JP2017525663A5 - - Google Patents
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- JP2017525663A5 JP2017525663A5 JP2016573956A JP2016573956A JP2017525663A5 JP 2017525663 A5 JP2017525663 A5 JP 2017525663A5 JP 2016573956 A JP2016573956 A JP 2016573956A JP 2016573956 A JP2016573956 A JP 2016573956A JP 2017525663 A5 JP2017525663 A5 JP 2017525663A5
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- Prior art keywords
- reagent
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- 238000000034 method Methods 0.000 claims description 86
- 239000003153 chemical reaction reagent Substances 0.000 claims description 63
- 239000007788 liquid Substances 0.000 claims description 43
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 claims description 10
- 239000012159 carrier gas Substances 0.000 claims description 10
- 239000000047 product Substances 0.000 claims description 9
- 235000019387 fatty acid methyl ester Nutrition 0.000 claims description 6
- 239000007789 gas Substances 0.000 claims description 6
- 239000012528 membrane Substances 0.000 claims description 6
- 230000003647 oxidation Effects 0.000 claims description 6
- 238000007254 oxidation reaction Methods 0.000 claims description 6
- 238000005949 ozonolysis reaction Methods 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 3
- 229930003658 monoterpene Natural products 0.000 claims description 3
- 150000002773 monoterpene derivatives Chemical class 0.000 claims description 3
- 235000002577 monoterpenes Nutrition 0.000 claims description 3
- 150000003505 terpenes Chemical class 0.000 claims description 3
- 235000007586 terpenes Nutrition 0.000 claims description 3
- 239000007795 chemical reaction product Substances 0.000 claims description 2
- 239000002826 coolant Substances 0.000 claims description 2
- 238000001816 cooling Methods 0.000 claims description 2
- 239000011552 falling film Substances 0.000 claims description 2
- 239000010408 film Substances 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims description 2
- 150000003512 tertiary amines Chemical class 0.000 claims description 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 239000000839 emulsion Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- MOQGCGNUWBPGTQ-UHFFFAOYSA-N 2,6,6-trimethyl-1-cyclohexene-1-carboxaldehyde Chemical group CC1=C(C=O)C(C)(C)CCC1 MOQGCGNUWBPGTQ-UHFFFAOYSA-N 0.000 description 2
- 241000220317 Rosa Species 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 229930004069 diterpene Natural products 0.000 description 2
- 150000004141 diterpene derivatives Chemical class 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 2
- -1 methoxy citronellene Chemical compound 0.000 description 2
- GYHFUZHODSMOHU-UHFFFAOYSA-N nonanal Chemical compound CCCCCCCCC=O GYHFUZHODSMOHU-UHFFFAOYSA-N 0.000 description 2
- 239000002351 wastewater Substances 0.000 description 2
- ATVJXMYDOSMEPO-UHFFFAOYSA-N 3-prop-2-enoxyprop-1-ene Chemical compound C=CCOCC=C ATVJXMYDOSMEPO-UHFFFAOYSA-N 0.000 description 1
- BTXXTMOWISPQSJ-UHFFFAOYSA-N 4,4,4-trifluorobutan-2-one Chemical group CC(=O)CC(F)(F)F BTXXTMOWISPQSJ-UHFFFAOYSA-N 0.000 description 1
- BQACOLQNOUYJCE-FYZZASKESA-N Abietic acid Natural products CC(C)C1=CC2=CC[C@]3(C)[C@](C)(CCC[C@@]3(C)C(=O)O)[C@H]2CC1 BQACOLQNOUYJCE-FYZZASKESA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- 125000000815 N-oxide group Chemical class 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 229930002839 ionone Natural products 0.000 description 1
- 150000002499 ionone derivatives Chemical group 0.000 description 1
- 235000001510 limonene Nutrition 0.000 description 1
- 229940087305 limonene Drugs 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229930004725 sesquiterpene Natural products 0.000 description 1
- 150000004354 sesquiterpene derivatives Chemical class 0.000 description 1
- 241000894007 species Species 0.000 description 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201462015311P | 2014-06-20 | 2014-06-20 | |
| US62/015,311 | 2014-06-20 | ||
| US201562163022P | 2015-05-18 | 2015-05-18 | |
| US62/163,022 | 2015-05-18 | ||
| PCT/US2015/036589 WO2015196019A1 (en) | 2014-06-20 | 2015-06-19 | Film ozonolysis in a tubular or multitubular reactor |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2020022255A Division JP7104083B2 (ja) | 2014-06-20 | 2020-02-13 | 管式又は多管式反応器における膜オゾン分解 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2017525663A JP2017525663A (ja) | 2017-09-07 |
