US2788307A - Stabilized non-corrosive pesticidal composition - Google Patents
Stabilized non-corrosive pesticidal composition Download PDFInfo
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- US2788307A US2788307A US342999A US34299953A US2788307A US 2788307 A US2788307 A US 2788307A US 342999 A US342999 A US 342999A US 34299953 A US34299953 A US 34299953A US 2788307 A US2788307 A US 2788307A
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- US
- United States
- Prior art keywords
- corrosion
- corrosive
- inhibitor
- containers
- concentrate
- 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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- 230000000361 pesticidal effect Effects 0.000 title claims description 7
- 239000000203 mixture Substances 0.000 title description 18
- 230000009972 noncorrosive effect Effects 0.000 title description 2
- 230000007797 corrosion Effects 0.000 claims description 26
- 238000005260 corrosion Methods 0.000 claims description 26
- 239000012141 concentrate Substances 0.000 claims description 10
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical class CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 claims description 10
- 239000003995 emulsifying agent Substances 0.000 claims description 6
- JLYXXMFPNIAWKQ-GNIYUCBRSA-N gamma-hexachlorocyclohexane Chemical compound Cl[C@H]1[C@H](Cl)[C@@H](Cl)[C@@H](Cl)[C@H](Cl)[C@H]1Cl JLYXXMFPNIAWKQ-GNIYUCBRSA-N 0.000 claims description 5
- JLYXXMFPNIAWKQ-UHFFFAOYSA-N gamma-hexachlorocyclohexane Natural products ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 claims description 5
- 229960002809 lindane Drugs 0.000 claims description 5
- 150000002790 naphthalenes Chemical class 0.000 claims description 5
- 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 claims description 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 4
- 229910052700 potassium Inorganic materials 0.000 claims description 4
- 239000011591 potassium Substances 0.000 claims description 4
- 229910052708 sodium Inorganic materials 0.000 claims description 4
- 239000011734 sodium Substances 0.000 claims description 4
- 230000003993 interaction Effects 0.000 claims description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 2
- 229910017053 inorganic salt Inorganic materials 0.000 claims description 2
- DHCDFWKWKRSZHF-UHFFFAOYSA-L thiosulfate(2-) Chemical compound [O-]S([S-])(=O)=O DHCDFWKWKRSZHF-UHFFFAOYSA-L 0.000 claims 1
- 239000003112 inhibitor Substances 0.000 description 15
- 238000009472 formulation Methods 0.000 description 14
- 239000007788 liquid Substances 0.000 description 12
- 239000005028 tinplate Substances 0.000 description 11
- 235000008504 concentrate Nutrition 0.000 description 8
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 8
- 150000004764 thiosulfuric acid derivatives Chemical class 0.000 description 8
- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 7
- 235000019345 sodium thiosulphate Nutrition 0.000 description 7
- 239000004495 emulsifiable concentrate Substances 0.000 description 6
- 239000013049 sediment Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 238000000354 decomposition reaction Methods 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- 230000006866 deterioration Effects 0.000 description 4
- 230000000749 insecticidal effect Effects 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- 239000000575 pesticide Substances 0.000 description 3
- 239000011521 glass Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- PODWXQQNRWNDGD-UHFFFAOYSA-L sodium thiosulfate pentahydrate Chemical compound O.O.O.O.O.[Na+].[Na+].[O-]S([S-])(=O)=O PODWXQQNRWNDGD-UHFFFAOYSA-L 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 241000256113 Culicidae Species 0.000 description 1
- 241000255925 Diptera Species 0.000 description 1
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical class C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 239000011280 coal tar Substances 0.000 description 1
- 230000002844 continuous effect Effects 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 229910001504 inorganic chloride Inorganic materials 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 231100000956 nontoxicity Toxicity 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000005201 scrubbing Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 231100000820 toxicity test Toxicity 0.000 description 1
- WCLDITPGPXSPGV-UHFFFAOYSA-N tricamba Chemical compound COC1=C(Cl)C=C(Cl)C(Cl)=C1C(O)=O WCLDITPGPXSPGV-UHFFFAOYSA-N 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
Definitions
- This invention relates to the improvement in the storage of liquid pesticidal formulations and the inhibiting of the corrosion of metallic containers.
- An object of this invention is to stabilize emulsifiable concentrates so that the components of the concentrates do not react with each other and with the container with a resultant decrease in efiectiveness.
