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Changes in the microstructure and hardness after heat treatment of a billet made of powder high-speed steel R6M5K5 containing a diffusion-alloyed additive 含扩散合金添加剂的粉末高速钢R6M5K5坯热处理后显微组织和硬度的变化
Pub Date : 2023-01-01 DOI: 10.30791/1028-978x-2023-3-43-48
A. Akhmetov, Z. Eremeeva
In this work, a study was made of the change in the microstructure of a hot-pressed billet from a powder mixture of high-speed steel grade R6M5K5 containing a diffusion-alloyed additive based on tungsten, molybdenum, cobalt and iron after heat treatment processes: quenching in oil at a temperature of 1230 °C and double high tempering at 550 °C for 60 min. The study was carried out using electron microscopy and energy dispersive X-ray spectroscopy. After quenching, dissolution of small-sized carbides in the matrix is observed, and after two-fold tempering, secondary carbides of the M6C and MC types are already precipitated. The second type of carbides is formed from a separate structural component — a phase based on ferrovanadium, whose powder was used as a source of vanadium. Also, cobalt is unevenly distributed in the matrix, which is concentrated in a separate phase based on a diffusion-alloyed additive. These phases practically do not dissolve, and are quite stable under these conditions of hot pressing and heat treatment. It is shown that the hardness of blanks changes from 63.1 HRA after hot pressing to 67.2 HRA after quenching and up to 66.3 HRA after double tempering.
本文研究了含钨、钼、钴、铁扩散合金添加剂的高速钢R6M5K5粉末混合物在1230℃油中淬火,550℃双高温回火60 min后热压坯的显微组织变化。采用电子显微镜和能量色散x射线能谱进行了研究。淬火后,观察到基体中细小碳化物的溶解,两次回火后,M6C型和MC型次生碳化物已经析出。第二种碳化物是由一种单独的结构成分形成的——一种基于钒铁的相,其粉末被用作钒的来源。此外,钴在基体中的分布不均匀,在扩散合金添加剂的作用下,钴被集中在一个单独的相中。这些相实际上不溶解,在热压和热处理条件下相当稳定。结果表明:坯料硬度由热压后的63.1 HRA提高到淬火后的67.2 HRA,再经二次回火后达到66.3 HRA。
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引用次数: 0
Traditional and new approaches to the creation of biomedical materials based on polyhydroxyalkanoates with antimicrobial activity 以具有抗菌活性的聚羟基烷酸酯为基础的生物医学材料的传统和新方法
Pub Date : 2023-01-01 DOI: 10.30791/1028-978x-2023-4-5-30
P. Tyubaeva, A. Popov, A. A. Olkhov
This thematic review considers the principles of creating biomedical materials based on biopolymers and their compositions for various medical needs. The direction of creating materials with antimicrobial activity is especially emphasized using the example of polyhydroxyalkanoates. These biopolymers and composites based on them occupy leading positions in the production of medical devices. Polyhydroxyalkanoates as a class of biopolymers, as well as polyhydroxybutyrate, the most suitable representative of this class for biomedical products, were analyzed from the point of view of increasing resistance to microorganisms. Progress in this direction has been reported in recent years. The influence of the supramolecular and molecular structure of materials on the ability to biodegrade in the environment and in a living organism is considered in sufficient detail. The advantage of mixtures of biopolymers for achieving high degradation rates compared to the original polymers was noted. Promising antiseptics based on porphyrin metal complexes in combination with biopolymer nonwoven fibrous matrices have been demonstrated. Features of preclinical tests of antiseptic materials are considered. Based on this review of research papers, it can be concluded that the structural organization of a polymeric material or composite determines the level of intermolecular interactions during the formation of the material and thereby programs the complex of functional properties and the degradation mechanism under the influence of aggressive external factors.
