JP2013256429A - Gas generation material and micropump - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a gas generation material which promotes the simplification and miniaturization of the structure of a micropump and evolves a large amount of gas per unit time in order to mount a pump in high density.SOLUTION: A gas generation material 11a includes a gas generating agent comprising an azo compound or an azide compound, a compound having a hydrogen atom bonded to a heteroatom, and a photosensitizer. The heteroatom is preferably a nitrogen atom, an oxygen atom, or a sulfur atom. The compound having the hydrogen atom bonded to the heteroatom is preferably a compound having a primary or secondary amino group, a hydroxy group, a carboxyl group, or a thiol group.

Description

  The present invention relates to a gas generating material and a micropump including the same.

  In recent years, analyzers using microfluidic devices have come to be used as analyzers that are small and have excellent portability. In the analysis apparatus using this microfluidic device, it is possible to send, dilute, and analyze a sample in the microchannel.

  In the microfluidic device, a micropump is provided for feeding a sample in the microchannel. For example, Patent Document 1 discloses a micropump using a photoresponsive gas generating material. Patent Document 2 discloses a gas generating agent containing an aliphatic polyether having an azidomethyl group and a hydroxyl group in the side chain. Patent Document 3 discloses a composition containing a glycidyl azide polymer. Non-Patent Document 1 discloses a glycidyl azide polymer (GAP) having a methyl azide group in the side chain and a method for producing the terminal hydroxyl polyether.

JP 2010-89259 A JP-A-8-310888 JP-A-8-109093

Industrial explosives Vol. 51, no. 4, 1990, p. 216-217

  In recent years, as the microdevices become more complex, there is a desire to mount the pumps at high density by advancing simplification and miniaturization of the structure of the micropump.

  The main object of the present invention is to provide a gas generating material that generates a large amount of gas per unit time.

  The gas generating material of the present invention includes a gas generating agent comprising an azo compound or an azide compound, a compound having a hydrogen atom bonded to a hetero atom, and a photosensitizer.

  The hetero atom is preferably a nitrogen atom, an oxygen atom or a sulfur atom.

  The compound having a hydrogen atom bonded to a hetero atom is preferably a compound having any one of a primary or secondary amino group, a hydroxyl group, a carboxyl group, and a thiol group.

  The content of the compound having a hydrogen atom bonded to a hetero atom is preferably 5 parts by mass to 95 parts by mass with respect to 100 parts by mass of the gas generating agent.

  It is preferable that content of the gas generating agent which consists of an azo compound or an azide compound in a gas generating material is 30 mass%-92 mass%.

  The gas generating agent comprising an azide compound is preferably a compound having a sulfonyl azide group or an azidomethyl group.

  The content of the photosensitizer in the gas generating material is preferably 0.5 parts by mass to 20 parts by mass with respect to 100 parts by mass of the gas generating agent.

  The gas generating material preferably further contains a binder resin.

  The content of the gas generating agent comprising an azo compound or an azide compound is 30% by mass to 80% by mass, the content of the photosensitizer is 0.1% by mass to 17% by mass, and the binder resin is contained. The amount is preferably 6% by mass to 65% by mass.

  The micropump of the present invention includes the gas generating material and a base material on which a microchannel is formed. The gas generating material is arranged so that the gas generated in the gas generating material is supplied to the microchannel.

  ADVANTAGE OF THE INVENTION According to this invention, the gas generating material with much gas generation amount per unit time can be provided.

1 is a schematic cross-sectional view of a micropump according to an embodiment of the present invention. It is a schematic sectional drawing of the micropump which concerns on a modification.

  Hereinafter, an example of the preferable form which implemented this invention is demonstrated. However, the following embodiment is merely an example. The present invention is not limited to the following embodiments.

  The drawings referred to in the embodiments are schematically described, and the ratio of the dimensions of the objects drawn in the drawings may be different from the ratio of the dimensions of the actual objects. The specific dimensional ratio of the object should be determined in consideration of the following description.

