CN109852195A - A kind of preparation method of anti-static coatings - Google Patents

A kind of preparation method of anti-static coatings Download PDF

Info

Publication number
CN109852195A
CN109852195A CN201910029266.1A CN201910029266A CN109852195A CN 109852195 A CN109852195 A CN 109852195A CN 201910029266 A CN201910029266 A CN 201910029266A CN 109852195 A CN109852195 A CN 109852195A
Authority
CN
China
Prior art keywords
parts
stirred
modified
under
conditions
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
Application number
CN201910029266.1A
Other languages
Chinese (zh)
Inventor
陈可
仲华
薛丞
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to CN201910029266.1A priority Critical patent/CN109852195A/en
Publication of CN109852195A publication Critical patent/CN109852195A/en
Pending legal-status Critical Current

Links

Abstract

The invention discloses a kind of preparation methods of anti-static coatings, belong to technical field of polymer materials.Sisal fiber, Bacillus pasteurii bacterium solution, urea, water mixed fermentation are then added dropwise to iron nitrate solution, are stirred by the present invention, are filtered, freezing, and ball milling is sieved, dry, and charing heats up, high-temperature process is to get modified fibre step by step;According to parts by weight, by 40~60 parts of modified epoxies, 40~60 parts of diluents, 10~20 parts of pretreatment mica powders, 10~20 parts of modified fibres, 10~20 parts of modified additives, 5~8 parts of curing agent, 5~8 parts of modified meerschaums, 20~30 parts of alkalescent phenol resins, 10~20 parts of modification infusorial earths, are stirred to get anti-static coatings.Anti-static coatings provided by the invention have excellent antistatic performance.

