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Stability of permanent connection of deformable high-temperature nickel based and cast intermetallic alloys obtained by pressure welding under superplasticity conditions 超塑性条件下压力焊接可变形高温镍基合金与铸造金属间合金永久连接的稳定性
Pub Date : 2022-01-01 DOI: 10.30791/1028-978x-2022-2-17-28
O. Bazyleva, V. Valitov, E. Arginbaeva, N. S. Dmitriev, A. N. Raevskikh, E. Galieva
The article presents a study of welded joints of cast intermetallic single-crystal rhenium containing VKNA-25 alloy with crystallographic orientation [001] and deformable high-temperature disk nickel alloy EP975, depending on the parameters of pressure welding under superplasticity conditions and standart heat treatment for high-temperature disk nickel alloy with regulated single-phase cooling. The study was carries out for the interdendritic region. The results of X-ray micro-spectral analysis of a solid-phase joint in the welding zone and at distances of up to 140 μm are presented in comparison with the initial chemical composition of the alloys. Found that before and after heat treatment in the welding zone and near-weld zone particles of topologically cloth-packed phases are not observed. Balance of alloying is better maintained in deformable high-temperature disk nickel alloy EP975 and this is natural, since pressure under superplasticity conditions takes place due to the disk alloy and at cast intermetallic single-crystal alloy only diffusion processes take place. Thus, high-quality one-piece connection of a disk and a blade for blisk-type structures is feasible under superplasticity only of one deformable fine-grained disk alloy and it is relevant for blisk type constructions. Blade intermetallic alloy VKNA-25 keeps thermally stable single-crystal structure.
本文根据超塑性条件下的压力焊接参数和高温盘状镍合金单相调节冷却的标准热处理,研究了具有晶相取向的铸造含金属间化合物铼VKNA-25合金[001]与可变形高温盘状镍合金EP975的焊接接头。这项研究是在树突间区域进行的。本文给出了在焊接区和140 μm范围内对固相接头进行x射线显微光谱分析的结果,并与合金的初始化学成分进行了比较。发现在焊接区和近焊区热处理前后均未观察到拓扑布填充相的颗粒。在可变形的高温圆盘镍合金EP975中,合金的平衡得到了更好的保持,这是很自然的,因为在超塑性条件下,压力是由圆盘合金产生的,而在铸造时,金属间单晶合金只发生扩散过程。因此,仅在一种可变形细晶盘合金的超塑性条件下,圆盘与叶片的高质量一体连接是可行的,并且适用于圆盘结构。叶片金属间合金VKNA-25保持热稳定的单晶结构。
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引用次数: 0
Study of electrochemical, electrical properties and temperature dependences of azomethine-Zn (II) ligand complexes based on pyrazolone 吡唑酮类偶氮胺- zn (II)配体配合物的电化学、电学性质及温度依赖性研究
Pub Date : 2022-01-01 DOI: 10.30791/1028-978x-2022-3-36-45
A. Tyutyunik, V. Gurchenko, A. Mazinov
Comprehensive study of the electrochemical, electrical properties and temperature dependences of the Zn (II) hybrid organic complex based on Schiff (C48H42N6O2Zn) is carried out. In order to determine the prospects for using this compound as a semiconductor material, thin films were obtained using the centrifugation method. The method of preparation, synthesis, microscopy of the surface, as well as the method of measuring the temperature dependences of the electrical properties of the obtained thin films are described. The temperature measurement range ranged from 270 to 330 K. The energy levels of the lowest unoccupied molecular orbital and the highest occupied molecular orbital were determined using cyclic voltammetry. The activation energy calculated from linear approximations of the current-voltage characteristics in Arrhenius coordinates was 0.65 eV. Analysis of the current-voltage characteristics of the ITO – PBAL – Al structure showed that they correspond to the typical characteristics of Schottky diodes with a charge mobility of ~ 1,18·10–11 cm2·V–1·s–1.To study the mechanisms of charge transfer, the C – V characteristics of the samples were investigated at a frequency of 1 kHz. The concentration of charge carriers was calculated using the Mott – Schottky relationship.
