CN111909615B - Water-based flame-retardant coating for fireproof cotton textile rope - Google Patents
Water-based flame-retardant coating for fireproof cotton textile rope Download PDFInfo
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- CN111909615B CN111909615B CN202010820945.3A CN202010820945A CN111909615B CN 111909615 B CN111909615 B CN 111909615B CN 202010820945 A CN202010820945 A CN 202010820945A CN 111909615 B CN111909615 B CN 111909615B
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- 239000003063 flame retardant Substances 0.000 title claims abstract description 103
- 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 101
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims abstract description 61
- 239000004753 textile Substances 0.000 title claims abstract description 54
- 229920000742 Cotton Polymers 0.000 title claims abstract description 52
- 238000000576 coating method Methods 0.000 title claims abstract description 47
- 239000011248 coating agent Substances 0.000 title claims abstract description 39
- 229920002451 polyvinyl alcohol Polymers 0.000 claims abstract description 47
- 239000004372 Polyvinyl alcohol Substances 0.000 claims abstract description 46
- 239000002131 composite material Substances 0.000 claims abstract description 44
- 239000004327 boric acid Substances 0.000 claims abstract description 31
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims abstract description 30
- 239000012796 inorganic flame retardant Substances 0.000 claims abstract description 9
- 239000000853 adhesive Substances 0.000 claims abstract description 8
- 230000001070 adhesive effect Effects 0.000 claims abstract description 8
- 239000002518 antifoaming agent Substances 0.000 claims abstract description 7
- 239000002270 dispersing agent Substances 0.000 claims abstract description 7
- 239000000945 filler Substances 0.000 claims abstract description 7
- 239000002994 raw material Substances 0.000 claims abstract description 6
- 238000004132 cross linking Methods 0.000 claims abstract description 5
- 239000007864 aqueous solution Substances 0.000 claims description 33
- 238000003756 stirring Methods 0.000 claims description 26
- 239000000463 material Substances 0.000 claims description 21
- 239000006185 dispersion Substances 0.000 claims description 20
- 230000009970 fire resistant effect Effects 0.000 claims description 18
- 239000004114 Ammonium polyphosphate Substances 0.000 claims description 17
- 235000019826 ammonium polyphosphate Nutrition 0.000 claims description 17
- 229920001276 ammonium polyphosphate Polymers 0.000 claims description 17
- 239000007788 liquid Substances 0.000 claims description 16
- 238000000227 grinding Methods 0.000 claims description 14
- 239000000839 emulsion Substances 0.000 claims description 12
- 238000001035 drying Methods 0.000 claims description 11
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 claims description 10
- 238000002360 preparation method Methods 0.000 claims description 10
- 239000005995 Aluminium silicate Substances 0.000 claims description 9
- 229910052582 BN Inorganic materials 0.000 claims description 9
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 claims description 9
- 235000012211 aluminium silicate Nutrition 0.000 claims description 9
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 claims description 9
- 238000005406 washing Methods 0.000 claims description 9
- 238000001914 filtration Methods 0.000 claims description 8
- 238000009210 therapy by ultrasound Methods 0.000 claims description 8
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 7
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 claims description 7
- 229910000388 diammonium phosphate Inorganic materials 0.000 claims description 7
- 235000019838 diammonium phosphate Nutrition 0.000 claims description 7
- 229910052710 silicon Inorganic materials 0.000 claims description 7
- 239000010703 silicon Substances 0.000 claims description 7
- 239000008367 deionised water Substances 0.000 claims description 6
- 229910021641 deionized water Inorganic materials 0.000 claims description 6
- -1 polyethylene Polymers 0.000 claims description 6
- 239000004576 sand Substances 0.000 claims description 6
- 238000005303 weighing Methods 0.000 claims description 6
- 239000004698 Polyethylene Substances 0.000 claims description 5
- 238000007599 discharging Methods 0.000 claims description 5
- 229920000573 polyethylene Polymers 0.000 claims description 5
- 239000011259 mixed solution Substances 0.000 claims description 4
