JP2008059990A - Cooling liquid composition for fuel cell - Google Patents
Cooling liquid composition for fuel cell Download PDFInfo
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- JP2008059990A JP2008059990A JP2006237799A JP2006237799A JP2008059990A JP 2008059990 A JP2008059990 A JP 2008059990A JP 2006237799 A JP2006237799 A JP 2006237799A JP 2006237799 A JP2006237799 A JP 2006237799A JP 2008059990 A JP2008059990 A JP 2008059990A
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- fuel cell
- cooling liquid
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- liquid composition
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- 239000000203 mixture Substances 0.000 title claims abstract description 32
- 239000000446 fuel Substances 0.000 title claims abstract description 25
- 239000000110 cooling liquid Substances 0.000 title abstract description 7
- 239000002826 coolant Substances 0.000 claims description 20
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 12
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 claims description 6
- 150000002334 glycols Chemical class 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
- 150000001298 alcohols Chemical class 0.000 claims description 5
- -1 glycol ethers Chemical class 0.000 claims description 5
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 3
- HTJDQJBWANPRPF-UHFFFAOYSA-N Cyclopropylamine Chemical compound NC1CC1 HTJDQJBWANPRPF-UHFFFAOYSA-N 0.000 claims description 2
- KZZKOVLJUKWSKX-UHFFFAOYSA-N cyclobutanamine Chemical compound NC1CCC1 KZZKOVLJUKWSKX-UHFFFAOYSA-N 0.000 claims description 2
- HBGGBCVEFUPUNY-UHFFFAOYSA-N cyclododecanamine Chemical compound NC1CCCCCCCCCCC1 HBGGBCVEFUPUNY-UHFFFAOYSA-N 0.000 claims description 2
- HSOHBWMXECKEKV-UHFFFAOYSA-N cyclooctanamine Chemical compound NC1CCCCCCC1 HSOHBWMXECKEKV-UHFFFAOYSA-N 0.000 claims description 2
- NISGSNTVMOOSJQ-UHFFFAOYSA-N cyclopentanamine Chemical compound NC1CCCC1 NISGSNTVMOOSJQ-UHFFFAOYSA-N 0.000 claims description 2
- 230000003647 oxidation Effects 0.000 abstract description 10
- 238000007254 oxidation reaction Methods 0.000 abstract description 10
- 230000007774 longterm Effects 0.000 abstract description 3
- 239000003795 chemical substances by application Substances 0.000 abstract 2
- 150000003973 alkyl amines Chemical class 0.000 abstract 1
- 230000000052 comparative effect Effects 0.000 description 10
- 239000002253 acid Substances 0.000 description 7
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 230000007797 corrosion Effects 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000010248 power generation Methods 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
- BBMCTIGTTCKYKF-UHFFFAOYSA-N 1-heptanol Chemical compound CCCCCCCO BBMCTIGTTCKYKF-UHFFFAOYSA-N 0.000 description 2
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000012809 cooling fluid Substances 0.000 description 2
- 150000001923 cyclic compounds Chemical class 0.000 description 2
- 230000005611 electricity Effects 0.000 description 2
- 238000007710 freezing Methods 0.000 description 2
