Gel-type thermal interface material

Information

  • Patent Grant
  • 10501671
  • Patent Number
    10,501,671
  • Date Filed
    Wednesday, July 5, 2017
    6 years ago
  • Date Issued
    Tuesday, December 10, 2019
    4 years ago
Abstract
A thermal interface material that is useful in transferring heat from heat generating electronic devices, such as computer chips, to heat dissipating structures, such as heat spreaders and heat sinks. The thermal interface material includes at least one silicone oil, and at least one thermally conductive filler.
Description
FIELD OF THE INVENTION

The present disclosure relates generally to thermal interface materials, and more particularly to gel-type thermal interface materials.


DESCRIPTION OF THE RELATED ART

Thermal interface materials (TIMs) are widely used to dissipate heat from electronic components, such as central processing units, video graphics arrays, servers, game consoles, smart phones, LED boards, and the like. Thermal interface materials are typically used to transfer excess heat from the electronic component to a heat spreader, such as a heat sink.


A typical electronics package structure 10 including thermal interface materials is illustrated in FIG. 1. The electronics package structure 10 illustratively includes a heat generating component, such as an electronic chip 12, and one or more heat dissipating components, such as a heat spreader 14, and a heat sink 16. Illustrative heat spreaders 14 and heat sinks comprise a metal, metal alloy, or metal-plated substrate, such as copper, copper alloy, aluminum, aluminum alloy, or nickel-plated copper. TIM materials, such as TIM 18 and TIM 20, provide a thermal connection between the heat generating component and the one or more heat dissipating components. Electronics package structure 10 includes a first TIM 18 connecting the electronic chip 12 and heat spreader 14. TIM 18 is typically referred to as a “TIM 1”. Electronics package structure 10 includes a second TIM 20 connecting the heat spreader 14 and heat sink 16, TIM 20 is typically referred to as a “TIM 2”. In another embodiment, electronics package structure 10 does not include a heat spreader 14, and a TIM (not shown) connects the electronic chip 12 directly to the heat sink 16. Such a TIM connecting the electronic chip 12 directly to the heat sink 16 is typically referred to as a TIM 1.5.


Traditional thermal interface materials include components such as gap pads. However, gap pads have certain disadvantages, such as inability to meet very small thickness requirements and being difficult to use in automated production.


Other thermal interface materials include gel products. Gel products may be automatically dispensed for large scale production, and can be formed to desired shapes and thicknesses. However, typical gel products have issues with dripping and cracking in temperature cycling tests, including that the product may potentially be more likely to fail in extreme cases.


Improvements in the foregoing are desired.


SUMMARY OF THE INVENTION

The present disclosure provides thermal interlace materials that are useful in transferring heat from heat generating electronic devices, such as computer chips, to heat dissipating structures, such as heat spreaders and heat sinks. The thermal interface material includes at least one silicone oil, at least one thermally conductive filler, and at least one addition inhibitor.


In one exemplary embodiment, a thermal interface material is provided. The thermal interface material includes at least one low molecular weight silicone oil having a weight (Mw) average molecular weight less than 50,000 Daltons; at least one thermally conductive filler; at least one addition catalyst; and at least one high molecular weight silicone oil, wherein the high molecular weight silicone oil comprises a vinyl functional silicone oil having a weight (Mw) average molecular weight of at least 60,000 Daltons. In a more particular embodiment, the at least one low molecular weight silicone oil comprises a first silicone oil and a second silicone oil, wherein the first silicone oil is a vinyl functional silicone oil and the second silicone oil is a hydride functional silicone oil.


In a more particular embodiment, the thermally conductive filler includes a first thermally conductive filler and a second thermally conductive filler, wherein the first thermally conductive filer is a metal oxide having a particle size greater than 1 micron and the second thermally conductive filler is a metal oxide have a particle size less than 1 micron. In another more particular embodiment, the thermally conductive filler includes a first thermally conductive filler, a second thermally conductive filler, and a third thermally conductive filler, wherein the first thermally conductive filler is a metal oxide having an average particle size greater than 10 microns, the second thermally conductive flier is a metal oxide having an average particle size between 1 micron and 10 microns, and the third thermally conductive filler is a metal oxide having an average particle size less than 1 micron.


In still another more particular embodiment, the thermal interface material comprises: from 2 wt % to 20 wt. % of the low molecular weight silicone oil; from 50 wt % to 95 wt % of the thermally conductive filler; and from 0.1 wt % to 5 wt % of the high molecular weight silicone oil. In still another more particular embodiment, the low molecular weight silicone oil comprises a first silicone oil and a second silicone oil, wherein the first silicone oil is a vinyl functional silicone oil and the second silicone oil is a hydride functional silicone oil.


In a more particular embodiment of any of the above embodiments, a thermal interface material is provided. The thermal interface material comprises: at least one silicone oil; at least one thermally conductive tiller; and at least one addition inhibitor, wherein the addition inhibitor comprises an alkynyl compound. In a still more particular embodiment, the addition inhibitor is selected from the group consisting of: a multivinyl functional polysiloxane, polydimethylsiloxane vinyl terminated in ethynyl cyclohexanol, 2-methyl-3-butyn-2-ol, and 3-methyl-1-pentyn-3-ol. In a more particular embodiment of any of the above embodiments, the at least one silicone oil comprises a first silicone oil and a second silicone oil, wherein the first silicone oil is a vinyl functional silicone oil and the second silicone oil is a hydride functional silicone oil.


In a more particular embodiment of any of the above embodiments, the thermally conductive filler includes a first thermally conductive filler and a second thermally conductive filler, wherein the first thermally conductive filer is a metal having a particle size greater than 1 micron and the second thermally conductive filler is a metal oxide having a particle size less than 1 micron. In a more particular embodiment of any of the above embodiments, a ratio of the first thermally conductive filler to the second thermally conductive filler is from 1.5:1 to 3:1.


In a more particular embodiment of any of the above embodiments, the thermal interface material comprises: from 2 wt. % to 20 wt. % of the silicone oil; from 0.1 wt. % to 5 wt. % of a silane coupling agent; from 50 wt. % to 95 wt. % of the thermally conductive filler; and from 0.01 wt. % to 5 wt. % of the addition inhibitor. In a more particular embodiment, the addition inhibitor is polydimethylsiloxane vinyl terminated in ethynyl cyclohexanol. In a more particular embodiment, the silicone oil comprises a first silicone oil and a second silicone oil, wherein the first silicone oil is a vinyl functional silicone oil and the second silicone oil is a hydride functional silicone oil.


In one exemplary embodiment, an electronic component is provided. The electronic component includes a heat sink; an electronic chip; a thermal interface material having a first surface layer and a second surface layer, the thermal interface material positioned between the heat sink and electronic chip, the thermal interface material including: at least one silicone oil; at least one thermally conductive filler; and at least one addition inhibitor, wherein the addition inhibitor comprises an alkynyl compound. In a more particular embodiment, the at least one silicone comprises at least one low molecular weight silicone oil and at least one high molecular weight silicone oil.


In a more particular embodiment, the at least one high molecular weight silicone oil comprises a vinyl functional silicone oil having a weight (Mw) average molecular weight of at least 60,000 Daltons. In another more particular embodiment, the first surface layer is in contact with a surface of the electronic chip and the second surface layer is in contact with the heat sink. In another more particular embodiment, the electronic component further comprises a heat spreader positioned between the heat sink and the electronic chip, wherein the first surface layer is in contact with a surface of the electronic chip and the second surface layer is in contact with the heat spreader. In a further more particular embodiment, the electronic component further comprises a heat spreader positioned between the heat sink and the electronic chip, wherein the first surface layer is in contact with a surface of the heat spreader and the second surface layer is in contact with the heat sink.





BRIEF DESCRIPTION OF THE DRAWINGS

The above-mentioned and other features and advantages of this disclosure, and the manner of attaining them, will become more apparent and the invention itself will be better understood by reference to the following description of embodiments of the invention taken in conjunction with the accompanying drawings, wherein:



FIG. 1 schematically illustrates a typical electronics package structure;



FIG. 2A is related to Example 1 and shows the sample formed from Example 1 before the thermal cycling test;



FIG. 2B is related to Example 1 and shows the sample formed from the comparative example before the thermal cycling test;



FIG. 3A is related to Example 1 and shows the sample formed from Example 1 after the thermal cycling test;



FIG. 3B is related to Example 1 and shows the sample formed from Example 1 after the thermal cycling test;



FIG. 4A is related to Example 2 and shows the sample formed from Comparative Example 2 before the thermal cycling test;



FIG. 4B is related to Example 2 and shows the sample formed from Example 2A before the thermal cycling test;



FIG. 4C is related to Example 2 and shows the sample formed from Example 2B before the thermal cycling test;



FIG. 5A is related to Example 2 and shows the sample formed from Comparative Example 2 after the thermal cycling test;



FIG. 5B is related to Example 2 and shows the sample formed from Example 2A after the thermal cycling test;



FIG. 5C is related to Example 2 and shows the sample formed from Example 2B after the thermal cycling test;



FIG. 6A shows a dispenser apparatus according to an embodiment of the present disclosure;



FIG. 6B shows the dispenser apparatus of FIG. 6A in operation; and



FIG. 7 is a schematic diagram showing the interaction of exemplary coupling agents with exemplary fillers.





Corresponding reference characters indicate corresponding parts throughout the several views. The exemplifications set out herein illustrate exemplary embodiments of the invention and such exemplifications are not to be construed as limiting the scope of the invention in any manner.


