CN114016282A - Manufacturing method of flame-retardant antibacterial polyester-cotton blended fabric - Google Patents
Manufacturing method of flame-retardant antibacterial polyester-cotton blended fabric Download PDFInfo
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- CN114016282A CN114016282A CN202111309330.5A CN202111309330A CN114016282A CN 114016282 A CN114016282 A CN 114016282A CN 202111309330 A CN202111309330 A CN 202111309330A CN 114016282 A CN114016282 A CN 114016282A
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- Prior art keywords
- flame
- cotton
- retardant
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- 229920000742 Cotton Polymers 0.000 title claims abstract description 212
- 239000004744 fabric Substances 0.000 title claims abstract description 155
- 239000003063 flame retardant Substances 0.000 title claims abstract description 136
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 title claims abstract description 134
- 230000000844 anti-bacterial effect Effects 0.000 title claims abstract description 49
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 24
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims abstract description 69
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 claims abstract description 50
- 239000000499 gel Substances 0.000 claims abstract description 39
- 239000005020 polyethylene terephthalate Substances 0.000 claims abstract description 39
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 33
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims abstract description 25
- 235000017557 sodium bicarbonate Nutrition 0.000 claims abstract description 25
- 229910000030 sodium bicarbonate Inorganic materials 0.000 claims abstract description 25
- 239000007864 aqueous solution Substances 0.000 claims abstract description 24
- 239000000022 bacteriostatic agent Substances 0.000 claims abstract description 23
- 235000011121 sodium hydroxide Nutrition 0.000 claims abstract description 23
- 229920001817 Agar Polymers 0.000 claims abstract description 22
- 239000008272 agar Substances 0.000 claims abstract description 22
- SNIVVKDUMQYBAV-UHFFFAOYSA-M tetrakis(hydroxymethyl)phosphanium;urea;chloride Chemical compound [Cl-].NC(N)=O.OC[P+](CO)(CO)CO SNIVVKDUMQYBAV-UHFFFAOYSA-M 0.000 claims abstract description 19
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 claims abstract description 17
- 229920000139 polyethylene terephthalate Polymers 0.000 claims abstract description 14
- 239000002994 raw material Substances 0.000 claims abstract description 10
- -1 polyethylene terephthalate Polymers 0.000 claims abstract description 7
- 238000003756 stirring Methods 0.000 claims description 48
- 239000010410 layer Substances 0.000 claims description 41
- 238000002156 mixing Methods 0.000 claims description 36
- 238000010438 heat treatment Methods 0.000 claims description 25
- 238000007710 freezing Methods 0.000 claims description 21
- 230000008014 freezing Effects 0.000 claims description 21
- 239000000843 powder Substances 0.000 claims description 19
- 238000001816 cooling Methods 0.000 claims description 17
- 238000007731 hot pressing Methods 0.000 claims description 16
- 239000002202 Polyethylene glycol Substances 0.000 claims description 15
- 229920001223 polyethylene glycol Polymers 0.000 claims description 15
- 238000002791 soaking Methods 0.000 claims description 15
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 claims description 15
- 239000002344 surface layer Substances 0.000 claims description 13
- 239000000203 mixture Substances 0.000 claims description 12
- 239000000243 solution Substances 0.000 claims description 12
- 108010010803 Gelatin Proteins 0.000 claims description 11
- 229920002472 Starch Polymers 0.000 claims description 11
- 239000011248 coating agent Substances 0.000 claims description 11
- 238000000576 coating method Methods 0.000 claims description 11
- 239000008273 gelatin Substances 0.000 claims description 11
- 229920000159 gelatin Polymers 0.000 claims description 11
- 235000019322 gelatine Nutrition 0.000 claims description 11
- 235000011852 gelatine desserts Nutrition 0.000 claims description 11
- 239000002245 particle Substances 0.000 claims description 11
- 235000019698 starch Nutrition 0.000 claims description 11
- 239000008107 starch Substances 0.000 claims description 11
- 238000007654 immersion Methods 0.000 claims description 10
- 238000009987 spinning Methods 0.000 claims description 9
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 claims description 8
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 8
- 238000005057 refrigeration Methods 0.000 claims description 7
- 229940080313 sodium starch Drugs 0.000 claims description 7
- 238000002360 preparation method Methods 0.000 claims description 6
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- 238000001125 extrusion Methods 0.000 claims description 5
- 239000001103 potassium chloride Substances 0.000 claims description 4
- 235000011164 potassium chloride Nutrition 0.000 claims description 4
- 239000011780 sodium chloride Substances 0.000 claims description 4
- 239000004254 Ammonium phosphate Substances 0.000 claims description 3
- 238000010306 acid treatment Methods 0.000 claims description 3
- 229910000148 ammonium phosphate Inorganic materials 0.000 claims description 3
- 235000019289 ammonium phosphates Nutrition 0.000 claims description 3
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 claims description 3
- 238000004321 preservation Methods 0.000 claims description 3
- 235000002639 sodium chloride Nutrition 0.000 claims description 3
- 238000003860 storage Methods 0.000 claims description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 abstract description 32
- 239000001569 carbon dioxide Substances 0.000 abstract description 16
- 229910002092 carbon dioxide Inorganic materials 0.000 abstract description 16
- 229920000728 polyester Polymers 0.000 description 34
- 229920004933 Terylene® Polymers 0.000 description 23
- 238000000034 method Methods 0.000 description 20
- 230000000694 effects Effects 0.000 description 17
- 239000000835 fiber Substances 0.000 description 16
- 239000000463 material Substances 0.000 description 14
- 230000008569 process Effects 0.000 description 12
- 239000007787 solid Substances 0.000 description 11
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 10
- 150000001875 compounds Chemical class 0.000 description 8
- 238000009833 condensation Methods 0.000 description 8
- 230000005494 condensation Effects 0.000 description 8
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 6
- CKNGMMSBYBSTLC-UHFFFAOYSA-N [chloro-tris(hydroxymethyl)-$l^{5}-phosphanyl]methanol Chemical compound OCP(Cl)(CO)(CO)CO CKNGMMSBYBSTLC-UHFFFAOYSA-N 0.000 description 6
- 230000009471 action Effects 0.000 description 6
- 230000003385 bacteriostatic effect Effects 0.000 description 6
- 239000004202 carbamide Substances 0.000 description 6
- 238000002844 melting Methods 0.000 description 6
- 230000008018 melting Effects 0.000 description 6
- 238000007765 extrusion coating Methods 0.000 description 5
- 238000005507 spraying Methods 0.000 description 4
- 229940032147 starch Drugs 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 238000002485 combustion reaction Methods 0.000 description 3
- 238000005336 cracking Methods 0.000 description 3
- 239000000446 fuel Substances 0.000 description 3
- 230000035699 permeability Effects 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- 229920004934 Dacron® Polymers 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 230000000903 blocking effect Effects 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 238000011049 filling Methods 0.000 description 2
- 238000001879 gelation Methods 0.000 description 2
- 238000002955 isolation Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000001294 propane Substances 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- CNOVKBXLGAQOJR-UHFFFAOYSA-N NC(=O)N.C(O)P(CO)(CO)(CO)Cl Chemical compound NC(=O)N.C(O)P(CO)(CO)(CO)Cl CNOVKBXLGAQOJR-UHFFFAOYSA-N 0.000 description 1
- ZRIUUUJAJJNDSS-UHFFFAOYSA-N ammonium phosphates Chemical compound [NH4+].[NH4+].[NH4+].[O-]P([O-])([O-])=O ZRIUUUJAJJNDSS-UHFFFAOYSA-N 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000001877 deodorizing effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229920005615 natural polymer Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000012795 verification Methods 0.000 description 1
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- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
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- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
The invention belongs to the technical field of flame-retardant fabrics, and particularly relates to a manufacturing method of a flame-retardant antibacterial polyester-cotton blended fabric, which comprises the following raw materials: 45-50 parts of polyethylene terephthalate (PET), 60-65 parts of cotton fibers, 8-12 parts of caustic soda, 62-66 parts of dilute hydrochloric acid, 10-12 parts of a tetramethylolphosphonium chloride urea condensate aqueous solution and 8-10 parts of a plant source bacteriostatic agent; the concentration of the aqueous solution of the tetramethylolphosphonium chloride urea condensate is 400-500 g/L; according to the invention, the flame-retardant gel is added, the agar, the water, the aluminum sulfate and the sodium bicarbonate are matched to prepare the component A and the component B, the aluminum sulfate and the sodium bicarbonate in the component A and the component B can react after contacting with each other to generate a large amount of carbon dioxide gas, and after the temperature is increased, the large amount of carbon dioxide gas is generated and sprayed to a fire source.
