SU436043A1 - - Google Patents
Info
- Publication number
- SU436043A1 SU436043A1 SU1311880A SU1311880A SU436043A1 SU 436043 A1 SU436043 A1 SU 436043A1 SU 1311880 A SU1311880 A SU 1311880A SU 1311880 A SU1311880 A SU 1311880A SU 436043 A1 SU436043 A1 SU 436043A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- zone
- oxidation
- extraction
- hydrocarbons
- weight
- Prior art date
Links
- 239000000047 product Substances 0.000 description 15
- 229930195733 hydrocarbon Natural products 0.000 description 12
- 238000000034 method Methods 0.000 description 12
- 238000000605 extraction Methods 0.000 description 11
- 238000007254 oxidation reaction Methods 0.000 description 11
- 239000002994 raw material Substances 0.000 description 11
- 150000002430 hydrocarbons Chemical class 0.000 description 10
- 230000003647 oxidation Effects 0.000 description 10
- 239000012296 anti-solvent Substances 0.000 description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 229910052760 oxygen Inorganic materials 0.000 description 5
- 239000001301 oxygen Substances 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 239000012535 impurity Substances 0.000 description 4
- 239000012188 paraffin wax Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 150000003464 sulfur compounds Chemical class 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- XSBJUSIOTXTIPN-UHFFFAOYSA-N aluminum platinum Chemical compound [Al].[Pt] XSBJUSIOTXTIPN-UHFFFAOYSA-N 0.000 description 1
- 239000010426 asphalt Substances 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- UBAZGMLMVVQSCD-UHFFFAOYSA-N carbon dioxide;molecular oxygen Chemical compound O=O.O=C=O UBAZGMLMVVQSCD-UHFFFAOYSA-N 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 150000001728 carbonyl compounds Chemical class 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000008396 flotation agent Substances 0.000 description 1
- -1 hydrocarbon hydrocarbons Chemical class 0.000 description 1
- 150000001261 hydroxy acids Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 150000002926 oxygen Chemical class 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000010902 straw Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU1311880A SU436043A1 (cs) | 1969-03-17 | 1969-03-17 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU1311880A SU436043A1 (cs) | 1969-03-17 | 1969-03-17 |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU894767112A Addition SU1710243A2 (ru) | 1989-12-11 | 1989-12-11 | Па льник дл групповой пайки |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU436043A1 true SU436043A1 (cs) | 1974-07-15 |
Family
ID=20444954
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1311880A SU436043A1 (cs) | 1969-03-17 | 1969-03-17 |
Country Status (1)
| Country | Link |
|---|---|
| SU (1) | SU436043A1 (cs) |
-
1969
- 1969-03-17 SU SU1311880A patent/SU436043A1/ru active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2814448C2 (cs) | ||
| SU1176840A3 (ru) | Способ получени фурфурола | |
| US3531376A (en) | Purification of acetone by extractive distillation and rectification with simultaneous alkali-containing acetone solution contact and halogen impurity side stream removal | |
| SU436043A1 (cs) | ||
| US3859335A (en) | Process for obtaining esters from cyclohexanone waste | |
| US2698336A (en) | Purification of crude wax oxidates | |
| US2815355A (en) | Method for preparing carboxylic acids | |
| US2269467A (en) | Recovery of solvent from hydrocarbon oils | |
| US4098838A (en) | Process for obtaining sulfur free pure naphthalene from bituminous coal tar and thionaphthene as a by-product | |
| US2611740A (en) | Distillation of furfural | |
| SU465780A3 (ru) | Способ получени 1,3-диацетокси-2метиленпропана | |
| US4021493A (en) | Vanillin recovery process | |
| US1450984A (en) | Process of making condensation products of aliphatic aldehydes | |
| US2571759A (en) | Continuous process for polymerizing aliphatic aldehydes | |
| US3432557A (en) | Aldoling process | |
| US2610977A (en) | Recovery of alcohols from hydrocarbon oils | |
| US3277168A (en) | Isolation of epsilon-hydroxycaproic acid | |
| US1940146A (en) | Process of purifying phenolphthalein | |
| BE496062A (cs) | ||
| US3052727A (en) | Oxidation of petroleum distillates to obtain higher crystallized ethers, and higher liquid ethers | |
| US2564433A (en) | Xrecovering o of pyridine from acid | |
| RU1795967C (ru) | Способ экстракции С @ - С @ - н -парафинов из их смеси с С @ - С @ - парафинсульфокислотами | |
| US4278503A (en) | Low bromine content glacial acetic acid | |
| US1858151A (en) | Process for concentrating volatile aliphatic acids | |
| SU172751A1 (ru) | СПОСОБ ПОЛУЧЕНИЯ ЖИРНЫХ КИСЛОТBDiCoicc;;;,.К*- n,\7EiiTi;Q -«•* т:::;;ичЕс:;,':1 f':;jA;::7z:;A |