CN117924855A - Breathable black mask for automobile and preparation method thereof - Google Patents
Breathable black mask for automobile and preparation method thereof Download PDFInfo
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- CN117924855A CN117924855A CN202410338073.5A CN202410338073A CN117924855A CN 117924855 A CN117924855 A CN 117924855A CN 202410338073 A CN202410338073 A CN 202410338073A CN 117924855 A CN117924855 A CN 117924855A
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- breathable
- zinc oxide
- diatomite
- black mask
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- 238000002360 preparation method Methods 0.000 title claims abstract description 21
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims abstract description 108
- 239000011787 zinc oxide Substances 0.000 claims abstract description 54
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 49
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 42
- 239000004594 Masterbatch (MB) Substances 0.000 claims abstract description 20
- 239000004014 plasticizer Substances 0.000 claims abstract description 18
- 239000002994 raw material Substances 0.000 claims abstract description 16
- 239000006087 Silane Coupling Agent Substances 0.000 claims abstract description 13
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 claims abstract description 13
- 235000013539 calcium stearate Nutrition 0.000 claims abstract description 13
- 239000008116 calcium stearate Substances 0.000 claims abstract description 13
- 239000006229 carbon black Substances 0.000 claims abstract description 13
- 238000003756 stirring Methods 0.000 claims description 42
- 238000011282 treatment Methods 0.000 claims description 22
- 238000001035 drying Methods 0.000 claims description 21
- 238000005406 washing Methods 0.000 claims description 21
- 238000002156 mixing Methods 0.000 claims description 18
- 239000007788 liquid Substances 0.000 claims description 17
- 229920001661 Chitosan Polymers 0.000 claims description 15
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 14
- FYDKNKUEBJQCCN-UHFFFAOYSA-N lanthanum(3+);trinitrate Chemical compound [La+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O FYDKNKUEBJQCCN-UHFFFAOYSA-N 0.000 claims description 13
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical group CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 claims description 12
- 238000001125 extrusion Methods 0.000 claims description 12
- 238000010438 heat treatment Methods 0.000 claims description 12
- 238000001132 ultrasonic dispersion Methods 0.000 claims description 12
- SIWVEOZUMHYXCS-UHFFFAOYSA-N oxo(oxoyttriooxy)yttrium Chemical compound O=[Y]O[Y]=O SIWVEOZUMHYXCS-UHFFFAOYSA-N 0.000 claims description 9
- 238000001816 cooling Methods 0.000 claims description 7
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 claims description 7
- 230000004048 modification Effects 0.000 claims description 7
- 238000012986 modification Methods 0.000 claims description 7
- 239000012286 potassium permanganate Substances 0.000 claims description 7
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 6
- 238000002715 modification method Methods 0.000 claims description 6
- 239000001509 sodium citrate Substances 0.000 claims description 6
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 claims description 6
- 238000009210 therapy by ultrasound Methods 0.000 claims description 6
- 239000012856 weighed raw material Substances 0.000 claims description 6
- 238000005303 weighing Methods 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
- 239000005909 Kieselgur Substances 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims 1
- 230000002195 synergetic effect Effects 0.000 abstract description 2
- 230000000052 comparative effect Effects 0.000 description 8
- 230000035699 permeability Effects 0.000 description 5
- 230000003138 coordinated effect Effects 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 230000006866 deterioration Effects 0.000 description 3
- 230000006872 improvement Effects 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000005034 decoration Methods 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- RNWHGQJWIACOKP-UHFFFAOYSA-N zinc;oxygen(2-) Chemical class [O-2].[Zn+2] RNWHGQJWIACOKP-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/18—Manufacture of films or sheets
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2327/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers
- C08J2327/02—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers not modified by chemical after-treatment
- C08J2327/04—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
- C08J2327/06—Homopolymers or copolymers of vinyl chloride
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2475/00—Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
- C08J2475/04—Polyurethanes
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- 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
- C08K13/00—Use of mixtures of ingredients not covered by one single of the preceding main groups, each of these compounds being essential
- C08K13/06—Pretreated ingredients and ingredients covered by the main groups C08K3/00 - C08K7/00
