IL303430A - תרכובות מייצרות עשן - Google Patents
תרכובות מייצרות עשןInfo
- Publication number
- IL303430A IL303430A IL303430A IL30343023A IL303430A IL 303430 A IL303430 A IL 303430A IL 303430 A IL303430 A IL 303430A IL 30343023 A IL30343023 A IL 30343023A IL 303430 A IL303430 A IL 303430A
- Authority
- IL
- Israel
- Prior art keywords
- solvent
- smoke
- red
- yellow
- pigment
- Prior art date
Links
- 239000000779 smoke Substances 0.000 title claims description 30
- 150000001875 compounds Chemical class 0.000 title description 3
- 239000000203 mixture Substances 0.000 claims description 39
- 239000000975 dye Substances 0.000 claims description 27
- 238000002485 combustion reaction Methods 0.000 claims description 7
- 238000000354 decomposition reaction Methods 0.000 claims description 6
- -1 nitrobenzamines Chemical class 0.000 claims description 6
- 230000001590 oxidative effect Effects 0.000 claims description 6
- 239000002904 solvent Substances 0.000 claims description 5
- 238000000859 sublimation Methods 0.000 claims description 5
- 230000008022 sublimation Effects 0.000 claims description 5
- NIDFGXDXQKPZMA-UHFFFAOYSA-N 14h-benz[4,5]isoquino[2,1-a]perimidin-14-one Chemical compound C1=CC(N2C(=O)C=3C4=C(C2=N2)C=CC=C4C=CC=3)=C3C2=CC=CC3=C1 NIDFGXDXQKPZMA-UHFFFAOYSA-N 0.000 claims description 4
- COHYTHOBJLSHDF-UHFFFAOYSA-N Indigo Chemical compound N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 claims description 4
- 239000003638 chemical reducing agent Substances 0.000 claims description 4
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 claims description 4
- 239000000843 powder Substances 0.000 claims description 4
- 239000007800 oxidant agent Substances 0.000 claims description 3
- XBYRMPXUBGMOJC-UHFFFAOYSA-N 1,2-dihydropyrazol-3-one Chemical class OC=1C=CNN=1 XBYRMPXUBGMOJC-UHFFFAOYSA-N 0.000 claims description 2
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 claims description 2
- 239000004375 Dextrin Substances 0.000 claims description 2
- 229920001353 Dextrin Polymers 0.000 claims description 2
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims description 2
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 claims description 2
- 229920002472 Starch Polymers 0.000 claims description 2
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 claims description 2
- 229930006000 Sucrose Natural products 0.000 claims description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical class OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims description 2
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 claims description 2
- 235000019425 dextrin Nutrition 0.000 claims description 2
- 239000008121 dextrose Substances 0.000 claims description 2
- 239000008101 lactose Substances 0.000 claims description 2
- 150000004780 naphthols Chemical class 0.000 claims description 2
- 150000002979 perylenes Chemical class 0.000 claims description 2
