WO2022113197A1 - Compression sensor - Google Patents
Compression sensor Download PDFInfo
- Publication number
- WO2022113197A1 WO2022113197A1 PCT/JP2020/043790 JP2020043790W WO2022113197A1 WO 2022113197 A1 WO2022113197 A1 WO 2022113197A1 JP 2020043790 W JP2020043790 W JP 2020043790W WO 2022113197 A1 WO2022113197 A1 WO 2022113197A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- compression
- spacer
- sensor
- mpa
- compression sensor
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
Images
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01L—MEASURING FORCE, STRESS, TORQUE, WORK, MECHANICAL POWER, MECHANICAL EFFICIENCY, OR FLUID PRESSURE
- G01L1/00—Measuring force or stress, in general
- G01L1/14—Measuring force or stress, in general by measuring variations in capacitance or inductance of electrical elements, e.g. by measuring variations of frequency of electrical oscillators
Definitions
- the present invention relates to a compression sensor.
- Patent Document 1 a pair of panel electrodes integrally molded inside the outer skin cover, an elastic frame spacer provided inside the peripheral edge of the outer skin cover, and an elastic frame spacer provided inside the frame spacer between the panel electrodes.
- a weight sensor with multiple elastic support spacers has been described, and it has been proposed to measure the force acting on the sensor by measuring the capacitance between a pair of panel electrodes separated by spacers. There is.
- Patent Document 1 it was difficult for the spacer of Patent Document 1 to have both the flexibility to compress and deform with a slight force and the compression resistance when a large force is repeatedly applied. For this reason, it has been difficult to apply it to the hand part of an industrial robot or a construction machine that grips a heavy object, or to measure the load on the sole of a walking / traveling robot to which a high load is applied.
- an object of the present invention is to provide a compression sensor capable of achieving both flexibility of compression and deformation with a small force and compression resistance when a large force is repeatedly applied.
- the present invention includes a spacer and a pair of electrodes separated by a gas layer, and the spacer material is a compression sensor that measures the compressive force acting on the sensor by measuring the electrostatic capacitance between the electrodes.
- the compression limit stress is 1.0 ⁇ 10 1 MPa or more, and the compressive elastic modulus is 5.0 ⁇ 10 2 MPa or less.
- the spacer material preferably has a compression limit ratio of 20% or more.
- the spacer material preferably has a compression limit stress of 2.0 ⁇ 10 1 MPa or more.
- the spacer material preferably has a compressive elastic modulus of 2.0 ⁇ 10 2 MPa or less.
- the spacer material is preferably a material formed of crosslinked polyrotaxane.
- the dielectric elastomer layer is preferably formed of crosslinked polyrotaxane.
- the compressive elastic modulus is as low as 5.0 ⁇ 10 2 MPa or less, it can be easily compressed and deformed with a slight force, and this slight force can be measured. Since the compression limit stress is as high as 1.0 ⁇ 10 1 MPa or more, large repetitive forces can be measured with good reproducibility. When the compression limit ratio is 20% or more, the resolution of the sensor is high. When a crosslinked polyrotaxane having a high dielectric constant is used for the dielectric elastomer layer, the capacitance greatly fluctuates even at the stage where the gas layer is compressed, and the resolution is improved.
- FIG. 1 is a perspective view showing a crosslinked polyrotaxane molded product used in Examples and a compression test method thereof.
- FIG. 2 is a graph showing a load-displacement curve in a compression test of the crosslinked polyrotaxane molded product.
- FIG. 3 is a micrograph of the crosslinked polyrotaxane molded product after a predetermined load is applied and unloaded.
- FIG. 4A is a graph showing a load-displacement curve in a compression test of a polyurethane molded product as a comparative example
- FIG. 4B is a graph showing an enlarged curve of the IVb portion of FIG. 4A.
- FIG. 5 is a micrograph of the polyurethane molded product after a predetermined load is loaded and unloaded.
- FIG. 6A is a cross-sectional view of the compression sensor of the first embodiment
- FIG. 6B is a cross-sectional view of the compression sensor of the second embodiment.
- FIG. 7A is a perspective view using the compression sensor of the embodiment for the robot hand
- FIG. 7B is a perspective view of using the compression sensor of the embodiment for the shoe insole.
- the material of the spacer is not particularly limited as long as it has the above-mentioned compression characteristics, and various dielectric elastomers can be used.
- the dielectric elastomer is not particularly limited, and examples thereof include silicone elastomer, styrene-based thermoplastic elastomer, natural rubber, nitrile rubber, acrylic rubber, urethane rubber, urea rubber, fluororubber, and crosslinked polyrotaxane. Of these, crosslinked polyrotaxane is particularly preferable because it is easy to obtain the above-mentioned compression characteristics.
- polyrotaxane is a molecular assembly having a structure in which a linear molecule penetrates a cyclic molecule so as to be relatively slidable, and the cyclic molecule is not detached by the blocking groups arranged at both ends of the linear molecule (for example).
- International Publication No. 2005/080469 also known as a slide ring material.
- the polyrotaxane is not limited to those having a specific cyclic molecule, a linear molecule, and a blocking group.
- the cyclic molecule include cyclodextrin, crown ether, cyclophane, calixarene, cucurbituril, cyclic amide and the like.
- linear molecule examples include polyethers such as polyethylene glycol, polypropylene glycol and polytetrachloride, polyesters such as polylactic acid, polyamides such as 6-nylon, diene polymers such as polyisoprene and polybutadiene, polyethylene and polypropylene. , Polyvinyl alcohol, polyvinyl methyl ether, vinyl polymers such as polyisobutylene, polydimethylsiloxane, and the like can be exemplified.
- the blocking groups include dinitrophenyl groups, cyclodextrins, adamantan groups, trityl groups, fluoresceins, pyrenes, and substituted benzenes (alkyl, alkyloxy, hydroxy, halogen, cyano, sulfonyl, carboxyl as substituents).
- Amino, phenyl and the like can be exemplified), polynuclear aromatics which may be substituted (the same as above can be exemplified as the substituent), steroids and the like can be exemplified.
- the most common polyrotaxane uses cyclodextrin as a cyclic molecule and polyethylene glycol as a linear molecule.
- the crosslinked polyrotaxane is one in which the cyclic molecules of adjacent polyrotaxanes are crosslinked with a crosslinking agent.
- the cross-linking agent is not limited to a specific one.
- examples of the cross-linking agent include cyanul chloride, trimeoyl chloride, terephthaloyl chloride, epichlorohydrin, dibromobenzene, glutaaldehyde, aliphatic polyfunctional isocyanate, aromatic polyfunctional isocyanate, trilein diisosocyanate, hexamethylene diisocyanate, and divinyl.
- Block copolymers containing sulfones, 1,1'-carbonyldiimidazoles, alkoxysilanes and their derivatives, and polysiloxanes (polycaprolactone-polysiloxane block copolymers, polyadipates-polysiloxane block copolymers, Polyethylene glycol-polysiloxane block copolymer, etc.) can be exemplified.
- the material of the dielectric elastomer layer is not particularly limited, and various dielectric elastomers can be used.
