CN108252104A - A kind of preparation method for smooth agent of weaving - Google Patents

A kind of preparation method for smooth agent of weaving Download PDF

Info

Publication number
CN108252104A
CN108252104A CN201711410071.9A CN201711410071A CN108252104A CN 108252104 A CN108252104 A CN 108252104A CN 201711410071 A CN201711410071 A CN 201711410071A CN 108252104 A CN108252104 A CN 108252104A
Authority
CN
China
Prior art keywords
parts
temperature
mixed
smooth agent
weaving
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CN201711410071.9A
Other languages
Chinese (zh)
Other versions
CN108252104B (en
Inventor
董晓
乔舍
程依
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
ZHEJIANG KAILUOQI GARMENTS Co.,Ltd.
Original Assignee
董晓
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 董晓 filed Critical 董晓
Priority to CN201711410071.9A priority Critical patent/CN108252104B/en
Publication of CN108252104A publication Critical patent/CN108252104A/en
Application granted granted Critical
Publication of CN108252104B publication Critical patent/CN108252104B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/643Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
    • D06M15/647Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain containing polyether sequences
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/42Block-or graft-polymers containing polysiloxane sequences
    • C08G77/46Block-or graft-polymers containing polysiloxane sequences containing polyether sequences
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M11/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
    • D06M11/77Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with silicon or compounds thereof
    • D06M11/79Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with silicon or compounds thereof with silicon dioxide, silicic acids or their salts
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/244Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus
    • D06M13/248Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus with compounds containing sulfur
    • D06M13/256Sulfonated compounds esters thereof, e.g. sultones
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/01Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with natural macromolecular compounds or derivatives thereof
    • D06M15/03Polysaccharides or derivatives thereof
    • D06M15/05Cellulose or derivatives thereof
    • D06M15/09Cellulose ethers
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2200/00Functionality of the treatment composition and/or properties imparted to the textile material
    • D06M2200/50Modified hand or grip properties; Softening compositions

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Abstract

The invention discloses a kind of preparation methods for smooth agent of weaving, and belong to weaving additive agent field.The present invention, which is additionally added, have been carried out nano-silica surface with dimethyl silicone polymer in graft modification addition lotion, since dimethyl silicone polymer is coated on the surface of nanometer titanium dioxide carbon in the form of silicon oxygen bond, so as to increase the organic principle of particle surface, reduce the content of its surface hydroxyl, reduce elecrtonegativity, so as to improve its hydrophobic performance, defoaming and suds suppressing properties are better, so as to preferably solve the problems, such as organosilicon emulsification hardly possible, easily layering.The smooth agent that the present invention solves at present on the market belongs to organosilicon flexible smooth agent more, and application effect is general, and there is the problem of easily layering, stability of emulsion is poor.