对基于Schiff (C48H42N6O2Zn)的Zn (II)杂化有机配合物的电化学、电学性质和温度依赖性进行了全面研究。为了确定该化合物作为半导体材料的应用前景,采用离心法获得了薄膜。描述了制备、合成、表面显微镜的方法,以及测量所获得薄膜电性能的温度依赖性的方法。温度测量范围为270 ~ 330k。用循环伏安法测定了最低未占据分子轨道和最高已占据分子轨道的能级。根据Arrhenius坐标下的电流-电压特性线性近似计算得到的活化能为0.65 eV。ITO - PBAL - Al结构的电流-电压特性分析表明,它们符合肖特基二极管的典型特性,电荷迁移率为~ 1,18·10-11 cm2·V-1·s-1。为了研究电荷转移的机理,在1 kHz频率下对样品的C - V特性进行了研究。利用莫特-肖特基关系计算载流子的浓度。
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引用次数: 0
Obtaining hybrid nanostructures based on graphene and nano-ZrO2 基于石墨烯和纳米zro2的杂化纳米结构的制备
Pub Date : 2022-01-01 DOI: 10.30791/1028-978x-2022-10-52-63
A. Afzal, E. A. Trusova, A. Konovalov
A technologically promising method for obtaining nanostructured graphene/ZrO2 has been proposed. Its main idea is to use suspensions of graphene and nano-ZrO2 and create conditions for the interaction of graphene sheets and ZrO2 crystallites to form a hybrid nanostructured powder without the formation of new chemical bonds. The oxygen-free graphene sheets with thickness of several nanometers were obtained by sonochemical method in N,N-dimethyloctylamine-aqua emulsion. Nano-ZrO2 powder with average crystallite size of 8.1 nm was synthesized by sol-gel method. The morphology and phase composition of all synthesized objects (nano-ZrO2, graphene, composite) were studied by using a set of instrumental methods (transmission electron microscopy (TEM) and electron diffraction, x-ray diffraction (XRD), electron energy loss spectroscopy (EELS), nitrogen adsorption-desorption, diffusion aerosol spectrometry (DAS) and elemental analysis). It was shown that the proposed method allows obtain chemically homogeneous mesoporous hybrid powders consisting of graphene sheets and ZrO2 crystallites with a size of 8 – 13 nm fixed on them. We investigated an effect of duration of ultrasonic impact to graphite on the morphology of the hybrid and the mechanism of its formation. According to the results of a comprehensive analysis of the obtained data, the mechanisms for the formation of graphene suspension in emulsion and a nanostructured hybrid during the interaction of crystalline ZrO2 and oxygen-free graphene sheets in an aqueous-organic medium was proposed. The developed hybrid nanostructures are highly demanded innovative raw-products in the production of (photo)catalysts for a wide range of processes, sensor, ceramic and electrical materials, and materials for medical and biological purposes.
提出了一种技术上有前途的制备纳米结构石墨烯/ZrO2的方法。其主要思路是利用石墨烯和纳米ZrO2的悬浮液,为石墨烯片和ZrO2晶体相互作用创造条件,在不形成新的化学键的情况下形成混合纳米结构粉末。采用声化学方法在N,N-二甲基辛基胺-水乳液中制备了厚度为几纳米的无氧石墨烯薄膜。采用溶胶-凝胶法制备了平均晶粒尺寸为8.1 nm的zro2纳米粉体。采用透射电子显微镜(TEM)和电子衍射、x射线衍射(XRD)、电子能量损失谱(EELS)、氮吸附-解吸、扩散气溶胶谱(DAS)和元素分析等仪器方法,研究了所有合成物(纳米zro2、石墨烯、复合材料)的形貌和相组成。结果表明,该方法可以获得由石墨烯片和固定尺寸为8 - 13 nm的ZrO2晶体组成的化学均匀的介孔杂化粉末。研究了超声冲击时间对石墨杂化形貌的影响及其形成机理。通过对实验数据的综合分析,提出了ZrO2晶体与无氧石墨烯片在有机水介质中相互作用形成乳状石墨烯悬浮液和纳米结构杂化物的机理。所开发的混合纳米结构在生产(光)催化剂、传感器、陶瓷和电气材料以及医疗和生物用途材料等各种工艺中都是非常需要的创新原材料。
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引用次数: 0
Investigation of the formation of a multilayer functional composite material with a gradient structure titanium nitride – titanium – base 氮化钛-钛基梯度结构多层功能复合材料的形成研究
Pub Date : 2022-01-01 DOI: 10.30791/1028-978x-2022-7-75-86
M. A. Sudarchikova
Composite materials based on aluminum alloy D16 and titanium alloy Ti – 10 Nb – 3 Mo with surface layers of titanium, titanium nitride and a multilayer composition consisting of alternating layers of titanium and titanium nitride for biomedical and tribological purposes by high-vacuum magnetron sputtering at direct current in inert and reactive media were obtained. The structure and phase composition were studied using SEM, AES, X-ray diffractometry and probe microscopy. The rate of formation of a surface layer of pure titanium on a substrate made of alloy D16 was 185 nm/min, and the rate of synthesis of a surface layer of titanium in a reactive medium was significantly slowed down and was no more than 70 nm/min due to nitrogen poisoning of the target. The transition layer formed as a result of the synthesis of a titanium layer on an aluminum alloy substrate had a thickness of about 600 nm, which is significantly greater than the thickness of the transition layer when titanium is obtained on a titanium alloy substrate. During the formation of titanium nitride on a titanium sublayer, a greater concentration of nitrogen was observed than during the formation of nitride on a substrate with the same deposition parameters. The intensity of the TiN phase reflexes in the X-ray diffractometry diagrams were weakly expressed in all variants of the applied ratios of working gases Ar/N2 during spraying. The speed of the titanium sublayer makes it possible to form a greater thickness of the titanium nitride layer than without the sublayer, as well as a more nitrogen–saturated surface layer - up to 38% by weight.
