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首页> 外文期刊>Journal of porous materials >Simultaneous control of rod length and pore diameter of SBA-15 for PPL loading
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Simultaneous control of rod length and pore diameter of SBA-15 for PPL loading

机译:用于PPL加载的SBA-15杆长度和孔径的同时控制

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摘要

Mesoporous silica materials are attractive materials for immobilizing enzymes because of their well-ordered structures, large surface area are pore volume. Diffusion of large enzyme molecules such as porcine pancreatic lipase (PPL) through the lengthy channels of MPS takes place too slowly. Therefore, the squat of the enzyme at the pore mouth entrance, actually makes the rest of the channel useless. In this study, to overcome this problem, synthesis parameters of SBA-15 were changed, since along with pore diameter increasing, the mesochannel length becomes shorter. The main point to obtain a well-ordered 2D hexagonal pore structure was the pre-hydrolysis of tetraethyl orthosilicate (TEOS) before the addition of 1,3,5-trimethyl benzene as a micelle swelling agent. Due to the strong effect of zirconium in changing the morphology of SBA-15 particles, we modified SBA-15 in the presence of a small amount of ZrOCl2 in the synthesis solution under acidic conditions. As a result, mesochannel length of SBA-15-Zr was shortened from 600 to < 200 nm. The morphology of mesoporous silica was also changed from rod-like to platelet, because of the accelerating effect of Zr(IV) on the self-assembly rate of P123 and TEOS condensation. Characteristic results conducted by low angle XRD, high resolution transmission electron microscopy and nitrogen adsorption, confirmed tuning effect of Zr(IV) in SBA-15. Furthermore, it was shown that the number of pore entrances increases with decreasing the length of SBA-15 mesochannels, leading to obvious improvement of enzyme uptake. PPL has been successfully immobilized in the mesoporous channels of SBA-15-Zr. The total amount of lipase adsorbed on the mesoporous SBA-15-Zr was measured by thermal gravimetric analysis. The largest PPL adsorption capacity was 784 mg/g belonging to the SBA-15-Zr with the length of 150 nm and the mean pore size diameter of 9.22 nm.
机译:介孔二氧化硅材料是固定化酶的有吸引力的材料,因为它们的结构井然有序,大的表面积是孔体积。大型酶分子(例如猪胰脂肪酶(PPL))通过MPS的漫长通道扩散的速度太慢。因此,酶在孔口入口处的下蹲实际上使其余通道无效。在这项研究中,为克服这个问题,改变了SBA-15的合成参数,因为随着孔径的增加,介孔长度变短了。获得井井有条的2D六角孔结构的要点是在添加1,3,5-三甲基苯作为胶束膨胀剂之前对原硅酸四乙酯(TEOS)进行预水解。由于锆在改变SBA-15颗粒形态方面的强大作用,因此在酸性条件下,在合成溶液中存在少量ZrOCl2的情况下,我们对SBA-15进行了改性。结果,SBA-15-Zr的中通道长度从600缩短到<200 nm。由于Zr(IV)对P123的自组装速率和TEOS缩合的促进作用,介孔二氧化硅的形态也从棒状变为血小板。通过低角度XRD,高分辨率透射电子显微镜和氮吸附进行的特性结果证实了Zr(IV)在SBA-15中的调谐效果。此外,已经表明,随着SBA-15介孔长度的减少,孔入口的数量增加,从而导致酶吸收的明显改善。 PPL已成功固定在SBA-15-Zr的介孔通道中。通过热重量分析法测量了吸附在中孔SBA-15-Zr上的脂肪酶的总量。属于SBA-15-Zr的最大PPL吸附容量为784 mg / g,长度为150 nm,平均孔径直径为9.22 nm。

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