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- 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
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K2003/2296—Oxides; Hydroxides of metals of zinc
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- 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
- C08K2201/00—Specific properties of additives
- C08K2201/011—Nanostructured additives
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- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/02—Elements
- C08K3/04—Carbon
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- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
- C08K5/098—Metal salts of carboxylic acids
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- C08K5/10—Esters; Ether-esters
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- C08K7/00—Use of ingredients characterised by shape
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Abstract
The invention relates to the technical field of automobile films, and in particular discloses a breathable black mask for an automobile and a preparation method thereof, wherein the breathable black mask comprises the following raw materials in parts by weight: 25-30 parts of PVC master batch, 15-20 parts of TPU master batch, 2-5 parts of plasticizer, 1-3 parts of calcium stearate, 2-5 parts of carbon black, 5-10 parts of modified nano zinc oxide, 4-7 parts of diatomite agent and 1-2 parts of silane coupling agent KH 560. According to the breathable black shielding film, PVC master batches, TPU master batches, plasticizers, calcium stearate, carbon black and a silane coupling agent KH560 are adopted, modified nano zinc oxide and diatomite agents are added, and the PVC master batches, the TPU master batches, the calcium stearate, the carbon black and the silane coupling agent KH560 are matched and synergistic together, so that the breathability, the glossiness and the scratch resistance of the obtained product can be improved in a coordinated manner.
Description
Technical Field
The invention relates to the technical field of automobile films, in particular to a breathable black shielding film for an automobile and a preparation method thereof.
Background
The black film is also called as black shielding film, belongs to one kind of functional automobile film, is used in the inner and outer frames, driving window, automobile body, etc. of automobile to replace paint for decoration, and may be used in expanding the vision of automobile window and driving window. In order to improve the air permeability of the product, the traditional black mask is easy to cause the reduction of the glossiness and scratch resistance of the product, and the performance coordination improvement of the product is difficult to realize, so that the use efficiency of the product is limited.
Disclosure of Invention
In view of the drawbacks of the prior art, an object of the present invention is to provide a breathable black mask for an automobile and a method for preparing the same, so as to solve the problems set forth in the background art.
The invention solves the technical problems by adopting the following technical scheme:
the invention provides a breathable black mask for an automobile, which comprises the following raw materials in parts by weight:
25-30 parts of PVC master batch, 15-20 parts of TPU master batch, 2-5 parts of plasticizer, 1-3 parts of calcium stearate, 2-5 parts of carbon black, 5-10 parts of modified nano zinc oxide, 4-7 parts of diatomite agent and 1-2 parts of silane coupling agent KH 560.
Preferably, the breathable black mask for automobiles comprises the following raw materials in parts by weight:
27.5 parts of PVC master batch, 17.5 parts of TPU master batch, 3.5 parts of plasticizer, 2 parts of calcium stearate, 3.5 parts of carbon black, 7.5 parts of modified nano zinc oxide, 5.5 parts of diatomite agent and 1-2 parts of silane coupling agent KH 560.
Preferably, the plasticizer is di (2-ethylhexyl) phthalate;
Preferably, the modification method of the modified nano zinc oxide comprises the following steps:
S101: the nano zinc oxide is irradiated for 10 to 15 minutes in a proton irradiation box, and then is stirred and mixed uniformly in a sufficient amount of 10 percent potassium permanganate solution, and finally, the zinc oxide agent is obtained after water washing and drying;
S102: adding 3-5 parts of chitosan solution and 1-3 parts of sodium dodecyl benzene sulfonate into 7-10 parts of lanthanum nitrate solution, then adding 1-3 parts of yttrium oxide, and stirring and mixing uniformly to obtain a modified liquid;
S103: and (3) stirring and modifying the zinc oxide agent and the modifying liquid according to the weight ratio of 2:5, and washing and drying after stirring is finished to obtain the modified nano zinc oxide.
Preferably, the irradiation power is 350-400W.
Preferably, the mass fraction of the chitosan solution is 4-7%; the mass fraction of the lanthanum nitrate solution is 2-5%.
Preferably, the stirring temperature of the stirring modification treatment is 48-52 ℃, the stirring rotation speed is 450-500r/min, and the stirring time is 35-40min.
