US2166812A - Process for the separation of the constituents of organic mixtures containing both resin acids and fatty acids, particularly tall oil - Google Patents
Process for the separation of the constituents of organic mixtures containing both resin acids and fatty acids, particularly tall oil Download PDFInfo
- Publication number
- US2166812A US2166812A US169654A US16965437A US2166812A US 2166812 A US2166812 A US 2166812A US 169654 A US169654 A US 169654A US 16965437 A US16965437 A US 16965437A US 2166812 A US2166812 A US 2166812A
- Authority
- US
- United States
- Prior art keywords
- resin
- acids
- fatty acids
- mixture
- separation
- 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
Links
- 235000014113 dietary fatty acids Nutrition 0.000 title description 78
- 239000000194 fatty acid Substances 0.000 title description 78
- 229930195729 fatty acid Natural products 0.000 title description 78
- 238000000034 method Methods 0.000 title description 60
- 239000002253 acid Substances 0.000 title description 59
- 239000011347 resin Substances 0.000 title description 56
- 229920005989 resin Polymers 0.000 title description 56
- 150000007513 acids Chemical class 0.000 title description 53
- 150000004665 fatty acids Chemical class 0.000 title description 52
- 239000000203 mixture Substances 0.000 title description 46
- 238000000926 separation method Methods 0.000 title description 29
- 239000003784 tall oil Substances 0.000 title description 22
- 239000000470 constituent Substances 0.000 title description 5
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 56
- 239000002904 solvent Substances 0.000 description 40
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 31
- -1 cyclic alcohols Chemical class 0.000 description 29
- 229930195733 hydrocarbon Natural products 0.000 description 28
- 150000002430 hydrocarbons Chemical class 0.000 description 28
- 239000000344 soap Substances 0.000 description 28
- RSWGJHLUYNHPMX-UHFFFAOYSA-N 1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid Chemical compound C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 27
- 239000004215 Carbon black (E152) Substances 0.000 description 27
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 26
- 235000019441 ethanol Nutrition 0.000 description 23
- 238000005886 esterification reaction Methods 0.000 description 20
- 230000032050 esterification Effects 0.000 description 19
- 239000000243 solution Substances 0.000 description 16
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 238000004821 distillation Methods 0.000 description 11
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 10
- 239000003960 organic solvent Substances 0.000 description 10
- 230000003472 neutralizing effect Effects 0.000 description 9
- 230000015572 biosynthetic process Effects 0.000 description 8
- LBPYPRXFFYUUSI-UHFFFAOYSA-N furan-2-carbaldehyde;hydrate Chemical compound O.O=CC1=CC=CO1 LBPYPRXFFYUUSI-UHFFFAOYSA-N 0.000 description 8
- 150000002148 esters Chemical class 0.000 description 7
- 150000001298 alcohols Chemical class 0.000 description 6
- 238000000605 extraction Methods 0.000 description 6
- 239000012071 phase Substances 0.000 description 6
- 239000007788 liquid Substances 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 238000011084 recovery Methods 0.000 description 4
- 239000011369 resultant mixture Substances 0.000 description 4
- 239000001117 sulphuric acid Substances 0.000 description 4
- 235000011149 sulphuric acid Nutrition 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 238000004040 coloring Methods 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 239000010802 sludge Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 229910021653 sulphate ion Inorganic materials 0.000 description 3
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000008240 homogeneous mixture Substances 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 238000000638 solvent extraction Methods 0.000 description 2
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 2
- 238000013019 agitation Methods 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 229940053200 antiepileptics fatty acid derivative Drugs 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- 239000012456 homogeneous solution Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000002655 kraft paper Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 229940068065 phytosterols Drugs 0.000 description 1
- 239000012261 resinous substance Substances 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 239000008149 soap solution Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000001256 steam distillation Methods 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11C—FATTY ACIDS FROM FATS, OILS OR WAXES; CANDLES; FATS, OILS OR FATTY ACIDS BY CHEMICAL MODIFICATION OF FATS, OILS, OR FATTY ACIDS OBTAINED THEREFROM
- C11C1/00—Preparation of fatty acids from fats, fatty oils, or waxes; Refining the fatty acids
- C11C1/007—Preparation of fatty acids from fats, fatty oils, or waxes; Refining the fatty acids using organic solvents
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09F—NATURAL RESINS; FRENCH POLISH; DRYING-OILS; OIL DRYING AGENTS, i.e. SICCATIVES; TURPENTINE
- C09F1/00—Obtaining purification, or chemical modification of natural resins, e.g. oleo-resins
Definitions
- This invention relates to an improved process for the separation and recovery of the major constituents of organic mixtures or oils containing both resin acids and fatty acids, and particularly to the clean, sharp and economic separation and recovery of the resin acids and the fatty acids from such mixtures or oils, and particularly from tall oil.
