1539 results about "Anthraquinone glycoside" patented technology

The present invention provides a treatment composition comprising a hydrophobic dye, having an anthraquinone structure and surfactant. A method of treating a textile with said composition is also claimed.

A method for marking a liquid petroleum hydrocarbon. The method comprises adding to the liquid petroleum hydrocarbon at least one substituted anthraquinone dry having formula (I) wherein X is O or S; Y is O, NR<7 >or S; R<1 >and R<2 >independently are hydrogen, alkyl, aryl, aralkyl, heteroalkyl, heterocyclic or alkanoyl; R<3 >and R<5 >independently are alkyl, aryl, aralkyl, heteroalkyl or heterocyclic; R<4 >and R<6 >independently are hydrogen or alkyl; R<7 >is hydrogen or alkyl; and wherein the substituted anthraquinone dye(s) has an absorption maximum in the range from 600 nm to 750 nm.

A hydrogenation process for producing fluidized bed with hydrogen peroxide by anthraquinone method is carried out by taking empty tower hydrogenation reactor with amplification section on top, moving operating liquid and hydrogen upward at specific speed, floating powdery catalyst in tower body, hydrogenation reacting by free contacting, separating hydrogenated liquid by gas-liquid separating system, filtering by filter system and oxidizing. It has fast hydrogenation speed, low resistance, homogenous distribution and higher utilization rate.

Laundry detergent compositions comprise (a) surfactant, and (b) a hueing dye selected from triarylmethane blue and violet basic dyes, methine blue and violet basic dyes, anthraquinone blue and violet basic dyes, azo dyes basic blue 16, basic blue 65, basic blue 66 basic blue 67, basic blue 71, basic blue 159, basic violet 19, basic violet 35, basic violet 38, basic violet 48, oxazine dyes, basic blue 3, basic blue 75, basic blue 95, basic blue 122, basic blue 124, basic blue 141, Nile blue A and xanthene dye basic violet 10, and mixtures thereof.

A polymerizable polymeric photoinitiator according to Formula (I):

wherein:

• • PL represents an n+m+p-functional polymeric core;
  • n and m independently represent an integer from 1 to 30;
  • p represents an integer from 0 to 10;
  • o is 0 or 1;
  • INI represents a group selected from the group consisting of a benzophenone, a thioxanthone, a carbazole, a anthraquinone, a camphor quinone, an α-hydroxyalkylphenone, an α-aminoalkylphenone, an acylphosphine oxide, a bisacyl phosphine oxide, an acylphosphine sulfide, a phenyl glyoxalate, a benzoin ether, a benzyl ketal, an α-dialkoxyacetophenone, a carbazolyl-O-acyl-oxime, an α-haloarylketone and an α-haloaryl sulfone;
  • L₃ and L₄ represent a substituted or unsubstituted divalent linking group comprising 1 to 14 carbon atoms;
  • A represents a radically polymerizable functional group selected from the group consisting of an acrylate, a methacrylate, a styrene, an acryl amide, a methacryl amide, a maleate, a fumarate, an itaconate, an vinyl ether, an allyl ether, an allyl ester, a maleimide, a vinyl nitrile and a vinyl ester; and
  • R4 represents a substituted or unsubstituted alkyl group.

Radiation curable compositions containing the polymerizable polymeric photoinitiator and methods for preparing the polymerizable polymeric photoinitiator are also disclosed.

A blue colorant comprising a chromophore having at least one poly(oxyalkylene) chain attached, through aromatic amino group (or groups), to the 1-position, the 4-position, or both, of an anthraquinone backbone is provided. Such colorants exhibit excellent amine/base stability and thermal stability, effective colorations, excellent low extraction rates, and high lightfastness levels, particularly when incorporated within certain media and/or on the surface of certain substrates, particularly polyesters, polyolefins, and polyurethanes. The poly(oxyalkylene) chain or chains can be conveniently tailored to increase the solubility or compatibility in different solvents or resins thereby permitting the introduction of such excellent coloring chromophores within diverse media and/or or diverse substrates as well as provides a liquid colorant which facilitates handling. Compositions and articles comprising such colorants are provided as well as methods for producing such inventive colorants.

This invention relates to polymerizable ultraviolet light absorbers and yellow colorants and their use in ophthalmic lenses. In particular, this invention relates to polymerizable ultraviolet light absorbing methine compounds and yellow compounds of the methine and anthraquinone classes that block ultraviolet light and/or violet-blue light transmission through ophthalmic lenses.

The invention provides a monolithic catalyst for oxydol production and a preparation method thereof. The catalyst uses ceramic monolithic honeycomb or metal monolithic honeycomb as a substrate, one or more of Al2O3, SiO2, CaO, MgO, TiO2, ZrO2, La2O3, CeO2, Fe2O3 and Cr2O3 as a coating material, and noble metal palladium as an active component to be used in an anthraquinone hydrogenation reaction of oxydol production. The monolithic catalyst adopts a preparation method of fractional support so as to effectively control depth of impregnation of the active component. The monolithic catalyst used in the anthraquinone hydrogenation process has the advantages of high activity, good selectivity and 82.21kg (100 percent of H2O2) /mcat.h of space-time yield of the oxydol, which is over 3 times more than a commercial bead catalyst.

