is improved and developed and because of environmental standards become more stringent. The article presents the proposed mechanism of action of additives in the fuel. Today, there is a trend in the production of engines that operate at higher temperatures and it expects that the content of antioxidant additives will grow, and it will be use in the systems with higher temperatures. Analysis of world literature over the past 30 years has shown that in the process of creating effective additives for fuels and oils, the possibility of using numerous organic compounds for this purpose was a investigated. The possibility of using for this purpose numerous organic compounds was used. Without exaggeration, we can say that all classes of organic compounds containing various functional groups are used like additives. As an effective antioxidant additive for fuels and oils is phenol-type additives and alkylphenol isomers. It’s effect depends on the position of the alkyl radical in the benzene ring, significantly improve the performance, since the mechanism of action (radical-type antioxidants) is to transfer the free radical from the active peroxide molecule to the phenol molecule to form a low-active, highly shielded radical on the oxygen atom of phenol. For citation: Alexanyan K.G., Stokolos O.A., Solodova E.V., Zaytseva Y.N., Salmanov S.Yu., Yarullin N.R., Naletova A.V., Mikhailov E.R. History of development and applying of antioxidant additives for fuel and oil. Izv. Vyssh. Uchebn. Zaved. Khim. Khim. Tekhnol. 2018. V. 61. N 9-10. P. 120-125
抗氧化添加剂的发展和改进的历史随着工程工业和石油化学的发展而发展变化。本文阐述了燃料和油品添加剂的重要性。由于对环境的要求和对汽车运行的要求,对燃料质量的要求变得越来越严格。通常,新添加剂的开发是因为技术的改进和发展,因为环境标准变得更加严格。本文提出了添加剂在燃料中的作用机理。如今,发动机生产的趋势是在更高的温度下运行,预计抗氧化添加剂的含量将会增加,它将在更高温度的系统中使用。对过去30年世界文献的分析表明,在为燃料和油创造有效添加剂的过程中,研究了为此目的使用多种有机化合物的可能性。为了达到这个目的,可以使用许多有机化合物。毫不夸张地说,含有各种官能团的各类有机化合物都被当作添加剂使用。酚类添加剂和烷基酚异构体是燃料和油类的有效抗氧化添加剂。它的作用取决于烷基自由基在苯环上的位置,显著提高性能,因为(自由基型抗氧化剂)的作用机制是将自由基从活性过氧化物分子转移到苯酚分子上,在苯酚的氧原子上形成低活性、高屏蔽的自由基。引文:Alexanyan k.g., Stokolos o.a., Solodova e.v., Zaytseva y.n., Salmanov s.u yu。,亚鲁林N.R,纳列托娃a.v.,米哈伊洛夫e.r。燃料和石油抗氧化添加剂的发展和应用历史。Izv。Vyssh。Uchebn。Zaved。Khim。Khim。Tekhnol》2018。v . 61。N 9。p . 120 - 125
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引用次数: 2
BIODEGRADATION OF SOLUTIONS FOR CHEMICAL NICKELATION 化学镍化溶液的生物降解
IF 0.9 Q4 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2018-10-22 DOI: 10.6060/ivkkt.20186109-10.5792
G. M. Mukhametova, E. G. Vinokurov, E. Babusenko, V. D. Skopintsev
In this article, we examined the susceptibility of biodegradation of nickel-containing processing solutions and selected fungicidal products which meet the requirements. Technological solutions are characterized by such a priority parameter as the high deposition rate of the nickel coating were subject to biofouling by mycelial fungi, despite the presence of heavy metal ions in solutions. It is established that the development of mycelial fungi in solutions leads to their decomposition and deterioration of technological characteristics. The purpose of the study was to select the fungicide and its corresponding concentrations, which do not adversely affect the process rate and the quality of the coating. The following tasks were posed: investigation of the stability of various solutions for nickel plating to the action of microorganisms; identification of taxonomic affiliation of microorganisms that populate