CN114213698A - Electromagnetic shielding composite foam with oriented filler structure and preparation method thereof - Google Patents
Electromagnetic shielding composite foam with oriented filler structure and preparation method thereof Download PDFInfo
- Publication number
- CN114213698A CN114213698A CN202111678195.1A CN202111678195A CN114213698A CN 114213698 A CN114213698 A CN 114213698A CN 202111678195 A CN202111678195 A CN 202111678195A CN 114213698 A CN114213698 A CN 114213698A
- Authority
- CN
- China
- Prior art keywords
- fiber
- composite material
- polymer
- magnetic conductive
- magnetic
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000002131 composite material Substances 0.000 title claims abstract description 87
- 239000000945 filler Substances 0.000 title claims abstract description 53
- 239000006260 foam Substances 0.000 title claims abstract description 35
- 238000002360 preparation method Methods 0.000 title claims abstract description 35
- 239000002245 particle Substances 0.000 claims abstract description 47
- 229920000642 polymer Polymers 0.000 claims abstract description 24
- 238000005187 foaming Methods 0.000 claims abstract description 13
- 238000009738 saturating Methods 0.000 claims abstract description 9
- 238000002156 mixing Methods 0.000 claims abstract description 7
- 239000006249 magnetic particle Substances 0.000 claims abstract description 6
- 238000001816 cooling Methods 0.000 claims abstract description 3
- 239000000835 fiber Substances 0.000 claims description 53
- 229910052751 metal Inorganic materials 0.000 claims description 37
- 239000002184 metal Substances 0.000 claims description 37
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 30
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 20
- 239000000126 substance Substances 0.000 claims description 20
- 238000007747 plating Methods 0.000 claims description 19
- 238000001035 drying Methods 0.000 claims description 18
- -1 polypropylene Polymers 0.000 claims description 18
- 238000003756 stirring Methods 0.000 claims description 17
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 16
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 claims description 15
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 15
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 claims description 14
- 239000007789 gas Substances 0.000 claims description 14
- 239000002904 solvent Substances 0.000 claims description 14
- 238000005406 washing Methods 0.000 claims description 14
- 239000000919 ceramic Substances 0.000 claims description 13
- 239000010941 cobalt Substances 0.000 claims description 13
- 229910017052 cobalt Inorganic materials 0.000 claims description 13
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 13
- 229920000049 Carbon (fiber) Polymers 0.000 claims description 12
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 12
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 12
- 239000004917 carbon fiber Substances 0.000 claims description 12
- 229910052759 nickel Inorganic materials 0.000 claims description 12
- 229910001220 stainless steel Inorganic materials 0.000 claims description 12
- 239000010935 stainless steel Substances 0.000 claims description 12
- 229920000747 poly(lactic acid) Polymers 0.000 claims description 11
- 239000004626 polylactic acid Substances 0.000 claims description 11
- 229920001971 elastomer Polymers 0.000 claims description 10
- 229910052742 iron Inorganic materials 0.000 claims description 10
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 9
- 229920002379 silicone rubber Polymers 0.000 claims description 9
- 229920002748 Basalt fiber Polymers 0.000 claims description 8
- 239000004698 Polyethylene Substances 0.000 claims description 8
- 229920006231 aramid fiber Polymers 0.000 claims description 8
- 239000000806 elastomer Substances 0.000 claims description 8
- 239000003822 epoxy resin Substances 0.000 claims description 8
- 229920000647 polyepoxide Polymers 0.000 claims description 8
- 229920000573 polyethylene Polymers 0.000 claims description 8
- 239000004642 Polyimide Substances 0.000 claims description 7
- 239000003365 glass fiber Substances 0.000 claims description 7
- 229920001721 polyimide Polymers 0.000 claims description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 6
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical group CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 6
- 239000004743 Polypropylene Substances 0.000 claims description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 6
- 229920001155 polypropylene Polymers 0.000 claims description 6
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 claims description 4
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims description 4
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims description 4
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 claims description 4
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims description 4
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 claims description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 4
- 239000004952 Polyamide Substances 0.000 claims description 4
- 239000004793 Polystyrene Substances 0.000 claims description 4
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 4
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 claims description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 claims description 4
- 229910052755 nonmetal Inorganic materials 0.000 claims description 4
- 229920002647 polyamide Polymers 0.000 claims description 4
- 239000004417 polycarbonate Substances 0.000 claims description 4
- 229920000515 polycarbonate Polymers 0.000 claims description 4
- 229920005594 polymer fiber Polymers 0.000 claims description 4
- 229920002223 polystyrene Polymers 0.000 claims description 4
- 239000004800 polyvinyl chloride Substances 0.000 claims description 4
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 4
- 239000004945 silicone rubber Substances 0.000 claims description 4
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 claims description 4
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 claims description 3
- 239000001273 butane Substances 0.000 claims description 3
- 239000001569 carbon dioxide Substances 0.000 claims description 3
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 3
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 claims description 3
- 229910052757 nitrogen Inorganic materials 0.000 claims description 3
- 239000003208 petroleum Substances 0.000 claims description 3
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 claims description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 claims description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 2
- 229920002972 Acrylic fiber Polymers 0.000 claims description 2
- 101000878595 Arabidopsis thaliana Squalene synthase 1 Proteins 0.000 claims description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 2
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 claims description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 2
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 claims description 2
- 229920000181 Ethylene propylene rubber Polymers 0.000 claims description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims description 2
- 229920000877 Melamine resin Polymers 0.000 claims description 2
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 2
- 239000004696 Poly ether ether ketone Substances 0.000 claims description 2
- 229920000954 Polyglycolide Polymers 0.000 claims description 2
- 239000004734 Polyphenylene sulfide Substances 0.000 claims description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 2
- 229920000297 Rayon Polymers 0.000 claims description 2
