512 results about "Quaternary ammonium surfactant" patented technology

Electrolyte solutions of soluble bifunctional redox dyes in molten salt solvent may be used to prepare electrooptic devices with enhanced stability toward ultraviolet radiation. The solvents include lithium or quaternary ammonium cations, and perfluorinated sulfonylimide anions selected from trifluoromethylsulfonate (CF₃SO₃⁻), bis(trifluoromethylsulfonyl)imide ((CF₃SO₂)₂N⁻), bis(perfluoroethylsulfonyl)imide ((CF₃CF₂SO₂)₂N⁻) and tris(trifluoromethylsulfonyl)methide ((CF₃SO₂)₃C⁻).

Crystalline molecular sieves are prepared using a mixture comprising an organic structure directing agent capable of forming the molecular-sieve and an N,N,N-trialkyl benzyl quaternary ammonium cation.

The invention discloses a preparation method for a Beta zeolite molecular sieve with a hierarchical porous structure. Ethyl orthosilicate is used as a silicon source, sodium metaaluminate is used as an aluminum source, hexaammonio cationic quaternary ammonium surfactant is used as a template, and then the hierarchical porous zeolite molecular sieve containing meso pores and Beta zeolite micropores is prepared by using a hydro-thermal synthesis process under an alkaline condition. According to the invention, the hexaammonio cationic quaternary ammonium surfactant is used as a Beta zeolite structure guiding agent and generates micropores, aggregation of hydrophobic long-chain alkyl groups on the surfactant forms the meso pores, so the prepared Beta zeolite molecular sieve has both meso pores and the crystalline micropores. The structure with both the meso pores and the micropores enables defects of a single pore structure to be avoided and mass transfer efficiency to be improved, and the Beta zeolite molecular sieve has a wide application prospect in aspects of macro-molecular catalysis, adsorption, separation, etc.

Electrolyte solutions for electrochromic devices such as rear view mirrors and displays with low leakage currents are prepared using inexpensive, low conductivity conductors. Preferred electrolytes include bifunctional redox dyes and molten salt solvents with enhanced stability toward ultraviolet radiation. The solvents include lithium or quaternary ammonium cations, and perfluorinated sulfonylimide anions selected from trifluoromethylsulfonate (CF₃SO₃⁻), bis(trifluoromethylsulfonyl)imide ((CF₃SO₂)₂N⁻), bis(perfluoroethylsulfonyl)imide ((CF₃CF₂SO₂)₂N⁻) and tris(trifluoromethylsulfonyl)methide ((CF₃SO₂)₃C⁻). Electroluminescent, electrochromic and photoelectrochromic devices with nanostructured electrodes include ionic liquids with bifunctional redox dyes. Some of the electrolyte solutions color to red when devices employing the solutions are powered, leading to red or neutral electrooptic devices.

An aqueous hard surface cleaner with improved soil removal is provided and has, as components, the following:(a) either an anionic, nonionic, amphoteric surfactant, and mixtures thereof with optionally, a quaternary ammonium surfactant, the total amount of the surfactants being present in a cleaning effective amount;(b) at least one water-soluble or dispersible organic solvent having a vapor pressure of at least 0.001 mm Hg at 25° C., present in a solubilizing-or dispersion-effective amount;(c) Tetrapotassium ethylenediamine-tetraacetate (potassium EDTA) as a chelating agent, present in an amount effective to enhance soil removal in said cleaner; and(d) the remainder, water.

