US1844998A - Production of valuable hydrocarbons of low boiling point - Google Patents
Production of valuable hydrocarbons of low boiling point Download PDFInfo
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- US1844998A US1844998A US263581A US26358128A US1844998A US 1844998 A US1844998 A US 1844998A US 263581 A US263581 A US 263581A US 26358128 A US26358128 A US 26358128A US 1844998 A US1844998 A US 1844998A
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- production
- boiling point
- hydrogen
- oxid
- low boiling
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- 238000009835 boiling Methods 0.000 title description 15
- 229930195733 hydrocarbon Natural products 0.000 title description 10
- 150000002430 hydrocarbons Chemical class 0.000 title description 10
- 238000004519 manufacturing process Methods 0.000 title description 8
- 239000003054 catalyst Substances 0.000 description 23
- 229910052751 metal Inorganic materials 0.000 description 19
- 239000002184 metal Substances 0.000 description 19
- 239000001257 hydrogen Substances 0.000 description 15
- 229910052739 hydrogen Inorganic materials 0.000 description 15
- 238000006243 chemical reaction Methods 0.000 description 13
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 11
- 239000000463 material Substances 0.000 description 11
- 239000004411 aluminium Substances 0.000 description 10
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 10
- 229910052782 aluminium Inorganic materials 0.000 description 10
- 238000000034 method Methods 0.000 description 10
- 239000003921 oil Substances 0.000 description 9
- 239000002480 mineral oil Substances 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- 230000001427 coherent effect Effects 0.000 description 5
- 230000008021 deposition Effects 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 4
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- 229910052804 chromium Inorganic materials 0.000 description 4
- 239000011651 chromium Substances 0.000 description 4
- VNNRSPGTAMTISX-UHFFFAOYSA-N chromium nickel Chemical compound [Cr].[Ni] VNNRSPGTAMTISX-UHFFFAOYSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 230000001066 destructive effect Effects 0.000 description 4
- 150000002431 hydrogen Chemical class 0.000 description 4
- 150000002739 metals Chemical class 0.000 description 4
- 235000010446 mineral oil Nutrition 0.000 description 4
- 230000000737 periodic effect Effects 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 229910052709 silver Inorganic materials 0.000 description 4
- 239000004332 silver Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 239000011269 tar Substances 0.000 description 4
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 3
- XHCLAFWTIXFWPH-UHFFFAOYSA-N [O-2].[O-2].[O-2].[O-2].[O-2].[V+5].[V+5] Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[V+5].[V+5] XHCLAFWTIXFWPH-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 229910045601 alloy Inorganic materials 0.000 description 3
- 239000000956 alloy Substances 0.000 description 3
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 3
- 239000004327 boric acid Substances 0.000 description 3
- 230000003197 catalytic effect Effects 0.000 description 3
- 239000008187 granular material Substances 0.000 description 3
- 238000005984 hydrogenation reaction Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 229910052748 manganese Inorganic materials 0.000 description 3
- 239000011572 manganese Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 210000002268 wool Anatomy 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 229910052793 cadmium Inorganic materials 0.000 description 2
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- PQQKPALAQIIWST-UHFFFAOYSA-N oxomolybdenum Chemical compound [Mo]=O PQQKPALAQIIWST-UHFFFAOYSA-N 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 229910002007 uranyl nitrate Inorganic materials 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- KYARBIJYVGJZLB-UHFFFAOYSA-N 7-amino-4-hydroxy-2-naphthalenesulfonic acid Chemical compound OC1=CC(S(O)(=O)=O)=CC2=CC(N)=CC=C21 KYARBIJYVGJZLB-UHFFFAOYSA-N 0.000 description 1
- 229910000851 Alloy steel Inorganic materials 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 241000543381 Cliftonia monophylla Species 0.000 description 1
- 241001676573 Minium Species 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- 229910052770 Uranium Inorganic materials 0.000 description 1
- WZECUPJJEIXUKY-UHFFFAOYSA-N [O-2].[O-2].[O-2].[U+6] Chemical compound [O-2].[O-2].[O-2].[U+6] WZECUPJJEIXUKY-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 239000003463 adsorbent Substances 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical group [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- -1 aluminium Chemical compound 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 239000002802 bituminous coal Substances 0.000 description 1
