CN114086407A - Novel environment-friendly color modifier and preparation method thereof - Google Patents

Novel environment-friendly color modifier and preparation method thereof Download PDF

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CN114086407A
CN114086407A CN202111255547.2A CN202111255547A CN114086407A CN 114086407 A CN114086407 A CN 114086407A CN 202111255547 A CN202111255547 A CN 202111255547A CN 114086407 A CN114086407 A CN 114086407A
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friendly
environment
reaction
color modifier
stirring
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CN114086407B (en
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申彦彬
葛江波
唐昌军
沈伟
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Zhejiang Hanbang New Materials Co ltd
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Zhejiang Hanbang New Materials Co ltd
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    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P1/00General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
    • D06P1/44General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
    • D06P1/64General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing low-molecular-weight organic compounds without sulfate or sulfonate groups
    • D06P1/642Compounds containing nitrogen
    • D06P1/649Compounds containing carbonamide, thiocarbonamide or guanyl groups
    • D06P1/6495Compounds containing carbonamide -RCON= (R=H or hydrocarbons)
    • D06P1/6498Compounds containing -CONCO-, e.g. phthalimides, hydantoine; Compounds containing RCONHSO2R (R=H or hydrocarbon)
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P1/00General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
    • D06P1/44General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
    • D06P1/60General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing polyethers
    • D06P1/613Polyethers without nitrogen
    • D06P1/6136Condensation products of esters, acids, oils, oxyacids with oxiranes
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P1/00General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
    • D06P1/44General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
    • D06P1/62General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing low-molecular-weight organic compounds with sulfate, sulfonate, sulfenic or sulfinic groups

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  • Textile Engineering (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

The invention relates to the technical field of color modifiers, in particular to a novel environment-friendly color modifier and a preparation method thereof, wherein the novel environment-friendly color modifier comprises the following components in percentage by mass: the high-temperature leveling agent comprises 20-30% of an environment-friendly carrier BPI, 30-40% of an oleic acid glycerol ether sulfonate intermediate A, 10-20% of polyethylene glycol oleate, 5-10% of an auxiliary component, 0.1-0.3% of a preservative and the balance of water, and the high-temperature leveling agent can meet dual-function environment-friendly performance of leveling and color repairing simultaneously by adopting a self-made environment-friendly carrier BPI, the oleic acid glycerol ether sulfonate intermediate A, polyepoxides, the auxiliary component and the like.

Description

Novel environment-friendly color modifier and preparation method thereof
Technical Field
The invention relates to the technical field of color modifiers, in particular to a novel environment-friendly color modifier and a preparation method thereof.
Background
The terylene is an important variety in synthetic fibers and is also the synthetic fiber with the largest market share in the world at present, and is the commodity name of the polyester fiber in China. The basic component of terylene is polyethylene glycol terephthalate with molecular formula [ -OC-Ph-COOCH2CH2O-]nAnd small amounts of monomers and cyclic oligomers. Because of the presence of a large number of ester groups on the molecular chain,and is therefore referred to as polyester fiber (PET). The terylene has compact molecular structure, high crystallinity and orientation degree, the glass transition temperature is higher than 80 ℃, so that the terylene is difficult to dye, and dye molecules are difficult to diffuse into fibers, so disperse dyes with simple structures are usually adopted for dyeing, the dyeing method of the disperse dyes comprises a hot melting method, a carrier dyeing method and a high-temperature high-pressure method, the hot melting method is generally applied to a continuous pad dyeing process for dyeing the polyester-cotton blended woven fabric, the carrier dyeing method mainly aims at an intermittent dyeing process of the polyester-wool blended fabric and the like, the dyeing temperature of which can not exceed 105 ℃, the high-temperature high-pressure method belongs to an intermittent high-temperature dyeing process, the dyeing process is generally completed under the condition of 125 ℃ and 135 ℃, various varieties such as yarns, loose fibers, fabrics and the like can be dyed, and the terylene and the blended fabric thereof are the most extensive dyeing processing mode at present.
In actual production, color spots, stains and stains are problems which are often encountered in high-temperature and high-pressure dyeing methods. The slight color can be repaired in a stripping and re-dyeing mode, and the serious color can not be repaired frequently, so that defects can be picked, trimming can be avoided, goods can be supplemented or the products can be folded in the subsequent process, and great economic loss is caused to a factory.
