DE1593704A1 - Sicher handhabbare Diacylperoxydzusammensetzungen - Google Patents
Sicher handhabbare DiacylperoxydzusammensetzungenInfo
- Publication number
- DE1593704A1 DE1593704A1 DE19661593704 DE1593704A DE1593704A1 DE 1593704 A1 DE1593704 A1 DE 1593704A1 DE 19661593704 DE19661593704 DE 19661593704 DE 1593704 A DE1593704 A DE 1593704A DE 1593704 A1 DE1593704 A1 DE 1593704A1
- Authority
- DE
- Germany
- Prior art keywords
- peroxide
- aliphatic
- safety
- solvent
- compositions
- 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
- 239000000203 mixture Substances 0.000 title claims description 45
- 239000012933 diacyl peroxide Substances 0.000 title claims description 16
- 239000002904 solvent Substances 0.000 claims description 38
- 150000002978 peroxides Chemical class 0.000 claims description 37
- ZQMIGQNCOMNODD-UHFFFAOYSA-N diacetyl peroxide Chemical compound CC(=O)OOC(C)=O ZQMIGQNCOMNODD-UHFFFAOYSA-N 0.000 claims description 30
- -1 acyl peroxide Chemical class 0.000 claims description 14
- 238000009835 boiling Methods 0.000 claims description 14
- 238000001704 evaporation Methods 0.000 claims description 13
- 230000008020 evaporation Effects 0.000 claims description 13
- 125000001931 aliphatic group Chemical group 0.000 claims description 12
- KOPQZJAYZFAPBC-UHFFFAOYSA-N propanoyl propaneperoxoate Chemical compound CCC(=O)OOC(=O)CC KOPQZJAYZFAPBC-UHFFFAOYSA-N 0.000 claims description 9
- RPBWMJBZQXCSFW-UHFFFAOYSA-N 2-methylpropanoyl 2-methylpropaneperoxoate Chemical compound CC(C)C(=O)OOC(=O)C(C)C RPBWMJBZQXCSFW-UHFFFAOYSA-N 0.000 claims description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 239000012808 vapor phase Substances 0.000 claims description 4
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 3
- 150000002576 ketones Chemical class 0.000 claims description 3
- 239000007791 liquid phase Substances 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims 1
- 125000003158 alcohol group Chemical group 0.000 claims 1
- 150000007824 aliphatic compounds Chemical class 0.000 claims 1
- RXKJFZQQPQGTFL-UHFFFAOYSA-N dihydroxyacetone Chemical compound OCC(=O)CO RXKJFZQQPQGTFL-UHFFFAOYSA-N 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 238000012360 testing method Methods 0.000 description 25
- 238000000034 method Methods 0.000 description 22
- 239000000243 solution Substances 0.000 description 21
- 230000035939 shock Effects 0.000 description 15
- 238000000354 decomposition reaction Methods 0.000 description 14
- 230000035945 sensitivity Effects 0.000 description 11
- NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 description 10
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 8
- 230000009965 odorless effect Effects 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 239000000523 sample Substances 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 6
- 238000001816 cooling Methods 0.000 description 5
- FBSAITBEAPNWJG-UHFFFAOYSA-N dimethyl phthalate Natural products CC(=O)OC1=CC=CC=C1OC(C)=O FBSAITBEAPNWJG-UHFFFAOYSA-N 0.000 description 5
- 229960001826 dimethylphthalate Drugs 0.000 description 5
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 239000003513 alkali Substances 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 230000009172 bursting Effects 0.000 description 4
- NGAZZOYFWWSOGK-UHFFFAOYSA-N heptan-3-one Chemical compound CCCCC(=O)CC NGAZZOYFWWSOGK-UHFFFAOYSA-N 0.000 description 4
- 239000012074 organic phase Substances 0.000 description 4
- 238000010998 test method Methods 0.000 description 4
- PTTPXKJBFFKCEK-UHFFFAOYSA-N 2-Methyl-4-heptanone Chemical compound CC(C)CC(=O)CC(C)C PTTPXKJBFFKCEK-UHFFFAOYSA-N 0.000 description 3
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000004880 explosion Methods 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 description 3
- 239000011707 mineral Substances 0.000 description 3
- 235000010755 mineral Nutrition 0.000 description 3
- 230000007935 neutral effect Effects 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- FFWSICBKRCICMR-UHFFFAOYSA-N 5-methyl-2-hexanone Chemical compound CC(C)CCC(C)=O FFWSICBKRCICMR-UHFFFAOYSA-N 0.000 description 2
