CN115975235A - Anti-slip woven bag - Google Patents
Anti-slip woven bag Download PDFInfo
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- CN115975235A CN115975235A CN202211689252.0A CN202211689252A CN115975235A CN 115975235 A CN115975235 A CN 115975235A CN 202211689252 A CN202211689252 A CN 202211689252A CN 115975235 A CN115975235 A CN 115975235A
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- Prior art keywords
- woven bag
- portions
- parts
- silica
- antiskid
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 42
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 29
- -1 aliphatic isocyanate Chemical class 0.000 claims abstract description 16
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 15
- 239000004925 Acrylic resin Substances 0.000 claims abstract description 13
- 239000003085 diluting agent Substances 0.000 claims abstract description 13
- 239000012948 isocyanate Substances 0.000 claims abstract description 13
- 229920005906 polyester polyol Polymers 0.000 claims abstract description 13
- 239000002518 antifoaming agent Substances 0.000 claims abstract description 10
- GKTNLYAAZKKMTQ-UHFFFAOYSA-N n-[bis(dimethylamino)phosphinimyl]-n-methylmethanamine Chemical compound CN(C)P(=N)(N(C)C)N(C)C GKTNLYAAZKKMTQ-UHFFFAOYSA-N 0.000 claims abstract description 10
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000003054 catalyst Substances 0.000 claims abstract description 9
- 239000003963 antioxidant agent Substances 0.000 claims abstract description 7
- 230000003078 antioxidant effect Effects 0.000 claims abstract description 7
- 238000000576 coating method Methods 0.000 claims description 22
- 239000010410 layer Substances 0.000 claims description 22
- 239000011248 coating agent Substances 0.000 claims description 21
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 15
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical group CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims description 15
- 238000002156 mixing Methods 0.000 claims description 15
- 238000003756 stirring Methods 0.000 claims description 14
- 238000001035 drying Methods 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 7
- 238000010438 heat treatment Methods 0.000 claims description 7
- 239000005543 nano-size silicon particle Substances 0.000 claims description 7
- 229920000178 Acrylic resin Polymers 0.000 claims description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 6
- 238000006243 chemical reaction Methods 0.000 claims description 6
- 239000006185 dispersion Substances 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 238000002360 preparation method Methods 0.000 claims description 6
- 238000005406 washing Methods 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical group CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 claims description 5
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 claims description 5
- KORSJDCBLAPZEQ-UHFFFAOYSA-N dicyclohexylmethane-4,4'-diisocyanate Chemical group C1CC(N=C=O)CCC1CC1CCC(N=C=O)CC1 KORSJDCBLAPZEQ-UHFFFAOYSA-N 0.000 claims description 5
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 claims description 5
- 229920001451 polypropylene glycol Polymers 0.000 claims description 5
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims description 4
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 claims description 4
- 235000011114 ammonium hydroxide Nutrition 0.000 claims description 4
- 238000007865 diluting Methods 0.000 claims description 4
- 238000010790 dilution Methods 0.000 claims description 4
- 239000012895 dilution Substances 0.000 claims description 4
- 238000004321 preservation Methods 0.000 claims description 4
- 235000012239 silicon dioxide Nutrition 0.000 claims description 4
- 239000008367 deionised water Substances 0.000 claims description 3
- 229910021641 deionized water Inorganic materials 0.000 claims description 3
- 239000012153 distilled water Substances 0.000 claims description 3
- 229910052757 nitrogen Inorganic materials 0.000 claims description 3
- 239000011241 protective layer Substances 0.000 claims description 3
- 239000000463 material Substances 0.000 description 8
- 238000005299 abrasion Methods 0.000 description 7
- 239000000126 substance Substances 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- 239000004033 plastic Substances 0.000 description 4
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical group CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 3