The invention relates to a cleaning process for extracting high quality fiber with high efficiency, high yield and low energy consumption from plant raw materials by a combination method of chemistry and machinery in a sectional type. The process comprises the following steps: a raw material is fully immersed in a NaOH solution or a KOH solution or limewater with low concentration (black liquor is used for supplementing into the corresponding alkaline for repeated and circular use) under the normal temperature or certain temperature, wherein the concrete immersion temperature and immersion time can be determined according to the types and the water content of the raw materials so that the alkaline liquor is fully, uniformly and properly absorbed and diffused into plants; steaming under normal pressure or steaming with pressure or no liquid steaming with pressure is used; the steamed material can be selected according to the paper quality requirement by using a blowout slurrying mode or a mode of pulp refining after blowing to form slurry or by using thread rolling and pulp refining to relief material once or multitime to prepare slurry. The novel process combines the advantages of chemical treatment and mechanical pulping, so that the uniform mass transfer and uniform heat transfer can be ensured and the damage to cellulose and hemicellulose by excessive alkali can be reduced, the yield of fiber is raised to about 75% from about 45% of the prior art, so that the novel pulping process is capable of avoiding the usage of auxiliary agents like sulfured and anthraquinone, conveniently extracting and using the cellulose and lignin in black liquor, and overcoming the influence on environment during the process of pulping and post-treating lignin.

A textile ink composition and a method of manufacturing a textile ink composition are disclosed. The textile ink composition is formed from a cationically charged metal oxide and a dye, and is capable of durably dyeing different types of fabric. The cationically charged metal oxide is typically an oligomer, such as an alumina oligomer. A suitable alumina oligomer is aluminum chlorohydrate. Typical dyes have anthraquinone, catechol, hydroxyazo or salicylic acid groups or are mordant dyes, such as Carminic Acid, Alizarin Red, Acid Blue 45, Acid Green 41, Hematoxylin, Chromoxane Cyanine R, Calconcarboxylic Acid, Plasmocorinth B, Pyrocatechol, Acid Alizarin Violet N, Alizarin Yellow GG, Mordant Yellow 12 and Mordant Blue 9.

The invention disclosed a anthraquinone hydrogenation catalyst; its character is the catalyst is made up of the matrix, support body and active component. The said matrix have openings at both ends of the rules parallel channel structure cordierite or foam alumina, the said support body coat on the surface of the matrix, mainly made up of gamma - alumina, zirconia and selected from cerium oxide, lanthanum oxide and oxidized protactinium in one or more, the weight is 5% to 35% of the body weight, the said active ingredient is loaded on the surface of the support body, made from A component or components A and B components of the mixture composition, Group A is Pd and/or platinum, it's weight is 0.5% to 5% of the support body, Group B is selected from titanium, zirconium, hafnium, manganese, drilling, cerium, lanthanum in one or more, it's weight is 0% to 1% of the support body.

The invention provides novel anthraquinone compositions that are useful as broad-spectrum quenchers of fluorescence and provides methods for making and using them. The anthraquinone quenchers can be conjugated to a variety of biologically relevant compounds, including lipids, nucleic acids, polypeptides, and more specifically antigens, steroids, vitamins, drugs, haptens, metabolites, toxins, environmental pollutants, amino acids, peptides, proteins, nucleotides, oligonucleotides, polynucleotides, carbohydrates, and their analogs. The invention also provides kits comprising, in one or more containers, at least one anthraquinone quencher dye composition of the present invention, and instructions for using that composition.

The invention relates to a method for production of an aqueous dispersion of polymer-encapsulated pigments, characterised in that (a) an aqueous pigment dispersion, containing at least one organic pigment (P), selected from the group of azo, isoindolinone, isoindoline, anthanthrone, thioindigo, thiazinindigo, triarylcarbonium, quinophthalone, anthraquinone, dioxazine, phthalocyanine, quinacridone, quinacridonquinone, indanthrone, perylene, perinone, pyranthrone, diketopyrrolopyrrole, isoviolanthrone and azomethine pigments, at least one detergent (T), and water is prepared, (b) a monomer miniemulsion, stabilised by a hydrophobic organic compound with a water solubility at 20 DEG C of at most 5x10<-5> g/l, is prepared from a polymerisable monomer (M) and at least one detergent (T) in water, (c) a monomer pigment emulsion is prepared, whereby the aqueous dispersion from (a) and the monomer miniemulsion from (b) are mixed and homogenised and (d) the pigment-containing monomer from (c) is polymerised in the presence of a polymerisation initiator and/or by heat, whereupon an encapsulation of the pigment with the polymer thus formed occurs.

