EP4058405A1 - Electromagnetic interference shielding composition, article and methods thereof - Google Patents
Electromagnetic interference shielding composition, article and methods thereofInfo
- Publication number
- EP4058405A1 EP4058405A1 EP20887102.0A EP20887102A EP4058405A1 EP 4058405 A1 EP4058405 A1 EP 4058405A1 EP 20887102 A EP20887102 A EP 20887102A EP 4058405 A1 EP4058405 A1 EP 4058405A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- composition
- article
- present disclosure
- ferrite
- absorbing material
- 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.)
- Withdrawn
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 142
- 238000000034 method Methods 0.000 title claims abstract description 43
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- 239000002184 metal Substances 0.000 claims abstract description 54
- 239000002086 nanomaterial Substances 0.000 claims abstract description 46
- 229920001971 elastomer Polymers 0.000 claims abstract description 44
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 41
- 239000000806 elastomer Substances 0.000 claims abstract description 40
- 229910021389 graphene Inorganic materials 0.000 claims abstract description 31
- 239000011358 absorbing material Substances 0.000 claims abstract description 22
- 239000011248 coating agent Substances 0.000 claims abstract description 22
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- 239000002079 double walled nanotube Substances 0.000 claims description 14
- 239000004945 silicone rubber Substances 0.000 claims description 14
- 239000002109 single walled nanotube Substances 0.000 claims description 14
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 12
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 8
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 8
- 229910017052 cobalt Inorganic materials 0.000 claims description 8
- 239000010941 cobalt Substances 0.000 claims description 8
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 8
- 229910052802 copper Inorganic materials 0.000 claims description 8
- 239000010949 copper Substances 0.000 claims description 8
- 229910052709 silver Inorganic materials 0.000 claims description 8
- 239000004332 silver Substances 0.000 claims description 8
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims description 7
- 229910052748 manganese Inorganic materials 0.000 claims description 7
- 239000011572 manganese Substances 0.000 claims description 7
- NQNBVCBUOCNRFZ-UHFFFAOYSA-N nickel ferrite Chemical compound [Ni]=O.O=[Fe]O[Fe]=O NQNBVCBUOCNRFZ-UHFFFAOYSA-N 0.000 claims description 7
- 238000000748 compression moulding Methods 0.000 claims description 6
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 6
- 238000005516 engineering process Methods 0.000 abstract description 2
- 229920000642 polymer Polymers 0.000 abstract description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 27
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 18
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 16
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 15
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 12
- 230000008569 process Effects 0.000 description 11
- 239000002904 solvent Substances 0.000 description 11
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 10
- 239000012154 double-distilled water Substances 0.000 description 10
- 239000002105 nanoparticle Substances 0.000 description 10
- 238000002360 preparation method Methods 0.000 description 10
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- 239000008367 deionised water Substances 0.000 description 8
- 229910021641 deionized water Inorganic materials 0.000 description 8
- 229910002804 graphite Inorganic materials 0.000 description 8
- 239000010439 graphite Substances 0.000 description 8
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 8
- 239000011541 reaction mixture Substances 0.000 description 7
- 229910052742 iron Inorganic materials 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- 239000012265 solid product Substances 0.000 description 6
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 5
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 5
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 5
- VCJMYUPGQJHHFU-UHFFFAOYSA-N iron(3+);trinitrate Chemical compound [Fe+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O VCJMYUPGQJHHFU-UHFFFAOYSA-N 0.000 description 5
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- 239000005060 rubber Substances 0.000 description 4
- 238000004729 solvothermal method Methods 0.000 description 4
- 238000001354 calcination Methods 0.000 description 3
- 230000006835 compression Effects 0.000 description 3
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- 239000010935 stainless steel Substances 0.000 description 3
- 239000004944 Liquid Silicone Rubber Substances 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 238000003917 TEM image Methods 0.000 description 2
- 230000005540 biological transmission Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- UFMZWBIQTDUYBN-UHFFFAOYSA-N cobalt(II) nitrate Inorganic materials [Co+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O UFMZWBIQTDUYBN-UHFFFAOYSA-N 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
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- 230000005670 electromagnetic radiation Effects 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- MIVBAHRSNUNMPP-UHFFFAOYSA-N manganese(II) nitrate Inorganic materials [Mn+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O MIVBAHRSNUNMPP-UHFFFAOYSA-N 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- KBJMLQFLOWQJNF-UHFFFAOYSA-N nickel(II) nitrate Inorganic materials [Ni+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O KBJMLQFLOWQJNF-UHFFFAOYSA-N 0.000 description 2
