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设计了2组高分子材料组合实验:石墨型氮化碳/聚苯胺(g-C3N4/PANI)复合催化剂的制备及其催化性能研究和孔状g-C3N4/PANI复合催化剂的制备及其催化性能研究。在学生查阅文献及了解实验原理后,确定实验方案,即首先通过直接加热双氰胺制备g-C3N4(或孔状g-C3N4),然后通过界面聚合法制备复合催化剂。在对所得材料进行结构表征基础上,研究其催化性能及影响因素。该实验集仪器分析、高分子材料制备与高分子物理性能分析于一体,不仅能够全面提高学生综合实验能力,而且能够串联学科间知识点,为培养全面型人才提供支撑。 相似文献
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综合设计性实验是培养大学生综合素质和创新能力最重要的途径之一。根据化学与材料相关专业的特点,开设"硫掺杂碳纳米球的制备、表征及其储氢性能"综合设计性实验项目,通过文献调研、原理阐述、方案制定、材料制备、结构表征、性能测试、数据处理与分析等实验环节,使学生充分掌握与化学和材料相关的多门课程内涉及的纳米材料制备、结构表征、性能分析等关键知识点,培养学生的综合能力和创新能力。实践表明,通过综合设计性实验的实践,学生的实践能力、创新能力、基本科学素养和综合素质得到明显提高。 相似文献
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将CR2032型锂离子电池的制作及电化学性能测试实验设计为大学化学本科生的综合实验并将其应用于本科教学中,建立起基于锂离子电池用正极材料的合成、表征、电极制备及电池组装和性能测试的综合性开放实验。实验以无机材料制备为实验基础,以电化学原理为理论基础,通过文献查阅、确立合成路线、材料制备及表征、锂离子电池制作与测试等多项综合实验内容,使学生了解目前常见的正极材料种类、合成方法、电池的基本结构以及电池性能的测试方法。在教学过程中以学生主动探索为主体,培养学生的科学探究素养,锻炼学生查阅文献、自主设计实验和合作开发的能力。 相似文献
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为将导电聚合物超级电容器电极材料引入到本科教学实验中,设计了综合探究性高分子材料制备实验——电化学沉积制备聚苯胺纳米阵列及性能研究。首先采用电化学法构筑导电高分子聚苯胺纳米阵列;然后运用紫外光谱、拉曼光谱、扫描电子显微镜和电化学工作站等,分别对聚苯胺阵列的化学结构、形貌和电化学性能进行表征。从材料的合成角度来看,该实验可以使学生了解和掌握电化学合成导电聚合物的机理与方法;从材料的结构和性能表征方面来看,可以使学生学习和操作科研类的大型仪器设备,对学生的动手操作能力具有实质性的锻炼。此外,该综合性实验很好地将化学制备与材料的应用相结合,方法简单,耗时短,重复性好,可作为高分子类专业本科生综合探究性实验开设。 相似文献
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Extensive computer simulations of multicomponent ion exchange processes in fixed beds are reported. The simulations are based on the local equilibrium theory developed by Helfferich and Klein. The simulations illustrate through computer graphics how the various ions separate and migrate in a column. Detailed concentration profiles as a function of time are shown for cyclic chromatographic operations such as elution, displacement, and selective displacement processes. The simulations elucidate the main features of the interference phenomena as a result of solute competition for the sorbent sites. These simulations also provide important guidelines for designing bulk separation processes, for example, the strategies of recovery, the choices of cyclic operations, feed size, presaturant, eluant, and displacer. 相似文献
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《Arabian Journal of Chemistry》2020,13(1):557-567
Reducing carbon dioxide (CO2) is an area of great interest in current international efforts geared toward lowering emissions and combating global warming. In this work, amino-silica composite membranes were prepared and used to capture carbon dioxide. The surface of silica particles was chemically modified with amine to efficiently capture carbon dioxide. The phase separation technique was used to prepare the membranes from a composite containing polyvinylidene-fluoride-hexafluoropropylene (PVDF-HFP), amino-silica particles, acetone and water. SEM images revealed that the membranes composed of multilayers of porous polymer uniformly impregnated with silica particles. Both XRD and FTIR results have validated the perfect integration of silica particles within the polymeric network. The mechanical properties of the membrane are improved by the presence of silica particles as proved by the high tensile strength value (1.5 N/cm2) obtained for the PVDF-HFP/SiO2 membrane compared to 0.9 N/cm2 obtained for bare PVDF-HFP membrane. Also, we succeeded in recording SEM images to show that the plastic deformation of the film is associated with the formation of macro-holes. To the best of our knowledge this is the first time for such results to be monitored with SEM to observe the macroscopic evolution of the structure. Additionally, the surface area was significantly increased from 3.8 m2/g for bare PVDF-HFP membrane to 116.4 m2/g for PVDF-HFP impregnated with silica particles. Moreover, the CO2 separation efficiency depends on both surface area and the quantity of amino-SiO2 added to the membrane. The addition of amino-silica particles leads to a significant uptake of carbon dioxide compared to non-modified polymer membrane. The results obtained indicated that combing the phase separation with amino silica particles provided a cost-effective route to scaling up the synthesis of membranes that were mechanically stable and highly efficient at CO2 capture. 相似文献
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膜分离现状及发展趋向 总被引:6,自引:0,他引:6
本文简要综述了近年来国内外反渗透、超过滤、微孔过滤、扩散渗析、电渗析、气体分离、液膜、渗透蒸发、蒸发渗透等一些主要膜分离过程,特别是有关新膜研制方面的开发现状及其发展趋向。 相似文献
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Zeolite X membranes were investigated by in-situ hydrothermal synthesis on porous ceramic tubes precoated with zeolite X seeds or precursor amorphous aluminosilicate, and porous α-Al2O3 ceramic tubes with a pore size of 50 200 nm were employed as supports. Zeolite X crystals were synthesized by the classic method and mixed into deionized water as a slurry with a concentration of 0.2 0.5wt%, having a range of crystal sizes from 0.2 to 2μm. Crystal seeds were pressed into the pores near the inner surface of the ceramic tubes, and crystallization took place at 95℃ for 24-96 h. It was also investigated that Boehmite sol added with zeolite X seeds was precoated on ceramic supports to form a layer of γ-Al2O3 by heating, and hydrothermal crystallization could then take place to prepare the zeolite membranes on the composite ceramic tubes. The crystal species were characterized by XRD, and the morphology of the supports subjected to crystallization was characterized by SEM. The composite zeolite membranes have zeolitic top-layers with a thickness of 10-25 μm, and zeolite crystals can be intruded into pores of the supports as deeply as 100μm. The experimental results indicate that the precoating of zeolitic seeds on supports is beneficial to crystallization by shortening the synthesis time and improving the membrane strength. The resulting zeolite X membrane shows permselectivity to tri-n-butylamine((C4H9)3N) over perfluro-tributyl-amine ((C4Fg)3N), and a permeance ratio of 57 for ((C4Hg)3N to (C4F9)3N could be reached at 350℃. Permeances of BZ, EB and TIPB through the zeolite membrane were also measured and were found to slightly increase with temperature. 相似文献