US2424628A - Process of extracting resinous wood - Google Patents

Process of extracting resinous wood Download PDF

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US2424628A
US2424628A US552449A US55244944A US2424628A US 2424628 A US2424628 A US 2424628A US 552449 A US552449 A US 552449A US 55244944 A US55244944 A US 55244944A US 2424628 A US2424628 A US 2424628A
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alcohol
wood
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petroleum
chips
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Robert C Palmer
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Newport Industries Inc
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09FNATURAL RESINS; FRENCH POLISH; DRYING-OILS; OIL DRYING AGENTS, i.e. SICCATIVES; TURPENTINE
    • C09F1/00Obtaining purification, or chemical modification of natural resins, e.g. oleo-resins

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  • This invention relates to a process of extracting resinous wood. More particularly the invention rela-tes to a process of extracting resinous wood with a mixture of a petroleum solvent and an alcohol to obtain a resinous product in much higher yield than petroleum solvent alone. From such a product can b-e recovered a resin that is substantially petroleum-insoluble and the yield of this resin is several times that when petroleum solvent alone is used for extraction. Also a rosin may be recovered in higher yield from the wood than when. using petroleum solvent that may be further puried in ⁇ accordance with well-known processes to yield a pale wood rosin. n
  • Ethyl alcohol in the form of ordinary commercial denatured alcohol, is preferred because of its availability and the ease with which it may be handled, but the process is not limited to ethyl alcohol.
  • MethylA alcohol, isopropyl alcohol, secondary butyl alcohol and others can be used so long as the alcohol exhibits the desired solvent power when diluted with the petroleum solvent.
  • Ordinary 95% ethyl alcohol is lmiscible in all proportions with a petroleum solvent at temperatures above about 35 C.
  • the mixture of alcohol and petroleum solvent that I prefer to use is one containing between v30 and 35% of alcohol and between and '70% of petroleum solvent, by volume. These proportions, however, are not critical, since my process operates satisfactorily so long as the mixed alcohol-petroleum solvent contains at least 30% by volume of 95% ethyl alcohol, or the equivalent of another alcohol.
  • the advantages of my process are not fully realized, however, if more than about '75% of alcohol by volume of the mixed alcohol-petroleum solvent is used.
  • Mixtures of yalcohol and petroleum can be readily kept from separating into two layers if the strength of the alcohol with respect to the water content is kept sufficiently high. While it would be possible, although not so economical, to allow separation to occur between the alcohol and petroleum solvent, and then recover the alcohol by rectification, and reintroduce the alcohol into the hot naphtha at the point of extraction, the use of a premixture of the alcohol and petroleum solvent is greatly to be preferred for ease of recovery and re-use, as will be apparent from the following description,
  • the chips are immersed in a petroleum solvent and the solvent brought-to.a.,boil .under distillation conditions.
  • the 'chips may be first steamed to remove turpentine and some of the high boiling terpenes and then: boiled with a petroleum solvent under distillation conditions. Water distills olic as vapor with the pe troleum solvent vapor, thereby-reducing the water content of the chips. sible by carrying the distillation far enoughto reduce the water content of the chips to below 10% by weight.
  • the drawing comprises a flow sheet illustrating the process of my invention.
  • a resinous wood such as pine stumps
  • the chips maygif desired-be rststeamed to remove-some turpentine and pine oil, and then subjected to the rstvstage ofthe process illustrated on the accompanying flow sheet, or the preliminary steamingmay be omitted.
  • rlhe petroleum solvent that-is preferred is a naphtha that is-not so llow vboiling as to give excessive vapor losses and yet one the dryvpoint'of which is sufficiently low Vto permit complete separation from pinenes,
  • the water content of the wood chips can be reduced from the normal value of from ⁇ 15m-20% by weight down to below 10% by weight.
  • that portion of the liquid petroleum solvent extract that will readily drain from the wood chips is discharged from the extractor.
  • a substantial portion, as much as from 20 to 35%, of the solvent necessary to immerse the chips is left behind adsorbed in the wood.