Description
Technical Field
The invention belongs to the technical field of flame-retardant fabrics, and particularly relates to a manufacturing method of a flame-retardant antibacterial polyester-cotton blended fabric.
Background
In the prior art, when the polyester-cotton blended fabric is heated, the polyester component which is heated and melted can cover the surface of the polyester fiber, the polyester fiber and the carbon generated by cracking the polyester fiber form a framework to prevent the fabric from shrinking, so that the molten polyester becomes a fuel of an ignition area, the fabric burns more intensely, and a flame retardant can migrate between the polyester and the cotton during the combustion process, therefore, the flame retardant property of the polyester-cotton fabric is difficult, in the prior art, in order to improve the flame retardant property of the polyester-cotton blended fabric, the polyester fiber and the cotton fiber are modified by using the flame retardant, but because the polyester-cotton fabric ensures the comfort, the content of the cotton fibers is high, and the polyester fibers and the cotton fibers are mutually supported, so that flame in the ignited polyester-cotton fabric is easy to spread along the cotton fibers, and the ignition speed of the polyester-cotton fabric is high.
A method for manufacturing a flame-retardant antibacterial polyester-cotton blended fabric published by Chinese patent application No. comprises the following steps: CN2020106827155, using aqueous solution of tetra-hydroxymethyl phosphorus chloride urea condensate to perform secondary flame retardant treatment on the cotton-polyester blended fabric, and then using natural polymer shell polysaccharide antibacterial agent to treat the flame retardant cotton-polyester blended fabric to finally obtain the flame retardant antibacterial cotton-polyester blended fabric. The flame-retardant antibacterial polyester-cotton blended fabric prepared by the method has good flame-retardant, antibacterial, mildew-proof, deodorizing, moisture-absorbing and antistatic effects, has an inhibiting effect on various bacteria and fungi, and has a high-efficiency antibacterial effect.
In view of the above, the invention provides a method for manufacturing a flame-retardant antibacterial polyester-cotton blended fabric, which is used for solving the technical problems.
Disclosure of Invention
The invention provides a manufacturing method of a flame-retardant antibacterial polyester-cotton blended fabric, aiming at making up for the defects of the prior art and solving the problem that the flame retardant property of the fabric is poor when the polyester-cotton blended fabric is heated and combusted in the prior art.
The technical scheme adopted by the invention for solving the technical problems is as follows: the invention relates to a manufacturing method of a flame-retardant antibacterial polyester-cotton blended fabric, which comprises the following raw materials:
45-50 parts of polyethylene terephthalate (PET), 60-65 parts of cotton fibers, 8-12 parts of caustic soda, 62-66 parts of dilute hydrochloric acid, 10-12 parts of a tetramethylolphosphonium chloride urea condensate aqueous solution and 8-10 parts of a plant source bacteriostatic agent;
the concentration of the dilute hydrochloric acid is 2.6-2.8%; the concentration of the aqueous solution of the tetramethylolphosphonium chloride urea condensate is 400-500 g/L;
the manufacturing method of the flame-retardant antibacterial polyester-cotton blended fabric comprises the following steps:
s1: introducing polyethylene glycol terephthalate into a stirring kettle, controlling the temperature in the stirring kettle to be 275-295 ℃, pouring the aqueous solution of the tetramethylolphosphonium chloride urea condensate into the stirring kettle after the temperature is raised, controlling the stirring speed of the stirring kettle to be 120-160 r/min, and keeping the temperature and heating for 25-30 min;
s2: after heat preservation and heating are finished, introducing caustic soda particles which are milled to be 0.08-0.1 mm in particle size into a stirring kettle, continuously stirring for 10-12min, introducing the mixture into a double-screw extruder, and controlling the extrusion temperature of the double-screw extruder to be 175-195 ℃;
s3: twisting cotton fibers to form 0.75-0.8 mm cotton threads, soaking half of the cotton threads in warm water with a temperature of 45-65 ℃ added with a plant source bacteriostatic agent for 2-3H, transferring the cotton threads into a cold storage, freezing the cotton threads at a temperature of-15 to-12 ℃ for 30-45 min, and extruding and coating the mixture in a double-screw extruder on the surfaces of the cotton threads after the freezing treatment is finished;
s4: controlling the thickness of the coating layer to be 0.25-0.3 mm, extruding and coating to obtain a double-layer silk thread, cooling the double-layer silk thread at normal temperature, immersing the double-layer silk thread in a dilute hydrochloric acid solution, controlling the immersion time to be 3-4H, overturning at an interval of 0.5H, preparing a flame-retardant silk thread after immersion is finished, and co-spinning the flame-retardant silk thread and the residual cotton threads to obtain the flame-retardant antibacterial polyester-cotton blended fabric;
in the prior art, when the polyester-cotton blended fabric is heated, the polyester component which is heated and melted can cover the surface of the polyester fiber, the polyester fiber and the carbon generated by cracking the polyester fiber form a framework to prevent the fabric from shrinking, so that the molten polyester becomes a fuel of an ignition area, the fabric burns more intensely, and a flame retardant can migrate between the polyester and the cotton during the combustion process, therefore, the flame retardant property of the polyester-cotton fabric is difficult, in the prior art, in order to improve the flame retardant property of the polyester-cotton blended fabric, the polyester fiber and the cotton fiber are modified by using the flame retardant, but because the polyester-cotton fabric ensures the comfort, the content of the cotton fibers is high, and the polyester fibers and the cotton fibers are mutually supported, so that flame in the ignited polyester-cotton fabric is easy to spread along the cotton fibers, and the ignition speed of the polyester-cotton fabric is high;
when the invention works, firstly, the aqueous solution of the condensation compound of the tetramethylol phosphorus chloride and the urea is added into the terylene base material, the flame retardance of the terylene is effectively improved, simultaneously, the modified terylene base material is coated on the surface of the cotton thread, the modified cotton thread and the rest cotton thread are blended and woven into the fabric, compared with the ratio of the terylene to the cotton thread in the polyester-cotton blended fabric in the prior art, the area occupied by the terylene in the fabric is effectively increased, simultaneously, after the moisture in the terylene base material added with the condensation compound of the tetramethylol phosphorus chloride and the urea is evaporated in the continuous heating process, the caustic soda powder is added, because the melting point temperature of the caustic soda solid is higher than the melting point of the terylene base material (polyethylene glycol terephthalate), the caustic soda powder is uniformly dispersed on the surface layer of the double-layer silk thread under the extrusion coating effect of a double screw extruder, and in the process of soaking in the dilute hydrochloric acid solution, the caustic soda is alkaline and reacts with the dilute hydrochloric acid to be dissolved, so that uniform micropores are formed on the surface of the double-layer silk thread, the conductivity of the prepared flame-retardant silk thread is better, the polyester is used for covering, the specific area of the polyester in the fabric is increased, and meanwhile, the micropores can also enable cotton threads inside the flame-retardant silk thread to be better conducted with the outside, so that the prepared fabric is better in air permeability and moisture absorption.
