CN116731377A - Antistatic sponge prepared from single-walled carbon nanotubes and preparation method thereof - Google Patents
Antistatic sponge prepared from single-walled carbon nanotubes and preparation method thereof Download PDFInfo
- Publication number
- CN116731377A CN116731377A CN202310704753.XA CN202310704753A CN116731377A CN 116731377 A CN116731377 A CN 116731377A CN 202310704753 A CN202310704753 A CN 202310704753A CN 116731377 A CN116731377 A CN 116731377A
- Authority
- CN
- China
- Prior art keywords
- parts
- antistatic
- sponge
- carbon nanotube
- mixture
- 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.)
- Granted
Links
- 239000002109 single walled nanotube Substances 0.000 title claims abstract description 60
- 238000002360 preparation method Methods 0.000 title abstract description 35
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 97
- 239000002041 carbon nanotube Substances 0.000 claims abstract description 86
- 229910021393 carbon nanotube Inorganic materials 0.000 claims abstract description 86
- 238000003756 stirring Methods 0.000 claims abstract description 81
- 239000000203 mixture Substances 0.000 claims abstract description 69
- -1 amine compounds Chemical class 0.000 claims abstract description 57
- 239000000178 monomer Substances 0.000 claims abstract description 54
- 239000003431 cross linking reagent Substances 0.000 claims abstract description 53
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims abstract description 50
- 229920002545 silicone oil Polymers 0.000 claims abstract description 42
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 42
- 229920000609 methyl cellulose Polymers 0.000 claims abstract description 37
- 239000001923 methylcellulose Substances 0.000 claims abstract description 37
- 235000010981 methylcellulose Nutrition 0.000 claims abstract description 37
- 238000005187 foaming Methods 0.000 claims abstract description 25
- 238000001723 curing Methods 0.000 claims abstract description 16
- 239000006185 dispersion Substances 0.000 claims description 57
- 239000002994 raw material Substances 0.000 claims description 30
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 claims description 30
- 229920005862 polyol Polymers 0.000 claims description 28
- 150000003077 polyols Chemical class 0.000 claims description 28
- 239000011159 matrix material Substances 0.000 claims description 24
- 238000000034 method Methods 0.000 claims description 16
- ZYWUVGFIXPNBDL-UHFFFAOYSA-N n,n-diisopropylaminoethanol Chemical compound CC(C)N(C(C)C)CCO ZYWUVGFIXPNBDL-UHFFFAOYSA-N 0.000 claims description 15
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 14
- 229920000570 polyether Polymers 0.000 claims description 14
- 238000005303 weighing Methods 0.000 claims description 12
- 239000011135 tin Substances 0.000 claims description 11
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 claims description 9
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 claims description 9
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 claims description 9
- 230000000694 effects Effects 0.000 abstract description 15
- 239000000463 material Substances 0.000 abstract description 5
- 238000010521 absorption reaction Methods 0.000 abstract description 4
- 230000002045 lasting effect Effects 0.000 abstract description 3
- 238000009413 insulation Methods 0.000 abstract description 2
- 230000035699 permeability Effects 0.000 abstract description 2
- 238000004321 preservation Methods 0.000 abstract description 2
- 230000035939 shock Effects 0.000 abstract description 2
- 230000002411 adverse Effects 0.000 abstract 1
- 238000009776 industrial production Methods 0.000 abstract 1
- 239000000047 product Substances 0.000 description 21
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 14
- 150000001875 compounds Chemical class 0.000 description 12
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 10
- 238000005520 cutting process Methods 0.000 description 10
- 239000012975 dibutyltin dilaurate Substances 0.000 description 10
- 230000000052 comparative effect Effects 0.000 description 9
- 239000012467 final product Substances 0.000 description 8
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical group OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 6
- 150000005846 sugar alcohols Polymers 0.000 description 6
- KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 description 6
- 238000012360 testing method Methods 0.000 description 5
- GODZNYBQGNSJJN-UHFFFAOYSA-N 1-aminoethane-1,2-diol Chemical compound NC(O)CO GODZNYBQGNSJJN-UHFFFAOYSA-N 0.000 description 4
- 238000005054 agglomeration Methods 0.000 description 4
- 230000002776 aggregation Effects 0.000 description 4
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
- 238000007906 compression Methods 0.000 description 3
- 230000006835 compression Effects 0.000 description 3
- 239000006260 foam Substances 0.000 description 3
- 239000002216 antistatic agent Substances 0.000 description 2
- 230000005611 electricity Effects 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 239000005022 packaging material Substances 0.000 description 2
- 229920001451 polypropylene glycol Polymers 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 230000003068 static effect Effects 0.000 description 2
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 229920001940 conductive polymer Polymers 0.000 description 1
- 238000005034 decoration Methods 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- 238000011066 ex-situ storage Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000002085 persistent effect Effects 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/0066—Use of inorganic compounding ingredients
- C08J9/0071—Nanosized fillers, i.e. having at least one dimension below 100 nanometers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/32—Polyhydroxy compounds; Polyamines; Hydroxyamines
- C08G18/3203—Polyhydroxy compounds
- C08G18/3206—Polyhydroxy compounds aliphatic
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/32—Polyhydroxy compounds; Polyamines; Hydroxyamines
- C08G18/3225—Polyamines
- C08G18/3228—Polyamines acyclic
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/32—Polyhydroxy compounds; Polyamines; Hydroxyamines
- C08G18/3271—Hydroxyamines
- C08G18/3275—Hydroxyamines containing two hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/4009—Two or more macromolecular compounds not provided for in one single group of groups C08G18/42 - C08G18/64
- C08G18/4081—Mixtures of compounds of group C08G18/64 with other macromolecular compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/64—Macromolecular compounds not provided for by groups C08G18/42 - C08G18/63
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/65—Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
- C08G18/66—Compounds of groups C08G18/42, C08G18/48, or C08G18/52
- C08G18/6666—Compounds of group C08G18/48 or C08G18/52