- BFDHFSHZJLFAMC-UHFFFAOYSA-L nickel(ii) hydroxide Chemical class [OH-].[OH-].[Ni+2] BFDHFSHZJLFAMC-UHFFFAOYSA-L 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
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- 150000003839 salts Chemical class 0.000 description 2
- 235000011149 sulphuric acid Nutrition 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 229920001875 Ebonite Polymers 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 239000002041 carbon nanotube Substances 0.000 description 1
- ASKVAEGIVYSGNY-UHFFFAOYSA-L cobalt(ii) hydroxide Chemical class [OH-].[OH-].[Co+2] ASKVAEGIVYSGNY-UHFFFAOYSA-L 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000005672 electromagnetic field Effects 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000696 magnetic material Substances 0.000 description 1
- IPJKJLXEVHOKSE-UHFFFAOYSA-L manganese dihydroxide Chemical class [OH-].[OH-].[Mn+2] IPJKJLXEVHOKSE-UHFFFAOYSA-L 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- 239000002082 metal nanoparticle Substances 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 238000005325 percolation Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000012279 sodium borohydride Substances 0.000 description 1
- 229910000033 sodium borohydride Inorganic materials 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
Classifications
-
- 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
- H05K9/0083—Electromagnetic shielding materials, e.g. EMI, RFI shielding comprising electro-conductive non-fibrous particles embedded in an electrically insulating supporting structure, e.g. powder, flakes, whiskers
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B32/00—Carbon; Compounds thereof
- C01B32/15—Nano-sized carbon materials
- C01B32/158—Carbon nanotubes
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B32/00—Carbon; Compounds thereof
- C01B32/15—Nano-sized carbon materials
- C01B32/182—Graphene
- C01B32/198—Graphene oxide
-
- 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
- C08K3/042—Graphene or derivatives, e.g. graphene oxides
-
- 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
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions 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; Compositions of derivatives of such polymers
- C08L83/04—Polysiloxanes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y30/00—Nanotechnology for materials or surface science, e.g. nanocomposites
-
- 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
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
Definitions
- the present disclosure generally relates to the field of polymer engineering, applied industrial technology and Electromagnetic interference (EMI) shielding materials. Particularly, the present disclosure relates to a low-density EMI shielding composition comprising soft elastomer, conductive nanostructure and metal ferrite doped reduced graphene oxide (RGO) and method of preparing the composition. The present disclosure also relates to articles comprising the composition and methods of obtaining the same.
- EMI Electromagnetic interference
- EMI shields are typically inserted within electronic modules both to confine the EM energy within a source device and prevent it from interfering with other nearby devices.
- the spaces between the adjacent panels and openings inside the electronic modules should be properly sealed so as to prevent the leakage of electromagnetic energy.
- the prior arts provide for high density EMI shielding compositions with lower efficiency in terms of total shielding effectiveness.
- the density of conventional EMI shielding gaskets is found to be more than 2.5 which adds to the weight of electronic gadgets.
- the composition and methods of the prior art require higher concentration of nanomaterials, have higher costs, and lower shielding effectiveness. Therefore, there is a strong urge to develop low density gasket compositions which will also help to reduce the final weight of the electronic devices and achieve high shielding effectiveness.
- the present disclosure aims at overcoming the limitations of the prior art.
- the present disclosure relates to a composition comprising soft elastomer, conductive nanostructure and metal ferrite doped reduced graphene oxide (RGO); a method of preparing the said composition, comprising acts of: contacting the conductive nanostructure with the soft elastomer, and optionally mixing, to obtain a mixture; and adding the metal ferrite doped reduced graphene oxide (RGO) to the mixture, and optionally mixing, to obtain the composition; an article comprising the said composition; a method of obtaining an article comprising the said composition, comprising the act of compression moulding the said composition to obtain the article; and a method of obtaining an article comprising the said composition, comprising the act of combining and optionally mixing the said composition with an industrially acceptable excipient to obtain the article.
- RGO metal ferrite doped reduced graphene oxide
- FIGURES 1A & IB illustrate the transmission electron microscopic (TEM) images of the NiFdCft nanoparticle at 10 nm and 50 nm magnification respectively.
- FIGURE 2 illustrates the synthesis strategy of NiFdGi doped RGO.
- FIGURE 3 A & B illustrates the transmission electron microscopic (TEM) images ofNiFe 2 04 doped RGO at 50nm and 20 nm magnification respectively.
- FIGURE 4 illustrates the EMI shielding performance of silicone rubber gasket in X band region (8.2- 12.4 GHz).