Preferably, the raw materials also comprise 15-18 parts of flame-retardant gel; the flame-retardant gel is formed by mixing the component A and the component B according to the proportion of 1: 6; the component A is prepared from agar, water and aluminum sulfate according to the proportion of 5:3: 1; the component B is prepared from agar, water, sodium bicarbonate and starch according to the proportion of 5:15:6: 3; the flame retardant gel is combined with cotton threads;
when the fabric is in work, the flame-retardant gel is added, the agar is matched with water to prepare the component A and the component B by the aluminum sulfate and the sodium bicarbonate, the agar is in a solid state at normal temperature and can be melted into a solid state when being heated to more than 95 ℃, the agar solution is used to prepare the aluminum sulfate and the sodium bicarbonate into the gel, the component A and the component B are both solid gels at normal temperature and can not react with each other, after the surface temperature of the fabric is increased, the moisture in the gel is gradually evaporated along with the increase of the temperature, the fabric is cooled, the flame-retardant gel is converted into a liquid state from the solid state along with the continuous increase of the temperature, the aluminum sulfate and the sodium bicarbonate in the component A and the component B can react after being contacted with each other to generate a large amount of carbon dioxide gas, after the temperature is increased, the generation of the large amount of the carbon dioxide gas is sprayed to a fire source, and the carbon dioxide has the flame-retardant effect, the flame-retardant fabric can effectively prevent open fire from being generated, and further improves the flame-retardant effect of the fabric.
Preferably, the preparation method of the flame-retardant gel comprises the following steps:
a1: mixing agar and water, heating to 98-102 ℃, preserving heat, stirring uniformly, naturally cooling to 55-60 ℃, mixing with aluminum sulfate, and mixing uniformly to obtain a component A;
a2: mixing sodium bicarbonate and starch, introducing into a refrigeration house, freezing for 0.5-1H at the low temperature of-30 to-25 ℃, crushing after freezing, mixing agar and water, heating to 98-102 ℃, preserving heat, stirring uniformly, naturally cooling to 65-70 ℃, and blending with crushed sodium bicarbonate powder to obtain a component B;
a3: respectively soaking the cotton threads in the S3 in the component A and the component B according to the ratio of 1:1, naturally cooling to normal temperature, removing redundant gel on the surface layer to obtain the cotton threads A and the cotton threads B, soaking the cotton threads B in warm water added with a plant-derived bacteriostatic agent, and directly blending the cotton threads A;
when in work, the component A and the component B are respectively solidified in the cotton thread to prepare the cotton thread A and the cotton thread B, the component A and the component B are effectively isolated, in the manufacturing process of the fabric, the component B can be temporarily dissolved at high temperature at the moment that the cotton thread B is extruded and coated on the surface of the terylene base material, but the cotton thread B is frozen at low temperature before being extruded and coated, can effectively reduce the dissolution of the component B, and can effectively reduce the difficulty of the component A and the component B in the preparation of the flame-retardant antibacterial polyester-cotton fabric due to the mutual isolation of the component A and the component B, meanwhile, in the preparation process of the component B, the viscosity and the filling property of the starch can be effectively utilized by mixing the sodium bicarbonate and the starch, so that the component B prepared from the sodium bicarbonate is effectively prevented from being decomposed under the short-time heating effect of extrusion coating, and the effect of flame-retardant gel is further reduced.
Preferably, the double-layer silk threads and the residual cotton threads are co-spun to obtain the fabric in S4, then the fabric is placed in a hot press, a single-side pressing plate of the hot press is controlled to be heated to 280-300 ℃, the hot pressing time is 0.5-0.8S, and dilute hydrochloric acid treatment is carried out after the hot pressing is finished;
when the double-layer silk thread fabric is in operation, the cotton thread B of the inner layer of the double-layer silk thread contains the component B in the flame-retardant gel, the double-layer silk thread is blended with the rest cotton thread A to prepare the fabric, then the fabric is placed in a hot press to be quickly hot-pressed, in the process of quick hot-pressing, under the action of high temperature, the polyethylene glycol terephthalate on one side of the fabric is dissolved, so that gaps between the flame-retardant silk thread and the cotton thread are further reduced, the conductivity of the one side of the fabric is reduced, the component A and the component B in the cotton thread A and the cotton thread B are partially dissolved under the action of high temperature, but at the moment, the polyethylene glycol terephthalate on the surface layer of the double-layer silk thread is softened and slightly dissolved, but still covers the surface of the cotton thread B, so that the cotton thread A and the cotton thread B are isolated, and dilute sulfuric acid washing is carried out after hot-pressing, so that the surface layer of the double-layer silk thread has micropores, and the component A and the component B are solidified, and then effectively avoiding the component A and the component B from reacting in advance to reduce the flame retardance of the finally prepared flame-retardant antibacterial polyester-cotton blended fabric, and simultaneously, the unilateral hot pressing enables the gaps on one side of the fabric to be small and the gaps on one side to be large, the blocking effect of the small side of the gap on the air to be strong, the fabric has strong flame retardance, the conduction area of the large side of the gap and the air is large, the fabric has strong hygroscopicity, and the performance of the fabric is further enhanced.
