WO2024254770A1 - Dispersion of a wax in an alkyl methyl siloxane fluid - Google Patents

Dispersion of a wax in an alkyl methyl siloxane fluid Download PDF

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Publication number
WO2024254770A1
WO2024254770A1 PCT/CN2023/100044 CN2023100044W WO2024254770A1 WO 2024254770 A1 WO2024254770 A1 WO 2024254770A1 CN 2023100044 W CN2023100044 W CN 2023100044W WO 2024254770 A1 WO2024254770 A1 WO 2024254770A1
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Prior art keywords
alkyl
dispersion
wax
composition
phase change
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PCT/CN2023/100044
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French (fr)
Inventor
Peng Wei
Dorab Bhagwagar
Zhengming TANG
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Dow Global Technologies LLC
Dow Silicones Corp
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Dow Global Technologies LLC
Dow Silicones Corp
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Priority to KR1020257041626A priority Critical patent/KR20260022320A/en
Priority to CN202380098285.4A priority patent/CN121127519A/en
Priority to EP23941008.7A priority patent/EP4727991A1/en
Priority to PCT/CN2023/100044 priority patent/WO2024254770A1/en
Priority to TW113119452A priority patent/TW202506892A/en
Publication of WO2024254770A1 publication Critical patent/WO2024254770A1/en
Anticipated expiration legal-status Critical
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K5/00Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
    • C09K5/02Materials undergoing a change of physical state when used
    • C09K5/06Materials undergoing a change of physical state when used the change of state being from liquid to solid or vice versa
    • C09K5/063Materials absorbing or liberating heat during crystallisation; Heat storage materials
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/01Hydrocarbons
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L83/00Compositions 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
    • C08L83/04Polysiloxanes
    • GPHYSICS
    • G06COMPUTING OR CALCULATING; COUNTING
    • G06FELECTRIC DIGITAL DATA PROCESSING
    • G06F1/00Details not covered by groups G06F3/00 - G06F13/00 and G06F21/00
    • G06F1/16Constructional details or arrangements
    • G06F1/20Cooling means
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/04Polysiloxanes
    • GPHYSICS
    • G06COMPUTING OR CALCULATING; COUNTING
    • G06FELECTRIC DIGITAL DATA PROCESSING
    • G06F2200/00Indexing scheme relating to G06F1/04 - G06F1/32
    • G06F2200/20Indexing scheme relating to G06F1/20
    • G06F2200/201Cooling arrangements using cooling fluid

