WO2017104813A1 - Composite particles and method for manufacturing same - Google Patents

Composite particles and method for manufacturing same Download PDF

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WO2017104813A1
WO2017104813A1 PCT/JP2016/087581 JP2016087581W WO2017104813A1 WO 2017104813 A1 WO2017104813 A1 WO 2017104813A1 JP 2016087581 W JP2016087581 W JP 2016087581W WO 2017104813 A1 WO2017104813 A1 WO 2017104813A1
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hydrogen
particles
hydrogen detection
composite particles
detection member
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PCT/JP2016/087581
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French (fr)
Japanese (ja)
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致維 胡
山田　保誠
吉村　和記
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国立研究開発法人産業技術総合研究所
致維 胡
山田　保誠
吉村　和記
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Priority to JP2017556471A priority Critical patent/JP6552015B2/en
Publication of WO2017104813A1 publication Critical patent/WO2017104813A1/en

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    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/75—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/75—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated
    • G01N21/77—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated by observing the effect on a chemical indicator
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/75—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated
    • G01N21/77—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated by observing the effect on a chemical indicator
    • G01N21/78—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated by observing the effect on a chemical indicator producing a change of colour
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N31/00—Investigating or analysing non-biological materials by the use of the chemical methods specified in the subgroup; Apparatus specially adapted for such methods

