CN109797581A - A kind of few water dyeing of cotton fabric - Google Patents
A kind of few water dyeing of cotton fabric Download PDFInfo
- Publication number
- CN109797581A CN109797581A CN201910095227.1A CN201910095227A CN109797581A CN 109797581 A CN109797581 A CN 109797581A CN 201910095227 A CN201910095227 A CN 201910095227A CN 109797581 A CN109797581 A CN 109797581A
- Authority
- CN
- China
- Prior art keywords
- dyeing
- few water
- cotton fabric
- concentration
- soaping
- 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
Links
Landscapes
- Coloring (AREA)
Abstract
The invention discloses a kind of few water dyeing of cotton fabric, include the steps that being dyed cotton fabric addition navy dye bath and the cotton fabric soaping steps of dyeing;The soaping agent that uses soaped is the mixed solution of maleic acid-acrylic acid copolymer sodium salt, potassium peroxydisulfate, urea and sodium metasilicate.The technique can improve the homogenized diet of reactive dye;Wet friction color fastness is better than the prior art.
Description
Technical field
The invention belongs to printing technology fields, are related to a kind of dyeing of cotton fabric, and in particular to a kind of cotton is fine
Tie up few water dyeing of fabric.
Background technique
Dip method progress is usually taken in traditional cotton fabric dyeing, and cotton fabric is immersed in reactive dye dye bath
And add alkali fixation, to form firm covalent bond in cotton fiber row.However, in dyeing course, cotton fiber and the equal band of dyestuff
Negative electrical charge, it is necessary to the electrical charge rejection effect that electrolyte such as anhydrous sodium sulphate etc. weakens the two be added.The use of a large amount of electrolyte is no doubt
The dye-uptake of cotton fiber is improved, but can not recycle and degrade, causes modifying porcelain difficult.In addition to electrolyte, dye
Color waste water usually also comprising not fixed dyestuff more than one third, causes dyeing waste-water COD value to be up to 104mg/L.Therefore, it contaminates
Color waste water is always a great problem for perplexing dyeing.
In order to solve wastewater problem from the root, people gradually develop a variety of based on non-aqueous solvent system or few aqueous solvent
The colouring method of system, such as supercritical CO2Dyeing, organic solvent dyeing, suspension system dyeing and reverse micelle dyeing.These dyes
Color method, as dyeing medium, avoids or reduces the usage amount of water by using other dicyandiamide solutions substitution water;It can also subtract simultaneously
The usage amount of few salt.It among these, the use of more dicyandiamide solution is atoleine and organosiloxane.
Chinese patent application CN106368016A discloses a kind of atoleine colouring method of cotton fiber, and the method will
Leuco vat dye is scattered in atoleine, and in dyeing course, leuco vat dye is spontaneously transferred to cotton fiber
Above and through being contaminated in oxidation.Dyestuff dye-uptake is high, and auxiliary agent consumption is few, and dyeing is simple.However, the level-dyeing property of this method is not
It is good, while wet friction color fastness is poor.
Chinese patent application CN101922121B discloses a kind of non-aqueous dyeing method of reactive dye to textile, the party
Method by reactive dye, surfactant, coupling agent and as solvent cyclic methyl siloxane mix, make active dye by ball milling
Material is evenly dispersed in cyclic methyl siloxane, stable dye media suspension system dye bath is prepared into, using certain dye
Color technique is dyed.The not salt-free dyeing using water as the reactive dye of medium to cellulose fibre may be implemented in this method, Du
Exhausted electrolyte pollution, and dyestuff hydrolysis is greatly decreased, improve dyestuff fixation rate.The wet friction color fastness of this method and traditional water
Bath dyeing method is suitable, but still the level-dyeing property problem of unresolved dyestuff.
In view of the above drawbacks of the prior art, it is still desirable to for the dye based on non-aqueous solvent system or few aqueous solvent
Color technique makes sustained improvement.
Summary of the invention
The purpose of the present invention is to provide a kind of few water dyeings of navy cotton fabric.Few water dye of the invention
Color technique is able to solve the one or more of following technical problem: improving the homogenized diet of reactive dye;Wet friction color fastness with
Traditional water bath colouring method is suitable;Or it is better than the prior art.
