CN1058986A - The method of unsaponifiables in the separating naphthenic acid - Google Patents
The method of unsaponifiables in the separating naphthenic acid Download PDFInfo
- Publication number
- CN1058986A CN1058986A CN 90105528 CN90105528A CN1058986A CN 1058986 A CN1058986 A CN 1058986A CN 90105528 CN90105528 CN 90105528 CN 90105528 A CN90105528 A CN 90105528A CN 1058986 A CN1058986 A CN 1058986A
- Authority
- CN
- China
- Prior art keywords
- acid
- unsaponifiables
- naphthenic
- naphthenic acid
- soap
- 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.)
- Granted
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Detergent Compositions (AREA)
Abstract
The method of unsaponifiables in the separating naphthenic acid.Naphthenic acid is the by-product of petroleum refinement, and it is used for terebine, chemical catalyst, chemical assistant, petroleum additive, plant-growth regulator etc.Contain 10～55% unsaponifiables in the crude naphthenic acid, feature of the present invention be with boiling range less than 400 ℃ crude naphthenic acid saponification after the direct unsaponifiables in the underpressure distillation separating naphthenic acid, the unsaponifiables acid number that reclaims can be lower than the acidifying at high temperature of 0.02mgKOH/g naphthenic soap, cyclocarboxylic acid content after the acidifying can be greater than 95%, thick acid number can be greater than 195mgKOH/g, the naphthenic acid yield has remarkable economic efficiency and social benefit greater than 90%.
Description
The present invention relates to the separation method of unsaponifiables in the naphthenic acid.
Crude naphthenic acid is the by-product of petroleum refinement, contains 10～55% unsaponifiable matter, influences the use properties of naphthenic acid.Unsaponifiables in the separating naphthenic acid, generally adopt following method:
1, sodium salt-tube oven method
With after the naphthenic acid saponification, settlement separate part unsaponifiables is heated to 300～360 ℃ through tube furnace then, naphthenic soap and water and unsaponifiables flash separation among USSR992510 and the USSR527416.Use sulfuric acid acidation behind the naphthenic soap dilute with water, prepare the naphthenic acid of high acid content, but separate with water, and also have small amounts of soap, must further separate with the isolating unsaponifiable matter of this method.
2, extraction process
With after the naphthenic acid saponification, add coagent and solvent among JP58-22138 and the US2296039, unsaponifiables is separated, the aqueous solution sulfuric acid acidation of soap with soap.But need to use a large amount of solvent and auxiliary agent.
Direct underpressure distillation divides dried up and unsaponifiable matter respectively after the objective of the invention is to make the crude naphthenic acid saponification, makes it to obtain acid number and is lower than 0.02mgKOH/g, does not contain the unsaponifiables of soap and obtain acid content to be higher than 95% naphthenic acid.
The present invention handles boiling range at the crude naphthenic acid below 400 ℃.
The present invention is achieved in that at first after the crude naphthenic acid saponification, directly underpressure distillation divides dried up and unsaponifiables in stainless steel cauldron.The used alkali of saponification can be sodium hydroxide, potassium hydroxide or their carbonate.The alkali consumption of saponification naphthenic acid should be higher by 0～3% than theoretical value.The not moisture and soap by isolating like this unsaponifiables, acid number is lower than 0.02mgKOH/g, the naphthenic acid that acidifying obtains, thick acid number is greater than 185mgKOH/g, and acid content is greater than 85%, and the naphthenic acid yield is greater than 95%.However, be difficult to obtain the naphthenic acid of high acid content.Because, if separate boiling point, then need high separation temperature greater than the unsaponifiables more than 370 ℃, if chuck uses the elevated temperature heat carrier, the selection of elevated temperature heat carrier will be met difficulty.Also have, when still temperature above 300 ℃, naphthenic soap very easily decomposes.Therefore, the present invention divides the unsaponifiables in the two step decompression separation naphthenic soaps, to prepare the naphthenic acid of high acid content.The first step is with after the crude naphthenic acid saponification, divides dried up and unsaponifiables in direct underpressure distillation below 50～300 ℃; Second step was heated to 360 ℃ with naphthenic soap through pipeline, and material is 2～10 minutes in the ducted residence time, was heated to height in 360 ℃ the naphthenic soap flash separation naphthenic soap unsaponifiables that boils.Also can separate unsaponifiables through a step underpressure distillation.Naphthenic soap after the second step flash distillation, its acid content is 95%, and thick acid number can be greater than 200mgKOH/g, and the naphthenic acid yield can be greater than 95%, and naphthenic soap is lower than 200 ℃ and just loses flowability.With the naphthenic soap acidifying, generally with screw rod naphthenic soap is added in the entry on the engineering, be made into 30% the aqueous solution, add sulfuric acid acidation then, souring temperature is lower than 100 ℃, yet, at high temperature make the naphthenic soap acidifying.Run into following problem on the engineering: 1, under the situation that naphthenic soap loses flowability, how to make the rapid acidifying of naphthenic soap; 2, at high temperature how to avoid the bumping problem of water in the acidizing fluid.The present invention take have low-carbon alcohol (methyl alcohol, ethanol, Virahol, isopropylcarbinol etc.), toluene, dimethylbenzene and boiling range be 120～180 ℃ naphthenic oil acidification adjuvant in the presence of, under 100～250 ℃ of temperature naphthenic soap is carried out acidifying, the consumption of acidification adjuvant is 0～6% of a pure acid amount.The used acid of naphthenic soap acidifying can be sulfuric acid, hydrochloric acid, phosphoric acid, nitric acid, and the add-on of acidifying acid should be bigger by 0～3% than theoretical add-on.The present invention also is applicable to the unsaponifiables that separates in the normal fatty acid.