Definitions

  • the present invention relates to composite particles, a method for producing composite particles, a hydrogen detection member, a hydrogen detection method, and a method for processing a hydrogen detection member.
  • a hydrogen detection member In order to detect hydrogen, a hydrogen detection member is used as an indispensable element.
  • a hydrogen detection member As a hydrogen detection member, a hydrogen sensor that detects hydrogen by a change in electrical resistance of the surface of a semiconductor (tin oxide) due to adsorption of hydrogen is often used.
  • the operating temperature is about 400 ° C. and heating is required.
  • Patent Document 1 discloses an element having a stacked structure of a metal that adsorbs and dissociates hydrogen or a hydrogen-containing compound gas and a solid compound that is reduced by hydrogen atoms in the metal, and changes in light absorption of the solid compound due to reduction.
  • a gas sensor comprising optical means for detection is disclosed.
  • Patent Document 2 discloses a hydrogen sensor in which a catalyst layer is formed in contact with a magnesium thin film having a thickness of 40 nm or less.
  • Patent Document 3 on the substrate, are a thickness of 10 ⁇ 200 nm magnesium-palladium alloy MgPd x (0.05 ⁇ x ⁇ 0.3 ) thin film is formed, on the substrate, or A hydrogen sensor in which a catalyst layer is further formed on a thin film is disclosed.
  • One embodiment of the present invention provides composite particles capable of detecting hydrogen in a short time by visual observation and maintaining the state in which hydrogen is detected even when temporarily exposed to an atmosphere containing hydrogen. With the goal.
  • nanopalladium particles are attached to the surface of nickel oxyhydroxide particles in a composite particle, and the molar ratio of Pd to Ni is 0.01 to 0.03.
  • FIG. 2 is an FT-IR spectrum of the composite particles of Example 1.
  • 2 is an X-ray photoelectron spectroscopy spectrum around Ni 2p of the composite particle of Example 1.
  • FIG. 2 is an X-ray photoelectron spectroscopy spectrum around Pd 3d of the composite particles of Example 1.
  • FIG. 2 is an X-ray diffraction spectrum of a composite particle of Example 1.
  • FIG. 2 is a scanning electron micrograph (2000 times) of the composite particles of Example 1.
  • FIG. 2 is a scanning electron micrograph (10,000 times) of the composite particles of Example 1.
  • FIG. FIG. 3 is a schematic view showing an optical device for measuring the light transmittance of the hydrogen detection member of Example 1. It is a figure which shows the measurement result of the light transmittance of the hydrogen detection member of Example 1.
  • FIG. It is the photograph before and behind detecting the hydrogen of the hydrogen detection member of Example 1.
  • nanopalladium particles are attached to the surface of the nickel oxyhydroxide particles.
  • the molar ratio of Pd to Ni in the composite particles is 0.01 to 0.03, preferably 0.15 to 0.025.
  • hydrogen cannot be detected in a short time by visual observation, and when it exceeds 0.03, hydrogen cannot be detected by visual observation.
  • the composite particles When the composite particles are exposed to an atmosphere containing hydrogen, nickel oxyhydroxide is reduced to nickel hydroxide by the catalytic action of nanopalladium particles adhering to the surface of the composite particles, and the wavelength ranges from 400 to 800 nm. Thus, the light transmittance or reflectance changes.
  • the nickel oxyhydroxide particles are black.
  • the particle diameter of the nickel oxyhydroxide particles is preferably 2 to 5 ⁇ m.
  • the method for synthesizing the nickel oxyhydroxide particles is not particularly limited, and examples thereof include a chemical bath deposition method, a coprecipitation method, and a uniform precipitation method.
  • Nickel oxyhydroxide particles can be synthesized by dropping an aqueous solution of a metal compound containing, an aqueous solution of potassium persulfate, and an aqueous solution of ammonium hydroxide.
  • a sufficient amount of an aqueous solution of an alkali metal hydroxide is preferably added appropriately.
  • the catalytic properties of nanopalladium particles are dramatically improved compared to normal palladium particles due to the increase in surface area accompanying the nanosize of the particle size.
  • the number average particle diameter of the nanopalladium particles is preferably 20 to 40 nm.
  • the nanopalladium particles preferably have a protective layer formed on the surface.
  • the protective layer preferably contains a water-soluble polymer.
  • the water-soluble polymer is not particularly limited, and examples thereof include polyvinyl pyrrolidone and polyol.
  • the method for synthesizing the nanopalladium particles is not particularly limited, and examples thereof include a chemical reduction method and a solution method.
  • reaction solution for example, in a reaction vessel at 70 ° C., an aqueous solution of a metal compound containing palladium as a main component, a water-soluble polymer as a material constituting the protective layer, and an aqueous solution of sodium hydroxide (NaOH) are reacted. By doing so, nanopalladium particles can be synthesized. At that time, the reaction solution is preferably made alkaline.
  • FIG. 1 shows an example of a method for producing composite particles of the present embodiment.
  • the composite particles 1 can be produced by mixing the nickel oxyhydroxide particles 1a and the nanopalladium particles 1b in a solvent.
  • the solvent is not particularly limited, and examples thereof include water and ethanol. Among these, water is particularly preferable.
  • FIG. 2 shows an example of the hydrogen detection member of this embodiment.
  • the hydrogen detection member detects hydrogen by a change in optical properties, and a hydrogen detection film 2 including the composite particles 1 is formed on the substrate 3.
  • the hydrogen detection film 2 changes in light transmittance or reflectance according to an atmosphere containing hydrogen to be exposed.
  • the film thickness of the hydrogen detection film 2 is preferably 20 to 100 ⁇ m.
  • the thickness of the hydrogen detection film 2 is 20 ⁇ m or more, the black color of the hydrogen detection film 2 is easily recognized by visual observation.
  • the thickness is 100 ⁇ m or less, the white color of the hydrogen detection film 2 is easily recognized by visual observation.
  • the hydrogen detection film 2 can be formed by a wet coating method.
  • the wet coating method is not particularly limited, and examples thereof include a spin coating method, a spray coating method, a dip coating method, and a drop coating method.
  • the hydrogen detection film 2 can be formed by a wet coating method, the hydrogen detection film 2 having a large surface area can also be formed at high speed. Further, since an expensive vacuum device or the like is not used, the hydrogen detection member of the present embodiment can be manufactured at a very low cost compared to the conventional hydrogen detection member.
  • the material constituting the substrate 3 is not particularly limited, but is an oxide such as glass, quartz, sapphire, and lithium niobate, polymer such as polyethylene terephthalate (PET), and cellophane tape that transmits light in the visible light region. Examples thereof include metals and opaque plastics that reflect light in the visible light region.
  • FIG. 3 shows an example of the hydrogen detection method of the present embodiment.
  • the hydrogen detection film 2 is black in a state before detecting hydrogen (see FIG. 3A), but changes to white when hydrogen is detected by exposure to an atmosphere containing hydrogen (FIG. 3B). )reference). Therefore, the hydrogen detection member of the present embodiment has a greater contrast before and after hydrogen detection than the conventional hydrogen detection member, so that even when a small amount of hydrogen is contained in the atmosphere, hydrogen can be detected visually. .
  • the hydrogen detection film 2 has a memory property that retains white color once it is detected and changes to white color. Therefore, even when hydrogen leakage has occurred in the past and then no longer occurs, hydrogen leakage can be visually confirmed. For this reason, a hydrogen detection member can be used for the use which detects a hydrogen leak. Furthermore, even if the hydrogen detection film 2 changes to white once, by treating with ozone (O 3 ), nickel hydroxide in the composite particles is oxidized to nickel oxyhydroxide and can be returned to black. . This makes it possible to reuse the hydrogen detection member.
  • Example 1 ⁇ Synthesis of nickel oxyhydroxide particles> 1.0M and nickel (II) sulfate hexahydrate (NiSO 4 ⁇ 6H 2 O) aqueous solution of 25 ml, 0.25M potassium persulfate (K 2 S 2 O 8) with stirring an aqueous solution 18.25ml mixed, mixed A liquid was obtained.
  • FT-IR apparatus Frontier Fourier transform near-infrared / mid-infrared / far-infrared spectrometer (Perkin Elmer Japan) was used to measure the FT-IR spectrum of the composite particles.
  • FIG. 4 shows the FT-IR spectrum of the composite particles.
  • the X-ray photoelectron spectroscopy spectrum of the composite particles was measured using an X-ray photoelectron spectrometer Theta Probe Angle-Resolved Spectrometer system (manufactured by Thermo Fisher Scientific).
  • FIG. 5 shows an X-ray photoelectron spectroscopy spectrum around Ni 2p of the composite particle.
  • the composite particles had a molar ratio of Pd to Ni of 0.025.
  • FIG. 6 shows an X-ray photoelectron spectrum around Pd 3d of the composite particle.
  • the X-ray diffraction spectrum of the composite particles was measured using an X-ray diffractometer X'Pert-MRD (manufactured by Philip).
  • FIG. 7 shows an X-ray diffraction spectrum of the composite particle.
  • FIG. 8 shows a scanning electron micrograph (2000 ⁇ magnification) of the composite particles.
  • FIG. 8 shows that nickel oxyhydroxide particles having a particle diameter of about 2 to 3 ⁇ m are aggregated.
  • FIG. 9 shows a scanning electron micrograph (10,000 times) of the composite particles.
  • FIG. 9 shows that the individual nickel oxyhydroxide particles have irregular sheet flakes on the surface.
  • 150 ⁇ l of the composite particle aqueous dispersion was drop-coated on a 3 cm ⁇ 3 cm silica glass substrate to form a hydrogen detection film having a thickness of 50 ⁇ m to obtain a hydrogen detection member.
  • the light transmittance of the hydrogen detection member before and after being exposed to an atmosphere having a hydrogen content of 4% was measured using the optical apparatus shown in FIG.
  • the optical device includes a light source 4 and a spectroscope 5, and a base material 3 on which a hydrogen detection film 2 is formed, that is, a hydrogen detection member is disposed between the light source 4 and the spectroscope 5 to transmit light. Measure the rate.
  • FIG. 11 shows the measurement results of the light transmittance of the hydrogen detection member.
  • FIG. 12 shows photographs before and after detecting the hydrogen of the hydrogen detection member.
  • the hydrogen detection film was black (see FIG. 12B) before being exposed to the hydrogen atmosphere, but changed to white (see FIG. 12A) when exposed to the hydrogen atmosphere.
  • the time required for the hydrogen detection film to change to white after being exposed to the hydrogen atmosphere that is, the time for visually detecting hydrogen was 3 minutes.
  • the hydrogen detection film returned to black in 5 seconds when ozone treatment was performed under the conditions of an ozone output of 70 mg / h and an air flow rate of 5 L / min using an ozone generator Soec V350 (manufactured by Marco Co., Ltd.). For this reason, the hydrogen detection member can be reused.
  • Composite particles and a hydrogen detection member were produced in the same manner as in Example 1 except that the amount of the nanopalladium particle dispersion added was changed to 0.1 ml.
  • the composite particles had a molar ratio of Pd to Ni of 0.0015.
  • Example 2 ⁇ Production of composite particles and hydrogen detection member> Composite particles and a hydrogen detection member were produced in the same manner as in Example 1 except that the amount of the nanopalladium particle dispersion added was changed to 0.5 ml. The composite particles had a molar ratio of Pd to Ni of 0.01.
  • the hydrogen detection film was black before being exposed to an atmosphere containing hydrogen, but turned white when exposed to a hydrogen atmosphere. At this time, the hydrogen detection film had a time of 15 minutes for visually detecting hydrogen. Moreover, even if the hydrogen detection film was stopped from being exposed to the hydrogen atmosphere, it did not return to black and maintained white. On the other hand, the hydrogen detection film returned to black in 5 seconds when ozone treatment was performed under the conditions of an ozone output of 70 mg / h and an air flow rate of 5 L / min using an ozone generator Soec V350 (manufactured by Marco Co., Ltd.). For this reason, the hydrogen detection film can be reused.
  • this embodiment relates to a hydrogen detection material, a hydrogen detection member, and a hydrogen detection method using a nickel oxyhydroxide-nanopalladium thin film, and according to this embodiment, heating is not required.
  • a hydrogen detector that operates at room temperature can be produced.
  • the hydrogen detection member of the present embodiment can be manufactured at low cost because its basic constituent material is inexpensive and an expensive noble metal material is used in a very small amount.
  • this embodiment can be manufactured by a simple process using only a wet method and has a simple structure, it is possible to realize a hydrogen detector that is excellent in performance and inexpensive.

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Abstract

One aspect of the present invention is composite particles, wherein nano-palladium particles are bonded to the surface of nickel oxyhydroxide particles, the molar ratio of Pd to Ni being 0.01-0.03.