- 229920000604 Polyethylene Glycol 200 Polymers 0.000 claims description 2
- 239000013530 defoamer Substances 0.000 claims description 2
- 239000002245 particle Substances 0.000 claims description 2
- 229940113115 polyethylene glycol 200 Drugs 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims 2
- 239000005696 Diammonium phosphate Substances 0.000 claims 1
- 230000000694 effects Effects 0.000 abstract description 4
- 239000011258 core-shell material Substances 0.000 abstract description 2
- 238000009776 industrial production Methods 0.000 abstract 1
- 238000003672 processing method Methods 0.000 abstract 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 34
- 238000012360 testing method Methods 0.000 description 15
- 238000000034 method Methods 0.000 description 8
- 239000003973 paint Substances 0.000 description 8
- 238000002485 combustion reaction Methods 0.000 description 6
- 239000010410 layer Substances 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- 229910052799 carbon Inorganic materials 0.000 description 5
- 239000007789 gas Substances 0.000 description 4
- 238000004062 sedimentation Methods 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 239000006260 foam Substances 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 238000011056 performance test Methods 0.000 description 3
- 229920001296 polysiloxane Polymers 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000011241 protective layer Substances 0.000 description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- 208000003251 Pruritus Diseases 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000006136 alcoholysis reaction Methods 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 238000003763 carbonization Methods 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 230000007803 itching Effects 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000001338 self-assembly Methods 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 230000004584 weight gain Effects 0.000 description 1
- 235000019786 weight gain Nutrition 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D183/00—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Coating compositions based on derivatives of such polymers
- C09D183/04—Polysiloxanes
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/18—Fireproof paints including high temperature resistant paints
- C09D5/185—Intumescent paints
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/60—Additives non-macromolecular
- C09D7/61—Additives non-macromolecular inorganic
-
- D—TEXTILES; PAPER
- D07—ROPES; CABLES OTHER THAN ELECTRIC
- D07B—ROPES OR CABLES IN GENERAL
- D07B7/00—Details of, or auxiliary devices incorporated in, rope- or cable-making machines; Auxiliary apparatus associated with such machines
- D07B7/02—Machine details; Auxiliary devices
- D07B7/14—Machine details; Auxiliary devices for coating or wrapping ropes, cables, or component strands thereof
- D07B7/145—Coating or filling-up interstices
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/32—Phosphorus-containing compounds
- C08K2003/321—Phosphates
- C08K2003/322—Ammonium phosphate
- C08K2003/323—Ammonium polyphosphate
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/38—Boron-containing compounds
- C08K2003/382—Boron-containing compounds and nitrogen
- C08K2003/385—Binary compounds of nitrogen with boron
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/02—Flame or fire retardant/resistant
Abstract
The invention belongs to the technical field of coatings, and particularly relates to a water-based flame-retardant coating for a fireproof cotton textile rope. The water-based flame-retardant coating comprises the following raw material components: 8-10 parts of an adhesive, 3-4 parts of an intumescent composite flame retardant, 7-10 parts of a refractory filler, 0.1-0.15 part of a dispersing agent, 0.1-0.2 part of a defoaming agent and 40-50 parts of water; the intumescent composite flame retardant is a core-shell structure obtained by wrapping an inorganic flame retardant with a polyvinyl alcohol and boric acid crosslinking structure. The water-based flame-retardant coating for the fireproof cotton textile rope provided by the invention has the advantages of good flame-retardant effect, low price and simple processing method, and is suitable for large-scale industrial production.
Description
Technical Field
The invention belongs to the technical field of coatings, and particularly relates to a water-based flame-retardant coating for a fireproof cotton textile rope.