The present invention separates in the cycloalkanes unsaponifiables and compares with extraction process, do not have to add a large amount of solvents and solubility promoter, and it is uncomplicated that solvent and solubility promoter reclaim technology, and rate of recovery height, production cost are low, can prepare the characteristics such as naphthenic acid of high acid content.
Embodiment 1:
At volume is to add thick acid number 132mgKOH/g in 8.5 cubic metres the stainless steel cauldron, pure acid number 200mgKOH/g, moisture 0.5%, positive structure fatty compounds content is 13.5% naphthenic acid 4210kg, add and stir that to add concentration down be 30% aqueous sodium hydroxide solution 1347kg(excessive 2%), heat by the chuck thermal barrier, water and the unsaponifiables in the separating naphthenic acid soap under reduced pressure, vacuum tightness-0.09MPa, in underpressure distillation, separate water outlet 1128kg, unsaponifiables 1170kg, unsaponifiables acid number 0.02mgKOH/g.Naphthenic soap is cooled to 220 ℃, add acidification adjuvant A139kg, add 18% hydrochloric acid 2087kg(excessive 2% again), acidification adjuvant B139kg, acidifying 1.5 hours, the isolating naphthenic acid of acidifying is through underpressure distillation, getting thick acid number is 186mgKOH/g, and pure acid number is 215mgKOH/g, and positive structure fatty compounds content is 9.5% naphthenic acid 2800kg, calculate by acid content, the naphthenic acid yield is 93.7%.
Embodiment 2:
At volume is that to add thick acid number in 4 cubic metres the stainless steel cauldron be 130mgKOH/g, and pure acid number is 198mgKOH/g, moisture 0.5%, and positive structure fatty compounds content is 13% cycloalkanes 2200kg.Under agitation add concentration and be 30% aqueous sodium hydroxide solution 693.3kg(excessive 2%), material underpressure distillation under the heating of chuck thermal barrier, vacuum tightness-0.09MPa separates water outlet 577kg, unsaponifiables 560kg.Unsaponifiables acid number 0.02mgKOH/g when the still temperature is 290 ℃, makes the still temperature maintain 290～300 ℃.In 1.5 hours, naphthenic soap is heated to 360 ℃ through pipeline heater, the residence time of naphthenic soap in pipeline heater is 1.5 minutes.Get unsaponifiables 126kg, acid number 0.01mgKOH/g after the flash distillation.The naphthenic soap that is captured by the flash distillation still is cooled to 220 ℃, add acidification adjuvant A72.2kg, the hydrochloric acid 378.4kg(excessive 2% of adding 18%), acidification adjuvant B72.2kg, acidificatoin time 1.5 hours, the isolating naphthenic acid of acidifying is through underpressure distillation, get thick acid number 202mgKOH/g, pure acid number 210mgKOH/g, the naphthenic acid 1317kg of positive structure fatty compounds content 9.2%, press the cyclocarboxylic acid cubage, naphthenic acid yield 93%.
Embodiment 3:
Adopting the process equipment thick acid number identical with embodiment 2 is 130mgKOH/g, and pure acid number is 198mgKOH/g, moisture 0.5% normal fatty acid, get unsaponifiables acid number 0.01mgKOH/g, the thick acid number 215mgKOH/g of normal fatty acid, pure acid number 225mgKOH/g, lipid acid yield 90%.
Claims (3)
1, the method of unsaponifiables in a kind of separating naphthenic acid, it is characterized in that, divide the direct underpressure distillation of two steps to separate unsaponifiables after the crude naphthenic acid saponification, the first step is separated unsaponifiables in reactor under 280～300 ℃, second step was heated to 300～360 ℃ through pipe, unsaponifiables in the vacuum flashing separating naphthenic acid, also can separate unsaponifiables through a step underpressure distillation hundreds of, the naphthenic soap that has separated unsaponifiables, under 100～250 ℃, add acidification adjuvant and carry out acidifying, the add-on of the used acid of acidifying is bigger by 0～3% than theoretical add-on, and the consumption of acidification adjuvant is 0～6% of a pure acid amount.