- 239000003575 carbonaceous material Substances 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000011280 coal tar Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- XTVVROIMIGLXTD-UHFFFAOYSA-N copper(II) nitrate Chemical compound [Cu+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O XTVVROIMIGLXTD-UHFFFAOYSA-N 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical compound [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- PPNAOCWZXJOHFK-UHFFFAOYSA-N manganese(2+);oxygen(2-) Chemical compound [O-2].[Mn+2] PPNAOCWZXJOHFK-UHFFFAOYSA-N 0.000 description 1
- 229910001092 metal group alloy Inorganic materials 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- NQLVQOSNDJXLKG-UHFFFAOYSA-N prosulfocarb Chemical compound CCCN(CCC)C(=O)SCC1=CC=CC=C1 NQLVQOSNDJXLKG-UHFFFAOYSA-N 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- JFALSRSLKYAFGM-UHFFFAOYSA-N uranium(0) Chemical compound [U] JFALSRSLKYAFGM-UHFFFAOYSA-N 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 1
- 229910001935 vanadium oxide Inorganic materials 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 230000003245 working effect Effects 0.000 description 1
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
Definitions
- a parsuitable catalysts are the oxids or compounds ticular advantage of the catalysts according furnishing the same under the conditions of to the present invention is also their hi h Working of theelements from groups 3 to 7 heat-conducting capacity which enables t 39 of the periodic system, such as uranium oxid, otherwise readily occurring local superhea Vanadium oxid, chromic acid anhydride, 'ing within the reaction zone to be more. or Y manganese oxid, molybdenum oxid, boric less completely prevented.
- the said catalyst may be preapplied to the metal and surpasses that of the pared by treating the' metals, such as comsubstance applied when the latter is used flipal granular aluminium, preferably alone or on non metallic carriers such as charafter etclnng, for example, with hydrochlocoal, pumicestone and the like.
- the aforesaid catalysts are very well adapted for the production of low-boiling products of the benzine type, and are also very suitable for dehydrogenating hydrocarbons, tars, mineral oils, their distillation, conversion, extraction products and the like, or for converting the same into aromatic hydrocarbons.
- the working temperatures are generally higher for example 550 to 650 centrigrade than those necessary for the production of benzines.
- the methods already known for converting coals, tars, mineral oils and the like into valuable hydrocarbons may also be applied in connection with the present process, for example such as the operation in a c tun system, prepurifying the gases, puri ying the gases in circulation, separatin the reaction products by cooling and/or y adsorbent masses or by washing with suitable liquids, means for heating the reaction components and avoiding, in those parts of the apparatus coming into contact with the hot reaction components, the presence of substances which promote the deposition of carbon or the ormation of methane this being achieved, for example, by lining the apparatus with irll1 ⁇ 1minium,-high-grade steel alloys and the
- the operations may be conducted in such a way that the hydrocarbons or the like are brought into reaction in the state of vapor wherein the operation is preferably carried out with a large excess of hydrogen, or the hydrocarbons and the like may be brought into reaction, wholly or partially in a liquid condition, in the presence of the'above de-- scribed catalysts.
- reaction components may also be ad- I mitted into the reaction chamber in the form of mist or in an atomized condition, or they may be in thin la ers, or the gases may be introduced into t e substances under treatment througha porous stratum.
- reaction components may also be sub- 0 jected to repeated treatment by heat, .with or without the presence of hydrogen or gases giving off hydrogen.
- Example 1 A mineral oil fraction boiling above 270 an aluminium-lined pressure vessel containing a catalyst consisting of fine granules of aluminium activiated with 1 to 2 per cent of uranyl nitrate with the aid of h drochloric acid. The nitrate is converted un er the 0011-. ditions of working. In this way an oil is obtained consisting to the extent of 80 per cent and over of benzines boiling up to 200 centigrade. Similar action is exerted by a catalyst prepared by activating aluminium with boric acid.
- Example 2 Elwerath oil, boiling at above 300 centigrade, and mixed with an equal amount of an ash-free middle oil, is forced, with the aid of hydrogen, through an aluminium-lined pressure vessel at 450 centigrade.
- suitable spiral ribbons of aluminium are arranged, so that the oil takes a spiral course.
- the aluminium parts are previously activated with hydrochloric acid and boric acid. In a single passage, 40 per cent and more of the crude oil is converted into benzine, and further large proportions into middle oil.
- the yield obtained in a single passage is generally somewhat lower, and moreoverthe resulting product is partially unsaturated.