solutions; selection of fungicide, meeting the requirements for neutrality to the components of the solution, as there is no effect on the rate of the process. Based on the results of the experiment, the influence of microorganisms on the technological characteristics of solutions was determined. After the appearance and development of the colonies of mycelial fungi in time solutions, the pH changed to an alkaline region, the deposition rate of the Ni-P coating dropped. Copper sulfate, sodium tetraborate, lactic acid, chloroform was used as inhibitors. The use of copper sulfate fungicide in concentrations of 0.002-0.005 mol/l led to the inhibition of growth of the fungal colonies, but insignificant. Fungicide sodium tetraborate at a concentration of 0.03 mol/l had a noticeable inhibitory effect on the growth of fungi, and also had a positive effect on the rate of the process, which meets all the requirements for this compound. For citation: Mukhametova G.M., Vinokurov E.G., Babusenko E.S., Skopintsev V.D. Biodegradation of solutions for chemical nickelation. Izv. Vyssh. Uchebn. Zaved. Khim. Khim. Tekhnol. 2018. V. 61. N 9-10. P. 89-97
在本文中,我们检测了含镍加工溶液的生物降解敏感性,并选择了符合要求的杀菌产品。技术解决方案的特征在于这样一个优先参数,即尽管溶液中存在重金属离子,但镍涂层的高沉积速率会受到菌丝真菌的生物污染。研究表明,菌丝真菌在溶液中的发育会导致其分解和工艺特性的恶化。本研究的目的是选择不会对工艺速率和涂层质量产生不利影响的杀菌剂及其相应浓度。提出了以下任务:研究各种镀镍溶液对微生物作用的稳定性;确定溶液中微生物的分类隶属关系;杀菌剂的选择,要满足对溶液中性成分的要求,因为对工艺的速率没有影响。根据实验结果,确定了微生物对溶液工艺特性的影响。菌丝真菌菌落在时间溶液中出现和发育后,pH值变为碱性区域,Ni-P涂层的沉积速率下降。使用硫酸铜、四硼酸钠、乳酸、氯仿作为抑制剂。使用浓度为0.002-0.005摩尔/升的硫酸铜杀菌剂可抑制真菌菌落的生长,但不显著。浓度为0.03mol/l的杀菌剂四硼酸钠对真菌的生长有显著的抑制作用,对该过程的速率也有积极影响,满足了该化合物的所有要求。引用:Mukhametova G.M.、Vinokurov E.G.、Babusenko E.S.、Skopintsev V.D.化学镀镍溶液的生物降解。伊兹夫。维什。Uchebn。扎维德。Khim。Khim。Tekhnol。2018年第61条。N 9-10。第89-97页
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引用次数: 1
DEVELOPMENT AND INDUSTRIAL APPROBATION OF TECHNOLOGIES OF COBALT CATALYSTS FOR SYNTHESIS OF LONG CHAIN HYDROCARBONS FROM SYNTHESIS GAS 合成气合成长链烃用钴催化剂技术的开发与产业化评价
IF 0.9 Q4 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2018-10-22 DOI: 10.6060/IVKKT20186109-10.5864A
A. Savost’yanov, R. Yakovenko, Grigory B. Narochny, V. G. Bakun, A. A. Merkin
The compositions, methods of preparation and specific technological parameters of the production processes of cobalt catalysts for the synthesis of long chain hydrocarbons from synthesis gas were justified. To obtain C35+ selective catalysts by coprecipitation of active components, the carrier must provide a polydisperse distribution of the pore volume along the radii. This is achieved by hydrothermal treatment of the aluminosilicate carrier. To increase the strength of catalysts, it is possible to incorporate natural bentonites and diatomite of Roctov region deposits into the composition of coprecipitated catalysts. Effective catalytic systems are impregnated catalysts on Al2O3 and SiO2 supports with aluminum oxide promotion. The insertion of 5% - Al2O3 of cobalt metal mass allows to form crystallites of Co-CoO system with a size of 8 nm on the SiO2 surface, which provides high activity and selectivity for ceresin. Aluminum oxide is stabilized with Co3O4 in a structure with a high degree of ordering, without hindering its reduction, with the formation of cobalt predominantly with the crystalline structure of hexagonal close packing. Catalyst technologies are implemented in industry. The catalysts underwent continuous continuous testing (1000 h) in laboratory and