The invention discloses a preparation method of fewer-layer graphene, which comprises the following steps of: putting graphite into solution containing a tetraalkyl-substituted quaternary ammonium cation and OH- for ultrasonic treatment in combination with a liquid phase intercalation technology and a microwave irradiation technology, so that the tetraalkyl-substituted quaternary ammonium cation is inserted into the middle of a graphite layer to form an intercalation layer, and the spacing of the graphite layer is increased; then carrying out microwave irradiation on the treated graphite, so that the graphite intercalation layer is decomposed to generate a large quantity of gas and further increase the spacing of the graphite layer; successively dispersing the treated graphite in a low-polarity organic solvent for ultrasonic treatment, so that the graphite is stripped to generate the grapheme; and finally carrying out centrifugal treatment to obtain upper-layer liquid after treatment, i.e. fewer-layer graphene dispersion liquid. The preparation method has the advantages of simplicity in operation, short time consumption, low cost, high grapheme yield, good repeatability and easy realization of industrialized mass production; and the fewer-layer graphene prepared by the preparation method is below 10 in quantity of layers and has the advantages of fewer defects, fewer oxygen-contained groups and high conductivity.

A process for forming a solder bump on an under bump metal structure in the manufacture of a microelectronic device comprising exposing the under bump metal structure to an electrolytic bath comprising a source of Sn²⁺ ions, a source of Ag⁺ ions, a thiourea compound and/or a quaternary ammonium surfactant; and supplying an external source of electrons to the electrolytic bath to deposit a Sn—Ag alloy onto the under bump metal structure.

The present invention is directed to a process for producing crystalline zeolites from a reaction mixture containing an N,N,N-trialkyl benzyl quaternary ammonium cation as a structure directing agent.

A single-compartment reversible mirror device having a solution of aprotic molten salt, at least one soluble metal-containing species comprising metal capable of being electrodeposited, and at least one anodic compound capable of being oxidized was prepared. The aprotic molten salt is liquid at room temperature and includes lithium and/or quaternary ammonium cations, and anions selected from trifluoromethylsulfonate (CF₃SO₃⁻), bis(trifluoromethylsulfonyl)imide ((CF₃SO₂)₂N⁻), bis(perfluoroethylsulfonyl)imide ((CF₃CF₂SO₂)₂N⁻) and tris(trifluoromethylsulfonyl)methide ((CF₃SO₂)₃C⁻). A method for preparing substantially pure molten salts is also described.

The invention provides an improved, liquid aqueous hard surface cleaner containing a fluoropolymer having a molecular weight of no less than 5,000, further containing preferably a nonionic surfactant, optionally, a quaternary ammonium compound, a chelating agent/buffer and water to provide enhanced cleaning of hard surfaces, especially vitreous surfaces, in which the thus cleaned surface is rendered soil and stain repellent.

The invention discloses a rosinyl bis-quaternary ammonium surfactant, the general molecular formula of which is as follows. In the formula, R is a rosinyl ricyclic diterpene structure, X is Br or I, and n is larger than or equal to 1 and smaller than or equal to 10. The invention also discloses a method for preparing the compound: firstly, dehydroabietic acid or disproportionated rosin is adopted to prepare rosinyl tertiary amine, and then the rosinyl tertiary amine and saturated dihalide are prepared into the rosinyl bis-quaternary ammonium surfactant through quaternization. The synthesis of the rosinyl tertiary amine comprises the following steps: the dehydroabietic acid or the disproportionated rosin is converted into active acyl chloride intermediate, and then the acyl chloride intermediate and N,N-dimethyl ethanolamine are prepared into the rosinyl tertiary amine in the presence of the triethylamine which is used as the acid-binding agent. The rosinyl tertiary amine and the saturated dihalide are reacted in the solvent isopropyl alcohol, and then vacuum drying is performed after filtration. The prepared surface active agent has good surface activity performance; the raw material is inexpensive and easy to obtain, and can be biodegraded; the synthetic method is assisted with microwave, the reaction time is short, and the product purity is high.