In order to solve the above-mentioned technical problem, the invention adopts the following technical scheme:
A kind of few water dyeing of cotton fabric, including dye cotton fabric addition navy dye bath
The cotton fabric soaping steps of step and dyeing.
Few water dyeing above-mentioned according to the present invention, wherein the soaping agent used of soaping is maleic-acrylic acid
Copolymer sodium salt, potassium peroxydisulfate, urea and sodium metasilicate mixed solution.
Wherein, the number-average molecular weight of maleic acid-acrylic acid copolymer sodium salt is 22000-28000.
In a specific embodiment, the number-average molecular weight of maleic acid-acrylic acid copolymer sodium salt is 25000.
Few water dyeing above-mentioned according to the present invention, wherein the concentration of maleic acid-acrylic acid copolymer sodium salt is 0.8-
1.2g/L;The concentration of potassium peroxydisulfate is 0.2-0.4g/L;The concentration of urea is 0.4-0.8g/L;The concentration of sodium metasilicate is
0.05-0.3g/L。
In a specific embodiment, the concentration of maleic acid-acrylic acid copolymer sodium salt is 1g/L;Potassium peroxydisulfate
Concentration is 0.3g/L;The concentration of urea is 0.6g/L;The concentration of sodium metasilicate is 0.2g/L.
Few water dyeing above-mentioned according to the present invention, wherein the soaping condition is 60-80 DEG C, bath raio 1:(20-
40), pH=9.5-11, time 10-30min.Preferably, the soaping condition is 60-75 DEG C, pH=9.5-10.5, the time
For 10-20min.
In a specific embodiment, the soaping condition is 70 DEG C, bath raio 1:30, pH=10, and the time is
15min。
Few water dyeing above-mentioned according to the present invention, wherein the step of further comprising cotton fabric swelling treatment.
Few water dyeing above-mentioned according to the present invention, wherein the swelling treatment step are as follows: use cotton fabric
Lye swelling, control liquid carrying rate are 80-160%.
Preferably, cotton fabric is swollen using lye, control liquid carrying rate is 90-150%;It is highly preferred that by cotton fibre
Dimension fabric is swollen using lye, and control liquid carrying rate is 100-140%;And most preferably, cotton fabric is molten using lye
Swollen, control liquid carrying rate is 110-130%.
In a specific embodiment, cotton fabric is swollen using lye, control liquid carrying rate is 120%.
Wherein, the alkali in the lye is selected from inorganic weak bases, including but not limited to, carbonate, phosphate, silicate, phosphorus
Sour hydrogen salt, dihydric phosphate and pyrophosphate.
Preferably, the inorganic weak bases are selected from carbonate, phosphate, silicate and dihydric phosphate;It is highly preferred that described
Inorganic weak bases are selected from carbonate, phosphate and silicate;And most preferably, the inorganic weak bases are selected from carbonate and silicic acid
Salt.
In a specific embodiment, the inorganic weak bases are selected from carbonate.
As the cation of inorganic weak bases, lithium, sodium, potassium and ammonium ion can be.
Preferably, the concentration of the lye is 10-50g/L;It is highly preferred that the concentration of the lye is 20-45g/L;With
And most preferably, the concentration of the lye is 30-40g/L.
In a specific embodiment, the lye is selected from the aqueous sodium carbonate of 35g/L.
Few water dyeing above-mentioned according to the present invention, wherein the navy dye bath is by navy dye high concentration water
Solution and atoleine reverse micelle system composition.
Few water dyeing above-mentioned according to the present invention, wherein the navy dye is selected from chemical combination shown in formula (I)
Object;
Wherein, R1-R4It is each independently selected from H, C1-C4Alkyl, C1-C4Alkoxy and SO3M;Y1-Y2It selects each independently
From SO2CH=CH2Or SO2CH2CH2OSO3M;M is selected from H or alkali metal.
Preferably, in formula (I) compound represented, R1-R4It is each independently selected from H, C1-C4Alkyl and C1-C4Alcoxyl
Base;Y1-Y2It is each independently selected from SO2CH=CH2Or SO2CH2CH2OSO3M;M is selected from H or alkali metal.
