222 results about "Hydrophilic-lipophilic balance" patented technology

Composition for pharmaceutical or cosmetic use, capable of forming a microemulsion, comprising at least: an active principle, a lipophilic phase consisting of a mixture of fatty acid esters and glycerides, a surfactant (SA), a cosurfactant (CoSA), a hydrophilic phase, characterized: in that the lipophilic phase consists of a mixture of C8 to C18 polyglycolized glycerides having a hydrophilic-lipophilic balance (HLB) of less than 16, this lipophilic phase representing from 30 to 75% of the total weight of the composition; in that the surfactant (SA) is chosen from the group comprising saturated C8-C10 olyglycolized glycerides and oleic esters of polyglycerol, this surfactant having an HLB of less than 16; in that the cosurfactant (CoSA) is chosen from the group comprising lauric esters of propylene glycol, oleic esters of polyglycerol and ethyl diglycol; in that the SA/CoSA ratio is between 0.5 and 6; and in that the hydrophilic phase of the final microemulsion is supplied after ingestion by the physiological fluid of the digestive milieu.

The present invention relates to the development of tracer fluids, more generally, that of aqueous liquids, intended to be injected under pressure in an oil reservoir, for example from an injection well up to a production well.

The object of the invention is to propose a new method of study of a solid medium, i.e. an oil reservoir, by diffusion of a liquid (i.e. injection waters) containing tracers, through said solid medium, which is simple to implement and economical and which remedies the drawbacks of the known tracers for injection waters of oil reservoirs.

This method essentially consisting of injecting, in this solid medium, an injection liquid comprising a nanoparticle-based tracer having average dimensions comprised between 20 and 200 nm, detectable by means of one or several S signals at dilutions of less than or equal to 10⁻⁷, adapted to form a stable colloidal suspension in a saline medium, at least a portion of which is constituted of a core and a coating provided with an adjustable hydrophilic-lipophilic balance (HLB) and comprising at least one organic and/or organosilicon component; recovering the liquid having diffused; and analyzing this liquid having diffused to measure the quantity of tracer by detection of the signal or signals S.

The present invention relates to biocompatible microemulsion systems designed for controlled release drug delivery applications formulated with phospholipids such as lecithin (surfactant), a lipophilic additive (linker) containing 9 or more carbons in their alkyl group and hydrophilic-lipophilic balance (HLB) of 5 or less, and a surfactant-like hydrophilic additive (linker) containing between 6 to 9 carbon atoms in their alkyl tail. The combination of linkers and phospholipids produce formulations capable of delivering high concentrations of poorly soluble drugs into epithelial tissue using low surfactant concentrations, with minimum cytotoxic side effects.

Disclosed and claimed is a microemulsion flowback aid composition and a method of enhancing recovery of oil or gas during fracturing or stimulation processes. The microemulsion flowback aid composition includes (i) an oil-like phase comprising at least one nonionic surfactant having a hydrophilic-lipophilic balance (HLB) of less than about 9; (ii) a coupling agent capable of stabilizing the microemulsion flowback aid composition; (iii) at least one water-soluble or dispersible nonionic surfactant that is different from the at least one nonionic surfactant in the oil-like phase; (iv) at least one additional surfactant selected from anionic, cationic, amphoteric, and combinations thereof; and (v) water.

A well treatment microemulsion includes an oil external phase, an internal aqueous phase and a hydrophilic surfactant. The surfactant has a hydrophile lipophile balance of between 8-18. The oil external phase may include d-Limonene, xylenes, light mineral oil, or kerosene. The surfactant is configured to emulsify the water of the internal aqueous phase into the oil of the external (continuous) phase. The surfactant may include polyoxyethylene sorbitan monooleate, polyoxyethylene sorbitan tristearate, polyoxyethylene hydrogenated castor oil, polyoxyethylene sorbitan monostearate, polyoxyethylene sorbitan monooleate, polyoxyethylene sorbitan monolaurate or mixtures therebetween. The use of hydrophilic surfactants to emulsify an internal aqueous phase within an oil external microemulsion produces unexpected and beneficial results.