Preferably, the surface of the cotton thread frozen in the step S3 is coated with a layer of sodium chloride, potassium chloride and ammonium phosphate salt according to a ratio of 1: 1:1, mixing to obtain flame-retardant powder;
when the fabric is in operation, a layer of flame-retardant powder is adhered to the surface of the cotton thread B subjected to freezing treatment in S3, when the temperature of the fabric is raised, the flame-retardant gel begins to melt, the sodium bicarbonate in the component A is decomposed to generate carbon dioxide, the carbon dioxide carries the flame-retardant powder in the outward spraying process and is converged with the component B, and after the component A and the component B react, more carbon dioxide gas is generated, so that the spraying range of the flame-retardant powder is enlarged, the flame-retardant effect is effectively generated, and the flame-retardant performance of the prepared fabric is enhanced.
Preferably, 3-4 parts of gelatin are dissolved in warm water at 45-65 ℃ added with the plant-derived bacteriostatic agent in S3;
when the flame-retardant bacteriostatic polyester-cotton blended fabric works, a certain amount of gelatin is added into warm water at 45-65 ℃ added with a plant-source bacteriostatic agent, the gelatin is melted at the temperature of the warm water, the gelatin causes gelation of a solution in which the plant-source bacteriostatic agent is dissolved in the process of freezing after the cotton threads are soaked, and the gel formed by the gelatin is dissolved at a temperature of over 22 ℃, so that the volatilization rate of the plant-source bacteriostatic agent can be effectively controlled, and the bacteriostatic property of the prepared flame-retardant bacteriostatic polyester-cotton blended fabric is more durable.
The invention has the following beneficial effects:
1. according to the manufacturing method of the flame-retardant antibacterial polyester-cotton blended fabric, the flame-retardant gel is added, the agar and the water are matched with the aluminum sulfate and the sodium bicarbonate to prepare the component A and the component B, the aluminum sulfate and the sodium bicarbonate in the component A and the component B are contacted with each other and then react to generate a large amount of carbon dioxide gas, and after the temperature is increased, the large amount of carbon dioxide gas is generated and sprayed to a fire source.
2. The invention relates to a method for manufacturing a flame-retardant antibacterial polyester-cotton blended fabric, which comprises the steps of blending a double-layer silk thread with the rest cotton thread A to prepare the fabric, then placing the fabric in a hot press for quick hot pressing, dissolving polyethylene glycol terephthalate on one side of the fabric under the action of high temperature in the quick hot pressing process to further reduce gaps between the flame-retardant silk thread and the cotton thread and reduce the conductivity of the one side of the fabric, partially dissolving the component A and the component B in the cotton thread A and the cotton thread B under the action of high temperature, but because the polyethylene glycol terephthalate on the surface layer of the double-layer silk thread is softened and slightly dissolved and still covers the surface of the cotton thread B, the cotton thread A and the cotton thread B are isolated, and washing with dilute sulfuric acid is carried out after the hot pressing, the surface layer of the double-layer silk thread has micropores, and the component A and the component B are solidified, further effectively avoiding the component A and the component B from reacting in advance, so that the flame retardance of the finally prepared flame-retardant antibacterial polyester-cotton blended fabric is reduced.
Drawings
The invention will be further explained with reference to the drawings.
FIG. 1 is a method flow chart of a manufacturing method of the flame-retardant antibacterial polyester-cotton blended fabric;
FIG. 2 is a process flow diagram of a method of making a flame retardant gel;
Detailed Description
In order to make the technical means, the creation characteristics, the achievement purposes and the effects of the invention easy to understand, the invention is further described with the specific embodiments.
As shown in fig. 1 to 2, the method for manufacturing the flame-retardant antibacterial polyester-cotton blended fabric comprises the following raw materials:
45-50 parts of polyethylene terephthalate (PET), 60-65 parts of cotton fibers, 8-12 parts of caustic soda, 62-66 parts of dilute hydrochloric acid, 10-12 parts of a tetramethylolphosphonium chloride urea condensate aqueous solution and 8-10 parts of a plant source bacteriostatic agent;
the concentration of the dilute hydrochloric acid is 2.6-2.8%; the concentration of the aqueous solution of the tetramethylolphosphonium chloride urea condensate is 400-500 g/L;
the manufacturing method of the flame-retardant antibacterial polyester-cotton blended fabric comprises the following steps:
s1: introducing polyethylene glycol terephthalate into a stirring kettle, controlling the temperature in the stirring kettle to be 275-295 ℃, pouring the aqueous solution of the tetramethylolphosphonium chloride urea condensate into the stirring kettle after the temperature is raised, controlling the stirring speed of the stirring kettle to be 120-160 r/min, and keeping the temperature and heating for 25-30 min;
s2: after heat preservation and heating are finished, introducing caustic soda particles which are milled to be 0.08-0.1 mm in particle size into a stirring kettle, continuously stirring for 10-12min, introducing the mixture into a double-screw extruder, and controlling the extrusion temperature of the double-screw extruder to be 175-195 ℃;
s3: twisting cotton fibers to form 0.75-0.8 mm cotton threads, soaking half of the cotton threads in warm water with a temperature of 45-65 ℃ added with a plant source bacteriostatic agent for 2-3H, transferring the cotton threads into a cold storage, freezing the cotton threads at a temperature of-15 to-12 ℃ for 30-45 min, and extruding and coating the mixture in a double-screw extruder on the surfaces of the cotton threads after the freezing treatment is finished;
s4: controlling the thickness of the coating layer to be 0.25-0.3 mm, extruding and coating to obtain a double-layer silk thread, cooling the double-layer silk thread at normal temperature, immersing the double-layer silk thread in a dilute hydrochloric acid solution, controlling the immersion time to be 3-4H, overturning at an interval of 0.5H, preparing a flame-retardant silk thread after immersion is finished, and co-spinning the flame-retardant silk thread and the residual cotton threads to obtain the flame-retardant antibacterial polyester-cotton blended fabric;
in the prior art, when the polyester-cotton blended fabric is heated, the polyester component which is heated and melted can cover the surface of the polyester fiber, the polyester fiber and the carbon generated by cracking the polyester fiber form a framework to prevent the fabric from shrinking, so that the molten polyester becomes a fuel of an ignition area, the fabric burns more intensely, and a flame retardant can migrate between the polyester and the cotton during the combustion process, therefore, the flame retardant property of the polyester-cotton fabric is difficult, in the prior art, in order to improve the flame retardant property of the polyester-cotton blended fabric, the polyester fiber and the cotton fiber are modified by using the flame retardant, but because the polyester-cotton fabric ensures the comfort, the content of the cotton fibers is high, and the polyester fibers and the cotton fibers are mutually supported, so that flame in the ignited polyester-cotton fabric is easy to spread along the cotton fibers, and the ignition speed of the polyester-cotton fabric is high;
when the invention works, firstly, the aqueous solution of the condensation compound of the tetramethylol phosphorus chloride and the urea is added into the terylene base material, the flame retardance of the terylene is effectively improved, simultaneously, the modified terylene base material is coated on the surface of the cotton thread, the modified cotton thread and the rest cotton thread are blended and woven into the fabric, compared with the ratio of the terylene to the cotton thread in the polyester-cotton blended fabric in the prior art, the area occupied by the terylene in the fabric is effectively increased, simultaneously, after the moisture in the terylene base material added with the condensation compound of the tetramethylol phosphorus chloride and the urea is evaporated in the continuous heating process, the caustic soda powder is added, because the melting point temperature of the caustic soda solid is higher than the melting point of the terylene base material (polyethylene glycol terephthalate), the caustic soda powder is uniformly dispersed on the surface layer of the double-layer silk thread under the extrusion coating effect of a double screw extruder, and in the process of soaking in the dilute hydrochloric acid solution, the caustic soda is alkaline and reacts with the dilute hydrochloric acid to be dissolved, so that uniform micropores are formed on the surface of the double-layer silk thread, the conductivity of the prepared flame-retardant silk thread is better, the polyester is used for covering, the specific area of the polyester in the fabric is increased, and meanwhile, the micropores can also enable cotton threads inside the flame-retardant silk thread to be better conducted with the outside, so that the prepared fabric is better in air permeability and moisture absorption.