Definitions

  • the present invention relates to a composition
  • a composition comprising a dispersion of a wax in an alkyl methyl siloxane fluid continuous phase.
  • the composition is useful as an immersion cooling fluid for data centers.
  • Immersion cooling where all the data center components are immersed in a dielectric (non-electrically conducting) fluid, is expected to replace air-cooling in the next few years.
  • dielectric fluids suitable as immersion coolants include fluorinated fluids such as hydrofluoroethers and fluoroketones.
  • fluorinated fluids such as hydrofluoroethers and fluoroketones.
  • the dielectric and chemical inertness of fluorinated fluids make them particularly attractive as heat transfer media, along their wide range of boiling points, low viscosities, low pour points, low surface tension, high thermal and chemical stability as well as compatibility with metals, plastics, and elastomers.
  • These fluids are further advantaged by being odorless, non-flammable, non-explosive, and virtually non-toxic.
  • fluorinated fluids use the latent heat of the phase transition to extract heat from CPUs and GPUs.
  • Silicone fluids are another class dielectric fluids that show promise as immersion cooling fluids. Like fluorinated fluids, they exhibit low viscosity, low dielectric properties, thermal stability, low flammability, chemical inertness, and low toxicity. Silicone fluids have the additional advantage of being environmentally impermanent; however, as single-phase fluids, they extract heat much less efficiently than fluorinated fluids. It would therefore be an advantage in the field of immersion cooling fluids to discover a medium that meets property and environmental demands.
  • the present invention addresses a need by providing a composition comprising a dispersion of a C 16 -C 28 hydrocarbon wax in an alkyl methyl silicone fluid continuous phase of Formula 1:
  • R and R 1 are each independently methyl or C 6 -C 18 -alkyl, with the proviso that at least one of R and R 1 is C 6 -C 18 -alkyl; where m is from 1 to 20; and n is from 0 to 10; with the further proviso that when n is 0, one or both of the R 1 groups is C 6 -C 18 -alkyl; where the relative amounts of the wax and the alkyl methyl silicone fluid are such that the viscosity of the dispersion is in the range of from 10 cSt to 100 cSt and the phase change energy absorbed of the dispersion is at least 12 J/g.
  • the composition of the present invention is useful as a 2-phase immersion coolant.
  • the present invention is a composition comprising a dispersion of a C 16 -C 28 hydrocarbon wax in an alkyl methyl silicone fluid continuous phase of Formula 1:
  • R and R 1 are each independently methyl or C 6 -C 18 -alkyl, with the proviso that at least one of R and R 1 is C 6 -C 18 -alkyl; where m is from 1 to 20; and n is from 0 to 10; with the further proviso that when n is 0, one or both of the R 1 groups is C 6 -C 18 -alkyl; where the relative amounts of the wax and the alkyl methyl silicone fluid are such that the viscosity of the dispersion is in the range of from 10 cSt to 100 cSt and the phase change energy absorbed of the dispersion is at least 12 J/g.
  • the composition of the present invention is useful as a 2-phase immersion coolant.
  • the wax may be a single wax or a combination of C 16 -C 28 hydrocarbon waxes having a melting point preferably in the range of from 18 °C to 65 °C.
  • each R 1 is methyl, n is from 1 to 10, m is from 1 or from 2, to 10 or to 5; and each R is C 6 -C 18 alkyl, preferably C 8 -C 16 alkyl; in a second aspect, n is 0; and at least one of R 1 is C 6 -C 18 alkyl, preferably each of R 1 is C 8 -C 16 alkyl; and in a third aspect, n is from 1 to 10; at least one of R 1 is C 6 -C 18 alkyl, preferably each of R 1 is C 8 -C 16 alkyl; and each R is C 6 -C 18 alkyl, preferably C 8 -C 16 alkyl.
  • R and R 1 are C 6 -C 18 groups
  • R and R 1 are preferably linear C 6 -C 18
  • Compounds of Formula 1 can be prepared by the catalytic hydrosilylation of a 1-alkene with an organohydrogenpolysiloxane containing internal Si-H groups:
