US1317868A - Of hxkdto mnatahtb - Google Patents
Of hxkdto mnatahtb Download PDFInfo
- Publication number
- US1317868A US1317868A US1317868DA US1317868A US 1317868 A US1317868 A US 1317868A US 1317868D A US1317868D A US 1317868DA US 1317868 A US1317868 A US 1317868A
- Authority
- US
- United States
- Prior art keywords
- chlorin
- products
- unsaturated
- hydrocarbons
- conditions
- 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 - Lifetime
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- 239000000047 product Substances 0.000 description 80
- WGSLWEXCQQBACX-UHFFFAOYSA-N Chlorin Chemical compound C=1C(C=C2)=NC2=CC(C=C2)=NC2=CC(C=C2)=NC2=CC2=NC=1CC2 WGSLWEXCQQBACX-UHFFFAOYSA-N 0.000 description 58
- 150000002430 hydrocarbons Chemical class 0.000 description 50
- 239000000463 material Substances 0.000 description 44
- 238000000034 method Methods 0.000 description 38
- 239000003208 petroleum Substances 0.000 description 30
- 150000001336 alkenes Chemical class 0.000 description 26
- 239000011780 sodium chloride Substances 0.000 description 20
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 18
- 150000002148 esters Chemical class 0.000 description 18
- 239000003350 kerosene Substances 0.000 description 16
- 150000007524 organic acids Chemical class 0.000 description 14
- 239000003153 chemical reaction reagent Substances 0.000 description 12
- 229910052783 alkali metal Inorganic materials 0.000 description 10
- -1 alkali metal salt Chemical class 0.000 description 10
- 150000004035 chlorins Chemical class 0.000 description 10
- 238000005336 cracking Methods 0.000 description 10
- 239000007788 liquid Substances 0.000 description 10
- 150000003839 salts Chemical class 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- PPKPKFIWDXDAGC-IHWYPQMZSA-N (Z)-1,2-dichloroprop-1-ene Chemical class C\C(Cl)=C\Cl PPKPKFIWDXDAGC-IHWYPQMZSA-N 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 8
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 8
- 239000003921 oil Substances 0.000 description 8
- 239000004215 Carbon black (E152) Substances 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N HCl Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 238000005660 chlorination reaction Methods 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 238000004508 fractional distillation Methods 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 229910052742 iron Inorganic materials 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- PGMYKACGEOXYJE-UHFFFAOYSA-N Amyl acetate Chemical compound CCCCCOC(C)=O PGMYKACGEOXYJE-UHFFFAOYSA-N 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 229940072049 amyl acetate Drugs 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-M benzoate Chemical compound [O-]C(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-M 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000012320 chlorinating reagent Substances 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 230000000875 corresponding Effects 0.000 description 2
- 238000006298 dechlorination reaction Methods 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 150000001993 dienes Chemical class 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- 239000000295 fuel oil Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 230000001788 irregular Effects 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-M methanoate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- 238000009738 saturating Methods 0.000 description 2
- VMHLLURERBWHNL-UHFFFAOYSA-M sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 2
- 239000001632 sodium acetate Substances 0.000 description 2
- 235000017281 sodium acetate Nutrition 0.000 description 2
- 241000894007 species Species 0.000 description 2
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/10—Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides with ester groups or with a carbon-halogen bond
- C07C67/11—Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides with ester groups or with a carbon-halogen bond being mineral ester groups
Definitions
- splittingoperatio ing oil vapors were maintained at a temperathe latter were pumped UNITED. STATES PATENT ormon. j
- This invention relates to'a process of making derivatives of gasolene and relates in particular to the treatment of gasolene like material obtainedthrough the heat decomposition of kerosene or heavier oil and which contain large amounts of unsaturated materials and in chlorinating such unsaturated products to form dichlor compounds or higher chlorinated bodies as the case may be and furthermore in converting such chlorinated bodies by contact-with alkali material into dechlorinated bodies of acter,
- the unsaturated hydrocarbon material is preferably prepared by passing a saturated hydrocarbon such-as kerosenethrough a heatedtube, as for example, an iron pipe which is preferably heated to 425 or 480 C.