- Another object of this invention is to inhibit the corrosion of the container and prevent the deterioration of the emulsifiable concentrate by adding a material that does not interfere with the proper emulsification of the concen trate or reduce the efficacy of the emulsion as an insecticide.
- Another object of this invention is to stabilize pesticidal emulsifiable concentrates and prevent corrosion of their containers.
- Another object of this invention is to prevent the loss due to the corrosion of metals in contact with corrosive oils, such as certain synthetic products, petroleum fractions, coal tar fractions, and other products of similar nature derived from these.
- Another object of this invention is to prevent the loss due to corrosion in industrial concens Where corrosive liquids are held in metal pipes, vats, and tanks, and an inhibitor is needed which is sparingly soluble or not soluble in the liquids.
- This invention is based on the surprising discovery that 2,788,307 Patented Apr. 9, 1957 the addition of small amounts of certain metallic thio sulfates and polythionates to emulsifiable concentrate formulations of insecticidal materials will stabilize these concentrates so that the reaction between the components with deterioration and the ensuing corrosion is greatly retarded.
- Sodium thiosulfate has been found to be an inhibitor of the deterioration of a formulation consisting of lindane20%, isophorone-40%, an alkylated naphthalene mixture, in this case Velsicol AR-6032.5%, and an emulsifier, in this case Triton X1007.5%.
- This particular formulation is hereinafter referred to as LIVT. Tests have been made at ordinary or natural temperatures and accelerated or elevated temperatures. The results of a series of insecticidal packages in accelerated storage at 49 C. are presented in Table 1.
- Table 3 are shown the results of 7 months con tinuous storage at room temperature.
- Anhydrous sodium thiosulfate has shown slightly better value as an inhibtor at ordinary temperatures while sodium thiosulfate pentahydrate has given better protection at elevated temperatures.
- the finely divided thiosulfate salt is added freely or in' a porous retainer in the calculate quantity to the emulsifiable concentrate immediately after it has been placed in the container in which it is to be stored.
- the container is closed tightly and the contents mixed well by shaking.
- a DDT formulation composed of DDT25%, 'alkylated naphthalene-%, and an emulsifier is also protected against deterioration in storage by the addition of sodium thiosulfate.
- sodium thiosulfates as the inhibitor
- other water soluble thiosulfates and polythionates such as ammonium and potassium
- ammonium and potassium may be used.
- Thelthiosulfate salts protect the stability of the pesticidalformulation in glass and metal containers. These thio sulfate salts also inhibit the corrosion of metallic containers, thus insuring a decrease in loss of the contents through leakage.
- the thiosulfate salts may also be used to inhibit corrosion in industrial installations of pipes and tanks, Where normally corrosion will occur.
- the optimum amount of the inhibitor to add depends on the specific conditions under which it is used, such as flow rate through pipes, size of vats or tanks, and time the liquids are going to be kept in the vats or tanks.
- In tin-coated containers We have been able to stop corrosion by acid organic solvents for 3 to 5 months when the inhibitor sodium thiosulfate was used in concentrations of 1% to 0.1% under accelerated storage temperature of 120 F. Under normal room temperature conditions corrosion has been stopped for 9 months at least.
- concentrations of 0.01% to 0.001% or lower may sufiice.
- the inhibitor may be added freely or in porous bags and any part remaining in the liquid, if necessary, may be eliminated by scrubbing with water and a phase separation.
- a pesticide comprising lindane2030%, isophorone-40%, alkylated napthalenes30-3S%, emulsifier-3-l0%, and sodium thiosulfate-0.1-2.0%.
- a pesticide comprising 20% of lindane, of isophorone, 32% of alkylated naphthalene, 7.5% of emulsifier, and 0.5% of sodium thiosulfate pentahydrate.
- An emulsifiable pesticidal concentrate comprising lindane, alkylated naphthalenes, isophorone, an emulsifier and an amount of sodium thiosulfate suflicient to prevent the interaction of the components of the concentrate and to prevent corrosion of metallic containers holding the same.
- An emulsifiable pesticidal concentrate comprising lindane, alkylated naphthalenes, isophorone, an emulsifier, and an amount sufficient to prevent interaction of the components of the concentrate and to prevent corrosion of metallic containers holding the same of a water-soluble inorganic salt selected from the group consisting of the thiosulfates and polythionates of a member selected from the group consisting of sodium, potassium, and ammomum.
