DE697949C - Process for the production of hydrocarbon oils from coals, tars, mineral oils, their distillation or extraction products - Google Patents
Process for the production of hydrocarbon oils from coals, tars, mineral oils, their distillation or extraction productsInfo
- Publication number
- DE697949C DE697949C DE1935I0061735 DEI0061735D DE697949C DE 697949 C DE697949 C DE 697949C DE 1935I0061735 DE1935I0061735 DE 1935I0061735 DE I0061735 D DEI0061735 D DE I0061735D DE 697949 C DE697949 C DE 697949C
- Authority
- DE
- Germany
- Prior art keywords
- coals
- tars
- distillation
- oils
- production
- 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.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G1/00—Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal
- C10G1/08—Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal with moving catalysts
- C10G1/086—Characterised by the catalyst used
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Description
Verfahren zur Herstellung von Kohlenwasserstoffölen aus Kohlen, Teeren, Mineralölen, deren Destillations- oder Extraktionsprodukten Im Hauptpatent 695 209 wird vorge$chlagen, bei der Herstellung wertvoller Kohlenwasserstoffe aus Kohlen, Teeren, Mineralölen, deren Destillations- oder Extraktionsprodukten sowie Rückständen durch Behandlung mit Wasserstoff in strömendem Zustand bei erhöhter Temperatur und unter Druck, Halogenide von Kupfer, Silber, Zink, Zinn, Titan, Rhenium, Nickel, Kobalt oder Eisen zusammen mit Halogen oder Halogenwasserstoff als Katalysatoren zu verwenden.A process for the production of hydrocarbon oils, from coal tars, mineral oils, their distillation and extraction products in the main patent 695,209 pre $ is chlagen, in the preparation of valuable hydrocarbons from coals, tars, mineral oils, their distillation and extraction products and residues by treatment with hydrogen in flowing state at elevated temperature and under pressure to use halides of copper, silver, zinc, tin, titanium, rhenium, nickel, cobalt or iron together with halogen or hydrogen halide as catalysts.
Es wurde nun gefunden, daß bei der spaltenden Druckhydrierung der genannten Stoffe während langer Betriebszeiten gleichmäßig hohe Ausbeuten erzielt werden, wenn als Katalysator Zinnammoniumchlorid zusammen mit Halogen oder Halogenwasserstoff verwendet wird.It has now been found that the cracking pressure hydrogenation mentioned substances achieved consistently high yields over long periods of operation if tinammonium chloride is used as a catalyst together with halogen or hydrogen halide is used.
Das Zinnammoniumchlorid kann in gemahlenem oder gelöstem Zustand, gegebenenfalls auch auf Trägern, wie aktiver Kohle, aktivierter Grude, Bimsstein, Bleicherde oder Tonscherben, dem Ausgangsstoff zugegeben werden. Mitunter ist es zweckmäßig, den Katalysator erst nach Aufh.eizung, des Ausgangsstoffes auf Reaktionstemperatur an einer oder mehreren Stellen der Apparatur- zuzuführen. Bei der Verarbeitung hochsiedender oder nicht destillierbarer Ausgangsstoffe, z. B. von Kohlen, kohlenstoffhaltigen Rückständen, Asphalten, Pechen oder Harzen, ist es vorteilhaft, :den Katalysator in fein gemahlenen Zustand in Menge von z. B. o,oi bis io °/o, insbesondere o,oi bis 3 °/o, zuzugeben. Die Ausgangsstoffe werden zweckmäßig zusammen mit dem Katalysator kontinuierlich durch den Reaktionsofen geführt. Dabei kann das Zinnammoniumchlorid entweder in dem zu behandelnden Ausgangsstoff oder in einem asphalt- oder harzfreien Mittelöl suspendiert angewendet werden.The tin ammonium chloride can be ground or dissolved, possibly also on carriers such as active charcoal, activated green, pumice stone, Fuller's earth or potsherds are added to the starting material. Sometimes it is expediently, the catalyst only after heating up the starting material to the reaction temperature to be supplied at one or more points of the apparatus. When processing high-boiling or non-distillable starting materials, e.g. B. of coals, carbonaceous Residues, asphalt, pitch or resins, it is beneficial to: the catalyst in finely ground state in the amount of e.g. B. o, oi to io ° / o, in particular o, oi up to 3 ° / o to be added. The starting materials are expediently used together with the catalyst passed continuously through the reaction furnace. The tin ammonium chloride can be used either in the raw material to be treated or in an asphalt-free or resin-free one Medium oil can be used in suspension.