- 239000004743 Polypropylene Substances 0.000 description 3
- 238000000227 grinding Methods 0.000 description 3
- 238000004806 packaging method and process Methods 0.000 description 3
- 239000003973 paint Substances 0.000 description 3
- 229920001155 polypropylene Polymers 0.000 description 3
- KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 description 3
- 241000270295 Serpentes Species 0.000 description 2
- 238000006555 catalytic reaction Methods 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 239000002985 plastic film Substances 0.000 description 2
- 229920006255 plastic film Polymers 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 238000007151 ring opening polymerisation reaction Methods 0.000 description 2
- 238000012935 Averaging Methods 0.000 description 1
- AFCARXCZXQIEQB-UHFFFAOYSA-N N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CCNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 AFCARXCZXQIEQB-UHFFFAOYSA-N 0.000 description 1
- 239000002390 adhesive tape Substances 0.000 description 1
- 238000009954 braiding Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 238000009941 weaving Methods 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
- Polyurethanes Or Polyureas (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
Abstract
The invention discloses an anti-skid woven bag which comprises a woven bag layer, wherein an anti-skid layer is coated outside the woven bag layer; the anti-skid layer comprises the following components in parts by weight: acrylate resin: 30-50 parts; polyester polyol: 10-30 parts; antioxidant: 1-2 parts; defoaming agent: 1-2 parts; leveling agent: 1-2 parts; diluent agent: 30-50 parts; catalyst: 0.2-1 part; aliphatic isocyanate: 20-50 parts; accelerator (b): 0.5-5 parts; aminated nano-silica: 5-10 parts; caprolactone: 20-30 parts; phosphazene base: 0.2 to 1 portion. The invention aims to provide an anti-skidding woven bag.
Description
Technical Field
The invention relates to the field of polymers, in particular to an anti-skidding woven bag.
Background
A woven bag is a kind of plastic bag for packing, and is made up of polypropylene (English name pp) as main raw material through extruding out, stretching to become flat filament, weaving, braiding and making bag. The anti-slip woven bag is used for packaging bulk commodities, the bulk commodities are often stacked in practical use, and the polypropylene has poor anti-slip effect, so that the polypropylene is easy to slip, and the anti-slip woven bag is continued.
Disclosure of Invention
Aiming at the defects in the prior art, the invention aims to provide an anti-skidding woven bag.
In order to realize the purpose, the invention provides the following technical scheme:
an anti-skid woven bag, which comprises a woven bag,
the anti-skid woven bag comprises a woven bag layer, wherein an anti-skid layer is coated outside the woven bag layer;
the anti-skid layer comprises the following components in parts by weight:
acrylate resin: 30 to 50 portions of
Polyester polyol: 10 to 30 portions of
Antioxidant: 1 to 2 portions of
Defoaming agent: 1 to 2 portions of
Leveling agent: 1 to 2 portions of
Diluent agent: 30 to 50 portions of
Catalyst: 0.2 to 1 portion
Aliphatic isocyanate: 20 to 50 portions of
Accelerator (b): 0.5 to 5 portions of
Aminated nano-silica: 5 to 10 portions of
Caprolactone: 20 to 30 portions of
Phosphazene base: 0.2 to 1 portion.
As a further improvement of the present invention,
the acrylic resin is ethyl methacrylate.
As a further improvement of the present invention,
the polyester polyol is polypropylene glycol.
As a further improvement of the present invention,
the catalyst is triethylamine.
As a further improvement of the present invention,
the aliphatic isocyanate is dicyclohexylmethane-4, 4' -diisocyanate.
As a further improvement of the present invention,
the diluent is methyl isobutyl ketone.
As a further improvement of the present invention,
the preparation method of the aminated nano silicon dioxide comprises the following steps:
adding 250 parts by volume of absolute ethyl alcohol, 5 parts by volume of deionized water and 15 parts by volume of 28% ammonia water into a flask, preserving heat for 2 hours at 40 ℃, then quickly adding 14 parts by volume of tetraethyl orthosilicate, stirring for 12 hours at 40 ℃, centrifugally separating a product, washing the product with distilled water, then washing with absolute ethyl alcohol, and drying for 24 hours at 110 ℃ to obtain the aminated nano-silicon dioxide.