Description

A kind of preparation method of anti-static coatings
Technical field
The invention discloses a kind of preparation methods of anti-static coatings, belong to technical field of polymer materials.
Background technique
Using polymer matrix composites as nonmetal structure/functional material of representative there is light, performance can design, easily in batches The features such as production, application range are growing.The volume resistivity of polymer matrix composites is higher, generally higher than 109 Ω cm, Surface by air-flow, solid particle and liquid friction and shock when, be also easy to produce and accumulate electrostatic.Accumulation of static electricity reaches certain journey Degree, will cause static discharge, cause the breakdown of instrument and equipment component to be scrapped, control system failure, accuracy at target reduces, seriously When have cause weapon system explode danger, cause serious accident.Simultaneously as accumulation of static electricity, composite material surface is easy to inhale Dust in attached air, and be difficult to thoroughly it is cleared, influence product appearance.
Anti-static coatings are coated, anti-static coating is formed, are the effective measures for eliminating composite material surface electrostatic.Coating When volume resistivity is less than 107 Ω cm, the electrostatic charge of generation can be dissipated with moment, will not be accumulated, because higher without causing Electrostatic field.The anti-static coatings of actual use, volume resistivity general control have preferable warp in 104~107 Ω cm Ji property and craftsmanship.Whether anti-static coatings are made of film forming matter, paint filler, auxiliary agent and solvent, led according to film forming matter Electricity can be divided into Intrinsical anti-static coatings and addition type anti-static coatings.Film forming matter itself is conductive, is not required to addition and leads Electric component, this coating are known as Intrinsical anti-static coatings;Film forming matter itself is insulator, since addition filler or auxiliary agent make Coating has antistatic performance, and this coating is known as addition type anti-static coatings.
Addition type anti-static coatings are made of conductive filler (pigment), insulation film forming matter, auxiliary agent and solvent, electric conductivity Can be related with the resistance of conductive filler, it is related with volume fraction of the conductive filler in paint film, it is also related with environment temperature.Due to Film forming matter is insulator, and conducting particles must be in contact with each other or closely in dry film, electronics can just overcome between particle at The blocking of membrane substance forms electric current, therefore the volume fraction of conductive filler is generally very high.Conductive filler can be divided into metal class, carbon Class, metal oxide-type, inorganic salts, conductive polymer subclass and organic salt.The most study that metal class conductive filler is subject to, Using most mature, but it is universal oxidizable, and color is deep, can not prepare white or light-colored anti-static coatings;Carbons conductive filler is conductive Property it is good and stablize, but color is single, can only prepare dark paint;Metal oxide-type and inorganic salts conductive filler it is common Feature is stable conductivity, and color is shallower, is the direction developed in recent years, but resistivity is higher;Conductive polymer subclass conduction is filled out Expect best with the compatibility of matrix resin, be conducive to the raising of coating mechanical mechanics property, but its preparation process complexity, cost compared with It is high;Organic salt conductive filler belongs to surfactant, relies primarily on the coefficient of friction and adsorbed water molecule for reducing coating surface And antistatic, effect are poor.
It is current to there is researcher to mix following ingredients in the prior art, 25% modified epoxy (mass fraction, under Together), 5% curing agent, 70% silver-colored packet glass microballoon (silver content 30%), solvent are the mixed solution of n-butanol and dimethylbenzene, are dried Dry temperature 60 C, drying time 2h.Thus the epoxy conductive corrosion-inhibiting coating that technique obtains is creamy white, and film is smooth, resistivity For 0.03~0.05 cm, 2 grades of adhesive force.There are also researchers to use substep mixing method, by diatomite, concavo-convex rod soil, conduction Mica powder, nanometer iron powder, talcum powder conducing composite material are mixed together so that between the different five kinds of substances of granularity, density with The network connection of diatomite, concavo-convex rod soil, conductive mica powder and nanometer iron powder is got up, is uniformly mixed as skeleton by talcum powder, from And guaranteeing prepared coating uniformity, application performance is good, static conductive excellent effect.But antistatic traditional at present applies Material, since there are biggish interface resistances between each conductive filler, cause the antistatic performance of coating bad, therefore also need to its into Row research.
Summary of the invention
The present invention solves the technical problem of: for traditional anti-static coatings, due to exist between each conductive filler compared with Big interface resistance, the problem for causing the antistatic performance of coating bad provide a kind of preparation method of anti-static coatings.
In order to solve the above-mentioned technical problem, the technical scheme adopted by the invention is that:
(1) according to parts by weight, by 20~30 parts of sisal fibers, 2~3 parts of Bacillus pasteurii bacterium solutions, 2~3 parts of urea, 30~ 40 parts of water mixed fermentations are then added dropwise to 0.1~0.2 times of sisal fiber quality of iron nitrate solution, are stirred, filtering, cold Freeze, ball milling, be sieved, dry, charing heats up, high-temperature process is to get modified fibre step by step;
(2) according to parts by weight, by 40~60 parts of modified epoxies, 40~60 parts of diluents, 10~20 parts of pretreatment micas Powder, 10~20 parts of modified fibres, 10~20 parts of modified additives, 5~8 parts of curing agent, 5~8 parts of modified meerschaums, 20~30 parts Alkalescent phenol resin, 10~20 parts of modification infusorial earths, is stirred to get anti-static coatings.
The preparation process of step (1) the Bacillus pasteurii bacterium solution are as follows: according to parts by weight, by 2~3 parts of Pasteur's gemma Bacillus, 1~2 part of glycerol, 1~2 part of polyethylene glycol, 20~30 parts of water termostats are stirred, and obtain Bacillus pasteurii bacterium solution.
The preparation process of step (2) described modified epoxy are as follows: epoxy resin is heated, and epoxy resin quality is added 0.2~0.3 times of paraphenylene terephthalamide and 0.2~0.4 times of epoxy resin quality of acrylonitrile-butadiene rubber latex after being stirred, must change Property epoxy resin.
Step (2) described diluent is formed by dimethylbenzene and acetone 1:10~1:20 mixed preparing in mass ratio.
The preparation process of step (2) the pretreatment mica powder are as follows: according to parts by weight, by 20~30 parts of mica powders, 10 ~20 parts of starch, 1~2 part of yeast, 20~30 parts of water mixed fermentations are subsequently added into sodium hydroxide solution and are stirred, dry, powder Broken, ball milling, sieving is to get pretreatment mica powder;The starch is potato starch, any in tapioca or wheaten starch It is a kind of.
The process of step (2) the modified additive are as follows: (N- amidino groups) dodecylacrylamide spreads out with polyethylene glycol Biology 2:1~4:1 in mass ratio mixing, and 0.2~0.4 times of polyethyleneglycol derivative quality of paracide and poly- second two is added The ferrocene that 0.12~0.18 times of 01 derivatives quality, is stirred, and obtains mixed processing agent, according to parts by weight, by 20~30 Part graphene oxide, 10~20 parts of mixed processing agents, 40~60 parts of water mixing ultrasounds, be subsequently added into ammonium hydroxide adjust pH to 8.1~ 8.4, it is stirred, is subsequently added into 0.01~0.02 times of graphene oxide quality of isocyanates, is stirred, filter, washing, Drying is to get modified additive;The polyethyleneglycol derivative is novel Y-shaped polyethylene glycol, multi-arm polyethylene glycol or methoxyl group Any one in polyethylene glycol;The isocyanates is toluene di-isocyanate(TDI), methyl diphenylene diisocyanate or front three Any one in base hexane diisocyanate.
Step (2) described curing agent is by dihexyl triamine and diethylaminopropylamine 1:3~1:5 mixed preparing in mass ratio It forms.
The preparation process of step (2) described modified meerschaum are as follows: according to parts by weight, by 20~30 parts of sepiolites, 2~3 Part secondary settling tank sludge, 1~2 portion of sucrose, 40~60 parts of water, mixed fermentation, being subsequently added into 0.1~0.2 times of sepiolite quality has Machine acid, is stirred, and ammonium hydroxide is then added dropwise and adjusts pH to 8.1~8.3, is stirred, filters, dry to get modified meerschaum; The organic acid is formed by malic acid and citric acid 1:3~1:5 mixed preparing in mass ratio.
The preparation process of step (2) described alkalescent phenol resin are as follows: according to parts by weight, 30~40 parts of glyoxals are molten Liquid, 10~20 parts of potassium hydroxide solutions, 30~40 parts of hydroquinone constant temperature are stirred to react, and glyoxal solution volume is added in cooling 0.2~0.3 times of ethylene urea is stirred to react, and 0.1~0.2 times of glyoxal solution volume of silane coupling agent KH- is added in cooling 570 are stirred to react, and cool down to get alkalescent phenol resin.
Step (2) described modification infusorial earth the preparation method comprises the following steps: diatomite and hydrochloric acid 1:10~1:20 in mass ratio are stirred Mixing is mixed, is filtered, is washed, it is dry, single treatment diatomite is obtained, according to parts by weight, by 30~40 parts of single treatment diatomite, 8~10 parts of biogas slurries, 3~5 portions of sucrose, 40~60 parts of water mixed fermentations are filtered, and are washed, dry, obtain secondary treatment diatomite, By low-melting alloy and secondary treatment diatomite 1:3~1:5 Hybrid Heating ball milling in mass ratio to get modification infusorial earth;Institute Stating low-melting alloy is bismuth tin alloy, each component mass content in bismuth tin alloy are as follows: bismuth accounts for 51%(ω), tin accounts for 30%(ω), lead Account for 8%(ω), indium accounts for 11%(ω).
The beneficial effects of the present invention are:
(1) present invention is by addition modified fibre and modification infusorial earth, in modified fibre preparation process, firstly, by sisal hemp fibre Dimension, Bacillus pasteurii bacterium solution, urea, water mixed fermentation, on the one hand, decomposed using the enzyme that microorganism generates organic in fiber Matter is conducive to the entrance of moisture so that the bond strength between fibrocyte declines, on the other hand, Bacillus pasteurii cell table Face is negatively charged, can be enriched with the iron ion of later period addition, then, then in refrigerating process, water and fibre between fiber gap The water of dimension cell interior build-ups ice, and grinds using stone mill, makes the ice crystal effect of being under pressure and ruptures, and is broken into micro/nano level Fibrous crystal must, then, under the high temperature conditions, organic matter in system charing, as system temperature is gradually increasing, in system Carbonaceous makes iron ion be reduced into fe by carbonaceous, while a large amount of tar is generated in system, in heat curing process, changes Property diatomite in low-melting alloy melted by heat, and disperse in system, meanwhile, the heated exudation of tar in modified fibre, Attraction of the low-melting alloy by tar after fusing, is able to enter in modified fibre, effectively improves interfibrous interface electricity Resistance, after low-melting alloy solidification, so that conductive communication network is formed between modified fibre, so that the electric conductivity of system is mentioned It rises, so that the antistatic performance of system gets a promotion;
(2) present invention is by adding modified additive, modified fibre and alkalescent phenol resin, in modified additive preparation process In, molecular structure is the block copolymer with parents' performance in additive effective component, which can self assembly shape At imitated vesicle structure, to make to be dispersed with the imitated vesicle structure inside system, then by addition, isocyanates can be reacted with water, raw At carbon dioxide and amine substance, the generation of carbon dioxide can be reacted with the amidine group in the block copolymer, and make amidine group Take charge, on the one hand, since imitated vesicle structure surface has positive charge, negatively charged graphene oxide can be attracted, so that Graphene oxide good can be dispersed in system, on the other hand, be made inside imitated vesicle structure since like charges are mutually exclusive Volume increases, so that graphene oxide is further dispersed, in heat curing process, expansion vesica is heated to release dioxy Change carbon, the graphene oxide for being adsorbed on the surface of vesica is able to get rid of the constraint of vesica, under the promotion of carbon dioxide, in system In dispersion, meanwhile, the heated exudation of tar in modified fibre can adhere to the graphene oxide dispersed in the system of being dispersed in, To effectively reduce interfibrous interface resistance, so that the antistatic performance of system is further promoted.
Specific embodiment