本专题综述考虑了基于生物聚合物及其组合物为各种医疗需求创造生物医学材料的原则。以聚羟基烷酸酯为例,特别强调了创造具有抗菌活性材料的方向。这些生物聚合物和基于它们的复合材料在医疗器械的生产中占据领先地位。从增强微生物抗性的角度分析了聚羟基烷酸酯类生物聚合物,以及聚羟基丁酸酯类生物医药产品的最合适代表。近年来在这方面取得了进展。材料的超分子和分子结构对其在环境和生物体中的生物降解能力的影响被充分详细地考虑。指出了与原始聚合物相比,生物聚合物混合物在实现高降解率方面的优势。基于卟啉金属配合物与生物高聚物非织造纤维基质结合的有前途的防腐剂已经被证明。考虑了防腐材料临床前试验的特点。通过对研究论文的回顾,可以得出结论,聚合物材料或复合材料的结构组织决定了材料形成过程中分子间相互作用的水平,从而规划了功能性质复合物和在侵略性外部因素影响下的降解机制。
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引用次数: 0
Effects of mesenchymal stem cells on the physical and mechanical properties of polyester scaffolds of different architectonics 间充质干细胞对不同结构聚酯支架物理力学性能的影响
Pub Date : 2023-01-01 DOI: 10.30791/1028-978x-2023-5-22-34
I. Arutyunyan, A. Dunaev, E. M. Trifanova, M. Khvorostina, A. Elchaninov, A. Soboleva, T. Fatkhudinov, V. Popov
The biocompatibility of polylactic-co-glycolic acid (PLGA) scaffolds for tissue engineering constructions can be significantly improved by autologous mesenchymal stem cells (MSCs) colonization. However, the features of the cell colonization procedure can generally affect the changes in the physical and mechanical properties of these scaffolds, which are mostly determined by their architectonics. To study this issue, in this work, we have formed and investigated three types of experimental PLGA samples: 1). molded monolithic blocks; 2). porous scaffolds formed by plasticization in supercritical CO2 followed by foaming; and 3). electrospun fibrous non-woven scaffolds. The quantitative XTT test showed the nontoxicity of all studied samples, as well as the greater efficiency of the dynamic cell colonization method compared to the static one. After 48 hours of samples incubation with cell cultures, their physical and mechanical properties were noted to change both at macro- and microlevels. These changes, in our opinion, occur due to the processes of hydrolytic and enzymatic PLGA hydrolysis, as well as the effect of adhered MSCs on the scaffold internal structure and surface morphology. Similar transformations of certain physical, mechanical and structural properties of scaffolds based on other biodegradable polymers or their compositions can also occur as a result of their colonization with various cell cultures, which should be taken into account when applying the scaffolds to develop tissue engineering constructions.
自体间充质干细胞(MSCs)定植可显著提高组织工程用聚乳酸-羟基乙酸(PLGA)支架的生物相容性。然而,细胞定植过程的特点通常会影响这些支架的物理和机械性能的变化,这些变化主要由它们的结构决定。为了研究这一问题,在本工作中,我们形成并研究了三种类型的实验PLGA样品:1)模压整体块;2).在超临界CO2中塑化后发泡形成多孔支架;3).电纺纤维无纺布支架。定量XTT试验表明,所研究的所有样品均无毒,并且动态细胞定殖方法比静态定殖方法效率更高。样品与细胞培养物孵育48小时后,其物理和机械性能在宏观和微观水平上都发生了变化。我们认为,这些变化是由于水解和酶促PLGA水解过程以及粘附的MSCs对支架内部结构和表面形态的影响而发生的。基于其他可生物降解聚合物或其组成物的支架的某些物理、机械和结构性能的类似转变也可能由于它们与各种细胞培养物的定植而发生,在应用支架开发组织工程结构时应考虑到这一点。
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引用次数: 0
Ion-beam formation of a silver-containing surface of porous silicon 多孔硅含银表面的离子束形成
Pub Date : 2023-01-01 DOI: 10.30791/1028-978x-2023-4-31-41
V. Perinsky, I. Perinskaya, I. Rodionov, L. Kuts
The results of a study of the formation of a silver-containing porous layer on the surface of single-crystal silicon KEF-4,5 by ion-beam alloying are presented. A computer simulation of the process of ion doping of silicon with KEF-4,5, high-energy helium and silver ions was carried out using the TRIM/SRIM software package in order to determine the dose and energy neighborhoods of helium and silver ions necessary and sufficient in the experiment. The relief of the porous surface, the density of quasi-pores on the surface of implanted silicon, the elemental composition of the obtained porous composite silver-containing layers, taking into account the effect of intermediate heat treatment on it, are studied. The ion-beam formation of a silver-containing coating ensures the creation of a developed surface relief at the nanoscale with high reproducibility and controllability inherent in the ion doping method, which contributes to an increase in the yield of usable solar cell products. The technological modes of high reproducibility and controllability inherent in the ion doping method are determined based on the experimental data obtained for studying the relief of a porous surface and the density of quasi-pores on the surface of implanted silicon from the energy and dose of helium ions. Based on the study of the elemental composition of the quasi-porous composite silver-containing layer obtained by implantation of silver ions, the recommended parameters of implantation of silver ions have been established.
