US1810660A - Method of and composition for increasing the conductivity of - Google Patents
Method of and composition for increasing the conductivity of Download PDFInfo
- Publication number
- US1810660A US1810660A US1810660DA US1810660A US 1810660 A US1810660 A US 1810660A US 1810660D A US1810660D A US 1810660DA US 1810660 A US1810660 A US 1810660A
- Authority
- US
- United States
- Prior art keywords
- composition
- conductivity
- oleate
- naphtha
- alkyl group
- 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
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- 239000000203 mixture Substances 0.000 title description 20
- 238000000034 method Methods 0.000 title description 6
- 125000000217 alkyl group Chemical group 0.000 description 15
- 239000003209 petroleum derivative Substances 0.000 description 13
- 230000005611 electricity Effects 0.000 description 10
- 229930195733 hydrocarbon Natural products 0.000 description 9
- 150000002430 hydrocarbons Chemical class 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- 239000002904 solvent Substances 0.000 description 9
- 239000000126 substance Substances 0.000 description 9
- 238000006467 substitution reaction Methods 0.000 description 8
- 229940049964 oleate Drugs 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- 238000004880 explosion Methods 0.000 description 6
- 235000014113 dietary fatty acids Nutrition 0.000 description 5
- 229930195729 fatty acid Natural products 0.000 description 5
- 239000000194 fatty acid Substances 0.000 description 5
- 150000004665 fatty acids Chemical class 0.000 description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 5
- 239000000344 soap Substances 0.000 description 5
- 239000003350 kerosene Substances 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 230000003068 static effect Effects 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000004140 cleaning Methods 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- AXLHVTKGDPVANO-UHFFFAOYSA-N methyl 2-amino-3-[(2-methylpropan-2-yl)oxycarbonylamino]propanoate Chemical compound COC(=O)C(N)CNC(=O)OC(C)(C)C AXLHVTKGDPVANO-UHFFFAOYSA-N 0.000 description 3
- 239000003208 petroleum Substances 0.000 description 3
- ICLYJLBTOGPLMC-KVVVOXFISA-N (z)-octadec-9-enoate;tris(2-hydroxyethyl)azanium Chemical compound OCCN(CCO)CCO.CCCCCCCC\C=C/CCCCCCCC(O)=O ICLYJLBTOGPLMC-KVVVOXFISA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 241000282461 Canis lupus Species 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- KGWDUNBJIMUFAP-KVVVOXFISA-N Ethanolamine Oleate Chemical compound NCCO.CCCCCCCC\C=C/CCCCCCCC(O)=O KGWDUNBJIMUFAP-KVVVOXFISA-N 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- 239000004020 conductor Substances 0.000 description 2
- 238000004043 dyeing Methods 0.000 description 2
- ARNAHNTWKSJFHG-KVVVOXFISA-N ethanamine;(z)-octadec-9-enoic acid Chemical compound CCN.CCCCCCCC\C=C/CCCCCCCC(O)=O ARNAHNTWKSJFHG-KVVVOXFISA-N 0.000 description 2
- 229940031124 ethanolamine oleate Drugs 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 229960005068 monoethanolamine oleate Drugs 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 229940117013 triethanolamine oleate Drugs 0.000 description 2
- BTXXTMOWISPQSJ-UHFFFAOYSA-N 4,4,4-trifluorobutan-2-one Chemical compound CC(=O)CC(F)(F)F BTXXTMOWISPQSJ-UHFFFAOYSA-N 0.000 description 1
- BQACOLQNOUYJCE-FYZZASKESA-N Abietic acid Natural products CC(C)C1=CC2=CC[C@]3(C)[C@](C)(CCC[C@@]3(C)C(=O)O)[C@H]2CC1 BQACOLQNOUYJCE-FYZZASKESA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- BAVYZALUXZFZLV-UHFFFAOYSA-O Methylammonium ion Chemical compound [NH3+]C BAVYZALUXZFZLV-UHFFFAOYSA-O 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- FVFJGQJXAWCHIE-UHFFFAOYSA-N [4-(bromomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CBr)C=C1 FVFJGQJXAWCHIE-UHFFFAOYSA-N 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- -1 benzine Chemical class 0.000 description 1
