CN116926970A - Dyeing method of high-density nylon woven fabric - Google Patents
Dyeing method of high-density nylon woven fabric Download PDFInfo
- Publication number
- CN116926970A CN116926970A CN202210373476.4A CN202210373476A CN116926970A CN 116926970 A CN116926970 A CN 116926970A CN 202210373476 A CN202210373476 A CN 202210373476A CN 116926970 A CN116926970 A CN 116926970A
- Authority
- CN
- China
- Prior art keywords
- dyeing
- woven fabric
- nylon woven
- density nylon
- ceramic powder
- 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.)
- Pending
Links
- 229920001778 nylon Polymers 0.000 title claims abstract description 87
- 238000004043 dyeing Methods 0.000 title claims abstract description 78
- 239000004677 Nylon Substances 0.000 title claims abstract description 71
- 239000002759 woven fabric Substances 0.000 title claims abstract description 60
- 238000000034 method Methods 0.000 title claims abstract description 38
- 239000004744 fabric Substances 0.000 claims abstract description 77
- 239000000980 acid dye Substances 0.000 claims abstract description 33
- 238000010438 heat treatment Methods 0.000 claims abstract description 25
- 238000004321 preservation Methods 0.000 claims abstract description 21
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 68
- 239000000919 ceramic Substances 0.000 claims description 60
- 239000000843 powder Substances 0.000 claims description 60
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 51
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 37
- 229920001690 polydopamine Polymers 0.000 claims description 35
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 34
- 239000011259 mixed solution Substances 0.000 claims description 34
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 34
- 229960000583 acetic acid Drugs 0.000 claims description 28
- 238000001035 drying Methods 0.000 claims description 24
- 229920001732 Lignosulfonate Polymers 0.000 claims description 20
- CTENFNNZBMHDDG-UHFFFAOYSA-N Dopamine hydrochloride Chemical compound Cl.NCCC1=CC=C(O)C(O)=C1 CTENFNNZBMHDDG-UHFFFAOYSA-N 0.000 claims description 16
- 229960001149 dopamine hydrochloride Drugs 0.000 claims description 16
- 239000012362 glacial acetic acid Substances 0.000 claims description 16
- 239000002245 particle Substances 0.000 claims description 14
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims description 13
- 238000006136 alcoholysis reaction Methods 0.000 claims description 13
- 235000011114 ammonium hydroxide Nutrition 0.000 claims description 13
- 239000000243 solution Substances 0.000 claims description 12
- 238000003756 stirring Methods 0.000 claims description 11
- 230000001105 regulatory effect Effects 0.000 claims description 9
- 238000001914 filtration Methods 0.000 claims description 8
- JEGUKCSWCFPDGT-UHFFFAOYSA-N h2o hydrate Chemical compound O.O JEGUKCSWCFPDGT-UHFFFAOYSA-N 0.000 claims description 8
- 238000002360 preparation method Methods 0.000 claims description 8
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims description 7
- 238000001816 cooling Methods 0.000 claims description 3
- 239000000975 dye Substances 0.000 abstract description 30
- 238000004040 coloring Methods 0.000 abstract description 13
- 241000218998 Salicaceae Species 0.000 abstract description 4
- 230000009286 beneficial effect Effects 0.000 abstract 1
- LRWZZZWJMFNZIK-UHFFFAOYSA-N 2-chloro-3-methyloxirane Chemical compound CC1OC1Cl LRWZZZWJMFNZIK-UHFFFAOYSA-N 0.000 description 12
- 239000011248 coating agent Substances 0.000 description 10
- 238000000576 coating method Methods 0.000 description 10
- 230000000052 comparative effect Effects 0.000 description 7
- 230000008569 process Effects 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000000835 fiber Substances 0.000 description 5
- 125000003277 amino group Chemical group 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 238000004132 cross linking Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000001179 sorption measurement Methods 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 238000005299 abrasion Methods 0.000 description 2
- 238000002835 absorbance Methods 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 238000011534 incubation Methods 0.000 description 2
- 239000010985 leather Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 125000000542 sulfonic acid group Chemical group 0.000 description 2
- 239000002344 surface layer Substances 0.000 description 2
- 238000002834 transmittance Methods 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 1
- 230000006750 UV protection Effects 0.000 description 1
- 238000005411 Van der Waals force Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000003490 calendering Methods 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000009990 desizing Methods 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 230000004224 protection Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 230000003746 surface roughness Effects 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/39—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using acid dyes
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06B—TREATING TEXTILE MATERIALS USING LIQUIDS, GASES OR VAPOURS
- D06B23/00—Component parts, details, or accessories of apparatus or machines, specially adapted for the treating of textile materials, not restricted to a particular kind of apparatus, provided for in groups D06B1/00 - D06B21/00
- D06B23/20—Arrangements of apparatus for treating processing-liquids, -gases or -vapours, e.g. purification, filtration or distillation
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06B—TREATING TEXTILE MATERIALS USING LIQUIDS, GASES OR VAPOURS
- D06B23/00—Component parts, details, or accessories of apparatus or machines, specially adapted for the treating of textile materials, not restricted to a particular kind of apparatus, provided for in groups D06B1/00 - D06B21/00
- D06B23/20—Arrangements of apparatus for treating processing-liquids, -gases or -vapours, e.g. purification, filtration or distillation
- D06B23/22—Arrangements of apparatus for treating processing-liquids, -gases or -vapours, e.g. purification, filtration or distillation for heating
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
- D06P1/46—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing natural macromolecular substances or derivatives thereof