- 239000004433 Thermoplastic polyurethane Substances 0.000 claims description 2
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 claims description 2
- 229920001807 Urea-formaldehyde Polymers 0.000 claims description 2
- 229920002978 Vinylon Polymers 0.000 claims description 2
- QXZUUHYBWMWJHK-UHFFFAOYSA-N [Co].[Ni] Chemical compound [Co].[Ni] QXZUUHYBWMWJHK-UHFFFAOYSA-N 0.000 claims description 2
- 239000003570 air Substances 0.000 claims description 2
- 229910052786 argon Inorganic materials 0.000 claims description 2
- 229910052796 boron Inorganic materials 0.000 claims description 2
- 229920005549 butyl rubber Polymers 0.000 claims description 2
- 239000003638 chemical reducing agent Substances 0.000 claims description 2
- 239000004020 conductor Substances 0.000 claims description 2
- 229920001577 copolymer Polymers 0.000 claims description 2
- 239000010949 copper Substances 0.000 claims description 2
- 229910052802 copper Inorganic materials 0.000 claims description 2
- 229940117389 dichlorobenzene Drugs 0.000 claims description 2
- 239000011737 fluorine Substances 0.000 claims description 2
- 229910052731 fluorine Inorganic materials 0.000 claims description 2
- 235000019253 formic acid Nutrition 0.000 claims description 2
- 239000007849 furan resin Substances 0.000 claims description 2
- 239000001307 helium Substances 0.000 claims description 2
- 229910052734 helium Inorganic materials 0.000 claims description 2
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 claims description 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 claims description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 claims description 2
- 229920003049 isoprene rubber Polymers 0.000 claims description 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 claims description 2
- NDLPOXTZKUMGOV-UHFFFAOYSA-N oxo(oxoferriooxy)iron hydrate Chemical compound O.O=[Fe]O[Fe]=O NDLPOXTZKUMGOV-UHFFFAOYSA-N 0.000 claims description 2
- 239000005011 phenolic resin Substances 0.000 claims description 2
- 229920003229 poly(methyl methacrylate) Polymers 0.000 claims description 2
- 229920002492 poly(sulfone) Polymers 0.000 claims description 2
- 229920001230 polyarylate Polymers 0.000 claims description 2
- 229920001610 polycaprolactone Polymers 0.000 claims description 2
- 239000004632 polycaprolactone Substances 0.000 claims description 2
- 229920000728 polyester Polymers 0.000 claims description 2
- 229920002530 polyetherether ketone Polymers 0.000 claims description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 claims description 2
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 2
- 239000004633 polyglycolic acid Substances 0.000 claims description 2
- 239000004926 polymethyl methacrylate Substances 0.000 claims description 2
- 229920000069 polyphenylene sulfide Polymers 0.000 claims description 2
- 239000004810 polytetrafluoroethylene Substances 0.000 claims description 2
- 229920001343 polytetrafluoroethylene Polymers 0.000 claims description 2
- 229920002635 polyurethane Polymers 0.000 claims description 2
- 239000004814 polyurethane Substances 0.000 claims description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 2
- 239000001294 propane Substances 0.000 claims description 2
- 239000005060 rubber Substances 0.000 claims description 2
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 claims description 2
- 229910010271 silicon carbide Inorganic materials 0.000 claims description 2
- 229920002050 silicone resin Polymers 0.000 claims description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 claims description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 2
- 229920001169 thermoplastic Polymers 0.000 claims description 2
- 229920006344 thermoplastic copolyester Polymers 0.000 claims description 2
- 229920002397 thermoplastic olefin Polymers 0.000 claims description 2
- 229920006345 thermoplastic polyamide Polymers 0.000 claims description 2
- 229920002803 thermoplastic polyurethane Polymers 0.000 claims description 2
- 239000004416 thermosoftening plastic Substances 0.000 claims description 2
- UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 claims description 2
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 claims description 2
- 229940029284 trichlorofluoromethane Drugs 0.000 claims description 2
- 239000008096 xylene Substances 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims 3
- 229960001701 chloroform Drugs 0.000 claims 2
- 239000000463 material Substances 0.000 abstract description 24
- 239000000243 solution Substances 0.000 description 13
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 12
- 239000007864 aqueous solution Substances 0.000 description 12
- 238000001914 filtration Methods 0.000 description 12
- QVYYOKWPCQYKEY-UHFFFAOYSA-N [Fe].[Co] Chemical compound [Fe].[Co] QVYYOKWPCQYKEY-UHFFFAOYSA-N 0.000 description 8
- NVIVJPRCKQTWLY-UHFFFAOYSA-N cobalt nickel Chemical compound [Co][Ni][Co] NVIVJPRCKQTWLY-UHFFFAOYSA-N 0.000 description 8
- SZVJSHCCFOBDDC-UHFFFAOYSA-N ferrosoferric oxide Chemical compound O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 8
- TXUICONDJPYNPY-UHFFFAOYSA-N (1,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) heptanoate Chemical compound C1CC2CC(=O)C=C(C)C2(C)C2C1C1CCC(OC(=O)CCCCCC)C1(C)CC2 TXUICONDJPYNPY-UHFFFAOYSA-N 0.000 description 6
- 229910021626 Tin(II) chloride Inorganic materials 0.000 description 6
- 229910052799 carbon Inorganic materials 0.000 description 6
- 239000012153 distilled water Substances 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 238000003760 magnetic stirring Methods 0.000 description 6
- 230000007935 neutral effect Effects 0.000 description 6
- 229920003225 polyurethane elastomer Polymers 0.000 description 6
- 239000001509 sodium citrate Substances 0.000 description 6
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 6
- 239000001119 stannous chloride Substances 0.000 description 6
- 235000011150 stannous chloride Nutrition 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- KWSLGOVYXMQPPX-UHFFFAOYSA-N 5-[3-(trifluoromethyl)phenyl]-2h-tetrazole Chemical compound FC(F)(F)C1=CC=CC(C2=NNN=N2)=C1 KWSLGOVYXMQPPX-UHFFFAOYSA-N 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 239000004760 aramid Substances 0.000 description 4
- 229920003235 aromatic polyamide Polymers 0.000 description 4
- 239000011231 conductive filler Substances 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 229910001379 sodium hypophosphite Inorganic materials 0.000 description 4
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 235000011114 ammonium hydroxide Nutrition 0.000 description 3
- 229940044175 cobalt sulfate Drugs 0.000 description 3
- 229910000361 cobalt sulfate Inorganic materials 0.000 description 3
- KTVIXTQDYHMGHF-UHFFFAOYSA-L cobalt(2+) sulfate Chemical compound [Co+2].[O-]S([O-])(=O)=O KTVIXTQDYHMGHF-UHFFFAOYSA-L 0.000 description 3
- 238000007723 die pressing method Methods 0.000 description 3
- 239000003517 fume Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000005670 electromagnetic radiation Effects 0.000 description 2
- RUTXIHLAWFEWGM-UHFFFAOYSA-H iron(3+) sulfate Chemical compound [Fe+3].[Fe+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O RUTXIHLAWFEWGM-UHFFFAOYSA-H 0.000 description 2
- 229910000360 iron(III) sulfate Inorganic materials 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 239000007769 metal material Substances 0.000 description 2
- 238000001000 micrograph Methods 0.000 description 2
- LJCNRYVRMXRIQR-OLXYHTOASA-L potassium sodium L-tartrate Chemical compound [Na+].[K+].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O LJCNRYVRMXRIQR-OLXYHTOASA-L 0.000 description 2
- 229940074439 potassium sodium tartrate Drugs 0.000 description 2
