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Features of the defect structure and photoluminescence of nominally pure LiNbO3 crystals grown from boron doped charge 掺杂硼的名义纯LiNbO3晶体的缺陷结构和光致发光特性
Pub Date : 2023-01-01 DOI: 10.30791/1028-978x-2023-2-32-43
N. V. Sidorov, A. Kadetova, M. Smirnov, R. Titov, N. Teplyakova, M. Palatnikov
Features of the defect structure of nominally pure LiNbO3:В crystals were investigated by X-ray diffraction analysis and photoluminescence. Crystals were grown by the Czochralski from a mixture of congruent composition charge containing 0.08 and 0.12 wt. % boron. At this, the concentration of boron in crystals is at the level of trace amounts of metallic impurities and is ~ 10–4 wt%. MeO6 oxygen-octahedral clusters are responsible for the ferroelectric and nonlinear optical properties of the crystal. It has been found that in LiNbO3:B crystals, the lengths of O–O, Me–O, and Me–Me (Me–Li, Nb) bonds in clusters, the arrangement of Me cations, vacancies, and NbLi point defects along the polar axis differ significantly from those for nominally pure congruent crystal. NbLi defects and transition metals are deep electron traps responsible for the photorefraction effect. The photoluminescence spectra showed that the concentration of defects and metals in the investigated LiNbO3:B crystals is lower than in the congruent crystal. these differences can be due to both a change in the properties of the boron-containing melt and the localization of trace amounts of boron in the O4 tetrahedral gaps of the LiNbO3 crystal structure. In the first case, reactive boron binds cations of niobium and transition metals in the melt into stable complexes.
通过x射线衍射分析和光致发光研究了名义纯LiNbO3:В晶体的缺陷结构特征。晶体是由含有0.08 wt. %和0.12 wt. %硼的相同组成电荷的混合物通过zzochralski生长的。此时,晶体中硼的浓度达到微量金属杂质的水平,为~ 10-4 wt%。MeO6氧八面体团簇对晶体的铁电性质和非线性光学性质负责。研究发现,在LiNbO3:B晶体中,簇中O-O、Me - o和Me - Me (Me - li, Nb)键的长度、Me阳离子的排列、空位和沿极轴的NbLi点缺陷与名义上纯全等晶体有很大的不同。NbLi缺陷和过渡金属是引起光折射效应的深层电子陷阱。光致发光光谱表明,在所研究的LiNbO3:B晶体中缺陷和金属的浓度低于同晶。这些差异可能是由于含硼熔体性质的变化和微量硼在LiNbO3晶体结构的O4四面体间隙中的局部化造成的。在第一种情况下,反应性硼将熔体中的铌和过渡金属阳离子结合成稳定的配合物。
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引用次数: 0
Effect of synthesis conditions on the physicochemical properties of хerogels, nanopowders and ceramic materials in the CeO2 – Nd2O3 system 合成条件对хerogels、纳米粉体和陶瓷材料在CeO2 - Nd2O3体系中理化性质的影响
Pub Date : 2023-01-01 DOI: 10.30791/1028-978x-2023-7-23-33
M. Kalinina, D. A. Dyuskina, T. V. Khamova, L. N. Yefimova, I. Kruchinina, O. Shilova
By liquid-phase methods of synthesis: by the method of co-precipitation of hydroxides and co-crystallization of nitrate salts, highly dispersed mesoporous powders of the composition are synthesized: (SeO2)1 – x(Nd2O3)x (х = 0,05; 0,10; 0,15; 0,20, 0,25), having a specific pore volume of 0.030 – 0.111 cm3/g and a specific surface area of 7.40 – 119.26 m2/g. Based on them, ceramic nanomaterials of a given composition with CSR ~ 69 – 88 nm (1300 °С) were obtained. The physicochemical properties of the resulting ceramics have been studied; it was revealed that it is a solid solution with open porosity in the range of 17 – 30 %, high values of relative density of 89 – 96 %. In terms of their physicochemical properties (density, thermal expansion coefficient), the resulting ceramic materials are promising as solid oxide electrolytes for medium-temperature fuel cells.
