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30 results about "Superbase" patented technology

In chemistry, a superbase is an extremely basic compound or caustic substance that has a high affinity for protons. The hydroxide ion is the strongest base possible in aqueous solutions, but bases exist with much greater strengths than can exist in water. Such bases are valuable in organic synthesis and are fundamental to physical organic chemistry. Superbases have been described and used since the 1850s. Reactions involving superbases often require special techniques since they are destroyed by water and atmospheric carbon dioxide as well as oxygen. Inert atmosphere techniques and low temperatures minimize these side reactions. The strongest base is CH3CH2- [ CH3CH3 pka= 50]

Superbase-Derived Protic Ionic Liquids

Protic ionic liquids having a composition of formula (A−)(BH+) wherein A− is a conjugate base of an acid HA, and BH+ is a conjugate acid of a superbase B. In particular embodiments, BH+ is selected from phosphazenium species and guanidinium species encompassed, respectively, by the general formulas:The invention is also directed to films and membranes containing these protic ionic liquids, with particular application as proton exchange membranes for fuel cells.
Owner:UT BATTELLE LLC

Methods for preparation and use of strong base catalysts

Methods for preparation of a unique superbase catalyst consisting of mixture of polyether alcohol and base in which a polyether alcohol superbase is produced by the removal of water or alcohol at elevated temperatures to form a polyether alcohol alkoxide. The superbase catalyst is useful in, but not limited to, quantitative isomerization of alkyl esters of vegetable oils containing interrupted double bond systems to yield esters with conjugated double bond systems.
Owner:AGRI & AGRI FOOD

Preparation method and application of mild reaction type aldehyde ketone resin

ActiveCN103333302AReduce volatilityOvercoming the disadvantage of being prone to bumpingBuilding insulationsEpoxyKetone
The invention discloses a preparation method of mild reaction type aldehyde ketone resin. The mild reaction type aldehyde ketone resin is prepared by adding a quantitative superbase catalyst into mixed liquid of aldehyde and ketone compounds under the condition of stirring at normal temperature, wherein the reaction process is mild and stable, so the defect that the traditional furfuraldehyde acetone system is easy to implode is overcome. The invention also discloses an application of the mild reaction type aldehyde ketone resin to preparation of an aldehyde ketone resin modified epoxy grouting material. The prepared grouting material can completely exert the flexibility of the aldehyde ketone resin, solves the problem that epoxy resin has high brittleness, can further improve excellent mechanical properties, adhesive property, ageing resistance and corrosion resistance of the epoxy resin, and also has the characteristics of low toxicity, environmental friendliness and the like. In addition, according to the preparation method, the aldehyde ketone resin is prepared in advance and has higher viscosity and thixotropism when being used together with fillers, so the construction process is simple and the aldehyde ketone resin can be applied to concrete surface corrosion of basic facilities such as bridges and ports, restoration of cultural relic, water and seepage prevention, reinforcement and strengthening of buildings and the like.
Owner:东莞微积分新材料科技有限公司

Process for preparing solid strong base and superbase catalysts

The invention relates to a process for preparing solid strong base and superbase catalysts, and belongs to the field of catalysts. The process is characterized by comprising the following steps: (1) adding a particle type carrier containing active hydroxy in a reaction kettle; (2) in vacuum condition, stirring and heating to a temperature of between 80 and 200 DEG C, and removing adsorbed water on the surface of the carrier; (3) raising the temperature to between 200 and 300 DEG C, and adding NaOH or KOH with equivalent mol number to that of the hydroxyl on the surface of the carrier to dehydrate in pressure reduction condition; and (4) preserving heat at a temperature of between 200 and 300 DEG C, and preparing the solid strong base catalyst when no water is generated. The super strong catalysts prepared by the method have high catalytic activity on various organic chemical reactions, can be used for ester exchange reaction, ester condensation reaction, aldol condensation reaction, alkylations of acyl compounds, double bond isomerization of alkene, double bond transfer of unsaturated compounds containing heteroatom, branch alkylation of alkylbenzene, partial hydrogenization of conjugated dienes, amine adding catalytical reaction and the like, and has the advantages of recycling and reuse, simple operation, no environmental pollution and the like.
Owner:ZIBO TED CHEM TECH

