WO2022102217A1 - Amortisseur à fluide électro-visqueux - Google Patents

Amortisseur à fluide électro-visqueux Download PDF

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Publication number
WO2022102217A1
WO2022102217A1 PCT/JP2021/031972 JP2021031972W WO2022102217A1 WO 2022102217 A1 WO2022102217 A1 WO 2022102217A1 JP 2021031972 W JP2021031972 W JP 2021031972W WO 2022102217 A1 WO2022102217 A1 WO 2022102217A1
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Prior art keywords
electrorheological fluid
mol
emulsifier
amount
damper
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PCT/JP2021/031972
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English (en)
Japanese (ja)
Inventor
ソクチョル 申
裕一郎 山本
智弘 岡田
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日立Astemo株式会社
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Publication of WO2022102217A1 publication Critical patent/WO2022102217A1/fr

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    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M149/00—Lubricating compositions characterised by the additive being a macromolecular compound containing nitrogen
    • C10M149/12—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M149/14—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds a condensation reaction being involved
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16F—SPRINGS; SHOCK-ABSORBERS; MEANS FOR DAMPING VIBRATION
    • F16F9/00—Springs, vibration-dampers, shock-absorbers, or similarly-constructed movement-dampers using a fluid or the equivalent as damping medium
    • F16F9/32—Details
    • F16F9/53—Means for adjusting damping characteristics by varying fluid viscosity, e.g. electromagnetically
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2010/00—Metal present as such or in compounds
    • C10N2010/02—Groups 1 or 11
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2010/00—Metal present as such or in compounds
    • C10N2010/04—Groups 2 or 12
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00—Specified use or application for which the lubricating composition is intended
    • C10N2040/14—Electric or magnetic purposes

Definitions

  • the present invention relates to an electrorheological fluid and an electrorheological fluid damper using the same.
  • An electrorheological fluid is a fluid whose apparent viscosity changes rapidly and reversibly in the presence of an applied electric field. Electrorheological fluids are roughly classified into uniform systems and particle dispersion systems, and the latter is generally dispersed in a hydrophobic and electrically non-conductive oil (dispersion medium) in which finely divided solids (particles, etc.) are dispersed. Has a body aspect. When an electrorheological fluid is exposed to an electric field, its flow resistance changes and generally becomes highly viscous, and when the electric field is removed, it returns to a normal liquid state.
  • the electrorheological fluid is characterized in that the current density of the leakage current is small and the power consumption is small when a voltage is applied, and can be advantageously used in applications such as dampers in which it is desirable to control the transmission of force by a low power level.
  • the characteristics required for the electrorheological fluid mainly include damping force and responsiveness, and in addition to these, there are a plurality of characteristics including heat resistance, current density, damping force fluctuation characteristics, and the like.
  • damping force damping force
  • damping force fluctuation characteristics damping force fluctuation characteristics
  • an electrorheological fluid having a high maximum shear stress and a low current density is desired.
  • Patent Document 1 describes 1 selected from the group consisting of Al, Si, Ti, V, Cr, Mn, Fe, Co, Ga, Ge, Zr, In, Sn, and Hf in order to improve the induced shear stress.
  • An electrically viscous fluid in which a zinc oxide powder containing a seed or two or more kinds of doped metal elements is dispersed in an electrically insulating oily medium is disclosed.
  • this document does not disclose the Li—Zn mixed system containing Li as a doped metal element, and the dispersion (powder) in the medium disclosed in the same document is zinc oxide powder. Resin particles, especially polyurethane particles, are not disclosed.
  • Non-Patent Document 1 discloses that the Li ion concentration is 0.00306 mol / kg and the Zn ion concentration is 0.00614 mol / kg, which are dispersed in silicone oil.
  • An electrically viscous fluid consisting of doped polyurethane particles is disclosed.
  • this document does not disclose an electrorheological fluid using polyurethane particles whose doped Li ion concentration exceeds the Zn ion concentration.
  • Non-Patent Document 1 An electrically viscous fluid using polyurethane particles having a Zn ion concentration higher than the Li ion concentration disclosed in Non-Patent Document 1 cannot exhibit a sufficient damping force, and when this is applied to a damper, the damper is damped. The force cannot be kept constant. When the electrorheological fluid cannot sufficiently exert its damping force in the damper, a "fluctuation” phenomenon occurs in which the damping force fluctuates. This "fluctuation” phenomenon can be confirmed from the Lissajous waveform of the stroke (piston displacement) and damping force in the damper test.
  • An object of the present invention is to provide an electrorheological fluid that exhibits a sufficient damping force and suppresses a fluctuation phenomenon, and an electrorheological fluid damper using the electrorheological fluid.
  • One aspect of the present invention is an electrically viscous fluid in which polyurethane particles are dispersed in an electrically insulating medium, wherein the polyurethane particles are contained in the particles or adhered to the surface of the particles. It contains metal ions, and the metal ions are characterized by containing lithium ions and zinc ions in a smaller amount than the lithium ions.
  • the lithium ion is in the range of 0.001 to 0.006 mol / kg with respect to the polyurethane particles, and the zinc ion is in the range of 0.00004 to 0.0004 mol / kg. Can be done.
  • the polyurethane particles can be a reaction product of a mixture containing polyols, isocyanates and an emulsifier having an alkoxy group.
  • the present invention also relates to an electrorheological fluid damper having a piston, a cylinder in which the piston is housed, and the electrorheological fluid enclosed in the cylinder.
  • an electrorheological fluid that exhibits a sufficient damping force and suppresses a fluctuation phenomenon, and an electrorheological fluid damper using the electrorheological fluid.
  • FIG. 1 is a diagram showing an example of a flow chart of an electrorheological fluid synthesis process according to the present invention.
  • FIG. 2 is a schematic diagram illustrating the structure of the electrorheological fluid damper according to the embodiment of the present invention.
  • FIG. 3 is a diagram showing the relationship between the amount of lithium ions in the electrorheological fluid used for the electrorheological fluid damper and the standard deviation of the damping force when a voltage of 5 kV is applied to the damper.
  • FIG. 4 is a diagram showing the relationship between the amount of lithium ions in the electrorheological fluid used for the electrorheological fluid damper and the current value when a voltage of 5 kV is applied to the damper.
  • FIG. 1 is a diagram showing an example of a flow chart of an electrorheological fluid synthesis process according to the present invention.
  • FIG. 2 is a schematic diagram illustrating the structure of the electrorheological fluid damper according to the embodiment of the present invention.
  • FIG. 3 is a diagram
  • FIG. 5 is a diagram showing the relationship between the amount of zinc ions in the electrorheological fluid and the polyurethane particle size.