液相法合成:采用氢氧化物共沉淀法和硝酸盐共结晶法,合成了高度分散的介孔粉末,其组成为:(SeO2)1 - x(Nd2O3)x (p = 0.05;0, 10;0, 15;0、20、0、25),比孔容为0.030 ~ 0.111 cm3/g,比表面积为7.40 ~ 119.26 m2/g。在此基础上,获得了具有一定组成的陶瓷纳米材料,其CSR为69 ~ 88 nm(1300°С)。对所得陶瓷的理化性质进行了研究;结果表明,它是一种固溶体,孔隙度为17 ~ 30%,相对密度高达89 ~ 96%。就其物理化学性质(密度,热膨胀系数)而言,所得到的陶瓷材料很有希望作为中温燃料电池的固体氧化物电解质。
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引用次数: 0
Laser-ultrasonic study of local porosity distribution in CFRP stringer panels CFRP弦板局部孔隙率分布的激光超声研究
Pub Date : 2023-01-01 DOI: 10.30791/1028-978x-2023-7-73-83
Yu. G. Sokolovskaya, N. Podymova, A. Karabutov
The paper presents a method for quantifying the porosity of carbon fiber structures based on laser excitation of probing ultrasonic pulses. A method for estimating the porosity of a material from the experimentally measured phase velocity of longitudinal acoustic waves propagating in it is proposed. Using the example of control samples and real structures made of carbon fiber, the possibility of obtaining distributions of local porosity values in the studied section of the structure is demonstrated. It is shown that in the studied structures there are regions with a significant variation in the value of local porosity. The proposed method can be used to control the quality of manufactured composite structures, as well as to study the internal changes in structure during operation.
提出了一种基于激光激发探测超声脉冲的碳纤维结构孔隙度定量测量方法。提出了一种利用实验测量的纵波在材料中传播的相速度来估计材料孔隙率的方法。通过对照样品和实际碳纤维结构的实例,证明了在结构研究截面上获得局部孔隙度值分布的可能性。结果表明,在研究的构造中存在局部孔隙度值变化较大的区域。该方法可用于控制复合材料制造结构的质量,也可用于研究结构在运行过程中的内部变化。
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引用次数: 0
Investigation of the effect of LiCl and LiF additives on the kinetics of Spark Plasma Sintering of fine-grained alumina LiCl和LiF添加剂对细晶氧化铝放电等离子烧结动力学影响的研究
Pub Date : 2023-01-01 DOI: 10.30791/1028-978x-2023-1-66-79
M. Boldin, A. Popov, G. Shcherbak, K. Smetanina, D. Permin, V. A. Koshkin, A. Nokhrin, V. Chuvil’deev, А. А. Moskvichev, A. Murashov
The effect of the lithium chloride and lithium fluoride additives (2 wt. %) on the kinetics of Spark Plasma Sintering of industrial fine alumina powder was investigated. The Al2O3 + 2 % LiF powder was obtained by mixing the α-Al2O3 fine powders with the aqueous solution of LiF. The Al2O3 + 2 % LiCl fine powder was obtained by joint grinding of the components in a planetary mill. The sintering of the powders was performed with the heating rates of 10 and 50 °C/min up to the temperature corresponding to the end of the shrinkage. The ceramics sintered with the heating rate of 10 °C/min had the relative density of 97.4 – 98.7 %. The addition of lithium fluoride into the alumina powder was found to allow reducing the temperature of the beginning of the intensive powder shrinkage from 1400 – 1500 °C down to 1255 – 1335 °C. LiCl was shown to evaporate at low heating temperatures and not to affect the compaction intensity of the Al2O3 powder. The presence of the overheated LiF melt (not having enough time to evaporate from the specimen volume completely) in the ceramics leads to the appearance of the residual porosity and to the reduction of the hardness of the ceramics. Using the Young – Cutler equation, the powder compaction mechanisms were determined for pure alumina α-Al2O3 and for the powder compositions with the LiCl and LiF additives in the rapid heating conditions. The sintering activation energy was shown to be close to the one of the grain boundary diffusion. The LiF melt was found to promote the sliding of the Al2O3 fine particles during the low-temperature compaction stage.
