US3035887A - Method for inhibiting bacterial activity in petroleum - Google Patents
Method for inhibiting bacterial activity in petroleum Download PDFInfo
- Publication number
- US3035887A US3035887A US13418A US1341860A US3035887A US 3035887 A US3035887 A US 3035887A US 13418 A US13418 A US 13418A US 1341860 A US1341860 A US 1341860A US 3035887 A US3035887 A US 3035887A
- Authority
- US
- United States
- Prior art keywords
- petroleum
- borate
- sodium
- water
- tank
- 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/30—Organic compounds compounds not mentioned before (complexes)
- C10L1/301—Organic compounds compounds not mentioned before (complexes) derived from metals
- C10L1/303—Organic compounds compounds not mentioned before (complexes) derived from metals boron compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M1/00—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
- C10M1/08—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2227/00—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
- C10M2227/06—Organic compounds derived from inorganic acids or metal salts
- C10M2227/061—Esters derived from boron
- C10M2227/062—Cyclic esters
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2227/00—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
- C10M2227/09—Complexes with metals
Definitions
- a further object of this invention is to provide a method for adding a bactericide to petroleum and petroleum fractions which substantially completely eliminates the need for aqueous solutions.
- the invention then comprises the features hereinafter fully described and particularly pointed out in the claims, the following description setting forth in detail certain illustrative embodiments of the invention, these being indicative, however, of but a few of the Ways in which the principle of the invention may be employed.
- the present invention comprises the method of preventing bacterial action in stored petroleum which comprises adding to said stored petroleum a liquid alkali metal organoborate selected from the group consisting of the condensation products of an alkali metal borate and a material selected from the group consisting of an ethylene glycol, diethylene glycol, triethylene glycol, 1,4-butanediol, 2,3-butanediol, and 1,2-propanediol, said glycol borate condensation products consisting essentially of a mole ratio of from about 6:1 to about 20:1 of diol to equivalent alkali metal tetraborate, and said condensation products added to tank in bactericidal amounts.
- a liquid alkali metal organoborate selected from the group consisting of the condensation products of an alkali metal borate and a material selected from the group consisting of an ethylene glycol, diethylene glycol, triethylene glycol, 1,4-butanediol, 2,3-butanediol, and 1,2-
- the glycol borate condensation product is added in an amount equivalent to that amount necessary to completely cover the bottom of the tank to be protected against bacterial action. If the tank is substantially water-free, an amount of condensation product is added which would substantially completely cover the bottom of the tank. If the tank already contains water, an amount of condensation product is used which is equivalent to that amount necessary to substantially completely cover the bottom of the tank if no water were present.
- petroleum as used herein, is intended to include crude oil, kerosene, gasoline, lubricating oils, diesel fuels, and the like, as well as other hydrocarbons that are susceptible to bacterial degradation during storage.
- condensation products useful in the present inven tion are readily prepared using condensation processes well known to those skilled in the art.
- the condensation product of sodium tetraborate and ethylene glycol is simply prepared by adding 1.0 mole of borax and 9.0 moles of the glycol to a reaction vessel and heating it to about to C. for sufiicient time to drive out water and give a product having a 9:1 mole ratio of glycol to equivalent sodium tetraborate.
- the condensation product is a clear liquid which can be added directly to the petroleum storage tank.
- the present invention has provided an efficient means for inhibiting bacterial growth in storage tanks, and which means is independent of the amount of Water present in the storage tank.
- the present products are substantially inert with respect to the liquid contained in the storage tank and they are substantially completely compatible with any water which may be present in the tank.
- the improvement which comprises adding to the stored petroleum in bactericidal amounts a liquid alkali metal glycol borate having an alkylene group of 2 to 6 carbon atoms in length and containing a total of 2 to 20 carbon atoms.
- liquid alkali metal glycol borate selected from the class consisting of sodium ethylene glycol borate, potassium ethylene glycol borate, sodium dietbylene glycol borate, potassium diethylene glycol borate, sodium 1,2-propanediol borate, potassium 1,2-propanediol borate, sodium 2,3-butanediol borate, potassium 2,3-butanediol borate, sodium 1,4-butanedio1 borate, potassium 1,4-butanediol borate, and sodium triethylene glycol borate.
- a composition comprising a major proportion of petroleum in contact With an aqueous phase and tending to undergo degradation and to deposit a sludge due to the presence in at least one of said petroleum and said aqueous phase of microorganisms that promote degradation of petroleum and a bactericidal amount of a liquid alkali metal glycol borate having an alkylene group of 2 to 6 carbon atoms in length and containing a total of 2 to 20 carbon atoms.
- composition of claim 3 where said alkali metal glycol borate comprises sodium ethylene glycol borate.
