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67 results about "Ferriporphyrin" patented technology

Ferriporphyrin definition is - a red-brown to black ferric derivative of a porphyrin that differs from a ferroporphyrin by the additional combination of a univalent anion (as chloride) with the iron atom.

Preparation method of iron molybdenum based catalyst for preparing formaldehyde by methanol oxidation and application

The invention relates to a preparation method of an iron molybdenum based catalyst for preparing formaldehyde by methanol oxidation and application. The method is characterized in that macromolecularheterocyclic compounds such as ferriporphyrin molybdenum porphyrin are treated as the raw materials and subjected to nano self-assembling to prepare nano structures with different appearance and sizeand regular and stable structures; the nano structures are thermally treated to obtain a series of iron molybdenum based catalysts for preparing formaldehyde by methanol oxidation; the size and appearance of the regular ferrum-molybdenum nano structures can be changed to realize the control of binary activity center spacing, ratio and distribution of ferrum and molybdenum, and thus the effective contact area of ferrum and molybdenum is increased. With the adoption of the catalyst, methyl alcohol can be efficiently converted under the condition that the pressure is normal pressure, the reactiontemperature is 230-420 DEG C, the volume content of input methyl alcohol is 1-15%, and the gas carrying airspeed is 3000-15000h<-1>. The preparation method is simple to operate, and easy to widely apply; the method is applicable to the fields such as methanol oxidation type formaldehyde preparation and has a good industrial application prospect.
Owner:DALIAN INST OF CHEM PHYSICS CHINESE ACAD OF SCI

High-sensitivity photoelectrochemical sensor made from iridium oxide-ferriporphyrin-titanium oxide and preparation method for sensor

The invention belongs to the technical field of photoelectrochemical sensors, and in particular relates to a high-sensitivity glutathione photoelectrochemical sensor made from iridium oxide-ferriporphyrin-titanium oxide and a preparation method for the sensor. The photoelectrochemical sensor takes an iridium oxide-ferriporphyrin-titanium oxide nano wire array as a working electrode, an Ag / AgCl electrode as a reference electrode and a platinum wire as a counter electrode; a PBS (phosphate buffer solution) with the pH of 7.4 is used as reaction electrolyte; the irradiation light intensity is equal to the sunshine, and the irradiation sectional area is 0.02-0.06cm<2>; the lowest sensitivity is 10nM. The preparation method comprises the steps of preparing a titanium oxide nano wire by adopting a hydrothermal method, bonding upper ferriporphyrin through chemical coupling, finally performing chemical immersion deposition on iridium oxide to prepare the iridium oxide-ferriporphyrin-titanium oxide nano wire array, and then preparing the photoelectrochemical sensor. The raw materials of the photoelectrochemical sensor are readily available; the preparation method is simple, environmentally-friendly, low in cost, high in response speed, large in linear range, high in selectivity and favorable for popularization and application.
Owner:FUDAN UNIV

Application of ferric iron ferriporphyrin compound in preparation of anti-type-2 diabetes drug

ActiveCN102935222AHigh ascorbate peroxidase activityReduce cholesterolDipeptide ingredientsMetabolism disorderPeroxidaseSuperoxide
The invention provides application of a ferric iron ferriporphyrin compound in preparation of an anti-type-2 diabetes drug and belongs to the technical field of biological pharmacy. The ferric iron ferriporphyrin compound consists of heme and oligopeptide. A carboxyl of the heme is connected with an amino on a peptide chain through an amido bond to achieve connection of the heme and the oligopeptide. Other type-2 diabetes treating or preventing drugs can be applied to the drug preparation. The ferric iron ferriporphyrin compound serves as a peroxidase stimulant, has small molecular weight, can enter cells to effectively remove internal superoxide, super-oxygen ions and free radicals and has the effects of reducing blood sugar, cholesterol and triglycerides activity.
Owner:吉林省润宝生物科技有限公司

Preparation method of fullerene/tetraphenylferriporphyrin self-assembled structure oxygen reduction electrocatalyst

