CN108329798A - Anti-flaming dope for new-energy automobile - Google Patents
Anti-flaming dope for new-energy automobile Download PDFInfo
- Publication number
- CN108329798A CN108329798A CN201810157362.XA CN201810157362A CN108329798A CN 108329798 A CN108329798 A CN 108329798A CN 201810157362 A CN201810157362 A CN 201810157362A CN 108329798 A CN108329798 A CN 108329798A
- Authority
- CN
- China
- Prior art keywords
- parts
- new
- energy automobile
- flaming dope
- additive
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Classifications
-
- 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
- C09D163/00—Coating compositions based on epoxy resins; Coating compositions based on derivatives of epoxy resins
-
- 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
-
- 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
-
- 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
- C09D7/62—Additives non-macromolecular inorganic modified by treatment with other compounds
-
- 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
- C09D7/63—Additives non-macromolecular organic
-
- 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
- C09D7/65—Additives macromolecular
-
- 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
- C09D7/66—Additives characterised by particle size
- C09D7/67—Particle size smaller than 100 nm
-
- 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
- C09D7/70—Additives characterised by shape, e.g. fibres, flakes or microspheres
-
- 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
- C08K2201/00—Specific properties of additives
- C08K2201/011—Nanostructured additives
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
- C08L2205/035—Polymer mixtures characterised by other features containing three or more polymers in a blend containing four or more polymers in a blend
Abstract
A kind of anti-flaming dope for new-energy automobile is made of the raw material of following parts by weight：10 15 parts of bisphenol A epoxide resin, 5 10 parts of diatom ooze, 5 10 parts of propylene glycol, 5 10 parts of ammonium polyphosphate, 15 parts of sepiolite powder, 15 parts of ammonium dihydrogen phosphate, 0.5 1 parts of silica, 0.5 1 parts of polyaspartic, 0.5 1 parts of zinc stearate, 0.1 1 parts of modified glass-fiber, 0.01 0.05 parts of N methyl morpholine N oxides, 25 parts of additive；The made anti-flaming dope of the present invention is suitable for the shell of new-energy automobile, and the anti-flaming dope is remarkably improved the anti-flammability of new-energy automobile shell when its quality additive amount is 2.5%, flame retardant rating reaches 0 grade of V, oxygen index (OI) reaches 44.5%, therefore the impact of performance of the made new-energy automobile shell with excellent flame retardancy of sening as an envoy to can be played on the basis of its low dosage.
Description
Technical field：
The present invention relates to technical field of new energy, and in particular to a kind of anti-flaming dope for new-energy automobile.
Background technology：
New-energy automobile refers to all other energy automobile in addition to gasoline, diesel engine.Including fuel cell car,
Hybrid vehicle, hydrogen-powered vehicles and solar telephone etc..It has relatively low exhaust emission.According to incompletely statistics, entirely
Existing more than 4,000,000 liquefied petroleum gas automobiles in the world, more than 100 ten thousand gas-fueled vehicles.It is on sale new in Chinese market at present
Energy automobile is mostly hybrid vehicle and pure electric automobile.It is public according to People's Republic of China's national development and the reform committee
Definition is accused, new-energy automobile refers to using unconventional vehicle fuel as a source of power, the dynamic Control of comprehensive vehicle and drive
The advanced technology of dynamic aspect, the advanced automobile with new technology, new construction of the technical principle of formation.
Invention content：
Technical problem to be solved by the present invention lies in provide a kind of anti-flaming dope for new-energy automobile.
The technical problems to be solved by the invention are realized using technical solution below：
A kind of anti-flaming dope for new-energy automobile is made of the raw material of following parts by weight：
10-15 parts of bisphenol A epoxide resin, 5-10 parts of diatom ooze, 5-10 parts of propylene glycol, 5-10 parts of ammonium polyphosphate, sepiolite
1-5 parts of powder, 0.5-1 parts of silica, 0.5-1 parts of polyaspartic, 0.5-1 parts of zinc stearate, is modified 1-5 parts of ammonium dihydrogen phosphate
0.1-1 parts of glass fibre, 0.01-0.05 parts of N-methylmorpholine-N- oxides, 2-5 parts of additive.
The raw material of the above-mentioned anti-flaming dope for new-energy automobile, preferably following parts by weight is made：
13 parts of bisphenol A epoxide resin, 8 parts of diatom ooze, 8 parts of propylene glycol, 8 parts of ammonium polyphosphate, 3 parts of sepiolite powder, di(2-ethylhexyl)phosphate
3 parts of hydrogen ammonium, 0.8 part of silica, 0.8 part of polyaspartic, 0.8 part of zinc stearate, 0.5 part of modified glass-fiber, N- methyl
0.03 part of quinoline-N- oxides, 4 parts of additive.