  • FIG. 6 is a diagram showing the relationship between the amount of zinc ions in the electrorheological fluid and the rate of increase in viscosity of the electrorheological fluid after heat loading.
  • FIG. 7 is a diagram showing Lissajous waveforms before and after the fluctuation improvement (comparative example) and after the improvement (example) using the actual damper.
  • FIG. 8 is a diagram showing the relationship between the current value at 45 ° C. and the current value at 65 ° C. when a voltage of 5 kV is applied to the electrorheological fluid damper.
  • FIG. 9 is a diagram showing a Lissajous waveform at 80 ° C. when a voltage of 5 kV is applied to an electrorheological fluid damper.
  • FIG. 10 is a diagram showing the time variation of the damping force and the current value observed when the fluctuation of the damper damping force occurs.
  • FIG. 11 is a schematic diagram showing the mechanism of the electrorheological fluid (ER) effect when a voltage is applied to the damper.
  • FIG. 12 is a diagram showing a schematic diagram in which a capacitor is introduced into an electric circuit of an electrorheological fluid damper.
  • FIG. 13 is a diagram showing a resage waveform using an actual damper, and as a result of using (a) an electrorheological fluid containing an emulsifier for improving redispersibility, (b) electricity without an emulsifier for improving redispersibility. It is a figure which shows the result using the viscous fluid respectively.
  • FIG. 14 is a diagram showing the standard deviation of the damping force. As a result of using (a) an electrorheological fluid containing an emulsifier for improving redispersibility, (b) an electrorheological fluid not containing an emulsifier for improving redispersibility was used. It is a figure which shows each of the results used.
  • 15 is a diagram showing measured values of current densities at measured temperatures: 10 ° C, 30 ° C, 50 ° C, and 80 ° C when a voltage of 5 kV is applied to an electrorheological fluid damper according to the amount of lithium ions.
  • the electrorheological fluid of the present invention has an embodiment in which polyurethane particles containing specific metal ions are dispersed in an electrically insulating medium.
  • the present inventions are in the process of doping the polyurethane particles in an electrorheological fluid containing the polyurethane particles as a dispersoid.
  • the polarizability of the polyurethane particles was increased by controlling the amount of metal ions and improving the mobility of the ions.
  • the damping force of the damper using the polyurethane particles can be strengthened, and as a result, the fluctuation of the damper damping force can be reduced.
  • the inventors have found that the fluctuation reduction can be achieved by adjusting the amount of lithium ions having high ion mobility in the polyurethane particles in the electrorheological fluid to a state higher than the amount of zinc ions.
  • the present inventors use modified silicone containing an alkoxy group such as a methoxy group or an ethoxy group as an emulsifier in the production of an electrorheological fluid containing polyurethane particles as a dispersoid, whereby the alkoxy group is used.
  • the water contained as an impurity in the raw material of the electrorheological fluid is consumed, so that the water content can be removed from the reaction system, that is, the electrorheological fluid in which the content of water content is suppressed can be obtained.
  • the electrorheological fluid in addition to the improvement of durability, the decrease of the current density at the time of applying a voltage can be achieved.
  • each component of the electrorheological fluid according to the present invention and an electrorheological fluid damper in which the electrorheological fluid is enclosed will be described in detail.
  • Examples of the electrically insulating medium used in the present invention include paraffins (eg n-nonene), olefins (eg l-nonene, (cis, trans) -4-nonene) and aromatic hydrocarbons (eg xylene).
  • Liquid hydrocarbons such as: Polydimethylsiloxane having a viscosity of 3 mPa ⁇ s to 300 mPa ⁇ s, silicone oil such as liquid methylphenylsiloxane, and the like. Silicone oil is used as the preferred electrically insulating medium.
  • the electrically insulating medium can be used alone or in combination with other electrically insulating media.
  • the freezing point of the electrically insulating medium is preferably less than ⁇ 30 ° C., and the boiling point is preferably 150 ° C. or higher.
  • the polyurethane particles according to the present invention contain at least one kind of metal ion described later, which is encapsulated in the form of a molecule or an ion or adheres to the surface of the particle.
  • the polyurethane particles according to the present invention are reaction products of a mixture containing polyols, isocyanates, and an emulsifier having an alkoxy group.
  • the amount of the polyurethane particles contained in the electrorheological fluid can be, for example, 30% by mass to 70% by mass based on the total mass of the electrorheological fluid.
  • polyols examples include polyether polyols, polyester polyols, polymer polyols and the like.
  • examples of the polyether polyols include ethylene glycol, diethylene glycol, propylene glycol, 1,4-butylene glycol, dihydroxydiphenylpropane, glycerin, hexanetriol, trimethylolpropane, pentaerythritol, sorbitol, sucrose, dipropylene glycol and dihydroxy.
  • polyester polyols examples include ethylene glycol, diethylene glycol, propylene glycol, dipropylene glycol, trimethylene glycol, 1,3- or 1,4-butylene glycol, neopentyl glycol, 1,6-hexamethylene glycol, and deca.
  • Polyhydric alcohols such as methylene glycol, bisphenol A, bisphenol F, p-xylylene glycol, 1,4-cyclohexanediol, 1,4-cyclohexanedimethanol, glycerin, trimethylolpropane, hexanetriol, pentaerythlit, etc.
  • One or two of polyvalent carboxylic acids such as malonic acid, maleic acid, succinic acid, adipic acid, glutaric acid, pimelli acid, sebacic acid, oxalic acid, phthalic acid, isophthalic acid, terephthalic acid, hexahydrophthalic acid, etc.
  • polyvalent carboxylic acids such as malonic acid, maleic acid, succinic acid, adipic acid, glutaric acid, pimelli acid, sebacic acid, oxalic acid, phthalic acid, isophthalic acid, terephthalic acid, hexahydrophthalic acid, etc.
  • polyester polyol which is a condensate of the above, or a polyester polyol obtained by ring-opening polymerization of a cyclic ester such as propiolactone, butyrolactone, and caprolactone.
  • polyester polyols produced from the above-mentioned polyols and cyclic esters polyester polyols produced from the above-mentioned polyols, dibasic acids, and three types of cyclic esters can also be mentioned.
  • the polymer polyols include 1,2-polybutadiene polyol, 1,4-polybutadiene polyol, polychloroprene polyol, butadiene-acrylonitrile copolymer polyol, polydimethylsiloxane dicarbinol, polytetramethylene ether glycol and Himashi.