As an embodiment of the invention, the raw materials further comprise 15-18 parts of flame-retardant gel; the flame-retardant gel is formed by mixing the component A and the component B according to the proportion of 1: 6; the component A is prepared from agar, water and aluminum sulfate according to the proportion of 5:3: 1; the component B is prepared from agar, water, sodium bicarbonate and starch according to the proportion of 5:15:6: 3; the flame retardant gel is combined with cotton threads;
when the fabric is in work, the flame-retardant gel is added, the agar is matched with water to prepare the component A and the component B by the aluminum sulfate and the sodium bicarbonate, the agar is in a solid state at normal temperature and can be melted into a solid state when being heated to more than 95 ℃, the agar solution is used to prepare the aluminum sulfate and the sodium bicarbonate into the gel, the component A and the component B are both solid gels at normal temperature and can not react with each other, after the surface temperature of the fabric is increased, the moisture in the gel is gradually evaporated along with the increase of the temperature, the fabric is cooled, the flame-retardant gel is converted into a liquid state from the solid state along with the continuous increase of the temperature, the aluminum sulfate and the sodium bicarbonate in the component A and the component B can react after being contacted with each other to generate a large amount of carbon dioxide gas, after the temperature is increased, the generation of the large amount of the carbon dioxide gas is sprayed to a fire source, and the carbon dioxide has the flame-retardant effect, the flame-retardant fabric can effectively prevent open fire from being generated, and further improves the flame-retardant effect of the fabric.
As an embodiment of the present invention, the method for preparing the flame retardant gel comprises the steps of:
a1: mixing agar and water, heating to 98-102 ℃, preserving heat, stirring uniformly, naturally cooling to 55-60 ℃, mixing with aluminum sulfate, and mixing uniformly to obtain a component A;
a2: mixing sodium bicarbonate and starch, introducing into a refrigeration house, freezing for 0.5-1H at the low temperature of-30 to-25 ℃, crushing after freezing, mixing agar and water, heating to 98-102 ℃, preserving heat, stirring uniformly, naturally cooling to 65-70 ℃, and blending with crushed sodium bicarbonate powder to obtain a component B;
a3: respectively soaking the cotton threads in the S3 in the component A and the component B according to the ratio of 1:1, naturally cooling to normal temperature, removing redundant gel on the surface layer to obtain the cotton threads A and the cotton threads B, soaking the cotton threads B in warm water added with a plant-derived bacteriostatic agent, and directly blending the cotton threads A;
when in work, the component A and the component B are respectively solidified in the cotton thread to prepare the cotton thread A and the cotton thread B, the component A and the component B are effectively isolated, in the manufacturing process of the fabric, the component B can be temporarily dissolved at high temperature at the moment that the cotton thread B is extruded and coated on the surface of the terylene base material, but the cotton thread B is frozen at low temperature before being extruded and coated, can effectively reduce the dissolution of the component B, and can effectively reduce the difficulty of the component A and the component B in the preparation of the flame-retardant antibacterial polyester-cotton fabric due to the mutual isolation of the component A and the component B, meanwhile, in the preparation process of the component B, the viscosity and the filling property of the starch can be effectively utilized by mixing the sodium bicarbonate and the starch, so that the component B prepared from the sodium bicarbonate is effectively prevented from being decomposed under the short-time heating effect of extrusion coating, and the effect of flame-retardant gel is further reduced.
As an embodiment of the invention, the double-layer silk yarns in S4 are co-spun with the rest cotton yarns to obtain the fabric, then the fabric is placed in a hot press, the single-side press plate of the hot press is controlled to be heated to 280-300 ℃, the hot pressing time is 0.5-0.8S, and dilute hydrochloric acid treatment is performed after the hot pressing is finished;
when the double-layer silk thread fabric is in operation, the cotton thread B of the inner layer of the double-layer silk thread contains the component B in the flame-retardant gel, the double-layer silk thread is blended with the rest cotton thread A to prepare the fabric, then the fabric is placed in a hot press to be quickly hot-pressed, in the process of quick hot-pressing, under the action of high temperature, the polyethylene glycol terephthalate on one side of the fabric is dissolved, so that gaps between the flame-retardant silk thread and the cotton thread are further reduced, the conductivity of the one side of the fabric is reduced, the component A and the component B in the cotton thread A and the cotton thread B are partially dissolved under the action of high temperature, but at the moment, the polyethylene glycol terephthalate on the surface layer of the double-layer silk thread is softened and slightly dissolved, but still covers the surface of the cotton thread B, so that the cotton thread A and the cotton thread B are isolated, and dilute sulfuric acid washing is carried out after hot-pressing, so that the surface layer of the double-layer silk thread has micropores, and the component A and the component B are solidified, and then effectively avoiding the component A and the component B from reacting in advance to reduce the flame retardance of the finally prepared flame-retardant antibacterial polyester-cotton blended fabric, and simultaneously, the unilateral hot pressing enables the gaps on one side of the fabric to be small and the gaps on one side to be large, the blocking effect of the small side of the gap on the air to be strong, the fabric has strong flame retardance, the conduction area of the large side of the gap and the air is large, the fabric has strong hygroscopicity, and the performance of the fabric is further enhanced.