- the dielectric elastomer is not particularly limited, but the one exemplified in the above [1] can also be exemplified. Of these, crosslinked polyrotaxane is particularly preferable because it has a high dielectric constant.
- Electrode The material of the electrode is not particularly limited, but can be deformed according to compression deformation, such as a conductive film made of conductive particles, a conductive coating film containing conductive particles, and conductivity including conductive particles. Examples thereof include a sex elastomer molded product.
- the conductive particles are not particularly limited, and examples thereof include particles such as carbon black, carbon nanotubes, platinum, gold, silver, copper, and nickel.
- the resin component of the conductive coating film is not particularly limited, and examples thereof include phthalic acid-based, acrylic-based, urethane-based, epoxy-based, and vinyl-based resins.
- the elastomer component of the conductive elastomer molded product is not particularly limited, but the dielectric elastomer exemplified in the above [1] can be exemplified.
- Gas layer The gas in the gas layer is not particularly limited, and examples thereof include air and a low dielectric constant gas having a dielectric constant lower than that of air.
- Examples of the low dielectric constant gas include nitrogen and carbon dioxide gas.
- the polyrotaxane A of this example has a caprolactone group in order to further obtain solubility and compatibility.
- the block copolymer B containing polysiloxane has improved moisture resistance by polysiloxane (silicone component), and specifically, a block of polycaprolactone-polydimethylsiloxane-polycaprolactone having a terminal block isocyanate group. It is a copolymer.
- the addition of the copolymer B is optional.
- Polymer C which does not contain polysiloxane, has high compatibility with polyrotaxane, and by including this, high dielectric constant and low elasticity are realized. Specifically, polypropylene glycol having a terminal block isocyanate group is used. be.
- polymer C is optional. These and other components were added in the following formulation (formulation value is parts by mass), stirred, and defoamed well to prepare a polyrotaxane composition solution.
- Polyrotaxane A 10 Polysiloxane block copolymer B 10.6
- Polymer C 9 Polypropylene glycol diol 4.7 Methyl cellosolve 25.3 Dibutyltin dilauryl acid 0.015 DBL-C31 (manufactured by GELEST) 0.15 IRGANOX1726 (manufactured by BASF) 0.45
- the above polyrotaxane composition solution was applied onto a polyethylene terephthalate (PET) plate by a slit die coater method to form a polyrotaxane molded product (film) having a thickness of 50 ⁇ m. Subsequently, the polyrotaxane molded product with a PET plate was crosslinked and cured in an oven at 130 ° C. under reduced pressure for 5 hours, and the cured crosslinked polyrotaxane molded product (dielectric elastomer molded product) was peeled off from the PET plate.
- PET polyethylene terephthalate
- Polyurethane molded product as a comparative example As the polyurethane molded product as a comparative example, a polyurethane film (trade name “Touch Grace Film”, thickness 25 ⁇ m) manufactured by Takeda Sangyo Co., Ltd. was used.
- a polyurethane film (trade name “Touch Grace Film”, thickness 25 ⁇ m) manufactured by Takeda Sangyo Co., Ltd. was used.
- FIG. 2 shows the displacement-load curve of the crosslinked polyrotaxane molded product in the above compression test, and the compression characteristics were obtained from the curve and shown in Table 1 below.
- the compression limit stress (referred to as b) was obtained by dividing a by the indenter area.
- the displacement at the yield point is defined as the compression limit displacement (c)
- the displacement at the a / 2 load is defined as the 1/2 compression limit displacement (e)
- the displacement difference c-. e (referred to as f) was obtained.
- 2 ⁇ f / t was defined as the compression limit rate (referred to as g)
- b / g was defined as the compressive elastic modulus (referred to as h).
- 3 (a) to 3 (d) show a predetermined load ((a) 100 mN, (b) 200 mN, (c) 300 mN, (d) 400 mN) on the crosslinked polyrotaxane molded product with the indenter, apart from the compression test.
- FIG. 4 (a) is a displacement-load curve of the polyurethane molded product in the compression test
- FIG. 4 (b) is an enlarged curve of the IVb portion of (a), and the compression characteristics are obtained from the enlarged curve. It is shown in Table 1 above.
- the load at the bending point where the curve of FIG. 4A rises is about 710 mN, which seems to be stronger than that of the crosslinked polyrotaxane molded product.
- the load at the bending point was not set as the compression limit load, and the internal structural change point of the enlarged curve in FIG. 4 (b) was used.
- the load of 50 mN was evaluated as the compression limit load (referred to as a), and a was divided by the indenter area to obtain the compression limit stress (referred to as b). Further, the displacement due to the internal structural change is defined as the compression limit displacement (c), the displacement due to the a / 2 load (d) is defined as the 1/2 compression limit displacement (e), and the displacement difference c between them. -E (referred to as f) was obtained. Then, 2 ⁇ f / t was defined as the compression limit rate (referred to as g), and b / g was defined as the compressive elastic modulus (referred to as h).
- 5 (a) to 5 (d) show that, apart from the compression test, a predetermined load ((a) 20 mN, (b) 50 mN, (c) 100 mN, (d) 200 mN) is applied to the polyurethane molded product with the indenter.
- a predetermined load ((a) 20 mN, (b) 50 mN, (c) 100 mN, (d) 200 mN) is applied to the polyurethane molded product with the indenter.
- a 20 mN micrograph did not show a clear internal structural change along the compressed edge, but a 50 mN micrograph began to show a clear internal structural change with a large number of granular precipitates appearing along the compressed edge.
- the precipitate is considered to be a polyol component that did not react with the is
- the compression limit load is evaluated by the smaller of the load at the yield point and the load at the internal structural change point. It can be said that the crosslinked polyrotaxane molded product has a higher compression limit stress than polyurethane and does not change to a larger pressure.
- Example 1 Fabrication of Compression Sensor of Example 1 As shown in FIG. 6A, an insulator, an electrode, a dielectric elastomer layer, a frame-shaped spacer, an electrode, and an insulator are laminated in this order from bottom to top.
- the compression sensor of Example 1 having an air layer as a gas layer sandwiched between a lower electrode and a dielectric elastomer layer and surrounded by a frame of a spacer was produced.
- the two insulators are polycarbonate sheets.
- the two electrodes are obtained by applying a silicone elastomer composition solution having the following composition (the compounding value is parts by mass) to an insulator by the slit die coater method, and cross-linking and curing the insulator at 100 ° C. for 24 hours. It is 20 ⁇ m. Silicone elastomer 10 Organic solvent (heptane) 300 Carbon particles (Ketchen black) 1
- the dielectric elastomer layer is obtained by applying the polyrotaxane composition solution to the upper electrode by a slit die coater method, cross-linking and curing at 130 ° C. ⁇ 5 hours (cross-linked polyrotaxane), and has a thickness of 50 ⁇ m. Therefore, the dielectric elastomer layer has a compression limit stress of 3.8 ⁇ 10 1 MPa and a compressive elastic modulus of 1.0 ⁇ 10 2 MPa.
