JPH06306392A - Azeotropic or azeotrope-like composition and detergent comprising same - Google Patents
Azeotropic or azeotrope-like composition and detergent comprising sameInfo
- Publication number
- JPH06306392A JPH06306392A JP12054393A JP12054393A JPH06306392A JP H06306392 A JPH06306392 A JP H06306392A JP 12054393 A JP12054393 A JP 12054393A JP 12054393 A JP12054393 A JP 12054393A JP H06306392 A JPH06306392 A JP H06306392A
- Authority
- JP
- Japan
- Prior art keywords
- composition
- azeotropic
- azeotrope
- detergent
- pentanol
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 35
- 239000003599 detergent Substances 0.000 title claims abstract description 7
- JYVLIDXNZAXMDK-UHFFFAOYSA-N pentan-2-ol Chemical compound CCCC(C)O JYVLIDXNZAXMDK-UHFFFAOYSA-N 0.000 claims abstract description 18
- CXQXSVUQTKDNFP-UHFFFAOYSA-N octamethyltrisiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)O[Si](C)(C)C CXQXSVUQTKDNFP-UHFFFAOYSA-N 0.000 claims description 10
- 238000004140 cleaning Methods 0.000 abstract description 8
- 150000001875 compounds Chemical class 0.000 abstract description 2
- 230000000779 depleting effect Effects 0.000 abstract 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 12
- -1 IPA and ethanol Chemical class 0.000 description 9
- 229910052801 chlorine Inorganic materials 0.000 description 8
- 239000000460 chlorine Substances 0.000 description 8
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 7
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 6
- AJDIZQLSFPQPEY-UHFFFAOYSA-N 1,1,2-Trichlorotrifluoroethane Chemical compound FC(F)(Cl)C(F)(Cl)Cl AJDIZQLSFPQPEY-UHFFFAOYSA-N 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- 239000012459 cleaning agent Substances 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- HMMGMWAXVFQUOA-UHFFFAOYSA-N octamethylcyclotetrasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 HMMGMWAXVFQUOA-UHFFFAOYSA-N 0.000 description 5
- 238000004821 distillation Methods 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 238000005238 degreasing Methods 0.000 description 3
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- RKMGAJGJIURJSJ-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidine Chemical compound CC1(C)CCCC(C)(C)N1 RKMGAJGJIURJSJ-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 2
- MKUWVMRNQOOSAT-UHFFFAOYSA-N but-3-en-2-ol Chemical compound CC(O)C=C MKUWVMRNQOOSAT-UHFFFAOYSA-N 0.000 description 2
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 description 2
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 2
- LPIQUOYDBNQMRZ-UHFFFAOYSA-N cyclopentene Chemical compound C1CC=CC1 LPIQUOYDBNQMRZ-UHFFFAOYSA-N 0.000 description 2
- 238000004817 gas chromatography Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N n-propyl alcohol Natural products CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 230000035699 permeability Effects 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- MGSRCZKZVOBKFT-UHFFFAOYSA-N thymol Chemical compound CC(C)C1=CC=C(C)C=C1O MGSRCZKZVOBKFT-UHFFFAOYSA-N 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- PMJHHCWVYXUKFD-SNAWJCMRSA-N (E)-1,3-pentadiene Chemical compound C\C=C\C=C PMJHHCWVYXUKFD-SNAWJCMRSA-N 0.000 description 1