- 235000011006 sodium potassium tartrate Nutrition 0.000 description 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- 229910021586 Nickel(II) chloride Inorganic materials 0.000 description 1
- AYRXSINWFIIFAE-UHFFFAOYSA-N O6-alpha-D-Galactopyranosyl-D-galactose Natural products OCC1OC(OCC(O)C(O)C(O)C(O)C=O)C(O)C(O)C1O AYRXSINWFIIFAE-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 229960002089 ferrous chloride Drugs 0.000 description 1
- 238000013012 foaming technology Methods 0.000 description 1
- DLRVVLDZNNYCBX-CQUJWQHSSA-N gentiobiose Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC[C@@H]1[C@@H](O)[C@H](O)[C@@H](O)C(O)O1 DLRVVLDZNNYCBX-CQUJWQHSSA-N 0.000 description 1
- NMCUIPGRVMDVDB-UHFFFAOYSA-L iron dichloride Chemical compound Cl[Fe]Cl NMCUIPGRVMDVDB-UHFFFAOYSA-L 0.000 description 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 239000012762 magnetic filler Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- QMMRZOWCJAIUJA-UHFFFAOYSA-L nickel dichloride Chemical compound Cl[Ni]Cl QMMRZOWCJAIUJA-UHFFFAOYSA-L 0.000 description 1
- LGQLOGILCSXPEA-UHFFFAOYSA-L nickel sulfate Chemical compound [Ni+2].[O-]S([O-])(=O)=O LGQLOGILCSXPEA-UHFFFAOYSA-L 0.000 description 1
- 229910000363 nickel(II) sulfate Inorganic materials 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000001878 scanning electron micrograph Methods 0.000 description 1
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 1
- 229940048086 sodium pyrophosphate Drugs 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 1
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1
Images
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
- C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
- C08J9/12—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent
- C08J9/122—Hydrogen, oxygen, CO2, nitrogen or noble gases
-
- 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
- C08J9/009—Use of pretreated compounding ingredients
-
- 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
- C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
- C08J9/12—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent
- C08J9/14—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent organic
- C08J9/141—Hydrocarbons
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K9/00—Screening of apparatus or components against electric or magnetic fields
- H05K9/0073—Shielding materials
- H05K9/0081—Electromagnetic shielding materials, e.g. EMI, RFI shielding
-
- 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
- C08J2203/00—Foams characterized by the expanding agent
- C08J2203/06—CO2, N2 or noble gases
-
- 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
- C08J2203/00—Foams characterized by the expanding agent
- C08J2203/14—Saturated hydrocarbons, e.g. butane; Unspecified hydrocarbons
-
- 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
- C08J2323/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
- C08J2323/02—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
- C08J2323/04—Homopolymers or copolymers of ethene
- C08J2323/06—Polyethene
-
- 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
- C08J2363/00—Characterised by the use of epoxy resins; Derivatives of epoxy resins
-
- 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
- C08J2367/00—Characterised by the use of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Derivatives of such polymers
- C08J2367/04—Polyesters derived from hydroxy carboxylic acids, e.g. lactones
-
- 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
- C08J2383/00—Characterised by the use of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen, or carbon only; Derivatives of such polymers
- C08J2383/04—Polysiloxanes
-
- 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
- C08J2477/00—Characterised by the use of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Derivatives of such polymers
- C08J2477/10—Polyamides derived from aromatically bound amino and carboxyl groups of amino carboxylic acids or of polyamines and polycarboxylic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Polymers & Plastics (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Organic Chemistry (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Electromagnetism (AREA)
- Physics & Mathematics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Shielding Devices Or Components To Electric Or Magnetic Fields (AREA)
Abstract
The invention discloses an electromagnetic shielding composite foam with an oriented filler structure and a preparation method thereof, wherein the electromagnetic shielding composite foam comprises the following steps: s1: attaching magnetic particles to the surface of the filler particles with the length-diameter ratio to obtain magnetic conductive particles; s2: blending the magnetic conductive particles and a polymer to prepare a magnetic conductive particle-polymer composite material; s3: placing the composite material obtained in the S2 in a magnetic field, and orienting the magnetic particles with the length-diameter ratio along the direction of the magnetic field at the temperature of 0-300 ℃; s4: and (3) placing the composite material obtained in the step (S3) in a foaming gas environment, saturating the composite material at the temperature of 30-300 ℃ and under the pressure of 0.2-50 MPa for 1 min-24 h, then relieving the pressure to normal pressure at the speed of 0.1-30 MPa/S, and cooling the pressure to room temperature to obtain the composite material. The composite foam prepared by the invention has good electromagnetic shielding performance, the density of the material is reduced by introducing the foam holes, the preparation method is simple, and the cost is low.
Description
Technical Field
The invention belongs to the technical field of electromagnetic shielding composite materials, and particularly relates to electromagnetic shielding composite foam with an oriented filler structure and a preparation method thereof.
Background
With the continuous progress of society, a large number of electronic products are rushed into the daily life and work of people. The use of electronic components provides a lot of convenience for people on one hand, and causes pollution caused by excessive electromagnetic radiation on the other hand, so that a series of social and environmental problems are caused, and various electromagnetic shielding protective materials are developed for preventing various problems caused by the excessive electromagnetic radiation. At present, metal materials are the most widely used electromagnetic shielding materials, and the traditional metal-based electromagnetic shielding materials have very excellent electric conduction and electromagnetic shielding properties. However, the metal material has the defects of high density, easy corrosion, poor processability and the like in the practical application process, and compared with the traditional metal-based electromagnetic shielding material, the polymer-based electromagnetic shielding composite material has the advantages of light weight, easy processing, corrosion resistance, adjustable conductivity and the like, and has wide application prospect.
In order to provide a good shielding effect for the material, a large amount of conductive filler is generally required to be added into the polymer matrix, so as to increase the electrical conductivity of the material and increase the shielding effectiveness of the material. The preparation cost of the material is greatly increased, the density of the material is greatly improved, and the application of the material in related fields of electronic appliances, communication equipment, aerospace and the like is greatly limited.
