US2279499A - Process of combining hardenable phenol-aldehyde condensation products with air-drying fatty oils - Google Patents
Process of combining hardenable phenol-aldehyde condensation products with air-drying fatty oils Download PDFInfo
- Publication number
- US2279499A US2279499A US427993A US42799330A US2279499A US 2279499 A US2279499 A US 2279499A US 427993 A US427993 A US 427993A US 42799330 A US42799330 A US 42799330A US 2279499 A US2279499 A US 2279499A
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- air
- oil
- drying
- oils
- condensation products
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- 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
- 238000007605 air drying Methods 0.000 title description 23
- 239000007859 condensation product Substances 0.000 title description 15
- 239000010685 fatty oil Substances 0.000 title description 15
- 238000000034 method Methods 0.000 title description 8
- 239000003921 oil Substances 0.000 description 26
- 235000019198 oils Nutrition 0.000 description 26
- 229920003987 resole Polymers 0.000 description 22
- 239000002904 solvent Substances 0.000 description 20
- 239000000047 product Substances 0.000 description 14
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- 239000000203 mixture Substances 0.000 description 12
- 239000000944 linseed oil Substances 0.000 description 10
- 235000021388 linseed oil Nutrition 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 6
- 239000002966 varnish Substances 0.000 description 6
- 241000779819 Syncarpia glomulifera Species 0.000 description 5
- 239000001739 pinus spp. Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 229940036248 turpentine Drugs 0.000 description 5
- 230000003647 oxidation Effects 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 3
- QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 description 3
- 229910021529 ammonia Inorganic materials 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 229930003836 cresol Natural products 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 238000007792 addition Methods 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- AMWRITDGCCNYAT-UHFFFAOYSA-L hydroxy(oxo)manganese;manganese Chemical compound [Mn].O[Mn]=O.O[Mn]=O AMWRITDGCCNYAT-UHFFFAOYSA-L 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000004922 lacquer Substances 0.000 description 2
- 229910000464 lead oxide Inorganic materials 0.000 description 2
- 229920003986 novolac Polymers 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- YEXPOXQUZXUXJW-UHFFFAOYSA-N oxolead Chemical compound [Pb]=O YEXPOXQUZXUXJW-UHFFFAOYSA-N 0.000 description 2
- 229920001195 polyisoprene Polymers 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 239000011877 solvent mixture Substances 0.000 description 2
- 239000002383 tung oil Substances 0.000 description 2
- 229920001342 Bakelite® Polymers 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- MKYBYDHXWVHEJW-UHFFFAOYSA-N N-[1-oxo-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propan-2-yl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(C(C)NC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 MKYBYDHXWVHEJW-UHFFFAOYSA-N 0.000 description 1
- -1 PHENOL ALDEHYDE Chemical class 0.000 description 1
- 235000004347 Perilla Nutrition 0.000 description 1
- 244000124853 Perilla frutescens Species 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000004637 bakelite Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- 238000006385 ozonation reaction Methods 0.000 description 1
- 239000010491 poppyseed oil Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000012262 resinous product Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L61/00—Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
- C08L61/04—Condensation polymers of aldehydes or ketones with phenols only
- C08L61/06—Condensation polymers of aldehydes or ketones with phenols only of aldehydes with phenols
- C08L61/14—Modified phenol-aldehyde condensates
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L61/00—Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
- C08L61/04—Condensation polymers of aldehydes or ketones with phenols only
- C08L61/06—Condensation polymers of aldehydes or ketones with phenols only of aldehydes with phenols
Definitions
- Patented Apr. 14, 1942 UNITED STATES PATENT OFjFlCE" PROCESS OF COMBINING HARDENABLE PHENOL ALDEHYDE CONDENSATION PRODUCTS WITH AIR-DRYING FATTY OILS Fritz Seebach, Erkner, near Berlin, Germany, assignor, by mesne assignments, to Bakelite v Corporation, a corporation of New Jersey No Drawing. Application February 12, 1930, Serial No. 427,993. In Germany February 25,
- Resoles i. e. synthetic resinous products of a hardenable nature in their fusible and-soluble initial condition, and air-drying, fatty oils cannot be mixed or are insoluble in each other. This "constitutes a serious disadvantage, for resoles .ably changed in imparting the oil-soluble property thereto.