- 230000008014 freezing Effects 0.000 description 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000010525 oxidative degradation reaction Methods 0.000 description 2
- DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 description 1
- HGRCFOLSTCZSJR-UHFFFAOYSA-N (cyclohexylamino)methanol Chemical compound OCNC1CCCCC1 HGRCFOLSTCZSJR-UHFFFAOYSA-N 0.000 description 1
- FVCWZBVQRLEGDH-UHFFFAOYSA-N 1,2,2-trimethylcyclohexan-1-amine Chemical compound CC1(C)CCCCC1(C)N FVCWZBVQRLEGDH-UHFFFAOYSA-N 0.000 description 1
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 1
- PAJPWUMXBYXFCZ-UHFFFAOYSA-N 1-aminocyclopropanecarboxylic acid Chemical compound OC(=O)C1(N)CC1 PAJPWUMXBYXFCZ-UHFFFAOYSA-N 0.000 description 1
- QOECBYFRUBDAEP-UHFFFAOYSA-N 1-cyclohexylpropane-1,1-diamine Chemical compound CCC(N)(N)C1CCCCC1 QOECBYFRUBDAEP-UHFFFAOYSA-N 0.000 description 1
- VSRXAWSAKJABKW-UHFFFAOYSA-N 1-methylcyclopropan-1-amine Chemical compound CC1(N)CC1 VSRXAWSAKJABKW-UHFFFAOYSA-N 0.000 description 1
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 1
- MGUMZJAQENFQKN-UHFFFAOYSA-N 2-(cyclohexylamino)ethanol Chemical compound OCCNC1CCCCC1 MGUMZJAQENFQKN-UHFFFAOYSA-N 0.000 description 1
- ZSENYWITPNLAQQ-UHFFFAOYSA-N 2-(cyclooctylamino)ethanol Chemical compound OCCNC1CCCCCCC1 ZSENYWITPNLAQQ-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- COBPKKZHLDDMTB-UHFFFAOYSA-N 2-[2-(2-butoxyethoxy)ethoxy]ethanol Chemical compound CCCCOCCOCCOCCO COBPKKZHLDDMTB-UHFFFAOYSA-N 0.000 description 1
- WFSMVVDJSNMRAR-UHFFFAOYSA-N 2-[2-(2-ethoxyethoxy)ethoxy]ethanol Chemical compound CCOCCOCCOCCO WFSMVVDJSNMRAR-UHFFFAOYSA-N 0.000 description 1
- MXVMODFDROLTFD-UHFFFAOYSA-N 2-[2-[2-(2-butoxyethoxy)ethoxy]ethoxy]ethanol Chemical compound CCCCOCCOCCOCCOCCO MXVMODFDROLTFD-UHFFFAOYSA-N 0.000 description 1
- GTAKOUPXIUWZIA-UHFFFAOYSA-N 2-[2-[2-(2-ethoxyethoxy)ethoxy]ethoxy]ethanol Chemical compound CCOCCOCCOCCOCCO GTAKOUPXIUWZIA-UHFFFAOYSA-N 0.000 description 1
- RNMCCPMYXUKHAZ-UHFFFAOYSA-N 2-[3,3-diamino-1,2,2-tris(carboxymethyl)cyclohexyl]acetic acid Chemical compound NC1(N)CCCC(CC(O)=O)(CC(O)=O)C1(CC(O)=O)CC(O)=O RNMCCPMYXUKHAZ-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- XBPCUCUWBYBCDP-UHFFFAOYSA-N Dicyclohexylamine Chemical compound C1CCCCC1NC1CCCCC1 XBPCUCUWBYBCDP-UHFFFAOYSA-N 0.000 description 1
- SVYKKECYCPFKGB-UHFFFAOYSA-N N,N-dimethylcyclohexylamine Chemical compound CN(C)C1CCCCC1 SVYKKECYCPFKGB-UHFFFAOYSA-N 0.000 description 1
- GSCCALZHGUWNJW-UHFFFAOYSA-N N-Cyclohexyl-N-methylcyclohexanamine Chemical compound C1CCCCC1N(C)C1CCCCC1 GSCCALZHGUWNJW-UHFFFAOYSA-N 0.000 description 1
- XTUVJUMINZSXGF-UHFFFAOYSA-N N-methylcyclohexylamine Chemical compound CNC1CCCCC1 XTUVJUMINZSXGF-UHFFFAOYSA-N 0.000 description 1
- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 150000001642 boronic acid derivatives Chemical class 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000006388 chemical passivation reaction Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- VXVVUHQULXCUPF-UHFFFAOYSA-N cycloheptanamine Chemical compound NC1CCCCCC1 VXVVUHQULXCUPF-UHFFFAOYSA-N 0.000 description 1
- YMHQVDAATAEZLO-UHFFFAOYSA-N cyclohexane-1,1-diamine Chemical compound NC1(N)CCCCC1 YMHQVDAATAEZLO-UHFFFAOYSA-N 0.000 description 1