- D06P1/48—Derivatives of carbohydrates
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
- D06P1/52—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing synthetic macromolecular substances
- D06P1/5207—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- D06P1/5214—Polymers of unsaturated compounds containing no COOH groups or functional derivatives thereof
- D06P1/5228—Polyalkenyl alcohols, e.g. PVA
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
- D06P1/64—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing low-molecular-weight organic compounds without sulfate or sulfonate groups
- D06P1/651—Compounds without nitrogen
- D06P1/65106—Oxygen-containing compounds
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
- D06P1/673—Inorganic compounds
- D06P1/67383—Inorganic compounds containing silicon
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
- D06P3/02—Material containing basic nitrogen
- D06P3/04—Material containing basic nitrogen containing amide groups
- D06P3/24—Polyamides; Polyurethanes
- D06P3/241—Polyamides; Polyurethanes using acid dyes
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06B—TREATING TEXTILE MATERIALS USING LIQUIDS, GASES OR VAPOURS
- D06B2700/00—Treating of textile materials, e.g. bleaching, dyeing, mercerising, impregnating, washing; Fulling of fabrics
- D06B2700/36—Devices or methods for dyeing, washing or bleaching not otherwise provided for
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
- Y02P70/50—Manufacturing or production processes characterised by the final manufactured product
- Y02P70/62—Manufacturing or production processes characterised by the final manufactured product related technologies for production or treatment of textile or flexible materials or products thereof, including footwear
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Molecular Biology (AREA)
- Inorganic Chemistry (AREA)
- Coloring (AREA)
Abstract
The invention relates to the technical field of nylon fabric dyeing methods, and discloses a dyeing method of a high-density nylon woven fabric, which comprises the following steps: immersing the high-density nylon woven fabric into an acid dye solution for dyeing, adjusting the pH to 3.5-5, and adopting staged heat preservation treatment, wherein the heat preservation is carried out for 10-20 min at 70-80 ℃, 20-30 min at 90-100 ℃ and 45-55 min at 110-120 ℃ in sequence. The staged heat preservation treatment of the acid dye is beneficial to level dyeing and cover dyeing of the dye, so that the color ratio of the dye is improved, and the color fastness is also improved; the stepped heating is adopted to ensure the uniformity of dye-uptake, so that the dyeing problems of colored flowers, colored willows and the like are avoided; by adopting the low bath ratio to obtain the high dye amount of the nylon fiber, the higher the dye amount on the nylon fiber is, the better the coloring rate of the fabric is.
Description
Technical Field
The invention relates to the technical field of nylon fabric dyeing methods, in particular to a dyeing method of a high-density nylon woven fabric.
Background
The bags in the current market are various in variety and full of eyes, and the materials of the bags comprise leather, PU and the like. However, the leather trunk has a single style, is quite troublesome in later maintenance, depends on animal sources, and is expensive and has a complex animal skin treatment process. The PU case is generally obtained by adopting a coating fabric or a laminating fabric, but the fabrics are thick and heavy, and the problem of poor stripping performance possibly occurs between the fabrics and a resin film layer.
Therefore, nylon fibers are more suitable for use in bags from the viewpoint of environmental protection and practical factors such as abrasion resistance, tear resistance, lightweight, water repellency, and discoloration. Nylon fiber has good mechanical properties, heat resistance, abrasion resistance, flame retardance, chemical resistance and other properties, and bags made of woven fabrics woven by nylon fiber are popular with consumers. However, the high-density nylon case fabric has the problems of coloring, and the durability and the color fastness after coloring are difficult to be qualified, and the problems of high water consumption, high steam consumption, low production efficiency, high rejection rate and the like in the traditional dyeing production process are solved. The Chinese patent with publication number of CN111996808A discloses a production process of a light and thin high-strength luggage nylon fabric, which comprises the following steps: s1, preparing a surface fabric, wherein the surface fabric is made of 20D nylon ultra-light fabric, and the warp yarn is 40D/24F, the warp density is 180T, the weft yarn is 40D/24F and the weft density is 120T; s2, desizing the fabric; s3, dyeing the surface fabric to form color fabric; s4, performing clear water shaping on the dyed color cloth; s5, calendaring the front surface of the color cloth; s6, coating a first coating on the facing fabric; s7, coating a second coating on the surface fabric, specifically the surface fabric after the first coating, and coating the second coating on the front surface of the surface fabric. The dyeing process of the face fabric does not improve the dyeing problem of the nylon fabric, and the problems of uneven dyeing and poor durable color fastness still exist.
Disclosure of Invention
In order to solve the coloring problems of uneven coloring and poor durable color fastness of the high-density nylon woven fabric, the invention provides a dyeing method of the high-density nylon woven fabric, and the dyed nylon fabric has the excellent characteristics of high coloring rate and high color fastness and can also save energy and reduce consumption by optimizing the dyeing and heat-preserving treatment process.
The specific technical scheme of the invention is as follows: the invention provides a dyeing method of a high-density nylon woven fabric, which comprises the following steps: immersing the high-density nylon woven fabric into an acid dye solution for dyeing, adjusting the pH value to 3.5-5, adopting staged heat preservation treatment, and sequentially preserving heat at 70-80 ℃ for 10-20 min, 90-100 ℃ for 20-30 min and 110-120 ℃ for 45-55 min.
