779 results about "Crown ether" patented technology

This invention describes a new concept of flexible template-directed microporous partially pyrolyzed polymeric membranes which have greatly improved performance in separation of gas pairs compared to their precursor polymeric membranes. Organic hosts, such as crown ethers, cyclodextrins (CDs), calixarenes (CXs), and spherands, or polymeric additives, such as poly(ethylene glycol) (PEG) and polyvinylpyrrolidone (PVP) were used as the micropore-forming templates. Micropore-forming template/polymer blend membranes comprising organic micropore-forming templates embedded in a polymer matrix were prepared by dissolving the organic micropore-forming templates in the polymer solution followed by solution-casting and solvent evaporation or solvent exchange. Low-temperature selectively pyrolyzing micropore-forming templates in the micropore-forming template/polymer blend membranes at a nitrogen flow resulted in the formation of flexible microporous partially pyrolyzed polymeric membranes.

An inkjet ink is provided that employs one or more water-soluble colorants or water-insoluble colorants, such as solvent dyes, disperse dyes, or pigments. The colorant, whether water-soluble or water-insoluble, is derivatized with one or more crown ethers to render the water-insoluble colorants soluble in water and in water-miscible organic solvents commonly employed in inkjet printing, particularly thermal inkjet printing, and to impart improved properties to the colorants, such as lightfastness, smearfastness, and waterfastness. The inkjet ink comprises a vehicle and at least one crown ether derivatized colorant. The resulting inkjet ink evidences improved print quality properties, compared to inkjet inks containing colorants that are not so derivatized.

The present invention is related to glucose sensors that are capable of detecting the concentration or level of glucose in a solution or fluid having either low or high ionic strength. The glucose sensors of the present invention comprise a polymerized crystalline colloidal array (PCCA) and a molecular recognition component capable of responding to glucose. The molecular recognition component may be a boronic acid, such as a phenylboronic acid, glucose oxidase, a combination of phenylboronic acid and poly(ethylene)glycol or crown ether, or another component capable of detecting glucose in various fluids and solutions. The glucose sensors of the present invention may be useful in the development of noninvasive or minimally invasive in vivo glucose sensors for patients having diabetes mellitus.

The invention provides a benzocrown ether graft polymer with a lithium isotopic separation effect and a preparation method thereof. As for the polymer, hydroxyl-contained polyvinyl alcohol or polyethylene-vinyl alcohol is adopted to serve as a main chain; benzocrown ether is adopted to serve as a side hung group; and the main chain and the side hung group are connected together through chemical bonds so as to form the benzocrown ether graft polymer. The preparation method comprises the following steps: dissolving the active hydroxyl-contained polyvinyl alcohol or the polyethylene-vinyl alcohol and the benzocrown ether with an active carboxyl functional group or an aldehyde group in a solvent; performing esterification or aldolization under the action of a catalyst at a certain temperature; completing the chemical grafting of the benzocrown ether with the polyvinyl alcohol or the polyethylene-vinyl alcohol; and finally adding a precipitating agent so as to obtain the graft polymer through precipitation. The graft polymer provided by the invention, which contains the benzocrown ether group, has a good lithium isotopic separation effect. Moreover, through adjusting the size of the crown ether ring, the graft polymer can be used for recognition and separation of heavy metal ions, and has an extensive application prospect.

A composition for removing metals from masrolar D contains chelating agent, precipitant, optional surfactant and demulsifier, and at least one of mono-alcohol or biol polymer, quaternary ammonium salt, quaternary phosphonium salt and crown ether.