  • Other compounds of Formula 1 can be prepared from the hydrosilylation of an alkene with an organohydrogenpolysiloxane containing terminal Si-H groups or terminal and internal Si-H groups.
  • the dispersion exhibits a phase change energy absorbed as determined by dynamic scanning calorimetric thermal analysis (DSC) of greater than 12 J/g, preferably in the range of from 12 J/g to 150 J/g or to 120 J/g or to 110 J/g.
  • the dispersion has a phase change temperature maximum, as determined by DSC preferably in the range of from 5 °C to 60 °C for both heating and cooling cycles.
  • FIG. 1 is a DSC of a dispersion containing 77 parts by weight (pbw) of a compound of Formula 1, where R is n-hexadecyl, m is 3, and n is 6; 18 pbw of a C 18 hydrocarbon wax, and 5 pbw of a C 22 hydrocarbon wax.
  • the peak temperature of the cooling scan (10.3 °C) , the peak temperature of the heating scan (19.9 °C) , and the phase change energy absorbed (105.9 J/g) all exceeded the physical property requirements for the composition.
  • composition of the present invention addresses a need in the art by providing compositions that have all the property advantages of fluorinated fluids without the environmental drawbacks.
  • the example and comparative example cooling fluids were prepared by mixing an alkyl methyl silicone fluid with one or more waxes for 30 min using a magnetic stirrer. Sample viscosities at 25 °C, phase change temperature maxima for the cool and heating cycles, and phase change energy absorbed were measured by the following methods.
  • Viscosity was measured with a DHR-III viscometer using a 25-mm parallel plate. The flow temperature was ramped from 25 °C to 150 °C at a rate of 3 °C/min and a shear rate of 200 s -1 .
  • Phase change temperature maxima and phase change energy absorbed were measured using a DSC-Q2000 instrument as follows:
  • the sample was equilibrated at -80.00 °C. Data storage was turned on and the temperature was ramped to 70.00 °C at a rate of 10 °C/min to complete the first cycle. The temperature was then decreased to 80.00 °C at the rate of 10 °C/min and maintained at this temperature for 3.00 min to complete the second cycle. Finally, the temperature was ramped to 70.00 °C at a rate of 10 °C/min to complete the third cycle.
  • Heat removal from a device using the two-phase immersion coolant of the present invention is accomplished in two ways.
  • the alkyl methyl silicone fluid continuous phase removes heat from the hot device by virtue of having a lower temperature than the device.
  • the phase change energy absorbed by virtue of the melting of the wax disperse phase upon heating provides a second mechanism for heat removal. The higher the phase change energy absorbed, the more efficient the heat removal from the device.
  • Phase change energy absorbed is calculated by integrating the area under the fusion heat flow endotherm as a function of temperature (enthalpy, See FIG. 1) , then dividing the enthalpy by the mass of the test specimen.
  • Silicone oil is a silicone fluid with a viscosity of 20 cSt. at 25 °C.
  • AMS-C8 refers to an alkyl methyl silicone of Formula 1 where R is n-octyl, each R 1 is methyl, m is 3, and n is 6; and
  • AMS-C16 refers to an alkyl methyl silicone of Formula 1 where R is n-hexadecyl, each R 1 is methyl, m is 3, and n is 6.
  • the C 16 hydrocarbon wax (C 16 wax) had a melting point (m. p. ) of 18.2 °C; the C 18 hydrocarbon wax (C 18 wax) had an m. p. of 28.18 °C; the C 22 hydrocarbon wax (C 22 wax) had an m. p. of 42 °C to 45 °C; and the C 24-28 hydrocarbon wax (C 24-28 wax) had an m. p. of 49 °C to 64 °C.
  • refers to the viscosity in cSt at 25 °C
  • T c max refers to the phase change maximum temperature for the cooling cycle
  • T h max refers to the phase change maximum temperature for the heating cycle
  • E a refers to the phase change energy absorbed in J/g.
  • Viscosities in the range of 10 cSt. to 100 cSt., temperatures of phase change maxima in the range of 5°C to 60 °C, and phase change energy absorbed values of > 12 J/g were targeted properties of the immersion coolant. All amounts are weight percentages based on the weight of the composition.