采用直流高真空磁控溅射技术,在惰性介质和反应介质中制备了以钛合金D16和钛合金Ti - 10nb - 3mo为基材,表面为钛和氮化钛,表面为钛和氮化钛交替层的复合材料,用于生物医学和摩擦学研究。采用扫描电子显微镜(SEM)、原子发射光谱(AES)、x射线衍射仪(xrd)和探针显微镜(probe microscopy)对其结构和相组成进行了研究。在D16合金衬底上形成纯钛表面层的速率为185 nm/min,反应介质中钛表面层的合成速率由于靶物的氮中毒而明显减慢,不超过70 nm/min。在铝合金衬底上合成钛层形成的过渡层厚度约为600 nm,明显大于在钛合金衬底上获得钛时的过渡层厚度。在钛亚层上形成氮化钛的过程中,观察到的氮浓度高于在相同沉积参数的衬底上形成氮化钛的过程。x射线衍射图中的TiN相反射强度在喷涂过程中工作气体Ar/N2的应用比例的所有变量中都弱表达。钛子层的速度使得形成比没有子层更厚的氮化钛层成为可能,以及更含氮的表面层-高达重量的38%。
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引用次数: 0
Oxygen electrocatalytic reduction on glass-carbon electrodes coated with polyporphyrin films based on metal complexes of 5,10,15,20-tetrakis(3-aminophenyl)porphyrin 基于5,10,15,20-四(3-氨基苯基)卟啉金属配合物的聚卟啉膜涂覆玻璃碳电极的氧电催化还原
Pub Date : 2022-01-01 DOI: 10.30791/1028-978x-2022-7-14-24
M. V. Tesakova, S. Kuzmin, V. Parfenyuk
Carbon-based materials are widespread and promising in areas such as electrochemical and electrocatalytic power generation and can be excellent choices for use as electrode substrates. To increase the efficiency of using carbonaceous materials, the surface of the electrodes is modified with metal complexes of phthalocyanines and porphyrins with electrocatalytic properties. In this work polyporphyrin coatings were obtained on a glassy carbon electrode based on individual metal complexes of 5,10,15,20-tetrakis(3-aminophenyl)porphyrin and a composite based on two metal complexes Fe and Mn. Polymerization was carried out by the electrochemical method in the region of positive values of the potential in the potentiodynamic mode. Electrodeposited polyporphyrin coatings have a developed surface and exhibit catalytic activity in the reaction of oxygen electroreduction. The results of evaluating the catalytic activity of polyporphyrins obtained by various methods are in good agreement with each other and indicate a higher catalytic activity of a composite based on two metal complexes compared to films of individual porphyrins, which suggests the presence of a synergistic effect. Based on the results of our research, we propose potential directions for the creation of electrodes based on glassy carbon modified with polyporphyrins for electrocatalytic oxygen reduction.
