CN106118199A - A kind of preparation method of coating dedicated biomass antistatic filler - Google Patents

A kind of preparation method of coating dedicated biomass antistatic filler Download PDF

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CN106118199A
CN106118199A CN201610484418.3A CN201610484418A CN106118199A CN 106118199 A CN106118199 A CN 106118199A CN 201610484418 A CN201610484418 A CN 201610484418A CN 106118199 A CN106118199 A CN 106118199A
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walnut shell
biomass
antistatic
carbonization
coating
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陈建峰
林茂平
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D5/00Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/24Electrically-conducting paints
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/02Elements
    • C08K3/04Carbon
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K9/00Use of pretreated ingredients
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D163/00Coating compositions based on epoxy resins; Coating compositions based on derivatives of epoxy resins
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40Additives
    • C09D7/60Additives non-macromolecular
    • C09D7/61Additives non-macromolecular inorganic
    • C09D7/62Additives non-macromolecular inorganic modified by treatment with other compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K2201/00Specific properties of additives
    • C08K2201/011Nanostructured additives
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K2201/00Specific properties of additives
    • C08K2201/017Additives being an antistatic agent

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Inorganic Chemistry (AREA)
  • Paints Or Removers (AREA)
  • Pigments, Carbon Blacks, Or Wood Stains (AREA)

Abstract

The present invention relates to the preparation method of a kind of coating dedicated biomass antistatic filler, belong to antistatic material preparation field.The method is with walnut shell as raw material, carbonization after solution containing nickel soaks, compound that microorganism is modified i.e. obtains biomass antistatic filler again with Ipomoea batatas Lam. ginger liquid, the present invention is soaked by pure Ni solution and makes walnut shell powder nickel-loaded ion, and carry out carbonization with it as catalyst, the electric conductivity of biomass carbon can be improved, solve the problem that traditional biomass material with carbon element electric conductivity is weak, through Radix Ipomoeae Rhizoma Zingiberis Recens mixed liquor and the microorganism rich in various active function groups, walnut shell charcoal is modified, increase its surface functional group quantity, thus improve biomass carbon dispersibility in coating matrix, compensate for again having stronger cohesiveness between carbon system antistatic particle, it is difficult to dispersed in coating and the defect of mixing, there is splendid antistatic performance.

