NO327838B1 - Fremgangsmate for fremstilling av mykner - Google Patents
Fremgangsmate for fremstilling av mykner Download PDFInfo
- Publication number
- NO327838B1 NO327838B1 NO20020218A NO20020218A NO327838B1 NO 327838 B1 NO327838 B1 NO 327838B1 NO 20020218 A NO20020218 A NO 20020218A NO 20020218 A NO20020218 A NO 20020218A NO 327838 B1 NO327838 B1 NO 327838B1
- Authority
- NO
- Norway
- Prior art keywords
- reactor
- alkyl
- water
- approx
- ethanolamine
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 61
- 230000008569 process Effects 0.000 title claims description 16
- 239000004014 plasticizer Substances 0.000 title description 5
- 238000004519 manufacturing process Methods 0.000 claims abstract description 40
- 238000010924 continuous production Methods 0.000 claims abstract description 25
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 claims description 117
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical group [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 claims description 71
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 55
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims description 48
- 229910017604 nitric acid Inorganic materials 0.000 claims description 48
- 239000000203 mixture Substances 0.000 claims description 47
- 239000011592 zinc chloride Substances 0.000 claims description 33
- 235000005074 zinc chloride Nutrition 0.000 claims description 33
- 238000006243 chemical reaction Methods 0.000 claims description 28
- LJDSTRZHPWMDPG-UHFFFAOYSA-N 2-(butylamino)ethanol Chemical group CCCCNCCO LJDSTRZHPWMDPG-UHFFFAOYSA-N 0.000 claims description 16
- 238000005406 washing Methods 0.000 claims description 14
- 239000003054 catalyst Substances 0.000 claims description 12
- 239000002253 acid Substances 0.000 claims description 11
- HZAXFHJVJLSVMW-UHFFFAOYSA-N monoethanolamine hydrochloride Natural products NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 claims description 11
- 238000001816 cooling Methods 0.000 claims description 9
- 150000004820 halides Chemical class 0.000 claims description 8
- 238000009826 distribution Methods 0.000 claims description 7
- -1 alkyl ethanolamine Chemical compound 0.000 claims description 5
- 238000000926 separation method Methods 0.000 claims description 3
- 238000003860 storage Methods 0.000 claims description 3
- 238000002347 injection Methods 0.000 claims description 2
- 239000007924 injection Substances 0.000 claims description 2
- 238000011144 upstream manufacturing Methods 0.000 claims description 2
- 238000010626 work up procedure Methods 0.000 claims description 2
- 239000011541 reaction mixture Substances 0.000 description 31
- 239000000047 product Substances 0.000 description 26
- 239000007788 liquid Substances 0.000 description 21
- 235000015854 Heliotropium curassavicum Nutrition 0.000 description 17
- 244000301682 Heliotropium curassavicum Species 0.000 description 17
- 241000196324 Embryophyta Species 0.000 description 12
- 239000003721 gunpowder Substances 0.000 description 11
- 239000013067 intermediate product Substances 0.000 description 10
- 150000001875 compounds Chemical class 0.000 description 9
- 238000003756 stirring Methods 0.000 description 9
- 239000002360 explosive Substances 0.000 description 8
- 239000005457 ice water Substances 0.000 description 8
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 6
- 238000010923 batch production Methods 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 230000003197 catalytic effect Effects 0.000 description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- MIJDSYMOBYNHOT-UHFFFAOYSA-N 2-(ethylamino)ethanol Chemical compound CCNCCO MIJDSYMOBYNHOT-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- OPKOKAMJFNKNAS-UHFFFAOYSA-N N-methylethanolamine Chemical compound CNCCO OPKOKAMJFNKNAS-UHFFFAOYSA-N 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- 239000007791 liquid phase Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 239000007858 starting material Substances 0.000 description 4