It is highly preferred that in formula (I) compound represented, R1-R4It is each independently selected from H and C1-C4Alkyl;Y1-Y2Respectively
From independently selected from SO2CH=CH2Or SO2CH2CH2OSO3M;M is selected from H or alkali metal.
And most preferably, in formula (I) compound represented, R1-R4It is each independently selected from H;Y1-Y2It is respectively independent
Ground is selected from SO2CH=CH2Or SO2CH2CH2OSO3M;M is selected from alkali metal.
As alkali metal, M can be lithium, sodium, potassium;Preferably sodium and potassium.
In a specific embodiment, in formula (I) compound represented, R1-R4It is each independently selected from H;Y1-
Y2It is each independently selected from SO2CH2CH2OSO3M;M is selected from sodium.
In a more specific embodiment, formula (I) compound represented is selected from active black RB5 (CAS 17095-
24-8)。
Few water dyeing above-mentioned according to the present invention, wherein the concentration of the navy dye high concentration solution is
8-24g/L。
Preferably, the concentration of the navy dye aqueous solution is 10-22g/L;It is highly preferred that the navy dye is high
The concentration of concentration of aqueous solution is 12-20g/L;And most preferably, the concentration of the navy dye high concentration solution is
14-18g/L。
In a specific embodiment, the concentration of the navy dye high concentration solution is 15g/L.
Few water dyeing above-mentioned according to the present invention, wherein the atoleine reverse micelle system is organic solvent, table
Face activating agent, cosurfactant and atoleine mix.
Preferably, the organic solvent is selected from dimethyl sulfoxide and dimethylformamide;It is highly preferred that the organic solvent choosing
From dimethylformamide.
Preferably, the surfactant is selected from TWEEN Series surfactant, span series and Qula
Logical series of surfactants;It is highly preferred that the surfactant is selected from TWEEN Series surfactant and Span series surface
Activating agent;And most preferably, the surfactant is selected from span series.
In a specific embodiment, the surfactant is selected from sorbester p17.
Preferably, the cosurfactant is selected from n-hexyl alcohol, n-heptanol, n-octyl alcohol and isooctanol;It is highly preferred that described
Cosurfactant is selected from n-heptanol, n-octyl alcohol and isooctanol;And most preferably, the cosurfactant is selected from just pungent
Pure and mild isooctanol.
In a specific embodiment, the cosurfactant is selected from n-octyl alcohol.
Preferably as raw material, organic solvent, surfactant, cosurfactant and atoleine volume ratio be
1:(0.4-0.8): (1.2-1.8): (4-6).It is highly preferred that organic solvent, surfactant, cosurfactant and liquid stone
The volume ratio of wax is 1:(0.5-0.8): (1.4-1.8): (4.5-6);And most preferably, organic solvent, surfactant,
The volume ratio of cosurfactant and atoleine is 1:(0.5-0.7): (1.4-1.6): (4.5-5.5).
In a specific embodiment, the body of organic solvent, surfactant, cosurfactant and atoleine
Product is than being 1:0.6:1.5:5.
As hybrid mode, advantageously, it is uniformly mixed raw material using ultrasound and agitating mode.
Few water dyeing above-mentioned according to the present invention, wherein the navy dye high concentration solution and the liquid
The volume ratio of body paraffin reverse micelle system is 1:(8-12).
Preferably, the volume ratio of the navy dye high concentration solution and the atoleine reverse micelle system is 1:
(8.5-11);It is highly preferred that the volume ratio of the navy dye high concentration solution and the atoleine reverse micelle system
For 1:(8.5-10);And most preferably, the navy dye high concentration solution and the atoleine reverse micelle system
Volume ratio be 1:(8.5-9.5).
In a specific embodiment, the navy dye high concentration solution and the atoleine reverse micelle
The volume ratio of system is 1:9.
As hybrid mode, advantageously, it is uniformly mixed raw material using ultrasound and agitating mode.
Few water dyeing above-mentioned according to the present invention, wherein the bath raio of the dyeing course is 1:(10-30).
Preferably, the bath raio of the dyeing course is 1:(12-28);It is highly preferred that the bath raio of the dyeing course is 1:
(15-25);And most preferably, the bath raio of the dyeing course is 1:(18-22).
In a specific embodiment, the bath raio of the dyeing course is 1:20.