The subject invention provides a potentially economically viable method for the preparation of hydrogen peroxide (H₂O₂) in deep eutectic solvents (DES). H₂O₂ is then used for the destruction of small to large quantities of sulfur and nitrogen mustards and lewisite, their homologous/analogues, and similar chemical warfare agents at ambient conditions in DES without producing any toxic by-products. Furthermore, H₂O₂ has been used for the destruction of small to large quantities of halogenated hydrocarbons, their homologous/analogues, and similar hazardous chemicals at ambient conditions. H₂O₂ can be formed by either the electrochemical reduction of oxygen in DES in the presence of water or by dissolving Group 1 (alkali metals) or Group 2 (alkaline earth metals) superoxides, e.g. potassium superoxide, in DES in the presence of water, with/without chemicals used for the enhancement of the solubility of the metal superoxide in the DES, e.g. crown ethers.

The invention relates to a synthetic method for synthesizing ethylidene diacetate through carbonylation of methyl acetate, mainly solving the problems that the conversion rate of reactant methyl acetate during the synthesis of ethylidene diacetate through carbonylation of methyl acetate is low and the yield and selectivity of ethylidene diacetate are low when organic nitrogen or organic phosphorus is used as an accelerant in the prior art. The technical scheme of the synthetic method is as follows: methyl acetate, carbon monoxide and hydrogen are used as raw materials, acetate acid is used as a solvent, ethylidene diacetate is synthesized under the conditions that the reaction temperature is 130-200 DEG C, the reaction pressure is 2-10MPa and the reaction time is 3-10h, a main catalyst adopts ironic series metals or compounds thereof, a catalyst promoter is iodide and the accelerant is crown ether. By adopting the synthetic method, the problems are well solved, and the synthetic method can be used for production of vinyl acetate.

The invention provides a non-woven base composite membrane for lithium isotope separation and a preparation method thereof, as well as a lithium isotope separation method by using a membrane chromatography. The non-woven base composite membrane takes a non-woven fabric as a porous support body or a micropore membrane, a coating is prepared on the non-woven fabric by taking a crown ether graft polymer or a Kryptofix graft polymer with a lithium isotope separation effect as a film forming matter, or a coating can be prepared on the non-woven fabric by blending crown ether or Kryptofix and derivates of the crown ether or the Kryptofix into a film-formation polymer solution, and the coating and a base membrane are combined to form a composite separated membrane; the composite separated membrane is taken as a membrane chromatography medium stationary phase, so as to separate lithium isotopes by using the membrane chromatography. The non-woven base composite membrane or the lithium isotope separation method by using the membrane chromatography can effectively improve the contact and coupling efficiency of crown ether molecules and Lithium Ions in the separation process for solid-liquid extraction lithium isotopes, and realize the greenization, serialization and high efficient of the process of lithium isotope separation.

The invention relates to a preparation method for the two, four, six-three-chlorine fluorobenzene, belonging to fluorin chemical engineering technical field. The invention is characterized in that three and five-two chlorine and four fluorin are used as the materials, which are catalyzed and chlorinated with the chlorine under the action of a catalyst in order to make the two, four and six-three-chlorine fluorobenzene; the reaction temperature ranges from one hundred and fifty and two hundred and fifty DEG C; the catalyst is chosen from oxidation benzoyl, azobisisobutyronitrile, and crown ether; the dosage accounts for zero point zero three percent to one percent of the three and five-two-chlorine-four-nitrobenzene. The invention has the advantages that the defects of the preparation method in the prior art such as low yield, high reaction temperature and the rigorous equipment condition are overcome; the preparation method enables the reaction to be completed below two hundred and twenty DEG C; the reaction equipment and the corresponding matched auxiliary equipment has low cost; the material transformation rate and the yield are increased; the purity of the products can reach ninety-nine point eight percent; the materials of the invention can be chosen from the leftovers which can be seen commonly in chemical enterprises and the rectifying remaining, which can save the prior resources with good economic benefit, environmental benefits and social benefits.