Preferably, the preparation method of the diatomite agent comprises the following steps:
S11: fully mixing diatomite in a sufficient amount of hydrochloric acid solution with the mass fraction of 2%, and finally washing and drying;
S12: then heating to 150-160 ℃ at a speed of 1-3 ℃/min, preserving heat for 2-5min, then heating to 320-330 ℃ at a speed of 2-5 ℃/min, preserving heat for 5-10min, and finally air-cooling to room temperature for standby;
S13: and adding the standby diatomite into a sufficient amount of sodium citrate solution with the mass fraction of 10% for ultrasonic dispersion treatment, and washing and drying after ultrasonic treatment to obtain the diatomite agent.
Preferably, the ultrasonic power of the ultrasonic dispersion treatment is 300-350W, and the ultrasonic time is 20-30min.
The invention also provides a preparation method of the breathable black mask for the automobile, which comprises the following steps:
Weighing raw materials according to parts by weight, sequentially and fully mixing the weighed raw materials, then adding the mixture into a double-screw extruder for extrusion, wherein the extrusion temperature is 155-165 ℃, and thus the breathable black mask is obtained.
Compared with the prior art, the invention has the following beneficial effects:
According to the breathable black shielding film disclosed by the invention, PVC master batches, TPU master batches are matched with plasticizers, calcium stearate, carbon black and silane coupling agents KH560, modified nano zinc oxide and diatomite agents are added to realize coordinated improvement on breathability, glossiness and scratch resistance of the obtained product, the nano zinc oxide is treated by proton irradiation and potassium permanganate solution, the activity efficiency of the nano zinc oxide is optimized, chitosan solution, sodium dodecyl benzene sulfonate, lanthanum nitrate solution and yttrium oxide are mutually blended, the modified liquid obtained by the coordinated improvement on the nano zinc oxide, so that the overall performance stability of the system is enhanced in a distribution system, the surface glossiness of the system is optimized, the diatomite agents are heated to 150-160 ℃ by adopting hydrochloric acid solution and a combined 1-3 ℃/min rate, the temperature is kept for 2-5min, then the temperature is raised to 320-330 ℃ by adopting the combined 1-3 ℃/min rate, the temperature is kept for 5-10min, and finally the air cooling is carried out to room temperature by adopting a series of process treatment, so that the synergistic effect of the diatomite agents and the modified zinc oxide is optimized, and the coordinated effect of the product on the glossiness and the scratch resistance is further enhanced.
Detailed Description
The following description of the embodiments of the present invention will be made clearly and fully with reference to the accompanying drawings, in which it is evident that the embodiments described are only some, but not all embodiments of the invention. All other embodiments, which can be made by those skilled in the art based on the embodiments of the invention without making any inventive effort, are intended to be within the scope of the invention.
The breathable black mask for the automobile comprises the following raw materials in parts by weight:
25-30 parts of PVC master batch, 15-20 parts of TPU master batch, 2-5 parts of plasticizer, 1-3 parts of calcium stearate, 2-5 parts of carbon black, 5-10 parts of modified nano zinc oxide, 4-7 parts of diatomite agent and 1-2 parts of silane coupling agent KH 560.
The breathable black mask for automobiles of the embodiment comprises the following raw materials in parts by weight:
27.5 parts of PVC master batch, 17.5 parts of TPU master batch, 3.5 parts of plasticizer, 2 parts of calcium stearate, 3.5 parts of carbon black, 7.5 parts of modified nano zinc oxide, 5.5 parts of diatomite agent and 1-2 parts of silane coupling agent KH 560.
The plasticizer of this example is di (2-ethylhexyl) phthalate;
The modification method of the modified nano zinc oxide in the embodiment comprises the following steps:
S101: the nano zinc oxide is irradiated for 10 to 15 minutes in a proton irradiation box, and then is stirred and mixed uniformly in a sufficient amount of 10 percent potassium permanganate solution, and finally, the zinc oxide agent is obtained after water washing and drying;
S102: adding 3-5 parts of chitosan solution and 1-3 parts of sodium dodecyl benzene sulfonate into 7-10 parts of lanthanum nitrate solution, then adding 1-3 parts of yttrium oxide, and stirring and mixing uniformly to obtain a modified liquid;
S103: and (3) stirring and modifying the zinc oxide agent and the modifying liquid according to the weight ratio of 2:5, and washing and drying after stirring is finished to obtain the modified nano zinc oxide.