- WGQKYBSKWIADBV-UHFFFAOYSA-O benzylaminium Chemical compound [NH3+]CC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-O 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical class CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 1
- QUSNBJAOOMFDIB-UHFFFAOYSA-O ethylaminium Chemical compound CC[NH3+] QUSNBJAOOMFDIB-UHFFFAOYSA-O 0.000 description 1
- 239000003517 fume Substances 0.000 description 1
- YIWJUZGFAAAAKE-UHFFFAOYSA-N hexadecanoate triethylazanium Chemical compound C(CCCCCCCCCCCCCCC)(=O)[O-].C(C)[NH+](CC)CC YIWJUZGFAAAAKE-UHFFFAOYSA-N 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- GCVIWLTVOFILLW-KVVVOXFISA-N n,n-diethylethanamine;(z)-octadec-9-enoic acid Chemical compound CCN(CC)CC.CCCCCCCC\C=C/CCCCCCCC(O)=O GCVIWLTVOFILLW-KVVVOXFISA-N 0.000 description 1
- VUGKVBQHAGIDDN-UHFFFAOYSA-N n-ethyl-n-hydroxyethanamine oxide Chemical compound CC[N+](O)([O-])CC VUGKVBQHAGIDDN-UHFFFAOYSA-N 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 239000000615 nonconductor Substances 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000002942 palmitic acid derivatives Chemical class 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000000135 prohibitive effect Effects 0.000 description 1
- 239000011347 resin Chemical class 0.000 description 1
- 229920005989 resin Chemical class 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- CBXCPBUEXACCNR-UHFFFAOYSA-N tetraethylammonium Chemical compound CC[N+](CC)(CC)CC CBXCPBUEXACCNR-UHFFFAOYSA-N 0.000 description 1
- 229960004418 trolamine Drugs 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
- D06L1/00—Dry-cleaning or washing fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods
- D06L1/02—Dry-cleaning or washing fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods using organic solvents
- D06L1/04—Dry-cleaning or washing fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods using organic solvents combined with specific additives
Definitions
- Our invention relates to compositions such as described in the title, and particularly to a simple and cheaply produced chemical and process for use for accomplishing the desired result.
- the lighter hydrocarbons have a multitude of uses under conditions where static is formed, and in the absence of means for dissipating the accumulated elec tricity there is constant danger of sparking. This is illustrated in the transporting of quantities of gasoline and benzine, etc. in tanks by motor truck, in which the practice is to append a chain to the frame of the vehicle, allowing it to drag on the ground. In other cases, the possibility of grounding the charge is more difl icult danger from explosions from sparks. In some cases it is necessary to brush articles with metal brushes and gasoline and there are many cases of explosions taking place during this process.
- naphtha which is a petroleum hydrocarbon. It has been used for many years and there is constant 1929. Serial No. 372,534.
- the process consists in washing and rubbing garments in straight naphtha to which a benzine soluble soap has been added.
- naphtha is a nonconductor of electricity, having a resistance of about one million megohms. For this reason, silk or WOOl garments, when they are washed or rubbed in it form static electricity. This electricity, when it accumulates, forms sparks. These sparks ignite the naphtha vapors in the air and an explosion takes place. A number of accidents have happened and the result is that the insurance rate in dyeing and cleaning establishments is prohibitive. Lately, the cleaners are using a higher boiling fraction of naphtha, which is a kerosene. The disadvantage of using this kerosene is that it requires special equip.- ment to dry it out from the garments and to eliminate the odor of kerosene.