According to parts by weight, by 2~3 parts of Bacillus pasteuriis, 1~2 part of glycerol, 1~2 part of polyethylene glycol, 20~30 parts Water is placed in No. 1 beaker, and No. 1 beaker is then placed in digital display and is tested the speed in constant temperature blender with magnetic force, is 30~35 DEG C in temperature, is turned Under the conditions of speed is 200~300r/min, constant temperature is stirred 40~60min, obtains Bacillus pasteurii bacterium solution;In parts by weight Meter, by 20~30 parts of mica powders, 10~20 parts of starch, 1~2 part of yeast, 20~30 parts of water are placed in No. 1 fermentation cauldron, Yu Wendu It is 30~35 DEG C, under the conditions of revolving speed is 200~300r/min, is stirred fermentation 3~5 days, is then added into No. 1 fermentation cauldron The sodium hydroxide solution that mass fraction is 20~30%, under the conditions of revolving speed is 300~500r/min, it is stirred 40~ 60min obtains fermentation material, then fermentation material is placed in baking oven, dry to constant weight under the conditions of temperature is 105~110 DEG C, obtains Dry fermentation material is then placed in ball mill grinding in ball mill by dry fermentation material, crosses the sieve of 120 mesh to get pretreatment mica powder; (N- amidino groups) dodecylacrylamide and polyethyleneglycol derivative 2:1~4:1 in mass ratio are mixed in No. 2 beakers, and 0.2~0.4 times of polyethyleneglycol derivative quality of paracide and polyethyleneglycol derivative quality 0.12 are added into No. 2 beakers ~0.18 times of ferrocene is 28~38 DEG C in temperature, revolving speed is stirred 45 under conditions of being 250~320r/min~ After 80min, mixed processing agent is obtained, according to parts by weight, by 20~30 parts of graphene oxides, 10~20 parts of mixed processing agents, 40 ~60 parts of water are placed in single-necked flask, and then single-necked flask is placed in ultrasonic disperse instrument, in supersonic frequency be 55~75kHz Under the conditions of, mix 40~60min of ultrasound, then in case single-necked flask be added mass fraction be 20~30% ammonium hydroxide adjusting pH to 8.1~8.4, under the conditions of revolving speed is 400~600r/min, it is stirred 40~60min, oxygen is then added into single-necked flask The isocyanates of 0.01~0.02 times of graphite alkene quality, under the conditions of revolving speed is 400~600r/min, it is stirred 40~ After 60min, filtering obtains No. 1 filter cake, then with deionized water by No. 1 Washing of Filter Cake 5~8 times, then by No. 1 after washing filter Cake is placed in baking oven, and under the conditions of temperature is 105~110 DEG C, drying to constant weight is to get modified additive;According to parts by weight, By 20~30 parts of sepiolites, 2~3 parts of secondary settling tank sludge, 1~2 portion of sucrose, 40~60 parts of water are placed in No. 2 fermentation cauldrons, Yu Wendu It is 30~35 DEG C, under the conditions of revolving speed is 100~200r/min, is stirred fermentation 3~5 days, is then added into No. 2 fermentation cauldrons The organic acid that 0.1~0.2 times of sepiolite quality is stirred 40~60min, connects under the conditions of revolving speed is 500~600r/min Into No. 2 fermentation cauldrons be added dropwise mass fraction be 20~30% ammonium hydroxide adjust pH to 8.1~8.3, in revolving speed be 400~600r/ Under the conditions of min, after being stirred 40~60min, filtering obtains No. 2 filter cakes, then No. 2 filter cakes is placed in baking oven, are in temperature Under the conditions of 105~110 DEG C, drying is to constant weight to get modified meerschaum;It by epoxy resin plus moves into No. 3 beakers, and by No. 3 Beaker moves into digital display and tests the speed constant temperature blender with magnetic force, and epoxy resin in No. 3 beakers is heated to 70~80 DEG C, and to No. 3 beakers The middle paraphenylene terephthalamide for being added 0.2~0.3 times of epoxy resin quality and 0.2~0.4 times of epoxy resin quality of nitrile rubber cream Liquid is 70~85 DEG C in temperature, after revolving speed is stirred 30~50min under conditions of being 200~300r/min, obtains modified epoxy Resin;According to parts by weight, the glyoxal solution for being 40~50% by 30~40 parts of mass fractions, 10~20 parts of mass fractions are 20~30% potassium hydroxide solution, 30~40 parts of hydroquinones are placed in four-hole boiling flask, and four-hole boiling flask is placed in digital display and is tested the speed It is 76~78 DEG C in temperature, under the conditions of revolving speed is 300~500r/min, constant temperature is stirred to react 3~4h in constant temperature blender with magnetic force Afterwards, temperature in four-hole boiling flask is down to 60~62 DEG C, then 0.2~0.3 times of glyoxal solution volume is added into four-hole boiling flask Ethylene urea is 60~62 DEG C in temperature, under the conditions of revolving speed is 300~500r/min, after constant temperature is stirred to react 40~60min, incites somebody to action Temperature is down to 50~52 DEG C in four-hole boiling flask, and 0.1~0.2 times of glyoxal solution volume of silane is then added into four-hole boiling flask Coupling agent kh-570 is 50~52 DEG C in temperature, under the conditions of revolving speed is 300~500r/min, constant temperature is stirred to react 40~ Temperature in four-hole boiling flask is down to 40~42 DEG C by 50min, is 40~42 DEG C in temperature, revolving speed is 300~500r/min condition Under, continue constant temperature and is stirred to react 20~30min to get alkalescent phenol resin;The salt for being 20~30% by diatomite and mass fraction Acid 1:10~1:20 in mass ratio is placed in No. 4 beakers, under the conditions of revolving speed is 400~600r/min, it is stirred 40~ After 60min, filtering obtains No. 3 filter cakes, during No. 3 Washing of Filter Cake to cleaning solutions are by the ammonium hydroxide for being then 20~30% with mass fraction Property, then No. 3 after washing are placed in baking oven, it is dry to constant weight under the conditions of being 105~110 DEG C in temperature, obtain single treatment Diatomite, according to parts by weight, by 30~40 parts of single treatment diatomite, 8~10 parts of biogas slurries, 3~5 portions of sucrose, 40~60 parts Water is placed in No. 3 fermentation cauldrons, is 30~35 DEG C in temperature, under the conditions of revolving speed is 100~200r/min, is stirred fermentation 3~5 After it, filtering obtains No. 4 filter cakes, is then neutrality by No. 4 filter cake to cleaning solutions with deionized water, then by No. 4 filters after washing Cake is placed in baking oven, dry to constant weight under the conditions of temperature is 105~110, secondary treatment diatomite is obtained, by low-melting alloy It is placed in ball mill with secondary treatment diatomite 1:3~1:5 in mass ratio, under the conditions of temperature is 120~140 DEG C, mixing 40~60min of ball milling is to get modification infusorial earth;According to parts by weight, by 20~30 parts of sisal fibers, 2~3 parts of Pasteur's gemma bars Bacterium bacterium solution, 2~3 parts of urea, 30~40 parts of water are placed in No. 4 fermentation cauldrons, are 30~35 DEG C in temperature, revolving speed is 100~200r/ Under the conditions of min, it is stirred fermentation 3~5 days, is then added dropwise to 0.1~0.2 times of quality of sisal fiber quality to No. 4 fermentation cauldrons The iron nitrate solution that score is 10~20% after being stirred 40~60min, obtains 5 under the conditions of revolving speed is 400~600r/min No. 5 filter cakes, are then placed in liquid nitrogen and freeze, obtain freezing filter cake by number filter cake, will then freeze filter cake ball milling, and cross the sieve of 300 mesh, Crushed material is obtained, then crushed material is placed in baking oven, it is dry to constant weight under the conditions of temperature is 105~110 DEG C, obtain xeraphium Xeraphium particle is then placed in tube furnace by particle, and nitrogen, Yu Wen are passed through into tube furnace with 60~90mL/min rate Under the conditions of degree is 650~750 DEG C, after carbonizing 2~3h, under the conditions of being warming up to 1400~1500 DEG C with 10~15 DEG C/min rate, After 2~3h of high-temperature process, room temperature is down to get modified fibre with furnace;According to parts by weight, by 40~60 parts of modified epoxy trees Rouge, 40~60 parts of diluents, 10~20 parts of pretreatment mica powders, 10~20 parts of modified fibres, 10~20 parts of modified additives, 5 ~8 parts of curing agent, 5~8 parts of modified meerschaums, 20~30 parts of alkalescent phenol resins, 10~20 parts of modification infusorial earths are placed in mixing In machine, under the conditions of revolving speed is 600~800r/min, 40~60min is stirred to get anti-static coatings.The diluent It is to be formed by dimethylbenzene and acetone 1:10~1:20 mixed preparing in mass ratio.The starch is potato starch, tapioca Or any one in wheaten starch.The polyethyleneglycol derivative is novel Y-shaped polyethylene glycol, multi-arm polyethylene glycol or methoxy Any one in base polyethylene glycol.The isocyanates is toluene di-isocyanate(TDI), methyl diphenylene diisocyanate or three Any one in methyl hexane diisocyanate.The organic acid is mixed by malic acid and citric acid 1:3~1:5 in mass ratio Conjunction is formulated.The low-melting alloy is bismuth tin alloy, each component mass content in bismuth tin alloy are as follows: bismuth accounts for 51%(ω), tin Account for 30%(ω), lead accounts for 8%(ω), indium accounts for 11%(ω).
According to parts by weight, by 3 parts of Bacillus pasteuriis, 2 parts of glycerol, 2 parts of polyethylene glycol, 30 parts of water are placed in No. 1 beaker In, No. 1 beaker is then placed in digital display and is tested the speed in constant temperature blender with magnetic force, is 35 DEG C in temperature, revolving speed is 300r/min condition Under, constant temperature is stirred 60min, obtains Bacillus pasteurii bacterium solution;According to parts by weight, by 30 parts of mica powders, 20 parts of starch, 2 Part yeast, 30 parts of water are placed in No. 1 fermentation cauldron, are 35 DEG C in temperature, under the conditions of revolving speed is 300r/min, are stirred fermentation 5 It, is then added the sodium hydroxide solution that mass fraction is 30% into No. 1 fermentation cauldron, under the conditions of revolving speed is 500r/min, stirs Mixing 60min is mixed, fermentation material is obtained, then fermentation material is placed in baking oven, it is dry to constant weight under the conditions of temperature is 110 DEG C, it obtains Dry fermentation material is then placed in ball mill grinding in ball mill by dry fermentation material, crosses the sieve of 120 mesh to get pretreatment mica powder; (N- amidino groups) dodecylacrylamide and polyethyleneglycol derivative 4:1 in mass ratio are mixed in No. 2 beakers, and to No. 2 0.4 times of polyethyleneglycol derivative quality of paracide and the two of 0.18 times of polyethyleneglycol derivative quality cyclopentadienyls are added in beaker Iron is 38 DEG C in temperature, after revolving speed is stirred 80min under conditions of being 320r/min, obtains mixed processing agent, in parts by weight Meter, by 30 parts of graphene oxides, 20 parts of mixed processing agents, 60 parts of water are placed in single-necked flask, are then placed in single-necked flask super In in sound separating apparatus, under the conditions of supersonic frequency is 75kHz, ultrasound 60min is mixed, quality point is then added in case single-necked flask Number adjusts pH to 8.4 for 30% ammonium hydroxide, under the conditions of revolving speed is 600r/min, 60min is stirred, then to single-necked flask The middle isocyanates for being added 0.02 times of graphene oxide quality, under the conditions of revolving speed is 600r/min, after being stirred 60min, Filtering, obtain No. 1 filter cake, then with deionized water by No. 1 Washing of Filter Cake 8 times, No. 1 filter cake after washing is then placed in baking oven In, under the conditions of temperature is 110 DEG C, drying to constant weight is to get modified additive;According to parts by weight, by 30 parts of sepiolites, 3 Part secondary settling tank sludge, 2 portions of sucrose, 60 parts of water are placed in No. 2 fermentation cauldrons, in temperature be 35 DEG C, under the conditions of revolving speed is 200r/min, Be stirred fermentation 5 days, 0.2 times of sepiolite quality of organic acid be then added into No. 2 fermentation cauldrons, in revolving speed be 600r/min Under the conditions of, be stirred 60min, then into No. 2 fermentation cauldrons be added dropwise mass fraction be 30% ammonium hydroxide adjust pH to 8.3, in turn Under the conditions of speed is 600r/min, after being stirred 60min, filtering obtains No. 2 filter cakes, then No. 2 filter cakes is placed in baking oven, in Under the conditions of temperature is 110 DEG C, drying is to constant weight to get modified meerschaum;It by epoxy resin plus moves into No. 3 beakers, and by No. 3 Beaker moves into digital display and tests the speed constant temperature blender with magnetic force, and epoxy resin in No. 3 beakers is heated to 80 DEG C, and into No. 3 beakers plus Enter 0.3 times of epoxy resin quality of paraphenylene terephthalamide and 0.4 times of epoxy resin quality of acrylonitrile-butadiene rubber latex, in temperature be 85 DEG C, after revolving speed is stirred 50min under conditions of being 300r/min, obtain modified epoxy;According to parts by weight, by 40 parts of matter The glyoxal solution that score is 50%, the potassium hydroxide solution that 20 parts of mass fractions are 30% are measured, 40 parts of hydroquinones are placed in four mouthfuls In flask, and four-hole boiling flask is placed in digital display and is tested the speed in constant temperature blender with magnetic force, is 78 DEG C in temperature, revolving speed is 500r/min item Under part, after constant temperature is stirred to react 4h, temperature in four-hole boiling flask is down to 62 DEG C, then glyoxal solution body is added into four-hole boiling flask 0.3 times of ethylene urea of product, in temperature be 62 DEG C, under the conditions of revolving speed is 500r/min, after constant temperature is stirred to react 60min, Jiang Sikou Temperature is down to 52 DEG C in flask, and 0.2 times of glyoxal solution volume of Silane coupling reagent KH-570 is then added into four-hole boiling flask, It is 52 DEG C in temperature, under the conditions of revolving speed is 500r/min, constant temperature