Description

A kind of preparation method of coating dedicated biomass antistatic filler
Technical field
The present invention relates to the preparation method of a kind of coating dedicated biomass antistatic filler, belong to antistatic material preparation neck Territory.
Background technology
Static discharge is a kind of phenomenon the most common in daily life, and in a dry environment, human body is in contact sometimes Can feel there is electricity during metal object, the most also can be appreciated that electric spark, here it is static discharge phenomenon, namely ESD phenomenon.Quiet Discharge of electricity can produce of short duration discharge current and the strongest electric discharge magnetic field, can cause the electronic equipment misoperation of operation, even interior Portion's components and parts are damaged, and cause equipment loss of function.One of approach reducing electrostatic hazard increases electric-charge-dissipating speed exactly, Prevent charge buildup, reduce surface resistivity.
Coating major part is the non-conductor of electricity, at present, has metal-doped electrically-conducting paint.Being doping in electrically-conducting paint Dividing and should have good electric conductivity, the doping component being typically chosen is silver or copper, but silver and copper are precious metal, are prepared as This is higher.Meanwhile, the oxidative resistance of metallic conduction coating is very poor, uses time length copper powder, argentum powder to be easily formed oxide layer, doping The electric conductivity of material changes, and makes it become insulator from conductor, thus loses or reduce electric conductivity.Carbon system filler tool There are superior weatherability and chemical-resistant, low cost, abundance, as consumption is proper, the physical property of coating affected not Greatly, thus carbon conductive filler is most widely used in anti-static coatings.But have stronger cohesiveness between carbon system particle, he and have Between the coating matrixs such as machine macromolecule, affinity is weak, is difficult to dispersed in coating and mixing, and the most common carbon system leads Electricity filler is graphite and carbon black, and they are with non-renewable oil fossil energy as raw material, and the leading of biomass carbon material The most weak, therefore prepare a kind of efficient biomass carbon antistatic filler and there is splendid application prospect.
Summary of the invention
The technical problem that present invention mainly solves: have stronger cohesiveness between current carbon system antistatic particle, it and have Between the coating matrixs such as machine macromolecule, affinity is weak, is difficult to dispersed in coating and mixing, and the most common carbon system leads Electricity filler is graphite and carbon black, and they are with non-renewable oil fossil energy as raw material, and the leading of biomass carbon material The most weak defect, it is provided that the preparation method of a kind of coating dedicated biomass antistatic filler.The method is former with walnut shell Material, carbonization after solution containing nickel soaks, then compound the modified biomass antistatic filler that i.e. obtains of microorganism with Ipomoea batatas Lam. ginger liquid, this Invent to be soaked by pure Ni solution and make walnut shell powder nickel-loaded ion, and carry out carbonization with it as catalyst, biology can be improved The electric conductivity of matter charcoal, solves the problem that traditional biomass material with carbon element electric conductivity is weak, through the Radix Ipomoeae rich in various active function groups Walnut shell charcoal is modified by Rhizoma Zingiberis Recens mixed liquor and microorganism, increases its surface functional group quantity, thus improves biomass carbon and exist Dispersibility in coating matrix, compensate for again having stronger cohesiveness between carbon system antistatic particle, is difficult in coating dispersed With the defect of mixing, there is splendid antistatic performance.
In order to solve above-mentioned technical problem, the technical solution adopted in the present invention is:
(1) weigh 1~2kg walnut shell to put into jet mill is pulverized after 15~20min and proceed in ball mill, by ratio of grinding media to material be 20:1 adds stainless steel ball-milling pearl in ball mill, crosses 200 mesh standard sieves, obtain walnut shell powder after continuing ball milling 50~70min End;
(2) be 1:10 by walnut shell powder obtained above immersion mass concentration by solid-to-liquid ratio it is in 40% nickel nitrate solution, puts into Sonic oscillation instrument is with 300~400W power ultrasonic vibration steeped overnight, and dipping pours dipping mixed liquor into horizontal centrifugal after terminating Machine, is centrifuged 15~20min with 3000~4000r/min rotating speeds, isolated lower sediment;
(3) above-mentioned precipitation is first put into baking oven, at 105~110 DEG C, be dried 3~5h, more dried precipitation is moved into carbonization Be passed through argon in stove and in stove until displacement come out of the stove in all air, first pre-to 300~400 DEG C with 5 DEG C/min ramp Carbonization 40~60min, then it is warming up to 900~1000 DEG C with 10 DEG C/min rate program, naturally cool to after insulation carbonization 2~3h Room temperature, discharging, obtain nanometer walnut shell carbon powder, standby;
(4) weigh 400~500g Radix Ipomoeae peelings to clean, be manually cut into the thin slice that thickness is 1~2mm, put into clear water soaked overnight Remove starch, put into iron pan after ginger slice, remelt sugar and Radix Ipomoeae thin slice being mixed for 1:1:5 in mass ratio, add appropriate distilled water Until being totally submerged by mixture, being heated to 95~100 DEG C of infusions 1~2h, filtering and removing filtering residue, obtaining filtrate;
(5) be that standby nanometer walnut shell carbon powder is joined in above-mentioned filtrate by 1:8 by solid-to-liquid ratio, with magnetic stirrer with 200~300r/min rotating speeds obtain fermentation substrate and are proceeded in pottery fermentation tank after being uniformly mixed, then add in tank Fermentation substrate gross mass 0.5~2.0% yeast extract, put in the greenhouse of 25~35 DEG C after stirring by stirring rod, insulation is sent out Modified 1~2 week of ferment;
