CN106555335B - Fibrous material processing method and fibrous material inorganic agent - Google Patents
Fibrous material processing method and fibrous material inorganic agent Download PDFInfo
- Publication number
- CN106555335B CN106555335B CN201611080067.6A CN201611080067A CN106555335B CN 106555335 B CN106555335 B CN 106555335B CN 201611080067 A CN201611080067 A CN 201611080067A CN 106555335 B CN106555335 B CN 106555335B
- Authority
- CN
- China
- Prior art keywords
- fibrous material
- coupling agent
- processing method
- aqueous coupling
- aqueous
- 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.)
- Active
Links
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating 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 nitrogen
- D06M13/46—Compounds containing quaternary nitrogen atoms
- D06M13/47—Compounds containing quaternary nitrogen atoms derived from heterocyclic compounds
- D06M13/477—Compounds containing quaternary nitrogen atoms derived from heterocyclic compounds having six-membered heterocyclic rings
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/564—Polyureas, polyurethanes or other polymers having ureide or urethane links; Precondensation products forming them
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M2101/00—Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
- D06M2101/02—Natural fibres, other than mineral fibres
- D06M2101/04—Vegetal fibres
- D06M2101/06—Vegetal fibres cellulosic
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M2101/00—Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
- D06M2101/16—Synthetic fibres, other than mineral fibres
- D06M2101/30—Synthetic polymers consisting of macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M2101/34—Polyamides
- D06M2101/36—Aromatic polyamides
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
- D06M2200/20—Treatment influencing the crease behaviour, the wrinkle resistance, the crease recovery or the ironing ease
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
- D06M2200/45—Shrinking resistance, anti-felting properties
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
The present invention relates to textile technology field more particularly to a kind of fibrous material processing method and fibrous material inorganic agents.The fibrous material processing method includes the following steps: to provide containing chloro- 4,6- bis- (3 '-sodium formate) pyridyl group-S-1 of 2-, the aqueous coupling agent of 3,5- triazines;Prepare the dipping solution containing the aqueous coupling agent of preset concentration;The fibrous material is immersed in the dipping solution;The dipping solution for being soaked with fibrous material is heated to preset temperature, and keeps the temperature a preset time;Drain, washing, drying are carried out to warm fibrous material.The processing method and fibrous material inorganic agent of fibrous material provided by the invention, fibrous material is not only set to obtain good formaldehydeless crease-resistant, shrinkproof, ironing-free performance, and there is preferable durable scourability, it can be far smaller than that the washing times using conventional functionalization processing method.
Description
Technical field
The present invention relates to textile technology field more particularly to a kind of fibrous material processing method and fibrous material inorganic agents.
Background technique
The textile (clothes, home textile etc.) of fiber (cotton, fiber crops, viscose glue, Modal, tencel) material production has pro-skin, inhales
The excellent comfort property such as penetrable ventilated, is favored by the majority of consumers, but can generate shrink, corrugation, deformation equidimension after washing
How unstable phenomenon makes such textile dimensionally stable for a long time, and constantly meet that the majority of consumers constantly promote wants
It asks, is textile industry key subjects of interest.