Description

A kind of preparation method for smooth agent of weaving
Technical field
The invention belongs to additive agent fields of weaving, and in particular to a kind of preparation method for smooth agent of weaving.
Background technology
Smooth agent is a kind of weaving additive in textile industry, and in textile printing and dyeing industry, smooth agent can assign hair The smooth feel of pile fabric, Textileather, cotton fabric can make textile become soft, smooth, bright.It is suitable for various fibers Manufactured goods, have excellent glossiness, Bearable dry and wet wipe, flexibility, strong adhesive force, waterproof anti-pollution, fast drying, resistance to height Temperature and the smooth exquisiteness of feel, some smooth agent solid contents are high, good dispersion, dilution can be watered by arbitrary proportion, so as to have Effect extends the shelf life.The smooth dose of glossiness that can improve fabric simultaneously assigns the good smoothness of fabric and glossiness, thus extensively It is the optimal selection of grade textiles soft finishing agent of new generation applied to the finishing process of each kind fabric.
After weaving smooth agent currently on the market is mainly by compoundings such as dimethicone, hydroxy silicon oil, amido silicon oils It is made through emulsifying, although there is certain effect to fabric, such smooth agent application effect is general, and there is easily layering, lotion Stability difference the problems such as, to environmental requirement height.Therefore, it is good and be not easy the weaving smooth agent being layered to produce a kind of using effect It is a necessary thing.
Invention content
The technical problems to be solved by the invention:Belong to organosilicon flexible smooth agent for smooth agent at present on the market more, Application effect is general, and there is the problem of easily layering, stability of emulsion is poor, provides a kind of preparation method for smooth agent of weaving.
In order to solve the above technical problems, the present invention is using technical solution as described below:
A kind of preparation method for smooth agent of weaving, the preparation method include the following steps:
(1)It counts in parts by weight, takes 10 ~ 15 parts of octamethylcy-clotetrasiloxanes, 5 ~ 6 parts of epoxychloropropane, 2 ~ 3 parts of anhydrous four chlorinations Tin, 1 ~ 2 part of sodium hydroxide, octamethylcy-clotetrasiloxane, epoxychloropropane, anhydrous stannic chloride are mixed, it is warming up to 70 ~ 80 DEG C, 5 ~ 6h is kept the temperature, treats that temperature is reduced to 50 ~ 60 DEG C, sodium hydroxide is added in and is mixed, stand, then be evaporated under reduced pressure, obtain Distillation, in mass ratio 3 ~ 4:5~6:7 ~ 8, distillation, toluene, sodium hydroxide solution are mixed, stood, then depressurized Distillation, obtains distillate;
(2)It counts in parts by weight, takes 10 ~ 15 parts of organic amines, 7 ~ 8 parts of polyglycol ethers, 5 ~ 6 parts of distillates, 3 ~ 4 parts of isopropanols, Organic amine, polyglycol ether, isopropanol are mixed, and are stirred at 45 ~ 50 DEG C of temperature, is warming up to 80 ~ 90 DEG C, drop Add distillate, 5 ~ 6 h are kept the temperature at 80 ~ 85 DEG C of temperature, adjust pH value to 4 ~ 5, obtain heat preservation object, it is spare;
(3)In mass ratio 1:2:8 ~ 10, ethyl orthosilicate, ammonium hydroxide, absolute ethyl alcohol are mixed, stirred at 25 ~ 30 DEG C of temperature It mixes, filters, obtain filter residue, by filter residue ethyl alcohol centrifuge washing 2 ~ 3 times, dried at 35 ~ 40 DEG C of temperature, obtain drying object, by weight Number meter takes 10 ~ 15 parts of methanol, 5 ~ 6 parts of deionized waters, 3 ~ 4 parts of dimethyl silicone polymers, 3 ~ 4 parts of ammonium hydroxide, 1 ~ 2 part of drying object, Methanol, deionized water, dimethyl silicone polymer, drying object are put into container, stirred at 50 ~ 65 DEG C of temperature, adds in ammonium hydroxide, Reflux, is cooled to room temperature, centrifuges, obtains sediment, sediment wash 3 ~ 4 times with ethanol solution, dry at 40 ~ 50 DEG C of temperature It is dry, obtain dried object;
(4)It counts in parts by weight, takes 20 ~ 30 parts of deionized waters, 10 ~ 15 parts of steps(2)Spare heat preservation object, 7 ~ 8 parts of emulsifiers, 1 ~ 2 part of dried object, 0.5 ~ 0.8 part of hydroxymethyl cellulose, 0.1 ~ 0.2 part of catalyst, 0.1 ~ 0.2 part of formaldehyde, by step(2)It is spare Heat preservation object, emulsifier, catalyst, deionized water mixed, be warming up to 150 ~ 180 DEG C, stirring is cooled to 50 ~ 60 DEG C, Stirring adds in dried object, hydroxymethyl cellulose, formaldehyde, is stirred for, and is uniformly mixed to get weaving smooth agent.
The step(2)Middle organic amine is hexamethylene diamine, N, N- diethyl propyldiamines, ethanol amine it is therein any one.
The step(4)Middle emulsifier is in mass ratio 1:1, by dodecyl benzene sulfonic acid, anhydrous sorbitol mono laurate Ester is uniformly mixed to get emulsifier.
The step(4)Middle catalyst is hydrochloric acid.
Compared with other methods, advantageous effects are the present invention:
(1)The present invention is combined amino oriented alignment in the entire molecule to be formed with siloxanes using polyethers, and polyether segment is also one Determine to increase flatness in degree, number of amino groups is more, and molecule is positively charged more, big with fiber binding capacity, so as to make smooth agent not It is only good in fiber surface film forming, make fabric that there is good feel and flatness, and can penetrate into fabric and be allowed to have Have a certain bulkiness and preferable hydrophily, gas permeability, while it is under hydrochloric acid catalysis, in solution containing free hydrogen from Son, hydrogen ion are then attracted to by emulsion particle on its surface, make its surface positively charged, so as to effectively eliminate oil slick phenomenon, Layering will not be generated, then to be polymerize under anion, nonionic emulsifier collective effect, under the action of its emulsifier, Its emulsion particle is substantially anion, and the intramolecular of emulsion particle and intermolecular electrostatic force are great, and is caused in chain Stage, the hydrogen ion that dodecyl benzene sulfonic acid ionizes out can combine on the oxygen of siloxanes, reduce the bond energy of silicon oxygen bond, weak SiClx oxygen key so as to further improve the stabilization between latex particle, obtains uniform and stable emulsion system, it is easy to solve smooth agent The problem of demulsification.
(2)The present invention, which is additionally added, has carried out nano-silica surface with dimethyl silicone polymer graft modification addition breast In liquid, since dimethyl silicone polymer is coated on the surface of nanometer titanium dioxide carbon in the form of silicon oxygen bond, so as to increase particle table The organic principle in face reduces the content of its surface hydroxyl, reduces elecrtonegativity, so as to improve its hydrophobic performance, defoaming and suds Can be better, so as to preferably solve the problems, such as that organosilicon emulsification is difficult, is easily layered.
Specific embodiment
Organic amine is hexamethylene diamine, N, N- diethyl propyldiamines, ethanol amine it is therein any one.
Emulsifier is in mass ratio 1:1, dodecyl benzene sulfonic acid, sorbitan mono-laurate mix It is even to get emulsifier.
Catalyst is hydrochloric acid.
A kind of preparation method for smooth agent of weaving, the preparation method include the following steps:
(1)It counts in parts by weight, takes 10 ~ 15 parts of octamethylcy-clotetrasiloxanes, 5 ~ 6 parts of epoxychloropropane, 2 ~ 3 parts of anhydrous four chlorinations Tin, 1 ~ 2 part of sodium hydroxide, octamethylcy-clotetrasiloxane, epoxychloropropane, anhydrous stannic chloride are mixed, it is warming up to 70 ~ 80 DEG C, 5 ~ 6h is kept the temperature, treats that temperature is reduced to 50 ~ 60 DEG C, sodium hydroxide is added in and is mixed, stand 4 ~ 5h, then in vacuum degree 13.3Pa is evaporated under reduced pressure under the conditions of 55 ~ 65 DEG C of temperature, obtains distillation, in mass ratio 3 ~ 4:5~6:7 ~ 8, by distillation, first Benzene, sodium hydroxide solution are mixed, and stand 1 ~ 2h, then carry out decompression steaming under the conditions of vacuum degree 13.3Pa, 55 ~ 65 DEG C of temperature It evaporates, obtains distillate;
(2)It counts in parts by weight, takes 10 ~ 15 parts of organic amines, 7 ~ 8 parts of polyglycol ethers, 5 ~ 6 parts of distillates, 3 ~ 4 parts of isopropanols, Organic amine, polyglycol ether, isopropanol being mixed, and in 45 ~ 50 DEG C of temperature, 200 ~ 300r/min is stirred 1 ~ 2h, It is warming up to 80 ~ 90 DEG C, distillate is added dropwise, 5 ~ 6h is kept the temperature at 80 ~ 85 DEG C of temperature, adjust pH value to 4 ~ 5, obtain heat preservation object, it is spare;
(3)In mass ratio 1:2:8 ~ 10, ethyl orthosilicate, ammonium hydroxide, absolute ethyl alcohol are mixed, in 25 ~ 30 DEG C of temperature, 600 ~ Stirring 20 under 800r/min ~ for 24 hours, filtering obtains filter residue, and filter residue ethyl alcohol centrifuge washing 2 ~ 3 times dries at 35 ~ 40 DEG C of temperature Dry 2 ~ 3h, obtains drying object, counts in parts by weight, take 10 ~ 15 parts of methanol, 5 ~ 6 parts of deionized waters, 3 ~ 4 parts of dimethyl silicone polymers, 3 ~ 4 parts of ammonium hydroxide, 1 ~ 2 part of drying object, methanol, deionized water, dimethyl silicone polymer, drying object are put into container, in temperature 50 ~ 65 DEG C, 30 ~ 40min is stirred under the conditions of 200 ~ 300r/min, adds in ammonium hydroxide, flow back 0.8 ~ 1h at 70 ~ 80 DEG C of temperature, treats It is cooled to room temperature, to centrifuge 3 ~ 5 min under 3000 ~ 4000r/min, obtains sediment, sediment is washed 3 ~ 4 with ethanol solution It is secondary, it is dry at 40 ~ 50 DEG C of temperature, obtain dried object;
(4)It counts in parts by weight, takes 20 ~ 30 parts of deionized waters, 10 ~ 15 parts of steps(2)Spare heat preservation object, 7 ~ 8 parts of emulsifiers, 1 ~ 2 part of dried object, 0.5 ~ 0.8 part of hydroxymethyl cellulose, 0.1 ~ 0.2 part of catalyst, 0.1 ~ 0.2 part of formaldehyde, by step(2)It is spare Heat preservation object, emulsifier, catalyst, deionized water mixed, 150 ~ 180 DEG C are warming up to, to be stirred under 700 ~ 800r/min 100 ~ 120 min are cooled to 50 ~ 60 DEG C, stir 8 ~ 10min with the rotating speed of 4000 ~ 5000r/min, add in dried object, hydroxyl first Base cellulose, formaldehyde, then 3 ~ 5min is stirred with the rotating speed of 400 ~ 500r/min, it is uniformly mixed to get weaving smooth agent.
