73 results about "Carboxylic acid anion" patented technology

A method for increasing the permeability of a subterranean formation is disclosed in which an amount of an aqueous mixture, sufficient to increase the permeability of the formation, comprising specified aminopolycarboxylic anionic species, and specified cationic species, is injected into the formation matrix.

There is provided a resist underlayer film forming composition for lithography for forming a resist underlayer film capable of being used as a hardmask. A resist underlayer film forming composition for lithography comprising a silane compound containing an anion group, wherein the silane compound containing an anion group is a hydrolyzable organosilane in which an organic group containing an anion group is bonded to a silicon atom and the anion group forms a salt structure, a hydrolysis product thereof, or a hydrolysis-condensation product thereof. The anion group may be a carboxylic acid anion, a phenolate anion, a sulfonic acid anion, or a phosphonic acid anion. The hydrolyzable organosilane may be a compound of Formula (1): R¹_aR²_bSi(R³)_4−(a+b) (1). A composition comprising a mixture of a hydrolyzable organosilane of Formula (1), and at least one organic silicon compound selected from the group consisting of a compound of Formula (2): R⁴_aSi(R⁵)_4−a (2) and a compound of Formula (3): [R⁶_cSi(R⁷)_3−c]₂Y_b (3); a hydrolysis product of the mixture; or a hydrolysis-condensation product of the mixture.

The invention relates to a preparation method of quaternary ammonium ionic liquid, belongs to the field of chemical synthesis and solves the problems of complicated process and long reaction period in the conventional preparation method of the quaternary ammonium ionic liquid. The method comprises the following steps: reacting quaternary ammonium salt with alkali solution, generating anion exchange reaction to generate quaternary ammonium base and generating acid and alkali neutralization reaction with corresponding phosphonic acid anions or carboxylic acid anions to generate the quaternary ammonium ionic liquid. The method has the advantages of simple preparation process, short time, high product conversion rate and easiness in purification, an alcohol solvent can be recycled through distillation, extraction and other methods. The preparation method of the ionic liquid is wide in applicable scope. Compared with the prior art, the preparation method has briefer preparation steps, and the large-scale production is easy.

The invention belongs to the technical field of nano-materials, and particularly relates to ZnO luminous nanoparticles synthesized in polyethylene glycol and a preparation method thereof. The nanoparticles consist of ZnO monocrystal particles and external polymer radicals, and have high stability and photoluminescence performance. The preparation method comprises the following steps of: dissolving zinc acetate and basic hydroxide in a solvent together with stirring; and reacting at the room temperature for a period of time. The ZnO luminous nanoparticles can be purified by adopting a non-solvent precipitation method. In the stirring reaction process, a reaction mixture is fully contacted with the air, polyethylene glycol is oxidized by the air to form a carboxylic acid anion structure under the alkali catalyzing condition, and carboxylic acid anions can be coordinated onto the surfaces of the ZnO nanoparticles to make the ZnO nanoparticles illuminate stably. The preparation method has the advantages of low cost, environmental friendliness and high yield.

The present invention discloses a high water soluble carbon nanotube and a preparation method of the same. In the present invention, the carbon nanotube experiences noncovalent bond combinative coating modification by using the pi-pi conjugation between the hydrolysis styrene-maleic anhydride copolymer and the carbon nanotube; the dispersion stability of the carbon nanotube in water is improved by using the carboxylic acid anion with good water solubility of the copolymers; so that the water solubility of the carbon nanotube is greatly improved. The water solubility carbon nanotube coated by hydrolysis styrene-maleic anhydride copolymer is obtained by using hydrolysis styrene-maleic anhydride copolymer, carbon nanotube and water as raw material, adopting a circular fashion to inject hydrolysis styrene-maleic anhydride copolymers, and using an ultra sonic dispersion method and centrifugal method. The present invention has the advantages of that the technology is simple, the obtained water solubility carbon nanotube has a solubility of 29.2 mg/ml and an excellent stability, and the styrene-maleic anhydride copolymer has a simple preparation process and a lower cost, so that the large scale preparation and the industrial application of the water solubility carbon nanotube can be greatly improved.

The invention discloses a highly connected coordination polymer and a preparation method thereof. The highly connected coordination polymer adopts the following chemical formula: [Zn5(3,3'-tmbpt)(btec)2(OH)2], wherein betc is deprotonated 1,2,4,5-pyromellitic acid; 3,3'-tmbpt is 1-((1H-1,2,4-triazole)methyl)-3,5-bis(3-pyridyl)-1,2,4-triazole. Carboxyl groups of polycarboxylic acid anions can coordinate with metal ions to form metal clusters with larger size; the metal clusters serve as nodes, so that connections of the nodes can be greatly increased. In addition, distances among several coordinating groups of a polydentate nitrogen-containing ligand 3,3'-tmbpt is relatively large, so that steric hindrance is relatively small during coordination, and the metal clusters can further expand easily to form the coordination polymer adopting highly connected structure. The coordination polymer can serve as a broadband semiconductor material and a molecular-based light emitting material to be further developed and applied.