With the development of the times, people are broadly divided into following five stages for the crease-resistant research of fibrous material:
1, the general shrink-proof anti-crease finishing stage: the stage is intended to make smooth cotton fabric, dimensionally stable, wrinkle resistant, principle
Are as follows: urea element and formaldehyde reaction generate low molecule condensation product, penetrate into fiberoptic fiber, then under the action of acidic catalyst, lead to
Overheating Treatment makes its resinification, deposition and crosslinking is formed in fiberoptic fiber, creasy recovery angle index is by not collated processing
150 °~160 ° of fabric, promoted after arrangement processing to 220 °~230 °, this cotton fabric also needs after washing is dried
Want slight ironing;
2, the Wash-and-wear stage: with improve improve natural fabric Wet-resilient based on, and finishing effect not because
It washs and disappears, fabric still has good wrinkle resistance after dress and washing, and fabric is not required to ironing, and drying after washing can wear
, crease recovery angle index is further promoted to 250 °~280 °;
3, the durable press finish stage: the crease-resistant level of fabric increases than the Wash-and-wear stage, and flat appearance is not
Corrugation, the more smooth stabilization of apparent size, and play the role of keeping formation of clothing and rivel setting, the stage crease recovery angle index
280 °~300 ° are reached;
4, the low-methoxyl aldehyde arrangement stage: the stage, which largely works, is concentrated mainly on the spy of the novel finishing technique of etherified resin
Rope more successfully forms new technological flow, after conventional desizing, kiering, bleaching, mercerization finish, in conjunction with adjustment of equipment
Promotion increase Liquid Ammonia Treatment, in addition by the original dry crosslinking technique padding resin solution and then baking, with padding resin
Then solution contains the wet damp crosslinking process banked up, then baked, so that ironing-free performance is basically reached 2D resin finishing level, make simultaneously
Fabric formaldehyde burst size drops to 50mg/kg or so by 300-500mg/Kg, and the arrangement of low-methoxyl aldehyde is by hemiacetal hydroxyl
Etherificate, greatly reduces the burst size of formaldehyde, and to reduce stimulation and harm to human body, but textile is in dress and washing process
In, part it is uncrosslinked or hydrolysis generate free formaldehyde can still release, endanger environmental and human health impacts;
5, the green arrangement stage: with environmental protection and the proposition of green ecological textile concept in recent years, more brand clothes
Dress enterprise has proposed: realizing global zero-emission to the year two thousand twenty textile and its processing link, this will fundamentally be limited containing first
Contact and use of the aldehydes auxiliary agent with textile, the development and application technical study without (zero) formaldehyde DP finish agent obtain quickly
Development.It is shrinkproof, anti-in fiber-like textile as the 2D resin of high burst size of methanal and the etherified 2D resin of low burst size of methanal
Wrinkle, non-ironing technical field played important function, but since there are Form aldehyde releases to be eventually prohibited from using, and formaldehydeless class is anti-
It contracts, is crease-resistant, non-ironing technology is currently mainly dimethyl dihydroxy ethylene urea (such as: holding high the Arkofx NZK of high BASF) and BTCA
(butane tetracarboxylic acid), since only there are two crosslinked groups in molecule, dosage is big and effect is poor, is unable to satisfy wash and wear and wants for the former
It asks;The latter since crosslinking condition requires accurate control PH=2-2.8, when treatment temperature be higher than 40 DEG C, PH less than 4 when, fiber exists
Can occur to degrade strongly under this condition, so that textile be made to lose wearability, along with fabric crease-resistant performance raising and
Improve, other performances of fabric, which have, largely to be declined, and the decline of fabric tear strength is mainly manifested in, with wrinkle resistance
The raising of energy is in apparent negative correlativing relation, that is, the creasy recovery angle of fabric is higher after arranging, and tearing brute force is lower, substantially
Being that creasy recovery angle is every improves 20 °, and corresponding tearing brute force retention rate will decline 7%, although BTCA is formaldehydeless crease-resistant whole
Reason agent can obtain preferable wrinkle resistance, but 300 ° be increased to after arranging from initial 150 ° of unfinished creasy recovery angle reach
It rolls boiling hot to durable, can strongly damage 50% or more, so there are many product theoretical research article, but there is no practical application valence substantially
Value, and because its price is high, strength damage is big, technique reproducing stability is poor can not industrial applications.
In addition, being handled using Functional Chemicals textile fiber material, obtaining all kinds of textiles has height attached
Value added functionality is an important directions of textile product development in recent years, such product is also deep to be favored by market, but is used
Conventional functions of textile fabrics treatment process at present, these functionality do not have lasting washing resistance performance.
Summary of the invention
The present invention provides a kind of fibrous material processing method and fibrous material inorganic agent, so that made of fibrous material
Textile has good formaldehydeless crease-resistant, shrinkproof, non-ironing, durable scourability.