The simpler the molecular structure of the acid dye is, the smaller the relative molecular mass is, the larger the ratio of the water-soluble groups is, and the better the leveling property is. In the dyeing process, on one hand, the macromolecule chain segments are enabled to rotate through high-temperature treatment on the nylon fibers, tiny holes in the fibers are combined into larger holes, so that dye molecules penetrate into the nylon fibers along the continuously-changing holes, the combination of the dye molecules and the tail end amino groups of the nylon fibers is enhanced, and then the combination is carried out by stage-wise heat preservation treatment, so that the dye obtains certain mobility, the dye level dyeing and cover dyeing are facilitated, the dye color ratio is improved, the color ratio of the dye with color fastness is also improved, and the color fastness is further improved.
In addition, the dyeing conditions used are also particularly important in order to obtain a good degree of coloration. The dye adsorption quantity is greatly reduced along with the rise of the pH value of the dye liquor under the condition of a certain temperature, but the pH value is too low, so that the phthalein amino groups of the fiber are easy to adsorb H + Protons, forming positively charged-NH 3+ The problem of super equivalent adsorption is likely to occur, and the phenomenon of nylon fiber degradation occurs, so that the adsorption quantity of the fabric to the dye liquor can be ensured by controlling the pH value of the dye liquor to 3.5-5.
Preferably, the gram weight of the high-density nylon woven fabric is 300-400 g/m 2 。
Preferably, the acid dye liquor comprises an acid dye and acetic acid.
Preferably, the bath ratio at the time of dyeing is 1:4 to 6.
By adopting the low bath ratio to obtain the high dye amount of the nylon fiber, the higher the dye amount on the nylon fiber is, the better the coloring rate of the fabric is.
Preferably, the dyeing also adopts sectional heating; the sectional type intensification is: heating from room temperature to 60 ℃ at a rate of 2-3 ℃/min, heating from 60 ℃ to 70-80 ℃ at a rate of 1-1.5 ℃/min, preserving heat, heating from 70-80 ℃ to 80-100 ℃ at a rate of 1-2 ℃/min, preserving heat, heating from 80-100 ℃ to 110-120 ℃ at a rate of 0.5-1.5 ℃/min, preserving heat, and finally cooling from 110-120 ℃ to room temperature at a rate of-2 to-1 ℃/min.
Nylon fiber belongs to thermoplastic fiber, dye-uptake is very slow at low temperature, and when the glass transition temperature is higher than 60%, the fiber can expand sharply, dye-uptake is increased linearly, and at the moment, the temperature rising rate is too fast, so that dyeing problems such as colored flowers, colored willows and the like are easy to occur. Thus, a stepped temperature increase is employed to ensure uniformity of dye-uptake.
Preferably, the high-density nylon woven fabric further comprises surface pretreatment of the high-density nylon woven fabric before dyeing; the surface pretreatment comprises the following steps:
immersing the high-density nylon woven fabric in a mixed solution I of polyvinyl alcohol and water, carrying out heat preservation treatment at 70-90 ℃ for 20-50 min, adding epichlorohydrin and lignosulfonate, and stirring for 10-30 min; then taking out the fabric and drying, immersing the fabric in a mixed solution II of glacial acetic acid, citric acid and water, adding polydopamine coated nano ceramic powder, reacting for 30-60 min at 60-70 ℃, and then taking out the fabric again and drying.
The polyvinyl alcohol on the surface layer of the nylon fabric has good film forming property, and the hydroxyl groups which are rich in the polyvinyl alcohol can have good affinity with both the nylon fabric and the acid dye, so that the dyeing and coloring rate can be improved by virtue of Van der Waals force and hydrogen bonding. The added sulfonic acid group on the lignosulfonate can gradually reduce the pH value of the dye liquor, so that the nylon fiber can gradually release the terminal amino group, the ionic bond between the acid dye and the polyamide fiber is facilitated, the crosslinking effect between the polyvinyl alcohol and the lignosulfonate is realized through epichlorohydrin, and the bonding stability is improved. In addition, the nano ceramic powder can form a rough uneven surface on the surface layer of the nylon fabric, the dyeing efficiency is improved by increasing the specific surface area, and the nano ceramic powder also has better ultraviolet resistance, so that the added value of the nylon fabric can be increased, and the durability is improved. The polydopamine coated on the surface of the nano ceramic powder can provide amino ends to improve dyeing efficiency, and can also be combined with polyvinyl alcohol on the surface of nylon fabric through citric acid crosslinking, so that the combination stability of the nano ceramic powder is improved. Therefore, after the surface pretreatment of the high-density nylon woven fabric, the dyeing and coloring rate can be improved, so that the dyed fabric has high coloring rate and high color fastness.
Preferably, the molecular weight of the polyvinyl alcohol is 100000 ~ 130000, and the alcoholysis degree is 97-99%; the concentration of the polyvinyl alcohol in the mixed solution I is 10-14%; the mass ratio of the polyvinyl alcohol to the epichlorohydrin to the lignosulfonate is 1:0.05 to 0.1:0.2 to 0.5; the mass ratio of the glacial acetic acid, the citric acid, the water and the polydopamine coated nano ceramic powder is 0.1-1: 3-10: 80-120: 1 to 4.