A two-part foam hair dye which comprises a first part comprising an alkali agent, a second part comprising hydrogen peroxide, and a non-aerosol foamer container, wherein the first part comprises the components (A) to (D), an equivalent ratio of a anion site of the component (A) to a cation site of the component (B) (anion/cation) is more than 1, a mass ratio of a content of the component (C) to the content of the component (D) ((C)/(D)) is 5 or less, and the liquid mixture has a viscosity (25° C.) of 1 to 300 mPa·s:

• • (A) a carboxylic acid anionic surfactant,
  • (B) a polymer or copolymer having a mole fraction of diallyldimethyl quaternary ammonium salt monomer of 70% or more,
  • (C) 0.5 to 1.5% by mass of an oxidation dye having a meta-dihydroxybenzene structure, and
  • (D) 0.1 to 9% by mass of polypropyleneglycol of Mw 200 to 1200.

Disclosed is a cost-effective method for purifying and acidifying carboxylic acids, including organic acids and amino acids. The method involves removing impurities by allowing the anionic form of the carboxylic acid to bind to an anion exchange column and washing the column. The carboxylic anion is displaced as carboxylic acid by washing the resin with a strong inorganic anion. This method is effective in removing organic carboxylic acids and amino acids from a variety of industrial sources, including fermentation broths, hydrolysates, and waste streams.

The invention discloses a preparing method of a titanium salt surface conditioning agent. The preparing method comprises the following steps that firstly, 30 parts of anhydrous disodium hydrogen phosphate is prepared into a water solution with the concentration of 50%; secondly, 1-2 parts of sodium pyrophosphate, 0.8 part of titanyl sulfate, 3.5 parts of sodium pyrophosphate, 2.1 parts of sodium bicarbonate, 1.8 parts of sodium tetraborate, 3.6 parts of sodium hexametaphosphate, 0.3 part of polycarboxylic acid anion organic matter and 0.3 part of N-butyl naphthalene sulfonate are sequentially added in the water solution of disodium hydrogen phosphate, and a mixed solution is obtained; thirdly, the mixed solution is heated to 70 DEG C and fully stirred, and white powder with the water content below 2% is obtained; and fourthly, powder continues to be stirred at the temperature of 75 DEG C, 2.7 parts of sodium pyrophosphate, 1.2 parts of acetic acid, 0.7 part of methyltrimethoxysilane and 3.3 parts of magnesium sulfate are added into the powder at the same time, stirring continues, and drying is carried out till the water content is smaller than 1%. The prepared surface conditioning agent is good in scattering stability and can be stored for a long term.

The present invention relates to the pharmaceutical industry and more particularly to the provision of an agent for inhibiting membrane virus replication. The object of the invention is to provide an agent based on fullerene polycarboxylic anions for suppressing the activity of membrane viruses in treating diseases caused by these viruses. For accomplishing said subject, there is proposed a group of inventions united by a common inventive concept, said group comprising a method for preparing compounds, studying the mechanisms of action, provision of pharmaceutical compositions, and developing methods of treating with their use. Said object t is accomplished by selecting such quantitative ratios of the components and reaction conditions, which ensure the preparation of polyaddition products. It has been established that in carrying out the synthesis the amount of the amino acid must exceed the amount of fullerene by more than 50 times. The product prepared by the proposed method has an unlimited solubility in water, required bioavailability, high efficiency of action on non-infected cells, low toxicity. The content of the main substance in the target product is at least 90%. The process is adaptable to streamline production and can be used in the pharmaceutical industry. Compositions of drugs for and methods of treating infectious diseases caused by human immunodeficiency virus (HIW), herpes simplex virus (HSC) and hepatitis C virus (HCV) have been developed.

The invention discloses a perovskite quantum dot-polymer complex, a preparation method of a wavelength conversion film and a light-emitting device. The preparation method of the perovskite quantum dot-polymer complex comprises the following steps: a step of providing precursors, including: a first precursor composed of at least one of Rb <+>, Cs <+>, NR4 <+> or [CH (NH2) 2] <+> and at least one ofcarboxylate anions or halogen anions, wherein in the NR4 <+>, R is independently a hydrogen atom or a substituted or unsubstituted C1-C10 linear or branched alkyl group; a second precursor includinga Pb halide, a Ge halide, a Si halide, a Sn halide, or a combination thereof; and a polymer; and a step of mixing the precursors at a first temperature at or above the melting point of the polymer, and then cooling the mixed precursors. According to the invention, the problem of poor stability of existing perovskite quantum dots can be effectively solved.