Further, the additive is made of the raw material of following parts by weight：3-6 parts of nano zine oxide, mica powder 2-4
Part, ceramic fibre 2-4's, 1-3 parts of nano-sized iron oxide, 1-2 parts of bamboo charcoal fiber, 0.8-1.2 parts of chitin, 0.3-0.8 parts of pitch,
0.5-1 parts of aromatic naphtha.
Further, the raw material of the preferably following parts by weight of the additive is made：5 parts of nano zine oxide, mica powder 3
Part, ceramic fibre 3,2 parts of nano-sized iron oxide, 1.5 parts of bamboo charcoal fiber, 1 part of chitin, 0.5 part of pitch, 0.8 part of aromatic naphtha.
The modified glass-fiber is modified through alkyd resin by glass fibre, and method of modifying is：To glass fibers
Rosin and hexamethylolmelamine pregnancy ether are added in dimension, microwave treater microwave treatment 5min is utilized after being sufficiently mixed, then
Alkyd resin, nano-titanium dioxide and crospovidone is added, is uniformly mixed and continues microwave treatment 5min, and be transferred to 5-10 DEG C of ring
Sealing and standing 30min in border, again microwave treatment 5min, then cooled to room temperature, 5-10 DEG C of water water of gained mixture
It washes twice, is finally sent into freeze drier, fiber is made to get modified glass fibre through the broken machine of superfluorescent fiber in dry obtained solid
Dimension.
The glass fibre, rosin, hexamethylolmelamine pregnancy ether, alkyd resin, nano-titanium dioxide and crosslinking
The quality amount ratio of povidone is 10-15:0.5-1:0.3-0.5:3-5:1-3:0.5-1.
The operating condition of the microwave treater is microwave frequency 2250MHz, output power 800W.
Preparation method includes the following steps：
A, bisphenol A epoxide resin, diatom ooze, ammonium polyphosphate, silica, zinc stearate are mixed, is heated to molten
State, is stirred reaction, and mixing time is 20-30 minutes；
B, sepiolite powder, ammonium dihydrogen phosphate, polyaspartic, modified glass-fiber, N-methylmorpholine-N- oxides are added
Into reaction kettle, temperature setting is reacted in 120-150 degree, and the reaction time is 30-40 minutes；
C, the mixture of step a mixtures and b are added in blender and are stirred, mixing speed 800-1000r/
Min, temperature setting 80-90, mixing time are 20-30 minutes；
D, additive is added in the blender of step c, continues to stir, mixing speed 1200-1400r/min, temperature
Degree is set as 40-60, and mixing time is 30-40 minutes；
E, the mixture for handling step d well is ground to get to finished product.
Further, described to be ground to three sections of grindings, grinding rate is respectively：90-100/rpm, 100-120/rpm,
120-150/rpm。
The beneficial effects of the invention are as follows：The made anti-flaming dope of the present invention is suitable for the shell of new-energy automobile, the fire-retardant painting
The shell of material and new-energy automobile has good comixing compatibility, and the blending for effectively facilitating raw material is compatible；And this is fire-retardant
Coating is remarkably improved the anti-flammability of new-energy automobile shell when its quality additive amount is 2.5%, and flame retardant rating reaches V-0
Grade, oxygen index (OI) reach 44.5%, therefore can play made new-energy automobile shell of sening as an envoy to excellent on the basis of its low dosage
The impact of performance of different anti-flammability.
Specific implementation mode：
In order to make the technical means, the creative features, the aims and the efficiencies achieved by the present invention be easy to understand, tie below
Specific embodiment is closed, the present invention is further explained.
Embodiment 1
A kind of anti-flaming dope for new-energy automobile is made of the raw material of following parts by weight：
10 parts of bisphenol A epoxide resin, 5 parts of diatom ooze, 5 parts of propylene glycol, 5 parts of ammonium polyphosphate, 1 part of sepiolite powder, di(2-ethylhexyl)phosphate
1 part of hydrogen ammonium, 0.5 part of silica, 0.5 part of polyaspartic, 0.5 part of zinc stearate, 0.1 part of modified glass-fiber, N- methyl
0.01 part of quinoline-N- oxides, 2 parts of additive.