The molecular weight of the polyvinyl alcohol and its concentration in the aqueous solution affect the viscosity and thus the film forming properties. The alcoholysis degree of the polyvinyl alcohol can influence the solubility of the polyvinyl alcohol in an aqueous solution, so that the effect of surface pretreatment of the fabric is further influenced, and the polyvinyl alcohol after film formation is not easy to be swelled or dissolved in the dyeing process under the influence of the alcoholysis degree and the polymerization degree, so that the higher coloring rate can be achieved. The mass ratio of the raw materials determines the cross-linking structure and the bonding stability, and the best surface pretreatment effect of the fabric can be achieved under the ratio.
Preferably, the preparation method of the polydopamine coated nano ceramic powder comprises the following steps: adding the nano ceramic powder into a mixed solution of dopamine hydrochloride, water and ammonia water, regulating the pH value to 8-9, stirring and reacting for 12-20 h at 20-40 ℃, and then sequentially filtering and drying to obtain the polydopamine coated nano ceramic powder.
Preferably, the grain size of the nano ceramic powder is 50-100 nm; the mass ratio of the nano ceramic powder to the dopamine hydrochloride is 1-2: 1.
the particle size of the nano ceramic powder can influence the coating property of polydopamine, the combination stability between substances exceeding the range can be reduced, more importantly, the particle size can influence the degree of roughness of the surface of the fabric, the smaller the particle size is, the weaker the effect of improving the dye coloring rate caused by the surface roughness is, the larger the particle size is, the dyeing uniformity can be influenced, and the appearance quality of the fabric is further influenced.
Compared with the prior art, the invention has the following advantages:
(1) The acid dye is subjected to the staged heat preservation treatment, so that the dye obtains certain mobility, the level dyeing and cover dyeing of the dye are facilitated, the color ratio of the dye is improved, and the color fastness is also improved;
(2) The stepped heating is adopted to ensure the uniformity of dye-uptake, so that the dyeing problems of colored flowers, colored willows and the like are avoided;
(3) By adopting the low bath ratio to obtain the high dye amount of the nylon fiber, the higher the dye amount on the nylon fiber is, the better the coloring rate of the fabric is.
Detailed Description
The invention is further described below with reference to examples.
General examples
A dyeing method of a high-density nylon woven fabric comprises the following steps: the gram weight is 300 to 400g/m 2 The high-density nylon woven fabric is immersed into acid dye liquor for dyeing, and the bath ratio is 1: 4-6, regulating pH to 3.5-5, heating from room temperature to 60 ℃ at a rate of 2-3 ℃/min, heating from 60 ℃ to 70-80 ℃ at a rate of 1-1.5 ℃/min, preserving heat for 10-20 min, heating from 70-80 ℃ to 80-100 ℃ at a rate of 1-2 ℃/min, preserving heat for 20-30 min, heating from 80-100 ℃ to 110-120 ℃ at a rate of 0.5-1.5 ℃/min, preserving heat for 45-55 min, and finally cooling from 110-120 ℃ to room temperature at a rate of-2 to-1 ℃/min. Wherein the acid dye solution comprises acid dye and acetic acid.
In addition, the high-density nylon woven fabric can also comprise surface pretreatment of the high-density nylon woven fabric before dyeing, and the method comprises the following steps:
preparing a mixed solution I with the concentration of 10-14% from polyvinyl alcohol with the molecular weight of 100000 ~ 130000 and the alcoholysis degree of 97-99% and water, then immersing the high-density nylon woven fabric in the mixed solution I, carrying out heat preservation treatment for 20-50 min at 70-90 ℃, adding epichlorohydrin and lignosulfonate, and stirring for 10-30 min, wherein the mass ratio of the polyvinyl alcohol to the epichlorohydrin to the lignosulfonate is 1:0.05 to 0.1:0.2 to 0.5; then taking out the fabric and drying, immersing the fabric in a mixed solution II of glacial acetic acid, citric acid and water, adding polydopamine coated nano ceramic powder, and reacting for 30-60 min at 60-70 ℃, wherein the mass ratio of the glacial acetic acid, the citric acid, the water and the polydopamine coated nano ceramic powder is 0.1-1: 3-10: 80-120: 1-4, and then taking out the fabric again and drying.
The preparation method of the polydopamine coated nano ceramic powder comprises the following steps: adding nano ceramic powder with the particle size of 50-100 nm into a mixed solution of dopamine hydrochloride, water and ammonia water, wherein the mass ratio of the nano ceramic powder to the dopamine hydrochloride is 1-2: 1, regulating the pH value to 8-9, stirring and reacting for 12-20 h at 20-40 ℃, and then sequentially filtering and drying to obtain the polydopamine coated nano ceramic powder.
Example 1
A dyeing method of a high-density nylon woven fabric comprises the following steps: will have a gram weight of 350g/m 2 The high-density nylon woven fabric is immersed into acid dye liquor for dyeing, and the bath ratio is 1:5, adjusting the pH to about 4.3, wherein the acid dye liquor comprises Yellow S-GL 0.2% o.w.f, black 2S-LD 3.0% o.w.f and acetic acid 0.4% o.w.f. And then heating and heat preservation treatment is carried out according to the following table 1, and the fabric is taken out and dried after the treatment is finished.
Table 1 parameters of the heat-up and heat-preservation treatment in example 1
Example 2
High-density nylonThe dyeing method of the woven fabric comprises the following steps: the gram weight is 385g/m 2 The high-density nylon woven fabric is immersed into acid dye liquor for dyeing, and the bath ratio is 1:5, adjusting the pH to about 4.3, wherein the acid dye liquor comprises Yellow S-GL 0.2% o.w.f, black 2S-LD 3.0% o.w.f and acetic acid 0.4% o.w.f. And then heating and heat preservation treatment is carried out according to the following table 2, and the fabric is taken out and dried after the treatment is finished.
