化学
皮克林乳液
超强酸
亲脂性
沸石
两亲性
碳氢化合物
乳状液
催化作用
化学工程
有机化学
水溶液
煅烧
层状结构
共聚物
工程类
聚合物
结晶学
作者
Zhifeng Zeng,Fei Ma,Shuang-Jia Wang,Jiali Wen,Xiangqiong Jiang,Gaoyu Li,Tong Yan,Xiaolong Liu,Jiuxing Jiang
摘要
The formation of oil-in-water Pickering emulsions stabilized by lamellar zeolite MWW (International Zeolite Association, three-letters code) emulsifier without surface grafting is investigated. The crucial emulsification factors are the oligolayer morphology and amphiphilicity developed upon acidic treatment (NH4+ exchange/calcination, HNO3 treatment). In contrast with the readily available/abundant hydrophilic ≡Si–OH group in layer MWW, the lipophilicity generated by strong acid sites is another key to the success of emulsification. Hydrocarbon–strong acid site interaction is long known in petrochemistry and superacid research. However, to the best of our knowledge, this interaction was first introduced to gain lipophilicity in emulsion formation. Finally, the Pd-loaded acidic form of the MWW zeolite successfully stabilized the toluene/H2O emulsion system. The biphasic interfacial nitroarene hydrogenation demonstrated excellent catalytic performance. Overall, this work provided not only a new kind of intrinsic solid to emulsify the organic-aqueous biphase system but also a new mechanism to generate lipophilicity. Both are important for the applications and designs of Pickering emulsion materials.
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