Description

複合粒子及びその製造方法Composite particle and method for producing the same
　本発明は、複合粒子、複合粒子の製造方法、水素検知部材、水素検知方法及び水素検知部材の処理方法に関する。 The present invention relates to composite particles, a method for producing composite particles, a hydrogen detection member, a hydrogen detection method, and a method for processing a hydrogen detection member.
　近年、ＣＯ２等の温室効果ガスの放出による地球温暖化が問題となっており、水素エネルギーが大きな注目を集めている。水素は、酸素が存在する雰囲気中で爆発の危険性を持つため、今後、水素検知部材の需要が飛躍的に増大することが予想されるが、水素検知部材の取扱いには十分な安全対策が必要とされる。 In recent years, global warming due to the release of greenhouse gases such as CO 2 has become a problem, and hydrogen energy has attracted much attention. Hydrogen is expected to explode in the atmosphere where oxygen is present, so it is expected that the demand for hydrogen detection members will increase dramatically in the future. However, there are sufficient safety measures for handling hydrogen detection members. Needed.
　水素を検知するためには、水素検知部材が不可欠の要素として用いられる。 In order to detect hydrogen, a hydrogen detection member is used as an indispensable element.
　水素検知部材としては、水素の吸着による半導体（酸化スズ）の表面の電気抵抗の変化により水素を検知する水素センサがよく用いられている。 As a hydrogen detection member, a hydrogen sensor that detects hydrogen by a change in electrical resistance of the surface of a semiconductor (tin oxide) due to adsorption of hydrogen is often used.
　しかしながら、動作温度が４００℃程度であり、加熱を要するという問題がある。 However, there is a problem that the operating temperature is about 400 ° C. and heating is required.
　特許文献１には、水素又は含水素化合物ガスを吸着解離する金属と、金属中の水素原子により還元される固体化合物との積層構造を備えた素子と、還元による固体化合物の光吸収の変化を検出する光学手段とを備えたガスセンサが開示されている。 Patent Document 1 discloses an element having a stacked structure of a metal that adsorbs and dissociates hydrogen or a hydrogen-containing compound gas and a solid compound that is reduced by hydrogen atoms in the metal, and changes in light absorption of the solid compound due to reduction. A gas sensor comprising optical means for detection is disclosed.
　特許文献２には、厚さが４０ｎｍ以下であるマグネシウム薄膜に接して触媒層が形成されている水素センサが開示されている。 Patent Document 2 discloses a hydrogen sensor in which a catalyst layer is formed in contact with a magnesium thin film having a thickness of 40 nm or less.
　特許文献３には、基材の上に、厚さが１０～２００ｎｍであるマグネシウム・パラジウム合金ＭｇＰｄｘ（０．０５≦ｘ≦０．３）薄膜が形成されており、基材の上、又は、薄膜の上に触媒層がさらに形成されている水素センサが開示されている。 Patent Document 3, on the substrate, are a thickness of 10 ~ 200 nm magnesium-palladium alloy MgPd x (0.05 ≦ x ≦ 0.3 ) thin film is formed, on the substrate, or A hydrogen sensor in which a catalyst layer is further formed on a thin film is disclosed.
特開昭６０－３９５３６号公報Japanese Unexamined Patent Publication No. 60-39536 特開２００４－５３５４０号公報JP 2004-53540 A 特開２００７－７１５４７号公報JP 2007-71547 A
　しかしながら、水素を含む雰囲気に一時的に曝された場合でも、水素を検知した状態を維持することが望まれている。これにより、過去に水素漏れが発生し、その後、水素漏れが発生しなくなった場合でも、その事実を知ることができる。 However, it is desired to maintain a state in which hydrogen is detected even when it is temporarily exposed to an atmosphere containing hydrogen. Thereby, even if hydrogen leakage has occurred in the past and hydrogen leakage has not occurred thereafter, the fact can be known.
　また、目視により短時間で水素を検知することが望まれている。 Also, it is desired to detect hydrogen in a short time by visual inspection.
　本発明の一態様は、目視により短時間で水素を検知すると共に、水素を含む雰囲気に一時的に曝された場合でも、水素を検知した状態を維持することが可能な複合粒子を提供することを目的とする。 One embodiment of the present invention provides composite particles capable of detecting hydrogen in a short time by visual observation and maintaining the state in which hydrogen is detected even when temporarily exposed to an atmosphere containing hydrogen. With the goal.
　本発明の一態様は、複合粒子において、オキシ水酸化ニッケル粒子の表面にナノパラジウム粒子が付着しており、Ｎｉに対するＰｄのモル比が０．０１以上０．０３以下である。 In one embodiment of the present invention, nanopalladium particles are attached to the surface of nickel oxyhydroxide particles in a composite particle, and the molar ratio of Pd to Ni is 0.01 to 0.03.
　本発明の一態様によれば、目視により短時間で水素を検知すると共に、水素を含む雰囲気に一時的に曝された場合でも、水素を検知した状態を維持することが可能な複合粒子を提供することができる。 According to one embodiment of the present invention, it is possible to provide composite particles capable of detecting hydrogen in a short time by visual observation and maintaining the state in which hydrogen is detected even when temporarily exposed to an atmosphere containing hydrogen. can do.
本実施形態の複合粒子の作製方法の一例を示す模式図である。It is a schematic diagram which shows an example of the preparation methods of the composite particle of this embodiment. 本実施形態の水素検知部材の一例を示す模式図である。It is a schematic diagram which shows an example of the hydrogen detection member of this embodiment. 本実施形態の水素検知方法の一例を示す模式図である。It is a schematic diagram which shows an example of the hydrogen detection method of this embodiment. 実施例１の複合粒子のＦＴ－ＩＲスペクトルである。2 is an FT-IR spectrum of the composite particles of Example 1. 実施例１の複合粒子のＮｉ２ｐ周辺のＸ線光電子分光スペクトルである。2 is an X-ray photoelectron spectroscopy spectrum around Ni 2p of the composite particle of Example 1. FIG. 実施例１の複合粒子のＰｄ３ｄ周辺のＸ線光電子分光スペクトルである。2 is an X-ray photoelectron spectroscopy spectrum around Pd 3d of the composite particles of Example 1. FIG. 実施例１の複合粒子のＸ線回折スペクトルである。2 is an X-ray diffraction spectrum of a composite particle of Example 1. FIG. 実施例１の複合粒子の走査型電子顕微鏡写真（２０００倍）である。2 is a scanning electron micrograph (2000 times) of the composite particles of Example 1. FIG. 実施例１の複合粒子の走査型電子顕微鏡写真（１００００倍）である。2 is a scanning electron micrograph (10,000 times) of the composite particles of Example 1. FIG. 実施例１の水素検知部材の光の透過率を測定する光学装置を示す概略図である。FIG. 3 is a schematic view showing an optical device for measuring the light transmittance of the hydrogen detection member of Example 1. 実施例１の水素検知部材の光の透過率の測定結果を示す図である。It is a figure which shows the measurement result of the light transmittance of the hydrogen detection member of Example 1. FIG. 実施例１の水素検知部材の水素を検知する前後の写真である。It is the photograph before and behind detecting the hydrogen of the hydrogen detection member of Example 1. FIG.
　次に、本発明を実施するための形態を説明するが、本発明の範囲を逸脱することなく、下記の実施形態に種々の変形及び置換を加えることができる。 Next, modes for carrying out the present invention will be described, but various modifications and substitutions can be made to the following embodiments without departing from the scope of the present invention.
　［複合粒子］
　複合粒子は、オキシ水酸化ニッケル粒子の表面にナノパラジウム粒子が付着している。 [Composite particles]
In the composite particles, nanopalladium particles are attached to the surface of the nickel oxyhydroxide particles.
　複合粒子のＮｉに対するＰｄのモル比は、０．０１～０．０３であり、０.１５～０.０２５であることが好ましい。複合粒子のＮｉに対するＰｄのモル比が０．０１未満であると、目視により短時間で水素を検知することができなくなり、０．０３を超えると、目視により水素を検知することができなくなる。 The molar ratio of Pd to Ni in the composite particles is 0.01 to 0.03, preferably 0.15 to 0.025. When the molar ratio of Pd to Ni in the composite particles is less than 0.01, hydrogen cannot be detected in a short time by visual observation, and when it exceeds 0.03, hydrogen cannot be detected by visual observation.
　複合粒子を、水素を含む雰囲気に曝すと、複合粒子の表面に付着しているナノパラジウム粒子の触媒作用により、オキシ水酸化ニッケルが還元されて水酸化ニッケルになり、波長が４００～８００ｎｍの範囲で、光の透過率又は反射率が変化する。 When the composite particles are exposed to an atmosphere containing hydrogen, nickel oxyhydroxide is reduced to nickel hydroxide by the catalytic action of nanopalladium particles adhering to the surface of the composite particles, and the wavelength ranges from 400 to 800 nm. Thus, the light transmittance or reflectance changes.
　オキシ水酸化ニッケル粒子は、黒色である。 The nickel oxyhydroxide particles are black.
　オキシ水酸化ニッケル粒子の粒径は、２～５μｍであることが好ましい。 The particle diameter of the nickel oxyhydroxide particles is preferably 2 to 5 μm.
　オキシ水酸化ニッケル粒子の合成方法としては、特に限定されないが、化学浴析出法、共沈法、均一沈殿法等が挙げられる。 The method for synthesizing the nickel oxyhydroxide particles is not particularly limited, and examples thereof include a chemical bath deposition method, a coprecipitation method, and a uniform precipitation method.