- Tall oil is a by-product of sulphate or kraft paper. manufacture, and is obtained by acidification of the black liquor soap, which is salted out and rises to the surface of the black liquor on standing.
- the main constituents of tall oil include fatty acids, resin acids and unsaponifiable substances. While the bulk of the unsaponifiable matter consists of hydrocarbons, it also contains a considerable proportion of high-molecular weight cyclic alcohols belonging to the group of phytosterols.
- Tall oil as such has found relatively little commerical use. It is not suited for soap making on account of its dark color, its odor and its high resin acid content, not can it be used as a substitute for rosin or other natural resins on account of its fatty acid content.
- the components of tall oil, especially the resin acids, fatty acids and phytosterol are of considerable commercial value. Therefore, a process for the sharp separation of the components of tall oil would be of great commercial value, especially in view of the vast potential supply oftall oil, resulting from the increasing importance of the sulphate process for paper making. Due to its low commercial value, tall oil is usually not even recovered in the present sulphate pulp establishments.
- United States Patent No. 1,986,815 proposes to refine tall .011 by allowing a portion of those components possessing a higher melting point, such as resin acids and higher saturated fatty acids, to settle out onjstanding. It is obvious that no separation of resin and fatty acids can be effected by such a process.
- a well known method for the separation of resin and fatty acids of tall oil is based on.distilla-' tion in vacuo, as exemplified by United States Patent No. 1,826,224. Since the fatty acids distill at a lower temperature than the resin acids, it is possible to effect a rough separation by distillation. However, the .methodhas the limitation of all distillation methods,- and even when using expensive fractionating equipment will not give a profitable yield of fatty acids free of resin 111., a corpora- Application October 18,1937, Serial No. 169,654
- the resin acids are separated by an aqueous alkali solution as water soluble soaps.
- the shortcomings of this method are the retention of a portion of the resin acid soaps in the hydrocarbon-ester layer, and the unavoidable formation of stubborn emulsions preventing a clear separation into layers even after adding a considerable proportion of alcohol to the aqueous layer.
- Acid number Original V 116 After minutes.. 87 After 30 minutes '77 After 45 minutes 73 After 60 minutes 72 After 120 minutes 70 After 180 minutes 68 After 240 minutes 68 should cause the mixture to have an acid number of 6'7. Thus at the end of 3 to 4 hours the esterification of the fatty acids can be considered complete.
- the first step of our process contemplates the esterification of the fatty acids contained in tall oil, which may be effected by several methods, such as refluxing or otherwise reacting the tall oil with a monohydric alcohol such as absolute methylor ethyl alcohol, or a higher monohydric alcohol.
- a monohydric alcohol such as absolute methylor ethyl alcohol, or a higher monohydric alcohol.
- the alcohol we find, is preferably used in excess over that required for the quantitative 'es'terification of the fatty acids.
- Esterification can be eflected at or below the boiling point of the esteriflcation mixture in the presence of catalysts, such as sulphuric acid, etc., or by any other conventional or suitable method.
- our next step consists of separating the mixture into layers.
- the upper, hydrocarbon layer contains the bulk of the fatty acid esters and a portion of the unsaponifiable matter
- the lower layer contains the resin acid soaps dissolved in a mixture of furfural and water.
- the furfural layer may be extracted one or more times with smaller portions of the hydrocarbon solvent in order to extract any fatty acid esters that may remain in the lower layer as completely as is considered economical.
- fatty acid esters so obtained from our improved process are of a light yellow color and contain approximately onehalf of the unsaponifiable matter originally present in the tall oil.
- the esters can be purified and obtained substantially free from unsaponiflable matter by distillation, the
- esters so obtained by our process are either used industrially as starting materials for fatty acid derivatives, or are subjected to splitting or saponification by wellknown methods such as hydrolysis by the Twitchell process, or splitting by the autoclave process, or saponiflcation with sodium hydroxide and subsequent liberation of the fatty acids. It is, therefore, clear to those skilled in the art that fatty acids free of resin acids are thus obtained by a direct and simple process not previously known or practiced.
- the next major step in our inventive procedure consists of the recovery of the resin acids from their soaps contained in the furfural-water solution. This is effected by adding the theoretical amount of acid, preferably but not necessarily a mineral acid, to the furfural water layer to liberate the resin acids from their soaps, and extracting the resin acids with a hydrocarbon solvent. By distilling off the solvent and any furfural dissolved therein, resin acids of light yellow color are obtained.
- acid preferably but not necessarily a mineral acid
- the furfural is then subsequently recovered from the furfural-water mixture left after the extraction of the resin acids by steam distillation or by any other convenient method, and the still residue left after the distillation of furfural is a dark colored, brittle, resinous substance which contains a small proportion of resin acids, some unsaponifiable matter and practically all of the coloring matter of tall oil.