The additive is made of the raw material of following parts by weight：3 parts of nano zine oxide, 2 parts of mica powder, ceramic fibre 2
, 1 part of nano-sized iron oxide, 1 part of bamboo charcoal fiber, 0.8 part of chitin, 0.3 part of pitch, 0.5 part of aromatic naphtha.
Preparation method includes the following steps：
A, bisphenol A epoxide resin, diatom ooze, propylene glycol, ammonium polyphosphate, silica, zinc stearate are mixed, is heated to
Molten condition, is stirred reaction, and mixing time is 20 minutes；
B, sepiolite powder, ammonium dihydrogen phosphate, polyaspartic, modified glass-fiber, N-methylmorpholine-N- oxides are added
Into reaction kettle, temperature setting is reacted at 120 degree, and the reaction time is 30 minutes；
C, the mixture of step a mixtures and b are added in blender and are stirred, mixing speed 800r/min, temperature
Degree is set as 80, and mixing time is 20 minutes；
D, additive is added in the blender of step c, continues to stir, mixing speed 1200r/min, temperature setting
It is 40, mixing time is 30 minutes；
E, the mixture for handling step d well carries out segmentation grinding to get to finished product.
Further, the segmentation grinding is divided into three sections, and grinding rate is respectively：90/rpm, 100/rpm, 120/rpm.
Embodiment 2
A kind of anti-flaming dope for new-energy automobile is made of the raw material of following parts by weight：
15 parts of bisphenol A epoxide resin, 10 parts of diatom ooze, 10 parts of propylene glycol, 10 parts of ammonium polyphosphate, 5 parts of sepiolite powder, phosphoric acid
5 parts of ammonium dihydrogen, silica 1 part, 1 part of polyaspartic, 1 part of zinc stearate, 1 part of modified glass-fiber, N-methylmorpholine-N- oxygen
0.05 part of compound, 5 parts of additive.
Further, the additive is made of the raw material of following parts by weight：6 parts of nano zine oxide, 4 parts of mica powder,
Ceramic fibre 4,3 parts of nano-sized iron oxide, 2 parts of bamboo charcoal fiber, 1.2 parts of chitin, 0.8 part of pitch, 1 part of aromatic naphtha.
Preparation method includes the following steps：
A, bisphenol A epoxide resin, diatom ooze, propylene glycol, ammonium polyphosphate, silica, zinc stearate are mixed, is heated to
Molten condition, is stirred reaction, and mixing time is 30 minutes；
B, sepiolite powder, ammonium dihydrogen phosphate, polyaspartic, modified glass-fiber, N-methylmorpholine-N- oxides are added
Into reaction kettle, temperature setting is reacted at 150 degree, 40 minutes reaction time；
C, the mixture of step a mixtures and b are added in blender and are stirred, mixing speed 1000r/min, temperature
Degree is set as 90, and mixing time is 30 minutes；
D, additive is added in the blender of step c, continues to stir, mixing speed 1400r/min, temperature setting
It is 60, mixing time is 40 minutes；
E, the mixture for handling step d well carries out segmentation grinding to get to finished product.
Further, the segmentation grinding is divided into three sections, and grinding rate is respectively：100/rpm, 120/rpm, 150/rpm.
Control group 1
A kind of anti-flaming dope for new-energy automobile is made of the raw material of following parts by weight：
10 parts of bisphenol A epoxide resin, 5 parts of diatom ooze, 5 parts of propylene glycol, 5 parts of ammonium polyphosphate, 1 part of sepiolite powder, di(2-ethylhexyl)phosphate
1 part of hydrogen ammonium, 0.5 part of silica, 0.5 part of polyaspartic, 0.5 part of zinc stearate, 0.1 part of modified glass-fiber, N- methyl
0.01 part of quinoline-N- oxides.
Preparation method includes the following steps：
A, bisphenol A epoxide resin, diatom ooze, propylene glycol, ammonium polyphosphate, silica, zinc stearate are mixed, is heated to
Molten condition, is stirred reaction, and mixing time is 20 minutes；
B, sepiolite powder, ammonium dihydrogen phosphate, polyaspartic, modified glass-fiber, N-methylmorpholine-N- oxides are added
Into reaction kettle, temperature setting is reacted at 120 degree, and the reaction time is 30 minutes；
C, the mixture of step a mixtures and b are added in blender and are stirred, mixing speed 800r/min, temperature
Degree is set as 80, and mixing time is 20 minutes；
D, additive is added in the blender of step c, continues to stir, mixing speed 1200r/min, temperature setting
It is 40, mixing time is 30 minutes；
E, the mixture for handling step d well is ground to get to finished product.