　例えば、室温の反応槽中に、主成分としての、ニッケルと、副成分としての、他の遷移金属元素、１族元素、２族元素及び１３族元素からなる群より選択される一種以上の元素を含む金属化合物の水溶液と、過硫酸カリウムの水溶液と、水酸化アンモニウムの水溶液とを滴下することにより、オキシ水酸化ニッケル粒子を合成することができる。その際、反応液をアルカリ性、好ましくはｐＨを１０～１４に保持するために、十分な量のアルカリ金属の水酸化物の水溶液を適宜滴下することが好ましい。 For example, in a reaction chamber at room temperature, one or more elements selected from the group consisting of nickel as a main component and other transition metal elements, group 1, element 2 and group 13 elements as subcomponents Nickel oxyhydroxide particles can be synthesized by dropping an aqueous solution of a metal compound containing, an aqueous solution of potassium persulfate, and an aqueous solution of ammonium hydroxide. At that time, in order to keep the reaction solution alkaline, preferably at a pH of 10 to 14, a sufficient amount of an aqueous solution of an alkali metal hydroxide is preferably added appropriately.
　ナノパラジウム粒子は、粒径のナノサイズ化に伴う表面積の増加により、通常のパラジウム粒子と比較して、その触媒特性が劇的に向上する。 The catalytic properties of nanopalladium particles are dramatically improved compared to normal palladium particles due to the increase in surface area accompanying the nanosize of the particle size.
　ナノパラジウム粒子の個数平均粒径は、２０～４０ｎｍであることが好ましい。 The number average particle diameter of the nanopalladium particles is preferably 20 to 40 nm.
　ナノパラジウム粒子は、表面に保護層が形成されていることが好ましい。 The nanopalladium particles preferably have a protective layer formed on the surface.
　保護層は、水溶性高分子を含むことが好ましい。 The protective layer preferably contains a water-soluble polymer.
　水溶性高分子としては、特に限定されないが、ポリビニルピロリドン、ポリオール等が挙げられる。 The water-soluble polymer is not particularly limited, and examples thereof include polyvinyl pyrrolidone and polyol.
　ナノパラジウム粒子の合成方法としては、特に限定されないが、化学還元法、溶液法等が挙げられる。 The method for synthesizing the nanopalladium particles is not particularly limited, and examples thereof include a chemical reduction method and a solution method.
　例えば、７０℃の反応槽中に、主成分としての、パラジウムを含む金属化合物の水溶液と、保護層を構成する材料としての、水溶性高分子と、水酸化ナトリウム（ＮａＯＨ）の水溶液とを反応させることにより、ナノパラジウム粒子を合成することができる。その際、反応液をアルカリ性にすることが好ましい。 For example, in a reaction vessel at 70 ° C., an aqueous solution of a metal compound containing palladium as a main component, a water-soluble polymer as a material constituting the protective layer, and an aqueous solution of sodium hydroxide (NaOH) are reacted. By doing so, nanopalladium particles can be synthesized. At that time, the reaction solution is preferably made alkaline.
　図１に、本実施形態の複合粒子の作製方法の一例を示す。 FIG. 1 shows an example of a method for producing composite particles of the present embodiment.
　複合粒子１は、オキシ水酸化ニッケル粒子１ａとナノパラジウム粒子１ｂを溶媒中で混合することにより作製することができる。 The composite particles 1 can be produced by mixing the nickel oxyhydroxide particles 1a and the nanopalladium particles 1b in a solvent.
　溶媒としては、特に限定されないが、水、エタノール等が挙げられる。これらの中でも、特に水が好ましい。 The solvent is not particularly limited, and examples thereof include water and ethanol. Among these, water is particularly preferable.
　［水素検知部材］
　図２に、本実施形態の水素検知部材の一例を示す。 [Hydrogen detection member]
FIG. 2 shows an example of the hydrogen detection member of this embodiment.
　水素検知部材は、光学的性質の変化により水素を検知し、複合粒子１を含む水素検知膜２が基材３上に形成されている。水素検知膜２は、曝される水素を含む雰囲気に応じて、光の透過率又は反射率が変化する。 The hydrogen detection member detects hydrogen by a change in optical properties, and a hydrogen detection film 2 including the composite particles 1 is formed on the substrate 3. The hydrogen detection film 2 changes in light transmittance or reflectance according to an atmosphere containing hydrogen to be exposed.
　水素検知膜２の膜厚は、２０～１００μｍであることが好ましい。水素検知膜２の膜厚が２０μｍ以上であると、水素検知膜２の黒色を目視により認識しやすくなるため、１００μｍ以下であると、水素検知膜２の白色を目視により認識しやすくなる。 The film thickness of the hydrogen detection film 2 is preferably 20 to 100 μm. When the thickness of the hydrogen detection film 2 is 20 μm or more, the black color of the hydrogen detection film 2 is easily recognized by visual observation. When the thickness is 100 μm or less, the white color of the hydrogen detection film 2 is easily recognized by visual observation.
　水素検知膜２は、湿式塗布法により形成することができる。 The hydrogen detection film 2 can be formed by a wet coating method.
　湿式塗布法としては、特に限定されないが、スピンコート法、スプレーコート法、ディップコート法、ドロップコート法等が挙げられる。 The wet coating method is not particularly limited, and examples thereof include a spin coating method, a spray coating method, a dip coating method, and a drop coating method.
　本実施形態では、湿式塗布法により、水素検知膜２を形成することができるため、表面積が大きい水素検知膜２も高速で形成することができる。また、高価な真空装置等を用いないため、従来の水素検知部材に比べて、非常に低コストで、本実施形態の水素検知部材を製造することが可能となる。 In this embodiment, since the hydrogen detection film 2 can be formed by a wet coating method, the hydrogen detection film 2 having a large surface area can also be formed at high speed. Further, since an expensive vacuum device or the like is not used, the hydrogen detection member of the present embodiment can be manufactured at a very low cost compared to the conventional hydrogen detection member.
　基材３を構成する材料としては、特に限定されないが、可視光領域の光を透過する、ガラス、石英、サファイア、ニオブ酸リチウム等の酸化物、ポリエチレンテレフタレート（ＰＥＴ）、セロハンテープ等の高分子、可視光領域の光を反射する、金属及び不透明なプラスチック等が挙げられる。 The material constituting the substrate 3 is not particularly limited, but is an oxide such as glass, quartz, sapphire, and lithium niobate, polymer such as polyethylene terephthalate (PET), and cellophane tape that transmits light in the visible light region. Examples thereof include metals and opaque plastics that reflect light in the visible light region.
　［水素検知方法］
　図３に、本実施形態の水素検知方法の一例を示す。 [Hydrogen detection method]
FIG. 3 shows an example of the hydrogen detection method of the present embodiment.
　水素検知膜２は、水素を検知する前の状態では、黒色であるが（図３（ａ）参照）、水素を含む雰囲気に曝して、水素を検知すると、白色に変化する（図３（ｂ）参照）。したがって、本実施形態の水素検知部材は、従来の水素検知部材よりも、水素を検知する前後のコントラストが大きいため、雰囲気に微量の水素が含まれる場合でも、目視により水素を検知することができる。 The hydrogen detection film 2 is black in a state before detecting hydrogen (see FIG. 3A), but changes to white when hydrogen is detected by exposure to an atmosphere containing hydrogen (FIG. 3B). )reference). Therefore, the hydrogen detection member of the present embodiment has a greater contrast before and after hydrogen detection than the conventional hydrogen detection member, so that even when a small amount of hydrogen is contained in the atmosphere, hydrogen can be detected visually. .
　また、水素検知膜２は、水素を検知して、一旦白色に変化すると、白色を保持するメモリー性がある。そのため、過去に水素漏れが発生し、その後、水素漏れが発生しなくなった場合でも、水素漏れを目視により確認することができる。このため、水素検知部材は、水素漏れを検知する用途で用いることができる。
　さらに、水素検知膜２は、一旦白色に変化しても、オゾン（Ｏ３）処理することで、複合粒子中の水酸化ニッケルが酸化されてオキシ水酸化ニッケルになり、黒色に戻すことができる。これにより、水素検知部材を再利用することが可能になる。 In addition, the hydrogen detection film 2 has a memory property that retains white color once it is detected and changes to white color. Therefore, even when hydrogen leakage has occurred in the past and then no longer occurs, hydrogen leakage can be visually confirmed. For this reason, a hydrogen detection member can be used for the use which detects a hydrogen leak.
Furthermore, even if the hydrogen detection film 2 changes to white once, by treating with ozone (O 3 ), nickel hydroxide in the composite particles is oxidized to nickel oxyhydroxide and can be returned to black. . This makes it possible to reuse the hydrogen detection member.
　（実施例１）
　＜オキシ水酸化ニッケル粒子の合成＞
　１．０Ｍ硫酸ニッケル（ＩＩ）六水和物（ＮｉＳＯ４・６Ｈ２Ｏ）水溶液２５ｍｌと、０．２５Ｍ過硫酸カリウム（Ｋ２Ｓ２Ｏ８）水溶液１８．２５ｍｌを撹拌しながら混合し、混合液を得た。 Example 1
<Synthesis of nickel oxyhydroxide particles>
1.0M and nickel (II) sulfate hexahydrate (NiSO 4 · 6H 2 O) aqueous solution of 25 ml, 0.25M potassium persulfate (K 2 S 2 O 8) with stirring an aqueous solution 18.25ml mixed, mixed A liquid was obtained.
