JP2021004353A5 - - Google Patents
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- JP2021004353A5 JP2021004353A5 JP2020066779A JP2020066779A JP2021004353A5 JP 2021004353 A5 JP2021004353 A5 JP 2021004353A5 JP 2020066779 A JP2020066779 A JP 2020066779A JP 2020066779 A JP2020066779 A JP 2020066779A JP 2021004353 A5 JP2021004353 A5 JP 2021004353A5
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- 239000002904 solvent Substances 0.000 claims 54
- 239000000203 mixture Substances 0.000 claims 50
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 claims 10
- IIEWJVIFRVWJOD-UHFFFAOYSA-N ethylcyclohexane Chemical compound CCC1CCCCC1 IIEWJVIFRVWJOD-UHFFFAOYSA-N 0.000 claims 8
- LDTMPQQAWUMPKS-UPHRSURJSA-N (z)-1-chloro-3,3,3-trifluoroprop-1-ene Chemical compound FC(F)(F)\C=C/Cl LDTMPQQAWUMPKS-UPHRSURJSA-N 0.000 claims 7
- 238000004140 cleaning Methods 0.000 claims 7
- ZUBZATZOEPUUQF-UHFFFAOYSA-N isononane Chemical compound CCCCCCC(C)C ZUBZATZOEPUUQF-UHFFFAOYSA-N 0.000 claims 7
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 claims 6
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 claims 6
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 claims 6
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 claims 5
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 4
- 150000001336 alkenes Chemical class 0.000 claims 4
- 125000004429 atom Chemical group 0.000 claims 4
- 238000009835 boiling Methods 0.000 claims 4
- 125000004432 carbon atom Chemical group C* 0.000 claims 4
- 229910052801 chlorine Inorganic materials 0.000 claims 4
- 125000001309 chloro group Chemical group Cl* 0.000 claims 4
- 239000012459 cleaning agent Substances 0.000 claims 4
- 229930195733 hydrocarbon Natural products 0.000 claims 4
- 150000002430 hydrocarbons Chemical class 0.000 claims 4
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 claims 4
- BGVYPLBZJNTJEH-UHFFFAOYSA-N 1,3-dichloro-2,3,3-trifluoroprop-1-ene Chemical compound ClC=C(F)C(F)(F)Cl BGVYPLBZJNTJEH-UHFFFAOYSA-N 0.000 claims 3
- USCSECLOSDIOTA-UHFFFAOYSA-N 1-chloro-2,3,3-trifluoroprop-1-ene Chemical compound FC(F)C(F)=CCl USCSECLOSDIOTA-UHFFFAOYSA-N 0.000 claims 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 3
- GDPWRLVSJWKGPJ-UPHRSURJSA-N (z)-1-chloro-2,3,3,3-tetrafluoroprop-1-ene Chemical compound Cl\C=C(/F)C(F)(F)F GDPWRLVSJWKGPJ-UPHRSURJSA-N 0.000 claims 2
- FDMFUZHCIRHGRG-UHFFFAOYSA-N 3,3,3-trifluoroprop-1-ene Chemical compound FC(F)(F)C=C FDMFUZHCIRHGRG-UHFFFAOYSA-N 0.000 claims 2
- 239000000443 aerosol Substances 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- FFTOUVYEKNGDCM-OWOJBTEDSA-N (e)-1,3,3-trifluoroprop-1-ene Chemical compound F\C=C\C(F)F FFTOUVYEKNGDCM-OWOJBTEDSA-N 0.000 claims 1
- USCSECLOSDIOTA-OWOJBTEDSA-N (e)-1-chloro-2,3,3-trifluoroprop-1-ene Chemical compound FC(F)C(\F)=C/Cl USCSECLOSDIOTA-OWOJBTEDSA-N 0.000 claims 1
