Preparation of Hollow Silica Nanoparticles Using Fluorinated Surfactant and Fluorocarbon Solvents

In this study, we used a new class of fluorinated surfactant as a soft template for the preparation of the hollow silica nanoparticles. The size of the hollow silica nanoparticles was enlarged by incorporating a variety of swelling agents (perfluorodecalin, perfluorotributylamine, perfluorooctane, and perfluorooctyl bromide) into the cores of the micelles of the fluorinated surfactant. However, once we used the perfluorinated acids (perfluorooctadecanoic acid and perfluorodecanoic acid) as swelling agents, the structure of silica nanoparticles is solid without the formation of hollow voids. The TEM analysis combined with copper elemental mapping of the hollow silica loaded with copper hexadecafluorophthalocyanine indicated that the cores of the hollow silica nanoparticles are hydrophobic. The formation mechanism of the hollow silica nanoparticles is similar to that prepared by hydrocarbon surfactant/hydrocarbon, which was supported by the zeta potential measurements. The prepared hollow silica nanoparticles had the type IV isotherm with the H3 hysteresis loop.

Milling Performance of Fluorinated Surfactants-Based Coating Tools in Processing Particleboard

To investigate the cutting performance of tools with fluorinated surfactant-based coatings, the milling performance of melamine-coated particleboard was characterized by means of the cutting force, tool wear and surface quality. A scanning electron microscope (SEM) and a three-dimensional super field microscope were used to observe the morphologies of coated and uncoated tool wear and machined surfaces. The results showed that (1) the surface wettability of the coated tool is lower than that of the uncoated tool; (2) the main wear mechanisms for tools with a fluorinated surfactant-based coating are abrasive wear and microchipping. The fluorinated surfactant-based coating acts as a solid lubricant, which can obviously reduce adhesion wear; (3) the surface roughness obtained by machining using coated tools is much smaller than that found for uncoated tools.

Thermo-responsive fluorinated surfactant for on-demand demulsification of microfluidic droplets

Thermo-responsive fluorinated surfactant can lead to destabilization of droplets and subsequently cause droplet coalescence. Thus, the encapsulated cargoes can be retrieved on-demand from the droplets without complicated processing.

Fluorinated Surfactant Adsorption on Mineral Surfaces: Implications for PFAS Fate and Transport in the Environment

Fluorinated surfactants, which fall under the class of per- and polyfluoroalkyl substances (PFAS), are amphiphilic molecules that comprise hydrophobic fluorocarbon chains and hydrophilic head-groups. Fluorinated surfactants have been utilized in many applications, e.g., fire-fighting foams, paints, household/kitchenware items, product packaging, and fabrics. These compounds then made their way into the environment, and have been detected in soil, fresh water, and seawater. From there, they can enter human bodies. Fluorinated surfactants are persistent in water and soil environments, and their adsorption onto mineral surfaces contributes to this persistence. This review examines how fluorinated surfactants adsorb onto mineral surfaces, by analyzing the thermodynamics and kinetics of adsorption, and the underlying mechanisms. Adsorption of fluorinated surfactants onto mineral surfaces can be explained by electrostatic interactions, hydrophobic interactions, hydrogen bonding, and ligand and ion exchange. The aqueous pH, varying salt or humic acid concentrations, and the surfactant chemistry can influence the adsorption of fluorinated surfactants onto mineral surfaces. Further research is needed on fluorinated surfactant adsorbent materials to treat drinking water, and on strategies that can modulate the fate of these compounds in specific environmental locations.

Effect of a synthesized anionic fluorinated surfactant on wettability alteration for chemical treatment of near-wellbore zone in carbonate gas condensate reservoirs

The pressure drop during production in the near-wellbore zone of gas condensate reservoirs causes condensate formation in this area. Condensate blockage in this area causes an additional pressure drop that weakens the effective parameters of production, such as permeability. Reservoir rock wettability alteration to gas-wet through chemical treatment is one of the solutions to produce these condensates and eliminate condensate blockage in the area. In this study, an anionic fluorinated surfactant was synthesized and used for chemical treatment and carbonate rock wettability alteration. The synthesized surfactant was characterized by Fourier transform infrared spectroscopy and thermogravimetric analysis. Then, using surface tension tests, its critical micelle concentration (CMC) was determined. Contact angle experiments on chemically treated sections with surfactant solutions and spontaneous imbibition were performed to investigate the wettability alteration. Surfactant adsorption on porous media was calculated using flooding. Finally, the surfactant foamability was investigated using a Ross–Miles foam generator. According to the results, the synthesized surfactant has suitable thermal stability for use in gas condensate reservoirs. A CMC of 3500 ppm was obtained for the surfactant based on the surface tension experiments. Contact angle experiments show the ability of the surfactant to chemical treatment and wettability alteration of carbonate rocks to gas-wet so that at the constant concentration of CMC and at 373 K, the contact angles at treatment times of 30, 60, 120 and 240 min were obtained 87.94°, 93.50°, 99.79° and 106.03°, respectively. However, this ability varies at different surfactant concentrations and temperatures. The foamability test also shows the suitable stability of the foam generated by the surfactant, and a foam half-life time of 13 min was obtained for the surfactant at CMC.

Perfluorooctanoate in Aqueous Urea Solutions: Micelle Formation, Structure, and Microenvironment

Fluorinated surfactants are used in a wide range of applications that involve aqueous solvents incorporating various additives. The presence of organic compounds such as urea is expected to affect the self-assembly of fluorinated surfactants, however, very little is known about this. We investigated the effect of urea on the micellization in water of the common fluorinated surfactant ammonium perfluorooctanoate (APFO), and on the structure and microenvironment of the micelles that APFO forms. Addition of urea to aqueous APFO solution decreased the critical micellization concentration (CMC) and increased the counterion dissociation. The observed increase in surface area per APFO headgroup and decrease in packing density at the micelle surface suggest the localization of urea at the micelle surface in a manner that reduces headgroup repulsions. Micropolarity data further support this picture. The results presented here indicate that significant differences exist between urea effects on fluorinated surfactant and on hydrocarbon surfactant micellization in aqueous solution. For example, the CMC of sodium dodecyl sulfate (SDS) increased with urea addition, while the increase in surface area per headgroup and packing density of SDS with urea addition are much lower than those observed for APFO. This study informs fluorinated surfactant fate and transport in the environment, and also applications involving aqueous media in which urea or similar additives are present.