The invention discloses a preparing method for a manganese series phosphatisation surface conditioning agent. The preparing method includes the following steps that firstly, 35 parts of anhydrous sodium hydrogen phosphate is prepared into a water solution with the concentration being 55%; secondly, 1-2 parts of N-methyl pyrrolidone, 0.4 part of titanyl sulfate, 4.3 parts of sodium pyrophosphate, 3.8 parts of sodium bicarbonate, 0.7 part of sodium tetraborate, 2.1 parts of sodium tripolyphosphate, 0.3 part of polycarboxylic acid anion organic matter and 0.9 part of lauroyl aminoethyl sodium sulfate are sequentially added into the water solution of the sodium hydrogen phosphate, and a mixed solution is obtained; thirdly, the mixed solution is heated to 75 DEG C and sufficiently stirred, and white powder with the water content below 2% is obtained; fourthly, the powder is stirred continuously at the temperature being 80 DEG C, 0.9 part of sodium pyrophosphate, 1.2 parts of glacial acetic acid, 0.4 part of methyl triethoxysilane and 1.7 parts of magnesium sulfate are added into the powder at the same time, and stirring and drying are conducted continuously till the water content is smaller than 1%. The surface conditioning agent prepared through the preparing method is good in dispersion stability and capable of being stored for a long time.

The invention discloses a polycarboxylic acid and europium complex luminescent material and a preparation method thereof. The complex luminescent material is a three-dimensional coordination polymer containing two types of organic polycarboxylic acid anion ligand, and the general formula of the three-dimensional coordination polymer is [Eu2(1, 2-bdc)2(3, 5-pdc) (H2O)4]n, wherein 1, 2-bdc is phthalic acid di-anion; 3, 5-pdc is 3, 5-pyridinedicarboxylic acid di-anion; n is natural number not less than 100. The preparation method comprises the following steps: weighting 3, 5-pyridinedicarboxylic acid and potassium acid phthalate or phthalic acid, wherein the amount ratio of 3, 5-pyridinedicarboxylic acid substance to potassium acid phthalate or phthalic acid substance is 0.00008-0.00012mol to 0.00016-0.00024mol; adding deionized water to an europium compound; regulating the pH value to be 4-6; transferring into an oven to react for 48-80h; then decreasing the temperature at the speed of 1-5 DEG C per hour, wherein an europium complex obtained when the temperature is decreased to be less than 100 DEG C is a colorless crystal; then washing with absolute ethyl alcohol to obtain the complex luminescent material.

The invention discloses application of a carboxylate compound as an absorbent for capturing carbon dioxide. The carboxylate compound provided by the invention is used as an absorbent for capturing carbon dioxide and/or is applied to preparation of the absorbent for capturing carbon dioxide; carboxylic acid anions in the carboxylate compound are carboxylate radicals with carbon chains with more than 3 carbon atoms, and cations are substituted quaternary ammonium ions and/or quaternary phosphonium ions. The method for efficiently trapping carbon dioxide in an energy-saving manner by adopting a carboxylate compound stable to water comprises the following steps: placing an aqueous solution of the carboxylate compound in a carbon dioxide atmosphere to absorb carbon dioxide, so as to obtain a conjugate of carboxylate and carbon dioxide separated out from water. The invention is used for solving the problems of corrosivity, volatility and high energy consumption of the existing system, and can obtain higher carbon dioxide capture capacity at high temperature, low pressure of carbon dioxide pressure and high pressure; the conjugate of carboxylate and carbon dioxide is stable to water; the carboxylate can be regenerated.

The invention discloses a method for catching sulfur dioxide by adopting a halogenated carboxylic acid ion liquid. According to the halogenated carboxylic acid ion liquid, halogen is introduced onto carboxylic acid negative ions of a functionalized ionic liquid, the absorbing capacity of sulfur dioxide is improved by utilization of the action of halogen reinforced onto the negative ions and sulfur dioxide, and the electron absorption property of the halogen on the negative ions is utilized to improve the desorption property of carboxylic acid ion liquid, so that efficient reversible absorption of the sulfur dioxide can be realized.