- SSJXIUAHEKJCMH-UHFFFAOYSA-N cyclohexane-1,2-diamine Chemical compound NC1CCCCC1N SSJXIUAHEKJCMH-UHFFFAOYSA-N 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 229940028356 diethylene glycol monobutyl ether Drugs 0.000 description 1
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- 229940075557 diethylene glycol monoethyl ether Drugs 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- TUEYHEWXYWCDHA-UHFFFAOYSA-N ethyl 5-methylthiadiazole-4-carboxylate Chemical compound CCOC(=O)C=1N=NSC=1C TUEYHEWXYWCDHA-UHFFFAOYSA-N 0.000 description 1
- 229940051250 hexylene glycol Drugs 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- MEFBJEMVZONFCJ-UHFFFAOYSA-N molybdate Chemical compound [O-][Mo]([O-])(=O)=O MEFBJEMVZONFCJ-UHFFFAOYSA-N 0.000 description 1
- HKJBEFFYTGZZIN-UHFFFAOYSA-N n'-(1,2,2-trimethylcyclohexyl)methanediamine Chemical compound CC1(C)CCCCC1(C)NCN HKJBEFFYTGZZIN-UHFFFAOYSA-N 0.000 description 1
- CIXSDMKDSYXUMJ-UHFFFAOYSA-N n,n-diethylcyclohexanamine Chemical compound CCN(CC)C1CCCCC1 CIXSDMKDSYXUMJ-UHFFFAOYSA-N 0.000 description 1
- UYZWCDKHEOBGLW-UHFFFAOYSA-N n-butylhexan-1-amine Chemical compound CCCCCCNCCCC UYZWCDKHEOBGLW-UHFFFAOYSA-N 0.000 description 1
- GUQRKZPMVLRXLT-UHFFFAOYSA-N n-cyclohexylhydroxylamine Chemical compound ONC1CCCCC1 GUQRKZPMVLRXLT-UHFFFAOYSA-N 0.000 description 1
- AGVKXDPPPSLISR-UHFFFAOYSA-N n-ethylcyclohexanamine Chemical compound CCNC1CCCCC1 AGVKXDPPPSLISR-UHFFFAOYSA-N 0.000 description 1
- HHQZLSKAOKGKKL-UHFFFAOYSA-N n-ethynylcyclohexanamine Chemical compound C#CNC1CCCCC1 HHQZLSKAOKGKKL-UHFFFAOYSA-N 0.000 description 1
- KKTBUCVHSCATGB-UHFFFAOYSA-N n-methylcyclopentanamine Chemical compound CNC1CCCC1 KKTBUCVHSCATGB-UHFFFAOYSA-N 0.000 description 1
- SQGBZKZDUMBTIJ-UHFFFAOYSA-N n-prop-2-enylcyclohexanamine Chemical compound C=CCNC1CCCCC1 SQGBZKZDUMBTIJ-UHFFFAOYSA-N 0.000 description 1
- UYYCVBASZNFFRX-UHFFFAOYSA-N n-propan-2-ylcyclohexanamine Chemical compound CC(C)NC1CCCCC1 UYYCVBASZNFFRX-UHFFFAOYSA-N 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 150000002826 nitrites Chemical class 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- JCGNDDUYTRNOFT-UHFFFAOYSA-N oxolane-2,4-dione Chemical compound O=C1COC(=O)C1 JCGNDDUYTRNOFT-UHFFFAOYSA-N 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 150000003557 thiazoles Chemical class 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- JLGLQAWTXXGVEM-UHFFFAOYSA-N triethylene glycol monomethyl ether Chemical compound COCCOCCOCCO JLGLQAWTXXGVEM-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/30—Hydrogen technology
- Y02E60/50—Fuel cells
Landscapes
- Fuel Cell (AREA)
Abstract
Description
本発明は、燃料電池、特には自動車用燃料電池の冷却に使用される冷却液組成物に関する。詳細には長期の使用によっても基剤の酸化による導電率の上昇が小さく、初期の導電率を維持することができる燃料電池用冷却液組成物に関する。 The present invention relates to a coolant composition used for cooling a fuel cell, particularly an automobile fuel cell. More specifically, the present invention relates to a fuel cell coolant composition capable of maintaining the initial conductivity with little increase in conductivity due to oxidation of the base material even after long-term use.