Background
Textile cords are textile materials made by twisting a plurality of yarns or threads and are widely used, including clothing, household and specialty materials, and the like. Cotton is one of the most commonly used textile materials, and compared with some synthetic polymer fibers, the main advantages of cotton fibers are fluffiness, softness, temperature sensitivity, no itching feeling (the fiber ends are extremely thin), moisture dispersion, no static electricity under ordinary environment, and no generation of molten drops during combustion. However, the textile rope made of cotton fiber has the main disadvantages of flammability and environmental pollution in the combustion process, and limits the application of the cotton fiber textile rope in special textiles.
In order to reduce the inflammability of the material and improve the flame durability of the material, the flame-retardant method of the cotton textile rope is to react cotton with an organic flame retardant before the rope is formed and graft the material containing the flame-retardant component on the surface of the cotton textile rope; or the principle of layer-by-layer self-assembly is utilized to paste organic/inorganic flame-retardant components with opposite charges on the surface of the cotton textile rope, and a waterproof protective layer is coated on the basis of the organic/inorganic flame-retardant components.
Therefore, there is a need for a flame retardant coating for cotton textile ropes, which has a good flame retardant effect, is low in cost and is convenient to process.
Disclosure of Invention
Aiming at the defects of the prior art, the invention aims to provide the water-based flame-retardant coating for the fire-resistant cotton textile rope, which can solve the problems of low flame-retardant efficiency, and strict cost and processing conditions of the flame-retardant method for the cotton textile rope in the prior art.
The technical scheme adopted for solving the technical problem is to provide the water-based flame retardant coating for the fireproof cotton textile rope, which comprises the following raw materials in parts by weight: 8-10 parts of an adhesive, 3-4 parts of an intumescent composite flame retardant, 7-10 parts of a refractory filler, 0.1-0.15 part of a dispersing agent, 0.1-0.2 part of a defoaming agent and 40-50 parts of water;
the intumescent composite flame retardant is obtained by wrapping an inorganic flame retardant by a polyvinyl alcohol and boric acid crosslinking structure.
Preferably, the mass ratio of the polyvinyl alcohol to the boric acid to the inorganic flame retardant is 5: (1-2): (10-15).
As a preferred technical scheme, the inorganic flame retardant is ammonium polyphosphate.
As a preferable technical scheme, the preparation method of the intumescent composite flame retardant comprises the following steps:
1) dissolving polyvinyl alcohol in water to prepare a polyvinyl alcohol aqueous solution with the mass concentration of 4-6%;
2) dispersing ammonium polyphosphate in the polyvinyl alcohol aqueous solution obtained in the step 1), and performing ultrasonic treatment until a uniform dispersion liquid is formed;
3) slowly dropwise adding a boric acid aqueous solution with the mass concentration of 4-6% into the dispersion liquid obtained in the step 2) under stirring to obtain a mixed solution, wherein the boric acid aqueous solution is prepared by dissolving boric acid in water;
4) and (3) washing, filtering, drying and grinding the mixed solution obtained in the step 3) to obtain the intumescent composite flame retardant.
Preferably, the preparation method of the intumescent composite flame retardant comprises the following steps:
s1, preparing 500 parts by weight of 5% polyvinyl alcohol aqueous solution and 100-200 parts by weight of 5% boric acid aqueous solution;
s2, weighing 50-75 parts by weight of ammonium polyphosphate, dispersing into the polyvinyl alcohol aqueous solution in S1, and carrying out ultrasonic treatment until a uniform dispersion liquid is formed;
s3, slowly dripping the boric acid aqueous solution in the S1 into the dispersion liquid, and stirring continuously;
and S4, finally, washing, filtering, drying and grinding the obtained material to obtain the intumescent composite flame retardant.