The invention relates to a preparation method of a fullerene/tetraphenyl ferriporphyrin self-assembled structure oxygen reduction electrocatalyst. The preparation method comprises the following steps: carrying out condensation reflux on tetraphenyl porphyrin, iron nitrate nonahydrate and a DMF solvent, and carrying out vacuum drying to obtain tetraphenyl ferriporphyrin; preparing a fullerene toluene solution, mixing the fullerene toluene solution with the isopropyl alcohol suspension of tetraphenyl ferriporphyrin, performing standing, carrying out suction filtration, washing, and carrying out vacuum drying to obtain a sample with a self-assembly structure; taking a self-assembled sample and flatly spreading in a magnetic boat, putting the magnetic boat into a quartz tube protected by hydrogen and argon mixed gas, performing a heat preservation reaction at the temperature of 600-800 DEG C, performing natural cooling to the room temperature, and obtaining the fullerene/tetraphenylferriporphyrin self-assembled structure oxygen reduction electrocatalyst. The process for preparing the C60/FeTPP self-assembly structure through a liquid-liquid interface precipitation method is mature, simple to operate, low in production cost and easy for industrial production. A donor-acceptor system with charge transfer can be effectively constructed, and the half-wave potential of the donor-acceptor system can reach 0.86 V (vs.RHE).
Owner:SHAANXI UNIV OF SCI & TECH

Preparation method and use of cadmium sulfide-immobilized tetra(4-carboxyphenyl)ferriporphyrin catalysis material

The invention discloses a preparation method and use of a cadmium sulfide-immobilized tetra(4-carboxyphenyl)ferriporphyrin catalysis material. The preparation method comprises preparing cadmium sulfide through a microwave method, stirring and dispersing the generated cadmium sulfide in waterless ethanol, adding a waterless ethanol solution of tetra(4-carboxyphenyl)ferriporphyrin into the waterless ethanol solution of cadmium sulfide, heating the mixed solution to a temperature of 60-70 DEG C, carrying out stirring for 5-6h, carrying out pressure reduction pumping filtration to obtain filter cake, carrying out Soxhlet extraction on the filter cake through cyclohexane until the filtrate is colorless, and drying the obtained solids at a temperature of 120-140 DEG C for 10-12h to obtain the catalysis material. The preparation method has simple processes, low energy consumption and a low cost, can be used for production of cyclohexanol and cyclohexanone through catalytic oxygen oxidation of cyclohexane and has a conversion rate of 27.3%. The catalysis material has good catalysis effects, basically keeps catalysis efficiency after cyclic catalysis eight times, has a practical application value and is an ideal biomimetic catalyst.
Owner:GUANGXI UNIV

Preparation method of graphene/ferriporphyrin/gold nanoparticle composite material

The invention discloses a preparation method of a graphene/ferriporphyrin/gold nanoparticle composite material. The preparation method includes the following steps that oxidized graphene is prepared; 5 mL of a 1.0 mg/mL oxidized graphene water solution and 5 mL of 1.5 mg/mL ferriporphyrin turbid liquid are ultrasonically treated for 20 min at normal temperature, and the oxidized graphene water solution and the ferriporphyrin turbid liquid are mixed and then ultrasonically treated for 10 min; 40 microliters of a 0.025 mol/L HAuCl4 solution is added, ultrasonic mixing is conducted for 10 min, a NaOH solution is added dropwise, the pH value is adjusted to be about 10, and mixed liquid is ultrasonically treated for 10 min; the mixed liquid is magnetically stirred in a 90 DEG C water bath, and a condensation backflow reaction is conducted for 3 h; sublayer sediment is acquired centrifugally at the 12,000 r/min rotating speed; residual ferriporphyrin is washed away through tetrahydrofuran, the sublayer sediment is washed away through deionized water, and centrifugal separation is conducted and repeated multiple times till the pH value of supernatant liquid is about 7; a sublayer product is transferred to a small glass bottle and set to certain constant volume through deionized water; whether the reaction is complete or not is confirmed through color distinguishment and instrument analysis, and the required material is prepared after the reaction is complete.
Owner:YANCHENG INST OF TECH

Preparation method of composite structure oxygen reduction electrocatalyst for fuel cell cathode