- a great advantage of our method, and a necessary requirementfor practical and economical operation, is that the materials involved in the esterification and extraction procedures, such as excess alcohol and solvents, be capable of being completely recovered by very simple and economical methods such as by distillation.
- Our experiments show that about one-fourth of the excess alcohol is contained in the sludge separated after the esterification. Other than this, it can be seen that the balance of the excess alcohol can be recovered by distillation of the esterified mixture before subjecting it to solvent extraction, or may be recovered together with the furfural at the end of the process.
- Example I Three kilograms of tall oil containing 50% fatty acids, 40% resin acids, 10% unsapo'niflable and coloring matter, are mixed with 600 cc. of ethyl alcohol and grams of sulphuric acid. The mixture is refluxed for four hours and let stand to settle. The sludge which is drawn of! contains water, 70% of the sulphuric acid added, and '70 cc. of alcohol. is treated with 350 cc. of a sodium hydroxide solution containing 1'75 grams of sodium hydroxide. Three liters of naphtha and one and one-half liter of furfural are now added and the mixture lightly stirred until a homogeneous solution results.
- suflicient dilute sulphuric acid is now added to liberate the resin acids from their soaps and the resin acids extracted with three liters, and subsequently with smaller quantities of naphtha.
- the united naphtha solutions of the resin acids are distilled to remove the naphtha and the dissolved furfural.
- Light colored resin acids are obtained (1.15 kg.)
- On distilling the residual furfural-water layer 200 cc. of alcohol and the furfural are recovered; and as a residue 200 gms. of a mixture of unsaponifiable, resin acids and coloring matter are obtained.
- Example II One kilogram of tall oil from a Southern coour processes disclosed in our co-pending applications No. 169,655 and No. 169,656, from which we obtained 92'! grams of a refined oil of light yellow color as our starting point.
- 9 hundred grams of this refined oil are reacted by refluxing with 376 cc. absolute alcohol in the presence of 33 grams sulfuric acid. After neutralizing the sulfuric acid, the excess alcohol is recovered by distillation and we obtain 933 grams of the esterified mixture having an acid number of 71.
- the resin acids in this mixture are now neutralized with cc. of a solution containing 48 grams sodium hydroxide. Addition of 1000 cc. of naphtha and 500 cc. of furfural causes the formation of a single phase, which on adding-600 cc. water separates into two layers. After removing the naptha-ester layer, the extraction is repeated twice with smaller quantities of naphtha.
- the resin acids are liberated from their soaps contained in the furfural layer by adding cc. of 8 N. sulfuric acid, and the resin acids are extracted from the furfural-water layer with several portions of naphtha. Distillation of the naphtha solutions yields 546 grams esters and 299 grams resin acids respectively. Both esters and resin acids contain a small proportion of unsaponifiable matter. Distillation of the furfuralwater mixture yields 70 grams of a dark colored brittle substance composed mainly of resin acids.
- the neutralized esteriilcation mixture with two 20 niferous wood source was refined according to organic solvents, said solvents being substantially immiscible in each other and separable into'two layers upon the addition of water, and then causing the separation of said solvent solution into two layers by the addition of water, whereby the fatty acid esters are precisely dissolved in only one of the organic solvents, and resin acidsoaps are dissolved only in the other solvent.
- step 11 which comprises the formation of a two-phase liquid system, comprising an upper layer of a hydrocarbon solvent and monohydric alcohol esters of tall oil fatty acids, and a lower layer of furfural; water and resin acid soaps.
- step 12 which comprises the formation of a two-phase liquid system, comprising an upper layer of a hydrocarbon solvent and monohydric alcohol esters of tall oil fatty acids substantially free of resin acid compounds and a lower layer of furfural; water and resin acid soaps substantially free of fatty acid compounds.
- step 13 which comprises the formation of a two-phase liquid system, comprising an upper layer of a hydrocarbon solvent and monohydric alcohol esters of mixed fatty acids and a lower layer of furfural; water and resin acid soaps.
- step 14 which comprises the formation of a two-phase liquid system, comprising an upper layer of a hydrocarbon solvent and monohydric alcohol esters of mixed fatty acids substantially free of resin acid compounds and a lower layer of furfural, water and resin acid soaps substantially free of fatty acid compounds.
- the process of separating and recovering fatty acids and resin acids from their mixtures which comprises esterifying the fatty acids in said mixture by means of a monohydric alcohol and an esterification catalyst, adding an aqueous alkaline solution to said mixture to neutralize it and to form a homogeneous mixture comprising resin acid soap and fatty acid ester, adding thereto furfural and a hydrocarbon solvent to form a homogeneous mixture, adding an excess of water to form an upper layer of essentially fatty acid esters in hydrocarbon solvent, and a lower layer of essentially resin acid soap in furfural, separating the said layers by decantation, and recovering therefrom respectively fatty acid and resin acids.