Few water dyeing above-mentioned according to the present invention, wherein the dyeing course includes liter of the room temperature to target temperature
The heat preservation fixation stage under Wen Shangran stage and target temperature.
Few water dyeing above-mentioned according to the present invention, wherein the target temperature is 50-80 DEG C.
Preferably, the target temperature is 50-75 DEG C;It is highly preferred that the target temperature is 55-70 DEG C;And it is optimal
Selection of land, the target temperature are 60-70 DEG C.
In a specific embodiment, the target temperature is 65 DEG C.
Few water dyeing above-mentioned according to the present invention, wherein the heat preservation under stage and target temperature is contaminated in the heating
The duration in fixation stage is 10-120min.
Preferably, the heating rate that the stage is contaminated in the heating is 0.5-3 DEG C/min;It is highly preferred that being contaminated in the heating
The heating rate in stage is 0.5-2.5 DEG C/min;And most preferably, the heating rate that the stage is contaminated in the heating is 0.5-2
℃/min。
In a specific embodiment, the heating rate that the stage is contaminated in the heating is 1 DEG C/min.
Preferably, the when a length of 10-90min in the heat preservation fixation stage;It is highly preferred that it is described heat preservation the fixation stage when
A length of 10-60min;And most preferably, the when a length of 10-40min in the heat preservation fixation stage.
In a specific embodiment, the when a length of 30min in the heat preservation fixation stage.
Few water dyeing above-mentioned according to the present invention, wherein the dyeing course further comprises target temperature to room
The temperature-fall period of temperature.
The temperature-fall period can take Temperature fall or program to cool down.
Advantageously, the rate of temperature fall is 0.5-5 DEG C/min;It is highly preferred that the rate of temperature fall is 0.5-4 DEG C/min;
And most preferably, the rate of temperature fall is 1-3 DEG C/min.
In a specific embodiment, the rate of temperature fall is 2 DEG C/min.
In another embodiment, the soaping agent used of soaping can be containing 2-4g/L standard soap flakes and 2-
The soap boiling liquid of 4g/L sodium carbonate.
In a specific embodiment, the soaping agent used of soaping is containing 3g/L standard soap flakes and 3g/L carbon
The soap boiling liquid of sour sodium.
Advantageously, the soaping condition is 90-95 DEG C, bath raio 1:(40-60), time 5-20min.
In a specific embodiment, the soaping condition is 95 DEG C, bath raio 1:50, time 10min.
The navy dye bath for the reverse micelle system that inventor is improved based on atoleine, passes through polarized light microscope observing
To micella drop average-size in 200nm hereinafter, and size distribution it is more uniform.It is not intended to limited to any theory, this
The dyeing that invention takes above-mentioned dye bath to carry out can be effectively improved level-dyeing property.On the other hand, the present invention passes through specific soap
It washes one's hands section, washes away the not upper dyestuff and partial hydrolysis dyestuff contaminated, so that wet friction color fastness at least quite (is used with the prior art
The situation of soap flakes), or it is better than the prior art (using the situation of maleic acid-acrylic acid copolymer sodium salt).
Specific embodiment
The invention will be further elucidated with reference to specific embodiments.
It should be understood that a specific embodiment of the invention is only used for illustrating the spirit and principles in the present invention, rather than limitation
The scope of the present invention.In addition, it should also be understood that, after reading the contents of the present invention, those skilled in the art can be to of the invention
Technical solution make it is various change, replace, delete, correct or adjust, these equivalents thereofs equally fall within right of the present invention
Claim limited range.
Level-dyeing property test is carried out according to literature method, and the specific method is as follows: by cotton fabric few water according to the invention
Dyeing is dyed, and the navy cotton fabric is obtained, and is then bisected into two parts, referred to as A fabric.Then
The fabric B that is unstained of a A fabric and identical weight few water dyeing according to the invention is dyed again with bath.Point
Not Ce Ding A fabric dye again before initial apparent color depth (K/S value) and again dye after K/S value and B fabric it is same
K/S value after bath dyeing, is denoted as (K/S) respectivelyO、(K/S)A(K/S)B.According to formula L=(K/S)B/[(K/S)B+(K/S)A-
(K/S)O] * 100% calculating level dyeing sex index L.L value is higher, and level-dyeing property is better.