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  • Polymers & Plastics (AREA)
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Abstract

Disclosed is a composition which comprising a dispersion of a C 16-C 28 hydrocarbon wax in an alkyl methyl silicone fluid continuous phase of Formula 1: Formula 1 where R, R 1, m, and n are defined herein. The relative amounts of the wax and the alkyl methyl silicone fluid are such that the viscosity of the dispersion is in the range of from 10 cSt to 100 cSt and the phase change energy absorbed of the dispersion is at least 12 J/g. The composition is useful as a 2-phase immersion cooling fluid.

Description

Dispersion of a Wax in an Alkyl Methyl Siloxane Fluid Background of the Invention
The present invention relates to a composition comprising a dispersion of a wax in an alkyl methyl siloxane fluid continuous phase. The composition is useful as an immersion cooling fluid for data centers.
Data centers consume vast amounts of energy. Currently, most data centers are air cooled, which is highly inefficient. In a typical data center, only 60%of the total energy is consumed for computation/information requests, data storage, and networking, while 40%is used to remove heat generated by electronic components.
Immersion cooling, where all the data center components are immersed in a dielectric (non-electrically conducting) fluid, is expected to replace air-cooling in the next few years. Examples of dielectric fluids suitable as immersion coolants include fluorinated fluids such as hydrofluoroethers and fluoroketones. The dielectric and chemical inertness of fluorinated fluids make them particularly attractive as heat transfer media, along their wide range of boiling points, low viscosities, low pour points, low surface tension, high thermal and chemical stability as well as compatibility with metals, plastics, and elastomers. These fluids are further advantaged by being odorless, non-flammable, non-explosive, and virtually non-toxic. Moreover, as two-phase immersion fluids that transition from a liquid phase to a vapor phase below the operating temperature of the heat generating components in the server (CPUs and GPUs) , fluorinated fluids use the latent heat of the phase transition to extract heat from CPUs and GPUs.
Nevertheless, fluorinated fluids are encumbered by their relatively high vapor pressures, long atmospheric lifetimes, and relatively strong absorbance of infra-red radiation, all of which contribute to severe global warming potential of these fluids. Losses due to evaporation or leakage due to the low fluid surface tension also pose environmental hazards.
Silicone fluids are another class dielectric fluids that show promise as immersion cooling fluids. Like fluorinated fluids, they exhibit low viscosity, low dielectric properties, thermal stability, low flammability, chemical inertness, and low toxicity. Silicone fluids have the additional advantage of being environmentally impermanent; however, as single-phase fluids, they extract  heat much less efficiently than fluorinated fluids. It would therefore be an advantage in the field of immersion cooling fluids to discover a medium that meets property and environmental demands.
Background of the Invention
The present invention addresses a need by providing a composition comprising a dispersion of a C16-C28 hydrocarbon wax in an alkyl methyl silicone fluid continuous phase of Formula 1:
where R and R1 are each independently methyl or C6-C18-alkyl, with the proviso that at least one of R and R1 is C6-C18-alkyl; where m is from 1 to 20; and n is from 0 to 10; with the further proviso that when n is 0, one or both of the R1 groups is C6-C18-alkyl; where the relative amounts of the wax and the alkyl methyl silicone fluid are such that the viscosity of the dispersion is in the range of from 10 cSt to 100 cSt and the phase change energy absorbed of the dispersion is at least 12 J/g. The composition of the present invention is useful as a 2-phase immersion coolant.
Brief Description of Drawings
FIG. 1 is a dynamic scanning calorimetric thermal analysis of a dispersion of waxes in an alkyl methyl silicone fluid continuous phase.
Detailed Description of the Invention
The present invention is a composition comprising a dispersion of a C16-C28 hydrocarbon wax in an alkyl methyl silicone fluid continuous phase of Formula 1:
where R and R1 are each independently methyl or C6-C18-alkyl, with the proviso that at least one of R and R1 is C6-C18-alkyl; where m is from 1 to 20; and n is from 0 to 10; with the further proviso that when n is 0, one or both of the R1 groups is C6-C18-alkyl; where the relative amounts of the wax and the alkyl methyl silicone fluid are such that the viscosity of the dispersion is in the range of from 10 cSt to 100 cSt and the phase change energy absorbed of the dispersion is at least 12 J/g. The composition of the present invention is useful as a 2-phase immersion coolant.
The wax may be a single wax or a combination of C16-C28 hydrocarbon waxes having a melting point preferably in the range of from 18 ℃ to 65 ℃. In one aspect, each R1 is methyl, n is from 1 to 10, m is from 1 or from 2, to 10 or to 5; and each R is C6-C18 alkyl, preferably C8-C16 alkyl; in a second aspect, n is 0; and at least one of R1 is C6-C18 alkyl, preferably each of R1 is C8-C16 alkyl; and in a third aspect, n is from 1 to 10; at least one of R1 is C6-C18 alkyl, preferably each of R1 is C8-C16 alkyl; and each R is C6-C18 alkyl, preferably C8-C16 alkyl. Where R and R1 are C6-C18 groups, R and R1 are preferably linear C6-C18 groups.