industrial conditions, showed high stability of operation. During the entire operation, the yield of C5+ hydrocarbons was 159-171 g/Nm3 based on the processed synthesis gas. The long-chain hydrocarbons C35+ (ceresin) obtained are of high quality: the dropping point was 114-116 °C (37-40% ceresin content). Operation during the year of two industrial reactors at the Novocherkassk plant of synthetic products with a total volume of catalyst loading of 18 m3 confirmed the results of laboratory tests. For citation: Savostyanov A.P., Yakovenko R.E., Narochny G.B., Bakun V.G., Merkin A.A. Development and industrial approbation of technologies of cobalt catalysts for synthesis of long chain hydrocarbons from synthesis gas. Izv. Vyssh. Uchebn. Zaved. Khim. Khim. Tekhnol. 2018. V. 61. N 9-10. P. 53-58
对合成气合成长链烃用钴催化剂的组成、制备方法和具体工艺参数进行了论证。为了通过活性组分的共沉淀获得C35+选择性催化剂,载体必须沿半径提供多分散的孔体积分布。这是通过水热处理铝硅酸盐载体来实现的。为了提高催化剂的强度,可以将罗克托夫地区沉积物的天然膨润土和硅藻土加入共沉淀催化剂的组成中。有效的催化体系是在Al2O3和SiO2载体上浸渍催化剂,并由氧化铝促进。加入5% - Al2O3的钴金属质量可以在SiO2表面形成尺寸为8 nm的Co-CoO体系,具有较高的树脂活性和选择性。氧化铝与Co3O4稳定在一个高度有序的结构中,而不妨碍其还原,形成的钴主要是六方紧密堆积的晶体结构。催化剂技术在工业上得到了应用。催化剂在实验室和工业条件下连续测试(1000 h),表现出较高的运行稳定性。在整个操作过程中,以加工的合成气为基准,C5+烃的产率为159 ~ 171 g/Nm3。得到了高质量的长链烃C35+(蜡质),其落点为114-116℃(蜡质含量为37-40%)。在新切尔卡斯克合成产品工厂的两个工业反应器(催化剂装载总量为18立方米)一年内的运行证实了实验室测试的结果。引用本文:Savostyanov a.p., Yakovenko R.E, Narochny g.b., Bakun v.g., Merkin A.A.。合成气合成长链烃用钴催化剂技术的开发与工业认可。Izv。Vyssh。Uchebn。Zaved。Khim。Khim。Tekhnol》2018。v . 61。N 9。p . 53-58
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引用次数: 0
EXPERIMENTAL STUDY OF FLUID DYNAMIC BEHAVIOR OF BIOMASS PARTICLES IN FLUIDIZED BEDS: A REVIEW 生物质颗粒在流化床中流体动力学行为的实验研究综述
IF 0.9 Q4 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2018-10-22 DOI: 10.6060/IVKKT.20186109-10.5895
K. Tannous, A. G. D. Mitri, V. Mizonov
Decease of natural resources and increase of price of fossil fuels at growing energy consumption, toughening of ecological standards and necessity of the increase of the level of energetics diversification motivates mankind to more wide usage of renewable energy resources including the solid fuel of biological origin. The potential of biofuel usage is rather considerable because the energy equivalent of the biomass harvest on the land exceeds the worldwide energy consumption several times as much. The biomass application as a renewable fuel is already a reality worldwide with the development of policies and technologies that turn viable the transformation of biomass into energy. The aims of this work is to present a literature experimental review on the studies concerning to the use of fluidized beds taking into account their design and scale-up. Initially, the usual solid particle terminology and some important biomass properties are presented. A brief description of conversion technologies and the fluidization phenomena are introduced, followed by an explanation of the different experimental techniques. The characteristic velocities (initial, apparent, of segregation, and complete) are discussed based on different biomass properties, as well as a number of empirical correlations for these velocities are described. Finally, some considerations are made about characteristic bed porosities (apparent and complete) and bed expansion. Based on the literature analysis, an improvement has been done on the understanding of the biomass fluidization phenomena, however, further research is needed to comprehend the effect of biomass characteristics on the bed operational parameters, besides more accurate and general correlations must be developed to improve these technologies. For citation: Tannous K., De Mitri A.G., Mizonov V. Experimental study of fluid dynamic behavior of biomassparticles in fluidized beds: a review. Izv. Vyssh. Uchebn. Zaved. Khim. Khim. Tekhnol. 2018. V. 61. N 9-10. P. 4-14