A barrier composition which is injection mouldable and able to be made into a transparent film or incorporated (by co-extrusion and/or lamination) into multi-layer film products, the composition on dry basis: a) from 45 to 90% by weight of a starch and/or a modified starch selected from starches modified by reaction with a hydroxyl alkyl group, an acetate or a dicarboxylic acid anhydride or a grafting polymer; b) from 4 to 12% by weight of a water soluble polymer selected from polyvinyl alcohol, polyvinylacetate, and copolymers of ethylene and vinylalcohol which have a melting point compatible with the molten state of the starch components c) from 5 to 45% by weight of a non-crystallising mixture of sorbitol and at least one other plasticizer selected from glycerol, maltitol, xylitol, mannitol, glycerol trioleate, epoxidised linseed or soybean oil, tributyl citrate, acetyl tri-ethyl citrate, glyceryl triacetate, 2,2,4-trimethyl-1,3-pentanediol diisobutyrate; polyethylene oxide or polyethylene glycol; d) from 0.3 to 2.5 % by weight of a C12-22 fatty acid or salt; e) from 0.25% to 3% of an emulsifier system having a hydrophilic lipophilic balance value between 2 and 10. The barrier film may be co-injection moulded with polyethylene terephthalate (PET) or polylactic acid (PLA) for blow moulding into beverage bottles, with polyethylene (PE) or polypropylene (PP) or biodegradable polymers for high gas-barrier containers or closures, or may be co-extruded with polyethylene, polypropylene or polylactic acid for thin film packaging applications or for blow-moulded containers.

The invention discloses a preparation method of a polyether modified polysiloxane foam stabilizer and relates to a preparation method of a foam stabilizer for flexible polyurethane foam. The polyether modified polysiloxane foam stabilizer is generated through reaction between allyl epoxyethane and methyloxirane methyl ethers with different molecular weights and silicone oil with low hydrogen content under the conditions that methylbenzene as a solvent and chloroplatinic acid as a catalyst. Through controlling the degree of polymerization of a hydrophilic polyether chain segment and a hydrophobic polysiloxane chain segment of polyether modified polysiloxane, the foam stabilizer has precise hydrophilic-lipophilic balance property, better emulsifying property and a favorable foam stabilizing effect, so that a flexible polyurethane foam mixture has enough stability in a coring stage, a form hole growing stage, a punching stage and an early-stage crosslinking stage, and foam collapse cannot be caused.

A nanoemulsion having reversible continuous and dispersed phases. The nanoemulsion includes an aqueous phase and an oil phase, a weight ratio of the aqueous phase to the oil phase being 1:40-100:1. In the nanoemulsion, the aqueous phase is dispersed as nanosized droplets in the oil phase or the oil phase is dispersed as nanosized droplets in the aqueous phase. The aqueous phase contains water or a water solution and a water-soluble organic nanostructure stabilizer. The oil phase contains an oil or an oil solution, an organic gel thickener, and a hydrophilic surfactant having a hydrophilic-lipophilic balance value greater than 8.0. Also disclosed is a method for preparing the above-described nanoemulsion.

A new method of improving the process of dewatering fine particulate materials is disclosed. In this method, an aqueous slurry of fine particles is treated with appropriate hydrophobizing reagents so that the particulate material becomes moderately hydrophobic with its water contact angle considerably below 90°. A low hydrophile-lipophile balance (HLB) number surfactant is then added to the slurry, so that the surfactant molecules adsorb on the moderately hydrophobic surface primarily by hydrophobic attraction and, thereby, increase its contact angle close to or above 90°. By virtue of the greatly enhanced hydrophobicity, the water molecules adhering to the surface are destabilized and removed more readily by a mechanical dewatering process. Any nonionic surfactant with its HLB number below about 15 may be used for the hydrophobicity enhancement. The surfactants may be used in conjunction with appropriate solvents such as light hydrocarbon oils and short-chain alcohols. The moisture reduction can be further improved by using appropriate electrolytes in conjunction with the low HLB surfactants, spraying surface tension lowering reagents onto the filter cake, subjecting the cake to a suitable vibratory means, and by using combinations thereof.

The invention provides methanol diesel fuel, which comprises the following components in percentage by volume: 40 to 85 percent of diesel fuel, 5 to 40 percent of methanol, 0.1 to 2 percent of surfactant with the hydrophile-lipophile balance value of 3 to 6, 5 to 30 percent of cosurfactant and 0.1 to 1 percent of aid. The invention also provides a preparation method for the methanol diesel fuel, which comprises the following steps of: uniformly mixing the diesel fuel and the surfactant with the hydrophile-lipophile balance value of 3 to 6, adding the methanol, and uniformly mixing to prepare microemulsion; and adding the cosurfactant and the aid into the microemulsion, and uniformly mixing to prepare the methanol diesel fuel. In the methanol diesel fuel, the methanol and the diesel fuel form the transparent and stable microemulsion under the action of the surfactant and the cosurfactant, so that the prepared methanol diesel fuel has better stability and no demixing after a long time.