  • lOrdinary denatured ethyl alcohol (95% ethyl alcohol) as shown in the second stage of the extraction in the accompanying ilow sheet, is next introduced into the extraction vessel in an amount sufficient to bring the residual petroleum solvent up tothe desired alcohol concentration of the mixed solvent, which concentration will ordinarily be at least 30% of 95% alcohol by volume of the mixed solvent.
  • the alcohol is allowed to reux for a short period to effect a uniform admixture with the residual petroleum solvent.
  • the extractor is then filled With a mixed alcoholpetroleum solvent from another source and the extraction step carried out either at atmospheric pressure or under superatmospheric pressure, as desired.
  • the percentage of 95% alcohol in the extracting solvent may be considerably higher than 30% by volume, but, in general, no increase in resin yield has been observed even when the percentage of alcohol is carried as high as 50% by volume of the mixed solvent.V
  • the extraction may suitably be carried out at a gauge pressure of pounds per sq. in., which required a temperature of only about to 100 C.
  • the extraction of the Vchips is carried to substantially complete removal of the resinous content of the wood by dissolution into the extracting solvent.
  • the liquid contents of the extractor are discharged, preierablyby downward displacement, into a receiver,
  • alcoholV is readily concentrated-by fractionation even without the benet-o'f Aa iractionating column.
  • This is particularly true of alcohol-petroleum solvent mixtures Where the concentration of alcohol with respect to water pre-sent is above All of the alcolici froma 33% alcohol, 67% petroleum solvent mixture can be distilled oil before all of the naphtha is distilled oil. This makes it possible to recover terpenes, which may have been extracted, since af-terthe alcohol has been distilled ofi there is left in the concentrated extract naphtha and terpenes free of alcohol.
  • a-naphtha is preferably used that can be readily '75' fractionated from terpenes.
  • the chips are given a final rinse with straight petroleum solvent, containing no alcohol.
  • the next step in the process is to free the extracted wood from alcohol. This is done by supplying indirect heat, such as steam under pressure in a jacket or coil located aroundor in the extractor, and distilling out the alcohol by boiling oli the petroleum solvent. This may be done under pressure or at atmospheric pressure, as desired. The use of pressure haste-ns the rate of distilling oli the alcohol. Any residual water not removed from the wood in the iirst extractiondehydration stage, as well as water adsorbed from the alcohol, is distilled oil? along with the alcohol. In usual practice, if the distillation of the petroleum solvent and alcohol and/or water is conducted at, say, about 25 lbs. gauge pressure, all of the alcohol and/or water is removed from the wood chips by the time approximately two.
  • wood chips are then freed of any remaining petroleum solve-nt ⁇ by any of the methods commonly practiced in the pinew'ood extraction industry, such as by direct steaming.
  • the alcohol-petroleum solvent distilled from the wood in this step of the process is below a 30% alcohol content (95%) by volume of the mixed alcohol-petroleum solvent, and the alcohol itself is below 95% concentration with respect to the water present.
  • the alcohol is then recovered free of petroleum solvent by further washing of the distillate with water, after which the weak alcohol recovered is rectied back to concentration. Enough 95% alcohol is thus provided to introduce into the extraction step in the second stage, as illustrated in the flow sheet. rIhe rectified 95% alcohol can also be used in the system to make up for vapor losses,
  • the resin recovered from the liquid resin extract contains an abnormally high proportion of naphtha-insoluble resin and, of course, wood rosin.
  • the naphtha-insoluble resin fraction may be separated by adding naphtha gradually, with agitation, to the hot liquid resin, and continuing dilution with cold naphtha to the desired concentration. After settling and cooling, the bulk of the clear solution containing wood rosin can be decanted to tanks for water washing.
  • the petroleum-insoluble resin is melted out of the settling cone and removed to recovery stills, from which it is recovered free from naphtha.
  • the resulting petroleum-insoluble resin is not soluble in alcohol.
  • the clear naphtha solution containing wood resin can be further processed in the usual manner for the production of pale wood rosin.