- Richterol A preparation to increase the conductivity of naphtha was suggested some years ago by a German chemist, Dr. Richter, and this preparation has been named after him, Richterol. Richterol has not attained a Very great degree of success for many reasons.
- the composition of Richterol is magnesium oleate, which is known to increase the conductivity of cleaners naphtha. Magnesium oleate made by the wet process will not dissolve in gasoline or naphtha and for this reason will not increase the conductivity of either of them. Even properly prepared oleate of magnesium is very sparinglysoluble in naphtha; traces of Water will precipitate it. In general, it has proven to be .Very unreliable and its use has been quite limited. Other metallic salts of fattyacids have been tried and have proven to be still less adaptable than magnesium oleate.
- di, tri and tetra derivatives can be formed or their mixtures.
- any soap compound which is an organic substitution product of the (ammonium salt of a fatty acid can be formed or their mixtures.
- the solvent in which the chemical used for increasing conductivity is combined need not necessarily be a petroleum hydrocarbon. It may be propyl alcohol, ethyl acetate, acetone, or any other organic solvent that will act as a metal brush on metal surfaces a solvent for these particular chemicals and that will dissolve in petroleum hydrocarbons.
- R hydrogen, an alkyl group, the hydroxy derivatives of an alkyl group, the substitution products of an alkyl group
- X equals an alkyl group, the hydroxy derivatives of an alkyl group, the substitution products of an alkyl group
- N equals nitrogen
- FA equals any fatty acid or resin acids like abietic acid.
- R hydrogen, an alkyl group, the hydroxy derivatives of an alkyl group, the substitution products of an alkyl group
- X equals an alkyl group, the hydroxy derivatives of an alkyl group, the substitution products of an alkyl group
- N equals nitrogen
- FA equals any fatty acid or resin acids like abietic acid.
- this formula may indicate tetra-ethyl-amine oleate, triethyl-amine-palmitate, or mono-ethyl-aminesteal-ate, etc.
- a composition of matter that is a conductor of electricity consisting of a light petroleum distillate, and a chemical of the general formula Ra in which R equals hydrogen, an alkyl group, hydroxy derivatives of an alkyl group, the
- substitution products of any alkyl group X equals an alkyl group, hydroxy derivatives of any alkyl group, the substitution products of any alkyl group, N equals nitrogen, and FA equals any soap forming higher fatty acid, said chemical being soluble in said distillate.
- composition of matter that is a conductor of electricity consisting of a chemical of the general formula substitution products of any al yl group, N equals nitrogen, FA is any soap forming higher fatty acid, X equals an alkyl group,
- a composition of matter for increasing the conductivity of a light petroleum distillate consisting of tri-ethanol amine oleate, and a solvent therefor, the composition being soluble in said distillate.
- a composition of matter for increasing the conductivity of light petroleum distillates consisting of tri-ethanol amine oleate and a solvent therefor that is not a light petroleum distillate, the composition being soluble in said distillate.
- composition of matter for increasing the conductivity of light petroleum distillate consisting of mono-ethanol amine oleate,
- a composition of matter for increasing the conductivity of light petroleum distillates consisting of mono-ethanol amine oleate and a solvent therefor that is not a light petroleum distillate, the composition being soluble in said distillate.
- a composition of matter for increasing the conductivity of light petroleum distillates consistin of di-ethanol amine oleate and a solvent 1: erefor that is not a light petroleum distillate, the composition being soluble in said distillate.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Detergent Compositions (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Liquid Carbonaceous Fuels (AREA)
Description
, electricity Patented June 16, 1931 UNITED STATES PATENT OFFICE WOLF KRITCHEVSKY AND ELLIOTT MORRILL, OF CHICAGO, ILLINOIS, ASSIGNORS, BY
MESN E ASSIGNMENTS, TO ILLINOIS SPARKLESS METHOD OF AND COMPOSITION FOR INCREASING THE CLEANER COMPANY, .A CORPORATION OF CON DUCTIVITY OF HYDROCARIBON S No Drawing. Application filed June 20,
Our invention relates to compositions such as described in the title, and particularly to a simple and cheaply produced chemical and process for use for accomplishing the desired result.