Control group 2
A kind of anti-flaming dope for new-energy automobile is made of the raw material of following parts by weight：
15 parts of bisphenol A epoxide resin, 10 parts of diatom ooze, 10 parts of propylene glycol, 10 parts of ammonium polyphosphate, 5 parts of sepiolite powder, phosphoric acid
5 parts of ammonium dihydrogen, silica 1 part, 1 part of polyaspartic, 1 part of zinc stearate, 1 part of modified glass-fiber, N-methylmorpholine-N- oxygen
0.05 part of compound.
Preparation method includes the following steps：
A, all material is heated to molten condition, is stirred reaction, mixing time is 30 minutes；
B, the material of step a molten conditions is stirred, mixing speed 1000r/min, temperature setting 90, is stirred
Time is 30 minutes.
C, the mixture for handling step b well carries out segmentation grinding to get to finished product.
Table 1 is that the present invention is added to control group in the production process of new-energy automobile, performance test
The above shows and describes the basic principles and main features of the present invention and the advantages of the present invention.The technology of the industry
Personnel are it should be appreciated that the present invention is not limited to the above embodiments, and the above embodiments and description only describe this
The principle of invention, without departing from the spirit and scope of the present invention, various changes and improvements may be made to the invention, these changes
Change and improvement all fall within the protetion scope of the claimed invention.The claimed scope of the invention by appended claims and its
Equivalent thereof.
Claims (6)
1. a kind of anti-flaming dope for new-energy automobile, which is characterized in that be made of the raw material of following parts by weight：
10-15 parts of bisphenol A epoxide resin, 5-10 parts of diatom ooze, 5-10 parts of propylene glycol, 5-10 parts of ammonium polyphosphate, sepiolite powder 1-5
Part, 1-5 parts of ammonium dihydrogen phosphate, 0.5-1 parts of silica, 0.5-1 parts of polyaspartic, 0.5-1 parts of zinc stearate, modified glass fibre
0.1-1 parts of dimension, 0.01-0.05 parts of N-methylmorpholine-N- oxides, 2-5 parts of additive.
2. the anti-flaming dope according to claim 1 for new-energy automobile, it is characterised in that：It is preferred that following parts by weight
Raw material be made：13 parts of bisphenol A epoxide resin, 8 parts of diatom ooze, 8 parts of propylene glycol, 8 parts of ammonium polyphosphate, 3 parts of sepiolite powder, phosphoric acid
3 parts of ammonium dihydrogen, 0.8 part of silica, 0.8 part of polyaspartic, 0.8 part of zinc stearate, 0.5 part of modified glass-fiber, N- methyl
0.03 part of methylmorpholine-N-oxide, 4 parts of additive.
3. the anti-flaming dope according to claim 1 for new-energy automobile, it is characterised in that：The additive is by as follows
The raw material of parts by weight is made：3-6 parts of nano zine oxide, 2-4 parts of mica powder, ceramic fibre 2-4's, 1-3 parts of nano-sized iron oxide,
1-2 parts of bamboo charcoal fiber, 0.8-1.2 parts of chitin, 0.3-0.8 parts of pitch, 0.5-1 parts of aromatic naphtha.
4. the anti-flaming dope according to claim 2 for new-energy automobile, it is characterised in that：The additive is preferably such as
The raw material of lower parts by weight is made：5 parts of nano zine oxide, 3 parts of mica powder, ceramic fibre 3,2 parts of nano-sized iron oxide, bamboo charcoal fibre
1.5 parts of dimension, 1 part of chitin, 0.5 part of pitch, 0.8 part of aromatic naphtha.
5. the anti-flaming dope according to claim 1 or 2 for new-energy automobile, it is characterised in that：Preparation method packet
Include following steps：
A, bisphenol A epoxide resin, diatom ooze, propylene glycol, ammonium polyphosphate, silica, zinc stearate are mixed, is heated to melting
State, is stirred reaction, and mixing time is 20-30 minutes；
B, sepiolite powder, ammonium dihydrogen phosphate, polyaspartic, modified glass-fiber, N-methylmorpholine-N- oxides are added to instead
It answers in kettle, temperature setting is reacted in 120-150 degree, and the reaction time is 30-40 minutes；
C, the mixture of step a mixtures and b are added in blender and are stirred, mixing speed 800-1000r/min, temperature
Degree is set as 80-90, and mixing time is 20-30 minutes；
D, additive is added in the blender of step c, continues to stir, mixing speed 1200-1400r/min, temperature is set
It is set to 40-60, mixing time is 30-40 minutes；
E, the mixture for handling step d well is ground to get to finished product.