Cause analysis of color spots, stains and stains: one is that the cyclic trimer (about 75 percent, the solubility is less than 2mg/kg) with low degree of polymerization associated in the process of synthesizing the polyester fiber is gradually resolved and dissociated from the fiber after the dyeing temperature exceeds 120 ℃, because the solubility is ultralow, the cyclic trimer is often combined with dye in the process of dyeing and cooling, and is deposited on the surface of fabric or equipment during liquid discharge to form dyeing defects; and the other is related to the added dispersant in the disperse dye. The molecules of the disperse dye mainly contain hydrophobic groups, the solubility in water is low, and a large amount of anionic dispersant (more than 40-60%) is usually added in the commercialization process to disperse and suspend the disperse dye in an aqueous solution to complete the dyeing process. However, due to cost and market competition factors, different choices of dispersants by various manufacturers result in differentiation of dyes.
In order to achieve better dyeing effect, a proper amount of high-temperature resistant dispersant is usually required to be additionally supplemented during dyeing so as to obtain uniform dyeing effect. Such as carriers, polyepoxide compounds, and other anionic/nonionic type dispersion leveling compounds. The action mechanism is as follows:
a. the polyepoxy compound can increase the solubility of the disperse dye, and the components of the polyepoxy compound contain a large number of polyethylene glycol chain segments, so that the polyepoxy compound has a strong solubilizing effect on the dye and can promote the adsorption of the disperse dye on the fiber surface; but has the disadvantages of low dye utilization rate (low dye uptake percentage), cloud point problem, poor dispersibility at high temperature and easy dye agglomeration;
b. the carrier can plasticize the fiber, reduce the Tg of the fiber, accelerate the diffusion speed of the disperse dye in the fiber and achieve the aim of uniformity; the disadvantages are that the initial dyeing rate is high, the dyeing is easy to cause colored flowers, and the environmental protection performance of part of carriers is not enough (such as large toxicity and odor residue);
c. the anionic component in the anionic/nonionic type dispersing leveling agent can be adsorbed on the surface of dye molecules to form an electric double layer, dye ions form a stable dispersed state due to strong electrostatic repulsion, the nonionic component has a leveling effect, and the two components meet the requirement of dyeing leveling in a copolymerization or compounding manner; the anionic/nonionic disperse leveling agent is a widely used dyeing leveling agent product at present, but has the defects of non-ideal reconditioning effect, capability of guaranteeing normal dyeing requirements and difficulty in meeting the reconditioning requirements once dyeing is reconditioned.
Therefore, it is necessary to develop a novel environment-friendly level dyeing and color modifying agent which can simultaneously realize level dyeing and color modification, does not contain prohibited components, has low (no) air temperature, low ammonia nitrogen and no phosphorus, and meets the market demand.
Disclosure of Invention
The invention provides a novel environment-friendly color modifier and a preparation method thereof, aiming at solving the problem of the color modifier in the prior art.
The invention also discloses a novel environment-friendly color modifier and a preparation method thereof, and the preparation method has the advantages of simple process steps, strong operability, low requirement on equipment, low investment and suitability for large-scale industrial production.
In order to achieve the purpose, the invention adopts the following technical scheme:
the novel environment-friendly color modifier comprises the following components in percentage by mass: 20-30% of an environment-friendly carrier BPI, 30-38% of an oleic acid glycerol ether sulfonate intermediate A, 10-20% of polyethylene glycol oleate, 5-10% of an auxiliary component, 0.1-0.3% of a preservative, and the balance of water.
Preferably, the environment-friendly carrier BPI is prepared by the following method:
(1) under ice bath conditions, the isopropyl amine: 0.1-0.26 mol, dimethylformamide: 0.1-0.2 mol of phthalic anhydride and 0.01-0.1 mol of a small amount of triethylamine are placed into a reaction bottle to be mixed and stirred in proportion, then the mixture is kept warm for 0.5-2 h through the reaction bottle, the temperature is raised to 110-130 ℃, reflux reaction is carried out for 3-5 h, the mixture is poured into an ice water bath to precipitate white crystals after reaction, and the reactants are added with 2-10 g of emulsifier to be heated and stirred to obtain yellow transparent liquid, namely the environment-friendly carrier BPI.