- reaction product contains 30 per cent and more of aromatic hydrocarbons.
- Example 4 A'middle-oil fraction from bituminous coal tar, boiling between 200 and 350 centigrade is passed in a current of hydrogen at 450 centigrade and 200 atmospheres pressure over a-catalyst consisting of zinc wool activated by evaporating an aqueous suspension of. blue molybdenum oxid containing the zinc wool. Even in a single passage, more than 50 per' cent of the initial materials is converted into benzine, and complete conversion into benzine is effected by further treatment in circulation.
- middleoil may also be replaced by corresponding mineraloils.
- middle Example 5 A brown-coal-tar oil boiling substantially above 250 C. is passed at a temperature of 460 C. and at a pressure of 200 atmospheres together with hydrogen over a catalyst consisting of small compact aluminium granules on which 1 per cent of metallic silicon, and
- a process for the production of valuable hydrocarbons of low boiling point from a distillable bituminous material which comprises subjecting said material to a heat treatment at a temperature of between 450 to 650 C. and at a pressure of the order of the pressures employed in destructive hydrogenation, in the presence of a catalyst comprising small quantities of an oxid of a 'metal of groups 3 to 7 of the periodic. system deposited on ametal, which is in a dense coherent state under the conditions of working and which, under said conditions, does not cause deposition of carbon, selected from the class consisting of aluminium, chromiumnickel, silver, manganese and chromium.
- a process for the production of valuable hydrocarbons of low boiling point from a distillable bituminous material which comprises subjecting said material to a heat treatment with hydrogen at a temperature of between 450 and 650 C. and ata pressure of the order/of the pressures employed in destructive hydrogenation, in the presence of a catalyst comprising small quantities of an oxid of a metal of groups 3 to 7 of the periddic system, deposited on a metal, which'is in a dense coherent state under the conditions of work ing and under said conditions does not cause deposition of'carbon, selected from the class consisting of aluminium, chromium-nickel, silver, manganese and chromium.
- a metal which is in a dense coherent state under the conditions of working and which, under said conditions, does not cause deposition of carbon, selected from the class consisting of aluminium, chromiumnickel, silver, manganese and chromium, by
- a process for the roduction of valuable hydrocarbons of lowv oiling point from a mineral oil fraction boiling above 270 C. which comprises passing said mineral oil fraction, with an excess of hydrogen, at a temperature of about 450 C. and a pressure of 200 atmospheres, over, a catalyst comprising' an oxid of uranium deposited on granules of aluminium.
- a process for the production of valuable hydrocarbons of low boiling point from a dis-, tillable bituminous material which comprises subjectingsaid material to a heat treatment with hydrogen at a temperature between 450 and 650. C. and at a. pressure of about 200 atm spheres in the presence of a catalyst compr sing small quantities of an oxid of a metal of group 6 of the periodic system deposited on chromium-nickel which is in a' dense coherent state, under the conditions of working.
- a process for the production of valuable distillable bituminous material which comprises subj ecting said material to a heat treatmentwith hydrogen at a temperature "between 450 and.650 C. and a pressure of the order of pressures employed in destructive hydrogenation, in the presence of a catalyst hydrocarbons of low boiling point from a.
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- 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
Description
Patented Feb. 16, 1932 1,844,998
UNITED ST TES PATENT OFFICE BUDOLF wIE'rznL, on LUDWIGSEAFEN-ON-THE-BHINE, Aim connan rr'nunnnnn, or OPPAU, GERMANY, nssmuons no I. G. r'nnnnnmnus'rnm anrrmrensnnnscnnrr, or FRANKFQRT-ON-THE-MAIN, GERMANY, A CORPORATION or GERMANY PRODUCTION OF VALUABLE HYDBOCAKBONS OF LOW BOILING POINT No Drawing. Application filed l iarch 21, 1928, Serial-Ho. 263,581, and in Germany March 31, 1927.