In the preparation process of the intumescent composite flame retardant, the dispersion containing the ammonium polyphosphate and the polyvinyl alcohol is dripped into the aqueous solution of the boric acid, the hydroxyl on the polyvinyl alcohol and the carboxyl on the boric acid are esterified and crosslinked, the ammonium polyphosphate is wrapped in a crosslinking structure formed by the polyvinyl alcohol and the boric acid, thereby obtaining the intumescent composite flame retardant with the core-shell structure, in the ternary integrated intumescent flame retardant composite material prepared, the boric acid is used as an acid source, the polyvinyl alcohol is used as a carbon source, the ammonium polyphosphate is used as a gas source, the ammonium polyphosphate treated by the water-soluble polymer polyvinyl alcohol has better compatibility with the organic silicon emulsion, and the contact with the cotton textile rope is firmer under the action of the organic silicon emulsion after drying, and simultaneously, due to the cross-linking action of the boric acid and the polyvinyl alcohol, the hydroxyl on the polyvinyl alcohol is partially sealed, and the water washing resistance of the water-based flame-retardant coating is effectively improved.
The polyvinyl alcohol PVA is an environment-friendly material, is non-toxic and harmless to a human body, contains a large amount of carbon-hydroxyl in a molecular structure, and can serve as a carbon source in an expansion flame-retardant system. Boric acid is an excellent boron flame retardant, and can catalyze dehydration and carbonization of polyvinyl alcohol and dipentaerythritol during combustion, and the polyvinyl alcohol and the dipentaerythritol are attached to the surface of a protected base material.
In the present application, the polyvinyl alcohol may be selected from conventional polyvinyl alcohols, and preferably, the polyvinyl alcohol used is PVA 2088.
The applicant finds that the intumescent composite flame retardant prepared by PVA2088 has good dispersibility in the water-based flame retardant coating, and has good water resistance when being coated on the surface of a cotton textile rope. The other polyvinyl alcohol which is not at the molecular weight and has low alcoholysis degree is used for preparing the intumescent composite flame retardant, so that the dispersibility and the water resistance of the intumescent composite flame retardant and the water-based flame retardant coating are poor.
According to a preferable technical scheme, the average particle size of the composite flame retardant obtained by grinding is 100-200 μm.
As a preferred technical scheme, the adhesive is an aqueous silicone emulsion, and the aqueous silicone emulsion used in the present application is an UltrateX FSA silicone emulsion produced by basjia corporation, switzerland.
As a preferable technical scheme, the refractory filler is selected from at least one of diammonium hydrogen phosphate, kaolin, boron nitride and dipentaerythritol.
As a preferred technical scheme, the dispersing agent is polyethylene glycol-200.
As a preferred technical scheme, the defoaming agent selected by the application is T503.
According to the water-based flame-retardant coating for the fireproof cotton textile rope, which is provided by the preferred embodiment of the invention, the water-based flame-retardant coating comprises the following raw material components in parts by weight: 8 parts of UltrateX FSA organosilicon emulsion, 4 parts of intumescent composite flame retardant, 2 parts of diammonium hydrogen phosphate, 2.3 parts of kaolin, 1.2 parts of boron nitride, 2.2 parts of dipentaerythritol, 2000.15 parts of polyethylene glycol-5030.1-0.2 parts of deionized water and 42kg of deionized water;
the preparation method of the intumescent composite flame retardant comprises the following steps:
s1, firstly, preparing 500 parts by weight of a 5% polyvinyl alcohol 2088 type polyvinyl alcohol aqueous solution and 100 parts by weight of a 5% boric acid aqueous solution;
s2, weighing 50 parts by weight of ammonium polyphosphate, dispersing into a polyvinyl alcohol aqueous solution in S1, and carrying out ultrasonic treatment until a uniform dispersion liquid is formed;
s3, slowly dripping the boric acid aqueous solution in the S1 into the S2 dispersion liquid, and stirring continuously;
and S4, finally, washing, filtering, drying and grinding the obtained material to obtain the intumescent composite flame retardant.
Tests prove that the water-based flame-retardant coating with the formula has good dispersibility, is used for the flame-retardant coating of cotton textile ropes, and has the best flame retardance and water resistance effects.