- RBACIKXCRWGCBB-UHFFFAOYSA-N 1,2-Epoxybutane Chemical compound CCC1CO1 RBACIKXCRWGCBB-UHFFFAOYSA-N 0.000 description 1
- QTYUSOHYEPOHLV-FNORWQNLSA-N 1,3-Octadiene Chemical compound CCCC\C=C\C=C QTYUSOHYEPOHLV-FNORWQNLSA-N 0.000 description 1
- HIZVCIIORGCREW-UHFFFAOYSA-N 1,4-dioxene Chemical compound C1COC=CO1 HIZVCIIORGCREW-UHFFFAOYSA-N 0.000 description 1
- BMVXCPBXGZKUPN-UHFFFAOYSA-N 1-hexanamine Chemical compound CCCCCCN BMVXCPBXGZKUPN-UHFFFAOYSA-N 0.000 description 1
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 1
- JSZOAYXJRCEYSX-UHFFFAOYSA-N 1-nitropropane Chemical compound CCC[N+]([O-])=O JSZOAYXJRCEYSX-UHFFFAOYSA-N 0.000 description 1
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 1
- XRUGBBIQLIVCSI-UHFFFAOYSA-N 2,3,4-trimethylphenol Chemical compound CC1=CC=C(O)C(C)=C1C XRUGBBIQLIVCSI-UHFFFAOYSA-N 0.000 description 1
- LOCOMRPWMOCMPV-UHFFFAOYSA-N 2,3-dichloro-1,1,1,2-tetrafluoropropane Chemical group FC(F)(F)C(F)(Cl)CCl LOCOMRPWMOCMPV-UHFFFAOYSA-N 0.000 description 1
- FXNDIJDIPNCZQJ-UHFFFAOYSA-N 2,4,4-trimethylpent-1-ene Chemical compound CC(=C)CC(C)(C)C FXNDIJDIPNCZQJ-UHFFFAOYSA-N 0.000 description 1
- STMDPCBYJCIZOD-UHFFFAOYSA-N 2-(2,4-dinitroanilino)-4-methylpentanoic acid Chemical compound CC(C)CC(C(O)=O)NC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O STMDPCBYJCIZOD-UHFFFAOYSA-N 0.000 description 1
- LKMJVFRMDSNFRT-UHFFFAOYSA-N 2-(methoxymethyl)oxirane Chemical compound COCC1CO1 LKMJVFRMDSNFRT-UHFFFAOYSA-N 0.000 description 1
- MVRPPTGLVPEMPI-UHFFFAOYSA-N 2-cyclohexylphenol Chemical compound OC1=CC=CC=C1C1CCCCC1 MVRPPTGLVPEMPI-UHFFFAOYSA-N 0.000 description 1
- NJBCRXCAPCODGX-UHFFFAOYSA-N 2-methyl-n-(2-methylpropyl)propan-1-amine Chemical compound CC(C)CNCC(C)C NJBCRXCAPCODGX-UHFFFAOYSA-N 0.000 description 1
- CEBKHWWANWSNTI-UHFFFAOYSA-N 2-methylbut-3-yn-2-ol Chemical compound CC(C)(O)C#C CEBKHWWANWSNTI-UHFFFAOYSA-N 0.000 description 1
- NGKNMHFWZMHABQ-UHFFFAOYSA-N 4-chloro-2h-benzotriazole Chemical compound ClC1=CC=CC2=NNN=C12 NGKNMHFWZMHABQ-UHFFFAOYSA-N 0.000 description 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- CTKINSOISVBQLD-UHFFFAOYSA-N Glycidol Chemical compound OCC1CO1 CTKINSOISVBQLD-UHFFFAOYSA-N 0.000 description 1
- BJIOGJUNALELMI-ONEGZZNKSA-N Isoeugenol Natural products COC1=CC(\C=C\C)=CC=C1O BJIOGJUNALELMI-ONEGZZNKSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- FQYUMYWMJTYZTK-UHFFFAOYSA-N Phenyl glycidyl ether Chemical compound C1OC1COC1=CC=CC=C1 FQYUMYWMJTYZTK-UHFFFAOYSA-N 0.000 description 1
- 239000005844 Thymol Substances 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000003463 adsorbent Substances 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- CZBZUDVBLSSABA-UHFFFAOYSA-N butylated hydroxyanisole Chemical compound COC1=CC=C(O)C(C(C)(C)C)=C1.COC1=CC=C(O)C=C1C(C)(C)C CZBZUDVBLSSABA-UHFFFAOYSA-N 0.000 description 1
- BJIOGJUNALELMI-ARJAWSKDSA-N cis-isoeugenol Chemical compound COC1=CC(\C=C/C)=CC=C1O BJIOGJUNALELMI-ARJAWSKDSA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000010730 cutting oil Substances 0.000 description 1
- ZWAJLVLEBYIOTI-UHFFFAOYSA-N cyclohexene oxide Chemical compound C1CCCC2OC21 ZWAJLVLEBYIOTI-UHFFFAOYSA-N 0.000 description 1