燃料電池は、一般に発電単位である単セルを多数積層した構造のスタックとして構成されている。発電時にはスタックから熱が発生するので、このスタックを冷却するために数セル毎に冷却板が挿入されていた。そして、この冷却板内部には冷却液通路が形成されており、この通路を冷却液が流れることにより、スタックが冷却されるようになっていた。 A fuel cell is generally configured as a stack having a structure in which a large number of single cells as power generation units are stacked. Since heat is generated from the stack during power generation, a cooling plate is inserted every several cells to cool the stack. A cooling fluid passage is formed inside the cooling plate, and the stack is cooled by flowing the cooling fluid through the passage.
このように、燃料電池の冷却液は、発電を実行しているスタック内を循環してスタックを冷却するため、冷却液の電気伝導率が高いと、スタックで生じた電気が冷却液側へと流れて電気を損失し、当該燃料電池における発電力を低下させることになる。そこで、従来の燃料電池の冷却液には導電率が低い、換言すれば電気絶縁性が高い純水が使用されていた。 In this way, the coolant of the fuel cell circulates in the stack that is generating power to cool the stack, so if the electrical conductivity of the coolant is high, the electricity generated in the stack will move to the coolant side. It flows and loses electricity, and the power generation in the fuel cell is reduced. Therefore, pure water having low electrical conductivity, in other words, high electrical insulation, has been used as a conventional fuel cell coolant.
ところが、例えば自動車用燃料電池や家庭用コージェネレーションシステム用燃料電池を考慮した場合、非作動時に冷却液は周囲の温度まで低下してしまう。特に氷点下での使用可能性がある場合、純水では凍結してしまい、冷却液の体積膨張による冷却板の破損など、燃料電池の電池性能を損なう恐れがあった。 However, for example, when considering a fuel cell for automobiles and a fuel cell for household cogeneration systems, the cooling liquid is lowered to the ambient temperature during non-operation. In particular, when there is a possibility of use below freezing point, there is a possibility that the battery performance of the fuel cell is impaired, such as freezing in pure water and damage to the cooling plate due to volume expansion of the coolant.
このような事情から、燃料電池用冷却液には、不凍性を目的としてグリコール類やアルコール類などの基剤を使用することが考えられる。従来、例えば水とグリコール類の混合溶液からなる基剤と、冷却液の導電率を低導電率に維持するアミン系のアルカリ性添加剤を含む燃料電池用冷却液組成物が提案されている(特許文献1参照)。
しかし、従来の燃料電池用冷却液組成物にあっては、燃料電池作動中に冷却液中において基剤として使用されているグリコール類やアルコール類が酸化してイオン性物質を生成する。このため、長期に渡って使用することにより、冷却液中のイオン性物質の量が増加し、この結果、初期の導電率が維持できなくなるという事態を招く恐れがあった。 However, in the conventional fuel cell coolant composition, glycols and alcohols used as a base in the coolant are oxidized during fuel cell operation to produce an ionic substance. For this reason, when used for a long period of time, the amount of the ionic substance in the cooling liquid increases, and as a result, there is a possibility that the initial conductivity cannot be maintained.
本発明は、このような事情に鑑みなされたものであり、基剤の酸化による導電率の上昇が小さく、長期に渡って初期の導電率を維持することができる燃料電池用冷却液組成物を提供することを目的とするものである。 The present invention has been made in view of such circumstances, and provides a coolant composition for a fuel cell in which the increase in conductivity due to oxidation of the base is small and the initial conductivity can be maintained over a long period of time. It is intended to provide.
本発明の燃料電池用冷却液組成物(以下、単に組成物という)は、環式化合物であるシクロアルキルアミン又はその誘導体を含有することで特徴づけられたものである。 The fuel cell coolant composition of the present invention (hereinafter simply referred to as a composition) is characterized by containing a cyclic compound, cycloalkylamine, or a derivative thereof.
本発明の組成物はシクロアルキルアミン又はその誘導体を含有することから、該シクロアルキルアミン又はその誘導体が基剤の酸化を抑制し、基剤の酸化による冷却液の導電率の上昇が効果的に抑制され、長期に渡って使用した場合でも初期の導電率を維持することができる。 Since the composition of the present invention contains a cycloalkylamine or a derivative thereof, the cycloalkylamine or a derivative thereof suppresses the oxidation of the base, and the increase in the conductivity of the coolant due to the oxidation of the base is effective. Even when used over a long period of time, the initial conductivity can be maintained.