It is already known that valuable liquid uranyl nitrate is converted into the oxid by h drocarbons may be produced from distillsplitting off of oxids of nitrogen. 'The depa le carbonaceous material, such as any osition onto the metal may also be effected kind of coals, tars, mineral oils, their disin any other way, such as by evaporating a tillation, conversion and extraction products, salt solution in the presence of the fragments 65' residues, and the like, by heating, especially of metal, by electro-chemical means or also in contact with hydrogen or gases giving off by intimately mixing in a ball mill the metal hydrogen which are equivalents for the purgranules, which may be etched beforehand, pose of the present invention, to high temwith small quantities of moistened vanadium peratures, under pressure and by the use of oxidand the like. It may also s'ometimesbe catalysts. -.of advantage to render catalytic, by activa- We have now found that it is particularly tion in the above manner, the metal walls, advantageous to employ for this process catpipes, stirring or paddle devices and the like alysts which are deposited in small quansituated in the reaction zone in which caseit 15 tities on, metals or metallic alloys which do is..not necessary that additional catalysts be not meltunder the conditions of working. employed, since the walls themselvesiserveas These metals or alloys as for example alucatalysts, but additional catalysts may of minium, silver,'manganese, chromium, chrocourse be added. This last procedure withmium nickel, silicon and the like, are prefout the employment of additional catalysts erablyused in aform presenting a dense and may be of importance, when using initial coherent surface, such for example as grains, materials containing ash liable to"produce balls, chips, ribbons, wire, wool and the like. obstructions and the deposition of coke when A great variety of substances may be used passed through. a catalyst layer. These last as catalysts, the amount of which need often drawbacks may also be more or less elimibe merely fractions of one per cent of the nated by the employment of stirring mechaamount of metal or alloy used. Particularly nisms or of a high velocity of flow. A parsuitable catalysts are the oxids or compounds ticular advantage of the catalysts according furnishing the same under the conditions of to the present invention is also their hi h Working of theelements from groups 3 to 7 heat-conducting capacity which enables t 39 of the periodic system, such as uranium oxid, otherwise readily occurring local superhea Vanadium oxid, chromic acid anhydride, 'ing within the reaction zone to be more. or Y manganese oxid, molybdenum oxid, boric less completely prevented.
' I acid, and the like,'either alone or in admix- In many instances the metal or alloy not ture with one another or with other subonly acts as a carrier, but may also possess stances. -Other substances eiiective as catacatalytic properties or acquire same by realysts comprise oxids or compounds furnishson of the treatment herein described. Many ing the same of platinum, ruthenium, cobalt, metals, such as aluminium, ossess a certain gold, cadmium, and the like. A mixture of catalytic capacity, especia y after being iron oxid, copper nitrate and cadmium nietched with acids and the like. This capacity trate may be mentioned as examples of such is considerably increased by the substances compounds. The said catalyst may be preapplied to the metal and surpasses that of the pared by treating the' metals, such as comsubstance applied when the latter is used mercial granular aluminium, preferably alone or on non metallic carriers such as charafter etclnng, for example, with hydrochlocoal, pumicestone and the like. Not only the ric acid or mercuric chlorid, with, preferably proportion of substances of lowboiling point acidified, solutions of salts of catalytic eleproduced in a single passage is increased ments, as for example by moistening with thereby but also the output capacity, Inthe 7 solutions of uranyln1trate,boric acid and the manner herein described it is easy to convert like. The said compounds furnish oxids 80 per cent and more of a petroleum fraction 50 under the conditions of working. ,Thus of a boiling point above 300 centigrade by passing it only once with hydrogen over the catalyst under a pressure of the order of pressures employed in destructive h dro enation and at about 450 centigrade into enzines boiling below 200 centigrade, even when working continuously f0 weeks with the same catalyst. I
The aforesaid catalysts are very well adapted for the production of low-boiling products of the benzine type, and are also very suitable for dehydrogenating hydrocarbons, tars, mineral oils, their distillation, conversion, extraction products and the like, or for converting the same into aromatic hydrocarbons. In such cases, the working temperatures are generally higher for example 550 to 650 centrigrade than those necessary for the production of benzines.
The methods already known for converting coals, tars, mineral oils and the like into valuable hydrocarbons, may also be applied in connection with the present process, for example such as the operation in a c clic system, prepurifying the gases, puri ying the gases in circulation, separatin the reaction products by cooling and/or y adsorbent masses or by washing with suitable liquids, means for heating the reaction components and avoiding, in those parts of the apparatus coming into contact with the hot reaction components, the presence of substances which promote the deposition of carbon or the ormation of methane this being achieved, for example, by lining the apparatus with irll1{1minium,-high-grade steel alloys and the The operations may be conducted in such a way that the hydrocarbons or the like are brought into reaction in the state of vapor wherein the operation is preferably carried out with a large excess of hydrogen, or the hydrocarbons and the like may be brought into reaction, wholly or partially in a liquid condition, in the presence of the'above de-- scribed catalysts.