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 2
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000013068 control sample Substances 0.000 description 2
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 230000009931 harmful effect Effects 0.000 description 2
- AOGQPLXWSUTHQB-UHFFFAOYSA-N hexyl acetate Chemical compound CCCCCCOC(C)=O AOGQPLXWSUTHQB-UHFFFAOYSA-N 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- NTRZCEWBQFVIPC-UHFFFAOYSA-N methyl pentaneperoxoate Chemical compound CCCCC(=O)OOC NTRZCEWBQFVIPC-UHFFFAOYSA-N 0.000 description 2
- 150000001451 organic peroxides Chemical class 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 230000001376 precipitating effect Effects 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 235000015096 spirit Nutrition 0.000 description 2
- 230000004580 weight loss Effects 0.000 description 2
- WOYWLLHHWAMFCB-UHFFFAOYSA-N 2-ethylhexyl acetate Chemical compound CCCCC(CC)COC(C)=O WOYWLLHHWAMFCB-UHFFFAOYSA-N 0.000 description 1
- CPIVYSAVIPTCCX-UHFFFAOYSA-N 4-methylpentan-2-yl acetate Chemical compound CC(C)CC(C)OC(C)=O CPIVYSAVIPTCCX-UHFFFAOYSA-N 0.000 description 1
- 229910001369 Brass Inorganic materials 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 241001432959 Chernes Species 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229920006328 Styrofoam Polymers 0.000 description 1
- 206010057040 Temperature intolerance Diseases 0.000 description 1
- IEZGWZLXZLMRAZ-UHFFFAOYSA-N acetyl pentaneperoxoate Chemical class CCCCC(=O)OOC(C)=O IEZGWZLXZLMRAZ-UHFFFAOYSA-N 0.000 description 1
- CMMQQIFVGYKMCA-UHFFFAOYSA-N acetyl propaneperoxoate Chemical compound CCC(=O)OOC(C)=O CMMQQIFVGYKMCA-UHFFFAOYSA-N 0.000 description 1
- 229910001854 alkali hydroxide Inorganic materials 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- KQNZLOUWXSAZGD-UHFFFAOYSA-N benzylperoxymethylbenzene Chemical compound C=1C=CC=CC=1COOCC1=CC=CC=C1 KQNZLOUWXSAZGD-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 230000008543 heat sensitivity Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- VLAGSAGYAIGJSU-UHFFFAOYSA-N hexanoyl hexaneperoxoate Chemical class CCCCCC(=O)OOC(=O)CCCCC VLAGSAGYAIGJSU-UHFFFAOYSA-N 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 238000009863 impact test Methods 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- RXTNIJMLAQNTEG-UHFFFAOYSA-N methylamyl acetate Natural products CCCCC(C)OC(C)=O RXTNIJMLAQNTEG-UHFFFAOYSA-N 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- NWXPHYAWPBZQMX-UHFFFAOYSA-N pentanoyl pentaneperoxoate Chemical class CCCCC(=O)OOC(=O)CCCC NWXPHYAWPBZQMX-UHFFFAOYSA-N 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- WYVAMUWZEOHJOQ-UHFFFAOYSA-N propionic anhydride Chemical compound CCC(=O)OC(=O)CC WYVAMUWZEOHJOQ-UHFFFAOYSA-N 0.000 description 1
- 239000013558 reference substance Substances 0.000 description 1
- 238000011076 safety test Methods 0.000 description 1
- 238000009781 safety test method Methods 0.000 description 1
- 238000005204 segregation Methods 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 239000004449 solid propellant Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000008261 styrofoam Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 210000003462 vein Anatomy 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C409/00—Peroxy compounds
- C07C409/32—Peroxy compounds the —O—O— group being bound between two >C=O groups
- C07C409/34—Peroxy compounds the —O—O— group being bound between two >C=O groups both belonging to carboxylic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US46052865A | 1965-06-01 | 1965-06-01 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1593704A1 true DE1593704A1 (de) | 1970-11-26 |
Family
ID=23829074
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19661593704 Pending DE1593704A1 (de) | 1965-06-01 | 1966-03-24 | Sicher handhabbare Diacylperoxydzusammensetzungen |
Country Status (6)
| Country | Link |
|---|---|