碳基材料广泛应用于电化学和电催化发电等领域,是电极衬底的绝佳选择。为了提高碳质材料的使用效率,在电极表面用具有电催化性能的酞菁和卟啉的金属配合物进行修饰。本文在玻碳电极上制备了以5、10、15、20-四(3-氨基苯基)卟啉的金属配合物和以铁、锰两种金属配合物为基础的复合材料制备的多卟啉涂层。在动电位模式下,通过电化学方法在电位正值区域进行聚合。电沉积多卟啉涂层表面发达,在氧电还原反应中表现出催化活性。各种方法对多卟啉催化活性的评价结果一致,表明两种金属配合物复合的催化活性比单个卟啉膜的催化活性更高,表明存在协同效应。基于我们的研究结果,我们提出了基于多卟啉修饰的玻璃碳电极用于电催化氧还原的潜在方向。
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引用次数: 0
Properties of a light structural magnesium IMV7-1 type alloy of the Mg – Y – Gd – Zr system with the additions of cerium-group rare-earth metals such as samarium, neodymium, and lanthanum 添加钐、钕、镧等铈族稀土金属后Mg - Y - Gd - Zr体系轻结构IMV7-1型镁合金的性能
Pub Date : 2022-01-01 DOI: 10.30791/1028-978x-2022-10-5-13
L. Rokhlin, T. Dobatkina, I. Tarytina, E. Lukyanova, O. A. Ovchinnikova
The effect of small additions of cerium-group rare-earth metals such as samarium (Sm), neodymium (Nd) and lanthanum (La) on the properties of a light high-strength structural magnesium IMV7-1 type alloy of the Mg – Y – Gd – Zr system, where yttrium (Y) and gadolinium (Gd) are yttrium-group rare earth metals, has been studied. It is established that the presence of small quantities of samarium in the IMV7-1 alloy contributes to an increase in its strength properties upon heat treatment (aging) and makes it possible to reduce the time to reach the maximum strengthening. In the case where two other cerium-group rare earth metals, neodymium and lanthanum, are present in the IMV7-1 type alloy, the strengthening upon heat treatment (aging) is also observed, but to a much lesser extent. It has also been established that, as the contents of the main alloying elements (yttrium and gadolinium) are simultaneously increased and samarium is added, the maximum strengthening of the alloys under study gradually increases, and the time to its achievement decreases. The fact that the alloying with samarium results in substantially higher strengthening of the IMV7-1 type alloy than that provided by neodymium and lanthanum is explained by a much higher solubility of samarium compared to these of neodymium and lanthanum in solid magnesium.
研究了少量添加钐(Sm)、钕(Nd)和镧(La)等铈族稀土金属对Mg - Y - Gd - Zr体系(其中钇(Y)和钆(Gd)为钇族稀土金属)轻质高强结构镁IMV7-1型合金性能的影响。结果表明,少量钐在IMV7-1合金中的存在有助于提高其热处理(时效)时的强度性能,并有可能缩短达到最大强化的时间。在IMV7-1型合金中存在另外两种铈族稀土金属(钕和镧)的情况下,也观察到热处理(时效)的强化,但程度要小得多。同时增加主要合金元素(钇和钆)的含量并加入钐,合金的最大强化强度逐渐增大,达到最大强化强度所需的时间逐渐缩短。在IMV7-1型合金中,与钕和镧合金相比,与钐合金的合金化导致了更高的强化,这一事实是由于钐在固体镁中的溶解度比钕和镧合金高得多。
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引用次数: 0
Study of high-temperature deformation features of binderless tungsten carbide with various initial particle size 不同初始粒径无粘结剂碳化钨的高温变形特性研究
Pub Date : 2022-01-01 DOI: 10.30791/1028-978x-2022-4-40-52
Е. Lantsev, А. Nokhrin, V. Chuvil’deev, M. Boldin, Yu. V. Blagoveshchenskiy, P. Andreev, K. Smetanina, A. Murashov, N. Isaeva, A. V. Terentev
The mechanism of high-temperature creep deformation during compression tests of binderless tungsten carbide specimens with different initial particle size was studied. Tungsten carbide samples with high relative density (96.1 – 99.2 %) were obtained by high-speed spark plasma sintering (SPS) from nano-, submicron-, and micron-sized α-WC powders. The creep tests were carried out in two modes: isothermal soaking at different temperatures (1300 – 1375 °C) at a given stress, allowing to estimate the activation energy of creep, and tests by “stress jumps” at 1325 °C, allowing to estimate the value of the coefficient n in the creep equation. It is shown that the value of creep activation energy in ultrafine grained tungsten carbide with grain size ~ 0.15 µm sintered from plasma chemical nanopowders is ~ 31 kTm. This value is 1.5 – 2 times higher than the creep activation energy in fine-grained tungsten carbide samples obtained by SPS from submicron (~ 0.8 μm) and micron (~ 3 μm) industrial powders. It was found that the value of the coefficient n varies from 2.4 to 3.1, which corresponds to the case of motion of lattice dislocations in the field of uniformly located point obstacles. It has been suggested that one of the reasons for the increase in creep activation energy in tests of tungsten carbide is an increased volume fraction of W2C low carbide particles formed during high-speed sintering of plasma-chemical α-WC nanopowders with an increased concentration of adsorbed oxygen.
