JP2000302752A5 - - Google Patents
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- Publication number
- JP2000302752A5 JP2000302752A5 JP1999115744A JP11574499A JP2000302752A5 JP 2000302752 A5 JP2000302752 A5 JP 2000302752A5 JP 1999115744 A JP1999115744 A JP 1999115744A JP 11574499 A JP11574499 A JP 11574499A JP 2000302752 A5 JP2000302752 A5 JP 2000302752A5
- Authority
- JP
- Japan
- Prior art keywords
- oxidation reaction
- hydroperoxides
- oxidation
- hydroperoxide
- hydrocarbon
- 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.)
- Pending
Links
- 238000007254 oxidation reaction Methods 0.000 description 12
- 238000000034 method Methods 0.000 description 8
- 229930195733 hydrocarbon Natural products 0.000 description 7
- 150000002432 hydroperoxides Chemical class 0.000 description 6
- 239000004215 Carbon black (E152) Substances 0.000 description 4
- -1 arylalkyl hydrocarbon Chemical class 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- 150000002430 hydrocarbons Chemical class 0.000 description 4
- 230000003647 oxidation Effects 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 230000001590 oxidative effect Effects 0.000 description 3
- FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 2
- IAUKWGFWINVWKS-UHFFFAOYSA-N 1,2-di(propan-2-yl)naphthalene Chemical compound C1=CC=CC2=C(C(C)C)C(C(C)C)=CC=C21 IAUKWGFWINVWKS-UHFFFAOYSA-N 0.000 description 1
- VUMCUSHVMYIRMB-UHFFFAOYSA-N 1,3,5-tri(propan-2-yl)benzene Chemical compound CC(C)C1=CC(C(C)C)=CC(C(C)C)=C1 VUMCUSHVMYIRMB-UHFFFAOYSA-N 0.000 description 1
- UNEATYXSUBPPKP-UHFFFAOYSA-N 1,3-Diisopropylbenzene Chemical compound CC(C)C1=CC=CC(C(C)C)=C1 UNEATYXSUBPPKP-UHFFFAOYSA-N 0.000 description 1
- SPPWGCYEYAMHDT-UHFFFAOYSA-N 1,4-di(propan-2-yl)benzene Chemical compound CC(C)C1=CC=C(C(C)C)C=C1 SPPWGCYEYAMHDT-UHFFFAOYSA-N 0.000 description 1
- AMBHHSBRXZAGDZ-UHFFFAOYSA-N 1-phenyl-2,3-di(propan-2-yl)benzene Chemical group CC(C)C1=CC=CC(C=2C=CC=CC=2)=C1C(C)C AMBHHSBRXZAGDZ-UHFFFAOYSA-N 0.000 description 1
- HKTCLPBBJDIBGF-UHFFFAOYSA-N 1-phenyl-2-propan-2-ylbenzene Chemical group CC(C)C1=CC=CC=C1C1=CC=CC=C1 HKTCLPBBJDIBGF-UHFFFAOYSA-N 0.000 description 1
- PMPBFICDXLLSRM-UHFFFAOYSA-N 1-propan-2-ylnaphthalene Chemical compound C1=CC=C2C(C(C)C)=CC=CC2=C1 PMPBFICDXLLSRM-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 229930007927 cymene Natural products 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- HFPZCAJZSCWRBC-UHFFFAOYSA-N p-cymene Chemical compound CC(C)C1=CC=C(C)C=C1 HFPZCAJZSCWRBC-UHFFFAOYSA-N 0.000 description 1
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11574499A JP2000302752A (ja) | 1999-04-23 | 1999-04-23 | ヒドロペルオキシド類の製造方法 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11574499A JP2000302752A (ja) | 1999-04-23 | 1999-04-23 | ヒドロペルオキシド類の製造方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2000302752A JP2000302752A (ja) | 2000-10-31 |
JP2000302752A5 true JP2000302752A5 (enrdf_load_stackoverflow) | 2006-02-09 |
Family
ID=14669992
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11574499A Pending JP2000302752A (ja) | 1999-04-23 | 1999-04-23 | ヒドロペルオキシド類の製造方法 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2000302752A (enrdf_load_stackoverflow) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4770200B2 (ja) * | 2004-03-04 | 2011-09-14 | 三菱化学株式会社 | クメンハイドロパーオキサイドの製造方法 |
CN101384548A (zh) * | 2006-02-16 | 2009-03-11 | 住友化学株式会社 | 二烷基氢过氧基苯的制造方法 |
JP5076529B2 (ja) * | 2006-02-16 | 2012-11-21 | 住友化学株式会社 | ジアルキルハイドロパーオキシベンゼンの製造方法 |
WO2010069586A1 (en) | 2008-12-17 | 2010-06-24 | Borealis Ag | Improving cumene oxidation |
US8952202B2 (en) * | 2008-12-17 | 2015-02-10 | Borealis Ag | Multistage cumene oxidation |
EP2657192B1 (en) | 2012-04-26 | 2019-03-20 | Borealis AG | Reducing organic impurities in waste water |
RU2740017C1 (ru) * | 2020-03-03 | 2020-12-30 | Общество с ограниченной ответственностью "Научно-производственное объединение ЕВРОХИМ" | Способ получения гидроперекиси кумола |
-
1999
- 1999-04-23 JP JP11574499A patent/JP2000302752A/ja active Pending
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