As a further improvement of the present invention,
the preparation method of the protective layer comprises the following steps:
the method comprises the following steps: mixing aminated nano-silica with toluene to form a dispersion, heating to 80 ℃, stirring and preserving heat for 1h under the protection of nitrogen, then adding caprolactone and phosphazene base into the dispersion to react for 24h, and drying in vacuum to obtain modified nano-silica;
step two: stirring and mixing acrylate resin and polyester polyol, adding a diluent for dilution, adding an antioxidant, a defoaming agent and a flatting agent, and stirring and mixing to obtain a mixture A;
step three: adding aliphatic isocyanate, an accelerator, modified nano-silica and a catalyst into the mixture A for mixing, adding the rest diluent for diluting, heating to 85 ℃, and carrying out heat preservation reaction for 2 hours to obtain the anti-skid layer coating.
The anti-slip coating mainly adopts acrylic resin and polyester polyol as main materials and produces the coating through reaction of aliphatic isocyanate serving as a curing agent, wherein the key point is that modified nano-silica and aminated nano-silica are added and can be subjected to ring-opening polymerization with caprolactone under the catalysis of phosphazene base so as to form a chemical bond with the nano-silica, and then the modified nano-silica and the aminated nano-silica are added into the curing polymerization of the acrylic resin, the polyester polyol and the aliphatic isocyanate so that the silica and the main materials are better combined, and the wear resistance and the anti-slip performance are improved.
Detailed Description
The first embodiment is as follows: preparation of aminated nano-silica
Adding 250 parts by volume of absolute ethyl alcohol, 5 parts by volume of deionized water and 15 parts by volume of ammonia water with the mass fraction of 28%, preserving heat for 2 hours at 40 ℃, then quickly adding 14 parts by volume of tetraethyl orthosilicate, stirring for 12 hours at 40 ℃, centrifugally separating a product, washing the product with distilled water, then washing with absolute ethyl alcohol, and drying for 24 hours at 110 ℃ to obtain the aminated nano-silicon dioxide.
Example two:
an anti-skid woven bag, which comprises a bag body,
the anti-skid woven bag comprises a woven bag layer, wherein an anti-skid layer is coated outside the woven bag layer;
the woven bag layer adopts a commercially available woven bag.
The woven bag is a pp plastic woven snake skin bag of Linyi Naojie packaging Limited company;
the anti-skid layer comprises the following components in parts by weight:
ethyl methacrylate: 40 portions of
Polypropylene glycol ppg-2000:20 portions of
Antioxidant T-501:1 part of
Defoaming agent BYK-070:1 part of
Leveling agent BYK-330:1 part of
Methyl isobutyl ketone: 40 portions of
Triethylamine: 0.5 portion
Dicyclohexylmethane-4, 4' -diisocyanate: 30 portions of
Accelerator stannous octoate: 0.5 part of
Aminated nano-silica: 10 portions of
Caprolactone: 20 portions of
Phosphazene base: 0.2 part
The preparation method of the protective layer comprises the following steps:
the method comprises the following steps: mixing the aminated nano-silica obtained in the first embodiment with toluene (10 g of aminated nano-silica is mixed with 10ml of toluene per se) to form a dispersion, heating to 80 ℃, stirring and preserving heat for 1h under the protection of nitrogen, then adding caprolactone and phosphazene base into the dispersion to react for 24h, and carrying out vacuum drying to obtain modified nano-silica;
step two: stirring and mixing acrylate resin and polyester polyol, adding 30 parts of diluent for dilution, adding an antioxidant, a defoaming agent and a flatting agent, and stirring and mixing to obtain a mixture A;
step three: and adding aliphatic isocyanate, an accelerator, modified nano-silica and a catalyst into the mixture A for mixing, adding the rest 10 parts of diluent for diluting, heating to 85 ℃, and carrying out heat preservation reaction for 2 hours to obtain the anti-skid layer coating.
And coating the coating on the woven surface, and drying for 1h to obtain the woven bag containing the coating.