The irradiation power of this example was 350-400W.
The mass fraction of the chitosan solution in the embodiment is 4-7%; the mass fraction of the lanthanum nitrate solution is 2-5%.
Preferably, the stirring temperature of the stirring modification treatment is 48-52 ℃, the stirring rotation speed is 450-500r/min, and the stirring time is 35-40min.
The preparation method of the diatomite agent in the embodiment comprises the following steps:
S11: fully mixing diatomite in a sufficient amount of hydrochloric acid solution with the mass fraction of 2%, and finally washing and drying;
S12: then heating to 150-160 ℃ at a speed of 1-3 ℃/min, preserving heat for 2-5min, then heating to 320-330 ℃ at a speed of 2-5 ℃/min, preserving heat for 5-10min, and finally air-cooling to room temperature for standby;
S13: and adding the standby diatomite into a sufficient amount of sodium citrate solution with the mass fraction of 10% for ultrasonic dispersion treatment, and washing and drying after ultrasonic treatment to obtain the diatomite agent.
The ultrasonic power of the ultrasonic dispersion treatment of the embodiment is 300-350W, and the ultrasonic time is 20-30min.
The preparation method of the breathable black mask for the automobile comprises the following steps:
Weighing raw materials according to parts by weight, sequentially and fully mixing the weighed raw materials, then adding the mixture into a double-screw extruder for extrusion, wherein the extrusion temperature is 155-165 ℃, and thus the breathable black mask is obtained.
Example 1
The breathable black mask for the automobile comprises the following raw materials in parts by weight:
25 parts of PVC master batch, 15 parts of TPU master batch, 2 parts of plasticizer, 1 part of calcium stearate, 2 parts of carbon black, 5 parts of modified nano zinc oxide, 4 parts of diatomite agent and 1 part of silane coupling agent KH 560.
The plasticizer of this example is di (2-ethylhexyl) phthalate;
The modification method of the modified nano zinc oxide in the embodiment comprises the following steps:
S101: the nano zinc oxide is firstly irradiated for 10min in a proton irradiation box, then is stirred and mixed uniformly in a sufficient amount of potassium permanganate solution with the mass fraction of 10%, and finally is washed with water and dried to obtain a zinc oxide agent;
S102: adding 3 parts of chitosan solution and 1 part of sodium dodecyl benzene sulfonate into 7 parts of lanthanum nitrate solution, then adding 1 part of yttrium oxide, and stirring and mixing uniformly to obtain a modified liquid;
S103: and (3) stirring and modifying the zinc oxide agent and the modifying liquid according to the weight ratio of 2:5, and washing and drying after stirring is finished to obtain the modified nano zinc oxide.
The irradiation power of this example was 350W.
The mass fraction of the chitosan solution of this example was 4%; the mass fraction of the lanthanum nitrate solution is 2%.
The stirring temperature for the stirring modification treatment in this example was 48℃and the stirring speed was 450r/min, and the stirring time was 35min.
The preparation method of the diatomite agent in the embodiment comprises the following steps:
S11: fully mixing diatomite in a sufficient amount of hydrochloric acid solution with the mass fraction of 2%, and finally washing and drying;
S12: then heating to 150 ℃ at a speed of 1 ℃/min, preserving heat for 2min, heating to 320 ℃ at a speed of 2 ℃/min, preserving heat for 5min, and finally air-cooling to room temperature for later use;
S13: and adding the standby diatomite into a sufficient amount of sodium citrate solution with the mass fraction of 10% for ultrasonic dispersion treatment, and washing and drying after ultrasonic treatment to obtain the diatomite agent.
The ultrasonic power of the ultrasonic dispersion treatment in this embodiment was 300W, and the ultrasonic time was 20min.
The preparation method of the breathable black mask for the automobile comprises the following steps:
Weighing raw materials according to parts by weight, sequentially and fully mixing the weighed raw materials, then adding the mixture into a double-screw extruder for extrusion, wherein the extrusion temperature is 155 ℃, and obtaining the breathable black mask.