Disclosure of Invention
Aiming at the prior art, the invention provides an electromagnetic shielding composite foam with an oriented filler structure and a preparation method thereof, and aims to solve the problems of large addition amount of conductive filler, high preparation cost, large density, limited application and the like of the conventional electromagnetic shielding material.
In order to achieve the purpose, the invention adopts the technical scheme that: the preparation method of the electromagnetic shielding composite foam with the oriented filler structure comprises the following steps:
s1: attaching magnetic particles to the surface of the filler particles with the length-diameter ratio to obtain magnetic conductive particles;
s2: blending the magnetic conductive particles and a polymer to prepare a magnetic conductive particle-polymer composite material;
s3: placing the composite material obtained in the S2 in a magnetic field, and orienting the magnetic particles with the length-diameter ratio along the direction of the magnetic field at the temperature of 0-300 ℃;
s4: and (3) placing the composite material obtained in the step (S3) in a foaming gas environment, saturating the composite material at the temperature of 30-300 ℃ and under the pressure of 0.2-50 MPa for 1 min-24 h, then relieving the pressure to normal pressure at the speed of 0.1-30 MPa/S, and cooling the pressure to room temperature to obtain the composite material.
The electromagnetic shielding composite foam with the oriented filler structure is prepared by combining the action of a magnetic field and a high-pressure gas foaming technology, and the method effectively realizes high performance and light weight of the electromagnetic shielding composite material. The filler is oriented and orderly distributed in the polymer matrix through an external magnetic field, so that the lapping efficiency among filler particles can be effectively increased, and the electric conduction and electromagnetic shielding performance of the material are improved. According to the invention, a porous structure is introduced into the polymer composite material by using a high-pressure gas foaming method with simple and efficient process, so that the preparation cost of the material can be effectively reduced, the lightweight design of the composite material is realized, and the high-performance electromagnetic shielding composite foam is obtained.
On the basis of the technical scheme, the invention can be further improved as follows.
Further, the magnetic conductive particles are prepared by the following steps:
SS 1: surface treating filler particles having an aspect ratio;
SS 2: adding the treated filler particles into chemical iron plating solution, chemical cobalt plating solution, chemical nickel plating solution, chemical ferric oxide plating solution, chemical cobalt plating solution, chemical nickel plating solution or chemical nickel cobalt plating solution according to the material-to-solution ratio of 1g: 5-200 mL, then adding a reducing agent, stirring and reacting for 1 min-24 h, and finally washing and drying to obtain the magnetic conductive particles.
Further, the filler particles are polymer fibers, inorganic nonmetal fibers or metal fibers.
Further, the polymer fiber is at least one of polypropylene fiber, aramid fiber, polyester fiber, polyamide fiber, polypropylene fiber, vinylon fiber, acrylic fiber, polyvinyl chloride fiber and viscose; the inorganic nonmetal fibers are at least one of carbon fibers, basalt fibers, glass fibers, ceramic fibers, silicon carbide fibers and boron fibers; the metal fiber is at least one of stainless steel fiber, copper fiber, nickel fiber and iron-chromium-aluminum fiber.
Further, the magnetic conductive particle-polymer composite material is prepared by the following steps: and (2) blending the polymer and the magnetic conductive particles according to the mass ratio of 1-100: 1 at 30-300 ℃ for 1 min-12 h under the condition of 5-500 r/min.
Further, the magnetic conductive particle-polymer composite material is prepared by the following steps: dissolving a polymer in a solvent, adding magnetic conductive particles with the mass being 1/100-1 time that of the polymer into the solvent, uniformly dispersing the magnetic conductive particles, and volatilizing the solvent to obtain the conductive material.
Further, the solvent is ethanol, methanol, isopropanol, ethylene glycol, diethyl ether, acetone, hexane, cyclohexane, pentane, heptane, octane, aniline, butanone, chloroform, dimethylamine, carbon tetrachloride, N-heptanol, tetrahydrofuran, benzene, toluene, xylene, ethylbenzene, butyl acetate, chloroform, formic acid, dimethyl sulfoxide, chlorobenzene, dichlorobenzene, dichloromethane, trichloroethylene, or N-methylpyrrolidone.
Further, the polymer is polyethylene, polypropylene, polycarbonate, polystyrene, polyvinyl chloride, polytetrafluoroethylene, polyamide, vinyl acetate copolymer, polyethylene terephthalate, polymethyl methacrylate, polycarbonate, polyurethane, polylactic acid, polyglycolic acid, polycaprolactone, polyvinyl alcohol, epoxy resin, urea resin, furan resin, melamine formaldehyde resin, silicone resin, polyarylate, acrylate, phenol resin, polyether ether ketone, polysulfone, polyphenylene sulfide, polyimide, styrene-butadiene rubber, isoprene rubber, butyl rubber, ethylene-propylene rubber, fluorine rubber, silicone rubber, thermoplastic polystyrene elastomer, thermoplastic polyolefin elastomer, thermoplastic copolyester elastomer, thermoplastic polyamide elastomer, or thermoplastic polyurethane elastomer.
Further, the foaming gas is air, nitrogen, carbon dioxide, helium, argon, petroleum ether, methane, ethane, propane, butane, pentane, hexane, heptane, n-pentane, n-hexane, n-heptane, dichloromethane, or trichlorofluoromethane.
The invention has the beneficial effects that:
1. the invention obtains the magnetic conductive filler by a chemical loading method, compounds the magnetic filler and the polymer and places the compound in a magnetic field, so that the filler is oriented and arranged along the direction of the magnetic field, thereby effectively enhancing the lap joint passage of filler particles and improving the conductivity and the electromagnetic shielding efficiency of the composite material.
2. The electromagnetic shielding composite foam with the oriented filler structure prepared by the invention has good electromagnetic shielding performance, the density of the material is further reduced by introducing the foam holes, the electromagnetic shielding efficiency of the prepared composite foam can exceed 30dB, and the density of the material can be as low as 0.5g/cm3The use requirement of electromagnetic shielding materials for commercial application is met, and the application of the materials in related fields is widened.
3. The high-pressure gas foaming method used by the invention has the advantages of simple operation and low cost.
Drawings
FIG. 1 is a scanning electron microscope image of a metallic nickel-loaded carbon fiber prepared in example 2;
FIG. 2 is a scanning electron microscope image of a cross section of the electro-magnetic shielding composite foam with an oriented filler structure prepared in example 2;
fig. 3 shows the electromagnetic shielding effectiveness of the electromagnetic shielding composite foam with the oriented filler structure prepared in example 2.
