264 results about "ALCOHOL/SULFUR" patented technology

A method of forming mono-disperse iron-oxide core metal shell nanoparticles is disclosed. Particle size of the oxide core seeds is controlled and capped seeds are formed. The capping layer is desorbed by a thermally activated process and metal such as gold is chemically deposited on the core seeds in situ. This process can be repeated to produce multi-metal or different metal shells. A second capping layer is applied on the core / shell composite nanoparticles. In another step, the particles are sized by centrifuging to obtain a tightly controlled and narrow particle size distribution. The water-dispersibility of the particles is achieved by a thiol exchange reaction on the gold shell of the core / shell nanoparticles or by deposition of gold on ferritin-derived iron oxide cores in aqueous solution. Mono and multilayer thin films are assembled on different substrates using the core / shell particles and linking molecules.

The invention relates to a catalytically cracked gasoline deep desulfurization method which comprises the following steps: 1. carrying out thiolation reaction, wherein the gasoline is divided into a light component and a heavy component by a rectification tower after reaction; 2. carrying out selective hydrodesulfurization and isomerization on the heavy component; 3. after the selective hydrodesulfurization process, carrying out hydrodesulfurization on secondary mercaptan; 4. etherifying the light gasoline; and 5. finally, blending the light and heavy components to obtain the ultralow-sulfur gasoline product which conforms to the national V gasoline quality standard. The technique is suitable for hydrogenation modification of the catalytically cracked gasoline, and has the advantages of high desulfurization percent, high liquid yield, high catalyst stability of all units, long service life and no discharge of caustic sludge in the whole process.

A backlight unit for a liquid crystal display device, the backlight unit including: an light emitting diode (“LED”) light source; a light conversion layer disposed separate from the LED light source to convert light emitted from the LED light source to white light and to provide the white light to the liquid crystal panel; and a light guide panel disposed between the LED light source and the light conversion layer, wherein the light conversion layer includes a semiconductor nanocrystal and a polymer matrix, and wherein the polymer matrix includes a first polymerized polymer of a first monomer including at least two thiol (—SH) groups, each located at a terminal end of the first monomer, and a second monomer including at least two unsaturated carbon-carbon bonds, each located at a terminal end of the second monomer.

An electrochemical sensor for measuring the amount of hydrogen sulphide or thiols in a fluid in a wellbore comprises a temperature- and pressure-resistant housing containing a flow path for the fluids. The fluids flow over one side of a gas permeable membrane made of zeolite or a suitable ceramic material, the other side of the membrane being exposed to a chamber containing a reaction solution which together with the hydrogen sulphide or thiols create a redox reaction resulting in an electrical current dependent upon the amount of hydrogen sulphide or thiols in the fluid.

Provided is an optoelectronic device that includes: a light source; an emission layer disposed on the light source and including light emitting particles dispersed in a matrix polymer; and a polymer film disposed on the emission layer. The polymer film includes two layers: a first layer including a first polymer and a second layer including a second polymer. The first polymer includes a polymerized product of a first monomer including at least two thiol (—SH) groups and a siloxane-based second monomer or oligomer including at least one carbon-carbon unsaturated bond at a terminal end, and the second polymer includes a polymerized product of a third monomer including at least two thiol (—SH) groups and a fourth monomer including at least two carbon-carbon unsaturated bonds at a terminal end.

A printable metal nanoparticle having a self-assembled monolayer (SAM) composed of a compound containing a thiol (—SH), isocyanide (—CN), amino (—NH2), carboxylate (—COO) or phosphate group, as a linker, formed on the surface thereof, and a method for formation of a conductive pattern using the same are provided. The metal nanoparticles of an exemplary embodiment can be easily formed into a conductive film or pattern by a printing method, and the resulting film or pattern exhibits excellent conductivity which optimally may be adjusted if desired. Therefore, the resulting metal nanoparticles of can be used to advantage in the fields such as antistatic washable sticky mats, antistatic shoes, conductive polyurethane printer rollers, electromagnetic interference shielding materials, etc.

The invention belongs to the technical field of chemical material preparation, and particularly relates to a method for modifying an elastomer by using click reaction of thiol-ene. The method is characterized in that isolate double bonds in an elastomer material are crosslinked with an elastomer compound system by using click chemistry of thiol-ene with the participation of polythiol organic molecules under an UV-irradiation condition so as to achieve the purpose of modifying the elastomer material. The method for modifying the elastomer is simple, easy in obtaining of raw materials and relatively low in cost. The obtained composite material has excellent mechanical property and can be widely applied.