Colorless or colored coatings can be ink jetted onto a substrate using an aqueous particle-free inkjet ink composition that has a viscosity of less than 5 centipoises, and that includes a combination of an anionic polyether polyurethane and an anionic acrylic polymer or anionic styrene-acrylic polymer, in a total amount of less than or equal to 20 weight %. The composition can be colorless (free of colorants) or it can contain a suitable colorant to provide a color image. The composition also includes a defoamer that has a hydrophilic-lipophilic balance value of at least 3 and up to and including 5, and which is present in an amount of at least 0.15 weight % and up to and including 1 weight %. Such composition can be used in inkjet printing methods including recirculation apparatus and methods, and can be provided as part of an ink set.

A color-appearing ink composition includes a surfactant blend of at least two non-ionic surfactants having hydrophilic-lipophilic balance values greater than 10, or a non-ionic surfactant having a hydrophilic-lipophilic balance value greater than 10 and a charged surfactant. The composition includes one or more water-insoluble leuco dyes, a developer and a desensitizer. The composition may be applied to a substrate to form a sensor.

This invention provides a self-emulsifying composition comprising 50 to 95% by weight in total of at least one compound selected from the group consisting of ω3 polyunsaturated fatty acids and their pharmaceutically acceptable salts and esters; and 5 to 50% by weight of an emulsifier having a hydrophilic lipophilic balance of at least 10. The composition has no or reduced ethanol content, and exhibits excellent self-emulsifying property, dispersibility in the composition, emulsion stability, and absorption property. The composition is adapted for use as a drug.

The invention provides a polyurethane coating, which comprises the following components: A) surface-modified nanometer titania, B) polyalcohol and C) isocyanate, wherein the surface-modified nanometer titania consists of nanometer titania particles serving as a matrix and a nonionic surfactant which is coated on the surface of the nanometer titania matrix; the grain size of the nanometer titania matrix is 1 to 100nm; the hydrophilic-lipophilic balance value of the nonionic surfactant is 1 to 10; the nonionic surfactant is 1 to 20 percent based on the weight of the nanometer titania matrix; the surface-modified nanometer titania is 2 to 15 percent based on the weight of the polyalcohol; and the weight ratio of the polyalcohol to the isocyanate is 10:1-2:1. The invention also provides a method for preparing the polyurethane coating.

This invention relates to a method of using boied hemp or papermaking waste liquor to extract lignosulphonate. Firstly boied hemp or papermaking waste liquor proceed microfiltration and hyperfiltration; take lignin concentrated solution 25 to 50 parts by weight, put at reactor; unlock whipper, add 10% sulfuric acid 5 to 15 parts by weight, at 60 to 80 deg take reaction for 2 to 4hours, then add sulfite 10 to 30 parts by weight, ferric chloride or bluestone 2 to 6 parts by weight, at 80 to 100deg take reaction for 3 to 5hours, adjust pH value 7 to 8, gain lignosulphonate solution. The lignosulphonate has many active group, possess good surface activity and hydrophile-lipophile balance, good solubility and dispersibility, higher yield and good quality.

A method for producing a colored cosmetic composition having inorganic pigments resistant to agglomeration in an oil-in-water emulsion. The method includes the following: preparing an oil dispersion by adding inorganic pigments directly to an oil; preparing an aqueous base that includes water; combining the oil dispersion and aqueous base; and partitioning the inorganic pigments between the oil and the aqueous phase under controlled conditions, for example, hydrophile-lipophile balance, agitation time and speed, and cooling rate. The present invention provides a process to easily disperse iron-oxide pigments, even black iron-oxide pigments, in oil-in-water emulsions. The present invention provides colored cosmetic compositions that have excellent properties, such as smoothness, adhesion to skin, uniform color, ease of removal, smudge resistance and non-oiliness.

