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Release kinetics of tebuconazole from porous hollow silica nanospheres prepared by miniemulsion method

机译:细乳液法制备的戊唑醇从多孔空心二氧化硅纳米球中的释放动力学。

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摘要

Triazole fungicide tebuconazole was incorporated in porous hollow silica nanospheres (PHSNs) by the miniemulsion method to obtain controlled release properties. PHSNs were fabricated using tetraethyl orthosilicate (TEOS) as the silica source and an ethyl acetate as droplet templates. The tebuconazole was dissolved in droplet templates and wrapped into PHSNs as the volatilization of droplet templates, instead of a loading procedure such as the simple immersing loading method or supercritical fluids technology. The factors related to loading efficiency and controlled release behaviors of free tebuconazole from tebu-PHSNs were investigated. Results showed that the loading efficiency could reach about 45% (w/w) by changing the concentration of hexadecyl trimethyl ammonium bromide (CTAB) and the ratio of TEOS to ethyl acetate. The values for the diffusion exponent "n" Were in the range of 0.29-0.61, which indicated that the release of tebuconazole was diffusion-controlled. The time taken for 50% of the active ingredient to be released into water, T_(50), was also calculated for the comparison of formulation in different conditions. The results showed that the formulation with the lower temperature, pH value, and larger particle size had lower values of T_(50), which meant a slower release of the active ingredient.
机译:通过细乳液法将三唑类杀菌剂戊唑醇掺入多孔中空二氧化硅纳米球(PHSN)中,以获得控释性能。 PHSN是使用原硅酸四乙酯(TEOS)作为二氧化硅源和乙酸乙酯作为液滴模板制备的。将戊唑醇溶解在液滴模板中,并随着液滴模板的挥发而包裹在PHSN中,而不是采用诸如简单的浸入式加载方法或超临界流体技术之类的加载程序。研究了与tebu-PHSNs游离的tebuconazole的负载效率和控释行为有关的因素。结果表明,通过改变十六烷基三甲基溴化铵(CTAB)的浓度和TEOS与乙酸乙酯的比例,负载效率可以达到约45%(w / w)。扩散指数“ n”的值在0.29-0.61的范围内,这表明戊唑醇的释放是扩散控制的。还计算了50%的活性成分释放到水中所需的时间T_(50),用于比较不同条件下的制剂。结果表明,具有较低温度,pH值和较大粒径的制剂具有较低的T_(50)值,这意味着活性成分的释放较慢。

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