Compounds of Formula 1 can be prepared by the catalytic hydrosilylation of a 1-alkene with an organohydrogenpolysiloxane containing internal Si-H groups:
Other compounds of Formula 1 can be prepared from the hydrosilylation of an alkene with an organohydrogenpolysiloxane containing terminal Si-H groups or terminal and internal Si-H groups.
The viscosity and the phase change energy absorbed of the dispersion can be readily tuned to the desired levels by adjusting the proportion of the wax to the alkyl methyl silicone fluid. In general, the weight-to-weight ratio of the wax to the alkyl methyl silicone fluid is in the range of from 3∶97 or from 5∶95 or from 7∶93, to 25∶75 or to 20∶80 or to 15∶85. The wax and the alkyl methyl silicone fluid preferably comprise at least 90 or 95 or 99 or 100 percent of the composition. The composition may optionally further comprise low dielectric and low viscosity fluids such as hydrocarbon and fluorocarbon fluids.
The dispersion exhibits a phase change energy absorbed as determined by dynamic scanning calorimetric thermal analysis (DSC) of greater than 12 J/g, preferably in the range of from 12 J/g to 150 J/g or to 120 J/g or to 110 J/g. The dispersion has a phase change temperature maximum, as determined by DSC preferably in the range of from 5 ℃ to 60 ℃ for both heating and cooling cycles. FIG. 1 is a DSC of a dispersion containing 77 parts by weight (pbw) of a compound of Formula 1, where R is n-hexadecyl, m is 3, and n is 6; 18 pbw of a C18 hydrocarbon wax, and 5 pbw of a C22 hydrocarbon wax. The peak temperature of the cooling scan (10.3 ℃) , the peak temperature of the heating scan (19.9 ℃) , and the phase change energy absorbed (105.9 J/g) all exceeded the physical property requirements for the composition.
The composition of the present invention addresses a need in the art by providing compositions that have all the property advantages of fluorinated fluids without the environmental drawbacks.
Examples
The example and comparative example cooling fluids were prepared by mixing an alkyl methyl silicone fluid with one or more waxes for 30 min using a magnetic stirrer. Sample viscosities at 25 ℃, phase change temperature maxima for the cool and heating cycles, and phase change energy absorbed were measured by the following methods.
Viscosity measurements
Viscosity was measured with a DHR-III viscometer using a 25-mm parallel plate. The flow temperature was ramped from 25 ℃ to 150 ℃ at a rate of 3 ℃/min and a shear rate of 200 s-1.
Phase Change Measurements
Phase change temperature maxima and phase change energy absorbed were measured using a DSC-Q2000 instrument as follows:
The sample was equilibrated at -80.00 ℃. Data storage was turned on and the temperature was ramped to 70.00 ℃ at a rate of 10 ℃/min to complete the first cycle. The temperature was then decreased to 80.00 ℃ at the rate of 10 ℃/min and maintained at this temperature for 3.00 min to complete the second cycle. Finally, the temperature was ramped to 70.00 ℃ at a rate of 10 ℃/min to complete the third cycle.
Heat removal from a device using the two-phase immersion coolant of the present invention is accomplished in two ways. First, the alkyl methyl silicone fluid continuous phase removes heat from the hot device by virtue of having a lower temperature than the device. Second, the phase change energy absorbed by virtue of the melting of the wax disperse phase upon heating provides a second mechanism for heat removal. The higher the phase change energy absorbed, the more efficient the heat removal from the device.
Phase change energy absorbed is calculated by integrating the area under the fusion heat flow endotherm as a function of temperature (enthalpy, See FIG. 1) , then dividing the enthalpy by the mass of the test specimen.
Table 1 illustrates the properties of the immersion fluids. Silicone oil (Silicone) is a silicone fluid with a viscosity of 20 cSt. at 25 ℃. AMS-C8 refers to an alkyl methyl silicone of Formula 1 where R is n-octyl, each R1 is methyl, m is 3, and n is 6; and AMS-C16 refers to an alkyl methyl silicone of Formula 1 where R is n-hexadecyl, each R1 is methyl, m is 3, and n is 6.
The C16 hydrocarbon wax (C16 wax) had a melting point (m. p. ) of 18.2 ℃; the C18 hydrocarbon wax (C18 wax) had an m. p. of 28.18 ℃; the C22 hydrocarbon wax (C22 wax) had an m. p. of 42 ℃ to 45 ℃; and the C24-28 hydrocarbon wax (C24-28 wax) had an m. p. of 49 ℃ to 64 ℃.
η refers to the viscosity in cSt at 25 ℃; Tc max refers to the phase change maximum temperature for the cooling cycle; Th max refers to the phase change maximum temperature for the heating cycle; and Ea refers to the phase change energy absorbed in J/g. Viscosities in the range of 10 cSt. to 100 cSt., temperatures of phase change maxima in the range of 5℃ to 60 ℃, and  phase change energy absorbed values of > 12 J/g were targeted properties of the immersion coolant. All amounts are weight percentages based on the weight of the composition.
Table 1-Properties of Immersion Fluids
The data show that the viscosity, the phase change maximum temperatures, and the phase change energy absorbed can be tuned to the desired targets by adjusting the relative amounts and types of waxes and alkyl methyl siloxanes. In contrast, the blend of silicone oil and wax gave unacceptably low phase change maximum cooling and heating temperatures as well as unacceptably low phase change energy absorbed.