- the obtained products show a novolak character, that is, they remain fusible and soluble under the application ofheat, and they can as a result be combined with oils at the usual high temperatures employed in the lacquer or varnish practice.
- the resole character is to be retained such methods of working are out of the question on account of the readily initiated conversion of theresoles to their infusible and'insoluble condition which takes place under application of heat.
- Air-drying oils which are in some manner combinedwith more 'or less I oxygen show an entirely different behavio'r[towards resoles.
- Air-drying fatty oils for example', which contain a small proportion of their own oxidation products in solution, or which have undergone a mild oxidation throughout their mass, may be incorporated with resoles in any proportion and used in lacquers'to yield surfaces that remain glossy.
- the composite oil and resole products have the surprising property of solution in or dilution with solvents that are otherwise non-solvents for one of the two components, either the oil or the'resole. For instance, a varnish made with such products can be diluted with turpentine aloneor with wood alcohol alone. Films deposited therefrom are hardenable to an exceptional degree. They are resistant to mechanical and chemical influences; as an instance they are not changed ,when sub- Jected for days to the action of organic solvents such as benzene-alcohol, etc.
- Resales for incorporation. with air-drying oils according to this invention can be produced in any suitable manner, for example, by-the condensation of phenol or cresol with an aldehyde such as formaldehyde, using ammonia as a condensing agent.
- Resoles'made by the addition of hardening agents to novolaks can be used, or a mixture of several resoles.
- Suitable air-drying oils are linseed oils, China wood oil, perilla oil, poppyseed oil, linseed-stand oil or mixtures of these oils.
- Oxidation of these oils can be accomplishedin the usual manner, for example, by the action of air at ordinary or, elevated temperatures, simple exposure to the air, short-wave rays, ozonization, etc.'-.
- Several air-drying oils 7 can 'be mixed together and then oxidized or the or a suitable solvent mixture at ordinary'tem-j peratures. Coatings obtained with such oil var-- nishes remain glossy under all conditions, whether they be air dried or hardened by heat at elevated temperatures, and therefore exceptionally desirable.
- a similar mixture in solutioncontaining linseed oil varnish instead of linoxin would upon air drying as well in hardening by heat become turbid and therefore not usable.
- the heating temperature and the-heating period may be decreased in proportion to the increased absorption'ofoxygen by the air-dryin oil.
- the combination of air-drying fatty oils with resoles can be'hastened by the presence of certain catalysts, such'aslead oxide. Catalysts are especially desirable if the air-drying oils contain but a small amount of oxidation products.
- resoles can be combined with linseed oil or the like by boiling the'oil with a solution of the resole in'the presence of oxygen bearins catalysts, such as lead oxide, manganese oxide, etc., or combinations ofthese substances with fatty oils or resins.
- catalysts can be used in admixture or twoor more of them used consecutively.
- the quantity of catalyst to with be added varies with the different oils. linseed oils, for-example, more catalyst is re- 1 part by weight of a solvent dissolving both subin the air and after hardening on metal yield --mixture and it yields "clear drying and clear Resole prepared from technical cresol Solvents as per Example 1..
- the residue is bright and i l-part by weight of a resole prepared by con- 5 ,densation. 1 part by weight of an air-blown linseed oil.
- ' stances equally well, for example, cyclohexanol or a 1:1 mixture of turpentine and wood alcohol or a 1:1 mixture of benzolwood alcohol.
- films obtained from such solutions quickly dry elastic coatings resistant to organic solvents, such as carbon disulfide.
- Example 2 Theprocedure is the same as in Example 1, however, instead of air-blown linseed oil a mixturefof equal portions 'of'ordinary China wood oil and air-blown linseed oil are-applied.
- the finished product is clearly soluble in oil 0 turpentine or in an oil of turpentine-wood alcohol hardening films.