DETAILED DESCRIPTION

A. Thermal Interface Material


The present invention relates to thermal interface materials (TIMs) useful in transferring heat away from electronic components. In one exemplary embodiment, the TIM comprises at least one silicone oil, at least one catalyst, at least one thermally conductive filler, and at least one adhesion promoter including both amine and alkyl functional groups.


In some embodiments, the TIM may optionally include one or more of the following components: a silane coupling agent, an organic plasticizer, a surfactant, and a flux agent.


1. Silicone Oil


a. General Description


The present disclosure provides a matrix for a TIM material that includes at least one low molecular weight silicone oil and at least one high molecular weight silicone oil. The silicone oil includes one or more crosslinkable groups, such as vinyl, hydride, hydroxyl and acrylate functional groups, that are crosslinked by a catalyst. In one embodiment, one or more silicone oils include a first silicone oil and a second silicone oil, where the first silicone oil is a vinyl functional silicone oil and the second silicone oil is a hydride functional silicone oil. The silicone oil wets the thermally conductive filler and forms a dispensable fluid for the TIM.


In one exemplary embodiment, the silicone oil includes a silicone rubber such as the KE series products available from Shin-Etsu, such as SILBIONE® available from Bluestar, such as ELASTOSIL®, SILPURAN®, and SEMICOSIL® available from Wacker, such as Silopren® available from Momentive, such as Dow Corning®, Silastic®, XIAMETER®, Syl-off® and SYLGARD® available from Dow Corning, such as SQUARE® available from Square Silicone, such as Andril® available from AB specialty Silicones. Other polysiloxanes are available from Wacker, Shin-etsu, Dowcoring, Momentive, Bluestar, RUNHE, AB Specialty Silicones, Gelest, and United Chemical Technologies.


b. Low Molecular Weight Silicone Oil


1. Vinyl Functional Silicone Oil


The TIM includes a low weight average molecular weight silicone oil as measured by gel permeation chromatography (GPC). Exemplary low molecular weight silicone oils may include a vinyl silicone oil having a general formula as shown below:




embedded image


An exemplary low molecular weight vinyl silicone oil may also include a small amount of platinum catalyst.


Vinyl functional silicone oils include an organo-silicone component with Si—CH═CH2 groups. Exemplary vinyl functional silicone oils include vinyl-terminated silicone oils and vinyl-grafted silicone oils in which the Si—CH═CH2 group is grafted onto the polymer chain, and combinations thereof.


Exemplary vinyl-terminated silicone oils include vinyl terminated polydimethylsiloxane, such as DMS-V00 (having a weight average molecular weight (Mw) of 186 Daltons), DMS-V03 (having a Mw of about 500 Daltons), DMS-V05 (having a Mw of about 800 Daltons), DMS-V21 (having a Mw of about 6,000 Daltons), DMS-V22 (having a Mw of about 9400 Daltons), DMS-V25 (having a Mw of about 17,200 Daltons), DMS-V25R (having a Mw of about 17,200 Daltons), DMS-V35 (having a Mw of about 49,500 Daltons), DMS-V35R (having a Mw of about 49,500 Daltons), each available from Gelest, Inc. Exemplary vinyl-terminated silicone oils include vinyl terminated diphenylsiloxane-dimethylsiloxane copolymer, such as PDV-0325 (having a Mw of about 15,500 Daltons), PDV-0331 (having a Mw of about 27,000 Daltons), PDV-0525 (having a Mw of about 14,000 Daltons), PDV-1625 (having a Mw of about 9,500 Daltons), PDV-1631 (having a Mw of about 19,000 Daltons), PDV-2331 (having a Mw of about 12,500 Daltons), each available from Gelest, Inc. Exemplary vinyl-terminated silicone oils include vinyl terminated polyphenylmethylsiloxane, such as PMV-9925 (having a Mw of about 2000-3000 Daltons) available from Gelest, Inc. Exemplary vinyl-terminated silicone oils include vinyl terminated diethylsiloxane-dimethylsiloxane copolymer, such as EDV-2025 (having a Mw of about 16,500-19,000 Daltons) available from Gelest, Inc.


Exemplary vinyl-grafted silicone oils include vinylmethylsiloxane homopolymers, such as VMS-005 (having a Mw of about 258-431 Dalton), VMS-T11 (having a Mw of about 1000-1500 Daltons), both available from Gelest, Inc. Exemplary vinyl-grafted silicone oils include vinylmethylsiloxane-dimethylsiloxane copolymers, such as trimethylsiloxyl terminated silicone oils, silanol terminated silicone oils, and vinyl terminated silicone oils.


In one exemplary embodiment, the vinyl-grafted silicone oil is a vinylmethylsiloxane terpolymers, including a vinylmethylsiloxane-octylmethylsiloxane-dimethylsiloxane terpolymer, such as VAT-4325 (having a Mw of about 10,000-12,000 Daltons), or a vinylmethylsiloxane-methoxypolyethylenoxypropylmethylsiloxane-dimethylsiloxane terpolymer, such as VBT-1323 (having a M of about 8,000-12,000 Daltons), or a vinylmethylsiloxane-phenylmethylsiloxane-dimethylsiloxane (having a Mw of about 2,500-3,000 Daltons); each available from Gelest, Inc.


In one exemplary embodiment, the vinyl-functional silicone oil comprises a vinyl T resin or a vinyl Q resin.


In one exemplary embodiment, the silicone oil is a vinyl functional oil, such as RSI-V1303, RH-V1301 from RUNHE, such as Andril® VS 200, Andril® VS 1000 from AB Specialty Silicones.


2. Hydride Functional Silicone Oil


Another exemplary low molecular weight silicone oil may include a hydrosilicone oil having a general formula as shown below:




embedded image


In one exemplary embodiment, the silicone oil comprises a hydride functional silicone oil having an organo-silicone component and Si—H groups. Exemplary hydride functional silicone oils include hydride-terminated silicone oils and hydride-grafted silicone oils in which the Si—H group is grafted onto the polymer chain, and combinations thereof.


In one exemplary embodiment, the hydride-terminated silicone oil is a hydride terminated polydimethylsiloxane such as DMS-H03 (having a Mw of about 400-500 Daltons), DMS-H11 (having a Mw of about 1,0004,100 Daltons), DMS-H21 (having a Mw of about 6,000 Daltons), DMS-H25 (having a Mw of about 17,200 Daltons), or DMS-H31 (having a Mw of about 28,000 Daltons), each available from Gelest, Inc. In one exemplary embodiment, the hydride-terminated silicone oil is a methylhydrosiloxane-dimethylsiloxane copolymer, such as a trimethylsiloxyl terminated or hydride terminated. Exemplary trimethylsiloxyl terminated copolymers include HMS-031 (having a Mw of about 1,900-2,000 Daltons), HMS-071 (having a Mw of about 1,900-2,000 Daltons), HMS-082 (having a M of about 5,500-6,500 Daltons), HMS-151 (having a Mw of about 1,900-2,000 Daltons), HMS-301 (having a Mw of about 1,900-2,000 Daltons), HMS-501 (having a Mw of about 900-1200 Daltons); exemplary hydride terminated copolymers include HMS-H271 (having a Mw of about 2,000-2,600 Daltons); each of which is available from Gelest, Inc. In one exemplary embodiment, the hydride-grafted silicone oil is polymethylhydrosiloxane with trimethylsiloxyl terminated, such as HMS-991 (having a Mw of about 1,400-1,800 Daltons), HMS-992 (having a Mw of about 1,800-2,100 Daltons), HMS-993 (having a Mw of about 2,100-2,400 Daltons), each available from Gelest, Inc.


Exemplary low molecular weight silicone oils may have a weight (Mw) average molecular weight as little as 50 Daltons, 500 Daltons, 1000 Daltons, as great as 5000 Daltons, 10,000 Daltons, 50,000 Daltons, or within any range defined between any two of the foregoing values.


Exemplary low molecular weight silicone oils may have a kinematic viscosity as little as 0.5 cSt, 5 cSt, 100 cSt, as great as 5,000 cSt, 10,000 at, 50,000 cSt, or within any range defined between any two of the foregoing values as measured according to ASTM D445.


The TIM comprises one or more low molecular weight silicone oils in an amount as little as 0.1 wt %, 0.5 wt. %, 0.67 wt %, 1 wt. %, as great as 3 wt. %, 5 wt. %, 10 wt. %, 20 wt %, or within any range defined between any two of the foregoing values, based on the total weight of the TIM, such as 0.1 wt. % to 15 wt. %, 0.1 wt. % to 3 wt. %, or 0.67 wt. % to 10 wt. %.


c. High Molecular Weight Silicone Oil


The TIM includes a high molecular weight silicone oil as measured by gel permeation chromatography (GPC). Exemplary high molecular weight silicone oils may include a vinyl silicone oil having a general formula as shown below, similar to the low molecular weight silicone oils described above:




embedded image


Vinyl functional silicone oils include an organo-silicone component with Si-CH═CH2 groups. Exemplary vinyl functional silicone oils include vinyl-terminated silicone oils and vinyl-grafted silicone oils in which the Si—CH═CH2 group is grafted onto the polymer chain, and combinations thereof.


Exemplary vinyl-terminated silicone oils include vinyl terminated polydimethylsiloxane, such as DMS-V41 (having a Mw of about 62,700 Daltons), DMS-V42 (having a Mw of about 72,000 Daltons), DMS-V46 (having a Mw of about 117,000 Daltons), DMS-V51 (having a Mw of about 140,000 Daltons), and DMS-V52 (having a Mw of about 155,000 Daltons), each available from Gelest, Inc.