- FWFSEYBSWVRWGL-UHFFFAOYSA-N cyclohexene oxide Natural products O=C1CCCC=C1 FWFSEYBSWVRWGL-UHFFFAOYSA-N 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 229940043279 diisopropylamine Drugs 0.000 description 1
- NKDDWNXOKDWJAK-UHFFFAOYSA-N dimethoxymethane Chemical compound COCOC NKDDWNXOKDWJAK-UHFFFAOYSA-N 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- MCPKSFINULVDNX-UHFFFAOYSA-N drometrizole Chemical compound CC1=CC=C(O)C(N2N=C3C=CC=CC3=N2)=C1 MCPKSFINULVDNX-UHFFFAOYSA-N 0.000 description 1
- 150000002118 epoxides Chemical class 0.000 description 1
- 239000004210 ether based solvent Substances 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000005453 ketone based solvent Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 231100001231 less toxic Toxicity 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- QXLPXWSKPNOQLE-UHFFFAOYSA-N methylpentynol Chemical compound CCC(C)(O)C#C QXLPXWSKPNOQLE-UHFFFAOYSA-N 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- MCSAJNNLRCFZED-UHFFFAOYSA-N nitroethane Chemical compound CC[N+]([O-])=O MCSAJNNLRCFZED-UHFFFAOYSA-N 0.000 description 1
- LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical compound C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- DOIRQSBPFJWKBE-UHFFFAOYSA-N phthalic acid di-n-butyl ester Natural products CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000005437 stratosphere Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229960000790 thymol Drugs 0.000 description 1
- BJIOGJUNALELMI-UHFFFAOYSA-N trans-isoeugenol Natural products COC1=CC(C=CC)=CC=C1O BJIOGJUNALELMI-UHFFFAOYSA-N 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 1
- 239000005436 troposphere Substances 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
Landscapes
- Detergent Compositions (AREA)
- Cleaning And De-Greasing Of Metallic Materials By Chemical Methods (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明はフロン、トリクロロエタ
ン等の塩素系脱脂洗浄剤の代替剤として使用できると共
に、アルミニウムや鉄などの金属部品、レンズやプリズ
ム等の光学部品さらには電子部品などに対する精密洗浄
に好適に使用することができる共沸及び共沸様組成物
と、その洗浄剤に関する。INDUSTRIAL APPLICABILITY The present invention can be used as a substitute for chlorine-based degreasing detergents such as CFCs and trichloroethane, and can be used as precision parts for metal parts such as aluminum and iron, optical parts such as lenses and prisms and electronic parts. The present invention relates to an azeotropic and azeotrope-like composition that can be suitably used for cleaning, and a cleaning agent therefor.
【0002】[0002]
【従来の技術】光学部品、電子部品等の部品の洗浄用溶
剤としては、従来より1,1,2−トリクロロ−1,
2,2−トリフルオロエタン(フロン113)やトリク
ロロエタンが使用されている。これはフロン113が不
燃性である;生体に対する毒性が低い;プラスチック,
ゴムなどの高分子材料を侵食しないが、油脂等を溶解す
るという選択的溶解性を有する;乾燥速度が早い;等の
優れた特性を有しており、トリクロロエタンも優れた脱
脂洗浄力を有し、不燃性であるためである。2. Description of the Related Art As a solvent for cleaning optical parts, electronic parts and the like, 1,1,2-trichloro-1,
2,2-trifluoroethane (Freon 113) and trichloroethane are used. This is because Freon 113 is nonflammable; has low toxicity to living organisms; plastic,
It does not corrode polymer materials such as rubber, but has selective solubility that it dissolves fats and oils; it has a fast drying rate; and so on. Trichloroethane also has excellent degreasing and detergency. , Because it is nonflammable.