A method for producing a joint member between a carbon fiber composite material containing a thermoplastic resin as a matrix and a metal, includes: forming a layer containing a triazine thiol derivative on a surface of the metal; providing a thermoplastic resin layer between the layer containing a triazine thiol derivative and the carbon fiber composite material; and melting the thermoplastic resin layer to join the metal to the carbon fiber composite material.

This invention provides a process for accumulating different organic molecular films on oxidized III-V-group compound semiconductor substrates in order to produce a stable, high-quality organic monomolecular film that is three-dimensionally regularly arranged, as well as a process for producing a fine pattern of such organic films. This organic film is formed by immersing a III-V group compound semiconductor substrates in a vessel containing a solution containing phosphonic acid dissolved into a solvent in order to form a self-assembled film, and placing the substrate into a different solution to adsorb metal ions to the surface of the film, or immersing the substrate in a bromide or an acid or alkali solution to denature functional groups, then immersing it in a solution containing organic molecules that are selectively chemically adsorbed to the modified functional groups. These steps are repeated to form a stable, high-quality multilayer film that is three-dimensionally regularly arranged, while controlling film thickness with an accuracy on the scale of thickness of a molecular layer.In addition, the present invention realizes the formation of a fine composite three-dimensional organic self-assembled film of the order of nanometer, characterized in that the process comprises using a cleavage method or a very-high-vacuum vessel to form on a substrate with different types of III-V-group semiconductor materials mixed thereon by means of the heteroepitaxial process such as the MBE or MOCVD process, a self-assembled film of the molecules having thiol groups in a non-oxidized area and then forming on an oxidized surface a self-assembled film of molecules having phosphoric acid group, trichlorosilyl groups or alkoxylyl groups.

A circuit board having high adhessiveness contact between electrically insulating layers and having a low interlayer electric resistance is provided. A circuit board is provided with a first conductive layer formed on a core (1) and a first electrically insulating layer formed thereon. In the circuit board, a first conductor layer has a surface roughness Ra of 0.1 nm or more but less than 100 nm, and a first primer layer having a thiol compound as a main material is provided between the first conductive layer and the first electrically insulating layer. Thus, the circuit board which has excellent adhesiveness between the first conductor layer and the first electrically insulating layer and is also applicable to high frequency signal is provided.

The invention relates to a preparation method of a step hole ZSM-5 zeolite composite material-based low-temperature sulfur transfer catalyst for FCC (Fluid Catalytic Cracking) petroleum. The method comprises the following steps of: mixing deionized water, an alkali source and a substrate, adding an aluminum source, a microporous template agent and a silicon source, uniformly stirring to obtain aninitial sol mixed system, adding a mesoporous template agent, uniformly stirring, aging, and performing hydrothermal crystallization; cleaning a hydrothermal crystallization product, washing, separating, drying and baking to obtain a step hole ZSM-5 zeolite composite material; performing ammonium exchange treatment on the step hole ZSM-5 zeolite composite material, cleaning, washing, separating, drying and baking to obtain a hydrogen-type step hole ZSM-5 zeolite composite material; and stepwise soaking an aid and active ingredients onto the hydrogen-type step hole ZSM-5 zeolite composite material by adopting an equal-volume soaking method, airing at the room temperature, drying, and baking to obtain the step hole ZSM-5 zeolite composite material-based low-temperature sulfur transfer catalyst for FCC petroleum. The sulfur transfer removing rates of mercaptan and thiophene can be over 90 percent.

A method for dispersing conductive particles is provided, which takes advantages of simplified process and lower cost. The present invention is in applying of chemical bonding between metal and thiol with electric charge, thereby makes conductive particles and chip bumps carry charges. The conductive particles are then migrated and fixed to the bonding locations on the bumps of a chip through an electrophoresis procedure. The conductive particles will not come off during subsequent processes. The present invention can be applied to flip-chip packaging or other fine-pitch applications. With the present invention, the distance between bumps is smaller than 20 μm and the density of conductive particles is larger than 15 particles per bump.

Provided are an organosilicon surfactant and a thiol-ene click chemistry process preparation method thereof. The organosilicon surfactant is of a structure shown in a formula (I) (shown in the description), wherein the m and the n are integers, the sum of the m and the n is greater than 20 but is smaller than 100, the x is 10-100, the y is 0-80, the x and the y are integers, and the R is C1-10 straight-chain or heterogeneous long-chain alkyl or alkyl phenyl. The preparation method comprises the steps that thiol polyether and vinyl polysiloxane serve as raw materials and are dissolved in a benign solvent, a light initiator is added under stirring for reaction, the reaction materials are subjected to vacuum rotary evaporation at the temperature of 25-45 DEG C to remove the solvent after the reaction is completed, then vacuum drying is performed at the temperature of 30-60 DEG C for 2-48 hour to obtain the organosilicon surfactant having structural characteristics shown in the formula (I). Precious metal catalysts (such as a metal platinum catalyst) used for synthesis of organosilicon surfactants in the prior art are abandoned, and environmental protection and safety and widening of the product application field are guaranteed.