The reaction components may also be ad- I mitted into the reaction chamber in the form of mist or in an atomized condition, or they may be in thin la ers, or the gases may be introduced into t e substances under treatment througha porous stratum.
The reaction components may also be sub- 0 jected to repeated treatment by heat, .with or without the presence of hydrogen or gases giving off hydrogen.
The following examples will further illustrate the nature of the said invention which however is not limited thereto.
, Example 1 A mineral oil fraction boiling above 270 an aluminium-lined pressure vessel containing a catalyst consisting of fine granules of aluminium activiated with 1 to 2 per cent of uranyl nitrate with the aid of h drochloric acid. The nitrate is converted un er the 0011-. ditions of working. In this way an oil is obtained consisting to the extent of 80 per cent and over of benzines boiling up to 200 centigrade. Similar action is exerted by a catalyst prepared by activating aluminium with boric acid.
Example 2 Example 3 Elwerath oil, boiling at above 300 centigrade, and mixed with an equal amount of an ash-free middle oil, is forced, with the aid of hydrogen, through an aluminium-lined pressure vessel at 450 centigrade. In order to obtain a high velocity of flow, suitable spiral ribbons of aluminium are arranged, so that the oil takes a spiral course. The aluminium parts are previously activated with hydrochloric acid and boric acid. In a single passage, 40 per cent and more of the crude oil is converted into benzine, and further large proportions into middle oil.
If the initial material is forced through the apparatus without the aid of hydrogen, the yield obtained in a single passage is generally somewhat lower, and moreoverthe resulting product is partially unsaturated.
f a working temperature of about 600 centigrade or higher be employed, the reaction product contains 30 per cent and more of aromatic hydrocarbons.
Example 4 A'middle-oil fraction from bituminous coal tar, boiling between 200 and 350 centigrade is passed in a current of hydrogen at 450 centigrade and 200 atmospheres pressure over a-catalyst consisting of zinc wool activated by evaporating an aqueous suspension of. blue molybdenum oxid containing the zinc wool. Even in a single passage, more than 50 per' cent of the initial materials is converted into benzine, and complete conversion into benzine is effected by further treatment in circulation.
The said middleoil may also be replaced by corresponding mineraloils. such as middle Example 5 A brown-coal-tar oil boiling substantially above 250 C. is passed at a temperature of 460 C. and at a pressure of 200 atmospheres together with hydrogen over a catalyst consisting of small compact aluminium granules on which 1 per cent of metallic silicon, and
- 0.1 per centof vanadium oxid is deposited .in a fine state of division by treatment with a solution of a salt of vanadium oxide. 'If the oil is passed over the catalyst only once, an oil is obtained per cent of which boils below 250 C.
What we claim is: v
1. A process for the production of valuable hydrocarbons of low boiling point from a distillable bituminous material which comprises subjecting said material to a heat treatment at a temperature of between 450 to 650 C. and at a pressure of the order of the pressures employed in destructive hydrogenation, in the presence of a catalyst comprising small quantities of an oxid of a 'metal of groups 3 to 7 of the periodic. system deposited on ametal, which is in a dense coherent state under the conditions of working and which, under said conditions, does not cause deposition of carbon, selected from the class consisting of aluminium, chromiumnickel, silver, manganese and chromium.
2. A process for the production of valuable hydrocarbons of low boiling point from a distillable bituminous material which comprises subjecting said material to a heat treatment with hydrogen at a temperature of between 450 and 650 C. and ata pressure of the order/of the pressures employed in destructive hydrogenation, in the presence of a catalyst comprising small quantities of an oxid of a metal of groups 3 to 7 of the periddic system, deposited on a metal, which'is in a dense coherent state under the conditions of work ing and under said conditions does not cause deposition of'carbon, selected from the class consisting of aluminium, chromium-nickel, silver, manganese and chromium.
comprising small quantities'of an oxid of a metal of roups 3 to 7 of the periodic system,
deposite on a metal, which is in a dense coherent state under the conditions of working and which, under said conditions, does not cause deposition of carbon, selected from the class consisting of aluminium, chromiumnickel, silver, manganese and chromium, by
treating said metal with an acidified solution of a-salt of-a metal of the 3rd to 7th groups of the periodicsystem, which salt yields the said oxid under the conditions of working.
