共查询到20条相似文献,搜索用时 593 毫秒
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在实验室研究了循环利用电炉粉尘造泡沫渣过程中,FeO还原速度的影响因素,同时分析了 FeO 还原速度与炉渣发泡高度的关系. 结果表明,随着粉尘和煤粉加入量增加以及反应温度提高,渣中FeO的还原速度加快;渣中FeO被固体碳还原的反应为表观一级反应;渣中FeO还原反应速率常数与泡沫渣的最大发泡高度存在很好的相关性,还原速度增加,泡沫渣的最大发泡高度也随之提高. 相似文献
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小通道填充泡沫金属成为近几年强化换热方向的研究热点。以空气和水为工作介质,将PPI为10和20的泡沫金属分别填充到截面为2.5 mm×2.5 mm的T型小通道内,改变泡沫金属的亲疏水性,分别研究弹状流和环状流下气液两相表观流速及亲疏水性对相分离的影响机制。比较亲水、疏水处理及未处理这三种泡沫金属的分离特性发现:无论是弹状流还是环状流,分离效果最好的是亲水处理后的泡沫金属,其次是未经处理的泡沫金属,而进行疏水处理后的分离效果最差,填充泡沫金属的T型通道相分离效果要明显好于未填充的通道。对于亲疏水处理过的T型通道,无论是弹状流还是环状流,T型小通道内侧支管气相采出分率占优,液相采出分率随着液体表观速度的增加而降低,但气相表观速度对液相采出分率影响很小。而泡沫金属PPI的减小会降低气相采出分率,使分配效果更加趋近于均匀分布线。 相似文献
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为了加强泡沫相排液,提高目的产物的富集比,设计了一种新型泡沫分离塔即泡沫相部分水平泡沫分离塔.以传统泡沫相垂直泡沫分离塔为对照塔,以牛血清蛋白(BSA)为体系,考察了表观气速、装液量、物料初始浓度和初始pH对牛血清蛋白(BSA)富集比和回收率的影响.结果表明泡沫相部分水平泡沫分离塔有效减小了泡沫相排液的阻力,提高了BS... 相似文献
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分别利用K2Ti6O13晶须、短玻璃纤维对酚醛泡沫(PF)进行改性,并制备了不同短玻璃纤维含量的酚醛泡沫,考察了不同改性方法对酚醛泡沫的表观形貌、力学性能和保温性能的影响。表观形貌结果表明,添加4%K2Ti6O13晶须可以显著改变酚醛泡沫的表观形貌,使得泡孔更规则、均匀。力学性能测试表明,短玻璃纤维含量在8%以内,压缩强度和弯曲强度都随着短玻璃纤维含量的增加而增大;短玻璃纤维和短玻璃纤维/4%K2Ti6O13晶须可以显著提高酚醛泡沫的压缩强度和弯曲强度,压缩强度和弯曲强度最高分别提高了126%和208%;加入短玻璃纤维稍稍提高了酚醛泡沫的导热系数,降低了酚醛泡沫的保温性能;加入相同量的短玻璃纤维,短玻璃纤维/4%K2Ti6O13晶须改性的酚醛泡沫相比于短玻璃纤维改性酚醛泡沫具有更高的压缩强度、弯曲强度和保温性能。 相似文献
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Shirley K. García‐Castillo Brenda L. Buitrago Enrique Barbero 《Polymer Composites》2011,32(2):290-296
This work evaluates the behavior of sandwich and spaced plates subjected to high‐velocity impacts. The sandwich structures were made of glass/polyester face‐sheet and a PVC foam core. The spaced plates were made of two plates of the same material of the sandwich face‐sheet at a distance equal to the core thickness. The residual velocity, the ballistic limit, and the damage area were selected to compare the response of both structures. The residual velocity and ballistic limit was very similar in both cases. Nevertheless, the damage area of sandwich structures and spaced plates differed due to the dissimilar properties between the sandwich core and the air inside of the spaced plates. An analytical model, based on energy criteria, was applied to estimate the residual velocity of the projectile, the absorbed energy by each face‐sheet, and the ballistic limit in the spaced plates. POLYM. COMPOS., 2011. © 2010 Society of Plastics Engineers 相似文献
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Nathan Reed Nha Uyen Huynh Brooke Rosenow Kristoffer Manlulu George Youssef 《应用聚合物科学杂志》2020,137(26):48839
Polymeric foams are ubiquitous in impact mitigation for civilian and military applications; the performance in such loading scenarios can be elucidated through quasi-static and dynamic mechanical testing. The present study reports on the complex microstructure of newly synthesized polyurea foams exhibiting a hierarchical structure consisting of large perforated semi-closed spherical cells with a mean diameter of 370 ± 162 μm surrounded by smaller closed, spherical cells with size distribution of 69 ± 18 μm. The stress–strain curves were used to calculate the basic mechanical properties and to predict the dynamic behavior of the foams. Nonlinear regression and finite element analyses were used to calibrate the Ogden hyperfoam model to explicate the hyperelastic behavior. The performance of the polyurea foam was found to outperform a benchmark foam in nearly all the elastic and energy absorbing properties. For example, one variation of the newly synthesized foam stored nearly doubled the energy of the benchmark foam while being 12% lighter. Low-density polyurea foam was found to decelerate an incoming impact mass with a minimum G-level that was nearly one third lower than the higher density polyurea and benchmark foams. In all, the behavior of the foam is dependent on the parameters of the fabrication process. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48839. 相似文献
