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1.
制备参数对ZrO2气凝胶超细粉织构和结构性质的影响 Ⅰ.水凝胶pH值 总被引:5,自引:4,他引:5
用超临界流体干燥(SCFD)法制备出大孔高比表面ZrO2气凝胶超细粉,详细考察了初始水凝胶pH值对ZrO2超细粉形貌、晶相组成、颗粒大小与分布、比表面积及孔结构等织构和结构性质的影响。在实验范围内,当水凝胶pH值为10.30时,所制得的ZrO2超细粉具有最大的比表面积和孔体积,最小的表观堆密度和平均粒径,颗粒分布均匀狭窄,颗粒间连接成三维网络构状态,较好地保持了凝胶原始织构。 相似文献
2.
采用无机盐作为前驱物,利用溶胶凝胶超临界流体干燥(SCFD)法,制备出大孔、高比表面纳米级TiO2超细粉。详细考察了初始水凝胶pH值对TiO2超细粉形貌、晶相、颗粒大小、比表面积及孔结构等的影响。实验结果发现:当在酸性环境中,所制得的TiO2超细粉的比表面积随着pH值的减小而增大;而在碱性环境中,则随着pH值的增大而增大。TiO2超细粉的比表面积和孔体积由pH为6.5时的SBET=142.2m2·g1,VPN=0.45cm3·g1,增大到pH值为13.0时的SBET=425.6m2·g1,VPN=1.79cm3·g1,且颗粒分布均匀狭窄,颗粒间的三维网络织构更为规整清晰。 相似文献
3.
M(Fe,CO,Ni)ZrO2气凝胶超细粒子催化剂织构和结构热稳定性的研究 总被引:4,自引:0,他引:4
用超临界流体干燥(SCFD)法制备出高比表面纳米级ZrO2和M(Fe,Co,Ni)/ZrO2气凝胶超细原粉.详细考察了其在空气中450℃焙烧后织构和结构的变化,表明ZrO2气凝胶原粉织构和结构的热稳定性较差,而添加铁、钴、镍的M/ZrO2气凝胶原粉织构和结构的热稳定性明显增强,稳定作用依钴、镍、铁次序增加.焙烧后所得的M/ZrO2气凝胶超细催化剂颗粒增长不大,颗粒间仍较大程度地保持着原有凝胶三维网络织构状态.与常规法制备的催化剂相比,其比表面积和孔体积高出甚多. 相似文献
4.
采用pH摆动法,以硫酸铝为铝源,以氢氧化钠为碱沉淀剂,考察了添加SiO2对沉淀氧化铝物性的影响.通过孔结构分析、粒度测定和电镜观察等证实,加入少量SiO2可使沉淀粒子分散、变小,颗粒相对均匀,从而提高了氧化铝的比表面积和孔集中的程度.当加入2.5%的SiO时,pH仅摆动2次,即可使氧化铝粉体的孔体积高达1.2ml/g,比表面积达380m2/g.这类氧化铝的孔结构适宜,粒子小,易直接成型为孔径集中和耐压强度好的载体,故用于重油高压加氢脱氮反应具有较好的性能.沉淀时酸侧pH值降低,尽管沉淀氧化铝的孔径向较小的方面集中,但此时沉淀粒子呈紧密堆积,颗粒变大,比表面积下降,氧化铝沉淀粒子的结构发生改变.不同结构的氧化铝表现出不同的催化活性. 相似文献
5.
用超临界流体干燥法制备出大孔高比表面高分散态Fe/ZrO_2气凝胶超细粒子催化剂,研究了在其制备过程中织构性质、颗粒大小、体相和表面结构的变化,并与普通浸渍法制备的Fe/ZrO_2催化剂作了对比。对几种Fe/ZrO_2催化剂的F-T反应性能考察表明,Fe/ZeO_2气凝胶超细催化剂显示出高的反应活性;随载体ZrO_2颗粒尺寸减小,活性组分铁的分散度变大,其颗粒尺寸变小,催化剂比表面积增大,反应活性增大,甲烷和低碳烃生成量增加,重质组分减少,认为产物烃分布主要受催化剂活性相颗粒尺寸效应制约。 相似文献
6.
CuO/ZrO_2超细粒子催化剂的制备和物性结构表征Ⅰ.水凝胶pH值的影响 总被引:1,自引:0,他引:1
用乙醇超临界流体干燥法制备了CuO/ZrO2超细粒子催化剂,考察了制备过程中水凝胶pH值对催化剂物性参数如比表面积、孔结构和晶相等的影响,并与干凝胶进行了对比.结果表明,pH值在6.5~10.0范围内对晶相影响不大,但对物性结构的影响较大,比表面积和孔体积很快增大,孔形由椭圆形转变为均一的圆柱形,最可几孔径减小,微孔增多;与干凝胶相比,气凝胶表现出高比表面积和多孔结构的特点.pH=10.0时,气凝胶型催化剂的物性参数最佳 相似文献
7.