随着能源消耗的增长,自然资源的减少和化石燃料价格的上涨,生态标准的加强以及能源多样化水平提高的必要性促使人类更广泛地使用可再生能源,包括生物来源的固体燃料。生物燃料的使用潜力相当可观,因为土地上收获的生物质的能源当量超过了全球能源消耗的数倍。随着将生物质转化为能源的政策和技术的发展,生物质作为可再生燃料的应用已经成为世界各地的现实。这项工作的目的是在考虑流化床设计和放大的情况下,对有关流化床使用的研究进行文献实验综述。首先,介绍了常用的固体颗粒术语和一些重要的生物质性质。简要介绍了转化技术和流化现象,然后解释了不同的实验技术。基于不同的生物质性质,讨论了特征速度(初始、表观、分离和完全),并描述了这些速度的一些经验相关性。最后,对特征床孔隙率(表观和完全)和床膨胀进行了一些考虑。在文献分析的基础上,对生物质流化现象的理解有所提高,但还需要进一步的研究来理解生物质特性对床层操作参数的影响,此外,还必须建立更准确和通用的相关性来改进这些技术。引用:Tannous K.,De Mitri A.G.,Mizonov V.流化床中生物颗粒流体动力学行为的实验研究:综述。伊兹夫。维什。Uchebn。扎维德。Khim。Khim。Tekhnol。2018年第61条。N 9-10。第4-14页
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引用次数: 0
ANALYSIS OF THE CATALYST OF THE MEDIUM-TEMPERATURE CONVERSION OF CARBON MONOXIDE BY WATER VAPOR 水蒸气中温转化一氧化碳催化剂的分析
IF 0.9 Q4 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2018-10-22 DOI: 10.6060/IVKKT.20186109-10.5876A
R. Rumyantsev, M. Lebedev, D. Popov, A. A. Il’in, U. S. Uzhevskaya, A. P. Il’in
The work is devoted to the investigation of the iron-chromium catalyst, which is used at the stage of medium-temperature conversion of carbon monoxide by steam in large-capacity ammonia and hydrogen production. S brand catalyst was chosen аs the object for research. Literature data on the properties of this object are absent. In carrying out the work, such research methods as X-ray phase, synchronous thermal and laser analysis, scanning electron spectroscopy, gas chromatography, and the method of low-temperature adsorption-desorption of nitrogen were used. It is shown that, in addition to the main components (Fe, Cr, Cu) the catalyst contains promoters (Ca, Mn) in the form of compounds in the nanodispersed X-ray diffraction phase.The investigated catalyst has a rather developed specific surface, which is 96.4 ± 0.5 m2/g. By processing nitrogen adsorption-desorption isotherms, it has been found that there are no micro- and macropores in the sample, and the available mesopores have sizes from 3 to 15 nm. The catalytic activity of the sample was evaluated by the degree of CO conversion in the catalytic high-pressure unit PKU-2. The maximum degree of CO conversion is reached 91% at 360 °C. Analysis of the steam condensate formed during the conversion revealed the presence of methyl acetate, methanol, ethanol, butanol in it. The results of the work performed can be used to develop new, more efficient, catalytic systems for the process of medium-temperature conversion of carbon monoxide by steam. For citation: Rumyantsev R.N., Lebedev M.A., Popov D.S., Il’in A.A., Uzhevskaya U.S., Il’in A.P. Analysis of catalyst of medium-temperature conversion of carbon monoxide by water vapor. Izv. Vyssh. Uchebn. Zaved. Khim. Khim. Tekhnol. 2018. V. 61. N 9-10. P. 83-88
本工作致力于研究用于大容量氨和氢气生产中蒸汽转化一氧化碳的中温阶段的铁铬催化剂。选择S牌催化剂作为研究对象。没有关于该物体性质的文献数据。在这项工作中,使用了X射线相、同步热分析和激光分析、扫描电子能谱、气相色谱和氮的低温吸附-解吸方法等研究方法。结果表明,除了主要成分(Fe、Cr、Cu)外,催化剂还含有纳米分散X射线衍射相中化合物形式的促进剂(Ca、Mn)。所研究的催化剂具有相当发达的比表面积,为96.4±0.5m2/g。通过处理氮吸附-解吸等温线,发现样品中没有微孔和大孔,可用的中孔尺寸为3至15nm。样品的催化活性通过催化高压单元PKU-2中的CO转化率来评估。在360°C时,CO的最大转化率达到91%。对转化过程中形成的蒸汽冷凝物的分析表明,其中存在乙酸甲酯、甲醇、乙醇和丁醇。所做工作的结果可用于开发新的、更有效的催化系统,用于中温蒸汽转化一氧化碳的过程。引用:Rumyantsev R.N.,Lebedev M.A.,Popov D.S.,Il’in A.A.,Uzhevskaya U.S.,Il‘in A.P.水蒸气中温转化一氧化碳的催化剂分析。伊兹夫。维什。Uchebn。扎维德。Khim。Khim。Tekhnol。2018年第61条。N 9-10。第83-88页