Synthetic methods pertaining to tert-butyl-benzene-based compounds

According to some aspects, the present disclosure pertains to methods of forming dimethyl 5-tert-butylisophthalate which comprise comprising converting 5-tert-butylisophthalic acid into dimethyl 5-tert-butylisophthalate in synthesis procedures that comprises methanol and a dehydrating agent as chemical reagents. In other aspects, the present disclosure pertains to methods of forming 5-tert-butyl-1,3-bis(1-methoxy-1-methylethyl)benzene that comprise deprotonating 5-tert-butyl-1,3-bis(1-hydroxy-1-methylethyl)benzene with a Brønsted-Lowry superbase and methylating the deprotonated 5-tert-butyl-1,3-bis(1-hydroxy-1-methylethyl)benzene to form the 5-tert-butyl-1,3-bis(1-methoxy-1-methylethyl)benzene.
Owner:BOSTON SCI SCIMED INC

Method of Charge Reduction of Electron Transfer Dissociation Product Ions

ActiveUS20140110576A1Decrease in state of chargeSimplifying improving qualityPositive/negative analyte ion analysis/introduction/generationIsotope separationNitrogenProton
A mass spectrometer is disclosed wherein highly charged fragment ions resulting from Electron Transfer Dissociation fragmentation of parent ions are reduced in charge state within a Proton Transfer Reaction cell by reacting the fragment ions with a neutral superbase reagent gas such as Octahydropyrimidolazepine.
Owner:MICROMASS UK LTD

Method for preparing fatty acid amide dimethyl tertiary amine compounds from solid superbase

The invention discloses a method for preparing fatty acid amide dimethyl tertiary amine compounds from solid superbase, and belongs to the field of organic chemical synthesis. According to the method,one or several kinds of fatty acids and N,N-dimethylamino compounds are used as raw materials; solid superbase with the advantages of high catalysis activity, cyclic use and environment-friendly effect is used as a catalyst for preparing the fatty acid amide dimethyl tertiary amine compounds. The method has the advantages that the operation is simple and convenient; the post treatment is simple;the reaction conditions are mild; the yield is high; the method belongs to a green novel method for synthesizing the fatty acid amide dimethyl tertiary amine compounds.
Owner:HIGH & NEW TECH RES CENT OF HENAN ACAD OF SCI

Synthetic method of 2,3-pentanedione

The invention relates to a synthetic method of 2,3-pentanedione. The synthetic method of the 2,3-pentanedione comprises the following steps: mixing a lactic acid solution with a solid alkali catalystM / N and carrying out catalytic reaction for 2-10 hours at the temperature being 100-400 DEG C to obtain 2,3-pentanedione. M is an active load and is any one of K2CO3, KHCO3, KNO3, KPO4 and KF, N is acarrier and is any one of Al2O3, a zeolite molecular sieve and ZrO2, and the mole ratio of the active load to the carrier is 1: (0.1-10); and the mass ratio of the solid alkali catalyst M / N to lacticacid is 1: (5-100). Load type superbase is a catalyst, the 2,3-pentanedione is synthesized by catalyzing the lactic acid, the selectivity and the conversion ratio can be high, and the yield of directly synthesized 2,3-pentanedione reaches 60-80%.
Owner:HEFEI UNIV OF TECH

Method for removing chlorobenzene from underground water through nanosolid superbase-activated sodium persulfate

The invention discloses a method for removing chlorobenzene from underground water through nanosolid superbase-activated sodium persulfate. The method concretely comprises the following steps: feeding a nanosolid superbase activator and sodium persulfate into chlorobenzene-polluted underground water so as to conduct oxidization reaction, thus realizing the restoration of the chlorobenzene-polluted underground water. The prepared nanoscale solid superbase can enable aquifer media to fast, effectively and uniformly to achieve a strong basic environment, so that not only can the basic activation condition be continuously maintained, but also sulfate free radical (SO4<->) and hydroxyl free radical (OH) which have strong oxidative activity can be achieved through base-activated sodium persulfate so as to reach the obvious oxidization treatment effect on the chlorobenzene in the underground water, and the oxidization products have no secondary pollution on the underground water. The nanosolid superbase activator not only is low in the cost of raw materials, and environment-friendly, but also is simple and convenient in manufacturing process.
Owner:JIANGSU SUNTIME ENVIRONMENTAL REMEDIATION