以廉价的四氯化钛和工业水玻璃为原料,通过溶胶-凝胶法制得TiO2-SiO2复合湿凝胶,用三甲基氯硅烷(TMCS)/乙醇(EtOH)/正己烷(Hexane)混合溶液对湿凝胶进行改性,常压干燥制备了TiO2-SiO2复合气凝胶.利用扫描电子显微镜(SEM)、透射电子显微镜(TEM)、红外光谱(FTIR)、X射线衍射(XRD)及N2吸附/脱附法对复合气凝胶的形貌和性质进行了分析.结果表明,TiO2-SiO2复合气凝胶具有连续多孔结构,150℃干燥后复合气凝胶的比表面积为1 076 m2·g-1,孔体积为4.96 cm3·g-1;经550 ℃热处理后,复合气凝胶仍然具有高的孔隙率,比表面积为856 m2·g-1,孔体积为3.46 cm3·g-1.吸附和光催化降解罗丹明B的结果表明,复合气凝胶同时具有较好的吸附和光催化性能,其吸附/光催化协同作用活性优于纯SiO2气凝胶和锐钛矿TiO2粉末;且重复利用四次降解率仍然可达到89%. 相似文献
8.
用超临界流体干燥法制备纳米级二氧化锆 总被引:4,自引:0,他引:4
本文采用超临界流体干燥技术(Supercriticalfliuddryingtechnique),用超临界乙醇作干燥(脱水)剂制备了纳米粒子ZrO_2,并用X-射线衍射和透射电镜对其进行了表征.结果表明,用超临界流体干燥法能获得颗粒细、大小均匀和抗团聚性能好的纳米粒子。 相似文献
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10.
SnCl2制备超细二氧化锡及其表征 总被引:9,自引:0,他引:9
本工作以二氯化锡为主要制备原料,通过多种测试表征手段比较了分析了不同制备方法,尤其是不同干燥方式对合成SnO2粉体性能的影响,结果表明,采用有机溶剂醇解胶,溶胶-凝胶-超临界流体干燥法可以制得大比表面、小粒径、大孔超细二氧化锡粉体,其中超细粉体粒度6-10nm,比表面为40-80m^2/g,且具有类双峰宽孔分布。 相似文献
11.
Gbolahan O. Shitta-Bey Mojtaba Mirzaeian Peter J. Hall 《Journal of Sol-Gel Science and Technology》2011,57(2):178-184
Organic gels have been synthesized by sol–gel polycondensation of phenol (P) and formaldehyde (F) catalyzed by sodium carbonate
(C). The effect of synthesis parameters such as phenol/catalyst ratio (P/C), solvent exchange liquid and drying method, on
the porous structure of the gels have been investigated. The total and mesopore volumes of the PF gels increased with increasing
P/C ratio in the range of P/C ≤ 8, after this both properties started to decrease with P/C ratio for P/C > 8 and the gel with
P/C = 8 showed the highest total and mesopore volumes of 1.281 and 1.279 cm3 g−1 respectively. The gels prepared by freeze drying possessed significantly higher porosities than the vacuum dried gels. The
pore volume and average pore diameter of the freeze dried gels were significantly higher than those of the vacuum dried gels.
T-butanol emerged as the preferred solvent for the removal of water from the PF hydrogel prior to drying, as significantly
higher pore volumes and specific surface areas were obtained in the corresponding dried gels. The results showed that freeze
drying with t-butanol and lower P/C ratios were favourable conditions for the synthesis of highly mesoporous phenol–formaldehyde
gels. 相似文献
12.
Synthesis of Highly Porous Organic/Inorganic Hybrids by Ambient Pressure Sol-Gel Processing 总被引:6,自引:0,他引:6
This paper reports the synthesis of highly porous organic/inorganic hybrids by a two-step acid-base catalyzed sol-gel process and ambient pressure drying. In the method organic and inorganic precursors are copolymerized so as to incorporate organic ligands into the solid network. The two-step acid-base catalyzed process was used to prevent phase segregation during the hydrolysis and co-condensation of organic and inorganic precursors. The organic ligands incorporated into the solid gel network modify the surface chemistry. Thus, the wetting angle is significantly increased so that the collapse of the gel network is greatly reduced upon the removal of pore fluid during drying. Organic/inorganic hybrids with BET surface areas above 1250 m2/g, porosities above 75% and pore sizes of 8 nm have been synthesized. 相似文献
13.