- -1 1,1,2,2-tetrafluoroethyl-2,2,2-trifluoroethyl Chemical group 0.000 claims 1
- VJGCZWVJDRIHNC-UHFFFAOYSA-N 1-fluoroprop-1-ene Chemical compound CC=CF VJGCZWVJDRIHNC-UHFFFAOYSA-N 0.000 claims 1
- DJXNLVJQMJNEMN-UHFFFAOYSA-N 2-[difluoro(methoxy)methyl]-1,1,1,2,3,3,3-heptafluoropropane Chemical compound COC(F)(F)C(F)(C(F)(F)F)C(F)(F)F DJXNLVJQMJNEMN-UHFFFAOYSA-N 0.000 claims 1
- FNUBKINEQIEODM-UHFFFAOYSA-N 3,3,4,4,5,5,5-heptafluoropentanal Chemical compound FC(F)(F)C(F)(F)C(F)(F)CC=O FNUBKINEQIEODM-UHFFFAOYSA-N 0.000 claims 1
- 239000004215 Carbon black (E152) Substances 0.000 claims 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 claims 1
- 239000005456 alcohol based solvent Substances 0.000 claims 1
- 230000004907 flux Effects 0.000 claims 1
- 238000002347 injection Methods 0.000 claims 1
- 239000007924 injection Substances 0.000 claims 1
- 229920005668 polycarbonate resin Polymers 0.000 claims 1
- 239000004431 polycarbonate resin Substances 0.000 claims 1
- ZDCRNXMZSKCKRF-UHFFFAOYSA-N tert-butyl 4-(4-bromoanilino)piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)(C)C)CCC1NC1=CC=C(Br)C=C1 ZDCRNXMZSKCKRF-UHFFFAOYSA-N 0.000 claims 1
Claims (24)
（Ｂ）ノルマルオクタン、イソオクタン、イソノナン、メチルシクロヘキサン及びエチルシクロヘキサンからなる群より選択される１種以上の溶剤と
を含む溶剤組成物であって、
前記組成物の総量を１００重量部としたときに、
（Ａ）の含有量が５重量部超９５重量部未満であり、
（Ｂ）の含有量が５重量部超９５重量部未満であり、そして
（Ａ）及び（Ｂ）の含有量の合計が９５重量部以上１００重量部以下である、溶剤組成物（但し、１−クロロ−２，３，３−トリフルオロプロペンと、沸点が６０〜１００℃の炭化水素との組合せを含む溶剤組成物を除き、シス−１−クロロ−３，３，３−トリフルオロプロペンと、炭素原子数が５若しくは６である、直鎖状若しくは分岐状のアルケンとの組合せを含む溶剤組成物を除き、及び、（Ａ）が、１−クロロ−２，３，３，３−テトラフルオロ−１−プロペンのＺ体、１−クロロ−２，３，３，４，４，５，５−ヘプタフルオロ−１−ペンテン、又は１，３−ジクロロ−２，３，３−トリフルオロプロペンである場合を除く。）。 (A) Hydrofluoroolefins which may contain one or more atoms selected from the group consisting of (a1) chlorine atom and bromine atom, (a2) chlorofluoroolefins, and (a3) bromofluoroolefins. One or more solvents selected from the group consisting of
(B) A solvent composition containing one or more solvents selected from the group consisting of normal octane, isooctane, isononan, methylcyclohexane and ethylcyclohexane.
When the total amount of the composition is 100 parts by weight,
The content of (A) is more than 5 parts by weight and less than 95 parts by weight.
A solvent composition in which the content of (B) is more than 5 parts by weight and less than 95 parts by weight, and the total content of (A) and (B) is 95 parts by weight or more and 100 parts by weight or less (however, 1). With the exception of solvent compositions containing a combination of −chloro-2,3,3-trifluoropropene and hydrocarbons with a boiling point of 60-100 ° C., cis-1-chloro-3,3,3-trifluoropropene. , Except for solvent compositions containing combinations with linear or branched alkenes having 5 or 6 carbon atoms, and (A) are 1-chloro-2,3,3,3-tetra. Z form of fluoro-1-propene, 1-chloro-2,3,3,4,5,5-heptafluoro-1-pentene, or 1,3-dichloro-2,3,3-trifluoropropene Except when it is.) .