To solve the above-mentioned problems, the present invention provides a kind of fibrous material processing method, include the following steps: offer one
Aqueous coupling agent, the aqueous coupling agent include chloro- 4,6- bis- (3 '-sodium formate) pyridyl group-S-1 of 2-, 3,5- triazines, molecule
Structure is shown below:
Prepare the dipping solution containing the aqueous coupling agent of preset concentration;The fibrous material is immersed into the dipping solution
In;The dipping solution for being soaked with fibrous material is heated to preset temperature, and keeps the temperature a preset time;To warm fibrous material
Carry out drain processing;The fibrous material handled through drain is washed;Fibrous material through washing is dried.
Preferably, the fibrous material is cotton, fiber crops, viscose glue, Modal or tencel.
Preferably, the preset concentration is 50g/L-500g/L, and the preset temperature is 70 DEG C -130 DEG C, when described default
Between be 30min-60min.
Preferably, the fibrous material is natural fiber material, recycled fibrous material, composite fibre materials.
Preferably, the preset concentration is 5g/L-150g/L, and the preset temperature is 70 DEG C -130 DEG C, when described default
Between be 30min-60min.
Preferably, further include in the dipping solution concentration be 1g/L-5g/L aqueous polyurethane.
The present invention also provides a kind of fibrous material inorganic agent, the fibrous material inorganic agent includes aqueous coupling agent, institute
Stating aqueous coupling agent includes chloro- 4,6- bis- (3 '-sodium formate) pyridyl group-S-1 of 2-, 3,5- triazines, molecular structure such as following formula institute
Show:
Preferably, the aqueous coupling agent is prepared using following steps: preparing the sodium hydrate aqueous solution of preset concentration;It will
The sodium hydrate aqueous solution is added in 3- pyridine first carboxylic, and stirs to dissolution;Three are added portionwise into reaction system under stiring
Polychlorostyrene piperazine;It is stirred to react to the transparent solution of system;Adjusting the clear solution pH value with sodium hydroxide is 7-8 to get to water
Property coupling agent 2- chloro- 4,6- bis- (3 '-sodium formate) pyridyl group-S-1,3,5- triazine solution.
The processing method and fibrous material inorganic agent of fibrous material provided by the invention include 2- chloro- 4,6- by preparation
The aqueous coupling agent and the use aqueous coupling agent of two (3 '-sodium formate) pyridyl group-S-1,3,5- triazines are straight to fibrous material
Capable processing is tapped into, fibrous material is not only made to obtain good crease-resistant, shrinkproof, ironing-free performance, but also there is preferable durable washing
Performance can be far smaller than that the washing times using conventional functionalization processing method.
Detailed description of the invention
Attached drawing 1 is the processing method flow chart of the fibrous material of the specific embodiment of the invention.
Specific embodiment
Processing method to fibrous material provided by the invention and the specific reality of fibrous material inorganic agent with reference to the accompanying drawing
The mode of applying elaborates.
Present embodiment provides a kind of processing method of fibrous material, and attached drawing 1 is the specific embodiment of the invention
Fibrous material processing method flow chart.As shown in Figure 1, the processing method packet for the fibrous material that present embodiment provides
Include following steps:
Step S11, provides an aqueous coupling agent, and the aqueous coupling agent includes chloro- 4,6- bis- (3 '-sodium formate) pyridine of 2-
Base-S-1,3,5- triazine.Wherein, chloro- 4,6- bis- (3 '-sodium formate) pyridyl group-S-1 of the 2-, the molecular structure of 3,5- triazines
It is shown below:
Step S12 prepares the dipping solution containing the aqueous coupling agent of preset concentration.
Step S13 immerses the fibrous material in the dipping solution.
The dipping solution for being soaked with fibrous material is heated to preset temperature, and keeps the temperature a preset time by step S14.
Step S15 carries out drain processing to warm fibrous material.
Step S16 washes the fibrous material handled through drain.
Step S17 dries the fibrous material through washing.