本発明の組成物に用いる基剤としては、低導電率であって、不凍性を有するものが望ましい。具体的には水、アルコール類、グリコール類、及びグリコールエーテル類の中から選ばれる1種若しくは2種以上の混合物からなるものが望ましい。 As the base used in the composition of the present invention, those having low electrical conductivity and having antifreezing properties are desirable. Specifically, those composed of one or a mixture of two or more selected from water, alcohols, glycols, and glycol ethers are desirable.
アルコール類としては、例えばメタノール、エタノール、プロパノール、ブタノール、ペンタノール、ヘキサノール、ヘプタノール、オクタノールの中から選ばれる1種若しくは2種以上の混合物からなるものを挙げることができる。 Examples of the alcohols include those composed of one or a mixture of two or more selected from methanol, ethanol, propanol, butanol, pentanol, hexanol, heptanol, and octanol.
グリコール類としては、例えばエチレングリコール、ジエチレングリコール、トリエチレングリコール、プロピレングリコール、1,3−プロパンジオール、1,3−ブタンジオール、1,5−ペンタンジオール、ヘキシレングリコールの中から選ばれる1種若しくは2種以上の混合物からなるものを挙げることができる。 Examples of glycols include one selected from ethylene glycol, diethylene glycol, triethylene glycol, propylene glycol, 1,3-propanediol, 1,3-butanediol, 1,5-pentanediol, and hexylene glycol, or The thing which consists of 2 or more types of mixtures can be mentioned.
グリコールエーテル類としては、例えばエチレングリコールモノメチルエーテル、ジエチレングリコールモノメチルエーテル、トリエチレングリコールモノメチルエーテル、テトラエチレングリコールモノメチルエーテル、エチレングリコールモノエチルエーテル、ジエチレングリコールモノエチルエーテル、トリエチレングリコールモノエチルエーテル、テトラエチレングリコールモノエチルエーテル、エチレングリコールモノブチルエーテル、ジエチレングリコールモノブチルエーテル、トリエチレングリコールモノブチルエーテル、テトラエチレングリコールモノブチルエーテルの中から選ばれる1種若しくは2種以上の混合物からなるものを挙げることができる。 Examples of glycol ethers include ethylene glycol monomethyl ether, diethylene glycol monomethyl ether, triethylene glycol monomethyl ether, tetraethylene glycol monomethyl ether, ethylene glycol monoethyl ether, diethylene glycol monoethyl ether, triethylene glycol monoethyl ether, tetraethylene glycol monoethyl ether. Mention may be made of one or a mixture of two or more selected from ethyl ether, ethylene glycol monobutyl ether, diethylene glycol monobutyl ether, triethylene glycol monobutyl ether, and tetraethylene glycol monobutyl ether.
上記基剤の中でもエチレングリコールおよび又はプロピレングリコールは、取り扱い性、価格、入手容易性の点から好ましい。 Among the above bases, ethylene glycol and / or propylene glycol are preferable from the viewpoints of handleability, cost, and availability.
上記基剤中にシクロアルキルアミン又はその誘導体が含まれているのである。シクロアルキルアミンは抗酸化剤であり、これを基剤中に含有させることにより、基剤の酸化が効果的に抑制され、基剤の酸化によるイオン性物質の生成が抑えられる。このため、長期使用によっても冷却液中のイオン性物質の量が少なくすることができ、この結果、初期の導電率が維持されるという効果を奏することになる。 The above base contains cycloalkylamine or a derivative thereof. Cycloalkylamine is an antioxidant, and by containing it in the base, the oxidation of the base is effectively suppressed, and the production of ionic substances due to the oxidation of the base is suppressed. For this reason, even if it is used for a long time, the amount of the ionic substance in the cooling liquid can be reduced, and as a result, the initial conductivity is maintained.