The invention relates to a preparation of a double-long-chain non-ionic oil-removing surfactant and applications, belonging to colloid and interface chemistry fields. In the invention, by reacting fatty alcohol with chloropropylene oxide and ethylene oxide, a novel non-ionic surfactant-double-long-chain alkyl glyceryl ether ethoxy compound is prepared. The surfactant has excellent chemical stability, acid and alkali resistance and inorganic electrolyte, wherein the hydrophile lipophile balance can be regulated by controlling alkyl chain length of the raw material fatty alcohol and ethylene oxide number of added on each molecule. The surfactant has big saturation adsorption quantity on a water/air and oil/water interface, thereby high efficiency reducing a tensile force of a crude oil/water interface. The surfactant can be matched to other surfactants, wherein a mol fraction of the surfactant is 0.1-0.5, and a total mass fraction of the surfactant is in a range of 0.05-0.5%, under an oil reservoir temperature 45 DEG C, the interface tension force of Daqing crude oil/stratum water is reduced to 10-3mN/m order of magnitude, without addition of any acid salt, basic salt, neutral electrolyte and cosurfactant. Therefore, the surfactant is suitable for being used as an alkali-free oil displacement agent.

The invention belongs to the technical field of potato cultivation, and discloses an application of a biodegradable weeding mulching film in potato cultivation. The mulching film comprises the following components in percentage by mass: 70-97% of biodegradable resin A and 3-30% of biodegradable herbicide master batches, wherein the biodegradable herbicide master batches are prepared by a method comprising the following steps: mixing 10-60% of a herbicide with 0.5-7% of a surfactant A, and performing ultrasonic activation; and mixing 25-75% of biodegradable resin B and 1-10% of a surfactant B at a high speed, and performing extrusion and granulation, thereby obtaining the herbicide master batches, wherein the mass ratio of the surfactant A (the hydrophilic-lipophilic balance value is 7-10) to the surfactant B (the hydrophilic-lipophilic balance value is 3-6) is (1:1)-(1:2). As the biodegradable weeding mulching film is used in potato cultivation, the problems that weeds can grow out from furrow surfaces and environment pollution can be caused by common plastics can be effectively prevented, and the labor cost can be lowered.

The invention discloses a coenzyme Q10 self-emulsifying composition, a preparation method and the application thereof. The composition comprises the components with the mass parts: 0.5-20 parts of coenzyme Q10, more than 0 parts and less than or equal to 30 parts of medium chain fatty acid triglycercide, 0.5-50 parts of phospholipid, 5-50 parts of surface active agent and 10-60 parts of latent solvent; wherein the surface active agent has the hydrophile-lipophile balance value being more than 10, and the latent solvent is alcohol having 1-3 carbon atoms in a carbon chain. The components are heated at the temperature of 50-55 DEG C and stirred to be evenly mixed, so that the coenzyme Q10 self-emulsifying composition can be obtained; the whole preparation process requires to be kept in dark place. The coenzyme Q10 self-emulsifying composition can be fully self-emulsified to form nano-emulsion with the grain diameter of below 200nm in aqueous medium, so that the problem of insolubility of the coenzyme Q10 can be solved; meanwhile, the bioavailability and the stability of the coenzyme Q10 are obviously improved, so that the coenzyme Q10 self-emulsifying composition can be used for the drugs, health-care foods and cosmetic additive which take the coenzyme Q10 as active ingredient.

Aqueous blood-sample diluting reagent and method of its use for compelling a morphological change in a blood sample to yield an MCV value assayed at elapsed time after the sample is drawn to be consistent within a diagnostically acceptable range with the original, immediate post-drawing MCV value. Selection of a small amount of a predetermined surfactant added within a limited range of concentration, and of a salt for adjusting osmotic pressure of the sample is thereby determined. The blood sample is treated with an anti-coagulant agent immediately post-drawing, and for assay in a particle analyzer at post-drawing elapsed time is diluted with the reagent solution. The reagent has an osmotic pressure (pi) of approximately 150-400 mOsm/kg and a pH of 6.0-8.5. The surfactant is present in a 0.0005% to 0.5% concentration and has a hydrophile-lipophile balance (HLB) of 10-20.

Disclosed is a three-phase emulsion comprising an aqueous-gel outer phase; and a water-in-oil inner phase, wherein the emulsion is stable. The aqueous-gel outer phase can include 10% to 50% by weight of the total weight of the emulsion. This phase can also include 70% to 95% by weight of water based on the total weight of the aqueous-gel outer phase, a gelling agent, and an emulsifier having a hydrophilic-lipophilic balance (HLB) value of 10 to 19. The water-in-oil inner phase can include 50% to 95% by weight based on the total weight of the three-phase emulsion. This phase can also include 50% to 80% by weight of water based on the total weight of the water-in-oil inner phase, 20% to 50% by weight of oil based on the total weight of the water-in-oil inner phase, and an emulsifier.