Example 2
The breathable black mask for the automobile comprises the following raw materials in parts by weight:
30 parts of PVC master batch, 20 parts of TPU master batch, 5 parts of plasticizer, 3 parts of calcium stearate, 5 parts of carbon black, 10 parts of modified nano zinc oxide, 7 parts of diatomite agent and 2 parts of silane coupling agent KH 560.
The plasticizer of this example is di (2-ethylhexyl) phthalate;
The modification method of the modified nano zinc oxide in the embodiment comprises the following steps:
S101: the nano zinc oxide is irradiated for 15min in a proton irradiation box, and then is stirred and mixed uniformly in a sufficient amount of potassium permanganate solution with the mass fraction of 10%, and finally is washed with water and dried to obtain a zinc oxide agent;
S102: adding 5 parts of chitosan solution and 3 parts of sodium dodecyl benzene sulfonate into 10 parts of lanthanum nitrate solution, then adding 3 parts of yttrium oxide, and stirring and mixing uniformly to obtain a modified liquid;
S103: and (3) stirring and modifying the zinc oxide agent and the modifying liquid according to the weight ratio of 2:5, and washing and drying after stirring is finished to obtain the modified nano zinc oxide.
The irradiation power of this example was 400W.
The mass fraction of the chitosan solution of this example was 7%; the mass fraction of the lanthanum nitrate solution is 5%.
The stirring temperature for the stirring modification treatment in this example was 52℃and the stirring speed was 500r/min, and the stirring time was 40min.
The preparation method of the diatomite agent in the embodiment comprises the following steps:
S11: fully mixing diatomite in a sufficient amount of hydrochloric acid solution with the mass fraction of 2%, and finally washing and drying;
S12: then heating to 160 ℃ at the speed of 3 ℃/min, preserving heat for 5min, heating to 330 ℃ at the speed of 5 ℃/min, preserving heat for 10min, and finally air-cooling to room temperature for later use;
S13: and adding the standby diatomite into a sufficient amount of sodium citrate solution with the mass fraction of 10% for ultrasonic dispersion treatment, and washing and drying after ultrasonic treatment to obtain the diatomite agent.
The ultrasonic power of the ultrasonic dispersion treatment in this embodiment was 350W and the ultrasonic time was 30min.
The preparation method of the breathable black mask for the automobile comprises the following steps:
Weighing raw materials according to parts by weight, sequentially and fully mixing the weighed raw materials, then adding the mixture into a double-screw extruder for extrusion, wherein the extrusion temperature is 165 ℃, and obtaining the breathable black mask.
Example 3
The breathable black mask for the automobile comprises the following raw materials in parts by weight:
27.5 parts of PVC master batch, 17.5 parts of TPU master batch, 3.5 parts of plasticizer, 2 parts of calcium stearate, 3.5 parts of carbon black, 7.5 parts of modified nano zinc oxide, 5.5 parts of diatomite agent and 1-2 parts of silane coupling agent KH 560.
The plasticizer of this example is di (2-ethylhexyl) phthalate;
The modification method of the modified nano zinc oxide in the embodiment comprises the following steps:
S101: the nano zinc oxide is irradiated for 12 minutes in a proton irradiation box, then is stirred and mixed uniformly in a sufficient amount of 10% potassium permanganate solution, and finally is washed and dried to obtain a zinc oxide agent;
s102: adding 4 parts of chitosan solution and 2 parts of sodium dodecyl benzene sulfonate into 8.5 parts of lanthanum nitrate solution, then adding 2 parts of yttrium oxide, and stirring and mixing uniformly to obtain a modified liquid;
S103: and (3) stirring and modifying the zinc oxide agent and the modifying liquid according to the weight ratio of 2:5, and washing and drying after stirring is finished to obtain the modified nano zinc oxide.
The irradiation power of this example was 370W.
The mass fraction of the chitosan solution of the embodiment is 5.5%; the mass fraction of the lanthanum nitrate solution is 3.5%.
The stirring temperature for the stirring modification treatment in this example was 50℃and the stirring speed was 4700r/min, and the stirring time was 37min.