  • Examples thereof include a ricinol acid ester such as oil, a polymer polyol obtained by graft-polymerizing an ethylenically unsaturated compound such as acrylonitrile, styrene, and methyl methacrylate with the polyether polyol or the polyester polyol.
  • a ricinol acid ester such as oil
  • a polymer polyol obtained by graft-polymerizing an ethylenically unsaturated compound such as acrylonitrile, styrene, and methyl methacrylate with the polyether polyol or the polyester polyol.
  • polyether polyols are preferable.
  • isocyanates examples include toluene diisocyanate (TDI), hexamethylene diisocyanate (HDI), diphenylmethane diisocyanate (MDI), polymethylene polyphenyl polyisocyanate (p-MDI), isophorone diisocyanate (IPDI), methyl isocyanate and the like. ..
  • the molar ratio [(NCO group) / (OH group)] of the hydroxy group (OH group) of the polyols and the isocyanate group (NCO group) of the isocyanates is 1 to 1.5. It is desirable to use it for.
  • the water content in the reaction system is consumed by the reaction between the isocyanate groups of the curing agent and water, and it has an alkoxy group described later.
  • the water removing effect from the electroviscous fluid can be enhanced.
  • the emulsifier (surfactant) having an alkoxy group is not particularly limited, and for example, a polysiloxane having an alkoxy group at the side chain and / or the terminal may be mentioned because of its affinity with silicone oil as an electrically insulating medium. Can be done.
  • polysiloxane represented by the following formula can be mentioned.
  • A represents an aminoalkyl group, for example, an aminoethyl group (-(CH 2 ) 2 NH 2 ), an aminopropyl group (-(CH 2 ) 3 NH 2 ), an aminoethyl aminopropyl group (-(CH)). 2 ) 3 NH (CH 2 ) 2 NH 2 ) etc.
  • B represents an alkoxy group, for example, a methoxy group (CH 3O ⁇ ), an ethoxy group ( C2H 5O ⁇ ), or the like.
  • Examples of commercially available emulsifiers (surfactants) having an alkoxy group include reactive silicone oils manufactured by Shin-Etsu Silicone Co., Ltd. (trade names: KF-857, KF-8001, KF-862, KF-858) and the like. However, it is not limited to these.
  • the emulsifier having an alkoxy group may be used alone or in combination of two or more.
  • the emulsifier having an alkoxy group is preferably blended in a proportion of 1 to 2% by mass with respect to the mass of the above-mentioned electrically insulating medium.
  • the blending amount of the emulsifier having an alkoxy group By setting the blending amount of the emulsifier having an alkoxy group to 1% by mass or more with respect to the mass of the electrorheological insulating medium, a sufficient dispersed state is ensured, and by setting it to 2% by mass or less, the particle size of the polyurethane particles is in a suitable range.
  • the characteristics of the electrorheological fluid can be made suitable.
  • emulsifiers other than the above-mentioned emulsifier having an alkoxy group may be used in combination as long as the effect of the present invention is not impaired.
  • Other emulsifiers include surfactants that are soluble in the electrical insulating medium and derived from, for example, amines, imidazolines, oxazolines, alcohols, glycols or sorbitol. Polymers soluble in the electrical insulating medium can also be used, for example having a N (nitrogen atom) and / or OH (hydroxy group) content of 0.1-10% by weight and 25-83% by weight.
  • Examples thereof include polymers containing% C 4-24 alkyl groups and having a weight average molecular weight of 5,000 to 1,000,000.
  • Examples of the N and OH functional compounds in these polymers include amines, amides, imides, nitrilos, 5- to 6-membered N-containing heterocycles or alcohols, and C 4-24 alkyl esters of acrylic acid or methacrylic acid. be able to.
  • Examples of the N and OH functional compounds are N, N-dimethylaminoethyl methacrylate, tert-butylacrylamide, maleic acidimide, acrylonitrile, N-vinylpyrrolidone, vinylpyridine, 2-hydroxyethylmethacrylate and the like.
  • the polymer emulsifiers described above have the advantage that the systems prepared using them are generally more stable with respect to sedimentation dynamics compared to low molecular weight surfactants.
  • Modified silicone oils such as amino-modified silicone and fluorine-modified silicone can also be used.
  • the polyurethane particles according to the present invention contain metal ions in the particles.
  • the inclusion of the metal ion may mean that the metal ion is dissolved or dispersed in the particle or is in a non-dispersed state (unevenly distributed), that is, in a form enclosed in the particle, or the particle surface. It may be an aspect attached to.
  • metal ions dissolved or dispersed in the electrorheological insulating medium or in a non-dispersed (unevenly distributed) state may be present.
  • the metal ion examples include ions of metal elements such as lithium, zinc, chromium, copper, nickel, cobalt, iron, manganese, and tungsten, and in the present invention, lithium ion and zinc ion are essentially contained. do.
  • the present invention is characterized in that the amount of lithium ions is larger than that of zinc ions, for example, the lithium ions are in the range of 0.001 to 0.006 mol / kg in an electroviscous fluid, or 0. It is preferably in the range of .003 to 0.006 mol / kg or 0.001 to 0.003 mol / kg, and the zinc ion is preferably used in the range of 0.00004 to 0.0004 mol / kg. Is.
  • the amount of lithium ions in the above range it can be expected that the damping force of the obtained electrorheological fluid is enhanced, the generation of fluctuations is suppressed, and at the same time, the current value at the time of applying a voltage is suppressed within an allowable range.
  • the amount of zinc ions in the above range the particle size of the polyurethane particles can be controlled, and it can be expected that the increase in viscosity can be suppressed even after the heat load of the electrorheological fluid.
  • the particle size of the polyurethane particles may increase beyond a desired range (for example, 10 ⁇ m), and as a result, the contact area between the particles may decrease and the electrorheological effect may decrease.
  • the emulsifier having the alkoxy group is used as the emulsifier, no other emulsifier is used, the lithium ion amount is in the range of 0.001 to 0.003 mol / kg, and the zinc ion amount is 0.
  • the range is in the range of 0.0004 to 0.0004 mol / kg, it can be expected that the damping force is increased in the obtained electroviscous fluid to suppress the occurrence of fluctuations, and at the same time, the current value when a voltage is applied is suppressed to an allowable range.
  • the other emulsifiers particularly the above-mentioned polymer emulsifiers and modified silicone oils such as amino-modified silicones or fluorine-modified silicones, have the advantage that the systems prepared using them as described above are more stable with respect to sedimentation dynamics. This is because by preparing the polyurethane particles using the emulsifier, long molecular chains derived from the emulsifier are present on the surface of the obtained polyurethane particles, whereby the polyurethane particles are easily separated from each other. (Aggregation is suppressed). Therefore, these emulsifiers can be classified as emulsifiers for improving redispersibility.