【0003】一方、これらの塩素系溶剤の使用量削減お
よび不燃化、脱脂力の向上のため、種々の混合物や共沸
組成物が開発されている。例えば、特開平1−3180
94号公報には洗浄溶剤としてフロン113とイソプロ
ピルアルコール,メチルエチルケトンとの混合物が記載
されている。また、特開平2−289693号公報には
ジクロロテトラフルオロプロパン(フロン234)とエ
タノール等の脂肪族低級アルコールとの共沸組成物が開
示されている。さらには、IPA,エタノール等の脂肪
族低級アルコール,アセトン等のケトン単体,エーテル
系も検討されている。On the other hand, various mixtures and azeotropic compositions have been developed in order to reduce the use amount of these chlorine-based solvents, to make them incombustible, and to improve the degreasing power. For example, Japanese Patent Laid-Open No. 1-3180
JP-A-94 discloses a mixture of Freon 113, isopropyl alcohol, and methyl ethyl ketone as a cleaning solvent. Further, JP-A-2-289693 discloses an azeotropic composition of dichlorotetrafluoropropane (CFC 234) and an aliphatic lower alcohol such as ethanol. Furthermore, aliphatic lower alcohols such as IPA and ethanol, simple ketones such as acetone, and ethers are also being studied.
【0004】[0004]
【発明が解決しようとする課題】ところが、フロン11
3やトリクロロエタン等の塩素系溶剤は化学的に特に安
定であるため対流圏内での寿命が長く、拡散して成層圏
に達し、ここで太陽光線により分解して発生する塩素ラ
ジカルがオゾンと連鎖反応を起こし、オゾン層を破壊す
ることから、これらの使用の削減が求められている。こ
のため既述のように、フロン113等の塩素系溶剤と、
塩素系溶剤以外の有機溶剤との共沸組成物を開発するこ
とにより、その使用量の削減を図っているが、塩素系溶
剤を必須とするため、その使用量をある程度以上減らす
ことができない問題がある。また、フロン113に比
べ、オゾン層の破壊性が比較的小さいフロン234との
共沸組成物の開発されているがオゾン層の破壊を完全に
無くすことはできない。一方、脂肪族低級アルコール
は、乾燥性に問題があり、ケトン系、エーテル系の溶剤
はプラスチック等の被洗浄物を劣化させるため、実用性
に乏しいものとなっている。However, the CFC 11
Chlorine-based solvents such as 3 and trichloroethane are chemically particularly stable, so they have a long life in the troposphere and diffuse to reach the stratosphere where the chlorine radicals decomposed by sunlight cause a chain reaction with ozone. There is a need to reduce their use, as they wake up and destroy the ozone layer. Therefore, as described above, a chlorine-based solvent such as Freon 113,
We are trying to reduce the amount used by developing an azeotropic composition with organic solvents other than chlorine-based solvents, but since chlorine-based solvents are essential, it is not possible to reduce the amount used to a certain extent. There is. Further, although an azeotropic composition with Freon 234, which has a relatively low ozone depletion property as compared with Freon 113, has been developed, it is impossible to completely eliminate the destruction of the ozone layer. On the other hand, an aliphatic lower alcohol has a problem in drying property, and a ketone-based or ether-based solvent deteriorates an object to be cleaned such as a plastic, so that it is not practical.
【0005】本発明は、これらの問題点を考慮してなさ
れたものであり、オゾン層の破壊がなく、しかも優れた
洗浄性および乾燥性を有した共沸及び共沸様組成物と、
その洗浄剤を提供することを目的とする。The present invention has been made in consideration of these problems, and is an azeotropic and azeotrope-like composition which does not destroy the ozone layer and has excellent cleaning and drying properties.
The purpose is to provide the cleaning agent.
【0006】[0006]
【課題を解決するための手段および作用】本発明の共沸
及び共沸様組成物は、化1で示す構造を有したオクタメ
チルトリシロキサンと、2−プロパノールとから構成さ
れる。Means and Actions for Solving the Problems The azeotropic and azeotrope-like composition of the present invention comprises octamethyltrisiloxane having the structure shown in Chemical formula 1 and 2-propanol.