The invention relates to a preparation method of a composite structure oxygen reduction electrocatalyst for a fuel cell cathode. The preparation method comprises the following steps: condensing and refluxing tetrapyridyl porphyrin, ferric trichloride hexahydrate and a DMF (Dimethyl Formamide) solvent, removing a solution by using rotary evaporation, putting residues into a culture dish, freezing, transferring a solid into a freeze dryer, and drying to obtain tetrapyridyl ferriporphyrin; adding fullerene C70 and tetrapyridyl ferriporphyrin into a toluene solution, and carrying out ultrasonic dispersion to obtain a mixed solution; adding isopropanol into the mixed solution, standing for reaction, then carrying out suction filtration and washing, and carrying out vacuum drying to obtain a composite sample precursor; and uniformly spreading the composite sample precursor in a magnetic boat, putting the magnetic boat into a quartz tube taking hydrogen-argon mixed gas as a protective atmosphere, keeping the temperature at 700-900 DEG C for 2-4 hours, naturally cooling to room temperature, and grinding to obtain the composite structure oxygen reduction electrocatalyst. The process is simple to operate, the selected raw materials are low in production cost, and industrial production is easy. The obtained C70 / FeTPPy composite structure is expected to become a substitute of a noble metal catalyst. And the half-wave potential can reach 0.87 V (vs.RHE).
Owner:SHAANXI UNIV OF SCI & TECH

Method for preparing cyclic carbonate by transforming carbon dioxide with iron-based catalyst

The invention discloses a method for preparing cyclic carbonate by transforming carbon dioxide with an iron-based catalyst. The carbon dioxide and epoxide are taken as raw materials, a conjugated ferriporphyrin microporous polymer material is taken as a multiphase catalyst, and tetra-n-butylammonium bromide is taken as a co-catalyst to realize high-efficiency green catalytic synthesis of the cyclic carbonate under a normal-temperature, normal-pressure and solvent-free condition. The method has the major advantages of simple preparation method, low cost, high catalytic activity, stable structural performance, easiness in recycling and reusability of the catalyst, mild reaction conditions, high rate and safety in operation, and is suitable for large-scale industrial production.
Owner:HENAN INST OF ENG

Polyacrylonitrile fiber-hemin biomimetic catalyst and preparation method thereof

The invention discloses a polyacrylonitrile fiber-hemin biomimetic catalyst and a preparation method thereof. The biomimetic catalyst is in a shape of fibers and is prepared after 2-aminooimidazole modified polyacrylonitrile fibers and natural ferriporphyrin compound hemin react. The preparation method comprises steps as follows: firstly, polyacrylonitrile fibers are subjected to a modification reaction by the aid of 2-aminooimidazole under the conditions that the pH is 9.5 and the temperature is 95 DEG C, an active group containing an imidazole ring structure is obtained, the obtained modified acrylic fibers and a DMF solution of hemin are subjected to a coordination reaction, and the polyacrylonitrile fiber-hemin biomimetic catalyst simulating the structure of horseradish peroxidase is obtained. The biomimetic catalyst is applicable to an oxidation degradation reaction of dye and other organic pollutants in water; compared with treated hemin, the polyacrylonitrile fiber-hemin biomimetic catalyst has the advantages that the catalysis activity of the catalyst is remarkably enhanced due to introduction of a polyacrylonitrile fiber carrier, and the pH adaptability and the use stability of the catalyst are greatly improved.
Owner:TIANJIN POLYTECHNIC UNIV

Nitric oxide reductase analogs and preparation method thereof

The invention discloses nitric oxide reductase analogs and a preparation method thereof. Chemical names of the analogs comprise ferriporphyrin NO complexes and ferriporphyrin chlorides, bound ferriporphyrin NO complexes comprising C2-C5 alkyl are 1-FeNO to 4-FeNO, and corresponding precursor compounds, i.e., ferriporphyrin chlorides are 1-FeCl to 4-FeCl. The preparation method comprises the stepsof applying alkyl bridged bis(5-tert-butyl salicylaldehyde), synthesizing the ferriporphyrin chlorides by using a metal template method, carrying out decomposition by using nitrous acid to produce NO,and subjecting the NO to axial substitution, thereby obtaining the ferriporphyrin NO complexes. According to the method, by using the characteristic that a metal electron structure is regulated and controlled through porphyrin ring deformation, the interconversion of axial NO ligands to nucleophilic from electrophilic is achieved. The analogs are of nonplanar-structure continuous variation whichare similar to variation of structures and functions of nitric oxide reductase, the synthesis steps are few, the raw materials are economical and readily available, separation and purification costs are relatively low, and thus, the analogs are relatively ideal analogs of the nitric oxide reductase.
Owner:HUNAN UNIV OF SCI & TECH