is stirred to react 50min, temperature in four-hole boiling flask is down to 42 DEG C, It is 42 DEG C in temperature, under the conditions of revolving speed is 500r/min, continues constant temperature and be stirred to react 30min to get alkalescent phenol resin;By silicon The hydrochloric acid 1:20 in mass ratio that diatomaceous earth and mass fraction are 30% is placed in No. 4 beakers, under the conditions of revolving speed is 600r/min, is stirred After mixing mixing 60min, filtering obtains No. 3 filter cakes, No. 3 Washing of Filter Cake to cleaning solutions are by the ammonium hydroxide for being then 30% with mass fraction No. 3 after washing are then placed in baking oven by neutrality, dry to constant weight under the conditions of temperature is 110 DEG C, obtain single treatment silicon Diatomaceous earth, according to parts by weight, by 40 parts of single treatment diatomite, 10 parts of biogas slurries, 5 portions of sucrose, 60 parts of water are placed in No. 3 fermentation cauldrons In, it is 35 DEG C in temperature, under the conditions of revolving speed is 200r/min, after being stirred fermentation 5 days, filtering obtains No. 4 filter cakes, then uses Deionized water by No. 4 filter cakes to cleaning solution be neutrality, then No. 4 filter cakes after washing are placed in baking oven, in temperature be 110 It is dry to constant weight under part, secondary treatment diatomite is obtained, low-melting alloy and secondary treatment diatomite 1:5 in mass ratio are set In ball mill, under the conditions of temperature is 140 DEG C, mixing and ball milling 60min is to get modification infusorial earth;According to parts by weight, by 30 Part sisal fiber, 3 parts of Bacillus pasteurii bacterium solutions, 3 parts of urea, 40 parts of water are placed in No. 4 fermentation cauldrons, are 35 DEG C in temperature, are turned Under the conditions of speed is 200r/min, it is stirred fermentation 5 days, is then added dropwise to 0.2 times of quality of sisal fiber quality to No. 4 fermentation cauldrons The iron nitrate solution that score is 20% after being stirred 60min, obtains No. 5 filter cakes under the conditions of revolving speed is 600r/min, then will No. 5 filter cakes are placed in liquid nitrogen and freeze, and obtain freezing filter cake, will then freeze filter cake ball milling, and cross the sieve of 300 mesh, obtain crushed material, then Crushed material is placed in baking oven, it is dry to constant weight under the conditions of temperature is 110 DEG C, xeraphium particle is obtained, then by drying and crushing Material is placed in tube furnace, and nitrogen is passed through into tube furnace with 90mL/min rate, under the conditions of temperature is 750 DEG C, carbonizes 3h Afterwards, under the conditions of being warming up to 1500 DEG C with 15 DEG C/min rate, after high-temperature process 3h, room temperature is down to get modified fibre with furnace;It presses Parts by weight meter, by 60 parts of modified epoxies, 60 parts of diluents, 20 parts of pretreatment mica powders, 20 parts of modified fibres, 20 parts change Property additive, 8 parts of curing agent, 8 parts of modified meerschaums, 30 parts of alkalescent phenol resins, 20 parts of modification infusorial earths are placed in batch mixer, Under the conditions of revolving speed is 800r/min, 60min is stirred to get anti-static coatings.The diluent is by dimethylbenzene and third Ketone 1:20 mixed preparing in mass ratio forms.The starch is potato starch.The polyethyleneglycol derivative is poly- for novel Y-shaped Ethylene glycol.The isocyanates is toluene di-isocyanate(TDI).The organic acid is mixed by malic acid and citric acid 1:5 in mass ratio Conjunction is formulated.The low-melting alloy is bismuth tin alloy, each component mass content in bismuth tin alloy are as follows: bismuth accounts for 51%(ω), tin Account for 30%(ω), lead accounts for 8%(ω), indium accounts for 11%(ω).
According to parts by weight, by 3 parts of Bacillus pasteuriis, 2 parts of glycerol, 2 parts of polyethylene glycol, 30 parts of water are placed in No. 1 beaker In, No. 1 beaker is then placed in digital display and is tested the speed in constant temperature blender with magnetic force, is 35 DEG C in temperature, revolving speed is 300r/min condition Under, constant temperature is stirred 60min, obtains Bacillus pasteurii bacterium solution;According to parts by weight, by 30 parts of mica powders, 20 parts of starch, 2 Part yeast, 30 parts of water are placed in No. 1 fermentation cauldron, are 35 DEG C in temperature, under the conditions of revolving speed is 300r/min, are stirred fermentation 5 It, is then added the sodium hydroxide solution that mass fraction is 30% into No. 1 fermentation cauldron, under the conditions of revolving speed is 500r/min, stirs Mixing 60min is mixed, fermentation material is obtained, then fermentation material is placed in baking oven, it is dry to constant weight under the conditions of temperature is 110 DEG C, it obtains Dry fermentation material is then placed in ball mill grinding in ball mill by dry fermentation material, crosses the sieve of 120 mesh to get pretreatment mica powder; (N- amidino groups) dodecylacrylamide and polyethyleneglycol derivative 4:1 in mass ratio are mixed in No. 2 beakers, and to No. 2 0.4 times of polyethyleneglycol derivative quality of paracide and the two of 0.18 times of polyethyleneglycol derivative quality cyclopentadienyls are added in beaker Iron is 38 DEG C in temperature, after revolving speed is stirred 80min under conditions of being 320r/min, obtains mixed processing agent, in parts by weight Meter, by 30 parts of graphene oxides, 20 parts of mixed processing agents, 60 parts of water are placed in single-necked flask, are then placed in single-necked flask super In in sound separating apparatus, under the conditions of supersonic frequency is 75kHz, ultrasound 60min is mixed, quality point is then added in case single-necked flask Number adjusts pH to 8.4 for 30% ammonium hydroxide, under the conditions of revolving speed is 600r/min, 60min is stirred, then to single-necked flask The middle isocyanates for being added 0.02 times of graphene oxide quality, under the conditions of revolving speed is 600r/min, after being stirred 60min, Filtering, obtain No. 1 filter cake, then with deionized water by No. 1 Washing of Filter Cake 8 times, No. 1 filter cake after washing is then placed in baking oven In, under the conditions of temperature is 110 DEG C, drying to constant weight is to get modified additive;According to parts by weight, by 30 parts of sepiolites, 3 Part secondary settling tank sludge, 2 portions of sucrose, 60 parts of water are placed in No. 2 fermentation cauldrons, in temperature be 35 DEG C, under the conditions of revolving speed is 200r/min, Be stirred fermentation 5 days, 0.2 times of sepiolite quality of organic acid be then added into No. 2 fermentation cauldrons, in revolving speed be 600r/min Under the conditions of, be stirred 60min, then into No. 2 fermentation cauldrons be added dropwise mass fraction be 30% ammonium hydroxide adjust pH to 8.3, in turn Under the conditions of speed is 600r/min, after being stirred 60min, filtering obtains No. 2 filter cakes, then No. 2 filter cakes is placed in baking oven, in Under the conditions of temperature is 110 DEG C, drying is to constant weight to get modified meerschaum;It by epoxy resin plus moves into No. 3 beakers, and by No. 3 Beaker moves into digital display and tests the speed constant temperature blender with magnetic force, and epoxy resin in No. 3 beakers is heated to 80 DEG C, and into No. 3 beakers plus Enter 0.3 times of epoxy resin quality of paraphenylene terephthalamide and 0.4 times of epoxy resin quality of acrylonitrile-butadiene rubber latex, in temperature be 85 DEG C, after revolving speed is stirred 50min under conditions of being 300r/min, obtain modified epoxy;According to parts by weight, by 40 parts of matter The glyoxal solution that score is 50%, the potassium hydroxide solution that 20 parts of mass fractions are 30% are measured, 40 parts of hydroquinones are placed in four mouthfuls In flask, and four-hole boiling flask is placed in digital display and is tested the speed in constant temperature blender with magnetic force, is 78 DEG C in temperature, revolving speed is 500r/min item Under part, after constant temperature is stirred to react 4h, temperature in four-hole boiling flask is down to 62 DEG C, then glyoxal solution body is added into four-hole boiling flask 0.3 times of ethylene urea of product, in temperature be 62 DEG C, under the conditions of revolving speed is 500r/min, after constant temperature is stirred to react 60min, Jiang Sikou Temperature is down to 52 DEG C in flask, and 0.2 times of glyoxal solution volume of Silane coupling reagent KH-570 is then added into four-hole boiling flask, It is 52 DEG C in temperature, under the conditions of revolving speed is 500r/min, constant temperature is stirred to react 50min, temperature in four-hole boiling flask is down to 42 DEG C, It is 42 DEG C in temperature, under the conditions of revolving speed is 500r/min, continues constant temperature and be stirred to react 30min to get alkalescent phenol resin;By silicon The hydrochloric acid 1:20 in mass ratio that diatomaceous earth and mass fraction are 30% is placed in No. 4 beakers, under the conditions of revolving speed is 600r/min, is stirred After mixing mixing 60min, filtering obtains No. 3 filter cakes, No. 3 Washing of Filter Cake to cleaning solutions are by the ammonium hydroxide for being then 30% with mass fraction No. 3 after washing are then placed in baking oven by neutrality, dry to constant weight under the conditions of temperature is 110 DEG C, obtain single treatment silicon Diatomaceous earth, according to parts by weight, by 40 parts of single treatment diatomite, 10 parts of biogas slurries, 5 portions of sucrose, 60 parts of water are placed in No. 3 fermentation cauldrons In, it is 35 DEG C in temperature, under the conditions of revolving speed is 200r/min, after being stirred fermentation 5 days, filtering obtains No. 4 filter cakes, then uses Deionized water by No. 4 filter cakes to cleaning solution be neutrality, then No. 4 filter cakes after washing are placed in baking oven, in temperature be 110 It is dry to constant weight under part, secondary treatment diatomite is obtained, low-melting alloy and secondary treatment diatomite 1:5 in mass ratio are set In ball mill, under the conditions of temperature is 140 DEG C, mixing and ball milling 60min is to get modification infusorial earth;According to parts by weight, by 60 Part modified epoxy, 60 parts of diluents, 20 parts of pretreatment mica powders, 20 parts of modified additives, 8 parts of curing agent, 8 parts of modified seas Afrodite, 30 parts of alkalescent phenol resins, 20 parts of modification infusorial earths are placed in batch mixer, under the conditions of revolving speed is 800r/min, stirring 60min is mixed to get anti-static coatings.The diluent is formed by dimethylbenzene and acetone 1:20 mixed preparing in mass ratio. The starch is potato starch.The polyethyleneglycol derivative is novel Y-shaped polyethylene glycol.The isocyanates is toluene two Isocyanates.The organic acid is formed by malic acid and citric acid 1:5 mixed preparing in mass ratio.The low-melting alloy is Bismuth tin alloy, each component mass content in bismuth tin alloy are as follows: bismuth accounts for 51%(ω), tin accounts for 30%(ω), lead accounts for 8%(ω), indium accounts for 11%(ω).
According to parts by weight, by 3 parts of Bacillus pasteuriis, 2 parts of glycerol, 2 parts of polyethylene glycol, 30 parts of water are placed in No. 1 beaker In, No. 1 beaker is then placed in digital display and is tested the speed in constant temperature blender with magnetic force, is 35 DEG C in temperature, revolving speed is 300r/min condition Under, constant temperature is stirred 60min, obtains Bacillus pasteurii bacterium solution;According to parts by weight, by 30 parts of mica powders, 20 parts of starch, 2 Part yeast, 30 parts of water are placed in No. 1 fermentation cauldron, are 35 DEG C in temperature, under the conditions of revolving speed is 300r/min, are stirred fermentation 5 It, is then added the sodium hydroxide solution that mass fraction is 30% into No. 1 fermentation cauldron, under the conditions of revolving speed is 500r/min, stirs Mixing 60min is mixed, fermentation material is obtained, then fermentation material is placed in baking oven, it is dry to constant weight under the conditions of temperature is 110 DEG C, it obtains Dry fermentation material is then placed in ball mill grinding in ball mill by dry fermentation material, crosses the sieve of 120 mesh to get pretreatment mica powder; According to parts by weight, by 30 parts of sepiolites, 3 parts of secondary settling tank sludge, 2 portions of sucrose, 60 parts of water are placed in No. 2 fermentation cauldrons, Yu Wendu It is 35 DEG C, under the conditions of revolving speed is 200r/min, is stirred fermentation 5 days, sepiolite quality is then added into No. 2 fermentation cauldrons 0.2 times of organic acid is stirred 60min, quality then is added dropwise into No. 2 fermentation cauldrons under the conditions of revolving speed is 600r/min The ammonium hydroxide that score is 30% adjusts pH to 8.3, and under the conditions of revolving speed is 600r/min, after being stirred 60min, filtering obtains No. 2 No. 2 filter cakes are then placed in baking oven by filter cake, and under the conditions of temperature is 110 DEG C, drying is to constant weight to get modified meerschaum;It will Epoxy resin, which adds, to be moved into No. 3 beakers, and No. 3 beakers are moved into digital displays and are tested the speed constant temperature blender with magnetic force, by epoxy in No. 3 beakers Resin is heated to 80 DEG C, and 0.3 times of epoxy resin quality of paraphenylene terephthalamide and epoxy resin quality are added into No. 3 beakers 0.4 times of acrylonitrile-butadiene rubber latex is 85 DEG C in temperature, after revolving speed is stirred 50min under conditions of being 300r/min, obtains modification Epoxy resin;According to parts by weight, the glyoxal solution for being 50% by 40 parts of mass