Landscapes
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Agronomy & Crop Science (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
STABILIZED NON-CORROSIVE PESTICIDAL COMPOSITION Ralph Rodriguez-Torrent, Winter Park, and Robert N: Fitzwater, Orlando, F121,; dedicated to the free use ot the People in the territory oi the United States No Drawing. Application March 17, 1953., Serial No. 342,999
4 Claims. (Cl. 167-42) (Granted under Title 35, U. 8. Code (1952), sec. 266) A non-exclusive, irrevocable, royalty-free license in the invention herein described, for all governmental purposes, throughout the world, with the power to grant sublicenses for such purposes, is hereby granted to the Government of the United States of America.
We hereby dedicate the invention herein described to the free use of the People in the territory of the United States to take efiect on the granting of a patent to us.
This invention relates to the improvement in the storage of liquid pesticidal formulations and the inhibiting of the corrosion of metallic containers.
An object of this invention is to stabilize emulsifiable concentrates so that the components of the concentrates do not react with each other and with the container with a resultant decrease in efiectiveness.
Another object of this invention is to inhibit the corrosion of the container and prevent the deterioration of the emulsifiable concentrate by adding a material that does not interfere with the proper emulsification of the concen trate or reduce the efficacy of the emulsion as an insecticide. Another object of this invention is to stabilize pesticidal emulsifiable concentrates and prevent corrosion of their containers.
Another object of this invention is to prevent the loss due to the corrosion of metals in contact with corrosive oils, such as certain synthetic products, petroleum fractions, coal tar fractions, and other products of similar nature derived from these.
Another object of this invention is to prevent the loss due to corrosion in industrial concens Where corrosive liquids are held in metal pipes, vats, and tanks, and an inhibitor is needed which is sparingly soluble or not soluble in the liquids.
In many commercial plants the corrosion problem when certain corrosive liquids run through metal pipes or are held in tanks is serious. Any organic liquid or mixture which is of an acid nature, or has an acidity due to hydrogen bonding will tend to corrode metals. The exact mechanism by which oily liquids and organic solvents attack metals is rather obscure and of a controversial nature. We have found samples of isophorone with a pH as low as 3.0 and an acidity which cannot be exhausted by violent water washings. Our invention will minimize, retard, and control the ensuing corrosion, and has the added advantages of being either not soluble or sparingly soluble in the liquids, of stable nature, unreactive towards the liquids, and easily washed out with water or eliminated from the liquids.
This invention is based on the surprising discovery that 2,788,307 Patented Apr. 9, 1957 the addition of small amounts of certain metallic thio sulfates and polythionates to emulsifiable concentrate formulations of insecticidal materials will stabilize these concentrates so that the reaction between the components with deterioration and the ensuing corrosion is greatly retarded. We have found that in certain formulations of insecticidal emulsifiable concentrates the components will react with each other even in glass containers.
Sodium thiosulfate has been found to be an inhibitor of the deterioration of a formulation consisting of lindane20%, isophorone-40%, an alkylated naphthalene mixture, in this case Velsicol AR-6032.5%, and an emulsifier, in this case Triton X1007.5%. This particular formulation is hereinafter referred to as LIVT. Tests have been made at ordinary or natural temperatures and accelerated or elevated temperatures. The results of a series of insecticidal packages in accelerated storage at 49 C. are presented in Table 1.
Table 1.-Efiect of various concentrations of inhibitor on the rate of decomposition of LIVT formulations stored in difierent types of containers at 49 C.
Container Percent identlfl- Type of can N 21 8 0 Remarks 1 cation Electrolytic tinplate... 0.05 Severe corrosion, blackish, black sediment.
.- ..do .05 Removed from oven after 104 days.
do .1 Moderate to severe corrosion, black, black sediment.
d do .1 Removed from oven after 124 days.
e ..do .2 Moderate to severe corrosion, black, black sediment.
f do .2 Removed from oven after 128 days.
g do .2 o.
h "do .5 Very slightly darker in color 1.0 Severe corrosion, darker,
sediment.
1. 0 Removed from oven after days.
1. 0 Removed from oven after 107 days.
1.0 Removed from oven after 96 days.
No significant changes.
Slight precipitate on walls.
Removed from even after 28 days.
Removed from oven after 48 days.
Removed from oven after 63 days.
m 1.25-pound tinplate 1. 0 Terneplate 1. 0
lectrolytic tinplate... 0 1.25-pound tinplate 0 Terneplate 0 Check.