The present invention relates to a method of shaping a fibrous material and treatment compositions therefor. The method comprises providing a treatment composition comprising an active agent and a photocatalyst, applying the treatment composition to the fibrous material to form a treated fibrous material, mechanically shaping the treated fibrous material, and exposing the treated fibrous material to electromagnetic radiation. The treatment composition comprises an active agent, wherein the active agent comprises a thiol; and a photocatalyst.

The invention discloses a preparation method of a anticorrosive film for metal surface, which is characterized by comprising the following steps: dissolving dopamine in a aqueous solution of tris(hydroxymethyl)aminomethane hydrochloride or phosphate, stirring, dipping metal, contacting for 12-90 h and then taking out, flushing by deionized water, drying by nitrogen and then putting in a solution containing alkane thiol, carrying out water bathing at 20-30 DEG C for 24-48 h and then taking out, flushing by the solution containing the alkane thiol, drying by the nitrogen, and then forming an anticorrosive film on the surface of the metal. By adopting the method, a stable anticorrosive film layer can be formed on a metal substrate with strong cohesion; the preparation method does not need long reaction time and does not need to etch the metal; and the prepared metal surface anticorrosive film has good anticorrosive performance and high protection efficiency as high as 99%.

A capacitor and a manufacturing method thereof are provided. Two electrodes are disposed opposite to each other. Two electrode protection layers are respectively disposed on inner sides of the electrodes and include carbon particles each covered and bonded with a polymer shell. Active carbon layers are disposed on opposite inner sides of the electrode protection layers. The separator is disposed between the active carbon layers. The electrolyte fills between the electrode protection layers. The polymer shells of each electrode protection layer are bonded to the surface of the corresponding electrode by first and second functional groups. The first functional groups include thiol groups. The second functional groups include epoxy groups or carboxylic groups. The electrode protection layers serve as adhesion layers between the active carbon layers and the electrodes, and protect the electrodes from being corroded by the acid electrolyte solution.

The invention relates to a micro-nano orderly through-hole array metal film sensor based on a piezoelectric substrate sheet. The micro-nano orderly through-hole array metal film sensor structurally comprises a micro-nano orderly through-hole array metal film, the piezoelectric substrate sheet and an annular metal film from top to bottom, wherein the substrate is made of piezoelectric quartz crystals or piezoelectric ceramic. A manufacturing method is further provided. According to the manufacturing method, micro-nano orderly array patterns and annular patterns are machined on a silicon wafer through photoetching, and then a composite stamp with a hard PDMS (A:B=1:3) pattern layer and an elastic PDMS (A:B=1:10) substrate layer is copied through polydimethylsiloxane (PDMS, obtained by mixing the component A and the component B); thiol ink is smeared on the surface of the stamp, the stamp is pressed on the piezoelectric substrate plated with a gold film, and then anti-corrosion patterns of a compact thiol monomolecular layer is formed through self assembly; a porous gold film and an annular gold film are manufactured through wet method etching. The micro-nano orderly through-hole array metal film sensor can be applied to the field of combined sensing through the optical abnormal transmission technology, the quartz crystal microbalance technology and the electrochemistry technology and other fields. The manufacturing method has the advantages of being easy and convenient to perform, low in cost, controllable, high in repeatability and the like.

The invention discloses a method for simultaneously detecting hydrogen sulfide and thiol in crude oil by using photoelectric double signals and a detector thereof. The invention has the advantages of simple structure, easy operation, low operating cost (using air as the carrier gas), favorable stability and reproducibility, and high detection efficiency and precision. The nano catalysis luminescent detector is used for detection; the nano material is cerium oxide / aluminum oxide composite material, and cerium oxide accounts for 10-30% of the total mass of the composite material; the detection wavelength is 400-460 nm; the heating temperature range for the nano material is 200-300 DEG C; the flow rate of the carrier gas is 20-200 ml / min; a voltage is applied to both ends of the nano material; and the current value is taken as the detection signal. Compared with the prior art, the detector is characterized in that both ends of the nano semiconductor metal oxide are respectively provided with a positive electrode and a negative electrode, and a current output and photoelectric signal conversion device between the positive electrode and the negative electrode is connected with an electric signal detection circuit.