Embodiment 1
Organic amine is hexamethylene diamine.
Emulsifier is in mass ratio 1:1, dodecyl benzene sulfonic acid, sorbitan mono-laurate mix It is even to get emulsifier.
Catalyst is hydrochloric acid.
A kind of preparation method for smooth agent of weaving, the preparation method include the following steps:
(1)Count in parts by weight, take 10 parts of octamethylcy-clotetrasiloxanes, 5 parts of epoxychloropropane, 2 parts of anhydrous stannic chlorides, 1 part Sodium hydroxide mixes octamethylcy-clotetrasiloxane, epoxychloropropane, anhydrous stannic chloride, is warming up to 70 DEG C, heat preservation 5h treats that temperature is reduced to 50 DEG C, adds in sodium hydroxide and is mixed, stands 4h, then in vacuum degree 13.3Pa, 55 DEG C of conditions of temperature Under be evaporated under reduced pressure, obtain distillation, in mass ratio 3:5:7, distillation, toluene, sodium hydroxide solution are mixed, stood 1h, then be evaporated under reduced pressure under the conditions of vacuum degree 13.3Pa, 55 DEG C of temperature, obtain distillate;
(2)Count in parts by weight, take 10 parts of organic amines, 7 parts of polyglycol ethers, 5 parts of distillates, 3 parts of isopropanols, by organic amine, Polyglycol ether, isopropanol are mixed, and in temperature 45 C, and 200r/min is stirred 1h, are warming up to 80 DEG C, and distillation is added dropwise Liquid keeps the temperature 5h at 80 DEG C of temperature, adjusts pH value to 4, obtains heat preservation object, spare;
(3)In mass ratio 1:2:8, ethyl orthosilicate, ammonium hydroxide, absolute ethyl alcohol are mixed, in 25 DEG C of temperature, under 600r/min 20h is stirred, filtering obtains filter residue, by filter residue ethyl alcohol centrifuge washing 2 times, dries 2h at 35 DEG C of temperature, drying object is obtained, by weight Number meter is measured, 10 parts of methanol, 5 parts of deionized waters, 3 parts of dimethyl silicone polymers, 3 parts of ammonium hydroxide, 1 part of drying object is taken, by methanol, goes Ionized water, dimethyl silicone polymer, drying object are put into container, and 30min is stirred under the conditions of temperature 50 C, 200r/min, are added Enter ammonium hydroxide, flow back 0.8h under temperature 70 C, is cooled to room temperature, to centrifuge 3 min under 3000r/min, obtains sediment, will be heavy Starch is washed 3 times with ethanol solution, dry at 40 DEG C of temperature, obtains dried object;
(4)It counts in parts by weight, takes 20 parts of deionized waters, 10 parts of steps(2)Spare heat preservation object, 7 parts of emulsifiers, 1 part of drying Object, 0.5 part of hydroxymethyl cellulose, 0.1 part of catalyst, 0.1 part of formaldehyde, by step(2)Spare heat preservation object, emulsifier, catalysis Agent, deionized water are mixed, and are warming up to 150 DEG C, to stir 100min under 700r/min, 50 DEG C are cooled to, with 4000r/ The rotating speed stirring 8min of min, adds in dried object, hydroxymethyl cellulose, formaldehyde, then stir 3min with the rotating speed of 400r/min, mixes It closes uniformly to get weaving smooth agent.
Embodiment 2
Organic amine is N, N- diethyl propyldiamines.
Emulsifier is in mass ratio 1:1, dodecyl benzene sulfonic acid, sorbitan mono-laurate mix It is even to get emulsifier.
Catalyst is hydrochloric acid.
A kind of preparation method for smooth agent of weaving, the preparation method include the following steps:
(1)Count in parts by weight, take 15 parts of octamethylcy-clotetrasiloxanes, 6 parts of epoxychloropropane, 3 parts of anhydrous stannic chlorides, 2 parts Sodium hydroxide mixes octamethylcy-clotetrasiloxane, epoxychloropropane, anhydrous stannic chloride, is warming up to 80 DEG C, heat preservation 6h treats that temperature is reduced to 60 DEG C, adds in sodium hydroxide and is mixed, stands 5h, then in vacuum degree 13.3Pa, 65 DEG C of conditions of temperature Under be evaporated under reduced pressure, obtain distillation, in mass ratio 4:6:8, distillation, toluene, sodium hydroxide solution are mixed, stood 2h, then be evaporated under reduced pressure under the conditions of vacuum degree 13.3Pa, 65 DEG C of temperature, obtain distillate;
(2)Count in parts by weight, take 15 parts of organic amines, 8 parts of polyglycol ethers, 6 parts of distillates, 4 parts of isopropanols, by organic amine, Polyglycol ether, isopropanol are mixed, and in temperature 50 C, and 300r/min is stirred 2h, are warming up to 90 DEG C, and distillation is added dropwise Liquid keeps the temperature 6h at 85 DEG C of temperature, adjusts pH value to 5, obtains heat preservation object, spare;
(3)In mass ratio 1:2:10, ethyl orthosilicate, ammonium hydroxide, absolute ethyl alcohol are mixed, in 30 DEG C of temperature, 800r/min For 24 hours, filtering obtains filter residue for lower stirring, by filter residue ethyl alcohol centrifuge washing 3 times, dries 3h at 40 DEG C of temperature, obtains drying object, press Parts by weight meter takes 15 parts of methanol, 6 parts of deionized waters, 4 parts of dimethyl silicone polymers, 4 parts of ammonium hydroxide, 2 parts of drying object, by methanol, Deionized water, dimethyl silicone polymer, drying object are put into container, and in 65 DEG C of temperature, 40min is stirred under the conditions of 300r/min, Ammonium hydroxide is added in, flow back 1h at 80 DEG C of temperature, is cooled to room temperature, to centrifuge 5 min under 4000r/min, obtains sediment, will be heavy Starch is washed 4 times with ethanol solution, dry under temperature 50 C, obtains dried object;
