US2170644A - Wetting and spreading agent for oils - Google Patents
Wetting and spreading agent for oils Download PDFInfo
- Publication number
- US2170644A US2170644A US158374A US15837437A US2170644A US 2170644 A US2170644 A US 2170644A US 158374 A US158374 A US 158374A US 15837437 A US15837437 A US 15837437A US 2170644 A US2170644 A US 2170644A
- Authority
- US
- United States
- Prior art keywords
- oils
- water
- phenol
- wetting
- alkyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000003921 oil Substances 0.000 title description 16
- 238000009736 wetting Methods 0.000 title description 2
- 239000003795 chemical substances by application Substances 0.000 title 1
- -1 alkyl phenol Chemical compound 0.000 description 21
- 239000002480 mineral oil Substances 0.000 description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
- 235000019198 oils Nutrition 0.000 description 15
- 235000010446 mineral oil Nutrition 0.000 description 10
- 238000000034 method Methods 0.000 description 9
- 230000008020 evaporation Effects 0.000 description 8
- 238000001704 evaporation Methods 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- 229920006395 saturated elastomer Polymers 0.000 description 8
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 5
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 230000002401 inhibitory effect Effects 0.000 description 4
- 239000010409 thin film Substances 0.000 description 4
- MGSRCZKZVOBKFT-UHFFFAOYSA-N thymol Chemical compound CC(C)C1=CC=C(C)C=C1O MGSRCZKZVOBKFT-UHFFFAOYSA-N 0.000 description 4
- ABMULKFGWTYIIK-UHFFFAOYSA-N 2-hexylphenol Chemical group CCCCCCC1=CC=CC=C1O ABMULKFGWTYIIK-UHFFFAOYSA-N 0.000 description 3
- 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
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 229930003836 cresol Natural products 0.000 description 3
- 239000010408 film Substances 0.000 description 3
- 150000002989 phenols Chemical class 0.000 description 3
- MEEKGULDSDXFCN-UHFFFAOYSA-N 2-pentylphenol Chemical group CCCCCC1=CC=CC=C1O MEEKGULDSDXFCN-UHFFFAOYSA-N 0.000 description 2
- 239000005844 Thymol Substances 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 229940100630 metacresol Drugs 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 229960000790 thymol Drugs 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- KFZXVMNBUMVKLN-UHFFFAOYSA-N 4-chloro-5-methyl-2-propan-2-ylphenol Chemical compound CC(C)C1=CC(Cl)=C(C)C=C1O KFZXVMNBUMVKLN-UHFFFAOYSA-N 0.000 description 1
- PHYYLQOZCQBTOL-UHFFFAOYSA-N ClC1=C(C)C=CC(C(C)C)=C1O.C1=C(C)C=CC(C(C)C)=C1O Chemical compound ClC1=C(C)C=CC(C(C)C)=C1O.C1=C(C)C=CC(C(C)C)=C1O PHYYLQOZCQBTOL-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229940031956 chlorothymol Drugs 0.000 description 1
- 229940013361 cresol Drugs 0.000 description 1
- 210000002249 digestive system Anatomy 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S516/00—Colloid systems and wetting agents; subcombinations thereof; processes of
- Y10S516/01—Wetting, emulsifying, dispersing, or stabilizing agents
Definitions
- This invention relates to the preparation of oils having superiorwetting and spreading properties, and it relates particularly to the preparation of blends of mineral oils with compounds of the alkyl phenol type which are adapted to wet and spread in a thin film.
- oils having superiorwetting and spreading properties
- it relates particularly to the preparation of blends of mineral oils with compounds of the alkyl phenol type which are adapted to wet and spread in a thin film.
- the surface may be covered with oil layers and these oil layers will inhibit the evaporation.
- the disadvantages of using oils are that unsaturated oils of the vegetable or mineral oil types which will readily spread in thin-films are easily oxidized,
- saturated mineral oils it has been found that it-is very diiiicult 'to form continuous layers or films of the oils of this type unless very large amounts of the oils are used. These saturated mineral oils tend to gather in globules and leave large portions of the surface exposed to the atmosphere, unless large volumes are used.