The invention discloses an ionic liquid mixed electrolyte for a lithium ion battery. The ionic liquid mixed electrolyte comprises lithium salt, ionic liquid and a non-aqueous organic solvent, wherein the lithium salt is one or mixture of two of lithium bis borate and lithium difluoroborate; cations in the ionic liquid are selected from one of imidazole cations, piperidine cations, pyridine cations, pyrrole cations, quaternary ammonium cations and quaternary phosphine cations; anions in the ionic liquid are selected from one of tetrafluoroborate radicals, hexafluorophate radicals, difluorosulfimide anions and diperfluoroalkylsulfimide anions; and the non-aqueous organic solvent is selected from any one or mixture of several of linear carbonate, cyclic carbonate, linear ether and cyclic ether. The ionic liquid mixed electrolyte is high in thermal stability, wide for an electrochemical stability window, high in conductivity, low in viscosity and good in compatibility with an anode material and a cathode material of the lithium ion battery at the same time.

A method for preparing a spiro quaternary ammonium system and electrolytes containing spiro quaternary ammonium cations, comprising a synthesizing step wherein a spiro ammonium system is formed in a medium that can serve as both the reaction solvent and as an electrolyte solvent.

Drilling fluids are provided that comprise an organophilic clay treated with a quaternary ammonium surfactant having an amide linkage. The quaternary ammonium surfactant may comprise a compound generally represented by the following formula:

where M⁻ is an anion such as a chloride, methyl sulfate, bromide, acetate, or iodide ion; R₁ is an alkyl group such as a saturated hydrocarbon with 10 or more carbons; R₂, R₃, and R₄ are the same or different alkyl groups such as a methyl, ethyl, or benzyl group, and x is greater than or equal to 1. The organophilic clay treated in this manner is substantially biodegradable. In embodiments, the drilling fluids comprise the foregoing organophilic clay, an oil-based fluid and a weighting agent. In still embodiments, the drilling fluids comprise the foregoing organophilic clay, an invert emulsion, an emulsifier, and a weighting agent.

Electrolyte solutions for electrochromic devices such as rear view mirrors and displays with low leakage currents are prepared using inexpensive, low conductivity conductors. Preferred electrolytes include bifunctional redox dyes and molten salt solvents with enhanced stability toward ultraviolet radiation. The solvents include lithium or quaternary ammonium cations, and perfluorinated sulfonylimide anions selected from trifluoromethylsulfonate (CF₃SO₃⁻), bis(trifluoromethylsulfonyl)imide ((CF₃SO₂)₂N⁻), bis(perfluoroethylsulfonyl)imide ((CF₃CF₂SO₂)₂N⁻) and tris(trifluoromethylsulfonyl)methide ((CF₃SO₂)₃C⁻). Electroluminescent, electrochromic and photoelectrochromic devices with nanostructured electrodes include ionic liquids with bifunctional redox dyes.

The invention discloses composite modified starch as a hematite reverse flotation inhibitor and a preparation method thereof. The composite modified starch comprises 100 weight portions of raw material starch, 0.5-10 weight portions of sodium hypochlorite as an oxidizing agent, 1.2-7.0 weight portions of sodium hydrosulphite, 0.2-1.2 weight portions of sodium nitrite as esterification reagents, 0.5-3.5 weight portions of 3-chloro-2-hydroxypropyl-trimethyl quaternary ammonium salt as a cationic reagent, 3.0-7.0 weight portions of caustic alkali, and 25-40 weight portions of water. The composite modified starch contains carboxylic groups, sulfonic anions, and quaternary ammonium cations, and has the advantages of cold water solubility and low viscosity, and has the advantages of increasing the yield of hematite concentrate, improving the filtering conditions of iron ore pulp, and the like.

A power storage device using an organic solvent as a nonaqueous solvent for a nonaqueous electrolyte, in which a CV charging period in CCCV charging can be prevented from being extended and which has high performance, can be provided. The power storage device includes a positive electrode, a negative electrode, and a nonaqueous electrolyte. The nonaqueous electrolyte includes an ionic liquid including an alicyclic quaternary ammonium cation having one or more substituents and a counter anion to the alicyclic quaternary ammonium cation, a cyclic ester, and an alkali metal salt. In particular, in the power storage device, the ionic liquid content is greater than or equal to 70 wt % and less than 100 wt % per unit weight of the ionic liquid and the cyclic ester in the nonaqueous electrolyte, or greater than or equal to 50 wt % and less than 80 wt % per unit weight of the nonaqueous electrolyte.

