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61 results about "Lewis acids and bases" patented technology

A Lewis acid is a chemical species that contains an empty orbital which is capable of accepting an electron pair from a Lewis base to form a Lewis adduct. A Lewis base, then, is any species that has a filled orbital containing an electron pair which is not involved in bonding but may form a dative bond with a Lewis acid to form a Lewis adduct. For example, NH₃ is a Lewis base, because it can donate its lone pair of electrons. Trimethylborane (Me₃B) is a Lewis acid as it is capable of accepting a lone pair. In a Lewis adduct, the Lewis acid and base share an electron pair furnished by the Lewis base, forming a dative bond. In the context of a specific chemical reaction between NH₃ and Me₃B, the lone pair from NH₃ will form a dative bond with the empty orbital of Me₃B to form an adduct NH₃•BMe₃. The terminology refers to the contributions of Gilbert N. Lewis.

Special catalyst for preparing p-chlorobenzonitrile by ammonoxidation process, preparation method and use

The invention discloses a special catalyst for preparing p-chlorobenzonitrile by an ammonoxidation process. Organosilicone modified silica gel serves as a carrier of the special catalyst, a main catalyst comprises vanadium and phosphorus, a cocatalyst comprises at least one of an ingredient G, an ingredient D and an ingredient E, and an active ingredient of the special catalyst is represented as VPbGcDdEeOx; and the G is molybdenum, chromium, titanium, nickel or bismuth, the D is boron, manganese, ferrum, cobalt, copper, zinc or tin, and the E is potassium, lithium, sodium, cesium, magnesium or calcium. The invention further discloses a preparation method for the catalyst and use of the catalyst. According to the special catalyst, the preparation method and the use, electron donating groups on organosilicone and inorganic elements are subjected to an Lewis acid alkali reaction, and thus, actions of inorganic oxides and the carrier are strengthened; and meanwhile, the inorganic oxides can be more uniformly dispersed, catalyst ingredients are low in loss, the catalytic activity is high, the selectivity is good, and the service life of a commercial catalyst is prolonged to 2 years ormore from 1 year. The catalyst is simple in preparation method, low in cost and good in thermal stability and mechanical strength and can be applied to fixed-bed and fluidized-bed reactors.
Owner:SOUTH CENTRAL UNIVERSITY FOR NATIONALITIES

MgAl LDO/nitrogen vacancy carbon nitride-based photocatalyst as well as preparation method and application thereof

The invention belongs to the field of nano materials, and relates to an MgAl LDO / nitrogen vacancy carbon nitride-based photocatalyst as well as a preparation method and application thereof. According to the preparation method, a carbon nitride (g-C3N4) nanosheet rich in nitrogen vacancies is prepared, magnesium-aluminum bimetallic layered hydroxide (MgAl LDH) is deposited on the surface of the carbon nitride (g-C3N4) nanosheet in situ, and the magnesium-aluminum bimetallic layered oxide (MgAl LDH) / nitrogen vacancy carbon nitride composite photocatalytic CO2 reduction material which is low in cost, easy to obtain, stable in structure and high in catalytic activity is prepared through continuous calcination. The surface of MgAlLDO has abundant Lewis base / acid sites, O<2->, Mg<2+>-O<2-> and OH groups are used as Lewis base sites to improve the adsorption activation capacity of CO2, Al<3+> and Al<3+>-O<2-> are used as Lewis acid sites to improve the adsorption / dissociation of H2O, the oxidation semi-reaction of H2O is accelerated, more protons are provided, and the CO2 reduction activity is further improved. Meanwhile, surface nitrogen vacancies are beneficial to separation of photo-induced electrons and holes, and the Lewis acid / alkali and the nitrogen vacancies cooperate to enable the composite photocatalytic material to have excellent CO2 photocatalytic performance.
Owner:JIANGSU UNIV

Active hydrogen tolerant catalyst, preparation method thereof and ultralow-molecular-weight poly(carbonate-ether) polyol