- C08G18/667—Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38
- C08G18/6681—Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/32 or C08G18/3271 and/or polyamines of C08G18/38
- C08G18/6688—Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/32 or C08G18/3271 and/or polyamines of C08G18/38 with compounds of group C08G18/3271
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/02—Elements
- C08K3/04—Carbon
- C08K3/041—Carbon nanotubes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2101/00—Manufacture of cellular products
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2110/00—Foam properties
- C08G2110/0083—Foam properties prepared using water as the sole blowing agent
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2375/00—Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
- C08J2375/04—Polyurethanes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2375/00—Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
- C08J2375/04—Polyurethanes
- C08J2375/08—Polyurethanes from polyethers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K2201/00—Specific properties of additives
- C08K2201/011—Nanostructured additives
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K2201/00—Specific properties of additives
- C08K2201/017—Additives being an antistatic agent
Abstract
The application relates to the technical field of functional sponge materials, and particularly discloses an antistatic sponge prepared from single-walled carbon nanotubes and a preparation method thereof, wherein the antistatic sponge comprises carbon nanotube dispersoid, functional monomers, methylcellulose, amine compounds, silicone oil, organic tin, a cross-linking agent and water; the preparation method of the antistatic sponge comprises the steps of stirring and premixing a carbon nano tube dispersoid, an amine compound, silicone oil, organic tin, a cross-linking agent and water to obtain a mixture; adding functional monomers and methyl cellulose into the mixture, stirring, foaming and curing to obtain the required antistatic sponge; the preparation method is simple, the preparation conditions are mild, the preparation method is suitable for industrial production, the obtained antistatic sponge has remarkable antistatic effect, can realize lasting antistatic, and can not cause adverse effects on the performances of the sponge such as heat preservation, heat insulation, sound absorption, shock absorption, air permeability and the like.
Description
Technical Field
The application relates to the technical field of functional sponge materials, in particular to an antistatic sponge prepared from single-walled carbon nanotubes and a preparation method thereof.
Background
Polymer products such as foam, sponge, plate and the like have the advantages of good appearance, light weight, good electrical insulation, easy dyeing, easy molding and the like, and are widely applied to industries such as packaging materials, decoration and the like. However, most of plastic products are dry and insulating, when the plastic products are used as packaging materials, friction is easily generated between the plastic products and packaged objects in the cargo carrying process, static electricity is naturally generated in the friction process, when the packaged objects are sensitive electronic parts, the generated static electricity can influence or even damage the electronic parts, and electric shock accidents or fires can be generated when the packaged objects are severe. The plate and other hard materials have high density, and are convenient to carry out antistatic treatment, so that the antistatic plate is manufactured. Because the inside air holes of such plastics as foam, sponge and the like are rich, the pores are relatively large, and the antistatic treatment is inconvenient, the preparation of the antistatic sponge is not perfect so far.
In the related art, in order to reduce the surface resistance value of the sponge product, an ex-situ method such as soaking, dipping, spraying, coating and the like (for example, a preparation method of hydrophobic and oleophilic polyurethane sponge is disclosed in Chinese patent with publication number of CN 103342827A) is often adopted, and an antistatic agent component is loaded on the surface of a skeleton of an internal pore canal agent of the sponge product; in addition, in order to reduce the surface resistance value of the sponge product, a method of adding an antistatic component into the raw material before foaming the sponge product is adopted, wherein the added antistatic agent mainly comprises carbon black, carbon fiber, alkali metal salt or conductive polymer (for example, an antistatic sponge is disclosed in Chinese patent publication No. CN 102134302A), and the method has poor compatibility of the antistatic component and the sponge raw material, is difficult to uniformly disperse in the foaming material, is easy to agglomerate, and causes the finally prepared sponge product to have unsatisfactory antistatic effect. Based on the above statement, the application provides an antistatic sponge prepared from single-walled carbon nanotubes and a preparation method thereof, aiming at improving the antistatic effect of a sponge product and achieving the effects of lasting antistatic and delaying the service life of the sponge product.
Disclosure of Invention
The application provides an antistatic sponge prepared from single-walled carbon nanotubes and a preparation method thereof, aiming at solving the problems that the antistatic effect of the prior sponge product is poor and the lasting antistatic effect cannot be achieved.
In a first aspect, the application provides an antistatic sponge, which adopts the following technical scheme:
an antistatic sponge prepared from single-walled carbon nanotubes comprises the following raw materials in parts by weight: 10-100 parts of carbon nanotube dispersoid, 40-50 parts of functional monomer, 0-20 parts of methyl cellulose, 0.4-0.6 part of amine compound, 0.6-1 part of silicone oil, 0.1-0.3 part of organic tin, 1.5-8 parts of cross-linking agent and 1-5 parts of water.
Preferably, the antistatic sponge prepared from the single-walled carbon nanotubes comprises the following raw materials in parts by weight: 30-80 parts of carbon nanotube dispersoid, 42-48 parts of functional monomer, 5-15 parts of methyl cellulose, 0.45-0.55 part of amine compound, 0.7-0.9 part of silicone oil, 0.15-0.25 part of organic tin, 3-6 parts of cross-linking agent and 2-4 parts of water.
Preferably, the antistatic sponge prepared from the single-walled carbon nanotubes comprises the following raw materials in parts by weight: 50 parts of carbon nanotube dispersion, 45 parts of functional monomer, 10 parts of methyl cellulose, 0.5 part of amine compound, 0.8 part of silicone oil, 0.2 part of organic tin, 5 parts of cross-linking agent and 3 parts of water.