fractions, the hydrogen-oxygen that 20 parts of mass fractions are 30% Change potassium solution, 40 parts of hydroquinones are placed in four-hole boiling flask, and four-hole boiling flask is placed in digital display and is tested the speed in constant temperature blender with magnetic force, It is 78 DEG C in temperature, under the conditions of revolving speed is 500r/min, after constant temperature is stirred to react 4h, temperature in four-hole boiling flask is down to 62 DEG C, 0.3 times of glyoxal solution volume of ethylene urea is added into four-hole boiling flask again, is 62 DEG C in temperature, revolving speed is 500r/min condition Under, after constant temperature is stirred to react 60min, temperature in four-hole boiling flask is down to 52 DEG C, it is molten that glyoxal is then added into four-hole boiling flask The Silane coupling reagent KH-570 of 0.2 times of liquid product is 52 DEG C in temperature, and under the conditions of revolving speed is 500r/min, constant temperature is stirred to react Temperature in four-hole boiling flask is down to 42 DEG C by 50min, is 42 DEG C in temperature, under the conditions of revolving speed is 500r/min, is continued constant temperature stirring 30min is reacted to get alkalescent phenol resin;The hydrochloric acid 1:20 in mass ratio that diatomite and mass fraction are 30% is placed in No. 4 burnings In cup, under the conditions of revolving speed is 600r/min, after being stirred 60min, filtering obtains No. 3 filter cakes, is then with mass fraction 30% ammonium hydroxide by No. 3 Washing of Filter Cake to cleaning solution be neutrality, then No. 3 after washing are placed in baking oven, in temperature be 110 It is dry to constant weight under the conditions of DEG C, single treatment diatomite is obtained, according to parts by weight, by 40 parts of single treatment diatomite, 10 parts of natural ponds Liquid, 5 portions of sucrose, 60 parts of water are placed in No. 3 fermentation cauldrons, are 35 DEG C in temperature, under the conditions of revolving speed is 200r/min, are stirred hair After ferment 5 days, filtering obtains No. 4 filter cakes, is then neutrality by No. 4 filter cake to cleaning solutions with deionized water, then by 4 after washing Number filter cake is placed in baking oven, dry to constant weight under the conditions of temperature is 110, obtains secondary treatment diatomite, by low-melting alloy with Secondary treatment diatomite 1:5 in mass ratio is placed in ball mill, under the conditions of temperature is 140 DEG C, mixing and ball milling 60min, i.e., Obtain modification infusorial earth;According to parts by weight, by 30 parts of sisal fibers, 3 parts of Bacillus pasteurii bacterium solutions, 3 parts of urea, 40 parts of water are set In No. 4 fermentation cauldrons, it is 35 DEG C in temperature, under the conditions of revolving speed is 200r/min, is stirred fermentation 5 days, then ferments to No. 4 Kettle is added dropwise to the iron nitrate solution that 0.2 times of mass fraction of sisal fiber quality is 20%, under the conditions of revolving speed is 600r/min, stirs After mixing mixing 60min, No. 5 filter cakes are obtained, then No. 5 filter cakes are placed in liquid nitrogen and are freezed, freezing filter cake is obtained, will then freeze filter cake Ball milling crosses the sieve of 300 mesh, obtains crushed material, then crushed material is placed in baking oven, dry to perseverance under the conditions of temperature is 110 DEG C Weight, obtains xeraphium particle, then xeraphium particle is placed in tube furnace, and be passed through nitrogen into tube furnace with 90mL/min rate Gas, under the conditions of temperature is 750 DEG C, after carbonizing 3h, under the conditions of being warming up to 1500 DEG C with 15 DEG C/min rate, high-temperature process 3h Afterwards, room temperature is down to get modified fibre with furnace;According to parts by weight, by 60 parts of modified epoxies, 60 parts of diluents, 20 parts Pre-process mica powder, 20 parts of modified fibres, 8 parts of curing agent, 8 parts of modified meerschaums, 30 parts of alkalescent phenol resins, 20 parts of modified silicons Diatomaceous earth is placed in batch mixer, under the conditions of revolving speed is 800r/min, is stirred 60min to get anti-static coatings.The dilution Agent is formed by dimethylbenzene and acetone 1:20 mixed preparing in mass ratio.The starch is potato starch.The polyethylene glycol Derivative is novel Y-shaped polyethylene glycol.The isocyanates is toluene di-isocyanate(TDI).The organic acid is by malic acid and lemon Lemon acid 1:5 mixed preparing in mass ratio forms.The low-melting alloy is bismuth tin alloy, each component mass content in bismuth tin alloy Are as follows: bismuth accounts for 51%(ω), tin accounts for 30%(ω), lead accounts for 8%(ω), indium accounts for 11%(ω).
According to parts by weight, by 3 parts of Bacillus pasteuriis, 2 parts of glycerol, 2 parts of polyethylene glycol, 30 parts of water are placed in No. 1 beaker In, No. 1 beaker is then placed in digital display and is tested the speed in constant temperature blender with magnetic force, is 35 DEG C in temperature, revolving speed is 300r/min condition Under, constant temperature is stirred 60min, obtains Bacillus pasteurii bacterium solution;According to parts by weight, by 30 parts of mica powders, 20 parts of starch, 2 Part yeast, 30 parts of water are placed in No. 1 fermentation cauldron, are 35 DEG C in temperature, under the conditions of revolving speed is 300r/min, are stirred fermentation 5 It, is then added the sodium hydroxide solution that mass fraction is 30% into No. 1 fermentation cauldron, under the conditions of revolving speed is 500r/min, stirs Mixing 60min is mixed, fermentation material is obtained, then fermentation material is placed in baking oven, it is dry to constant weight under the conditions of temperature is 110 DEG C, it obtains Dry fermentation material is then placed in ball mill grinding in ball mill by dry fermentation material, crosses the sieve of 120 mesh to get pretreatment mica powder; (N- amidino groups) dodecylacrylamide and polyethyleneglycol derivative 4:1 in mass ratio are mixed in No. 2 beakers, and to No. 2 0.4 times of polyethyleneglycol derivative quality of paracide and the two of 0.18 times of polyethyleneglycol derivative quality cyclopentadienyls are added in beaker Iron is 38 DEG C in temperature, after revolving speed is stirred 80min under conditions of being 320r/min, obtains mixed processing agent, in parts by weight Meter, by 30 parts of graphene oxides, 20 parts of mixed processing agents, 60 parts of water are placed in single-necked flask, are then placed in single-necked flask super In in sound separating apparatus, under the conditions of supersonic frequency is 75kHz, ultrasound 60min is mixed, quality point is then added in case single-necked flask Number adjusts pH to 8.4 for 30% ammonium hydroxide, under the conditions of revolving speed is 600r/min, 60min is stirred, then to single-necked flask The middle isocyanates for being added 0.02 times of graphene oxide quality, under the conditions of revolving speed is 600r/min, after being stirred 60min, Filtering, obtain No. 1 filter cake, then with deionized water by No. 1 Washing of Filter Cake 8 times, No. 1 filter cake after washing is then placed in baking oven In, under the conditions of temperature is 110 DEG C, drying to constant weight is to get modified additive;By epoxy resin plus move into No. 3 beakers, and No. 3 beakers are moved into digital displays to test the speed constant temperature blender with magnetic force, epoxy resin in No. 3 beakers is heated to 80 DEG C, and to No. 3 beakers 0.3 times of epoxy resin quality of paraphenylene terephthalamide of middle addition and 0.4 times of epoxy resin quality of acrylonitrile-butadiene rubber latex are in temperature 85 DEG C, after revolving speed is stirred 50min under conditions of being 300r/min, obtain modified epoxy;According to parts by weight, by 40 parts The glyoxal solution that mass fraction is 50%, the potassium hydroxide solution that 20 parts of mass fractions are 30%, 40 parts of hydroquinones are placed in four In mouthful flask, and four-hole boiling flask is placed in digital display and is tested the speed in constant temperature blender with magnetic force, in temperature be 78 DEG C, revolving speed 500r/min Under the conditions of, after constant temperature is stirred to react 4h, temperature in four-hole boiling flask is down to 62 DEG C, then glyoxal solution is added into four-hole boiling flask The ethylene urea that 0.3 times of volume, in temperature be 62 DEG C, revolving speed be 500r/min under the conditions of, after constant temperature is stirred to react 60min, by four Temperature is down to 52 DEG C in mouth flask, and 0.2 times of glyoxal solution volume of silane coupling agent KH- is then added into four-hole boiling flask 570, it is 52 DEG C in temperature, under the conditions of revolving speed is 500r/min, constant temperature is stirred to react 50min, and temperature in four-hole boiling flask is down to 42 DEG C, it is 42 DEG C in temperature, under the conditions of revolving speed is 500r/min, continues constant temperature and be stirred to react 30min to get alkaline phenol formaldehyde tree Rouge;The hydrochloric acid 1:20 in mass ratio that diatomite and mass fraction are 30% is placed in No. 4 beakers, in revolving speed be 600r/min item Under part, after being stirred 60min, filtering, obtain No. 3 filter cakes, then with mass fraction be 30% ammonium hydroxide by No. 3 Washing of Filter Cake extremely Cleaning solution is neutrality, and then No. 3 after washing are placed in baking oven, dry to constant weight under the conditions of temperature is 110 DEG C, obtains one Secondary processing diatomite, according to parts by weight, by 40 parts of single treatment diatomite, 10 parts of biogas slurries, 5 portions of sucrose, 60 parts of water are placed in No. 3 It is 35 DEG C in temperature in fermentation cauldron, under the conditions of revolving speed is 200r/min, after being stirred fermentation 5 days, filtering obtains No. 4 filter cakes, Then it is neutrality by No. 4 filter cake to cleaning solutions with deionized water, then No. 4 filter cakes after washing is placed in baking oven, Yu Wendu It is dry to constant weight under the conditions of 110, secondary treatment diatomite is obtained, low-melting alloy and secondary treatment diatomite are pressed into quality It is placed in ball mill than 1:5, under the conditions of temperature is 140 DEG C, mixing and ball milling 60min is to get modification infusorial earth;In parts by weight Meter, by 30 parts of sisal fibers, 3 parts of Bacillus pasteurii bacterium solutions, 3 parts of urea, 40 parts of water are placed in No. 4 fermentation cauldrons, are in temperature 35 DEG C, under the conditions of revolving speed is 200r/min, it is stirred fermentation 5 days, is then added dropwise to sisal fiber quality to No. 4 fermentation cauldrons The iron nitrate solution that 0.2 times of mass fraction is 20% after being stirred 60min, obtains No. 5 filters under the conditions of revolving speed is 600r/min No. 5 filter cakes are then placed in liquid nitrogen and freeze, obtain freezing filter cake by cake, will then freeze filter cake ball milling, and cross the sieve of 300 mesh, obtain powder Crushed material is then placed in baking oven by particle, dry to constant weight under the conditions of temperature is 110 DEG C, obtains xeraphium particle, then Xeraphium particle is placed in tube furnace, and nitrogen is passed through into tube furnace with 90mL/min rate, in temperature be 750 DEG C of conditions Under, after carbonizing 3h, under the conditions of being warming up to 1500 DEG C with 15 DEG C/min rate, after high-temperature process 3h, room temperature is down to furnace to get changing Property fiber;According to parts by weight, by 60 parts of modified epoxies, 60 parts of diluents, 20 parts of pretreatment mica powders, 20 parts modified fine Dimension, 20 parts of modified additives, 8 parts of curing agent, 30 parts of alkalescent phenol resins, 20 parts of modification infusorial earths are placed in batch mixer, in turn Under the conditions of speed is 800r/min, 60min is stirred to get anti-static coatings.The diluent be by dimethylbenzene and acetone by Mass ratio 1:20 mixed preparing forms.The starch is potato starch.The polyethyleneglycol derivative is the poly- second two of novel Y-shaped Alcohol.The isocyanates is toluene di-isocyanate(TDI).The organic acid is to be mixed to match with citric acid 1:5 in mass ratio by malic acid It makes.The low-melting alloy is bismuth tin alloy, each component mass content in bismuth tin alloy are as follows: bismuth accounts for 51%(ω), tin accounts for 30%(ω), lead accounts for 8%(ω), indium accounts for 11%(ω).