  FIG. 1 is a schematic cross-sectional view of a micropump according to the present embodiment. As shown in FIG. 1, the micropump 1 includes a plate-like base material 10. The base material 10 can be comprised with resin, glass, ceramics etc., for example. As resin which comprises the base material 10, an organic siloxane compound, polymethacrylate resin, cyclic polyolefin resin etc. are mentioned, for example. Specific examples of the organic siloxane compound include polydimethylsiloxane (PDMS) and polymethylhydrogensiloxane.

  The base 10 is formed with a microchannel 10b that is open to the main surface 10a.

  Here, the “micro flow channel” refers to a flow channel formed in a shape and dimension in which a so-called micro effect is expressed in the liquid flowing through the micro flow channel. Specifically, the term “microchannel” means that the liquid flowing through a microchannel is strongly affected by surface tension and capillary action, and has a different shape from that of a liquid flowing through a normal channel. It refers to the flow path that is formed.

  A film-like gas generating material 11a is stuck on the main surface 10a. The opening of the microchannel 10b is covered with the gas generating material 11a. For this reason, the gas generated from the gas generating material 11a when an external stimulus such as light or heat is applied to the gas generating material 11a is guided to the microchannel 10b.

  Although the thickness of the gas generating material 11a is not specifically limited, For example, it can be set as about 5 micrometers-5 mm, Preferably it can be set as about 10 micrometers-500 micrometers.

  The gas generating material 11 a is covered with a gas barrier layer 12. The gas barrier layer 12 suppresses the gas generated in the gas generating material 11a from flowing out to the side opposite to the main surface 10a, and is efficiently supplied to the microchannel 10b. For this reason, it is preferable that the gas barrier layer 12 has a low permeability of the gas generated in the gas generating material 11a.

  The gas barrier layer 12 can be made of, for example, polyacrylic resin, polyolefin resin, polycarbonate resin, vinyl chloride resin, ABS resin, polyethylene terephthalate (PET) resin, nylon resin, urethane resin, polyimide resin, glass, or the like.

  In addition, although the thickness of the gas barrier layer 12 changes with materials etc. of the gas barrier layer 12, it can be set as about 10 micrometers-1 mm, for example, Preferably it can be set as about 25 micrometers-100 micrometers. When the gas barrier layer 12 transmits light, it is preferable that the light in the ultraviolet region hardly attenuates.

  The gas generating material 11a contains a gas generating agent. The gas generating agent is composed of an azo compound or an azide compound. The gas generating agent is not particularly limited as long as it is an azo compound or an azide compound that generates gas when an external stimulus such as heat or light is applied, and may be a known azo compound or an azide compound.

  Specific examples of the azo compound serving as the gas generating agent include, for example, 2,2′-azobis (N-cyclohexyl-2-methylpropionamide), 2,2′-azobis [N- (2-methylpropyl) -2. -Methylpropionamide], 2,2'-azobis (N-butyl-2-methylpropionamide), 2,2'-azobis [N- (2-methylethyl) -2-methylpropionamide], 2,2 '-Azobis (N-hexyl-2-methylpropionamide), 2,2'-azobis (N-propyl-2-methylpropionamide), 2,2'-azobis (N-ethyl-2-methylpropionamide) 2,2′-azobis {2-methyl-N- [1,1-bis (hydroxymethyl) -2-hydroxyethyl] propionamide}, 2,2′-azobis {2- Til-N- [2- (1-hydroxybutyl)] propionamide}, 2,2′-azobis [2-methyl-N- (2-hydroxyethyl) propionamide], 2,2′-azobis [N— (2-propenyl) -2-methylpropionamide], 2,2′-azobis [2- (5-methyl-2-imidazolin-2-yl) propane] dihydrochloride, 2,2′-azobis [2- (2-Imidazolin-2-yl) propane] dihydrochloride, 2,2′-azobis [2- (2-imidazolin-2-yl) propane] disulfate dihydrolate, 2,2′-azobis [2 -(3,4,5,6-tetrahydropyrimidin-2-yl) propane] dihydrochloride, 2,2'-azobis {2- [1- (2-hydroxyethyl) -2-imidazolidin-2-yl] propane} dihydrochloride, 2,2′-azobis [2- (2-imidazolin-2-yl) propane], 2,2′-azobis (2-methylpropionamidine) Hydrochloride, 2,2′-azobis (2-aminopropane) dihydrochloride, 2,2′-azobis [N- (2-carboxyacyl) -2-methyl-propionamidyne], 2,2′-azobis {2- [N- (2-carboxyethyl) amidyne] propane}, 2,2′-azobis (2-methylpropionamidoxime), dimethyl 2,2′-azobis (2-methylpropionate), dimethyl 2 , 2′-azobisisobutyrate, 4,4′-azobis (4-cyancarbonic acid), 4,4′-azobis (4-si Anopentanoic acid), 2,2'-azobis (2,4,4-trimethylpentane) and the like. These azo compounds generate nitrogen gas by being stimulated by light, heat, etc. in a specific wavelength range.