Der zweite Katalysatorbestandteil Halogen bder Halogenwasserstoff wird dem Ausgangsstoff oder dem Hydriergas vor dem Vorheizen oder nach diesem oder zweckmäßig im Reaktionsgefäß selbst, gegebenenfalls an mehreren Stellen, in. Mengen von o,oi bis 5 °/o zugegeben. Man kann auch Gennische von Halogen mit organischen Halogenverbindungen, z. B. Tetrachlorkohlenstoff, Chloroform, Methyl-, Äthyl-, Methylen- oder Athylenchlorid, -bromid oder -jödid oder Chlor-, Brom- oder jadverbindungen von Benzol oder Toluol, verwenden, Das Halogen kann auch in gelöster Form, z. B. in einem organischen Lösungsmittel, angewendet werden.The second catalyst component is halogen or hydrogen halide is the starting material or the hydrogenation gas before preheating or after this or expediently in the reaction vessel itself, if appropriate in several places, in amounts from o, oi to 5% added. You can also mix halogen with organic Halogen compounds, e.g. B. carbon tetrachloride, chloroform, methyl, ethyl, methylene or ethylene chloride, bromide or iodide or chlorine, Bromine or jad compounds of benzene or toluene, use, the halogen can also be dissolved in Shape, e.g. B. in an organic solvent can be used.
Neben den genannten Katalysatoren können auch andere katalytisch wirkende Metallverbindungen zugegeben werden.In addition to the catalysts mentioned, other catalytically active catalysts can also be used Metal compounds are added.
Die Arbeitsbedingungen sind die für die spaltende Druckhydrierung üblichen. ES kommen Temperaturen von Zoo bis 6oo° und Drucke von 2o at an, zweckmäßig 50 bis Zoo at oder mehr, z. B. 5oo at, in Frage.The working conditions are those customary for the pressure-splitting hydrogenation. ES come temperatures of Zoo to 6oo ° and pressures of at 2o to, suitably at 50 to Zoo or more, eg. B. 5oo at, in question.
Beispiel Fein gemahlene Steinkohle wird mit o,i ofo -Zinnammoniumchlorid gemischt, mit einem aus der gleichen Kohle stammenden Schweröl im Verhältnis i : i angepastet, zusammen mit Wasserstoff unter einem Druck von 250 at in einem gasgeheizten Vorheizer auf q.60° erhitzt und dann in ein 450 mm weites Reaktionsgefäß eingeführt. In dieses Gefäß wird, auf Kohle bezogen, 0,7$ ofo Chlor eingeleitet. Die Reaktionsprodukte werden in einem Abscheidegefäß in leichter flüchtige Anteile, Schweröl und feste Stoffe zerlegt. Der Abbau der Kohle beträgt 96 ofo; das Verflüssigungsprodukt enthält 62 °/o bis 325° siedende Bestandteile.Example Finely ground hard coal is mixed with o, i ofo tin ammonium chloride, made into a paste with a heavy oil from the same coal in the ratio i: i, heated to 60 ° together with hydrogen under a pressure of 250 atm in a gas-heated preheater and then introduced into a 450 mm wide reaction vessel. 0.7% ofo chlorine, based on coal, is introduced into this vessel. The reaction products are broken down in a separator into more volatile components, heavy oil and solid substances. The mining of coal is 96 ofo; the liquefaction product contains 62% to 325 ° boiling components.
Claims (1)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE1935I0061735 DE697949C (en) | 1935-11-06 | 1935-11-06 | Process for the production of hydrocarbon oils from coals, tars, mineral oils, their distillation or extraction products |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE1935I0061735 DE697949C (en) | 1935-11-06 | 1935-11-06 | Process for the production of hydrocarbon oils from coals, tars, mineral oils, their distillation or extraction products |
Publications (1)
Publication Number | Publication Date |
---|---|
DE697949C true DE697949C (en) | 1940-10-30 |
Family
ID=7195523
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE1935I0061735 Expired DE697949C (en) | 1935-11-06 | 1935-11-06 | Process for the production of hydrocarbon oils from coals, tars, mineral oils, their distillation or extraction products |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE697949C (en) |
-
1935
- 1935-11-06 DE DE1935I0061735 patent/DE697949C/en not_active Expired
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