12 results about "Proton acceptor" patented technology

The invention belongs to the field of new energy material synthesis and electro-catalysis, and particularly relates to a chiral molecule coupling layered hydroxide catalyst and a preparation method and application thereof. The invention innovatively provides a synergistic strategy fusing chiral molecular engineering and a bionic design principle to improve the oxygen evolution performance of the nickel-iron layered hydroxide, a one-step hydrothermal method is adopted for preparation, controllable anchoring of chiral molecules between layers of the nickel-iron layered hydroxide is realized, and the performance of the nickel-iron layered hydroxide is improved. Chiral molecules with a proton acceptor function are introduced into a NiFe-LDH interlayer; due to the steric hindrance and coordination characteristics of chiral molecules, regular growth of NiFe-LDH laminates can be disrupted, and more lattice defects, edge sites and unsaturated coordination metal centers are induced to be generated. The coordination effect of chiral molecules and metal centers (Ni and Fe) can adjust the electronic state and valence state of metal, so that the reaction energy barrier is reduced, and the reaction kinetics is accelerated.

This document describes a pharmaceutical composition comprising a therapeutic agent, an absorption enhancer, a polymer comprising multiple basic groups, and a non-polymeric (small molecule) proton acceptor. The absorption enhancer is preferably a substituted fatty acid or a salt thereof. This document also describes a method of treating a condition treatable by the therapeutic agent, comprising oral administration of the pharmaceutical composition.

The invention provides a method of continuous electrochemical dinitrogen reduction to produce ammonia, the method comprising: supplying dinitrogen to an electrochemical cell comprising an electrolyte in contact with at least a cathode; introducing protons to the electrolyte by anodic oxidation of a hydrogen-containing species; and cathodically reducing the dinitrogen in the presence of a metal selected from lithium, magnesium, calcium, strontium, barium, zinc, aluminium and vanadium to produce ammonia, wherein the electrolyte comprises a cationic proton carrier capable of reversible deprotonation to form a neutral proton acceptor, wherein the neutral proton acceptor is an ylide.

The application discloses an organic superlattice material, a lithium-doped organic superlattice material and a preparation method and application thereof, and relates to the technical field of superlattice materials.The organic superlattice material comprises a first organic crystal layer and a second organic crystal layer which are alternately stacked, the first organic crystal layer comprises a network structure formed by a first small-molecule organic compound, and the second organic crystal layer comprises a network structure formed by a second small-molecule organic compound; wherein the first small-molecule organic compound comprises a first monocyclic aromatic compound, and the first monocyclic aromatic compound has a proton donor group; and the second small-molecule organic compound comprises a second monocyclic aromatic compound, and the second monocyclic aromatic compound has a proton acceptor group.A new organic superlattice material is provided, which is applied to a solid-state electrolyte and can improve ionic conductivity.

This invention relates to the field of acyclic or carbocyclic compounds and discloses a method for preparing 6-bromo-2,3-difluorotrifluorotoluene, comprising: dissolving 2,3-difluorotrifluorotoluene in a mixed solvent composed of a polar modifier containing a proton acceptor site and a nonpolar solvent; adding a polyether stabilizer and an iron-based catalyst; and dropwise adding liquid bromine to trigger a directional bromination reaction. The method utilizes the protonated ion-pair complex formed by the in-situ generation of hydrogen bromide and the polar modifier, which, in conjunction with the polyether stabilizer, constructs a sterically hindered shielding structure at positions 4 and 5 of the substrate molecule. This invention forces the electrophilic substitution pathway to be directed towards position 6 of the substrate molecule, overcoming the bottleneck of extremely low positioning accuracy in passivated aromatic ring systems, transforming disordered isomers into a single dominant isomer, thereby reducing separation energy consumption.

The application discloses an absorption-delivery system for flue gas carbon dioxide capture, which is composed of a hydrophobic high-boiling point hydrophilic absorbent with a very high absorption rate and a high cycle load, and is used for absorbing and delivering carbon dioxide; the absorption-delivery process is that the hydrophobic absorbent directly contacts the flue gas, quickly absorbs CO2, and then reacts to generate a product, then the hydrophobic absorbent contacts the hydrophilic absorbent, the CO2 molecules in the product are delivered to the hydrophilic absorbent by using the strong interaction between the hydrophilic absorbent and the CO2 molecules or the strong proton acceptor characteristics of the hydrophilic absorbent, so that the hydrophobic absorbent is released and reduced, and then contacts the flue gas again to absorb CO2, thereby realizing the recycling of the absorbent. Compared with traditional hydrophilic absorbents, the CO2 absorption-delivery system has the advantages of a fast absorption rate, a low regeneration energy consumption and long-term stability.

The invention belongs to the technical field of inorganic gelling agent additives, and particularly relates to a strength deterioration resistant additive for flocculation and dehydration of cement residues, a synchronous grouting material and a preparation method of the synchronous grouting material, and the synchronous grouting material comprises the following components in parts by mass: 0.1-2 parts of a strong electron acceptor; 0.1-1 part of a strong proton acceptor; 0.1-2 parts of a high-charge metal ion compound; 90-180 parts of industrial solid waste; the strong electron acceptor is persulfate; the strong proton acceptor is cesium hydroxide or / and rubidium hydroxide; the high-charge metal ion compound is selected from at least one of ferric nitrate, ferric sulfate, aluminum nitrate or aluminum sulfate; the industrial solid waste is common industrial solid waste and superfine industrial solid waste. The synchronous grouting material has the advantages of being high in stability, excellent in mechanical property, low in cost, environmentally friendly, low in carbon and the like, and high-added-value utilization of dewatered cement slag type waste is achieved easily.

A composition usable for removing biofilm and necrotic or infected tissue from a skin lesion, comprising ethanesulfonic acid or 1-propanesulfonic acid and a proton acceptor. The proton acceptor is selected from the group consisting of dimethyl sulfoxide, silicon dioxide, tetraethoxysilane, and mixtures thereof. This composition can be prepared in gel form.

A CO2 absorbent, an enhanced amine-based flue gas decarbonization method, and a decarbonization device. The absorbent is mainly composed of a shuttle agent and a proton acceptor; the molar ratio of the shuttle agent to the proton acceptor is 1:1-1:5; and the molar ratio of the shuttle agent to the proton acceptor is 1:3. By preparing the absorbent and introducing, into the absorbent, flue gas that has been broken into micro-bubbles, the micro-bubbles, under the action of a drag force, can move in synchrony with a liquid phase, thereby forming a uniform gas-liquid mixture, enhancing the cyclic loading of the absorbent, reducing the overall energy consumption of a decarbonization process, and improving CO2 removal efficiency.

The present invention relates to a method for purifying a nucleic acid from a sample containing the nucleic acid in a simple, short-time and high-purity manner, and a kit for the purification. This method for purifying a nucleic acid comprises a step for bringing a sample containing a nucleic acid into contact with a zeolite and a proton acceptor.

The present invention further relates to a composition comprising methanesulfonic acid and a non-aqueous proton acceptor for use in a method for the treatment and management of one or more of fistula, pilonidal sinus, herpes labialis, pyogenic granuloma, fungal nail infection and onicocriptosis.

Aqueous anolytes for redox flow batteries are disclosed. The anolytes include a fluorenone-fluorenol derivative, an additive comprising an organic compound including one or more proton acceptor groups, an alkali metal hydroxide, and water. The additive functions as a homogeneous organocatalyst and may increase the current density of an aqueous redox flow battery including the anolyte.