Preferably, the carbon nanotube dispersion is obtained by uniformly dispersing carbon nanotubes and polyalcohol.
Preferably, the dispersing rotating speed is 1500-4500r/min, and the dispersing time is 10-20min.
Preferably, the carbon nanotubes are TUBALL TM MATRIX 209 single-walled carbon nanotubes.
Preferably, the polyol is a polyether polyol and/or a rosin polyol.
Preferably, the carbon nanotube content of the carbon nanotube dispersion is 5-10%.
Preferably, the functional monomer is at least one of MDI2412, TDI, lexomer TM 50.
Preferably, the amine compound is a compound of triethylenediamine and diisopropylethanolamine.
Preferably, the mass ratio of the triethylenediamine to the diisopropylethanolamine is 2-3:1.
Preferably, the organotin is dibutyltin dilaurate and/or stannous octoate.
Preferably, the cross-linking agent is diethanolamine and/or ethylene glycol.
In a second aspect, the application provides a method for preparing antistatic sponge by single-wall carbon nanotubes, which adopts the following technical scheme:
the preparation method of the antistatic sponge prepared by the single-wall carbon nano tube comprises the following preparation steps:
s1, weighing raw materials of carbon nanotube dispersoid, functional monomer, methyl cellulose, amine compound, silicone oil, organic tin, cross-linking agent and water according to parts by weight for standby;
s2, stirring and premixing the carbon nanotube dispersoid, amine compounds, silicone oil, organic tin, a cross-linking agent and water to obtain a mixture;
s3, adding the functional monomer and the methylcellulose into the mixture, stirring, foaming and curing to obtain the required antistatic sponge.
Preferably, in the step S2, the stirring speed is 2000-3000r/min, and the stirring time is 10-30S.
Preferably, in the step S3, the stirring speed is 1000-1500r/min, the stirring temperature is 35-55 ℃, and the stirring time is 8-20S.
Preferably, the curing temperature in the step S3 is 55-65 ℃ and the curing time is 20-40min.
In summary, the application has the following beneficial effects:
the application selects TUBALL TM The MATRIX 209 single-walled carbon nanotube is added as an antistatic component, so that a permanent and stable antistatic effect of the sponge material can be provided, and meanwhile, the performances of heat preservation, heat insulation, sound absorption, shock absorption, air permeability and the like of the sponge product can be ensured not to be influenced.
According to the application, the carbon nanotubes are prepared into the carbon nanotube dispersion in advance by adding the polyalcohol, so that excellent dispersion performance of the carbon nanotubes can be provided, uniform dispersion of the carbon nanotubes in a formula system is ensured, and layering and agglomeration phenomena are avoided; by controlling the dosage of the carbon nano tube in the formula, the sponge product can not cause soft stickiness or shrinkage while the excellent antistatic performance can be ensured, and the obtained sponge product has excellent comprehensive performance and long service life.
The amine compound of the application adopts the compound of triethylenediamine and diisopropylethanolamine, can ensure that the foam of the finally prepared sponge product is stable, uniform, fine, small in gap, high in porosity, high in sponge strength, good in compression rebound resilience and 10 in sponge resistance 6-9 Omega, has stable and durable antistatic effect.
Drawings
FIG. 1 TUBALL at 10% level TM Figure of the dispersion effect of MATRIX 209 single-walled carbon nanotubes in rosin polyol (2000 x under microscope).
FIG. 2 shows TUBALL at various levels TM Figure of the dispersion effect of MATRIX 209 single-walled carbon nanotubes in polyether polyol 330N (2000 x under microscope).
Detailed Description
The present application will be described in further detail with reference to examples.
Examples 1-6 provide an antistatic sponge prepared from single-walled carbon nanotubes and a preparation method thereof, and the following description is given by taking example 1 as an example.
Example 1
An antistatic sponge prepared from single-walled carbon nanotubes comprises the following raw materials in parts by weight: 100 parts of carbon nanotube dispersion, 50 parts of functional monomer, 0.4 part of amine compound, 1 part of silicone oil, 0.1 part of organic tin, 1.5 parts of cross-linking agent and 2.5 parts of water;
wherein the carbon nanotube dispersion is prepared by the following method:
control of TUBALL in carbon nanotube dispersions TM MATRIX 209 single-walled carbon nanotube content of 5% by weight, TUBALL TM Adding MATRIX 209 single-walled carbon nanotube into polyether polyol 330N, controlling the dispersion rotation speed to 1500r/min, and dispersingThe time is 17min, and the dispersion is uniform;
the functional monomer is Lexomer TM50;
the amine compound is a compound of triethylenediamine and diisopropylethanolamine in a mass ratio of 2:1;
the organic tin is dibutyl tin dilaurate;
the cross-linking agent is diethanolamine.
The preparation method of the antistatic sponge prepared by the single-wall carbon nano tube comprises the following preparation steps:
s1, weighing raw materials of carbon nanotube dispersoid, functional monomer, methyl cellulose, amine compound, silicone oil, organic tin, cross-linking agent and water according to parts by weight for standby;
s2, controlling the stirring rotation speed to be 2000r/min and the stirring time to be 30S, and stirring and premixing the carbon nano tube dispersoid, the amine compound, the silicone oil, the organic tin, the cross-linking agent and the water to obtain a mixture;
s3, adding the functional monomer and the methylcellulose into the mixture, controlling the stirring speed to be 1500r/min, the stirring temperature to be 35 ℃, the stirring time to be 20S, pouring the mixture into a foaming mold after stirring, curing the mixture for 40min at the temperature of 55 ℃ after foaming, and cutting the mixture to obtain the required antistatic sponge.