(4)It counts in parts by weight, takes 30 parts of deionized waters, 15 parts of steps(2)Spare heat preservation object, 8 parts of emulsifiers, 2 parts of dryings Object, 0.8 part of hydroxymethyl cellulose, 0.2 part of catalyst, 0.2 part of formaldehyde, by step(2)Spare heat preservation object, emulsifier, catalysis Agent, deionized water are mixed, and are warming up to 180 DEG C, to stir 120 min under 800r/min, 60 DEG C are cooled to, with 5000r/ The rotating speed stirring 10min of min, adds in dried object, hydroxymethyl cellulose, formaldehyde, then stir 5min with the rotating speed of 500r/min, mixes It closes uniformly to get weaving smooth agent.
Embodiment 3
Organic amine is ethanol amine.
Emulsifier is in mass ratio 1:1, dodecyl benzene sulfonic acid, sorbitan mono-laurate mix It is even to get emulsifier.
Catalyst is hydrochloric acid.
A kind of preparation method for smooth agent of weaving, the preparation method include the following steps:
(1)It counts in parts by weight, takes 12.5 parts of octamethylcy-clotetrasiloxanes, 5.5 parts of epoxychloropropane, 2.5 parts of anhydrous four chlorinations Tin, 1.5 parts of sodium hydroxides, octamethylcy-clotetrasiloxane, epoxychloropropane, anhydrous stannic chloride are mixed, are warming up to 75 DEG C, 5.5h is kept the temperature, treats that temperature is reduced to 55 DEG C, sodium hydroxide is added in and is mixed, stands 4.5h, then in vacuum degree 13.3Pa, It is evaporated under reduced pressure under the conditions of temperature 60 C, obtains distillation, in mass ratio 3.5:5.5:7.5, by distillation, toluene, hydroxide Sodium solution is mixed, and is stood 1.5h, then be evaporated under reduced pressure under the conditions of vacuum degree 13.3Pa, temperature 60 C, is obtained distillate;
(2)It counts in parts by weight, takes 12.5 parts of organic amines, 7.5 parts of polyglycol ethers, 5.5 parts of distillates, 3.5 parts of isopropanols, it will Organic amine, polyglycol ether, isopropanol are mixed, and in 47 DEG C of temperature, and 250r/min is stirred 1.5h, is warming up to 85 DEG C, distillate is added dropwise, 5.5h is kept the temperature at 83 DEG C of temperature, adjusts pH value to 4.5, obtains heat preservation object, it is spare;
(3)In mass ratio 1:2:9, ethyl orthosilicate, ammonium hydroxide, absolute ethyl alcohol are mixed, in 27 DEG C of temperature, under 700r/min 22h is stirred, filtering obtains filter residue, by filter residue ethyl alcohol centrifuge washing 2 times, dries 2.5h at 37 DEG C of temperature, obtains drying object, press Parts by weight meter takes 12.5 parts of methanol, 5.5 parts of deionized waters, 3.5 parts of dimethyl silicone polymers, 3.5 parts of ammonium hydroxide, 1.5 parts of drying Methanol, deionized water, dimethyl silicone polymer, drying object are put into container by object, in 57 DEG C of temperature, under the conditions of 250r/min 35min is stirred, adds in ammonium hydroxide, flow back 0.9h at 75 DEG C of temperature, is cooled to room temperature, to centrifuge 4min under 35000r/min, Sediment is obtained, sediment is washed 3 times with ethanol solution, it is dry under temperature 45 C, obtain dried object;
(4)It counts in parts by weight, takes 25 parts of deionized waters, 12.5 parts of steps(2)Spare heat preservation object, 7.5 parts of emulsifiers, 1.5 Part dried object, 0.65 part of hydroxymethyl cellulose, 0.15 part of catalyst, 0.15 part of formaldehyde, by step(2)Spare heat preservation object, breast Agent, catalyst, deionized water are mixed, and are warming up to 165 DEG C, to stir 110min under 750r/min, are cooled to 55 DEG C, 9min is stirred with the rotating speed of 4500r/min, adds in dried object, hydroxymethyl cellulose, formaldehyde, then stir with the rotating speed of 450r/min 4min is uniformly mixed to get weaving smooth agent.
Comparative example:The weaving smooth agent of company of Suzhou City production.
Same a batch of clothing that the smooth agent of the present invention and the smooth agent of comparative example produce same producer respectively into Exercise use, nursing, choose that 50 people fade to used clothes fabric, pilling etc. carries out overall merit after one month, partly Smooth agent delamination is evaluated after year, test result is shown in Table 1.
Table 1:
Test event Embodiment 1 Embodiment 2 Embodiment 3 Comparative example
Clothing discoloration Clothing is colour-fast Clothing is colour-fast Clothing is colour-fast It fades serious
Clothing pilling situation Without pilling effect Without pilling effect Without pilling effect Surface portion pilling
Fabric situation It is soft, smooth It is soft, smooth It is soft, smooth Quality is hardened
Smooth agent delamination No lamination occurs No lamination occurs No lamination occurs Layering is serious
Summary to clothing fanout free region after weaving smooth agent use of the invention, more can effectively prevent clothing colour fading pilling Phenomena such as generation.