- the present disclosure pertains to a composition
- a composition comprising soft elastomer, conductive nanostructure and metal ferrite doped reduced graphene oxide (RGO).
- the soft elastomer is silicone rubber or its analogue.
- soft elastomer refers to silicone rubber or its analogue which has a shore A hardness 30.
- Shore A hardness is the measure of softness.
- the conductive nanostructure is selected from a group comprising single walled carbon nanotubes (SWCNTs), double walled carbon nanotubes (DWCNTs), multiwalled carbon nanotubes (MWCNTs) or any combinations thereof.
- SWCNTs single walled carbon nanotubes
- DWCNTs double walled carbon nanotubes
- MWCNTs multiwalled carbon nanotubes
- the metal ferrite is selected from a group comprising nickel ferrite, copper ferrite, silver ferrite, cobalt ferrite, and manganese ferrite or any combination thereof.
- the conductive nanostructures is at a concentration ranging from about 1 to 2.88 weight percent.
- the metal ferrite doped reduced graphene oxide is at a concentration ranging from about 0.1 to 0.96 weight percent.
- the soft elastomer is at a concentration ranging from about 96.16 to 98.9 weight percent.
- the composition is used for manufacturing an article selected from a group comprising coating, adhesive, sheet, absorber, gasket, Microwave Absorbing Material, Radar Absorbing Material and soft electromagnetic interference shielding material or any combination thereof.
- the present disclosure also pertains to the use of the said composition for manufacturing an article selected from a group comprising coating, adhesive, sheet, absorber, gasket, Microwave Absorbing Material, Radar Absorbing Material and soft electromagnetic interference shielding material or any combination thereof.
- the present disclosure also pertains to a method of preparing the said composition, comprising acts of: contacting conductive nanostructure with soft elastomer, and optionally mixing, to obtain a mixture; and adding metal ferrite doped reduced graphene oxide (RGO) to the mixture, and optionally mixing, to obtain the composition.
- a method of preparing the said composition comprising acts of: contacting conductive nanostructure with soft elastomer, and optionally mixing, to obtain a mixture; and adding metal ferrite doped reduced graphene oxide (RGO) to the mixture, and optionally mixing, to obtain the composition.
- RGO metal ferrite doped reduced graphene oxide
- the mixing is carried out at a temperature ranging from about 95°C to about 120°C, preferably about 100°C for a time period ranging from about 15 to about 30 minutes, preferably about 25 minutes at about 60 rpm to about 100 rpm, preferably about 80 rpm.
- the present disclosure also pertains to an article comprising the said composition.
- the article is selected from a group comprising coating, adhesive, sheet, absorber, gasket, Microwave Absorbing Material, Radar Absorbing Material and soft electromagnetic interference shielding material or any combination thereof.
- density of the afore -described composition or article is less than 2.5, preferably ranging from about 1.14 to 1.25.
- the article has total shielding effectiveness of at least -20 dB at frequency range of about 8.2 to about 12.4 GHz.
- the article has total shielding effectiveness of about -74 dB at frequency range of about 8.2 to about 12.4 GHz.
- the present disclosure also pertains to a method of obtaining an article comprising the said composition, wherein the method comprises the act of compression moulding the said composition to obtain the article.
- the article is selected from a group comprising sheet, absorber, gasket, Microwave Absorbing Material, Radar Absorbing Material and a soft electromagnetic interference shielding gasket material.
- the compression moulding is carried out at a temperature ranging from about 130°C to about 160°C, preferably about 150°C.
- the present disclosure also pertains to a method of obtaining an article comprising the said composition, wherein the method comprises the act of combining, and optionally mixing, the said composition with an industrially acceptable excipient to obtain the article.
- the article is a coating or an adhesive.
- the term “about” means to be nearly the same as a referenced number or value. As used herein, the term “about” should be generally understood to encompass ⁇ 10% of a specified amount or value.
- hybrid nanomaterial or “hybrid combination” are used interchangeably and refer to combination of the conductive nanostructure and metal ferrite doped reduced graphene oxide employed in the present disclosure.
- the conductive nanostructure includes but are not limited to single walled carbon nanotubes (SWCNTs), double walled carbon nanotubes (DWCNTs), multiwalled carbon nanotubes (MWCNTs) or any combinations thereof.
- the metal ferrite doped reduced graphene oxide include reduced graphene oxide doped with dopents such as but not limited to metal ferrites selected from a group comprising nickel ferrite, copper ferrite, silver ferrite, cobalt ferrite, manganese ferrite, etc. or any combination thereof.