研究了氯化锂和氟化锂添加剂(2 wt. %)对工业细铝粉火花等离子烧结动力学的影响。将α-Al2O3细粉与LiF水溶液混合,得到Al2O3 + 2% LiF粉体。在行星磨机上对各组分进行联合研磨,得到了Al2O3 + 2% LiCl细粉。将粉末以10和50℃/min的升温速率烧结至相应的收缩结束温度。升温速率为10℃/min时,烧结陶瓷的相对密度为97.4% ~ 98.7%。在氧化铝粉末中加入氟化锂可以将粉末开始剧烈收缩的温度从1400 - 1500℃降低到1255 - 1335℃。LiCl在低温下蒸发,不影响Al2O3粉末的压实强度。在陶瓷中存在过热的liff熔体(没有足够的时间从试样体积中完全蒸发),导致残余孔隙的出现和陶瓷硬度的降低。利用Young - Cutler方程,确定了在快速加热条件下纯氧化铝α-Al2O3和添加LiCl和LiF的粉末组分的粉末压实机理。烧结活化能与晶界扩散活化能相近。在低温压实阶段,LiF熔体促进了Al2O3细颗粒的滑动。
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引用次数: 0
Percutaneous delivery system for nicotinamide transdermal therapeutic system 用于烟酰胺透皮治疗系统的经皮给药系统
Pub Date : 2023-01-01 DOI: 10.30791/1028-978x-2023-7-46-56
E. G. Kuznetsova, V. A. Ryzhikova, L. A. Salomatina, O. M. Kuryleva, V. Sevastianov
Recently, antioxidants, one of which is nicotinamide, have often been used in the treatment of a number of chronic cardiovascular, autoimmune, skin diseases, and diabetes mellitus. Taking into account the frequent and long-term use of nicotinamide, it seems appropriate to the authors to create a new dosage form of a transdermal therapeutic system (TTS) capable of maintaining the required level of the drug concentration in the blood for a long time. The aim of the work was to develop and to study the functional properties of a system for percutaneous delivery of nicotinamide in vitro. Four compositions of the percutaneous delivery emulsion system for the nicotinamide TTS were suggested, in which the amount of the percutaneous carrier of sodium docusate was varied. Studies of the diffusion of nicotinamide in vitro through unconserved rabbit skin have shown that an increase in the concentration of sodium docusate by three times (from 3.3 % to 9.8 %) significantly increases the amount of the diffused drug substance by 15% and decreases the amount of nicotinamide remaining in the TTS. The amount of the antioxidant founded in the skin flap was lower than the therapeutic dose (~ 1.46 % of its initial amount in TTS) 24 hours after the start of the in vitro experiment. It indicates the absence of a possible aftereffect of nicotinamide TTS in its clinical use after detaching from the patient’s skin.
近年来,抗氧化剂(其中之一是烟酰胺)已被广泛用于治疗多种慢性心血管疾病、自身免疫性疾病、皮肤病和糖尿病。考虑到烟酰胺的频繁和长期使用,作者似乎应该创建一种新的透皮治疗系统(TTS)剂型,能够长时间维持血液中所需的药物浓度水平。本研究的目的是开发和研究经皮烟酰胺体外给药系统的功能特性。提出了烟酰胺TTS经皮给药乳剂体系的四种组成,其中docusate钠的经皮载体量不同。烟酰胺在体外通过未保存的兔皮肤扩散的研究表明,将docusate钠的浓度增加三倍(从3.3%增加到9.8%),可使扩散的原料药的量显著增加15%,并减少残留在TTS中的烟酰胺的量。体外实验开始24小时后,皮瓣中抗氧化剂的含量低于治疗剂量(约为TTS初始量的1.46%)。这表明烟酰胺TTS在临床使用中从患者皮肤分离后没有可能的后遗症。
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引用次数: 0
Research of nanosized iron oxide powder as a biologically active material 纳米氧化铁粉作为生物活性材料的研究
Pub Date : 2023-01-01 DOI: 10.30791/1028-978x-2023-4-42-49
V. Kataev, M. A. Fedotov, N. A. Andreeva, A. Fomina, V. A. Volchenkova, A. A. Alpatov
A polydisperse nanopowder of iron oxide, consisting of hematite α-Fe2O3 and magnetite Fe3O4, was obtained by the method of solid-phase reduction of iron hydroxide Fe(OH)3. On the basis of the obtained iron oxide nanopowder, aqueous suspensions were prepared in the concentration range of 0.25 – 1.25 mg/l with a particle dispersion of 100 – 400 nm. To assess the biological activity of iron oxide nanopowder, pre-sowing treatment of corn seeds Zéa máys was carried out. It has been established that the treatment with nanoparticles has a stimulating effect on the development of the plant organism, making it possible to achieve an increase in germination by 15% and root mass by 23%. Determination of the quantitative content of iron in different parts of the plant was carried out using atomic emission and atomic absorption spectroscopy. It was shown that as a result of treatment of plants with iron nanoparticles, its accumulation in the root mass with subsequent redistribution to the leaves to stimulate the process of photosynthesis is observed.