Methods and compositions to extract radionuclides such as various actinides and lanthanides from organic and/or aqueous solutions by utilizing extractant functionalized carbon nanotubes are disclosed. More particularly, phosphorous-containing (such as phosphine oxides, phosphoric acids or phosphates) organic extractants and other predesigned extractants (such as crown ethers, calncrown derivatives, malonamide and diglycolamide derivatives, polyethylene glycol derivatives, cobalt dicarbollite derivatives, and N-donating heterocyclic ligands) can be covalently and/or non-covalently employed on the surfaces and/or ends (tips) of carbon nanotubes for the purpose of removal radionuclides such as various actinides and lanthanides from organic and/or aqueous solutions. Extractant functionalized carbon nanotubes can be used for extracting radioactive nuclides from nuclear waste or spent nuclear fuel, which are produced and/or reprocessed from the nuclear power generation or other nuclear application. The invention also relates to the solid-liquid separation process based on the contact of liquid radioactive waste by using the invention extracting agents as the solid phase.

The invention relates to a crown ether micropore containing polyimide intrinsic microporosity polymer membrane and a preparation method thereof. The preparation method comprises the following steps of: firstly, preparing a diamine solution from aromatic diamine; adding aromatic dianhydride into the diamine solution, and stirring for 9-13 hours at the room temperature; further adding a dehydration agent and a catalyst, stirring for 3-6 hours at 40-65 DEG C, removing the solvent, and drying, so as to obtain a crown ether micropore containing polyimide intrinsic microporosity polymer; and dissolving the polymer by using an organic solvent so as to obtain a membrane casting liquid, and performing membrane casting and drying, thereby obtaining the crown ether micropore containing polyimide intrinsic microporosity polymer membrane. As crown ether micropores are introduced into the polymer membrane provided by the invention, dense accumulation of polymer chain segments can be effectively prevented by virtue of steric hindrance of a cyclic structure of crown ether, an intrinsic microporosity polymer membrane material has a relatively large free volume, and in addition ether bonds of the crown ether have very good affinity with CO2, so that the prepared crown ether micropore containing polyimide intrinsic microporosity polymer membrane is relatively high in gas permeability coefficient and good in selectivity.

The invention provides a monocrystalline silicon wafer texture surface making additive. The monocrystalline silicon wafer texture surface making additive comprises the following components in percentages by mass: 0.1%-3% of a component A, 0.01%-10% of a component B and the balance of water. The component A is selected from one or more of crown ether, crown ether derivatives and alkali metal complex of the crown ether; and the component B is alcohol ether. The invention further provides texture surface making liquid for monocrystalline silicon wafer texture surface making. The texture surface making liquid contains an alkali solution and the monocrystalline silicon wafer texture surface making additive. The invention further provides a monocrystalline silicon wafer texture surface making method. Texture surface making on a monocrystalline silicon wafer is carried out by the texture surface making liquid. The additive is added in the monocrystalline silicon wafer texture surface making liquid, so that texture surface making reaction becomes fast, quick texture surface making on the monocrystalline silicon wafer cut by a diamond wire can be carried out, the capacity is improved, uniform and compact texture surface pyramids can be obtained, the reflectivity is reduced, and the efficiency of a battery is improved.

This invention relates to lithium ion battery electrolyte with high times and discloses the main components as following: vinylene carbonate for 10 to 30 percentage; propylene carbonate for 4 to 20 percentage; dimethyl carbonate for 35 to 50 percentage; methyl carbonate for 10 t0 20 percentage; lithium salt for 12.5 to 16 percentage and B(OR)<3> with R representing carbon atoms less than 4 or crown ether of one or more function addictives for 0.1 to 5.0 percentage.