The invention provides a gasoline desulfuration and deodorization process, which adopts a fiber liquid film mass transfer mode and a fixed bed reactor series connection mode to conduct gasoline desulfuration and deodorization purification. Gasoline is firstly contacted with alkali liquor in a fiber liquid film device, hydrogen sulfide and a large part of mercaptan in the gasoline are extracted to enter the alkali liquor and then are sent to a fixed bed reactor; under effects of oxidation air and activating agents, remained mercaptan is oxidized to be corresponding disulphide; and finally the gasoline desulfuration and deodorization purification is achieved. The gasoline desulfuration and deodorization process can not only improve efficiency of gasoline alkali wash in advance, but also achieve the purpose of effectively reducing equipment investment of a fixed bed, reducing use amounts of catalytic agents and the activating agents, and effectively guaranteeing product sulphur contents to reach the standard and the like.

The invention discloses a reinforced heat plastic composite material of preparing method of glass fiber needled felt, which comprises the following steps: (1) blending polyvinyl chloride paste resin and water with rate at 1: 2-4, adding 1-4% modifier and 3-6% methyl thiol tin stabilizer of PVX paste resin, stirring evenly to prepare water suspension, soaking 30-35% single-layer continuous glass fiber felt in the water suspension, drying, draining, punching to obtain the pre-soak belt, (2) placing the pre-soak belt in the three-layer mould, preheating for 10 min at 190-200 deg.c under 10Mpa for 25min, stripping to obtain the composite material.

Provided is a light- and heat-curable resin composition that has a sufficiently long pot life. The resin composition contains (A) an acrylic resin, (B) a thiol compound, (C) a latent curing agent, (D) a radical polymerization inhibitor, and (E) an anionic polymerization suppressor. The resin composition preferably further contains (F) a radical polymerization initiator. The resin composition preferably also contains (G) a compound other than an acrylic resin having at least two double bonds.

The present invention describes a new synthetic strategy that permits to produce 2D 1D, e OD hybrid organic-inorganic nanocrystals of tungsten / molybdenum chalcogenides. The innovative chemical approach is based on the thermal decomposition of a molecular precursor containing both metal and sulphur, in a mixture of long chain amines and / or fatty acids and / or long chain thiols. By the control of reaction conditions is possible to address the synthesis can be driven towards the formation of nanosystems with different morphologies such as sheets, particles, rods, tubes.

A phthalocyanine dye of formula (I) is provided: wherein: M is a metal group or is absent; n is 1 or 2; X is selected from —CHR3—, —NR3—, —O— or —S—; R1, R2 and R3 are independently selected from hydrogen, C1-8 alkyl, C1-8 alkoxy, carboxy, carboxy-C1-8 alkyl, hydroxyl, hydroxy-C1-8 alkyl; or R1 and R2, or R2 and R3 together are joined to form a C4-12 aryl or C3-12 heteroaryl group, optionally substituted with 1, 2, 3 or 4 substituent groups, the or each substituent group being independently selected from C1-12 alkyl, C1-12 alkoxy, phenyl-C1-8 alkyl, phenyl-C1-8 alkoxy, —(OCH2CH2)dORd, cyano, halogen, amino, hydroxyl, thiol, —SRv, —NRuRv, nitro, phenyl, phenoxy, —CO2Rv, —C(O)Rv, —OCORv, —SO2Rv, —OSO2Rv, —NHC(O)Rv, —CONRuRv, —CONRuRv, sulfonic acid, sulfonic acid salt and sulfonamide; d is an integer from 2 to 5000; Rd is H, C1-8 alkyl or C(O)C1-8 alkyl and Ru and Rv are independently selected from hydrogen, C1-12 alkyl, phenyl or phenyl-C1-8 alkyl. Dyes of this type are especially suitable for use in netpage and Hyperlabel™ systems.

The invention discloses a method for producing low sulfur gasoline by using by inferior gasoline fractions. The method comprises the following steps of: pretreating a full-range inferior gasoline material to remove diene and thiol; performing fractionation to obtain light fractions and heavy fractions; performing selective hydrodesulfurization on the heavy fractions by using a selective hydrodesulfurization catalyst; and mixing a desulfurization product and the light fractions to obtain a clean gasoline product. In a pretreatment catalyst adopted, alumina or silicon-containing alumina is taken as a carrier, copper and zinc are taken as active ingredients, and phosphorus is taken as an aid. Compared with the prior art, the method has the advantages that: deep desulfurization can be achieved, the loss of octane number is small, the catalysts have high activity and stability, and the running period of a device is long.