Preferably, the fibrous material can be cotton, fiber crops, viscose glue, Modal or tencel.When fibrous material is above-mentioned material
One of when, in order to obtain preferable crease-resistant, shrinkproof, ironing-free performance, the preset concentration is 50g/L-500g/L, described pre-
If temperature is 70 DEG C -130 DEG C, the preset time is 30min-60min.Present embodiment provides a control experiment,
To illustrate the performance through treated the fibrous material of method described in present embodiment.The control experiment includes two
Group:
First group, be control group, and the cotton fabric Jing Guo desizing, kiering, bleaching, mercerising pre-treatment is carried out Liquid Ammonia Treatment,
High-count and high-density cotton poplin cloth (warp × latitude weave specification: yarn count 80s × 80s, 685 × 512/10cm of density) is obtained, to process
The high-count and high-density cotton poplin cloth of above-mentioned processing carries out resurgence test under room temperature, as a result as shown in Table 1.
Second group, it is experimental group, the high-count and high-density cotton poplin cloth obtained after first group of processing is directlyed adopt into dipping
Fabric is immersed the solution containing the aqueous coupling agent 200g/L, is heated to 100 DEG C, keeps the temperature 60min, drain, water by method processing
It washes, dry, region carries out resurgence test under room temperature after cooling, as a result as shown in Table 1.
Table one
As can be seen from Table I, method through the present embodiment fibrous material that carries out that treated the, through+wet reply of latitude
There is great promotion at angle, this is absolutely proved, the dipping solution containing aqueous coupling agent provided using present embodiment
After directly handling the fibrous material, the fibrous material obtains good formaldehydeless crease-resistant, shrinkproof, easy-care properties
Can, operating method is simple, has achieved the effect that get twice the result with half the effort.
Preferably, the fibrous material is natural fiber material, recycled fibrous material, composite fibre materials.Work as undulation degree
When material is one of above-mentioned material, in order to obtain preferably crease-resistant, shrinkproof, non-ironing and durable scourability, it is described preset it is dense
Degree is 5g/L-150g/L, and the preset temperature is 70 DEG C -130 DEG C, and the preset time is 30min-60min.It is furthermore preferred that
Further include in the dipping solution concentration be 1g/L-5g/L aqueous polyurethane.For this purpose, present embodiment additionally provides a pair
It according to the facts tests, to illustrate the performance through treated the fibrous material of method described in present embodiment.The control experiment
Including three groups:
Third group is control group, will be implemented at waterproof (water repellent) by oil removal treatment, dyeing treated kevlar fabric
Reason directly carries out conventional factory's water-proof treatment technology: padding waterproofing agent treatment liquid that is, by above-mentioned processed kevlar fabric
(80g/L Japan is bright at company waterproofing agent SG-601, and 10g/L Japan is bright at company crosslinking agent FM-1, pick-up 65%), then passes through
110 DEG C of drying, 220 DEG C × 10min bake heat treatment, will carry out washing test through treated kevlar fabric, as a result such as
Shown in table two.
4th group, be experimental group, will by oil removal treatment, dyeing treated kevlar fabric using infusion process pretreatment,
Fabric is immersed into the mixed solution containing the aqueous coupling agent 20g/L, aqueous polyurethane 2g/L, is heated to 130 DEG C, heat preservation
60min, drain, washing, drying;Through above-mentioned pretreated kevlar fabric, carry out padding waterproofing agent treatment liquid (80g/L Japan
It is bright at company waterproofing agent SG-601, pick-up 65%), then bake heat treatment through 110 DEG C of drying, 220 DEG C × 10min, i.e.,
The kevlar fabric of group first uses the dipping solution comprising aqueous coupling agent of present embodiment to be pre-processed, then carries out function
Energyization handles (such as water-proofing treatment), will carry out washing test through treated kevlar fabric, as a result as shown in Table 2.
5th group, be experimental group, will by oil removal treatment, dyeing treated kevlar fabric using infusion process pretreatment,
Fabric is immersed into the mixed solution containing the aqueous coupling agent 20g/L, aqueous polyurethane 2g/L, is heated to 130 DEG C, heat preservation
60min, drain, washing, through above-mentioned pretreated kevlar fabric, carrying out dipping waterproofing agent treatment liquid, (8%o.w.f Japan is bright
Cheng company waterproofing agent SG-601,130 DEG C × 60min), then drain bakes heat treatment through 110 DEG C of drying, 220 DEG C × 10min,
I.e. the kevlar fabric of this group first uses the dipping solution comprising aqueous coupling agent of present embodiment to be pre-processed, then into
Row functionalization (such as water-proofing treatment) will carry out washing test through treated kevlar fabric, as a result as shown in Table 2.