  The azo compound is extremely easy to handle because it does not generate gas upon impact. Further, the azo compound does not cause a chain reaction and explosively generate a gas, but can interrupt the generation of gas by interrupting the irradiation of light. For this reason, control of gas generation amount becomes easy by using an azo compound as a gas generating agent.

  Examples of the azide compound serving as the gas generating agent include compounds having a sulfonyl azide group or an azidomethyl group.

  As a compound which has a sulfonyl azide group, the compound represented by following General formula (1) is mentioned, for example.

In the general formula (1), R ^{1 to} R ⁵ are the same or different and each is a saturated or unsaturated straight chain which may have a hydrogen atom, a halogen atom, an amino group, an amide group or a substituent. , A branched or cyclic hydrocarbon group, or a linear or branched alkoxy group which may have a substituent.

In R ^{1 to} R ⁵ of the general formula (1), the saturated or unsaturated linear, branched or cyclic hydrocarbon group which may have a substituent has about 1 to 30 carbon atoms. It is preferable that it is a range, It is more preferable that it is the range of about 3-20, It is further more preferable that it is the range of about 6-18. Examples of the substituent include an alkyl group having 1 to 3 carbon atoms and a halogen atom.

In R ^{1 to} R ⁵ of the general formula (1), the linear or branched alkoxy group which may have a substituent preferably has a carbon number in the range of about 1 to 20. More preferably, it is in the range of about ˜16, more preferably in the range of about 6-12. Examples of the substituent include an alkyl group having 1 to 3 carbon atoms and a halogen atom.

In the general formula (1), R ³ may have an amide group, a saturated or unsaturated linear, branched or cyclic hydrocarbon group which may have a substituent, or a substituent. It is preferably a good linear or branched alkoxy group. R ¹ , R ² , R ⁴ , and R ⁵ are each preferably a hydrogen atom.

  Examples of the compound having an azidomethyl group include a glycidyl azide polymer. As the glycidyl azide polymer, an aliphatic polyether having an azidomethyl group in the side chain and a hydroxyl group at the terminal is preferable. Examples of the aliphatic polyether having an azidomethyl group in the side chain and a hydroxyl group at the terminal include compounds represented by the following general formula (2-1).

H (B) _q (A) _n OR ¹ O (A) _m (B) _r H (2-1)
[Wherein, m + n = 2 to 20, m ≧ 1, n ≧ 1, q + r = 10 to 35, q ≧ 5, r ≧ 5. The A unit is —OR ² —. The B unit is —CH ₂ CH (CH ₂ N ₃ ) O—. R ¹ is —CH ₂ CH ₂ —, —CH ₂ CH ₂ CH ₂ CH ₂ —, —CH ₂ CH (CH ₃ ) —, — [(CH ₂ CH ₂ O) _x CH ₂ CH ₂ ] —, or - _{[(CH 2 CH 2 CH 2 CH} 2 O) y CH 2 CH 2 CH 2 CH 2 ] - a. x is 10 to 25, and y is 5 to 20. R ² is —CH ₂ CH ₂ CH ₂ CH ₂ —, —CH ₂ CH ₂ —, or —CH ₂ CH (CH ₃ ) —. ]

一般式（２−２）において、ｍは、１〜２０の整数であり、３〜１５の整数であることが好ましい。ｌ＋ｎは、７〜５０の整数であり、１０〜３０の整数であることが好ましい。 Moreover, as an aliphatic polyether which has an azidomethyl group in a side chain and has a hydroxyl group in the terminal, the compound represented by the following general formula (2-2) is mentioned, for example.