（Ｂ）ノルマルオクタン、イソオクタン、イソノナン、メチルシクロヘキサン及びエチルシクロヘキサンからなる群より選択される１種以上の溶剤と、
（Ｃ）（ｃ１）ハイドロフルオロカーボン類、（ｃ２）ハイドロフルオロエーテル類及び（ｃ３）１−メトキシ−２−プロパノールからなる群より選択される１種以上の溶剤とを含む溶剤組成物であって、
前記組成物の総量を１００重量部としたときに、
（Ａ）及び（Ｂ）の含有量の合計が１０重量部超１００重量部未満であり、そして
（Ａ）、（Ｂ）及び（Ｃ）の含有量の合計が９５重量部以上１００重量部以下である、溶剤組成物（但し、１−クロロ−２，３，３−トリフルオロプロペンと、沸点が６０〜１００℃の炭化水素との組合せを含む溶剤組成物を除き、シス−１−クロロ−３，３，３−トリフルオロプロペンと、炭素原子数が５若しくは６である、直鎖状若しくは分岐状のアルケンとの組合せを含む溶剤組成物を除き、及び、（Ａ）が、１−クロロ−２，３，３，３−テトラフルオロ−１−プロペンのＺ体、１−クロロ−２，３，３，４，４，５，５−ヘプタフルオロ−１−ペンテン、又は１，３−ジクロロ−２，３，３−トリフルオロプロペンである場合を除く。）。 (A) Hydrofluoroolefins which may contain one or more atoms selected from the group consisting of (a1) chlorine atom and bromine atom, (a2) chlorofluoroolefins, and (a3) bromofluoroolefins. One or more solvents selected from the group consisting of
(B) One or more solvents selected from the group consisting of normal octane, isooctane, isononan, methylcyclohexane and ethylcyclohexane.
A solvent composition comprising (C) (c1) hydrofluorocarbons, (c2) hydrofluoroethers and one or more solvents selected from the group consisting of (c3) 1-methoxy-2-propanol.
When the total amount of the composition is 100 parts by weight,
The total content of (A) and (B) is more than 10 parts by weight and less than 100 parts by weight, and the total content of (A), (B) and (C) is 95 parts by weight or more and 100 parts by weight or less. Is, except for solvent compositions containing a combination of 1-chloro-2,3,3-trifluoropropene and a hydrocarbon having a boiling point of 60-100 ° C., cis-1-chloro-. Except for solvent compositions containing a combination of 3,3,3-trifluoropropene and a linear or branched alkene having 5 or 6 carbon atoms, and (A) is 1-chloro. Z-form of -2,3,3,3-tetrafluoro-1-propene, 1-chloro-2,3,3,4,5,5-heptafluoro-1-pentene, or 1,3-dichloro -2,3,3-Except when it is trifluoropropene.)
（Ｂ）ノルマルオクタン、イソオクタン、イソノナン、メチルシクロヘキサン及びエチルシクロヘキサンからなる群より選択される１種以上の溶剤と(B) With one or more solvents selected from the group consisting of normal octane, isooctane, isononan, methylcyclohexane and ethylcyclohexane.
を含む溶剤組成物であって、A solvent composition containing
前記組成物の総量を１００重量部としたときに、When the total amount of the composition is 100 parts by weight,
（Ａ）の含有量が５重量部超９５重量部未満であり、The content of (A) is more than 5 parts by weight and less than 95 parts by weight.
