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Preparation and application performance of lignin-polyurea composite microcapsule with controlled release of avermectin

机译:木质素 - 聚脲复合微胶囊的制备及应用性能,具有温度素控制释放

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Pickering emulsion stabilized by lignin/sodium dodecyl sulfate composite nanoparticles (LSNP) was used as template to prepare the avermectin @ lignin/polyurea composite microcapsules (AVM@LPMC) through ion cross-linking and interfacial polymerization. The inner wall of the microcapsules is a firm and compact polyurea layer, and the outer wall is a loose lignin layer. The effects of stirring speed, dosage of sodium dodecyl sulfate (SDS), and pH value in aqueous phase on the formation of microcapsules were systematically studied. The results showed that the optimal stirring speed was 200 rpm, and the optimal dosage ratio in water phase was HCl (mmol):SDS (mmol):lignin AL (g) = 0.375:1.25:1 in fixed oil-water ratio (1:9) and oil phase composition. In this way, the encapsulation efficiency of microcapsules could reach up to 85.4%, while it would slightly decrease with the increase of lignin content in the wall materials. The polyurea layer played a key role in supporting the spherical structure of the capsule wall and delaying the release of avermectin, while the loose lignin layer contributed less to the slow release performance of microcapsule. By changing the amount of lignin, the polyurea-layer thickness could be regulated to adjust the release rate of microcapsule. Remarkably, a small amount of lignin introduced in the wall material could significantly improve the anti-photolysis performance of avermectin in microcapsules.
机译:用木质素/十二烷基硫酸钠复合纳米颗粒(LSNP)稳定的皮克林乳液用作模板,通过离子交联和界面聚合制备Avermectin / Polyurea复合微胶囊(AVM-LPMC)。微胶囊的内壁是固件和紧凑的聚脲层,外壁是松散的木质素层。系统地研究了搅拌速度,十二烷基硫酸钠(SDS)的剂量和水相的pH值的影响。结果表明,最佳搅拌速度为200 rpm,水相中的最佳剂量比为HCl(mmol):SDS(mmol):Lignin Al(g)= 0.375:1.25:1,固定油水比(1 :9)和油相组成。以这种方式,微胶囊的封装效率可达85.4%,而壁材料中木质素含量的增加会略微降低。聚脲层在支撑胶囊壁的球形结构中起着关键作用,并延迟了Avermectin的释放,而松散的木质素层对微胶囊的缓慢释放性能较低。通过改变木质素的量,可以调节聚脲层厚度以调节微胶囊的释放速率。值得注意的是,在墙壁材料中引入的少量木质素可以显着提高微胶囊中的Avermectin的抗光解性能。

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