  • the process oi extracting resinous wood which comprises extracting resinous wood in the form of chips containing less than 10% moisture by weight with a mixed solvent comprising a petroleum hydrocarbon and a hydrous monohydric alcohol containing less than ve carbon atoms, said solvent containing from 28.5% to 71.25% ofr said alcohol and the ratio of alcohol to water in said solvent being at least 19 to 1, separating the resulting liquid resinous extract from the wood and recovering the resin content from said extract.
  • the process of recovering from resinous Wood aresin that is relatively insoluble in a light petroleum hydrocarbon which comprises partially dehydrating chips of such resinous Wood to less than 10% moisture content by weight, extracting the partially dehydrated chips with a hot mixture containing from 28.5% to 71.25% of a hydrous monohydric alcohol containing less than ve carbon atoms and a liquid aliphatic hydrocarbon, the ratio of alcohol to Water in said mixture being at least 19 to l, separating a resinous residue from the resulting extract, and recovering a petroleum hydrocarbon-insoluble resin from said resinous residue.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Extraction Or Liquid Replacement (AREA)
  • Processing Of Solid Wastes (AREA)

Description

lR; C. PAL-MER PRocEss oF EXTRACTING REsINoUs wooDA July 29, 1947.
wferrcvwmfff Patented Juiy 29, 1947 UNITED STATES PATENT OFFICE 2,424,628 n rsoonss oF ExTRAoTiNo RnsiNoUs Robert C. Palmer, Pensacola, Fla., assigner to Newport Industries, Inc., Pensacola, Fla., a corporation of Delaware Application September 2, 1944, Serial No. 552,449
This invention relates to a process of extracting resinous wood. More particularly the invention rela-tes to a process of extracting resinous wood with a mixture of a petroleum solvent and an alcohol to obtain a resinous product in much higher yield than petroleum solvent alone. From such a product can b-e recovered a resin that is substantially petroleum-insoluble and the yield of this resin is several times that when petroleum solvent alone is used for extraction. Also a rosin may be recovered in higher yield from the wood than when. using petroleum solvent that may be further puried in` accordance with well-known processes to yield a pale wood rosin. n
It has heretofore been proposed to employ an alcohol in the extraction oi resinous woods, and also to extract resinous woods with a coal tar hydrocarbon to obtain a resin that is insoluble in light petroleum hydrocarbons, but to the best of my knowledge 'no one has heretofore proposed to extract resinous woods with a mixture of an alcohol and a petroleum solvent.
I have found that there are several advantages in the use of a mixed solvent comprising an alcohol and a petroleum solvent. Such a mixed solpine stumpwood chips were completely extracted` 13 Claims. (Cl. Zlle-110) hoi the yield was 23.3% and with secondary butyi with a petroleum solvent to yield 20.5% resin' (free of terpenes) by weight, based upon wood of 15% moisture content by weight. A sample of this same wood was completely extracted with benzene to yield 24% of resin on the same basis. Another sample of the same wood was completely extracted with a mixture of 95% denatured alcohol and a petroleum solvent, the mixture containing 33% by volume of 95% alcohol, to yield 26% of resin on the same basis. In another series of complete extractions of wood chips taken from j the same lot to compare the extraction eiliciency of diierent alcohols in each case, using 33% by volmne of the alcohol and 67% by volume of the petroleum solvent, in the case of 95% ethyl alcohol, the yield was 24.5% of resin; with methyl alcohol the yield was 25.1%; with isopropyl alcoalcohol the yield `was 24%.
Ethyl alcohol, in the form of ordinary commercial denatured alcohol, is preferred because of its availability and the ease with which it may be handled, but the process is not limited to ethyl alcohol. MethylA alcohol, isopropyl alcohol, secondary butyl alcohol and others can be used so long as the alcohol exhibits the desired solvent power when diluted with the petroleum solvent.
Ordinary 95% ethyl alcohol is lmiscible in all proportions with a petroleum solvent at temperatures above about 35 C. The mixture of alcohol and petroleum solvent that I prefer to use is one containing between v30 and 35% of alcohol and between and '70% of petroleum solvent, by volume. These proportions, however, are not critical, since my process operates satisfactorily so long as the mixed alcohol-petroleum solvent contains at least 30% by volume of 95% ethyl alcohol, or the equivalent of another alcohol. The advantages of my process are not fully realized, however, if more than about '75% of alcohol by volume of the mixed alcohol-petroleum solvent is used.
