Additional hydrophilic surfactants are generally introduced into W/O emulsion drag reducer systems to enhance the dissolution capacity of polymers. The hydrophilic surfactants may decrease the stability of W/O emulsion, which leads to deterioration of polymer emulsions in the storage and transport process instead. Herein, a pH-switchable surfactant, N-(2-morpholinoethyl) oleamide (NMEO) was designed for stabilizing a W/O emulsion drag reducer. The surface activity and solubility changes occurring at pH < 6 of NMEO guaranteed the phase inversion from W/O to O/W of emulsions upon pH stimulation. Based on optimal conditions (oil-water ratio of 0.429, NMEO concentration of 3 wt%, and pH of 6.5), the inverse emulsion polymerization of poly(acrylamide--acrylic acid--2-acrylamide-2-methylpropane sulfonic acid) was proceeded to obtain a W/O polymer emulsion with the pH-switchable behavior. It was demonstrated that the polymer emulsions were provided with prolonged storage stability by NMEO and could be stored for at least 30 days due to the absence of hydrophilic surfactants. The polymers were released and completely dissolved within 2.5 min by pH stimulation, compared with traditional emulsion polymers and powder polymers that require 4 and 17 min, respectively. In addition, the emulsion drag reducer prepared by NMEO provided drag-reduction performance of 64.67% at 0.021 wt% concentration. The pH-switchable behavior of NMEO promotes the validity of W/O polymer emulsions along with the capacity of rapid release and solubilization, which eliminates the imbalance between the long-term storage stability and rapid solubility of traditional drag reducers. Thus, NMEO-stabilized emulsion drag reducers are expected to be a promising alternative for traditional products.
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http://dx.doi.org/10.1021/acs.langmuir.3c01672 | DOI Listing |
Soft Matter
January 2025
Soft Condensed Matter Group, Raman Research Institute, C. V. Raman Avenue, Sadashivanagar, Bangalore 560 080, India.
The adsorption of charged clay nanoplatelets plays an important role in stabilizing emulsions by forming a barrier around the emulsion droplets and preventing coalescence. In this work, the adsorption of charged clay nanoplatelets on a preformed Latex microsphere in an aqueous medium is investigated at high temporal resolution using optical tweezer-based single-colloid electrophoresis. Above a critical clay concentration, charged clay nanoplatelets in an aqueous medium self-assemble gradually to form gel-like networks that become denser with increasing medium salinity.
View Article and Find Full Text PDFLangmuir
January 2025
National Key Laboratory of Oil and Gas Reservoir Geology and Exploitation, Southwest Petroleum University, Chengdu 610500, P. R. China.
To balance the stability and dissolution of polyacrylamide (PAM), emulsion drag reducers dominate the successful operation of volumetric fracturing. Herein, a pH-switchable four-tailed ionic liquid surfactant (OA/Cyclen) is synthesized by oleic acid (OA) and 1,4,7,10-tetraazacyclododecane (Cyclen). The four-tailed structure of OA/Cyclen enhances the stability of the emulsion polymerization reactor and supplies enough switchable sites for triggering the intensified release of the PAM emulsion.
View Article and Find Full Text PDFCarbohydr Polym
January 2025
State Key Laboratory of Materials-Oriented Chemical Engineering, School of Pharmaceutical Sciences, Nanjing Tech university, Nanjing 210009, Jiangsu Province, PR China.
Stimuli-responsive Pickering emulsions are promising in biocatalysis for their ease of product separation and emulsifier recovery. However, pH responsiveness, though simple and cost-effective, faces challenges in precise control and narrow transition ranges, limiting its use in enzymatic catalysis. Herein we introduced amorphous octenyl succinic anhydride-modified debranched starch chains (Am-OSA-St) to control emulsion properties within a pH range suitable for enzymatic catalysis.
View Article and Find Full Text PDFPhys Rev Lett
September 2024
New Cornerstone Science Laboratory, Center for Combustion Energy, Key Laboratory for Thermal Science and Power Engineering of Ministry of Education, Department of Energy and Power Engineering, Tsinghua University, 100084 Beijing, China.
Catastrophic phase inversion, the breakdown of a concentrated emulsion characterized by the most puzzling sudden feature, is crucial in numerous industrial applications. Here we combine well-controlled experiments and fully resolved numerical simulations to study the critical dynamics of catastrophic phase inversion in oil-water emulsions under turbulent flow as the phase-inversion volume fraction is approached. We reveal that the phase inversion is characterized by the critical power-law divergence of fluctuations in the global drag force.
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