高越, 郭瑞峰, 史高川, 张鹏九, 刘中芳, 范仁俊. 高效氯氰菊酯聚(N-正丙基丙烯酰胺)温敏微球的制备关键工艺研究[J]. 农药学学报, 2017, 19(2): 266-272. DOI: 10.16801/j.issn.1008-7303.2017.0035
    引用本文: 高越, 郭瑞峰, 史高川, 张鹏九, 刘中芳, 范仁俊. 高效氯氰菊酯聚(N-正丙基丙烯酰胺)温敏微球的制备关键工艺研究[J]. 农药学学报, 2017, 19(2): 266-272. DOI: 10.16801/j.issn.1008-7303.2017.0035
    GAO Yue, GUO Ruifeng, SHI Gaochuan, ZHANG Pengjiu, LIU Zhongfang, FAN Renjun. Study on the key preparation process of beta-cypermethrin poly (N-propylacrylamide) temperature-sensitive microsphere[J]. Chinese Journal of Pesticide Science, 2017, 19(2): 266-272. DOI: 10.16801/j.issn.1008-7303.2017.0035
    Citation: GAO Yue, GUO Ruifeng, SHI Gaochuan, ZHANG Pengjiu, LIU Zhongfang, FAN Renjun. Study on the key preparation process of beta-cypermethrin poly (N-propylacrylamide) temperature-sensitive microsphere[J]. Chinese Journal of Pesticide Science, 2017, 19(2): 266-272. DOI: 10.16801/j.issn.1008-7303.2017.0035

    高效氯氰菊酯聚(N-正丙基丙烯酰胺)温敏微球的制备关键工艺研究

    Study on the key preparation process of beta-cypermethrin poly (N-propylacrylamide) temperature-sensitive microsphere

    • 摘要: 为获得防治桃小食心虫Carposina niponensis Walsingham的控释化农药产品,根据温敏材料聚(N-正丙基丙烯酰胺)(PNNPAM)的体积相转变温度与桃小食心虫出土高峰温度相近的特点,采用无皂乳液聚合法制备了高效氯氰菊酯PNNPAM温敏微球,并考察了反应温度及N-正丙基丙烯酰胺(NNPAM)、N,N-亚甲基双丙烯酰胺(MBA)质量浓度对温敏微球制备工艺的影响。结果表明:当反应温度为70~80℃时,可制得粒径为(601.3±5.6)~(638.6±8.9)nm、载药量和包埋率均较高的高效氯氰菊酯PNNPAM温敏微球,且载药量和包埋率随着NNPAM、MBA质量浓度的增加而增大,温度对该微球累积释放率有显著影响。

       

      Abstract: In order to develop a pesticide product for the control of Carposina niponensis Walsingham, beta-cypermethrin poly (N-propylacrylamide) (PNNPAM) temperature-sensitive microsphere was developed. Given that the volume phase transition of PNNPAM and the peak emergence of C. niponensis happen at similar temperature, the microsphere was prepared by a surfactant-free emulsion polymerization method. Effects of temperature, the concentration of N-propylacrylamide (NNPAM) and the concentration of N,N'-methylene diacrylamide (MBA) on the preparation of the microsphere were investigated. The results showed that, when the reaction temperature was 70-80℃, the particle size of the temperature-sensitive microsphere prepared was (601.3±5.6)-(638.6±8.9) nm, and the drug-loading and embedding rate of the microsphere were both relatively high. The drug-loading and embedding rate increased with the increase of the concentration of NNPAM and MBA. In addition, temperature had a significant influence on the cumulative release rate of microsphere.

       

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