The invention provides a polishing liquid for polishing a barrier layer of a semiconductor integrated circuit, the polishing liquid comprising: a diquaternary ammonium cation; a corrosion inhibiting agent; and a colloidal silica, wherein the pH of the polishing liquid is in the range of 2.5 to 5.0. According to the invention, a polishing liquid capable of achieving a superior barrier layer polishing rate, as well as suppressing the occurrence of scratching due to the agglomeration of solid abrasive grains can be provided.

The invention discloses a flame retardation catalyst and a supported flame retardation catalyst composed of same. The flame retardation catalyst has a structural formula of (A)nB, wherein A<+> is an imidazoliumcation, a quaternary ammonium cation, a quaternary phosphoniumcation, a pyrrolidoniumcation, a pyrazoliumcation or a pyridyliumcation, and B<n-> is a polyoxometallate anion. The supported flame retardation catalyst is composed of the flame retardation catalyst and clay as a supported, and the load capacity of the flame retardation catalyst is 1-50 wt% of clay. The supported flame retardation catalyst has good compatibility with polymer matrixes, helps to improve char yield and flame retardation performance of a flame retardation polymer system, and has the advantages of good thermostability and migration resistance, being friendly to environment and the like. By employing clay to support the flame retardation catalyst, the flame retardation catalyst can be uniformly dispersed in the polymer, and the char yield is improved. By employing an immersion method and without complex reaction steps, the preparation method is economical, simple, low in cost and easy to popularize.

The invention discloses a preparation method for a mesoporous ZSM-5 zeolite molecular sieve. The mesoporous zeolite molecular sieve with ZSM-5 microporous crystalline pore walls is prepared by using tetraethoxysilane as a silicon source, sodium metaaluminate as an aluminum source and a difunctional triammonio quaternary ammonium salt cationic surfactant as a template through a hydrothermal synthesis process under an alkaline condition. According to the invention, the quaternary ammonium surfactant is used as a ZSM-5 zeolite structure directing agent and generates micropores, and aggregation of long hydrophobic alkyl groups at two ends of the surfactant forms meso pores. The method provided by the invention effectively changes an amorphous pore wall structure of traditional mesoporous materials and allows the ZSM-5 zeolite molecular sieve to have crystalline pore walls, which enables acidity and hydrothermal stability of mesoporous materials to be greatly improved; the prepared mesoporous ZSM-5 zeolite molecular sieve has a unique mesoporous/microporous multiple pore structure, so defects of a single pore structure are avoided, mass transfer efficiency is improved, and the ZSM-5 zeolite molecular sieve has a wide application prospect in aspects like macro-molecular catalysis, adsorption, separation, etc.

A cationic polymer salt composition is provided that includes a reaction product derived from reaction of a polyamine or a polyalkyleneimine and a substituted alkyl trialkyl quaternary ammonium salt. Also provided are surfactant compositions. The compositions may also include carriers, such as water, methanol, ethanol, propanol, isopropanol, butanol, isobutanol, monoethyleneglycol, an ethyleneglycol monobutyl ether, and hexylene glycol.

According to this invention, a process for producing fluorine containing polymer to obtain composite polymer electrolyte composition having excellent ion transport number, that is, ion transfer coefficient, for example, excellent transport number of lithium ion, is provided.

A process for producing fluorine containing polymer comprising graft-polymerizing a molten salt monomer having a polymerizable functional group and a quaternary ammonium salt structure having a quaternary ammonium cation and anion, with a polymer having the following unit;

• • —(CR¹R²—CFX)—
  • X means halogen atom except fluorine atom,
  • R¹ and R² mean hydrogen or fluorine atom, each is same or different atom.