Example 2
An antistatic sponge prepared from single-walled carbon nanotubes comprises the following raw materials in parts by weight: carbon nanotube dispersion 50 parts of carbon nanotube dispersion, 45 parts of functional monomer, 10 parts of methyl cellulose, 0.5 part of amine compound, 0.8 part of silicone oil, 0.2 part of organic tin, 5 parts of cross-linking agent and 3 parts of water;
wherein the carbon nanotube dispersion is prepared by the following method:
control of TUBALL in carbon nanotube dispersions TM MATRIX 209 single-walled carbon nanotube content of 8% was used to prepare TUBALL TM Adding MATRIX 209 single-walled carbon nanotube into rosin polyol (model: laote A220E), controlling the dispersion speed to 3000r/min, and dispersing for 15min to obtain the final product;
the functional monomer is MDI2412;
the amine compound is a compound of triethylenediamine and diisopropylethanolamine in a mass ratio of 2.5:1;
the organic tin is a mixture of dibutyl tin dilaurate and stannous octoate in a mass ratio of 1:1;
the cross-linking agent is a mixture of glycol amine and glycol in a mass ratio of 1:1.
The preparation method of the antistatic sponge prepared by the single-wall carbon nano tube comprises the following preparation steps:
s1, weighing raw materials of carbon nanotube dispersoid, functional monomer, methyl cellulose, amine compound, silicone oil, organic tin, cross-linking agent and water according to parts by weight for standby;
s2, controlling the stirring rotation speed to 2500r/min and the stirring time to 20S, and stirring and premixing the carbon nano tube dispersoid, the amine compound, the silicone oil, the organic tin, the cross-linking agent and the water to obtain a mixture;
s3, adding the functional monomer and the methylcellulose into the mixture, controlling the stirring speed to 1250r/min, the stirring temperature to 45 ℃, the stirring time to 14S, pouring the mixture into a foaming mold after stirring, curing the mixture for 30min at the temperature of 60 ℃ after foaming, and cutting the mixture to obtain the required antistatic sponge.
Example 3
An antistatic sponge prepared from single-walled carbon nanotubes comprises the following raw materials in parts by weight: 10 parts of carbon nanotube dispersion, 50 parts of functional monomer, 20 parts of methyl cellulose, 0.4 part of amine compound, 0.6 part of silicone oil, 0.3 part of organic tin, 8 parts of cross-linking agent and 5 parts of water;
wherein the carbon nanotube dispersion is prepared by the following method:
control of TUBALL in carbon nanotube dispersions TM MATRIX 209 single-walled carbon nanotube content of 10% by weight, TUBALL TM Adding MATRIX 209 single-walled carbon nanotube into polyether polyol 330N, controlling the dispersion speed to 4500r/min, and dispersing for 10min to obtain the final product;
the functional monomer is TDI;
the amine compound is a compound of triethylenediamine and diisopropylethanolamine in a mass ratio of 3:1;
the organic tin is stannous octoate;
the cross-linking agent is ethylene glycol.
The preparation method of the antistatic sponge prepared by the single-wall carbon nano tube comprises the following preparation steps:
s1, weighing raw materials of carbon nanotube dispersoid, functional monomer, methyl cellulose, amine compound, silicone oil, organic tin, cross-linking agent and water according to parts by weight for standby;
s2, controlling the stirring rotation speed to be 2000-3000r/min and the stirring time to be 10-30S, and stirring and premixing the carbon nano tube dispersoid, the amine compound, the silicone oil, the organotin, the cross-linking agent and the water to obtain a mixture;
s3, adding the functional monomer and the methylcellulose into the mixture, controlling the stirring speed to be 1000-1500r/min, the stirring temperature to be 35-55 ℃ and the stirring time to be 8-20S, pouring the mixture into a foaming mold after stirring, curing for 20-40min at the temperature of 55-65 ℃ after foaming and curing molding, and cutting to obtain the required antistatic sponge.
Example 4
An antistatic sponge prepared from single-walled carbon nanotubes comprises the following raw materials in parts by weight: carbon nanotube dispersion 50 parts of carbon nanotube dispersion, 45 parts of functional monomer, 10 parts of methyl cellulose, 0.5 part of amine compound, 0.8 part of silicone oil, 0.2 part of organic tin, 5 parts of cross-linking agent and 3 parts of water;
wherein the carbon nanotube dispersion is prepared by the following method:
control of TUBALL in carbon nanotube dispersions TM MATRIX 209 single-walled carbon nanotube content of 8% was used to prepare TUBALL TM Adding MATRIX 209 single-walled carbon nanotube into a mixture of polyether polyol 330N and rosin polyol (model: laote A220E) in a mass ratio of 3:1, controlling the dispersion rotating speed to 3000r/min, and dispersing for 15min to obtain the final product;
the functional monomer is MDI2412;
the amine compound is a compound of triethylenediamine and diisopropylethanolamine in a mass ratio of 2.5:1;
the organic tin is a mixture of dibutyl tin dilaurate and stannous octoate in a mass ratio of 1:1;
the cross-linking agent is a mixture of glycol amine and glycol in a mass ratio of 1:1.
The preparation method of the antistatic sponge prepared by the single-wall carbon nano tube comprises the following preparation steps:
s1, weighing raw materials of carbon nanotube dispersoid, functional monomer, methyl cellulose, amine compound, silicone oil, organic tin, cross-linking agent and water according to parts by weight for standby;
s2, controlling the stirring rotation speed to 2500r/min and the stirring time to 20S, and stirring and premixing the carbon nano tube dispersoid, the amine compound, the silicone oil, the organic tin, the cross-linking agent and the water to obtain a mixture;
s3, adding the functional monomer and the methylcellulose into the mixture, controlling the stirring speed to 1250r/min, the stirring temperature to 45 ℃, the stirring time to 14S, pouring the mixture into a foaming mold after stirring, curing the mixture for 30min at the temperature of 60 ℃ after foaming, and cutting the mixture to obtain the required antistatic sponge.