Table two
As can be seen from Table II, fibrous material is carried out at dipping using the aqueous coupling agent that present embodiment provides
After reason, then functionalization, such as water-proofing treatment are carried out, the durable scourability of the fibrous material finally obtained has greatly
It is promoted.
The processing method of fibrous material provided by the invention, by using including chloro- 4,6- bis- (3 '-sodium formate) pyridine of 2-
The aqueous coupling agent of base-S-1,3,5- triazines directly handle fibrous material, and fibrous material can be made to obtain good no first
Aldehyde is crease-resistant, shrinkproof, ironing-free performance, and has preferable durable scourability;Or use aqueous coupling agent provided by the invention
Various fibrous materials (each fiber material such as fiber, wool, silk, terylene, nylon, aramid fiber) are first pre-processed, after again
Functionalization is carried out, can be far smaller than that the washing times using conventional functionalization processing method.
Moreover, present embodiment additionally provides a kind of fibrous material inorganic agent, the fibrous material inorganic agent
Including aqueous coupling agent, the aqueous coupling agent includes chloro- 4,6- bis- (3 '-sodium formate) pyridyl group-S-1 of 2-, 3,5- triazines,
Molecular structure is shown below:
Preferably, the aqueous coupling agent is prepared using following steps: preparing the sodium hydrate aqueous solution of preset concentration;It will
The sodium hydrate aqueous solution is added in 3- pyridine first carboxylic, and stirs to dissolution;Three are added portionwise into reaction system under stiring
Polychlorostyrene piperazine;It is stirred to react to the transparent solution of system;Adjusting the clear solution pH value with sodium hydroxide is 7-8 to get to water
Property coupling agent 2- chloro- 4,6- bis- (3 '-sodium formate) pyridyl group-S-1,3,5- triazine solution.Such as: it is added in 900 milliliters of water
40 grams of piece alkali, stirring and dissolving, 61 grams of niacin (acidum nicotinicum) are added in (controlling temperature, the step heat release) in batches, stir molten
Solution, after cooling, is added portionwise and (controls temperature, the step heat release) 45 grams of trichloro-triazines (Cyanuric Chloride), be stirred to react
To the transparent solution of system, PH=7-8, discharging are adjusted with piece alkali.Wherein, during the preparation process, sodium hydroxide: niacin (3- pyrrole
Pyridine formic acid): the molar ratio of trichloro-triazine (Cyanuric Chloride) is 2:2:1.
The processing method and fibrous material inorganic agent of fibrous material provided by the invention include 2- chloro- 4,6- by preparation
Two (3 '-sodium formate) pyridyl group-S-1, the aqueous coupling agent of 3,5- triazines and use include chloro- 4,6-, the bis- (3 '-formic acid of 2-
Sodium) pyridyl group-S-1, the aqueous coupling agent of 3,5- triazines handles fibrous material, not only obtains fibrous material good
Crease-resistant, shrinkproof, ironing-free performance, and there is preferable durable scourability, it can be far smaller than that and handled using conventional functionalization
The washing times of method.
The above is only a preferred embodiment of the present invention, it is noted that for the ordinary skill people of the art
Member, various improvements and modifications may be made without departing from the principle of the present invention, these improvements and modifications also should be regarded as
Protection scope of the present invention.
Claims (3)
1. a kind of fibrous material processing method, which comprises the steps of:
One aqueous coupling agent is provided, the aqueous coupling agent includes bis- (3 '-sodium formate) pyridyl group-S-1 of chloro- 4, the 6- of 2-, and 3,5-
Triazine, molecular structure are shown below:
Prepare the dipping solution containing the aqueous coupling agent of preset concentration;The fibrous material is cotton, fiber crops, viscose glue, Modal or day
Silk, the preset concentration are 50g/L-500g/L;
The fibrous material is immersed in the dipping solution;
The dipping solution for being soaked with fibrous material is heated to preset temperature, and keeps the temperature a preset time;The preset temperature is 70
DEG C -130 DEG C, the preset time is 30min-60min;
Drain processing is carried out to warm fibrous material;
The fibrous material handled through drain is washed;
Fibrous material through washing is dried.