- the spacer is a molded product formed in a frame shape by the crosslinked polyrotaxane, and has a thickness of 300 ⁇ m. Therefore, the spacer has a compression limit stress of 3.8 ⁇ 10 1 MPa and a compressive elastic modulus of 1.0 ⁇ 10 2 MPa.
- the air layer is made of air and has a thickness of 300 ⁇ m, which is equal to that of the spacer.
- the compression sensor of Example 1 is easily compressed and deformed by an external force, and the air layer is first compressed, and then the dielectric elastomer layer is in contact with the lower electrode and then compressed, and is static at any stage. External force can be detected by fluctuating the electric capacity.
- Example 1 Fabrication of Compression Sensor of Example 2
- the air layer of Example 1 is a gas layer made of a low dielectric constant gas having a dielectric constant lower than that of air. It is replaced with a low dielectric constant gas layer, and the others are the same as in Example 1.
- the compression sensors of Examples 1 and 2 have a low compressive elastic modulus of 5.0 ⁇ 10 2 MPa or less, so that they are easily compressed and deformed with a slight force, and this slight amount is obtained. Force can be measured.
- the compression limit stress is as high as 1.0 ⁇ 101 MPa or more, a large force that repeatedly works can be measured with good reproducibility.
- the compression limit rate is as high as 20% or more, the resolution of the sensor is high. Since the crosslinked polyrotaxane having a high dielectric constant is used for the dielectric elastomer layer, the capacitance greatly fluctuates even at the stage where the air layer is compressed, and the resolution is improved.
- the compression sensors of Examples 1 and 2 have the following effects. -Has durability that can measure vertical stress without breaking. -Since the compression sensor itself contains an elastomer, it enhances the grip on the gripped object. -From the amount of deformation of the compression sensor, the gripping force, the weight of the gripping object, etc. can be measured in the stationary state, and the moment of inertia, the speed, the moving amount, etc. can be measured when the gripping object moves so as to cause inertia. -High resolution, wide dynamic range measurement, and high S / N ratio make it possible to reduce the size of the sensor, and it is possible to mount it in a narrow space and measure the load distribution by arranging it.
- the contact surface with the gripping object can be grasped, and the posture and gripping position of the gripping object can be measured and monitored.
- These measurement information can be used for reinforcement learning in combination with AI, and can be used for stable gripping of an object, optimization of a transportation method, and the like.
- the compression sensor of the first and second embodiments can be used in the following embodiments, for example, by taking advantage of the above-mentioned effects.
- a compression sensor is attached to the finger of the hand part of an industrial robot or a construction machine for use.
- a compression sensor is attached to the shoe insole or the sole of a heavy-duty robot, posture monitoring during walking / running and measurement of weight transfer during sports can be performed. .. -In addition, by arranging the compression sensor on the mat-shaped sheet, it is possible to measure the load on the mat and the movement of the center of gravity, and to use it according to various shapes that were difficult with the conventional mat sensor. ..
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
本発明は、圧縮センサに関するものである。 The present invention relates to a compression sensor.
従来のひずみゲージ(金属線式や圧電式)は、柔軟性に乏しいため、ずれが生じるようなせん断応力で破損する危険があり、ロボットハンドの表面等に適用することは困難であった。 Since conventional strain gauges (metal wire type and piezoelectric type) lack flexibility, there is a risk of damage due to shear stress that causes displacement, and it has been difficult to apply them to the surface of robot hands.
特許文献1には、外皮カバーの内側に一体成形された一対のパネル電極と、外皮カバーの周縁内側に設けられた弾性体の枠スペーサと、枠スペーサの内側であってパネル電極間に設けられた複数の弾性体の支持スペーサとを備えた重量センサーが記載され、スペーサで離間された一対のパネル電極間の静電容量を測定することで、センサに働く力を測定することが提案されている。
In
しかし、特許文献1のスペーサは、僅かな力で圧縮変形する柔軟性と、大きな力が繰り返しかかった場合の耐圧縮性との両立が難しかった。このため、高重量物を把持する産業用ロボットや建設機械のハンド部分に適用したり、高荷重がかかる歩行・走行ロボットの足裏の荷重測定に適用したりすることは困難であった。
However, it was difficult for the spacer of
そこで、本発明の目的は、僅かな力で圧縮変形する柔軟性と、大きな力が繰り返しかかった場合の耐圧縮性との両立が可能な圧縮センサを提供することにある。 Therefore, an object of the present invention is to provide a compression sensor capable of achieving both flexibility of compression and deformation with a small force and compression resistance when a large force is repeatedly applied.
本発明は、スペーサと、スペーサにより気体層をおいて離間された一対の電極とを含み、電極間の静電容量を測定することでセンサに働く圧縮力を測定する圧縮センサにおいて、スペーサ材料は、圧縮限界応力が1.0×101 MPa以上であり、圧縮弾性率が5.0×102MPa以下であることを特徴とする。 The present invention includes a spacer and a pair of electrodes separated by a gas layer, and the spacer material is a compression sensor that measures the compressive force acting on the sensor by measuring the electrostatic capacitance between the electrodes. The compression limit stress is 1.0 × 10 1 MPa or more, and the compressive elastic modulus is 5.0 × 10 2 MPa or less.
ここで、スペーサ材料は、圧縮限界率が20%以上であることが好ましい。 Here, the spacer material preferably has a compression limit ratio of 20% or more.
スペーサ材料は、圧縮限界応力が2.0×101 MPa以上であることが好ましい。 The spacer material preferably has a compression limit stress of 2.0 × 10 1 MPa or more.
スペーサ材料は、圧縮弾性率が2.0×102 MPa以下であることが好ましい。 The spacer material preferably has a compressive elastic modulus of 2.0 × 10 2 MPa or less.
スペーサ材料は、架橋されたポリロタキサンで形成されている物が好ましい。 The spacer material is preferably a material formed of crosslinked polyrotaxane.
一対の電極間には、気体層に加えて、誘電体エラストマー層とを有することが好ましい。誘電体エラストマー層は架橋されたポリロタキサンで形成されているものが好ましい。 It is preferable to have a dielectric elastomer layer in addition to the gas layer between the pair of electrodes. The dielectric elastomer layer is preferably formed of crosslinked polyrotaxane.
<作用>
圧縮弾性率が5.0×102 MPa以下と低いため、僅かな力で容易に圧縮変形し、この僅かな力を測定することができる。
圧縮限界応力が1.0×101MPa以上と高いため、繰り返し働く大きな力も、再現性良く測定できる。
圧縮限界率が20%以上であると、センサの分解能が高い。
誘電エラストマー層に誘電率の高い架橋ポリロタキサンを使用すると、気体層が圧縮される段階でも、静電容量が大きく変動し、分解能が向上する。
<Action>
Since the compressive elastic modulus is as low as 5.0 × 10 2 MPa or less, it can be easily compressed and deformed with a slight force, and this slight force can be measured.
Since the compression limit stress is as high as 1.0 × 10 1 MPa or more, large repetitive forces can be measured with good reproducibility.
When the compression limit ratio is 20% or more, the resolution of the sensor is high.