Example 5
An antistatic sponge prepared from single-walled carbon nanotubes comprises the following raw materials in parts by weight: carbon nanotube dispersion 50 parts of carbon nanotube dispersion, 45 parts of functional monomer, 10 parts of methyl cellulose, 0.5 part of amine compound, 0.8 part of silicone oil, 0.2 part of organic tin, 5 parts of cross-linking agent and 3 parts of water;
wherein the carbon nanotube dispersion is prepared by the following method:
control of TUBALL in carbon nanotube dispersions TM MATRIX 209 single-walled carbon nanotube content of 8% was used to prepare TUBALL TM Adding MATRIX 209 single-walled carbon nanotube into a mixture of polyether polyol 330N and rosin polyol (model: laote A220E) in a mass ratio of 3:1, controlling the dispersion rotating speed to 3000r/min, and dispersing for 15min to obtain the final product;
the functional monomer is a mixture of MDI2412 and TDI in a mass ratio of 1:1;
the amine compound is a compound of triethylenediamine and diisopropylethanolamine in a mass ratio of 2.5:1;
the organic tin is a mixture of dibutyl tin dilaurate and stannous octoate in a mass ratio of 1:1;
the cross-linking agent is a mixture of glycol amine and glycol in a mass ratio of 1:1.
The preparation method of the antistatic sponge prepared by the single-wall carbon nano tube comprises the following preparation steps:
s1, weighing raw materials of carbon nanotube dispersoid, functional monomer, methyl cellulose, amine compound, silicone oil, organic tin, cross-linking agent and water according to parts by weight for standby;
s2, controlling the stirring rotation speed to 2500r/min and the stirring time to 20S, and stirring and premixing the carbon nano tube dispersoid, the amine compound, the silicone oil, the organic tin, the cross-linking agent and the water to obtain a mixture;
s3, adding the functional monomer and the methylcellulose into the mixture, controlling the stirring speed to 1250r/min, the stirring temperature to 45 ℃, the stirring time to 14S, pouring the mixture into a foaming mold after stirring, curing the mixture for 30min at the temperature of 60 ℃ after foaming, and cutting the mixture to obtain the required antistatic sponge.
Example 6
An antistatic sponge prepared from single-walled carbon nanotubes comprises the following raw materials in parts by weight: carbon nanotube dispersion 50 parts of carbon nanotube dispersion, 45 parts of functional monomer, 10 parts of methyl cellulose, 0.5 part of amine compound, 0.8 part of silicone oil, 0.2 part of organic tin, 5 parts of cross-linking agent and 3 parts of water;
wherein the carbon nanotube dispersion is prepared by the following method:
control of TUBALL in carbon nanotube dispersions TM MATRIX 209 single-walled carbon nanotube content of 8% was used to prepare TUBALL TM Adding MATRIX 209 single-walled carbon nanotube into a mixture of polyether polyol 330N and rosin polyol (model: laote A220E) in a mass ratio of 3:1, controlling the dispersion rotating speed to 3000r/min, and dispersing for 15min to obtain the final product;
the functional monomer is a mixture of MDI2412, TDI and Lexomer TM50 in a mass ratio of 1:1:1;
the amine compound is a compound of triethylenediamine and diisopropylethanolamine in a mass ratio of 2.5:1;
the organic tin is a mixture of dibutyl tin dilaurate and stannous octoate in a mass ratio of 1:1;
the cross-linking agent is a mixture of glycol amine and glycol in a mass ratio of 1:1.
The preparation method of the antistatic sponge prepared by the single-wall carbon nano tube comprises the following preparation steps:
s1, weighing raw materials of carbon nanotube dispersoid, functional monomer, methyl cellulose, amine compound, silicone oil, organic tin, cross-linking agent and water according to parts by weight for standby;
s2, controlling the stirring rotation speed to 2500r/min and the stirring time to 20S, and stirring and premixing the carbon nano tube dispersoid, the amine compound, the silicone oil, the organic tin, the cross-linking agent and the water to obtain a mixture;
s3, adding the functional monomer and the methylcellulose into the mixture, controlling the stirring speed to 1250r/min, the stirring temperature to 45 ℃, the stirring time to 14S, pouring the mixture into a foaming mold after stirring, curing the mixture for 30min at the temperature of 60 ℃ after foaming, and cutting the mixture to obtain the required antistatic sponge.
To verify the performance of the antistatic sponges prepared in examples 1-4 of the present application, the applicant set comparative examples 1-2, which are specifically as follows:
comparative example 1
An antistatic sponge prepared from single-walled carbon nanotubes comprises the following raw materials in parts by weight: 100 parts of carbon nanotube dispersion, 50 parts of functional monomer, 0.4 part of amine compound, 1 part of silicone oil, 0.1 part of organic tin, 1.5 parts of cross-linking agent and 2.5 parts of water;
wherein the carbon nanotube dispersion is prepared by the following method:
control of TUBALL in carbon nanotube dispersions TM MATRIX 209 single-walled carbon nanotube content of 5% by weight, TUBALL TM Adding MATRIX 209 single-walled carbon nanotube into polypropylene glycol 3000, controlling the dispersion speed to 1500r/min, and dispersing for 17min to obtain the final product;
the functional monomer is Lexomer TM50;
the amine compound is a compound of triethylenediamine and diisopropylethanolamine in a mass ratio of 2:1;
the organic tin is dibutyl tin dilaurate;
the cross-linking agent is diethanolamine.