(6) take out modified product after modification terminates, put into sterilizing 30~40min in autoclave, then with high speed centrifuge with 4000~5000r/min rotating speeds are centrifugally separating to obtain lower black precipitation, put into baking oven and are dried after 3~5h at 105~110 DEG C Discharging, packs and i.e. obtains coating dedicated biomass antistatic filler.
The concrete application process of the present invention: be that the 10% biomass antistatic filler that the present invention prepared mixes by incorporation In epoxy resin varnish, putting in mixing kettle and manually brush at inner wall of oil tank after mix homogeneously, brushing thickness is 2~4mm, through inspection Surveying, the biomass antistatic filler resistivity that the present invention prepares is 0.05~0.10 Ω cm, and its electric conductivity is ordinary student material 10~15 times of Carbon Materials electric conductivity, and favorable dispersibility be difficult to reunite, there is splendid antistatic effect.
The invention has the beneficial effects as follows:
(1) the biomass antistatic filler material that the present invention prepares is easy to get, and preparation process is simple to operation and with low cost;
(2) the biomass antistatic filler resistivity that the present invention prepares is for for 0.05~0.10 Ω cm, and its electric conductivity is common 10~15 times of biomass carbon material conductivity;
(3) the biomass antistatic filler good dispersion that the present invention prepares, will not reunite, and has splendid antistatic effect Really.
Detailed description of the invention
Weigh 1~2kg walnut shell to put into jet mill is pulverized after 15~20min and proceed in ball mill, by ratio of grinding media to material In ball mill, add stainless steel ball-milling pearl for 20:1, cross 200 mesh standard sieves after continuing ball milling 50~70min, obtain walnut shell Powder;Be 1:10 by walnut shell powder obtained above immersion mass concentration by solid-to-liquid ratio it is in 40% nickel nitrate solution, puts into super Sound oscillation instrument pours dipping mixed liquor into horizontal centrifuge with 300~400W power ultrasonic vibration steeped overnight, dipping after terminating, It is centrifuged 15~20min, isolated lower sediment with 3000~4000r/min rotating speeds;Above-mentioned precipitation is first put into baking oven, It is dried 3~5h at 105~110 DEG C, more dried precipitation is moved in retort and is passed through argon in stove until displacing All air in stove, first with 5 DEG C/min ramp to 300~400 DEG C of pre-carbonizations 40~60min, then with 10 DEG C/min speed Temperature programming, to 900~1000 DEG C, naturally cools to room temperature, discharging after insulation carbonization 2~3h, obtains nanometer walnut shell powdered carbon End, standby;Weigh 400~500g Radix Ipomoeae peelings to clean, be manually cut into the thin slice that thickness is 1~2mm, put into clear water soaked overnight Remove starch, put into iron pan after ginger slice, remelt sugar and Radix Ipomoeae thin slice being mixed for 1:1:5 in mass ratio, add appropriate distilled water Until being totally submerged by mixture, being heated to 95~100 DEG C of infusions 1~2h, filtering and removing filtering residue, obtaining filtrate;By solid Liquor ratio is that standby nanometer walnut shell carbon powder is joined in above-mentioned filtrate by 1:8, with magnetic stirrer with 200~300r/min Rotating speed obtains fermentation substrate and is proceeded in pottery fermentation tank after being uniformly mixed, then adds fermentation substrate gross mass in tank 0.5~2.0% yeast extract, put in the greenhouse of 25~35 DEG C after stirring by stirring rod, modified 1~2 week of heat-preservation fermentation; Modification takes out modified product after terminating, and puts into sterilizing 30~40min in autoclave, then with high speed centrifuge with 4000~ 5000r/min rotating speed is centrifugally separating to obtain lower black precipitation, puts into discharging after baking oven is dried 3~5h at 105~110 DEG C, Pack and i.e. obtain coating dedicated biomass antistatic filler.
Example 1
Weigh 1kg walnut shell to put into jet mill is pulverized after 15min and proceed in ball mill, be that 20:1 is to ball milling by ratio of grinding media to material Machine adds stainless steel ball-milling pearl, crosses 200 mesh standard sieves after continuing ball milling 50min, obtain walnut shell powder;It is 1 by solid-to-liquid ratio: 10 by walnut shell powder obtained above immersion mass concentration be in 40% nickel nitrate solution, put into sonic oscillation instrument with 300W merit Rate sonic oscillation steeped overnight, dipping is poured dipping mixed liquor into horizontal centrifuge after terminating, is centrifuged with 3000r/min rotating speed 15min, isolated lower sediment;Above-mentioned precipitation is first put into baking oven, at 105 DEG C, is dried 3h, then by dried precipitation Move into be passed through argon in retort and in stove until displacement come out of the stove in all air, first with 5 DEG C/min ramp to 300 DEG C Pre-carbonization 40min, then be warming up to 900 DEG C with 10 DEG C/min rate program, naturally cools to room temperature after insulation carbonization 2h, discharging, Obtain nanometer walnut shell carbon powder, standby;Weigh the peeling of 400g Radix Ipomoeae to clean, be manually cut into the thin slice that thickness is 1mm, put into clear Water soaking overnight removes starch, puts into iron pan after ginger slice, remelt sugar and Radix Ipomoeae thin slice being mixed for 1:1:5 in mass ratio, adds Appropriate distilled water, until being totally submerged by mixture, is heated to 95 DEG C of infusion 1h, filters and removes filtering residue, obtains filtrate;Press Solid-to-liquid ratio is that standby nanometer walnut shell carbon powder is joined in above-mentioned filtrate by 1:8, turns with 200r/min with magnetic stirrer Speed obtains fermentation substrate and is proceeded in pottery fermentation tank after being uniformly mixed, then adds fermentation substrate gross mass in tank 0.5% yeast extract, puts in the greenhouse of 25 DEG C after stirring by stirring rod, modified 1 week of heat-preservation fermentation;Modification takes after terminating Go out modified product, put into sterilizing 30min in autoclave, then obtain with 4000r/min rotating speed centrifugation with high speed centrifuge Precipitate to lower black, put into baking oven at 105 DEG C, be dried discharging after 3h, pack and i.e. obtain coating dedicated biomass antistatic and fill out Material.