When a crosslinked polyrotaxane having a high dielectric constant is used for the dielectric elastomer layer, the capacitance greatly fluctuates even at the stage where the gas layer is compressed, and the resolution is improved.
本発明によれば、僅かな力で圧縮変形する柔軟性と、大きな力が繰り返しかかった場合の耐圧縮性との両立が可能な圧縮センサを提供できる。 According to the present invention, it is possible to provide a compression sensor capable of achieving both flexibility of compression and deformation with a small force and compression resistance when a large force is repeatedly applied.
[1]スペーサ
スペーサの材料は、上記圧縮特性を有するものであれば特に限定されず、各種の誘電エラストマーを用いることができる。
誘電エラストマーとしては、特に限定されないが、シリコーンエラストマー、スチレン系熱可塑性エラストマー、天然ゴム、ニトリルゴム、アクリルゴム、ウレタンゴム、ウレアゴム、フッ素ゴム、架橋ポリロタキサン等を例示できる。これらのうち架橋ポリロタキサンが、上記圧縮特性を得やすい点で特に好ましい。
[1] Spacer The material of the spacer is not particularly limited as long as it has the above-mentioned compression characteristics, and various dielectric elastomers can be used.
The dielectric elastomer is not particularly limited, and examples thereof include silicone elastomer, styrene-based thermoplastic elastomer, natural rubber, nitrile rubber, acrylic rubber, urethane rubber, urea rubber, fluororubber, and crosslinked polyrotaxane. Of these, crosslinked polyrotaxane is particularly preferable because it is easy to obtain the above-mentioned compression characteristics.
上記において、ポリロタキサンは、環状分子に直鎖状分子が相対スライド可能に貫通し、直鎖状分子の両末端に配された封鎖基により環状分子が脱離しない構造の分子集合体であり(例えば国際公開第2005/080469号)、スライドリングマテリアルとも称されている。ポリロタキサンは、特定の環状分子、直鎖状分子、封鎖基を有するものに限定されない。
環状分子としては、シクロデキストリン、クラウンエーテル、シクロファン、カリックスアレーン、ククルビットウリル、環状アミド等を例示できる。
直鎖状分子としては、ポリエチレングリコール、ポリプロピレングリコール、ポリテトラヒドロフラン等のポリエーテル類、ポリ乳酸等のポリエステル類、6-ナイロン等のポリアミド類、ポリイソプレン、ポリブタジエン等のジエン系重合体、ポリエチレン、ポリプロピレン、ポリビニルアルコール、ポリビニルメチルエーテル、ポリイソブチレン等のビニル重合体や、ポリジメチルシロキサン等を例示できる。
封鎖基としては、ジニトロフェニル基類、シクロデキストリン類、アダマンタン基類、トリチル基類、フルオレセイン類、ピレン類、置換ベンゼン類(置換基として、アルキル、アルキルオキシ、ヒドロキシ、ハロゲン、シアノ、スルホニル、カルボキシル、アミノ、フェニルなどを例示できる。)、置換されていてもよい多核芳香族類(置換基として、上記と同じものを例示できる。)、ステロイド類等を例示できる。
現在、最も一般的なポリロタキサンは、環状分子としてシクロデキストリン、直鎖状分子としてポリエチレングリコールを用いたものである。
In the above, polyrotaxane is a molecular assembly having a structure in which a linear molecule penetrates a cyclic molecule so as to be relatively slidable, and the cyclic molecule is not detached by the blocking groups arranged at both ends of the linear molecule (for example). International Publication No. 2005/080469), also known as a slide ring material. The polyrotaxane is not limited to those having a specific cyclic molecule, a linear molecule, and a blocking group.
Examples of the cyclic molecule include cyclodextrin, crown ether, cyclophane, calixarene, cucurbituril, cyclic amide and the like.
Examples of the linear molecule include polyethers such as polyethylene glycol, polypropylene glycol and polytetrachloride, polyesters such as polylactic acid, polyamides such as 6-nylon, diene polymers such as polyisoprene and polybutadiene, polyethylene and polypropylene. , Polyvinyl alcohol, polyvinyl methyl ether, vinyl polymers such as polyisobutylene, polydimethylsiloxane, and the like can be exemplified.
The blocking groups include dinitrophenyl groups, cyclodextrins, adamantan groups, trityl groups, fluoresceins, pyrenes, and substituted benzenes (alkyl, alkyloxy, hydroxy, halogen, cyano, sulfonyl, carboxyl as substituents). , Amino, phenyl and the like can be exemplified), polynuclear aromatics which may be substituted (the same as above can be exemplified as the substituent), steroids and the like can be exemplified.
Currently, the most common polyrotaxane uses cyclodextrin as a cyclic molecule and polyethylene glycol as a linear molecule.
そして、架橋ポリロタキサンは、隣接するポリロタキサンの環状分子間が架橋剤で架橋されたものである。架橋剤は、特定のものに限定されない。
架橋剤としては、塩化シアヌル、トリメソイルクロリド、テレフタロイルクロリド、エピクロロヒドリン、ジブロモベンゼン、グルタールアルデヒド、脂肪族多官能イソシアネート、芳香族多官能イソシアネート、ジイソシアン酸トリレイン、ヘキサメチレンジイソシアネート、ジビニルスルホン、1,1‘-カルボニルジイミダゾール、アルコキシシラン類、およびそれらの誘導体、ポリシロキサンを含有するブロック共重合体(ポリカプロラクトン-ポリシロキサンブロック共重合体、ポリアジペート-ポリシロキサンブロック共重合体、ポリエチレングリコール-ポリシロキサンブロック共重合体等)等を例示できる。
The crosslinked polyrotaxane is one in which the cyclic molecules of adjacent polyrotaxanes are crosslinked with a crosslinking agent. The cross-linking agent is not limited to a specific one.
Examples of the cross-linking agent include cyanul chloride, trimeoyl chloride, terephthaloyl chloride, epichlorohydrin, dibromobenzene, glutaaldehyde, aliphatic polyfunctional isocyanate, aromatic polyfunctional isocyanate, trilein diisosocyanate, hexamethylene diisocyanate, and divinyl. Block copolymers containing sulfones, 1,1'-carbonyldiimidazoles, alkoxysilanes and their derivatives, and polysiloxanes (polycaprolactone-polysiloxane block copolymers, polyadipates-polysiloxane block copolymers, Polyethylene glycol-polysiloxane block copolymer, etc.) can be exemplified.
[2]誘電エラストマー層
誘電エラストマー層の材料は、特に限定されず、各種の誘電エラストマーを用いることができる。
誘電エラストマーとしては、特に限定されないが、上記[1]に例示したものを同じく例示できる。これらのうち架橋ポリロタキサンが、誘電率が高い点で特に好ましい。
[2] Dielectric Elastomer Layer The material of the dielectric elastomer layer is not particularly limited, and various dielectric elastomers can be used.
The dielectric elastomer is not particularly limited, but the one exemplified in the above [1] can also be exemplified. Of these, crosslinked polyrotaxane is particularly preferable because it has a high dielectric constant.
