WO2013183175A1 - ガス発生材及びマイクロポンプ - Google Patents
ガス発生材及びマイクロポンプ Download PDFInfo
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- WO2013183175A1 WO2013183175A1 PCT/JP2012/074511 JP2012074511W WO2013183175A1 WO 2013183175 A1 WO2013183175 A1 WO 2013183175A1 JP 2012074511 W JP2012074511 W JP 2012074511W WO 2013183175 A1 WO2013183175 A1 WO 2013183175A1
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- gas generating
- generating material
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- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B43/00—Compositions characterised by explosive or thermic constituents not provided for in groups C06B25/00 - C06B41/00
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
- B01L3/50—Containers for the purpose of retaining a material to be analysed, e.g. test tubes
- B01L3/502—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
- B01L3/5027—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip
- B01L3/50273—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip characterised by the means or forces applied to move the fluids
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82B—NANOSTRUCTURES FORMED BY MANIPULATION OF INDIVIDUAL ATOMS, MOLECULES, OR LIMITED COLLECTIONS OF ATOMS OR MOLECULES AS DISCRETE UNITS; MANUFACTURE OR TREATMENT THEREOF
- B82B1/00—Nanostructures formed by manipulation of individual atoms or molecules, or limited collections of atoms or molecules as discrete units
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06D—MEANS FOR GENERATING SMOKE OR MIST; GAS-ATTACK COMPOSITIONS; GENERATION OF GAS FOR BLASTING OR PROPULSION (CHEMICAL PART)
- C06D5/00—Generation of pressure gas, e.g. for blasting cartridges, starting cartridges, rockets
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- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06D—MEANS FOR GENERATING SMOKE OR MIST; GAS-ATTACK COMPOSITIONS; GENERATION OF GAS FOR BLASTING OR PROPULSION (CHEMICAL PART)
- C06D5/00—Generation of pressure gas, e.g. for blasting cartridges, starting cartridges, rockets
- C06D5/04—Generation of pressure gas, e.g. for blasting cartridges, starting cartridges, rockets by auto-decomposition of single substances
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F04—POSITIVE - DISPLACEMENT MACHINES FOR LIQUIDS; PUMPS FOR LIQUIDS OR ELASTIC FLUIDS
- F04B—POSITIVE-DISPLACEMENT MACHINES FOR LIQUIDS; PUMPS
- F04B19/00—Machines or pumps having pertinent characteristics not provided for in, or of interest apart from, groups F04B1/00 - F04B17/00
- F04B19/20—Other positive-displacement pumps
- F04B19/24—Pumping by heat expansion of pumped fluid
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2400/00—Moving or stopping fluids
- B01L2400/04—Moving fluids with specific forces or mechanical means
- B01L2400/0403—Moving fluids with specific forces or mechanical means specific forces
- B01L2400/046—Chemical or electrochemical formation of bubbles
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T137/00—Fluid handling
- Y10T137/0318—Processes
- Y10T137/0396—Involving pressure control
Definitions
- the present invention relates to a gas generating material and a micro pump provided with the same.
- analyzers using microfluidic devices have come to be used as analyzers that are small and have excellent portability.
- the analysis apparatus using this microfluidic device it is possible to send, dilute, concentrate, and analyze a sample in the microchannel.
- 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.
- GAP glycidyl azide polymer
- Patent Documents 4 and 5 do not disclose the use of the micropump, but disclose a composition containing a gas generating agent.
- Patent Document 4 describes that the surface of a glass plate to which a layer containing a gas generating agent is attached is surface-treated with a silane coupling agent.
- the silane coupling agent is not mix
- Patent Document 5 discloses a multilayer sheet including a layer containing a gas generating agent and a layer containing an amino silane coupling agent.
- each layer of the multilayer sheet is formed using different compositions, and the gas generating agent and the amino silane coupling agent are used separately in different layers.
- the main object of the present invention is to provide a gas generating material that generates a large amount of gas per unit time and has high storage stability. Moreover, this invention provides a micropump provided with the said gas generating material.
- the gas generating material of the present invention includes a gas generating agent that is an azo compound or an azide compound, a tertiary amine, a photosensitizer, and a binder resin.
- the tertiary amine preferably contains at least one selected from the group consisting of cyclic amines, trialkylamines, and aromatic amines.
- the content of the tertiary amine is preferably 0.1 parts by mass or more and 50 parts by mass or less with respect to 100 parts by mass of the gas generating agent.
- the azide compound preferably has a sulfonyl azide group or an azidomethyl group.
- the content of the photosensitizer is preferably 0.1 parts by mass or more and 50 parts by mass or less with respect to 100 parts by mass of the gas generating agent.
- the photosensitizer preferably contains at least one selected from the group consisting of thioxanthone compounds, phenothiazine compounds, anthracene compounds, and acridone compounds.
- the gas generating material of the present invention preferably further contains a silane coupling agent.
- 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.
- a gas generating material having a large amount of gas generation per unit time and high storage stability can be provided.
- FIG. 1 is a schematic cross-sectional view of a micropump according to a first embodiment of the present invention.
- FIG. 2 is a schematic cross-sectional view of a micropump according to a modification.
- FIG. 3 is a graph showing the gas generation amount (integrated value) of the micropumps produced in Example 19 and Comparative Examples 3 to 5.
- FIG. 4 is a graph showing the gas generation amount (integrated value) of the micropumps produced in Example 20 and Comparative Example 6.
- FIG. 5 is a graph showing the gas generation amount (integrated value) of the micropumps produced in Example 21 and Comparative Example 7.
- FIG. 6 is a graph showing the gas generation amount (integrated value) of the micropumps produced in Example 22 and Comparative Example 8.
- FIG. 1 is a schematic cross-sectional view of a micropump according to a first embodiment of the present invention.
- FIG. 2 is a schematic cross-sectional view of a micropump according to a modification.
- FIG. 3 is a
- FIG. 7 is a graph showing the gas generation amount (integrated value) of the micropumps produced in Example 23 and Comparative Example 9.
- FIG. 8 is a graph showing the gas generation amount (integrated value) of the micropumps produced in Example 24 and Comparative Example 10.
- FIG. 9 is a graph showing the gas generation amount (integrated value) of the micropumps produced in Example 25 and Comparative Example 11.
- FIG. 10 is a graph showing the gas generation amount (integrated value) of the micropumps produced in Example 26 and Comparative Example 12.
- FIG. 11 is a graph showing the gas generation amount (integrated value) of the micropumps produced in Example 27 and Comparative Examples 13-15.