ActiveCN111471134AHigh proton tolerancePolymer sciencePtru catalyst
The invention provides an active hydrogen tolerant catalyst shown as a formula (I). The invention also provides a preparation method of ultralow-molecular-weight poly(carbonate-ether) polyol, which comprises: carrying out chain transfer polymerization reaction on carbon dioxide, an epoxy compound and an initiator under the action of the active hydrogen tolerant catalyst or the active hydrogen tolerant catalyst prepared by the preparation method to obtain the ultralow-molecular-weight poly(carbonate-ether) polyol. The active hydrogen tolerant catalyst provided by the invention is an alternatingmulti-center Lewis acid-base pair catalyst; the catalyst has high proton tolerance, so that the catalyst is not limited by the concentration of the initiator any more and can be used for preparing the ultralow-molecular-weight carbon dioxide polyol. The molecular weight of the ultralow-molecular-weight poly(carbonate-ether) polyol is 500-1000 g / mol, and the molecular weight distribution is 1.07-1.15; a carbonate segment and an ether segment exist on a main chain at the same time, and the functionality is 2-10; and the content of byproduct cyclic carbonate is lower than 1%.
Owner:CHANGCHUN INST OF APPLIED CHEMISTRY - CHINESE ACAD OF SCI

Preparation method of lanthanum-modified activated carbon and method for removing fluorine ions in water

The invention relates to the field of wastewater treatment, in particular to a preparation method of lanthanum modified activated carbon and a method for removing fluorine ions in water. The method comprises the following steps: immersing activated carbon in a lanthanum salt solution with a concentration of 0.05-0.15 mol/L, adjusting a pH value to 4-12, and conducting reacting at 25-55 DEG C. As the activated carbon is subjected to lanthanum modification, lanthanum loading can be performed on the surface of the activated carbon. The metal lanthanum can increase metal cations on the surface ofthe activated carbon and improve adsorption of anion pollutants such as fluorine ions and the like. The lanthanum element is large in atomic radius and easily loses electrons of an outer layer s, 5d or 4f'; the lanthanum element has very high affinity to fluorine ions with high electronegativity; and according to the Lewis acid-base theory, La<3+> is typical Lewis acid, F<-> is typical Lewis base,and La<3+> and F<-> form coordination covalent bond combination through coordination effect. The lanthanum-modified activated carbon can effectively improve the adsorption efficiency of an activatedcarbon adsorbent on fluorine.
Owner:CHINA UNIV OF MINING & TECH (BEIJING)

Catalyst for preparing para-Phthalonitrile by using ammoxidation method and preparation method and application

The invention discloses a special catalyst for preparing para-Phthalonitrile by using an ammoxidation method. Silica sol is adopted as a carrier of the special catalyst, the catalyst comprises an active component of an inorganic composite oxide with at least six of vanadium, molybdenum, chromium, boron, titanium, phosphorus, antimony and an alkali metal, the active component of the catalyst is shown in a formula VMoaCrbTicBdPeSbfMgOx, in the formula, x represents the alkali metal, and the alkali metal is sodium, potassium, rubidium or caesium. The invention furthermore discloses a preparationmethod and application of the catalyst. According to the catalyst, groups with lone electron pairs on silicon and inorganic elements are subjected to a Lewis acid-alkali reaction, so that functions ofinorganic oxides with carriers are enhanced; and meanwhile, the inorganic oxides can be uniformly dispersed, the catalyst is small in component loss, high in catalytic activity and good in selectivity, and the service life of the industrial catalyst is prolonged to two years or longer from one year. The catalyst is simple in preparation method, good in thermal stability and high in mechanical strength, and can be applied to fixed bed reactors and fluidized bed reactors.
Owner:SOUTH CENTRAL UNIVERSITY FOR NATIONALITIES

Method for catalyzing vinyl monomer polymerization by using hindered Lewis acid-base pairs based on binuclear aluminum Lewis acid

ActiveCN111320717ABlock copolymerizationImplementor random co-aggregationElastomerPolymer science
The invention discloses a method for catalyzing vinyl monomer polymerization by using hindered Lewis acid-base pairs based on binuclear aluminum Lewis acid, which belong to the technical field of polymer synthesis. According to the method, the vinyl monomer is efficiently catalyzed under mild conditions, the molecular weight and molecular weight distribution of the polymer are controllable, and anew strategy and the method are provided for controllable synthesis of the polymer. The polymerization mechanism in the invention relates to conjugate addition under the synergistic catalytic action of binuclear aluminum. The binuclear aluminum catalytic system disclosed by the invention has the advantages of low cost, easiness in obtaining, convenience in operation, mild reaction conditions, widemonomer adaptability and the like. In addition, efficient conversion of different monomers can be achieved by adjusting pKa of Lewis acid/base, the molecular weight and molecular weight distributionof the polymer can be accurately regulated and controlled, and the initiation efficiency is close to 100%. The catalytic system can efficiently catalyze homopolymerization and copolymerization reactions of methyl methacrylate and butyl acrylate, and also provides a new synthesis strategy and approach for copolymer thermoplastic elastomers of methyl methacrylate and butyl acrylate.
Owner:QINGDAO INST OF BIOENERGY & BIOPROCESS TECH CHINESE ACADEMY OF SCI