- a saturated hydrocarbon such-as kerosenethrough a heatedtube, as for example, an iron pipe which is preferably heated to 425 or 480 C.
- fragments of contact material such as nickel plated fragments of iron of irregular shape.
- the gravity of the the heated tube was 1 lighter than the of products lighter and heavier than keroof bodies ap material was distilled and the product collected below 150 C. ,was redistilled in an ordinary distilling apparatus equipped with a rectifying column tions were obtained.
- the dechlorination may take place with replacement of the chlorih by some other element or radical as for example by an acid radical to form an ester.
- the chlorinated compounds formed by treatment with chlorin or by union with hydrochloric acid or in any other suitable way may be treated with sodium acetate or other salt of acetic acid toform amyl acetate and other esters according to the nature of the materials used.
- the salts of other organic acids such as formate, benzoate, etc, similar corresponding esters can be secured.
- these same esters and other complex esters may be secured from thechlorination prod ucts obtained by direct chlorination.
- chlorin in the cold r oo ' 785,855 filed troleum oil through a heated form an iodin number not less than 30 but preferably is higher and may be in excess of 100.
- the products of higher iodin number absorb chlorin with avidity and dichlor compounds are formed when a single double bond is present while in the case of diolefins and the like the chlorination may progress further as desired.
- What I claim is l 1.
- the process of making derivatives of hydrocarbons which comprises passing petroleum oil through a heated zone maintained at a decomposing temperature under such conditions as to form lighter products of unsaturated character, in combining these unsaturated products, after fractional distillation, with chlorin, in reacting on the chlorinated body with an alkali metal salt of an organic acid and in separating the ester formed from other products of reaction.
- hydrocarbons which comprises cracking a petroleum oil in a heated-zone under such conditions as'to form lighter products of an unsaturated character, in chlorinatin" these unsaturated. products with free chlorin and in subsequently replacing the chlorin.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Fire-Extinguishing Compositions (AREA)
Description
,ing the splittingoperatio ing oil vapors were maintained at a temperathe latter were pumped UNITED. STATES PATENT ormon. j
GARLETON ELLIS, or MONTCLAIR, NEW JERSEY, ASSIGNOR TO ELLIS-FOSTER COMPANY, A CORPORATION on NEW JERSEY.
PROQESS OF MAKING DERIVATIVES 0F PETROLEUM-HYDROGARBONS.
No Drawing. Original application filed August 21, 1913, Serial No. 785,855.
filed September 19, 1916, Serial No. 121,010.
To all whom it may concern: 7
Be it known that I, CARLETON ELLIS, a citizen of the UnitedStates, and a resident of Montclair, in the county of Essex and State of New Jersey, have invented certain new and useful Improvements in Processes of Making Derivatives of Petroleum-Hydrocarbons, of which the following is a speci' fication.
This invention relates to'a process of making derivatives of gasolene and relates in particular to the treatment of gasolene like material obtainedthrough the heat decomposition of kerosene or heavier oil and which contain large amounts of unsaturated materials and in chlorinating such unsaturated products to form dichlor compounds or higher chlorinated bodies as the case may be and furthermore in converting such chlorinated bodies by contact-with alkali material into dechlorinated bodies of acter,
The unsaturated hydrocarbon material is preferably prepared by passing a saturated hydrocarbon such-as kerosenethrough a heatedtube, as for example, an iron pipe which is preferably heated to 425 or 480 C.
and in some cases maybe filled with fragments of contact material such as nickel plated fragments of iron of irregular shape.
' cases water maybe introduced Also in some with the kerosene or other raw 011 used and allowed to react with the hydrocarbons dur- The product obtained by such heat treatmentor other suitable heat treatment of a more or less similar ch'aracter may then be separated into its lighter and heavier parts by fractional condensation and if desired the fractions obtained in this or other manner are subjected to fractionaldistillation to obtain particularly certain relatively lowboilin fractions of an unsaturated character. Tor example kerosene of 42 passed through a tube of considerable length heated to such a temperature that. the escaptureof about 4655; (3., which required a temperature about the tube of approximately 630 C. The vapors were passed through an air condenser, then through a water con-' denser and finally the gases escaping from through heavy oil in order to remove some of the entrained Specification of Letters Patent.