[3]電極
電極の材料は、特に限定されないが、圧縮変形に追従して変形できるものとして、導電性粒子からなる導電性膜、導電性粒子を含む導電性塗膜、導電性粒子を含む導電性エラストマー成形体等を例示できる。
ここで、導電性粒子としては、特に限定されないが、カーボンブラック、カーボンナノチューブ、白金、金、銀、銅、ニッケル等の粒子等を例示できる。
導電性塗膜の樹脂成分としては、特に限定されないが、フタル酸系、アクリル系、ウレタン系、エポキシ系、ビニル系等の樹脂を例示できる。
導電性エラストマー成形体のエラストマー成分としては、特に限定されないが、上記[1]で例示した誘電エラストマーを例示できる。
[3] Electrode The material of the electrode is not particularly limited, but can be deformed according to compression deformation, such as a conductive film made of conductive particles, a conductive coating film containing conductive particles, and conductivity including conductive particles. Examples thereof include a sex elastomer molded product.
Here, the conductive particles are not particularly limited, and examples thereof include particles such as carbon black, carbon nanotubes, platinum, gold, silver, copper, and nickel.
The resin component of the conductive coating film is not particularly limited, and examples thereof include phthalic acid-based, acrylic-based, urethane-based, epoxy-based, and vinyl-based resins.
The elastomer component of the conductive elastomer molded product is not particularly limited, but the dielectric elastomer exemplified in the above [1] can be exemplified.
[3]気体層
気体層の気体は、特に限定されないが、空気、空気よりも誘電率が低い低誘電率ガス等を例示できる。低誘電率ガスとしては、窒素、炭酸ガス等を例示できる。
[3] Gas layer The gas in the gas layer is not particularly limited, and examples thereof include air and a low dielectric constant gas having a dielectric constant lower than that of air. Examples of the low dielectric constant gas include nitrogen and carbon dioxide gas.
以下、本発明を具体化した圧縮センサの実施例について、次の順に説明する。なお、本発明は本実施例に限定されるものではない。
<1>実施例に用いる架橋ポリロタキサン成形体の作製
<2>比較例としてのポリウレタン成形体
<3>架橋ポリロタキサン成形体とポリウレタン成形体の圧縮特性の測定
<4>実施例1の圧縮センサの作製
<5>実施例2の圧縮センサの作製
<6>実施例の圧縮センサの作用効果
<7>実施例の圧縮センサの使用態様
Hereinafter, examples of the compression sensor embodying the present invention will be described in the following order. The present invention is not limited to the present embodiment.
<1> Fabrication of crosslinked polyrotaxane molded article used in Examples <2> Polyurethane molded article as a comparative example <3> Measurement of compression characteristics of crosslinked polyrotaxane molded article and polyurethane molded article <4> Fabrication of compression sensor of Example 1 <5> Fabrication of compression sensor of Example 2 <6> Operation and effect of compression sensor of Example <7> Usage of compression sensor of Example
<1>実施例に用いる架橋ポリロタキサン成形体の作製
本出願人が先に提案した、特開2017-66318号公報の実施例2と同様のポリロタキサン組成物を作製した。
すなわち、まず、同公報に開示された、ポリロタキサンAと、ポリシロキサンを含有するブロック共重合体Bと、ポリシロキサンを含有しない重合体Cとを作製した。
ポリロタキサンAは、具体的には、環状分子としてシクロデキストリンを含有し、直鎖状分子としてポリエチレングリコールを含有し、直鎖状分子の両末端に封鎖基が配置されたものである。本例のポリロタキサンAは、さらに溶化性や相溶性を得るため、カプロラクトン基を有するものである。
ポリシロキサンを含有するブロック共重合体Bは、ポリシロキサン(シリコーン成分)により耐湿性を向上させるものであり、具体的には、末端ブロックイソシアネート基を有するポリカプロラクトン-ポリジメチルシロキサン-ポリカプロラクトンのブロック共重合体である。同共重合体Bの添加は任意である。
ポリシロキサンを含有しない重合体Cは、ポリロタキサンとの相溶性が高く、これを含むことで高誘電率と低弾性を実現するものであり、具体的には、末端ブロックイソシアネート基を有するポリプロピレングリコールである。同重合体Cの添加は任意である。
これらとその他の成分を、次に示す配合(配合数値は質量部)で加えて攪拌し、よく脱泡して、ポリロタキサン組成物溶液を調製した。
ポリロタキサンA 10
ポリシロキサンブロック共重合体B 10.6
重合体C 9
ポリプロピレングリコールジオール 4.7
メチルセロソルブ 25.3
ジラウリル酸ジブチルスズ 0.015
DBL-C31(GELEST社製) 0.15
IRGANOX1726(BASF社製) 0.45
<1> Preparation of Crosslinked Polyrotaxane Molded Product Used in Examples A polyrotaxane composition similar to Example 2 of JP-A-2017-66318, which was previously proposed by the present applicant, was prepared.
That is, first, the polyrotaxane A disclosed in the same publication, the block copolymer B containing polysiloxane, and the polymer C not containing polysiloxane were prepared.
Specifically, polyrotaxane A contains cyclodextrin as a cyclic molecule, polyethylene glycol as a linear molecule, and blocking groups are arranged at both ends of the linear molecule. The polyrotaxane A of this example has a caprolactone group in order to further obtain solubility and compatibility.
The block copolymer B containing polysiloxane has improved moisture resistance by polysiloxane (silicone component), and specifically, a block of polycaprolactone-polydimethylsiloxane-polycaprolactone having a terminal block isocyanate group. It is a copolymer. The addition of the copolymer B is optional.
Polymer C, which does not contain polysiloxane, has high compatibility with polyrotaxane, and by including this, high dielectric constant and low elasticity are realized. Specifically, polypropylene glycol having a terminal block isocyanate group is used. be. The addition of the polymer C is optional.
These and other components were added in the following formulation (formulation value is parts by mass), stirred, and defoamed well to prepare a polyrotaxane composition solution.
Polysiloxane block copolymer B 10.6
Polymer C 9
Polypropylene glycol diol 4.7
Methyl cellosolve 25.3
Dibutyltin dilauryl acid 0.015
DBL-C31 (manufactured by GELEST) 0.15
IRGANOX1726 (manufactured by BASF) 0.45
上記ポリロタキサン組成物溶液を、ポリエチレンテレフタラート(PET)板の上にスリットダイコータ法により塗布し、厚さ50μmのポリロタキサン成形体(膜)を形成した。続いて、PET板付きのポリロタキサン成形体を、130℃のオーブン内に減圧条件下で5時間おいて架橋・硬化させ、硬化した架橋ポリロタキサン成形体(誘電エラストマー成形体)をPET板から剥がした。 The above polyrotaxane composition solution was applied onto a polyethylene terephthalate (PET) plate by a slit die coater method to form a polyrotaxane molded product (film) having a thickness of 50 μm. Subsequently, the polyrotaxane molded product with a PET plate was crosslinked and cured in an oven at 130 ° C. under reduced pressure for 5 hours, and the cured crosslinked polyrotaxane molded product (dielectric elastomer molded product) was peeled off from the PET plate.