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Microbiology (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Fats And Perfumes (AREA)
Description
Patented July 18, 1939 UNITED STATES PATENT OFFICE Frederick H. Ga er and Charles E. Fawkes, Chicage, 111., as gnors to Continental Research Corporation; Chicago Heights,
tion of Illinois No Drawing.
17 Claims.
This invention relates to an improved process for the separation and recovery of the major constituents of organic mixtures or oils containing both resin acids and fatty acids, and particularly to the clean, sharp and economic separation and recovery of the resin acids and the fatty acids from such mixtures or oils, and particularly from tall oil.
Tall oil is a by-product of sulphate or kraft paper. manufacture, and is obtained by acidification of the black liquor soap, which is salted out and rises to the surface of the black liquor on standing. The main constituents of tall oil include fatty acids, resin acids and unsaponifiable substances. While the bulk of the unsaponifiable matter consists of hydrocarbons, it also contains a considerable proportion of high-molecular weight cyclic alcohols belonging to the group of phytosterols.
Tall oil as such has found relatively little commerical use. It is not suited for soap making on account of its dark color, its odor and its high resin acid content, not can it be used as a substitute for rosin or other natural resins on account of its fatty acid content. On the other hand, the components of tall oil, especially the resin acids, fatty acids and phytosterol are of considerable commercial value. Therefore, a process for the sharp separation of the components of tall oil would be of great commercial value, especially in view of the vast potential supply oftall oil, resulting from the increasing importance of the sulphate process for paper making. Due to its low commercial value, tall oil is usually not even recovered in the present sulphate pulp establishments.
Numerous processes have been described relating to the separation of the components of tall oil. For example, United States Patent No. 1,986,815 proposes to refine tall .011 by allowing a portion of those components possessing a higher melting point, such as resin acids and higher saturated fatty acids, to settle out onjstanding. It is obvious that no separation of resin and fatty acids can be effected by such a process. A well known method for the separation of resin and fatty acids of tall oil is based on.distilla-' tion in vacuo, as exemplified by United States Patent No. 1,826,224. Since the fatty acids distill at a lower temperature than the resin acids, it is possible to effect a rough separation by distillation. However, the .methodhas the limitation of all distillation methods,- and even when using expensive fractionating equipment will not give a profitable yield of fatty acids free of resin 111., a corpora- Application October 18,1937, Serial No. 169,654
acids. Another method, proposed by United States Patent No.- 1,921,566, is based on the esterification of the fatty and resin acids with a polyhydric alcohol. The separation in this case is effected by subjecting the mixture of esters to hydrolysis in such a way that only the fatty acid esters will be hydrolyzed. The resulting fatty acids are separated from the unchanged resin acid esters and the unsaponifiable matter by distillation. A simpler method is proposed by United States Patent No. 1,736,802. According to this method, only the fatty acids are esterified with ethyl alcohol. The mixture of fatty acid esters and resin acids is dissolved in a hydrocarbon solvent. From this solution the resin acids are separated by an aqueous alkali solution as water soluble soaps. The shortcomings of this method are the retention of a portion of the resin acid soaps in the hydrocarbon-ester layer, and the unavoidable formation of stubborn emulsions preventing a clear separation into layers even after adding a considerable proportion of alcohol to the aqueous layer.
We have found that all these processes constituting the prior art either do not result in a clean separation, or are entirely too long and tedious to be commercially useful. So far as we are aware, no process has heretofore been devised by which products of sufficient purity can be obtained from tall oil to meet commercial demands, at a cost sufficiently low to meet market prices of other sources of fatty acids, rosin, etc. In contrast to the processesof the prior art, the process forming the subject of our present application costs little to operate, gives excellent yields, and the final products are of a high degree of purity and commercially useful and valuable.
According to the present invention the separation and recovery of the major components "of tall oil, such as fatty acids and resin acids,
is effected by an entirely novel method. This method involves a combined process of esterififatty acids in tall 011- may be readily esterified with monohydric alcohols, such as methyl-, ethylor higher alcohols, whereas the resin acids remain unchanged. This known chemical principle has been made the basis of a new and useful process of separation and is an integral part thereof, as hereinafter set forth. That is, the essence of this invention resides in taking together the old process of selective esterification of the fatty acid components carried out under controlled and specified conditions in combination with the new step of subjecting the highly specific esterification mixture to selective solvent extraction.