In General formula (2-2), m is an integer of 1-20, and it is preferable that it is an integer of 3-15. l + n is an integer of 7 to 50, and preferably an integer of 10 to 30.

  These azide compounds are decomposed by being stimulated by light in a specific wavelength range, heat, ultrasonic waves, impact, etc., and generate nitrogen gas.

  In the gas generating material 11a, the gas generating agent is preferably contained in the range of about 30% by mass to 92% by mass, more preferably in the range of about 40% by mass to 90% by mass, 55 More preferably, it is contained in the range of about mass% to 90 mass%. When the gas generating agent is 30% by mass or more, a sufficient gas generation amount can be obtained. Since the gas generating material 11a needs to contain a photosensitizer and a compound having a hydrogen atom bonded to a hetero atom, the upper limit of the gas generating agent is about 92% by mass.

  The gas generating material 11a includes a compound having a hydrogen atom bonded to a hetero atom in addition to a gas generating agent composed of an azo compound or an azide compound. A compound having a hydrogen atom bonded to a heteroatom is a compound that can trap radicals generated when a gas generating agent receives a stimulus such as light and generates nitrogen gas or the like. A compound having a hydrogen atom bonded to a heteroatom is a compound that can function as a hydrogen donor.

  In the gas generating material 11a, by containing a compound capable of scavenging radicals such as a compound having a hydrogen atom bonded to a hetero atom, the above-described generation of nitrogen gas can be performed smoothly and the amount of gas generated can be increased. It becomes possible.

  Examples of the hetero atom of the compound having a hydrogen atom bonded to the hetero atom include a nitrogen atom, an oxygen atom, and a sulfur atom.

  The compound having a hydrogen atom bonded to a hetero atom is preferably a compound having any of a primary or secondary amino group, a hydroxyl group, a carboxyl group, or a thiol group. From the viewpoint of the function of scavenging radicals, the compound having a hydrogen atom bonded to a heteroatom is preferably a compound having either a primary or secondary amino group or a thiol group.

  Examples of the compound having a hydrogen atom bonded to a heteroatom include aliphatic hydrocarbons having any of primary or secondary amino groups, hydroxyl groups, carboxyl groups, or thiol groups. The number of carbon atoms of the aliphatic hydrocarbon is preferably in the range of about 1-30, more preferably in the range of about 3-20, and still more preferably in the range of about 4-18.

  Specific examples of the aliphatic hydrocarbon having a primary or secondary amino group include methylamine, ethylamine, butylamine, dodecylamine, propylamine, pentylamine, hexylamine, heptylamine, octylamine, nonylamine, decylamine, Examples include undecylamine (primary amine), diethylamine, dipropylamine, ethylpropylamine, dibutylamine, dipentylamine, and dihexylamine (secondary amine). Specific examples of the aliphatic hydrocarbon having a hydroxyl group include methanol, ethanol, 1-propanol, 1-butanol, 1-pentanol, 1-hexanol, 1-heptanol, 1-octanol, 1-nonanol, 1-decanol, Examples include 1-undecanol and 1-dodecanol. Specific examples of the aliphatic hydrocarbon having a carboxyl group include formic acid, acetic acid, propionic acid, butyric acid, valeric acid, caproic acid, enanthic acid, caprylic acid, pelargonic acid, capric acid, lauric acid, myristic acid, palmitic acid, Examples include margaric acid and stearic acid. Specific examples of the aliphatic hydrocarbon having a thiol group include ethanethiol, methanethiol, 1-propanethiol, 1-butanethiol, 1-pentanethiol, 1-hexanethiol, 1-heptanethiol, 1-octanethiol, Examples include 1-nonanethiol, 1-decanethiol, 1-undecanethiol, 1-dodecanethiol, and the like.