  • the emulsifier having an alkoxy group has a large emulsifying ability and can impart a molecular chain having an appropriate length to the surface of the polyurethane particles.
  • a polysiloxane having an alkoxy group represented by the above formula as an emulsifying agent having an alkoxy group has an alkoxy group at both ends and an alkylamino group (NH 2 R-) in the side chain.
  • an emulsifier having an alkoxy group to which a monoamino group having a relatively short chain length such as an aminoethyl group is bonded has good adhesion to polyurethane particles and improves dispersibility of polyurethane particles. , Does not excessively deprive particles of frictional force. Therefore, even without using an emulsifier for improving redispersibility, it is possible to achieve both the electrorheological viscosity effect and the improvement of redispersibility even in a range where the amount of ions is relatively small.
  • a lubricant may be further added to the electrorheological fluid of the present invention.
  • the lubricant include polydimethylsiloxane, polytrifluoropropylmethylsiloxane, and oil-based lubricants such as a copolymer of dimethylsiloxane and trifluoropropylmethylsiloxane.
  • oil-based lubricants such as a copolymer of dimethylsiloxane and trifluoropropylmethylsiloxane.
  • the polyurethane particles according to the present invention can be particles having an average particle diameter of, for example, about 2 ⁇ m to 5 ⁇ m.
  • the electroviscosity fluid of the present invention disperses and emulsifies a mixture containing, for example, the above-mentioned electrically insulating medium, polyols, metal ions, emulsifiers, and optionally other additives (lubricant, catalyst for polyurethane synthesis, etc.), and is used therein. It can be produced by adding isocyanates as a curing agent.
  • an example of the method for preparing the electrorheological fluid of the present invention will be described with reference to the manufacturing flowchart (outline) shown in FIG.
  • This step is a step of separately preparing a solution containing polyols and metal ions (electrolyte-containing polyol solution) and a solution containing an electrically insulating medium and an emulsifier (electrically insulating medium-containing solution). ..
  • the prepared electrolyte-containing polyol solution and electrically insulating medium-containing solution are individually stored at room temperature and mixed in the next step (emulsification). The preparation of each solution is described below.
  • Preparation of electrolyte-containing polyol solution Weigh the polyols and metal ions, add them to a compounding bottle (such as a bottle with a stopper) or a glass beaker / flask of an appropriate size, and add them to a magnetic stirrer and a magnetic stirrer, or a stirrer such as a homogenizer. Is used to mix and dissolve each material by heating and stirring.
  • a compounding bottle such as a bottle with a stopper
  • a glass beaker / flask of an appropriate size and add them to a magnetic stirrer and a magnetic stirrer, or a stirrer such as a homogenizer. Is used to mix and dissolve each material by heating and stirring.
  • the following operations can be performed in the glove box as needed.
  • the metal ion can be prepared as a salt of the above metal element, for example, a halide, preferably as a chloride, and in the present invention, lithium chloride and zinc chloride can be preferably used as a source of lithium ion and zinc ion. Therefore, lithium chloride and zinc chloride are preferably weighed, and if used, a synthetic catalyst for polyurethane is weighed. Since salts of metal elements have deliquescent properties depending on the type, care must be taken when handling them.
  • the polyols are heated and stirred to, for example, 50 ° C. to 80 ° C., and after confirming that the desired temperature has been reached, salts of metal elements are sequentially added thereto.
  • lithium chloride is added to the polyols. While maintaining the desired temperature, lithium chloride is mixed and stirred, and the mixture is stirred and dissolved until no undissolved matter or precipitate can be visually confirmed from the appearance.
  • zinc chloride is added, and the mixture is mixed and stirred while maintaining the desired temperature, and the mixture is stirred and dissolved until no undissolved matter or precipitate can be visually confirmed from the appearance.
  • a synthetic catalyst for polyurethane When a synthetic catalyst for polyurethane is used, it is added after the salt of the metal element is dissolved, and the mixture is mixed and stirred while maintaining the desired temperature to obtain an electrolyte-containing polyol solution.
  • the stirring time can be appropriately set until no undissolved substance or precipitate is confirmed in the electrolyte and each component is dissolved or dispersed, and can be, for example, 8 hours or more in total.
  • lithium ions are present in a larger amount than zinc ions, and in a preferred embodiment, the lithium ions are in the range of 0.001 to 0.006 mol / kg in the electrically viscous fluid.
  • the amount of the salt of the above-mentioned metal element can be adjusted so that the zinc ion is in the range of 0.00004 to 0.0004 mol / kg.
  • a polyurethane synthesis catalyst When a polyurethane synthesis catalyst is used, it is preferably added into the system after the metal ions (that is, salts of metal elements) are completely dissolved, as shown in the above specific operating procedure.
  • the catalyst include amine-based catalysts, and specific examples thereof include triethylamine, benzyldiethylamine, 1,4-diazabicyclo [2,2,2] octane, and 1,8-diazabicyclo [5,4,0]. Examples thereof include undecene, N, N, N', N'-tetramethyl-1,3-butanediamine, N-ethylmorpholine and the like.
  • the catalyst When the catalyst is used, it can be blended in a proportion of up to about 0.2% by mass with respect to the amount of polyurethane finally obtained. However, if a large amount is added, a decomposition reaction may occur due to the catalyst, so caution is required.
  • an electrically insulating medium silicone oil, etc.
  • an emulsifier having an alkoxy group emulsifier 1
  • another emulsifier emulsifier 2
  • a lubricant if desired
  • these emulsifiers / lubricants are added / mixed to the electrically insulating medium to be added / mixed to the electrically insulating medium.
  • the emulsifier having an alkoxy group emulsifier 1
  • the temperature at the time of stirring can be set to room temperature (20 ⁇ 10 ° C.).
  • Temporary curing process and 5. This is a step of preparing a curing agent used in the main curing step, that is, isocyanates.
  • the above-mentioned isocyanates as a curing agent can be used in combination of two or more, and for example, toluene diisocyanate (TDI) and polymethylene polyphenyl polyisocyanate (p-MDI) can be used in combination.
  • TDI toluene diisocyanate
  • p-MDI polymethylene polyphenyl polyisocyanate
  • Another kind of isocyanates can be added thereto to prepare a mixed solution.
  • the weighing and prepared curing agents (isocyanates) will be described later in 4.
  • Temporary curing process and 5 Since it is used separately in the main curing step in two steps, for example, 4. A 10% to 20% amount can be set aside in advance for use in the temporary curing step.