研究了不同初始粒度的无粘结碳化钨试样在压缩试验中的高温蠕变变形机理。采用高速放电等离子烧结(SPS)技术,将纳米级、亚微米级和微米级α-WC粉末制备成相对密度较高(96.1 ~ 99.2%)的碳化钨样品。蠕变试验以两种模式进行:在给定应力下,在不同温度(1300 - 1375°C)下进行等温浸泡,从而可以估计蠕变的活化能;在1325°C下进行“应力跳变”试验,从而可以估计蠕变方程中的系数n的值。结果表明,等离子体化学纳米粉末烧结的晶粒尺寸为~ 0.15 μ m的超细碳化钨的蠕变活化能为~ 31 kTm。该数值比用SPS从亚微米(~ 0.8 μm)和微米(~ 3 μm)工业粉末中得到的细晶碳化钨样品的蠕变活化能高1.5 ~ 2倍。结果表明,系数n的取值范围为2.4 ~ 3.1,对应于点状障碍物场中晶格位错运动的情况。本文认为,随着吸附氧浓度的增加,等离子化学α-WC纳米粉体在高速烧结过程中形成的W2C低碳化颗粒体积分数增加,是导致碳化钨蠕变活化能升高的原因之一。
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引用次数: 0
Synthesis of zirconium(IV) oxyacrylate complexes with polypyridine ligands and their use as precursors of nanomaterials with antiwear properties 聚吡啶配体氧化丙烯酸锆配合物的合成及其在纳米抗磨材料中的应用
Pub Date : 2022-01-01 DOI: 10.30791/1028-978x-2022-12-62-75
G. Dzhardimalieva, I. Uflyand, V. Zhinzhilo, E. Drogan, V. Burlakova
In the present work, complexes of zirconium(IV) oxyacrylate with polypyridine ligands 2,2’-bipyridine, 1,10-phenanthroline, and 4’-phenyl-2,2’:6’,2’’-terpyridine were obtained for the first time and characterized by elemental analysis, IR spectroscopy, thermogravimetry and differential scanning calorimetry. Thermolysis of these complexes at 600 °C made it possible to obtain nanosized zirconium oxides, which were studied by X-ray diffraction analysis, scanning electron microscopy, high-resolution transmission electron microscopy, and atomic force microscopy. The average crystallite size of the obtained zirconium oxide nanoparticles is 5.63 – 6.06 nm. Zirconium oxide nanoparticles are characterized by spherical and oval shapes. The products have been tested as anti-wear additives in lubricating oils. The optimal concentrations of nanoparticles were determined, at which the antiwear properties of the lubricant are best manifested.
本文首次获得了氧丙烯酸锆与多吡啶配体2,2′-联吡啶、1,10-菲罗啉和4′-苯基2,2′:6′,2′-三吡啶的配合物,并用元素分析、红外光谱、热重法和差示扫描量热法对其进行了表征。在600℃下对这些配合物进行热裂解,可以得到纳米级氧化锆,并通过x射线衍射分析、扫描电子显微镜、高分辨率透射电子显微镜和原子力显微镜对其进行了研究。所得氧化锆纳米颗粒的平均晶粒尺寸为5.63 ~ 6.06 nm。氧化锆纳米颗粒具有球形和椭圆形的特征。该产品已作为润滑油抗磨添加剂进行了试验。确定了纳米颗粒的最佳浓度,在此浓度下,润滑油的抗磨性能得到了最好的体现。
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引用次数: 0
Component selection and nano-structuring of WS2/MoS2/a-C thin-film coatings for effective friction reduction in difficult conditions of sliding 在困难滑动条件下有效减少摩擦的WS2/MoS2/a-C薄膜涂层的组分选择和纳米结构
Pub Date : 2022-01-01 DOI: 10.30791/1028-978x-2022-9-64-76
R. Romanov, D. Fominski, V. Nevolin, V. A. Kasianenko, V. Fominski
The possibility of forming new solid-lubricating thin-film coatings consisting of nanosized layers of WS2, MoS2 and amorphous carbon (a-C) with improved antifriction properties has been studied. To control the tribological properties of coatings, the conditions for obtaining layers of 2Н-WS2 and 2Н-MoS2 with a thickness of 5 – 20 nm with a crystalline laminar structure with a basal orientation to the substrate were determined. Nanolayers were created by reactive pulsed laser deposition from metal and metal oxide targets in hydrogen sulfide at elevated temperatures. It is shown that when alternating the processes of selected films deposition, no noticeable solid-phase reactions were observed at the interfaces. Tribological tests were carried out at room temperature using the method of sliding a steel ball over a coated disk without lubrication in an atmosphere enriched with nitrogen (~ 9 % relative humidity). The structural state of the coatings before and after the tribotests was studied by Raman spectroscopy. The lowest friction coefficient ~ 0,015 was found for the WS2 coatings deposited at 500 °C. The tribological properties of the MoS2 coatings turned out to be much worse. The coating, consisting of the WS2 and carbon nanolayers, showed a slightly higher friction coefficient (0,021), but it had the enhanced wear resistance.