2. a kind of fibrous material inorganic agent, which is characterized in that the fibrous material inorganic agent includes aqueous coupling agent, described aqueous
Coupling agent includes chloro- 4,6- bis- (3 '-sodium formate) pyridyl group-S-1 of 2-, 3,5- triazines, and molecular structure is shown below:
3. fibrous material inorganic agent according to claim 2, which is characterized in that the aqueous coupling agent uses following steps
Preparation:
Prepare the sodium hydrate aqueous solution of preset concentration;
The sodium hydrate aqueous solution is added in 3- pyridine first carboxylic, and is stirred to dissolution;
Three polychlorostyrene piperazines are added portionwise into reaction system under stiring;
It is stirred to react to the transparent solution of system;
Adjusting the clear solution pH value with sodium hydroxide is 7-8 to get to chloro- 4,6-, the bis- (3 '-formic acid of aqueous coupling agent 2-
Sodium) pyridyl group-S-1,3,5- triazine solution.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201611080067.6A CN106555335B (en) | 2016-11-29 | 2016-11-29 | Fibrous material processing method and fibrous material inorganic agent |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201611080067.6A CN106555335B (en) | 2016-11-29 | 2016-11-29 | Fibrous material processing method and fibrous material inorganic agent |
Publications (2)
Publication Number | Publication Date |
---|---|
CN106555335A CN106555335A (en) | 2017-04-05 |
CN106555335B true CN106555335B (en) | 2019-01-08 |
Family
ID=58445286
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201611080067.6A Active CN106555335B (en) | 2016-11-29 | 2016-11-29 | Fibrous material processing method and fibrous material inorganic agent |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN106555335B (en) |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS49125379A (en) * | 1973-03-09 | 1974-11-30 | ||
JP2003176275A (en) * | 2001-12-12 | 2003-06-24 | Toshio Hagiwara | Method for producing stabilized shape-stabilizing agent |
CN101130578A (en) * | 2007-08-07 | 2008-02-27 | 西南大学 | Polyvinyl alcohol dichloro s-triazine crosslinking agent and synthesis method of the same |
FR2920984B1 (en) * | 2007-09-19 | 2010-03-26 | Oreal | COMPOSITION COMPRISING A CONTINUOUS FATTY PHASE AND A PARTICULAR ESTER |
CN102558078A (en) * | 2011-12-27 | 2012-07-11 | 苏州大学 | Cyanuric chloride derivative as well as preparation method and application in anti-wrinkle finishing agent of cyanuric chloride derivative and finishing method of pure silk fabric |
CN103526551A (en) * | 2013-09-27 | 2014-01-22 | 昆山培新服装有限公司 | Noniron finishing method for pure cotton fabric |
CN104195819A (en) * | 2014-08-06 | 2014-12-10 | 浙江理工大学 | Natural silk anti-crease agent and preparation method and application thereof |
CN105113252A (en) * | 2015-08-28 | 2015-12-02 | 浙江理工大学 | Anti-crease agent containing isodigeranyl active groups as well as preparation method and application of anti-crease agent |
-
2016
- 2016-11-29 CN CN201611080067.6A patent/CN106555335B/en active Active
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS49125379A (en) * | 1973-03-09 | 1974-11-30 | ||
JP2003176275A (en) * | 2001-12-12 | 2003-06-24 | Toshio Hagiwara | Method for producing stabilized shape-stabilizing agent |
CN101130578A (en) * | 2007-08-07 | 2008-02-27 | 西南大学 | Polyvinyl alcohol dichloro s-triazine crosslinking agent and synthesis method of the same |
FR2920984B1 (en) * | 2007-09-19 | 2010-03-26 | Oreal | COMPOSITION COMPRISING A CONTINUOUS FATTY PHASE AND A PARTICULAR ESTER |
CN102558078A (en) * | 2011-12-27 | 2012-07-11 | 苏州大学 | Cyanuric chloride derivative as well as preparation method and application in anti-wrinkle finishing agent of cyanuric chloride derivative and finishing method of pure silk fabric |