（Ｂ）の含有量が５重量部超９５重量部未満であり、そしてThe content of (B) is more than 5 parts by weight and less than 95 parts by weight, and
（Ａ）及び（Ｂ）の含有量の合計が９０重量部以上１００重量部以下である、溶剤組成物（但し、１−クロロ−２，３，３−トリフルオロプロペンと、沸点が６０〜１００℃の炭化水素との組合せを含む溶剤組成物を除き、シス−１−クロロ−３，３，３−トリフルオロプロペンと、炭素原子数が５若しくは６である、直鎖状若しくは分岐状のアルケンとの組合せを含む溶剤組成物を除き、及び、（Ａ）が、１−クロロ−２，３，３，３−テトラフルオロ−１−プロペンのＺ体、１−クロロ−２，３，３，４，４，５，５−ヘプタフルオロ−１−ペンテン、又は１，３−ジクロロ−２，３，３−トリフルオロプロペンである場合を除く。）。A solvent composition having a total content of (A) and (B) of 90 parts by weight or more and 100 parts by weight or less (however, 1-chloro-2,3,3-trifluoropropene and a boiling point of 60 to 100). With the exception of solvent compositions containing a combination with hydrocarbons at ° C, cis-1-chloro-3,3,3-trifluoropropene and linear or branched alkenes with 5 or 6 carbon atoms. Except for the solvent composition containing the combination with, and (A) is the Z form of 1-chloro-2,3,3,3-tetrafluoro-1-propene, 1-chloro-2,3,3. 4,4,5,5-heptafluoro-1-pentene, or 1,3-dichloro-2,3,3-trifluoropropene).
（Ｂ）ノルマルオクタン、イソオクタン、イソノナン、メチルシクロヘキサン及びエチルシクロヘキサンからなる群より選択される１種以上の溶剤と、(B) One or more solvents selected from the group consisting of normal octane, isooctane, isononan, methylcyclohexane and ethylcyclohexane.
（Ｃ）（ｃ１）ハイドロフルオロカーボン類、（ｃ２）ハイドロフルオロエーテル類及び（ｃ３）１−メトキシ−２−プロパノールからなる群より選択される１種以上の溶剤とを含む溶剤組成物であって、A solvent composition comprising (C) (c1) hydrofluorocarbons, (c2) hydrofluoroethers and one or more solvents selected from the group consisting of (c3) 1-methoxy-2-propanol.
前記組成物の総量を１００重量部としたときに、When the total amount of the composition is 100 parts by weight,
（Ａ）及び（Ｂ）の含有量の合計が１０重量部超１００重量部未満であり、そしてThe total content of (A) and (B) is greater than 10 parts by weight and less than 100 parts by weight, and
（Ａ）、（Ｂ）及び（Ｃ）の含有量の合計が９０重量部以上１００重量部以下である、溶剤組成物（但し、１−クロロ−２，３，３−トリフルオロプロペンと、沸点が６０〜１００℃の炭化水素との組合せを含む溶剤組成物を除き、シス−１−クロロ−３，３，３−トリフルオロプロペンと、炭素原子数が５若しくは６である、直鎖状若しくは分岐状のアルケンとの組合せを含む溶剤組成物を除き、及び、（Ａ）が、１−クロロ−２，３，３，３−テトラフルオロ−１−プロペンのＺ体、１−クロロ−２，３，３，４，４，５，５−ヘプタフルオロ−１−ペンテン、又は１，３−ジクロロ−２，３，３−トリフルオロプロペンである場合を除く。）。A solvent composition having a total content of (A), (B) and (C) of 90 parts by weight or more and 100 parts by weight or less (however, 1-chloro-2,3,3-trifluoropropene and boiling point). Is linear or linear or having 5 or 6 carbon atoms with cis-1-chloro-3,3,3-trifluoropropene, except for solvent compositions containing a combination of hydrocarbons at 60-100 ° C. Except for solvent compositions containing a combination with branched alkenes, and (A) is the Z form of 1-chloro-2,3,3,3-tetrafluoro-1-propene, 1-chloro-2, 3,3,4,5,5-heptafluoro-1-pentene, or 1,3-dichloro-2,3,3-trifluoropropene).
