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Sulfluramid volatility reduction by beta-cyclodextrin

机译:β-环糊精可降低磺胺类药物的挥发性

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Sulfluramid is an expensive active principle of insecticidal baits that is lost by volatilization during the pelletization of baits. To increase the thermal stability of sulfluramid, we tested its molecular encapsulation in beta-cyclodextrin (beta-CD), using molar ratios of 1:1 and 1:2 (sulfluramid:beta-CD), using the complex preparation techniques of coprecipitation and kneading. The physical mixture of sulfluramid and P-CD was also tested for comparison. The products of complexation were characterized by differential scanning calorimetry, thermogravimetry, and derivative thermogravimetry, indicating the formation of a sulfluramid/beta-CD complex and showing that the release of the complexed sulfluramid occurs in the range of 270-300 degreesC, a temperature range that is well above the temperature at which sulfluramid sublimates (40 degreesC). This result warrants a reduced sulfluramid loss in the preparation of insecticidal baits. The preparation of the complex by kneading with molar ratio of 1:2 gave the highest yield of complex, about 64%, in relation to the theoretical maximum.
机译:磺胺嘧啶是杀虫诱饵的昂贵的有效成分,在诱饵造粒期间会因挥发而丢失。为了提高磺胺嘧啶的热稳定性,我们使用了共沉淀法和共沉淀法的复杂制备技术,以1:1和1:2的摩尔比(磺酰胺:β-CD)测试了其在β-环糊精(β-CD)中的分子包封性。揉捏。还测试了巯草胺和P-CD的物理混合物以进行比较。通过差示扫描量热法,热重法和导数热重法对络合产物进行表征,表明形成了磺胺嘧啶/β-CD络合物,并表明络合的磺胺嘧啶的释放发生在270-300℃的温度范围内。这远高于磺胺嘧啶升华的温度(40摄氏度)。该结果保证了在制备杀虫诱饵中减少了磺胺嘧啶的损失。通过以1:2的摩尔比捏合来制备配合物,相对于理论最大值,配合物的最高产率为约64%。

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