1 When a can became severely eorrod ed and leaked, and the formulation became black, acid, and contained sediment, it was removed from thetest. All others were observed at the end of 19 weeks.
The LIVT formulation without inhibitor showed 26 C.) with different quantities of sodium thiosulfate in.
LIVT are shown'in Table 2.
Table 2. -Efi ect of various concentrations of; inhibitor. on the decomposition of LI VT formulations in difierent types containers after 4 months storage at room temperature ELECTROLYTIC TINPLATE Chemical analysis Container Percent Internal Crystaldesignation NazSzO; corrosion lization Color Inorganic Percent 01 lindane 1 O. K Nona... 20.5 0.05 O. K
.2.. .0. K .5 O'.K. 0' SexteroL... Heavy. DaIk.1'ed-.. 5.0 1 4.
1.25-POUND TINPLATEv 1 None e .i 1 do None 20.2 0 Severe dq. Darkernn do 18.9
TERNEPLATE a 1 None -No11e o.K'. Ghee- O Slight do 0. Ken.
STANDARD O c... s.
1 Milligrams of inorganic chloride per 0.34 2-gram sample. I u 1 Accelerated storage.
At the end of 4 months in normal storage there were no significant difference in the samples in various containers with different amounts of inhibitor, but as in the accelerated storage test, all of those with the inhibitor were superior to the check samples. The check samples in all types of containers showed from slight to severe corrosion of the cans, and the chemical analysis and" biological tests on the formulation corroborated this visual estimation of decomposition. The formulations with inhibitor in electrolytic tinplate in normal and in 1.25-pound dipped tinplate in accelerated storage were equal to a freshly prepared standard in both the analytical and toxicity tests against mosquito larvae and flies.
In Table 3 are shown the results of 7 months con tinuous storage at room temperature.
Table 3.--Ejfect of various concentrations of inhibitor on the decomposition of LIVT formulations in different types of containers after 7 months storage at room temperature V V ELECTROLYTIC TINPLATE Internal COITOSIOH Container Percent Crystal- Color designation NElnSzO a lization 1 Slightly darker;
I2 01 K5 6O 5 None O. K. 0 Severe-derailed Reddlsh-black.
1.25-POUND TINPLATE I .65 t 1.0 None None". O.K.' Check .0 Severe .-do Darker.
'T'E'RN'EPLA'TE 1.0 None. None... 0. K. 70 Check .0 Slight general.-- do. O. K.
1 Eliminated from the test at 5 months. he m am l t er-. 99 h? i WW1?! Storage showed only slight or no corrosion of containers no 7 visible sediment, and a normal color. The check samples in the three types of containers showed for the terneplate slight general corrosion, for the 1.25-pon'nd dipped tinplate severe corrosion, and for the (LS-pound electrolytic tinplate elimination'because of leaking at the end of 4 months of normal storage. From the experimental evidence in the check samples it is evident that the inhibitor is offering satisfactory protection under normal temperature conditions.
Anhydrous sodium thiosulfate has shown slightly better value as an inhibtor at ordinary temperatures while sodium thiosulfate pentahydrate has given better protection at elevated temperatures.
In carrying into practice this invention the finely divided thiosulfate salt is added freely or in' a porous retainer in the calculate quantity to the emulsifiable concentrate immediately after it has been placed in the container in which it is to be stored. The container is closed tightly and the contents mixed well by shaking.
A DDT formulation composed of DDT25%, 'alkylated naphthalene-%, and an emulsifier is also protected against deterioration in storage by the addition of sodium thiosulfate.
Although the examples given herein have contained sodium thiosulfates as the inhibitor, other water soluble thiosulfates and polythionates, such as ammonium and potassium may be used. The sodium, potassium, and ammonium salts or inorganic polysulfur acids of varying oxygen content,'such as thiosulfates and polythionates, possess no toxicity in themselvespand do not interfere with the proper emulsifi c ation of the concentrate in the quantities used. They are water soluble and will not clog the spray nozzle when used in the spray.
It has. been observed that the addition of Water soluble thiosulfates, viz., sodium thiosulfate, inhibit the decomposition and corrosion of the container in the case of formulations containing other chlorinated hydrocarbon pesticides. a
Thelthiosulfate salts protect the stability of the pesticidalformulation in glass and metal containers. These thio sulfate salts also inhibit the corrosion of metallic containers, thus insuring a decrease in loss of the contents through leakage.