Preferably, the oleic acid glycerol ether sulfonate intermediate A is prepared by the following method:
600-800 g of glyceryl oleate is placed in a heating barrel to be heated to 90-120 ℃, 60-85 g of urea is added, heat preservation stirring is carried out for 0.5-1 h, then 110-150 g of sulfamic acid is added for three times, after the addition is finished at intervals of 20-30 min, heat preservation stirring is carried out at 110-130 ℃ for 2-3 h to measure cloud point (the cloud point is required to reach more than 100 ℃), and then the glyceryl oleate sulfonate intermediate A is obtained by cooling and discharging materials in a cooling chamber.
Preferably, the polyethylene glycol oleate is prepared by the following method:
putting polyethylene glycol and oleic acid into a dry four-neck flask according to a molar ratio of 1: 1.5-2, adding 2-10 g of catalyst, heating to 210-220 ℃ for reaction for 7-9h, introducing nitrogen gas at the initial stage to carry away water produced by the reaction, vacuumizing at the later stage in the reaction, maintaining negative pressure to obtain a crude product, and then performing suction filtration, wherein the reaction yield is controlled to be more than 95%, so as to obtain polyethylene glycol oleate.
Preferably, the auxiliary component is a catalyst, and the catalyst is a solid super acid.
Preferably, the environment-friendly carrier BPI is a compound of N-isopropyl phthalic diamide (NIP) and N-N-butyl phthalimide (NBP).
A method for preparing a novel environment-friendly color modifier is characterized by comprising the following steps: the method comprises the following steps:
firstly, feeding 10-20L of water into a reaction kettle, sealing a discharge port with liquid, starting stirring, stirring at a low speed, sequentially adding 20-30% of environment-friendly carrier BPI, 30-38% of oleic acid glycerol ether sulfonate intermediate A and 10-20% of polyethylene glycol oleate, stirring for 5-10 min to be uniform, adding 5-10% of auxiliary components, stirring for 3-5 min to be uniform, supplementing the balance of deionized water, finally adding 0.1-0.3% of preservative in total, stirring uniformly, and detecting qualified discharge to obtain the environment-friendly color modifier.
Therefore, the invention has the following beneficial effects:
(1) the novel environment-friendly color modifier is a high-temperature leveling agent which can simultaneously meet the dual-function environment-friendly performance of leveling and color modifying and is mainly prepared by a self-made environment-friendly carrier BPI, an oleic acid glycerol ether sulfonate intermediate A, a polyepoxide, an auxiliary component and the like.
(2) A novel environment-friendly level dyeing color modifier with low (no) air temperature, low ammonia nitrogen and no phosphorus.
Detailed Description
The invention is further described below by means of specific embodiments.
In the present invention, all percentages are by weight unless otherwise specified, all equipment and materials are commercially available or commonly used in the industry, and the methods in the following examples are conventional in the art unless otherwise specified.
Example 1
The novel environment-friendly color modifier comprises the following components in percentage by mass: 20% of an environment-friendly carrier BPI, 30% of an oleic acid glycerol ether sulfonate intermediate A, 10% of polyethylene glycol oleate, 5% of an auxiliary component, 0.1% of a preservative and the balance of water.
(1) The environment-friendly carrier BPI is prepared by the following steps:
under ice bath conditions, the isopropyl amine: 0.1mol, dimethylformamide: 0.1mol, 0.01mol of phthalic anhydride and 0.01mol of triethylamine are put into a reaction bottle to be mixed and stirred according to a proportion, then the mixture is kept warm for 0.5h through the reaction bottle, the temperature is raised to 110 ℃ for reaction for 3h, the reaction is finished, the reaction is poured into an ice water bath to precipitate white crystals, and the reactant is added with 2g of emulsifier to be heated and stirred to obtain yellow transparent liquid, namely the environment-friendly carrier BPI.