Exemplary vinyl-grafted silicone oils include vinylmethylsiloxane-dimethylsiloxane copolymers, such as trimethylsiloxyl terminated silicone oils, silanol terminated silicone oils, and vinyl terminated silicone oils.


In one exemplary embodiment, the vinyl-grafted silicone oil is a vinylmethylsiloxane terpolymers. In one exemplary embodiment, the vinyl-functional silicone oil comprises a vinyl T resin or a vinyl Q resin.


Another exemplary high molecular weight silicone oil may include a hydride functional silicone oil having an organo-silicone component and Si—H groups. Exemplary hydride functional silicone oils include hydride-terminated silicone oils, hydride-grafted silicone oils in which the Si—H group is grafted onto the polymer chain, and combinations thereof.


In one exemplary embodiment, the hydride-terminated silicone oil is a hydride terminated polydimethylsiloxane such as DMS-H41 (having a Mw of about 62,700 Daltons), available from Gelest, Inc. In one exemplary embodiment, the hydride-terminated silicone oil is a methylhydrosiloxane-dimethylsiloxane copolymer, such as a trimethylsiloxyl terminated or hydride terminated. Exemplary trimethylsiloxyl terminated copolymers include HMS-064 (having a Mw of about 60,000-65,000 Daltons), available from Gelest, Inc.


Exemplary low molecular weight silicone oils may have a weight (Mw) average molecular weight as little as 60,000 Daltons, 70,000 Daltons, 100,000 Daltons, as great as 1,000,000 Daltons, 10,000,000 Daltons, 100,000,000 Daltons, or within any range defined between any two of the foregoing values.


Exemplary high molecular weight silicone oils may have a kinematic viscosity as little as 10,000 cSt, 20,000 cSt, 100,000 cSt, as great as 1,000,000 cSt, 10,000,000 cSt, 100,000,000 cSt, or within any range defined between any two of the foregoing values as measured according to ASTM D445. In one exemplary embodiment, an exemplary high molecular weight silicone oil is a high molecular weight vinyl silicone oil having a kinematic viscosity of 2,000,000 cSt.


The TIM may comprise one or more high molecular weight silicone oils in an amount as little as 0.01 wt %, 0.1 wt. %, 0.25 wt. %, 0.5 wt. %, 0.67 wt. %, 0.75 wt. %, as great as 1 wt %, 1.5 wt. %, 2 wt. %, 5 wt. %, or within any range defined between any two of the foregoing values, based on the total weight of the TIM, such as 0.1 wt. % to 5 wt. %, 0.1 wt. % to 1 wt. %, or 0.25 wt. % to 0.67 wt %. In one exemplary embodiment, the TIM includes a high molecular weight silicone oil in the amount of about 0.6 wt. %. In another exemplary embodiment, the TIM includes a high molecular weight silicone oil in the amount of about 2.68 wt. %.


2. Catalyst


The TIM further includes one or more catalyst for catalyzing the addition reaction. Exemplary catalysts comprise platinum containing materials and rhodium containing materials. Exemplary platinum containing catalysts may have the general formula shown below:




embedded image


Exemplary platinum contain catalysts include: Platinum cyclovinylmethylsiloxane complex (Ashby Karstedt Catalyst), Platinum carbonyl cyclovinylmethylsiloxane complex (Ossko catalyst), Platinum divinyltetramethyldisiloxane dimethyl fumarate complex, Platinum divinyltetramethyldisiloxane dimethyl maleate complex and the like. Exemplary of Platinum carbonyl cyclovinylmethylsiloxane complexes include SIP6829.2, exemplary of Platinum divinyltetramethyldisiloxane complex include SIP6830.3 and SIP6831.2, exemplary of platinum cyclovinylmethylsiloxane complex include SIP6833.2, all available from Gelest, Inc. Further exemplary platinum containing material catalysts include Catalyst OL available from Wacker Chemie AG, and PC065, PC072, PC073, PC074, PC075, PC076, PC085, PC086, PC087, PC088 available from United Chemical Technologies Inc.


Exemplary rhodium containing materials include Tris(dibutylsulfide)Rhodium trichloride with product code INRH078, available from Gelest, Inc.


Without wishing to be held to any particular theory it is believed that the platinum catalyst reacts with a vinyl silicone oil and a hydrosilicone oil as shown below.




embedded image


The TIM may comprise the one or more catalyst in an amount as little as 5 ppm, 10 ppm, 15 ppm, 20 ppm, as great as 25 ppm, 30 ppm, 40 ppm, 50 ppm, 100 ppm, 200 ppm, 500 ppm, 1000 ppm, or within any range defined between any two of the foregoing values, based on the total weight of the silicone oil, such as 10 ppm to 30 ppm, 20 ppm to 100 ppm, or 5 ppm to 500 ppm.


In one exemplary embodiment, the catalyst is provided as a mixture with one or more of the silicone oils. In one exemplary embodiment, the platinum containing material catalyst is combined to a functional silicone oil, such as KE-1012-A, KE-1031-A, KE-109E-A, KE-1051J-A, KE-1800T-A, KE1204A, KE1218A available from Shin-Etsu, such as SILBIONE® RT Gel 4725 SLID A available from Bluestar, such as SilGel® 612 A, ELASTOSIL® LR 3153A, ELASTOSIL® LR 3003A, ELASTOSIL® LR 3005A, SEMICOSIL® 981A, SEMICOSIL® 927A, SEMICOSIL® 205A, SEMICOSIL® 9212A, SILPURAN® 2440 available from Wacker, such as Silopren® LSR 2010A available from Momentive, such as XIAMETER® RBL-9200 A, XIAMETER® R812004 A, XIAMETER® RBL-9050 A, XIAMETER® RBL-1552 A, Silastic® FL 30-9201 A, Silastic® 9202 A, Silastic® 9204 A, Silastic® 9206 A, SYLGARD® 184A, Dow Corning® QP-1 A, Dow Corning® C6 A, Dow Corning® CV9204 A available from Dow Corning.


The TIM may comprise a catalyst in an amount as little as 0.01 wt %, 0.1 wt. %, 0.2 wt. %, as great as 0.3 wt %, 0.4 wt. %, 0.5 wt. %, or within any range defined between any two of the foregoing values, based on the total weight of the TIM. In one exemplary embodiment, the TIM includes a catalyst in the amount of about 0.04 wt %. In another exemplary embodiment, the TIM includes a catalyst in the amount of about 0.4 wt. %.


In another embodiment, the platinum containing material catalyst is combined to a high molecular weight vinyl functional silicone oil.


3. Thermally Conductive Filler


The TIM includes one or more thermally conductive fillers. Exemplary thermally conductive fillers include metals, alloys, nonmetals, metal oxides and ceramics, and combinations thereof. The metals include, but are not limited to, aluminum, copper, silver, zinc, nickel, tin, indium, and lead. The nonmetal include, but are not limited to, carbon, graphite, carbon nanotubes, carbon fibers, graphenes, boron nitride and silicon nitride. The metal oxide or ceramics include but not limited to alumina (aluminum oxide), aluminum nitride, boron nitride, zinc oxide, and tin oxide.


The TIM may comprise the one or more thermally conductive fillers in an amount as little as 10 wt. %, 20 wt %, 25 wt. %, 50 wt. %, as great as 75 wt. %, 80 wt %, 85 wt. %, 90 wt. %, 95 wt. %, 97 wt. %, or within any range defined between any two of the foregoing values, based on the total weight of the TIM, such as 10 wt. % to 95 wt %, 50 wt. % to 95 wt. %, or 85 wt % to 97 wt %.


Exemplary thermally conductive fillers may have an average particle size of as little as 0.1 microns, 1 micron, 10 microns, as great as 50 microns, 75 microns, 100 microns or within any range defined between any two of the foregoing values.


In one exemplary embodiment, the TIM may include a first thermally conductive filler and a second thermally conductive filler, wherein the first thermally conductive filer has an average particle size greater than 1 micron and the second thermally conductive filler has an average particle size less than 1 micron. In a more particular embodiment, a ratio of the first thermally conductive filler to the second thermally conductive filler may be as little as 1:5, 1:4, 1:3, 1:2, as great as 1:1, 1,5:1, 2:1, 3:1, 4:1, 5:1, or within any range defined between any two of the foregoing values, such as 1:5 to 5:1 1:1 to 3:1, or 1.5:1 to 3:1.


In one exemplary embodiment, the TIM may include a first thermally conductive filler, a second thermally conductive filler, and a third thermally conductive filler, wherein the first thermally conductive filer has a particle size greater than 10 micron, the second thermally conductive filler has an average particle size as little as 1 micron, 2 microns, 4 microns, as great as 6 microns, 8 microns, 10 microns, or within any range defined therebetween, and the third thermally conductive filler has an average particle size less than 1 micron.


In one exemplary embodiment, the TIM includes a first thermally conductive filler in the amount of as little as 30 wt. %, 35 wt. %, 40 wt %, as great as 45 wt. %, 50 wt. %, 60 wt % or within any range defined between any two of the foregoing values with respect to the total TIM composition. The first thermally conductive filler has an average particle size of as little as 30 microns. 35 microns, 40 microns, as great as 45 microns, 50 microns, 60 microns, or within any range defined between any two of the foregoing values. The exemplary TIM further includes a second thermally conductive filler in the amount of as little as 5 wt. %, 10 wt %, 15 wt. %, as great as 25 wt. %, 30 wt. %, 40 wt % or within any range defined between any two of the foregoing values with respect to the total TIM composition. The second thermally conductive filler has an average particle size of as little as 1 micron, 3, microns. 5 microns, as great as 10 microns, 15 microns, 20 microns, or within any range defined between any two of the foregoing values. The exemplary TIM further includes a third thermally conductive filler in the amount of as little as 5 wt. %, 10 wt. %, 15 wt. %, as great as 25 wt. %, 30 wt %, 40 wt % or within any range defined between any two of the foregoing values with respect to the total TIM composition. The third thermally conductive filler has an average particle size of as little as 0.1 microns, 0.3, microns. 0.5 microns, as great as 1 micron, 1.5 microns, 2 microns, or within any range defined between any two of the foregoing values.