本文报道了离子束合金化在单晶硅kef -4,5表面形成含银多孔层的研究结果。利用TRIM/SRIM软件包对KEF-4、5、高能氦离子和银离子掺杂硅的过程进行了计算机模拟,以确定实验中氦离子和银离子的剂量和能量邻域是必要的和充分的。考虑中间热处理对多孔复合含银层元素组成的影响,研究了多孔表面的起伏程度、注入硅表面准孔的密度以及所得多孔复合含银层的元素组成。含银涂层的离子束形成确保了在纳米尺度上形成一个成熟的表面浮雕,具有离子掺杂方法固有的高再现性和可控性,这有助于提高可用太阳能电池产品的产量。根据氦离子能量和剂量对注入硅表面多孔表面的释放和准孔密度的实验数据,确定了离子掺杂方法固有的高重现性和可控性的工艺模式。通过对银离子注入获得的准多孔复合含银层元素组成的研究,建立了银离子注入的推荐参数。
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引用次数: 0
High-strength fluoroplastic composites with increased resistance to deformation under load 高强度氟塑料复合材料,在载荷下抗变形能力增强
Pub Date : 2023-01-01 DOI: 10.30791/1028-978x-2023-1-80-88
P. N. Petrova, M. Markova, A. Fedorov
This paper presents the results of research on the development of technology for plastic deformation of polymer blanks based on polytetrafluoroethylene (PTFE) and carbon fibers of the UVIS-AK-P brand in order to increase their strength and creep resistance. The dependence of the physico-mechanical and tribotechnical characteristics of the obtained composites is investigated and compared with a composite of the same composition, but obtained using a previously developed technology. It is established that the use of plastic deformation technology for the properties of PCM based on PTFE and carbon fibers of the brand UVIS-AK-P is an effective solution for obtaining high-strength, wear-resistant composites, characterized by increased resistance to tensile loads. The developed composites obtained using plastic deformation are characterized by 3 times increased tensile strength and 22 – 29 times reduced creep compared to the original PTFE obtained by standard technology. Structural studies of the technology of plastic deformation of polymer blanks have shown that this technology leads to the orientation of the carbon fiber (CF) in the direction of the flow of the material and a change in the spiral conformation of macromolecules with a transition to a more stable conformation, which favorably affects its operational properties. The use of this method will make it possible to obtain high-strength polymer materials with increased resistance to deformation, promising for use for loading schemes with high tensile loads.