采用氢氧化铁Fe(OH)3固相还原法制备了由赤铁矿α-Fe2O3和磁铁矿Fe3O4组成的多分散纳米氧化铁粉体。在得到氧化铁纳米粉的基础上,制备了浓度为0.25 ~ 1.25 mg/l,颗粒分散为100 ~ 400 nm的水相悬浮液。为评价氧化铁纳米粉的生物活性,对玉米种子z máys进行了播前处理。已经证实,纳米颗粒处理对植物有机体的发育有刺激作用,可以使发芽率增加15%,根质量增加23%。采用原子发射光谱法和原子吸收光谱法测定了该植物不同部位铁的定量含量。结果表明,铁纳米粒子处理植物后,其在根质量中积累,随后再分配到叶片,以刺激光合作用过程。
{"title":"Research of nanosized iron oxide powder as a biologically active material","authors":"V. Kataev, M. A. Fedotov, N. A. Andreeva, A. Fomina, V. A. Volchenkova, A. A. Alpatov","doi":"10.30791/1028-978x-2023-4-42-49","DOIUrl":"https://doi.org/10.30791/1028-978x-2023-4-42-49","url":null,"abstract":"A polydisperse nanopowder of iron oxide, consisting of hematite α-Fe2O3 and magnetite Fe3O4, was obtained by the method of solid-phase reduction of iron hydroxide Fe(OH)3. On the basis of the obtained iron oxide nanopowder, aqueous suspensions were prepared in the concentration range of 0.25 – 1.25 mg/l with a particle dispersion of 100 – 400 nm. To assess the biological activity of iron oxide nanopowder, pre-sowing treatment of corn seeds Zéa máys was carried out. It has been established that the treatment with nanoparticles has a stimulating effect on the development of the plant organism, making it possible to achieve an increase in germination by 15% and root mass by 23%. Determination of the quantitative content of iron in different parts of the plant was carried out using atomic emission and atomic absorption spectroscopy. It was shown that as a result of treatment of plants with iron nanoparticles, its accumulation in the root mass with subsequent redistribution to the leaves to stimulate the process of photosynthesis is observed.","PeriodicalId":20003,"journal":{"name":"Perspektivnye Materialy","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89707492","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
Preparation of thin nanostructured n-WSe2 films and their application in semiconductor p-Si photocathodes for hydrogen production by water splitting 纳米结构n-WSe2薄膜的制备及其在半导体p-Si光电阴极中的应用
Pub Date : 2023-01-01 DOI: 10.30791/1028-978x-2023-6-5-16
O. Rubinkovskaya, D. Fominski, V. Nevolin, R. Romanov, P. Kartsev, Hualin Jiang, V. Fominski
The possibilities of modification of the structure and type of conductivity of WSe2 films formed on p-type silicon by thermal treatment of a thin-film precursor, which was preliminarily created by pulsed laser deposition, are studied. Pulsed laser ablation of WSe2 and rhenium targets made it possible to obtain amorphous films WSex (x > 2) containing rhenium atoms and inclusions of β-W nanoparticles. Heat treatment at 450 °C caused the crystallization of the amorphous matrix and the formation of a layered 2H-WSe2 shell surrounded the metal nanoparticles. Doping with rhenium led to the production of n-type WSe2 semiconductor films, which, in terms of their properties (band gap ~ 1.2 eV, high catalytic activity, low resistance to current transport), represent a promising material for creating p-Si photocathodes for efficient light-activated hydrogen evolution in acid solution. Theoretical calculations are carried out, which make it possible to identify local areas on the surface of the formed WSe2 films with enhanced catalytic activity in hydrogen evolution reaction.