It is a well-known fact that aliphatic hydrocarbons do not conduct electricity, like for instance naphtha, gasoline, kerosene, benzine, pctrolatum etc. The result is that when they come in contact with materials that are electrically charged, sparks are formed due to the accumulation of static electricity and it is discharged into the air. For instance, if a quantity of benzine is drawn through pipes that are electrically charged, sparks will be formed, or by brushing metallic surfaces against each other in benzine of other petroleum hydrocarbons.
There may be no harm from spark formation when higher hydrocarbons are used, and the flash point is high, as there would be no danger of explosion or ignition. On the other hand, when this happens to all hydrocarbons like benzine, cleaners naphtha, or gasoline, where the. flash point is about room temperature, the sparks 'lormcd ignite the hydrocarbon and especially the fumes in the air, and an explosion takes place.
The lighter hydrocarbons have a multitude of uses under conditions where static is formed, and in the absence of means for dissipating the accumulated elec tricity there is constant danger of sparking. This is illustrated in the transporting of quantities of gasoline and benzine, etc. in tanks by motor truck, in which the practice is to append a chain to the frame of the vehicle, allowing it to drag on the ground. In other cases, the possibility of grounding the charge is more difl icult danger from explosions from sparks. In some cases it is necessary to brush articles with metal brushes and gasoline and there are many cases of explosions taking place during this process.
very important use for naphtha is in the cleaning and dyeing industry. It is well known that the best known cleaner for garments is naphtha which is a petroleum hydrocarbon. It has been used for many years and there is constant 1929. Serial No. 372,534.
for professional cleaning and also by the general public. The process consists in washing and rubbing garments in straight naphtha to which a benzine soluble soap has been added.
One of the main disadvantages of the use of naphtha is that it is a nonconductor of electricity, having a resistance of about one million megohms. For this reason, silk or WOOl garments, when they are washed or rubbed in it form static electricity. This electricity, when it accumulates, forms sparks. These sparks ignite the naphtha vapors in the air and an explosion takes place. A number of accidents have happened and the result is that the insurance rate in dyeing and cleaning establishments is prohibitive. Lately, the cleaners are using a higher boiling fraction of naphtha, which is a kerosene. The disadvantage of using this kerosene is that it requires special equip.- ment to dry it out from the garments and to eliminate the odor of kerosene.
The general public which has not any special cleaners equipment is still confined to the use of naphtha and accidents due to eXplosions are frequent.
A preparation to increase the conductivity of naphtha was suggested some years ago by a German chemist, Dr. Richter, and this preparation has been named after him, Richterol. Richterol has not attained a Very great degree of success for many reasons. The composition of Richterol is magnesium oleate, which is known to increase the conductivity of cleaners naphtha. Magnesium oleate made by the wet process will not dissolve in gasoline or naphtha and for this reason will not increase the conductivity of either of them. Even properly prepared oleate of magnesium is very sparinglysoluble in naphtha; traces of Water will precipitate it. In general, it has proven to be .Very unreliable and its use has been quite limited. Other metallic salts of fattyacids have been tried and have proven to be still less adaptable than magnesium oleate.
We have found that the organic ammonium salts of fatty acidswhich are soluble in petroleum hydrocarbons remarkably increase the conductivity of those hydrocarbons; this includes the organic substitution products of ammonia that are soluble in the described medium. For instance, by substituting one of the hydrogens of ammonium oleate with the methyl oup, the substance taking the place of the ydrogen linked to the nitrogen atom, we get methyl ammonium oleate the same way we can obtain the ethyl ammonium oleate, the phenyl ammonium oleate, the hydroXy alkyl ammonium oleate, benzyl ammonium oleate, or instead of the oleates, the linoleatcs, stcaratcs, palmitates, laurates, ricinoleates, resina-tes of an caid capable of forming a so-called soap. Instead of monoderivatives, di, tri and tetra derivatives can be formed or their mixtures. For instance, We can have tri-ethyl ammonium oleate, dihydroxy diethyl ammonium resinate, etc. In other words, any soap compound which is an organic substitution product of the (ammonium salt of a fatty acid.