Claims (4)

1. a kind of preparation method for smooth agent of weaving, which is characterized in that the preparation method includes the following steps:
(1)It counts in parts by weight, takes 10 ~ 15 parts of octamethylcy-clotetrasiloxanes, 5 ~ 6 parts of epoxychloropropane, 2 ~ 3 parts of anhydrous four chlorinations Tin, 1 ~ 2 part of sodium hydroxide, octamethylcy-clotetrasiloxane, epoxychloropropane, anhydrous stannic chloride are mixed, it is warming up to 70 ~ 80 DEG C, 5 ~ 6h is kept the temperature, treats that temperature is reduced to 50 ~ 60 DEG C, sodium hydroxide is added in and is mixed, stand, then be evaporated under reduced pressure, obtain Distillation, in mass ratio 3 ~ 4:5~6:7 ~ 8, distillation, toluene, sodium hydroxide solution are mixed, stood, then depressurized Distillation, obtains distillate;
(2)It counts in parts by weight, takes 10 ~ 15 parts of organic amines, 7 ~ 8 parts of polyglycol ethers, 5 ~ 6 parts of distillates, 3 ~ 4 parts of isopropanols, Organic amine, polyglycol ether, isopropanol are mixed, and are stirred at 45 ~ 50 DEG C of temperature, is warming up to 80 ~ 90 DEG C, drop Add distillate, 5 ~ 6 h are kept the temperature at 80 ~ 85 DEG C of temperature, adjust pH value to 4 ~ 5, obtain heat preservation object, it is spare;
(3)In mass ratio 1:2:8 ~ 10, ethyl orthosilicate, ammonium hydroxide, absolute ethyl alcohol are mixed, stirred at 25 ~ 30 DEG C of temperature It mixes, filters, obtain filter residue, by filter residue ethyl alcohol centrifuge washing 2 ~ 3 times, dried at 35 ~ 40 DEG C of temperature, obtain drying object, by weight Number meter takes 10 ~ 15 parts of methanol, 5 ~ 6 parts of deionized waters, 3 ~ 4 parts of dimethyl silicone polymers, 3 ~ 4 parts of ammonium hydroxide, 1 ~ 2 part of drying object, Methanol, deionized water, dimethyl silicone polymer, drying object are put into container, stirred at 50 ~ 65 DEG C of temperature, adds in ammonium hydroxide, Reflux, is cooled to room temperature, centrifuges, obtains sediment, sediment wash 3 ~ 4 times with ethanol solution, dry at 40 ~ 50 DEG C of temperature It is dry, obtain dried object;
(4)It counts in parts by weight, takes 20 ~ 30 parts of deionized waters, 10 ~ 15 parts of steps(2)Spare heat preservation object, 7 ~ 8 parts of emulsifiers, 1 ~ 2 part of dried object, 0.5 ~ 0.8 part of hydroxymethyl cellulose, 0.1 ~ 0.2 part of catalyst, 0.1 ~ 0.2 part of formaldehyde, by step(2)It is spare Heat preservation object, emulsifier, catalyst, deionized water mixed, be warming up to 150 ~ 180 DEG C, stirring is cooled to 50 ~ 60 DEG C, Stirring adds in dried object, hydroxymethyl cellulose, formaldehyde, is stirred for, and is uniformly mixed to get weaving smooth agent.
2. the preparation method for smooth agent of weaving according to claim 1, which is characterized in that the step(2)Middle organic amine is Hexamethylene diamine, N, N- diethyl propyldiamines, ethanol amine it is therein any one.
3. the preparation method for smooth agent of weaving according to claim 1, which is characterized in that the step(4)Middle emulsifier is In mass ratio 1:1, dodecyl benzene sulfonic acid, sorbitan mono-laurate are uniformly mixed to get emulsifier.
4. the preparation method for smooth agent of weaving according to claim 1, which is characterized in that the step(4)Middle catalyst is Hydrochloric acid.
CN201711410071.9A 2017-12-23 2017-12-23 Preparation method of textile smoothing agent Active CN108252104B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201711410071.9A CN108252104B (en) 2017-12-23 2017-12-23 Preparation method of textile smoothing agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201711410071.9A CN108252104B (en) 2017-12-23 2017-12-23 Preparation method of textile smoothing agent