The invention relates to a cadmium ion fluorescence probe and a preparation method thereof. The cadmium ion fluorescence probe consists of a derivative of quinoline with a position 2 which is modified by aza-crown ether. An aza-crown ether group is bonded onto a quinoline chromophoric group with an auxiliary coordination function to synthesize the cadmium ion fluorescence probe with a specific response function. As homologous transition metal ions, the interaction of cadmium and zinc with S, O and N donors is very close. Comparatively, the connection of the cadmium with the S and N donors is closer than the connection of the zinc with the S and N donors. The novel fluorescence probe is designed by using the characteristics. The influence of zinc ions on the unique response of the cadmium ion fluorescence probe is overcome. The fluorescence probe can be used for the selective rapid fluorescence detection of the cadmium ions in water bodies, the selectivity is very good, the resistance to interference of other metal ions is strong and the cadmium ion fluorescence probe consists of ideal sensing molecules for the field detection of the cadmium ions.

The invention provides a benzo crown ether graft polymer material with lithium isotope separation effect and a preparation method of the material. The polymer is a benzo crown ether graft polymer which is formed by taking polysulfone, polyethersulfone or polyetheretherketone containing a chloromethyl group as a substrate and benzo crown ether as a side hanging group and connecting by chemical bonds. The preparation process of the polymer is as follows: preparing chloromethylated polymer under the action of proper catalyst and chloromethylation reagent; and carrying out unimolecular nucleophilic substitution reaction on the chloromethylated polymer and benzo crown ether with an active functional group at certain temperature under the action of an acid-binding agent to finish chemical graft so as to prepare the benzo crown ether graft polymer. The benzo crown ether graft polymer contains a crown ether group, thereby having excellent lithium isotope separation characteristic; and in addition, by adjusting the size of the crown ether ring, the graft polymer can be used for identification and separation of heavy metal ions and has wide application prospects.

The invention provides a preparation method and application of a lithium-ion-imprinted polyethersulfone composite membrane, belonging to the technical field of preparation of functional materials. The lithium-ion-imprinted polyethersulfone composite membrane is prepared with a polyethersulfone membrane as a substrate membrane material, lithium ions as a template, 12-crown-4-ether as a binding site, methacrylic acid as a functional monomer, ethylene glycol dimethacrylate as a cross-linking agent and azodiisobutyronitrile as an initiator by using a combination of dopamine surface modification technology, silica nanometer compounding technology and imprinted polymerization technology. Static adsorption experiments are conducted to research the adsorption equilibrium, kinetic performance and selective recognition performance of the prepared lithium-ion-imprinted polyethersulfone composite membrane; and selective permeation experiments are carried out to research the permeation action of the prepared lithium-ion-imprinted polyethersulfone composite membrane on target ions (lithium ions) and non-target ions (sodium ions and potassium ions). The lithium-ion-imprinted polyethersulfone composite membrane prepared in the invention has high specific lithium ion adsorption capability and lithium ion recognition and separation capability.

The invention discloses a method for producing a polymer membrane silver ion selective electrode. Crown ether compound which comprises amide groups and sulfur heteroatoms is used as silver ion carrier and is mixed with polyvinyl chloride, plasticizer and ion exchanging agent according to a certain proportion. Inorganic salt which comprises anions which can form slightly soluble matters with silver ions is used to adjust the concentration of interfering ions and main ions in internally filled liquid. The polymer membrane silver ion selective electrode membrane forming and activating conditions are optimized, the seepage of main irons of an inner membrane phase to sample solution is effectively reduced, and the polymer membrane silver ion selective electrode detection limit is made to comply with theoretical prediction value (less than 10-10mol/L). The polymer membrane silver ion selective electrode has good silver ion nernst response and silver ion selectivity. The method for producing the polymer membrane silver ion selective electrode overcomes the defect that the complexing agent used for the internally filled liquid of a polymer membrane electrode of low detection limit is easy to seep into a polymer membrane and the iron exchange resin is hard to miniaturize. The performance of the polymer membrane silver ion selective electrode can not be reduced in one month.