Mixtures of yalcohol and petroleum can be readily kept from separating into two layers if the strength of the alcohol with respect to the water content is kept sufficiently high. While it would be possible, although not so economical, to allow separation to occur between the alcohol and petroleum solvent, and then recover the alcohol by rectification, and reintroduce the alcohol into the hot naphtha at the point of extraction, the use of a premixture of the alcohol and petroleum solvent is greatly to be preferred for ease of recovery and re-use, as will be apparent from the following description,
An important discovery, made in my study of the use of a mixed solvent such as above described, greatly simplifies the operation as regards the maintenance of a solvent system which will not separate into two layers at ordinary atmospheric temperatures, a phenomenon that would otherwise occur in actual practice. This discovery was that partially dehydrated pinewood chips act as a dehydrating agent for alcohol dissolved in a petroleum solvent where the alcohol is about strength, so that the mixed solvent recovalcohol-petroleum solvent is rst noticed when the water content of the wood chip-s being extracted goes below 10%, and is markedly noticeable when the water content of the chips is below 8%. When Wood chips having a water content as low as are extracted, the concentration of alcohol with respect to the alcohol-water solution recovered from the extract was found to be as high as 98%.
In order to bring the water content of the pine- Wood chips from its normal value of between and moisture by weight down to below 10% by Weight, the chips are immersed in a petroleum solvent and the solvent brought-to.a.,boil .under distillation conditions. Alternatively, the 'chips may be first steamed to remove turpentine and some of the high boiling terpenes and then: boiled with a petroleum solvent under distillation conditions. Water distills olic as vapor with the pe troleum solvent vapor, thereby-reducing the water content of the chips. sible by carrying the distillation far enoughto reduce the water content of the chips to below 10% by weight. By this method, it hasbeenpossible to devise a very practical extraction .process using an alcohol-petroleum solvent mixture.
It is, therefore, an important object ofthis invention'to provide a process for the extraction :of resinous ywood for the economical recoveryV of :a resinous product in good yield,
It is a further important object Aof .this invention to provide a .process of extracting resinous Wood that includes the preliminary partial dehydration of the woodfollowed by the extraction of the partially dehydrated Wood by means .of 'ahot mixed solvent containing an alcohol and a petroleum solvent.
'It is a further important object of thisfinvention-to provide an economical and practicallprocess -for the extraction of resinous Wood in 'which thesolvent used is a mixtureof an alcohol and a petroleum hydrocarbon in suchproportions as to =be --miscible under the temperature'conditions to which the mixture may be subjected in the system, whereby separation of the alcohol and pe-Y troleum hydrocarbon into layers is avoided.
It isa further important object of this invention to provide a process for the recoveryr of a resinous product from resinous wood, inaccordance with which the resinous Wood in the 'form of chipsis first partially dehydrated and then extracted with a mixture of ordinary denatured ethyl alcohol Yand petroleum naphtha, the partially dehydrated chips serving to maintain :the alcohol as at least 95% alcohol with respect to its water content and therebyk facilitating :the maintenance of the alcoholnaphtha vmixturein a single liquidphase under the temperature conditions obtaining in the system.
Other and further important objects ofthis-invention will become apparent from the-following description and` appended claims.
The drawing comprises a flow sheet illustrating the process of my invention. y
In accordance with my process, fresh chips of a resinous wood, such as pine stumps, are placed in asuitable extractor. The chips maygif desired-be rststeamed to remove-some turpentine and pine oil, and then subjected to the rstvstage ofthe process illustrated on the accompanying flow sheet, or the preliminary steamingmay be omitted. Av sumcient amountof a-petroleum solvent, such -as a light petroleum'hydrocarbon, is added to immerse the wood chips. rlhe petroleum solvent that-is preferred is a naphtha that is-not so llow vboiling as to give excessive vapor losses and yet one the dryvpoint'of which is sufficiently low Vto permit complete separation from pinenes,
fmospheric or superatmospheric pressure, and
Acontinued until the desired degree of dehydration Accordingly, it is posof vthe wood chips has been reached, as determined by measuring the Water obtained from the condensed vapor-s coming from the extractor. By
this Lmeans, the water content of the wood chips can be reduced from the normal value of from `15m-20% by weight down to below 10% by weight. When this point has been reached, that portion of the liquid petroleum solvent extract that will readily drain from the wood chips is discharged from the extractor. A substantial portion, as much as from 20 to 35%, of the solvent necessary to immerse the chips is left behind adsorbed in the wood.