The preparation method of the diatomite agent in the embodiment comprises the following steps:
S11: fully mixing diatomite in a sufficient amount of hydrochloric acid solution with the mass fraction of 2%, and finally washing and drying;
S12: then heating to 155 ℃ at the speed of 2 ℃/min, preserving heat for 3.5min, then heating to 325 ℃ at the speed of 3.5 ℃/min, preserving heat for 7.5min, and finally air-cooling to room temperature for later use;
S13: and adding the standby diatomite into a sufficient amount of sodium citrate solution with the mass fraction of 10% for ultrasonic dispersion treatment, and washing and drying after ultrasonic treatment to obtain the diatomite agent.
The ultrasonic power of the ultrasonic dispersion treatment in this example was 325W and the ultrasonic time was 25min.
The preparation method of the breathable black mask for the automobile comprises the following steps:
Weighing raw materials according to parts by weight, sequentially and fully mixing the weighed raw materials, then adding the mixture into a double-screw extruder for extrusion, wherein the extrusion temperature is 160 ℃, and obtaining the breathable black mask.
Comparative example 1.
The difference from example 3 is that no modified nano zinc oxide was added.
Comparative example 2.
The difference from example 3 is that the modified nano zinc oxide is replaced with nano zinc oxide.
Comparative example 3.
The difference from example 3 is that no modification liquid treatment is used in the preparation of the modified nano zinc oxide.
Comparative example 4.
The difference from example 3 is that yttrium oxide and chitosan solution are not added in the preparation of the modified liquid.
Comparative example 5.
The difference from example 3 is that no diatomite agent was added.
Comparative example 6.
The difference from example 3 is that the diatomaceous earth preparation was not treated with the step S12.
The products of examples 1-3 and comparative examples 1-6 were tested for performance, gloss according to GB/T8807 standard, moisture permeability was measured using a moisture permeameter, and the products were scratched 50 times, scratch stability was measured, and the test results are shown in Table 1;
Table 1, gloss, moisture permeability test table:
As can be seen from comparative examples 1 to 6 and examples 1 to 3; the glossiness and moisture permeability of the product can be improved in a coordinated manner, and the scratch resistance and stability effects of the product are obvious;
According to the invention, one of modified nano zinc oxide and diatomite agent is not added, the product has a trend of deterioration in glossiness and moisture permeability, meanwhile, the scratch resistance and stability effects of the product are a trend of deterioration, the modified nano zinc oxide is replaced by nano zinc oxide, modified liquid treatment is not adopted in the preparation of the modified nano zinc oxide, yttrium oxide, chitosan solution and diatomite agent are not added in the preparation of the modified liquid, S12 step treatment is not adopted in the preparation of the diatomite agent, the product has a trend of deterioration in performance, and the modified nano zinc oxide and diatomite agent prepared by the method have the most remarkable performance effects.
It will be evident to those skilled in the art that the invention is not limited to the details of the foregoing illustrative embodiments, and that the present invention may be embodied in other specific forms without departing from the spirit or essential characteristics thereof. The present embodiments are, therefore, to be considered in all respects as illustrative and not restrictive, the scope of the invention being indicated by the appended claims rather than by the foregoing description, and all changes which come within the meaning and range of equivalency of the claims are therefore intended to be embraced therein.
Furthermore, it should be understood that although the present disclosure describes embodiments, not every embodiment is provided with a separate embodiment, and that this description is provided for clarity only, and that the disclosure is not limited to the embodiments described in detail below, and that the embodiments described in the examples may be combined as appropriate to form other embodiments that will be apparent to those skilled in the art.
Claims (9)
1. The breathable black shielding film for the automobile is characterized by comprising the following raw materials in parts by weight:
25-30 parts of PVC master batch, 15-20 parts of TPU master batch, 2-5 parts of plasticizer, 1-3 parts of calcium stearate, 2-5 parts of carbon black, 5-10 parts of modified nano zinc oxide, 4-7 parts of diatomite agent and 1-2 parts of silane coupling agent KH 560; the modification method of the modified nano zinc oxide comprises the following steps:
S101: the nano zinc oxide is irradiated for 10 to 15 minutes in a proton irradiation box, and then is stirred and mixed uniformly in a sufficient amount of 10 percent potassium permanganate solution, and finally, the zinc oxide agent is obtained after water washing and drying;
S102: adding 3-5 parts of chitosan solution and 1-3 parts of sodium dodecyl benzene sulfonate into 7-10 parts of lanthanum nitrate solution, then adding 1-3 parts of yttrium oxide, and stirring and mixing uniformly to obtain a modified liquid;
S103: and (3) stirring and modifying the zinc oxide agent and the modifying liquid according to the weight ratio of 2:5, and washing and drying after stirring is finished to obtain the modified nano zinc oxide.