【0007】[0007]
【化1】 [Chemical 1]
【0008】オクタメチルトリシロキサンの粘度は、2
5℃において1CStであり、2−プロパノールのオク
タメチルトリシロキサンに対する組成比は78重量%で
ある。この共沸及び共沸様組成物及びこの共沸及び共沸
様組成物を有効成分として含有する本発明の洗浄剤は、
安定剤を適宜混合することができる。The viscosity of octamethyltrisiloxane is 2
It was 1 CSt at 5 ° C., and the composition ratio of 2-propanol to octamethyltrisiloxane was 78% by weight. The azeotropic and azeotrope-like composition and the cleaning agent of the present invention containing the azeotropic and azeotrope-like composition as an active ingredient,
Stabilizers can be mixed as appropriate.
【0009】安定剤としては、ニトロメタン、ニトロエ
タン、ニトロプロパンなどの脂肪族ニトロ合物、3−メ
チル−1−ブチン−3−オール、3−メチル−1−ペン
チン−3−オールなどのアセチルアルコール類、グリシ
ドール、メチルグリシジルエーテル、アリルグリシジル
エテール、フェニルグリシジルエーテル、1,2−ブチ
レンオキシド、シクロヘキセンオキシド、エピクロルヒ
ドリンなどのエポキシド類、ジメトキシメタン、1−2
ジメトキシエタン、1,4−ジオキセン、1,3,5−
トリオキセンなどのエーテル類、ヘキセン、ヘプタン、
オクテン、2,4,4−トリメチル−1−ペンテン、ペ
ンタジエン、オクタジエン、シクロヘキセン、シクロペ
ンテンなどの不飽和炭化水素類、アリルアルコール、1
−ブテン−3−オール、3−メチル−1−ブーテン−3
−オールなどのオレフィン系アルコール、アクリル酸メ
チル、アクリル酸エチル、アクリル酸ブチルなどのアク
リル酸エステル類をそれぞれ単独であるいは2種以上併
用して用いることができる。また、これらの化合物とフ
ェノール、トリメチルフェノール、シクロヘキシルフェ
ノール、チモール、2,6−ジ−t−ブチル−4−メチ
ルフェノール、ブチルヒドロキシアニソール、イソオイ
ゲノールなどのフェノール類や、ヘキシルアミン、ベン
チルアミン、ジプロピルアミン、ジイソプロピルアミ
ン、ジイソブチルアミン、トリエチルアミン、トリブチ
ルアミン、ピリジン、n−メチルモルマリン、シクロヘ
キシルアミン、2,2,6,6−テトラメチルピペリジ
ン、N,N′(−ジアリル−p−フェニレンジアミンな
どのアミン類、ベンゾトリアゾール、2−(2′−ヒド
ロキシ−5′−メチルフェニル)ベンゾトリアゾール、
クロロベンゾトリアゾールなどのトリアゾール類などと
併用して用いることもできる。これらの安定剤が備える
性質としては、本発明の組成物を安定化する効果の大き
いことが必要であるのは勿論であるが、蒸留操作により
同伴留出されるものや共沸を形成するものが望ましい。As stabilizers, aliphatic nitro compounds such as nitromethane, nitroethane and nitropropane, and acetyl alcohols such as 3-methyl-1-butyn-3-ol and 3-methyl-1-pentyn-3-ol. , Epoxides such as glycidol, methyl glycidyl ether, allyl glycidyl ether, phenyl glycidyl ether, 1,2-butylene oxide, cyclohexene oxide, epichlorohydrin, dimethoxymethane, 1-2
Dimethoxyethane, 1,4-dioxene, 1,3,5-
Ethers such as trioxene, hexene, heptane,
Unsaturated hydrocarbons such as octene, 2,4,4-trimethyl-1-pentene, pentadiene, octadiene, cyclohexene, cyclopentene, allyl alcohol, 1
-Buten-3-ol, 3-methyl-1-butene-3
-Olefin and other olefinic alcohols, and acrylic acid esters such as methyl acrylate, ethyl acrylate and butyl acrylate may be used alone or in combination of two or more. Further, these compounds and phenols such as phenol, trimethylphenol, cyclohexylphenol, thymol, 2,6-di-t-butyl-4-methylphenol, butylhydroxyanisole, and isoeugenol, hexylamine, ventilamine, and diamine. Propylamine, diisopropylamine, diisobutylamine, triethylamine, tributylamine, pyridine, n-methylmolmarin, cyclohexylamine, 2,2,6,6-tetramethylpiperidine, N, N '(-diallyl-p-phenylenediamine, etc.) Amines, benzotriazole, 2- (2'-hydroxy-5'-methylphenyl) benzotriazole,
It can also be used in combination with triazoles such as chlorobenzotriazole. As a property of these stabilizers, it is needless to say that they have a large effect of stabilizing the composition of the present invention, but those which are entrained by the distillation operation or those which form an azeotrope. Is desirable.