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引用次数: 1
INFLUENCE OF FORMATION OF THE COMPLEXES WITH DIFFERENT KIND OF LIGANDS ON KINETICS OF OXIDATIVE DISSOLUTION OF METALS 不同配体配合物的形成对金属氧化溶解动力学的影响
IF 0.9 Q4 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2018-08-21 DOI: 10.6060/IVKKT20186108.5690
V. Lutsik, Yu. V. Chursanov, Anatoly V. Starovoytov
Rotating disk method has been used to study the dissolution of gold in the presence of an oxidizer and a mixture of dissimilar ligandforming reagents. Kinetic regularities of gold dissolution were investigated in aqueous systems thiourea-thiocyanate with Fe (III) and Cu (II) ions as the oxidizer; thiosulfate-thiocyanatewithFe(III)EDTA oxidizing complex and thiosulfate-thiocyanate with ammonia complex [Cu(NH3)4]2+ asoxidizing agent. Peculiarities of these mixed systems is a possibility to form the monoligandas as well as geteroligand complexes of gold. The influence of gold complexes formation with different sorts of ligands on the metal dissolution rate have been considered. The dependence of the dissolution rate on the ratio of ligands concentrations and on the oxidizing agent nature was investigated.  Interrelation was established: the use of dissimilar ligandforming reagents - the higher thermodynamic stability of the geteroligand complexes of gold (relative to the homoligand ones) - synergistic increase of the gold dissolution rate. It was found that the heterophase reaction makromechanism for the thiourea-thiocyanate-Fe(III) system is determined by the proximity of the rates of chemical and diffusion stages (experimental activation energy - 21.6 kJ/mol; the reaction order in respect to the disk rotation frequency – 0.23). Diffusive limitation is due to the slow withdrawal of the reaction products -Au (I) compounds - from the solid phase surface. The formation of stronger heteroligand complexes and the corresponding increase in the reaction products concentration at the surface increases a rate of the metal diffusion into the solution. For the thiourea-thiosulfate-Fe(III)EDTA system a film formation of the reaction solid products on the gold surface was observed. To identify it the infrared reflection spectra of the polished gold surface after the etching were obtained. There is a strong absorption band on the spectra at 804 cm-1. Absorption in this area has been associated with the stretching vibrations of C=S bond of the thiourea molecules joined to the surface and the products of their oxidation.
旋转圆盘法已被用于研究金在氧化剂和不同配体形成试剂的混合物存在下的溶解。以硫氰酸硫脲为氧化剂,Fe(III)和Cu(II)离子为氧化剂研究了金在水中的溶解动力学规律;硫氰酸硫代硫酸盐与Fe(III)EDTA氧化络合物和硫氰酸硫代硫酸酯与氨络合物[Cu(NH3)4]2+作为氧化剂。这些混合体系的特点是有可能形成金的单配体和多配体络合物。考虑了不同配体形成金络合物对金属溶解速率的影响。研究了溶解速率对配体浓度比和氧化剂性质的依赖性。建立了相互关系:使用不同的配体形成试剂-金的geteroligand复合物(相对于同配体)具有更高的热力学稳定性-协同提高了金的溶解速率。研究发现,硫脲-硫氰酸盐-Fe(III)体系的异相反应主要由化学和扩散阶段速率的接近程度决定(实验活化能为21.6kJ/mol;相对于圆盘旋转频率的反应级数为0.23)。扩散限制是由于反应产物Au(I)化合物从固相表面。更强的杂配体配合物的形成和表面反应产物浓度的相应增加增加了金属扩散到溶液中的速率。对于硫代硫酸硫脲-Fe(III)-EDTA体系,观察到反应固体产物在金表面上的成膜。为了识别它,获得了蚀刻后抛光金表面的红外反射光谱。在804cm-1处有一个强吸收带。该区域的吸收与连接到表面的硫脲分子的C=S键的拉伸振动及其氧化产物有关。
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引用次数: 0