2. The breathable black mask for automobiles according to claim 1, wherein the breathable black mask for automobiles comprises the following raw materials in parts by weight:
27.5 parts of PVC master batch, 17.5 parts of TPU master batch, 3.5 parts of plasticizer, 2 parts of calcium stearate, 3.5 parts of carbon black, 7.5 parts of modified nano zinc oxide, 5.5 parts of diatomite agent and 1-2 parts of silane coupling agent KH 560.
3. A breathable black mask for automobiles according to claim 1, wherein the plasticizer is di (2-ethylhexyl) phthalate.
4. A breathable black mask for automobiles according to claim 1, wherein the irradiation power is 350 to 400W.
5. A breathable blackout film for automobiles according to claim 1, wherein the mass fraction of the chitosan solution is 4-7%; the mass fraction of the lanthanum nitrate solution is 2-5%.
6. The breathable black mask for automobiles according to claim 1, wherein the stirring temperature of the stirring modification treatment is 48-52 ℃, the stirring speed is 450-500r/min, and the stirring time is 35-40min.
7. The breathable black mask for automobiles according to claim 1, wherein the diatomaceous earth preparation method comprises:
S11: fully mixing diatomite in a sufficient amount of hydrochloric acid solution with the mass fraction of 2%, and finally washing and drying;
S12: then heating to 150-160 ℃ at a speed of 1-3 ℃/min, preserving heat for 2-5min, then heating to 320-330 ℃ at a speed of 2-5 ℃/min, preserving heat for 5-10min, and finally air-cooling to room temperature for standby;
S13: and adding the standby diatomite into a sufficient amount of sodium citrate solution with the mass fraction of 10% for ultrasonic dispersion treatment, and washing and drying after ultrasonic treatment to obtain the diatomite agent.
8. The breathable black mask for automobiles according to claim 7, wherein the ultrasonic power of the ultrasonic dispersion treatment is 300-350W and the ultrasonic time is 20-30min.
9. A method for producing a breathable black mask for automobiles according to any one of claims 1 to 8, comprising the steps of:
Weighing raw materials according to parts by weight, sequentially and fully mixing the weighed raw materials, then adding the mixture into a double-screw extruder for extrusion, wherein the extrusion temperature is 155-165 ℃, and thus the breathable black mask is obtained.
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Citations (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102807718A (en) * | 2011-10-12 | 2012-12-05 | 袁少山 | Automotive safety protective film and production process thereof |
CN105400177A (en) * | 2015-12-30 | 2016-03-16 | 浙江索凡胶粘制品有限公司 | Antibiosis protection film for automobiles, and making method thereof |
CN105419305A (en) * | 2015-12-30 | 2016-03-23 | 浙江索凡胶粘制品有限公司 | Automobile protection film and preparation method therefor |
CN105602236A (en) * | 2016-03-15 | 2016-05-25 | 江苏德威新材料股份有限公司 | PVC/TPU (polyvinyl chloride/thermoplastic polyurethane) oil-resistant flame-retardant thermoplastic elastomer for new energy automobile charging pile cables |
CN105670179A (en) * | 2016-04-07 | 2016-06-15 | 江苏德威新材料股份有限公司 | Wear-resistant high-specific-gravity PVC/TPU (polyvinyl chloride/thermoplastic polyurethane) composite material for high-speed elevator cables and preparation method thereof |
CN109054252A (en) * | 2018-08-10 | 2018-12-21 | 广东金斯迪新材料科技有限公司 | A kind of automobile film and preparation method thereof |
CN110951187A (en) * | 2019-12-10 | 2020-04-03 | 山东玉马遮阳科技股份有限公司 | Anion PVC polyester coated yarn for sun-shading material and production process thereof |