The thiosulfate salts may also be used to inhibit corrosion in industrial installations of pipes and tanks, Where normally corrosion will occur. The optimum amount of the inhibitor to add depends on the specific conditions under which it is used, such as flow rate through pipes, size of vats or tanks, and time the liquids are going to be kept in the vats or tanks. In tin-coated containers We have been able to stop corrosion by acid organic solvents for 3 to 5 months when the inhibitor sodium thiosulfate was used in concentrations of 1% to 0.1% under accelerated storage temperature of 120 F. Under normal room temperature conditions corrosion has been stopped for 9 months at least. The research does indicate that for shorter periods of time of storage or contact between corrosive liquids and metal, concentrations of 0.01% to 0.001% or lower may sufiice. The inhibitor may be added freely or in porous bags and any part remaining in the liquid, if necessary, may be eliminated by scrubbing with water and a phase separation.
It is to be understood that the above examples used in describing the use of these stabilizers and inhibitors are given only as examples and that this invention is not to be restricted by such use.
We claim:
1. A pesticide comprising lindane2030%, isophorone-40%, alkylated napthalenes30-3S%, emulsifier-3-l0%, and sodium thiosulfate-0.1-2.0%.
2. A pesticide comprising 20% of lindane, of isophorone, 32% of alkylated naphthalene, 7.5% of emulsifier, and 0.5% of sodium thiosulfate pentahydrate.
3. An emulsifiable pesticidal concentrate comprising lindane, alkylated naphthalenes, isophorone, an emulsifier and an amount of sodium thiosulfate suflicient to prevent the interaction of the components of the concentrate and to prevent corrosion of metallic containers holding the same.
4. An emulsifiable pesticidal concentrate comprising lindane, alkylated naphthalenes, isophorone, an emulsifier, and an amount sufficient to prevent interaction of the components of the concentrate and to prevent corrosion of metallic containers holding the same of a water-soluble inorganic salt selected from the group consisting of the thiosulfates and polythionates of a member selected from the group consisting of sodium, potassium, and ammomum.
References Cited in the file of this patent FOREIGN PATENTS 35,060 France June 18, 1929 (Addition to Patent 649,934) 844,003 Germany July 14, 1952
Claims (1)
- 4. AN EMULSIFIABLE PESTICIDAL CONCENTRATE COMPRISING LINDANE, ALKYLATED NAPHTHALENES, ISOPHORONE, AN EMULSIFIER, AND AN AMOUNT SUFFICIENT TO PREVENT INTERACTION OF THE COMPONENTS OF THE CONCENTRATE AND TO PREVENT CORROSION OF METALLIC CONTAINERS HOLDING THE SAME OF A WATER-SOLUBLE INORGANIC SALT SELECTED FROM THE GROU CONSISTING OF THE THIOSULFATES AD POLYTHIONATES OF A MEMBER SELECTED FROM THE GROUP CONSISTING OF SODIUM, POTASSIUM, AND AMMONIUM.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US342999A US2788307A (en) | 1953-03-17 | 1953-03-17 | Stabilized non-corrosive pesticidal composition |
| US630425A US2844507A (en) | 1953-03-17 | 1956-12-10 | Ddt stabilized compositions |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US342999A US2788307A (en) | 1953-03-17 | 1953-03-17 | Stabilized non-corrosive pesticidal composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2788307A true US2788307A (en) | 1957-04-09 |
Family
ID=23344240
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US342999A Expired - Lifetime US2788307A (en) | 1953-03-17 | 1953-03-17 | Stabilized non-corrosive pesticidal composition |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2788307A (en) |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR649934A (en) * | 1927-08-04 | 1928-12-29 | Process for the dehydration of carbon tetrachloride | |
| FR35060E (en) * | 1929-12-10 | |||
| DE844003C (en) * | 1942-08-28 | 1952-07-14 | Krupp Kohlechemie G M B H | Process for the stabilization of halogenated, especially chlorinated, higher molecular weight aliphatic hydrocarbons |
-
1953
- 1953-03-17 US US342999A patent/US2788307A/en not_active Expired - Lifetime
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR35060E (en) * | 1929-12-10 | |||
| FR649934A (en) * | 1927-08-04 | 1928-12-29 | Process for the dehydration of carbon tetrachloride | |
| DE844003C (en) * | 1942-08-28 | 1952-07-14 | Krupp Kohlechemie G M B H | Process for the stabilization of halogenated, especially chlorinated, higher molecular weight aliphatic hydrocarbons |
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