CN103526551A (en) * | 2013-09-27 | 2014-01-22 | 昆山培新服装有限公司 | Noniron finishing method for pure cotton fabric |
CN104195819A (en) * | 2014-08-06 | 2014-12-10 | 浙江理工大学 | Natural silk anti-crease agent and preparation method and application thereof |
CN105113252A (en) * | 2015-08-28 | 2015-12-02 | 浙江理工大学 | Anti-crease agent containing isodigeranyl active groups as well as preparation method and application of anti-crease agent |
Also Published As
Publication number | Publication date |
---|---|
CN106555335A (en) | 2017-04-05 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN102199803B (en) | High elastic non-ironing cellulose fiber and preparation method thereof | |
CN109577004B (en) | Processing method of easy-care shirt containing hemp or regenerated cellulose fiber | |
CN107142721A (en) | A kind of formaldehydeless non-ironing cellulose base fiber fabric dressing liquid of high whiteness and its application | |
CN105839414A (en) | A non-ironing finishing liquid for a ready-to-wear shirt and a non-ironing finishing method for a ready-to-wear shirt | |
WO2014100842A1 (en) | Non-fibrillating flame resistant cellulosic fabric, its use and method for producing the same | |
US3472606A (en) | Two-component wet fixation process for imparting durable press to cellulosecontaining materials | |
CN111601923B (en) | Use of non-formaldehyde technology to improve the balance of durable set properties of cotton fabrics | |
CN106555335B (en) | Fibrous material processing method and fibrous material inorganic agent | |
US3627556A (en) | Durable press finish for wool/cellulosic fabrics (melamine/dihydroxy-imidazolidinone resins) | |
US3656885A (en) | High strength wrinkle resistant cotton fabrics produced by a process involving both monosubstitution and crosslinking of the cotton | |
CN103243555A (en) | Noniron finishing method for purified cotton textiles with high strength retention | |
Galligan et al. | New Developments in Epoxide Wash-Wear Finishes for Cotton | |
US3402988A (en) | Chemical deactivation of catalyst at both faces of a cellulosic fabric impregnated with a resin-catalyst system to improve abrasion resistance of fabric after curing | |
Xu et al. | Durable press treatments to improve the durability and wrinkle resistance of cotton and other fabrics | |
Reid et al. | Durable Creasing of Wrinkle Resistant Cotton1 | |
US3533728A (en) | Inorganic and/or organic cellulose swelling agents used in conjunction with cross-linking agents in fabric modification process | |
IE872723L (en) | Treatment of fabric | |
US3041199A (en) | Wrinkle resistant cellulose fabric and method of production | |
CN111074609A (en) | Production method of polyurethane non-ironing cotton shirt | |
CN107724085A (en) | A kind of fibrous material processing method and fibrous material inorganic agent | |
US3166436A (en) | Treatment of fibrous materials | |
US3268291A (en) | Process for the production of permanent creases in cellulosic textiles utilizing inorganic salt solutions | |
US3563690A (en) | Production of dimensionally stable and shape-retaining garments of cellulosic fabrics | |
US3483570A (en) | Abrasion resistant wash-wear cellulosic products | |
US3660011A (en) | Dimethyl sulfoxide used as a solvent for textile treating compositions |
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 | ||
GR01 | Patent grant | ||
GR01 | Patent grant | ||
TR01 | Transfer of patent right | ||
TR01 | Transfer of patent right |
Effective date of registration: 20220729 Address after: Room 407-2-6, building C, Tian'an Digital City, 588 Changwu South Road, Wujin high tech Industrial Development Zone, Changzhou City, Jiangsu Province 213100 Patentee after: CHANGZHOU XIAOGUO INFORMATION SERVICES Co.,Ltd. Address before: 213164 No.53 Gehu Middle Road, Wujin District, Changzhou City, Jiangsu Province Patentee before: Changzhou Vocational Institute of Textile and Garment |