Arnab Sarkar S. Ray Chaudhuri Shiho Wang Fikret Kirkbir Hideaki Murata 《Journal of Sol-Gel Science and Technology》1994,2(1-3):865-870
The process of drying of a porous material as per the current phenomenological theory can be divided into two stages. At first the body shrinks by an amount equal to the volume of liquid that evaporates, and the liquid-vapor interface remains at the exterior surface of the body. The second stage begins when the body becomes too stiff to shrink and the liquid recedes into the interior, leaving air filled pores near the surface. We shall refer to this phenomenology as the drying front model. In our investigation of drying of alkoxide silica gels of less than 50 Angstroms pore radius, we have observed a different drying pattern, in which even after the gel body stops shrinking, drying continues to occur by evaporation on the exterior surface of the gel body, causing spontaneous nucleation of partially or fully dried opaque clusters, randomly distributed in the interior parts of the gel. These clusters than increase in number and size till they coalesce to form an opaque body. Upon further drying, the gel returns to its transparent form. We postulate that this is possible only if the rate of fluid flow in the pores by diffusion is faster than that by Darcy's flow, as well as the evaporation rate at the surface of the gel body. We shall refer to this as the cluster drying model. We shall present results of pin-hole drying experiments on cylindrical alkoxide gels showing that for identical gels the evaporation rate can be increased to change the phenomenology from cluster drying to one that exhibits both phenomenology simultaneously and finally to that of the drying front phenomenology. We shall also show the effect of gel pore size distribution on the phenomenology of drying under identical drying conditions. Finally, we will present evidence that for successful drying of large cylindrical alkoxide gels, drying conditions favoring cluster drying phenomenology is desirable. 相似文献
14.
非超临界干燥法制备SiO2气凝胶 总被引:26,自引:2,他引:26
应用廉价的国产硅溶胶为原料,通过凝胶过程和干燥过程条件的选择,以非超临界干燥技术最终获得了块状SiO2气凝胶.该气凝胶外观状态与应用正硅酸乙酯为原料制得的完全一致,其微观结构也相当良好,其直径和孔分布均匀.溶液的配比和pH对凝胶过程和气凝胶样品的密度有比较明显的影响,同时pH值与SiO2的粒径之间也有一定的关系.依据制备条件的变化,所得SiO2气凝胶的密度约在200~400 kg•m-3,比表面在250~300 m2•g-1之间变化,平均孔径约为11~20 nm,而孔隙率在91%左右. 相似文献
15.
Preparation of SnO2 Monolithic Gel by Sol-Gel Method 总被引:2,自引:0,他引:2
Haruhisa Shiomi Chisato Kakimoto Atsushi Nakahira Shinichi Takeda 《Journal of Sol-Gel Science and Technology》2000,19(1-3):759-763
The effects of aging of a wet gel at room temperature and a use of a drying control chemical additive (DCCA) were investigated on the prevention of cracking of the gel during drying. N,N-Dimethylformamide (DMF) having low surface tension was used as a DCCA in this study. Before drying, the aged wet gel was immersed in DMF for several days to replace the pore liquid in the wet gel with DMF.The longer the aging and DMF immersing times became, a fewer cracks generated during drying. Especially, the immersion in DMF for over 8 days made it possible to obtain the SnO2 gel monolith without cracking from the wet gel aged for short time (1 day). However, the wet gel aged for long time without immersing in DMF could not be dried without cracking. Therefore, the replacement of the pore liquid in the wet gel with DMF having low surface tension is thought to be more effective on avoiding a crack generation than aging. From a pore size distribution measurement by N2 gas adsorption, it was found that the pore size and the breadth of the pore size distribution of the dried gel became larger and narrower respectively with increasing DMF immersing time. DMF is thought to be capable of forming strong hydrogen bonding to hydroxyl groups remaining on the surface of the wet gel and providing a shielding cage around the reactants (Sn–OH), thus further condensation reaction is probably suppressed. Consequently, a large pore distribution is developed in the gel, which reduces the magnitude of capillary stress induced during drying. 相似文献
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Silica materials are synthesized by the sol–gel method including the deposition of tetraethoxysilane on various micro- and nanocarbon fibers. The use of nanofibrous carbon as a template makes it possible to prepare thermally stable mesoporous SiO2 samples with unusually high surface areas (up to 1255 m2/g) and high porosity (up to 5.6 cm3/g). These silica materials and aerogels prepared by supercritical drying have comparable pore volumes. It is found by high-resolution electron microscopy that a thin-wall matrix permeated by channels is a prevailing structure of silica materials. When some catalytic fibrous carbons are used as templates, silica nanotubes can be prepared. 相似文献
18.
Silica aerogels are very highly divided materials which are synthesised through the association of a chemical step, the so-called sol–gel chemistry, with a physical step which is a particular way of drying the wet gel, namely under supercritical conditions with respect to the liquid phase filling its porosity. This drying process preserves the texture of the dry material: in practice it strongly reduces the pore collapse. The resulting hyperporous solids that have bulk densities of the same magnitude as air develop new and very interesting physical and even chemical properties. Owing to their poor chemical reactivity, very large surface areas (of the order of 1,000 m 2/g), unusual porous volumes (greater than 95%), morphologies (monoliths or powders), optical properties (transparent, opaque or translucent), and very low thermal conductivity, they find high added-value applications in the physics of high-energy particles (Cherenkov emitters), transparent and superinsulating double windows, life and space science as well. 相似文献