In the present invention, the measurement of apparent colour depth K/S value carries out on Datacolor color measurement and color match instrument, will dye
Fabric builds up 4 layers, and every layer of front and back sides take a point, measures 8 points and is averaged.
Wet friction color fastness is tested and is measured according to GB/T3920-2008 and GB/T251-2008.
Embodiment 1
Cotton fabric is swollen using the aqueous sodium carbonate of 35g/L, by an immersing and rolling, controlling liquid carrying rate is
120%.The active black RB5 aqueous solution of compound concentration 15g/L.It is 1:0.6:1.5:5 according to volume ratio, measures dimethyl formyl
Amine, sorbester p17, n-octyl alcohol and atoleine;It is uniformly mixed raw material using ultrasonic power, obtains atoleine reverse micelle system.
Then the two is mixed under ultrasonication for 1:9 according to active black RB5 aqueous solution and atoleine reverse micelle system volume ratio
Uniformly, navy dye bath is obtained.By the average-size of polarized light microscope observing to micella drop in 200nm hereinafter, and big
Small distribution is more uniform.Cotton fabric addition navy dye bath is dyed.The bath raio of dyeing course is 1:20.First from
For room temperature to 65 DEG C, heating rate is 1 DEG C/min;Then fixation 30min is kept the temperature;Room temperature, rate of temperature fall are down to from 65 DEG C again
For 2 DEG C/min, contaminate out.
Embodiment 2
Embodiment 1 is gone out into the cotton fabric contaminated and first uses 60 DEG C of hot water wash 10min, is subsequently placed in soaping agent;Wherein, horse
The concentration for carrying out sour-acrylic copolymer sodium salt (Mn=25000) is 1g/L;The concentration of potassium peroxydisulfate is 0.3g/L;Urea it is dense
Degree is 0.6g/L;The concentration of sodium metasilicate is 0.2g/L;Soaping condition is 70 DEG C, bath raio 1:30, pH=10, time 15min.
Then 60 DEG C of hot water wash 10min, cold water wash 5min, and drying obtains the navy cotton fabric of embodiment 2.
Embodiment 3
Embodiment 1 is gone out into the cotton fabric contaminated and first uses 60 DEG C of hot water wash 10min, is subsequently placed in soaping agent;Wherein, soap
Lotion is the soap boiling liquid containing 3g/L standard soap flakes and 3g/L sodium carbonate;Soaping condition is 95 DEG C, bath raio 1:50, and the time is
10min.Then 60 DEG C of hot water wash 10min, cold water wash 5min, and drying obtains the navy cotton fabric of embodiment 3.
Embodiment 4
Cotton fabric is swollen using the aqueous sodium carbonate of 30g/L, by an immersing and rolling, controlling liquid carrying rate is
130%.The active black RB5 aqueous solution of compound concentration 14g/L.It is 1:0.5:1.4:4.5 according to volume ratio, measures dimethyl formyl
Amine, sorbester p17, n-octyl alcohol and atoleine;It is uniformly mixed raw material using ultrasonic power, obtains atoleine reverse micelle system.
It then is 1:9.5 the two is mixed under ultrasonication according to active black RB5 aqueous solution and atoleine reverse micelle system volume ratio
It closes uniformly, obtains navy dye bath.By the average-size of polarized light microscope observing to micella drop in 200nm hereinafter, and
Size distribution is more uniform.Cotton fabric addition navy dye bath is dyed.The bath raio of dyeing course is 1:18.First
From room temperature to 60 DEG C, heating rate is 1 DEG C/min;Then fixation 30min is kept the temperature;Room temperature, cooling speed are down to from 60 DEG C again
Rate is 2 DEG C/min, is contaminated out.
Embodiment 5
Embodiment 4 is gone out into the cotton fabric contaminated and first uses 60 DEG C of hot water wash 10min, is subsequently placed in soaping agent;Wherein, horse
The concentration for carrying out sour-acrylic copolymer sodium salt (Mn=25000) is 1g/L;The concentration of potassium peroxydisulfate is 0.3g/L;Urea it is dense
Degree is 0.6g/L;The concentration of sodium metasilicate is 0.2g/L;Soaping condition is 70 DEG C, bath raio 1:30, pH=10, time 15min.