2, method according to claim 1 is characterized in that, the acidification adjuvant that is added is low-carbon alcohol, toluene, dimethylbenzene, and boiling range is 120～180 ℃ a naphthenic oil.
3, method according to claim 1, it is characterized in that this method also is applicable to separates unsaponifiables in the normal fatty acid.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 90105528 CN1025493C (en) | 1990-08-16 | 1990-08-16 | Separating unsaponifiables from naphthenic acid |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 90105528 CN1025493C (en) | 1990-08-16 | 1990-08-16 | Separating unsaponifiables from naphthenic acid |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1058986A true CN1058986A (en) | 1992-02-26 |
| CN1025493C CN1025493C (en) | 1994-07-20 |
Family
ID=4879342
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN 90105528 Expired - Fee Related CN1025493C (en) | 1990-08-16 | 1990-08-16 | Separating unsaponifiables from naphthenic acid |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN1025493C (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102648271A (en) * | 2009-10-23 | 2012-08-22 | 普瓦图-夏朗德瓦拉格罗可再生碳公司 | Method for extracting unsaponifiables from renewable raw materials |
| CN113730954A (en) * | 2021-09-09 | 2021-12-03 | 福建省长汀金龙稀土有限公司 | Method for recovering isooctanol and sulfonated kerosene from waste organic of naphthenic acid system for extracting and separating yttrium |
-
1990
- 1990-08-16 CN CN 90105528 patent/CN1025493C/en not_active Expired - Fee Related
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102648271A (en) * | 2009-10-23 | 2012-08-22 | 普瓦图-夏朗德瓦拉格罗可再生碳公司 | Method for extracting unsaponifiables from renewable raw materials |
| CN102648271B (en) * | 2009-10-23 | 2015-03-11 | 普瓦图-夏朗德瓦拉格罗可再生碳公司 | Method for extracting unsaponifiables from renewable raw materials |
| CN113730954A (en) * | 2021-09-09 | 2021-12-03 | 福建省长汀金龙稀土有限公司 | Method for recovering isooctanol and sulfonated kerosene from waste organic of naphthenic acid system for extracting and separating yttrium |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1025493C (en) | 1994-07-20 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4652406A (en) | Process for the production of fatty acid alkyl esters | |
| CN104844456B (en) | A kind of n-butyl acrylate waste oil recovery process and device | |
| CN103724261A (en) | Novel industrial production method for hydroxychloroquine sulfate | |
| US2139179A (en) | Purification of alcohols | |
| CN112225634A (en) | Method for separating cyclohexane and tert-butyl alcohol by liquid-liquid extraction-flash evaporation | |
| CN1025493C (en) | Separating unsaponifiables from naphthenic acid | |
| US2861110A (en) | Procedure for the obtention of higher alcohols by condensation of lower alcohols | |
| US1851040A (en) | Production of chloropropionic esters | |
| CN112321543A (en) | Preparation method of alpha-chloro-alpha acetyl-gamma-butyrolactone | |
| CN100368377C (en) | Tech. of producing ortho nitro methyl-phenoxide para nitro methyl-phenoxide and meta nitro chlorobenzene from chlorobenzene | |
| Brown et al. | The Preparation of Ethyl ε-Bromocaproate | |
| CN1031706C (en) | Process for producing antioxidant | |
| CN205990356U (en) | A kind of novel distillation system | |
| CN104892416A (en) | 2-Ethylhexyl acrylate waste oil recovery technology | |
| CN204644234U (en) | A kind of n-butyl acrylate drain oil recovery equipment | |
| CN211753890U (en) | Recovery system of tail gas is hydrolysised to glyphosate synthetic liquid | |
| CN210786817U (en) | Device for recovering effective components of rectification residues and comprehensively treating waste gas in polyvinyl alcohol production process | |
| CN110451684A (en) | The processing method of Lauryl Alcohol ester production technology waste water | |
| CN112624925A (en) | Method for preparing dimethyl carbonate by using waste | |
| CN103112968A (en) | Method for treating high-COD (Chemical Oxygen Demand) components in phenoxyalkanoic acid production wastewater | |
| Barbour et al. | The reactions of highly fluorinated organic compounds. III. A heptafluoroadipic acid and its derivatives | |
| CA1190560A (en) | PROCESS FOR THE PRODUCTION OF 3-ALKYL-6-METHYL-.beta.- RESORCYCLIC ACID ESTERS | |
| CN104292080B (en) | The continuous distillation method of two-(2-chloro isopropyl) ether is extracted from epoxy propane slop | |
| CN220443807U (en) | Intermittent production system for 3-methoxy-N, N-dimethyl propionamide | |
| CN104403804A (en) | Method for removing methanol from crude methyl ester |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| C19 | Lapse of patent right due to non-payment of the annual fee | ||
| CF01 | Termination of patent right due to non-payment of annual fee |