Comparative example one:
the anti-skid woven bag comprises a woven bag layer, wherein an anti-skid layer is coated outside the woven bag layer;
the woven bag layer adopts a commercially available woven bag.
The woven bag is a pp plastic woven snake skin bag of Linyi Naojie packaging company Limited;
the anti-slip layer comprises the following components in parts by weight:
ethyl methacrylate: 40 portions of
Polypropylene glycol ppg-2000:20 portions of
Antioxidant T-501:1 part of
Defoaming agent BYK-070:1 part of
Leveling agent BYK-330:1 part of
Methyl isobutyl ketone: 40 portions of
Triethylamine: 0.5 portion
Dicyclohexylmethane-4, 4' -diisocyanate: 30 portions of
Accelerator stannous octoate: 0.5 portion
Commercially available nano-silica: 10 portions of
The method comprises the following steps: stirring and mixing acrylate resin and polyester polyol, adding a diluent for dilution, adding an antioxidant, a defoaming agent and a flatting agent, and stirring and mixing to obtain a mixture A;
step two: and adding aliphatic isocyanate, an accelerator, commercially available nano silicon dioxide and a catalyst into the mixture A for mixing, adding the rest diluent for diluting, heating to 85 ℃, and carrying out heat preservation reaction for 2 hours to obtain the anti-skid layer coating.
And (3) coating the coating on the woven surface, and drying for 1h to obtain the woven bag containing the coating.
Raw material table:
| anhydrous ethanol | SHANGHAI ALADDIN BIOCHEMICAL TECHNOLOGY Co.,Ltd. |
| Tetraethyl orthosilicate | Shanghai Mirui Biochemical technology Ltd |
| Ammonia water | SHANGHAI ALADDIN BIOCHEMICAL TECHNOLOGY Co.,Ltd. |
| Methacrylic acid ethyl ester | SHANGHAI ALADDIN BIOCHEMICAL TECHNOLOGY Co.,Ltd. |
| Polypropylene glycol ppg-2000 | Zhengzhou Jinnuo chemical products Co Ltd |
| Antioxidant T-501 | Shijiazhuang Ruitong chemical technology Co Ltd |
| Defoaming agent BYK-070 | German Bike chemical |
| Leveling agent BYK-330 | German Bick chemistry |
| Methyl isobutyl ketone | Jiangsu plerian Biotechnology Ltd |
| Triethylamine | Nantong Runfeng petrochemical Co., ltd |
| Dicyclohexylmethane-4, 4' -diisocyanate | SHANGHAI ALADDIN BIOCHEMICAL TECHNOLOGY Co.,Ltd. |
| Stannous octoate | SHANGHAI ALADDIN BIOCHEMICAL TECHNOLOGY Co.,Ltd. |
| Epsilon-caprolactone | SHANGHAI YUANYE BIOTECHNOLOGY Co.,Ltd. |
| Phosphazene bases | Sigma Aldrich trade company |
| Toluene | SHANGHAI ALADDIN BIOCHEMICAL TECHNOLOGY Co.,Ltd. |
| Nano silicon dioxide | Shanghai Jizhi Biochemical Technology Co.,Ltd. |
The coatings obtained in example two and comparative example one were tested:
test 1: the flexibility of the paint films was tested according to GB/T1731-93 using a flexibility tester.
And (3) testing 2: according to GB/T1720-89, the adhesion force of a paint film is tested by a circle forming method
And (3) testing: the test was carried out by the rubber grinding wheel method according to the national standard GB/T1768-89, and the measurement was carried out using a wear meter model JM-3. The sample is cut into 10 x 10cm, fixed on the rotatable base of the abrasion instrument according to requirements, and the rubber grinding wheel is pressed well with the surface of the coating. When the load capacity is 1 multiplied by 10 Fahrenheit, the sample plate is rotated according to the specified rotating speed, and the grinding is stopped after 100 revolutions. And weighing the weight of the sample plate before and after abrasion by using an analytical balance, wherein the difference value is the abrasion loss.