- Lead oxide or tjparts man se ,oxide 6 are heated to 120 Clfor l'hoiirfif desired under pressure. Then the'volatile solvent is driven oil! easily soluble in a turpentine-wood alcohol mixture.
- oils which. as specified in the example, are to be combined with the resoles one may dissolve other resins also, as for example,
- Example 5 Parts by weight Hardenable phenol-aldehyde condensation products 2 Melt of oxidized linseed oil and caoutchouc in the proportion of 1:1 2
- Solvents according to Example 1 4 are heated together at a temperature of 100l30 C. until the fusion is completed.
- the films thus produced ar bright.
- the varnishes or films may be vulcanized.
- the products obtained according to the invention may furthermore be used for impregnation. superposed layers of paper, that is, for example, saturated with a wood alcohol solution of the described combination products from resoles and air-drying oils may be molded under heat and pressure into solid pieces. Instead of a single solvent one may in this instance as in all the others use suitable solvent mixtures in the preparation and application of the combination products.
- compositions which comprises mixing a hardenable phenol-aldehyde condensation product with an oxidized air-drying fattyoil in a solvent for both components and thereafter removing the solvent.
- compositions which comprises mixing a hardenable phenol-aldehyde condensation product with an oxidized air-drying fatty oilina solvent for bothcomponents and thereafter removing the solvent under-reduced pressure.
- compositions which comprises mixing hardenable phenol-aldehyde condensation product with an oxidized air-drying fatty oil in a solvent for both components and with .the application of heat, and thereafter removinsthe solvent.
- condensation product with an oxidized air-drying fatty oil in a solvent for both tfimponents and with the application of heat, and'thereafter removing the solvent under reduced pressure.
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Paints Or Removers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Treatment And Processing Of Natural Fur Or Leather (AREA)
- Moulding By Coating Moulds (AREA)
Description
Patented Apr. 14, 1942 UNITED STATES PATENT OFjFlCE" PROCESS OF COMBINING HARDENABLE PHENOL ALDEHYDE CONDENSATION PRODUCTS WITH AIR-DRYING FATTY OILS Fritz Seebach, Erkner, near Berlin, Germany, assignor, by mesne assignments, to Bakelite v Corporation, a corporation of New Jersey No Drawing. Application February 12, 1930, Serial No. 427,993. In Germany February 25,
6 Claims.
Resoles, i. e. synthetic resinous products of a hardenable nature in their fusible and-soluble initial condition, and air-drying, fatty oils cannot be mixed or are insoluble in each other. This "constitutes a serious disadvantage, for resoles .ably changed in imparting the oil-soluble property thereto. The obtained products show a novolak character, that is, they remain fusible and soluble under the application ofheat, and they can as a result be combined with oils at the usual high temperatures employed in the lacquer or varnish practice. However, if the resole character is to be retained such methods of working are out of the question on account of the readily initiated conversion of theresoles to their infusible and'insoluble condition which takes place under application of heat. It has been proposed to simplymix a resole with an airdrying oil in a common solvent at temperatures which do not cause transformation oi! 'the resole. As a matter of fact such solutions are readily obtained; but a separation of oil and resole takes place to a degreecorresponding to the evaporation of the solvent either'from a coating made with the solution or from the solution.
We have now foundthat air-drying oils which are in some manner combinedwith more 'or less I oxygen show an entirely different behavio'r[towards resoles. Air-drying fatty oils, for example', which contain a small proportion of their own oxidation products in solution, or which have undergone a mild oxidation throughout their mass, may be incorporated with resoles in any proportion and used in lacquers'to yield surfaces that remain glossy. The composite oil and resole products have the surprising property of solution in or dilution with solvents that are otherwise non-solvents for one of the two components, either the oil or the'resole. For instance, a varnish made with such products can be diluted with turpentine aloneor with wood alcohol alone. Films deposited therefrom are hardenable to an exceptional degree. They are resistant to mechanical and chemical influences; as an instance they are not changed ,when sub- Jected for days to the action of organic solvents such as benzene-alcohol, etc.