Precursor solution for organic polymer film formation and method for forming organic polymer film

A precursor solution for use in forming an organic polymer film includes a first monomer which is a Lewis acid, a second monomer which is a Lewis base to be brought into a Lewis acid-base reaction, and a sacrificial organic molecule including a polar group.
Owner:PANASONIC CORP

Method for preparing amphiphilic block copolymer through cooperation of light-operated free radical polymerization and ring-opening copolymerization

The invention discloses a method for preparing an amphiphilic block copolymer through cooperation of light-operated free radical polymerization and ring-opening copolymerization, which comprises the following steps: simultaneously adding a Lewis acid-base pair catalytic system consisting of a reversible addition chain transfer reagent containing hydroxyl or carboxyl, a photoinitiator, a hydrophilic vinyl monomer, a Lewis acid-base pair system composed of Lewis acid and Lewis base, an epoxy compound, and a cyclic acid anhydride. The chain transfer reagent is used as a ring-opening polymerization initiator, and a Lewis acid-base pair is used as a catalyst to catalyze ring-opening copolymerization of cyclic anhydride and epoxide, so that the chain transfer agent is attached to the tail end of polyester. Meanwhile, visible light or ultraviolet light is irradiated, the photoinitiator is decomposed to generate free radicals, free radical polymerization of allyl monomers is achieved, and hydrophilic polyolefin chains and polyester chains are subjected to addition through reversible addition of a chain transfer agent, so that the amphiphilic block polymer is formed. The preparation method is simple and easy to operate, the production cost is low, certain biodegradability is achieved, the polymerization process is easy to control, and the product structure can be accurately regulated and controlled.
Owner:ANYANG INST OF TECH

Emodin solid dispersion as well as preparation method and application thereof

The invention belongs to the technical field of medicines, and particularly discloses an emodin solid dispersion as well as a preparation method and application thereof. The emodin solid dispersion disclosed by the invention is obtained by mixing emodin, a high polymer carrier and a bonding agent and then treating through a hot melt extrusion technology, and the drug loading capacity of the emodin solid dispersion is 5-20%. Through Lewis acid-base and hydrogen-bond interaction, an emodin molecular dimer structure is broken, so that an amorphous drug is in a supersaturated state; meanwhile, the emodin solid dispersion system is relatively low in Gibbs free energy and molecular mobility and relatively strong in intermolecular interaction, so that the physical stability of the amorphous preparation is enhanced, and the in-vitro dissolution of the amorphous preparation is prolonged; according to the emodin solid dispersion and the preparation method thereof, no organic solvent is used, the preparation is safe and efficient, the obtained emodin solid dispersion improves the dissolution rate and solubility of insoluble drugs, the drug loading capacity is high, the stability is good, a good intermediate is provided for other oral solid preparations of emodin, and the preparation process is simple, efficient, safe and suitable for industrial production.
Owner:NINGXIA MEDICAL UNIV

Application of Lewis acid-base pair in polymerization-induced self-assembly, fiber morphology amphiphilic block polymer as well as preparation method and application of fiber morphology amphiphilic block polymer

The invention provides application of a Lewis acid-base pair in polymerization-induced self-assembly, a fiber morphology amphiphilic block polymer as well as a preparation method and application of the fiber morphology amphiphilic block polymer, and relates to the technical field of liquid crystal polymers. The invention provides an application of a Lewis acid-base pair in polymerization induced self-assembly. The Lewis acid-base pair comprises Lewis acid and Lewis base. According to the invention, a polymerization-induced self-assembly method is adopted, a Lewis acid-base pair is used as a catalyst, and the catalyst has high catalytic activity on a methacrylate monomer, so that the time of a polymerization-induced self-assembly reaction can be remarkably shortened; the amphiphilic block polymer has good polymerization controllability on a polymerization induced self-assembly system, and the amphiphilic block polymer with uniform and adjustable fiber diameter can be prepared by controlling the ratio of the stable chain segment monomer to the nucleation chain segment monomer; according to the preparation method provided by the invention, the size-adjustable amphiphilic block polymer with the fiber morphology can be efficiently and rapidly synthesized through one-pot two-step, and the operation is simple.
Owner:JILIN UNIV

