DE296591C - - Google Patents
Info
- Publication number
- DE296591C DE296591C DENDAT296591D DE296591DA DE296591C DE 296591 C DE296591 C DE 296591C DE NDAT296591 D DENDAT296591 D DE NDAT296591D DE 296591D A DE296591D A DE 296591DA DE 296591 C DE296591 C DE 296591C
- Authority
- DE
- Germany
- Prior art keywords
- stability
- powder
- increase
- plasticity
- anilides
- 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.)
- Active
Links
- 239000000843 powder Substances 0.000 claims description 9
- 229940051881 Anilide analgesics and antipyretics Drugs 0.000 claims description 4
- 150000003931 anilides Chemical class 0.000 claims description 4
- ZTHRQJQJODGZHV-UHFFFAOYSA-N N-phenylpropanamide Chemical compound CCC(=O)NC1=CC=CC=C1 ZTHRQJQJODGZHV-UHFFFAOYSA-N 0.000 claims description 3
- 150000007524 organic acids Chemical class 0.000 claims description 3
- 235000005985 organic acids Nutrition 0.000 claims description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 150000003949 imides Chemical class 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 239000000020 Nitrocellulose Substances 0.000 description 4
- 229920001220 nitrocellulos Polymers 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 235000019271 petrolatum Nutrition 0.000 description 2
- SNIOPGDIGTZGOP-UHFFFAOYSA-N 1,2,3-propanetrioltrinitrate Chemical compound [O-][N+](=O)OCC(O[N+]([O-])=O)CO[N+]([O-])=O SNIOPGDIGTZGOP-UHFFFAOYSA-N 0.000 description 1
- GSODDLMZIJTUCX-UHFFFAOYSA-N 3,4-dipentylphthalic acid Chemical compound CCCCCC1=CC=C(C(O)=O)C(C(O)=O)=C1CCCCC GSODDLMZIJTUCX-UHFFFAOYSA-N 0.000 description 1
- DSSYKIVIOFKYAU-UHFFFAOYSA-N Camphor Chemical group C1CC2(C)C(=O)CC1C2(C)C DSSYKIVIOFKYAU-UHFFFAOYSA-N 0.000 description 1
- 229960000846 Camphor Drugs 0.000 description 1
- 241000723346 Cinnamomum camphora Species 0.000 description 1
- 241000182341 Cubitermes group Species 0.000 description 1
- 229940052296 Esters of benzoic acid for local anesthesia Drugs 0.000 description 1
- 239000000006 Nitroglycerin Substances 0.000 description 1
- 229940014995 Nitroglycerin Drugs 0.000 description 1
- DOOTYTYQINUNNV-UHFFFAOYSA-N Triethyl citrate Chemical compound CCOC(=O)CC(O)(C(=O)OCC)CC(=O)OCC DOOTYTYQINUNNV-UHFFFAOYSA-N 0.000 description 1
- 229940099259 Vaseline Drugs 0.000 description 1
- 230000000996 additive Effects 0.000 description 1
- 159000000032 aromatic acids Chemical class 0.000 description 1
- 229930007890 camphor Natural products 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- -1 diamylsuccinic acid ester Chemical class 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 230000002708 enhancing Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 230000002349 favourable Effects 0.000 description 1
- 229960003711 glyceryl trinitrate Drugs 0.000 description 1
- 239000003721 gunpowder Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000000087 stabilizing Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003899 tartaric acid esters Chemical class 0.000 description 1
- 235000013769 triethyl citrate Nutrition 0.000 description 1
Classifications
-
- 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
- C06B25/18—Compositions containing a nitrated organic compound the compound being nitrocellulose present as 10% or more by weight of the total composition
- C06B25/24—Compositions containing a nitrated organic compound the compound being nitrocellulose present as 10% or more by weight of the total composition with nitroglycerine
- C06B25/26—Compositions containing a nitrated organic compound the compound being nitrocellulose present as 10% or more by weight of the total composition with nitroglycerine with an organic non-explosive or an organic non-thermic component
Landscapes
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
■ft■ ft
KAISERLICHESIMPERIAL
PATENTAMT.PATENT OFFICE.
KLASSE 78 c. GRUPPECLASS 78 c. GROUP
in BERLIN.in Berlin.