Table 2 parameters of the heat-up and heat-preservation treatment in example 2
Sectional temperature | Rate of temperature change | Incubation temperature time |
Room temperature-60 DEG C | 2℃/min | / |
60℃—80℃ | 1℃/min | 80℃*15min |
80℃—100℃ | 1.5℃/min | 100℃*30min |
100℃—120℃ | 1℃/min | 120℃*50min |
120 ℃ to room temperature | -1℃/min | / |
Example 3
A dyeing method of a high-density nylon woven fabric comprises the following steps: will have a gram weight of 350g/m 2 The high-density nylon woven fabric is immersed into acid dye liquor for dyeing, and the bath ratio is 1:6, adjusting the pH to about 3.8, wherein the acid dye liquor comprises Yellow S-GL 0.2% o.w.f, black 2S-LD 3.0% o.w.f and acetic acid 0.4% o.w.f. And then heating and heat preservation treatment is carried out according to the following table 3, and the fabric is taken out and dried after the treatment is finished.
TABLE 3 temperature increasing and preserving treatment parameters in example 3
Sectional temperature | Rate of temperature change | Incubation temperature time |
Room temperature-60 DEG C | 2℃/min | / |
60℃—75℃ | 1.5℃/min | 75℃*15min |
75℃—95℃ | 1℃/min | 95℃*25min |
95℃—120℃ | 0.5℃/min | 120℃*45min |
120 ℃ to room temperature | -2℃/min | / |
Example 4
The difference from example 1 is that: the method also comprises a fabric surface pretreatment step.
A dyeing method of a high-density nylon woven fabric comprises the following steps:
polyvinyl alcohol with molecular weight of 110000 and alcoholysis degree of 98% and water are prepared into a mixed solution I with concentration of 12%, and then the gram weight of 350g/m 2 The high-density nylon woven fabric is immersed in the mixed solution I, is subjected to heat preservation treatment at 85 ℃ for 30min, is added with epoxy chloropropane and lignosulfonate and is stirred for 15min, and the mass ratio of polyvinyl alcohol to epoxy chloropropane to lignosulfonate is 1:0.07:0.3; then taking out the fabric and drying, immersing the fabric in a mixed solution II of glacial acetic acid, citric acid and water, adding polydopamine coated nano ceramic powder, and reacting for 35min at 70 ℃, wherein the mass ratio of the glacial acetic acid to the citric acid to the polydopamine coated nano ceramic powder is 0.2:5:100:2, taking out the fabric again and drying.
The preparation method of the polydopamine coated nano ceramic powder comprises the following steps: adding the nano ceramic powder with the average particle size of 60nm into a mixed solution of dopamine hydrochloride, water and ammonia water, wherein the mass ratio of the nano ceramic powder to the dopamine hydrochloride to the water is 1.5:1:100, ammonia water is used for regulating the pH value to 8-9, stirring is carried out at 30 ℃ for reaction for 18 hours, and then the polydopamine coated nano ceramic powder is obtained after filtration and drying are carried out sequentially.
Then, immersing the high-density nylon woven fabric subjected to surface pretreatment into an acid dye solution for dyeing, wherein the bath ratio is 1:5, adjusting the pH to about 4.3, wherein the acid dye liquor comprises Yellow S-GL 0.2% o.w.f, black 2S-LD 3.0% o.w.f and acetic acid 0.4% o.w.f. And then heating and heat preserving treatment is carried out according to the table 1, and the fabric is taken out and dried after the treatment is finished.
Example 5
The difference from example 1 is that: the method also comprises a fabric surface pretreatment step.
A dyeing method of a high-density nylon woven fabric comprises the following steps:
polyvinyl alcohol with molecular weight of 130000 and alcoholysis degree of 98% and water are prepared into a mixed solution I with concentration of 12%, and then the gram weight of 350g/m 2 The high-density nylon woven fabric is immersed in the mixed solution I and is subjected to heat preservation treatment at 75 ℃ for 40min, and then epoxy chloropropane and lignosulfonate are added and stirred for 30min, wherein the mass ratio of polyvinyl alcohol to epoxy chloropropane to lignosulfonate is 1:0.09:0.5; then taking out the fabric and drying, immersing the fabric in a mixed solution II of glacial acetic acid, citric acid and water, adding polydopamine coated nano ceramic powder, and reacting at 60 ℃ for 45min, wherein the mass ratio of the glacial acetic acid, the citric acid, the water and the polydopamine coated nano ceramic powder is 0.4:4:100:2, taking out the fabric again and drying.
The preparation method of the polydopamine coated nano ceramic powder comprises the following steps: adding nano ceramic powder with the average particle size of 75nm into a mixed solution of dopamine hydrochloride, water and ammonia water, wherein the mass ratio of the nano ceramic powder to the dopamine hydrochloride to the water is 1:1:100, ammonia water is used for regulating the pH value to 8-9, stirring is carried out at 20 ℃ for reaction for 20 hours, and then the polydopamine coated nano ceramic powder is obtained after filtration and drying are carried out sequentially.