介绍了基于聚四氟乙烯(PTFE)和UVIS-AK-P品牌碳纤维的聚合物毛坯塑性变形技术开发的研究成果,以提高其强度和抗蠕变性能。研究了所获得的复合材料的物理力学和摩擦技术特性的依赖性,并与使用先前开发的技术获得的相同成分的复合材料进行了比较。研究表明,利用塑性变形技术提高基于PTFE和UVIS-AK-P碳纤维的PCM的性能是获得高强度、耐磨复合材料的有效解决方案,其特点是增加抗拉伸载荷的能力。所研制的塑性变形复合材料的抗拉强度比原PTFE标准工艺提高3倍,蠕变降低22 ~ 29倍。聚合物毛坯塑性变形技术的结构研究表明,该技术使碳纤维的取向与材料的流动方向一致,使大分子的螺旋构象发生变化,向更稳定的构象过渡,有利于碳纤维的使用性能。这种方法的使用将使获得具有更高抗变形能力的高强度聚合物材料成为可能,有望用于具有高拉伸载荷的加载方案。
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引用次数: 0
Dopant ions’ behavior in solution synthesis of substituted calcium phosphates 掺杂离子在取代磷酸钙溶液合成中的行为
Pub Date : 2023-01-01 DOI: 10.30791/1028-978x-2023-6-34-41
I. Fadeeva, A. A. Forysenkova, V. A. Volchenkova, A. Fomina, V. B. Smirnova, S. Barinov
The dependence of the (Zn, Cu, Co, Ni, Mn)-substituted calcium phosphates’ composition on the water synthesis method has been studied. Cation-substituted tricalcium phosphates and hydroxyapatites were obtained by precipitation from an aqueous solution and by the mechanical activation’ method. The reaction products were dried, calcined at 400°C and investigated by ICP AES and flame AAS. The content of Zn, Cu, Co, Ni, Mn in samples and mother liquors was quantitatively determined. It has been established that the content of Cu2+, Zn2+, Co2+, Ni2+ ions in phosphates is greatly reduced compared to the calculated amounts. At the same time, for tricalcium phosphate, precipitation and the mechanical activation’ method gave comparable results for the content of dopant ions. At the same time, the mechanical activation’ method increase the content of the dopant ion in the substituted hydroxyapatites up to ≈ 48 %.
研究了(Zn, Cu, Co, Ni, Mn)取代磷酸钙的组成与水合成方法的关系。用机械活化法从水溶液中沉淀得到阳离子取代磷酸三钙和羟基磷灰石。将反应产物干燥,在400℃下煅烧,用ICP - AES和火焰原子吸收光谱对反应产物进行了表征。定量测定了样品及母液中Zn、Cu、Co、Ni、Mn的含量。与计算值相比,磷酸盐中Cu2+、Zn2+、Co2+、Ni2+离子的含量大大降低。同时,对于磷酸三钙,沉淀法和机械活化法对掺杂离子含量的测定结果相当。同时,机械活化法使取代羟基磷灰石中掺杂离子的含量提高了约48%。
{"title":"Dopant ions’ behavior in solution synthesis of substituted calcium phosphates","authors":"I. Fadeeva, A. A. Forysenkova, V. A. Volchenkova, A. Fomina, V. B. Smirnova, S. Barinov","doi":"10.30791/1028-978x-2023-6-34-41","DOIUrl":"https://doi.org/10.30791/1028-978x-2023-6-34-41","url":null,"abstract":"The dependence of the (Zn, Cu, Co, Ni, Mn)-substituted calcium phosphates’ composition on the water synthesis method has been studied. Cation-substituted tricalcium phosphates and hydroxyapatites were obtained by precipitation from an aqueous solution and by the mechanical activation’ method. The reaction products were dried, calcined at 400°C and investigated by ICP AES and flame AAS. The content of Zn, Cu, Co, Ni, Mn in samples and mother liquors was quantitatively determined. It has been established that the content of Cu2+, Zn2+, Co2+, Ni2+ ions in phosphates is greatly reduced compared to the calculated amounts. At the same time, for tricalcium phosphate, precipitation and the mechanical activation’ method gave comparable results for the content of dopant ions. At the same time, the mechanical activation’ method increase the content of the dopant ion in the substituted hydroxyapatites up to ≈ 48 %.","PeriodicalId":20003,"journal":{"name":"Perspektivnye Materialy","volume":"296 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75419848","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
The influence of the structure of azo compounds on the deposition process and the quality of copper coatings on Anodized aluminum alloys 偶氮化合物结构对阳极氧化铝合金沉积过程及铜镀层质量的影响
Pub Date : 2023-01-01 DOI: 10.30791/1028-978x-2023-3-64-74
T. I. Devyatkina, R. V. Taranets, V. V. Rogozhin, V. Isaev