- FIG. 1 is a schematic cross-sectional view of a micropump according to a first embodiment.
- the micropump 1 includes a plate-like base material 10.
- the base material 10 can be comprised by resin, glass, ceramics etc., for example.
- 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 organosiloxane compound include polydimethylsiloxane (PDMS) and polymethylhydrogensiloxane.
- the base 10 is formed with a microchannel 10b that is open to the main surface 10a.
- Micro channel refers to a channel formed in a shape and dimension in which a so-called micro effect is manifested in the liquid flowing through the micro channel.
- 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 affixed 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.
- the thickness of the gas generating material 11a is not particularly limited and is, for example, preferably 5 ⁇ m or more, more preferably 10 ⁇ m or more, preferably 5 mm or less, more preferably 500 ⁇ m or less.
- 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 is a layer with 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, and glass.
- the thickness of the gas barrier layer 12 varies depending on the material of the gas barrier layer 12 and is, for example, preferably 10 ⁇ m or more, more preferably 25 ⁇ m or more, preferably 1 mm or less, more preferably 100 ⁇ m or less.
- the gas barrier layer 12 is preferably a layer in which attenuation of light in the ultraviolet region hardly occurs when light is transmitted.
- the gas generating material 11a includes a gas generating agent.
- the gas generating agent is an azo compound or an azide compound.
- the gas generating agent generates gas when an external stimulus such as heat or light is applied.
- the azo compound or the azide compound is not particularly limited, and may be a known azo compound or azide compound.
- the gas generating agent is preferably the azo compound, and is preferably the azide compound.
- the gas generating agent may be used alone or in combination of two or more.
- the azo compound used 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-methyl) Propionamide), 2,2′-azobis ⁇ 2-methyl-N- [1,1-bis (hydroxymethyl) -2-hydroxyethyl] propionamide ⁇ , 2, '-Azobis ⁇ 2-methyl-N- [2- (1-hydroxybutyl)] propionamide ⁇ , 2,2'-azobis [2-methyl-N- (2-hydroxy)]
- the azo compound is extremely easy to handle because it does not generate gas upon impact. Moreover, the azo compound does not cause a chain reaction and generate gas explosively. If the said azo compound is used, generation
- Examples of the azide compound used as the gas generating agent include an azide compound having a sulfonyl azide group or an azidomethyl group.
- the azide compound preferably has a sulfonyl azide group or an azidomethyl group.
- the azide compound preferably has a sulfonyl azide group, and preferably has an azidomethyl group.
- Preferred examples of the compound having a sulfonyl azide group include a compound represented by the following formula (1).
- R 1 to R 5 are each a hydrogen atom, a halogen atom, an amino group, an amide group, a hydrocarbon group, a group in which a substituent is bonded to a hydrocarbon group, or an alkoxy group.
- R 1 to R 5 in the above formula (1) may be the same or different.
- the hydrocarbon group may be linear, branched, or cyclic.
- the hydrocarbon group may be a saturated hydrocarbon group or an unsaturated hydrocarbon group.
- the alkoxy group may have a substituent, may be linear, or may be branched.
- At least one group of R 1 to R 5 is preferably a hydrocarbon group or a group having a substituent bonded to a hydrocarbon group, and more preferably a hydrocarbon group.
- the hydrocarbon group has 1 or more, preferably 3 or more, more preferably 6 or more, preferably 30 or less. More preferably, it is 20 or less, More preferably, it is 18 or less.
- the substituent in the group in which the substituent is bonded to the hydrocarbon group include a halogen atom.
- the alkoxy group has 1 or more carbon atoms, preferably 3 or more, more preferably 6 or more, preferably 20 or less, more preferably 16 or less, still more preferably 12 or less. It is.
- examples of the substituent include a halogen atom.
- R 3 is preferably an amide group, a hydrocarbon group, a group in which a substituent is bonded to a hydrocarbon group, or an alkoxy group.
- R 1 , R 2 , R 4 and R 5 are each preferably a hydrogen atom.
- Examples of the azide compound having an azidomethyl group include glycidyl azide polymer.
- the glycidyl azide polymer is preferably an aliphatic polyether having an azidomethyl group in the side chain and a hydroxyl group at the terminal.
- Preferred examples of the aliphatic polyether having an azidomethyl group in the side chain and a hydroxyl group at the terminal include an azide compound represented by the following formula (2-1).
- aliphatic polyether having an azidomethyl group in the side chain and a hydroxyl group at the terminal include an azide compound represented by the following formula (2-2).
- m is an integer of 1 to 20, and l + n is an integer of 7 to 50.
- m is preferably 3 or more, and preferably 15 or less.
- l + n is preferably 10 or more, and preferably 30 or less.
- aliphatic polyether having an azidomethyl group in the side chain and a hydroxyl group at the terminal include an azide compound represented by the following formula (2-3).
- n1, n2 and n3 are each an integer from 1 to 20.
- the azide compound is preferably an azide compound represented by the above formula (1), (2-1), (2-2) or (2-3).
- the azide compound is preferably an azide compound represented by the above formula (1), and is an azide compound represented by the above formula (2-1), (2-2) or (2-3). Is also preferable.
- the above-mentioned azide compound is decomposed by receiving an external stimulus such as light, heat, ultrasonic waves or impact in a specific wavelength range, and generates nitrogen gas.
- the content of the gas generating agent is preferably 10% by mass or more, more preferably 15% by mass or more, still more preferably 20% by mass or more, preferably 90% by mass or less, more preferably 70% by mass. % Or less, more preferably 60% by mass or less.
- the content of the gas generating agent is not less than the above lower limit, a sufficient gas generating amount can be obtained. Since the gas generating material 11a needs to contain a tertiary amine, a photosensitizer, and a binder resin, a preferable upper limit of the gas generating agent is about 90% by mass.
- the above-described generation of nitrogen gas can be performed smoothly, and the amount of gas generated can be increased.
- the gas generating material 11a contains a tertiary amine.
- the kind of said tertiary amine is not specifically limited.
- Examples of the tertiary amine include cyclic amines, trialkylamines, and aromatic amines. Each of the cyclic amine and the aromatic amine has a tertiary amine structure.
- the above tertiary amine may be included in only one kind or in plural kinds.
- the gas generating material 11a preferably contains at least one selected from the group consisting of cyclic amines, trialkylamines, and aromatic amines.
- the tertiary amine is preferably a cyclic amine, preferably a trialkylamine, and preferably an aromatic amine.
- the cyclic amine has a cyclic skeleton excluding an aromatic skeleton and does not have an aromatic skeleton.