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 229910000029 sodium carbonate Inorganic materials 0.000 description 3
- POCJOGNVFHPZNS-ZJUUUORDSA-N (6S,7R)-2-azaspiro[5.5]undecan-7-ol Chemical group O[C@@H]1CCCC[C@]11CNCCC1 POCJOGNVFHPZNS-ZJUUUORDSA-N 0.000 description 2
- 239000004451 Ballistite Substances 0.000 description 2
- 229910002651 NO3 Inorganic materials 0.000 description 2
- 239000000020 Nitrocellulose Substances 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000000356 contaminant Substances 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 230000020169 heat generation Effects 0.000 description 2
- 238000006396 nitration reaction Methods 0.000 description 2
- 229920001220 nitrocellulos Polymers 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- BSPUVYFGURDFHE-UHFFFAOYSA-N Nitramine Natural products CC1C(O)CCC2CCCNC12 BSPUVYFGURDFHE-UHFFFAOYSA-N 0.000 description 1
- SNIOPGDIGTZGOP-UHFFFAOYSA-N Nitroglycerin Chemical compound [O-][N+](=O)OCC(O[N+]([O-])=O)CO[N+]([O-])=O SNIOPGDIGTZGOP-UHFFFAOYSA-N 0.000 description 1
- 239000000006 Nitroglycerin Substances 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 230000005587 bubbling Effects 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 239000000567 combustion gas Substances 0.000 description 1
- 238000011437 continuous method Methods 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- ZWWCURLKEXEFQT-UHFFFAOYSA-N dinitrogen pentoxide Inorganic materials [O-][N+](=O)O[N+]([O-])=O ZWWCURLKEXEFQT-UHFFFAOYSA-N 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 229960003711 glyceryl trinitrate Drugs 0.000 description 1
- QNVRIHYSUZMSGM-UHFFFAOYSA-N hexan-2-ol Chemical compound CCCCC(C)O QNVRIHYSUZMSGM-UHFFFAOYSA-N 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- POCJOGNVFHPZNS-UHFFFAOYSA-N isonitramine Natural products OC1CCCCC11CNCCC1 POCJOGNVFHPZNS-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- AHLHDIKRENEJHF-UHFFFAOYSA-N n-ethylnitramide Chemical compound CCN[N+]([O-])=O AHLHDIKRENEJHF-UHFFFAOYSA-N 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 208000018316 severe headache Diseases 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- 229940124549 vasodilator Drugs 0.000 description 1
- 239000003071 vasodilator agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C241/00—Preparation of compounds containing chains of nitrogen atoms singly-bound to each other, e.g. hydrazines, triazanes
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B25/00—Compositions containing a nitrated organic compound
- C06B25/34—Compositions containing a nitrated organic compound the compound being a nitrated acyclic, alicyclic or heterocyclic amine
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B45/00—Compositions or products which are defined by structure or arrangement of component of product
- C06B45/04—Compositions or products which are defined by structure or arrangement of component of product comprising solid particles dispersed in solid solution or matrix not used for explosives where the matrix consists essentially of nitrated carbohydrates or a low molecular organic explosive
- C06B45/06—Compositions or products which are defined by structure or arrangement of component of product comprising solid particles dispersed in solid solution or matrix not used for explosives where the matrix consists essentially of nitrated carbohydrates or a low molecular organic explosive the solid solution or matrix containing an organic component
- C06B45/10—Compositions or products which are defined by structure or arrangement of component of product comprising solid particles dispersed in solid solution or matrix not used for explosives where the matrix consists essentially of nitrated carbohydrates or a low molecular organic explosive the solid solution or matrix containing an organic component the organic component containing a resin