In one exemplary embodiment, the TIM includes a first thermally conductive filler in the amount of as little as 5 wt. %, 10 wt. %, 15 wt. %, as great as 25 wt. %, 30 wt. %, 40 wt % or within any range defined between any two of the foregoing values with respect to the total TIM composition. The first thermally conductive filler having an average particle size of as little as 30 microns. 35 microns, 40 microns, as great as 45 microns, 50 microns, 60 microns, or within any range defined between any two of the foregoing values. The exemplary TIM further includes a second thermally conductive filler in the amount of as little as 30 wt. %, 35 wt. %, 40 wt. %, as great as 45 wt. %, 50 wt. %, 60 wt % or within any range defined between any two of the foregoing values with respect to the total TIM composition. The second thermally conductive filler having an average particle size of as little as 1 micron, 3, microns. 5 microns, as great as 10 microns, 15 microns, 20 microns, or within any range defined between any two of the foregoing values. The exemplary TIM further includes a third thermally conductive filler in the amount of as little as 5 wt. %, 10 wt. %, 15 wt. %, as great as 25 wt. %, 30 wt. %, 40 wt % or within any range defined between any two of the foregoing values with respect to the total TIM composition. The third thermally conductive filler having an average particle size of as little as 0.1 microns, 0.3, microns. 0.5 microns, as great as 1 micron, 1.5 microns. 2 microns, or within any range defined between any two of the foregoing values.


Exemplary thermal conductive fillers include alumina oxide and zinc oxide.


4. Addition Inhibitor


The TIM comprises one or more addition inhibitors for inhibiting or limiting crosslinking of the silicone oils. The addition inhibitors includes at least one alkynyl compound, and optionally, the addition inhibitor further includes a multi-vinyl functional polysiloxane.


Exemplary addition inhibitors include acetylenic alcohols such as 1-ethynyl-1-cyclohexanol, 2-methyl-3-butyn-2-ol, 2-phenyl-3-butyn-2-ol, 2-ethynyl-isopropanol, 2-ethynyl-butane-2-ol, and 3,5-dimethyl-1-hexyn-3-ol; silylated acetylenic alcohols such as trimethyl (3,5-dimethyl-1-hexyn-3-oxy)silane, dimethyl-bis-(3-methyl-1-butyn-oxy)silane, methylvinylbis(3-methyl-1-butyn-3-oxy)silane, and ((1,1-dimethyl-2-propynyl)oxy)trimethylsilane; unsaturated carboxylic esters such as diallyl maleate, dimethyl maleate, diethyl fumarate, diallyl fumarate, and bis-2-methoxy-1-methylethylmaleate, mono-octylmaleate, mono-isooctylmaleate, mono-allyl maleate, mono-methyl maleate, mono-ethyl fumarate, mono-allyl fumarate, 2-methoxy-1-methylethylmaleate; fumarate/alcohol mixtures, such as mixtures where the alcohol is selected from benzyl alcohol or 1-octanol and ethenyl cyclohexyl-1-ol; conjugated ene-ynes such as 2-isobutyl-1-butene-3-yne, 3,5-dimethyl-3-hexene-1-yne, 3-methyl-3-pentene-1-yne, 3-methyl-3-hexene-1-yne, 1-ethynylcyclohexene, 3-ethyl-3-butene-1-yne, and 3-phenyl-3-butene-1-yne; vinylcyclosiloxanes such as 1,3,5,7-tetramethyl-1,3,5,7-tetravinylcyclotetrasiloxane, and mixtures of conjugated ene-yne and vinylcyclosiloxane. In one exemplary embodiment, the addition inhibitor is selected from 2-methyl-3-butyn-2-ol or 3-methyl-1-pentyn-3-ol.


In some exemplary embodiments, the addition inhibitor further includes a multi-vinyl functional polysiloxane. An exemplary multi-vinyl functional polysiloxane is a vinyl terminated polydimethylsiloxane in ethynyl cyclohexanol, such as Pt Inhibitor 88 available from Wacker Chemie AG. Without wishing to be held to any particular theory it is believed that the platinum catalyst forms a complex with ethynyl cyclohexanol and vinyl terminated polydimethylsiloxane as shown below.




embedded image


The formation of the complex is believed to decrease the catalyst activity in room temperature, and thus maintaining the dispensability and wettability of the TIM. At the higher temperatures of the curing step, the Pt is released from the complex and help the hydrosilylation of vinyl functional silicone oil and hydride functional silicone oil, provides greater control over the “crosslinking”.


In some exemplary embodiments, the TIM may comprise the one or more addition inhibitors in an amount as little as 0.01 wt. %, 0.02 wt %, 0.05 wt. %, 0.1 wt. %, 0.15 wt. %, as great as 0.2 wt. %, 0.25 wt. %, 0.3 wt. %, 0.5 wt. %, 1 wt. %, 3 wt %, 5 wt. %, or within any range defined between any two of the foregoing values, based on the total weight of the TIM, such as 0.01 wt. % to 1 wt. %, 0.01 wt. % to 0.5 wt. %, or 0.05 wt. % to 0.2 wt. %. In one exemplary embodiment, the TIM includes an addition inhibitor in the amount of 0.1 wt %. In another exemplary embodiment, the TIM includes an addition inhibitor in the amount of 0.13 wt. %.


Without wishing to be held to any particular theory, it is believed that, in the absence of an addition inhibitor, the vinyl functional silicone oil reacts with the hydride functional silicone oil very quickly based on the addition hydrosilylation mechanism to form a solid phase that cannot be automatically dispensed by typical methods.


In one exemplary embodiment, the addition inhibitor is combined to functional silicone oils, such as KE-1056, KE-1151, KE-1820, KE-1825, KE-1830, KE-1831, KE-1833, KE-1842, KE-1884, KE-1885, KE-1886, FE-57, FE-61 available from Shin-Etsu, such as Syl-off® 7395, Syl-off® 7610, Syl-off® 7817, Syl-off® 7612, Syl-off® 7780 available from Dow Corning.


5. Optional Components


In some embodiments, the TIM may optionally include one or more of the following components: a silane coupling agent, an organic plasticizer, a surfactant, and a flux agent.


In some exemplary embodiments, the TIM comprises one or more coupling agents. Exemplary coupling agents include silane coupling agents with general formula Y—(CH2)n—Si—X3, wherein Y is organofunctional group, X is hydrolysable group. Organofunctional group Y includes alkyl, glycidoxy, acryloxyl, methylacryloxyl, amine. Hydrolysable group X includes alkyloxy, acetoxy. In some exemplary embodiments, the silane coupling agent includes alkyltrialkoxysilanes. Exemplary alkytrialkoxy silane comprise decyltrimethoxylsilane, undecyltrimethoxylsilane, hexadecyltrimethoxysilane, octadecyltrimethoxysilane. In one exemplary embodiment, the TIM includes hexadecyltrimethoxysilane as the coupling agent's shown in the formula below.




embedded image


Exemplary coupling agents interact with exemplary fillers as shown in the example reaction in FIG. 7. Alumina is the representative filler used in the reaction below; however, other alternative fillers may be used. As shown, the coupling agent is added to water and undergoes hydrolysis to remove an ethoxide group. The products then undergo a modification reaction where water is removed and the coupling agent and alumina are bonded together.


In some exemplary embodiments, the TIM may comprise the one or more coupling agents in an amount as little as 0.1 wt. %, 0.25 wt. %, 0.5 wt %, 0.67 wt. %, 0.75 wt. %, as great as 1 wt. %, 1.5 wt. %, 2 wt. %, 5 wt. %, 10 wt. %, or within any range defined between any two of the foregoing values, based on the total weight of the TIM, such as 0.1 wt. % to 10 wt. %, 0.1 wt. % to 1 wt. %, or 0.25 wt. % to 0.67 wt %. In one exemplary embodiment, the TIM includes a coupling agent in the amount of 0.4 wt. %.


In some exemplary embodiments, the TIM comprises one or more organic plasticizers. Exemplary organic plasticizers include phthalate-based plasticizers such as Bis(2-ethylhexyl) phthalate (DEHP), Di-n-butyl phthalate (DnBP, DBP), Dioctyl phthalate (DOP or DnOP), Diethyl phthalate (DEP), Diisobutyl phthalate (DIBP), Diisodecyl phthalate (DIDP), Diisononyl phthalate (DINP), and Butyl benzyl phthalate (BBzP).


In some exemplary embodiments, the TIM may comprise the one or more organic plasticizers in an amount as little as 0.01%, 0.1 wt. %, 0.25 wt %, 0.5 wt %, 0.67 wt. %, 0.75 wt %, as great as 1 wt. %, 1.5 wt. %, 2 wt. %, 5 wt %, 10 wt. %, or within any range defined between any two of the foregoing values, based on the total weight of the TIM, such as 0.01 wt. % to 10 wt. %, 0.1 wt. % to 1 wt %, or 0.25 wt. % to 0.67 wt. %.


In some exemplary embodiments, the TIM comprises one or more surfactants. Exemplary surfactants include silicone based surface additives, such as the BYK surfactants available from BYK Chemie GmbH, including BYK-307, BYK-306, and BYK-222.