The preparation method of the antistatic sponge prepared by the single-wall carbon nano tube comprises the following preparation steps:
s1, weighing raw materials of carbon nanotube dispersoid, functional monomer, methyl cellulose, amine compound, silicone oil, organic tin, cross-linking agent and water according to parts by weight for standby;
s2, controlling the stirring rotation speed to be 2000r/min and the stirring time to be 30S, and stirring and premixing the carbon nano tube dispersoid, the amine compound, the silicone oil, the organic tin, the cross-linking agent and the water to obtain a mixture;
s3, adding the functional monomer and the methylcellulose into the mixture, controlling the stirring speed to be 1500r/min, the stirring temperature to be 35 ℃, the stirring time to be 20S, pouring the mixture into a foaming mold after stirring, curing the mixture for 40min at the temperature of 55 ℃ after foaming, and cutting the mixture to obtain the required antistatic sponge.
Comparative example 2
An antistatic sponge prepared from single-walled carbon nanotubes comprises the following raw materials in parts by weight: 5 parts of carbon nano tube, 95 parts of polyalcohol, 50 parts of functional monomer, 0.4 part of amine compound, 1 part of silicone oil, 0.1 part of organic tin, 1.5 parts of cross-linking agent and 2.5 parts of water;
wherein the carbon nanotubes are TUBALL TM MATRIX 209 single-walled carbon nanotubes;
the polyol is polyether polyol 330N;
the functional monomer is Lexomer TM50;
the amine compound is a compound of triethylenediamine and diisopropylethanolamine in a mass ratio of 2:1;
the organic tin is dibutyl tin dilaurate;
the cross-linking agent is diethanolamine.
The preparation method of the antistatic sponge prepared by the single-wall carbon nano tube comprises the following preparation steps:
s1, weighing raw materials including carbon nano tubes, polyalcohol, functional monomers, methylcellulose, amine compounds, silicone oil, organic tin, a cross-linking agent and water according to parts by weight for later use;
s2, controlling the stirring rotation speed to be 2000r/min and the stirring time to be 30S, and stirring and premixing the carbon nano tube, the polyalcohol, the amine compound, the silicone oil, the organotin, the cross-linking agent and the water to obtain a mixture;
s3, adding the functional monomer and the methylcellulose into the mixture, controlling the stirring speed to be 1500r/min, the stirring temperature to be 35 ℃, the stirring time to be 20S, pouring the mixture into a foaming mold after stirring, curing the mixture for 40min at the temperature of 55 ℃ after foaming, and cutting the mixture to obtain the required antistatic sponge.
Comparative example 3
An antistatic sponge prepared from single-walled carbon nanotubes comprises the following raw materials in parts by weight: 100 parts of carbon nanotube dispersion, 50 parts of functional monomer, 0.4 part of amine compound, 1 part of silicone oil, 0.1 part of organic tin, 1.5 parts of cross-linking agent and 2.5 parts of water;
wherein the carbon nanotube dispersion is prepared by the following method:
control of TUBALL in carbon nanotube dispersions TM MATRIX 209 single-walled carbon nanotube content of 5% by weight, TUBALL TM Adding MATRIX 209 single-walled carbon nanotube into polyether polyol 330N, controlling the dispersion speed to 1500r/min, and dispersing for 17min to obtain the final product;
the functional monomer is Lexomer TM50;
the amine compound is triethylenediamine;
the organic tin is dibutyl tin dilaurate;
the cross-linking agent is diethanolamine.
The preparation method of the antistatic sponge prepared by the single-wall carbon nano tube comprises the following preparation steps:
s1, weighing raw materials of carbon nanotube dispersoid, functional monomer, methyl cellulose, amine compound, silicone oil, organic tin, cross-linking agent and water according to parts by weight for standby;
s2, controlling the stirring rotation speed to be 2000r/min and the stirring time to be 30S, and stirring and premixing the carbon nano tube dispersoid, the amine compound, the silicone oil, the organic tin, the cross-linking agent and the water to obtain a mixture;
s3, adding the functional monomer and the methylcellulose into the mixture, controlling the stirring speed to be 1500r/min, the stirring temperature to be 35 ℃, the stirring time to be 20S, pouring the mixture into a foaming mold after stirring, curing the mixture for 40min at the temperature of 55 ℃ after foaming, and cutting the mixture to obtain the required antistatic sponge.
Comparative example 4
An antistatic sponge prepared from single-walled carbon nanotubes comprises the following raw materials in parts by weight: 100 parts of carbon nanotube dispersion, 50 parts of functional monomer, 0.4 part of amine compound, 1 part of silicone oil, 0.1 part of organic tin, 1.5 parts of cross-linking agent and 2.5 parts of water;
wherein the carbon nanotube dispersion is prepared by the following method:
control of TUBALL in carbon nanotube dispersions TM MATRIX 209 single-walled carbon nanotube content of 5% by weight, TUBALL TM Adding MATRIX 209 single-walled carbon nanotube into polyether polyol 330N, controlling the dispersion speed to 1500r/min, and dispersing for 17min to obtain the final product;
the functional monomer is Lexomer TM50;
the amine compound is diisopropylethanolamine;
the organic tin is dibutyl tin dilaurate;
the cross-linking agent is diethanolamine.
The preparation method of the antistatic sponge prepared by the single-wall carbon nano tube comprises the following preparation steps:
s1, weighing raw materials of carbon nanotube dispersoid, functional monomer, methyl cellulose, amine compound, silicone oil, organic tin, cross-linking agent and water according to parts by weight for standby;
s2, controlling the stirring rotation speed to be 2000r/min and the stirring time to be 30S, and stirring and premixing the carbon nano tube dispersoid, the amine compound, the silicone oil, the organic tin, the cross-linking agent and the water to obtain a mixture;
s3, adding the functional monomer and the methylcellulose into the mixture, controlling the stirring speed to be 1500r/min, the stirring temperature to be 35 ℃, the stirring time to be 20S, pouring the mixture into a foaming mold after stirring, curing the mixture for 40min at the temperature of 55 ℃ after foaming, and cutting the mixture to obtain the required antistatic sponge.