If a mixture of fatty and resin acids is esterifled, the progress of the esterification reaction can beeasily followed by the analysis of samples withdrawn at certain intervals of time. For example, on esterifying a tall oil of acid number 166, and containing 50% fatty acids, and 38% resin acids with ethyl alcohol, the following results were obtained:
Acid number Original V 116 After minutes.. 87 After 30 minutes '77 After 45 minutes 73 After 60 minutes 72 After 120 minutes 70 After 180 minutes 68 After 240 minutes 68 should cause the mixture to have an acid number of 6'7. Thus at the end of 3 to 4 hours the esterification of the fatty acids can be considered complete.
Now, the basis of our precise separation of tall oil consituents resides in the fact we have discovered that after the fatty acids are esterified it is possible by the process disclosed herein to successively extract first the fatty acid ester, and then the resin acid component with a preciseness never before obtained by formerly known methods.
The first step of our process contemplates the esterification of the fatty acids contained in tall oil, which may be effected by several methods, such as refluxing or otherwise reacting the tall oil with a monohydric alcohol such as absolute methylor ethyl alcohol, or a higher monohydric alcohol. The alcohol, we find, is preferably used in excess over that required for the quantitative 'es'terification of the fatty acids. Esterification can be eflected at or below the boiling point of the esteriflcation mixture in the presence of catalysts, such as sulphuric acid, etc., or by any other conventional or suitable method. After cooling, settling and separation of the sludge formed during the esteriflcation reaction, a strong aqueous solution of an alkali, preferably in excess over that required for the complete new tralization of the resin acids, is added to the solution to neutralize the mixture and form a resin acid soap. Our experiments show that it is 1m portant that the concentration of the alkali solution be high enough to cause the formation of a single, homogeneous phase, as no separation into layers of the resin and soap solution and fatty acid ester solution is desired at this point.
Specifically, we have found that the separation of the fatty acid esters from the resin acid soaps is effected very readily with the aid of selective solvents. More specifically, we have discovered that iurfural and a hydrocarbon solvent are especially adapted to effect a clean, rapid separation of the fatty acid esters from the resin acid soaps. A hydrocarbon solvent, and as the result of numerous experiments, preferably one of narrow boiling range, and furfurai are added to the mixture obtained after the neutralization of the resin acids. While furfural and hydrocarbon solvents possess only a limited solubility in each other, no separation of layers will take place when they are added to this mixture as long as the concentration of water is kept low. We thereby obtain a single liquid phase in which all of the components, including both the solvents and the mixture to be extracted, are intimately mixed, and no agitation or raising of the temperature is required to obtain such intimate contact as long as only one layer exists.
Having thus secured an intimate contact of solvents and matter to be extracted, our next step consists of separating the mixture into layers. We have found that on addition of water to the aforementioned mixture, two layers form. The upper, hydrocarbon layer contains the bulk of the fatty acid esters and a portion of the unsaponifiable matter, and the lower layer contains the resin acid soaps dissolved in a mixture of furfural and water. After separating the upper layer, the furfural layer may be extracted one or more times with smaller portions of the hydrocarbon solvent in order to extract any fatty acid esters that may remain in the lower layer as completely as is considered economical. We have found that approximately 90% of the esters are removed by the first extraction, and three or four extractions with smaller portions of hydrocarbon solvent will remove substantially all of the fatty acid esters from the furfurai layer. We also find it desirable to wash the hydrocarbon solutions of the fatty acid esters with small quantities of water in order to remove most of the furfural dissolved in the hydrocarbon.
Among the numerous and valuable advantages of this process is the clean, rapid separation of the fatty acid esters from the resin acid soaps. When water containing a considerable proportion of alcohol is employed as a solvent for the resin acid soaps, and the esters are taken up by a hydrocarbon solvent as in the gravimetric analytical method for the determination of resin acids, invariably the hydrocarbon solvent dissolves a portion of the soap which. has to be removed by protracted washing. As mentioned in the discussion of the prior art, this procedure also leads to the formation of troublesome emulsions which make operation on a large scale unfeasible. These disadvantages are, for the first time, successfully avoided in our process.
-We find, moreover-the retentive power of the furfural-water mixture for resin acid soaps is so great that no resin acid soap will be found in the hydrocarbon-ester layer. It is also of eminent practical importance that no emulsions .are formed during the course of the extraction.
In our process, the separation of the hydrocarhop and the furfural layers is extremely rapid, and a sharp separation into layers takes place within a few minutes.
These hydrocarbon solutions are then subjected to distillation, preferably with steam to remove the hydrocarbon and any residual small quantity of furfural. 'The fatty acid esters so obtained from our improved process are of a light yellow color and contain approximately onehalf of the unsaponifiable matter originally present in the tall oil. In our process, the esters can be purified and obtained substantially free from unsaponiflable matter by distillation, the
unsaponifiable portion remaining in the still residue.