In some exemplary embodiments, the TIM may comprise the one or more surfactants in an amount as little as 0.01%, 0.1 wt. %, 0.25 wt. %, 0.5 wt. %, 0.87 wt. %, 0.75 wt %, as great as 1 wt. %, 1.5 wt %, 2 wt. %, 5 wt. %, 10 wt. %, or within any range defined between any two of the foregoing values, based on the total weight of the TIM, such as 0.1 wt % to 10 wt. %, 0.1 wt % to 1 wt %, or 0.25 wt. % to 0.67 wt. %.


In some exemplary embodiments, the TIM comprises one or more flux agents. Exemplary flux agents include fumed silica.


In some exemplary embodiments, the TIM may comprise the one or more flux agents in an amount as little as 0.1 wt. %, 0.25 wt. %, 0.5 wt. %, 0.67 wt. %, 0.75 wt. %, as great as 1 wt %, 1.5 wt. %, 2 wt. %, 5 wt. %, 10 wt. %, or within any range defined between any two of the foregoing values, based on the total weight of the TIM, such as 0.1 wt % to 10 wt. %, 0.1 wt. % to 1 wt. %, or 015 wt % to 0.67 wt. %.


6. Exemplary Formulations of the Thermal Interface Material


In a first non-limiting illustrative embodiment, the TIM includes about 2 wt. % to about 20 wt % silicone oil, about 0.1 wt. % to about 5 wt. % coupling agent, about 50 wt. % to about 95 wt. % thermally conductive filler, about 0.1 wt. % to about 5 wt. % addition inhibitor, and about 0.1 wt. % to about 5 wt. % addition catalyst.


In a second non-limiting illustrative embodiment, the TIM includes about 2 wt. % to about 10 wt. % of a first low molecular silicone oil, about 2 wt. % to about 10 wt. % of a second low molecular silicone oil, about 0.1 wt. % to about 5 wt. % of a high molecular weight silicone oil, about 0.1 wt. % to about 5 wt. % of a coupling agent, about 25 wt. % to about 50 wt. % of a first thermally conductive filler, about 25 wt % to about 50 wt. % of a second thermally conductive filler, about 25 wt. % to about 50 wt. % of a third thermally conductive filler, about 0.1 wt. % to about 5 wt. % addition inhibitor, and about 0.1 wt. % to about 5 wt. % addition catalyst.


7. Exemplary Properties of the Thermal Interface Material


In some exemplary embodiments, a thermal interface material as described above has excellent resistance to highly-accelerated stress testing (HAST). HAST testing is typically understood to relate to the resistance of the thermal interface material to humidity and temperature on the thermal performance of the thermal interface material. An exemplary HAST test standard is JESD22-A110-B. In one particular embodiment, the thermal interface material shows no dripping when placed between a glass and exemplary copper heat sink at in a vertically oriented 1.6 mm gap and subjected to 10000 thermal cycles between −55° C. and +125° C. for over one week. In other embodiments, the thermal interface material shows little to no cracking following the thermal cycling test.


In some exemplary embodiments, a thermal interface material as described above has excellent resistance to temperature cycling. Temperature cycling is typically understood to relate to the resistance of the thermal interface material to extremes of high and low temperatures, as well as its ability to withstand cyclical thermal stresses. An exemplary temperature cycling test standard is JESD22-A104-B. In one particular embodiment, the thermal interface material shows no dripping when placed between a glass an exemplary copper heat sink at in a vertically oriented 1.6 mm gap and subjected to 10000 thermal cycles between −55° C. and +125° C. over one week. In other embodiments, the thermal interface material shows little to no cracking following the temperature cycling test.


In some exemplary embodiments, a thermal interface material as described above has the thermal conductivity at least 1 W/m·K. An exemplary thermal conductivity test method standard is ASTM D5470. In one exemplary amendment, a thermal interface material as described above has the thermal conductivity of about 4 W/m·K. In another exemplary embodiment, a thermal interface material as described above has the thermal conductivity of about 2 W/m·K.


In some exemplary embodiments, a thermal interface material as described above has the viscosity in the range of 10 Pas to 100,000 Pa·s, or more particularly in the range of 100 Pa·s to 10,000 Pa·s at room temperature. An exemplary viscosity test method standard is DIN 53018. In one particular embodiment, the viscosity is tested by Brookfield Rheometer with shear rate 2 s−1.


As applied, a thermal interface material can have a varied thickness as measured by a micrometer. In some exemplary embodiments, a thermal interface material as described above has a thickness of as little as 0.05 mm, 0.5 mm, 1 mm, as great as 3 mm, 5 mm, 7 mm, 10 mm or within any range defined between any two of the foregoing values, such as from 0.05 mm to 5 mm.


In some exemplary embodiments, a thermal interface material as described above is compressible at a given temperature when cured. In one exemplary embodiment, the thermal interface material is compressible by at least 10% at a temperature of about 25° C.


In some exemplary embodiments, a thermal interface material as described above has the dispense rate in the range of 1 g/min to 1000 g/min, or more particularly in the range of 10 g/min to 100 g/min. In one particular embodiment, the dispense rate is tested under 0.6 MPa pressure with a 10 ml syringe having a 0.1 inch diameter dispense header opening.


B. Methods of Forming a Thermal Interface Material


In some exemplary embodiments, the TIM is prepared by combining the individual components in a heated mixer and blending the composition together. The blended composition may then be applied directly to the substrate without baking.


C. Applications Utilizing the Thermal Interface Material


Referring again to FIG. 1, in some exemplary embodiments, the thermal interface material is positioned as a TIM 1 between an electronic component 12 and a heat spreader 14, as indicated by TIM 18. In some exemplary embodiments, the thermal interface material is positioned as a TIM 2 between a heat spreader 14 and a heat sink 16, as indicated by TIM 20. In some exemplary embodiments, the thermal interface material is positioned as a TIM 1.5 (not shown) between an electronic component 12 and a heat sink 16.


EXAMPLES
Example 1

A thermal interface material was prepared according to the formulation provided in Table 1.









TABLE 1







Formulations (wt. %) for Example 1










Component
Wt. %














Low MW silicone oil A
4.75



Low MW silicone oil B
4.75



Silane coupling agent
0.5



Thermal conductive filler A
60



Thermal conductive filler B
30



Addition inhibitor
0.1










Low molecular weight (MW) silicone oil A was a low molecular weight liquid silicone rubber comprising vinyl functional group. The molecular weight of the low MW silicone oil was below 50,000 Daltons and further included a platinum catalyst. Low MW silicone oil B is a liquid silicone rubber comprising hydride functional group and has a molecular weight below 58,000 Daltons. The silane coupling agent was hexadecyltrimethoxysilane. Thermal conductive filler A was aluminum particles having a particle diameter between 1 and 10 microns. Thermal conductive filler B was zinc oxide particles having a particle diameter less than 1 micron. The addition inhibitor was Pt Inhibitor 88 available from Wacker Chemie AG.


To prepare the formulation of Example 1, the silicone oil, silane coupling agent, and addition inhibitor were combined and blended with a speed mixer. The thermally conductive fillers were then added, and the mixture was blended again.


A GEL 30 Thermally Conductive Dispensable Gel from Parker Chomerics was obtained for use a comparative example. GEL 30 includes a partially cross-linked silicone rubber and alumina.


The formulation of Example 1 and the comparative example were each sandwiched between a glass and an exemplary heat sink in a vertically oriented 1.6 mm gap and subjected to thermal cycling between −55° C. and +125° C. for one week.



FIG. 2A shows the sample formed from Example 1 before the thermal cycling test and FIG. 2B shows the sample formed from the GEL 30 comparative example before the thermal cycling test. FIG. 3A shows the sample formed from Example 1 after the thermal cycling test and FIG. 3B shows the sample formed from the GEL 30 comparative example after the thermal cycling test.


As shown in FIG. 3A, the sample formed from Example 1 showed no dripping, as indicated by the sample maintaining its original vertical position between the glass and substrate during the test. In contrast, the sample formed from the comparative example showed significant dripping as indicated by the movement downward between FIGS. 2B and 3B.


In addition, FIG. 3A showed limited cracking of the sample formed from Example 1 due to the thermal cycling test. In contrast, FIG. 3B showed significantly more cracking in the comparative example.


Example 2

A thermal interface material was prepared according to the formulation provided in Table 2.









TABLE 2







Formulations (wt. %) for Example 2














Comp. Ex. 2
Ex. 2A
Ex. 2B
Ex. 2C



Component
(wt. %)
(wt. %)
(wt. %)
(wt. %)

















Low MW
5
4.2
4.6
3.14



silicone oil A







Low MW
5
4.4
4.6
3.3



silicone oil B







High MW

0.6

0.9



Silicone Oil







Silane
0.5
0.5
0.5
0.4



coupling







agent







Thermal
60
60
60




conductive







filler A







Thermal
30
30
30




conductive







filler B







Thermal



43.8



conductive







filler C







Thermal



21.9



conductive







filler D







Thermal



26.3



conductive







filler E







Addition

0.1
0.1
0.1



inhibitor







Addition

0.2
0.2
0.16



Catalyst














Low molecular weight (MW) silicone oil A was a low molecular weight liquid silicone rubber comprising vinyl functional group. The molecular weight of the low MW silicone oil A was below 50,000 Daltons and further Included a platinum catalyst. Low MW silicone oil B was a low molecular weight liquid silicone rubber comprising hydride functional group. The molecular weight of the low MW silicone oil B was below 50,000 Daltons. High MW silicone oil had the molecular weight higher than 60,000 Daltons. The silane coupling agent was hexadecyltrimethoxysilane. Thermal conductive filler A was aluminum oxide particles having a particle diameter between 1 and 10 microns. Thermal conductive filler B was aluminum oxide particles having a particle diameter less than 1 micron. The addition inhibitor was Pt Inhibitor 88 available from Wacker Chemie AG.