Detailed Description
The following examples are provided to illustrate specific embodiments of the present invention.
Example 1
A preparation method of electromagnetic shielding composite foam with an oriented filler structure comprises the following steps:
(1) preparation of magnetic conductive particles
Adding 1g of aramid fiber into 50mL of dilute sulfuric acid, mechanically stirring for 1h, repeatedly washing with distilled water, filtering to be neutral, adding the aramid fiber into a stannous chloride aqueous solution, mechanically stirring, adding the sensitized aramid fiber into 100mL of chemical iron plating solution (10 g/L of ferric sulfate and 5g/L of gentiobiose), slowly adding a sodium citrate aqueous solution, reacting for 10h under magnetic stirring, and washing, filtering and drying to obtain the metal iron-loaded aramid fiber magnetic conductive particles.
(2) Preparation of metal iron loaded aramid fiber-polyethylene composite material
Placing 8g of polyethylene and 1g of metal iron-loaded aramid fiber magnetic conductive particles into an internal mixer, blending for 5min at the temperature of 120 ℃ and at the speed of 100 r/min, and obtaining the metal iron-loaded aramid fiber-polyethylene composite material through a die pressing process.
(3) Preparation of oriented filler structure metal iron loaded aramid fiber-polyethylene composite material
And (3) placing the composite material prepared in the step (2) in a magnetic field, and enabling the metal iron loaded aramid fiber to be oriented and arranged along the direction of the magnetic field under the action of magnetic force at 150 ℃.
(4) High pressure gas foaming
Cutting the metal iron-loaded aramid fiber-polyethylene composite material with the oriented filler structure obtained in the step (3) into a regular shape, placing the material in a high-pressure reaction kettle, heating, introducing carbon dioxide gas, saturating at 80 ℃ and under the pressure of 10MPa for 30min, then reducing the pressure relief rate to normal pressure at the pressure of 5MPa/s, taking out a foamed sample, and drying in a drying oven to finally obtain the polyethylene electromagnetic shielding composite foam with the oriented filler structure.
Example 2
A preparation method of electromagnetic shielding composite foam with an oriented filler structure comprises the following steps:
(1) preparation of magnetic conductive particles
Adding 1g of carbon fiber into 10mL of dilute sulfuric acid, mechanically stirring for 2h, repeatedly washing with distilled water, filtering to be neutral, adding the carbon fiber into a stannous chloride aqueous solution, mechanically stirring, adding the sensitized carbon fiber into 50mL of chemical nickel plating solution (40 g/L of nickel sulfate, 10g/L of sodium pyrophosphate, 5g/L of sodium hypophosphite, 5g/L of thiourea and 5mL of ammonia water), slowly adding a sodium citrate aqueous solution, reacting for 10min under magnetic stirring, and washing, filtering and drying to obtain the metallic nickel-loaded carbon fiber magnetic conductive particles.
(2) Preparation of metallic nickel loaded carbon fiber-epoxy resin composite material
And (2) placing 10g of epoxy resin and 0.5g of metal nickel loaded carbon fiber magnetic conductive particles into an internal mixer, blending for 10min at 50 ℃ under the condition of 80 r/min, and obtaining the metal nickel loaded carbon fiber-epoxy resin composite material through a die pressing process.
(3) Preparation of oriented filler structure metal nickel loaded carbon fiber-epoxy resin composite material
And (3) placing the composite material prepared in the step (2) in a magnetic field, and enabling the metallic nickel loaded carbon fibers to be oriented and arranged along the direction of the magnetic field under the action of magnetic force at 0 ℃.
(4) High pressure gas foaming
Cutting the metal nickel-loaded carbon fiber-epoxy resin composite material with the oriented filler structure obtained in the step (3) into a regular shape, placing the material in a high-pressure reaction kettle, heating and introducing air, saturating the material at 30 ℃ and 5MPa for 10min, then reducing the pressure relief rate to normal pressure at 1MPa/s, taking out a foamed sample, and drying the sample in a drying oven to finally obtain the epoxy resin electromagnetic shielding composite foam with the oriented filler structure.
Example 3
A preparation method of electromagnetic shielding composite foam with an oriented filler structure comprises the following steps:
(1) preparation of magnetic conductive particles
Adding 1g of basalt fiber into 20mL of dilute sulfuric acid, mechanically stirring for 1h, repeatedly washing with distilled water, filtering to be neutral, adding the basalt fiber into a stannous chloride aqueous solution, mechanically stirring, adding the sensitized basalt fiber into 100mL of chemical cobalt plating solution (40 g/L of cobalt sulfate, 20g/L of potassium sodium tartrate, 2g/L of sodium hypophosphite, 10g/L of boric acid and 5mL of ammonia water), slowly adding a sodium citrate aqueous solution, reacting for 30min under magnetic stirring, and washing, filtering and drying to obtain the metallic cobalt-loaded basalt fiber magnetic conductive particles.
(2) Preparation of metallic cobalt-loaded basalt fiber-polyurethane elastomer composite material
10g of polyurethane elastomer and 2g of metal cobalt-loaded basalt fiber magnetic conductive particles are placed in an internal mixer, and are blended for 1h at the temperature of 120 ℃ and at the speed of 50 r/min, so that the metal cobalt-loaded basalt fiber-polyurethane elastomer composite material is obtained through a die pressing process.
(3) Preparation of oriented filler structure metal cobalt loaded basalt fiber-polyurethane elastomer composite material
And (3) placing the composite material prepared in the step (2) in a magnetic field, and enabling the metal cobalt-loaded basalt fibers to be oriented and arranged along the direction of the magnetic field under the action of magnetic force at 120 ℃.
(4) High pressure gas foaming
Cutting the metal cobalt-loaded basalt fiber-polyurethane elastomer composite material with the oriented filler structure obtained in the step (3) into a regular shape, placing the material in a high-pressure reaction kettle, heating, introducing nitrogen, saturating at 90 ℃ under the pressure of 15MPa for 1h, then reducing the pressure relief rate of 10MPa/s to normal pressure, taking out a foamed sample, and drying in an oven to finally obtain the polyurethane elastomer electromagnetic shielding composite foam with the oriented filler structure.