As an example, we wish to cite one that will be illustrative of all the combinations above stated. For instance, when we dissolve one part of tri-ethanol amine oleatein 2000 parts of cleaners naphtha, the resistance of the naphtha decreases from one million megohms to less than ten megohms. In other words, the conductivity has increased 100,000 times. Similar observations have been made on ethyl amine oleate and many other chemicals belonging to the same class.
We have added one ounce of ethyl amine oleate to 15 gallons of gasoline and have washed in it silk garments, rubbed them and treated them otherwise to produce static electricity, and yet there was not spark formation. We have taken a small portion of ordi nary gasoline and dipped the two balls of an electro-static machine therein, and by revolving it a few times, we have produced sparks in the gasoline which has ignited the hydrocarbon; we then took the same amount of gasoline treated as above described, and dippedthe two balls in this same mixture, and revolved the machine for a long time and no sparks were formed, either in the gasoline so treated or around the brushes. We have also used gasoline so treated and used it as a cleaner with and no sparks were formed. We have placed a motor in this solution and let it run and there was no spark formation whatever at the brushes, while otherwise there would have been continuous sparking at the brushes. We believe we have sufliciently described our invention to include the scope of chemicals we desire to use and have indicated in a general way applications and possibilities of it.
The solvent in which the chemical used for increasing conductivity is combined need not necessarily be a petroleum hydrocarbon. It may be propyl alcohol, ethyl acetate, acetone, or any other organic solvent that will act as a metal brush on metal surfaces a solvent for these particular chemicals and that will dissolve in petroleum hydrocarbons.
We prefer to represent the product by the following formula in which R equals hydrogen, an alkyl group, the hydroxy derivatives of an alkyl group, the substitution products of an alkyl group, X equals an alkyl group, the hydroxy derivatives of an alkyl group, the substitution products of an alkyl group, N equals nitrogen and FA equals any fatty acid or resin acids like abietic acid. In each case all the three Rs and the X may he the same group, or they may be different groups. For instance, this formula may indicate tetra-ethyl-amine oleate, triethyl-amine-palmitate, or mono-ethyl-aminesteal-ate, etc.
We claim:
1. A composition of matter that is a conductor of electricity consisting of a light petroleum distillate, and a chemical of the general formula Ra in which R equals hydrogen, an alkyl group, hydroxy derivatives of an alkyl group, the
substitution products of any alkyl group, X equals an alkyl group, hydroxy derivatives of any alkyl group, the substitution products of any alkyl group, N equals nitrogen, and FA equals any soap forming higher fatty acid, said chemical being soluble in said distillate.
2. A composition of matter that is a conductor of electricity consisting of a chemical of the general formula substitution products of any al yl group, N equals nitrogen, FA is any soap forming higher fatty acid, X equals an alkyl group,
hydroxy derivatives of any alkyl group, the substitution product-s of any alkyl group, and a solvent therefor, the finished product being soluble in light petroleum distillate.
3. A composition of matter for increasing the conductivity of a light petroleum distillate, consisting of tri-ethanol amine oleate, and a solvent therefor, the composition being soluble in said distillate.
4. A composition of matter for increasing the conductivity of light petroleum distillates, consisting of tri-ethanol amine oleate and a solvent therefor that is not a light petroleum distillate, the composition being soluble in said distillate.
5. A composition of matter for increasing the conductivity. of light petroleum distillate consisting of mono-ethanol amine oleate,
and a solvent therefor, the composition being soluble in said distillate.