Process for highly purified polyhedral oligomeric silsesquioxane monomers

InactiveUS20070065750A1Extended Synthetic MethodsLow resin contentSilicon organic compoundsPhotosensitive materialsSolvent freeSilanol
A synthesis process for polyhedral oligomeric silsesquioxanes that produces in high yield a low resin content, solvent free, and trace metal free monomer suitable for use in microelectronic applications. POSS silanols are reacted with a silane coupling agent in the presence of a solvent and a superbase.
Owner:SCHWAB JOSEPH J +3

Method of synthesizing isopentenol from butenol

The invention is applied to the technical field of synthetic methods of isopentenol, and provides a method of synthesizing the isopentenol from butenol, in particular to a method of generating the isopentenol by double-bond isomerization of 3-methyl-3-butenol under a catalytic action of a catalyst consisting of solid superbase and aluminum isopropoxide, wherein the solid superbase is Na-Na2CO3 / gamma-Al2O3; the dosage of the catalyst is 0.2 percent to 12 percent of the mass of the 3-methyl-3-butenol; the mass ratio of the solid superbase to the aluminum isopropoxide in the catalyst is 1:1 to 1:2; the pressure intensity of reaction is 0.5 to 4MPa, the temperature is 100DEG C to 140DEG C, and the time is 2 to 3h. The method disclosed by the invention has the advantages that reaction conditions are mild; the catalyst is high in activity, is easy to separate and can be repeatedly used; the production cost is low, and environment protection and safety in production are realized; the product is high in purity and selectivity, and is green and environment-friendly; the cost is greatly reduced; the method is a high-efficiency and economic synthetic method, and has a broad prospect.
Owner:SHANDONG CHENGTAI CHEM IND

Process for assembly of POSS monomers

InactiveUS20070232823A1Produce in highHigh yieldSilicon organic compoundsSolvent freeSuperbase
A synthesis process for polyhedral oligomeric silsesquioxanes using phosphazene superbases to produce in high yield a low resin content, solvent free, and trace metal free monomer suitable for use in microelectronic, biological, and medical applications involving polymerization, grafting, and alloying.
Owner:HYBRID PLASTICS INC

Treated Fillers And Uses Thereof

The various embodiments of the present invention relate to condensation curable silicone compositions comprising: a condensation curable polyorganosiloxane; and treated particles comprising a particulate solid having an effective amount of nitrogen-containing base (e.g., a nitrogen-containing superbase) disposed thereon. Other embodiments of the present invention relate to methods for preparing the aforementioned treated particles; the treated particles themselves; and methods of using the treated particles and compositions of the various embodiments of the present invention.
Owner:DOW SILICONES CORP

Method for preparing heptenoic acid cyclopentyl ester derivative

The invention discloses a method for preparing a heptenoic acid cyclopentyl ester product by taking (4R-cis)-6-[(acetoxy)methyl]-2,2-dimethyl-1,3-dioxane-4-tert butyl acetate as an initial raw material, and the product is prepared through steps of hydrolysis, replacement and oxidation. The synthesis step is simple, an intermediate can be subjected to a next reaction without refining and purifying steps, for a butt-coupling reaction, the conventional mild technology condition can replace ultralow temperature reaction condition, superbase with high danger is simultaneously replaced, reaction security is increased, the route total yield is high, and the method is suitable for large-scale industrial production.
Owner:NANTONG CHANGYOO PHARMATECH CO LTD

Process for assembly of POSS monomers

A synthesis process for polyhedral oligomeric silsesquioxanes using phosphazene superbases to produce in high yield a low resin content, solvent free, and trace metal free monomer suitable for use in microelectronic, biological, and medical applications involving polymerization, grafting, and alloying.
Owner:HYBRID PLASTICS INC

A kind of method utilizing solid super base to prepare fatty amide dimethyl tertiary amine compound

The invention discloses a method for preparing fatty acid amide dimethyl tertiary amine compounds from solid superbase, and belongs to the field of organic chemical synthesis. According to the method,one or several kinds of fatty acids and N,N-dimethylamino compounds are used as raw materials; solid superbase with the advantages of high catalysis activity, cyclic use and environment-friendly effect is used as a catalyst for preparing the fatty acid amide dimethyl tertiary amine compounds. The method has the advantages that the operation is simple and convenient; the post treatment is simple;the reaction conditions are mild; the yield is high; the method belongs to a green novel method for synthesizing the fatty acid amide dimethyl tertiary amine compounds.
Owner:HIGH & NEW TECH RES CENT OF HENAN ACAD OF SCI