Long-time chemiluminescence system based on ferriporphyrin metal-organic framework material/glucose oxidase

The invention discloses a long-time chemiluminescence system based on ferriporphyrin metal-organic framework material/glucose oxidase. The chemiluminiscence system takes a ferriporphyrin metal-organicframework material/glucose oxidase compound as a catalyst of chemiluminiscence reaction and luminol and glucose as chemiluminiscence substrates, and generates long-time chemiluminiscence by utilizinglocal cascade catalysis of the ferriporphyrin metal-organic framework material and the glucose oxidase. The ferriporphyrin metal-organic framework material is prepared by taking Zr < 4 + > as a metalcenter and ferriporphyrin as a ligand through a hydrothermal method, and has relatively high peroxidase activity and stability; the glucose oxidase is modified on the surface of the ferriporphyrin metal-organic framework material through electrostatic adsorption, and the ferriporphyrin metal-organic framework material/glucose oxidase compound is prepared. A mixed solution system containing the ferriporphyrin metal-organic framework material/glucose oxidase compound, the luminol and the glucose can generate 7.5-hour stable high-intensity chemiluminescence. The chemiluminiscence system can generate long-time stable high-intensity chemiluminiscence under physiological conditions, and has a good application prospect in the aspects of biological detection and imaging.
Owner:NANJING UNIV

Method for preparing cyclic carbonate by iron-based catalyst

The invention discloses a method for preparing cyclic carbonate by an iron-based catalyst. Carbon dioxide and epoxide serve as raw materials, a conjugate ferriporphyrin dipyridyl / conjugate ferriporphyrin dipyrrole microporous polymer material serves as a heterogeneous catalyst, tetra-n-butylammonium bromide serves as a co-catalyst, and efficient green catalytic synthesis of cyclic carbonate is realized at normal temperature and pressure in a solvent-free manner. The method mainly has the advantages that the catalyst is simple in preparation method, low in cost, high in catalytic activity, stable in structural performance, easy to recycle, reusable, mild in reaction condition, high in speed, safe to operate and applicable to large-scale industrial production.
Owner:HENAN INST OF ENG

Glass refining agent and preparation method thereof

The invention relates to a glass refining agent and a preparation method thereof, and belongs to the field of the glass refining agents. Catalytic oxygen evolution is performed through catalyst additive release by gas; meanwhile, the assembly is formed with ferriporphyrin; the catalysis active center sites are increased; the catalysis process is promoted; water steam and glass melt take reaction at the molten high temperature; the viscosity and surface tension of the glass are reduced; the bubble discharge is promoted; a branched structure is formed through an extrusion foam discharge agent; the flowability of a refining agent is improved; substances with elastic structures and good mechanical performance form elastic deformation, so that the extrusion discharging of bubbles is further promoted; the glass crystallization is induced through light transmission nucleation additives; the light effect of the glass is improved, so that the transparency of the glass is improved; auxiliary additives are added in an auxiliary way to realize the coordination participation into a glass silica network structure; the softening point of the glass is improved; the better melting is realized. Theglass refining agent and the preparation method solve the problems that by using the existing glass refining agent, micro bubbles liable to occur on the glass plate surface, and flaws are caused.
Owner:胡莉

Iron porphyrin-flaky bismuth tungstate two-dimensional composite material and preparation method thereof

The invention discloses an iron porphyrin-flaky bismuth tungstate two-dimensional composite material and a preparation method thereof, wherein the iron porphyrin-flaky bismuth tungstate two-dimensional composite material comprises iron porphyrin and flaky bismuth tungstate, and the iron porphyrin is immobilized on the surface of the flaky bismuth tungstate. The preparation method comprises: preparing a mixed solution of bismuth nitrate and sodium tungstate; preparing a precursor mixed solution; and carrying out a hydrothermal reaction on the precursor mixed solution. According to the present invention, the iron porphyrin-flaky bismuth tungstate two-dimensional composite material has advantages of good dispersibility, strong stability, easy recovery and reuse, excellent photocatalytic performance, environmental friendliness and the like, can efficiently degrade pollutants (such as antibiotics) in environment without the adding of H2O2, has good photocatalytic degradation effect, can significantly reduce the treatment cost, and has good application prospects and application range in the field of photocatalysis; and the preparation method has advantages of mild reaction conditions, simple process flow and environmental protection.
Owner:HUNAN UNIV
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