And (4) testing: coating the paint on the surface of plastic, drying for later use, cutting the coated plastic film into samples slightly larger than 63mm × 63mm (the size of a small slide block) and 80mm × 200mm, fixing the samples on the small slide block and a sliding plate by using double-sided adhesive tapes respectively, measuring the friction coefficient of the contact surface of the plastic film by using a friction coefficient tester, measuring each sample for three times on average, and then averaging.
| Flexibility/mm | Adhesion/grade | Abrasion loss per gram | Coefficient of friction | |
| Example two | 2 | 2 | 0.0325 | 0.942 |
| Comparative example 1 | 2 | 2 | 0.0742 | 0.627 |
From the test results, the coating material prepared in example two has substantially the same flexibility and adhesion as the coating material prepared in comparative example one, and it can be seen in the amount of abrasion that the amount of abrasion is greatly reduced after the nano-silica is modified, which indicates that the coating material prepared in example two has better durability because the nano-silica forms more stable chemical bonds with the whole coating material after being modified, and has better abrasion resistance than the nano-silica without modification. Of the coefficients of friction, the same example also had a better coefficient of friction than the comparative example one.
The core of the anti-slip coating is the anti-slip coating, the anti-slip coating is mainly produced by using acrylic resin and polyester polyol as main materials and using aliphatic isocyanate as a curing agent for reaction, wherein the key point is that modified nano-silica is added, aminated nano-silica can be subjected to ring-opening polymerization with caprolactone under the catalysis of phosphazene base so as to form a chemical bond with the nano-silica, and then the nano-silica is added into the curing polymerization of the acrylic resin, the polyester polyol and the aliphatic isocyanate so that the silica and the main materials are better combined, and the wear resistance and the anti-slip performance are improved.
The above description is only a preferred embodiment of the present invention, and the protection scope of the present invention is not limited to the above embodiments, and all technical solutions belonging to the idea of the present invention belong to the protection scope of the present invention. It should be noted that modifications and embellishments within the scope of the invention may occur to those skilled in the art without departing from the principle of the invention, and are considered to be within the scope of the invention.
Claims (8)
1. An antiskid braided bag which characterized in that:
the anti-skid woven bag comprises a woven bag layer, wherein an anti-skid layer is coated outside the woven bag layer;
the anti-slip layer comprises the following components in parts by weight:
acrylate resin: 30 to 50 portions of
Polyester polyol: 10 to 30 portions of
Antioxidant: 1 to 2 portions of
Defoaming agent: 1 to 2 portions of
Leveling agent: 1 to 2 portions of
Diluent agent: 30 to 50 portions of
Catalyst: 0.2 to 1 portion
Aliphatic isocyanate: 20 to 50 portions of
Accelerator (b): 0.5 to 5 portions of
Aminated nano-silica: 5 to 10 portions of
Caprolactone: 20 to 30 portions of
Phosphazene base: 0.2 to 1 portion.
2. The antiskid woven bag according to claim 1, wherein:
the acrylic resin is ethyl methacrylate.
3. The non-slip woven bag according to claim 1, wherein:
the polyester polyol is polypropylene glycol.
4. The antiskid woven bag according to claim 1, wherein:
the catalyst is triethylamine.
5. The antiskid woven bag according to claim 1, wherein:
the aliphatic isocyanate is dicyclohexylmethane-4, 4' -diisocyanate.
6. The antiskid woven bag according to claim 1, wherein:
the diluent is methyl isobutyl ketone.
7. The antiskid woven bag according to claim 1, wherein:
the preparation method of the aminated nano silicon dioxide comprises the following steps:
adding 250 parts by volume of absolute ethyl alcohol, 5 parts by volume of deionized water and 15 parts by volume of 28% ammonia water into a flask, preserving heat for 2 hours at 40 ℃, then quickly adding 14 parts by volume of tetraethyl orthosilicate, stirring for 12 hours at 40 ℃, centrifugally separating a product, washing the product with distilled water, then washing with absolute ethyl alcohol, and drying for 24 hours at 110 ℃ to obtain the aminated nano-silicon dioxide.