研究了对脉冲激光沉积制备的薄膜前驱体进行热处理后,在p型硅上形成的WSe2薄膜结构和电导率改变的可能性。脉冲激光烧蚀WSe2和铼靶可以获得含有铼原子和β-W纳米颗粒包体的非晶膜WSex (x >2)。450℃的热处理使非晶态基体结晶,并在金属纳米颗粒周围形成层状的2H-WSe2壳层。铼掺杂制备了n型WSe2半导体薄膜,其性能(带隙~ 1.2 eV,催化活性高,电流输运阻力低)是一种很有前途的材料,可用于制造在酸溶液中高效光活化析氢的p-Si光电阴极。通过理论计算,确定了生成的WSe2膜在析氢反应中催化活性增强的局部区域。
{"title":"Preparation of thin nanostructured n-WSe2 films and their application in semiconductor p-Si photocathodes for hydrogen production by water splitting","authors":"O. Rubinkovskaya, D. Fominski, V. Nevolin, R. Romanov, P. Kartsev, Hualin Jiang, V. Fominski","doi":"10.30791/1028-978x-2023-6-5-16","DOIUrl":"https://doi.org/10.30791/1028-978x-2023-6-5-16","url":null,"abstract":"The possibilities of modification of the structure and type of conductivity of WSe2 films formed on p-type silicon by thermal treatment of a thin-film precursor, which was preliminarily created by pulsed laser deposition, are studied. Pulsed laser ablation of WSe2 and rhenium targets made it possible to obtain amorphous films WSex (x > 2) containing rhenium atoms and inclusions of β-W nanoparticles. Heat treatment at 450 °C caused the crystallization of the amorphous matrix and the formation of a layered 2H-WSe2 shell surrounded the metal nanoparticles. Doping with rhenium led to the production of n-type WSe2 semiconductor films, which, in terms of their properties (band gap ~ 1.2 eV, high catalytic activity, low resistance to current transport), represent a promising material for creating p-Si photocathodes for efficient light-activated hydrogen evolution in acid solution. Theoretical calculations are carried out, which make it possible to identify local areas on the surface of the formed WSe2 films with enhanced catalytic activity in hydrogen evolution reaction.","PeriodicalId":20003,"journal":{"name":"Perspektivnye Materialy","volume":"106 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76084611","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
Effect of electron-beam treatment on the nature of fatigue crack propagation and formation of plastic zones on fracture surfaces in TiNi shape memory alloy 电子束处理对TiNi形状记忆合金疲劳裂纹扩展性质及断口塑性区形成的影响
Pub Date : 2023-01-01 DOI: 10.30791/1028-978x-2023-1-5-18
S. Meisner, L. Meisner
Influence of surface electron-beam processing on character of fatigue cracks propagation and crack growth rates under cyclic tension in a mode of low-cycle loading of TiNi samples before and after irradiation by low-energy high-current electron beam (LEHCEB) is studied in the work. Correlation between stages of fatigue cracks propagation and formation of plastic zones on surfaces of failure in TiNi samples before and after LEHCEB treatments is established. The LEHCEB treatment of specimen surfaces was carried out at the electron-beam installation “RITM-SP” with the electron beam parameters: energy density ES = 3.7 J/cm2, pulse duration τ = 2.5 μs, number of pulses n = 5. Differences in the stages of propagation of main fatigue cracks during cyclic stretching of TiNi samples before and after LEHCEB have been revealed. Preferential mechanisms of quasistatic and fatigue fracture at different stages of crack propagation are determined. It is shown that LEHCEB treatment leads to a shift of fatigue fracture initiation and the beginning of all stages by ∆N ≥ 3000, increasing the cyclic durability of the specimens by ~ 1.5 times. The greatest influence of surface modification is shown on Stage I of fatigue crack propagation. The lower rate of fatigue crack propagation at this stage in irradiated specimens leads to an increase in its duration as compared to unirradiated specimens. It is concluded that to effectively increase the fatigue life of TiNi specimens by means of LEHCEB treatments it is necessary to create conditions for increasing the number of cycles before the Stage I initiation and maximizing the duration of this stage.