6. A composition of matter for increasing the conductivity of light petroleum distillates, consisting of mono-ethanol amine oleate and a solvent therefor that is not a light petroleum distillate, the composition being soluble in said distillate.
7 A. composition of matter for increasing 10 the conductivity of a light petroleum distillate consisting of di-ethanol amine oleate, and a solvent therefor, the composition being soluble in said distillate.
8. A composition of matter for increasing the conductivity of light petroleum distillates, consistin of di-ethanol amine oleate and a solvent 1: erefor that is not a light petroleum distillate, the composition being soluble in said distillate. In testimony whereof we have aflixed our si gnatu res.
WOLF KRITGHEVSKY. ELLIOTT MORRILL.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US356717XA | 1929-06-20 | 1929-06-20 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1810660A true US1810660A (en) | 1931-06-16 |
Family
ID=21884088
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US1810660D Expired - Lifetime US1810660A (en) | 1929-06-20 | Method of and composition for increasing the conductivity of |
Country Status (3)
| Country | Link |
|---|---|
| US (1) | US1810660A (en) |
| DE (1) | DE546008C (en) |
| GB (1) | GB356717A (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2475418A (en) * | 1945-09-20 | 1949-07-05 | Fmc Corp | Dry cleaning |
| US2503744A (en) * | 1947-08-12 | 1950-04-11 | Great Lakes Carbon Corp | Method and agent for preventing linting in the dry cleaning of fabrics |
| US2729576A (en) * | 1953-09-29 | 1956-01-03 | Davies Young Soap Company | Method of dry cleaning fabric and simultaneously rendering the same antistatic |
| US2820719A (en) * | 1952-08-27 | 1958-01-21 | Davies Young Soap Company | Process for rendering fabrics water repellent |
| US3101239A (en) * | 1953-10-07 | 1963-08-20 | R R Street & Co Inc | Dry cleaning |
| US3101240A (en) * | 1953-06-29 | 1963-08-20 | Martin B Mathews | Dry cleaning |
| US3210148A (en) * | 1960-12-15 | 1965-10-05 | Extraction Continue De Smet Sa | Water, isopropanol and hexane scouring of wool |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3029136A (en) * | 1955-10-05 | 1962-04-10 | Gulf Research Development Co | Stabilized distillate fuel oils |
| US3033665A (en) * | 1958-08-01 | 1962-05-08 | Gulf Research Development Co | Nonstalling gasoline motor fuel |
-
0
- US US1810660D patent/US1810660A/en not_active Expired - Lifetime
-
1930
- 1930-06-06 GB GB17635/30A patent/GB356717A/en not_active Expired
- 1930-06-07 DE DE1930546008D patent/DE546008C/en not_active Expired
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2475418A (en) * | 1945-09-20 | 1949-07-05 | Fmc Corp | Dry cleaning |
| US2503744A (en) * | 1947-08-12 | 1950-04-11 | Great Lakes Carbon Corp | Method and agent for preventing linting in the dry cleaning of fabrics |
| US2820719A (en) * | 1952-08-27 | 1958-01-21 | Davies Young Soap Company | Process for rendering fabrics water repellent |
| US3101240A (en) * | 1953-06-29 | 1963-08-20 | Martin B Mathews | Dry cleaning |
| US2729576A (en) * | 1953-09-29 | 1956-01-03 | Davies Young Soap Company | Method of dry cleaning fabric and simultaneously rendering the same antistatic |
| US3101239A (en) * | 1953-10-07 | 1963-08-20 | R R Street & Co Inc | Dry cleaning |
| US3210148A (en) * | 1960-12-15 | 1965-10-05 | Extraction Continue De Smet Sa | Water, isopropanol and hexane scouring of wool |
Also Published As
| Publication number | Publication date |
|---|---|
| DE546008C (en) | 1932-03-09 |
| GB356717A (en) | 1931-09-07 |
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