A comparative analysis of the influence of the structure of azo compounds (on the example of methyl red (MKR) and nitroso-p-salt (NRS)) was carried out during copper plating of anodized aluminum alloys, on the microstructure, micro-roughness and quality of deposited copper coatings. It is shown that the choice of azo dye significantly depends on the charge of the surface of the oxide film in the solutions used. It is shown that the dyes used should have at least two functional groups in their composition, one of which should ensure the formation of complexes with copper ions, and the other – their adhesion to the surface of the oxide film due to the forces of electrostatic interaction. The adsorption of azo compounds changes the structure of the double electric layer at the film – electrolyte interface, which affects the speed of the copper plating process. At the same time, the mobility of the formed complexes in the adsorption layer increases, which leads to a better opening of the film surface. The studied indicators (dyes) positively affected the structure of the copper coating (eliminated defects and made it fine-crystalline), and also significantly smoothed the surface of the copper coating. The advantage of using the NRS over the MKR was revealed, which allowed not only to obtain a high-quality coating, but also to significantly intensify the copper plating process. A new composition of copper sulfuric acid electrolyte for coating anodized aluminum alloys at elevated cathode current densities with preservation of fine-crystalline structure and smoothed surface is proposed.
对比分析了阳极氧化铝合金镀铜过程中偶氮化合物(以甲基红(MKR)和亚硝基对盐(NRS)为例)结构对镀层显微组织、显微粗糙度和镀层质量的影响。结果表明,偶氮染料的选择在很大程度上取决于所使用溶液中氧化膜表面的电荷。结果表明,所使用的染料在其组成中应至少具有两个官能团,其中一个官能团应确保与铜离子形成配合物,另一个官能团应确保它们由于静电相互作用而粘附在氧化膜表面。偶氮化合物的吸附改变了膜-电解质界面的双电层结构,影响了镀铜过程的速度。同时,在吸附层中形成的配合物的迁移率增加,导致膜表面的开度更好。所研究的指示剂(染料)对铜涂层的结构产生了积极的影响(消除了缺陷,使其呈细晶状),并显著地光滑了铜涂层的表面。与MKR相比,使用NRS的优势被揭示出来,它不仅可以获得高质量的涂层,而且可以显着加强镀铜过程。提出了一种新的铜硫酸电解质,用于在高阴极电流密度下涂覆阳极氧化铝合金,同时保留了细晶结构和表面光滑。
{"title":"The influence of the structure of azo compounds on the deposition process and the quality of copper coatings on Anodized aluminum alloys","authors":"T. I. Devyatkina, R. V. Taranets, V. V. Rogozhin, V. Isaev","doi":"10.30791/1028-978x-2023-3-64-74","DOIUrl":"https://doi.org/10.30791/1028-978x-2023-3-64-74","url":null,"abstract":"A comparative analysis of the influence of the structure of azo compounds (on the example of methyl red (MKR) and nitroso-p-salt (NRS)) was carried out during copper plating of anodized aluminum alloys, on the microstructure, micro-roughness and quality of deposited copper coatings. It is shown that the choice of azo dye significantly depends on the charge of the surface of the oxide film in the solutions used. It is shown that the dyes used should have at least two functional groups in their composition, one of which should ensure the formation of complexes with copper ions, and the other – their adhesion to the surface of the oxide film due to the forces of electrostatic interaction. The adsorption of azo compounds changes the structure of the double electric layer at the film – electrolyte interface, which affects the speed of the copper plating process. At the same time, the mobility of the formed complexes in the adsorption layer increases, which leads to a better opening of the film surface. The studied indicators (dyes) positively affected the structure of the copper coating (eliminated defects and made it fine-crystalline), and also significantly smoothed the surface of the copper coating. The advantage of using the NRS over the MKR was revealed, which allowed not only to obtain a high-quality coating, but also to significantly intensify the copper plating process. A new composition of copper sulfuric acid electrolyte for coating anodized aluminum alloys at elevated cathode current densities with preservation of fine-crystalline structure and smoothed surface is proposed.","PeriodicalId":20003,"journal":{"name":"Perspektivnye Materialy","volume":"41 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85128647","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