Publications (2)

Publication Number Publication Date
CN108252104A true CN108252104A (en) 2018-07-06
CN108252104B CN108252104B (en) 2020-06-30

Family

ID=62723506

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201711410071.9A Active CN108252104B (en) 2017-12-23 2017-12-23 Preparation method of textile smoothing agent

Country Status (1)

Country Link
CN (1) CN108252104B (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111185977A (en) * 2020-02-29 2020-05-22 浙江省林业科学研究院 Production method of super-hydrophobic wood
CN112663332A (en) * 2020-12-23 2021-04-16 南通恒润新材料科技有限公司 Preparation method of high-stability high-temperature-resistant smoothing agent
CN113445318A (en) * 2021-07-28 2021-09-28 沂水祥腾化工有限公司 Yarn smoothing agent for spinning and preparation method thereof
CN117645728A (en) * 2024-01-29 2024-03-05 江苏恒力化纤股份有限公司 Preparation method of flexibility-enhanced flame retardant and high-strength flexibility flame-retardant polyester industrial yarn

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002092666A1 (en) * 2001-05-15 2002-11-21 Clariant International Ltd Modified polyorganosiloxanes, aqueous emulsions thereof, their production and their use
CN101392061A (en) * 2008-10-30 2009-03-25 上海大学 Method for synthesizing epoxy quaternized modified amido silicon oil
CN101509196A (en) * 2009-03-04 2009-08-19 深圳天鼎精细化工制造有限公司 Method of preparing epoxy modified amino-silicone oil softening agent
CN101550237A (en) * 2009-05-18 2009-10-07 安徽德佳有机硅有限公司 High springback silicone stiffening agent and preparation method thereof
CN101914206A (en) * 2010-08-13 2010-12-15 东华大学 Quaternized modified amino silicone oil softener and preparation and application thereof
CN105484045A (en) * 2015-11-19 2016-04-13 杭州美高华颐化工有限公司 Cationic smoothing agent for polyester fabric and preparation method thereof