- the ferrite particles are less than 50 nm.
- the ferrite particles are ranging from about 5-50 nm.
- total shielding effectiveness refers to the shielding value in decibel (dB) offered by a shield material at a particular frequency and thickness to measure attenuation.
- specific EMI shielding effectiveness means shielding effectiveness value in (db) divided by density of the composition.
- density indicated herein is Relative Density.
- the present disclosure overcomes the non-limited drawbacks of the prior art and provides for cost-effective, efficient composition, articles and methods thereof.
- the present disclosure provides for low density, cost-effective, efficient composition, articles and methods thereof for efficient absorption and attenuation of electromagnetic (EM) waves in X band frequency region (8.2-12.4 GHz) and/or providing technical enhancement in the shielding effectiveness value.
- EM electromagnetic
- the present disclosure relates to a composition comprising a soft elastomer and a process for obtaining the said composition.
- the present disclosure also relates to an article made from the composition comprising soft elastomer, methodology of obtaining the said article and applications thereof.
- the article drawn from the composition comprising the soft elastomer is selected from group comprising but not limiting to coating, adhesive, sheet, absorber, gasket, Microwave Absorbing Material, Radar Absorbing Material and soft electromagnetic interference shielding material or any combination thereof.
- the composition and the article drawn from the said composition has total shielding effectiveness of at least -20 dB at frequency range of about 8.2 to about 12.4 GHz.
- -20 dB is the minimum shielding requirement for application in electronics devices.
- the composition and the article drawn from the said composition has total shielding effectiveness ranging from about -63 dB to about -74 dB at frequency range of about 8.2 to about 12.4 GHz.
- the composition and the article drawn from the said composition has a maximum total shielding effectiveness of about -74 dB at frequency range of about 8.2 to about 12.4 GHz.
- the composition and the article drawn from the said composition is capable of absorbing microwave radiations, electromagnetic radiations, radio waves in frequency ranging from about 8.2 GHz to about 12.4 GHz.
- the composition and the article drawn from the said composition is capable of absorbing microwave (MW) radiation of at least about -20 decibels in frequency range of about 8.2 GHz to about 12.4 GHz.
- MW microwave
- the composition and the article drawn from the said composition is capable of absorbing electromagnetic radiation of at least about -20 decibels in frequency range of about 8.2 GHz to about 12.4 GHz.
- the composition and the article drawn from the said composition is capable of absorbing radio waves of at least about -20 decibels in frequency range of about 8.2 GHz to about 12.4 GHz.
- composition and the article of the present disclosure is a flexible Electromagnetic interference (EMI) shielding composition.
- EMI Electromagnetic interference
- Electromagnetic shielding refers to reducing the electromagnetic field in a space by blocking the field with barriers made of conductive or magnetic materials.
- the composition and the article of the present disclosure has a specific EMI shielding effectiveness value ranging from 63/1.1148 which is 55 db.g Vcm 3 to -74/1.148 which is -64 (db.g Vcm 3 ).
- the composition of the present disclosure comprises a soft elastomer, conductive nanostructure and metal ferrite doped reduced graphene oxide (RGO).
- the conductive nanostructure provides electric dipoles and the metal ferrite present in the doped RGO provides magnetic dipoles for the electromagnetic waves to interact with.
- Magnetic nanomaterial such as metal ferrites tend to agglomerate if added alone.
- doping the metal ferrites on RGO aids its uniform dispersion in the rubber matrix (soft elastomer).
- the soft elastomer employed in the present disclosure has a Shore A hardness of 35-45.
- the soft elastomer is silicone rubber/ polydimetyl siloxane (PDMS) or its analogue.
- the conductive nanostructure is selected from a group comprising single walled carbon nanotubes (SWCNTs), double walled carbon nanotubes (DWCNTs), multiwalled carbon nanotubes (MWCNTs) or any combinations thereof.
- SWCNTs single walled carbon nanotubes
- DWCNTs double walled carbon nanotubes
- MWCNTs multiwalled carbon nanotubes
- the conductive nanostructure is single walled carbon nanotubes (SWCNTs).
- the conductive nanostructure is double walled carbon nanotubes (DWCNTs).
- the conductive nanostructure is multiwalled carbon nanotubes (MWCNTs).
- MWCNTs multiwalled carbon nanotubes
- the reduced graphene oxide is doped with metal ferrites wherein the metal is selected from a group comprising nickel, copper, silver, cobalt, manganese, or any combination thereof.