- the trialkylamine does not have a cyclic skeleton and an aromatic skeleton.
- the aromatic amine has an aromatic skeleton and does not have a cyclic skeleton excluding the aromatic skeleton.
- the carbon number of the cyclic amine is preferably 6 or more, preferably 20 or less.
- Specific examples of the cyclic amine include 1,4-diazabicyclo [2.2.2] octane (DABCO), diazabicycloundecene (DBU), and diazabicyclononene (DBN).
- the three alkyl groups of the trialkylamine may be the same or different.
- the carbon number of the three alkyl groups of the trialkylamine is 1 or more, preferably 2 or more, preferably 20 or less, more preferably 6 or less.
- Specific examples of the trialkylamine include trimethylamine, N, N-diethylmethylamine, N, N-dimethylethylamine, triethylamine, N, N-dimethylpropylamine, tripropylamine and tributylamine.
- aromatic amine examples include N, N-dimethylaminotoluidine, N, N-diethylaminotoluidine, N, N-dimethylaminobenzene, N, N-diethylaminobenzene, and N, N, N′N′—. And tetramethyl-p-phenylenediamine.
- the tertiary amine is at 23 ° C. It is preferably liquid.
- the content of the tertiary amine is preferably 0.1 parts by mass or more, more preferably 0.5 parts by mass or more, further preferably 1 part by mass or more, preferably 100 parts by mass of the gas generating agent. 50 parts by mass or less, more preferably 40 parts by mass or less, and still more preferably 30 parts by mass or less.
- the content of the tertiary amine is not less than the above lower limit and not more than the above upper limit, the gas generation amount per unit time in the gas generating material 11a is effectively increased, and the storage stability is effectively increased.
- the gas generating material 11a contains a photosensitizer.
- the photosensitizer has an effect of amplifying light stimulation to the gas generating agent. Therefore, when the gas generating material 11a contains the photosensitizer, the gas can be generated and released with a small amount of light irradiation. Further, gas can be generated and emitted by light in a wider wavelength region.
- the said photosensitizer may be used independently and may be used together 2 or more types.
- the type of the photosensitizer is not particularly limited.
- a known photosensitizer can be used as the photosensitizer.
- Examples of the photosensitizer include thioxanthone compounds, phenothiazine compounds, anthracene compounds, and acridone compounds.
- the thioxanthone compound has a thioxanthone skeleton.
- the phenothiazine compound has a phenothiazine skeleton.
- the anthracene compound has an anthracene skeleton.
- the acridone compound has an acridone skeleton.
- thioxanthone compound examples include thioxanthone, 2-chlorothioxanthone, 2,4-dichlorothioxanthone, 1-chloro-4-propoxythioxanthone, 2-isopropylthioxanthone, 4-isopropylthioxanthone, and 2,4-diethylthioxanthone. Is mentioned.
- phenothiazine compound examples include phenothiazine, 2-chlorophenothiazine, 2-methylthiophenothiazine, 2-methoxyphenothiazine, and 2- (trifluoromethyl) phenothiazine.
- anthracene compound examples include anthracene, 9,10-diethoxyanthracene, 9,10-dipropoxyanthracene, 9,10-dibutoxyanthracene, 9-carboxyanthracene, 2-anthracenecarboxylic acid, and 1-anthracenecarboxylic acid.
- acridone compound examples include 10-methyl-9 (10H) acridone, 9 (10H) -acridone, and 10-butyl-2-chloro-9 (10H) -acridone.
- the photosensitizer preferably contains at least one selected from the group consisting of a thioxanthone compound, a phenothiazine compound, an anthracene compound, and an acridone compound.
- the photosensitizer is preferably a thioxanthone compound, is preferably a phenothiazine compound, is preferably an anthracene compound, and is preferably an acridone compound.
- examples of the photosensitizer include polycyclic aromatic compounds having an alkoxy group.
- the polycyclic aromatic compound may have two or more alkoxy groups.
- polycyclic aromatic compounds having an alkoxy group containing a glycidyl group or a hydroxyl group are preferred.
- This polycyclic aromatic compound is preferably a substituted alkoxy polycyclic aromatic compound having an alkoxy group in which a part of the alkoxy group is substituted with a glycidyl group or a hydroxyl group.
- Such a photosensitizer has high sublimation resistance and can be used at high temperatures.
- the solubility in the gas generating material 11a is increased, and bleeding out can be suppressed.
- Preferred examples of the polycyclic aromatic compound used as the photosensitizer include polycyclic aromatic compounds having an anthracene skeleton.
- the polycyclic aromatic compound having an anthracene skeleton is an anthracene compound having an alkoxy group, such as an anthracene derivative.
- the carbon number of the alkoxy group of the polycyclic aromatic compound having an alkoxy group is 1 or more, preferably 18 or less, more preferably 8 or less.
- polycyclic aromatic compound having an alkoxy group examples include 9,10-dimethoxyanthracene, 2-ethyl-9,10-dimethoxyanthracene, 2-t-butyl-9,10-dimethoxyanthracene, 2,3 -Dimethyl-9,10-dimethoxyanthracene, 9-methoxy-10-methylanthracene, 9,10-diethoxyanthracene, 2-ethyl-9,10-diethoxyanthracene, 2-t-butyl-9,10-di Ethoxyanthracene, 2,3-dimethyl-9,10-diethoxyanthracene, 9-ethoxy-10-methylanthracene, 9,10-dipropoxyanthracene, 2-ethyl-9,10-dipropoxyanthracene, 2-t- Butyl-9,10-dipropoxyanthracene, 2,3-dimethyl-9,10 Dipropoxyanthracen
- polycyclic aromatic compound having a glycidyl group or an alkoxy group containing a hydroxyl group examples include 9,10-di (glycidyloxy) anthracene, 2-ethyl-9,10-di (glycidyloxy) anthracene, 2- t-butyl-9,10-di (glycidyloxy) anthracene, 2,3-dimethyl-9,10-di (glycidyloxy) anthracene, 9- (glycidyloxy) -10-methylanthracene, 9,10-di ( 2-vinyloxyethoxy) anthracene, 2-ethyl-9,10-di (2-vinyloxyethoxy) anthracene, 2-t-butyl-9,10-di (2-vinyloxyethoxy) anthracene, 2,3- Dimethyl-9,10-di (2-vinyloxyethoxy) anthracene, 9
- the photosensitizer may be a material generally known as a photopolymerization initiator.
- Examples of such photosensitizers include compounds that are activated by irradiation with light having a wavelength of 250 to 800 nm.