このような作用効果を奏するシクロアルキルアミン又はその誘導体としては、例えばメチルシクロプロパンアミン、アミノシクロプロパンカルボン酸、メチルシクロペンチルアミン、シクロヘキサンジアミン、シクロヘキシルヒドロキシルアミン、メチルシクロヘキシルアミン、ジメチルシクロヘキシルアミン、トリメチルシクロヘキシルアミン、アミノメチルトリメチルシクロヘキシルアミン、ヒドロキシメチルシクロヘキシルアミン、エチルシクロヘキシルアミン、エチニルシクロヘキシルアミン、ジエチルシクロヘキシルアミン、ヒドロキシエチルシクロヘキシルアミン、イソプロピルシクロヘキシルアミン、シクロヘキシルプロパンジアミン、アリルシクロヘキシルアミン、ブチルヘキシルアミン、ジアセチルシクロヘキサンジアミン、シクロヘキサンジアミンテトラ酢酸、ジシクロヘキシルアミン、メチルジシクロヘキシルアミン、ジシクロヘプチルアミン、シクロオクチルヒドロキシエチルアミンなどを挙げることができ、これらの1種若しくは2種以上の混合物の形態で用いることができる。上記シクロアルキルアミン又はその誘導体の中でも、炭素数が3〜12のシクロプロピルアミン、シクロブチルアミン、シクロペンチルアミン、シクロヘキシルアミン、シクロオクチルアミン、シクロドデシルアミンは、酸化抑制効果に優れ、かつ取り扱い性や入手容易性が良好である点でより好ましい。 Examples of cycloalkylamines or derivatives thereof having such effects include methylcyclopropanamine, aminocyclopropanecarboxylic acid, methylcyclopentylamine, cyclohexanediamine, cyclohexylhydroxylamine, methylcyclohexylamine, dimethylcyclohexylamine, and trimethylcyclohexylamine. , Aminomethyltrimethylcyclohexylamine, hydroxymethylcyclohexylamine, ethylcyclohexylamine, ethynylcyclohexylamine, diethylcyclohexylamine, hydroxyethylcyclohexylamine, isopropylcyclohexylamine, cyclohexylpropanediamine, allylcyclohexylamine, butylhexylamine, diacetylcyclohexanediamine , Cyclohexanediamine tetraacetic acid, dicyclohexylamine, methyl dicyclohexylamine, di cycloheptylamine, and the like can be illustrated cyclooctyl hydroxyethylamine, it can be used in the form of these one or two or more thereof. Among the above cycloalkylamines or derivatives thereof, cyclopropylamine, cyclobutylamine, cyclopentylamine, cyclohexylamine, cyclooctylamine, and cyclododecylamine having 3 to 12 carbon atoms are excellent in oxidation-inhibiting effect and are easy to handle and obtain. It is more preferable in terms of ease.
シクロアルキルアミン又はその誘導体の含有量としては、基剤100重量部に対して0.001〜20重量部の範囲が好ましく、より好ましくは0.001〜15重量部であり、最適には0.01〜10重量部である。シクロアルキルアミン又はその誘導体の含有量が基剤100重量部に対して0.001重量部を下回る場合、十分な基剤の酸化抑制効果を得ることができず、20重量部を上回る場合には、上回っただけの酸化抑制効果が期待できず、不経済となる。 The content of cycloalkylamine or a derivative thereof is preferably in the range of 0.001 to 20 parts by weight, more preferably 0.001 to 15 parts by weight with respect to 100 parts by weight of the base. 01 to 10 parts by weight. When the content of cycloalkylamine or a derivative thereof is less than 0.001 part by weight with respect to 100 parts by weight of the base, a sufficient base oxidation inhibition effect cannot be obtained, and when the content exceeds 20 parts by weight. However, it is not possible to expect the effect of suppressing oxidation just exceeding the value, which is uneconomical.
また本発明の組成物には、燃料電池に使用されている金属の腐食を効果的に抑制するため、少なくとも1種以上の腐食抑制剤を導電率に影響を与えない範囲で含ませることができる。 In addition, the composition of the present invention can contain at least one or more types of corrosion inhibitors as long as they do not affect the conductivity in order to effectively suppress the corrosion of the metal used in the fuel cell. .
腐食抑制剤としては、リン酸及び又はその塩、脂肪族カルボン酸及び又はその塩、芳香族カルボン酸及び又はその塩、トリアゾール類、チアゾール類、ケイ酸塩、硝酸塩、亜硝酸塩、ホウ酸塩、モリブテン酸塩、及びアミン塩のいずれか1種若しくは2種以上の混合物を挙げることができる。 Corrosion inhibitors include phosphoric acid and / or salts thereof, aliphatic carboxylic acids and / or salts thereof, aromatic carboxylic acids and / or salts thereof, triazoles, thiazoles, silicates, nitrates, nitrites, borates, Any one or a mixture of two or more of molybdate and amine salts can be mentioned.