- the reduced graphene oxide is doped with metal ferrite selected from a combination of copper ferrite, silver ferrite, nickel ferrite, cobalt ferrite, manganese ferrite, etc. and combinations thereof.
- the metal ferrite/magnetically doped RGO is NiFdCri doped RGO.
- the present disclosure relates to low density soft elastomer composition
- low density soft elastomer composition comprising of hybrid nanostructures with multi walled carbon nanotubes and nickel ferrite doped graphene for efficient absorption and attenuation of electromagnetic waves in X band frequency region (8.2-12.4 GHz).
- the soft elastomer is at a concentration ranging from about 96.16 to 98.9 weight percent of the total weight of the composition.
- the conductive nanostructure (such as MWCNT) is at a concentration ranging from about 1 to 2.88 weight percent of the total weight of the composition.
- the metal ferrite doped RGO is at a concentration ranging from about 0.1 to 0.96 weight percent of the total weight of the composition.
- the hybrid combination is at a concentration ranging from about 1.1 to 3.84 weight percent of the total weight of the composition. In embodiments of the present disclosure, the hybrid combination is at a concentration ranging from about 3.5 Parts per Hundred Rubber (Phr)- to 5 Phr.
- the soft elastomer’s concentration is always 100 phr or 100 parts to which the hybrid combination is added.
- the conductive nanostructure is at a concentration ranging from about 3 Phr to 4 Phr.
- the metal ferrite doped RGO is at a concentration ranging from about 0.5 Phr to 1 Phr.
- a percolating network of the conductive nanostructure aids in proper distribution of the metal ferrite doped RGO.
- the present disclosure provides for a uniform distribution of the metal ferrite doped RGO and conductive nanostructure with the soft elastomer. This allows employing lower loading of the metal ferrite on the elastomer, which retains the flexibility of the elastomer and results in a product having much lower density compared to products known in the art.
- the density of the composition and/or the article drawn from the composition is very low. This reduces the overall weight of the final product, such as electronic product, into which it is inserted to serve as EMI shield.
- the density of the composition and/or the article drawn from the composition of the present disclosure is less than 2.5.
- the composition and/or the article of the present disclosure thus has high specific EMI shielding value i.e. shielding per unit density (db.g-d/cnG).
- the density of the composition and/or the article drawn from the composition is less than 1.25. In embodiments of the present disclosure, the density of the composition and/or the article drawn from the composition ranges from about 1.14 to 1.25, preferably 1.148.
- Graphite oxide is synthesized by oxidation of graphite according to Hummer’s method, wherein H2SO4 is cooled and added to a mixture of graphite flakes and NaNCb. The mixture is then kept at 0 °C followed by addition of KMnOu The reaction mixture is then heated and stirred followed by slow addition of water to increase the temperature. The reaction mixture is then cooled followed by the addition of water and H2O2 in order to terminate the reaction. The resulting solution is then allowed to settle down and washed with double distilled water until the pH becomes neutral. The solution is filtered. The filtrate is collected and vacuum -dried to obtain graphite oxide (GO).
- Hummer Hummer’s method
- the metal ferrite employed in the present disclosure may be prepared in accordance to any standard protocol known in the art.
- the process for preparing the metal ferrite comprises: contacting salts (such as nitrates) of metal selected from a group comprising nickel, copper, silver, cobalt, and manganese or any combinations thereof with salts of iron (preferably iron (III) nitrate) and dissolving in a suitable solvent such as water, the pH of the above reaction mixture is maintained to about 10-11 to aid precipitation of the iron and the metal hydroxides, the solution along with the precipitate thus obtained is heated and subsequently cooled, the resulting solid product is collected, washed, dried and optionally calcined to obtain the metal ferrite.
- salts such as nitrates
- iron preferably iron (III) nitrate
- spinal NiFciOr is prepared by mixing Fe(NC>3)2 ⁇ 9FhO and Ni(NC>3)2 ⁇ 6H2O and dissolved in water preferably deionized water.
- the pH is maintained at 10-11 by addition of KOH solution, to aid precipitation of iron and nickel hydroxides.
- the solution along with the precipitate is transferred into an autoclave.
- the autoclave is sealed and kept in an oven and subsequently cooled.
- the resulting solid product is collected and washed. The washed particles are then dried and calcined to obtain the spinal NiFerCh.
- the solid product is washed with deionized water and ethanol.
- the metal ferrite doped RGO is obtained by Solvothermal Synthesis for decorating the metal ferrite on graphene.