(2) The oleic acid glycerol ether sulfonate intermediate A is prepared by the following method:
600g of glyceryl oleate is put into a heating barrel to be heated to 90 ℃, 60g of urea is added, heat preservation and stirring are carried out for 0.5h, then 110g of sulfamic acid is added for three times, after 20min is added, heat preservation and stirring are carried out at 110 ℃ for 2h to measure the cloud point (the cloud point is required to reach more than 100 ℃), and then the glyceryl oleate sulfonate intermediate A is obtained by cooling and discharging materials through a cooling chamber.
(3) The polyethylene glycol oleate is prepared by the following method:
putting polyethylene glycol and oleic acid into a dry four-neck flask according to a molar ratio of 1:1.5, adding 2g of catalyst which is solid super acid, heating to 210 ℃ for reaction for 7h, introducing nitrogen gas at the initial stage to carry away water produced by the reaction, vacuumizing at the later stage in the reaction, maintaining negative pressure to obtain a crude product, and then carrying out suction filtration, wherein the reaction yield is controlled to be more than 95%, so as to obtain polyethylene glycol oleate.
A method for preparing a novel environment-friendly color modifier comprises the following steps: the composite material comprises the following components in percentage by mass: 20% of an environment-friendly carrier BPI, 30% of an oleic acid glycerol ether sulfonate intermediate A, 10% of polyethylene glycol oleate, 5% of an auxiliary component, 0.1% of a preservative and the balance of water.
Firstly, feeding 10L of water into a reaction kettle, sealing a discharge port with liquid, starting stirring, stirring at a low speed, sequentially adding 20% of environment-friendly carrier BPI, 30% of oleic acid glycerol ether sulfonated intermediate A and 10% of polyethylene glycol oleate, stirring for 5min to be uniform, adding 5% of auxiliary components, stirring for 3min to be uniform, supplementing the balance of deionized water, finally adding 0.1% of preservative in total, stirring uniformly, detecting qualified, and discharging to obtain the environment-friendly color modifier.
Example 2
The novel environment-friendly color modifier comprises the following components in percentage by mass: 30% of environment-friendly carrier BPI, 38% of oleic acid glycerol ether sulfonate intermediate A, 20% of polyethylene glycol oleate, 10% of auxiliary components, 0.3% of preservative and the balance of water.
(1) The environment-friendly carrier BPI is prepared by the following steps:
under ice bath conditions, the isopropyl amine: 0.26mol, dimethylformamide: 0.2mol, 0.1mol of phthalic anhydride and 0.05mol of triethylamine are put into a reaction bottle to be mixed and stirred according to a proportion, then the mixture is kept warm for 2h through the reaction bottle, the temperature is raised to 130 ℃ for reaction for 5h, the reaction product is poured into an ice water bath to precipitate white crystals after the reaction product is reacted, 10g of emulsifier is added into the reaction product, and the mixture is heated and stirred to obtain yellow transparent liquid, namely the environment-friendly carrier BPI.
(2) The oleic acid glycerol ether sulfonate intermediate A is prepared by the following method:
placing 800g of glyceryl oleate into a heating barrel, heating to 120 ℃, adding 85g of urea, stirring for 1 hour under heat preservation, adding 150g of sulfamic acid for three times, stirring for 3 hours under heat preservation at 130 ℃ after adding for 30 minutes at intervals, measuring cloud point (the cloud point is required to reach more than 100 ℃), and then cooling and discharging through a cooling chamber to obtain the glyceryl oleate sulfonate intermediate A.
(3) The polyethylene glycol oleate is prepared by the following method:
putting polyethylene glycol and oleic acid into a dry four-neck flask according to a molar ratio of 1:2, adding 10g of catalyst which is solid super acid, heating to 220 ℃ for reaction for 9 hours, introducing nitrogen to carry away water produced by the reaction at the initial stage, vacuumizing at the later stage in the reaction, maintaining negative pressure to obtain a crude product, and then carrying out suction filtration, wherein the reaction yield is controlled to be more than 95%, so as to obtain polyethylene glycol oleate.
A method for preparing a novel environment-friendly color modifier comprises the following steps: the composite material comprises the following components in percentage by mass: 30% of environment-friendly carrier BPI, 38% of oleic acid glycerol ether sulfonate intermediate A, 20% of polyethylene glycol oleate, 10% of auxiliary components, 0.3% of preservative and the balance of water.