Resales for incorporation. with air-drying oils according to this invention can be produced in any suitable manner, for example, by-the condensation of phenol or cresol with an aldehyde such as formaldehyde, using ammonia as a condensing agent. Resoles'made by the addition of hardening agents to novolaks can be used, or a mixture of several resoles. Suitable air-drying oils are linseed oils, China wood oil, perilla oil, poppyseed oil, linseed-stand oil or mixtures of these oils. Oxidation of these oils can be accomplishedin the usual manner, for example, by the action of air at ordinary or, elevated temperatures, simple exposure to the air, short-wave rays, ozonization, etc.'-. Several air-drying oils 7 can 'be mixed together and then oxidized or the or a suitable solvent mixture at ordinary'tem-j peratures. Coatings obtained with such oil var-- nishes remain glossy under all conditions, whether they be air dried or hardened by heat at elevated temperatures, and therefore exceptionally desirable. A similar mixture in solutioncontaining linseed oil varnish instead of linoxin would upon air drying as well in hardening by heat become turbid and therefore not usable. With the use of air-drying fatty oils which are oxidized to but a small percmtage of their oxygen absorbing capacity it is generally not 'sufllcient to mix resoles with them in any kind of solvent at ordinary temperatures: in such cases bothcompcnents should be heated for some time and preferably in .the presence of a diluting,
agent. The heating temperature and the-heating period may be decreased in proportion to the increased absorption'ofoxygen by the air-dryin oil. The combination of air-drying fatty oils with resoles can be'hastened by the presence of certain catalysts, such'aslead oxide. Catalysts are especially desirable if the air-drying oils contain but a small amount of oxidation products. For example, resoles can be combined with linseed oil or the like by boiling the'oil with a solution of the resole in'the presence of oxygen bearins catalysts, such as lead oxide, manganese oxide, etc., or combinations ofthese substances with fatty oils or resins. Several catalysts can be used in admixture or twoor more of them used consecutively. The quantity of catalyst to with be added varies with the different oils. linseed oils, for-example, more catalyst is re- 1 part by weight of a solvent dissolving both subin the air and after hardening on metal yield --mixture and it yields "clear drying and clear Resole prepared from technical cresol Solvents as per Example 1..
-'under avacuum. The residue is bright and i l-part by weight of a resole prepared by con- 5 ,densation. 1 part by weight of an air-blown linseed oil.
' stances equally well, for example, cyclohexanol or a 1:1 mixture of turpentine and wood alcohol or a 1:1 mixture of benzolwood alcohol.
are heated for or hour at 80-100"C. Then the volatile ingredients are removed under a vacuum while the temperature should not exceed 100'. .After removal of the'volatile ingredients a substance is obtained that is extremely tough at room temperature, yet perfectly clear, consisting of about equal proportions of resole and fatty oil. The product in this consistency is similar to softer kinds of resoles and in appearance is hardly to be distinguished from them.
The clear solubility of the product in wood alcohol or in oil of turpentine is remarkable. The
films obtained from such solutions quickly dry elastic coatings resistant to organic solvents, such as carbon disulfide.
Example 2 Theprocedure is the same as in Example 1, however, instead of air-blown linseed oil a mixturefof equal portions 'of'ordinary China wood oil and air-blown linseed oil are-applied. The finished product is clearly soluble in oil 0 turpentine or in an oil of turpentine-wood alcohol hardening films.
' Ezample-ti Parts y condensation with formaldehyde and ammonia 50 Solvents as per'Example 1 50 standeoil of airblown linseed oil 12 are heated to 100 C. for 1% hours or %.hour to 160 if desired under pressure, and the solvent "is driven off under a vacuum. The finished product is soluble in wood alcohol or in a mixture of wood alcohol and turpentine.
