US1936754A - Neutralizing aliphatic acids containing froth-producing substances - Google Patents
Neutralizing aliphatic acids containing froth-producing substances Download PDFInfo
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- US1936754A US1936754A US467391A US46739130A US1936754A US 1936754 A US1936754 A US 1936754A US 467391 A US467391 A US 467391A US 46739130 A US46739130 A US 46739130A US 1936754 A US1936754 A US 1936754A
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- Prior art keywords
- neutralizing
- acid
- froth
- liquor
- cellulose
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- Expired - Lifetime
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- 230000003472 neutralizing effect Effects 0.000 title description 23
- 239000000126 substance Substances 0.000 title description 11
- 125000001931 aliphatic group Chemical group 0.000 title description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 30
- 239000002253 acid Substances 0.000 description 28
- 229920002678 cellulose Polymers 0.000 description 15
- 239000000243 solution Substances 0.000 description 14
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 13
- 235000014113 dietary fatty acids Nutrition 0.000 description 11
- 229930195729 fatty acid Natural products 0.000 description 11
- 239000000194 fatty acid Substances 0.000 description 11
- 150000004665 fatty acids Chemical class 0.000 description 11
- 238000000034 method Methods 0.000 description 11
- 239000001913 cellulose Substances 0.000 description 10
- 238000006243 chemical reaction Methods 0.000 description 8
- 238000006386 neutralization reaction Methods 0.000 description 8
- 229910000029 sodium carbonate Inorganic materials 0.000 description 7
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 6
- 235000017550 sodium carbonate Nutrition 0.000 description 6
- 230000021736 acetylation Effects 0.000 description 5
- 238000006640 acetylation reaction Methods 0.000 description 5
- 229920002301 cellulose acetate Polymers 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical class [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- 239000002244 precipitate Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- 238000007792 addition Methods 0.000 description 3
- -1 alkalimetal acetates Chemical class 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical class [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 239000000701 coagulant Substances 0.000 description 3
- 229910052802 copper Inorganic materials 0.000 description 3
- 239000010949 copper Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000010802 sludge Substances 0.000 description 3
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 230000032050 esterification Effects 0.000 description 2
- 238000005886 esterification reaction Methods 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 229910052742 iron Chemical class 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 229920013683 Celanese Polymers 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 229940037003 alum Drugs 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229960004424 carbon dioxide Drugs 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 235000003891 ferrous sulphate Nutrition 0.000 description 1
- 239000011790 ferrous sulphate Substances 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 150000002506 iron compounds Chemical class 0.000 description 1
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 1
- RUTXIHLAWFEWGM-UHFFFAOYSA-H iron(3+) sulfate Chemical compound [Fe+3].[Fe+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O RUTXIHLAWFEWGM-UHFFFAOYSA-H 0.000 description 1
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 1
- 229910000360 iron(III) sulfate Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 150000002895 organic esters Chemical class 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 description 1
- 229910052939 potassium sulfate Inorganic materials 0.000 description 1
- 235000011151 potassium sulphates Nutrition 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 229940095574 propionic acid Drugs 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/41—Preparation of salts of carboxylic acids
- C07C51/412—Preparation of salts of carboxylic acids by conversion of the acids, their salts, esters or anhydrides with the same carboxylic acid part
Definitions
- a further object of our invention is to form alkalimetal acetates by the neutralization of the relatively dilute acetic acid obtained Whenwater is added to solutions of cellulose acetate in acetic acid to precipitate the cellulose acetate. Further objects of our invention will appear from the following detailed description.
- the dilute acid solutions may be heated in a batch the dilute acid is separated from the precipitated cellulose ester.
- dilute acid contains; either in suspension or in solution, certain organicmat-.
- the process maybefa continuous one and thismay be done bypassing the solutions of the fatty acids through tubes or coils that are heated to the neutralizing vat.
- the liquor does not cool to room tempera tures, but about one-half of the heat is. retained in the liquor when evaporationis commenced.
- acid obtained from the precipitation of cellulose acetate contains sulfuric acid that may have been employed as a catalyst, the same may be treated with the carbonate or hydroxide of barium to precipitate barium sulfate.