Firstly, feeding 10L of water into a reaction kettle, sealing a discharge port with liquid, starting stirring, stirring at a low speed, sequentially adding 30% of environment-friendly carrier BPI, 38% of oleic acid glycerol ether sulfonated intermediate A and 20% of polyethylene glycol oleate, stirring for 10min to be uniform, adding 10% of auxiliary components, stirring for 5min to be uniform, supplementing the balance of deionized water, finally adding 0.3% of preservative in total, stirring uniformly, detecting qualified, and discharging to obtain the environment-friendly color modifier.
Example 3
The novel environment-friendly color modifier comprises the following components in percentage by mass: 25% of an environment-friendly carrier BPI, 35% of an oleic acid glycerol ether sulfonate intermediate A, 15% of polyethylene glycol oleate, 8% of an auxiliary component, 0.2% of a preservative and the balance of water.
(1) The environment-friendly carrier BPI is prepared by the following steps:
under ice bath conditions, the isopropyl amine: 0.15mol, dimethylformamide: 0.15mol, 0.05mol of phthalic anhydride and 0.03mol of triethylamine are put into a reaction bottle to be mixed and stirred according to a proportion, then the mixture is kept warm for 1h through the reaction bottle, the temperature is raised to 120 ℃ for reaction for 4h, the reaction is finished, the reaction product is poured into an ice water bath to precipitate white crystals, and the reactant is added with 6g of emulsifier to be heated and stirred to obtain yellow transparent liquid, namely the environment-friendly carrier BPI.
(2) The oleic acid glycerol ether sulfonate intermediate A is prepared by the following method:
700g of glyceryl oleate is put into a heating barrel to be heated to 110 ℃, 75g of urea is added, heat preservation and stirring are carried out for 1 hour, then 130 sulfamic acid is added for three times, after 25min addition, heat preservation and stirring are carried out at 120 ℃ for 2.5 hours to measure the cloud point (the cloud point is required to reach more than 100 ℃), and then the glyceryl oleate sulfonate intermediate A is obtained by cooling and discharging through a cooling chamber.
(3) The polyethylene glycol oleate is prepared by the following method:
putting polyethylene glycol and oleic acid into a dry four-neck flask according to a molar ratio of 1:1.8, adding 6g of catalyst which is solid super acid, heating to 215 ℃ for reaction for 8h, introducing nitrogen to carry away water produced by the reaction at the initial stage, vacuumizing at the later stage in the reaction, maintaining negative pressure to obtain a crude product, and then carrying out suction filtration, wherein the reaction yield is controlled to be more than 95%, so as to obtain polyethylene glycol oleate.
A method for preparing a novel environment-friendly color modifier comprises the following steps: the composite material comprises the following components in percentage by mass: 25% of an environment-friendly carrier BPI, 35% of an oleic acid glycerol ether sulfonate intermediate A, 15% of polyethylene glycol oleate, 8% of an auxiliary component, 0.2% of a preservative and the balance of water.
Firstly, feeding 15L of water into a reaction kettle, sealing a discharge port with liquid, starting stirring, stirring at a low speed, sequentially adding 25% of an environment-friendly carrier BPI, 35% of an oleic acid glycerol ether sulfonated intermediate A and 15% of polyethylene glycol oleate, stirring for 8min to be uniform, adding 8% of auxiliary components, stirring for 4min to be uniform, supplementing the balance of deionized water, finally adding 0.2% of preservative in total, stirring uniformly, detecting qualified, and discharging to obtain the environment-friendly color modifier.