lOrdinary denatured ethyl alcohol (95% ethyl alcohol) as shown in the second stage of the extraction in the accompanying ilow sheet, is next introduced into the extraction vessel in an amount sufficient to bring the residual petroleum solvent up tothe desired alcohol concentration of the mixed solvent, which concentration will ordinarily be at least 30% of 95% alcohol by volume of the mixed solvent. The alcohol is allowed to reux for a short period to effect a uniform admixture with the residual petroleum solvent. The extractor is then filled With a mixed alcoholpetroleum solvent from another source and the extraction step carried out either at atmospheric pressure or under superatmospheric pressure, as desired. The percentage of 95% alcohol in the extracting solvent may be considerably higher than 30% by volume, but, in general, no increase in resin yield has been observed even when the percentage of alcohol is carried as high as 50% by volume of the mixed solvent.V The extraction may suitably be carried out at a gauge pressure of pounds per sq. in., which required a temperature of only about to 100 C. The extraction of the Vchips is carried to substantially complete removal of the resinous content of the wood by dissolution into the extracting solvent.
At the end of the extraction period, the liquid contents of the extractor are discharged, preierablyby downward displacement, into a receiver,
vfromwhich the liquid resin extract is conducted to evaporator stills, or any other conventional equipment, for the recovery of the resin extracted aswell as to separate the mixed solvent for recycling.
In kthe evaporation of the mixed solvent from the lliquid resinextract, alcoholV is readily concentrated-by fractionation even without the benet-o'f Aa iractionating column. This is particularly true of alcohol-petroleum solvent mixtures Where the concentration of alcohol with respect to water pre-sent is above All of the alcolici froma 33% alcohol, 67% petroleum solvent mixture can be distilled oil before all of the naphtha is distilled oil. This makes it possible to recover terpenes, which may have been extracted, since af-terthe alcohol has been distilled ofi there is left in the concentrated extract naphtha and terpenes free of alcohol. As pointed out above, a-naphtha is preferably used that can be readily '75' fractionated from terpenes.
After discharging the liquid resin extract from the extractor, as much more of the mixed solvent in a heated condition is introduced as will electively rinse the extracted Wood free of extract. This may be done either at atmospheric or at superatmospheric pressure, as desired, but is preferably carried out under pressure by downward displacement. lt may also be conducted in a cycle system with several extractors in series in different stages of extraction or rinsing. No attempt has been made in the accompanying flow sheet to illustrate a cycle system, but for the sake of simplicity the ilow sheet does show the extractor in three different stages: a first stage in which the extractor is charged with fresh chips and subjected to the action of boiling straight naphtha to partially dehydrate the chips; a second stage in which the partially dehydrated chips and naphtha remaining :from the rst stage are fortified with 95% alcohol and with an alcoholnaphtha mixture for effecting the extraction step; and a third stage in which the extracted chips containing extract from the second stage are rinsed with mixed solvent, then with straight naphtha, then heated to remove the remaining alcohol and nally steamed. It is thus obvious from the flow sheet that the partial dehydration ofthe chips, extraction of the chips and the rinsing of the extracted chips could be carried out in a cycle system,
After the rinsing of the extracted chips with mixed solvent is complete, the chips are given a final rinse with straight petroleum solvent, containing no alcohol. This amounts in effect to a displacement of the mixed solvent with the petroleum solvent, so that when the concentration of alcohol in the effluent shows a decrease as compared with the alcohol concentration in the preferred alcohol-petroleum solvent mixture, the displacement is stopped. This avoids reducing the alcohol content oi the eiiuent solvent, since this effluent solvent being displaced is to be used for extraction, as' indicated on the flow sheet, or for rinsing.