- 235000010333 potassium nitrate Nutrition 0.000 claims description 2
- 239000004323 potassium nitrate Substances 0.000 claims description 2
- 239000008107 starch Substances 0.000 claims description 2
- 235000019698 starch Nutrition 0.000 claims description 2
- 239000005720 sucrose Substances 0.000 claims description 2
- 150000005075 thioxanthenes Chemical class 0.000 claims description 2
- 150000003732 xanthenes Chemical class 0.000 claims description 2
- 239000000049 pigment Substances 0.000 claims 9
- SMKKEOQDQNCTGL-ZETCQYMHSA-N (2s)-2-[(2-nitrophenoxy)methyl]oxirane Chemical compound [O-][N+](=O)C1=CC=CC=C1OC[C@H]1OC1 SMKKEOQDQNCTGL-ZETCQYMHSA-N 0.000 claims 2
- XWZOKATWICIEMU-UHFFFAOYSA-N (3,5-difluoro-4-formylphenyl)boronic acid Chemical compound OB(O)C1=CC(F)=C(C=O)C(F)=C1 XWZOKATWICIEMU-UHFFFAOYSA-N 0.000 claims 2
- XCKGFJPFEHHHQA-UHFFFAOYSA-N 5-methyl-2-phenyl-4-phenyldiazenyl-4h-pyrazol-3-one Chemical compound CC1=NN(C=2C=CC=CC=2)C(=O)C1N=NC1=CC=CC=C1 XCKGFJPFEHHHQA-UHFFFAOYSA-N 0.000 claims 2
- NPGIHFRTRXVWOY-UHFFFAOYSA-N Oil red O Chemical compound Cc1ccc(C)c(c1)N=Nc1cc(C)c(cc1C)N=Nc1c(O)ccc2ccccc12 NPGIHFRTRXVWOY-UHFFFAOYSA-N 0.000 claims 2
- SJJISKLXUJVZOA-UHFFFAOYSA-N Solvent yellow 56 Chemical compound C1=CC(N(CC)CC)=CC=C1N=NC1=CC=CC=C1 SJJISKLXUJVZOA-UHFFFAOYSA-N 0.000 claims 2
- 239000011230 binding agent Substances 0.000 claims 2
- YLNJGHNUXCVDIX-UHFFFAOYSA-N bis(2-methylpropyl) perylene-3,9-dicarboxylate Chemical compound C=12C3=CC=CC2=C(C(=O)OCC(C)C)C=CC=1C1=CC=CC2=C1C3=CC=C2C(=O)OCC(C)C YLNJGHNUXCVDIX-UHFFFAOYSA-N 0.000 claims 2
- MRQIXHXHHPWVIL-UHFFFAOYSA-N chembl1397023 Chemical compound OC1=CC=C2C=CC=CC2=C1N=NC1=CC=CC=C1 MRQIXHXHHPWVIL-UHFFFAOYSA-N 0.000 claims 2
- NHXXLZBKTKNTEF-UHFFFAOYSA-N chembl1997306 Chemical compound CC1=CC=CC(N=NC=2C(=CC(=CC=2)N=NC=2C3=CC=CC=C3C=CC=2O)C)=C1 NHXXLZBKTKNTEF-UHFFFAOYSA-N 0.000 claims 2
- 239000003112 inhibitor Substances 0.000 claims 2
- RCTGMCJBQGBLKT-PAMTUDGESA-N scarlet red Chemical compound CC1=CC=CC=C1\N=N\C(C=C1C)=CC=C1\N=N\C1=C(O)C=CC2=CC=CC=C12 RCTGMCJBQGBLKT-PAMTUDGESA-N 0.000 claims 2
- NRBKWAQSLYBVSG-UHFFFAOYSA-N solvent red 26 Chemical compound CC1=CC=CC=C1N=NC1=CC(C)=C(N=NC=2C3=CC=CC=C3C=CC=2O)C=C1C NRBKWAQSLYBVSG-UHFFFAOYSA-N 0.000 claims 2
- 229940033816 solvent red 27 Drugs 0.000 claims 2
- UTTFXJZCRVZYQF-UHFFFAOYSA-N 3-(diethylamino)-7-oxo-7h-(1)benzopyrano(3',2':3,4)pyrido(1,2-a)benzimidazole-6-carbonitrile Chemical compound C1=CC=C2N(C(=O)C(C#N)=C3C4=CC5=CC=C(C=C5O3)N(CC)CC)C4=NC2=C1 UTTFXJZCRVZYQF-UHFFFAOYSA-N 0.000 claims 1
- QPQKUYVSJWQSDY-UHFFFAOYSA-N 4-phenyldiazenylaniline Chemical compound C1=CC(N)=CC=C1N=NC1=CC=CC=C1 QPQKUYVSJWQSDY-UHFFFAOYSA-N 0.000 claims 1
- ZLHGTHCCYUEAIK-UHFFFAOYSA-N 5,7-dibromo-2-(5,7-dibromo-3-hydroxy-1H-indol-2-yl)indol-3-one Chemical compound [O-]c1c([nH]c2c(Br)cc(Br)cc12)C1=[NH+]c2c(cc(Br)cc2Br)C1=O ZLHGTHCCYUEAIK-UHFFFAOYSA-N 0.000 claims 1