Test data
Figure BDA0003324022480000061
Figure BDA0003324022480000071
Raw material explanation:
an environment-friendly carrier BPI: the environment-friendly carrier BPI is a compound of N-isopropyl phthalic diamide (NIP) and N-N-butyl phthalimide (NBP);
isopropylamine: isopropylamine is an organic substance with the chemical formula of C3H9N, and the aqueous solution is alkaline, and the mixture of isopropylamine and air is highly explosive and can react with an oxidant strongly. The steam is heavier than air, can be diffused to a far away place at a lower position, can cause the back combustion when meeting open fire, has corrosivity, and can be used for synthesizing pesticides, medicines, dye intermediates, rubber vulcanization accelerators, emulsifiers, detergents, depilatories, hard water treatment agents, surfactants, textile auxiliaries and the like;
dimethylformamide: n, N-dimethylformamide is an organic compound, has a molecular formula of C3H7NO, is colorless transparent liquid, is a chemical raw material with wide application, is an excellent solvent with wide application range, can be randomly mixed with water and a plurality of organic solvents except halogenated hydrocarbon, and has good dissolving capacity for a plurality of organic compounds and inorganic compounds; phthalic anhydride: phthalic anhydride is an organic compound, has a molecular formula of C8H4O3, is cyclic anhydride formed by the intramolecular dehydration of phthalic acid, is a white solid, is an important raw material in chemical engineering, and is particularly used for the manufacture of plasticizers;
triethylamine: triethylamine, an organic compound, with a molecular formula of C6H15N, is a colorless oily liquid, strongly ammoniacal, flammable, slightly soluble in water, soluble in organic solvents such as ethanol and diethyl ether, irritant, toxic, poisoned by swallowing by mistake, and burns the skin, and the vapor thereof strongly irritates the eyelid and mucous membrane, and may cause combustion and explosion risks in case of open fire, high temperature and strong oxidants. The product is mainly used as solvent, curing agent, catalyst, polymerization inhibitor, preservative, synthetic dye and the like in industry;
emulsifier: the emulsifier reduces the interfacial tension of each component in the mixed system, forms a firmer film on the surface of the micro-droplets or forms an electric double layer on the surface of the micro-droplets due to the electric charge given by the emulsifier, prevents the micro-droplets from aggregating with each other, and maintains uniform emulsion. From a phase point of view, emulsions are still heterogeneous systems, the dispersed phase in emulsions can be either an aqueous phase or an oil phase, mostly an oil phase; the continuous phase can be an oil phase or an aqueous phase, most of which are aqueous phases, the emulsifier is a surfactant, and has a hydrophilic group and a lipophilic group in the molecule, in order to indicate the hydrophilicity or lipophilicity of the emulsifier, a "hydrophilic-lipophilic balance value (HLB value)" is generally adopted, and the lower the HLB value, the stronger the lipophilicity; conversely, the higher the HLB value, the stronger the hydrophilicity, and the different HLB values of the various emulsifiers, the proper emulsifier must be selected in order to obtain a stable emulsion;
DXF-A: glyceryl oleate (1-oleoyl glyceride) is an organic compound with the molecular formula of C21H40O4, is a polymerization product of oleic acid (octadecenoic acid) and glycerol (glycerol), and belongs to unsaturated glyceride. Can be hydrolyzed under acid and alkaline conditions, can be added with hydrogen to carry out nitration reaction with nitric acid, and is commonly used as a surfactant, a food stabilizer and a plastic rubber additive;
urea: urea can react with acid to form salts. Has hydrolysis effect. Can carry out condensation reaction at high temperature to generate biuret, triuret and cyanuric acid. Heating to 160 deg.C to decompose, generating ammonia gas and changing into isocyanic acid. Since this substance is contained in human urine, urea is named. The urea contains 46% of nitrogen (N), which is the highest nitrogen content in the solid nitrogen fertilizer, and can be hydrolyzed to generate ammonia and carbon dioxide under the action of acid, alkali and enzyme (acid and alkali need to be heated), and the ammonia and the carbon dioxide are unstable to heat and are deaminated to biuret when the temperature is heated to 150-160 ℃. The reaction of copper sulfate and biuret is purple, it can be used for identifying urea, if it is quickly heated, it can be deaminated and trimerized into six-membered ring compound cyanuric acid, and can be reacted with acetyl chloride or acetic anhydride to produce acetyl urea and diacetylurea, and reacted with diethyl malonate under the action of sodium ethoxide to produce malonyl urea (also called barbituric acid, because it has a certain acidity), and can be reacted with formaldehyde under the action of basic