4. A process for the roduction of valuable hydrocarbons of lowv oiling point from a mineral oil fraction boiling above 270 C. which comprises passing said mineral oil fraction, with an excess of hydrogen, at a temperature of about 450 C. and a pressure of 200 atmospheres, over, a catalyst comprising' an oxid of uranium deposited on granules of aluminium.
5. A process for the production of valuable hydrocarbons of low boiling point from a dis-, tillable bituminous material which comprises subjectingsaid material to a heat treatment with hydrogen at a temperature between 450 and 650. C. and at a. pressure of about 200 atm spheres in the presence of a catalyst compr sing small quantities of an oxid of a metal of group 6 of the periodic system deposited on chromium-nickel which is in a' dense coherent state, under the conditions of working.
6. The process as defi ned in claim 3 wherein the conversion is effected in the presence of an excess of hydrogen.
. thereon. a
In testimony whereof we have hereunto set our hands.
' RUDOLF WIETZEL. v
CONRAD PFAUNDLER.
.. 3. A process for the production of valuable distillable bituminous material which comprises subj ecting said material to a heat treatmentwith hydrogen at a temperature "between 450 and.650 C. and a pressure of the order of pressures employed in destructive hydrogenation, in the presence of a catalyst hydrocarbons of low boiling point from a.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE1844998X | 1927-03-31 |
Publications (1)
Publication Number | Publication Date |
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US1844998A true US1844998A (en) | 1932-02-16 |
Family
ID=7745738
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US263581A Expired - Lifetime US1844998A (en) | 1927-03-31 | 1928-03-21 | Production of valuable hydrocarbons of low boiling point |
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Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2436970A (en) * | 1944-12-28 | 1948-03-02 | Standard Oil Dev Co | Ferrous metal supported zinc oxide bismuth oxide catalyst |
US2441966A (en) * | 1942-12-16 | 1948-05-25 | Nat Agrol Company Inc | Dehydration process and catalyst |
US2507496A (en) * | 1947-12-31 | 1950-05-16 | Houdry Process Corp | Molded contact masses |
US2524357A (en) * | 1947-02-12 | 1950-10-03 | Socony Vacuum Oil Co Inc | Heat-resistant paint |
US2548159A (en) * | 1947-01-17 | 1951-04-10 | Shell Dev | Group viii silicate catalyst on nonsiliceous support |
US2912419A (en) * | 1955-03-08 | 1959-11-10 | Standard Oil Co | Hydrocarbon polymerization (group 5a metal oxide and air3 initiator) |
US3140148A (en) * | 1961-07-26 | 1964-07-07 | Lawrence J E Hofer | Method of treating exhaust gases with urania-containing catalysts |
US3923634A (en) * | 1974-03-22 | 1975-12-02 | Mobil Oil Corp | Liquefaction of coal |
US4033852A (en) * | 1975-06-26 | 1977-07-05 | Polygulf Associates | Process for treating coal and products produced thereby |
-
1928
- 1928-03-21 US US263581A patent/US1844998A/en not_active Expired - Lifetime
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2441966A (en) * | 1942-12-16 | 1948-05-25 | Nat Agrol Company Inc | Dehydration process and catalyst |
US2436970A (en) * | 1944-12-28 | 1948-03-02 | Standard Oil Dev Co | Ferrous metal supported zinc oxide bismuth oxide catalyst |
US2548159A (en) * | 1947-01-17 | 1951-04-10 | Shell Dev | Group viii silicate catalyst on nonsiliceous support |
US2524357A (en) * | 1947-02-12 | 1950-10-03 | Socony Vacuum Oil Co Inc | Heat-resistant paint |
US2507496A (en) * | 1947-12-31 | 1950-05-16 | Houdry Process Corp | Molded contact masses |
US2912419A (en) * | 1955-03-08 | 1959-11-10 | Standard Oil Co | Hydrocarbon polymerization (group 5a metal oxide and air3 initiator) |
US3140148A (en) * | 1961-07-26 | 1964-07-07 | Lawrence J E Hofer | Method of treating exhaust gases with urania-containing catalysts |
US3923634A (en) * | 1974-03-22 | 1975-12-02 | Mobil Oil Corp | Liquefaction of coal |
US4033852A (en) * | 1975-06-26 | 1977-07-05 | Polygulf Associates | Process for treating coal and products produced thereby |
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