| JP2017525663A5 true JP2017525663A5 (https=) | 2018-07-05 |
| JP6687547B2 JP6687547B2 (ja) | 2020-04-22 |
Family
ID=54936124
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016573956A Active JP6687547B2 (ja) | 2014-06-20 | 2015-06-19 | 管式又は多管式反応器における膜オゾン分解 |
| JP2020022255A Active JP7104083B2 (ja) | 2014-06-20 | 2020-02-13 | 管式又は多管式反応器における膜オゾン分解 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2020022255A Active JP7104083B2 (ja) | 2014-06-20 | 2020-02-13 | 管式又は多管式反応器における膜オゾン分解 |
Country Status (4)
| Country | Link |
|---|---|
| US (3) | US10071944B2 (https=) |
| EP (1) | EP3157898B1 (https=) |
| JP (2) | JP6687547B2 (https=) |
| WO (1) | WO2015196019A1 (https=) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2991337B1 (ja) | 1998-09-28 | 1999-12-20 | 鹿島建設株式会社 | 未利用熱源氷蓄熱ヒートポンプ装置 |
| US6902921B2 (en) | 2001-10-30 | 2005-06-07 | 454 Corporation | Sulfurylase-luciferase fusion proteins and thermostable sulfurylase |
| WO2015106293A1 (en) | 2014-01-13 | 2015-07-16 | P2 Science, Inc. | Terpene-derived acids and esters and methods for preparing and using same |
| US10071944B2 (en) | 2014-06-20 | 2018-09-11 | P2 Science, Inc. | Film ozonolysis in a tubular or multitubular reactor |
| CN105903424B (zh) * | 2016-05-16 | 2017-10-31 | 浙江大学 | 一种多层落管式降膜脱挥反应器 |
| JP7028457B2 (ja) * | 2016-06-21 | 2022-03-02 | ピー２・サイエンス・インコーポレイテッド | 過酸化物混合物の連続クエンチのためのフロースルー反応器およびそれを含む方法 |
| EP3512631B1 (en) | 2016-09-16 | 2022-03-23 | P2 Science, Inc. | Uses of vanadium to oxidize aldehydes and ozonides |
| EP3866968A4 (en) | 2018-10-19 | 2022-07-27 | P2 Science, Inc. | NEW METHODS FOR THE DISPROPORTIONATION DETERRENCE OF OZONIDES |
| IT202000032612A1 (it) * | 2020-12-29 | 2022-06-29 | Desmet Ballestra S P A | Reattore a film per reazioni gas-liquido, in particolare di solfatazione-solfonazione |
| FR3123356B1 (fr) | 2021-05-28 | 2023-04-28 | Melchior Material & Life Science France | Nouveau procédé de fabrication de phéromone en continu |
| US20240376038A1 (en) * | 2021-09-17 | 2024-11-14 | P2 Science, Inc. | Fragrance and flavor compositions comprising hydroxymelonal formate ester |
| CN114163293A (zh) * | 2021-11-09 | 2022-03-11 | 浙江诺亚氟化工有限公司 | 一种2h-全氟(2-甲基戊烷)的制备方法 |
| WO2024112938A1 (en) | 2022-11-22 | 2024-05-30 | P2 Science, Inc. | New method for the ozonolytic synthesis of high melting dicarboxylic acids and oxo-acids |
| EP4662194A1 (en) | 2023-02-06 | 2025-12-17 | P2 Science, Inc. | New method for ozonolysis and reductive quenching of ozonides |
| KR102755748B1 (ko) * | 2023-10-18 | 2025-01-21 | 한국지질자원연구원 | 토양시료 입도 선별을 위한 일체형 시브 장치 |
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| US4296258A (en) | 1979-01-26 | 1981-10-20 | Firmenich Sa | Process for the preparation of macrocyclic ketones |
| IT1166068B (it) | 1979-02-23 | 1987-04-29 | Ballestra Chim | Procedimento perfezionato per la solfonazione a film in un reattore multitubolare a reattore multitubolare atto a realizare detto procedimento |
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| DE3722566A1 (de) * | 1987-07-08 | 1989-01-19 | Henkel Kgaa | Verfahren zur kontinuierlichen ozonisierung von ungesaettigten organischen verbindungen |
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| PT972762E (pt) | 1993-07-09 | 2004-02-27 | Theramex | Novos analogos estruturais da vitamina d |
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| US10071944B2 (en) | 2014-06-20 | 2018-09-11 | P2 Science, Inc. | Film ozonolysis in a tubular or multitubular reactor |
| WO2016022803A2 (en) | 2014-08-06 | 2016-02-11 | P2 Science, Inc. | Fragrances from the esters of fatty acids |
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| JP7028457B2 (ja) | 2016-06-21 | 2022-03-02 | ピー２・サイエンス・インコーポレイテッド | 過酸化物混合物の連続クエンチのためのフロースルー反応器およびそれを含む方法 |
| EP3512631B1 (en) | 2016-09-16 | 2022-03-23 | P2 Science, Inc. | Uses of vanadium to oxidize aldehydes and ozonides |
-
2015
- 2015-06-19 US US15/320,250 patent/US10071944B2/en active Active
- 2015-06-19 JP JP2016573956A patent/JP6687547B2/ja active Active
- 2015-06-19 WO PCT/US2015/036589 patent/WO2015196019A1/en not_active Ceased
- 2015-06-19 EP EP15809565.3A patent/EP3157898B1/en active Active
-
2018
- 2018-08-07 US US16/057,235 patent/US10428001B2/en active Active
-
2019
- 2019-08-14 US US16/541,065 patent/US10934239B2/en active Active
-
2020
- 2020-02-13 JP JP2020022255A patent/JP7104083B2/ja active Active
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