' original kerosene.
sene with a certain amount proximatlng kerosene in boiling point. This a useful c'har- B., was
foregoing heat treatment has in its preferred Patented Oct. 7 1919. Divided and this application condensable material. product as drawn from about 43 B., or.only
The gravity of the the heated tube was 1 lighter than the of products lighter and heavier than keroof bodies ap material was distilled and the product collected below 150 C. ,was redistilled in an ordinary distilling apparatus equipped with a rectifying column tions were obtained.
and the following frac-- It consisted of a mixture Fractions Percentage Iodin Per cent.
. ficient to split off their chlorin in large measure forming different varieties of unsaturated bodies or other useful material.
'The dechlorination may take place with replacement of the chlorih by some other element or radical as for example by an acid radical to form an ester. Thus the chlorinated compounds formed by treatment with chlorin or by union with hydrochloric acid or in any other suitable way may be treated with sodium acetate or other salt of acetic acid toform amyl acetate and other esters according to the nature of the materials used. By employing the salts of other organic acids such as formate, benzoate, etc, similar corresponding esters can be secured. These same esters and other complex esters may be secured from thechlorination prod ucts obtained by direct chlorination.
The gasolene material obtained by the liquid the Chlorin-' by volume.! number.
chlorin in the cold r oo ' 785,855, filed troleum oil through a heated form an iodin number not less than 30 but preferably is higher and may be in excess of 100. As stated the products of higher iodin number absorb chlorin with avidity and dichlor compounds are formed when a single double bond is present while in the case of diolefins and the like the chlorination may progress further as desired.
This application is a division of Serial No. Aug. 21, 1913, entitled Motor fuel and process of making same.
What I claim is l 1. The process of making derivatives of hydrocarbons which comprises passing petroleum oil through a heated zone maintained at a decomposing temperature under such conditions as to form lighter products of unsaturated character, in combining these unsaturated products, after fractional distillation, with chlorin, in reacting on the chlorinated body with an alkali metal salt of an organic acid and in separating the ester formed from other products of reaction.
2. The process of making derivatives of hydrocarbons which comprises passing petroleum oil through a heated zone maintained at a decomposing temperature under such conditions as to form lighter products of unsaturated character, in reacting on these unsaturated products with a chlorinating agent, in reacting on the chlorinated body so formed, with an alkali metal salt of an organic acid and in separating the ester formed from other products of reaction.
3. The process of making derivatives of. hydrocarbons which comprises passing petube main tained at a decomposing temperature under such conditions as to form very light products of unsaturated character, in combining these unsaturated products with chlorin, in reacting on the chlorinated body with a salt of an organic acid and in separating the ester formed from other products of reaction.
1. The process of making derivatives of hydrocarbons which comprises passing petroleum oil through a heated zone maintained at'a decomposing temperature under such conditions as to form lighter products of unsaturated character, in combining these unsaturated products with chlorin, in reacting on the chlorinated body with a salt of acetic acid and in separating the ester formed from other products of reaction.
5. The process of making derivatives of hydrocarbons which comprises bringing petroleum oil into a heated zone maintained at a decomposingtemperature under such conditions as to form lighter products of unsaturated character, in combining the resulting' olefin products with chlorin and in reacting on the chlorinated body with an acetate.
6. The process of making derivatives of hydrocarbons which comprises passing petroleum oil with water through a heated zone maintained at a decomposing temperature under such conditions as to form lighter products of unsaturated character, in combining the resulting olefin products, with chlorin and in reacting on the chlorinated body with an alkali metal salt of an organic acid.
7. The process of making derivatives of hydrocarbons which comprises passing petroleum oil with water through a heated tube maintained at a decomposing temperature under such conditions as to form lighter products of unsaturated character, in combining the resulting olefin products with chlorin and in reacting with the chlorinated body with an alkali metal salt of an organic acid.
8. The process of making derivatives of hydrocarbons which comprises passing petroleum oil with water through a heated zone maintained at a decomposing temperature under such conditions as to form lighter products of unsaturated character, in G011.- bining the resulting olefin products with chlorin, and in reacting with the chlorinated body with a salt of an organic acid.