As a preferred technical scheme, the preparation method of the water-based flame-retardant coating comprises the following steps: adding the adhesive, the water, the intumescent composite flame retardant, the refractory filler and the dispersant into a stirring barrel, continuously stirring for 0.5-1 h to obtain coarse materials, fully grinding the coarse materials in a sand mill for 5-10 h, discharging, adding the defoamer according to the formula amount, and uniformly stirring.
Aiming at the defect that a cotton textile rope is easy to burn, the invention develops an expansion type flame-retardant water-based paint. The intumescent flame-retardant water-based paint has good flame retardance and dispersibility, and the flame-retardant and fireproof mechanism is as follows: during the combustion process, PVA and dipentaerythritol are quickly carbonized under the catalytic action of phosphoric acid and boric acid decomposed from ammonium polyphosphate and boric acid ester respectively, and meanwhile, ammonium polyphosphate can be decomposed into incombustible nitrogen-containing gas (NH) at high temperature3) When the gas escapes and passes through the carbon layer, the gas rapidly expands to form a thick protective layer, and kaolin and boron nitride are added into the coating to increase the compactness and the heat insulation of the expanded carbon layer, so that the internal cotton textile rope is protected.
Compared with the prior art, the invention has the beneficial effects that: the intumescent composite flame retardant prepared by the invention has good compatibility with the organic silicon emulsion, can be better fixed on a cotton textile rope, has good adhesion with the cotton textile rope, improves the water resistance of the flame retardant coating on the rope, and prolongs the service life of the cotton textile rope. In addition, the water-based flame-retardant coating can generate a thick expansion layer on the surface of the rope in the combustion process, has stronger fire resistance, widens the application field of the cotton textile rope, and improves the use value of the cotton textile rope. Tests prove that the limited oxygen index of the cotton textile rope treated by the coating can reach more than 35 percent, and the phenomenon of continuous open fire can not occur in a vertical combustion test. The cotton textile rope treated by the coating has the characteristics of good fireproof performance and less smoke.
Detailed Description
The experimental procedures in the following examples are conventional unless otherwise specified. The raw materials in the following examples are all commercially available products and are commercially available, unless otherwise specified. The present invention is described in further detail below with reference to examples:
example 1
S1, firstly, 500g of a 5% polyvinyl alcohol (2088 type) aqueous solution and 100g of a 5% boric acid aqueous solution are prepared.
S2, weighing 50g of ammonium polyphosphate to be dispersed in the PVA aqueous solution in S1, and carrying out ultrasonic treatment until a uniform dispersion liquid is formed.
S3, slowly dripping the boric acid aqueous solution in the S1 into the S2 dispersion liquid, and stirring continuously.
And S4, finally, washing, filtering, drying and grinding the obtained material to obtain the intumescent composite flame retardant.
Example 2
S1, firstly, 500g of a 5% polyvinyl alcohol (2088 type) aqueous solution and 200g of a 5% boric acid aqueous solution are prepared.
S2, weighing 75g of ammonium polyphosphate to be dispersed into the PVA aqueous solution in S1, and carrying out ultrasonic treatment until a uniform dispersion liquid is formed.
S3, slowly dripping the boric acid aqueous solution in the S1 into the S2 dispersion liquid, and stirring continuously.
And S4, finally, washing, filtering, drying and grinding the obtained material to obtain the intumescent composite flame retardant.
Example 3
S1, firstly, taking 10kg of organic silicon emulsion and 40kg of deionized water, and uniformly stirring for 5 min;
s2, respectively adding 3.5kg of the intumescent composite flame retardant, 2.5kg of diammonium hydrogen phosphate, 2kg of kaolin and 1kg of boron nitride in the embodiment 1, and stirring for 60 min;
s3, adding polyethylene glycol-2000.1 kg and dipentaerythritol 2kg, and continuously stirring for 30 min;
and S4, finally, adding the prepared coarse material into a sand mill, fully grinding for 10 hours, then discharging, adding 0.1kg of defoaming agent, and slowly stirring until no large amount of foam exists, thus obtaining the water-based paint for the refractory cotton textile rope.