The esters so obtained by our process are either used industrially as starting materials for fatty acid derivatives, or are subjected to splitting or saponification by wellknown methods such as hydrolysis by the Twitchell process, or splitting by the autoclave process, or saponiflcation with sodium hydroxide and subsequent liberation of the fatty acids. It is, therefore, clear to those skilled in the art that fatty acids free of resin acids are thus obtained by a direct and simple process not previously known or practiced.
The next major step in our inventive procedure consists of the recovery of the resin acids from their soaps contained in the furfural-water solution. This is effected by adding the theoretical amount of acid, preferably but not necessarily a mineral acid, to the furfural water layer to liberate the resin acids from their soaps, and extracting the resin acids with a hydrocarbon solvent. By distilling off the solvent and any furfural dissolved therein, resin acids of light yellow color are obtained.
The furfural is then subsequently recovered from the furfural-water mixture left after the extraction of the resin acids by steam distillation or by any other convenient method, and the still residue left after the distillation of furfural is a dark colored, brittle, resinous substance which contains a small proportion of resin acids, some unsaponifiable matter and practically all of the coloring matter of tall oil.
A great advantage of our method, and a necessary requirementfor practical and economical operation, is that the materials involved in the esterification and extraction procedures, such as excess alcohol and solvents, be capable of being completely recovered by very simple and economical methods such as by distillation. Our experiments show that about one-fourth of the excess alcohol is contained in the sludge separated after the esterification. Other than this, it can be seen that the balance of the excess alcohol can be recovered by distillation of the esterified mixture before subjecting it to solvent extraction, or may be recovered together with the furfural at the end of the process.
The following examples will illustrate our process, although we do not limit ourselves to the conditions as disclosed in these particular. examples:
Example I Three kilograms of tall oil containing 50% fatty acids, 40% resin acids, 10% unsapo'niflable and coloring matter, are mixed with 600 cc. of ethyl alcohol and grams of sulphuric acid. The mixture is refluxed for four hours and let stand to settle. The sludge which is drawn of! contains water, 70% of the sulphuric acid added, and '70 cc. of alcohol. is treated with 350 cc. of a sodium hydroxide solution containing 1'75 grams of sodium hydroxide. Three liters of naphtha and one and one-half liter of furfural are now added and the mixture lightly stirred until a homogeneous solution results. On adding 2.5 liters of water two layers are obtained, namely 4.85 liters of an upper, light yellow naphtha layer, and a larger volume of a lower, dark brown furfural layer. The latter is extracted twice more with 800 cc. and 400 cc. naphtha respectively, and the resulting upper layers (900 cc. and 420 cc.) separated. The united naphtha layers are washed The esterifled mixture with small quantities of water, and the naphtha distilled off preferably by steam. A clear, light yellow liquid (1.79 kg.) is obtained as residue representing the fatty acid esters and a few per cent of unsaponifiable matter. To the furfuralwater layer, suflicient dilute sulphuric acid is now added to liberate the resin acids from their soaps and the resin acids extracted with three liters, and subsequently with smaller quantities of naphtha. The united naphtha solutions of the resin acids are distilled to remove the naphtha and the dissolved furfural. Light colored resin acids are obtained (1.15 kg.) On distilling the residual furfural-water layer 200 cc. of alcohol and the furfural are recovered; and as a residue 200 gms. of a mixture of unsaponifiable, resin acids and coloring matter are obtained.
Example II One kilogram of tall oil from a Southern coour processes disclosed in our co-pending applications No. 169,655 and No. 169,656, from which we obtained 92'! grams of a refined oil of light yellow color as our starting point. Nine hundred grams of this refined oil are reacted by refluxing with 376 cc. absolute alcohol in the presence of 33 grams sulfuric acid. After neutralizing the sulfuric acid, the excess alcohol is recovered by distillation and we obtain 933 grams of the esterified mixture having an acid number of 71. The resin acids in this mixture are now neutralized with cc. of a solution containing 48 grams sodium hydroxide. Addition of 1000 cc. of naphtha and 500 cc. of furfural causes the formation of a single phase, which on adding-600 cc. water separates into two layers. After removing the naptha-ester layer, the extraction is repeated twice with smaller quantities of naphtha.
The resin acids are liberated from their soaps contained in the furfural layer by adding cc. of 8 N. sulfuric acid, and the resin acids are extracted from the furfural-water layer with several portions of naphtha. Distillation of the naphtha solutions yields 546 grams esters and 299 grams resin acids respectively. Both esters and resin acids contain a small proportion of unsaponifiable matter. Distillation of the furfuralwater mixture yields 70 grams of a dark colored brittle substance composed mainly of resin acids.