尚、本発明の組成物には、例えば水酸化ナトリウムや水酸化カリウムなどのpH調整剤、消泡剤、或いは着色剤などを導電率に影響を与えない範囲で適宜添加することができる。 In addition, for example, a pH adjusting agent such as sodium hydroxide or potassium hydroxide, an antifoaming agent, or a coloring agent can be appropriately added to the composition of the present invention as long as the electrical conductivity is not affected.
尚、本発明は、下記実施例に限定されるものではなく、「特許請求の範囲」に記載された範囲で自由に変更して実施することができる。 In addition, this invention is not limited to the following Example, It can implement freely by changing in the range described in the "Claims".
以下、本発明の組成物の好ましい実施例を挙げ、比較例と対比しつつ、その性能を評価した。表1には実施例1〜3並びに比較例1〜3の組成物を挙げた。実施例1〜3並びに比較例1〜3の各組成物は、いずれもイオン交換水及びエチレングリコールを基剤としており、この基剤中にシクロヘキシルアミンを添加したものを実施例1とし、メチルシクロヘキシルアミンを添加したものを実施例2、1,2−シクロヘキサンジアミンを添加したものを実施例3とした。 Hereafter, the preferable Example of the composition of this invention was given and the performance was evaluated, contrasting with a comparative example. Table 1 lists the compositions of Examples 1 to 3 and Comparative Examples 1 to 3. Each of the compositions of Examples 1 to 3 and Comparative Examples 1 to 3 is based on ion-exchanged water and ethylene glycol, and Example 1 was obtained by adding cyclohexylamine to this base. Example 2 was obtained by adding amine, and Example 3 by adding 1,2-cyclohexanediamine.
一方、上記基剤のみのものを比較例1とし、上記基剤中にエタノールアミンを添加したものを比較例2、アセトニトリルを添加したものを比較例3とした。 On the other hand, Comparative Example 1 was obtained by adding only the above-mentioned base, Comparative Example 2 was obtained by adding ethanolamine to the above-mentioned base, and Comparative Example 3 was obtained by adding acetonitrile.
Claims (4)
The fuel cell coolant composition according to any one of claims 1 to 3, wherein the content of the cycloalkylamine or a derivative thereof is 0.001 to 20 parts by weight with respect to 100 parts by weight of the base. .
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102015119448A1 (en) | 2014-11-14 | 2016-05-19 | Toyota Jidosha Kabushiki Kaisha | Coolant for fuel cell vehicle with improved storage stability and method for producing the same |
| US20220033700A1 (en) * | 2020-07-29 | 2022-02-03 | Toyota Jidosha Kabushiki Kaisha | Non-water coolant composition and cooling system |
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Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102015119448A1 (en) | 2014-11-14 | 2016-05-19 | Toyota Jidosha Kabushiki Kaisha | Coolant for fuel cell vehicle with improved storage stability and method for producing the same |
| US9929416B2 (en) | 2014-11-14 | 2018-03-27 | Toyota Jidosha Kabushiki Kaisha | Fuel cell vehicle coolant having improved storage stability and method for producing the same |
| DE102015119448B4 (en) | 2014-11-14 | 2020-08-06 | Toyota Jidosha Kabushiki Kaisha | Method for producing a stock solution composition for a coolant and a coolant composition for fuel cell vehicles with improved storage stability |
| US20220033700A1 (en) * | 2020-07-29 | 2022-02-03 | Toyota Jidosha Kabushiki Kaisha | Non-water coolant composition and cooling system |
| JP2022025572A (en) * | 2020-07-29 | 2022-02-10 | トヨタ自動車株式会社 | Non-water coolant composition and cooling system |
| CN114058340A (en) * | 2020-07-29 | 2022-02-18 | 丰田自动车株式会社 | Non-aqueous coolant composition and cooling system |
| JP7334691B2 (en) | 2020-07-29 | 2023-08-29 | トヨタ自動車株式会社 | Non-aqueous coolant composition and cooling system |
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