- sulfuric acid is not absolutely necessary; since the sodium sulfate or potassium sulfate formed during neutralization does not form any scale in the evaporators.
- soda ash sodium carbonate
- additions of both the acid and soda ash is carried on in such a manner thatthe liquor in the neutralizing vat is kept almost at the neutral point.
- aluminum sulfate .in amounts equal to about 0.015% of theliquor present is added.
- aluminum 'sulfate is usually added in the form of a solution in a small amount of water.
- liquor in the vat is then tested and adjustments are made'so that it has a slightly alkaline reac--' tion'corresponding to an excess of 0.05' to 0.1% of sodium carbonate.
- Method of neutralizing a relatively dilute lower aliphatic acid containing a'froth-producing substance comprising treating the-same at a tem
- the temperature of the acid is which generates gas upon neutralizing the acid.
- the dilute acid to be neutralized say acetic 3
- Method of neutralizing a relatively dilute lower fatty acid recovered from the reaction mass "r'esulting'from the esterification of cellulose and containing a froth producing substance comprising treating the same at a temperature above C. with an alkaline substance which gencrates gas upon neutralizing the acid and then settling the resulting liquor.
- Method of neutralizing relatively dilute acetic acid recovered from the reaction mass resulting from the esterification of. cellulose and containing a froth producing substance comprising treating the same-at a temperature above 60C. with an alkaline substance which generates gas upon'neutralizing the acid and then settling .the resultingliquor.
- Method. of neutralizing a relativelydilute lower fatty. acid containing a froth-producing substance comprising neutralizing the same at a temperature above 60? C. with an alkaline substance: which generates gas upon neutralizing with an alkaline, carbonate and towards the end of the reaction adding a coagulant thereto. 7 7 10.
- Method. of neutralizing relatively dilute acetic acid -recovered from the reaction mass resulting from the acetylation of cellulose and containing a froth-producing,substance comprising treating the same at a temperature above 60 C. withan alkaline carbonate and towards the end of the reactionadding a soluble iron compound.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
Description
Patented Nov. 28, 1933 T res 1,936,254 PAT 'r crrrca NEUTRALIZING ALIPHATIC. ACIDS coN ,TAINING FROTH PRODUCING SUB- STANCES Camille Dreyfus, New York, N.
Y., and Clifford I.
Haney, Brummondville, Quebec, Canada, assigners to Celanese Corporation of America, a p p is ccrporation of Delaware 1 No Drawing. Application July 11, 1930 Serial No. 467,391
11 Claims.
' or other lower aliphatic acids in an economical and expeditious manner. I i
A further object of our invention is to form alkalimetal acetates by the neutralization of the relatively dilute acetic acid obtained Whenwater is added to solutions of cellulose acetate in acetic acid to precipitate the cellulose acetate. Further objects of our invention will appear from the following detailed description.
In the formation of cellulose acetate or other organic esters of cellulose, the usual manner is to esterify the cellulose in the presence of the anhydride of the lower fatty acid corresponding to the cellulose ester to be formed and also in the presence of such lower fatty acid. When esterirfication is complete, the'cellulose ester dissolves in the lower fatty'acid'present. In order to'precipitate the cellulose ester, there is added at a subsequent stage ofthe process, water insufficient quantities to dilute the acid until it no longer retains the cellulose ester in solution, and
such as formic acid,'prop ionic acid or butyric acid.
In accordance with our invention, we neutralize relatively dilute solutions of lower fatty acids which contain froth-producing impurities by heating the same at elevated temperatures and then neutralizing them at such temperatures with an alkaline material, and then after settling, subjecting the solution to evaporation to recover the salts of the fatty acids. While' at present this invention is of greatest importance in connect-ion With the neutralization of dilute acetic acid ob tained after the acetylation of cellulose, it isap-= plicable to solutions of other lower fatty acids lhe invention is not confined to the neutraliza tion of such acids as are obtained from the esterif fication of cellulose, but is also applicableto the" neutralization of such acids obtained in any man ner. By relatively dilute solutions of the acids we intend to include solutions of 5,to' 50% or more concentration and particularly aqueous solutions of such acids.