- 239000006096 absorbing agent Substances 0.000 claims 1
- 239000000654 additive Substances 0.000 claims 1
- WYVHNCGXVPMYQK-UHFFFAOYSA-N fluorol yellow 088 Chemical compound C1=CC=C2C(C=3C(=CC=C(C=3)C)O3)=C4C3=CC=C(C)C4=CC2=C1 WYVHNCGXVPMYQK-UHFFFAOYSA-N 0.000 claims 1
- WTIFIAZWCCBCGE-UUOKFMHZSA-N guanosine 2'-monophosphate Chemical compound C1=2NC(N)=NC(=O)C=2N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1OP(O)(O)=O WTIFIAZWCCBCGE-UUOKFMHZSA-N 0.000 claims 1
- 239000002245 particle Substances 0.000 claims 1
- KXXXUIKPSVVSAW-UHFFFAOYSA-K pyranine Chemical compound [Na+].[Na+].[Na+].C1=C2C(O)=CC(S([O-])(=O)=O)=C(C=C3)C2=C2C3=C(S([O-])(=O)=O)C=C(S([O-])(=O)=O)C2=C1 KXXXUIKPSVVSAW-UHFFFAOYSA-K 0.000 claims 1
- 230000011664 signaling Effects 0.000 claims 1
- JXUKQCUPTNLTCS-UHFFFAOYSA-N vat green 1 Chemical compound C1=CC=C[C]2C(=O)C(C3=C45)=CC=C4C(C4=C67)=CC=C7C(=O)[C]7C=CC=CC7=C6C=C(OC)C4=C5C(OC)=CC3=C21 JXUKQCUPTNLTCS-UHFFFAOYSA-N 0.000 claims 1
- YKSGNOMLAIJTLT-UHFFFAOYSA-N violanthrone Chemical compound C12=C3C4=CC=C2C2=CC=CC=C2C(=O)C1=CC=C3C1=CC=C2C(=O)C3=CC=CC=C3C3=CC=C4C1=C32 YKSGNOMLAIJTLT-UHFFFAOYSA-N 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000002957 persistent organic pollutant Substances 0.000 description 4
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 3
- 150000004056 anthraquinones Chemical class 0.000 description 3
- 231100000252 nontoxic Toxicity 0.000 description 2
- 230000003000 nontoxic effect Effects 0.000 description 2
- 231100000956 nontoxicity Toxicity 0.000 description 2
- 125000005575 polycyclic aromatic hydrocarbon group Chemical group 0.000 description 2
- KVGZZAHHUNAVKZ-UHFFFAOYSA-N 1,4-Dioxin Chemical compound O1C=COC=C1 KVGZZAHHUNAVKZ-UHFFFAOYSA-N 0.000 description 1
- 241000282412 Homo Species 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 150000002013 dioxins Chemical class 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 239000010804 inert waste Substances 0.000 description 1
- 231100001231 less toxic Toxicity 0.000 description 1
- VKJKEPKFPUWCAS-UHFFFAOYSA-M potassium chlorate Chemical compound [K+].[O-]Cl(=O)=O VKJKEPKFPUWCAS-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B23/00—Compositions characterised by non-explosive or non-thermic constituents
- C06B23/001—Fillers, gelling and thickening agents (e.g. fibres), absorbents for nitroglycerine
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B23/00—Compositions characterised by non-explosive or non-thermic constituents
- C06B23/005—Desensitisers, phlegmatisers
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06D—MEANS FOR GENERATING SMOKE OR MIST; GAS-ATTACK COMPOSITIONS; GENERATION OF GAS FOR BLASTING OR PROPULSION (CHEMICAL PART)
- C06D3/00—Generation of smoke or mist (chemical part)
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Botany (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Combustion & Propulsion (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Compounds Of Unknown Constitution (AREA)