Example 4
A preparation method of electromagnetic shielding composite foam with an oriented filler structure comprises the following steps:
(1) particles of magnetic conductive fillers
Adding 1g of glass fiber into 50mL of dilute sulfuric acid, mechanically stirring for 1h, repeatedly washing with distilled water, filtering to be neutral, adding the obtained product into a stannous chloride aqueous solution, mechanically stirring, adding the sensitized glass fiber into 50mL of chemical iron-cobalt plating solution (30 g/L of ferric sulfate, 20g/L of cobalt sulfate, 20g/L of potassium sodium tartrate, 2g/L of sodium hypophosphite and 10mL of ammonia water), slowly adding a sodium citrate aqueous solution, reacting for 2h under magnetic stirring, and washing, filtering and drying to obtain the metal iron-cobalt loaded glass fiber magnetic conductive particles.
(2) Preparation of metal iron-cobalt loaded glass fiber-silicone rubber composite material
Adding 10g of silicon rubber and 10g of metal iron cobalt loaded glass fiber magnetic conductive particles into a cyclohexane solvent, mechanically stirring under an ultrasonic condition to fully dissolve the silicon rubber, pouring the mixture into a mold, and then placing the mold in a fume hood until the solvent is completely volatilized to obtain the metal iron cobalt loaded glass fiber-silicon rubber composite material.
(3) Preparation of oriented filler structure metal iron-cobalt loaded glass fiber-silicone rubber composite material
And (3) placing the composite material prepared in the step (2) in a magnetic field, and enabling the metal iron-cobalt loaded glass fibers to be oriented and arranged along the direction of the magnetic field under the action of magnetic force at 180 ℃.
(4) High pressure gas foaming
Cutting the metal iron-cobalt loaded glass fiber-silicon rubber composite material with the oriented filler structure obtained in the step (3) into a regular shape, placing the material in a high-pressure reaction kettle, heating, introducing methane, saturating at 30 ℃ and under the pressure of 0.2MPa for 1min, then reducing the pressure relief rate of 0.1MPa/s to the normal pressure, taking out a foamed sample, and drying in a drying oven to finally obtain the silicon rubber electromagnetic shielding composite foam with the oriented filler structure.
Example 5
A preparation method of electromagnetic shielding composite foam with an oriented filler structure comprises the following steps:
(1) preparation of highly conductive particles
Adding 1g of ceramic fiber into 5mL of dilute sulfuric acid, mechanically stirring for 24h, repeatedly washing with distilled water, filtering to be neutral, adding the ceramic fiber into a stannous chloride aqueous solution, mechanically stirring, adding the sensitized ceramic fiber into 200mL of chemical cobalt-nickel plating solution (40 g/L of nickel chloride, 10g/L of cobalt sulfate and 20g/L of sodium hypophosphite), slowly adding a sodium citrate aqueous solution, reacting for 1min under magnetic stirring, and washing, filtering and drying to obtain the metal cobalt-nickel loaded ceramic fiber conductive particles.
(2) Preparation of metal cobalt-nickel loaded ceramic fiber conductive particle-polylactic acid composite material
Adding 10g of polylactic acid and 0.1g of metal cobalt nickel loaded ceramic fiber magnetic conductive particles into a chloroform solvent, mechanically stirring to fully dissolve the polylactic acid, pouring the mixture into a mold, and then placing the mold in a fume hood until the solvent is completely volatilized to obtain the metal cobalt nickel loaded ceramic fiber-polylactic acid composite material.
(3) Preparation of oriented filler structure metal cobalt-nickel loaded ceramic fiber-polylactic acid composite material
And (3) placing the composite material prepared in the step (2) in a magnetic field, and enabling the metal cobalt nickel loaded ceramic fibers to be oriented and arranged along the direction of the magnetic field under the action of magnetic force at 220 ℃.
(4) High pressure gas foaming
Cutting the metal cobalt-nickel loaded ceramic fiber-polylactic acid composite material with the oriented filler structure obtained in the step (3) into a regular shape, placing the material in a high-pressure reaction kettle, heating, introducing butane, saturating at 30 ℃ and 50MPa for 24h, then reducing the pressure relief rate to normal pressure at 30MPa/s, taking out a foamed sample, and drying in an oven to finally obtain the polylactic acid electromagnetic shielding composite foam with the oriented filler structure.
Example 6
A preparation method of electromagnetic shielding composite foam with an oriented filler structure comprises the following steps:
(1) preparation of highly conductive particles
Adding 1g of stainless steel fiber into 200mL of dilute sulfuric acid, mechanically stirring for 1min, repeatedly washing with distilled water, filtering to be neutral, adding the stainless steel fiber into a stannous chloride aqueous solution, mechanically stirring, adding the sensitized stainless steel fiber into 100mL of chemically plated ferroferric oxide liquid (100 g/L of ferric chloride and 50g/L of ferrous chloride), slowly adding sodium hydroxide and sodium citrate aqueous solution, reacting for 24h under magnetic stirring, and washing, filtering and drying to obtain the magnetic ferroferric oxide loaded stainless steel fiber conductive particles.
(2) Preparation of ferroferric oxide-loaded stainless steel fiber conductive particle-polyimide composite material
Adding 10g of polyimide and 1g of ferroferric oxide-loaded stainless steel fiber magnetic conductive particles into a dimethylacetamide solvent, mechanically stirring under the ultrasonic condition of 1000W power to fully dissolve the polyimide, pouring the mixture into a mold, and then placing the mold in a fume hood until the solvent is completely volatilized to obtain the ferroferric oxide-loaded stainless steel fiber-polylactic acid composite material.
(3) Preparation of oriented filler structure ferroferric oxide loaded stainless steel fiber-polylactic acid composite material
And (3) placing the composite material prepared in the step (2) in a magnetic field, and enabling the ferroferric oxide loaded stainless steel fibers to be oriented and arranged along the direction of the magnetic field under the action of magnetic force at 300 ℃.
(4) High pressure gas foaming
Cutting the ferroferric oxide-loaded stainless steel fiber-polyimide composite material with the oriented filler structure obtained in the step (3) into a regular shape, placing the regular shape in a high-pressure reaction kettle, heating, introducing petroleum ether, saturating at 300 ℃ under the pressure of 20MPa for 24h, then reducing the pressure relief rate of 10MPa/s to normal pressure, taking out a foamed sample, and drying in a drying oven to finally obtain the polyimide electromagnetic shielding composite foam with the oriented filler structure.