We claim as our invention:
1. The process of separating fatty acids from resin acids, comprising esterifying the fatty acids, neutralizing the resultant mixture and treating the neutralized esterification mixture with two organic solvents and water, said solvents being substantially immiscible in each other and separable into two layers upon the addition of water, whereby the fatty acid esters are precisely dissolved in only one of the organic solvents.
2. The process of separating'fatty acids from resin acids, comprising esterifying the fatty acids, neutralizing the resultant mixture and treating the neutralized esterification mixture with two organic solvents and water, said solvents being substantially immiscible in each other and separable into two layers upon the addition of water, whereby the fatty acid esters are precisely dissolved in only one of the organic solvents, and resin acid soaps are dissolved only in the other solvent.
3. The process of separating fatty acids from resin acids, comprising esterifying the fatty acids,
.the neutralized esteriilcation mixture with two 20 niferous wood source, was refined according to organic solvents, said solvents being substantially immiscible in each other and separable into'two layers upon the addition of water, and then causing the separation of said solvent solution into two layers by the addition of water, whereby the fatty acid esters are precisely dissolved in only one of the organic solvents, and resin acidsoaps are dissolved only in the other solvent.
4. The process of separating fatty acids from resin acids, comprising esterifying the fatty acids,
neutralizing the resultant mixture and treating the neutralized esteriflcation mixture with two organic solvents and water, said solvents being substantially immiscible in each other and separable into two layers upon the addition of water, whereby the fatty acid esters are precisely dissolved in only one of the organic solvents, and resin acid soaps are dissolved only in the other solvent, the said solvent solutions being formed into two layers, and separately recovering the respective constituents of said solvent solution layers.
5. The process of separating fatty acids from resin acids, which comprises the esterification of the fatty acids with a monohydric alcohol, neutralizing the mixture and treating the neutralized esterification mixture with two organic solvents and water, said solvents being substantially immiscible in each other and separable into two layers upon the addition of water, whereby the fatty acid esters are precisely dissolved in only one of the organic solvents.
6. The process of separating fatty acids from resin acids, which comprises the esterification of the fatty acids with a monohydric alcohol, neutralizing the mixture, and treating the neutralized esterification' mixture with a hydrocarbon solvent, furfural and water, whereby the fatty acid esters are precisely dissolved into only the hydrocarbon solvent.
7. The process of separating fatty acids from resin acids, which comprises the esterification of the fatty acids with a monohydric alcohol, neutralizing the mixture, and treating the neutralized esterification mixture with a hydrocarbon solvent, furfural and water, whereby the fatty acid esters are precisely dissolved into only the hydrocarbon solvent, and the resin acid soaps are precisely dissolved into only the furfural and water.
8. The process of separating fatty acids from resin acids, which comprises the esterification of the fatty acids with a monohydric alcohol, neutralizing the mixture, and treating the neutralized esterification mixture with a hydrocarbon solvent and furfural, thereby forming a single homogeneous liquid phase, and adding water thereto to cause a separation of said mixture into two solvent solution layers, and separately recovering the respective constituent compounds of said layers.
9. The process of separating fatty acid esters from resin acid soaps in mixtures thereof which comprises treating the mixture with a hydrocarbon solvent, furfural and water.
10. The process of separating fatty acid esters from resin acid soaps in mixtures thereof, which comprises treating the mixture with a hydrocarbon solvent and furfural, adding. water to cause a separation into layers, and decanting the layers apart.
11. In the process of separation of fatty acids from resin acids the step which comprises the formation of a two-phase liquid system, comprising an upper layer of a hydrocarbon solvent and monohydric alcohol esters of tall oil fatty acids, and a lower layer of furfural; water and resin acid soaps.
12. In the process of separation of fatty acids from resin acids the step which comprises the formation of a two-phase liquid system, comprising an upper layer of a hydrocarbon solvent and monohydric alcohol esters of tall oil fatty acids substantially free of resin acid compounds and a lower layer of furfural; water and resin acid soaps substantially free of fatty acid compounds.
13. In the process of separation of fatty acids from resin acids the step which comprises the formation of a two-phase liquid system, comprising an upper layer of a hydrocarbon solvent and monohydric alcohol esters of mixed fatty acids and a lower layer of furfural; water and resin acid soaps.
14. In the process of separation of fatty acids from resin acids the step which comprises the formation of a two-phase liquid system, comprising an upper layer of a hydrocarbon solvent and monohydric alcohol esters of mixed fatty acids substantially free of resin acid compounds and a lower layer of furfural, water and resin acid soaps substantially free of fatty acid compounds.