【0010】本発明の組成物において、2−ペンタノー
ル単体では極性が強く、洗浄剤と優れているが、表面張
力が23.5dyn/cm(25℃)と大きく、良好な
浸透性が得られない。一方、オクタメチルトリシロキサ
ンは表面張力が16.9dyn/cm(25℃)と小さ
く浸透性が優れている。しかし、KB価(カウリブタノ
ール価)が15と小さく洗浄力が弱い。そこで、2−ペ
ンタノールとオクタメチルトリシロキサンとを混合する
ことにより両者の長所を引き出すものである。In the composition of the present invention, 2-pentanol alone has a strong polarity and is excellent as a detergent, but has a large surface tension of 23.5 dyn / cm (25 ° C.) and a good permeability can be obtained. Absent. On the other hand, octamethyltrisiloxane has a small surface tension of 16.9 dyn / cm (25 ° C.) and is excellent in permeability. However, the KB value (kauributanol value) is as small as 15 and the detergency is weak. Therefore, by mixing 2-pentanol and octamethyltrisiloxane, the advantages of both are brought out.
【0011】一方、洗浄剤として使用するためには、使
用時の液管理が容易で、かつ容易に回収,再使用できる
ことが重要な要件である。こうした要件を満たす混合溶
剤は単に2成分以上を混合しただけでは得られず、共沸
点を有する状態、すなわち共沸状態の組成にする必要が
ある。共沸状態の組成物は個々の成分の沸点と異なる一
定の沸点を示し(この場合、個々の成分の沸点より低い
ことが望まれる)、揮発速度が向上すると共に、蒸発の
結果として組成物または留出物の割合がほとんど変化し
ない等優れた特性を有するためである。760mmHg
おいて、オクタメチルトリシロキサン21〜23重量
%、2−ペンタノール79〜77重量%の組成比におい
て共沸となり、上記特性を得るためにはこの組成比に近
いものが望まれる。被洗浄対象物については、本発明の
組成物による基材へのアタック等がなく、実用レベルで
あれば特に限定されるものではない。構成物であるオク
タメチルトリシロン,2−ペンタノールは生体への毒性
が少なく、化学的にも安定であり、また、塩素等のハロ
ゲンを含んでいないためオゾン層への影響もない。On the other hand, in order to use it as a cleaning agent, it is an important requirement that the liquid be easily controlled during use and that it be easily recovered and reused. A mixed solvent satisfying these requirements cannot be obtained simply by mixing two or more components, and it is necessary to have a composition having an azeotropic point, that is, an azeotropic state. The azeotropic composition exhibits a constant boiling point that is different from the boiling points of the individual components (in this case, it is desirable that it is lower than the boiling points of the individual components), and the volatilization rate is improved, and the composition or This is because it has excellent characteristics such that the ratio of distillate hardly changes. 760 mmHg
In the composition ratio of 21 to 23% by weight of octamethyltrisiloxane and 79 to 77% by weight of 2-pentanol, azeotropy occurs, and in order to obtain the above characteristics, a composition close to this composition ratio is desired. The object to be cleaned is not particularly limited as long as it does not attack the substrate by the composition of the present invention and is at a practical level. The constituents, octamethyltrisilone and 2-pentanol, are less toxic to living organisms, are chemically stable, and have no effect on the ozone layer because they do not contain halogen such as chlorine.