研究了低能大电流电子束辐照前后的表面电子束处理对TiNi试样低周加载模式下循环拉伸疲劳裂纹扩展特性和裂纹扩展速率的影响。建立了LEHCEB处理前后TiNi试样疲劳裂纹扩展阶段与破坏表面塑性区形成的相关性。在“RITM-SP”电子束装置上对样品表面进行LEHCEB处理,电子束参数为能量密度ES = 3.7 J/cm2,脉冲持续时间τ = 2.5 μs,脉冲数n = 5。揭示了循环拉伸前后TiNi试样主疲劳裂纹扩展阶段的差异。确定了裂纹扩展不同阶段准静态断裂和疲劳断裂的优先机制。结果表明:LEHCEB处理使疲劳断裂起始和各阶段开始发生∆N≥3000的位移,使试件的循环耐久性提高~ 1.5 倍;表面改性对疲劳裂纹扩展的第一阶段影响最大。与未辐照试样相比,辐照试样在这一阶段的疲劳裂纹扩展速率较低,导致其持续时间增加。结果表明,要想通过LEHCEB处理有效提高TiNi试样的疲劳寿命,必须创造条件,增加第一阶段开始前的循环次数,并使该阶段的持续时间最大化。
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引用次数: 0
Magnetic properties of SMC materials based on iron powder with multilayer insulating coating 多层绝缘涂层铁粉基SMC材料的磁性研究
Pub Date : 2023-01-01 DOI: 10.30791/1028-978x-2023-5-66-71
G. Govor, A. Larin, O. Demidenko, A. L. Zheludkevich
Magnetic properties of composite magnetically soft (SMC) materials based on iron powder ABC100.30 depending on the thickness of the insulating coating based on phosphorus oxide are investigated. It was found that for SMC materials with a three-layer coating of particles, the magnitude of magnetic hysteresis is minimal. As a result, the remagnetization losses for a materials with three-layer insulating particles coating are reduced by an order of magnitude in comparison with composites based on powders with a single-layer coating. The developed materials with magnetic permeability µ = 100 – 150 and induction up to 1.8 T are promising for use in the frequency range up to 1 MHz in the manufacture of various types of electrical devices.
研究了ABC100.30铁粉基复合磁软材料的磁性能随氧化磷基绝缘涂层厚度的变化。结果表明,对于三层颗粒包覆的SMC材料,磁滞效应最小。结果表明,与基于单层涂层的粉末复合材料相比,具有三层绝缘颗粒涂层的材料的再磁化损失降低了一个数量级。所开发的磁导率μ = 100 - 150,感应强度高达1.8 T的材料有望在高达1 MHz的频率范围内用于制造各种类型的电气设备。
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引用次数: 0
Adsorption properties with respect to methane of a functional porous material based on coffee waste 基于咖啡渣的功能多孔材料对甲烷的吸附特性
Pub Date : 2023-01-01 DOI: 10.30791/1028-978x-2023-6-42-51
A. Memetova, A. Zelenin, N. Memetov, V. Yagubov, N. Chapaksov, R. Stolyarov, A. Gerasimova, E. Mkrtchyan
A new microporous carbon material (MUM-51) was obtained from waste coffee grounds by carbonization and activation of KOH. MUM-51 has been characterized by various methods, including N2 adsorption-desorption at 77 K, X-ray diffraction analysis, Fourier transform IR spectroscopy, and Raman spectroscopy. Methane adsorption was studied on the resulting adsorbent at pressures up to 10 MPa and temperatures of 298.15, 303.15, 308.15, 313.15, 318.15, and 323.15 K. The specific pore volume of the adsorbent according to DFT is VDFT = 1.604 cm3/g. The BET specific surface is SBET = 3456 m2/g. The maximum value of methane adsorption at a temperature of 298,15 K and a pressure of 10 MPa reaches ~ 19 mmol/g. Experimental data on methane adsorption on MUM-51 were analyzed using the Dubinin–Radushkevich adsorption model in the temperature range 298.15 – 323.15 K and pressures up to 10 MPa. It has been established that the average relative deviations between the experimental results and the results obtained using the Dubinin-Radushkevich model are less than 3%. The initial differential molar heat of methane adsorption on the MUM-51 adsorbent is 28.7 kJ/mol. The results of the work showed that the carbon material obtained from waste coffee grounds, which has a high specific surface area and porosity, can be effectively used as an adsorbent for greenhouse gases, in particular methane.