Performance testing
The antistatic sponges of examples 1 to 6 and comparative examples 1 to 2 of the present application were tested for their properties, respectively, as follows:
tensile strength testing is carried out by adopting GB/T6344-2008 standard;
the GB/T10808-2006 standard is adopted for carrying out tearing strength test;
compression set testing is carried out by adopting GB/T6669-2008 standard;
measuring a surface resistance value by adopting a surface resistance tester;
the specific test results are shown in table 1 below:
table 1:
as can be seen from the data shown in table 1: the antistatic sponges prepared in examples 1-6 of the present application have remarkable and durable antistatic effect, excellent tensile properties, tear properties and low compression set.
From examples 2 and 4, it can be seen that: under the condition that other factors are unchanged, the polyol is a mixture of polyether polyol and rosin polyol, so that the antistatic performance and the comprehensive mechanical performance of the sponge product can be remarkably improved, and particularly as shown in fig. 1 and 2, the polyether polyol 330N and the rosin polyol are singly used for prefabricating the carbon nanotube dispersion, although a good pre-dispersing effect can be achieved, a small amount of agglomeration exists, and in the embodiment 4 of the application, the two are mixed and jointly dispersed, so that the agglomeration problem can be well solved, and the overall performance is further improved.
As is clear from example 1 and comparative example 1, when the polyether polyol 330N is selected to be replaced by the polypropylene glycol 3000, the prepared carbon nanotube dispersion is used for formulation addition, which results in a decrease in mechanical properties of the sponge product, a decrease in antistatic stability, and a non-persistent antistatic effect.
As can be seen from example 1 and comparative example 2, the carbon nanotubes are prepared into carbon nanotube dispersion in advance by adding the polyalcohol, so that excellent dispersion performance of the carbon nanotubes can be provided, uniform dispersion of the carbon nanotubes in a formula system is ensured, layering and agglomeration phenomena are avoided, further, antistatic stability of the sponge product can be remarkably improved, the antistatic effect is remarkable and durable, and mechanical properties of the sponge product are not reduced.
As can be seen from example 1 and comparative examples 3 to 4, under the condition that other conditions are unchanged, the amine compound is a compound of triethylenediamine and diisopropylethanolamine, and compared with the compound of triethylenediamine or diisopropylethanolamine alone, the comprehensive performance of the sponge product can be further improved.
The present embodiment is only for explanation of the present application and is not to be construed as limiting the present application, and modifications to the present embodiment, which may not creatively contribute to the present application as required by those skilled in the art after reading the present specification, are all protected by patent laws within the scope of claims of the present application.
Claims (10)
1. An antistatic sponge prepared from single-walled carbon nanotubes is characterized by comprising the following raw materials in parts by weight: 10-100 parts of carbon nanotube dispersoid, 40-50 parts of functional monomer, 0-20 parts of methyl cellulose, 0.4-0.6 part of amine compound, 0.6-1 part of silicone oil, 0.1-0.3 part of organic tin, 1.5-8 parts of cross-linking agent and 1-5 parts of water.
2. The antistatic sponge prepared from single-walled carbon nanotubes according to claim 1, comprising the following raw materials in parts by weight: 30-80 parts of carbon nanotube dispersoid, 42-48 parts of functional monomer, 5-15 parts of methyl cellulose, 0.45-0.55 part of amine compound, 0.7-0.9 part of silicone oil, 0.15-0.25 part of organic tin, 3-6 parts of cross-linking agent and 2-4 parts of water.
3. The antistatic sponge prepared from single-walled carbon nanotubes according to claim 1, comprising the following raw materials in parts by weight: 50 parts of carbon nanotube dispersion, 45 parts of functional monomer, 10 parts of methyl cellulose, 0.5 part of amine compound, 0.8 part of silicone oil, 0.2 part of organic tin, 5 parts of cross-linking agent and 3 parts of water.
4. The antistatic sponge of claim 1 wherein the carbon nanotube dispersion is obtained by uniformly dispersing carbon nanotubes with a polyol.
5. The antistatic sponge of claim 4 wherein the carbon nanotubes are TUBALL TM MATRIX 209 single-walled carbon nanotubes.
6. The antistatic sponge of claim 5 wherein the polyol is a polyether polyol and/or a rosin polyol.
7. The antistatic sponge of claim 5 wherein the carbon nanotube dispersion comprises 5-10% carbon nanotubes.
8. The antistatic sponge of claim 1 wherein the functional monomer is at least one of MDI2412, TDI, lexomer TM 50.
9. The antistatic sponge of claim 1 wherein the amine compound is a complex of triethylenediamine and diisopropylethanolamine.