Then 60 DEG C of hot water wash 10min, cold water wash 5min, and drying obtains the navy cotton fabric of embodiment 5.
Embodiment 6
Cotton fabric is swollen using the aqueous sodium carbonate of 40g/L, by an immersing and rolling, controlling liquid carrying rate is
110%.The active black RB5 aqueous solution of compound concentration 18g/L.It is 1:0.6:1.6:5.5 according to volume ratio, measures dimethyl formyl
Amine, sorbester p17, n-octyl alcohol and atoleine;It is uniformly mixed raw material using ultrasonic power, obtains atoleine reverse micelle system.
It then is 1:8.5 the two is mixed under ultrasonication according to active black RB5 aqueous solution and atoleine reverse micelle system volume ratio
It closes uniformly, obtains navy dye bath.By the average-size of polarized light microscope observing to micella drop in 200nm hereinafter, and
Size distribution is more uniform.Cotton fabric addition navy dye bath is dyed.The bath raio of dyeing course is 1:22.First
From room temperature to 70 DEG C, heating rate is 1 DEG C/min;Then fixation 30min is kept the temperature;Room temperature, cooling speed are down to from 70 DEG C again
Rate is 2 DEG C/min, is contaminated out.
Embodiment 7
Embodiment 6 is gone out into the cotton fabric contaminated and first uses 60 DEG C of hot water wash 10min, is subsequently placed in soaping agent;Wherein, soap
Lotion is the soap boiling liquid containing 3g/L standard soap flakes and 3g/L sodium carbonate;Soaping condition is 95 DEG C, bath raio 1:50, and the time is
10min.Then 60 DEG C of hot water wash 10min, cold water wash 5min, and drying obtains the navy cotton fabric of embodiment 7.
Comparative example 1
Cotton fabric is swollen using the aqueous sodium carbonate of 35g/L, by an immersing and rolling, controlling liquid carrying rate is
120%.The active black RB5 aqueous solution of compound concentration 15g/L.It is 1:9 according to active black RB5 aqueous solution and atoleine volume ratio
The two is uniformly mixed under ultrasonication, obtains navy dye bath.Cotton fabric addition navy dye bath is dyed.
The bath raio of dyeing course is 1:20.First from room temperature to 65 DEG C, heating rate is 1 DEG C/min;Then fixation is kept the temperature
30min;Room temperature is down to from 65 DEG C again, rate of temperature fall is 2 DEG C/min, is contaminated out.Then, it is first then set with 60 DEG C of hot water wash 10min
In soaping agent;Wherein, soaping agent is the soap boiling liquid containing 3g/L standard soap flakes and 3g/L sodium carbonate;Soaping condition is 95 DEG C,
Bath raio 1:50, time 10min.Then 60 DEG C of hot water wash 10min, cold water wash 5min, and drying obtains the navy of comparative example 1
Cotton fabric.
According to present invention method above-mentioned measurement embodiment 2-3,5 and 7 and comparative example 1 level dyeing sex index L and wet rub
Wipe color fastness.As a result referring to table 1.
Table 1
Level dyeing sex index L | Wet friction color fastness | |
Embodiment 2 | 78% | 4-5 |
Embodiment 3 | 71% | 3-4 |
Embodiment 5 | 75% | 4-5 |
Embodiment 7 | 67% | 4 |
Comparative example 1 | 56% | 3-4 |
As can be seen from Table 1,2-3 of the embodiment of the present invention, 5 and 7 change relative to comparative example 1 due to taking atoleine
Into the navy dye bath of obtained reverse micelle system, level dyeing sex index L is significantly improved.In addition, the soap of embodiment 2 and 5
Chemical industry skill uses maleic acid-acrylic acid copolymer sodium salt, and wet friction color fastness relatively example 1 improves half grade or level-one.And it is real
The saponification process of example 3 and 7 is applied using soap flakes, wet friction color fastness and comparative example 1 are substantially quite.
The foregoing is only a preferred embodiment of the present invention, is not intended to restrict the invention, for the skill of this field
For art personnel, the invention may be variously modified and varied.All within the spirits and principles of the present invention, made any to repair
Change, equivalent replacement, improvement etc., is all included in the scope of protection of the present invention.