catalyst of ammonia water, etc. to produce urea-formaldehyde resin, and reacted with hydrazine hydrate to produce semicarbazide, urea (urea), also called urea and carbonamide, its chemical formula is CH4N2O, and is an organic compound formed from carbon, nitrogen, oxygen and hydrogen, and is a white crystal, one of the simplest organic compounds, and is the main nitrogen-containing end product of protein metabolic decomposition in the bodies of mammal and some fishes, and can be used as a neutral fertilizer, and the urea is applicable to various soils and plants, and is easy to store, convenient use and small damage to soil, and is a chemical nitrogen fertilizer with larger use amount and also a nitrogen fertilizer with the highest nitrogen content. Industrially synthesizing urea by ammonia gas and carbon dioxide under certain conditions;
sulfamic acid: the sulfuric acid is an inorganic solid acid formed by substituting hydroxyl of sulfuric acid with amino, the molecular formula is NH2SO3H, the molecular weight is 97.09, the crystal is generally white and odorless rhombus flaky crystal, the relative density is 2.126, the melting point is 205 ℃, the crystal is soluble in water and liquid ammonia, solid sulfamic acid does not absorb moisture and is relatively stable as long as the crystal is kept dry and does not contact with water at normal temperature, an aqueous solution of sulfamic acid has strong acidity equal to that of hydrochloric acid, sulfuric acid and the like, SO the crystal is called solid sulfuric acid, and the crystal has the characteristics of no volatilization, no odor and low toxicity to a human body, dust or solution has irritation to eyes and skin and can cause burn, and the maximum allowable concentration is 10mg/m < 3 >. Sulfamic acid can be used for synthesizing herbicides, fire retardants, sweeteners, preservatives, metal cleaning agents and the like, and is a common chemical raw material;
polyethylene glycol: is a high molecular polymer with a chemical formula of HO (CH2CH2O) nH, has no irritation, slightly bitter taste, good water solubility and good compatibility with a plurality of organic matter components. The lubricating oil has excellent lubricity, moisture retention, dispersibility and adhesiveness, can be used as an antistatic agent, a softening agent and the like, and has extremely wide application in industries such as cosmetics, pharmacy, chemical fiber, rubber, plastics, papermaking, paint, electroplating, pesticides, metal processing, food processing and the like;
oleic acid: oleic acid (Oleic acid), of the formula C18H34O2, is a monounsaturated Omega-9 fatty acid and is found in the bodies of animals and plants. And adding oleic acid by hydrogenation to obtain stearic acid. The double-bond trans isomer of oleic acid is known as elaidic acid; sulfamic acid: sulfamic acid is an inorganic solid acid formed by substituting hydroxyl of sulfuric acid with amino, has a molecular formula of NH2SO3H, a molecular weight of 97.09, is generally white and odorless rhombus flaky crystal, has a relative density of 2.126, a melting point of 205 ℃, is soluble in water and liquid ammonia, is stable and does not absorb moisture as long as being dried and not contacted with water at normal temperature, and an aqueous solution of sulfamic acid has strong acidity equal to that of hydrochloric acid, sulfuric acid and the like, SO the sulfamic acid is also called solid sulfuric acid, has the characteristics of no volatilization, no odor and low toxicity to a human body, dust or solution has irritation to eyes and skin and can cause burn, and the maximum allowable concentration is 10mg/m < 3 >. Sulfamic acid can be used for synthesizing herbicides, fire retardants, sweeteners, preservatives, metal cleaning agents and the like, and is a common chemical raw material;
catalyst: solid superacid, solid superacid refers to an acid which is more acidic than 100% sulfuric acid, as represented by the Hammett acidity function H, and an acid which is 100% sulfuric acid and has an H0 value of 11.93H0< -11.93 is a superacid. The solid superacid is divided into two types, one type contains halogen and fluorosulfonic acid resin to form fluoride immobilized matter; another type of halogen-free catalyst is prepared by high-temperature combustion of sulfate radicals adsorbed on the surface of metal oxides or hydroxides.
The above-described embodiments are only preferred embodiments of the present invention, and are not intended to limit the present invention in any way, and other variations and modifications may be made without departing from the spirit of the invention as set forth in the claims.

Claims (7)

1. A novel environment-friendly color modifier is characterized in that: the composite material comprises the following components in percentage by mass:
20-30% of an environment-friendly carrier BPI, 30-40% of an oleic acid glycerol ether sulfonate intermediate A, 10-20% of polyethylene glycol oleate, 5-10% of an auxiliary component, 0.1-0.3% of a preservative, and the balance of water.