CN110964308A (en) * | 2019-12-20 | 2020-04-07 | 山东一诺威聚氨酯股份有限公司 | Explosion-proof heat-insulation TPU film for automobile glass and preparation method thereof |
CN113024861A (en) * | 2021-03-03 | 2021-06-25 | 德星技术(苏州)有限公司 | High-toughness and high-tensile-strength TPU (thermoplastic polyurethane) film and preparation method thereof |
CN114426766A (en) * | 2022-01-21 | 2022-05-03 | 昆山红苹果塑胶新材料有限公司 | High-shading double-color TPU (thermoplastic polyurethane) film and production process thereof |
CN115012215A (en) * | 2022-06-09 | 2022-09-06 | 吴江罗太化纤有限公司 | Preparation method of antibacterial PVC polyester coated yarn |
CN117186588A (en) * | 2023-09-18 | 2023-12-08 | 同宇新材料(广东)股份有限公司 | High heat-resistant resin composition for electronic circuit substrate and preparation method thereof |
CN117343575A (en) * | 2023-11-30 | 2024-01-05 | 广东欧文莱陶瓷有限公司 | Composition for ceramic tile printing and preparation method thereof |
CN117511047A (en) * | 2023-11-07 | 2024-02-06 | 贵州省纳米材料工程中心 | Antibacterial and mildew-proof polypropylene edible fungus bag film and preparation method thereof |
-
2024
- 2024-03-25 CN CN202410338073.5A patent/CN117924855B/en active Active
Patent Citations (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102807718A (en) * | 2011-10-12 | 2012-12-05 | 袁少山 | Automotive safety protective film and production process thereof |
CN105400177A (en) * | 2015-12-30 | 2016-03-16 | 浙江索凡胶粘制品有限公司 | Antibiosis protection film for automobiles, and making method thereof |
CN105419305A (en) * | 2015-12-30 | 2016-03-23 | 浙江索凡胶粘制品有限公司 | Automobile protection film and preparation method therefor |
CN105602236A (en) * | 2016-03-15 | 2016-05-25 | 江苏德威新材料股份有限公司 | PVC/TPU (polyvinyl chloride/thermoplastic polyurethane) oil-resistant flame-retardant thermoplastic elastomer for new energy automobile charging pile cables |
CN105670179A (en) * | 2016-04-07 | 2016-06-15 | 江苏德威新材料股份有限公司 | Wear-resistant high-specific-gravity PVC/TPU (polyvinyl chloride/thermoplastic polyurethane) composite material for high-speed elevator cables and preparation method thereof |
CN109054252A (en) * | 2018-08-10 | 2018-12-21 | 广东金斯迪新材料科技有限公司 | A kind of automobile film and preparation method thereof |
CN110951187A (en) * | 2019-12-10 | 2020-04-03 | 山东玉马遮阳科技股份有限公司 | Anion PVC polyester coated yarn for sun-shading material and production process thereof |
CN110964308A (en) * | 2019-12-20 | 2020-04-07 | 山东一诺威聚氨酯股份有限公司 | Explosion-proof heat-insulation TPU film for automobile glass and preparation method thereof |
CN113024861A (en) * | 2021-03-03 | 2021-06-25 | 德星技术(苏州)有限公司 | High-toughness and high-tensile-strength TPU (thermoplastic polyurethane) film and preparation method thereof |
CN114426766A (en) * | 2022-01-21 | 2022-05-03 | 昆山红苹果塑胶新材料有限公司 | High-shading double-color TPU (thermoplastic polyurethane) film and production process thereof |
CN115012215A (en) * | 2022-06-09 | 2022-09-06 | 吴江罗太化纤有限公司 | Preparation method of antibacterial PVC polyester coated yarn |
CN117186588A (en) * | 2023-09-18 | 2023-12-08 | 同宇新材料(广东)股份有限公司 | High heat-resistant resin composition for electronic circuit substrate and preparation method thereof |
CN117511047A (en) * | 2023-11-07 | 2024-02-06 | 贵州省纳米材料工程中心 | Antibacterial and mildew-proof polypropylene edible fungus bag film and preparation method thereof |
CN117343575A (en) * | 2023-11-30 | 2024-01-05 | 广东欧文莱陶瓷有限公司 | Composition for ceramic tile printing and preparation method thereof |
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