The invention relates to a low-shrinkage high-strength polyester industrial yarn and a preparation method thereof. The preparation method comprises: carrying out solid phase condensation polymerization tackifying on a modified polyester, melting, metering, extruding, cooling, oiling, drawing, carrying out heat setting, and winding, wherein the unchanged longitudinal height is maintained during thecooling, the cross section area of the slow cooling chamber is increased while the plate surface temperature of the spinning plate is maintained by using the thermal insulation method, and the oil agent for oiling contains 67.30-85.58 wt% of crown ether. According to the present invention, the preparation method is simple; the material of the prepared low-shrinkage high-strength polyester industrial yarn is the modified polyester with the molecular chain including a terephthalic acid chain segment, an ethylene glycol chain segment and a diol chain segment having the branched chain, the fracture strength is more than or equal to 7.3 cN/dtex, and the dry heat shrinkage rates at the conditions comprising 177 DEG C, 10 min and 0.05 cN/dtex and the conditions comprising 190 DEG C, 15 min and 0.01 cN/dtex respectively are 1.8+/-0.5% and 3.5+/-0.5%.

A decalcification agent for crude oil contains at least one chelating agent chosen from monocarboxylic acid, binary carboxylic acid, organic phosphonic acid, amino acid or its derivative, polyphosphoric acid and hydroxy quinoline, optional surfactant and demulsifier, and at least one of monoalcohol or biol polymer quaternary ammonium salt, quaternary phosphonium salt and crown ether.

The invention discloses a ZSM-48 molecular sieve with a low silica-alumina ratio and a preparation method thereof. The molecular sieve has the following properties: the molar ratio of silica to alumina is 25-50; the specific surface is 250-400 m2/g; the pore volume is 0.25-0.35 cm3/g; the average pore size is 3-5 nm. The preparation method comprises the following steps: (1) well mixing a seed crystal S, a template R, a silicon source, an aluminium source, sodium hydroxide and water to prepare a reaction mixture, wherein the composition of the reaction mixture is as follows: on a basis of oxide, the molar ratio of R to SiO2 is 0.05-0.2, the molar ratio of SiO2 to Al2O3 is 30-50, the molar ratio of Na2O to SiO2 is 0.06-0.1, the molar ratio of H2O to SiO2 is 15-23, the mass ratio of S to SiO2 is 0.05-0.5, S is the ZSM-48 molecular sieve, and R is 12-crown ether-4; (2) performing hydrothermal crystallization of the reaction mixture prepared in step (1) at 150-170 DEG C for 4-8 days, performing filtration, washing, drying, and roasting of the crystallization product to obtain the ZSM-48 molecular sieve with a low silica-alumina ratio. The ZSM-48 molecular sieve prepared by the method of the invention has a low silica-alumina ratio, and has good application prospects in technical fields of isodewaxing and the like.

The invention discloses a method for quickly testing melamine content in milk powder by using a gold nanoparticle colorimetric method, which belongs to the technical field of analytical chemistry. The invention comprises the steps of preparing gold nanoparticles (AuNPs), derivatizing crown ether, conjugating gold nanoparticle and crown ether, self assembling by applying the gold nanoparticles, detecting melamine by molecular recognition, detecting the practical sampling and the like. The invention prepares a gold nanoparticle self-assembly material, can simply, quickly and flexibly detect the melamine content in the milk powder according to the color change of a gold nanoparticle system, simultaneously improves the detection sensitivity greatly, achieves the purpose of high flux, and provides convenience for the subsequent research, production, supervision and the like.

The subject invention provides a potentially economically viable method for the preparation of reactive superoxide ion in deep eutectic solvents (DES). The superoxide ion can be used for many applications, e.g. the degradation of hazardous chemicals at ambient conditions or in the synthesis of some special chemicals, e.g. carboxylic acids, aldehydes, and ketones from the corresponding alcohols. The superoxide ion can be formed by either the electrochemical reduction of oxygen in DES or by dissolving Group 1 (alkali metals) or Group 2 (alkaline earth metals) superoxides, e.g. potassium superoxide, in DES, with/without chemicals used for the enhancement of the solubility of the metal superoxide in the DES, e.g. crown ethers.