The invention discloses a method for capturing nitric oxide by means of carboxylic acid anion-functionalized ionic liquid. The method is characterized in that carboxylic acid anions with alkalinity are selected as a gas absorbent, and in the nitric oxide capturing process, the absorption pressure ranges from 0.0001 MPa to 0.2 MPa, the absorption temperature ranges from 20 DEG C to 100 DEG C, and the absorption time ranges from 2 hours to 16 hours; absorbed nitric oxide is easy to desorb, wherein the desorption temperature ranges from 60 DEG C to 120 DEG C, and the desorption time ranges from 0.1 hour to 40 hours. Compared with a traditional nitric oxide capturing method, the method has the main advantages that the efficiency and the capacity are high, desorption is easy, the purpose of efficient capturing is achieved through the chemical action between carboxylate radicals and nitric oxide, and the highest absorption capacity that every 1 mol of the ionic liquid absorbs 4.28 mol of nitric oxide is achieved.

The present invention relates to a method for preparing an ionic liquid having a carboxylic acid anion using a microreactor. More specifically, the present invention relates to a method for preparing, with high efficiency, an ionic liquid having a carboxylic acid anion as shown in FIG. 1, by having sodium butanoate, sodium 2-ethylhexanoate, or sodium octanoate undergo a substitution reaction with 1-alkyl-3-methylimidazolium, 1,1-alkylmethylpyrrolidinium, 1,2-dimethyl-3-alkylimidazolium, 1-alkyl-3-methylpyridinium, or tetramethylammonium, each of which being a cation. The ionic liquid prepared according to the present invention has high purity, containing residual halide at less than 10 ppm, and has high electrical conductivity, and therefore is capable of being used as an electrolyte or for a condenser.

The invention provides an electrolytic capacitor. The electrolytic capacitor comprises an electrolyte and a core package soaked in the electrolyte, the sparking voltage of the electrolyte is greater than 400V, the electrolyte comprises a main solvent and a main solute, the main solvent comprises a lactone compound, and the main solute comprises imidazolinium cations and organic carboxylic acid anions; the total carbon content of the organic carboxylic acid anions is 8-26, and the structural formula of the organic carboxylic acid anions is shown in the description, wherein P is a main carbon chain of 1-25 carbons, and the main carbon chain contains or does not contain unsaturated bonds; R1, R2, R3 and R4 are respectively and independently selected from hydrogen, benzene rings, alkyl benzenerings, nitrobenzene rings, carboxyl or straight carbon chains with 1-10 carbons or carbon chains with branched chains, and one or two of R1, R2, R3 and R4 are selected from carboxyl; the core packagecomprises an anode, a cathode and electrolytic paper, the tightness of the electrolytic paper is 0.30-0.75 g/cm <3>, and the thickness of the electrolytic paper is 40-120 microns; and the working voltage of the electrolytic capacitor is 350 to 500 V. The electrolytic capacitor provided by the invention widens the working temperature range and has the characteristic of high voltage resistance.

The present invention has its object to provide an electrolyte anion which is high in decomposition temperature, in order to inhibit the electrolyte anion in the electrolyte solution for electrolytic capacitors from undergoing decarboxylation in the lead-free solder reflowing step to thereby prevent valve opening.

The present invention uses an electrolyte solution comprising, as an electrolyte, the salt (A) composed of ammonium cation (a) and a polybasic carboxylic acid (b) anion, wherein the proton part charge of each carboxyl group in the polybasic carboxylic acid (b) as calculated by the quantum mechanics calculation software CAChe-based AM1 method is not higher than 0.243. Preferred is the polybasic carboxylic acid (b) represented by the general formula (1):

wherein R¹ to R⁴ may be the same or different and each represents a hydrogen atom, a functional group or a hydrocarbon group containing 1 to 3 carbon atoms, which may optionally contain a functional group, provided that at least one of R¹ to R⁴ is an electron-donating group.

The present disclosure relates to a curable composition to be prepared by mixing a base paste and a catalyst paste, the base paste comprising (A) a hardenable compound comprising at least two aziridine moieties, and (B) a metal containing component containing anions and/or ligands, the metal containing component being present in an amount of about 0.1 to about 5 wt.-%, the metal being selected from Zn, Cu, Co, Ni, Ag and combinations thereof, the anions or ligands being selected from oxide, hydroxyl, (hydro)carbonate, sulphate, nitrate, halide, lactate, benzoate, wolframate, linear or branched aliphatic carboxylic acid anions, ligands having not more than two coordinating moieties and combinations thereof, the catalyst paste comprising (C) a Lewis acid, the composition optionally further comprising (D) a retarder, (E) filler and (F) additive(s).

The present disclosure also relates to a kit of parts, the use of a metal containing component as a means for reducing the curing time of a cationically curable composition and a method of taking a dental impression.