- Specific examples of such photosensitizers include acetophenone compounds such as methoxyacetophenone; benzoin ether compounds such as benzoin propyl ether and benzoin isobutyl ether; ketal compounds such as benzyldimethyl ketal and acetophenone diethyl ketal; phosphine oxide compounds;
- Examples include titanocene compounds such as bis ( ⁇ 5-cyclopentadienyl) titanocene; benzophenone; Michler ketone; chlorothioxanthone; dodecylthioxanthone; dimethylthioxanthone; diethylthioxanthone; ⁇ -hydroxycyclohexylphenylket
- the content of the photosensitizer is preferably 0.1 parts by mass or more, more preferably 0.5 parts by mass or more, preferably 50 parts by mass or less, more preferably 100 parts by mass of the gas generating agent. 30 parts by mass or less.
- the content of the photosensitizer is preferably 0.5 parts by mass or more, more preferably 1 part by mass or more, preferably 30 parts by mass or less, more preferably 100 parts by mass of the binder resin described later. 15 parts by mass or less.
- the blending amount of the tertiary amine and the photosensitizer it is preferable to blend so that the tertiary amine is equimolar with respect to the photosensitizer. Moreover, since it is thought that the said tertiary amine is not consumed at the time of gas generation
- the molar equivalent of the tertiary amine is preferably not more than the molar equivalent of the gas generating material.
- the equivalent here means that one nitrogen atom in the amine is one equivalent, and one molecule of the photosensitizer is one equivalent.
- the gas generating material 11a may further contain a binder resin.
- the gas generating material 11a includes a binder resin, the gas generating material 11a can be easily formed into a tablet shape, a fine particle shape, a film shape, or the like. Further, the gas generating agent can be firmly held in the gas generating material 11a.
- the said binder resin may be used independently and may be used together 2 or more types.
- the bainter resin is not particularly limited.
- the binder resin an appropriate binder resin that can hold the gas generating agent, the tertiary amine, and the photosensitizer in the gas generating material 11a is used.
- the binder resin for example, polymer materials such as poly (meth) acrylate, polyester, polyethylene, polypropylene, polystyrene, polyether, polyurethane, polycarbonate, polyamide, and polyimide can be used.
- the copolymer of the monomer which comprises these polymer materials may be used, and these polymer materials may be used together.
- the said poly (meth) acrylate is preferable as binder resin, in order to improve the generation efficiency of gas further. That is, the binder resin is preferably a (meth) acrylic polymer.
- the (meth) acrylic polymer includes a (meth) acrylic copolymer.
- the SP value of the binder resin is preferably 7 or more, preferably 10.5 or less.
- the SP value of the binder resin is not less than the above lower limit and not more than the above upper limit, the compatibility is further improved.
- the SP value (solubility parameter) can be calculated using the Fedors method (R. F. Fedors, Polym. Eng. Sci., 14, 147 (1974)).
- the (meth) acrylate monomer constituting the poly (meth) acrylate may be a chain compound or a cyclic compound.
- the chain compound include methyl (meth) acrylate, ethyl acrylate, butyl (meth) acrylate, 2-methylhexyl (meth) acrylate, and lauryl (meth) acrylate.
- the cyclic compound include cyclohexyl (meth) acrylate and isobornyl (meth) acrylate. Among these, methyl (meth) acrylate is preferable.
- the poly (meth) acrylate may be, for example, a copolymer of a (meth) acrylate monomer and a vinyl monomer copolymerizable with the (meth) acrylate monomer.
- the vinyl monomer is not particularly limited.
- vinyl monomer Containing vinyl monomer: (meth) acrylonitrile, N-vinyl pyrrolidone, N-vinyl caprolactam, N-vinyl lauryl lactam, (meth) acryloylmorpholine, (meth) acrylamide, dimethyl (meth) actyl Ruamido, N- methylol (meth) acrylamide, N- butoxymethyl (meth) acrylamide, N- isopropyl (meth) acrylamide, such as nitrogen-containing vinyl monomers such as dimethylaminomethyl (meth) acrylate.
- the said vinyl monomer may be used independently and may be used together with 2 or more types.
- the combination of the (meth) acrylate monomer and the vinyl monomer is not particularly limited.
- butyl (meth) acrylate and (meth) acrylic acid butyl (meth) acrylate and (meth) acrylamide, and (meth) ) A combination of acrylic acid and N-isopropyl (meth) acrylamide.
- the copolymerization ratio (mass ratio) of the (meth) acrylate monomer and the vinyl monomer is preferably in the range of 98: 2 to 51:49.
- the poly (meth) acrylate includes polymethyl (meth) acrylate, butyl (meth) acrylate / (meth) acrylic acid copolymer, and butyl (meth) acrylate / At least one selected from the group consisting of (meth) acrylamide copolymers is preferred.
- the poly (meth) acrylate preferably has an amino group or a carbonyl group.
- the binder resin preferably has an ultraviolet light absorption band.
- the ultraviolet light absorption band of the binder resin preferably has a shorter wavelength than the ultraviolet light absorption bands of the gas generating agent and the photosensitizer.
- the binder resin may have photodegradability.
- the weight average molecular weight of the binder resin is preferably 50,000 or more, more preferably 600,000 or more, preferably 2 million or less, more preferably 1.6 million or less.
- the weight average molecular weight of the binder resin is equal to or more than the lower limit, a decrease in the cohesive force of the binder resin itself is suppressed, and the gas generating agent, the tertiary amine, and the photosensitizer are contained in the gas generating material 11a. Can be held firmly.
- the weight average molecular weight of the binder resin is not more than the above upper limit, the gas generating material 11a can be easily processed into various forms.
- the binder resin preferably has adhesiveness.
- adhesiveness can be provided to the gas generating material 11a.
- the gas generating material 11 a can be easily disposed in the micropump 1.
- the film-like gas generating material 11 a having adhesiveness can be easily attached to the substrate surface of the micropump 1 or the wall surface inside the substrate.
- the content of the binder resin is, for example, preferably 10 parts by mass or more, more preferably 20 parts by mass or more, and still more preferably with respect to 100 parts by mass of the gas generating agent. Is 30 parts by mass or more, preferably 300 parts by mass or less, more preferably 200 parts by mass or less, and still more preferably 150 parts by mass or less.
- the gas generating material 11a includes 100 parts by mass of the gas generating agent and 0.1 parts by mass or more and 50 parts by mass or less of the tertiary amine with respect to 100 parts by mass of the gas generating agent. 1 part by mass or more and 50 parts by mass or less, 11 parts by mass or more and 300 parts by mass or less of the binder resin, and the gas generating material 11a is 10% by mass of the gas generating agent in 100% by mass of the gas generating material 11a. % Or more and 90% by mass or less.
