A method for producing a click-active Janus particle includes combining seed particles with a monomer emulsion to obtain monomer-swollen seed particles; and polymerizing the monomer-swollen seed particles to obtain click-active Janus particles. A method for functionalizing a click-active Janus particle includes combining seed particles with a monomer emulsion to obtain monomer-swollen seed particles; polymerizing the monomer-swollen seed particles to obtain click-active Janus particles; and functionalizing the click-active Janus particles using one or more click chemistry reactions.

A method for producing a click-active Janus particle includes combining seed particles with a monomer emulsion to obtain monomer-swollen seed particles; and polymerizing the monomer-swollen seed particles to obtain click-active Janus particles. A method for functionalizing a click-active Janus particle includes combining seed particles with a monomer emulsion to obtain monomer-swollen seed particles; polymerizing the monomer-swollen seed particles to obtain click-active Janus particles; and functionalizing the click-active Janus particles using one or more click chemistry reactions.

Disclosed are compositions comprising HCFC-243db, HCFO-1233xf, HCFC-244 db and/or HFO-1234yf and at least one additional compound. For the composition comprising 1234yf, the additional compound is selected from the group consisting of HFO-1234ze, HFO-1243zf, HCFC-243db, HCFC-244db, HFC-245cb, HFC-245fa, HCFO-1233xf, HCFO-1233zd, HCFC-253fb, HCFC-234ab, HCFC-243 fa, ethylene, HFC-23, CFC-13, HFC-143a, HFC-152a, HFC-236fa, HCO-1130, HCO-1130a, HFO-1336, HCFC-133a, HCFC-254fb, CHF═CHCl, HFO-1141, HCFO-1242 zf, HCFO-1223xd, HCFC-233ab, HCFC-226ba, and HFC-227ca. Compositions comprising HCFC-243db, HCFO-1233xf, and/or HCFC-244db are useful in processes to make HFO-1234yf. Compositions comprising HFO-1234yf are useful, among other uses, as heat transfer compositions for use in refrigeration, air-conditioning and heat pump systems.

Various examples of systems and methods for making microspheres, microparticles, and emulsions are provided. In one example, a system and method for forming microspheres comprises: pumping a dispersed phase liquid and a continuous phase liquid into a levitating magnetic impeller pump to subject the dispersed phase liquid and continuous phase liquid to a high shear environment within the impeller pump's pump chamber. In another example, a system and method for forming an emulsion comprises: pumping a dispersed phase liquid and an inner aqueous phase liquid into a levitating magnetic impeller pump to subject the dispersed phase and the inner aqueous phase to a high shear environment within the impeller pump's pump chamber.

Various examples of systems and methods for making microspheres, microparticles, and emulsions are provided. In one example, a system and method for forming microspheres comprises: pumping a dispersed phase liquid and a continuous phase liquid into a levitating magnetic impeller pump to subject the dispersed phase liquid and continuous phase liquid to a high shear environment within the impeller pump's pump chamber. In another example, a system and method for forming an emulsion comprises: pumping a dispersed phase liquid and an inner aqueous phase liquid into a levitating magnetic impeller pump to subject the dispersed phase and the inner aqueous phase to a high shear environment within the impeller pump's pump chamber.

The present invention relates to a particulate carbon material that can be produced from renewable raw materials, in particular from biomass containing lignin, comprising: a 14C content that corresponds to that of the renewable raw materials, said content being preferably greater than 0.20 Bq/g carbon, especially preferably greater than 0.23 Bq/g carbon, but preferably less than 0.45 Bq/g carbon in each case; a carbon content in relation to the ash-free dry substance of between 60 ma. % and 80 ma. %; an STSA surface area of the primary particles of at least 5 m2/g and at most 200 m2/g; and an oil absorption value (OAN) of between 50 ml/100 g and 150 ml/100 g. The present invention also relates to a method for producing said carbon material and to the use thereof.

A method of the modification of the silicon surface that is used as an anode active material in lithium ion batteries, with all of the monomers and derivatives thereof (acrylate group, methacrylate group, styrene, vinyl acetate, acrylic acid and salts thereof) that contain an acrylic or methacrylic group.

A solid surfactant composition includes a water-wetting surfactant and a plant fiber carrying agent. A process includes forming a solid surfactant composition comprising a water-wetting surfactant and a plant fiber carrying agent and injecting the solid surfactant composition into a wellbore.

A liquid foam composition and a foam dispenser. The liquid foam composition includes a combination of water, a surfactant, and a emulsifier. The foam dispenser includes a container containing the liquid foam composition. The foam dispenser further includes a foam dispensing pump having mesh within a liquid passage, a closure securing the foam dispensing pump assembly within the container, and a nozzle operably connected to the foam dispensing pump and extending from the closure. The nozzle is fluidly connected to the liquid passage.

An aqueous radiation curable dispersant formulation includes water and styrene acrylic resin stabilized thioxanthone derivative photoinitiator particles dispersed in the water. The styrene acrylic resin stabilized thioxanthone derivative photoinitiator particles have a volume-weighted mean diameter of less than 40 nm. The styrene acrylic resin stabilized thioxanthone derivative photoinitiator particles include a water-insoluble, thioxanthone derivative photoinitiator core having one, two, or three units, wherein a structure of the unit is: and x=2-12. When the water-insoluble, thioxanthone derivative photoinitiator core includes two units or three units, the units are covalently bonded together.