以废咖啡渣为原料,经氢氧化钾碳化活化制备了一种新型微孔碳材料MUM-51。MUM-51通过各种方法进行了表征,包括77k下N2吸附-解吸、x射线衍射分析、傅里叶变换红外光谱和拉曼光谱。在压力为10 MPa,温度为298.15、303.15、308.15、313.15、318.15和323.15 K的条件下,对甲烷的吸附进行了研究。根据DFT得到吸附剂的比孔体积为VDFT = 1.604 cm3/g。BET比表面积为SBET = 3456 m2/g。在298℃、15 K、10 MPa压力下,甲烷吸附最大值达到~ 19 mmol/g。采用Dubinin-Radushkevich吸附模型对MUM-51在298.15 ~ 323.15 K、10 MPa压力下的甲烷吸附进行了实验分析。实验结果与杜比宁-拉都什克维奇模型计算结果的平均相对偏差小于3%。MUM-51吸附剂吸附甲烷的初始差摩尔热为28.7 kJ/mol。研究结果表明,从废咖啡渣中获得的碳材料具有较高的比表面积和孔隙率,可以有效地用作温室气体,特别是甲烷的吸附剂。
{"title":"Adsorption properties with respect to methane of a functional porous material based on coffee waste","authors":"A. Memetova, A. Zelenin, N. Memetov, V. Yagubov, N. Chapaksov, R. Stolyarov, A. Gerasimova, E. Mkrtchyan","doi":"10.30791/1028-978x-2023-6-42-51","DOIUrl":"https://doi.org/10.30791/1028-978x-2023-6-42-51","url":null,"abstract":"A new microporous carbon material (MUM-51) was obtained from waste coffee grounds by carbonization and activation of KOH. MUM-51 has been characterized by various methods, including N2 adsorption-desorption at 77 K, X-ray diffraction analysis, Fourier transform IR spectroscopy, and Raman spectroscopy. Methane adsorption was studied on the resulting adsorbent at pressures up to 10 MPa and temperatures of 298.15, 303.15, 308.15, 313.15, 318.15, and 323.15 K. The specific pore volume of the adsorbent according to DFT is VDFT = 1.604 cm3/g. The BET specific surface is SBET = 3456 m2/g. The maximum value of methane adsorption at a temperature of 298,15 K and a pressure of 10 MPa reaches ~ 19 mmol/g. Experimental data on methane adsorption on MUM-51 were analyzed using the Dubinin–Radushkevich adsorption model in the temperature range 298.15 – 323.15 K and pressures up to 10 MPa. It has been established that the average relative deviations between the experimental results and the results obtained using the Dubinin-Radushkevich model are less than 3%. The initial differential molar heat of methane adsorption on the MUM-51 adsorbent is 28.7 kJ/mol. The results of the work showed that the carbon material obtained from waste coffee grounds, which has a high specific surface area and porosity, can be effectively used as an adsorbent for greenhouse gases, in particular methane.","PeriodicalId":20003,"journal":{"name":"Perspektivnye Materialy","volume":"22 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83224092","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}
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