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002092666A1 (en) * 2001-05-15 2002-11-21 Clariant International Ltd Modified polyorganosiloxanes, aqueous emulsions thereof, their production and their use
CN101392061A (en) * 2008-10-30 2009-03-25 上海大学 Method for synthesizing epoxy quaternized modified amido silicon oil
CN101509196A (en) * 2009-03-04 2009-08-19 深圳天鼎精细化工制造有限公司 Method of preparing epoxy modified amino-silicone oil softening agent
CN101550237A (en) * 2009-05-18 2009-10-07 安徽德佳有机硅有限公司 High springback silicone stiffening agent and preparation method thereof
CN101914206A (en) * 2010-08-13 2010-12-15 东华大学 Quaternized modified amino silicone oil softener and preparation and application thereof
CN105484045A (en) * 2015-11-19 2016-04-13 杭州美高华颐化工有限公司 Cationic smoothing agent for polyester fabric and preparation method thereof

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111185977A (en) * 2020-02-29 2020-05-22 浙江省林业科学研究院 Production method of super-hydrophobic wood
CN112663332A (en) * 2020-12-23 2021-04-16 南通恒润新材料科技有限公司 Preparation method of high-stability high-temperature-resistant smoothing agent
CN113445318A (en) * 2021-07-28 2021-09-28 沂水祥腾化工有限公司 Yarn smoothing agent for spinning and preparation method thereof
CN117645728A (en) * 2024-01-29 2024-03-05 江苏恒力化纤股份有限公司 Preparation method of flexibility-enhanced flame retardant and high-strength flexibility flame-retardant polyester industrial yarn

Also Published As

Publication number Publication date
CN108252104B (en) 2020-06-30

Similar Documents

Publication Publication Date Title
CN108252104A (en) A kind of preparation method for smooth agent of weaving
CN102197950B (en) Terylene printed non-woven carpet and manufacturing method thereof
CN102587147B (en) Production process of fluoride-free waterproof breathable knitted fabric
CN110774683B (en) Fabric with low water washing shrinkage and preparation process thereof
CN104532589B (en) Weather resistance used for textiles is ventilative, antibacterial, reinforcement, absorbing fast-drying finishing composition and preparation method
WO2018099150A1 (en) Aqueous double-sided-suede microfiber pu synthetic leather and preparation method therefor
CN101105006A (en) Wet method transfer printing method for natural fiber and polyamide fibre
CN107558231A (en) A kind of umbrella cloth and its manufacture method
CN105951484B (en) Wool fabric wet method transfer printing method
CN107953497B (en) Preparation method of completely environment-friendly leather base cloth
CN109610191A (en) A kind of preparation method of organic/inorganic composite flame-proof cotton fabric coating
CN106436278A (en) Ammoniation modification method of ramine fibers and application method thereof in liquid ammonia solvent dyeing
CN105755813B (en) A kind of textile auxiliary for improving textile abrasion resistance and preparation method thereof
CN116084162A (en) Bio-based anti-pilling finishing agent and preparation method and application thereof
CN106750324A (en) A kind of poly- quaternary ammonium polyethers dimethyl silicone polymer and preparation method thereof and hand feel finishing agent
CN112127148A (en) High-water-absorption needle-punched non-woven decorative fabric and preparation method thereof
CN202069397U (en) Printed polyester non-woven carpet
CN106939512A (en) A kind of preparation method of terylene spinning finish
CN104761723B (en) A kind of polysiloxane soft agent with fixing property
CN107587346A (en) A kind of floride-free water repellent fabric and its manufacture method
Namboodri et al. Foam finishing of cotton-containing textiles
CN109267393B (en) A kind of preparation method of the oil removing level dyeing compound emulsifying agent for dacron
CN106521935A (en) Ultra-soft fast soluble film and preparation method thereof
CN109267355A (en) A kind of preparation method of silicone oil softener
CN101263259A (en) Method for coating surfaces and suitable particles therefor

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
TA01 Transfer of patent application right
TA01 Transfer of patent application right

Effective date of registration: 20200604

Address after: No.206, Tashan Road, industrial function zone, Fotang Town, Yiwu City, Jinhua City, Zhejiang Province 322000

Applicant after: ZHEJIANG KAILUOQI GARMENTS Co.,Ltd.

Address before: 213000 room 24, building 703, Fenghuang famous town, Xinbei District, Changzhou, Jiangsu

Applicant before: Dong Xiao

GR01 Patent grant
GR01 Patent grant