- the gas generating material 11a preferably contains a silane coupling agent.
- silane coupling agent By using the silane coupling agent, the adhesion of the gas generating material 11a to the member to be bonded is further increased.
- the said silane coupling agent only 1 type may be used and 2 or more types may be used together.
- the gas generating material 11a contains a silane coupling agent having an amino group.
- the silane coupling agent having an amino group By using the silane coupling agent having an amino group, not only the adhesion of the gas generating material 11a to the member to be bonded is further increased, but also the gas generating material 11a is generated by using the silane coupling agent. A decrease in the amount of gas generated can also be suppressed. That is, when the silane coupling agent having an amino group is used, the adhesive force of the gas generating material 11a to the member to be bonded is more effective than when the silane coupling agent having no amino group is used. In addition, a decrease in the amount of gas generated from the gas generating material 11a can be effectively suppressed.
- the tertiary amine preferably does not contain a silicon atom, and is preferably not a silane coupling agent.
- the silane coupling agent having an amino group is preferably not the tertiary amine.
- silane coupling agent having an amino group examples include N-2- (aminoethyl) -3-aminopropylmethyldimethoxysilane, N-2- (aminoethyl) -3-aminopropyltrimethoxysilane, N -2- (aminoethyl) -3-aminopropyltriethoxysilane, N, N′-bis [(3-trimethoxysilyl) propyl] ethylenediamine, 3-aminopropyltrimethoxysilane, 3-aminopropyltriethoxysilane, and N-phenyl-3-aminopropyltrimethoxysilane and the like can be mentioned.
- Silane coupling agents having amino groups other than these may be used.
- the said silane coupling agent which has an amino group may be used independently, and 2 or more types may be used together.
- silane coupling agent having no amino group examples include epoxy groups such as 3-glycidoxypropyltrimethoxysilane, 3-glycidoxypropylmethyldiethoxysilane, and 3-glycidoxypropyltriethoxysilane.
- the content of the silane coupling agent and the content of the silane coupling agent having an amino group are preferably 0.0001 parts by mass or more with respect to 100 parts by mass of the gas generating agent. More preferably, it is 0.0003 mass part or more, Preferably it is 1 mass part or less, More preferably, it is 0.3 mass part or less.
- the adhesive force of the gas generating material 11a to the bonding target member is further increased.
- the content of the silane coupling agent and the amino group-containing silane coupling agent is less than or equal to the upper limit, the amount of gas generated by the excess silane coupling agent and the amino group-containing silane coupling agent is reduced. It is further suppressed.
- the gas generating material 11a may contain a crosslinking agent, an adhesive, an inorganic filler, and the like. It is more preferable that the gas generating material 11a contains the crosslinking agent. However, the gas generating material 11a may not contain the crosslinking agent. By using the crosslinking agent, the adhesiveness of the gas generating material 11a is further increased.
- 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 11b and the shape of the base material 10.
- the micro flow path 10b is connected to a pump chamber 10c 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.
- micropump 2 As in the micropump 1, a high output and a long drive time can be realized.
- Binder resin synthesis example The binder resin used in the examples and comparative examples was synthesized as follows. 97 parts by mass of n-butyl acrylate (manufactured by Nippon Shokubai Co., Ltd.), 3 parts by mass of acrylic acid (manufactured by Nippon Shokubai Co., Ltd.), 0.05 part by mass of Irgacure 907 (manufactured by Nagase Sangyo Co., Ltd.), and 200 parts by mass of ethyl acetate Mixed to obtain a mixture. Next, this mixture was irradiated with ultraviolet rays for 4 hours to produce a binder resin A which was an acrylic copolymer. The weight average molecular weight of the binder resin A was about 700,000. The SP value of the obtained binder resin A is in the range of 7 or more and 10.5 or less.
- Example 1 190 parts by weight of binder resin A and 380 parts by weight of ethyl acetate as a solvent were blended.
- binder resin A (however, 380 parts by weight of ethyl acetate as a solvent is blended with binder resin A)
- GAP4006 glycol azide polymer, manufactured by NOF Corporation
- tripropylamine tri-n-propylamine
- tertiary amine 3.5 parts by mass of 2,4-diethylthioxanthone
- DETX-S 2,4-diethylthioxanthone
- Example 1 the tetrad X used as a crosslinking agent in Example 1 is represented by the following formula (X).
- a micropump having a configuration substantially similar to the micropump 1 of the first embodiment was manufactured.
- the cross-sectional shape of the microchannel 10b was a 0.5 mm square shape.
- the length of the microchannel 10b was 800 mm.
- the tip of the microchannel 10b was open to the atmosphere.
- the gas generating material was a film having a diameter of 0.6 cm and a thickness of 50 ⁇ m.
- the gas generation amount ( ⁇ L) after 24 hours and after 10 days were measured, respectively. Based on the gas generation amount ( ⁇ L) after 24 hours, the relative gas generation amount (increase / decrease in gas generation amount) (%) after 10 days was determined. The same evaluation was performed in Examples and Comparative Examples described later.
- 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 micro flow path 10b and the measuring pipette with a silicon tube, filling the inside with water, and then irradiating the gas generating material with ultraviolet rays, and changing the volume of the measuring pipette by the generated gas. It was set as the method of reading.
- Example 2 to 18 and Comparative Examples 1 and 2 A micropump was produced in the same manner as in Example 1 except that the type and blending amount (unit: parts by mass) of the blending components were changed as shown in Tables 1 and 2 below.
- Comparative Example 1 no tertiary amine was used.
- Comparative Example 2 a tertiary amine and a crosslinking agent were not used.
- tertiary amine Tripropylamine (tri-n-propylamine) 1,4-diazabicyclo [2.2.2] octane (DABCO) Diazabicycloundecene (DBU) Diazabicyclononene (DBN) N, N-diethylamino-p-toluidine
- Example 19 In a micropump manufactured in the same manner as in Example 1, light of 380 nm was irradiated from an ultraviolet LED (NS375L-5RFS manufactured by Nitride Semiconductor Co., Ltd.), and a gas generation amount ( ⁇ L) was measured.
- an ultraviolet LED N375L-5RFS manufactured by Nitride Semiconductor Co., Ltd.
- Comparative Example 3 A micropump produced in the same manner as in Comparative Example 1 was irradiated with 380 nm light from an ultraviolet LED in the same manner as in Example 19 to measure the amount of gas generated ( ⁇ L).