Example 4
S1, firstly, taking 8kg of organic silicon emulsion and 42kg of deionized water, and stirring for 2 min;
s2, respectively adding 4kg of the intumescent composite flame retardant, 2kg of diammonium hydrogen phosphate, 2.3kg of kaolin and 1.2kg of boron nitride in the embodiment 1, and stirring for 40 min;
s3, adding polyethylene glycol-2000.15 kg and 2.2kg of dipentaerythritol, and continuously stirring for 20 min;
and S4, finally, adding the prepared coarse material into a sand mill, fully grinding for 8 hours, then discharging, adding 0.12kg of defoaming agent, and slowly stirring until no large amount of foam exists, thus obtaining the water-based paint for the refractory cotton textile rope.
Example 5
S1, firstly, taking 10kg of organic silicon emulsion and 40kg of deionized water, and stirring for 3 min;
s2, respectively adding 3kg of the intumescent composite flame retardant, 3kg of diammonium hydrogen phosphate, 2.3kg of kaolin and 1.3kg of boron nitride in the embodiment 1, and stirring for 30 min;
s3, adding 2.5kg of polyethylene glycol-2000.1 kg of dipentaerythritol, and continuing to stir for 20 min;
and S4, finally, adding the prepared coarse material into a sand mill, fully grinding for 5 hours, then discharging, adding 0.1kg of defoaming agent, and slowly stirring until no large amount of foam exists, thus obtaining the water-based paint for the fire-resistant cotton textile rope.
Example 6
The intumescent composite flame retardant prepared according to the method provided by the example 1 is different from the example 1 only in that the type of polyvinyl alcohol used is PVA1788, and the prepared flame retardant is used for preparing the waterborne flame retardant coating instead of the intumescent composite flame retardant in the example 3.
Example 7
The intumescent composite flame retardant prepared according to the method provided by the example 1 is different from the method provided by the example 1 only in that the type of the polyvinyl alcohol used is PVA2099, and the prepared flame retardant is used for preparing the water-based flame retardant coating instead of the intumescent composite flame retardant in the example 3.
Example 8
The intumescent composite flame retardant prepared according to the method provided in example 1 is different from example 1 only in that the polyvinyl alcohol used is PVA2488, and the prepared flame retardant is used to prepare a water-based flame retardant coating instead of the intumescent composite flame retardant in example 3.
Test example 1
The flame retardant property test is carried out on the water-based flame retardant coating prepared in the embodiment 3-8, and the preparation method of the fireproof cotton textile rope comprises the following steps: firstly, the cotton textile rope passes through a sand frame, then is dipped in coating through a coating tank, then is rolled by two rollers, is dried through a high-temperature drying channel at 120 ℃, and finally is rolled at the speed of 20m/min to obtain the fire-resistant cotton textile rope, and meanwhile, a pure sample of the cotton textile rope which is not treated by the water-based flame-retardant coating is set as a reference, and the detection result is shown in table 1.
TABLE 1 flame retardancy test of aqueous flame retardant coatings
As can be seen from Table 1, the pure samples are very flammable, but after the samples are treated by the water-based coatings of the invention of the examples 3-8, continuous open fire does not appear under the heating of flame, and the limiting oxygen indexes are all over 35 percent. From the six examples it can be seen that the overall performance of example 4 is the best, and that example 3, 4 has a higher content of modified intumescent flame retardant than example 4, so that when the flame treated rope is tested it has a thicker intumescent layer, which is more favourable for the fire resistance of the rope, and in addition has a lower weight gain due to the use of less adhesive. The total intumescent flame retardant system of examples 3 and 5 was added in equal amounts, but example 5 contained more kaolin and boron nitride, which somewhat limited the expansion of the carbon layer and therefore the expanded thickness was seen to be less in the test results.