<2>比較例としてのポリウレタン成形体
比較例としてのポリウレタン成形体には、株式会社武田産業のポリウレタンフィルム(商品名「Tough Grace Film」、厚さ25μm)を用いた。
<2> Polyurethane molded product as a comparative example As the polyurethane molded product as a comparative example, a polyurethane film (trade name “Touch Grace Film”,
<3>架橋ポリロタキサン成形体とポリウレタン成形体の圧縮特性の測定
上記架橋ポリロタキサン成形体と上記ポリウレタン成形体を、それぞれ寸法10mm×10mmに切断して試験片とした。
図1に示すように、圧縮試験機の台に試験片を載せ、圧子を試験片に押し当てて変位させ、圧縮試験を行った。圧子先端は直径100μmの円形面であり、よって圧子面積は7.85×10-9m2 である。
<3> Measurement of Compression Characteristics of Crosslinked Polyrotaxane Molded Body and Polyurethane Molded Body The crosslinked polyrotaxane molded body and the polyurethane molded body were cut into test pieces having dimensions of 10 mm × 10 mm, respectively.
As shown in FIG. 1, a test piece was placed on the table of a compression tester, and an indenter was pressed against the test piece to displace it, and a compression test was performed. The tip of the indenter is a circular surface with a diameter of 100 μm, so the indenter area is 7.85 × 10 -9 m 2 .
図2は、架橋ポリロタキサン成形体の上記圧縮試験での変位-荷重曲線であり、同曲線から圧縮特性を求めて下記の表1に示した。まず、同曲線のカーブが立ち上がる屈伏点での荷重は約300mNであり、後述するように屈伏点以前に内部構造変化は見られなかったため、屈伏点での荷重を圧縮限界荷重(aとする)と評価し、aを圧子面積で除して圧縮限界応力(bとする)を求めた。また、屈伏点での変位を圧縮限界変位(cとする)とし、a/2荷重(dとする)での変位を1/2圧縮限界変位(eとする)とし、これらの変位差c-e(fとする)を求めた。そして、2×f/tを圧縮限界率(gとする)とし、b/gを圧縮弾性率(hとする)とした。 FIG. 2 shows the displacement-load curve of the crosslinked polyrotaxane molded product in the above compression test, and the compression characteristics were obtained from the curve and shown in Table 1 below. First, the load at the bending point where the curve of the same curve rises is about 300 mN, and as will be described later, no internal structural change was observed before the bending point, so the load at the bending point is the compression limit load (a). The compression limit stress (referred to as b) was obtained by dividing a by the indenter area. Further, the displacement at the yield point is defined as the compression limit displacement (c), the displacement at the a / 2 load (d) is defined as the 1/2 compression limit displacement (e), and the displacement difference c-. e (referred to as f) was obtained. Then, 2 × f / t was defined as the compression limit rate (referred to as g), and b / g was defined as the compressive elastic modulus (referred to as h).
図3(a)~(d)は、上記圧縮試験とは別に、架橋ポリロタキサン成形体に上記圧子で所定の荷重((a)100mN、(b)200mN、(c)300mN、(d)400mN)を載荷してから除荷したときの架橋ポリロタキサン成形体顕微鏡写真であり、円形の線は圧子による圧縮範囲の縁(以下「圧縮縁」という。)を写真に記入したものである(直径100μm)。いずれの顕微鏡写真を観察しても、圧縮縁に沿った内部構造変化は見られなかった。
3 (a) to 3 (d) show a predetermined load ((a) 100 mN, (b) 200 mN, (c) 300 mN, (d) 400 mN) on the crosslinked polyrotaxane molded product with the indenter, apart from the compression test. It is a photomicrograph of a crosslinked polyrotaxane molded product when it is loaded and then unloaded, and the circular line shows the edge of the compression range by the indenter (hereinafter referred to as "compression edge") in the photograph (
図4(a)は、ポリウレタン成形体の上記圧縮試験での変位-荷重曲線であり、図4(b)は(a)のIVb部の拡大曲線であり、同拡大曲線から圧縮特性を求めて上記の表1に示した。まず、図4(a)の曲線のカーブが立ち上がる屈伏点での荷重は約710mNであり、これだけからすると、上記架橋ポリロタキサン成形体よりも強いように思われる。しかし、後述するように屈伏点よりもはるか以前の荷重50mNで内部構造変化が見られたため、屈伏点での荷重を圧縮限界荷重とせず、図4(b)の拡大曲線の内部構造変化点での荷重50mNを圧縮限界荷重(aとする)と評価し、aを圧子面積で除して圧縮限界応力(bとする)を求めた。また、内部構造変化での変位を圧縮限界変位(cとする)とし、a/2荷重(dとする)での変位を1/2圧縮限界変位(eとする)とし、これらの変位差c-e(fとする)を求めた。そして、2×f/tを圧縮限界率(gとする)とし、b/gを圧縮弾性率(hとする)とした。 FIG. 4 (a) is a displacement-load curve of the polyurethane molded product in the compression test, and FIG. 4 (b) is an enlarged curve of the IVb portion of (a), and the compression characteristics are obtained from the enlarged curve. It is shown in Table 1 above. First, the load at the bending point where the curve of FIG. 4A rises is about 710 mN, which seems to be stronger than that of the crosslinked polyrotaxane molded product. However, as will be described later, since the internal structural change was observed at a load of 50 mN long before the bending point, the load at the bending point was not set as the compression limit load, and the internal structural change point of the enlarged curve in FIG. 4 (b) was used. The load of 50 mN was evaluated as the compression limit load (referred to as a), and a was divided by the indenter area to obtain the compression limit stress (referred to as b). Further, the displacement due to the internal structural change is defined as the compression limit displacement (c), the displacement due to the a / 2 load (d) is defined as the 1/2 compression limit displacement (e), and the displacement difference c between them. -E (referred to as f) was obtained. Then, 2 × f / t was defined as the compression limit rate (referred to as g), and b / g was defined as the compressive elastic modulus (referred to as h).
図5(a)~(d)は、上記圧縮試験とは別に、ポリウレタン成形体に上記圧子で所定の荷重((a)20mN、(b)50mN、(c)100mN、(d)200mN)を載荷してから除荷したときのポリウレタン成形体の顕微鏡写真であり、円形の線は圧縮縁である(直径100μm)。20mNの顕微鏡写真では圧縮縁に沿った明確な内部構造変化は見られなかったが、50mNの顕微鏡写真では圧縮縁に沿って多数の粒状の析出物が現れるという明確な内部構造変化が見られ始め、100mN・200nmの顕微鏡写真ではその内部構造変化が顕著になった。なお、析出物は、ウレタン反応時にイソシアネート成分と反応しなかったポリオール成分と考えられる。
5 (a) to 5 (d) show that, apart from the compression test, a predetermined load ((a) 20 mN, (b) 50 mN, (c) 100 mN, (d) 200 mN) is applied to the polyurethane molded product with the indenter. It is a micrograph of the polyurethane molded body when it was loaded and then unloaded, and the circular line is a compression edge (
以上のように、圧縮限界荷重は、屈伏点での荷重と内部構造変化点での荷重とのうち小さい方で評価される。そして、架橋ポリロタキサン成形体の方が、ポリウレタンよりも圧縮限界応力が高く、より大きな圧力まで変化しないといえる。 As described above, the compression limit load is evaluated by the smaller of the load at the yield point and the load at the internal structural change point. It can be said that the crosslinked polyrotaxane molded product has a higher compression limit stress than polyurethane and does not change to a larger pressure.