Then, immersing the high-density nylon woven fabric subjected to surface pretreatment into an acid dye solution for dyeing, wherein the bath ratio is 1:5, adjusting the pH to about 4.3, wherein the acid dye liquor comprises Yellow S-GL 0.2% o.w.f, black 2S-LD 3.0% o.w.f and acetic acid 0.4% o.w.f. And then heating and heat preserving treatment is carried out according to the table 1, and the fabric is taken out and dried after the treatment is finished.
Comparative example 1
The difference from example 4 is that: no nano ceramic powder is added.
A dyeing method of a high-density nylon woven fabric comprises the following steps:
polyvinyl alcohol with molecular weight of 110000 and alcoholysis degree of 98% and water are prepared into a mixed solution I with concentration of 12%, and then the gram weight of 350g/m 2 The high-density nylon woven fabric is immersed in the mixed solution I, is subjected to heat preservation treatment at 85 ℃ for 30min, is added with epoxy chloropropane and lignosulfonate and is stirred for 15min, and the mass ratio of polyvinyl alcohol to epoxy chloropropane to lignosulfonate is 1:0.07:0.3, then the fabric is taken out and dried.
Then, immersing the high-density nylon woven fabric subjected to surface pretreatment into an acid dye solution for dyeing, wherein the bath ratio is 1:5, adjusting the pH to about 4.3, wherein the acid dye liquor comprises Yellow S-GL 0.2% o.w.f, black 2S-LD 3.0% o.w.f and acetic acid 0.4% o.w.f. And then heating and heat preserving treatment is carried out according to the table 1, and the fabric is taken out and dried after the treatment is finished.
Comparative example 2
The difference from example 4 is that: the molecular weight of the added polyvinyl alcohol is 200000.
A dyeing method of a high-density nylon woven fabric comprises the following steps:
polyvinyl alcohol with molecular weight of 200000 and alcoholysis degree of 98% and water are prepared as a mixed solution I with concentration of 12%, and then the gram weight of 350g/m 2 The high-density nylon woven fabric is immersed in the mixed solution I, is subjected to heat preservation treatment at 85 ℃ for 30min, is added with epoxy chloropropane and lignosulfonate and is stirred for 15min, and the mass ratio of polyvinyl alcohol to epoxy chloropropane to lignosulfonate is 1:0.07:0.3; then taking out the fabric and drying, immersing the fabric in a mixed solution II of glacial acetic acid, citric acid and water, adding polydopamine coated nano ceramic powder, and reacting for 35min at 70 ℃, wherein the mass ratio of the glacial acetic acid to the citric acid to the polydopamine coated nano ceramic powder is 0.2:5:100:2, taking out the fabric again and drying.
The preparation method of the polydopamine coated nano ceramic powder comprises the following steps: adding the nano ceramic powder with the average particle size of 60nm into a mixed solution of dopamine hydrochloride, water and ammonia water, wherein the mass ratio of the nano ceramic powder to the dopamine hydrochloride to the water is 1.5:1:100, ammonia water is used for regulating the pH value to 8-9, stirring is carried out at 30 ℃ for reaction for 18 hours, and then the polydopamine coated nano ceramic powder is obtained after filtration and drying are carried out sequentially.
Then, immersing the high-density nylon woven fabric subjected to surface pretreatment into an acid dye solution for dyeing, wherein the bath ratio is 1:5, adjusting the pH to about 4.3, wherein the acid dye liquor comprises Yellow S-GL 0.2% o.w.f, black 2S-LD 3.0% o.w.f and acetic acid 0.4% o.w.f. And then heating and heat preserving treatment is carried out according to the table 1, and the fabric is taken out and dried after the treatment is finished.
Comparative example 3
The difference from example 4 is that: the alcoholysis degree of the added polyvinyl alcohol was 88%.
A dyeing method of a high-density nylon woven fabric comprises the following steps:
polyvinyl alcohol with molecular weight of 110000 and alcoholysis degree of 88% and water are prepared into a mixed solution I with concentration of 12%, and then the gram weight of 350g/m 2 The high-density nylon woven fabric is immersed in the mixed solution I, is subjected to heat preservation treatment at 85 ℃ for 30min, is added with epoxy chloropropane and lignosulfonate and is stirred for 15min, and the mass ratio of polyvinyl alcohol to epoxy chloropropane to lignosulfonate is 1:0.07:0.3; then taking out the fabric and drying, immersing the fabric in a mixed solution II of glacial acetic acid, citric acid and water, adding polydopamine coated nano ceramic powder, and reacting for 35min at 70 ℃, wherein the mass ratio of the glacial acetic acid to the citric acid to the polydopamine coated nano ceramic powder is 0.2:5:100:2, taking out the fabric again and drying.
The preparation method of the polydopamine coated nano ceramic powder comprises the following steps: adding the nano ceramic powder with the average particle size of 60nm into a mixed solution of dopamine hydrochloride, water and ammonia water, wherein the mass ratio of the nano ceramic powder to the dopamine hydrochloride to the water is 1.5:1:100, ammonia water is used for regulating the pH value to 8-9, stirring is carried out at 30 ℃ for reaction for 18 hours, and then the polydopamine coated nano ceramic powder is obtained after filtration and drying are carried out sequentially.
Then, immersing the high-density nylon woven fabric subjected to surface pretreatment into an acid dye solution for dyeing, wherein the bath ratio is 1:5, adjusting the pH to about 4.3, wherein the acid dye liquor comprises Yellow S-GL 0.2% o.w.f, black 2S-LD 3.0% o.w.f and acetic acid 0.4% o.w.f. And then heating and heat preserving treatment is carried out according to the table 1, and the fabric is taken out and dried after the treatment is finished.