After one of Comp. Ex. 2, Ex. 2A, 2B, or 2C are prepared, the prepared mixture is inserted into and sealed in a syringe 50 as shown in FIGS. 6A, 6B. Syringe 50 is connected to an automatic dispenser tool 52. The mixtures can be purged out of syringe 50 by air pressure generated by dispenser tool 52. Dispenser tool 52 also controls the orifice diameter. In effect, dispenser tool 52 controls the dispense rate of the mixtures from syringe 50 by varying the two parameters—orifice diameter and air pressure. In one embodiment, the formulation is dispensed from syringe 50 with no tip attachment at 10 cubic centimeters under a compression of 90 psi through a 0.100 inch orifice of syringe 50.


The formulation of Comp. Ex. 2, Ex. 2A, and Ex. 2B were each dispensed on an exemplary heat sink after which a glass plate was placed onto the exemplary heat sink where a 1.6 mm gap exists between the heat sink and the glass when the apparatus is vertically oriented as shown in FIG. 2A, for example. The pressure applied onto the formulation causes the formulation to spread to a desired area. There is a 1.6 mm gap between the heat sink and the glass. The glass and exemplary heat sink apparatus as described above is subjected thermal cycling between −55° C. and +125° C. for one week with each cycle having a duration of 40 minutes. A total of about 250 cycles were conducted, each individual cycle having a duration of 40 minutes.



FIGS. 4A-4C shows Comp. Ex. 2, Ex. 2A, and Ex. 2B formed from Example 2 before the thermal cycling test with the resulting formulations of Comp. Ex. 2, Ex. 2A, and Ex. 2B after the thermal cycling test shown in FIGS. 5A-5C.


As shown in FIGS. 5A and 5B, Comp, Ex. 2 and Ex. 2A each showed significant dripping as indicated by the samples not maintaining their respective original vertical positions between the glass and substrate during the test. By contrast, as shown in FIG. 5C, Ex. 2B showed limited dripping, as indicated by the sample maintaining its original vertical position between the glass and substrate during the test.


In addition, Ex. 2B (FIG. 5C) showed limited cracking of the sample formed from Example 1 due to the thermal cycling test. By contrast, Comp. Ex. 2 and Ex. 2A (FIGS. 5A and 5B respectively) showed significantly more cracking in the comparative example.


While this invention has been described as having exemplary designs, the present invention can be further modified within the spirit and scope of this disclosure. This application is therefore intended to cover any variations, uses, or adaptations of the invention using its general principles. Further, this application is intended to cover such departures from the present disclosure as come within known or customary practice in the art to which this invention pertains and which fail within the limits of the appended claims.

Claims
  • 1. A thermal interface material comprising: at least one low molecular weight silicone oil having a weight (Mw) average molecular weight less than 50,000 Daltons;at least one thermally conductive filler; andat least one high molecular weight silicone oil, wherein the high molecular weight silicone oil comprises a vinyl functional silicone oil having a weight (Mw) average molecular weight of at least 60,000 Daltons and having a kinematic viscosity of at least 100,000 cSt.
  • 2. The thermal interface material of claim 1, wherein the at least one low molecular weight silicone oil comprises a first silicone oil and a second silicone oil, wherein the first silicone oil is a vinyl functional silicone oil and the second silicone oil is a hydride functional silicone oil.
  • 3. The thermal interface material of claim 1, wherein the thermally conductive filler includes a first thermally conductive filler and a second thermally conductive filler, wherein the first thermally conductive filer is a metal oxide having a particle size greater than 1 micron and the second thermally conductive filler is a metal oxide having a particle size less than 1 micron.
  • 4. The thermal interface material of claim 1, wherein the thermally conductive filler includes a first thermally conductive filler, a second thermally conductive filler, and a third thermally conductive filler, wherein the first thermally conductive filler is a metal oxide having an average particle size greater than 10 microns, the second thermally conductive filler is a metal oxide having an average particle size between 1 micron and 10 microns, and the third thermally conductive filler is a metal oxide having an average particle size less than 1 micron.
  • 5. The thermal interface material of claim 1, wherein the thermal interface material comprises: from 2 wt. % to 20 wt. % of the low molecular weight silicone oil;from 50 wt. % to 95 wt. % of the thermally conductive filler; andfrom 0.1 wt. % to 5 wt. % of the high molecular weight silicone oil.
  • 6. The thermal interface material of claim 5, wherein the low molecular weight silicone oil comprises a first silicone oil and a second silicone oil, wherein the first silicone oil is a vinyl functional silicone oil and the second silicone oil is a hydride functional silicone oil.
  • 7. A thermal interface material comprising: at least one high molecular weight vinyl functional silicone oil having a weight (Mw) average molecular weight of at least 60,000 Daltons and a kinematic viscosity of at least 100,000 cSt;at least one low molecular weight silicone oil having a weight (Mw) average molecular weight less than 50,000 Daltons;at least one thermally conductive filler; andat least one addition inhibitor, wherein the addition inhibitor comprises an alkynyl compound.
  • 8. The thermal interface material of claim 7, wherein the addition inhibitor is selected from the group consisting of: a multivinyl functional polysiloxane, polydimethylsiloxane vinyl terminated in ethynyl cyclohexanol, 2-methyl-3-butyn-2-ol, and 3-methyl-1-pentyn-3-ol.
  • 9. The thermal interface material of claim 7, wherein the thermally conductive filler includes a first thermally conductive filler and a second thermally conductive filler, wherein the first thermally conductive filer is a metal having a particle size greater than 1 micron and the second thermally conductive filler is a metal oxide having a particle size less than 1 micron.
  • 10. The thermal interface material of claim 9, wherein a ratio of the first thermally conductive tiller to the second thermally conductive filler is from 1.5:1 to 3:1.
  • 11. The thermal interface material of claim 7, wherein the thermal interface material comprises: from 2 wt. % to 20 wt. % of the silicone oils;from 0.1 wt. % to 5 wt. % of a silane coupling agent;from 50 wt. % to 95 wt. % of the thermally conductive filler; andfrom 0.01 wt. % to 5 wt. % of the addition inhibitor.
  • 12. The thermal interface material of claim 11, wherein the addition inhibitor is polydimethylsiloxane vinyl terminated in ethynyl cyclohexanol.
  • 13. An electronic component comprising: a heat sink;an electronic chip;a thermal interface material having a first surface layer and a second surface layer, the thermal interface material positioned between the heat sink and electronic chip, the thermal interface material including: at least one silicone oil having a kinematic viscosity of at least 100,000 cSt;at least one thermally conductive filler; andat least one addition inhibitor, wherein the addition inhibitor comprises an alkynyl compound, wherein the at least one silicone comprises at least one low molecular weight silicone oil and at least one high molecular weight silicone oil.
  • 14. The electronic component of claim 13, wherein the at least one high molecular weight silicone oil comprises a vinyl functional silicone oil having a weight (Mw) average molecular weight of at least 60,000 Daltons.
  • 15. The electronic component of claim 13, wherein the first surface layer is in contact with a surface of the electronic chip and the second surface layer is in contact with the heat sink.
  • 16. The electronic component of claim 13, wherein the electronic component further comprises a heat spreader positioned between the heat sink and the electronic chip, wherein the first surface layer is in contact with a surface of the electronic chip and the second surface layer is in contact with the heat spreader.
  • 17. The electronic component of claim 13, the electronic component further comprises a heat spreader positioned between the heat sink and the electronic chip, wherein the first surface layer is in contact with a surface of the heat spreader and the second surface layer is in contact with the heat sink.
  • 18. The thermal interface of claim 1, wherein the at least one high molecular weight silicone oil has a weight (Mw) average molecular weight of at least 1,000,000 Daltons and having a kinematic viscosity of at least 1,000,000 cSt.
  • 19. The thermal interface of claim 1, wherein the at least one low molecular weight silicone oil has a kinematic viscosity of less than 5,000 cSt.
CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims priority to U.S. Provisional Patent Application Ser. No. 62/366,704, filed Jul. 26, 2016 and U.S. Provisional Patent Application Ser. No. 62/436,746, filed Dec. 20, 2016, the disclosures of which are hereby expressly incorporated by reference herein in their entireties.