- metal ferrite doped RGO is in situ- synthesized by coprecipitation of the metal ferrite in the presence of GO using hydrothermal reaction, wherein the metal ferrite is added to GO and dispersed in water.
- the mixture obtained is optionally sonicated and combined with NaBHr, transferred into a hydrothermal reactor half filled with water and heated. The mixture is then left to cool down to room temperature.
- the obtained metal ferrite doped RGO powder is filtered, rinsed with double distillated water several times, and optionally dried.
- the metal ferrite is selected from a group comprising nickel ferrite, copper ferrite, silver ferrite, cobalt ferrite, manganese ferrite, or any combination thereof.
- the composition of the present disclosure is prepared by contacting the conductive nanostructure with soft elastomer, and then adding metal ferrite doped reduced graphene oxide (RGO) to obtain the composition.
- RGO metal ferrite doped reduced graphene oxide
- the method of preparing the EMI shielding composition comprises acts of:
- RGO metal ferrite doped reduced graphene oxide
- the method of preparing the EMI shielding composition comprises acts of:
- RGO metal ferrite doped reduced graphene oxide
- the blending/mixing is carried out at temperature ranging from about
- the mixer is selected from a group comprising Haake mixer or barbender.
- the soft elastomer is silicone rubber or its analogue
- the conductive nanostructure is selected from a group comprising single walled carbon nanotubes (SWCNTs), double walled carbon nanotubes (DWCNTs), multiwalled carbon nanotubes (MWCNTs) or any combinations thereof
- the reduced graphene oxide is doped with metal ferrite selected from a group comprising nickel ferrite, copper ferrite, silver ferrite, cobalt ferrite, and manganese ferrite or any combination thereof.
- the conductive nanostructures is at a concentration ranging from about 1 to 2.88 weight percent; the metal ferrite doped reduced graphene oxide is at a concentration ranging from about 0.1 to 0.96 weight percent; and the soft elastomer is at a concentration ranging from about 96.16 to 98.9 weight percent.
- a percolating network of carbon nanotubes is obtained at about at least 3 phr of conductive nanostructure and followed by addition of magnetically doped RGO.
- the metal ferrite nanoparticles are stacked uniformly in between the graphene sheets in the metal ferrite doped RGO.
- the metal nanoparticles are not coated on graphene but stacked in between the sheets of graphene via weak Vander walls forces of interaction.
- the article of the present disclosure is prepared by compression moulding the well dispersed soft elastomer composition at about 130°C to 160°C to make EMI shielding articles with desired thickness.
- the thickness of the article may be varied as desired to provide at least -20 db shielding effectiveness, and hence a wide range of thickness may be employed.
- the thickness of the article is ranging from about 0.1 mm to 10 mm.
- the article is compression molded to different forms.
- the gasket is compression molded to different forms.
- the composition is manufactured into an article selected from a group comprising coating, adhesive, sheet, absorber, gasket, Microwave Absorbing Material, Radar Absorbing Material and soft electromagnetic interference shielding material or any combination thereof
- the total shielding effectiveness of an article of the composition is -74 dB at 12 Ghz.
- the method of obtaining the article such coating, adhesive etc. comprises the act of combining and optionally mixing the afore-described composition of the present disclosure with an industrially acceptable excipient to obtain the said article.
- the excipient used in the process of obtaining the article may be any industrially acceptable excipient such as but not limited to resin, solvent or any combination thereof.
- the resin is liquid silicone resin.
- the solvent is selected from a group comprising chloroform, THF, xylene, toluene, pentane, n-heptane, diisoproplyamine or any combination thereof.
- heating during the process is carried out in a hot water bath.
- cooling during the process is carried out in an ice bath.
- room temperature is about 28°C.
- the coating is prepared by combining the soft elastomer, the conductive nanostructure (such as SWCNT, DWCNT, and/or MWCNT) and the metal ferrite doped RGO in a suitable solvent.
- the solvent is selected from a group comprising chloroform, tetrahydrofuran (THF), xylene, toluene, pentane, n-heptane, and diisoproplyamine or any combination thereof.
- the silicone rubber based coating is prepared by dispersing the hybrid nanostructures in a solvent, and mixed with liquid silicone rubber to form the coating.
- the coating on drying at the desired thickness has total shielding effectiveness of at least -20 dB at frequency range of about 8.2 to about 12.4 GHz.
- the solvent for use in preparation of the coating is selected from a group comprising chloroform, tetrahydrofuran (THF), xylene, toluene, pentane, n-heptane and diisoproplyamine or any combination thereof.