Porosity of nickel nanopowder compacts consolidated by gas extrusion 气体挤压固结纳米镍粉末的孔隙率
Pub Date : 2023-01-01 DOI: 10.30791/1028-978x-2023-6-80-84
M. Alymov
The method of hot gas extrusion differs from other methods of metal pressure treatment in that the processed material is subjected to intense plastic deformation by extrusion under conditions of high isostatic pressure of inert gas and heating in the area of plastic deformation. The method makes it possible to process powder materials, while inevitably there is a need to control mechanical properties by controlling porosity and pressure inside the pores. The paper presents a method for calculating the pressure inside the pores from the minimum size of the closed pore. The pore pressure was evaluated on materials obtained by the consolidation of nickel nanopowders by hot gas extrusion. Quantitative processing of the material cross-section view images obtained by scanning electron microscopy showed that the minimum pore size is 220 nm. The formula for calculating the pore pressure is derived from the formula for calculating the critical pore radius. It takes into account the external impact pressure (the gas pressure during the extrusion process was equal to 400 MPa), the surface tension coefficient and the yield strength of nickel (at the extrusion start temperature of 910 °С), as well as the minimum pore radius. The proposed method for calculating the pressure inside a closed pore will allow us to evaluate the mechanical properties of materials obtained by various methods of powder metallurgy.
热气体挤压法与其他金属压力处理方法的不同之处在于,被加工的材料在惰性气体的高等静压和塑性变形区加热的条件下,通过挤压而受到强烈的塑性变形。该方法使加工粉末材料成为可能,但不可避免地需要通过控制孔隙率和孔隙内压力来控制机械性能。本文提出了一种从封闭孔的最小尺寸出发计算孔内压力的方法。研究了高温气体挤压法制备的纳米镍粉末固结材料的孔隙压力。通过扫描电镜对材料横截面图像进行定量处理,发现最小孔径为220 nm。由临界孔隙半径计算公式推导出孔隙压力计算公式。考虑了外部冲击压力(挤压过程中气体压力为400 MPa)、镍的表面张力系数和屈服强度(挤压起始温度为910°С)以及最小孔隙半径。所提出的计算封闭孔内压力的方法将使我们能够评价通过各种粉末冶金方法获得的材料的力学性能。
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引用次数: 0
Investigation of the polyvinylpyrrolidone amount as gelling agent to lanthanum cobaltite micropowders synthesize by sol-gel method 溶胶-凝胶法制备钴酸镧微粉的胶凝剂聚乙烯吡咯烷酮用量的研究
Pub Date : 2023-01-01 DOI: 10.30791/1028-978x-2023-3-75-84
E. Ermakova, S. S. Strelnikova, A. Anokhin, A. A. Konovalov, О. S. Antonova, M. Chuvikina
The paper focuses on lanthanum cobaltite micropowders LaCoO3-δ (LCO) synthesized by the sol-gel method using polyvinylpyrrolidone (PVP) as gelling agent. The PVP content has been varied from 0.5 to 5.0 wt. % when ionic solutions of the soluble raw components were prepared. The gels were dried in a microwave oven at microwave power 90 W for 2 h to evaporate water. Xerogels were thermally treated in a muffle furnace at temperatures 800°C and 900°C, the maximum holding time was 10 h and 30 h. After heat treatment of Xerogels at 800°C for 10 h LCO micropowders were slightly aggregated and particle size were in the range from 0.24 to 0.38 µm as well as specific surface area was in the range from 2.60 to 4.10 m2/g. After heat treatment 900°C for 10 h the specific surface area range of LCO micropowders decreased from 1.00 to 3.20 m2/g, but particle size range slightly increased from 0.31 up to 1.0 µm. Xerogels heat treatment at temperature 900° C for 30 h resulted to particles size range growing from 0.50 to 1.25 μm, and the specific surface area was 2.00 m2/g for all LCO micropowders. There was no effect of PVP content in the ionic solution on phase composition for all heat treated LCO micropowders.