According to parts by weight, by 3 parts of Bacillus pasteuriis, 2 parts of glycerol, 2 parts of polyethylene glycol, 30 parts of water are placed in No. 1 beaker In, No. 1 beaker is then placed in digital display and is tested the speed in constant temperature blender with magnetic force, is 35 DEG C in temperature, revolving speed is 300r/min condition Under, constant temperature is stirred 60min, obtains Bacillus pasteurii bacterium solution;According to parts by weight, by 30 parts of mica powders, 20 parts of starch, 2 Part yeast, 30 parts of water are placed in No. 1 fermentation cauldron, are 35 DEG C in temperature, under the conditions of revolving speed is 300r/min, are stirred fermentation 5 It, is then added the sodium hydroxide solution that mass fraction is 30% into No. 1 fermentation cauldron, under the conditions of revolving speed is 500r/min, stirs Mixing 60min is mixed, fermentation material is obtained, then fermentation material is placed in baking oven, it is dry to constant weight under the conditions of temperature is 110 DEG C, it obtains Dry fermentation material is then placed in ball mill grinding in ball mill by dry fermentation material, crosses the sieve of 120 mesh to get pretreatment mica powder; (N- amidino groups) dodecylacrylamide and polyethyleneglycol derivative 4:1 in mass ratio are mixed in No. 2 beakers, and to No. 2 0.4 times of polyethyleneglycol derivative quality of paracide and the two of 0.18 times of polyethyleneglycol derivative quality cyclopentadienyls are added in beaker Iron is 38 DEG C in temperature, after revolving speed is stirred 80min under conditions of being 320r/min, obtains mixed processing agent, in parts by weight Meter, by 30 parts of graphene oxides, 20 parts of mixed processing agents, 60 parts of water are placed in single-necked flask, are then placed in single-necked flask super In in sound separating apparatus, under the conditions of supersonic frequency is 75kHz, ultrasound 60min is mixed, quality point is then added in case single-necked flask Number adjusts pH to 8.4 for 30% ammonium hydroxide, under the conditions of revolving speed is 600r/min, 60min is stirred, then to single-necked flask The middle isocyanates for being added 0.02 times of graphene oxide quality, under the conditions of revolving speed is 600r/min, after being stirred 60min, Filtering, obtain No. 1 filter cake, then with deionized water by No. 1 Washing of Filter Cake 8 times, No. 1 filter cake after washing is then placed in baking oven In, under the conditions of temperature is 110 DEG C, drying to constant weight is to get modified additive;According to parts by weight, by 30 parts of sepiolites, 3 Part secondary settling tank sludge, 2 portions of sucrose, 60 parts of water are placed in No. 2 fermentation cauldrons, in temperature be 35 DEG C, under the conditions of revolving speed is 200r/min, Be stirred fermentation 5 days, 0.2 times of sepiolite quality of organic acid be then added into No. 2 fermentation cauldrons, in revolving speed be 600r/min Under the conditions of, be stirred 60min, then into No. 2 fermentation cauldrons be added dropwise mass fraction be 30% ammonium hydroxide adjust pH to 8.3, in turn Under the conditions of speed is 600r/min, after being stirred 60min, filtering obtains No. 2 filter cakes, then No. 2 filter cakes is placed in baking oven, in Under the conditions of temperature is 110 DEG C, drying is to constant weight to get modified meerschaum;It by epoxy resin plus moves into No. 3 beakers, and by No. 3 Beaker moves into digital display and tests the speed constant temperature blender with magnetic force, and epoxy resin in No. 3 beakers is heated to 80 DEG C, and into No. 3 beakers plus Enter 0.3 times of epoxy resin quality of paraphenylene terephthalamide and 0.4 times of epoxy resin quality of acrylonitrile-butadiene rubber latex, in temperature be 85 DEG C, after revolving speed is stirred 50min under conditions of being 300r/min, obtain modified epoxy;It is by diatomite and mass fraction 30% hydrochloric acid 1:20 in mass ratio is placed in No. 4 beakers, under the conditions of revolving speed is 600r/min, after being stirred 60min, and mistake Filter obtains No. 3 filter cakes, and No. 3 Washing of Filter Cake to cleaning solutions are neutrality by the ammonium hydroxide for being then 30% with mass fraction, then will washing No. 3 afterwards are placed in baking oven, dry to constant weight under the conditions of temperature is 110 DEG C, obtain single treatment diatomite, in parts by weight Meter, by 40 parts of single treatment diatomite, 10 parts of biogas slurries, 5 portions of sucrose, 60 parts of water are placed in No. 3 fermentation cauldrons, in temperature be 35 DEG C, Under the conditions of revolving speed is 200r/min, after being stirred fermentation 5 days, filtering obtains No. 4 filter cakes, then with deionized water by No. 4 filter cakes It is neutrality to cleaning solution, then No. 4 filter cakes after washing is placed in baking oven, under the conditions of temperature is 110, drying to constant weight, Secondary treatment diatomite is obtained, low-melting alloy and secondary treatment diatomite 1:5 in mass ratio are placed in ball mill, Yu Wendu Under the conditions of 140 DEG C, mixing and ball milling 60min is to get modification infusorial earth;According to parts by weight, by 30 parts of sisal fibers, 3 parts bars Family name's bacillus bacterium solution, 3 parts of urea, 40 parts of water are placed in No. 4 fermentation cauldrons, are 35 DEG C in temperature, revolving speed is 200r/min condition Under, it is stirred fermentation 5 days, is then added dropwise to the nitric acid that 0.2 times of mass fraction of sisal fiber quality is 20% to No. 4 fermentation cauldrons Ferrous solution after being stirred 60min, obtains No. 5 filter cakes, No. 5 filter cakes is then placed in liquid nitrogen under the conditions of revolving speed is 600r/min Middle freezing obtains freezing filter cake, will then freeze filter cake ball milling, and cross the sieve of 300 mesh, obtain crushed material, crushed material is then placed in baking It is dry to constant weight under the conditions of temperature is 110 DEG C in case, xeraphium particle is obtained, xeraphium particle is then placed in tube furnace In, and nitrogen is passed through into tube furnace with 90mL/min rate, under the conditions of temperature is 750 DEG C, after carbonizing 3h, with 15 DEG C/min Rate is warming up under the conditions of 1500 DEG C, after high-temperature process 3h, is down to room temperature with furnace to get modified fibre;According to parts by weight, will 60 parts of modified epoxies, 60 parts of diluents, 20 parts of pretreatment mica powders, 20 parts of modified fibres, 20 parts of modified additives, 8 parts Curing agent, 8 parts of modified meerschaums, 20 parts of modification infusorial earths are placed in batch mixer, and under the conditions of revolving speed is 800r/min, stirring is mixed 60min is closed to get anti-static coatings.The diluent is formed by dimethylbenzene and acetone 1:20 mixed preparing in mass ratio.Institute Stating starch is potato starch.The polyethyleneglycol derivative is novel Y-shaped polyethylene glycol.The isocyanates is that toluene two is different Cyanate.The organic acid is formed by malic acid and citric acid 1:5 mixed preparing in mass ratio.The low-melting alloy is bismuth Tin alloy, each component mass content in bismuth tin alloy are as follows: bismuth accounts for 51%(ω), tin accounts for 30%(ω), lead accounts for 8%(ω), indium accounts for 11% (ω).
According to parts by weight, by 3 parts of Bacillus pasteuriis, 2 parts of glycerol, 2 parts of polyethylene glycol, 30 parts of water are placed in No. 1 beaker In, No. 1 beaker is then placed in digital display and is tested the speed in constant temperature blender with magnetic force, is 35 DEG C in temperature, revolving speed is 300r/min condition Under, constant temperature is stirred 60min, obtains Bacillus pasteurii bacterium solution;According to parts by weight, by 30 parts of mica powders, 20 parts of starch, 2 Part yeast, 30 parts of water are placed in No. 1 fermentation cauldron, are 35 DEG C in temperature, under the conditions of revolving speed is 300r/min, are stirred fermentation 5 It, is then added the sodium hydroxide solution that mass fraction is 30% into No. 1 fermentation cauldron, under the conditions of revolving speed is 500r/min, stirs Mixing 60min is mixed, fermentation material is obtained, then fermentation material is placed in baking oven, it is dry to constant weight under the conditions of temperature is 110 DEG C, it obtains Dry fermentation material is then placed in ball mill grinding in ball mill by dry fermentation material, crosses the sieve of 120 mesh to get pretreatment mica powder; (N- amidino groups) dodecylacrylamide and polyethyleneglycol derivative 4:1 in mass ratio are mixed in No. 2 beakers, and to No. 2 0.4 times of polyethyleneglycol derivative quality of paracide and the two of 0.18 times of polyethyleneglycol derivative quality cyclopentadienyls are added in beaker Iron is 38 DEG C in temperature, after revolving speed is stirred 80min under conditions of being 320r/min, obtains mixed processing agent, in parts by weight Meter, by 30 parts of graphene oxides, 20 parts of mixed processing agents, 60 parts of water are placed in single-necked flask, are then placed in single-necked flask super In in sound separating apparatus, under the conditions of supersonic frequency is 75kHz, ultrasound 60min is mixed, quality point is then added in case single-necked flask Number adjusts pH to 8.4 for 30% ammonium hydroxide, under the conditions of revolving speed is 600r/min, 60min is stirred, then to single-necked flask The middle isocyanates for being added 0.02 times of graphene oxide quality, under the conditions of revolving speed is 600r/min, after being stirred 60min, Filtering, obtain No. 1 filter cake, then with deionized water by No. 1 Washing of Filter Cake 8 times, No. 1 filter cake after washing is then placed in baking oven In, under the conditions of temperature is 110 DEG C, drying to constant weight is to get modified additive;According to parts by weight, by 30 parts of sepiolites, 3 Part secondary settling tank sludge, 2 portions of sucrose, 60 parts of water are placed in No. 2 fermentation cauldrons, in temperature be 35 DEG C, under the conditions of revolving speed is 200r/min, Be stirred fermentation 5 days, 0.2 times of sepiolite quality of organic acid be then added into No. 2 fermentation cauldrons, in revolving speed be 600r/min Under the conditions of, be stirred 60min, then into No. 2 fermentation cauldrons be added dropwise mass fraction be 30% ammonium hydroxide adjust pH to 8.3, in turn Under the conditions of speed is 600r/min, after being stirred 60min, filtering obtains No. 2 filter cakes, then No. 2 filter cakes is placed in baking oven, in Under the conditions of temperature is 110 DEG C, drying is to constant weight to get modified meerschaum;It by epoxy resin plus moves into No. 3 beakers, and by No. 3 Beaker moves into digital display and tests the speed constant temperature blender with magnetic force, and epoxy resin in No. 3 beakers is heated to 80 DEG C, and into No. 3 beakers plus Enter 0.3 times of epoxy resin quality of paraphenylene terephthalamide and 0.4 times of epoxy resin quality of acrylonitrile-butadiene rubber latex, in temperature be 85 DEG C, after revolving speed is stirred 50min under conditions of being 300r/min, obtain modified epoxy;According to parts by weight, by 40 parts of matter The glyoxal solution that score is 50%, the potassium hydroxide solution that 20 parts of mass fractions are 30% are measured, 40 parts of hydroquinones are placed in four mouthfuls In flask, and four-hole boiling flask is placed in digital display and is tested the speed in constant temperature blender with magnetic force, is 78 DEG C in temperature, revolving speed is 500r/min item Under part, after constant temperature is stirred to react 4h, temperature in four-hole boiling flask is down to 62 DEG C, then glyoxal solution body is added into four-hole boiling flask 0.3 times of ethylene urea of product, in temperature be 62 DEG C, under the conditions of revolving speed is 500r/min, after constant temperature is stirred to react 60min, Jiang Sikou Temperature is down to 52 DEG C in flask, and 0.2 times of glyoxal solution volume of Silane coupling reagent KH-570 is then added into four-hole boiling flask, It is 52 DEG C in temperature, under the conditions of revolving speed is 500r/min, constant temperature is stirred to react 50min, temperature in four-hole boiling flask is down to 42 DEG C, It is 42 DEG C in temperature, under the conditions of revolving speed is 500r/min, continues constant temperature and be stirred to react 30min to get alkalescent phenol resin;By weight Number meter is measured, by 30 parts of sisal fibers, 3 parts of Bacillus pasteurii bacterium solutions, 3 parts of urea, 40 parts of water are placed in No. 4 fermentation cauldrons, in Temperature is 35 DEG C, under the conditions of revolving speed is 200r/min, is stirred fermentation 5 days, is then added dropwise to sisal fiber to No. 4 fermentation cauldrons The iron nitrate solution that 0.2 times of mass fraction of quality is 20% after being stirred 60min, obtains 5 under the conditions of revolving speed is 600r/min No. 5 filter cakes, are then placed in liquid nitrogen and freeze, obtain freezing filter cake by number filter cake, will then freeze filter cake ball milling, and cross the sieve of 300 mesh, Crushed material is obtained, then crushed material is placed in baking oven, under the conditions of temperature is 110 DEG C, drying to constant weight obtains xeraphium particle, Then xeraphium particle is placed in tube furnace, and nitrogen is passed through into tube furnace with 90mL/min rate, in temperature be 750 DEG C Under the conditions of, after carbonizing 3h, under the conditions of being warming up to 1500 DEG C with 15 DEG C/min rate, after high-temperature process 3h, it is down to room temperature with furnace, i.e., Obtain modified fibre;According to parts by weight, by 60 parts of modified epoxies, 60 parts of diluents, 20 parts of pretreatment mica powders, 20 parts change Property fiber, 20 parts of modified additives, 8 parts of curing agent, 8 parts of modified meerschaums, 30 parts of alkalescent phenol resins are placed in batch mixer, in Under the conditions of revolving speed is 800r/min, 60min is stirred to get anti-static coatings.The diluent is by dimethylbenzene and acetone 1:20 mixed preparing in mass ratio forms.The starch is potato starch.The polyethyleneglycol derivative is the poly- second of novel Y-shaped Glycol.The isocyanates is toluene di-isocyanate(TDI).The organic acid is to be mixed by malic acid with citric acid 1:5 in mass ratio It is formulated.The low-melting alloy is bismuth tin alloy, each component mass content in bismuth tin alloy are as follows: bismuth accounts for 51%(ω), tin accounts for 30%(ω), lead accounts for 8%(ω), indium accounts for 11%(ω).
1 to 6 gained anti-static coatings of example are subjected to performance detection, the specific detection method is as follows:
The resistivity of conductive coating is detected according to GB/T 26004.
Specific testing result is as shown in table 1:
Table 1: performance detection table
Detection project Example 1 Example 2 Example 3 Example 4 Example 5 Example 6
Resistivity/× 10-4Ω·cm 0.36 0.61 0.68 0.72 0.75 0.67
By 1 testing result of table it is found that anti-static coatings provided by the invention have excellent antistatic performance.