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Lubricants (AREA)
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
BE601086D BE601086A (de) | 1960-03-08 | ||
NL261886D NL261886A (de) | 1960-03-08 | ||
US13418A US3035887A (en) | 1960-03-08 | 1960-03-08 | Method for inhibiting bacterial activity in petroleum |
GB2472/61A GB931759A (en) | 1960-03-08 | 1961-01-20 | Improvements in or relating to the reduction in the susceptibility of petroleum and petroleum fractions to bacterial attack |
FR854909A FR1288969A (fr) | 1960-03-08 | 1961-03-08 | Perfectionnements au traitement des pétroles et fractions de pétrole |
DEU7861A DE1177763B (de) | 1960-03-08 | 1961-03-08 | Herabsetzung der Empfindlichkeit von Erdoel-produkten gegen bakteriellen Befall |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US13418A US3035887A (en) | 1960-03-08 | 1960-03-08 | Method for inhibiting bacterial activity in petroleum |
Publications (1)
Publication Number | Publication Date |
---|---|
US3035887A true US3035887A (en) | 1962-05-22 |
Family
ID=21759867
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US13418A Expired - Lifetime US3035887A (en) | 1960-03-08 | 1960-03-08 | Method for inhibiting bacterial activity in petroleum |
Country Status (5)
Country | Link |
---|---|
US (1) | US3035887A (de) |
BE (1) | BE601086A (de) |
DE (1) | DE1177763B (de) |
GB (1) | GB931759A (de) |
NL (1) | NL261886A (de) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3163506A (en) * | 1959-02-19 | 1964-12-29 | United States Borax Chem | Preparation of organic monoborate salts |
DE1247743B (de) * | 1965-04-28 | 1967-08-17 | Shell Int Research | Unter Normalbedingungen fluessige Kohlenwasserstoff-Kraftstoffe mit verbesserter Widerstandsfaehigkeit gegenueber einer Zersetzung durch Mikroorganismen |
DE1247742B (de) * | 1965-04-28 | 1967-08-17 | Shell Int Research | Unter Normalbedingungen fluessige Kohlenwasserstoffkraftstoffe mit Widerstandsfaehigkeit gegenueber Zersetzungen durch Mikroorganismen |
US3869388A (en) * | 1973-06-25 | 1975-03-04 | Continental Oil Co | Oil water separation |
US4265664A (en) * | 1978-05-12 | 1981-05-05 | Chemie Linz Aktiengesellschaft | Spirocyclic boron compounds, a process for their manufacture and their use as a flame-retardant additive |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1953741A (en) * | 1932-07-15 | 1934-04-03 | Bennett Harry | Reaction products of glycols and boric acid and method of producing the same |
US2882227A (en) * | 1954-02-23 | 1959-04-14 | Sinclair Refining Co | Corrosion prevention method and composition |
US2883412A (en) * | 1954-12-27 | 1959-04-21 | California Research Corp | P-xylylenediamine salts of glycol boric acids |
US2894020A (en) * | 1957-10-30 | 1959-07-07 | Monsanto Chemicals | Borates |
US2979524A (en) * | 1957-03-05 | 1961-04-11 | Us Borax & Chemcial Corp | Modified organic fluids of the glycol type and methods of producing the same |
-
0
- NL NL261886D patent/NL261886A/xx unknown
- BE BE601086D patent/BE601086A/xx unknown
-
1960
- 1960-03-08 US US13418A patent/US3035887A/en not_active Expired - Lifetime
-
1961
- 1961-01-20 GB GB2472/61A patent/GB931759A/en not_active Expired
- 1961-03-08 DE DEU7861A patent/DE1177763B/de active Pending
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1953741A (en) * | 1932-07-15 | 1934-04-03 | Bennett Harry | Reaction products of glycols and boric acid and method of producing the same |
US2882227A (en) * | 1954-02-23 | 1959-04-14 | Sinclair Refining Co | Corrosion prevention method and composition |
US2883412A (en) * | 1954-12-27 | 1959-04-21 | California Research Corp | P-xylylenediamine salts of glycol boric acids |
US2979524A (en) * | 1957-03-05 | 1961-04-11 | Us Borax & Chemcial Corp | Modified organic fluids of the glycol type and methods of producing the same |
US2894020A (en) * | 1957-10-30 | 1959-07-07 | Monsanto Chemicals | Borates |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3163506A (en) * | 1959-02-19 | 1964-12-29 | United States Borax Chem | Preparation of organic monoborate salts |
DE1247743B (de) * | 1965-04-28 | 1967-08-17 | Shell Int Research | Unter Normalbedingungen fluessige Kohlenwasserstoff-Kraftstoffe mit verbesserter Widerstandsfaehigkeit gegenueber einer Zersetzung durch Mikroorganismen |
DE1247742B (de) * | 1965-04-28 | 1967-08-17 | Shell Int Research | Unter Normalbedingungen fluessige Kohlenwasserstoffkraftstoffe mit Widerstandsfaehigkeit gegenueber Zersetzungen durch Mikroorganismen |
US3869388A (en) * | 1973-06-25 | 1975-03-04 | Continental Oil Co | Oil water separation |
US4265664A (en) * | 1978-05-12 | 1981-05-05 | Chemie Linz Aktiengesellschaft | Spirocyclic boron compounds, a process for their manufacture and their use as a flame-retardant additive |
Also Published As
Publication number | Publication date |
---|---|
DE1177763B (de) | 1964-09-10 |
GB931759A (en) | 1963-07-17 |
BE601086A (de) | |
NL261886A (de) |
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