Special catalyst for preparing isophthalonitrile by ammoxidation reaction, preparation method and application

The invention discloses a special catalyst for preparing isophthalonitrile by ammoxidation of m-xylene. The carrier is silica gel, the main catalyst is three components of V, Mo and Sb, and the co-catalyst is at least one of D and E components. species; its active components are expressed as: VMo b Sb c D. d E. e o x ; The D is boron, chromium, titanium, phosphorus, nickel, bismuth, manganese, iron, cobalt, copper, zinc or tin; E is potassium, lithium, sodium, cesium, magnesium or calcium. The invention also discloses the preparation method and application of the catalyst. In the present invention, groups containing lone electron pairs on silicon are used to carry out Lewis acid-base reaction with inorganic elements, thereby strengthening the effect of inorganic oxides and supports; at the same time, the dispersion of inorganic oxides is more uniform, the loss of catalyst components is small, and the catalytic activity is high. , good selectivity, prolonging the service life of industrial catalysts from one year to more than two years. The preparation method of the catalyst is simple, the thermal stability and mechanical strength are good, and the catalyst can be used in fixed-bed and fluidized-bed reactors.
Owner:SOUTH CENTRAL UNIVERSITY FOR NATIONALITIES

Preparation method of nanofiltration membrane based on polyamidoxime as boundary layer

The invention provides a preparation method of a nanofiltration membrane based on polyamidoxime as a boundary layer, and belongs to the field of nanofiltration membrane preparation. According to the invention, the polyamidoxime rich in amidoxime groups is used as an organic boundary layer, so that the hydrophilicity of the surface of a supporting layer can be obviously enhanced, the uniform spreading of a water solution of a water-phase monomer piperazine on the boundary layer is facilitated, a compact and thin PA layer with small surface aperture is prepared, and the polyamidoxime can generate hydrogen-bond interaction and Lewis acid-base interaction with piperazine, the diffusion of piperazine to an oil phase solution is effectively inhibited, the instability of interfacial polymerization is caused, a wrinkled PA layer with relatively strong electronegativity on the surface is formed, the effective permeation area is further remarkably increased, the permeation transmission channels of the finally obtained nanofiltration membrane are increased and the transmission resistance is reduced due to the reduction of the thickness of the PA layer and the increase of the effective permeation area of the PA layer, and the permeation flus is greatly improved. Meanwhile, the surface of the PA layer has relatively strong electronegativity and relatively small surface aperture, so that the solute rejection rate is increased.
Owner:EAST CHINA UNIV OF TECH

Method for synthesizing fluorescent functional polyester-based amphiphilic polymer

The invention discloses a method for synthesizing polyunsaturated side group-containing polyester and preparing a fluorescent functional amphiphilic polymer through post-modification of the polyunsaturated side group-containing polyester. Fluorescent functional small organic molecules such as rhodamine and the like are used as initiators, an organoboron compound is used as lewis acid and organic alkali to form different lewis acid-base pair catalytic systems, ring-opening copolymerization of cyclic anhydride and epoxide is catalyzed, and polyunsaturated side group-containing completely alternating polyesters with different molecular weights are prepared. Post-modification is conducted on unsaturated double bonds of side groups through a mercapto-alkene click reaction, and hydrophilic side groups or side chains are introduced, so as to prepare the fluorescent functional amphiphilic polymer. The catalyst is cheap and easy to obtain, the initiator is selected according to the requirement of fluorescence characteristics, different types of amphiphilic polymers can be obtained by adjusting the types of cyclic anhydride, epoxide and hydrophilic side groups, no metal is introduced in the preparation process, the main chain structure of the product is polyester, and the advantages of low toxicity, biodegradability and excellent biocompatibility are achieved.
Owner:ANYANG INST OF TECH
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