<4>実施例1の圧縮センサの作製
図6(a)に示すとおり、下から上へ順に、絶縁体、電極、誘電エラストマー層、枠状のスペーサ、電極及び絶縁体を積層してなり、下の電極と誘電エラストマー層とに挟まれ且つスペーサの枠内に囲まれた気体層としての空気層を有する、実施例1の圧縮センサを作製した。
<4> Fabrication of Compression Sensor of Example 1 As shown in FIG. 6A, an insulator, an electrode, a dielectric elastomer layer, a frame-shaped spacer, an electrode, and an insulator are laminated in this order from bottom to top. The compression sensor of Example 1 having an air layer as a gas layer sandwiched between a lower electrode and a dielectric elastomer layer and surrounded by a frame of a spacer was produced.
2つの絶縁体は、ポリカーボネートのシートである。 The two insulators are polycarbonate sheets.
2つの電極は、次に示す配合(配合数値は質量部)のシリコーンエラストマー組成物溶液を、絶縁体にスリットダイコータ法で塗布し、100℃×24時間で架橋・硬化させたものであり、厚さ20μmである。
シリコーンエラストマー 10
有機溶媒(ヘプタン) 300
カーボン粒子(ケッチェンブラック) 1
The two electrodes are obtained by applying a silicone elastomer composition solution having the following composition (the compounding value is parts by mass) to an insulator by the slit die coater method, and cross-linking and curing the insulator at 100 ° C. for 24 hours. It is 20 μm.
Organic solvent (heptane) 300
Carbon particles (Ketchen black) 1
誘電エラストマー層は、前記ポリロタキサン組成物溶液を上側の電極にスリットダイコータ法で塗布し、130℃×5時間で架橋・硬化させたもの(架橋ポリロタキサン)であり、厚さ50μmである。よって、誘電エラストマー層は、圧縮限界応力3.8×101 MPa、圧縮弾性率1.0×102 MPaである。 The dielectric elastomer layer is obtained by applying the polyrotaxane composition solution to the upper electrode by a slit die coater method, cross-linking and curing at 130 ° C. × 5 hours (cross-linked polyrotaxane), and has a thickness of 50 μm. Therefore, the dielectric elastomer layer has a compression limit stress of 3.8 × 10 1 MPa and a compressive elastic modulus of 1.0 × 10 2 MPa.
スペーサは、前記架橋ポリロタキサンで枠状に形成した成形体であり、厚さ300μmである。よって、スペーサは、圧縮限界応力3.8×101 MPa、圧縮弾性率1.0×102 MPaである。 The spacer is a molded product formed in a frame shape by the crosslinked polyrotaxane, and has a thickness of 300 μm. Therefore, the spacer has a compression limit stress of 3.8 × 10 1 MPa and a compressive elastic modulus of 1.0 × 10 2 MPa.
空気層は、空気よりなり、スペーサと等しく厚さ300μmである。 The air layer is made of air and has a thickness of 300 μm, which is equal to that of the spacer.
実施例1の圧縮センサは、外力で容易に圧縮変形し、まず空気層が圧縮される段階となり、続いて誘電エラストマー層が下の電極と接した後に圧縮される段階となり、いずれの段階でも静電容量が変動して、外力を検知できる。 The compression sensor of Example 1 is easily compressed and deformed by an external force, and the air layer is first compressed, and then the dielectric elastomer layer is in contact with the lower electrode and then compressed, and is static at any stage. External force can be detected by fluctuating the electric capacity.
<5>実施例2の圧縮センサの作製
図6(b)に示す実施例2の圧縮センサは、実施例1の空気層を空気よりも誘電率が低い低誘電率ガスよりなる気体層としての低誘電率ガス層に置換したものであり、その他は実施例1と共通である。
<5> Fabrication of Compression Sensor of Example 2 In the compression sensor of Example 2 shown in FIG. 6B, the air layer of Example 1 is a gas layer made of a low dielectric constant gas having a dielectric constant lower than that of air. It is replaced with a low dielectric constant gas layer, and the others are the same as in Example 1.
<6>実施例の圧縮センサの作用効果
実施例1,2の圧縮センサは、圧縮弾性率が5.0×102 MPa以下と低いため、僅かな力で容易に圧縮変形し、この僅かな力を測定することができる。
また、圧縮限界応力が1.0×101MPa以上と高いため、繰り返し働く大きな力も、再現性良く測定できる。
また、圧縮限界率が20%以上と高いため、センサの分解能が高い。
誘電エラストマー層に誘電率の高い架橋ポリロタキサンを使用したため、空気層が圧縮される段階でも、静電容量が大きく変動し、分解能が向上する。
<6> Actions and effects of the compression sensor of Examples The compression sensors of Examples 1 and 2 have a low compressive elastic modulus of 5.0 × 10 2 MPa or less, so that they are easily compressed and deformed with a slight force, and this slight amount is obtained. Force can be measured.
In addition, since the compression limit stress is as high as 1.0 × 101 MPa or more, a large force that repeatedly works can be measured with good reproducibility.
Moreover, since the compression limit rate is as high as 20% or more, the resolution of the sensor is high.
Since the crosslinked polyrotaxane having a high dielectric constant is used for the dielectric elastomer layer, the capacitance greatly fluctuates even at the stage where the air layer is compressed, and the resolution is improved.
その他にも、実施例1,2の圧縮センサは次の作用効果を奏する。
・垂直方向応力を壊れることなく測定することができる耐久性を有している。
・圧縮センサはそれ自体がエラストマーを含むため、把持物体へのグリップ力を高める。
・圧縮センサの変形量から、静止状態においては、把持力、把持物体の重量等を測定でき、慣性が生じるような把持物体の移動では、慣性モーメント、速度、移動量等を測定できる。
・高分解能、ワイドダイナミックレンジ測定、高S/N比であるため、センサの小型化が可能となり、狭小部への取り付けや、アレイ化による荷重分布測定が可能となる。荷重分布測定によって、把持物体への接触表面の把握ができ、把持物体の姿勢・把持位置の測定・モニタリングができる。
・これらの測定情報は、AIと組み合わせた強化学習に用いることができ、物体の安定把持、運搬方法等の最適化に用いることができる。
In addition, the compression sensors of Examples 1 and 2 have the following effects.
-Has durability that can measure vertical stress without breaking.
-Since the compression sensor itself contains an elastomer, it enhances the grip on the gripped object.
-From the amount of deformation of the compression sensor, the gripping force, the weight of the gripping object, etc. can be measured in the stationary state, and the moment of inertia, the speed, the moving amount, etc. can be measured when the gripping object moves so as to cause inertia.