- the adhesive is prepared by combining the soft elastomer, the conductive nanostructure (such as SWCNT, DWCNT, and/or MWCNT) and the metal ferrite doped RGO in a suitable solvent.
- the solvent is selected from a group comprising chloroform, tetrahydrofuran (THF), xylene, toluene, pentane, n-heptane, and diisoproplyamine or any combination thereof.
- composition of the present disclosure comprising the soft elastomer, the conductive nanostructure, and the metal ferrite doped reduced graphene oxide is synergistic in nature.
- replacement of the soft elastomer with hard rubber such as natural rubber or styrene -butadiene rubber (SBR) does not result in the desired shielding effectiveness due to increased hardness of the rubber matrix.
- SBR styrene -butadiene rubber
- excluding conductive nanostructures from the composition of the present disclosure i.e. resulting in a composition having only the soft elastomer and metal ferrite doped RGO does not result in the desired properties in the composition/ article.
- the conductive nanostructures are added first to form a percolating network followed by addition of the metal ferrite doped RGO.
- excluding metal ferrite doped RGO from the composition of the present disclosure i.e. resulting in a composition having only the soft elastomer and conductive nanostructure does not result in the desired properties in the composition article as the shielding value is found to be much lesser than -74 db.
- advantages of the present disclosure include but are not limiting to:
- composition and articles of the present disclosure provide for efficient absorption and attenuation of electromagnetic waves in X band frequency region (8.2-12.4 GHz)
- composition is advantageous as articles such as coating, adhesive, sheet, absorber, gasket, Microwave Absorbing Material, Radar Absorbing Material and soft electromagnetic interference shielding material or any combination thereof.
- composition and articles of the present disclosure provide for high shielding materials with lower hybrid combination loadings. Lower loading of the hybrid combination of the nanomaterials, results in reduction of costs. •
- the present disclosure provides for composition and articles having low density of about 1.14 to 1.25, preferably about 1.148.
- Graphite oxide was synthesized by oxidation of graphite according to Hummer’s method with slight modifications. 69 ml of H2SO4 was cooled to 0 °C in an ice bath and after 45 min of cooling, it was added to a mixture of graphite flakes (3.0 g) and NaNCb (1.5 g). The mixture was again kept in the ice bath at 0 °C followed by the slow addition of KMnCft (9.0 g). The slow addition process takes place for about 2-3 h. The reaction mixture was then heated to 35 °C in a hot water bath and stirred for 30 min followed by slow addition of double distilled water (138 ml) to increase the temperature to 95°C.
- the heating of the reaction mixture at 95 °C was continued for 15 min, after which the heat was removed.
- the reaction mixture was then cooled using an ice bath for 10 min followed by the addition of 420 ml double distilled water and 30 ml H2O2 in order to terminate the reaction.
- the resulting solution was allowed to settle down for 24 h and washed with double distilled water several times until the pH became neutral through settling and decantation process.
- the reaction mixture is allowed to slowly settle down the bottom of the flask post which it can be easily decanted.
- the solution was filtered with Whatman ® Grade 41 filter paper. The filtrate was collected and vacuum -dried at 60°C for 24 h to obtain GO.
- Spinal NiFe204 was prepared by using about 3.5 g of Fe(N03)2 ⁇ 93 ⁇ 40 and about 1.4 g of Ni(N03)2 ⁇ 6H2O which were mixed together in 2:1 molar ratio and dissolved in 20 ml deionized water. The pH was maintained at 10-11 with KOH solution, where iron and nickel hydroxides were precipitated. The solution along with the precipitate was transferred into a 100-ml Teflon-lined stainless steel autoclave. The autoclave was sealed and kept in an oven at 180°C for 6h and then cooled to room temperature. The resulting solid product was collected and washed with deionized water and ethanol.
- CoFdC nanoparticles were prepared by using about 3.5g of Fe(NC>3)2 ⁇ 9FhO and about 1.4 g of CO(NC>3)2 ⁇ 6FhO which were mixed together in 2:1 molar ratio and dissolved in 20 ml deionized water.
- the pH was maintained at 10-11 with KOH solution, where iron and cobalt hydroxides were precipitated.
- the solution along with the precipitate was transferred into a 100-ml Teflon-lined stainless steel autoclave. The autoclave was sealed and kept in an oven at 180°C for 6h and then cooled to room temperature. The resulting solid product was collected and washed with deionized water and ethanol. The washed particles were then dried at 70°C for 6 h followed by calcination at 600°C for 3h in air. iii) Preparation of MnFe 2Q4 nanoparticles
- MnFe204 nanoparticles were prepared by using about 3.5 g of Fe(NC>3)2 ⁇ 9H2O and about 1.4 g of Mh(Nq3)2 ⁇ 6H2O which were mixed together in 2:1 molar ratio and dissolved in 20 ml deionized water.