Comparative example 4
The difference from example 4 is that: the grain size of the nano ceramic powder is 300nm.
A dyeing method of a high-density nylon woven fabric comprises the following steps:
polyvinyl alcohol with molecular weight of 110000 and alcoholysis degree of 98% and water are prepared into a mixed solution I with concentration of 12%, and then the gram weight of 350g/m 2 The high-density nylon woven fabric is immersed in the mixed solution I, is subjected to heat preservation treatment at 85 ℃ for 30min, is added with epoxy chloropropane and lignosulfonate and is stirred for 15min, and the mass ratio of polyvinyl alcohol to epoxy chloropropane to lignosulfonate is 1:0.07:0.3; then taking out the fabric and drying, immersing the fabric in a mixed solution II of glacial acetic acid, citric acid and water, adding polydopamine coated nano ceramic powder, and reacting for 35min at 70 ℃, wherein the mass ratio of the glacial acetic acid to the citric acid to the polydopamine coated nano ceramic powder is 0.2:5:100:2, taking out the fabric again and drying.
The preparation method of the polydopamine coated nano ceramic powder comprises the following steps: adding the nano ceramic powder with the average particle size of 300nm into a mixed solution of dopamine hydrochloride, water and ammonia water, wherein the mass ratio of the nano ceramic powder to the dopamine hydrochloride to the water is 1.5:1:100, ammonia water is used for regulating the pH value to 8-9, stirring is carried out at 30 ℃ for reaction for 18 hours, and then the polydopamine coated nano ceramic powder is obtained after filtration and drying are carried out sequentially.
Then, immersing the high-density nylon woven fabric subjected to surface pretreatment into an acid dye solution for dyeing, wherein the bath ratio is 1:5, adjusting the pH to about 4.3, wherein the acid dye liquor comprises Yellow S-GL 0.2% o.w.f, black 2S-LD 3.0% o.w.f and acetic acid 0.4% o.w.f. And then heating and heat preserving treatment is carried out according to the table 1, and the fabric is taken out and dried after the treatment is finished.
Performance testing
Fastness to rubbing: testing was performed according to standard GB/T3920-1997;
dye-uptake rate: the residual liquid method is used for measurement on a 723 type spectrophotometer, and the dye uptake at the time T is calculated: dye uptake E= [ (A) 0 -A T )/A 0 ]X 100%; wherein: a is that 0 Absorbance of the original solution; a is that T Absorbance of the residual dyeing liquid at the time T;
average ultraviolet transmittance: and testing the average transmittance of the high-density nylon woven fabric with the ultraviolet wavelength of 280-400 nm.
Table 4 dyeing properties of the high density nylon woven fabrics of each group
As shown in Table 1, the dyeing method of the invention can obtain nylon fabric with high dye uptake, ensures the uniformity of dye-uptake, avoids the dyeing problems of color flowers, color willows and the like, and improves the rubbing color fastness. In addition, in combination with examples 1-5, surface pretreatment of the fabric can further improve dye coloration rate and color fastness, which is achieved mainly by increasing specific surface area of the dye and interacting functional groups. In combination with the embodiment 4 and the comparative example 1, the dyeing is carried out only by the interaction of hydroxyl groups, sulfonic acid groups and terminal amino groups of nylon fibers on the surface of the fabric and dye molecules without adding nano ceramic powder, so that the dyeing rate and the ultraviolet-proof additional value are reduced. In combination with the embodiment 4 and the comparative examples 2-3, when the molecular weight of the polyvinyl alcohol is too large, the viscosity is too large, the film forming property and the loading effect of the nano ceramic powder can be affected, and the dye uptake and the color fastness are reduced; and the polyvinyl alcohol with low alcoholysis degree is easy to dissolve, and the phenomenon of unstable combination is easy to occur in the dyeing process, so that the dye-uptake rate is reduced. In combination with example 4 and comparative example 4, the particle size of the nano ceramic powder affects the coating property of polydopamine, and the bonding stability between substances exceeding the range is lowered, more importantly, the particle size affects the degree of roughness of the surface of the fabric, and the larger the particle size is, the dyeing uniformity and color fastness are both affected.
The foregoing description is only a preferred embodiment of the present invention, and is not intended to limit the present invention, and any simple modification, variation and equivalent transformation of the above embodiment according to the technical substance of the present invention still fall within the scope of the technical solution of the present invention.
Claims (9)
1. The dyeing method of the high-density nylon woven fabric is characterized by comprising the following steps of: immersing the high-density nylon woven fabric into an acid dye solution for dyeing, adjusting the pH value to 3.5-5, adopting staged heat preservation treatment, and sequentially preserving heat at 70-80 ℃ for 10-20 min, 90-100 ℃ for 20-30 min and 110-120 ℃ for 45-55 min.
2. The dyeing method of high-density nylon woven fabric according to claim 1, wherein the gram weight of the high-density nylon woven fabric is 300-400 g/m 2 。
3. The method for dyeing a high-density nylon woven fabric of claim 1, wherein the acid dye solution comprises an acid dye and acetic acid.
4. The method for dyeing a high-density nylon woven fabric according to claim 1, wherein the bath ratio at the time of dyeing is 1:4 to 6.