8. The antiskid woven bag according to claim 1, wherein:
the preparation method of the protective layer comprises the following steps:
the method comprises the following steps: mixing aminated nano-silica with toluene to form a dispersion, heating to 80 ℃, stirring and preserving heat for 1h under the protection of nitrogen, then adding caprolactone and phosphazene base into the dispersion to react for 24h, and drying in vacuum to obtain modified nano-silica;
step two: stirring and mixing acrylate resin and polyester polyol, adding a diluent for dilution, adding an antioxidant, a defoaming agent and a flatting agent, and stirring and mixing to obtain a mixture A;
step three: and adding aliphatic isocyanate, an accelerator, modified nano-silica and a catalyst into the mixture A for mixing, adding the rest diluent for diluting, heating to 85 ℃, and carrying out heat preservation reaction for 2 hours to obtain the anti-skid layer coating.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202211689252.0A CN115975235A (en) | 2022-12-23 | 2022-12-23 | Anti-slip woven bag |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202211689252.0A CN115975235A (en) | 2022-12-23 | 2022-12-23 | Anti-slip woven bag |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN115975235A true CN115975235A (en) | 2023-04-18 |
Family
ID=85964432
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN202211689252.0A Pending CN115975235A (en) | 2022-12-23 | 2022-12-23 | Anti-slip woven bag |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN115975235A (en) |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20130261209A1 (en) * | 2011-02-14 | 2013-10-03 | Lg Chem Ltd | Uv-curable coating compositions with self-healing capabilities, coating films, and methods of producing coating films |
| CN103421167A (en) * | 2013-07-08 | 2013-12-04 | 常州大学 | One-step synthetic method of degradable branched polyester |
| CN108929455A (en) * | 2018-07-26 | 2018-12-04 | 枣阳市华星纺织有限公司 | A kind of manufacturing method of wear-resisting antiskid Polywoven Bag |
| CN113308174A (en) * | 2021-07-05 | 2021-08-27 | 安徽大学 | Dual-modified waterborne epoxy resin anticorrosive paint and preparation method thereof |
| CN114106683A (en) * | 2021-12-01 | 2022-03-01 | 安徽瑞联节能科技股份有限公司 | Waterproof and heat-insulating integrated material and production process thereof |
| CN114262560A (en) * | 2021-11-12 | 2022-04-01 | 海洋化工研究院有限公司 | Light corrosion-resistant anti-slip coating and construction method thereof |
| CN115011215A (en) * | 2022-04-26 | 2022-09-06 | 江西鼎春建设工程有限公司 | Functionalized silicon dioxide toughened epoxy resin coating and preparation method thereof |
-
2022
- 2022-12-23 CN CN202211689252.0A patent/CN115975235A/en active Pending
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20130261209A1 (en) * | 2011-02-14 | 2013-10-03 | Lg Chem Ltd | Uv-curable coating compositions with self-healing capabilities, coating films, and methods of producing coating films |
| CN103421167A (en) * | 2013-07-08 | 2013-12-04 | 常州大学 | One-step synthetic method of degradable branched polyester |
| CN108929455A (en) * | 2018-07-26 | 2018-12-04 | 枣阳市华星纺织有限公司 | A kind of manufacturing method of wear-resisting antiskid Polywoven Bag |
| CN113308174A (en) * | 2021-07-05 | 2021-08-27 | 安徽大学 | Dual-modified waterborne epoxy resin anticorrosive paint and preparation method thereof |
| CN114262560A (en) * | 2021-11-12 | 2022-04-01 | 海洋化工研究院有限公司 | Light corrosion-resistant anti-slip coating and construction method thereof |
| CN114106683A (en) * | 2021-12-01 | 2022-03-01 | 安徽瑞联节能科技股份有限公司 | Waterproof and heat-insulating integrated material and production process thereof |
| CN115011215A (en) * | 2022-04-26 | 2022-09-06 | 江西鼎春建设工程有限公司 | Functionalized silicon dioxide toughened epoxy resin coating and preparation method thereof |
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