The next step in the process is to free the extracted wood from alcohol. This is done by supplying indirect heat, such as steam under pressure in a jacket or coil located aroundor in the extractor, and distilling out the alcohol by boiling oli the petroleum solvent. This may be done under pressure or at atmospheric pressure, as desired. The use of pressure haste-ns the rate of distilling oli the alcohol. Any residual water not removed from the wood in the iirst extractiondehydration stage, as well as water adsorbed from the alcohol, is distilled oil? along with the alcohol. In usual practice, if the distillation of the petroleum solvent and alcohol and/or water is conducted at, say, about 25 lbs. gauge pressure, all of the alcohol and/or water is removed from the wood chips by the time approximately two.
thirds of the solvent required toimmerse the wood chips has been distilled off.
The wood chips are then freed of any remaining petroleum solve-nt `by any of the methods commonly practiced in the pinew'ood extraction industry, such as by direct steaming.
The alcohol-petroleum solvent distilled from the wood in this step of the process is below a 30% alcohol content (95%) by volume of the mixed alcohol-petroleum solvent, and the alcohol itself is below 95% concentration with respect to the water present. The alcohol is then recovered free of petroleum solvent by further washing of the distillate with water, after which the weak alcohol recovered is rectied back to concentration. Enough 95% alcohol is thus provided to introduce into the extraction step in the second stage, as illustrated in the flow sheet. rIhe rectified 95% alcohol can also be used in the system to make up for vapor losses,
By this novel system, therefore, only a minor proportion of the total alcohol necessary for the extraction need be separated from the petroleum solvent and recovered by rectification.
The resin recovered from the liquid resin extract contains an abnormally high proportion of naphtha-insoluble resin and, of course, wood rosin. The naphtha-insoluble resin fraction may be separated by adding naphtha gradually, with agitation, to the hot liquid resin, and continuing dilution with cold naphtha to the desired concentration. After settling and cooling, the bulk of the clear solution containing wood rosin can be decanted to tanks for water washing. The petroleum-insoluble resin is melted out of the settling cone and removed to recovery stills, from which it is recovered free from naphtha. The resulting petroleum-insoluble resin is not soluble in alcohol.
The clear naphtha solution containing wood resin can be further processed in the usual manner for the production of pale wood rosin.
It will, of course, be understood that various details of the process may be varied through a wide range without departing from the principles of this invention and it is, thereforanotthe purpose to limit the patent granted hereon otherwise than necessitated by the scope of the appended claims. Y
I claim as my invention:
1. The process of extracting resinous wood which comprises at an elevated temperature extracting the wood in subdivided form and containing less than 10% moisture by weight with a mixed solvent containing a petroleum solvent and from 28.5% to 71.25% of said mixture of a hydrous monohydric alcohol containing less than five carbon atoms, the ratio of alcohol to water in said solvent being at least 19 to 1, to form a liquid resin extract and separating a resin from said extract.
2. The process oi extracting resinous wood which comprises extracting resinous wood in the form of chips containing less than 10% moisture by weight with a mixed solvent comprising a petroleum hydrocarbon and a hydrous monohydric alcohol containing less than ve carbon atoms, said solvent containing from 28.5% to 71.25% ofr said alcohol and the ratio of alcohol to water in said solvent being at least 19 to 1, separating the resulting liquid resinous extract from the wood and recovering the resin content from said extract.
3. In the process of recovering from resinous Wood a resin that is relatively insoluble in a light petroleum hydrocarbon, the step of extracting the resinous wood in chip form and containing less than 10% of moisture by weight with a hot solution of a light petroleum hydrocarbon and a hydrous monohydric alcohol containing less than five carbon atoms, said solvent containing from 28.5% to 71.25% of said alcohol and the ratio of alcohol to water in said solvent being at least 19 to 1.
4...In the process of recovering from resinous wood a resin that is relatively insoluble in a light petroleum hydrocarbon, the steps of extracting the resinous wood with a hot solution of hydrous ethyl alcohol and a light petroleum hydrocarbonf said solution containing from 28.5% to 33.25% ethyl alcohol and from 70% to 65% of said light hydrocarbon by volume of said solution, the ratio of ethyl alcohol to Water in said solution being at least 19 to 1.