【0012】[0012]
【実施例1】市販されているオクタメチルシクロテトラ
シロキサンの純度はガスクロマトグラフィーで分析した
結果、98.0%レベルであり、不純物としてオクタメ
チルシクロテトラシロキサンより低分子のシロキサンあ
るいはシラン化合物また、オクタメチルシクロテトラシ
ロキサンより揮発しにくい炭化水素系化合物、シロキサ
ン等も含まれている。この内オクタメチルシクロテトラ
シロキサンよりも揮発しにくい不純物は被洗浄物上に残
渣となる可能性がある。このため、オクタメチルシクロ
テトラキサンより揮発しにくい成分を蒸留、精留、吸着
剤を用いて除去した。この不純物除去後の、オクタメチ
ルシクロテトラシロキサンと2−プロパノールのそれぞ
れ100gの混合物200gを蒸留フラスコにいれ、理
論段数30段の精留塔を用いて常圧下で蒸留を行った。
その結果、115〜110℃において共沸留分をえ、そ
の留分をガスクロマトグラフィーにより分析したとこ
ろ、組成はオクタメチルトリシロキサンが21〜23重
量%で、2−ペンタノールが79〜77重量%であっ
た。表1はオクタメチルトリシロキサン、2−ペンタノ
ールおよび本実施例の共沸組成物の表面張力(25
℃)、KB価を示す。Example 1 The purity of octamethylcyclotetrasiloxane on the market was 98.0% as a result of analysis by gas chromatography, and a siloxane or silane compound having a lower molecular weight than octamethylcyclotetrasiloxane as an impurity, It also contains hydrocarbon compounds, siloxanes, etc. that are less volatile than octamethylcyclotetrasiloxane. Of these, impurities that are less likely to volatilize than octamethylcyclotetrasiloxane may be residues on the object to be cleaned. Therefore, components that are less volatile than octamethylcyclotetraxane were removed by distillation, rectification, and an adsorbent. After removing the impurities, 200 g of a mixture of 100 g each of octamethylcyclotetrasiloxane and 2-propanol was placed in a distillation flask, and distillation was carried out under normal pressure using a rectification column having 30 theoretical plates.
As a result, an azeotropic fraction was obtained at 115 to 110 ° C., and the fraction was analyzed by gas chromatography to find that the composition was 21 to 23 wt% octamethyltrisiloxane and 79 to 77 wt% 2-pentanol. %Met. Table 1 shows the surface tension of octamethyltrisiloxane, 2-pentanol and the azeotropic composition of this Example (25
° C) and KB value are shown.
【0013】[0013]
【表1】 [Table 1]
【0014】[0014]
【実施例2】この実施例では洗浄に適用した場合を説明
する。硝子レンズ、アルミニウムを被洗浄物とし、汚れ
として硝子レンズには芯取り油,アルミニウムには切削
油を塗布し以下の手順により洗浄した。実施例1で得ら
れた組成物を第1槽にいれ超音波を加えながら洗浄物を
脱脂した後、第2槽にも実施例1で得られた組成物をい
れ、超音波を加えながら再度脱脂した。更に、第3槽に
実施例1で得られた組成物をいれ、超音波を加えた後、
冷風ブローを行い乾燥した。この洗浄後の仕上がり状態
を観察するため汚れ塗布前と洗浄後の接触角を測定し
た。比較例としてトリクロロエタンを実施例1の組成物
のかわりに用いて同様に洗浄・乾燥を行い、その洗浄物
との比較も行った。結果を表2に示す。表2より、実施
例1の組成物を用いた洗浄はトリクロロエタン洗浄より
良好な結果が得られた。Second Embodiment In this embodiment, a case of applying to cleaning will be described. A glass lens and aluminum were used as objects to be cleaned, and as stains, a glass lens was coated with centering oil and aluminum was coated with cutting oil, and cleaned by the following procedure. The composition obtained in Example 1 was put in the first tank to degrease the washed product while applying ultrasonic waves, and then the composition obtained in Example 1 was also put in the second tank and again added with ultrasonic waves. Degreased. Furthermore, after putting the composition obtained in Example 1 in a third tank and applying ultrasonic waves,
It was blown with cold air and dried. In order to observe the finished state after this washing, the contact angle before and after the stain application was measured. As a comparative example, trichloroethane was used instead of the composition of Example 1 and washing and drying were carried out in the same manner, and comparison with the washed product was also made. The results are shown in Table 2. From Table 2, the cleaning using the composition of Example 1 gave better results than the trichloroethane cleaning.