15. The process of separating and recovering fatty acids and resin acids from their mixtures, which comprises esterifying the fatty acids in said mixture by means of a monohydric alcohol and an esterification catalyst, adding an aqueous alkaline solution to said mixture to neutralize it and to form a homogeneous mixture comprising resin acid soap and fatty acid ester, adding thereto furfural and a hydrocarbon solvent to form a homogeneous mixture, adding an excess of water to form an upper layer of essentially fatty acid esters in hydrocarbon solvent, and a lower layer of essentially resin acid soap in furfural, separating the said layers by decantation, and recovering therefrom respectively fatty acid and resin acids.
16. The process of separating fatty acids from resin acids, comprising esterifying the fatty acids,
neutralizing the resultant mixture and diiferen-,
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US169654A US2166812A (en) | 1937-10-18 | 1937-10-18 | Process for the separation of the constituents of organic mixtures containing both resin acids and fatty acids, particularly tall oil |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US169654A US2166812A (en) | 1937-10-18 | 1937-10-18 | Process for the separation of the constituents of organic mixtures containing both resin acids and fatty acids, particularly tall oil |
Publications (1)
Publication Number | Publication Date |
---|---|
US2166812A true US2166812A (en) | 1939-07-18 |
Family
ID=22616605
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US169654A Expired - Lifetime US2166812A (en) | 1937-10-18 | 1937-10-18 | Process for the separation of the constituents of organic mixtures containing both resin acids and fatty acids, particularly tall oil |
Country Status (1)
Country | Link |
---|---|
US (1) | US2166812A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2423232A (en) * | 1945-12-27 | 1947-07-01 | Pittsburgh Plate Glass Co | Fractionation of tall oil |
US2486938A (en) * | 1947-01-22 | 1949-11-01 | Swift & Co | Manufacture of fatty acid esters |
US2509884A (en) * | 1947-05-24 | 1950-05-30 | Hercules Powder Co Ltd | Tall oil treatment |
WO2012112574A1 (en) * | 2011-02-14 | 2012-08-23 | Arizona Chemical Company, Llc | Fuel additives, fuels, methods of making and using same |
-
1937
- 1937-10-18 US US169654A patent/US2166812A/en not_active Expired - Lifetime
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2423232A (en) * | 1945-12-27 | 1947-07-01 | Pittsburgh Plate Glass Co | Fractionation of tall oil |
US2486938A (en) * | 1947-01-22 | 1949-11-01 | Swift & Co | Manufacture of fatty acid esters |
US2509884A (en) * | 1947-05-24 | 1950-05-30 | Hercules Powder Co Ltd | Tall oil treatment |
WO2012112574A1 (en) * | 2011-02-14 | 2012-08-23 | Arizona Chemical Company, Llc | Fuel additives, fuels, methods of making and using same |
CN103459574A (en) * | 2011-02-14 | 2013-12-18 | 阿利桑那化学公司 | Fuel additives, fuels, methods of making and using same |
CN103459574B (en) * | 2011-02-14 | 2015-12-23 | 阿利桑那化学公司 | Fuel dope, fuel and production and preparation method thereof |
US9828559B2 (en) | 2011-02-14 | 2017-11-28 | Kraton Chemical, Llc | Fuel additives, fuels, methods of making and using same |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2530810A (en) | Separation of unsaponifiable matter from tall oil residue | |
US2240365A (en) | Method of treating tall oil | |
US3804819A (en) | Recovery of fatty acids from tall oil heads | |
US2296952A (en) | Chemical treatment of black liquor and tall oil | |
US2166812A (en) | Process for the separation of the constituents of organic mixtures containing both resin acids and fatty acids, particularly tall oil | |
US2248346A (en) | Method for the recovery of phytosterol | |
US2389260A (en) | Producing unsaturated compounds | |
US1943427A (en) | Production of organic acids | |
US2610195A (en) | Recovery of unsaponifiables from concentrates containing the same | |
US2640823A (en) | Treatment of tall oil | |
US2866781A (en) | Separating non-acids from soap stocks | |
US2306547A (en) | Preparation of phytosterol glucosides | |
US2000244A (en) | Process for separation and recovery of naphthenic acids and phenols | |
US2679503A (en) | Extraction of sterols and antioxidants | |
US2223850A (en) | Process for refining and obtaining valuable products from tall oil | |
US1736802A (en) | Process of treating talloel | |
US2294446A (en) | Treatment of tall oil acids | |
US2356988A (en) | Process for the separation of the constituents of tall oil | |
US2348970A (en) | Process for the separation of acids contained in tall oil | |
US2437643A (en) | Separation of neutral fat from tall oil | |
US2268786A (en) | Process for refining fatty compounds | |
US2423232A (en) | Fractionation of tall oil | |
US2598269A (en) | Recovery of sterols | |
US2275186A (en) | Process for refining tall oil | |
US2288947A (en) | Conversion and separation of the constituents of organic mixtures containing both fatty and resin acids, particularly tall oil |