  In addition, the compound having a hydrogen atom bonded to a hetero atom may be, for example, a polymer having a plurality of primary or secondary amino groups, hydroxyl groups, carboxyl groups, or thiol groups. Examples of compounds and polymers having a plurality of primary or secondary amino groups include aminoethylated acrylic polymer, copolymerization of acrylamide monomer and N, N-dimethylaminoethyl acrylate monomer, acrylamide monomer and N, N-dimethylaminoethyl Examples include copolymerization of methacrylate monomers. Examples of the polymer having a plurality of hydroxyl groups include (poly) ethylene glycol, (poly) propylene glycol, (poly) tetramethylene glycol, a hydroxyethyl (meth) acrylate polymer, and glycerin. Examples of the compound polymer having a plurality of carboxyl groups include a copolymer of 2-ethylhexyl acrylate and acrylic acid, a copolymer of butyl acrylate and acrylic acid, and a copolymer of ethyl acrylate and acrylic acid. Examples of the compound or polymer having a plurality of thiol groups include trimethylolpropane tris (3-mercaptobutyrate), trimethylolethane tris (3-mercaptobutyrate), pentaerythritol tetrakis (3-mercaptobutyrate), and the like.

  In the gas generating material 11a, the compound having a hydrogen atom bonded to a hetero atom is preferably contained in a range of about 5 to 95 parts by mass with respect to 100 parts by mass of the gas generating agent. More preferably, it is contained in the range of about 70 parts by mass, and more preferably in the range of about 10 parts by mass to 50 parts by mass.

  The gas generating material 11a further contains a photosensitizer. Examples of the photosensitizer include benzophenone, diethylthioxanthone, anthraquinone, benzoin, and acridine derivatives.

  The photosensitizer is preferably contained in a range of about 0.5 to 20 parts by mass with respect to 100 parts by mass of the gas generant, and is contained in a range of about 1 to 10 parts by mass. More preferably.

  The photosensitizer is preferably contained in the gas generating material 11a in a range of about 0.1% by mass to 17% by mass, and contained in a range of about 1% by mass to 15% by mass. It is more preferable that it is contained in the range of about 1% by mass to 10% by mass.

  The gas generating material 11a may further contain a binder resin. Examples of the binder resin include acrylic resins and glycidyl azide polymers. The binder resin is preferably contained in a range that allows the shape of the gas generating material 11a to be maintained.

  When the gas generating material 11a includes a binder resin, the binder resin is preferably included in a range of about 20 parts by mass to 200 parts by mass with respect to 100 parts by mass of the gas generating agent, for example, 30 parts by mass to More preferably, it is contained in the range of about 150 parts by mass.

  Moreover, when the gas generating material 11a contains binder resin, it is preferable that binder resin is contained in the range of about 6 mass%-70 mass% in the gas generating material 11a, About 20 mass%-about 65 mass%. More preferably, it is contained in the range of about 40% by mass to 65% by mass. When an acrylic resin is used as the binder resin, it is preferable that the gas generating material 11a contains 20% by mass or more of the binder resin because it is possible to impart adhesiveness to the gas generating material 11a.

  Moreover, the gas generating material 11a may contain a tackifier together with the binder resin.

  The gas generating material 11a includes a compound having a hydrogen atom bonded to a hetero atom in addition to a gas generating agent composed of an azo compound or an azide compound. Thereby, in the gas generating material 11a, the amount of gas generation per unit time can be increased.

  Although the detailed mechanism by which the gas generation amount of the gas generating material 11a is increased by including a compound having a hydrogen atom bonded to a hetero atom is not clear, for example, the following mechanism is conceivable. When a gas generating agent comprising an azo compound or an azide compound is stimulated by light or the like to generate nitrogen gas, the reaction that generates nitrogen gas proceeds by including a compound having a hydrogen atom bonded to a heteroatom. It will be easier.

  The gas generating material 11a includes a compound having a hydrogen atom bonded to a hetero atom. For this reason, it is considered that the gas generation reaction easily proceeds, and as a result, the amount of gas generated per unit time of the gas generating material 11a can be increased.