Provided is a resin composition that is suitable as a one-component adhesive to be used during production of image sensor modules and electronic components due to being heat-curable at a temperature of approximately 80 DEG C and having exceptional PCT resistance. This resin composition is characterized by containing (A) an epoxy resin, (B) a compound shown by formula (1), (C) a curing accelerator, and (D) a silane coupling agent, the contained amount of the compound of component (B) being from 1:0.5 to 1:2.5 by equivalent ratio of epoxy groups in the epoxy resin of component (A) and thiol groups in the compound of component (B), the contained amount of the silane coupling agent of component (D) being from 0.2 to 50 parts by mass per 100 total parts by mass of component (A), component (B), component (C), and component (D), and the equivalent ratio of thiol groups in the compound of component (B) and Si in the silane coupling agent (D) being from 1:0.002 to 1:1.

A method for bonding two free surfaces, respectively of first and second different substrates, includes a formation step, on the free surface of the first substrate, of a self-assembled mono-molecular layer consisting of a thiol compound of the SH—R—X type, where —R is a carbonaceous chain and —X is a group selected from the group consisting in —H, —OH and —COOH, at least said free surface of the first substrate being formed by a material able to form molecular bonds with the —SH group of the thiol compound. The method also includes preparing the free surface of the second substrate consisting in saturating the free surface of the second substrate with —H groups if —X is a —H group or with —OH groups if —X is selected from the group consisting in —OH and —COOH, and placing the two free surfaces in contact.

A method and structure is provided for preventing wetting or bleed of an adhesive, such as an epoxy, onto noble metal wire bond pads on the surface of a dielectric substrate when attaching an I / C chip to the substrate. The method includes treating the wire bond pads with a chemical composition which prevents bleeding onto the surfaces of the wire bond pads by a component of the epoxy. The chemical composition is a chemical which will provide "Self-Assembled Monolayers" (SAMs) on the surface of the gold. These compositions are characterized by a molecule having at least one group, such as a mercaptan or disulfide, connected to a hydrocarbon moiety, such as a (CH2)x chain. The affinity of the thiol or sulfur-containing portion of the molecule chemically bonding with the noble metal provides a relatively strong attachment of the molecule to the metal surface. The hydrocarbon segment presents a surface on the noble metal that has the characteristics of the hydrocarbon portion of the molecule which has a low surface tension, and, thus, prevents wetting of the noble metal by an epoxy adhesive component.The SAMs, once they provide protection from the bleed of the die attach adhesives, self desorb during the wire bonding or soldering temperatures.

A process for reducing the sulfur content of a hydrocarbon stream, including: feeding a hydrocarbon stream including sulfur compounds to a catalytic distillation reactor having one or more hydrodesulfurization reaction zones; feeding hydrogen to the catalytic distillation reactor; concurrently in the catalytic distillation reactor: fractionating the hydrocarbon stream into a heavy fraction and a light fraction; contacting hydrogen and the light fraction to form H2S and a light fraction of reduced sulfur content; recovering the light fraction, H2S, and hydrogen as an overheads; recovering the heavy fraction; heating the overheads to a temperature from 500 to 700° F.; feeding the heated overheads and hydrogen to a high temperature low pressure reactor to form H2S and a reactor effluent of reduced mercaptan content; separating the reactor effluent, H2S, and unreacted hydrogen to form a light hydrocarbon fraction and a fraction including H2S and hydrogen; recycling a portion of the light hydrocarbon fraction to the catalytic distillation reactor.

The invention discloses a supported metal nano-cluster catalyst for CO oxidation. The formula of the supported metal nano-cluster catalyst for CO oxidation is (M1)n(SR)m / M'xOy, wherein (M1)n(SR)m is metal nano cluster, M1 is a metal such as Au, Ag or an alloy thereof, SR (R=CH2CH2Ph) is an organic thiol ligand of the metal nano cluster, and M'xOy is a metal oxide carrier such as CeO2, ZrO2 and the like. In the supported metal nano-cluster catalyst, the metal nano cluster composition (M1)n(SR)m has the characteristics that the thermal stability is good, the size distribution of active nano metal particles is controllable, and the like. The supported metal nano-cluster catalyst embodies an excellent CO oxidation performance, and especially shows a stable CO oxidation performance in the atmosphere of a raw material gas added with water vapor. When the supported metal nano-cluster catalyst such as Au25 (SR) 18 / CeO2 catalyst is used, the CO conversion rate at 80 DEG C is 94%, and the CO conversion rate at 100 DEG C is 100%.