A kind of preparation method and application of mild reaction type aldehyde and ketone resin

ActiveCN103333302BReduce volatilityOvercoming the disadvantage of being prone to bumpingBuilding insulationsEpoxyFuraldehyde
The invention discloses a preparation method of mild reaction type aldehyde ketone resin. The mild reaction type aldehyde ketone resin is prepared by adding a quantitative superbase catalyst into mixed liquid of aldehyde and ketone compounds under the condition of stirring at normal temperature, wherein the reaction process is mild and stable, so the defect that the traditional furfuraldehyde acetone system is easy to implode is overcome. The invention also discloses an application of the mild reaction type aldehyde ketone resin to preparation of an aldehyde ketone resin modified epoxy grouting material. The prepared grouting material can completely exert the flexibility of the aldehyde ketone resin, solves the problem that epoxy resin has high brittleness, can further improve excellent mechanical properties, adhesive property, ageing resistance and corrosion resistance of the epoxy resin, and also has the characteristics of low toxicity, environmental friendliness and the like. In addition, according to the preparation method, the aldehyde ketone resin is prepared in advance and has higher viscosity and thixotropism when being used together with fillers, so the construction process is simple and the aldehyde ketone resin can be applied to concrete surface corrosion of basic facilities such as bridges and ports, restoration of cultural relic, water and seepage prevention, reinforcement and strengthening of buildings and the like.
Owner:东莞微积分新材料科技有限公司

Technology of extracting triacontanol from natural beeswax by microwave and solid superalkali catalysis

The invention discloses a process for extracting triacontanol from natural beeswax by microwave and solid superalkali catalysis. Firstly, a certain quality of natural beeswax is placed in a container, and methanol is added at a solid-to-liquid ratio of 1:50. Then add KF / γ‑Al in an amount of 30% of the natural beeswax quality 2 o 3 Solid strong alkaline agent, the reaction of several grams of natural beeswax is heated to reflux for 10 minutes under the microwave power of 200-300W, and the reaction of kilograms of natural beeswax is refluxed and heated for 30 minutes under the microwave power of 6 to 9kw, and it is carried out under microwave catalysis Transesterification reaction to obtain a mixture of triacontanol+methanol+methyl oleate+catalyst; filter to recover KF / γ‑Al 2 o 3 Solid strong base agent, to obtain triacontanol+methanol+methyl oleate mixture; then rotary evaporation, recovery of methanol, to obtain triacontanol+methyl oleate mixture; and then recrystallization to obtain triacontanol . Compared with traditional catalysts such as sodium hydroxide and potassium hydroxide under microwave conditions, the present invention forms a high-efficiency, environment-friendly and low-cost production process for preparing triacontanol using natural beeswax as raw material.
Owner:GUANGXI NORMAL UNIV

Method for preparing biodiesel by solid superbase catalysis

The invention discloses a method for preparing biodiesel by solid superbase catalysis. A composite oxide solid superbase catalyst used has a small size, has a cubic shape and is not easy to agglomerate at high temperature. The catalyst has simple composition, high catalytic activity and simple preparation. When the catalyst is applied to various catalytic reactions, the catalyst is used in a smallamount and has no corrosion to a reactor, and the catalyst is an environmentally friendly catalyst. After the end of the reaction, the catalyst can be separated by centrifugation. The catalyst can bereused, the yield of the biodiesel is high, and can reach 96%, the preparation time is short, and the biodiesel meets the standard of European EN14214 biodiesel.
Owner:杭州更蓝生物科技有限公司

Compounded universal type disinfectant

The invention relates to a compounded universal type disinfectant. The compounded universal type disinfectant comprises a mixed solvent, caustic alkali and a complexing agent, wherein the mixed solvent comprises alkyl alcohol amine, alcohol and a polar nonprotic solvent, and the caustic alkali and the complexing agent are dissolved into the mixed solvent. The disinfectant provided by the inventionis one 'superbase' system, has extremely strong nucleophilicity, has extremely high reactivity on disinfection of military highly toxic chemicals and has relatively high solubility on insoluble gluemilitary highly toxic chemicals, so that disinfection efficiency of the disinfectant is enhanced; meanwhile, the disinfectant has extremely low conductivity, good storage stability, low corrosivenessand high safety and can be applied to disinfection of electronic sensitive equipment; besides, the disinfectant provided by the invention also has certain broad-spectrum property on microorganism disinfection, not only can be applied to the field of chemical defense and also can be applied to the fields of public health precaution and the like.
Owner:中国人民解放军陆军防化学院