- C06B45/105—The resin being a polymer bearing energetic groups or containing a soluble organic explosive
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C213/00—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton
- C07C213/06—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton from hydroxy amines by reactions involving the etherification or esterification of hydroxy groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dispersion Chemistry (AREA)
- Molecular Biology (AREA)
- Crystallography & Structural Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Steroid Compounds (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NO20020218A NO327838B1 (no) | 1999-10-14 | 2002-01-15 | Fremgangsmate for fremstilling av mykner |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/NO1999/000312 WO2001027073A1 (fr) | 1999-10-14 | 1999-10-14 | Procede de preparation d'un agent plastifiant de grande energie |
| NO20020218A NO327838B1 (no) | 1999-10-14 | 2002-01-15 | Fremgangsmate for fremstilling av mykner |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO20020218L NO20020218L (no) | 2002-01-15 |
| NO20020218D0 NO20020218D0 (no) | 2002-01-15 |
| NO327838B1 true NO327838B1 (no) | 2009-10-05 |
Family
ID=19907909
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20020218A NO327838B1 (no) | 1999-10-14 | 2002-01-15 | Fremgangsmate for fremstilling av mykner |
Country Status (8)
| Country | Link |
|---|---|
| EP (1) | EP1196374B1 (fr) |
| AT (1) | ATE235460T1 (fr) |
| AU (1) | AU1298800A (fr) |
| CA (1) | CA2370145C (fr) |
| DE (1) | DE69906393T2 (fr) |
| ES (1) | ES2194529T3 (fr) |
| NO (1) | NO327838B1 (fr) |
| WO (1) | WO2001027073A1 (fr) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102004007706A1 (de) * | 2004-02-16 | 2005-08-25 | Dynamit Nobel Gmbh Explosivstoff- Und Systemtechnik | Verfahren zur Herstellung von flüssigen Nitratestern |
| US8425703B1 (en) | 2010-03-24 | 2013-04-23 | The United States of Amierica as Represented by the Secretary of the Navy | Insensitive munitions primers |
| EP3539943A1 (fr) | 2018-03-15 | 2019-09-18 | Nitrochemie Aschau GmbH | Procédé de préparation de la n-alkyl-nitratoethylnitramine |
| CN111763154A (zh) * | 2019-04-01 | 2020-10-13 | 南京理工大学 | 一种二乙醇硝胺二硝酸酯的合成方法 |
| CN115784924A (zh) * | 2022-11-29 | 2023-03-14 | 天元航材(营口)科技股份有限公司 | 一种连续法制备高纯度Bu-NENA的新工艺 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2678946A (en) * | 1944-12-30 | 1954-05-18 | Us Navy | Process of preparing nitroxy alkyl nitramines |
| US2485855A (en) * | 1944-12-30 | 1949-10-25 | Us Seeretary Of The Navy | Nitramines |
| US5520757A (en) * | 1988-08-25 | 1996-05-28 | Ici Explosives Usa Inc. | Low vulnerability propellants |
-
1999
- 1999-10-14 AT AT99956364T patent/ATE235460T1/de not_active IP Right Cessation
- 1999-10-14 WO PCT/NO1999/000312 patent/WO2001027073A1/fr active IP Right Grant
- 1999-10-14 ES ES99956364T patent/ES2194529T3/es not_active Expired - Lifetime
- 1999-10-14 CA CA002370145A patent/CA2370145C/fr not_active Expired - Lifetime
- 1999-10-14 DE DE69906393T patent/DE69906393T2/de not_active Expired - Lifetime
- 1999-10-14 EP EP99956364A patent/EP1196374B1/fr not_active Expired - Lifetime
- 1999-10-14 AU AU12988/00A patent/AU1298800A/en not_active Abandoned
-
2002
- 2002-01-15 NO NO20020218A patent/NO327838B1/no not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| NO20020218L (no) | 2002-01-15 |
| CA2370145A1 (fr) | 2001-04-19 |
| ES2194529T3 (es) | 2003-11-16 |
| EP1196374B1 (fr) | 2003-03-26 |
| WO2001027073A1 (fr) | 2001-04-19 |
| DE69906393D1 (de) | 2003-04-30 |
| ATE235460T1 (de) | 2003-04-15 |
| EP1196374A1 (fr) | 2002-04-17 |
| DE69906393T2 (de) | 2003-10-30 |
| AU1298800A (en) | 2001-04-23 |
| CA2370145C (fr) | 2003-05-06 |
| NO20020218D0 (no) | 2002-01-15 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MK1K | Patent expired |