- An object of this invention is to provide a blend of mineral oils which will not only spread rapidly but also remain asthin films on the surfaces of the water
- the blends. of mineral oils 40 prepared for this particularv use are by adding tothe mineral oils a material of the type of alwl phenols such as normal alkyl phenols, secondary alkyl phenols, tertiary alwl phenols, halogenated phenols and the bi-cyclic group, as represented 5 by alpha nephthol, etc.
- alkyl phenols which are used according to this invention are cresol, thymol chlorothymol, ar'nyl-metacresol, alpha naphthol,
- the amount r these alkyl phenols added may be varied from about 0.5 to 2%. Where the oils have low solubility ratios, it may be necessary to add a mutual solvent, such as alcohol, to hold 'the materials in solution, when higher concentrations are desirable, although it was found that some of the solid materials may be, readily dissolved in the oil by means of heat, that is, heating the mixture of mineral oil and solidalkyl phenol until the solid alkyl phenol 5 goes into solution.
- a mutual solvent such as alcohol
- this mineral oil blend is when it becomes contaminated with dust, leaves, etc., it may be easily re- 20 moved from. the surface of the water and replaced with a new portion.
- These blends are stable, that is, they are not easily oxidized or reduced by exposure to the atmosphere.
- a saturated mineral oil with sufiiciently low volatility to be stable against ready evaporation on exposure to the atmosphere belongs to the class of highly refined mineral oilsoften referred to as white oils and medicinal oils. Such oils are ggiocuous to the digestive system of a human 30
- the invention is not to be limited to the specific embodiments, nor to any theories advanced as the operation of the invention, but in the appended claims it is intended to cla all inherent 35 novelty in the invention as broa as the prior art permits.
- a process for inhibiting evaporation from a body of water having a limited surface area which comprises coating the surface of the water with a stable solution of an alkyl phenol in a saturated mineral oil; said solvent being stable against oxidation and loss on exposure to the atmosphere, being free from ingredients which contaminate the water internally and acting as -'a uniformly and continuously spread protective coating between the atmosphere and the surface of the. water.
- alkyl phenol is a. tertiary alkyl phenol.
- alkyl phenol is selected from the group consisting of cresol, thymol, chlcrothymol, amyl- 'meta-cresol, alpha. naphthol, secondary hexyl phenol, tertiary amyl phenol, hept'al phenol.
- a process of inhibiting the evaporation of water which comprises dividing the surface area of the water into limited surface spaces andcoating the said limited surface spaces with a .stable blend of a saturated mineral oil and alkyl' phenol, v
- a process of inhibiting the evaporation of water which comprises dividing the surface of the water into limited surface areas and coating the said surfaces of the surface areas with a stable solution of saturated mineral oil containin; from, about 0.5 to 2% of an alkyl phenol.
- a process of inhibiting the evaporation of water which comprises dividing the surface of the (later into limited surface areas and coating the said surfaces of the'surface areas with a stable solution of saturated mineral oil containin: from about 0.5 to 2% of a compound of the type of an 'alkyl phenol selected from the group consisting of cresol, thymol, chlorothymol, amylineta-cresol, alpha naphthol, secondary hexyl phenol, tertiary amyl phenol, heptal phenol.
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Hydrology & Water Resources (AREA)
- Engineering & Computer Science (AREA)
- Environmental & Geological Engineering (AREA)
- Water Supply & Treatment (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Description
Patented Aug. 22, 1939 2.110.644 warms AND sPnsanlNG scam son one 0. Nelson, lie, N. 1., assignor to Stanco, Incorporated .No Bra. Application Serial No. 158,374
90mins.