As an embodiment of the present invention, the surface of the cotton thread frozen in S3 is coated with a layer of sodium chloride, potassium chloride and ammonium phosphate before the cotton thread is hot-pressed and coated, according to a ratio of 1: 1:1, mixing to obtain flame-retardant powder;
when the fabric is in operation, a layer of flame-retardant powder is adhered to the surface of the cotton thread B subjected to freezing treatment in S3, when the temperature of the fabric is raised, the flame-retardant gel begins to melt, the sodium bicarbonate in the component A is decomposed to generate carbon dioxide, the carbon dioxide carries the flame-retardant powder in the outward spraying process and is converged with the component B, and after the component A and the component B react, more carbon dioxide gas is generated, so that the spraying range of the flame-retardant powder is enlarged, the flame-retardant effect is effectively generated, and the flame-retardant performance of the prepared fabric is enhanced.
In one embodiment of the present invention, 3 to 4 parts of gelatin are further dissolved in 45 to 65 ℃ warm water to which the plant-derived bacteriostatic agent is added in S3;
when the flame-retardant bacteriostatic polyester-cotton blended fabric works, a certain amount of gelatin is added into warm water at 45-65 ℃ added with a plant-source bacteriostatic agent, the gelatin is melted at the temperature of the warm water, the gelatin causes gelation of a solution in which the plant-source bacteriostatic agent is dissolved in the process of freezing after the cotton threads are soaked, and the gel formed by the gelatin is dissolved at a temperature of over 22 ℃, so that the volatilization rate of the plant-source bacteriostatic agent can be effectively controlled, and the bacteriostatic property of the prepared flame-retardant bacteriostatic polyester-cotton blended fabric is more durable.
The specific implementation flow is as follows:
when the fabric is in work, firstly, the aqueous solution of the condensation compound of the tetramethylol phosphorus chloride and the urea is added into the terylene base material, the flame retardance of terylene is effectively improved, meanwhile, the modified terylene base material is coated on the surface of cotton threads, the modified cotton threads and the rest cotton threads are blended and woven into the fabric, compared with the ratio of the terylene to the cotton threads in the polyester-cotton blended fabric in the prior art, the occupied area of the terylene in the fabric is effectively increased, simultaneously, after the moisture in the terylene base material added with the condensation compound of the tetramethylol phosphorus chloride and the urea is evaporated in the continuous heating process, the caustic soda powder is added, because the melting point temperature of the caustic soda solid is higher than the melting point of the terylene base material (polyethylene glycol terephthalate), the caustic soda powder is uniformly dispersed on the surface layer of the double-layer silk threads under the extrusion coating effect of a double-screw extruder, and in the process of soaking in the dilute hydrochloric acid solution, the caustic soda is in an alkaline state and reacts and dissolves with the dilute hydrochloric acid, and then make the surface of double-deck silk thread produce even micropore, and then make the fire-retardant silk thread of making per se conductivity better, not only use dacron to cover, improve dacron in the area of occupation of area in the surface fabric, the micropore can also make the inside cotton thread of fire-retardant silk thread and external better switch on simultaneously, and then make the surface fabric of making per se gas permeability and hygroscopicity better.
In order to verify the flame retardance of the flame-retardant antibacterial polyester-cotton blended fabric prepared by the invention, the following groups of experiments are specially set for verification;
example 1
The flame-retardant antibacterial polyester-cotton blended fabric comprises the following raw materials:
45 parts of polyethylene terephthalate (PET), 95 parts of cotton fiber, 10 parts of a tetramethylolphosphonium chloride urea condensate aqueous solution and 10 parts of a plant source bacteriostatic agent;
the concentration of the aqueous solution of the tetramethylolphosphonium chloride urea condensate is 400-500 g/L;
introducing polyethylene glycol terephthalate into a stirring kettle, controlling the temperature in the stirring kettle to be 275-295 ℃, pouring a tetramethylol phosphorus chloride urea condensation compound aqueous solution into the stirring kettle after the temperature is raised, controlling the stirring speed of the stirring kettle to be 120-160 r/min, keeping the temperature and heating for 25-30 min, placing the mixture into a spinning machine after the heating is finished, spinning the mixture into polyester silk threads, twisting the cotton fibers into cotton threads with the diameter of 0.75-0.8 mm, co-spinning the cotton threads and the polyester silk threads to obtain the flame-retardant antibacterial polyester-cotton blended fabric, and repeating the steps to obtain five flame-retardant antibacterial polyester-cotton blended fabrics with the labels of A1-A5;
fixing the first 1 to the second 5 by using fixing clamps respectively, placing alcohol lamps below the first 1 to the second 5 respectively, controlling the distance between the flame of the alcohol lamps and the fabric to be 3cm, 6cm, 9cm, 12cm and 15cm respectively, recording the generation time of open fire on the surfaces of the first 1 to the second 5 respectively, removing the alcohol lamps after the open fire is generated, measuring the burning area of the fabric after the flame on the surface of the fabric is automatically extinguished, and recording and outputting a table;
TABLE 1
Example 2
The flame-retardant antibacterial polyester-cotton blended fabric comprises the following raw materials:
45 parts of polyethylene terephthalate (PET), 65 parts of cotton fiber, 8 parts of caustic soda, 62 parts of dilute hydrochloric acid, 10 parts of a tetramethylolphosphonium chloride urea condensate aqueous solution and 8 parts of a plant source bacteriostatic agent;
the concentration of the dilute hydrochloric acid is 2.6 percent; the concentration of the aqueous solution of the tetramethylolphosphonium chloride urea condensate is 400 g/L;