In the compound having a hydrogen atom bonded to a heteroatom, the hydrogen atom bonded to the heteroatom has hydrophilicity. On the other hand, for example, in a gas generating agent composed of an azide compound, a sulfonyl azide group or an azidomethyl group has hydrophilicity. Therefore, for example, in a gas generating agent composed of an azide compound, if a portion other than a sulfonyl azide group or an azidomethyl group is hydrophobic, it binds to a hydrophilic sulfonylazide group or an azidomethyl group and a hydrophilic heteroatom. This makes it easier for hydrogen atoms to gather. If it does so, the distance between the functional groups which have hydrophilicity will become near, and it will be thought that the radical which generate | occur | produced from the gas generating agent by stimuli, such as light, is efficiently trapped by the compound which has the hydrogen atom couple | bonded with the hetero atom. Therefore, it is considered that the amount of gas generated per unit time of the gas generating material 11a can be increased. From such a viewpoint, for example, when the gas generating material 11a is a compound represented by the general formula (1), at least one of R ^{1 to} R ⁵ may be a saturated or non-substituted group which may have a substituent. A saturated linear, branched or cyclic hydrocarbon group is preferred. The number of carbon atoms of the hydrocarbon group is more preferably in the range of about 3 to 16, and still more preferably in the range of about 6 to 12. From this point of view, when the gas generating material 11a is a compound represented by the general formula (2-2), m is an integer of 1 to 20, and l + n is an integer of 7 to 50. It is preferable that Further, for example, in a compound having a hydrogen atom bonded to a hetero atom, the aliphatic hydrocarbon having any of a primary or secondary amino group, a hydroxyl group, a carboxyl group, or a thiol group has 3 to 30 carbon atoms. It is preferable that the amount is within a range, particularly 6 to 20, because the hydrogen atom bonded to the heteroatom and the sulfonylazide group or azidomethyl group of the gas generating agent are more likely to gather. The number of carbon atoms of the aliphatic hydrocarbon is more preferably in the range of about 4-18.

(Modification)
FIG. 2 is a schematic cross-sectional view of a micropump according to a modification of the above embodiment.

  The micropump 2 according to this modification is different from the micropump 1 according to the above embodiment in the shape of the gas generating material and the shape of the base material 10.

  In the present modification, the microchannel 10 b is connected to a pump chamber 10 c formed in the base material 10. The gas generating material 11b is formed in a block shape and is arranged in the pump chamber 10c.

  Also in the micropump 2 according to the present embodiment, as in the micropump 1, a high output and a long drive time can be realized.

  Hereinafter, the present invention will be described in more detail based on specific examples. The present invention is not limited to the following examples, and can be implemented with appropriate modifications without departing from the scope of the invention.

Example 1
96.5 parts by mass of 2-ethylhexyl acrylate, 3 parts by mass of acrylic acid, and 0.5 parts by mass of 2-hydroxyethyl acrylate are mixed to prepare an acrylic copolymer (weight average molecular weight 700,000). Was made. 190 parts by mass of this acrylic copolymer as a binder resin, 100 parts by mass of 4-dodecylbenzenesulfonyl azide (DBSN manufactured by Toyobo Co., Ltd.) as a gas generating agent, and 1 as a compound having a hydrogen atom bonded to a hetero atom -Mixing 10 parts by weight of butanethiol, 3.5 parts by weight of diethylthioxanthone (DETX-S manufactured by Ciba Specialty Chemicals) as a photosensitizer, and 380 parts by weight of ethyl acetate as a solvent, and releasing the mold It was coated on a PET film and dried at 110 ° C. for 5 minutes. This was protected with mold release PET and cured for one day to obtain a film-like gas generating material having a thickness of 50 μm.

  Using this gas generating material, a micropump having a configuration substantially similar to the micropump 1 of the first embodiment was produced.