10. A method for preparing an antistatic sponge prepared from the single-walled carbon nanotubes according to any of claims 1-9, comprising the steps of:
s1, weighing raw materials of carbon nanotube dispersoid, functional monomer, methyl cellulose, amine compound, silicone oil, organic tin, cross-linking agent and water according to parts by weight for standby;
s2, stirring and premixing the carbon nanotube dispersoid, amine compounds, silicone oil, organic tin, a cross-linking agent and water to obtain a mixture;
s3, adding the functional monomer and the methylcellulose into the mixture, stirring, foaming and curing to obtain the required antistatic sponge.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202310704753.XA CN116731377B (en) | 2023-06-14 | 2023-06-14 | Antistatic sponge prepared from single-walled carbon nanotubes and preparation method thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202310704753.XA CN116731377B (en) | 2023-06-14 | 2023-06-14 | Antistatic sponge prepared from single-walled carbon nanotubes and preparation method thereof |
Publications (2)
Publication Number | Publication Date |
---|---|
CN116731377A true CN116731377A (en) | 2023-09-12 |
CN116731377B CN116731377B (en) | 2024-02-13 |
Family
ID=87907665
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202310704753.XA Active CN116731377B (en) | 2023-06-14 | 2023-06-14 | Antistatic sponge prepared from single-walled carbon nanotubes and preparation method thereof |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN116731377B (en) |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2029843A5 (en) * | 1969-01-28 | 1970-10-23 | Elekal | Flexible hydrophilic polyurethante foam - suitable as a sponge |
GB1372357A (en) * | 1970-11-17 | 1974-10-30 | Dunlop Holdings Ltd | Vehicle road wheels |
US4108791A (en) * | 1977-01-31 | 1978-08-22 | The Dow Chemical Company | High resiliency polyurethane foams |
KR20210106184A (en) * | 2020-02-20 | 2021-08-30 | 한국전기연구원 | Manufacturing method of highly dispersed polyurethane foam composites with carbon nanotubes and polyurethane foam composites manufactured by the method |
CN113527618A (en) * | 2021-08-06 | 2021-10-22 | 南京金栖化工集团有限公司 | Preparation method and application of flame-retardant flatulence slow-rebound combined polyether polyol |
US20220227917A1 (en) * | 2019-05-16 | 2022-07-21 | Basf Se | Low density polyurethane foam systems with high split tear |
CN115232287A (en) * | 2022-08-08 | 2022-10-25 | 南京金栖化工集团有限公司 | Flame-retardant slow-rebound polyurethane sponge and preparation method thereof |
-
2023
- 2023-06-14 CN CN202310704753.XA patent/CN116731377B/en active Active
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2029843A5 (en) * | 1969-01-28 | 1970-10-23 | Elekal | Flexible hydrophilic polyurethante foam - suitable as a sponge |
GB1372357A (en) * | 1970-11-17 | 1974-10-30 | Dunlop Holdings Ltd | Vehicle road wheels |
US4108791A (en) * | 1977-01-31 | 1978-08-22 | The Dow Chemical Company | High resiliency polyurethane foams |
US20220227917A1 (en) * | 2019-05-16 | 2022-07-21 | Basf Se | Low density polyurethane foam systems with high split tear |
KR20210106184A (en) * | 2020-02-20 | 2021-08-30 | 한국전기연구원 | Manufacturing method of highly dispersed polyurethane foam composites with carbon nanotubes and polyurethane foam composites manufactured by the method |
CN113527618A (en) * | 2021-08-06 | 2021-10-22 | 南京金栖化工集团有限公司 | Preparation method and application of flame-retardant flatulence slow-rebound combined polyether polyol |
CN115232287A (en) * | 2022-08-08 | 2022-10-25 | 南京金栖化工集团有限公司 | Flame-retardant slow-rebound polyurethane sponge and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
CN116731377B (en) | 2024-02-13 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN105238061A (en) | Foaming silicone rubber compound, low-density silicone rubber sponge and preparing method of low-density silicone rubber sponge | |
CN107541070B (en) | Thixotropic foam silicone rubber and preparation method thereof | |
CN113956667B (en) | Foaming silicone rubber and preparation method and application thereof | |
CA1295084C (en) | Foamable vinyl chloride resin composition for powder molding and method for producing same | |
CN113072735A (en) | Master batch material, foaming master batch preparation method and foaming material preparation method | |
CN1970598A (en) | Preparation of hard polyurethane conductive foam plastic for carbon nanotube filling | |
CN110256853A (en) | A kind of in-place molding foamed silastic sealing ring composition and preparation method thereof | |
CN111040104B (en) | Sound-absorbing flame-retardant vegetable oil-based polyurethane foam material and preparation method thereof | |
Jia et al. | Microstructure and properties of microcellular silicone rubber foams with improved surface quality | |
CN116731377B (en) | Antistatic sponge prepared from single-walled carbon nanotubes and preparation method thereof | |
CN114736505A (en) | Foaming polyphenyl ether polypropylene composite bead and wafer packaging box | |
CN111138864B (en) | Fluorine-containing oil-resistant anti-swelling silicone rubber foam material and preparation method thereof | |
CN113956543B (en) | Hyperbranched ionic liquid/CNFs hybrid particle, microporous foaming flame retardant TPV and preparation method thereof | |
CN111574678A (en) | Anti-static polyurethane foam base material, preparation method thereof and adhesive tape | |
CN110540626B (en) | Ultra-light macroporous reticular polyurethane foam plastic and ultra-low temperature preparation method thereof | |
CN111574673A (en) | Environment-friendly heat-conducting polyurethane foam, preparation method thereof and adhesive tape | |
CN114106718A (en) | Preparation method of PVA-based degradable adhesive tape | |
CN109517387B (en) | Soft organic silicon foam material and preparation method and application thereof | |
CN102408718A (en) | Silicon foaming adhesive composition and its preparation method, silicon foaming adhesive and ultrasonic sensor | |
CN109369993A (en) | A kind of butadiene styrene rubber foaming material prescription of uniform in foaming | |
CN114231031B (en) | Foaming polyphenylene sulfide composition and preparation method and application thereof | |
CN109369851B (en) | Preparation method of starch-based foaming buffer material | |
CN112876727B (en) | Foaming agent and preparation method thereof, composition for preparing hard foam, set and method for preparing hard foam | |
CN113429633B (en) | Rubber vulcanization activator and preparation method thereof | |
CN113736156B (en) | Epoxidized natural latex sponge and preparation method and application thereof |
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 | ||
GR01 | Patent grant | ||
GR01 | Patent grant |