5. In the process of recovering from resinous Wood a resin that is relatively insoluble in a light hydrocarbon, the steps of subjecting the resinous wood to the action of a hot liquid aliphatic hydrocarbon under distillation conditions to reduce the moisture content of the wood to less than by Weight, and extracting the partially dehydrated wood'with a hot mixed solvent comprising a liquid aliphatic hydrocarbon and from 28.5% to 71.25% of a'hydrous monohydric alcohol containing less than ve carbon atoms, the ratio of alcohol to water in said solvent being at least 19 to 1.
6. In the process of recovering from resinous wood a resin that is relatively insoluble in a light petroleum hydrocarbon, the steps of subjecting the resinous Wood to the action of a hot liquid aliphatic hydrocarbon under distillation conditions to reduce the moisture content of the Wood to less than 10% by Weight, and extracting the partially dehydrated Wood With a hot mixed solvent comprising frorn 28.5% to 71.25% of hydrous ethyl alcohol and a light petroleum hydrocarbon, the ratio of alcohol to water in said solvent being at least 19 to l.
7. In the process of recovering from resinous Wood a resin that is relatively insoluble in a light hydrocarbon, the steps of subjecting the resinous Wood to the action of a hot liquid aliphatic hydrocarbon under distillation conditions to reduce the moisture content of the Wood to less than 10%, and extracting the partially dehydrated Wood with a mixed solvent comprising from 28.5%
, to 71.25% of a hydrous monohydric alcohol containing less than ve carbon atoms and a light petroleum hydrocarbon, the ratio of said alcohol to Water in said solution being at least 19 to 1.
8. The process of recovering from resinous Wood aresin that is relatively insoluble in a light petroleum hydrocarbon, which comprises partially dehydrating chips of such resinous Wood to less than 10% moisture content by weight, extracting the partially dehydrated chips with a hot mixture containing from 28.5% to 71.25% of a hydrous monohydric alcohol containing less than ve carbon atoms and a liquid aliphatic hydrocarbon, the ratio of alcohol to Water in said mixture being at least 19 to l, separating a resinous residue from the resulting extract, and recovering a petroleum hydrocarbon-insoluble resin from said resinous residue.
9. The process of recovering from resinous Wood a resin that is relatively insoluble in a, light hydrocarbon, which comprises partially dehydrating chips of such resinous Wood to less than 10% moisture content by weight by the action of a hot liquid aliphatic hydrocarbon under distillation conditions, adding a hydrous monohydric alcohol containing less than five carbon atoms to the resulting mass of partially dehydrated chips and the hydrocarbon to forma liquid mixture containing from 28.5% to 71.25% of saidalcohol, the ratio of alcohol to Water in said mixture being at least `19 to l, separating a resinous residuefrom the resulting extract and recovering a petroleum hydrocarbon-insoluble resin from said resi-nous residue.
l0. vThe process of recovering from resinous Wood a resinthat is relatively insoluble ina light petroleum hydrocarbonywhich comprises partially dehydrating chips of such resinous wood to less than 10% moisture content by Weight, extracting the partially dehydrated chips with a hot mixture containing from 28.5% to 71.25% of a hydrous monohydric alcohol containing less than ve carbon atoms and a light petroleum hydrocarbon, the ratio of alcohol to Water in said mixture being at least 19 to 1, distilling the resulting extract to separate the alcohol, the petroleum hydrocarbon, terpenes, and a resinous residue, and recovering a petroleum hydrocarbon-insoluble resin from said resinous residue.
1l. In the process of extracting Wood in chip form containing less than 10% moisture by Weight With a mixture containing a petroleum solvent and from 28.5% to 71.25% of a hydrous monohydric alcohol containing less than iive carbon atoms to form a liquid resin extract, the ratio of alcohol to Water in said mixture being at least 19 to l, and recovering a resin from said extract, the step of recovering said alcohol petroleum solvent mixture Which comprises subjecting said liquid resin extract to distillation to distill off therefrom substantially all of the alcohol in admixture With petroleum solvent in proper proportion for reuse.