- Example 20 to 26 and Comparative Examples 4 and 5 In the micropump produced in the same manner as in Example 19 except that the photosensitizers and amines of the types shown in Tables 3 and 4 below were used, the light of 380 nm from the ultraviolet LED was obtained in the same manner as in Example 19. The amount of gas generation ( ⁇ L) was measured.
- Example 19 to 26 are shown in Table 3 below, and the results of Comparative Examples 3 to 12 are shown in Table 4 below. Further, the results of Example 19 and Comparative Examples 3, 4, and 5 are shown in FIG. 3, the results of Example 20 and Comparative Example 6 are shown in FIG. 4, and the results of Example 21 and Comparative Example 7 are shown in FIG. The results of Example 22 and Comparative Example 8 are shown in FIG. 6, the results of Example 23 and Comparative Example 9 are shown in FIG. 7, the results of Example 24 and Comparative Example 10 are shown in FIG. The results of Comparative Example 11 are shown in FIG. 9, and the results of Example 26 and Comparative Example 12 are shown in FIG. The gas generation amounts shown in Tables 3 and 4 and FIGS. 3 to 10 are integrated values.
- Example 27 About 6 micropumps produced in the same manner as in Example 1, 1 day after production, 3 days, 6 days, 9 days, 16 days, and 30 days from UV LED The amount of gas generated ( ⁇ L) when irradiated with light of 380 nm for 2 minutes was measured.
- Comparative Example 13 Six micropumps produced in the same manner as in Comparative Example 4 were each irradiated with 380 nm light from an ultraviolet LED for 2 minutes after 1 day, 3 days, 6 days, and 9 days after production. The amount of gas generated ( ⁇ L) was measured.
- Comparative Example 14 Six micropumps produced in the same manner as in Comparative Example 5 were each irradiated with 380 nm light from an ultraviolet LED for 2 minutes after 1 day, 3 days, 6 days, and 9 days after production. The amount of gas generated ( ⁇ L) was measured.
- Example 15 6 micropumps produced in the same manner as in Example 1 except that dodecylamine was used instead of tripropylamine, respectively, 1 day after the production, 3 days, 6 days, and 9 days Later, the amount of gas generated ( ⁇ L) when irradiated with light of 380 nm from an ultraviolet LED for 2 minutes was measured.
- Example 27 and Comparative Examples 13, 14, and 15 are shown in Table 5 and FIG.
- the gas generation amounts shown in Tables 5 and 11 are integrated values.
- the gas generating material containing a tertiary amine is more stable than the gas generating material containing a primary amine and a secondary amine. It turns out that it is excellent.
- Example 28 100 parts by weight of binder resin A and 567 parts by weight of ethyl acetate as a solvent were blended. 100 parts by weight of binder resin A (provided that 567 parts by weight of ethyl acetate as a solvent is blended together with binder resin A), 50 parts by weight of DBSN (4-dodecylbenzenesulfonyl azide manufactured by Toyobo Co., Ltd.) as a gas generating agent, Tertiary amine tripropylamine (tri-n-propylamine) 3.5 parts by mass, photosensitizer (IPX made by DKSH Japan) 2 parts by mass, and crosslinking agent (Soken Chemical Co., Ltd.) 0.5 parts by mass of E-AX Toluene 5% solution) was mixed and processed into a film.
- DBSN 4-dodecylbenzenesulfonyl azide manufactured by Toyobo Co., Ltd.
- This film was heated at 110 ° C. for 5 minutes to remove ethyl acetate as a solvent. This was protected with a release PET film and stored at room temperature for one day (24 hours) to obtain a film-like gas generating material. Using the obtained gas generating material, a micropump was obtained in the same manner as in Example 1.
- Example 29 to 31 A gas generating material was obtained and a micropump was produced in the same manner as in Example 28 except that the type and amount of the blending component (unit: parts by mass) were changed as shown in Table 6 below.
- GAP5003 glycol azide polymer, manufactured by NOF Corporation was used as a gas generating agent.
- Example 2 The same evaluation as in Example 1 was performed on the micropumps obtained in Examples 28 to 31.
- the evaluation results are shown in Table 6 below. Since the gas generating materials of Examples 28 to 31 also use a tertiary amine as in Examples 1 to 27, the decrease in the amount of gas generated is not limited even after 24 hours and after 10 days. Less, and relative to the amount of gas generated after 24 hours ( ⁇ L) ( ⁇ L) (100%), the relative amount of gas generated after 10 days (increase / decrease in gas generation) (%) is 95% or more and 105% or less The storage stability was excellent.
- Example 32 100 parts by weight of binder resin A and 567 parts by weight of ethyl acetate as a solvent were blended. 100 parts by weight of binder resin A (provided that 567 parts by weight of ethyl acetate as a solvent is blended with binder resin A), 110 parts by weight of GAP4006 (glycidyl azide polymer, manufactured by NOF Corporation) as a gas generating agent, and amino N-2- (aminoethyl) -3-aminopropylmethyldimethoxysilane (KBM-602 manufactured by Shin-Etsu Chemical Co., Ltd.) which is a silane coupling agent having a group, and triamine which is a tertiary amine 2 parts by mass of propylamine (tri-n-propylamine), 3.5 parts by mass of photosensitizer (IPX made by DKSH Japan), and a crosslinking agent (E-AX toluene 5 made by Soken Chemical Co.,
- This film was heated at 110 ° C. for 5 minutes to remove ethyl acetate as a solvent. This was protected with a release PET film and stored at room temperature for one day (24 hours) to obtain a film-like gas generating material. Using the obtained gas generating material, a micropump was obtained in the same manner as in Example 1.
- Example 33 to 38 A gas generating material was obtained and a micropump was produced in the same manner as in Example 32 except that the type and blending amount (unit: parts by mass) of the blending components were changed as shown in Table 7 below.
- a silane coupling agent having an amino group was used in Examples 33 to 35.
- a silane coupling agent having no amino group was used in Examples 36 and 37.
- no silane coupling agent was used in Example 38.
- silane coupling agent used is as follows. N, N-bis [(3-trimethoxysilyl) propyl] ethylenediamine (manufactured by Gelest) 3-Aminopropyltrimethoxysilane (KBM-903 manufactured by Shin-Etsu Chemical Co., Ltd.) 3-Aminopropyltriethoxysilane (KBE-903 manufactured by Shin-Etsu Chemical Co., Ltd.) 3-Glycidoxypropyltriethoxysilane (KBE-403 manufactured by Shin-Etsu Chemical Co., Ltd.) 3-Methacryloxypropylmethyldiethoxysilane (KBE-502 manufactured by Shin-Etsu Chemical Co., Ltd.)