6. the anti-flaming dope according to claim 5 for new-energy automobile, it is characterised in that：It is described to be ground to three sections and grind
Mill, grinding rate are respectively：90-100/rpm, 100-120/rpm, 120-150/rpm.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201810157362.XA CN108329798A (en) | 2018-02-24 | 2018-02-24 | Anti-flaming dope for new-energy automobile |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201810157362.XA CN108329798A (en) | 2018-02-24 | 2018-02-24 | Anti-flaming dope for new-energy automobile |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN108329798A true CN108329798A (en) | 2018-07-27 |
Family
ID=62929623
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201810157362.XA Pending CN108329798A (en) | 2018-02-24 | 2018-02-24 | Anti-flaming dope for new-energy automobile |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN108329798A (en) |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104312423B (en) * | 2014-11-07 | 2017-02-15 | 广东希贵光固化材料有限公司 | UV (ultraviolet) curing flame-retardant coating |
| CN107674533A (en) * | 2017-11-01 | 2018-02-09 | 安徽省金正塑业有限公司 | A kind of anti-flaming dope for refrigerator |
-
2018
- 2018-02-24 CN CN201810157362.XA patent/CN108329798A/en active Pending
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104312423B (en) * | 2014-11-07 | 2017-02-15 | 广东希贵光固化材料有限公司 | UV (ultraviolet) curing flame-retardant coating |
| CN107674533A (en) * | 2017-11-01 | 2018-02-09 | 安徽省金正塑业有限公司 | A kind of anti-flaming dope for refrigerator |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Ye et al. | Performance enhancement of rubber composites using VOC-Free interfacial silica coupling agent | |
| CN102617942B (en) | Ethylene-propylene-diene monomer rubber used for manufacturing wind energy cable and preparation method thereof | |
| CN106543560A (en) | High tenacity PP/PS/SBS composite and preparation method thereof | |
| CN105017740A (en) | Natural fiber composite material and preparation method thereof | |
| CN105062080A (en) | Arc-resistant silicon composite material, preparation method and use thereof | |
| CN105350107A (en) | Preparation method of light-colored PET polyester conductive fiber based on conductive zinc oxide | |
| CN115093608B (en) | Preparation method and application of core-shell structure boron nitride material | |
| CN111154233B (en) | Flame-retardant epoxy resin based on iron-containing nickel silicate and preparation method thereof | |
| CN112111094A (en) | Resin-coated diethyl aluminum hypophosphite flame-retardant low-density polyethylene and preparation method thereof | |
| CN102617944A (en) | Chlorinated polyethylene rubber for manufacturing wind energy cables and preparation method for chlorinated polyethylene rubber | |
| CN104927137A (en) | Nano carbon rubber material | |
| CN108329798A (en) | Anti-flaming dope for new-energy automobile | |
| CN102115076A (en) | Method for preparing carbon nanotube by use of biodegradable plastic | |
| CN111978523A (en) | Preparation method of flame-retardant unsaturated polyester | |
| CN104183852B (en) | Phenolic resin-graphite-graphene composite battery bipolar grid plate and preparation method thereof | |
| CN115044165B (en) | ABS resin composition and preparation method thereof | |
| CN114891272B (en) | Melamine formaldehyde resin microencapsulated flame retardant and preparation method thereof | |
| CN115232422A (en) | Insulating protective film for power battery | |
| CN108219638A (en) | For the anti-aging coating of new-energy automobile | |
| CN112920552B (en) | Flame-retardant epoxy resin and preparation method and application thereof | |
| CN100352859C (en) | Nano composite fire retardant parent material, preparation method and application | |
| KR20150130779A (en) | The preparing method of silica-polybutadiene composite material and the silica-polybutadiene composite material thereby | |
| CN109206755A (en) | A kind of spectacle-frame attapulgite-active calcium silicate modified EPT rubber composite material preparation method | |
| CN108164880A (en) | A kind of automotive wire cable and preparation method thereof | |
| CN108559240A (en) | A kind of anti-ageing cable jacket of new-energy automobile |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PB01 | Publication | ||
| PB01 | Publication | ||
| SE01 | Entry into force of request for substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| RJ01 | Rejection of invention patent application after publication |
Application publication date: 20180727 |
|
| RJ01 | Rejection of invention patent application after publication |