Claims (10)

1. a kind of preparation method of anti-static coatings, it is characterised in that referring specifically to north, steps are as follows:
(1) according to parts by weight, by 20~30 parts of sisal fibers, 2~3 parts of Bacillus pasteurii bacterium solutions, 2~3 parts of urea, 30~ 40 parts of water mixed fermentations are then added dropwise to 0.1~0.2 times of sisal fiber quality of iron nitrate solution, are stirred, filtering, cold Freeze, ball milling, be sieved, dry, charing heats up, high-temperature process is to get modified fibre step by step;
(2) according to parts by weight, by 40~60 parts of modified epoxies, 40~60 parts of diluents, 10~20 parts of pretreatment micas Powder, 10~20 parts of modified fibres, 10~20 parts of modified additives, 5~8 parts of curing agent, 5~8 parts of modified meerschaums, 20~30 parts Alkalescent phenol resin, 10~20 parts of modification infusorial earths, is stirred to get anti-static coatings.
2. a kind of preparation method of anti-static coatings according to claim 1, it is characterised in that: step (1) Pasteur's bud The preparation process of spore bacillus bacterium solution are as follows: according to parts by weight, by 2~3 parts of Bacillus pasteuriis, 1~2 part of glycerol, 1~2 part poly- Ethylene glycol, 20~30 parts of water termostats are stirred, and obtain Bacillus pasteurii bacterium solution.
3. a kind of preparation method of anti-static coatings according to claim 1, it is characterised in that: step (2) the modified ring The preparation process of oxygen resin are as follows: epoxy resin is heated, and be added 0.2~0.3 times of epoxy resin quality paraphenylene terephthalamide and The acrylonitrile-butadiene rubber latex that 0.2~0.4 times of epoxy resin quality after being stirred, obtains modified epoxy.
4. a kind of preparation method of anti-static coatings according to claim 1, it is characterised in that: step (2) described diluent It is to be formed by dimethylbenzene and acetone 1:10~1:20 mixed preparing in mass ratio.
5. a kind of preparation method of anti-static coatings according to claim 1, it is characterised in that: step (2) described pretreatment The preparation process of mica powder are as follows: according to parts by weight, by 20~30 parts of mica powders, 10~20 parts of starch, 1~2 part of yeast, 20~ 30 parts of water mixed fermentations, are subsequently added into sodium hydroxide solution and are stirred, dry, pulverize, ball milling, and sieving is to get pretreatment cloud Female powder;The starch is potato starch, any one in tapioca or wheaten starch.
6. a kind of preparation method of anti-static coatings according to claim 1, it is characterised in that: step (2) described modification adds The process of charging are as follows: (N- amidino groups) dodecylacrylamide is mixed with polyethyleneglycol derivative 2:1~4:1 in mass ratio, And be added 0.2~0.4 times of polyethyleneglycol derivative quality paracide and 0.12~0.18 times of polyethyleneglycol derivative quality Ferrocene, be stirred, obtain mixed processing agent, according to parts by weight, by 20~30 parts of graphene oxides, 10~20 parts of mixing Inorganic agent, 40~60 parts of water mixing ultrasounds, is subsequently added into ammonium hydroxide and adjusts pH to 8.1~8.4, be stirred, be subsequently added into oxidation The isocyanates that 0.01~0.02 times of graphene quality, is stirred, and filters, washing, dry to get modified additive;It is described Polyethyleneglycol derivative is novel Y-shaped polyethylene glycol, any one in multi-arm polyethylene glycol or methoxy poly (ethylene glycol);It is described Isocyanates is toluene di-isocyanate(TDI), any one in methyl diphenylene diisocyanate or trimethylhexane diisocyanate Kind.
7. a kind of preparation method of anti-static coatings according to claim 1, it is characterised in that: step (2) described curing agent It is to be formed by dihexyl triamine and diethylaminopropylamine 1:3~1:5 mixed preparing in mass ratio.
8. a kind of preparation method of anti-static coatings according to claim 1, it is characterised in that: step (2) the modified sea The preparation process of afrodite are as follows: according to parts by weight, by 20~30 parts of sepiolites, 2~3 parts of secondary settling tank sludge, 1~2 portion of sucrose, 40 ~60 parts of water, mixed fermentation are subsequently added into 0.1~0.2 times of sepiolite quality of organic acid, are stirred, ammonium hydroxide is then added dropwise PH to 8.1~8.3 is adjusted, is stirred, is filtered, it is dry to get modified meerschaum;The organic acid is by malic acid and lemon Sour 1:3~1:5 mixed preparing in mass ratio forms.
9. a kind of preparation method of anti-static coatings according to claim 1, it is characterised in that: step (2) the alkaline phenol The preparation process of urea formaldehyde are as follows: according to parts by weight, by 30~40 parts of glyoxal solutions, 10~20 parts of potassium hydroxide solutions, 30 ~40 parts of hydroquinone constant temperature are stirred to react, cooling, and 0.2~0.3 times of glyoxal solution volume of ethylene urea is added and is stirred to react, Cooling is added 0.1~0.2 times of glyoxal solution volume of Silane coupling reagent KH-570 and is stirred to react, cools down to get alkaline phenol formaldehyde Resin.
10. a kind of preparation method of anti-static coatings according to claim 1, it is characterised in that: step (2) described modified silicon Diatomaceous earth the preparation method comprises the following steps: diatomite and hydrochloric acid 1:10~1:20 in mass ratio are stirred, filter, wash, it is dry, obtain one Secondary processing diatomite, according to parts by weight, by 30~40 parts of single treatment diatomite, 8~10 parts of biogas slurries, 3~5 portions of sucrose, 40 ~60 parts of water mixed fermentations are filtered, and are washed, dry, secondary treatment diatomite are obtained, by low-melting alloy and secondary treatment silicon Diatomaceous earth 1:3~1:5 Hybrid Heating ball milling in mass ratio is to get modification infusorial earth;The low-melting alloy is bismuth tin alloy, bismuth tin Each component mass content in alloy are as follows: bismuth accounts for 51%(ω), tin accounts for 30%(ω), lead accounts for 8%(ω), indium accounts for 11%(ω).
CN201910029266.1A 2019-01-12 2019-01-12 A kind of preparation method of anti-static coatings Pending CN109852195A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201910029266.1A CN109852195A (en) 2019-01-12 2019-01-12 A kind of preparation method of anti-static coatings