| JP (1) | JPS5141610B1 (enrdf_load_stackoverflow) |
| BE (1) | BE678389A (enrdf_load_stackoverflow) |
| DE (1) | DE1593704A1 (enrdf_load_stackoverflow) |
| FR (1) | FR1472767A (enrdf_load_stackoverflow) |
| GB (1) | GB1128984A (enrdf_load_stackoverflow) |
| NL (1) | NL6604105A (enrdf_load_stackoverflow) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0810213A3 (en) * | 1996-05-31 | 1998-11-25 | Witco Corporation | Organic peroxide stabilization with beta-dicarbonyl or cyclic alpha-diketone compounds |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN116396200A (zh) * | 2023-04-12 | 2023-07-07 | 兰州助剂厂股份有限公司 | 一种过氧化二异丁酰的制备方法 |
-
0
- FR FR1472767D patent/FR1472767A/fr not_active Expired
-
1966
- 1966-03-24 DE DE19661593704 patent/DE1593704A1/de active Pending
- 1966-03-24 BE BE678389A patent/BE678389A/xx unknown
- 1966-03-29 NL NL6604105A patent/NL6604105A/xx unknown
- 1966-05-04 JP JP2814266A patent/JPS5141610B1/ja active Pending
- 1966-05-27 GB GB2398066A patent/GB1128984A/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0810213A3 (en) * | 1996-05-31 | 1998-11-25 | Witco Corporation | Organic peroxide stabilization with beta-dicarbonyl or cyclic alpha-diketone compounds |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5141610B1 (enrdf_load_stackoverflow) | 1976-11-11 |
| NL6604105A (enrdf_load_stackoverflow) | 1966-12-02 |
| GB1128984A (en) | 1968-10-02 |
| BE678389A (enrdf_load_stackoverflow) | 1966-09-26 |
| FR1472767A (enrdf_load_stackoverflow) | 1967-05-31 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2038320B2 (de) | Nichtwäßrige Wasserstoffperoxid-Lösungen | |
| EP3380552B1 (de) | Bchpc mit verringerter abbrandgeschwindigkeit | |
| DE2438898C3 (de) | Polyolefinmasse | |
| DE2823706C2 (de) | Polymere Diacylperoxyde, Verfahren zu ihrer Herstellung und ihre Verwendung | |
| CH196646A (de) | Verfahren zur Herstellung eines Zellulose-Essigsäure-Esters nach dem Nichtlöseverfahren mit höchstens 61,5% Essigsäuregehalt. | |
| DE2948152A1 (de) | Copolymeres mit peroxybindungen in seinem molekuel und verfahren zu dessen herstellung | |
| DE1593704A1 (de) | Sicher handhabbare Diacylperoxydzusammensetzungen | |
| DE920514C (de) | Verfahren zur Herstellung von zur Polymerisation von Carbonsaeurevinyl-estern geeigneten organischen Peroxyd-Polymerisations-Katalysatoren | |
| DE69701591T2 (de) | Stabilisierung von organischen Peroxiden mit Alpha-hydroxyalkylperoxiden | |
| DE1543466B1 (de) | Verfahren zum Stabilisieren von Acrylsaeureamid gegen Polymerisation | |
| DE861156C (de) | Verfahren zur Herstellung von Polymerisaten oder Mischpolymerisaten ungesaettigter Verbindungen | |
| DE69800578T2 (de) | Stabilisiering von organischen Peroxiden mit Oximen | |
| DE2148185B2 (enrdf_load_stackoverflow) | ||
| DE69706365T2 (de) | Stabilisierung von organischen Peroxiden mit Phosphomolybdänsäure | |
| DE69106299T2 (de) | Peroxyester und seine Verwendung als Polymerisationsinitiator und Härtungsmittel. | |
| DE69703001T2 (de) | Stabilisierung von organischen Peroxiden mit Beta-dicarbonyl oder Alpha-diketon Verbindungen | |
| DE1520011C3 (de) | Verfahren zur Herstellung von wärme- und lichtstabilen Hydroxylgruppen enthaltenden Vinylpolymeren | |
| DE2528492C2 (de) | Perester, Verfahren zu ihrer Herstellung und ihre Verwendung zur Initiierung chemischer Reaktionen | |
| DE2631910A1 (de) | Fluessige haltbare peroxidloesungen und ihre verwendung als initiatoren bei der polymerisation von vinylmonomeren | |
| EP0237946A1 (de) | Kupferhaltiges Mittel zur Bekämpfung von Pilzen und Bakterien | |
| DE1793809A1 (de) | Azopolymere und verfahren zu ihrer herstellung | |
| DE69821744T2 (de) | Substituierte tetrahydropyrimidin derative und ihre verwendung als polymerization hemmer für vinyl aromatische verbindungen | |
| DE862368C (de) | Verfahren zur Herstellung von Loesungen von Acrylnitrilpolymeren | |
| DE2050723A1 (de) | Verfahren zur Herstellung von Vinyl Chloridpolymerisaten | |
| DE3048081A1 (de) | Verfahren zur herstellung von polymeren und mischpolymeren aethylenisch ungesaettigter monomerer |