ABOUT ONE APPROACH TO CALCULATION OF PARAMETERS OF HEAT TRANSFER THROUGH WALL IN PRESENCE OF CONDENSING VAPOR 关于有冷凝蒸汽时壁面传热参数计算的一种方法
IF 0.9 Q4 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2018-08-21 DOI: 10.6060/ivkkt20186108.5672
A. I. Moshinskiy, P. G. Ganin, A. V. Markova, L. Rubtsova, V. Sorokin
The article is dedicated to the study of heat exchangers operation. The main goal of the work was to improve a standard method for calculating a typical heat exchanger based on dependencies approved in engineering practice. The noted technique is presented in educational literature for chemical engineers and it is included in the educational process for the training of engineers. On the basis of practical recommendations stated in literature the working formulas of the process are taken in approximate form. Further, a correction is calculated, which, as calculations show, leads (together with the initial approximation) to an almost exact satisfaction of the initial equations. It is expedient because traditional equations of a heat transfer have not really high precision, which is determined by the processing of numerous experiments. These experiments are rather rough. It is reasonable that the accuracy of the analysis has to be consistent with the model accuracy. This factor justifies the need to simplify the models (use of various recommendations based on the experience of equipment operation, etc.). At the same time, it is desirable to simplify the mathematical model equation so that it is possible to calculate the corrections, i.e. to clarify the solution. We clarify the equation solution meaning more and more exact satisfaction with the initial equation of the mathematical model. In this direction, various variants of perturbation methods can be used. The search for analytical solutions is complicated by the fact that the equations of the mathematical model of energy transfer in a heat exchanger are nonlinear. The three-layer heat transfer problem in a stationary mode is considered.  The first layer is the space of the heat exchanger where a phase transition (first heat transfer agent vapor condensation) occurs. The second layer is the space of the heat exchanger where convective movement of the second heat transfer agent takes place without phase transition. The third layer is a wall separating the heat transfer agent providing some resistance to the heat transfer process. As a result of the simplified model analysis, it became possible to obtain an analytical solution to the problem with such accuracy that the calculated correction turned out to be insignificant i.e. the correction is not appropriate to take into account. The solution found was almost exactly approximated by a simple analytic dependence.
本文主要研究换热器的运行。这项工作的主要目标是改进基于工程实践中批准的相关性计算典型换热器的标准方法。化学工程师的教育文献中介绍了上述技术,并将其纳入了工程师培训的教育过程中。根据文献中所述的实际建议,该过程的工作公式采用近似形式。此外,还计算了一个修正值,正如计算所示,该修正值(与初始近似值一起)几乎完全满足初始方程。这是有利的,因为传统的传热方程并没有真正高的精度,这是通过大量实验确定的。这些实验相当粗糙。分析的准确性必须与模型的准确性一致,这是合理的。这一因素证明了简化模型的必要性(根据设备操作经验使用各种建议等)。同时,简化数学模型方程是可取的,这样就可以计算修正值,即澄清解决方案。我们阐明了方程的解意味着对数学模型的初始方程越来越精确的满足。在这个方向上,可以使用扰动方法的各种变体。换热器中能量传递数学模型的方程是非线性的,这使得寻找解析解变得复杂。考虑了稳态模式下的三层传热问题。第一层是发生相变(第一传热剂蒸汽冷凝)的热交换器的空间。第二层是热交换器的空间,在该空间中第二传热剂发生对流运动而没有相变。第三层是分隔传热剂的壁,为传热过程提供一些阻力。作为简化模型分析的结果,有可能以这样的精度获得问题的分析解,即计算出的校正被证明是无关紧要的,即校正不适合考虑。找到的解决方案几乎完全近似于一个简单的分析相关性。
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引用次数: 0