  • the curing agent isocyanate
  • a neutralizing solution eg, a mixed solution of a 5% sodium carbonate aqueous solution and a neutral detergent
  • Emulsification process This process is described in 1. above.
  • the electrolyte-containing polyol solution and the electrically insulating medium-containing solution obtained in the preparation step of the above are dispersed and mixed by a stirrer such as a homogenizer or a disperser to obtain an electrolyte-containing polyol solution / an electrically insulating medium-containing solution mixture, and then the mixture is obtained.
  • a stirrer such as a homogenizer or a disperser to obtain an electrolyte-containing polyol solution / an electrically insulating medium-containing solution mixture, and then the mixture is obtained.
  • the average particle size of the polyurethane particles formed in the subsequent process is adjusted according to the type of agitator and disperser used in this process, the type of shear blades in the disperser, the number of rotations (speed), and the stirring (rotation) time. can do.
  • the electrolyte-containing polyol solution obtained in the step is weighed in a flask, and here, 1-2.
  • the solution containing the electrically insulating medium obtained in the step is weighed and added.
  • the flask is set in a constant temperature device such as a water bath, and the mixture is stirred and mixed with a homogenizer to obtain an emulsion.
  • the rotation speed at the time of stirring can be about 10,000 rpm to 20,000 rpm
  • the temperature at the time of stirring can be, for example, about 40 ° C.
  • the stirring time can be about 0.5 hours. Yes, but not limited to these conditions.
  • Temporary curing (hardener addition (1)) step This step is described in 3. above. This is a step of curing the emulsion (uncured emulsion particles) produced in the emulsification step to obtain semi-cured polyurethane particles. In this step, about 10% to 20% of the total amount of the curing agent (isocyanates) used to form the polyurethane particles is used.
  • a curing agent isocyanate in an amount of about 10% to 20% of the total addition amount is added dropwise using a tube pump or the like.
  • the emulsion is set in a constant temperature device such as a mantle heater so that the temperature becomes a predetermined temperature (for example, 50 ° C. or higher), stirring is continued, and after reaching the predetermined temperature, the curing agent (partly). ) Can be added.
  • the stirring time can be about 0.5 hours, but is not limited to such addition / stirring conditions.
  • several drops can be dropped (about 5 times) in order to confirm that the stirring does not stop.
  • Main curing (hardener addition (2)) step This step is described in 4. above. This is a step of further curing the semi-cured polyurethane particles (emulsion particles) formed by the temporary curing step. In this step, of the total amount of the curing agent (isocyanates) used for forming the polyurethane particles, the remaining amount of the one consumed in the previous step, that is, 80% to 90% of the total amount is used.
  • the curing agent isocyanates
  • the stirring time can be about 1.0 hour, but is not limited to such addition / stirring conditions.
  • the liquid temperature drops to about 70 ° C., and then the stirring device (homogenizer or the like) is stopped to obtain a fluid that can be said to be a crude product.
  • Filtration process 5 After the operation of this curing step is completed, the obtained fluid is filtered to obtain an electrorheological fluid.
  • filtration treatment may be performed in two steps.
  • the present invention also covers an electrorheological fluid damper having a piston, a cylinder in which the piston is housed, and the above-mentioned electrorheological fluid which is enclosed in the cylinder and whose viscosity is changed by applying a voltage.
  • an electrorheological fluid damper having a piston, a cylinder in which the piston is housed, and the above-mentioned electrorheological fluid which is enclosed in the cylinder and whose viscosity is changed by applying a voltage.
  • the electrorheological fluid damper is a damping force adjusting shock absorber that uses an electrorheological fluid as a working fluid.
  • FIG. 2 is a sectional view taken along a plane including an axis of the electrorheological fluid damper 11 of the preferred embodiment of the present invention.
  • the electrorheological fluid damper 11 has an inner cylinder 12 (cylinder), an outer cylinder 13, and an intermediate cylinder 14.
  • the vertical direction in FIG. 2 is the vertical direction in the electrorheological fluid damper 11.
  • the lower end of the outer cylinder 13 is closed by the bottom cap 15.
  • the lower end of the inner cylinder 12 is fitted to the valve body 17 of the bottom valve 16, and the upper end is fitted to the rod guide 18.
  • An annular reservoir chamber 19 is formed between the inner cylinder 12 and the outer cylinder 13.
  • the electrorheological fluid and gas according to the present invention are sealed in the reservoir chamber 19.
  • the gas in the reservoir chamber 19 is, for example, nitrogen gas or air.
  • a piston 20 is slidably provided inside the inner cylinder 12.
  • the lower end of the piston rod 23 is connected to the piston 20.
  • the upper end of the piston rod 23 extends to the outside of the outer cylinder 13 via the rod guide 18.
  • the piston 20 divides the inside of the inner cylinder 12 into two chambers, a cylinder upper chamber 21 and a cylinder lower chamber 22.
  • the piston 20 is provided with a contraction-side passage 24 and an extension-side passage 25 for communicating the cylinder upper chamber 21 and the cylinder lower chamber 22.
  • the electrorheological fluid damper 11 has a uniflow structure, and as an example, a double-cylinder uniflow structure is shown.
  • the electrorheological fluid damper may have a biflow structure or a single cylinder type, but the case where the electrorheological fluid damper 11 has a uniflow structure will be described below with reference to FIG. That is, the electrorheological fluid damper 11 transfers the electrorheological fluid from the cylinder upper chamber 21 through the passage 26 provided in the inner cylinder 12 in both the contraction stroke and the expansion stroke of the piston rod 23. It is circulated to the annular flow path 27 formed between the intermediate cylinder 14 and the intermediate cylinder 14.
  • a contraction-side check valve 28 is provided on the upper end surface of the piston 20, and a disc valve 32 is provided on the lower end surface of the piston 20.
  • the contraction-side check valve 28 opens during the contraction stroke of the piston rod 23, and allows the flow of electrorheological fluid from the cylinder lower chamber 22 to the cylinder upper chamber 21 via the contraction-side passage 24.
  • the disc valve 32 opens when the pressure in the cylinder upper chamber 21 reaches a predetermined pressure during the extension stroke of the piston rod 23, and the pressure in the cylinder upper chamber 21 is applied to the extension side passage 25. Relieve to the cylinder lower chamber 22 through.
  • the valve body 17 separates the reservoir chamber 19 and the cylinder lower chamber 22.
  • An annular holding member 29 is fitted to the outer periphery of the inner cylinder 12 fitted to the small diameter portion of the valve body 17.
  • the holding member 29 positions the lower end portion of the intermediate cylinder 14 in the axial direction (vertical direction) and the radial direction.