Analysis of results
Taking the example 2 as an example, the metallic nickel-loaded carbon fiber is characterized by adopting a scanning electron microscope, and the result is shown in fig. 1, and it can be seen from fig. 1 that a layer of perfect metallic nickel particles are attached to the surface of the prepared nickel-plated carbon fiber, which can endow the filler with good magnetic performance and promote the orientation arrangement of the carbon fiber in a magnetic field environment. Fig. 2 is a sectional SEM image of the oriented filler structure polymer electromagnetic shielding composite foam of example 2, and it can be seen from a that the fibers are diverged out of the plane in the direction perpendicular to the magnetic field direction, and the fibers are aligned in the plane in the direction parallel to the magnetic field direction, which helps to improve the lapping efficiency of the filler particles along the magnetic field direction.
The electromagnetic shielding composite foam of the oriented filler structure prepared in example 2 was cut into a regular shape, and the shielding effectiveness of the composite foam in different orientation directions was measured using an electromagnetic shielding test system, and fig. 3 is the electromagnetic shielding effectiveness of the composite foam in directions parallel and perpendicular to the magnetic field. Because the ceramic fiber surface has good magnetic strength after being adhered with metal cobalt and nickel, orientation arrangement can occur under the action of a magnetic field, the lapping efficiency between fibers is improved, and the shielding efficiency is enhanced. The average shielding effectiveness of the syntactic foam in the direction parallel to the magnetic field was over 30dB and the average shielding effectiveness in the direction perpendicular to the magnetic field was under 20dB, indicating that the fiber orientation had an enhanced effect on the shielding effectiveness.
While the present invention has been described in detail with reference to the embodiments, it should not be construed as limited to the scope of the patent. Various modifications and changes may be made by those skilled in the art without inventive step within the scope of the appended claims.
Claims (10)
1. A preparation method of electromagnetic shielding composite foam with an oriented filler structure is characterized by comprising the following steps:
s1: attaching magnetic particles to the surface of the filler particles with the length-diameter ratio to obtain magnetic conductive particles;
s2: blending the magnetic conductive particles and a polymer to prepare a magnetic conductive particle-polymer composite material;
s3: placing the composite material obtained in the S2 in a magnetic field, and orienting the magnetic particles with the length-diameter ratio along the direction of the magnetic field at the temperature of 0-300 ℃;
s4: and (3) placing the composite material obtained in the step (S3) in a foaming gas environment, saturating the composite material at the temperature of 30-300 ℃ and under the pressure of 0.2-50 MPa for 1 min-24 h, then relieving the pressure to normal pressure at the speed of 0.1-30 MPa/S, and cooling the pressure to room temperature to obtain the composite material.
2. The method of claim 1, wherein: the magnetic conductive particles are prepared by the following steps:
SS 1: surface treating filler particles having an aspect ratio;
SS 2: adding the treated filler particles into chemical iron plating solution, chemical cobalt plating solution, chemical nickel plating solution, chemical ferric oxide plating solution, chemical cobalt plating solution, chemical nickel plating solution or chemical nickel cobalt plating solution according to the material-to-solution ratio of 1g: 5-200 mL, then adding a reducing agent, stirring and reacting for 1 min-24 h, and finally washing and drying to obtain the magnetic conductive particles.
3. The production method according to claim 1 or 2, characterized in that: the filler particles are polymer fibers, inorganic nonmetal fibers or metal fibers.
4. The production method according to claim 3, characterized in that: the polymer fiber is at least one of polypropylene fiber, aramid fiber, polyester fiber, polyamide fiber, polypropylene fiber, vinylon fiber, acrylic fiber, polyvinyl chloride fiber and viscose; the inorganic nonmetal fibers are at least one of carbon fibers, basalt fibers, glass fibers, ceramic fibers, silicon carbide fibers and boron fibers; the metal fiber is at least one of stainless steel fiber, copper fiber, nickel fiber and iron-chromium-aluminum fiber.
5. The method of claim 1, wherein the magnetic conductive particle-polymer composite is prepared by the steps of: and (2) blending the polymer and the magnetic conductive particles according to the mass ratio of 1-100: 1 at 30-300 ℃ for 1 min-12 h under the condition of 5-500 r/min.
6. The method of claim 1, wherein the magnetic conductive particle-polymer composite is prepared by the steps of: dissolving a polymer in a solvent, adding magnetic conductive particles with the mass being 1/100-1 time that of the polymer into the solvent, uniformly dispersing the magnetic conductive particles, and volatilizing the solvent to obtain the conductive material.
7. The method of claim 6, wherein: the solvent is ethanol, methanol, isopropanol, ethylene glycol, diethyl ether, acetone, hexane, cyclohexane, pentane, heptane, octane, aniline, butanone, chloroform, dimethylamine, carbon tetrachloride, N-heptanol, tetrahydrofuran, benzene, toluene, xylene, ethylbenzene, butyl acetate, trichloromethane, formic acid, dimethyl sulfoxide, chlorobenzene, dichlorobenzene, dichloromethane, trichloroethylene or N-methylpyrrolidone.
8. The production method according to claim 1, 5 or 6, characterized in that: the polymer is polyethylene, polypropylene, polycarbonate, polystyrene, polyvinyl chloride, polytetrafluoroethylene, polyamide, vinyl acetate copolymer, polyethylene terephthalate, polymethyl methacrylate, polycarbonate, polyurethane, polylactic acid, polyglycolic acid, polycaprolactone, polyvinyl alcohol, epoxy resin, urea resin, furan resin, melamine formaldehyde resin, silicone resin, polyarylate, acrylate, phenol resin, polyether ether ketone, polysulfone, polyphenylene sulfide, polyimide, styrene-butadiene rubber, isoprene rubber, butyl rubber, ethylene-propylene rubber, fluorine rubber, silicone rubber, thermoplastic polystyrene elastomer, thermoplastic polyolefin elastomer, thermoplastic copolyester elastomer, thermoplastic polyamide elastomer, or thermoplastic polyurethane elastomer.
9. The method of claim 1, wherein: the foaming gas is air, nitrogen, carbon dioxide, helium, argon, petroleum ether, methane, ethane, propane, butane, pentane, hexane, heptane, n-pentane, n-hexane, n-heptane, dichloromethane or trichlorofluoromethane.