- Cosmetics (AREA)
- Artificial Filaments (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR2012672A FR3117112B1 (fr) | 2020-12-04 | 2020-12-04 | Compositions fumigenes |
| PCT/FR2021/052208 WO2022117975A1 (fr) | 2020-12-04 | 2021-12-03 | Compositions fumigenes |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| IL303430A true IL303430A (he) | 2023-08-01 |
Family
ID=75746727
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL303430A IL303430A (he) | 2020-12-04 | 2021-12-03 | תרכובות מייצרות עשן |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US20240010578A1 (he) |
| EP (1) | EP4255870A1 (he) |
| KR (1) | KR20230154792A (he) |
| CN (1) | CN116867756A (he) |
| AU (1) | AU2021391988A1 (he) |
| CA (1) | CA3203576A1 (he) |
| FR (1) | FR3117112B1 (he) |
| IL (1) | IL303430A (he) |
| WO (1) | WO2022117975A1 (he) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN114956923B (zh) * | 2022-06-30 | 2023-06-02 | 北京航空工程技术研究中心 | 一种飞行表演液体型彩色拉烟剂及其制备方法 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA1115167A (en) * | 1979-03-02 | 1981-12-29 | Joseph E.G. Couture | Coating of granulated organic dyes with an epoxy |
| GB2330896A (en) * | 1997-11-04 | 1999-05-05 | Mantsuna & Co Ltd S | Roman candle |
| JPH11201699A (ja) * | 1997-11-04 | 1999-07-30 | Mantsuna Shoten:Kk | 昼間用煙乱玉花火 |
| ES2302620B1 (es) * | 2006-07-10 | 2009-05-07 | Falken S.A. | Mezcla fumigena, composicion de encendido y dispositivo para su almacenaje. |
| CN105622300A (zh) * | 2016-01-13 | 2016-06-01 | 中国人民武装警察部队工程大学 | 一种黑色发烟剂及其制备方法 |
| US10759720B1 (en) * | 2018-09-20 | 2020-09-01 | The United States Of America As Represented By The Secretary Of The Army | Low toxicity, environmentally friendly red smoke generating composition and method of making the same |
| CN110627597B (zh) * | 2019-10-08 | 2020-08-07 | 颜谷科技发展（天津）有限公司 | 一种航空彩色拉烟剂及其制备方法 |
-
2020
- 2020-12-04 FR FR2012672A patent/FR3117112B1/fr active Active
-
2021
- 2021-12-03 AU AU2021391988A patent/AU2021391988A1/en not_active Abandoned
- 2021-12-03 US US18/255,863 patent/US20240010578A1/en active Pending
- 2021-12-03 IL IL303430A patent/IL303430A/he unknown
- 2021-12-03 KR KR1020237022302A patent/KR20230154792A/ko active Pending
- 2021-12-03 EP EP21839608.3A patent/EP4255870A1/fr active Pending
- 2021-12-03 WO PCT/FR2021/052208 patent/WO2022117975A1/fr not_active Ceased
- 2021-12-03 CA CA3203576A patent/CA3203576A1/fr active Pending
- 2021-12-03 CN CN202180081728.XA patent/CN116867756A/zh active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| CA3203576A1 (fr) | 2022-06-09 |
| US20240010578A1 (en) | 2024-01-11 |
| CN116867756A (zh) | 2023-10-10 |
| FR3117112B1 (fr) | 2023-04-14 |
| KR20230154792A (ko) | 2023-11-09 |
| AU2021391988A1 (en) | 2023-06-29 |
| EP4255870A1 (fr) | 2023-10-11 |
| WO2022117975A1 (fr) | 2022-06-09 |
| FR3117112A1 (fr) | 2022-06-10 |
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