2009
DOI: 10.1016/j.jcis.2009.08.010
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Adsorption of lysozyme on spherical mesoporous carbons (SMCs) replicated from colloidal silica arrays by chemical vapor deposition

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Cited by 12 publications
(7 citation statements)
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“…[38][39][40] Moreover, the pore volume at a relative pressure of 0.99 was calculated to be 3.56 cm 3 /g, in which 0.18 cm 3 /g was contributed by the micropores, according to the alpha-s plot analysis (see Table 1). These results suggest that the obtained HCS were generated by a surface-templating mechanism, 33,34 which allows a thin layer of carbon films to be deposited on the surface of the template. As a result, the carbon replicas displayed larger surface areas and pore volumes than those prepared via the volume-templating mechanism.…”
Section: Resultsmentioning
confidence: 88%
See 1 more Smart Citation
“…[38][39][40] Moreover, the pore volume at a relative pressure of 0.99 was calculated to be 3.56 cm 3 /g, in which 0.18 cm 3 /g was contributed by the micropores, according to the alpha-s plot analysis (see Table 1). These results suggest that the obtained HCS were generated by a surface-templating mechanism, 33,34 which allows a thin layer of carbon films to be deposited on the surface of the template. As a result, the carbon replicas displayed larger surface areas and pore volumes than those prepared via the volume-templating mechanism.…”
Section: Resultsmentioning
confidence: 88%
“…Colloidal silica spheres with a solid core and mesoporous shell were synthesized according to the previous recipe, in which the tetraethylorthosilicate and octadecyltrimethoxysilane were applied as a silica precursor and a porogen agent, respectively. The synthetic method of the hollow carbon spheres was similar to our previous procedures, , using silica spheres with a solid core/mesoporous shell as the template and ferrocene as the precursor. After chemical vapor deposition (CVD) at 550 °C for 60 min, the as-synthesized silica/carbon composites were annealed at 800 °C for an additional 90 min, to promote graphitization of the carbon materials.…”
Section: Methodsmentioning
confidence: 99%
“…3b displayed three well-developed peaks centered at 0.7 nm, 1.4 nm and 2.7 nm, which correspond to the adsorption of N 2 in ultrafine micropores, micropores and mesopores, respectively. Taking into account the pore confinement of silica template coupled with the surface-templating property of ferrocene when applied as a carbon precursor, 23,24 the micropores of 1.4 nm in the carbon nanospheres were most likely generated by the mesopores of 2.2 nm in the silica template (Fig. S1 †) via a surface-templating mechanism, by which the nanopores of silica were not completely filled by the pyrolytic carbon.…”
Section: Resultsmentioning
confidence: 99%
“…The mesoporous carbon nanospheres (MCS) were prepared by using the chemical vapor deposition (CVD) method with the calcined MSS as the template and ferrocene as the carbon precursor. 23,24 Typically, about 1.0 g of MSS was loaded on a quartz boat, which was placed in the center of a quartz tube heated by a furnace. The sublimation and the pyrolysis of the ferrocene were conducted in N 2 flow at 120 C and 550 C, respectively.…”
Section: Preparation Of the Monodispersed Mesoporous Carbon Spheresmentioning
confidence: 99%
“…定性, 可应用于不同 pH 的溶液中, 同时, 碳表面的 零电荷也有利于减弱吸附质与吸附剂之间的相互作 用, 因而碳材料更加适合作为吸附材料用于溶菌素 (Lz) [13][14] 和维生素 [15][16] 等生物大分子的吸附. 研究表 明,CMK鄄3 中孔碳材料可以吸附溶菌素分子 [14] , 而 CMK鄄5 中孔 碳对大分子吸附的研究报道则相对 较少.…”
Section: 相对于中孔硅材料 中孔碳材料具有较高的稳unclassified