9. The process of making derivatives of hydrocarbons which comprises passing petroleum oil through a heated zone maintained at a decomposing temperature under such conditions as to form light products of unsaturated character, in combining these unsaturated products with chlorin and in reacting on the chlorinated body with an. alkali metal salt of acetic acid.
10. The processof making derivatives of hydrocarbons which comprises cracking kerosene under such conditions as to form olefin material, in saturating said olefin material with chlorinto form chlorin compounds and in contacting said chlorin compounds with a reagent capable of replacing chlorin.
11. The process of making derivatives of hydrocarbons which comprises passing a petroleum oil into aheated zonemaintained at a decol'nposing temperature under such conditions as to form lighterproducts of an unsaturated character, in chlorinating these unsaturated products and in subsequently replacing the chlorin by another element or radical.
12. The process of making derivatives of hydrocarbons which comprises cracklng kerosene under such conditions as to form olefin material having an iodin number exceeding 30'. in chlor nating sald olefin material toform chlorin compounds and in hydrocarbons which comprises cracking a petroleum oil under such conditions as to form lighter products of an unsaturated character, in chlorinating these unsaturated products and in subsequently replacing the chlorin by a substituent. a
14. The process of making derivatives of hydrocarbons which com olefin material, in chlorinating said olefin in contacting said dichlor material to form dichlor compounds and compounds with a reagent capable of replacing chlorin.
15. The hydrocarbons which comprises cracking a petroleum oil in a heated-zone under such conditions as'to form lighter products of an unsaturated character, in chlorinatin" these unsaturated. products with free chlorin and in subsequently replacing the chlorin.
16. The process of making derivatives of hydrocarbons which comprises passing petroleum oil through a heated zone at a temperature between 425", and 480 C. under such conditions as to form o'lefin material and in chlorinating said olefin material;
17. The process of making derivatives of hydrocarbons which comprises cracking petroleum to form olefin material, in treating said olefin material under such conditions as to form chlorin compounds and in contacting said chlorin compounds with a reagent capable of replacing chlorin.
18. The process-of making derivatives of hydrocarbons which comprises passing a petroleum oil into a heated zone maintained ata decomposing temperature under such conditions as to form lighter products of an unsaturated character having an iodin number above 30; in chlorinating these unsaturated products and in subsequently replacing the chlorin. a
' 19. The process of making derivatives of hydrocarbons-which comprises cracking an prises cracking- Qing kerosene under such condltlons as to form process of makingderivatives of having an iodin oil under such conditions as to produce light volatile hydrocarbons of an unsaturated character having'an iodin number'-in excess of 30, in exposing said products to the action of chlorin in the cold whereby chlorin isabsorbed with the evolution of heat forma more or less non-inflammable liquid and-in bringing said liquid into contact with a' reagent capable of replacing chlorin.
20. In the preparation of derivatives of hydrocarbons from unsaturated hydrocar bons the step which comprises treating cracked petroleum having an iodin number of more than 30 with chlorin and in subsequently contacting the product vwith a reexposing said products to the action of chlorin in the cold whereby chlorin is absorbed with the evolution of heat. forming a relatively non-inflammable liquid and in contacting said liquid with a reagent. capable of replacing chlorin. I V
23.. In the preparation of hydrocarbons from unsaturated gasolene material the step which comprises treating gasolene material number of more than 100 in subsequently contacting a reagent capable of replacwith chlorin and the product with ing chlorin.
' CARLETON ELLIS]
Publications (1)
Publication Number | Publication Date |
---|---|
US1317868A true US1317868A (en) | 1919-10-07 |
Family
ID=3385346
Family Applications (1)
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US1317868D Expired - Lifetime US1317868A (en) | Of hxkdto mnatahtb |
Country Status (1)
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2957820A (en) * | 1958-05-09 | 1960-10-25 | Basf Ag | Removal of sulfur compounds from hydrocarbons with alpha-sodium-sodium acetate |
-
0
- US US1317868D patent/US1317868A/en not_active Expired - Lifetime
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2957820A (en) * | 1958-05-09 | 1960-10-25 | Basf Ag | Removal of sulfur compounds from hydrocarbons with alpha-sodium-sodium acetate |
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