以聚乙烯吡咯烷酮(PVP)为胶凝剂,采用溶胶-凝胶法制备了钴酸镧微粉LaCoO3-δ (LCO)。当制备可溶原料组分的离子溶液时,PVP含量在0.5 ~ 5.0 wt. %之间变化。将凝胶在微波炉中以90 W的微波功率干燥2 h以蒸发水分。在马弗炉中分别在800℃和900℃温度下对干凝胶进行热处理,最大保温时间分别为10 h和30 h。在800℃温度下热处理10 h后,LCO微粉呈微团聚状,粒径在0.24 ~ 0.38µm之间,比表面积在2.60 ~ 4.10 m2/g之间。900℃热处理10 h后,LCO微粉的比表面积范围从1.00 m2/g减小到3.20 m2/g,粒径范围从0.31µm略微增大到1.0µm。在900℃下干凝胶热处理30 h, LCO微粉的粒径范围从0.50 ~ 1.25 μm不等,比表面积为2.00 m2/g。离子溶液中PVP含量对热处理LCO微粉的相组成没有影响。
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引用次数: 0
Influence of the technological mode of mixing and curing system on the properties of compositions based on nitrile rubber and ultrahigh molecular weight polyethylene 混合和固化体系工艺模式对丁腈橡胶与超高分子量聚乙烯基组合物性能的影响
Pub Date : 2023-01-01 DOI: 10.30791/1028-978x-2023-2-77-86
N. V. Shadrinov, A. A. Borisova, A. R. Khaldeeva, K. P. Antoev
The results of a study of the influence of the mixing mode and curing system on the properties of low temperature and oil resistant rubber based on a composition of butadiene-nitrile rubber (BNKS-18AMN) and ultra-high molecular weight polyethylene (GUR 4113) are presented. Different ways of UHMWPE introducing into the rubber compound are considered: mixing before and after the introduction the main ingredients of the rubber compound at temperatures up to 80 °C (below the melting point of UHMWPE) and preliminary high-temperature (160 °C) mixing of rubber and UHMWPE. It was found that the preliminary high temperature mixing of rubber with UHMWPE leads to a decrease in the viscosity of the rubber compound, as well as a reduction in the scorch time and the achievement of an optimum vulcanization but does not lead to significant changes in the physical and mechanical properties and oil resistance of vulcanizates. The study of the influence of the curing system showed the effectiveness of using a combined sulfur-peroxide curing system, which is manifested in the improvement of the technical properties of vulcanizates, which is largely due to an increase in the density of rubber crosslinking through the formation of stronger and more heat-resistant C-C bonds. It has been shown that the best set of technical properties of vulcanizates, including high frost-resistance, physical and mechanical properties, resistance to hydrocarbon environment and retention of properties after thermal exposure, is achieved when using the sulfur-peroxide combination S/DCP – 1/2.
研究了丁腈橡胶(BNKS-18AMN)和超高分子量聚乙烯(GUR 4113)的混合方式和固化体系对低温耐油橡胶性能的影响。考虑了UHMWPE引入胶料的不同方式:在引入胶料的主要成分之前和之后,在高达80℃(低于UHMWPE的熔点)的温度下进行混炼,以及橡胶和UHMWPE的初步高温(160℃)混炼。研究发现,橡胶与超高分子量聚乙烯的初步高温混炼可以降低胶料的粘度,减少焦化时间,达到最佳硫化效果,但对硫化胶的物理机械性能和耐油性能没有显著影响。硫化体系影响的研究表明,采用硫-过氧化物复合硫化体系是有效的,表现在硫化胶技术性能的改善上,这主要是由于通过形成更强、更耐热的C-C键,提高了橡胶交联的密度。研究表明,硫-过氧化物组合S/DCP - 1/2可获得最佳的硫化胶技术性能,包括高抗冻性、物理力学性能、耐烃类环境和热暴露后的保持性。
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引用次数: 0
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