2. The novel environment-friendly color modifier as claimed in claim 1, wherein the environment-friendly carrier BPI is prepared by the following method:
under ice bath conditions, the isopropyl amine: 0.1-0.26 mol, dimethylformamide: 0.1-0.2 mol of phthalic anhydride and 0.01-0.1 mol of a small amount of triethylamine are placed into a reaction bottle to be mixed and stirred in proportion, then the mixture is kept warm for 0.5-2 h through the reaction bottle, the temperature is raised to 110-130 ℃, reflux reaction is carried out for 3-5 h, the mixture is poured into an ice water bath to precipitate white crystals after reaction, and the reactants are added with 2-10 g of emulsifier to be heated and stirred to obtain yellow transparent liquid, namely the environment-friendly carrier BPI.
3. The novel environment-friendly color modifier as claimed in claim 1, wherein the glycerol oleate sulfonate intermediate A is prepared by the following method:
600-800 g of glyceryl oleate is placed in a heating barrel to be heated to 90-120 ℃, 60-85 g of urea is added, heat preservation stirring is carried out for 0.5-1 h, then 110-150 g of sulfamic acid is added for three times, after the addition is finished at intervals of 20-30 min, heat preservation stirring is carried out at 110-130 ℃ for 2-3 h to measure cloud point (the cloud point is required to reach more than 100 ℃), and then the glyceryl oleate sulfonate intermediate A is obtained by cooling and discharging materials in a cooling chamber.
4. The novel environment-friendly color modifier as claimed in claim 1, wherein the polyethylene glycol oleate is prepared by the following method:
putting polyethylene glycol and oleic acid into a dry four-neck flask according to a molar ratio of 1: 1.5-2, adding 2-10 g of catalyst, heating to 210-220 ℃ for reaction for 7-9h, introducing nitrogen gas at the initial stage to carry away water produced by the reaction, vacuumizing at the later stage in the reaction, maintaining negative pressure to obtain a crude product, and then performing suction filtration, wherein the reaction yield is controlled to be more than 95%, so as to obtain polyethylene glycol oleate.
5. The novel environment-friendly color modifier as claimed in claim 1 or 4, wherein the auxiliary component is a catalyst, and the catalyst is a solid super acid.
6. The novel environment-friendly color modifier according to claim 1, wherein the environment-friendly carrier BPI is a compound of N-isopropyl phthalic acid amide (NIP) and N-N-butyl phthalimide (NBP).
7. A method for preparing a novel environment-friendly color modifier is characterized by comprising the following steps: the method comprises the following steps:
firstly, feeding 10-20L of water into a reaction kettle, sealing a discharge port with liquid, starting stirring, stirring at a low speed, sequentially adding 20-30% of environment-friendly carrier BPI, 30-40% of oleic acid glycerol ether sulfonate intermediate A and 10-20% of polyethylene glycol oleate, stirring for 5-10 min to be uniform, adding 5-10% of auxiliary components, stirring for 3-5 min to be uniform, supplementing the balance of deionized water, finally adding 0.1-0.3% of preservative in total, stirring uniformly, and detecting qualified discharge to obtain the environment-friendly color modifier.
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Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101413218A (en) * 2008-11-18 2009-04-22 东华大学 Method for preparing terylene environment protection type dye carrier
CN106245379A (en) * 2016-08-16 2016-12-21 嘉兴华晟助剂工业有限公司 Environment-friendly type level dyeing healant compositions and application thereof
CN111058318A (en) * 2019-12-13 2020-04-24 太仓宝霓实业有限公司 Environment-friendly polyester color modifier and preparation method thereof

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101413218A (en) * 2008-11-18 2009-04-22 东华大学 Method for preparing terylene environment protection type dye carrier
CN106245379A (en) * 2016-08-16 2016-12-21 嘉兴华晟助剂工业有限公司 Environment-friendly type level dyeing healant compositions and application thereof
CN111058318A (en) * 2019-12-13 2020-04-24 太仓宝霓实业有限公司 Environment-friendly polyester color modifier and preparation method thereof

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