  The cross-sectional shape of the microchannel 10b was a 0.5 mm square shape. The length of the microchannel 10b was 800 mm. Two openings were formed on the main surface 10a so that both ends of the microchannel 10b were open to the atmosphere. The gas generating material was a film having a diameter of 0.6 cm and a thickness of 50 μm. The gas generating material 11b was a disk shape having a diameter of 0.6 cm and a thickness of 50 μm, and was installed so as to cover one side of the opening. The gas barrier layer 12 was laminated on the gas generating material using a transparent PET film having a thickness of 200 μm. The other opening of the microchannel 10b was opened to the atmosphere.

  Next, the gas generation amount of the obtained micropump was measured. The results are shown in Table 1.

  In the measurement of the amount of gas generated, the amount of gas generated when irradiated with an ultraviolet LED of 380 nm (NS375L-5RFS manufactured by Nitride Semiconductor Co., Ltd.) for 2 minutes was measured. The gas generation amount is measured by connecting the opening of the microchannel 10b opened to the atmosphere and a pipette with a silicon tube, filling the inside with water, and then irradiating the gas generating material with ultraviolet rays. In this method, the volume change of the water in the measuring pipe due to the generated gas was read.

(Example 2)
A micropump was produced in the same manner as in Example 1 except that the acrylic copolymer was 150 parts by mass and 1-butanethiol was 50 parts by mass. Next, in the same manner as in Example 1, the gas generation amount of the obtained micropump was measured. The results are shown in Table 1.

(Example 3)
A micropump was produced in the same manner as in Example 1 except that 1-dodecanethiol was used instead of 1-butanethiol as a compound having a hydrogen atom bonded to a heteroatom. Next, in the same manner as in Example 1, the gas generation amount of the obtained micropump was measured. The results are shown in Table 1.

Example 4
A micropump was produced in the same manner as in Example 3, except that the acrylic copolymer was 150 parts by mass and 1-dodecanethiol was used in an amount of 50 parts by mass. Next, in the same manner as in Example 1, the gas generation amount of the obtained micropump was measured. The results are shown in Table 1.

(Example 5)
A micropump was produced in the same manner as in Example 1 except that butylamine was used in place of 1-butanethiol as a compound having a hydrogen atom bonded to a heteroatom. Next, in the same manner as in Example 1, the gas generation amount of the obtained micropump was measured. The results are shown in Table 1.

(Example 6)
A micropump was produced in the same manner as in Example 5 except that the acrylic copolymer was 150 parts by mass and 50 parts by mass of butylamine was used. Next, in the same manner as in Example 1, the gas generation amount of the obtained micropump was measured. The results are shown in Table 1.

(Example 7)
A micropump was produced in the same manner as in Example 1 except that dodecylamine was used in place of 1-butanethiol as a compound having a hydrogen atom bonded to a heteroatom. Next, in the same manner as in Example 1, the gas generation amount of the obtained micropump was measured. The results are shown in Table 1.

(Example 8)
A micropump was produced in the same manner as in Example 7 except that the acrylic copolymer was 150 parts by mass and 50 parts by mass of dodecylamine was used. Next, in the same manner as in Example 1, the gas generation amount of the obtained micropump was measured. The results are shown in Table 1.

(Comparative Example 1)
A micropump was produced in the same manner as in Example 1 except that the amount of the acrylic copolymer was 200 parts by mass and a compound having a hydrogen atom bonded to a hetero atom was not used. Next, in the same manner as in Example 1, the gas generation amount of the obtained micropump was measured. The results are shown in Table 1.

Example 9
96.5 parts by mass of 2-ethylhexyl acrylate, 3 parts by mass of acrylic acid, and 0.5 parts by mass of 2-hydroxyethyl acrylate are mixed to prepare an acrylic copolymer (weight average molecular weight 700,000). Got. A mixture of this acrylic copolymer and vinyl polymer (manufactured by Nippon Shokubai Co., Ltd .: product number AX4-HC-MO8) at a mass ratio of 8: 2 was used as a binder resin. 100 parts by mass of this binder resin, 200 parts by mass of glycidyl azide polymer (manufactured by NOF Corporation: GAP4006) as a gas generating agent, 100 parts by mass of dodecylamine (manufactured by Tokyo Chemical Industry Co., Ltd.) as a compound having a hydrogen atom bonded to a hetero atom, Diethylthioxanthone (DETX-S manufactured by Ciba Specialty Chemicals) as a photosensitizer is mixed with 3.5 parts by mass, ethyl acetate as a solvent is mixed with 380 parts by mass, processed into a film, and dried at 110 ° C. for 5 minutes. did. This was protected with mold release PET and cured for one day to obtain a film-like gas generating material. A micropump was produced in the same manner as in Example 1 by using the obtained gas generating material. Next, in the same manner as in Example 1, the gas generation amount of the obtained micropump was measured. The results are shown in Table 2.