As stated the relatively dilute solutions of the acids are heated at elevated temperatures, say
above 60 0., preferably between 90 and-100 C.
- The dilute acid solutions may be heated in a batch the dilute acid is separated from the precipitated cellulose ester.
However such dilute acid contains; either in suspension or in solution, certain organicmat-.
ters that cause frothing when-sodium carbonate is added thereto at room temperatures even while stirring. The froth so formed persists for hours and interferes with the'further working up of a solution of the metal salt thus formed on a commercial scale. Heretofore it has been theprac tice to distil the lower fatty acid, such as acetic acid, from such waste organic material, and then to neutralize the distillate. This distillation involves great expense, and moreover, even when copper stills are employed, the acid attacks the stills so that they depreciate rapidly.
-We have found that if such dilute lower fatty acid is neutralized, say with sodium carbonate,
while'at elevated temperatures, that the froth produced tends to breakdown quite readily, so that at such elevated temperatures, the neutralization can be carried outquickly enough for practical purposes. Contrary to expectation, there is noappreciable loss of acetic acid or other relatively volatile lower fatty acid during the neutralizing of the hot acid, owing to thefact that the froth that is formed acts as a fractionating column which permits only water vapor and carbondioxide to escape into the air,
liquor, so thatupon process in vessels of copper, wood, stainless steel and the like. If desired the process maybefa continuous one and thismay be done bypassing the solutions of the fatty acids through tubes or coils that are heated to the neutralizing vat.
For neutralizing the lower fatty acid, we prefer. to use sodium carbonate for economical reasons. However othercarbonates such as of potassium or calcium may be used as may the iii-carbonates v, v
of sodium and potassium. p H
During the neutralization'of the acid liquor, the organic products that are soluble in thedilute acid Often some of thisorganic material is so fine separate from the solution in a very fine form.
that it does notsettle outcompletely fromthe decantation it remains in the neutralized liquor and causes frothirig ofthe' same when it is evaporated. In such cases, we have found it preferable to add to the liquor. being neutralized small quantities of coagulatingagentssuch as soluble salts of aluminum and iron, examples of which are alum, aluminum sulfate, ferrous sulfate, ferric sulfate-or the doublesaltg of aluminum and ferric sulfate; liquor becomes slightly alkaline at the end of neutralization, these iron or aluminum compounds precipitate outas hydroxides and act as coagulants tobring down these organic bodies. J. In manycases there are enough organic impurities present in the dilute neutralizing'and act as coagulants for the gfine, organic precipitate, inwhich, case the additionof. other coagulantsis not'absolutely necessary.
As soon as the acid'which precipitate-out on time, the liquor does not cool to room tempera tures, but about one-half of the heat is. retained in the liquor when evaporationis commenced.
acid obtained from the precipitation of cellulose acetate, contains sulfuric acid that may have been employed as a catalyst, the same may be treated with the carbonate or hydroxide of barium to precipitate barium sulfate. However the removal of sulfuric acid is not absolutely necessary; since the sodium sulfate or potassium sulfate formed during neutralization does not form any scale in the evaporators.
In order further to illustrate our invention but without being limited thereto, thefollowing specific example is given.
7 Example Dilute acetic acid obtained from the precipitation of cellulose acetate by the addition of water to the acetylation mixture, and having a concentration of say 20%, is heated in a copper or wood container by means of a closed steam coil until it attains a temperature of 90 to 95 C. .When' this temperature is reached, the acid is run into a wooden neutralizing vat provided. with a me chanical agitator and asmall open steam connection. .As soon as the acid liquor starts to run into the 'vat, agitation is commenced and a small -amount of steam is injected into the liquor through the open steam connection to make up for the heat lost from the liquor to the vat and by radiation. maintained around 90 C.