INFLUENCE OF SODIUM HYDROXIDE ADDITIVES ON HYDROGENIZATION KINETICS OF 4-NITRO-2'-HYDROXY-5'-METYLAZOBENZENE ON SKELETAL NICKEL IN AQUEOUS SOLUTION OF 2-PROPANOL 氢氧化钠添加剂对4-硝基-2′-羟基-5′-甲基偶氮苯在2-丙醇水溶液中对骨架镍加氢动力学的影响
IF 0.9 Q4 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2018-08-21 DOI: 10.6060/IVKKT201861008.5752
A. Hoang, V. A. Kalashnikova, O. Lefedova, D. Filippov
The elucidation of the sequence of transformations in compounds containing several reactive groups and the development of approaches to controlling the selectivity of the processes with their participation is of interest both from the theoretical and practical points of view. The article is devoted to the analysis of the kinetics of hydrogenation of 4-nitro-2'-hydroxy-5'-methylazobenzene in aqueous solution of 2-propanol with addition of sodium hydroxide on skeletal nickel at different initial amounts of the starting compound. An increase in the initial amount of 4-nitro-2'-hydroxy-5'-methylazobenzene leads to an increase in the rate of conversion of the nitro group in the starting compound and to a decrease in the rate of conversion of the azo-group. The effect of the introduced sodium hydroxide in the neutral solvent 2-propanol-water on the rate of conversion of the nitro and azo-groups to 4-nitro-2'-hydroxy-5'-methylazobenzene is consistent with the nature of the rate changes for the hydrogenation of individual compounds containing nitro and azo-groups, in the quality of which 4-nitroaniline and 4-amino-2'-hydroxy-5'-methylazobenzene were chosen. The results obtained do not contradict the notion of a parallel-sequential scheme of 4-nitro-2'-hydroxy-5'-methylazobenzene transformations. One of the directions involves the conversion of 4-nitro-2'-hydroxy-5'-methylazobenzene due to the hydrogenation of the azo-group to 4-nitroaniline and PC, and the second one is the conversion of 4-nitro-2'-hydroxy-5'-methylazobenzene through 4-amino-2'-hydroxy-5'-methylazobenzene due to the reduction of the nitro group. By the end of the reaction, all the intermediate compounds are restored to PC and 1,4-phenylenediamine. When sodium hydroxide is introduced into the neutral solvent 2-propanol-water, the effect of the direction providing the formation of 4-amino-2'-hydroxy-5'-methylazobenzene to the overall reaction rate increases. It was experimentally established that the amount of 4-amino-2'-hydroxy-5'-methylazobenzene during the hydrogenation of 4-nitro-2'-hydroxy-5'-methylazobenzene in the presence of sodium hydroxide increases by 15%, on the contrary, the amount of 4-nitroaniline decreases by 4 % in comparison with the neutral solvent.
从理论和实践的角度来看,阐明含有几个反应性基团的化合物中的转化序列,以及开发在它们的参与下控制过程选择性的方法,都是令人感兴趣的。本文分析了在不同起始量的2-丙醇水溶液中,在骨架镍上加入氢氧化钠加氢4-硝基-2’-羟基-5’-甲基偶氮苯的动力学。4-硝基-2'-羟基-5'-甲基偶氮苯初始量的增加导致起始化合物中硝基的转化率的增加和偶氮基团的转化率降低。在中性溶剂2-丙醇-水中引入的氢氧化钠对硝基和偶氮基团转化为4-硝基-2'-羟基-5'-甲基偶氮苯的速率的影响与含有硝基和偶氮基的单个化合物的氢化速率变化的性质一致,其中选择了4-硝基苯胺和4-氨基-2’-羟基-5’-甲基偶氮苯。所获得的结果与4-硝基-2'-羟基-5'-甲基偶氮苯转化的平行顺序方案的概念并不矛盾。其中一个方向涉及由于偶氮基团氢化为4-硝基苯胺和PC而使4-硝基-2'-羟基-5'-甲基偶氮苯转化,第二个方向是由于硝基基团还原而使4-氨基-2'-羟-5'-甲偶氮苯通过4-氨基-2'-羟基-5'-甲偶氮苯转化。在反应结束时,所有中间化合物都还原为PC和1,4-苯二胺。当氢氧化钠被引入中性溶剂2-丙醇-水中时,提供4-氨基-2’-羟基-5’-甲基偶氮苯形成的方向对总反应速率的影响增加。实验证明,在氢氧化钠存在下,4-硝基-2'-羟基-5'-甲基偶氮苯加氢过程中,4-氨基-2'-羟-5'-甲偶氮苯的量增加了15%,而4-硝基苯胺的量与中性溶剂相比减少了4%。
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引用次数: 1
IMMOBILIZATION OF COBALT DISULFOPHTHALOCYANINATE ONTO POLYMETHYLOLACRYLAMIDE 聚甲基丙烯酰胺固定化二磺基酞菁钴
IF 0.9 Q4 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2018-08-21 DOI: 10.6060/IVKKT20186108.5712