US Referenced Citations (217)
Number Name Date Kind
4180498 Spivack Dec 1979 A
4446266 von Gentzkow et al. May 1984 A
4459185 Obata et al. Jul 1984 A
4565610 Nobel et al. Jan 1986 A
4604424 Cole et al. Aug 1986 A
5162555 Remmers et al. Nov 1992 A
5167851 Jamison et al. Dec 1992 A
5562814 Kirby Oct 1996 A
6040362 Mine et al. Mar 2000 A
6096414 Young Aug 2000 A
6238596 Nguyen et al. May 2001 B1
6339120 Misra et al. Jan 2002 B1
6372337 Takahashi et al. Apr 2002 B2
6372997 Hill et al. Apr 2002 B1
6391442 Duvall et al. May 2002 B1
6400565 Shabbir et al. Jun 2002 B1
6432320 Bonsignore et al. Aug 2002 B1
6432497 Bunyan Aug 2002 B2
6451422 Nguyen Sep 2002 B1
6475962 Khatri Nov 2002 B1
6496373 Chung Dec 2002 B1
6500891 Kropp et al. Dec 2002 B1
6562180 Bohin et al. May 2003 B1
6597575 Matayabas et al. Jul 2003 B1
6605238 Nguyen et al. Aug 2003 B2
6610635 Khatri Aug 2003 B2
6616999 Freuler et al. Sep 2003 B1
6617517 Hill et al. Sep 2003 B2
6620515 Feng et al. Sep 2003 B2
6624224 Misra Sep 2003 B1
6649325 Gundale et al. Nov 2003 B1
6657297 Jewram et al. Dec 2003 B1
6673434 Nguyen Jan 2004 B2
6706219 Nguyen Mar 2004 B2
6761928 Hill et al. Jul 2004 B2
6764759 Duvall et al. Jul 2004 B2
6783692 Bhagwagar Aug 2004 B2
6791839 Bhagwagar Sep 2004 B2
6797382 Nguyen et al. Sep 2004 B2
6797758 Misra et al. Sep 2004 B2
6811725 Nguyen et al. Nov 2004 B2
6815486 Bhagwagar et al. Nov 2004 B2
6835453 Greenwood et al. Dec 2004 B2
6838182 Kropp et al. Jan 2005 B2
6874573 Collins et al. Apr 2005 B2
6900163 Khatri May 2005 B2
6908669 Nguyen Jun 2005 B2
6908682 Mistele Jun 2005 B2
6913686 Hilgarth Jul 2005 B2
6926955 Jayaraman et al. Aug 2005 B2
6940721 Hill Sep 2005 B2
6946190 Bunyan Sep 2005 B2
6975944 Zenhausern Dec 2005 B1
6984685 Misra et al. Jan 2006 B2
7013965 Zhong et al. Mar 2006 B2
7056566 Freuler et al. Jun 2006 B2
7074490 Feng et al. Jul 2006 B2
7078109 Hill et al. Jul 2006 B2
7135232 Yamada et al. Nov 2006 B2
7147367 Balian et al. Dec 2006 B2
7172711 Nguyen Feb 2007 B2
7241707 Meagley et al. Jul 2007 B2
7244491 Nguyen Jul 2007 B2
7291396 Huang et al. Nov 2007 B2
7294394 Jayaraman et al. Nov 2007 B2
RE39992 Misra et al. Jan 2008 E
7328547 Mehta et al. Feb 2008 B2
7369411 Hill et al. May 2008 B2
7462294 Kumar et al. Dec 2008 B2
7465605 Raravikar et al. Dec 2008 B2
7550097 Tonapi et al. Jun 2009 B2
7572494 Mehta et al. Aug 2009 B2
7641811 Kumar et al. Jan 2010 B2
7682690 Bunyan et al. Mar 2010 B2
7695817 Lin et al. Apr 2010 B2
7700943 Raravikar et al. Apr 2010 B2
7744991 Fischer et al. Jun 2010 B2
RE41576 Bunyan et al. Aug 2010 E
7816785 Iruvanti et al. Oct 2010 B2
7646778 Rumer et al. Dec 2010 B2
7850870 Ahn et al. Dec 2010 B2
7867609 Nguyen Jan 2011 B2
7955900 Jadhav et al. Jun 2011 B2
7960019 Jayaraman et al. Jun 2011 B2
8039961 Suhir et al. Oct 2011 B2
8076773 Jewram et al. Dec 2011 B2
8081468 Hill et al. Dec 2011 B2
8105504 Gerster et al. Jan 2012 B2
8110919 Jewram et al. Feb 2012 B2
8138239 Prack et al. Mar 2012 B2
8223498 Lima Jul 2012 B2
8308861 Rolland et al. Nov 2012 B2
8324313 Funahashi Dec 2012 B2
8373283 Masuko et al. Feb 2013 B2
8431647 Dumont et al. Apr 2013 B2
8431655 Dershem Apr 2013 B2
8445102 Strader et al. May 2013 B2
8518302 Gerster et al. Aug 2013 B2
8535478 Pouchelon et al. Sep 2013 B2
8535787 Lima Sep 2013 B1
8557896 Jeong et al. Oct 2013 B2
8586650 Zhang et al. Nov 2013 B2
8587945 Hartmann et al. Nov 2013 B1
8618211 Bhagwagar et al. Dec 2013 B2
8632879 Weisenberger Jan 2014 B2
8633478 Cummings et al. Jan 2014 B2
8638001 Kimura et al. Jan 2014 B2
8647752 Strader et al. Feb 2014 B2
8758892 Bergin et al. Jun 2014 B2
8796068 Stender et al. Aug 2014 B2
8837151 Hill et al. Sep 2014 B2
8865800 Stammer et al. Oct 2014 B2
8917510 Boday et al. Dec 2014 B2
8937384 Bao et al. Jan 2015 B2
9055694 Lima Jun 2015 B2
9070660 Lowe et al. Jun 2015 B2
9080000 Ahn et al. Jul 2015 B2
9222735 Hill et al. Dec 2015 B2
9260645 Bruzda Feb 2016 B2
9392730 Hartmann et al. Jul 2016 B2
9481851 Matsumoto et al. Nov 2016 B2
9527988 Habimana et al. Dec 2016 B2
9537095 Stender et al. Jan 2017 B2
9593209 Dent et al. Mar 2017 B2
9593275 Tang et al. Mar 2017 B2
9598575 Bhagwagar et al. Mar 2017 B2
10155894 Liu et al. Dec 2018 B2
20020018885 Takahashi et al. Feb 2002 A1
20020132896 Nguyen Sep 2002 A1
20030112603 Roesner et al. Jun 2003 A1
20030128521 Matayabas, Jr. Jul 2003 A1
20030151030 Gurin Aug 2003 A1
20030159938 Hradil Aug 2003 A1
20030203181 Ellsworth et al. Oct 2003 A1
20030207064 Bunyan et al. Nov 2003 A1
20030207128 Uchiya et al. Nov 2003 A1
20030230403 Webb Dec 2003 A1
20040069454 Bonsignore et al. Apr 2004 A1
20040097635 Fan et al. May 2004 A1
20040149587 Hradil Aug 2004 A1
20040161571 Duvall et al. Aug 2004 A1
20040206941 Gurin Oct 2004 A1
20050020738 Jackson et al. Jan 2005 A1
20050025984 Odell et al. Feb 2005 A1
20050072334 Czubarow et al. Apr 2005 A1
20050148721 Tonapi et al. Jul 2005 A1
20050228097 Zhong Oct 2005 A1
20050287362 Garcia-Ramirez et al. Dec 2005 A1
20060057364 Nguyen Mar 2006 A1
20060094809 Simone May 2006 A1
20060208354 Liu et al. Sep 2006 A1
20060228542 Czubarow Oct 2006 A1
20060260948 Zschintzsch et al. Nov 2006 A2
20060264566 Cassar et al. Nov 2006 A1
20070051773 Ruchert et al. Mar 2007 A1
20070097651 Canale et al. May 2007 A1
20070131913 Cheng et al. Jun 2007 A1
20070161521 Sachdev et al. Jul 2007 A1
20070164424 Dean et al. Jul 2007 A1
20070179232 Collins et al. Aug 2007 A1
20070249753 Lin et al. Oct 2007 A1
20080044670 Nguyen Feb 2008 A1
20080116416 Chacko May 2008 A1
20080141629 Alper et al. Jun 2008 A1
20080149176 Sager et al. Jun 2008 A1
20080291634 Weiser Nov 2008 A1
20060302064 Rauch Dec 2008
20090111925 Burnham et al. Apr 2009 A1
20090184283 Chung et al. Jul 2009 A1
20100048435 Yamagata et al. Feb 2010 A1
20100048438 Carey et al. Feb 2010 A1
20100075135 Kendall Mar 2010 A1
20100129648 Xu et al. May 2010 A1
20100197533 Kendall et al. Aug 2010 A1
20110121435 Mitsukura et al. May 2011 A1
20110141698 Chiou et al. Jun 2011 A1
20110187009 Masuko et al. Aug 2011 A1
20110192564 Mommer et al. Aug 2011 A1
20110204280 Bruzda Aug 2011 A1
20110265979 Chen et al. Nov 2011 A1
20110294958 Ahn et al. Dec 2011 A1
20110308782 Merrill et al. Dec 2011 A1
20120060826 Weisenberger Mar 2012 A1
20120195822 Werner et al. Aug 2012 A1
20120253033 Boucher et al. Oct 2012 A1
20120285673 Cola et al. Nov 2012 A1
20120288725 Tanaka et al. Nov 2012 A1
20130199724 Dershem Aug 2013 A1
20130248163 Bhagwagar et al. Sep 2013 A1
20130265721 Strader et al. Oct 2013 A1
20130288462 Stender et al. Oct 2013 A1
20130299140 Ling et al. Nov 2013 A1
20140190672 Swaroop et al. Jul 2014 A1
20150125646 Tournilhac et al. May 2015 A1
20150138739 Hishiki May 2015 A1
20150158982 Saito et al. Jun 2015 A1
20150183951 Bhagwagar et al. Jul 2015 A1
20150275060 Kuroda et al. Oct 2015 A1
20150279762 Lowe et al. Oct 2015 A1
20160160102 Minegishi et al. Jun 2016 A1
20160160104 Bruzda et al. Jun 2016 A1
20160226114 Hartmann et al. Aug 2016 A1
20160272839 Yamamoto et al. Sep 2016 A1
20170009362 Werner et al. Jan 2017 A1
20170107415 Shiono Apr 2017 A1
20170137685 Liu et al. May 2017 A1
20170167716 Ezaki et al. Jun 2017 A1
20170226396 Yang et al. Aug 2017 A1
20170317257 Ezaki et al. Nov 2017 A1
20170321100 Zhang et al. Nov 2017 A1