introducing polyethylene glycol terephthalate into a stirring kettle, controlling the temperature in the stirring kettle to be 275-295 ℃, pouring an aqueous solution of a tetramethylolphosphonium chloride urea condensation compound into the stirring kettle after the temperature is raised, controlling the stirring speed of the stirring kettle to be 120-160 r/min, keeping the temperature and heating for 25-30 min, introducing caustic soda particles with the particle size of 0.08-0.1 mm into the stirring kettle after the temperature is kept and heating, continuously stirring for 10-12min, introducing the mixture into a double-screw extruder, controlling the extrusion temperature of the double-screw extruder to be 175-195 ℃, twisting cotton fibers into cotton threads with the particle size of 0.75-0.8 mm, soaking half of the cotton threads into warm water with the temperature of 45-65 ℃ added with a plant source bacteriostatic agent for 2-3H, transferring the cotton threads into a refrigeration house, carrying out refrigeration treatment at the temperature of-15-12 ℃ for 30-45 min, extruding the mixture in the double-screw extruder to coat the surfaces of the cotton threads after the refrigeration treatment is finished, controlling the thickness of the coating layer to be 0.25-0.3 mm, extruding and coating to obtain a double-layer silk thread, cooling the double-layer silk thread at normal temperature, immersing the double-layer silk thread in a dilute hydrochloric acid solution, controlling the immersion time to be 3-4H, overturning at an interval of 0.5H, preparing a flame-retardant silk thread after immersion is completed, co-spinning the flame-retardant silk thread and the residual cotton threads to obtain a flame-retardant antibacterial polyester-cotton blended fabric, and repeating the steps to obtain five flame-retardant antibacterial polyester-cotton blended fabrics with the labels of B1-B5 respectively;
respectively fixing the second 1 to the second 5 by using fixing clamps, respectively placing alcohol lamps below the second 1 to the second 5, controlling the distances between the flame of the alcohol lamps and the fabric to be 3cm, 6cm, 9cm, 12cm and 15cm, respectively recording the generation time of open fire on the surfaces of the second 1 to the second 5, removing the alcohol lamps after the open fire is generated, measuring the burning area of the fabric after the flame on the surface of the fabric is automatically extinguished, and recording and outputting a table;
TABLE 2
Example 3
The flame-retardant antibacterial polyester-cotton blended fabric comprises the following raw materials:
45 parts of polyethylene terephthalate (PET), 65 parts of cotton fiber, 8 parts of caustic soda, 62 parts of dilute hydrochloric acid, 10 parts of a tetramethylolphosphonium chloride urea condensate aqueous solution, 8 parts of a plant source bacteriostatic agent and 15 parts of a flame-retardant gel;
the concentration of the dilute hydrochloric acid is 2.6 percent; the concentration of the aqueous solution of the tetramethylolphosphonium chloride urea condensate is 400 g/L;
introducing polyethylene glycol terephthalate into a stirring kettle, controlling the temperature in the stirring kettle to be 275-295 ℃, pouring a tetramethylolphosphonium chloride urea condensate aqueous solution into the stirring kettle after the temperature is raised, controlling the stirring speed of the stirring kettle to be 120-160 r/min, keeping the temperature and heating for 25-30 min, introducing caustic soda particles with the particle size of 0.08-0.1 mm into the stirring kettle after the temperature is kept and heating, continuously stirring for 10-12min, introducing the mixture into a double-screw extruder, controlling the extrusion temperature of the double-screw extruder to be 175-195 ℃, twisting cotton fibers into 0.75-0.8 mm cotton threads, mixing agar and water, heating to 98-102 ℃, keeping the temperature and stirring uniformly, naturally cooling to 55-60 ℃, blending with aluminum sulfate, preparing a component A after uniform mixing, introducing sodium bicarbonate and starch into a refrigeration house after mixing, freezing for 0.5-1H at the low temperature of-30 to-25 ℃, after freezing, crushing, mixing agar and water, heating to 98-102 ℃, keeping the temperature, stirring uniformly, naturally cooling to 65-70 ℃ and blending with crushed sodium bicarbonate powder to obtain a component B, respectively soaking cotton threads into the component A and the component B according to the proportion of 1:1, naturally cooling to normal temperature, removing redundant gel on the surface layer to obtain the cotton threads A and the cotton threads B, soaking the cotton threads B into warm water with plant source bacteriostat and at the temperature of 45-65 ℃ for 2-3H, transferring the cotton threads B into a refrigerator, freezing for 30-45 min at the temperature of-15 to-12 ℃, extruding and coating the mixture in a double-screw extruder on the surface of the cotton threads after freezing, controlling the thickness of the coating layer to be 0.25-0.3 mm, preparing double-layer silk threads after extruding and coating, cooling at normal temperature, immersing the double-layer silk threads in dilute hydrochloric acid solution, controlling the immersion time to be 3-4H, overturning at an interval of 0.5H, preparing a flame-retardant silk thread after immersion, co-spinning the flame-retardant silk thread and the cotton thread A to obtain the flame-retardant antibacterial polyester-cotton blended fabric, and repeating the steps to obtain five pieces of flame-retardant antibacterial polyester-cotton blended fabric which are respectively marked as propane 1-propane 5;
respectively fixing the third to fourth fabrics 1 to 5 by using fixing clamps, respectively placing alcohol lamps below the third to fourth fabrics 1 to 5, controlling the distances between the flame of the alcohol lamps and the fabrics to be 3cm, 6cm, 9cm, 12cm and 15cm, respectively recording the generation time of open fire on the surfaces of the third to fourth fabrics 1 to 5, removing the alcohol lamps after the open fire is generated, measuring the burning area of the fabrics after the flame on the surfaces of the fabrics is automatically extinguished, and recording and outputting a table;
TABLE 3
According to the three groups of experimental data, under the same burning effect of the alcohol lamp, the comparison between the embodiment 1 and the embodiment 2 shows that the ignition difficulty and the flame retardant strength of the flame-retardant antibacterial polyester-cotton blended fabric prepared by using part of the formula of the flame-retardant antibacterial polyester-cotton blended fabric are improved compared with those of the prior art by coating and perforating the polyester fibers and the cotton fibers, and meanwhile, the comparison between the embodiment 2 and the embodiment 3 shows that the flame-retardant antibacterial polyester-cotton blended fabric prepared by completely using the formula and the method can quickly extinguish and retard fire due to the fact that the flame-retardant gel capable of reacting with each other is arranged in the flame-retardant antibacterial polyester-cotton blended fabric, and the flame-retardant antibacterial polyester-cotton blended fabric has a good flame retardant effect in the using process.
The foregoing illustrates and describes the principles, general features, and advantages of the present invention. It will be understood by those skilled in the art that the present invention is not limited to the embodiments described above, which are described in the specification and illustrated only to illustrate the principle of the present invention, but that various changes and modifications may be made therein without departing from the spirit and scope of the present invention, which fall within the scope of the invention as claimed. The scope of the invention is defined by the appended claims and equivalents thereof.