(Example 10)
96.5 parts by mass of 2-ethylhexyl acrylate, 3 parts by mass of acrylic acid, and 0.5 parts by mass of 2-hydroxyethyl acrylate are mixed to prepare an acrylic copolymer (weight average molecular weight 700,000). Got. 100 parts by mass of this acrylic copolymer as a binder resin, 200 parts by mass of glycidyl azide polymer (manufactured by NOF Corporation: GAP4006) as a gas generating agent, and aminoethylation as a compound having a hydrogen atom bonded to a hetero atom 100 parts by mass of an acrylic polymer (manufactured by Nippon Shokubai Co., Ltd .: Poliment NK-380), 3.5 parts by mass of diethylthioxanthone (DETX-S made by Ciba Specialty Chemicals) as a photosensitizer, and 380 of ethyl acetate as a solvent Mass parts were mixed, processed into a film, and dried at 110 ° C. for 5 minutes. This was protected with mold release PET and cured for one day to obtain a film-like gas generating material. A micropump was produced in the same manner as in Example 1 by using the obtained gas generating material. Next, in the same manner as in Example 1, the gas generation amount of the obtained micropump was measured. The results are shown in Table 2.

(Comparative Example 2)
A micropump was produced in the same manner as in Example 10 except that a compound having a hydrogen atom bonded to a hetero atom was not used. Next, in the same manner as in Example 1, the gas generation amount of the obtained micropump was measured. The results are shown in Table 2.

DESCRIPTION OF SYMBOLS 1, 2 ... Micro pump 10 ... Base material 10a ... Main surface 10b ... Micro flow path 10c ... Pump chamber 11a, 11b ... Gas generating material 12 ... Gas barrier layer

Claims (10)

  A gas generating material comprising a gas generating agent comprising an azo compound or an azide compound, a compound having a hydrogen atom bonded to a hetero atom, and a photosensitizer.   The gas generating material according to claim 1, wherein the hetero atom is a nitrogen atom, an oxygen atom, or a sulfur atom.   The gas generation according to claim 1 or 2, wherein the compound having a hydrogen atom bonded to the heteroatom is a compound having any one of a primary or secondary amino group, a hydroxyl group, a carboxyl group, and a thiol group. Wood.   Content of the compound which has the hydrogen atom couple | bonded with the said hetero atom is 5 mass parts-95 mass parts with respect to 100 mass parts of said gas generants, It is any one of Claims 1-3. Gas generating material.   The gas generating material according to any one of claims 1 to 4, wherein a content of the gas generating agent composed of the azo compound or the azide compound in the gas generating material is 30% by mass to 92% by mass.   The gas generating material according to any one of claims 1 to 5, wherein the gas generating agent comprising the azide compound has a sulfonyl azide group or an azidomethyl group.   The content of the photosensitizer in the gas generating material is 0.5 to 20 parts by mass with respect to 100 parts by mass of the gas generating agent. The gas generating material described.   Furthermore, the gas generating material as described in any one of Claims 1-7 containing binder resin.   The content of the gas generating agent comprising the azo compound or the azide compound is 30% by mass to 80% by mass, the content of the photosensitizer is 0.1% by mass to 17% by mass, and the binder. The gas generating material according to any one of claims 1 to 8, wherein the resin content is 6 mass% to 65 mass%. The gas generating material according to any one of claims 1 to 9,
A substrate on which a microchannel is formed;
With
The gas generating material is a micropump arranged such that gas generated in the gas generating material is supplied to the micro flow path.

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