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Michael Hajimichael Annette Lewis Dave Scholey Clive Simmonds 《Polymer International》1986,18(5):307-311
The development of low toxicity rigid epoxy foams as an alternative to polyurethane foams for electronics encapsulation is described. The basic foam components - epoxy resin, hardener, accelerator, blowing agent and surfactant - are blended to form a two part system which is mixed and foamed when required. Each foam component is selected for its contribution to the foaming reaction and the final foam properties. The balance of component miscibility, viscosity, reaction rate and exotherm determine foam quality. Foam properties are affected by (1) density (2) cell structure and (3) the molecular structure of the reactants. Initial foam development utilised epoxy/amine chemistry and produced two foams, Feldex F3 and F4. Subsequently, use of a more reactive polymercaptan hardener improved foam strength and process times, resulting in Feldex F5 and F6 which have been used successfully to prepare quality mouldings and encapsulated electronics. Recently, development has been extended to new areas of application, e.g. high temperature foams. The mechanical, electrical, thermal and chemical properties of the best epoxy foams have been evaluated; selected results are reported. The epoxy foams developed offer low density, high strength, low dielectric constant and loss tangent, high volume resistivity, good thermal insulation, low corrosivity and low toxicity. In addition, epoxy foams soften in acetone, an advantage over their polyurethane counterparts since encapsulated electronics may be retrieved without employing corrosive solvents. (Feldex is a registered trade mark of THORN EMI Electronics.) 相似文献
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Divinylbenzene (DVB) shells with a density of about 100 mg/cc were produced using a dual‐thermal initiator system. New high‐gain designs for direct‐drive ignition at the National Ignition Facility and the OMEGA laser facility at the Laboratory for Laser Energetics require low‐density foam shells such as these. Previous research using a single initiator system produced fragile DVB shells that cracked or imploded during the fabrication process. The dual‐initiator DVB system used in the present study enabled the shells to be robust enough to produce a high yield of intact shells. The two thermal initiators used were azobisisobutyronitrile (AIBN) and another azo‐type initiator, V‐70. The DVB shells were 800–3500 μm in diameter, with shell wall thickness 7%–10% of the diameter. Because the foam shells were porous, a full‐density permeation barrier of poly(vinyl phenol) was developed and deposited on the shells using two techniques to enable the shells to retain gas. The initial results show that the permeation barrier was pinhole free and could hold the gas in a gas‐filled shell. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 2523–2529, 2006 相似文献
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A simple, rapid and green method for fabrication of nanoporous metal (Ag and Pd) foams using electrochemically deposited nanoporous copper foam is presented. Ideally direct electrochemical formation of Ag and Pd foam structures without any additive reagent does not lead to a desired result; however, indirect fabrication starting from electrochemically fabricated Cu foam seems promising. Highly porous copper foam is fabricated electrochemically at a copper sheet and in turn serves as a hard template and a redox inducer for the deposition of Ag or Pd. The redox induced replacement of copper foam with Ag or Pd is done via simple immersion of as-fabricated nanoporous copper foam in cation aqueous solutions of Ag or Pd. The surface morphology of the as-fabricated foam is characterized by scanning electron microscopy (SEM), EDX and X-ray diffraction. The hydrogen evolution reaction is investigated as an example to demonstrate the electrocatalytic ability of as-fabricated foams. 相似文献
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