20180030328 Zhang et al. Feb 2018 A1
20180085977 Ezaki Mar 2018 A1
20180194982 Ezaki et al. Jul 2018 A1
20180267315 Yonemura Sep 2018 A1
20180358283 Zhang et al. Dec 2018 A1
20190048245 Liu et al. Feb 2019 A1
20190078007 Zhang et al. Mar 2019 A1
Foreign Referenced Citations (104)
Number Date Country
2311067 Jan 2001 CA
1407141 Apr 2003 CN
1456710 Nov 2003 CN
1549875 Nov 2004 CN
1970666 May 2007 CN
101067030 Nov 2007 CN
101090922 Dec 2007 CN
101445627 Jun 2009 CN
101735619 Jun 2010 CN
101835830 Sep 2010 CN
102134474 Jul 2011 CN
102341474 Feb 2012 CN
102627943 Aug 2012 CN
102634212 Aug 2012 CN
102348763 Apr 2013 CN
103087389 May 2013 CN
103102552 May 2013 CN
103102689 May 2013 CN
103131138 Jun 2013 CN
103214848 Jul 2013 CN
103254647 Aug 2013 CN
103333447 Oct 2013 CN
103409116 Nov 2013 CN
103436027 Dec 2013 CN
103709757 Apr 2014 CN
103756631 Apr 2014 CN
103773322 May 2014 CN
103849356 Jun 2014 CN
103865271 Jun 2014 CN
104098914 Oct 2014 CN
104140678 Nov 2014 CN
104152103 Nov 2014 CN
104449550 Mar 2015 CN
104497574 Apr 2015 CN
104513487 Apr 2015 CN
104804705 Jul 2015 CN
104861661 Aug 2015 CN
105111750 Dec 2015 CN
105349113 Feb 2016 CN
105419339 Mar 2016 CN
105670555 Jun 2016 CN
105838322 Aug 2016 CN
105925243 Sep 2016 CN
105980512 Sep 2016 CN
107057370 Aug 2017 CN
1224669 Jul 2002 EP
1149519 Nov 2004 EP
1514956 Mar 2005 EP
1629059 Mar 2006 EP
2194165 Jun 2010 EP
2848215 Jun 2004 FR
2508320 May 2014 GB
57027188 Jun 1982 JP
0543116 May 1986 JP
3662715 Jan 1991 JP
02611364 May 1997 JP
2000143808 May 2000 JP
2001139818 May 2001 JP
2002003830 Jan 2002 JP
100479857 Jul 2003 JP
2007002002 Jan 2007 JP
4016326 Dec 2007 JP
2008063412 Mar 2008 JP
5269366 Mar 2009 JP
2009102577 May 2009 JP
5137538 Jun 2009 JP
2009138036 Jun 2009 JP
4288469 Jul 2009 JP
5607298 Mar 2010 JP
5390202 Aug 2010 JP
2010248277 Nov 2010 JP
2010278115 Dec 2010 JP
5318733 Jun 2011 JP
2011165792 Aug 2011 JP
5687167 Apr 2013 JP
5463116 Apr 2014 JP
5944306 Jul 2014 JP
5372270 Sep 2014 JP
2014194006 Oct 2014 JP
20070116654 Dec 2007 KR
201527309 Jul 2015 TW
1997026297 Jul 1997 WO
WO0120618 Mar 2001 WO
WO03052818 Jun 2003 WO
2003064148 Aug 2003 WO
2004008497 Jan 2004 WO
2004022330 Mar 2004 WO
WO2005021257 Mar 2005 WO
200511146 Nov 2005 WO
2005119771 Dec 2005 WO
WO2006023860 Mar 2006 WO
2007027670 Mar 2007 WO
2006014171 Jan 2008 WO
WO2008103219 Aug 2008 WO
2008121491 Oct 2008 WO
2008121970 Oct 2008 WO
2009032212 Mar 2009 WO
2013191116 Dec 2013 WO
2014007119 Jan 2014 WO
2014160067 Oct 2014 WO
2015179056 Nov 2015 WO
2016004565 Jan 2016 WO
2016103424 Jun 2016 WO
WO2018068222 Apr 2018 WO
Non-Patent Literature Citations (33)
Entry
Wacker Silicones, Catalyst EP/Inhibitor PT 88 product data sheet, p. 1-3, Oct. 6, 2008.
“Dynasylan 1146: Oligomeric Diamino-Silane-System” Evonik Industries, pp. 1-3, 2008.
“Semicosil 9212A” Wacker Silicones Material Safety Data Sheet, pp. 1-8, printed Dec. 11, 2009.
“Semicosil 9212B.” Wacker Silicones Material Safety Data Sheet, pp. 1-8, printed Dec. 11, 2009.
Extended European Search Report issued in EP Application No. 14897036.1, dated Jul. 2, 2018, 7 pages.
Extended Search Report issued in EP Application 14907530.1, dated Jun. 27, 2018, 9 pages.
Fink, Johannes Karl. “Chapter 18: Metal Deactivators.” in: A Concise Introduction to Additives for Thermoplastic Polymers, Wiley-Scrivener, pp. 165-171, Jan. 1, 2010.
Singaporean Search Report and Written Opinion issued in SG Application No. 11201704238Y, completed May 18, 2018, 9 pages.
“Hi-Flow 225F-AC Reinforced, Phase Change Thermal Interlace Material,” The Bergquist Company, 1 page, available at least as early as the filing date of the present application.
“THERM-A-GAP HCS10,569,570,579 and 580 Thermally Conductive Gap Filler Pads,” Parker Chomerics, Engineering Your Success, pp. 11-12, available at least as early as the filing date of the present application.
Aranzabe, Estibaliz, et al. “More than Color: Pigments with Thermal Storage Capacity; Processing and Degradation Behavior.” Advances in Materials Physics and Chemistry, 5:171-184, 2015.
Extended European Search Report issued in EP Application 14867847.7, dated Jun. 26, 2017, 7 pages.
Gowda, Arun, et al. “Choosing the Right Thermal Interface Material.” Solid State Technology, Insights for Electronics Manufacturing, Online Blog, 9 pages, 2005. Retrieved May 25, 2017 from the Internet <http://electroiq.com/blog/2005/03/choosing-the-right-therrnal-interface-material/.
International Search Report and Written Opinion issued in PCT/CN2014/081724. dated Apr. 1, 2015, 12 pages.
International Search Report and Written Opinion issued in PCT/CN2014/093138, dated Sep. 6 2015, 8 pages.
International Search Report and Written Opinion issued in PCT/CN2016/101874, dated Apr. 28, 2017, 12 pages.
International Search Report and Written Opinion issued in PCT/US2014/068033, dated Mar. 26, 2015, 12 pages.
International Search Report and Written Opinion issued in PCT/US2017/041498, dated Oct. 20, 2017, 10 pages.
Martyak et al., On the oxidation of tin(II) in methanesulfonate solutions and the role of sulfate, Gaivanotechnik (2005), 96(3), 594-601 (Abstract).
Ping, Ding, et al, “Preparation and Application Research of Novel Silicone Gel for High-Power IGBT.” Insulating Materials, 47(2):52-55, Chinese text with English translation of Abstract, 2014.
Ramaswamy et al., Phase change materials as a viable thermal interface material for high-power electronic applications.
Ramaswamy, C., et al. “Phase Change Materials as a Viable Thermal Interface Material for High-Power Electronic Applications.” The Ninth Intersociety Conference on Thermal and Thermomechanical Phenomena in Electronic Systems, IEEE, 2:687-691, 2004.
Search Report issued in CN application 201480066502.2, dated May 18, 2017, 2 pages.
Dow Coming® Two-Part RTV Silicone Sealant: Total Assembly Solutions for Home Appliance Production; www.dowcoming.com; Form No. 80-3375-01; 6 pages.
Evonik, Silanes for Adhesives and Sealants, 2013, p. 1-24.
International Preliminary Report on Patentability issued in PCT/CN2016/075827, dated Sep. 20, 2018, 5 pages.
International Search Report and Written Opinion issued in PCT/CN2016/075827, dated Dec. 1, 2016, 7 pages.
International Search Report and Written Opinion issued in PCT/US2018/049218, dated Dec. 28, 2018, 13 pages.
International Search Report and Written Opinion issued in PCT/US2018/056870, dated Feb. 8, 2019, 9 pages.
Singaporean Written Opinion issued in SG Application No. 11201704238Y, completed Feb. 7, 2019, 7 pages.
Yasuhiro Aoyagi et al., “Effects of antioxidants and the solild component on the thermal stability of polyol-ester-based thermal pastes”, J Mater Sci (2007) 42:2358-2375; Mar. 12, 2007.
Yasuhiro Aoyagi et al., “Polyol-Based Phase-Change Thermal Interface Materials”, Journal of Electronic Materials, vol. 35, No. 3, (2006); pp. 416-424.
Yunsheng Xu et al., “Lithium Doped Polyethylene-Glycol-Based Thermal Interface Pastes for High Thermal Contact Conductance”, Transactions of the ASME; Journal of Electronic Packagiing, vol. 124, Sep. 2002; pp. 188-191.
Related Publications (1)
Number Date Country
20180030327 A1 Feb 2018 US
Provisional Applications (2)
Number Date Country
62436746 Dec 2016 US
62366704 Jul 2016 US