　２８質量％水酸化アンモニウム水溶液６．２５ｍｌと、混合液を撹拌しながら混合し、室温で約１時間反応させると、黒色のオキシ水酸化ニッケル粒子の沈澱が生成した。次に、８０００ｒｐｍで遠心分離した後、三回水洗し、オキシ水酸化ニッケル粒子を回収した。 When 6.25 ml of 28 mass% ammonium hydroxide aqueous solution was mixed with stirring and reacted at room temperature for about 1 hour, precipitation of black nickel oxyhydroxide particles was generated. Next, after centrifuging at 8000 rpm, it was washed with water three times to recover nickel oxyhydroxide particles.
　オキシ水酸化ニッケル粒子の合成化学反応式を以下に示す。 The synthetic chemical reaction formula of nickel oxyhydroxide particles is shown below.
　ＮＨ３＋Ｈ２Ｏ→ＮＨ４ ＋＋ＯＨ－・・・（１）
　Ｎｉ２＋＋ＯＨ－→ｘ［α－Ｎｉ（ＯＨ）２］＋ｙ［β－Ｎｉ（ＯＨ）２］（ｘ＋ｙ＝１）・・・（２）
　ｘ［α－Ｎｉ（ＯＨ）２］＋ｙ［β－Ｎｉ（ＯＨ）２］＋１／２Ｓ２Ｏ８ ２→γ－ＮｉＯＯＨ＋ＳＯ４ ２－＋Ｈ＋・・・（３）
　＜ナノパラジウム粒子の合成＞
　５０ｍＭ塩化パラジウム（ＩＩ）（ＰｄＣｌ２）水溶液６ｍｌと、ポリビニルピロリドン（ＰＶＰ）１９．８ｍｇと、１．５Ｍ水酸化ナトリウム（ＮａＯＨ）エチレングリコール溶液２０ｍｌを撹拌しながら混合し、７０℃で６時間反応させ、ナノパラジウム粒子の分散液を得た。このとき、反応前の液は薄い黄色を呈しているが、ナノパラジウム粒子が生成すると、液は濃い茶色に変化した。 NH 3 + H 2 O → NH 4 + + OH − (1)
Ni 2+ + OH − → x [α-Ni (OH) 2 ] + y [β-Ni (OH) 2 ] (x + y = 1) (2)
x [α-Ni (OH) 2 ] + y [β-Ni (OH) 2 ] + 1 / 2S 2 O 8 2 → γ-NiOOH + SO 4 2− + H + (3)
<Synthesis of nanopalladium particles>
50mM palladium (II) chloride and (PdCl 2) solution 6 ml, and polyvinylpyrrolidone (PVP) 19.8 mg, a 1.5M sodium hydroxide (NaOH) ethylene glycol solution 20ml and mixed with stirring, 6 hours at 70 ° C. To obtain a dispersion of nanopalladium particles. At this time, the liquid before the reaction had a light yellow color, but when nanopalladium particles were produced, the liquid turned dark brown.
　粒径分布分析装置Ｐｈｏｔａｌ　ＥＬＳＺ－１０００（大塚電子社製）を用いて、ナノパラジウム粒子の個数平均粒径の測定したところ、２８．９であった。 When the number average particle diameter of the nanopalladium particles was measured using a particle size distribution analyzer Photo ELSZ-1000 (manufactured by Otsuka Electronics Co., Ltd.), it was 28.9.
　ナノパラジウム粒子の合成化学反応式を以下に示す。 The synthetic chemical reaction formula of nanopalladium particles is shown below.
　２（ＣＨ２ＯＨ）２→２ＣＨ３ＣＨＯ＋２Ｈ２Ｏ・・・（４）
　２ＣＨ３ＣＨＯ＋Ｐｄ２＋＋３ＯＨ－＋Ｈ２Ｏ→ＣＨ３ＣＯＯ－＋２Ｈ２Ｏ＋Ｐｄ・・・（５）
　＜複合粒子の作製＞
　オキシ水酸化ニッケル粒子５００ｍｇと、水５０ｍｌと、ナノパラジウム粒子の分散液２ｍｌを３時間撹拌しながら混合した。次に、８０００ｒｐｍで遠心分離した後、三回水洗し、オキシ水酸化ニッケル粒子の表面にナノパラジウム粒子が付着している複合粒子を回収した。 2 (CH 2 OH) 2 → 2CH 3 CHO + 2H 2 O (4)
2CH 3 CHO + Pd 2+ + 3OH − + H 2 O → CH 3 COO − + 2H 2 O + Pd (5)
<Production of composite particles>
500 mg of nickel oxyhydroxide particles, 50 ml of water, and 2 ml of a dispersion of nanopalladium particles were mixed with stirring for 3 hours. Next, after centrifuging at 8000 rpm, it was washed with water three times, and composite particles in which nanopalladium particles were adhered to the surface of the nickel oxyhydroxide particles were recovered.
　＜複合粒子の特性＞
　ＦＴ－ＩＲ装置Ｆｒｏｎｔｉｅｒ　フーリエ変換近赤外/中赤外/遠赤外分光分析装置（パーキンエルマージャパン社製）を用いて、複合粒子のＦＴ－ＩＲスペクトルを測定した。 <Characteristics of composite particles>
FT-IR apparatus Frontier Fourier transform near-infrared / mid-infrared / far-infrared spectrometer (Perkin Elmer Japan) was used to measure the FT-IR spectrum of the composite particles.
　図４に、複合粒子のＦＴ－ＩＲスペクトルを示す。 FIG. 4 shows the FT-IR spectrum of the composite particles.
　図４から、オキシ水酸化ニッケルに起因する吸収ピーク（波数＝５６１ｃｍ－１）が観測されることがわかる。 FIG. 4 shows that an absorption peak (wave number = 561 cm −1 ) due to nickel oxyhydroxide is observed.
　Ｘ線光電子分光装置Ｔｈｅｔａ　Ｐｒｏｂｅ　Ａｎｇｌｅ－Ｒｅｓｏｌｖｅｄ　Ｓｐｅｃｔｒｏｍｅｔｅｒ　ｓｙｓｔｅｍ（サーモフィッシャーサイエンティフィック社製）を用いて、複合粒子のＸ線光電子分光スペクトルを測定した。 The X-ray photoelectron spectroscopy spectrum of the composite particles was measured using an X-ray photoelectron spectrometer Theta Probe Angle-Resolved Spectrometer system (manufactured by Thermo Fisher Scientific).
　図５に、複合粒子のＮｉ２ｐ周辺のＸ線光電子分光スペクトルを示す。 FIG. 5 shows an X-ray photoelectron spectroscopy spectrum around Ni 2p of the composite particle.
　図５から、オキシ水酸化ニッケルに起因するピーク（結合エネルギー＝８６０．０ｅＶ）が顕著に観測されることがわかる。 FIG. 5 shows that a peak due to nickel oxyhydroxide (binding energy = 860.0 eV) is remarkably observed.
　図４及び図５から、複合粒子は、Ｎｉに対するＰｄのモル比が０．０２５であった。 4 and 5, the composite particles had a molar ratio of Pd to Ni of 0.025.
　図６に、複合粒子のＰｄ３ｄ周辺のＸ線光電子分光スペクトルを示す。 FIG. 6 shows an X-ray photoelectron spectrum around Pd 3d of the composite particle.
　図６から、Ｐｄ０に起因するピーク（結合エネルギー＝３４２．１ｅＶ，３４７．２ｅＶ）が観測されることがわかる。 FIG. 6 shows that peaks due to Pd 0 (binding energy = 342.1 eV, 347.2 eV) are observed.
　Ｘ線回折装置Ｘ’Ｐｅｒｔ－ＭＲＤ（Ｐｈｉｌｉｐ社製）を用いて、複合粒子のＸ線回折スペクトルを測定した。 The X-ray diffraction spectrum of the composite particles was measured using an X-ray diffractometer X'Pert-MRD (manufactured by Philip).
　図７に、複合粒子のＸ線回折スペクトルを示す。 FIG. 7 shows an X-ray diffraction spectrum of the composite particle.
　図７から、オキシ水酸化ニッケルに起因するピーク（２θ＝１１．２°，２．６°，３３．２°，５２．０°）、パラジウムに起因するピーク（２θ＝４０．０°）が観測されることがわかる。 From FIG. 7, there are peaks attributable to nickel oxyhydroxide (2θ = 11.2 °, 2.6 °, 33.2 °, 52.0 °) and peaks attributable to palladium (2θ = 40.0 °). You can see that it is observed.
　＜複合粒子の電子顕微鏡写真＞
　走査型電子顕微鏡Ｓ－４３００（日立製作所社製）を用いて、複合粒子の走査型電子顕微鏡写真を撮影した。 <Electron micrograph of composite particles>
A scanning electron micrograph of the composite particles was taken using a scanning electron microscope S-4300 (manufactured by Hitachi, Ltd.).
　図８に、複合粒子の走査型電子顕微鏡写真（２０００倍）を示す。 FIG. 8 shows a scanning electron micrograph (2000 × magnification) of the composite particles.
　図８から、粒径が約２～３μｍのオキシ水酸化ニッケル粒子が凝集していることがわかる。 FIG. 8 shows that nickel oxyhydroxide particles having a particle diameter of about 2 to 3 μm are aggregated.
　図９に、複合粒子の走査型電子顕微鏡写真（１００００倍）を示す。 FIG. 9 shows a scanning electron micrograph (10,000 times) of the composite particles.
　図９から、個々のオキシ水酸化ニッケル粒子は、表面が不規則なシートフレーク状になっていることがわかる。 FIG. 9 shows that the individual nickel oxyhydroxide particles have irregular sheet flakes on the surface.
　＜水素検知部材の作製＞
　＜複合粒子の作製＞において、複合粒子を回収せずに、水で希釈し、１０質量％の複合粒子の水分散液を得た。 <Production of hydrogen detection member>
In <Production of Composite Particles>, the composite particles were not collected and diluted with water to obtain a 10% by mass aqueous dispersion of composite particles.
　複合粒子の水分散液１５０μｌを３ｃｍ×３ｃｍのシリカガラス基材上にドロップコートし、膜厚が５０μｍの水素検知膜を形成し、水素検知部材を得た。 150 μl of the composite particle aqueous dispersion was drop-coated on a 3 cm × 3 cm silica glass substrate to form a hydrogen detection film having a thickness of 50 μm to obtain a hydrogen detection member.
　＜水素検知部材による水素検知＞
　水素の含有量が４％である雰囲気（以下、水素雰囲気という）に曝される前後の水素検知部材の光の透過率を、図１０に示す光学装置を用いて測定した。光学装置は、光源４と分光器５で構成され、光源４と分光器５の間に、水素検知膜２が形成されている基材３、即ち、水素検知部材を配置して、光の透過率を測定する。 <Hydrogen detection by hydrogen detection member>
The light transmittance of the hydrogen detection member before and after being exposed to an atmosphere having a hydrogen content of 4% (hereinafter referred to as a hydrogen atmosphere) was measured using the optical apparatus shown in FIG. The optical device includes a light source 4 and a spectroscope 5, and a base material 3 on which a hydrogen detection film 2 is formed, that is, a hydrogen detection member is disposed between the light source 4 and the spectroscope 5 to transmit light. Measure the rate.
　図１１に、水素検知部材の光の透過率の測定結果を示す。 FIG. 11 shows the measurement results of the light transmittance of the hydrogen detection member.
　図１２に、水素検知部材の水素を検知する前後の写真を示す。 FIG. 12 shows photographs before and after detecting the hydrogen of the hydrogen detection member.