- Adhesive strength Using a tensile tester (manufactured by Shimadzu Corporation: AG-IS), the adhesive strength was evaluated by peeling off 180 degrees.
- the measurement conditions are a peel rate of 300 mm / min, a peel width of 25 mm, and a measurement temperature of 23 ° C.
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Abstract
Description
上記式(2-1)中、m+n=2~20、m≧1、n≧1、q+r=10~35、q≧5、r≧5であり、Aは、-OCH2CH2CH2CH2-、-OCH2CH2-、または-OCH2CH(CH3)-であり、Bは、-CH2CH(CH2N3)O-であり、R1は、-CH2CH2-、-CH2CH2CH2CH2-、-CH2CH(CH3)-、-[(CH2CH2O)xCH2CH2]-、または-[(CH2CH2CH2CH2O)yCH2CH2CH2CH2]-である。上記R1におけるxは10~25、yは5~20である。
図2は、上記の実施形態の変形例に係るマイクロポンプの略図的断面図である。
以下のようにして、実施例及び比較例で使用したバインダー樹脂を合成した。n-ブチルアクリレート(日本触媒社製)97質量部と、アクリル酸(日本触媒社製)3質量部と、イルガキュア907(長瀬産業社製)0.05質量部と、酢酸エチル200質量部とを混合して、混合物を得た。次に、この混合物に、紫外線を4時間照射して、アクリル共重合体であるバインダー樹脂Aを作製した。バインダー樹脂Aの重量平均分子量は、約70万であった。得られたバインダー樹脂AのSP値は7以上、10.5以下の範囲内である。
バインダー樹脂A190質量部と溶剤である酢酸エチル380重量部とを配合した。バインダー樹脂A190質量部(但し、溶剤である酢酸エチル380質量部をバインダー樹脂Aと共に配合してある)と、ガス発生剤であるGAP4006(グリシジルアジドポリマー、日油社製)100質量部と、第三級アミンであるトリプロピルアミン(トリn-プロピルアミン)10質量部と、光増感剤である2,4-ジエチルチオキサントン(日本化薬社製のDETX-S)3.5質量部と、架橋剤であるテトラッドX(三菱ガス化学社製)1質量部とを混合し、フィルム状に加工した。このフィルムを110℃で5分間加熱して、溶剤である酢酸エチルを除去した。これを離型PETフィルムで保護し、常温で一日(24時間)保管して、フィルム状のガス発生材を得た。なお、実施例1において架橋剤として用いたテトラッドXは、下記式(X)で表される。
配合成分の種類及び配合量(単位は質量部)を下記の表1,2に示すように変更したこと以外は実施例1と同様にして、マイクロポンプを作製した。なお、比較例1では、第三級アミンを用いなかった。比較例2では、第三級アミンと架橋剤とを用いなかった。
トリプロピルアミン(トリn-プロピルアミン)
1,4-ジアザビシクロ[2.2.2]オクタン(DABCO)
ジアザビシクロウンデセン(DBU)
ジアザビシクロノネン(DBN)
N,N-ジエチルアミノ-p-トルイジン
実施例1と同様にして作製したマイクロポンプにおいて、紫外線LED(ナイトレイドセミコンダクター社製のNS375L-5RFS)から380nmの光を照射して、ガス発生量(μL)を測定した。
比較例1と同様にして作製したマイクロポンプについて、実施例19と同様にして、紫外線LEDからの380nmの光を照射して、ガス発生量(μL)を測定した。
下記の表3,4に示す種類の光増感剤及びアミンを用いたこと以外は実施例19と同様にして作製したマイクロポンプにおいて、実施例19と同様にして、紫外線LEDからの380nmの光を照射して、ガス発生量(μL)を測定した。
下記の表4に示す種類の光増感剤を用いたこと、並びにアミンを用いなかったこと以外は実施例19と同様にして作製したマイクロポンプにおいて、実施例19と同様にして、紫外線LEDからの380nmの光を照射して、ガス発生量(μL)を測定した。
実施例1と同様にして作製した6つのマイクロポンプについて、それぞれ、作製してから1日経過後、3日経過後、6日経過後、9日経過後、16日経過後及び30日経過後に、紫外線LEDからの380nmの光を2分間照射したときのガス発生量(μL)を測定した。
比較例4と同様にして作製した6つのマイクロポンプについて、それぞれ、作製してから1日経過後、3日経過後、6日経過後及び9日経過後に、紫外線LEDからの380nmの光を2分間照射したときのガス発生量(μL)を測定した。
比較例5と同様にして作製した6つのマイクロポンプについて、それぞれ、作製してから1日経過後、3日経過後、6日経過後及び9日経過後に、紫外線LEDからの380nmの光を2分間照射したときのガス発生量(μL)を測定した。
トリプロピルアミンの代わりにドデシルアミンを用いたこと以外は実施例1と同様にして作製した6つのマイクロポンプについて、それぞれ、作製してから1日経過後、3日経過後、6日経過後及び9日経過後に、紫外線LEDからの380nmの光を2分間照射したときのガス発生量(μL)を測定した。
バインダー樹脂A100質量部と溶剤である酢酸エチル567重量部とを配合した。バインダー樹脂A100質量部(但し、溶剤である酢酸エチル567質量部をバインダー樹脂Aと共に配合してある)と、ガス発生剤であるDBSN(4-ドデシルベンゼンスルフォニルアジド 東洋紡社製)50質量部と、第三級アミンであるトリプロピルアミン(トリn-プロピルアミン)3.5質量部と、光増感剤である(DKSHジャパン社製のIPX)2質量部と、架橋剤である(綜研化学社製のE-AX トルエン5%液)0.5質量部とを混合し、フィルム状に加工した。このフィルムを110℃で5分間加熱して、溶剤である酢酸エチルを除去した。これを離型PETフィルムで保護し、常温で一日(24時間)保管して、フィルム状のガス発生材を得た。得られたガス発生材を用いて、実施例1と同様にしてマイクロポンプを得た。
配合成分の種類及び配合量(単位は質量部)を下記の表6に示すように変更したこと以外は実施例28と同様にして、ガス発生材を得て、マイクロポンプを作製した。実施例30,31では、ガス発生剤として、GAP5003(グリシジルアジドポリマー、日油社製)を用いた。
バインダー樹脂A100質量部と溶剤である酢酸エチル567重量部とを配合した。バインダー樹脂A100質量部(但し、溶剤である酢酸エチル567質量部をバインダー樹脂Aと共に配合してある)と、ガス発生剤であるGAP4006(グリシジルアジドポリマー、日油社製)110質量部と、アミノ基を有するシランカップリング剤であるN-2-(アミノエチル)-3-アミノプロピルメチルジメトキシシラン(信越化学工業社製のKBM-602)0.001質量部と、第三級アミンであるトリプロピルアミン(トリn-プロピルアミン)2質量部と、光増感剤である(DKSHジャパン社製のIPX)3.5質量部と、架橋剤である(綜研化学社製のE-AX トルエン5%液)0.5質量部とを混合し、フィルム状に加工した。このフィルムを110℃で5分間加熱して、溶剤である酢酸エチルを除去した。これを離型PETフィルムで保護し、常温で一日(24時間)保管して、フィルム状のガス発生材を得た。得られたガス発生材を用いて、実施例1と同様にしてマイクロポンプを得た。