Claims (10)
1. few water dyeing of a kind of cotton fabric, including the step for dyeing cotton fabric addition navy dye bath
Rapid and dyeing cotton fabric soaping steps;It is characterized in that, the soaping agent used of soaping is total for maleic-acrylic acid
Polymers sodium salt, potassium peroxydisulfate, urea and sodium metasilicate mixed solution.
2. few water dyeing according to claim 1, wherein the equal molecule of the number of maleic acid-acrylic acid copolymer sodium salt
Amount is 22000-28000.
3. few water dyeing according to claim 1, wherein the concentration of maleic acid-acrylic acid copolymer sodium salt is
0.8-1.2g/L;The concentration of potassium peroxydisulfate is 0.2-0.4g/L;The concentration of urea is 0.4-0.8g/L;The concentration of sodium metasilicate is
0.05-0.3g/L。
4. few water dyeing according to claim 1, wherein the soaping condition is 60-80 DEG C, bath raio 1:(20-
40), pH=9.5-11, time 10-30min.
5. few water dyeing according to claim 1, wherein the navy dye bath is by navy dye high concentration water
Solution and atoleine reverse micelle system composition.
6. few water dyeing according to claim 1, wherein the atoleine reverse micelle system is dimethyl formyl
Amine, sorbester p17, n-octyl alcohol and atoleine mix.
7. few water dyeing according to claim 6, wherein dimethylformamide, sorbester p17, n-octyl alcohol and liquid stone
The volume ratio of wax is 1:(0.4-0.8): (1.2-1.8): (4-6).
8. few water dyeing according to claim 1, wherein the dyeing course includes liter of the room temperature to target temperature
The heat preservation fixation stage under Wen Shangran stage and target temperature.
9. few water dyeing according to claim 8, wherein the target temperature is 50-80 DEG C.
10. few water dyeing according to claim 1, wherein further comprise the step of cotton fabric swelling treatment
Suddenly.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201910095227.1A CN109797581B (en) | 2019-01-31 | 2019-01-31 | Low-water dyeing process for cotton fiber fabric |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201910095227.1A CN109797581B (en) | 2019-01-31 | 2019-01-31 | Low-water dyeing process for cotton fiber fabric |
Publications (2)
Publication Number | Publication Date |
---|---|
CN109797581A true CN109797581A (en) | 2019-05-24 |
CN109797581B CN109797581B (en) | 2021-04-16 |
Family
ID=66560644
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201910095227.1A Active CN109797581B (en) | 2019-01-31 | 2019-01-31 | Low-water dyeing process for cotton fiber fabric |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN109797581B (en) |
Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101922121A (en) * | 2010-08-11 | 2010-12-22 | 浙江理工大学 | New dyeing method of active dye taking methylsiloxane as medium |
CN103203192A (en) * | 2013-02-05 | 2013-07-17 | 东华大学 | Nonionic reverse micelle system and method for modifying polar material by using same |
CN105442359A (en) * | 2014-09-01 | 2016-03-30 | 香港理工大学 | Cotton fabric non-aqueous dyeing process and reverse micelle encapsulated reactive dye liquid |
CN105442350A (en) * | 2015-12-23 | 2016-03-30 | 浙江丝科院轻纺材料有限公司 | All-cotton fabric dyeing method adopting two-phase medium |
CN106337303A (en) * | 2016-08-25 | 2017-01-18 | 浙江理工大学 | Reactive dye dyeing method for cotton fabric |
CN106368016A (en) * | 2016-08-25 | 2017-02-01 | 浙江理工大学 | Liquid paraffin bath dyeing method of cotton fiber |
CN107022908A (en) * | 2017-03-24 | 2017-08-08 | 合肥云都棉花有限公司 | A kind of colouring method of cotton cloth |
CN107326700A (en) * | 2016-04-29 | 2017-11-07 | 香港理工大学 | A kind of non-aqueous dyeing process methods of fabric |
CN109183460A (en) * | 2018-11-22 | 2019-01-11 | 香港理工大学 | A kind of colouring method of protein fibre non-aqueous media |
-
2019
- 2019-01-31 CN CN201910095227.1A patent/CN109797581B/en active Active