Synthesis method of mono-sulfhydryl bis-hexadecyl ether polyethylene glycol interchain oligosaccharide glycolipid

The invention discloses a synthesis method of mono-sulfhydryl bis-hexadecyl ether polyethylene glycol interchain oligosaccharide glycolipid. The method is characterized in that 2,3,4,6-O-acetyl-alpha-D-mannopyranose trichloroacetimidate and allyloxy triethylene glycol are used for synthesizing epoxypropyl triethylene glycol acyl mannose in the serial reaction in which chloroperoxybenzoic acid MCPBA and trimethylsilyl trifluoromethanesulfonate TMSOTf are adopted as catalysts; the mannose derivative is sequentially mixed with cetyl alcohol and triphenyl heptadecyl methanesulfonate, and triphenyl-dihexadecyl polyethylene glycol mannose is synthesized by taking sodium hydride as a strong base and adopting boron trifluoride diethyl ether BF3-C2H6O and tetrabutylammonium iodide TABI as catalysts; finally, triphenyl-dihexadecyl polyethylene glycol mannose is mixed with trifluoroacetic acid TFA under the condition of sodium superbase blocks and subjected to a reaction under the catalysis of aphase transfer catalyst benzyl triethyl ammonium chloride TEBA to obtain a target product, namely the mono-sulfhydryl bis-hexadecyl ether polyethylene glycol interchain oligosaccharide glycolipid. Themethod fills up the blank of the synthesis of amphiphilic oligosaccharide containing sulfhydryl difatty chains in the prior art.
Owner:JIANGSU INST OF METROLOGY

Treated fillers and uses thereof

The various embodiments of the present invention relate to condensation curable silicone compositions comprising: a condensation curable polyorganosiloxane; and treated particles comprising a particulate solid having an effective amount of nitrogen-containing base (e.g., a nitrogen-containing superbase) disposed thereon. Other embodiments of the present invention relate to methods for preparing the aforementioned treated particles; the treated particles themselves; and methods of using the treated particles and compositions of the various embodiments of the present invention.
Owner:DOW SILICONES CORP

Catalyst for producing propynyl alcohol by cracking butynediol and preparation method thereof

The invention belongs to the field of industrial catalysis, and in particular relates to a catalyst for producing propynyl alcohol by cracking butynediol and a preparation method thereof. A catalyst for producing propynyl alcohol by cracking butynediol. The catalyst is a solid superbase made of a carrier loaded with a main active component and a coagent. The main active component is one or more of an alkali metal and an alkaline earth metal. Various, the coagent is copper and / or bismuth. It can directly catalyze the cracking of butynediol in an aqueous solution of butynediol to prepare propynyl alcohol. The invention also provides the technological conditions for using the catalyst to catalyze the cracking of butynediol, which can increase the conversion rate of butynediol to 46.3% and the selectivity of propynyl alcohol to 57.4% in the tubular reaction.
Owner:CHONGQING UNIV OF TECH

Enzymatic resolution method for preparation of (R)-1-(1-naphthyl) ethylamine

The invention provides a chemical enzymatic method for preparing (R)-1-(1-naphthyl) ethylamine, wherein the nano palladium is supported by a solid superbase to obtain immobilized palladium; Candida Antarctica lipase B (CALB) was covalently bound to the surface of epoxy resin carrier to obtain immobilized CALB. In reaction system A, immobilized CALB was used as catalyst, toluene as solvent, ethoxyacetate as acyl donor, (R)-1-(1-naphthyl) ethylamine is selectively esterified, solid-liquid separation is carried out after the reaction, immobilized CALB is left in the reaction system A, liquid phase is removed from the reaction system A into the reaction system B, and the palladium catalyst is immobilized by the method, so that the reuse rate of the palladium catalyst is increased.
Owner:JIANGSU UNIV OF TECH
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