This invention relates to the preparation of oils having superiorwetting and spreading properties, and it relates particularly to the preparation of blends of mineral oils with compounds of the alkyl phenol type which are adapted to wet and spread in a thin film. In dry climates, such as desert regions, the storage of water is a serious problem due to the rapid evaporation. It is known that the surface may be covered with oil layers and these oil layers will inhibit the evaporation. The disadvantages of using oils are that unsaturated oils of the vegetable or mineral oil types which will readily spread in thin-films are easily oxidized,
form acidic compounds and sometimes hard layers which can be broken and the value of the oil films as evaporation inhibitors thereby lost. Therefore it is desirable to use saturated mineral oils but it has been found that it-is very diiiicult 'to form continuous layers or films of the oils of this type unless very large amounts of the oils are used. These saturated mineral oils tend to gather in globules and leave large portions of the surface exposed to the atmosphere, unless large volumes are used.
An object of this invention is to provide a blend of mineral oils which will not only spread rapidly but also remain asthin films on the surfaces of the water This and other objects of the invention will be understood on reading the following description:
Where a large area of water is exposed to the atmosphere, it may be desirable to first provide a floating .grill which is partly submerged and partly exposed and divides the surface of the water into small areas. On the surface of the water in these small areas is then added a blend of mineral oil which will rapidly spread and form a thin film. The blends. of mineral oils 40 prepared for this particularv use are by adding tothe mineral oils a material of the type of alwl phenols such as normal alkyl phenols, secondary alkyl phenols, tertiary alwl phenols, halogenated phenols and the bi-cyclic group, as represented 5 by alpha nephthol, etc.
The specific alkyl phenols which are used according to this invention are cresol, thymol chlorothymol, ar'nyl-metacresol, alpha naphthol,
secondary hexyl phenol, tertiary amyl phehol,'
50 heptal phenol, etc.
The amount r these alkyl phenols added may be varied from about 0.5 to 2%. Where the oils have low solubility ratios, it may be necessary to add a mutual solvent, such as alcohol, to hold 'the materials in solution, when higher concentrations are desirable, although it was found that some of the solid materials may be, readily dissolved in the oil by means of heat, that is, heating the mixture of mineral oil and solidalkyl phenol until the solid alkyl phenol 5 goes into solution.
The addition of these compounds to mineral oils, especially those having poor wetting and spreading properties on surfaces of water, metal, wood and other materials, causes a reduction in 10 the surface and interfacial tension which in turn causes the oil to spread and wet the surface as desired. Where a grill prepared of wood or any other light material is used to divide the surface ofthe small areas, it is necessary that this 15 mineral 'oil wets and forms a thin film at the point ofcontact of the water-and the material.
Another advantage obtained by the use of this mineral oil blend is when it becomes contaminated with dust, leaves, etc., it may be easily re- 20 moved from. the surface of the water and replaced with a new portion. These blends are stable, that is, they are not easily oxidized or reduced by exposure to the atmosphere. A saturated mineral oil with sufiiciently low volatility to be stable against ready evaporation on exposure to the atmosphere belongs to the class of highly refined mineral oilsoften referred to as white oils and medicinal oils. Such oils are ggiocuous to the digestive system of a human 30 The invention is not to be limited to the specific embodiments, nor to any theories advanced as the operation of the invention, but in the appended claims it is intended to cla all inherent 35 novelty in the invention as broa as the prior art permits. y
I claim:
l. A process for inhibiting evaporation from a body of water having a limited surface area which comprises coating the surface of the water with a stable solution of an alkyl phenol in a saturated mineral oil; said solvent being stable against oxidation and loss on exposure to the atmosphere, being free from ingredients which contaminate the water internally and acting as -'a uniformly and continuously spread protective coating between the atmosphere and the surface of the. water. o
2. A'process as described in claim 1 in which said stable solution contains from 0.5% to 2% of the alkyl phenol in the saturated mineral oil. 3. A process as described in claim 1 in which said alkyl phenol is asecondary alkyl phenol.
4. A process as described in claim 1 in which said alkyl phenol is a. tertiary alkyl phenol.
5. A process as described in claim 1 in which said alkyl phenol is a halogenated alkyl phenol.
6. A process as described in claim 1 in which said alkyl phenol is selected from the group consisting of cresol, thymol, chlcrothymol, amyl- 'meta-cresol, alpha. naphthol, secondary hexyl phenol, tertiary amyl phenol, hept'al phenol.