Claims (7)

  1. A composition comprising a dispersion of a C16-C28 hydrocarbon wax in an alkyl methyl silicone fluid continuous phase of Formula 1:
    where R and R1 are each independently methyl or C6-C18-alkyl, with the proviso that at least one of R and R1 is C6-C18-alkyl; where m is from 1 to 20; and n is from 0 to 10; with the further proviso that when n is 0, one or both of the R1 groups is C6-C18-alkyl; where the relative amounts of the wax and the alkyl methyl silicone fluid are such that the viscosity of the dispersion is in the range of from 10 cSt to 100 cSt and the phase change energy absorbed of the dispersion is at least 12 J/g.
  2. The composition of Claim 1 wherein the phase change energy absorbed of the dispersion is in the range of from 12 J/g to 150 J/g; the weight-to-weight ratio of the wax to the alkyl methyl silicone fluid is in the range of from 3: 97 to 25: 75.
  3. The composition of Claim 2 wherein n is from 1 to 10; m is from 2 to 10; and each R1 is a methyl group, wherein the weight-to-weight ratio of the wax to the alkyl methyl silicone fluid is in the range of from 5: 95 to 25: 75; wherein the phase change energy absorbed of the dispersion is in the range of from 12 J/g to 120 J/g; and wherein at least 90 weight percent of the composition comprises the wax and the alkyl methyl silicone fluid.
  4. The composition of Claim 2 where n is 0; m is from 2 to 10; and each R1 is a C8-C16-alkyl group; wherein at least 95 weight percent of the composition comprises the wax and the alkyl methyl silicone fluid.
  5. The composition of Claim 2 where n is from 1 to 10; m is from 2 to 10; and each R1 is a C8-C16-alkyl group; and wherein the phase change energy absorbed of the dispersion is in the range of from 12 J/g to 110 J/g.
  6. The composition of Claim 1 wherein the dispersion has a phase change temperature maximum for both heating and cooling cycles in a dynamic scanning calorimetry thermal analysis in the range of from 5 ℃ to 60 ℃.
  7. A composition that consists of a dispersion of a C16-C28 hydrocarbon wax in an alkyl methyl silicone fluid continuous phase of Formula 1:
    where R and R1 are each independently methyl or C6-C18-alkyl, with the proviso that at least one of R and R1 is C6-C18-alkyl; where m is from 1 to 20; and n is from 0 to 10; with the further proviso that when n is 0, one or both of the R1 groups is C6-C18-alkyl; where the relative amounts of the wax and the alkyl methyl silicone fluid are such that the viscosity of the dispersion is in the range of from 10 cSt to 100 cSt and the phase change energy absorbed of the dispersion is at least 12 J/g.
PCT/CN2023/100044 2023-06-13 2023-06-13 Dispersion of a wax in an alkyl methyl siloxane fluid Ceased WO2024254770A1 (en)

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EP23941008.7A EP4727991A1 (en) 2023-06-13 2023-06-13 Dispersion of a wax in an alkyl methyl siloxane fluid
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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN120965740A (en) * 2025-04-23 2025-11-18 江西海多有机硅材料股份有限公司 A single-phase immersion modified organosiloxane coolant and its preparation method

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3885984A (en) * 1973-12-18 1975-05-27 Gen Electric Methyl alkyl silicone thermoconducting compositions
EP0641849A2 (en) * 1993-09-07 1995-03-08 Dow Corning Corporation Heat transfer fluid containing organosiloxane compositions
CN104216490A (en) * 2014-09-10 2014-12-17 上海交通大学 Liquid cooling system for computer chip
WO2022087877A1 (en) * 2020-10-28 2022-05-05 Dow Global Technologies Llc Alkylmethylsiloxane liquid immersion cooling media
CN114641538A (en) * 2019-10-24 2022-06-17 信越化学工业株式会社 Heat-conductive silicone composition and method for producing same

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3885984A (en) * 1973-12-18 1975-05-27 Gen Electric Methyl alkyl silicone thermoconducting compositions
EP0641849A2 (en) * 1993-09-07 1995-03-08 Dow Corning Corporation Heat transfer fluid containing organosiloxane compositions
CN104216490A (en) * 2014-09-10 2014-12-17 上海交通大学 Liquid cooling system for computer chip
CN114641538A (en) * 2019-10-24 2022-06-17 信越化学工业株式会社 Heat-conductive silicone composition and method for producing same
WO2022087877A1 (en) * 2020-10-28 2022-05-05 Dow Global Technologies Llc Alkylmethylsiloxane liquid immersion cooling media
WO2022089214A1 (en) * 2020-10-28 2022-05-05 Dow Global Technologies Llc Alkylmethylsiloxane liquid immersion cooling media
CN116438502A (en) * 2020-10-28 2023-07-14 陶氏环球技术有限责任公司 Alkylmethylsiloxane Liquid Immersion Cooling Medium

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN120965740A (en) * 2025-04-23 2025-11-18 江西海多有机硅材料股份有限公司 A single-phase immersion modified organosiloxane coolant and its preparation method

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