Patent Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101922121A (en) * | 2010-08-11 | 2010-12-22 | 浙江理工大学 | New dyeing method of active dye taking methylsiloxane as medium |
CN103203192A (en) * | 2013-02-05 | 2013-07-17 | 东华大学 | Nonionic reverse micelle system and method for modifying polar material by using same |
CN105442359A (en) * | 2014-09-01 | 2016-03-30 | 香港理工大学 | Cotton fabric non-aqueous dyeing process and reverse micelle encapsulated reactive dye liquid |
CN105442350A (en) * | 2015-12-23 | 2016-03-30 | 浙江丝科院轻纺材料有限公司 | All-cotton fabric dyeing method adopting two-phase medium |
CN107326700A (en) * | 2016-04-29 | 2017-11-07 | 香港理工大学 | A kind of non-aqueous dyeing process methods of fabric |
CN106337303A (en) * | 2016-08-25 | 2017-01-18 | 浙江理工大学 | Reactive dye dyeing method for cotton fabric |
CN106368016A (en) * | 2016-08-25 | 2017-02-01 | 浙江理工大学 | Liquid paraffin bath dyeing method of cotton fiber |
CN107022908A (en) * | 2017-03-24 | 2017-08-08 | 合肥云都棉花有限公司 | A kind of colouring method of cotton cloth |
CN109183460A (en) * | 2018-11-22 | 2019-01-11 | 香港理工大学 | A kind of colouring method of protein fibre non-aqueous media |
Non-Patent Citations (3)
Title |
---|
SUXIN XU等: "An environmentally responsible polyester dyeing technology using liquid paraffin", 《JOURNAL OF CLEANER PRODUCTION》 * |
郭宝夫 等: "活性染料低温皂洗工艺", 《印染》 * |
黄良晨 等: "活性染料染色用皂洗剂概述", 《印染助剂》 * |
Also Published As
Publication number | Publication date |
---|---|
CN109797581B (en) | 2021-04-16 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN105908534B (en) | A kind of viscose cheese dyeing | |
CN104746361B (en) | A kind of method of Non-water washing reactive dye non-aqueous solvent dyeing | |
CN105421105B (en) | A kind of polyester-cotton blend disperse dyes and reactive dye One Bath Dyeing Process | |
CN103711008B (en) | Semi-material dyeing technology of silk-cotton interweaving garment material | |
CN103498348B (en) | A kind of salt-free low alkali colouring method shortening the reactive dyeing time | |
CN105332291B (en) | Dyeing method for calcium alginate fibers | |
CN102493223B (en) | A kind of composition of aqueous solution of reactive dye for pad dyeing and compound method | |
CN106436349A (en) | Inkjet printing technology for cotton and linen fiber fabric | |
CN103572621A (en) | Method for improving color fastness of photochromic fabric | |
CN104448927B (en) | A kind of composite reactive blue dye | |
CN109750528A (en) | Few water dyeing of cotton fabric | |
CN109853260A (en) | A kind of few water dyeing | |
Wang et al. | Solvent assisted dyeing of wool fibers with reactive dyes in a ternary solvent system for protecting fibers against damage | |
CN104736644B (en) | Acid dye composition and use its staining | |
CN104313919A (en) | Non-ionic mixed reversed micelles and preparation method thereof | |
CN109797581A (en) | A kind of few water dyeing of cotton fabric | |
CN109797575A (en) | A kind of few water dyeing of navy cotton fabric | |
CN106758378B (en) | A kind of textile dyeing increases deep functional agent and preparation method thereof, application | |
CN101349015B (en) | Preparation and application of colloidal sol dyeing liquor | |
CN107164114A (en) | A kind of antifouling soaping agent of the quaternary ammonium salt of chain containing APEO and preparation method thereof | |
Burkinshaw et al. | The clearing of poly (lactic acid) fibres dyed with disperse dyes using ultrasound: Part 3 | |
CN103255645B (en) | Goat cashmere/viscose blend fabric dyeing | |
CN109183447A (en) | The reactive dye salt-free dyeing method of calcium alginate fibre | |
CN113152121B (en) | Orange coupled disperse dye compound and dyeing process thereof | |
El-Shishtawy et al. | Anionic colouration of acrylic fibre. Part II: Printing with reactive, acid and direct dyes |
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 |