The concrete application process of the present invention: be that the 10% biomass antistatic filler that the present invention prepared mixes by incorporation In epoxy resin varnish, putting in mixing kettle and manually brush at inner wall of oil tank after mix homogeneously, brushing thickness is 2mm, after testing, The biomass antistatic filler resistivity that the present invention prepares is 0.05 Ω cm, and its electric conductivity is ordinary student material Carbon Materials conduction Property 10 times, and favorable dispersibility be difficult to reunite, there is splendid antistatic effect.
Example 2
Weigh 2kg walnut shell to put into jet mill is pulverized after 18min and proceed in ball mill, be that 20:1 is to ball milling by ratio of grinding media to material Machine adds stainless steel ball-milling pearl, crosses 200 mesh standard sieves after continuing ball milling 60min, obtain walnut shell powder;It is 1 by solid-to-liquid ratio: 10 by walnut shell powder obtained above immersion mass concentration be in 40% nickel nitrate solution, put into sonic oscillation instrument with 350W merit Rate sonic oscillation steeped overnight, dipping is poured dipping mixed liquor into horizontal centrifuge after terminating, is centrifuged with 3500r/min rotating speed 18min, isolated lower sediment;Above-mentioned precipitation is first put into baking oven, at 108 DEG C, is dried 4h, then by dried precipitation Move into be passed through argon in retort and in stove until displacement come out of the stove in all air, first with 5 DEG C/min ramp to 350 DEG C Pre-carbonization 50min, then be warming up to 905 DEG C with 10 DEG C/min rate program, naturally cools to room temperature after insulation carbonization 3h, discharging, Obtain nanometer walnut shell carbon powder, standby;Weigh the peeling of 450g Radix Ipomoeae to clean, be manually cut into the thin slice that thickness is 2mm, put into clear Water soaking overnight removes starch, puts into iron pan after ginger slice, remelt sugar and Radix Ipomoeae thin slice being mixed for 1:1:5 in mass ratio, adds Appropriate distilled water, until being totally submerged by mixture, is heated to 98 DEG C of infusion 2h, filters and removes filtering residue, obtains filtrate;Press Solid-to-liquid ratio is that standby nanometer walnut shell carbon powder is joined in above-mentioned filtrate by 1:8, turns with 250r/min with magnetic stirrer Speed obtains fermentation substrate and is proceeded in pottery fermentation tank after being uniformly mixed, then adds fermentation substrate gross mass in tank 1.3% yeast extract, puts in the greenhouse of 30 DEG C after stirring by stirring rod, modified 2 weeks of heat-preservation fermentation;Modification takes after terminating Go out modified product, put into sterilizing 35min in autoclave, then obtain with 4500r/min rotating speed centrifugation with high speed centrifuge Precipitate to lower black, put into baking oven at 108 DEG C, be dried discharging after 4h, pack and i.e. obtain coating dedicated biomass antistatic and fill out Material.
The concrete application process of the present invention: be that the 10% biomass antistatic filler that the present invention prepared mixes by incorporation In epoxy resin varnish, putting in mixing kettle and manually brush at inner wall of oil tank after mix homogeneously, brushing thickness is 3mm, after testing, The biomass antistatic filler resistivity that the present invention prepares is 0.08 Ω cm, and its electric conductivity is ordinary student material Carbon Materials conduction Property 13 times, and favorable dispersibility be difficult to reunite, there is splendid antistatic effect.
Example 3
Weigh 2kg walnut shell to put into jet mill is pulverized after 20min and proceed in ball mill, be that 20:1 is to ball milling by ratio of grinding media to material Machine adds stainless steel ball-milling pearl, crosses 200 mesh standard sieves after continuing ball milling 70min, obtain walnut shell powder;It is 1 by solid-to-liquid ratio: 10 by walnut shell powder obtained above immersion mass concentration be in 40% nickel nitrate solution, put into sonic oscillation instrument with 400W merit Rate sonic oscillation steeped overnight, dipping is poured dipping mixed liquor into horizontal centrifuge after terminating, is centrifuged with 4000r/min rotating speed 20min, isolated lower sediment;Above-mentioned precipitation is first put into baking oven, at 110 DEG C, is dried 5h, then by dried precipitation Move into be passed through argon in retort and in stove until displacement come out of the stove in all air, first with 5 DEG C/min ramp to 400 DEG C Pre-carbonization 60min, then be warming up to 1000 DEG C with 10 DEG C/min rate program, naturally cools to room temperature after insulation carbonization 3h, discharging, Obtain nanometer walnut shell carbon powder, standby;Weigh the peeling of 500g Radix Ipomoeae to clean, be manually cut into the thin slice that thickness is 2mm, put into clear Water soaking overnight removes starch, puts into iron pan after ginger slice, remelt sugar and Radix Ipomoeae thin slice being mixed for 1:1:5 in mass ratio, adds Appropriate distilled water, until being totally submerged by mixture, is heated to 100 DEG C of infusion 2h, filters and removes filtering residue, obtains filtrate;Press Solid-to-liquid ratio is that standby nanometer walnut shell carbon powder is joined in above-mentioned filtrate by 1:8, turns with 300r/min with magnetic stirrer Speed obtains fermentation substrate and is proceeded in pottery fermentation tank after being uniformly mixed, then adds fermentation substrate gross mass in tank 2.0% yeast extract, puts in the greenhouse of 35 DEG C after stirring by stirring rod, modified 2 weeks of heat-preservation fermentation;Modification takes after terminating Go out modified product, put into sterilizing 40min in autoclave, then obtain with 5000r/min rotating speed centrifugation with high speed centrifuge Precipitate to lower black, put into baking oven at 110 DEG C, be dried discharging after 5h, pack and i.e. obtain coating dedicated biomass antistatic and fill out Material.
The concrete application process of the present invention: be that the 10% biomass antistatic filler that the present invention prepared mixes by incorporation In epoxy resin varnish, putting in mixing kettle and manually brush at inner wall of oil tank after mix homogeneously, brushing thickness is 4mm, after testing, The biomass antistatic filler resistivity that the present invention prepares is 0.10 Ω cm, and its electric conductivity is ordinary student material Carbon Materials conduction Property 15 times, and favorable dispersibility be difficult to reunite, there is splendid antistatic effect.