【0015】[0015]
【表2】 [Table 2]
【0016】[0016]
【発明の効果】本発明の共沸及び共沸様組成物は、オゾ
ン層を破壊することなく、洗浄力が優れ、蒸発による組
成変化がなく、乾燥速度が優れており、これらの組成液
は洗浄剤として使用した場合に優れた効果を発揮するも
のである。The azeotropic and azeotrope-like compositions of the present invention have excellent detergency without destroying the ozone layer, have no composition change due to evaporation, and have an excellent drying rate. It exhibits an excellent effect when used as a cleaning agent.
Claims (2)
ロキサンとからなることを特徴とする共沸及び共沸様組
成物。1. An azeotropic and azeotrope-like composition comprising 2-pentanol and octamethyltrisiloxane.
ロキサンとからなる共沸及び共沸様組成物を有機成分と
して含有することを特徴とする洗浄剤。2. A detergent comprising an azeotropic and azeotrope-like composition comprising 2-pentanol and octamethyltrisiloxane as an organic component.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12054393A JPH06306392A (en) | 1993-04-23 | 1993-04-23 | Azeotropic or azeotrope-like composition and detergent comprising same |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12054393A JPH06306392A (en) | 1993-04-23 | 1993-04-23 | Azeotropic or azeotrope-like composition and detergent comprising same |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH06306392A true JPH06306392A (en) | 1994-11-01 |
Family
ID=14788905
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP12054393A Withdrawn JPH06306392A (en) | 1993-04-23 | 1993-04-23 | Azeotropic or azeotrope-like composition and detergent comprising same |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH06306392A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5454970A (en) * | 1994-08-11 | 1995-10-03 | Dow Corning Corporation | Octamethyltrisiloxane containing azeotropes |
| US5456856A (en) * | 1995-01-18 | 1995-10-10 | Dow Corning Corporation | Azeotrope and azeotrope-like compositions of octamethyltrisiloxane |
| US5478493A (en) * | 1994-06-15 | 1995-12-26 | Dow Corning Corporation | Hexamethyldisiloxane containing azeotropes |
| US5492647A (en) * | 1995-05-08 | 1996-02-20 | Dow Corning Corporation | Octamethylcyclotetrasiloxane azeotropes |
| US5501811A (en) * | 1995-04-24 | 1996-03-26 | Dow Corning Corporation | Azeotropes of octamethyltrisiloxane and aliphatic or alicyclic alcohols |
-
1993
- 1993-04-23 JP JP12054393A patent/JPH06306392A/en not_active Withdrawn
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5478493A (en) * | 1994-06-15 | 1995-12-26 | Dow Corning Corporation | Hexamethyldisiloxane containing azeotropes |
| US5454970A (en) * | 1994-08-11 | 1995-10-03 | Dow Corning Corporation | Octamethyltrisiloxane containing azeotropes |
| EP0696637A3 (en) * | 1994-08-11 | 1996-06-26 | Dow Corning | Octamethyltrisiloxane containing azeotropes |
| US5456856A (en) * | 1995-01-18 | 1995-10-10 | Dow Corning Corporation | Azeotrope and azeotrope-like compositions of octamethyltrisiloxane |
| US5501811A (en) * | 1995-04-24 | 1996-03-26 | Dow Corning Corporation | Azeotropes of octamethyltrisiloxane and aliphatic or alicyclic alcohols |
| US5507878A (en) * | 1995-04-24 | 1996-04-16 | Dow Corning Corporation | Azeotropes of octamethyltrisiloxane and aliphatic or alicyclic alcohols |
| EP0739998A3 (en) * | 1995-04-24 | 1997-03-05 | Dow Corning | Azeotropes of octamethyltrisiloxane and aliphatic or alicyclic alcohols |
| US5492647A (en) * | 1995-05-08 | 1996-02-20 | Dow Corning Corporation | Octamethylcyclotetrasiloxane azeotropes |
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