The invention discloses an oxidation method for preparing hydrogen peroxide by an anthraquinone method in the technical field of chemical reaction. The method comprises the following steps of: dispersing an oxygen-containing gaseous phase into hydrogenated anthraquinone derivative-containing working solution to prepare a micron-sized bubble-containing gas-liquid mixed fluid, and finishing oxidation reaction when the gas-liquid mixed fluid flows through a delay pipeline. The method can improve the oxidation efficiency of a hydrogenated anthraquinone derivative, shorten oxidation reaction time, reduce the hold-up of the oxidization working solution in a reaction system and improve the safety of the oxidation process.

One aspect of the invention relates to an article of manufacture made from a pulp composition comprising an ARF pulp. In one embodiment, the pulp composition made from agricultural renewable fibers (ARF) having low Kappa number with unexpected quality sufficient for papermaking (e.g., high strength parameters and high freeness). In another embodiment, the ARF pulp has ISO brightness of 60% or higher, and unexpected quality sufficient for papermaking (e.g. high strength.parameters and high freeness). In another embodiment, the ARF pulp is made from a pulping process comprising using a high concentration of anthraquinone (AQ).

The invention discloses a chitosan oligosaccharide capsule; chitosan oligosaccharide with 2000-10000 of molecular weight, radix salviae miltiorrhizae extract, pueraria root extract, obtuseleaf senna seed extract and schisandra extract are used as main materials; starch and magnesium stearate are taken as auxiliary raw materials; the weight components of the formula of the chitosan oligosaccharide capsule include the chitosan oligosaccharide, the radix salviae miltiorrhizae extract, the pueraria root extract, obtuseleaf senna seed extract, schisandra extract, the starch and the magnesium stearate; the production process of the capsule is that: sieving, weighting, mixing, capsule filling, polishing, screening, inside and outside package, warehouse-in inspection are carried out to prepare the health-care product. The chitosan oligosaccharide capsule has the advantages that the main composition of the capsule comprises the chitosan oligosaccharide, general flavone and total anthraquinone; the capsule is taken orally two times one day, 3 granules each time, and the capsule has auxiliary protection function to the chemical liver damage.

The invention belongs to the technical field of crossing of chemical engineering, materials engineering and environmental engineering, particularly relates to an improvement technology of cellulose membrane materials and a chemical grafting and fixing technology for treating anthraquinones compound carriers of wastewater containing nitrogen, and particularly relates to a method for preparing an anthraquinone functional cellulose membrane by fixing an anthraquinone compound on microcrystalline cellulose by chemical grafting. According to the method, the microcrystalline cellulose is used as a raw material; firstly, ionic liquid is used as a solvent for dissolving the microcrystalline cellulose; thionyl chloride modified cellulose is used for preparing cellulose chloride and then the cellulose chloride is reacted with amino anthraquinone in dimethylformamide to prepare an anthraquinone functional cellulose membrane material; the substitution degree of the prepared cellulose chloride can reach 1.89 and the anthraquinone grafting rate of the anthraquinone functional cellulose membrane reaches 82%; the anthraquinone functional cellulose is prepared by the two-step reaction; the content of anthraquinonyl is high and the grafting rate is high; the fixing effect is stable; finally, the anthraquinone functional cellulose is changed into the membrane by a phase transferring method; the membrane material can be used for accelerating and strengthening the biological degradation process in the treatment of the wastewater containing the nitrogen.

The invention provides the formula of a working liquid for hydrogen peroxide production based on the anthraquinone process. The working liquid comprises solvent and a working carrier, wherein the solvent comprises the following components by volume percentage: 65% to 80% of alkyl benzene, 5% to 25% of trioctylphosphate (TOP) and 4.5% to 17.8% of N-phenyl-N-ethyl-benzamide; the working carrier is particularly a mixture of alkyl anthraquinone and alkyl tetrahydroanthraquinone with the total content thereof being 130g/L to 200g/L in the working liquid. The working liquid of the invention has the advantages of high working carrier solubility, moderate density and high working load, and reduces the degradation rate of anthraquinone. Therefore, the produced hydrogen peroxide has high yield and low material consumption, and the production process is simple and easy-to-operate.

The invention discloses a preparation method of BiVO4-BiOBr photocatalyst has a visible-light response, wherein the catalyst may be used under visible light, ultraviolet light, or sunlight. The preparation method of BiVO4-BiOBr photocatalyst that is in a multilevel nest-like nanostructure and is formed by nanosheets is: heating for 8 to 24 h under an alcohol-heating temperature of 100 to 200 DEG C with pH of 5 to 10. The catalyst of the invention can decompose water-soluble organic pollutant containing chlorine and sulfur, water-soluble organic pollutant of azo, xanthene, and anthraquinone type, and biological contaminant microcystic toxins generated by harmful algal bloom.