Seit lange setzt man den rauchlosen Schießpulvern Körper zu, welche, ohne an sich ballistisch zu wirken, infolge ihres hohen Kohlenstoffgehalts geeignet sind, die Brisanz des Pulvers zu vermindern. Ein solcher Zusatzstoff ist beispielsweise die Vaseline. Mit den Fortschritten der modernen Fabrikation sind an derartige Zusätze noch weitere Forderungen gestellt worden, insbesondere soweit die Erhöhung der Stabilität, die Vermehrung der Plastizität usw. in Betracht kommt. Diesen Forderungen vermochte ein Körper wie die Vaseline nicht zu entsprechen. Man ist daher zu Estern aromatischer oder Fettsäuren übergegangen: Diamylphtalsäure-, Diamylbernsteinsäureester, Weinsäure- und Zitronensäureäthylester, Ester der Benzoesäure usw. Alle diese Körper haben infolge ihrer Eigenschaften, Nitrocellulose zu lösen, wohl die Fähigkeit, die Plastizität von rauchlosen Nitroglycerin- oder reinen Nitrocellulosepulvern zu erhöhen, es fehlt ihnen aber die Eigenschaft, stabilisierend zu wirken. Nach dem vorliegenden Verfahren werden dagegen Körper verwendet, welche gleichzeitig die Plastizität und die Stabilität der Pulvermasse erhöhen. Solche Verbindungen sind die Anilide organischer Säuren, in denen der Imidwasserstoff durch ein Radikal ersetzt ist, wie dies beispielsweise beim Methylbenzoylanilid und Äthylformanilid der Fall ist. Diese Anilide, ausgenommen solche, welche bei der Verseifung Essigsäure bzw. deren Homologen abzuspalten vermögen, wie Äthyloder Methylacetanilid, erhöhen die Stabilität der Pulver in ganz besonderem Grade, ohne selbst bei größerem Zusatz (5 bis 8 Prozent) die ballistische Leistung der Pulver so ungünstig zu beeinflussen, wie dies bei Vaseline und anderen Stoffen der Fall ist.For a long time, bodies have been added to smokeless gunpowder, which without being ballistic to act, due to their high carbon content, the explosive nature of the To reduce powder. Such an additive is, for example, petroleum jelly. With the Advances in modern manufacturing make additional demands on such additives been asked, especially as far as the increase in stability, the increase in Plasticity, etc. comes into consideration. A body like that could meet these demands Vaseline does not match. We have therefore switched to esters of aromatic or fatty acids: Diamylphthalic acid, diamylsuccinic acid ester, tartaric acid and citric acid ethyl ester, Esters of benzoic acid, etc. All of these bodies, owing to their properties of dissolving nitrocellulose, have the ability to dissolve the To increase the plasticity of smokeless nitroglycerin or pure nitrocellulose powders, it but they lack the property of having a stabilizing effect. According to the present proceedings on the other hand, bodies are used, which at the same time enhance the plasticity and the stability of the Increase powder mass. Such compounds are the anilides of organic acids in which the imide hydrogen is replaced by a radical, as is the case with methylbenzoylanilide, for example and ethylformanilide is the case. These anilides, with the exception of those which are acetic acid or their Able to split off homologues, such as ethyl or methylacetanilide, increase the stability the powder in a very special degree, without even with larger additions (5 to 8 percent) affect the ballistic performance of the powder as unfavorably as it does with petroleum jelly and other substances is the case.
Sehr gut eignen sich diese substituierten Anilide organischer Säuren wegen ihres großen Lösungsvermögens für Nitrocellulose und ihrer leichten Löslichkeit in Äther und Alkohol auch zum Ersatz des Kampfers in Nitrocellulosepulvern, wobei sie noch den Vorteil der geringeren Flüchtigkeit bieten, wodurch natürlich die Stabilität der Pulver gleichfalls günstig beeinflußt wird. . .These substituted anilides of organic acids are very suitable because of their large size Solvent power for nitrocellulose and its easy solubility in ether and alcohol also to replace the camphor in nitrocellulose powders, whereby they still have the advantage of the lower ones Offer volatility, which of course makes the stability of the powder equally favorable being affected. . .
Claims (1)
Publications (1)
Publication Number | Publication Date |
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DE296591C true DE296591C (en) |
Family
ID=550967
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DENDAT296591D Active DE296591C (en) |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE296591C (en) |
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0
- DE DENDAT296591D patent/DE296591C/de active Active
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