Test example 2
The flame-retardant water-based paint of the embodiment 3-8 is subjected to dispersion performance test, a control group is set during the test (the intumescent composite flame retardant in the embodiment 3 is replaced by equal amount of ammonium polyphosphate, and the rest is the same), and the test method comprises the steps of respectively measuring 100ml of the flame-retardant water-based paint in the embodiment 3-8 by using 100ml of test tubes, vertically placing the test tubes on an observation frame, and checking whether the paint in the test tubes is settled every 12 hours, wherein the results are shown in table 2.
TABLE 2 Dispersion Performance test of aqueous flame retardant coatings
As can be seen from Table 2, the control group has sedimentation within 12 hours, the dispersibility is the worst, the flame-retardant water-based coatings provided in examples 3 to 5 have good dispersibility, and have no sedimentation after 36 hours, while the intumescent composite flame retardants in examples 6 to 8 have slightly poor dispersibility, have no sedimentation within 24 hours, and have sedimentation within 36 hours as time goes on.
Test example 3
The method of test example 1 was used to prepare a fire-resistant cotton textile rope from the aqueous flame-retardant coating prepared in examples 3 to 8, the fire-resistant cotton textile rope was soaked in water for 12 hours and then taken out, after drying, the appearance of the coating film on the cotton textile rope was observed, and the flame-retardant performance test was performed, the test results are shown in table 3
TABLE 3 Water resistance of aqueous flame retardant coatings
As shown in Table 3, the water resistance of the fire-resistant cotton textile ropes in the examples 3 to 5 is better than that of the fire-resistant cotton textile ropes in the examples 6 to 8, after being soaked in water, the limiting oxygen index of the fire-resistant cotton textile ropes in the examples 6 to 8 is obviously lower than that of the fire-resistant cotton textile ropes in the examples 3 to 5, which indicates that the water-based fire-retardant coatings provided in the examples 6 to 8 are used for fire retardation of the textile ropes, the water resistance is poor, and the fire retardation effect after being soaked is obviously lower than that of the fire-resistant cotton textile ropes in the examples 3 to 5.
Finally, it should be emphasized that the above-described preferred embodiments of the present invention are merely examples of implementations, rather than limitations, and that many variations and modifications of the invention are possible to those skilled in the art, without departing from the spirit and scope of the invention.
Claims (7)
1. The water-based flame-retardant coating for the fireproof cotton textile rope is characterized by comprising the following raw material components in parts by weight: 8-10 parts of an adhesive, 3-4 parts of an intumescent composite flame retardant, 7-10 parts of a refractory filler, 0.1-0.15 part of a dispersing agent, 0.1-0.2 part of a defoaming agent and 40-50 parts of water;
the intumescent composite flame retardant is obtained by wrapping an inorganic flame retardant by a polyvinyl alcohol and boric acid crosslinking structure; the mass ratio of the polyvinyl alcohol to the boric acid to the inorganic flame retardant is 5: (1-2): (10-15); the inorganic flame retardant is ammonium polyphosphate; the adhesive is aqueous organic silicon emulsion;
the polyvinyl alcohol is PVA 2088;
the preparation method of the intumescent composite flame retardant comprises the following steps:
1) dissolving polyvinyl alcohol in water to prepare a polyvinyl alcohol aqueous solution with the mass concentration of 4-6%;
2) dispersing ammonium polyphosphate in the polyvinyl alcohol aqueous solution obtained in the step 1), and performing ultrasonic treatment until a uniform dispersion liquid is formed;
3) dropwise adding a boric acid aqueous solution with the mass concentration of 4-6% into the dispersion liquid obtained in the step 2) under stirring to obtain a mixed solution, wherein the boric acid aqueous solution is prepared by dissolving boric acid in water;
4) and (3) washing, filtering, drying and grinding the mixed solution obtained in the step 3) to obtain the intumescent composite flame retardant.