5. Dyeing method for high-density nylon woven fabric according to one of claims 1 to 4, characterized in that the dyeing also uses a sectional heating; the sectional type intensification is: heating from room temperature to 60 ℃ at a rate of 2-3 ℃/min, heating to 70-80 ℃ at a rate of 1-1.5 ℃/min, preserving heat, heating to 80-100 ℃ at a rate of 1-2 ℃/min, preserving heat, heating to 110-120 ℃ at a rate of 0.5-1.5 ℃/min, preserving heat, and finally cooling to room temperature at a rate of-2 to-1 ℃/min.
6. The method of dyeing a high-density nylon woven fabric of claim 1, wherein the high-density nylon woven fabric further comprises a surface pretreatment of the high-density nylon woven fabric prior to dyeing; the surface pretreatment comprises the following steps:
immersing the high-density nylon woven fabric in a mixed solution I of polyvinyl alcohol and water, carrying out heat preservation treatment at 70-90 ℃ for 20-50 min, adding epichlorohydrin and lignosulfonate, and stirring for 10-30 min; then taking out the fabric and drying, immersing the fabric in a mixed solution II of glacial acetic acid, citric acid and water, adding polydopamine coated nano ceramic powder, reacting for 30-60 min at 60-70 ℃, and then taking out the fabric again and drying.
7. The dyeing method of high-density nylon woven fabric according to claim 6, wherein the molecular weight of the polyvinyl alcohol is 100000 ~ 130000 and the alcoholysis degree is 97-99%; the concentration of the polyvinyl alcohol in the mixed solution I is 10-14%; the mass ratio of the polyvinyl alcohol to the epichlorohydrin to the lignosulfonate is 1:0.05 to 0.1:0.2 to 0.5; the mass ratio of the glacial acetic acid, the citric acid, the water and the polydopamine coated nano ceramic powder is 0.1-1: 3-10: 80-120: 1 to 4.
8. The dyeing method of the high-density nylon woven fabric according to claim 6, wherein the preparation method of the polydopamine coated nano ceramic powder comprises the following steps: adding the nano ceramic powder into a mixed solution of dopamine hydrochloride, water and ammonia water, regulating the pH value to 8-9, stirring and reacting for 12-20 h at 20-40 ℃, and then sequentially filtering and drying to obtain the polydopamine coated nano ceramic powder.
9. The dyeing method of high-density nylon woven fabric according to claim 8, wherein the particle size of the nano ceramic powder is 50-100 nm; the mass ratio of the nano ceramic powder to the dopamine hydrochloride is 1-2: 1.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202210373476.4A CN116926970A (en) | 2022-04-11 | 2022-04-11 | Dyeing method of high-density nylon woven fabric |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202210373476.4A CN116926970A (en) | 2022-04-11 | 2022-04-11 | Dyeing method of high-density nylon woven fabric |
Publications (1)
Publication Number | Publication Date |
---|---|
CN116926970A true CN116926970A (en) | 2023-10-24 |
Family
ID=88393116
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202210373476.4A Pending CN116926970A (en) | 2022-04-11 | 2022-04-11 | Dyeing method of high-density nylon woven fabric |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN116926970A (en) |
-
2022
- 2022-04-11 CN CN202210373476.4A patent/CN116926970A/en active Pending
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN110230216B (en) | Lyocell fiber fabric dyed by natural dye and preparation method thereof | |
CN106868890B (en) | Digital printing paste and digital printing method | |
CN103669041B (en) | A kind of fabric aldehyde-free colour stabilizer and preparation method thereof | |
CN102182077A (en) | Coating-dye composite staining method for ribbon product | |
CN108660810A (en) | A kind of polyamines class aldehyde-free colour stabilizer and its preparation and application | |
WO2021136411A1 (en) | Acid low-temperature dip dyeing method for polyamide 56 fiber and fabric | |
CN105019271A (en) | Wash-resisting polyamide fabric dyeing process | |
CN103485204A (en) | Interlayer dyeing method for dyeing superfine fiber synthetic leather | |
CN111085171A (en) | Preparation method of magnetic chitosan modified silk fabric | |
CN106192453B (en) | A kind of Monascus color colouring method of silk fabric | |
CN103276597B (en) | Dyeing process of dual-type cashmere fiber | |
CN116926970A (en) | Dyeing method of high-density nylon woven fabric | |
CN112813701A (en) | Preparation method of natural curcumin antibacterial fabric for cotton underwear | |
CN105061773A (en) | Novel chitosan-modified epoxy-resin-base high-polymer dye and preparation method thereof | |
US2206278A (en) | Textile and other materials | |
CN105155299A (en) | High-efficiency dyeing process for polyamide fabric | |
CN110983817A (en) | Blue plant dye for fiber fabric | |
CN113308916B (en) | Dyeing method of aramid fiber and dyed aramid fiber | |
CN115928461A (en) | Digital direct-injection printing process for cellulose fiber fabric by using plant dye ink | |
CN111270539B (en) | Color fixing agent and preparation method thereof | |
CN115010373A (en) | On-line dyed water-resistant colorful basalt fiber and preparation method thereof | |
CN109338757A (en) | A kind of colouring method improving aramid fiber light fastness | |
CN110886113B (en) | Disperse dye dyeing method for treating cotton fabric by using waterborne polyurethane | |
CN112553888B (en) | Zirconium carbide modified cloth and preparation method and application thereof | |
CN110080010B (en) | Preparation method of colored cellulose fibers |
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 |