G. V. Osipova, N. L. Pechnikova, T. A. Ageeva
Different character of usage the porphyrins and their analogs immobilized on carrier polymers stimulates an increased interest in the synthesis and research of physico-chemical properties of porphyrin-polymer immobilizates. In this paper the peculiarities of a synthesis of water-soluble polymer systems containing cobalt disulfophthalocyaninate with the components of a different ratio are described. The methylolation reaction of polyacrylamide to immobilize cobalt disulfophthalocyaninate onto water-soluble carrier polymer has been carried out. It is known that heating polymethylolacrylamide or its solutions leads to the formation of three-dimensional structures with ether and methylene bridges. Therefore, initially the conditions for the preparation of polymethylolacrylamide with preservation of its water solubility were selected. It was found to obtain a water-soluble polymethylolacrylamide, it is necessary that the initial concentration of polyacrylamide in water did not exceed 2% by weight. The immobilization of phthalocyanine metal complex onto the modified polyacrylamide was carried out in two ways. The first is the interaction of the phthalocyanine metal complex with methylated polyacrylamide. The second is functionalization of polyacrylamide and the immobilization of phthalocyaninate metal complex onto the polymer in one-step. The introduction conditions of the cobalt disulfophthalocyaninate introduced influenced the formation of cross-linked structures in the synthesized samples. The introduction of macroheterocycle as a powder was found to promote the formation of insoluble compounds in aqueous media. Therefore, phthalocyanine metal complex was introduced into the system as 1% aqueous solution. The immobilization of the phthalocyanine metal complex onto a carrier polymer has been realized through the formation of hydrogen bonds between the methylol groups of polymethylolacrylamide and sulfo groups of the phthalocyanine metal complex and it was due to coordination interaction between the functional groups of the polymer and metallophthalocyanine as well. The amount of bound cobalt disulfophthalocyanine in the samples was determined by the electronic absorption spectra of the solutions of immobilized phthalocyanine metal complex onto the polymer. The mass content of immobilized cobalt disulfophthalocyaninate onto the polymer in the samples obtained by one-step is greater than in case of the samples obtained in two steps, the ratio of the initial reagents being the same.
固定在载体聚合物上的卟啉及其类似物的不同使用特性激发了人们对卟啉聚合物固定化物的合成和物理化学性质研究的兴趣。本文介绍了不同配比的含二磺基酞菁钴的水溶性聚合物体系的合成特点。采用聚丙烯酰胺甲基化反应将二磺基酞菁钴固定在水溶性载体聚合物上。已知加热聚甲基丙烯酰胺或其溶液会形成具有醚和亚甲基桥的三维结构。因此,初步选择了在保持其水溶性的情况下制备聚甲基丙烯酰胺的条件。发现要获得水溶性聚甲基丙烯酰胺,必须使聚丙烯酰胺在水中的初始浓度不超过2重量%。采用两种方法将酞菁金属配合物固定在改性聚丙烯酰胺上。第一个是酞菁金属配合物与甲基化聚丙烯酰胺的相互作用。二是聚丙烯酰胺的功能化和酞菁金属配合物在聚合物上的一步固定化。引入的二磺基酞菁钴的引入条件影响了合成样品中交联结构的形成。发现引入大杂环作为粉末可以促进水性介质中不溶性化合物的形成。因此,酞菁金属配合物以1%的水溶液的形式引入到该体系中。酞菁金属络合物固定在载体聚合物上是通过在聚甲基丙烯酰胺的羟甲基和酞菁金属络合物的磺基之间形成氢键实现的,这也是由于聚合物的官能团和金属酞菁之间的配位相互作用。通过固定化酞菁金属络合物在聚合物上的溶液的电子吸收光谱测定了样品中结合的二磺基酞菁钴的量。在通过一步获得的样品中,固定在聚合物上的二磺基酞菁钴的质量含量大于通过两步获得的情况,初始试剂的比例相同。
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引用次数: 0
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Izvestiya Vysshikh Uchebnykh Zavedenii Khimiya i Khimicheskaya Tekhnologiya
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