  • the holding member 29 is made of an electrically insulating material and electrically insulates the inner cylinder 12, the bottom cap 15, and the valve body 17 from the intermediate cylinder 14.
  • the holding member 29 is formed with a passage 30 for communicating an annular flow path 27 formed between the inner cylinder 12 and the intermediate cylinder 14 to the reservoir chamber 19.
  • the check valve 33 opens during the extension stroke of the piston rod 23, and allows the flow of the electrorheological fluid from the reservoir chamber 19 to the cylinder lower chamber 22 via the extension side passage 34.
  • the disc valve (relief valve) 35 opens when the pressure in the cylinder lower chamber 22 reaches a predetermined pressure during the contraction stroke of the piston rod 23, and the pressure in the cylinder lower chamber 22 is contracted. Relief to the reservoir chamber 19 via the side passage 36.
  • the intermediate cylinder 14 is made of a conductive material.
  • the upper end portion of the intermediate cylinder 14 is radially positioned by the rod guide 18 via the holding member 31 fitted to the outer peripheral surface of the upper end portion of the inner cylinder 12.
  • the holding member 31 is made of an electrically insulating material and electrically insulates the intermediate cylinder 14 from the inner cylinder 12.
  • the intermediate cylinder 14 is connected to the positive electrode of the battery (not shown) via a high voltage driver (voltage generation unit, not shown). That is, the intermediate cylinder 14 constitutes a positive electrode (electrode) that applies an electric field (voltage) to the electrorheological fluid flowing in the flow path 27.
  • the inner cylinder 12 used as the negative electrode (ground electrode) is connected to the ground via the valve body 17, the bottom cap 15, the outer cylinder 13, and the high voltage driver 10.
  • the intermediate cylinder 14 is provided with an electrode connection portion with a positive electrode
  • the inner cylinder 12 is provided with a first ground connection portion with a negative electrode (ground electrode).
  • a first ground connection portion with the electrode (ground electrode) may be provided, and the inner cylinder 12 may be provided with an electrode connection portion with the positive electrode.
  • the electrode connection portion with the positive electrode is the inner cylinder 12 and the outer cylinder. It may be provided in 13.
  • the damping force generated when a voltage is applied to the electrorheological fluid is between the electrodes. Since it is determined by the amount of electrorheological fluid (cross-sectional area), it is better to provide the electrodes so that the voltage is applied between the inner cylinder 12 and the intermediate cylinder 14, because the cross-sectional area between the electrodes is smaller, the applied voltage is smaller, and by extension, more. The same damping force (braking force) can be obtained with a small current consumption.
  • the energization amount increases due to an increase in the liquid temperature, the energization amount is suppressed to be smaller, the load applied to the power supply is suppressed to be smaller, and the power supply is prevented from being overloaded.
  • the ground may be ground, a frame ground, a signal ground, or the like.
  • the current from the positive electrode may be connected to the reference potential point.
  • the amount of metal ions doped in the particles is controlled, specifically, lithium ions and zinc ions in a smaller amount than the lithium ions are contained or adhered to the particle surface.
  • the amount of water present as impurities in the reaction system is reduced, for example.
  • the water content can be reduced from the order of more than 1,000 ppm to the level of several hundred ppm to several tens of ppm. This leads to the suppression of side reactions between the residual water remaining in the system and the isoialates, and the efficient progress of the curing reaction of the polyurethane improves the degree of curing of the polyurethane, resulting in the durability of the electrorheological fluid. This leads to improved properties (heat resistance).
  • Deterioration of heat resistance in an electrorheological fluid can lead to an accelerated decrease in damping force, and can also affect the viscosity and current value, so it can be said to be one of the important solutions. Further, the reduction of the water content can lead to the suppression of the amount of current flowing in the electrorheological fluid when a voltage is applied to the electrorheological fluid, and particularly in the case of the present invention, it also suppresses the increase in the amount of current that can occur due to the increase in lithium ions. It can be expected to connect and reduce energy consumption.
  • the electrorheological fluid damper of the present invention can suppress an increase in the amount of current even when the operating temperature rises, and the damper can be operated in a higher temperature range. Become.
  • FIG. 10 shows the time variation of the damping force and the current value observed when the fluctuation of the damper damping force occurs. As shown in FIG. 10, it can be confirmed that the current value increases several milliseconds after the damping force decreases, and then the damping force recovers. As shown in FIG. 11, this phenomenon is caused by the column of polyurethane particles (polarizing particles) formed when the damping force is high (FIG. 11 (a)) collapses when the damping force decreases (FIG.
  • inrush current flows through the electrode in order to repolarize the polyurethane particles after the column collapse, and this is observed as an increase in the current value.
  • This inrush current has a problem of raising the upper limit of the power supply capacity, so countermeasures are required.
  • a countermeasure against inrush current for example, as shown in FIG. 12 (1), a resistor is inserted in series between the power supply and the electrodes, and a capacitor is connected in parallel between the electrodes to connect the column shown in FIG. 11 (b).
  • the electrorheological fluid is a fluid in which the fluctuation of the damping force itself is suppressed by adjusting the blending amount of the metal ions doped in the polyurethane particles, thereby suppressing the generation of the inrush power itself. Even if the inrush power is generated, its magnitude can be suppressed. That is, the suppression of the fluctuation phenomenon of the damping force in the electrorheological fluid of the present invention also leads to the suppression of the inrush current.
  • the electrorheological fluid of the example was prepared according to the flow chart for producing the electrorheological fluid shown in FIG.
  • Lithium chloride and zinc chloride were used as raw materials for metal ions (lithium ion and zinc ion), and an electrolyte-containing polyol solution (polyol: Polyol3165 manufactured by Perstop) in which this and a catalyst for polyurethane synthesis were dissolved was prepared.
  • the amount of lithium ions in the finally obtained electrorheological fluid is 0.0007 mol / kg to 0.007 mol / kg, and the amount of zinc ions is 0 mol / kg to 0.005 mol / kg. Adjustment was made to prepare an electrolyte-containing polyol solution.
  • silicone oil (KT-5 manufactured by Momentive) used as an electrically insulating medium
  • emulsifier 1 KF-862 manufactured by Shinetsu Chemical Industry Co., Ltd. or OF7747 manufactured by Momentive
  • emulsifier 2 Fludicon having an alkoxy group.
  • Fluorinated amino-modified polysiloxane manufactured by Momentive
  • a lubricant GPW2233 manufactured by Momentive
  • the emulsifier 1 having an alkoxy group was used in an amount of 1.5% by mass with respect to the silicone oil which is an electrically insulating medium.
