The Compressibility of pH- Sensitive Microgels at the Oil- Water Interface: Higher Charge Leads to Less Repulsion

被引:89
作者
Geisel, Karen [1 ]
Isa, Lucio [2 ]
Richtering, Walter [1 ]
机构
[1] Rhein Westfal TH Aachen, D-52056 Aachen, Germany
[2] ETH, Dept Mat, Lab Interfaces Soft Matter & Assembly, CH-8093 Zurich, Switzerland
关键词
compression isotherms; electrostatic interactions; interfaces; pH-sensitive microgels; Pickering emulsions; POLY-N-ISOPROPYLACRYLAMIDE; ANGLE NEUTRON-SCATTERING; CORE-SHELL MICROGELS; POLY(N-ISOPROPYLACRYLAMIDE) MICROGELS; SOFT MICROGELS; EMULSION STABILIZERS; PARTICLES; TEMPERATURE; BEHAVIOR; MONOLAYERS;
D O I
10.1002/anie.201402254
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
pH-responsive microgels are unique stabilizers for stimuli-sensitive emulsions that can be broken on demand by changing the pHvalue. However, recent experiments have indicated that electrostatic interactions play a different role to that in conventional Pickering emulsions. The influence of charges on the interactions between microgels at the oil-water interface is now described. Compression isotherms of microgels with different charge density and architecture were determined in a Langmuir trough, and counter-intuitive results were obtained: Charged microgels can be compressed more easily than uncharged microgels. The compressibility of microgels is thus not determined by direct Coulomb repulsion. Instead, the different swelling of the microgels in the charged and the uncharged states is proposed to be the key parameter.
引用
收藏
页码:4905 / 4909
页数:5
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