　水素検知膜は、水素雰囲気に曝す前の状態では、黒色（図１２（ｂ）参照）であるが、水素雰囲気に曝すと、白色（図１２（ａ）参照）に変化した。このとき、水素検知膜は、水素雰囲気に曝されてから白色に変化するのに要した時間、即ち、目視により水素を検知する時間が３分であった。また、水素検知膜は、水素雰囲気に曝すのを止めても、黒色には戻らず、白色を維持した。一方、水素検知膜は、オゾン発生装置ＳｏｅｃＶ３５０（マルコー社製）を用いて、オゾン出力７０ｍｇ／ｈ、風量５Ｌ／ｍｉｎの条件でオゾン処理すると、５秒で黒色に戻った。このため、水素検知部材を再利用することができる。 The hydrogen detection film was black (see FIG. 12B) before being exposed to the hydrogen atmosphere, but changed to white (see FIG. 12A) when exposed to the hydrogen atmosphere. At this time, the time required for the hydrogen detection film to change to white after being exposed to the hydrogen atmosphere, that is, the time for visually detecting hydrogen was 3 minutes. Moreover, even if the hydrogen detection film was stopped from being exposed to the hydrogen atmosphere, it did not return to black and maintained white. On the other hand, the hydrogen detection film returned to black in 5 seconds when ozone treatment was performed under the conditions of an ozone output of 70 mg / h and an air flow rate of 5 L / min using an ozone generator Soec V350 (manufactured by Marco Co., Ltd.). For this reason, the hydrogen detection member can be reused.
　水素検知膜と水素の化学反応式を以下に示す。 The chemical reaction formula of hydrogen detection membrane and hydrogen is shown below.
　Ｈ２→２Ｈ＋＋２ｅ－・・・（６）
　ＮｉＯＯＨ＋Ｈ＋＋ｅ－→Ｎｉ（ＯＨ）２・・・（７）
　水素と反応した後の水素検知膜とオゾンの化学反応式を以下に示す。 H 2 → 2H + + 2e − (6)
NiOOH + H + + e − → Ni (OH) 2 (7)
The chemical reaction formula between the hydrogen detection film after reacting with hydrogen and ozone is shown below.
　Ｎｉ（ＯＨ）２＋Ｏ３→ＮｉＯＯＨ＋Ｏ３ －＋Ｈ＋・・・（８）
　（比較例１）
　＜複合粒子及び水素検知部材の作製＞
　ナノパラジウム粒子の分散液の添加量を５ｍｌに変更した以外は、実施例１と同様にして、複合粒子及び水素検知部材を作製した。複合粒子は、Ｎｉに対するＰｄのモル比が０．０８であった。 Ni (OH) 2 + O 3 → NiOOH + O 3 − + H + (8)
(Comparative Example 1)
<Production of composite particles and hydrogen detection member>
Composite particles and a hydrogen detection member were produced in the same manner as in Example 1 except that the amount of the nanopalladium particle dispersion added was changed to 5 ml. The composite particles had a molar ratio of Pd to Ni of 0.08.
　＜水素検知部材による水素検知＞
　水素検知膜は、ナノパラジウム粒子の量が多すぎるため、水素雰囲気に曝すと、水素分子から解離した水素原子と、水素雰囲気に含まれる酸素との燃焼反応が発生した。このとき、水素検知膜は、温度が激しく上昇したが、色が変化せず、黒色のままであった。 <Hydrogen detection by hydrogen detection member>
Since the amount of nanopalladium particles in the hydrogen detection film was too large, when exposed to a hydrogen atmosphere, a combustion reaction between hydrogen atoms dissociated from the hydrogen molecules and oxygen contained in the hydrogen atmosphere occurred. At this time, although the temperature of the hydrogen detection film rose violently, the color did not change and remained black.
　（比較例２）
　＜複合粒子及び水素検知部材の作製＞
　ナノパラジウム粒子の分散液の添加量を０．１ｍｌに変更した以外は、実施例１と同様にして、複合粒子及び水素検知部材を作製した。複合粒子は、Ｎｉに対するＰｄのモル比が０．００１５であった。 (Comparative Example 2)
<Production of composite particles and hydrogen detection member>
Composite particles and a hydrogen detection member were produced in the same manner as in Example 1 except that the amount of the nanopalladium particle dispersion added was changed to 0.1 ml. The composite particles had a molar ratio of Pd to Ni of 0.0015.
　＜水素検知部材による水素検知＞
　水素検知膜は、ナノパラジウム粒子の量が少なすぎるため、水素雰囲気に曝すと、水素分子から解離した水素原子の量は少ない。このとき、水素検知膜は、水素雰囲気に曝してから６０分後でも、色が変化せず、黒色のままであった。 <Hydrogen detection by hydrogen detection member>
Since the amount of nanopalladium particles in the hydrogen detection film is too small, when exposed to a hydrogen atmosphere, the amount of hydrogen atoms dissociated from hydrogen molecules is small. At this time, even after 60 minutes from exposure to the hydrogen atmosphere, the color of the hydrogen detection film did not change and remained black.
　（比較例３）
　＜複合粒子及び水素検知部材の作製＞
　ナノパラジウム粒子の分散液の添加量を３．５ｍｌに変更した以外は、実施例１と同様にして、複合粒子及び水素検知部材を作製した。複合粒子は、Ｎｉに対するＰｄのモル比が０．０５であった。 (Comparative Example 3)
<Production of composite particles and hydrogen detection member>
Composite particles and a hydrogen detection member were produced in the same manner as in Example 1 except that the amount of the nanopalladium particle dispersion added was changed to 3.5 ml. The composite particles had a molar ratio of Pd to Ni of 0.05.
　＜水素検知部材による水素検知＞
　水素検知膜は、ナノパラジウム粒子の量が多すぎるため、水素雰囲気に曝すと、水素分子から解離した水素原子と、水素雰囲気に含まれる酸素との燃焼反応が発生した。このとき、水素検知膜は、温度がやや上昇したが、色が変化せず、黒色のままであった。 <Hydrogen detection by hydrogen detection member>
Since the amount of nanopalladium particles in the hydrogen detection film was too large, when exposed to a hydrogen atmosphere, a combustion reaction between hydrogen atoms dissociated from the hydrogen molecules and oxygen contained in the hydrogen atmosphere occurred. At this time, the temperature of the hydrogen detection film increased slightly, but the color did not change and remained black.
　（実施例２）
　＜複合粒子及び水素検知部材の作製＞
　ナノパラジウム粒子の分散液の添加量を０．５ｍｌに変更した以外は、実施例１と同様にして、複合粒子及び水素検知部材を作製した。複合粒子は、Ｎｉに対するＰｄのモル比が０．０１であった。 (Example 2)
<Production of composite particles and hydrogen detection member>
Composite particles and a hydrogen detection member were produced in the same manner as in Example 1 except that the amount of the nanopalladium particle dispersion added was changed to 0.5 ml. The composite particles had a molar ratio of Pd to Ni of 0.01.
　＜水素検知部材による水素検知＞
　水素検知膜は、水素を含む雰囲気に曝す前の状態では、黒色であるが、水素雰囲気に曝すと、白色に変化した。このとき、水素検知膜は、目視により水素を検知する時間が１５分であった。また、水素検知膜は、水素雰囲気に曝すのを止めても、黒色には戻らず、白色を維持した。一方、水素検知膜は、オゾン発生装置ＳｏｅｃＶ３５０（マルコー社製）を用いて、オゾン出力７０ｍｇ／ｈ、風量５Ｌ／ｍｉｎの条件でオゾン処理すると、５秒で黒色に戻った。このため、水素検知膜を再利用することができる。 <Hydrogen detection by hydrogen detection member>
The hydrogen detection film was black before being exposed to an atmosphere containing hydrogen, but turned white when exposed to a hydrogen atmosphere. At this time, the hydrogen detection film had a time of 15 minutes for visually detecting hydrogen. Moreover, even if the hydrogen detection film was stopped from being exposed to the hydrogen atmosphere, it did not return to black and maintained white. On the other hand, the hydrogen detection film returned to black in 5 seconds when ozone treatment was performed under the conditions of an ozone output of 70 mg / h and an air flow rate of 5 L / min using an ozone generator Soec V350 (manufactured by Marco Co., Ltd.). For this reason, the hydrogen detection film can be reused.
　以上詳述したように、本実施形態は、オキシ水酸化ニッケル－ナノパラジウム薄膜を用いた水素検知材料、水素検知部材及び水素検知方法に係るものであり、本実施形態により、加熱を必要とせず常温で作動する水素検知体を作製することができる。 As described above in detail, this embodiment relates to a hydrogen detection material, a hydrogen detection member, and a hydrogen detection method using a nickel oxyhydroxide-nanopalladium thin film, and according to this embodiment, heating is not required. A hydrogen detector that operates at room temperature can be produced.
　また、本実施形態の水素検知部材は、その基本構成材料が安価であり、高価な貴金属材料はごく少量の使用で足りるため、低コストで作製することが可能である。 Further, the hydrogen detection member of the present embodiment can be manufactured at low cost because its basic constituent material is inexpensive and an expensive noble metal material is used in a very small amount.
　更に、本実施形態は、湿式法のみを用いた簡便なプロセスで作製でき、構造も簡単なことから、性能に優れかつ安価な水素検知体を実現することができる。 Furthermore, since this embodiment can be manufactured by a simple process using only a wet method and has a simple structure, it is possible to realize a hydrogen detector that is excellent in performance and inexpensive.
　本国際出願は、２０１５年１２月１７日に出願された日本国特許出願２０１５－２４６３３２号に基づく優先権を主張するものであり、日本国特許出願２０１５－２４６３３２号の全内容を本国際出願に援用する。 This international application claims priority based on Japanese Patent Application No. 2015-246332 filed on December 17, 2015, and the entire contents of Japanese Patent Application No. 2015-246332 are incorporated herein by reference. Incorporate.
　１　　複合粒子
　１ａ　　オキシ水酸化ニッケル粒子
　１ｂ　　ナノパラジウム粒子
　２　　水素検知膜
　３　　基材
　４　　光源
　５　　分光器 DESCRIPTION OF SYMBOLS 1 Composite particle 1a Nickel oxyhydroxide particle 1b Nano palladium particle 2 Hydrogen detection film | membrane 3 Base material 4 Light source 5 Spectroscope