  • a silicone solution solution containing an electrically insulating medium under the same conditions except that emulsifier 2 was not used was also prepared.
  • a predetermined amount of the electrolyte-containing polyol solution and the electrically insulating medium-containing solution were weighed and filled in the container of the disperser. The concentration and amount of each solution were variously adjusted so that the amount of polyurethane particles in the finally obtained electrorheological fluid was 50% by mass. Then, as shown in the flow chart of FIG. 1, the electrolyte-containing polyol solution was dispersed in the electrically insulating medium-containing solution in the emulsification step.
  • the curing agent isocyanates a mixture of 2,4-diisocyanate toluene (TDI) manufactured by Tosoh Corporation and the multimer diphenylmethane diisocyanate (p-MDI)
  • TDI 2,4-diisocyanate toluene
  • p-MDI multimer diphenylmethane diisocyanate
  • the total amount of the curing agent added here is the molar ratio of the hydroxy group (OH group) of the polyol and the isocyanate group (NCO group) of the curing agent (isocyanates): (NCO group) / (OH group) of 1 to 1. It was adjusted to be .5.
  • the amount of the curing agent By making the amount of the curing agent larger than the equal amount of the polyol amount, in addition to the water removing effect of the emulsifier 1 having an alkoxy group, water removal by the reaction with the water content by the isocyanate group of the curing agent can be expected.
  • the obtained fluid was filtered using a filter having a mesh of 125 ⁇ m to obtain an electrorheological viscous fluid.
  • ⁇ Measuring device Vertical vibration machine (Tokyo Koki Co., Ltd.) ⁇ Amplitude type: sine wave ⁇ Frequency: 1Hz ⁇ Amplitude width: ⁇ 40 mm ⁇ Applied voltage: 5kV -Measurement temperature: 45 ° C -Temperature measurement: Sheath thermocouple K type In the electrorheological fluid damper system used in the examples, a power supply of 50 W is used and a maximum of 5,000 V is applied, so 10 mA is set as the upper limit current value.
  • FIG. 3 shows the relationship between the amount of lithium ions in the electrorheological fluid used for the electrorheological fluid damper and the standard deviation of the damping force when a voltage of 5 kV is applied to the damper (N number: about 500 in this example). It is a figure which shows.
  • the standard deviation of the damping force is an index that quantitatively expresses the fluctuation.
  • the amount of zinc ions in the electroviscous fluid is 0.005 mol / kg in the region where the lithium ion amount is less than 0.003 mol / kg, and 0.003 mol / kg or more in the region where the lithium ion amount is 0.003 mol / kg or more.
  • the lithium ion amount is preferably 0.003 mol / kg or more.
  • FIG. 4 shows the relationship between the amount of lithium ions (0.0007 mol / kg to 0.007 mol / kg) in the electrorheological fluid used for the electrorheological fluid damper and the current value when a voltage of 5 kV is applied to the damper. It is a figure which shows. At the measurement points shown in this figure, the amount of zinc ions in the electrorheological fluid is about 0.00035 mol / kg. As shown in FIG. 4, it was confirmed that the damper current value increased as the amount of lithium ions increased. In particular, from the approximate curve (see the broken line), it was confirmed that the damper current value increased sharply when the lithium ion amount exceeded 0.006 mol / kg.
  • the current value at 45 ° C. is 1.0 mA or less. From the results in this figure, it can be judged that it is preferable that the amount of lithium ions is 0.006 mol / kg or less.
  • FIG. 5 is a diagram showing the relationship between the amount of zinc ions in the electrorheological fluid and the particle size of the obtained polyurethane particles.
  • the particle size of the polyurethane particles increased as the amount of zinc ions decreased.
  • the polyurethane particle size dramatically increased when the zinc ion content was less than 0.00004 mol / kg.
  • the amount of lithium ions at the zinc ion amount: 0 mol / kg is 0.003 mol / kg
  • the amount of lithium ions in the region where the zinc ion amount exceeds 0 mol / kg is 0.004 mol / kg. ..
  • the surface area of particles having a large polyurethane particle size is reduced, and the contact area between the particles is reduced, so that the electrorheological effect is reduced. Further, particles having a large polyurethane particle size also have a problem that their sedimentation is accelerated. As described above, it is desirable that the particle size of the polyurethane particles is 5 ⁇ m or less in consideration of the electrorheological effect and the dispersion / sedimentation phenomenon. From the results shown in this figure, it can be judged that it is preferable that the zinc ion amount is 0.0004 mol / kg or more.
  • FIG. 6 is a diagram showing the relationship between the amount of zinc ions and the rate of increase in viscosity of the electrorheological fluid after heat loading. As shown in FIG. 6, it was confirmed that the viscosity increase rate increased as the amount of zinc ions increased.
  • An increase in the viscosity of the electrorheological fluid affects the damping force of the damper, and when the viscosity increases, the ride quality becomes worse in the vehicle body to which the damper is applied. Therefore, it is desirable that the amount of zinc ions is in a range in which the viscosity change rate is approximately ⁇ 5% or less, that is, 0.0004 mol / kg or less, where it can be judged that there is almost no change in viscosity.
  • Test Example 3 Electrorheological fluid performance test using an actual damper
  • An electrorheological fluid performance test was carried out using the electrorheological fluid damper 11 shown in FIG. 2 under the same conditions as in Test Example 1, but at measurement temperatures of 45 ° C., 60 ° C., and 80 ° C.
  • the electrorheological fluid used in this test was prepared by using emulsifier 1 and emulsifier 2 in combination.
  • FIG. 7 shows a Lissajous waveform (45 ° C.) of the stroke (piston displacement) and damping force using the actual damper machine before and after the fluctuation improvement (comparative example) and after the improvement (example).
  • the amount of lithium ions and the amount of zinc ions in the electrorheological fluid used in the electrorheological fluid damper 11 obtained from the resage waveform of FIG. 7 are as follows.
  • FIG. 8 is a diagram showing the relationship between the current value at 45 ° C. and the current value at 65 ° C. when a voltage of 5 kV is applied to the electrorheological fluid damper.
  • the horizontal axis and the vertical axis are current values measured at 45 ° C. and 65 ° C., respectively.
  • the results of Example ( ⁇ ) or Comparative Example ( ⁇ ) shown in FIG. 8 were obtained by using the electrorheological fluid having the lithium ion amount and the zinc ion amount shown in Formulations 1 to 7.
  • FIG. 1 The results of Example ( ⁇ ) or Comparative Example ( ⁇ ) shown in FIG. 8 were obtained by using the electrorheological fluid having the lithium ion amount and the zinc ion amount shown in Formulations 1 to 7.