12. In the process of extracting resinous Wood in chip form and containing less than 10% moisture by weight at an elevated temperature with 30; a mixture containing from 28.5% to 71.25% of a hydrous monohydric alcohol containing less than ve carbon atoms and a petroleum solvent to form a liquid resin extract, the ratio of alcohol to water in said mixture being at least 19 to 1,
, and recovering a resin from said extract, the
of alcohol and petroleum solvent from said rinsing operation as long as the Proportion of alcohol in said recovered mixture is at least 28.5%, adding Water to the mixture of alcohol and petroleum solvent thereafter recovered from said rinsing operation in suflicient amount to form a tertiary mixture separable into petroleum solvent and aqueous alcohol fractions, separating the petroleum solvent from the diluted mixture to leave a dilute aqueous alcohol solution and rectifying said dilute alcohol solution to strength alcohol.
13; In the process of recovering a resin by subjecting resinous Wood to the action of a hot hydrocarbon under distillation conditions to reduce the moisture content to less than 10% by Weight, extracting the partially dehydrated wood with a mixture containing from 28.5% to 71.25% of a hydrous monohydric alcohol containing less than iive carbon atoms and a petroleum solvent to form a liquid resin extract, the ratio of alcohol to water in said mixture being at least 19 to l and recovering a resin from said extract, the steps of recovering the alcohol and petroleum solvent for reuse, which comprise recovering petroleum solvent and water from the partially dehydrated Wood, separating and recovering said petroleum solvent and water from the partially dehydrated Wood, separating and recovering said petroleum solvent from said Water, and subjecting said liquid resin extract to distillation to distill off therefrom substantially all of the alcohol in NIT D E admixture with not more than 70% of petroleum U E STAT s PATENTS so1vent. Number Name Date ROBERT C. PALMER. 783,367 Craighill 13610.21, 1905 5 945,612 s257101* Jan. 4, 1910 REFERENCES CTED 1,505,438 SheIWOOd et a1.. Aug. 19, 1924 The following references are of record in the Re' 19,749 Bent NOV- 12, 1935
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2487263A (en) * 1945-10-12 1949-11-08 Us Rubber Co Coagulation of synthetic rubber latices
US2757169A (en) * 1953-07-09 1956-07-31 Hercules Powder Co Ltd Process of recovering rosin from resinous wood
US2757170A (en) * 1953-07-09 1956-07-31 Hercules Powder Co Ltd Process of recovering rosin from resinous wood

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US783367A (en) * 1903-10-06 1905-02-21 Charles E Heald Producing rosin.
US945612A (en) * 1908-04-18 1910-01-04 Standard Turpentine And Pulp Company Process of extracting turpentine and rosin.
US1505438A (en) * 1921-05-18 1924-08-19 Hercules Powder Co Ltd Process of extracting turpentine and rosin from resinous wood
USRE19749E (en) * 1935-11-12 Method of extracting rosin from
US2221540A (en) * 1940-03-30 1940-11-12 Hercules Powder Co Ltd Method of producing a resin

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
USRE19749E (en) * 1935-11-12 Method of extracting rosin from
US783367A (en) * 1903-10-06 1905-02-21 Charles E Heald Producing rosin.
US945612A (en) * 1908-04-18 1910-01-04 Standard Turpentine And Pulp Company Process of extracting turpentine and rosin.
US1505438A (en) * 1921-05-18 1924-08-19 Hercules Powder Co Ltd Process of extracting turpentine and rosin from resinous wood
US2221540A (en) * 1940-03-30 1940-11-12 Hercules Powder Co Ltd Method of producing a resin

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2487263A (en) * 1945-10-12 1949-11-08 Us Rubber Co Coagulation of synthetic rubber latices
US2757169A (en) * 1953-07-09 1956-07-31 Hercules Powder Co Ltd Process of recovering rosin from resinous wood
US2757170A (en) * 1953-07-09 1956-07-31 Hercules Powder Co Ltd Process of recovering rosin from resinous wood

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