- the pH was maintained at 10-11 with KOH solution, where iron and manganese hydroxides were precipitated.
- the solution along with the precipitate was transferred into a 100-ml Teflon-lined stainless steel autoclave. The autoclave was sealed and kept in an oven at 180°C for 6h and then cooled to room temperature. The resulting solid product was collected and washed with deionized water and ethanol. The washed particles were then dried at 70°C for 6 h followed by calcination at 600°C for 3h in air.
- NiFe2C>4 doped RGO was in situ-synthesized by coprecipitation of Ni(N03)2 ⁇ 6H2O, and Fe(N03)3 93 ⁇ 40 in the presence of GO using hydrothermal reaction.
- 3.5 g of [Fe3 (NO)3 9HO2], 1.4 g ofNi(N0 3 )26H2O were added to 200 mg of GO dispersed in 400 ml of double distilled water.
- the mixture was sonicated with a frequency of 20 KHz and power of 1500 Watt for lh. An ice bath was used in order to avoid increase in temperature during the sonication process.
- NiFdCU doped RGO powder (with black color) was filtered with Whatman ® Grade 41 filter paper, rinsed with double distillated water several times, and dried in an oven at 80 °C for 24 h.
- the synthesis protocol of NiFdCri doped RGO is shown in figure 2.
- NiFe204 nanoparticles are stacked uniformly in between the graphene sheets.
- the NiFe204 nanoparticles are not coated on graphene but stacked in between the sheets of graphene via weak Vander walls forces of interaction.
- CoFe204 doped RGO was in situ-synthesized by coprecipitation of Co(N03)2 ⁇ 6H2O and Fe(N03)3 ⁇ 9H2O in the presence of GO using hydrothermal reaction.
- 3.5 g of [Fe 3 (N0) 3 ⁇ 9HO2], 1.4 g of Co(N0 3 )2 ⁇ 6H2O were added to 200 mg of GO dispersed in 400 ml of double distilled water.
- the mixture was sonicated with a frequency of 20 KHz and power of 1500 Watt for lh.
- An ice bath was used in order to avoid increase in temperature during the sonication process.
- MnFdC doped RGO was in situ-synthesized by coprecipitation of Mn(N03)2 ⁇ 6H2O and Fe(N03)3 ⁇ 9FhO in the presence of GO using hydrothermal reaction.
- 3.5 g of [Fe 3 (N0) 3 9HO2], 1.4 g of Mn(N0 3 )2 ⁇ 6FhO were added to 200 mg of GO dispersed in 400 ml of double distilled water.
- the mixture was sonicated with a frequency of 20 KHz and power of 1500 Watt for lh.
- An ice bath was used in order to avoid increase in temperature during the sonication process.
- the silicone rubber based EMI shielding composition was prepared by blending 100 PHR -silicone rubber (PDMS) with 3 PHR multi walled carbon nanotubes in a Haake mixer, followed by adding 1 PHR NiFe204 doped RGO to the mixture and mixing at 100°C for 25 min at 80 rpm.
- PDMS PHR -silicone rubber
- the well dispersed silicone rubber composition obtained was then compression moulded at 150°C to make EMI shielding gaskets with 5mm thickness.
- the moulded gasket samples were measured for EMI shielding effectiveness by using a vector network analyzer coupled with a wave guide operating in X band (8.2 to 21.4 Ghz)
- the silicone rubber based coating is prepared by dispersing the hybrid nanostructures (comprising the multi walled carbon nanotubes and NiFdGi doped RGO or CoFdCU doped RGO or MnFdCU doped RGO) in the solvent chloroform, adding liquid silicone rubber (PDMS) and mixing to form the coating. The process is repeated for each of the metal ferrite doped RGO by replacing the chloroform with alternate solvents viz. THF, xylene, toluene, pentane, n-heptane or diisoproplyamine. Each coating thus obtained has total shielding effectiveness of at least -20 dB at frequency range of about 8.2 to about 12.4 GHz. The coating was found to have the same EMI shielding performance as the gasket.
- composition a method for preparing the composition comprising a soft elastomer, conductive nanostructures, and magnetically doped reduced graphene oxide (RGO), that exhibit efficient absorption and attenuation of electromagnetic waves in X band frequency region (8.2-12.4 GHz).
- RGO reduced graphene oxide
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