  • the comparative example group shows the results of prescriptions 1 to 5 in order from the result with the smallest damper current value (horizontal axis) at 45 ° C., and the example group has the damper current value (vertical axis) at 65 ° C.
  • a slightly higher result is the result of Formulation 6.
  • FIG. 8 it can be confirmed that the behavior of the result of the example shown by the square point ( ⁇ ) is completely different from the result of the comparative example shown by the round point ( ⁇ ).
  • the ratio of the 65 ° C. current value to the 45 ° C. current value is high, because the ion mobility at 65 ° C.
  • the electrorheological fluid of the present invention has achieved improved ion mobility and damping force at high temperatures, and as shown in FIG. 9 (using the electrorheological fluid of Formulation 7), the damping force fluctuates even at 80 ° C. A non-resage waveform is obtained.
  • Test Example 4 Electrorheological fluid performance test using an actual damper
  • An electrorheological fluid performance test was carried out on the electrorheological fluid damper 11 shown in FIG. 2 under the same conditions as in Test Example 1, but at a measurement temperature of 45 ° C.
  • the electroviscous fluid used in this test is an electroviscous fluid prepared by using emulsifier 1 and emulsifier 2 in combination (containing an emulsifier for improving redispersibility) and an electroviscous fluid prepared by using only emulsifier 1. No emulsifier for improving dispersibility).
  • FIG. 13 shows the stroke (piston displacement) and damping using an actual damper machine using (a) an electrorheological fluid containing an emulsifier for improving redispersibility and (b) an electrorheological fluid not containing an emulsifier for improving redispersibility.
  • the force resage waveform (45 ° C.) is shown (piston speed of the resage waveform shown in FIGS. 13 (a) and 13 (b): 0.02 m / s, 0.05 m / s, 0.1 m / s, 0.13 m / s, 0.15 m / s, 0.3 m / s, 0.6 m / s, 0.9 m / s).
  • the amount of lithium ions and the amount of zinc ions in the electrorheological fluid (both containing the emulsifier for improving redispersibility and not containing the emulsifier for improving redispersibility) used in the electrorheological fluid damper 11 obtained with the resage waveform of FIG. 13 It is as follows.
  • FIG. 14 shows the standard deviation of the damping force calculated from the resage waveform shown in FIG. 13 (calculated from the region where the piston speed is 0.1 m / s, the damping force is 0 kN or more, and the stroke is ⁇ 20 mm).
  • the standard deviation of the damping force is an index that quantitatively expresses the fluctuation, and under this condition, (a) the redispersibility is improved as compared with (a) the standard deviation of the emulsifier for improving the redispersibility.
  • the results were obtained that the standard deviation of the electroviscous fluid containing no emulsifier was small.
  • Test Example 5 Current density measurement using a rheometer
  • the current densities of the prepared various electrorheological fluids were measured using a rheometer while changing the measurement temperature.
  • the equipment and measurement conditions used for the measurement are shown below.
  • the electrorheological fluid used in this test is an electrorheological fluid prepared by using only emulsifier 1 (without emulsifier for improving redispersibility).
  • -Measuring device Rheometer MCR302 (Anton Pair) ⁇ Jig: CC27 -Measurement temperature: 10 ° C, 30 ° C, 50 ° C, 80 ° C ⁇ Applied voltage: 5kV ⁇ Sample volume: 15 mL ⁇ Measurement program: Current value 1 minute after the start of strain dispersion measurement (frequency: 0.2Hz) -Lithium ion amount in electrorheological fluid: 0.002 mol / kg, 0.0023 mol / kg, or 0.0038 mol / kg; Zinc ion amount: 0.00035 mol / kg (constant) Based on the above measurement results, FIG.
  • an electrorheological fluid having a lithium ion amount of 0.0038 mol / kg has a current density of 15 ⁇ A / cm 2 at 80 ° C. The result was much higher. From this result, it was determined that the upper limit of the amount of lithium ions was 0.003 mol / kg in the case of the electrorheological fluid containing no emulsifier for improving redispersibility.
  • ERF damper electroheological fluid damper
  • 12 inner cylinder cylinder
  • 13 outer cylinder 20 piston
  • 23 piston rod piston
  • 14 intermediate cylinder electrowetting rod

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Abstract

Le problème décrit par la présente invention est de fournir : un fluide électro-visqueux qui présente une force d'amortissement satisfaisante et dans lequel une fluctuation est supprimée ; et un amortisseur à fluide électro-visqueux dans lequel le fluide électro-visqueux est utilisé. La solution selon l'invention porte sur un fluide électro-visqueux dans lequel des particules de polyuréthane sont dispersées dans un milieu électriquement isolant, les particules de polyuréthane contenant au moins un type d'ions métalliques encapsulés dans les particules ou fixés à la surface des particules, et les ions métalliques comprennent des ions lithium et des ions zinc à une quantité inférieure à celle des ions lithium ; et un amortisseur à fluide électro-visqueux dans lequel le fluide électro-visqueux est scellé.
PCT/JP2021/031972 2020-11-12 2021-08-31 Amortisseur à fluide électro-visqueux WO2022102217A1 (fr)

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Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH1081758A (ja) * 1996-08-12 1998-03-31 Bayer Ag 非水性分散系の調製方法及びそれらの使用
JP2015511643A (ja) * 2012-03-09 2015-04-20 フルディコン・ゲゼルシヤフト・ミト・ベシユレンクテル・ハフツング 電気粘性組成物
WO2018025456A1 (fr) * 2016-08-01 2018-02-08 日立オートモティブシステムズ株式会社 Amortisseur
JP2018521165A (ja) * 2015-06-18 2018-08-02 ダウ グローバル テクノロジーズ エルエルシー 電気レオロジー流体の作製方法
JP2020158598A (ja) * 2019-03-26 2020-10-01 日立オートモティブシステムズ株式会社 電気粘性流体

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH1081758A (ja) * 1996-08-12 1998-03-31 Bayer Ag 非水性分散系の調製方法及びそれらの使用
JP2015511643A (ja) * 2012-03-09 2015-04-20 フルディコン・ゲゼルシヤフト・ミト・ベシユレンクテル・ハフツング 電気粘性組成物
JP2018521165A (ja) * 2015-06-18 2018-08-02 ダウ グローバル テクノロジーズ エルエルシー 電気レオロジー流体の作製方法
WO2018025456A1 (fr) * 2016-08-01 2018-02-08 日立オートモティブシステムズ株式会社 Amortisseur
JP2020158598A (ja) * 2019-03-26 2020-10-01 日立オートモティブシステムズ株式会社 電気粘性流体

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