Claims (5)

  1. 　オキシ水酸化ニッケル粒子の表面にナノパラジウム粒子が付着しており、
    　Ｎｉに対するＰｄのモル比が０．０１以上０．０３以下であることを特徴とする複合粒子。     Nanopalladium particles are attached to the surface of nickel oxyhydroxide particles,
    A composite particle having a molar ratio of Pd to Ni of 0.01 or more and 0.03 or less.
  2. 　請求項１に記載の複合粒子を製造する方法であって、
    　前記オキシ水酸化ニッケル粒子と、前記ナノパラジウム粒子を溶媒中で混合する工程を含むことを特徴とする複合粒子の製造方法。     A method for producing the composite particles according to claim 1,
    A method for producing composite particles, comprising a step of mixing the nickel oxyhydroxide particles and the nanopalladium particles in a solvent.
  3. 　光学的性質の変化により水素を検知する水素検知部材であって、
    　請求項１に記載の複合粒子を含む膜が基材上に形成されていることを特徴とする水素検知部材。     A hydrogen detection member that detects hydrogen by a change in optical properties,
    A hydrogen detection member, wherein a film containing the composite particles according to claim 1 is formed on a substrate.
  4. 　請求項３に記載の水素検知部材を用いて、水素を検知する工程を含むことを特徴とする水素検知方法。 A hydrogen detection method comprising a step of detecting hydrogen using the hydrogen detection member according to claim 3.
  5. 　請求項３に記載の水素検知部材をオゾン処理する工程を含むことを特徴とする水素検知部材の処理方法。 A method for treating a hydrogen detection member, comprising a step of ozone treatment of the hydrogen detection member according to claim 3.
PCT/JP2016/087581 2015-12-17 2016-12-16 Composite particles and method for manufacturing same WO2017104813A1 (en)