研究了由WS2、MoS2和非晶碳(a-C)纳米层组成的新型固体润滑薄膜涂层的可能性。为了控制涂层的摩擦学性能,确定了制备厚度为5 ~ 20 nm的2Н-WS2和2Н-MoS2层的条件,这些层具有与基体基底取向的晶体层状结构。纳米层是由反应性脉冲激光沉积金属和金属氧化物靶在高温硫化氢中形成的。结果表明,当选择不同的沉积工艺时,在界面处没有观察到明显的固相反应。摩擦学试验在室温下进行,在富氮(~ 9%相对湿度)的气氛中,使用钢球在涂有涂层的圆盘上滑动而不润滑的方法。用拉曼光谱研究了摩擦试验前后涂层的结构状态。在500℃时,WS2涂层的摩擦系数最低,为0.015。结果表明,二硫化钼涂层的摩擦学性能较差。由WS2和碳纳米层组成的涂层具有略高的摩擦系数(0.021),但具有增强的耐磨性。
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引用次数: 0
Microporous carbon material with high adsorption rates 具有高吸附率的微孔碳材料
Pub Date : 2022-01-01 DOI: 10.30791/1028-978x-2022-6-46-53
A. Memetova, A. Zelenin, N. Memetov, A. Babkin, A. Gerasimova
A compacted microporous carbon material (CMC-032) was obtained, which has a number of unique properties: a high specific surface area according to BET (SBET = 2384 m2/g), a large volume of micropores (~ 0.95 cm3/g), and a very high ability to retain methane 336 m3/v3. Sorbent CMC-032 is obtained by activating polymer raw materials with potassium hydroxide and compaction by hot pressing using polyvinyl alcohol as a binder. In the most demanded range of methane accumulation pressures of 3,5 – 10,0  MPa, the amount of accumulated methane in the system with CMC-032 reaches 270 m3/m3. The amount of methane stored in the system with and without CMC-032 adsorbent at 100 bar differs by about 3 times. The physicochemical properties of the obtained CMC-032 adsorbent were studied using methods including adsorption-desorption of N2 at 77 K, X-ray diffraction analysis, FTIR spectroscopy, Raman spectroscopy, and transmission electron microscopy. Based on the adsorption characteristics, it was found that CMC-032 is a promising material for storing natural gas methane. It is assumed that the high adsorption capacity is due to the high micropore volume and packing density.
获得了一种致密微孔碳材料(CMC-032),该材料具有许多独特的性能:根据BET (SBET = 2384 m2/g),具有高比表面积(SBET = 2384 m2/g),微孔体积大(~ 0.95 cm3/g),具有很高的甲烷截留能力(336 m3/v3)。以氢氧化钾活化高分子原料,聚乙烯醇为粘结剂,热压压实得到吸附剂CMC-032。在3,5 ~ 10,0 MPa最需要的甲烷富集压力范围内,CMC-032体系的甲烷富集量可达270 m3/m3。加CMC-032吸附剂和不加CMC-032吸附剂的系统在100 bar下的甲烷储存量相差约3倍。采用77 K氮气吸附-解吸、x射线衍射、FTIR光谱、拉曼光谱和透射电镜等方法研究了CMC-032吸附剂的理化性质。通过对CMC-032吸附特性的分析,发现CMC-032是一种很有前途的天然气甲烷储存材料。假设高吸附容量是由于高微孔体积和填料密度。
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引用次数: 0
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