配合成分の種類及び配合量(単位は質量部)を下記の表7に示すように変更したこと以外は実施例32と同様にして、ガス発生材を得て、マイクロポンプを作製した。なお、実施例33~35では、アミノ基を有するシランカップリング剤を用いた。実施例36,37では、アミノ基を有さないシランカップリング剤を用いた。実施例38では、シランカップリング剤を用いなかった。
N,N-ビス[(3-トリメトキシシリル)プロピル]エチレンジアミン(Gelest社製)
3-アミノプロピルトリメトキシシラン(信越化学工業社製のKBM-903)
3-アミノプロピルトリエトキシシラン(信越化学工業社製のKBE-903)
3-グリシドキシプロピルトリエトキシシラン(信越化学工業社製のKBE-403)
3-メタクリロキシプロピルメチルジエトキシシラン(信越化学工業社製のKBE-502)
ガス発生量の測定では、380nmの紫外線LED(ナイトレイドセミコンダクター社製のNS375L-5RFS)で120秒間照射したときのガスの発生量を測定した。なお、ガス発生量の測定方法は、実施例1と同じである。
引張試験機(島津製作所製:AG-IS)を用いて、180度ピール剥離を行うことにより接着力を評価した。測定条件は、剥離速度300mm/分、剥離幅25mm及び測定温度23℃の条件である。
セロファンテープの糊面と得られたフィルム状のガス発生材の糊面とを互いに貼り合わせ、90度剥離を行い、剥離強度を測定した。測定方法は接着力の測定に準じる。
10…基材
10a…主面
10b…マイクロ流路
10c…ポンプ室
11a、11b…ガス発生材
12…ガスバリア層
Claims (13)
- アゾ化合物またはアジド化合物であるガス発生剤、第三級アミン、光増感剤、及びバインダー樹脂を含む、ガス発生材。
- 前記第三級アミンが、環状アミン、トリアルキルアミン、及び芳香族アミンからなる群から選択された少なくとも1種を含む、請求項1に記載のガス発生材。
- 前記第三級アミンの含有量は、前記ガス発生剤100質量部に対して、0.1質量部以上、50質量部以下である、請求項1または2に記載のガス発生材。
- 前記アジド化合物は、スルフォニルアジド基またはアジドメチル基を有する、請求項1または2に記載のガス発生材。
- 前記光増感剤の含有量は、前記ガス発生剤100質量部に対して、0.1質量部以上、50質量部以下である、請求項1または2に記載のガス発生材。
- 前記光増感剤が、チオキサントン化合物、フェノチアジン化合物、アントラセン化合物、及びアクリドン化合物からなる群から選択された少なくとも1種を含む、請求項1または2に記載のガス発生材。
- シランカップリング剤をさらに含む、請求項1または2に記載のガス発生材。
- 請求項1または2のいずれか1項に記載のガス発生材と、
マイクロ流路が形成された基材と、
を備え、
前記ガス発生材は、前記ガス発生材において発生したガスが前記マイクロ流路に供給されるように配されている、マイクロポンプ。 - 前記ガス発生材において、前記第三級アミンの含有量は、前記ガス発生剤100質量部に対して、0.1質量部以上、50質量部以下である、請求項8に記載のマイクロポンプ。
- 前記アジド化合物は、スルフォニルアジド基またはアジドメチル基を有する、請求項8に記載のマイクロポンプ。
- 前記ガス発生材において、前記光増感剤の含有量は、前記ガス発生剤100質量部に対して、0.1質量部以上、50質量部以下である、請求項8に記載のマイクロポンプ。
- 前記光増感剤が、チオキサントン化合物、フェノチアジン化合物、アントラセン化合物、及びアクリドン化合物からなる群から選択された少なくとも1種を含む、請求項8に記載のマイクロポンプ。
- 前記ガス発生材が、シランカップリング剤をさらに含む、請求項8に記載のマイクロポンプ。
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CN201280001957.7A CN103717553B (zh) | 2012-06-08 | 2012-09-25 | 气体发生材料及微型泵 |
US13/822,634 US8986630B2 (en) | 2012-06-08 | 2012-09-25 | Gas-generating material and micro pump |
JP2012543404A JP5162731B1 (ja) | 2012-06-08 | 2012-09-25 | ガス発生材及びマイクロポンプ |
EP12878533.4A EP2860167B1 (en) | 2012-06-08 | 2012-09-25 | Gas generating material, and micropump |
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JP2012131386 | 2012-06-08 |
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US (1) | US8986630B2 (ja) |
EP (1) | EP2860167B1 (ja) |
JP (1) | JP2014012624A (ja) |
CN (1) | CN103717553B (ja) |
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WO2014061355A1 (ja) * | 2012-10-15 | 2014-04-24 | 積水化学工業株式会社 | ガス発生材及びマイクロポンプ |
JP2014080310A (ja) * | 2012-10-15 | 2014-05-08 | Sekisui Chem Co Ltd | ガス発生材及びマイクロポンプ |
JP5580923B1 (ja) * | 2013-03-18 | 2014-08-27 | 積水化学工業株式会社 | ガス発生材、ガス発生材の製造方法及びマイクロポンプ |
JP2015230184A (ja) * | 2014-06-03 | 2015-12-21 | 積水化学工業株式会社 | 懸濁液の移送方法 |
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US20140161687A1 (en) | 2014-06-12 |
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US8986630B2 (en) | 2015-03-24 |
EP2860167B1 (en) | 2020-04-29 |
EP2860167A1 (en) | 2015-04-15 |
CN103717553B (zh) | 2015-08-19 |
CN103717553A (zh) | 2014-04-09 |
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