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Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6039536A (en) * 1983-08-12 1985-03-01 Hochiki Corp Gas sensor
JP2004053540A (en) * 2002-07-24 2004-02-19 National Institute Of Advanced Industrial & Technology Hydrogen sensor using magnesium thin film and hydrogen concentration measuring method
JP2011112359A (en) * 2009-11-24 2011-06-09 Figaro Engineerign Inc METHOD OF MANUFACTURING SnO2 GAS SENSOR
JP2016024001A (en) * 2014-07-18 2016-02-08 国立大学法人東北大学 Novel stannic oxide material, method for synthesizing the same, and gas sensor material

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6039536A (en) * 1983-08-12 1985-03-01 Hochiki Corp Gas sensor
JP2004053540A (en) * 2002-07-24 2004-02-19 National Institute Of Advanced Industrial & Technology Hydrogen sensor using magnesium thin film and hydrogen concentration measuring method
JP2011112359A (en) * 2009-11-24 2011-06-09 Figaro Engineerign Inc METHOD OF MANUFACTURING SnO2 GAS SENSOR
JP2016024001A (en) * 2014-07-18 2016-02-08 国立大学法人東北大学 Novel stannic oxide material, method for synthesizing the same, and gas sensor material

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Title
CHIH-WEI HU ET AL.: "Fabrication of nickel oxyhydroxide/palladium (NiOOH/Pd) nanocomposite for gasochromic application", SOLAR ENERGY MATERIALS & SOLAR CELLS, vol. 4, no. 23, 20 January 2017 (2017-01-20), pages 5390 - 5397, XP055373110 *
CHIH-WEI HU ET AL.: "Fabrication of nickel oxyhydroxide/palladium (NiOOH/Pd) thin films for gasochromic application", JOURNAL OF MATERIALS CHEMISTRY C, vol. 4, no. 23, 1 January 2016 (2016-01-01), pages 5390 - 5397, XP055373110 *

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