While the acid is running into the vat the addition of soda ash (sodium carbonate) is commenced and additions of both the acid and soda ash is carried on in such a manner thatthe liquor in the neutralizing vat is kept almost at the neutral point. When the neutralizing vat is filled, aluminum sulfate .in amounts equal to about 0.015% of theliquor present is added. The
aluminum 'sulfateis usually added in the form of a solution ina small amount of water. The
. liquor in the vat is then tested and adjustments are made'so that it has a slightly alkaline reac--' tion'corresponding to an excess of 0.05' to 0.1% of sodium carbonate. g
lhe agitation is stopped after several minutes, 'and' the liquorinithe vat allowed to stand,
whereupon the precipitates settle, and after 12 hours or even less time, a liquor 7 or 8 feet'deep will have cleared. The sludge that collects at the bottom of the vat is not disturbed and the clear liquor is drawn off for evaporation. During the evaporation-no difiiculty with frothing is encountered; Without cleaning the vat, a number of-operations may beperformed, allowing the sludge torsettle each time, until it becomes severalinches deep, whereupon the sludge is removed-end a fresh series of operations commenced;
It is to'be understood that the foregoing example'xis'given merely by Way of illustration and that many variations may be made therein without departing from the spirit of our invention.
' Having described our invention, what we desire to secure by Letters Patent is:
1. Method of neutralizing a relatively dilute lower aliphatic acid containing a'froth-producing substancecomprising treating the-same at a tem The temperature of the acid is which generates gas upon neutralizing the acid. If the dilute acid to be neutralized, say acetic 3; Method of neutralizing a relatively dilute lower fatty acid recovered from the reaction mass "r'esulting'from the esterification of cellulose and containing a froth producing substance comprising treating the same at a temperature above C. with an alkaline substance which gencrates gas upon neutralizing the acid and then settling the resulting liquor.
4'. Method of neutralizing relatively dilute acetic acid recovered from the reaction mass resulting from the esterification of. cellulose and containing a froth producing substance comprising treating the same-at a temperature above 60C. with an alkaline substance which generates gas upon'neutralizing the acid and then settling .the resultingliquor.
5. 'Method "of neutralizing relatively dilute" acetic acidrecovered from the reaction mass resulting from the acetylation of cellulose and containing a froth-producing substance comprising treating the same with an alkaline carbonate at temperatures above 60 C. and then permitting the resulting liquor to settle.
6. Method of neutralizing relatively dilute acetic acid recovered from the reaction mass resulting from the acetylation of cellulose and containing a froth-producing substancecomprising treating. the same with an alkaline carbonate at temperatures between 90and' 100 C. and then permitting the resulting liquor to settle."
7.Method' of neutralizing a relativelydilute lower: fatty. acid containing a froth-producing substance comprising neutralizing the same at a temperature above 60? C. with an alkaline substance: which generates gas upon neutralizing with an alkaline, carbonate and towards the end of the reaction adding a coagulant thereto. 7 7 10. Method. of neutralizing relatively dilute acetic acid -recovered from the reaction mass resulting from the acetylation of cellulose and containing a froth-producing,substance comprising treating the same at a temperature above 60 C. withan alkaline carbonate and towards the end of the reactionadding a soluble iron compound.
1l.-Method of neutralizing relatively dilute acetic acid recovered from the reaction mass resulting from theacetylation of cellulose and con-- taining a froth-producing substance comprising treating the same at a temperature above 60 C.
with an alkaline carbonate and'towards the end of the reaction adding a soluble aluminum compound. 1
CAMILLE DRE YE US.
CLIFFORD I. HANEY.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US467391A US1936754A (en) | 1930-07-11 | 1930-07-11 | Neutralizing aliphatic acids containing froth-producing substances |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US467391A US1936754A (en) | 1930-07-11 | 1930-07-11 | Neutralizing aliphatic acids containing froth-producing substances |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1936754A true US1936754A (en) | 1933-11-28 |
Family
ID=23855496
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US467391A Expired - Lifetime US1936754A (en) | 1930-07-11 | 1930-07-11 | Neutralizing aliphatic acids containing froth-producing substances |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1936754A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3274105A (en) * | 1962-08-03 | 1966-09-20 | Soc Etu Chimiques Ind Et Agri | Fire extinguishing composition |
-
1930
- 1930-07-11 US US467391A patent/US1936754A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3274105A (en) * | 1962-08-03 | 1966-09-20 | Soc Etu Chimiques Ind Et Agri | Fire extinguishing composition |
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