10. Electromagnetic shielding composite foam with oriented filler structure prepared by the preparation method of any one of claims 1 to 9.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202111678195.1A CN114213698A (en) | 2021-12-31 | 2021-12-31 | Electromagnetic shielding composite foam with oriented filler structure and preparation method thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202111678195.1A CN114213698A (en) | 2021-12-31 | 2021-12-31 | Electromagnetic shielding composite foam with oriented filler structure and preparation method thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
CN114213698A true CN114213698A (en) | 2022-03-22 |
Family
ID=80707518
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202111678195.1A Pending CN114213698A (en) | 2021-12-31 | 2021-12-31 | Electromagnetic shielding composite foam with oriented filler structure and preparation method thereof |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN114213698A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN115991890A (en) * | 2023-02-15 | 2023-04-21 | 四川大学 | Non-skin polyphenylene sulfide foam and preparation and forming method thereof |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0548289A (en) * | 1991-08-08 | 1993-02-26 | Showa Denko Kk | Shield material for electromagnetic waves |
US20080311378A1 (en) * | 2007-02-06 | 2008-12-18 | Scott Simpson | Conductive polymer foams, method of manufacture, and articles thereof |
CN102112534A (en) * | 2008-08-05 | 2011-06-29 | 环球产权公司 | Conductive polymer foams, method of manufacture, and articles thereof |
CN102686652A (en) * | 2009-12-29 | 2012-09-19 | 罗杰斯公司 | Conductive polymer foams, method of manufacture, and uses thereof |
CN104327373A (en) * | 2014-10-08 | 2015-02-04 | 浙江工业大学 | Preparation method for polymer base nanometer composite material with highly oriented nanoparticles in polymer matrix |
CN110540729A (en) * | 2019-09-19 | 2019-12-06 | 深圳先进技术研究院 | light high-conductivity shielding material and preparation method thereof |
CN111267434A (en) * | 2020-03-06 | 2020-06-12 | 深圳先进技术研究院 | Heat-conducting electromagnetic shielding material with oriented structure and preparation method thereof |
CN111660641A (en) * | 2020-06-24 | 2020-09-15 | 四川大学 | Polymer electromagnetic shielding composite material with multilayer cellular structure and preparation method thereof |
-
2021
- 2021-12-31 CN CN202111678195.1A patent/CN114213698A/en active Pending
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0548289A (en) * | 1991-08-08 | 1993-02-26 | Showa Denko Kk | Shield material for electromagnetic waves |
US20080311378A1 (en) * | 2007-02-06 | 2008-12-18 | Scott Simpson | Conductive polymer foams, method of manufacture, and articles thereof |
CN102112534A (en) * | 2008-08-05 | 2011-06-29 | 环球产权公司 | Conductive polymer foams, method of manufacture, and articles thereof |
CN102686652A (en) * | 2009-12-29 | 2012-09-19 | 罗杰斯公司 | Conductive polymer foams, method of manufacture, and uses thereof |
CN104327373A (en) * | 2014-10-08 | 2015-02-04 | 浙江工业大学 | Preparation method for polymer base nanometer composite material with highly oriented nanoparticles in polymer matrix |
CN110540729A (en) * | 2019-09-19 | 2019-12-06 | 深圳先进技术研究院 | light high-conductivity shielding material and preparation method thereof |
CN111267434A (en) * | 2020-03-06 | 2020-06-12 | 深圳先进技术研究院 | Heat-conducting electromagnetic shielding material with oriented structure and preparation method thereof |
CN111660641A (en) * | 2020-06-24 | 2020-09-15 | 四川大学 | Polymer electromagnetic shielding composite material with multilayer cellular structure and preparation method thereof |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN115991890A (en) * | 2023-02-15 | 2023-04-21 | 四川大学 | Non-skin polyphenylene sulfide foam and preparation and forming method thereof |
CN115991890B (en) * | 2023-02-15 | 2024-02-23 | 四川大学 | Non-skin polyphenylene sulfide foam and preparation and forming method thereof |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN111660641B (en) | Polymer electromagnetic shielding composite material with multilayer cellular structure and preparation method thereof | |
Lee et al. | Low percolation 3D Cu and Ag shell network composites for EMI shielding and thermal conduction | |
CN111138706B (en) | Polymer electromagnetic shielding composite foam with gradient filler structure and preparation method thereof | |
CN114437396A (en) | Electromagnetic shielding composite foam with sandwich structure and preparation method thereof | |
CN112911920B (en) | Preparation method of MXene-carbon aerogel/TPU composite material | |
CN101362389B (en) | Wide band electromagnetic wave-shielded polyethylene compound film containing nickel-plating carbon nanotube and preparation method thereof | |
CN107722595B (en) | Preparation method of fiber-graphene-thermoplastic polyarylether multi-scale composite material | |
CN110157159B (en) | Metallic copper/nano-carbon multi-scale reinforcement modified carbon fiber composite material and preparation method thereof | |
CN102746823A (en) | Material with characteristics of fire retardation, thermal insulation and wave absorption, and preparation method thereof | |
CN101085842A (en) | Method for preparing electromagnetic shielding plastic master batch and composite plastic | |
CN105566857A (en) | Light-weight epoxy resin composite material and preparation method thereof | |
CN114213698A (en) | Electromagnetic shielding composite foam with oriented filler structure and preparation method thereof | |
CN104761897A (en) | Modified PBO fiber/cyanate ester resin wave-transparent composite material and preparation method thereof | |
CN112898608A (en) | Polyaniline-modified carbon fiber composite material, preparation method and application thereof | |
CN114685939B (en) | Wave-absorbing carbon fiber prepreg, preparation method thereof and wave-absorbing carbon fiber reinforced plastic | |
CN112795137B (en) | ZIF-8 nanocrystal modified carbon fiber reinforced poly-hexahydrotriazine composite material and preparation method thereof | |
CN107779851B (en) | Carbon fiber/amorphous alloy composite electromagnetic wave absorption material and preparation method thereof | |
CN111302324B (en) | Magnetic microporous carbon-based wave-absorbing composite material and preparation method thereof | |
CN113400763A (en) | Basalt fiber wave-transparent composite material and preparation method thereof | |
CN110194880A (en) | A kind of Ni-coated graphite alkene reinforced resin based composites and preparation method thereof with electromagnetic shielding performance | |
KR20190024275A (en) | Manufacturing method of conductive carbon papers/epoxy composites using electroless nickel-plating | |
CN114230975A (en) | Light anti-scorching conductive shielding material and preparation method thereof | |
CN111098372B (en) | Preparation method of wood-based graphene conductive composite material | |
Jia et al. | Preparation of microwave absorbing nickel-based activated carbon by electroless plating with palladium-free activation | |
CN111218091A (en) | Preparation method of nickel-plated graphene directionally-reinforced epoxy resin |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
RJ01 | Rejection of invention patent application after publication |
Application publication date: 20220322 |