-High resolution, wide dynamic range measurement, and high S / N ratio make it possible to reduce the size of the sensor, and it is possible to mount it in a narrow space and measure the load distribution by arranging it. By measuring the load distribution, the contact surface with the gripping object can be grasped, and the posture and gripping position of the gripping object can be measured and monitored.
-These measurement information can be used for reinforcement learning in combination with AI, and can be used for stable gripping of an object, optimization of a transportation method, and the like.
<7>実施例の圧縮センサの使用態様
実施例1,2の圧縮センサは、上記の作用効果を生かし、例えば次のような態様で使用できる。
・図7(a)に示すように、産業用ロボットや建設機械のハンド部分の指に圧縮センサを取り付けて使用する。
・図7(b)に示すように、シューズインソールや高重量ロボットの足裏に圧縮センサを取り付けて使用することにより、歩行・走行時の姿勢監視や、スポーツ時の体重移動等の測定が行える。
・その他、マット状のシートに圧縮センサを配置することで、そのマット上の荷重、重心移動の測定や、従来のマットセンサでは困難であった各種形状に沿わせて使用することが可能となる。
<7> Usage of the compression sensor of the embodiment The compression sensor of the first and second embodiments can be used in the following embodiments, for example, by taking advantage of the above-mentioned effects.
-As shown in FIG. 7 (a), a compression sensor is attached to the finger of the hand part of an industrial robot or a construction machine for use.
-As shown in Fig. 7 (b), by attaching a compression sensor to the shoe insole or the sole of a heavy-duty robot, posture monitoring during walking / running and measurement of weight transfer during sports can be performed. ..
-In addition, by arranging the compression sensor on the mat-shaped sheet, it is possible to measure the load on the mat and the movement of the center of gravity, and to use it according to various shapes that were difficult with the conventional mat sensor. ..
なお、本発明は前記実施例に限定されるものではなく、発明の趣旨から逸脱しない範囲で適宜変更して具体化することができる。 The present invention is not limited to the above embodiment, and can be appropriately modified and embodied without departing from the spirit of the invention.
Claims (7)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/JP2020/043790 WO2022113197A1 (en) | 2020-11-25 | 2020-11-25 | Compression sensor |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/JP2020/043790 WO2022113197A1 (en) | 2020-11-25 | 2020-11-25 | Compression sensor |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2022113197A1 true WO2022113197A1 (en) | 2022-06-02 |
Family
ID=81754231
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/JP2020/043790 Ceased WO2022113197A1 (en) | 2020-11-25 | 2020-11-25 | Compression sensor |
Country Status (1)
| Country | Link |
|---|---|
| WO (1) | WO2022113197A1 (en) |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS58173035A (en) * | 1982-04-02 | 1983-10-11 | Hitachi Ltd | Flaring method of tube end |
| US20060272429A1 (en) * | 2005-06-02 | 2006-12-07 | Ganapathi Srinivasan K | Flexible imaging pressure sensor |
| JP2010223953A (en) * | 2009-02-26 | 2010-10-07 | Tokai Rubber Ind Ltd | Capacitance-type pressure-sensitive sensor and manufacturing method thereof |
| JP2017066318A (en) * | 2015-10-01 | 2017-04-06 | 豊田合成株式会社 | Composition containing polyrotaxane and use thereof |
-
2020
- 2020-11-25 WO PCT/JP2020/043790 patent/WO2022113197A1/en not_active Ceased
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS58173035A (en) * | 1982-04-02 | 1983-10-11 | Hitachi Ltd | Flaring method of tube end |
| US20060272429A1 (en) * | 2005-06-02 | 2006-12-07 | Ganapathi Srinivasan K | Flexible imaging pressure sensor |
| JP2010223953A (en) * | 2009-02-26 | 2010-10-07 | Tokai Rubber Ind Ltd | Capacitance-type pressure-sensitive sensor and manufacturing method thereof |
| JP2017066318A (en) * | 2015-10-01 | 2017-04-06 | 豊田合成株式会社 | Composition containing polyrotaxane and use thereof |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Ying et al. | Waterproof, highly tough, and fast self-healing polyurethane for durable electronic skin | |
| Lozano-Pérez et al. | Influence of rigid segment and carbon nanotube concentration on the cyclic piezoresistive and hysteretic behavior of multiwall carbon nanotube/segmented polyurethane composites | |
| Ellingford et al. | Self-healing dielectric elastomers for damage-tolerant actuation and energy harvesting | |
| Shan et al. | Self-healing strain sensor based on silicone elastomer for human motion detection | |
| Li et al. | Biomimetic, recyclable, highly stretchable and self-healing conductors enabled by dual reversible bonds | |
| Lu et al. | High-toughness and intrinsically self-healing cross-linked polyurea elastomers with dynamic sextuple H-bonds | |
| Yang et al. | Self-healing and degradable polycaprolactone-based polyurethane elastomer for flexible stretchable strain sensors | |
| CN104937735B (en) | Polymer actuator | |
| JP2016153729A (en) | Deformation amount measuring structure | |
| Wu et al. | Stratum Corneum‐Inspired Zwitterionic Hydrogels with Intrinsic Water Retention and Anti‐Freezing Properties for Intelligent Flexible Sensors | |
| CN113272981B (en) | Buckling Dielectric Elastomer Actuator | |
| Lee et al. | Wrinkled elastomers for the highly stretchable electrodes with excellent fatigue resistances | |
| CN110408033A (en) | Self-healing thermoplastic silicone material and preparation method | |
| WO2022113197A1 (en) | Compression sensor | |
| Ma et al. | Bioinspired thermoplastic elastomer with flexible, self-healing capabilities | |
| CN110816008A (en) | Elastomer and method of making the same | |
| WO2020262017A1 (en) | Elastomer composition, and actuator and sensor | |
| Mathew et al. | Effects of silicone rubber on properties of dielectric acrylate elastomer actuator | |
| JP5243775B2 (en) | Dielectric film and actuator, sensor, and transducer using the same | |
| JP5317511B2 (en) | Actuator and its electrodes | |
| Aierken et al. | Reprocessable, Highly Transparent Ionic Conductive Elastomers Based on β-Amino Ester Chemistry for Sensing Devices | |
| WO2020066203A1 (en) | Polyrotaxane composition and sensor | |
| Zeng et al. | Effect of branched structure on microphase separation and electric field induced bending actuation behaviors of poly (urethane–urea) elastomers | |
| Encinas-Encinas et al. | Evaluation of Strain Sensors Based on Poly (acrylonitrile-co-butadiene) and Polypyrrole Synthesized by the Diffusion Method | |
| JP2020162283A (en) | Driving method of dielectric elastomer actuator and actuator device |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 20963462 Country of ref document: EP Kind code of ref document: A1 |
|
| NENP | Non-entry into the national phase |
Ref country code: DE |
|
| 122 | Ep: pct application non-entry in european phase |
Ref document number: 20963462 Country of ref document: EP Kind code of ref document: A1 |
|
| NENP | Non-entry into the national phase |
Ref country code: JP |