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/JP2020/015333 WO2020204166A1 (en) | 2019-04-04 | 2020-04-03 | Solvent composition and aerosol composition for cleaning containing same |
| JP2021086250A JP6945258B2 (en) | 2019-04-04 | 2021-05-21 | Solvent composition and cleaning aerosol composition containing it |
| JP2021117286A JP6945259B1 (en) | 2019-04-04 | 2021-07-15 | Solvent composition and cleaning aerosol composition containing it |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2019071945 | 2019-04-04 | ||
| JP2019071945 | 2019-04-04 | ||
| JP2019119990 | 2019-06-27 | ||
| JP2019119990 | 2019-06-27 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2021086250A Division JP6945258B2 (en) | 2019-04-04 | 2021-05-21 | Solvent composition and cleaning aerosol composition containing it |
| JP2021117286A Division JP6945259B1 (en) | 2019-04-04 | 2021-07-15 | Solvent composition and cleaning aerosol composition containing it |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2021004353A JP2021004353A (en) | 2021-01-14 |
| JP2021004353A5 true JP2021004353A5 (en) | 2021-02-25 |
Family
ID=74097108
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2020066779A Withdrawn JP2021004353A (en) | 2019-04-04 | 2020-04-02 | Solvent composition and aerosol composition for cleaning containing same |
| JP2021086250A Active JP6945258B2 (en) | 2019-04-04 | 2021-05-21 | Solvent composition and cleaning aerosol composition containing it |
| JP2021117286A Active JP6945259B1 (en) | 2019-04-04 | 2021-07-15 | Solvent composition and cleaning aerosol composition containing it |
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| Application Number | Title | Priority Date | Filing Date |
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| JP2021086250A Active JP6945258B2 (en) | 2019-04-04 | 2021-05-21 | Solvent composition and cleaning aerosol composition containing it |
| JP2021117286A Active JP6945259B1 (en) | 2019-04-04 | 2021-07-15 | Solvent composition and cleaning aerosol composition containing it |
Country Status (1)
| Country | Link |
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| JP (3) | JP2021004353A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2020183495A (en) * | 2019-05-09 | 2020-11-12 | セントラル硝子株式会社 | Solvent composition |
| JP7487673B2 (en) | 2021-01-14 | 2024-05-21 | トヨタ自動車株式会社 | Technology Notification System |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02204466A (en) * | 1989-02-03 | 1990-08-14 | Asahi Glass Co Ltd | Fluorinated hydrocarbon mixed solvent composition |
| JPH07278594A (en) * | 1994-04-05 | 1995-10-24 | Cosmo Petorotetsuku:Kk | Detergent composition |
| JP6813499B2 (en) * | 2015-12-18 | 2021-01-13 | 株式会社トクヤマＭｅｔｅｌ | Cleaning agent composition, rinsing agent composition and cleaning method |
| JP6969385B2 (en) * | 2016-01-15 | 2021-11-24 | Ａｇｃ株式会社 | Solvent composition, draining drying method and flux cleaning method |
| JP6942528B2 (en) * | 2017-03-10 | 2021-09-29 | 株式会社トクヤマＭｅｔｅｌ | Detergent composition, rinse composition and cleaning method |
| WO2019039521A1 (en) * | 2017-08-25 | 2019-02-28 | Ａｇｃ株式会社 | Solvent composition, cleaning method, method for producing coated substrate, and heat transfer medium |
| WO2019123759A1 (en) * | 2017-12-22 | 2019-06-27 | Ａｇｃ株式会社 | Solvent composition, cleaning method, coating forming composition, method for manufacturing coated substrate, aerosol composition, rinsing composition, method for cleaning member, and device for cleaning member |
| JP2020041090A (en) * | 2018-09-12 | 2020-03-19 | Ａｇｃ株式会社 | Solvent composition, cleaning method, composition for coating film formation, and manufacturing method of coating film |
| JP2020183495A (en) * | 2019-05-09 | 2020-11-12 | セントラル硝子株式会社 | Solvent composition |
-
2020
- 2020-04-02 JP JP2020066779A patent/JP2021004353A/en not_active Withdrawn
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2021
- 2021-05-21 JP JP2021086250A patent/JP6945258B2/en active Active
- 2021-07-15 JP JP2021117286A patent/JP6945259B1/en active Active
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