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201910029266.1A CN109852195A (en) 2019-01-12 2019-01-12 A kind of preparation method of anti-static coatings

Publications (1)

Publication Number Publication Date
CN109852195A true CN109852195A (en) 2019-06-07

Family

ID=66894512

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201910029266.1A Pending CN109852195A (en) 2019-01-12 2019-01-12 A kind of preparation method of anti-static coatings

Country Status (1)

Country Link
CN (1) CN109852195A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112951525A (en) * 2021-01-28 2021-06-11 平江县岳峰云母新材料有限公司 Preparation process of antistatic and corrosion-resistant mica tape
CN116102953A (en) * 2023-04-10 2023-05-12 山东省地质矿产勘查开发局第二水文地质工程地质大队(山东省鲁北地质工程勘察院) Drag-reduction coating material in geothermal conveying pipeline and preparation method thereof

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106243914A (en) * 2016-07-27 2016-12-21 陈红旗 A kind of antistatic terrace paint compositing formula
CN106634850A (en) * 2016-10-19 2017-05-10 北京恒通绿建节能科技有限公司 Heat-conducting composite solid-solid phase-change material and preparation method therefor
CN108148519A (en) * 2017-12-30 2018-06-12 张静 A kind of weather-proof conducting foam
CN108947413A (en) * 2018-09-17 2018-12-07 佛山市禅城区诺高环保科技有限公司 A kind of preparation method of bend resistance calcium silicate board
CN108976708A (en) * 2018-06-21 2018-12-11 广西秀美壮乡能源环保有限公司 A kind of antistatic modified fibre resin based reinforcement material
CN109133960A (en) * 2018-09-29 2019-01-04 佛山齐安建筑科技有限公司 A kind of preparation method of porous light ceramics abatvoix

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106243914A (en) * 2016-07-27 2016-12-21 陈红旗 A kind of antistatic terrace paint compositing formula
CN106634850A (en) * 2016-10-19 2017-05-10 北京恒通绿建节能科技有限公司 Heat-conducting composite solid-solid phase-change material and preparation method therefor
CN108148519A (en) * 2017-12-30 2018-06-12 张静 A kind of weather-proof conducting foam
CN108976708A (en) * 2018-06-21 2018-12-11 广西秀美壮乡能源环保有限公司 A kind of antistatic modified fibre resin based reinforcement material
CN108947413A (en) * 2018-09-17 2018-12-07 佛山市禅城区诺高环保科技有限公司 A kind of preparation method of bend resistance calcium silicate board
CN109133960A (en) * 2018-09-29 2019-01-04 佛山齐安建筑科技有限公司 A kind of preparation method of porous light ceramics abatvoix

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112951525A (en) * 2021-01-28 2021-06-11 平江县岳峰云母新材料有限公司 Preparation process of antistatic and corrosion-resistant mica tape
CN116102953A (en) * 2023-04-10 2023-05-12 山东省地质矿产勘查开发局第二水文地质工程地质大队(山东省鲁北地质工程勘察院) Drag-reduction coating material in geothermal conveying pipeline and preparation method thereof

Similar Documents

Publication Publication Date Title
CN102766304B (en) Three-dimensional graphene network-contained high conductivity polymer composite material and preparation method thereof
CN102140179A (en) Method for preparing styrene grafted silicon dioxide superhydrophobic thin film
CN108221382B (en) Electromagnetic shielding type shear thickening liquid and preparation method thereof
CN109852195A (en) A kind of preparation method of anti-static coatings
CN102492351A (en) Conductive super-hydrophobic paint and production method thereof
CN106279874A (en) A kind of preparation method of lignin-base polythene material
CN104229787A (en) Method for increasing yield of graphene prepared by supercritical fluid through pretreatment of natural graphite
CN109825037A (en) A kind of modified carbon nano-tube epoxy resin-base composite material
CN114957855B (en) Wave-absorbing heat-conducting thermoplastic composite material and preparation method thereof
CN110172260A (en) A kind of lightweight electromagnetic shielding sealing material and its preparation method and application
CN108831759A (en) One kind is based on graphene/chitosan multi-porous carbon composite and its preparation method and application
CN101891936B (en) Preparation method of composite material based on epoxy resin and phosphazene nanotubes
CN101260234A (en) High conductivity polyaniline water dispersion liquid and preparation method thereof
CN109824030A (en) A kind of hollow carbon sphere and its preparation method and application
CN101942103B (en) Preparation method of magnetic cellulose composite microsphere
CN109266130A (en) A kind of preparation method of conductive coating
CN110194929A (en) A kind of preparation method of heat-resisting heat radiating type powdery paints
CN108899429A (en) A kind of preparation method of graphene-based organic solar batteries boundary material
CN110184849A (en) A kind of preparation method of conductive paper of carbon fiber
CN106783237B (en) A kind of Co-Fe alloy/graphite alkene composite material and preparation method and application
CN115627040A (en) Sealing composite material capable of resisting low temperature of-50 ℃, preparation method and sensor
CN106928656B (en) Nano-silicon dioxide modified RFI epoxy resin film and preparation method thereof
CN102888028B (en) Method for preparing chitosan-ferroferric oxide (CS-Fe3O4) composite nanoparticles by self-assembly
CN109880369A (en) A kind of nano-TiO2Composite material and preparation method
CN114479184A (en) Preparation method of high-dispersion zinc oxide

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
WD01 Invention patent application deemed withdrawn after publication
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20190607