Example f Parts Hardenable condensation products from v cresol, formaldehyde and ammonia '15 Linseed oil varnish Lead oxide or tjparts man se ,oxide 6 are heated to 120 Clfor l'hoiirfif desired under pressure. Then the'volatile solvent is driven oil! easily soluble in a turpentine-wood alcohol mixture. In the oils, which. as specified in the example, are to be combined with the resoles one may dissolve other resins also, as for example,
' natural resins or synthetic resins and proceed analogous 'to the above examples. One may however dissolve in the oils such substances also that ordinarily do not combine with hardenable phenol condensation products, as for example, caoutchouc.
Example 5 Parts by weight Hardenable phenol-aldehyde condensation products 2 Melt of oxidized linseed oil and caoutchouc in the proportion of 1:1 2
Solvents according to Example 1 4 are heated together at a temperature of 100l30 C. until the fusion is completed. The films thus produced ar bright. The varnishes or films may be vulcanized.
One may also obtain molded parts from the combination products of hardenable phenolaldehyde condensation products and air-drying cils by charging the molds with the heated product if desired after admixture with fillers. dyes or other, suitable additions and by hardening for example at temperatures of -150" C. Perfectly clear, hard, elastic substances can thus be obtained The products obtained according to the invention may furthermore be used for impregnation. superposed layers of paper, that is, for example, saturated with a wood alcohol solution of the described combination products from resoles and air-drying oils may be molded under heat and pressure into solid pieces. Instead of a single solvent one may in this instance as in all the others use suitable solvent mixtures in the preparation and application of the combination products.
I claim:
,1. Process of preparing compositions which comprises mixing a hardenable phenol-aldehyde condensation product with an oxidized air-drying fattyoil in a solvent for both components and thereafter removing the solvent.
2. Process of preparing compositions which comprises mixing a hardenable phenol-aldehyde condensation product with an oxidized air-drying fatty oilina solvent for bothcomponents and thereafter removing the solvent under-reduced pressure.-
3. In a process of preparingcompositions from hardenable phenol-aldehyde condensation products and air-drying fatty oils the step which comprises oxidizing an air-drying fatty oil in the presence of the hardenable phenol-aldehyde condensation product.
4.-In a process of preparing compositions from hardenable phenol-aldehyde condensation products and air-drying fatty oils the step which comprises oxidizing an air-drying fatty oil in the presence of the hardenable phenol-aldehyde condensation product, said condensation product being distributed as a suspensionin the oil.
5. Process of preparing compositions which comprises mixing hardenable phenol-aldehyde condensation product with an oxidized air-drying fatty oil in a solvent for both components and with .the application of heat, and thereafter removinsthe solvent.
condensation product with an oxidized air-drying fatty oil in a solvent for both tfimponents and with the application of heat, and'thereafter removing the solvent under reduced pressure.
FRITZ SEEBACH.
murmu- OI" CORRECTION intent Io. 2,279.1;99. April 1h, 19m.
FRITZ SEEBACH. It 1; hreb eertifledthat error appears in the printed specifica tion bf'the, abeve. numbered patant rquiring corr'ecfiidnias follows; Page 2, second column, line 69, claim 6,1or phenoj-aldehyde read -'--phehd1-'aldehyde-j--; and that the said Letters Patent should be read with this cor I e c tion than in that the same may confom to the recordjof the cas ihfihTatnt Signed and sealed this 16th day of June, A. p. 1913.,
Hem-y van Arsdale, (Seal) A Acting Commissioner of Patehta.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2279499X | 1929-02-25 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2279499A true US2279499A (en) | 1942-04-14 |
Family
ID=7993508
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US427993A Expired - Lifetime US2279499A (en) | 1929-02-25 | 1930-02-12 | Process of combining hardenable phenol-aldehyde condensation products with air-drying fatty oils |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US2279499A (en) |
| DE (1) | DE561656C (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2419238A (en) * | 1947-04-22 | Blown wrinkle vaknish |
-
1929
- 1929-02-26 DE DE1929561656D patent/DE561656C/en not_active Expired
-
1930
- 1930-02-12 US US427993A patent/US2279499A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2419238A (en) * | 1947-04-22 | Blown wrinkle vaknish |
Also Published As
| Publication number | Publication date |
|---|---|
| DE561656C (en) | 1932-10-17 |
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