2. The water-based flame retardant coating for fire-resistant cotton textile rope according to claim 1,
the preparation method of the intumescent composite flame retardant comprises the following steps:
s1, preparing 500 parts by weight of 5% polyvinyl alcohol aqueous solution and 100-200 parts by weight of 5% boric acid aqueous solution;
s2, weighing 50-75 parts by weight of ammonium polyphosphate, dispersing into the polyvinyl alcohol aqueous solution in S1, and carrying out ultrasonic treatment until a uniform dispersion liquid is formed;
s3, slowly dripping the boric acid aqueous solution in the S1 into the dispersion liquid, and stirring continuously;
and S4, finally, washing, filtering, drying and grinding the obtained material to obtain the intumescent composite flame retardant.
3. The water-based flame retardant coating for the fire-resistant cotton textile rope according to claim 2, wherein the average particle size of the expanded composite flame retardant obtained by grinding is 100-200 μm.
4. The aqueous flame retardant coating for fire resistant cotton textile rope according to claim 1, wherein the fire resistant filler is selected from at least one of diammonium phosphate, kaolin, boron nitride and dipentaerythritol.
5. The aqueous flame retardant coating for fire-resistant cotton textile rope according to claim 1, wherein the dispersant is polyethylene glycol-200.
6. The water-based flame-retardant coating for the fire-resistant cotton textile rope is characterized by comprising the following raw material components in parts by weight: 8 parts of UltrateX FSA organosilicon emulsion, 4 parts of intumescent composite flame retardant, 2 parts of diammonium hydrogen phosphate, 2.3 parts of kaolin, 1.2 parts of boron nitride, 2.2 parts of dipentaerythritol, polyethylene glycol-2000.15 parts, T5030.1-0.2 parts and 42 parts of deionized water;
the preparation method of the intumescent composite flame retardant comprises the following steps:
s1, firstly, preparing 500 parts by weight of a 5% polyvinyl alcohol 2088 type polyvinyl alcohol aqueous solution and 100 parts by weight of a 5% boric acid aqueous solution;
s2, weighing 50 parts by weight of ammonium polyphosphate, dispersing into a polyvinyl alcohol aqueous solution in S1, and carrying out ultrasonic treatment until a uniform dispersion liquid is formed;
s3, slowly dripping the boric acid aqueous solution in the S1 into the S2 dispersion liquid, and stirring continuously;
and S4, finally, washing, filtering, drying and grinding the obtained material to obtain the intumescent composite flame retardant.
7. The water-based flame retardant coating for the fire-resistant cotton textile rope according to any one of claims 1 to 6, characterized in that the preparation method of the water-based flame retardant coating is to add the adhesive, the water, the intumescent composite flame retardant, the fire-resistant filler and the dispersant into a stirring barrel, continuously stir for 0.5 to 1 hour to obtain a coarse material, fully grind the coarse material in a sand mill for 5 to 10 hours, add the defoamer into the mixture after discharging, and stir the mixture uniformly.
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CN111118885A (en) * | 2019-12-25 | 2020-05-08 | 江西龙泰新材料股份有限公司 | High-flame-retardant cotton textile water-based flame-retardant coating, preparation method and rope filling process thereof |
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CN104403603A (en) * | 2014-10-22 | 2015-03-11 | 上海大学 | Flame-retardant cross-linked polyvinyl alcohol binder and preparation method thereof |
CN104862966A (en) * | 2015-05-04 | 2015-08-26 | 江苏耐斯数码科技股份有限公司 | Wide-range flame-retarding canvas and preparation method thereof |
CN110527206A (en) * | 2019-08-15 | 2019-12-03 | 安徽壹石通材料科技股份有限公司 | A kind of preparation and its application of nitrogen-phosphorus-boron expansion type flame retardant |
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Denomination of invention: A water-based flame-retardant coating for fire-resistant cotton textile ropes Effective date of registration: 20231012 Granted publication date: 20211203 Pledgee: Shangyou County Sub branch of Agricultural Bank of China Co.,Ltd. Pledgor: JIANGXI LONGTAI NEW MATERIAL Co.,Ltd. Registration number: Y2023980060962 |