Claims (1)

1. the preparation method of a coating dedicated biomass antistatic filler, it is characterised in that concrete preparation process is:
(1) weigh 1~2kg walnut shell to put into jet mill is pulverized after 15~20min and proceed to ball mill, by ratio of grinding media to material be 20:1 adds stainless steel ball-milling pearl in ball mill, crosses 200 mesh standard sieves, obtain walnut shell powder after continuing ball milling 50~70min End;
(2) be 1:10 by walnut shell powder obtained above immersion mass concentration by solid-to-liquid ratio it is in 40% nickel nitrate solution, puts into Sonic oscillation instrument is with 300~400W power ultrasonic vibration steeped overnight, and dipping pours dipping mixed liquor into horizontal centrifugal after terminating Machine, is centrifuged 15~20min with 3000~4000r/min rotating speeds, isolated lower sediment;
(3) above-mentioned precipitation is first put into baking oven, at 105~110 DEG C, be dried 3~5h, more dried precipitation is moved into carbonization Be passed through argon in stove and in stove until displacement come out of the stove in all air, first pre-to 300~400 DEG C with 5 DEG C/min ramp Carbonization 40~60min, then it is warming up to 900~1000 DEG C with 10 DEG C/min rate program, naturally cool to after insulation carbonization 2~3h Room temperature, discharging, obtain nanometer walnut shell carbon powder, standby;
(4) weigh 400~500g Radix Ipomoeae peelings to clean, be manually cut into the thin slice that thickness is 1~2mm, put into clear water soaked overnight Remove starch, put into iron pan after ginger slice, remelt sugar and Radix Ipomoeae thin slice being mixed for 1:1:5 in mass ratio, add appropriate distilled water Until being totally submerged by mixture, being heated to 95~100 DEG C of infusions 1~2h, filtering and removing filtering residue, obtaining filtrate;
(5) be that standby nanometer walnut shell carbon powder is joined in above-mentioned filtrate by 1:8 by solid-to-liquid ratio, with magnetic stirrer with 200~300r/min rotating speeds obtain fermentation substrate and are proceeded in pottery fermentation tank after being uniformly mixed, then add in tank Fermentation substrate gross mass 0.5~2.0% yeast extract, put in the greenhouse of 25~35 DEG C after stirring by stirring rod, insulation is sent out Modified 1~2 week of ferment;
(6) take out modified product after modification terminates, put into sterilizing 30~40min in autoclave, then with high speed centrifuge with 4000~5000r/min rotating speeds are centrifugally separating to obtain lower black precipitation, put into baking oven and are dried after 3~5h at 105~110 DEG C Discharging, packs and i.e. obtains coating dedicated biomass antistatic filler.
CN201610484418.3A 2016-06-28 2016-06-28 A kind of preparation method of coating dedicated biomass antistatic filler Pending CN106118199A (en)