Claims (6)
1. A manufacturing method of a flame-retardant antibacterial polyester-cotton blended fabric is characterized by comprising the following steps: the flame-retardant antibacterial polyester-cotton blended fabric comprises the following raw materials:
45-50 parts of polyethylene terephthalate (PET), 60-65 parts of cotton fibers, 8-12 parts of caustic soda, 62-66 parts of dilute hydrochloric acid, 10-12 parts of a tetramethylolphosphonium chloride urea condensate aqueous solution and 8-10 parts of a plant source bacteriostatic agent;
the concentration of the dilute hydrochloric acid is 2.6-2.8%; the concentration of the aqueous solution of the tetramethylolphosphonium chloride urea condensate is 400-500 g/L;
the manufacturing method of the flame-retardant antibacterial polyester-cotton blended fabric comprises the following steps:
s1: introducing polyethylene glycol terephthalate into a stirring kettle, controlling the temperature in the stirring kettle to be 275-295 ℃, pouring the aqueous solution of the tetramethylolphosphonium chloride urea condensate into the stirring kettle after the temperature is raised, controlling the stirring speed of the stirring kettle to be 120-160 r/min, and keeping the temperature and heating for 25-30 min;
s2: after heat preservation and heating are finished, introducing caustic soda particles which are milled to be 0.08-0.1 mm in particle size into a stirring kettle, continuously stirring for 10-12min, introducing the mixture into a double-screw extruder, and controlling the extrusion temperature of the double-screw extruder to be 175-195 ℃;
s3: twisting cotton fibers to form 0.75-0.8 mm cotton threads, soaking half of the cotton threads in warm water with a temperature of 45-65 ℃ added with a plant source bacteriostatic agent for 2-3H, transferring the cotton threads into a cold storage, freezing the cotton threads at a temperature of-15 to-12 ℃ for 30-45 min, and extruding and coating the mixture in a double-screw extruder on the surfaces of the cotton threads after the freezing treatment is finished;
s4: controlling the thickness of the coating layer to be 0.25-0.3 mm, extruding and coating to obtain a double-layer silk thread, cooling at normal temperature, immersing the double-layer silk thread in a dilute hydrochloric acid solution, controlling the immersion time to be 3-4H, overturning at an interval of 0.5H, preparing a flame-retardant silk thread after immersion is finished, and co-spinning the flame-retardant silk thread and the residual cotton threads to obtain the flame-retardant antibacterial polyester-cotton blended fabric.
2. The manufacturing method of the flame-retardant antibacterial polyester-cotton blended fabric according to claim 1, characterized by comprising the following steps: the raw materials also comprise 15-18 parts of flame-retardant gel; the flame-retardant gel is formed by mixing the component A and the component B according to the proportion of 1: 6; the component A is prepared from agar, water and aluminum sulfate according to the proportion of 5:3: 1; the component B is prepared from agar, water, sodium bicarbonate and starch according to the proportion of 5:15:6: 3; the flame retardant gel is combined with cotton.
3. The manufacturing method of the flame-retardant antibacterial polyester-cotton blended fabric according to claim 2, characterized by comprising the following steps: the preparation method of the flame-retardant gel comprises the following steps:
a1: mixing agar and water, heating to 98-102 ℃, preserving heat, stirring uniformly, naturally cooling to 55-60 ℃, mixing with aluminum sulfate, and mixing uniformly to obtain a component A;
a2: mixing sodium bicarbonate and starch, introducing into a refrigeration house, freezing for 0.5-1H at the low temperature of-30 to-25 ℃, crushing after freezing, mixing agar and water, heating to 98-102 ℃, preserving heat, stirring uniformly, naturally cooling to 65-70 ℃, and blending with crushed sodium bicarbonate powder to obtain a component B;
a3: respectively soaking the cotton threads in the S3 in the component A and the component B according to the ratio of 1:1, naturally cooling to normal temperature, removing redundant gel on the surface layer to obtain the cotton threads A and the cotton threads B, soaking the cotton threads B in warm water added with the plant-derived bacteriostatic agent, and directly blending the cotton threads A.
4. The manufacturing method of the flame-retardant antibacterial polyester-cotton blended fabric according to claim 3, characterized by comprising the following steps: and in the S4, co-spinning the double-layer silk yarns and the residual cotton yarns to obtain the fabric, then placing the fabric in a hot press, controlling a single-side press plate of the hot press to heat to 280-300 ℃, carrying out hot pressing for 0.5-0.8S, and carrying out dilute hydrochloric acid treatment after the hot pressing is finished.
5. The manufacturing method of the flame-retardant antibacterial polyester-cotton blended fabric according to claim 3, characterized by comprising the following steps: wherein the surface of the cotton thread subjected to the freezing treatment in the S3 is adhered with a layer of sodium chloride, potassium chloride and ammonium phosphate before hot-pressing and coating, and the weight ratio of the cotton thread to the sodium chloride to the potassium chloride to the ammonium phosphate is 1: 1:1, and mixing to obtain the flame-retardant powder.
6. The manufacturing method of the flame-retardant antibacterial polyester-cotton blended fabric according to claim 5, characterized by comprising the following steps: wherein 3-4 parts of gelatin is dissolved in warm water at 45-65 ℃ added with the plant-derived bacteriostatic agent in S3.
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN115506062A (en) * | 2022-10-21 | 2022-12-23 | 石狮市益明染织有限公司 | Environment-friendly flame-retardant polyester yarn and preparation method thereof |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103752187A (en) * | 2014-01-09 | 2014-04-30 | 天津工业大学 | Preparation method of glass hollow fiber nanofiltration membrane with asymmetric pore structure |
WO2015096211A1 (en) * | 2013-12-25 | 2015-07-02 | 深圳市联嘉祥科技股份有限公司 | Fire-resistant wire cable and manufacturing method therefor |
CN112126202A (en) * | 2020-09-30 | 2020-12-25 | 梁亚正 | High-flame-retardancy color master batch and preparation method thereof |
CN112941924A (en) * | 2021-01-25 | 2021-06-11 | 浙江荣莱纺织有限公司 | Anti-pilling polyester cotton knitted fabric and preparation method thereof |
CN113089312A (en) * | 2021-03-03 | 2021-07-09 | 潘少华 | High-strength flame-retardant elastic fabric and preparation method thereof |
CN113290982A (en) * | 2021-04-06 | 2021-08-24 | 李冬冬 | Fire-resistant silica gel material and preparation method thereof |
-
2021
- 2021-11-06 CN CN202111309330.5A patent/CN114016282A/en active Pending
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2015096211A1 (en) * | 2013-12-25 | 2015-07-02 | 深圳市联嘉祥科技股份有限公司 | Fire-resistant wire cable and manufacturing method therefor |
CN103752187A (en) * | 2014-01-09 | 2014-04-30 | 天津工业大学 | Preparation method of glass hollow fiber nanofiltration membrane with asymmetric pore structure |
CN112126202A (en) * | 2020-09-30 | 2020-12-25 | 梁亚正 | High-flame-retardancy color master batch and preparation method thereof |
CN112941924A (en) * | 2021-01-25 | 2021-06-11 | 浙江荣莱纺织有限公司 | Anti-pilling polyester cotton knitted fabric and preparation method thereof |
CN113089312A (en) * | 2021-03-03 | 2021-07-09 | 潘少华 | High-strength flame-retardant elastic fabric and preparation method thereof |
CN113290982A (en) * | 2021-04-06 | 2021-08-24 | 李冬冬 | Fire-resistant silica gel material and preparation method thereof |
Non-Patent Citations (2)
Title |
---|
李竹君等, 中国轻工业出版社 * |
杨栋梁: "两种棉织物耐久阻燃整理技术的解析", 印染, vol. 2, no. 6, pages 1118 - 477 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN115506062A (en) * | 2022-10-21 | 2022-12-23 | 石狮市益明染织有限公司 | Environment-friendly flame-retardant polyester yarn and preparation method thereof |
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