7. A process of inhibiting the evaporation of water which comprises dividing the surface area of the water into limited surface spaces andcoating the said limited surface spaces with a .stable blend of a saturated mineral oil and alkyl' phenol, v
8. A process of inhibiting the evaporation of water which comprises dividing the surface of the water into limited surface areas and coating the said surfaces of the surface areas with a stable solution of saturated mineral oil containin; from, about 0.5 to 2% of an alkyl phenol.
9. A process of inhibiting the evaporation of water which comprises dividing the surface of the (later into limited surface areas and coating the said surfaces of the'surface areas with a stable solution of saturated mineral oil containin: from about 0.5 to 2% of a compound of the type of an 'alkyl phenol selected from the group consisting of cresol, thymol, chlorothymol, amylineta-cresol, alpha naphthol, secondary hexyl phenol, tertiary amyl phenol, heptal phenol.
' FRANKLIN C. NELSON.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US158374A US2170644A (en) | 1937-08-10 | 1937-08-10 | Wetting and spreading agent for oils |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US158374A US2170644A (en) | 1937-08-10 | 1937-08-10 | Wetting and spreading agent for oils |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2170644A true US2170644A (en) | 1939-08-22 |
Family
ID=22567825
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US158374A Expired - Lifetime US2170644A (en) | 1937-08-10 | 1937-08-10 | Wetting and spreading agent for oils |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2170644A (en) |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2547236A (en) * | 1947-02-17 | 1951-04-03 | Carl E Swenson | Multiple-speed drive |
| US2822238A (en) * | 1954-12-31 | 1958-02-04 | Standard Oil Co | Surfactant treatment of microballoons to improve water resistance |
| US3127235A (en) * | 1964-03-31 | Method of forming and maintaining | ||
| US3549313A (en) * | 1969-06-04 | 1970-12-22 | Texaco Inc | Composition and method for retarding evaporation of water |
| US4099915A (en) * | 1977-07-13 | 1978-07-11 | Texaco Inc. | Method for retarding the evaporation of water |
| US4404013A (en) * | 1979-07-17 | 1983-09-13 | Fisons Limited | Plant growth medium |
| US4426003A (en) | 1982-02-08 | 1984-01-17 | Jack Zarov | Drain cleaner package |
| US4516981A (en) * | 1984-01-09 | 1985-05-14 | Nelson Jr Otis L | Residual oil sludge dispersant |
| US4613340A (en) * | 1984-01-09 | 1986-09-23 | Polar Molecular Corp. | Residual oil sludge dispersant |
| US4846847A (en) * | 1984-01-09 | 1989-07-11 | Polar Molecular Corp. | Antigel fuel composition |
-
1937
- 1937-08-10 US US158374A patent/US2170644A/en not_active Expired - Lifetime
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3127235A (en) * | 1964-03-31 | Method of forming and maintaining | ||
| US2547236A (en) * | 1947-02-17 | 1951-04-03 | Carl E Swenson | Multiple-speed drive |
| US2822238A (en) * | 1954-12-31 | 1958-02-04 | Standard Oil Co | Surfactant treatment of microballoons to improve water resistance |
| US3549313A (en) * | 1969-06-04 | 1970-12-22 | Texaco Inc | Composition and method for retarding evaporation of water |
| US4099915A (en) * | 1977-07-13 | 1978-07-11 | Texaco Inc. | Method for retarding the evaporation of water |
| US4147658A (en) * | 1977-07-13 | 1979-04-03 | Texaco Inc. | Composition for retarding the evaporation of water |
| US4404013A (en) * | 1979-07-17 | 1983-09-13 | Fisons Limited | Plant growth medium |
| US4426003A (en) | 1982-02-08 | 1984-01-17 | Jack Zarov | Drain cleaner package |
| US4516981A (en) * | 1984-01-09 | 1985-05-14 | Nelson Jr Otis L | Residual oil sludge dispersant |
| US4613340A (en) * | 1984-01-09 | 1986-09-23 | Polar Molecular Corp. | Residual oil sludge dispersant |
| US4846847A (en) * | 1984-01-09 | 1989-07-11 | Polar Molecular Corp. | Antigel fuel composition |
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