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Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1831089A (en) * 2004-12-27 2006-09-13 方明 Charcoal produced by shell of mountain walnut and its processing method
CN102040218A (en) * 2011-01-19 2011-05-04 成都信息工程学院 New method for producing active carbon by using biomass wastes
CN103979534A (en) * 2014-05-14 2014-08-13 石家庄金太阳生物有机肥有限公司 Active carbon preparing method by adopting walnut shell as raw material and application of the active carbon
CN104916452A (en) * 2015-04-21 2015-09-16 中国林业科学研究院林产化学工业研究所 Wooden active carbon composite material for super capacitor and preparing method of wooden activated carbon composite material
CN105692618A (en) * 2016-02-18 2016-06-22 柳州东侯生物能源科技有限公司 Production method of biomass-powder activated carbon

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1831089A (en) * 2004-12-27 2006-09-13 方明 Charcoal produced by shell of mountain walnut and its processing method
CN102040218A (en) * 2011-01-19 2011-05-04 成都信息工程学院 New method for producing active carbon by using biomass wastes
CN103979534A (en) * 2014-05-14 2014-08-13 石家庄金太阳生物有机肥有限公司 Active carbon preparing method by adopting walnut shell as raw material and application of the active carbon
CN104916452A (en) * 2015-04-21 2015-09-16 中国林业科学研究院林产化学工业研究所 Wooden active carbon composite material for super capacitor and preparing method of wooden activated carbon composite material
CN105692618A (en) * 2016-02-18 2016-06-22 柳州东侯生物能源科技有限公司 Production method of biomass-powder activated carbon

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