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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
  • C10L1/00—Liquid carbonaceous fuels
  • C10L1/10—Liquid carbonaceous fuels containing additives
  • C10L1/14—Organic compounds
  • C10L1/18—Organic compounds containing oxygen
  • C10L1/19—Esters ester radical containing compounds; ester ethers; carbonic acid esters
• • 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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
  • C10L10/00—Use of additives to fuels or fires for particular purposes
  • C10L10/04—Use of additives to fuels or fires for particular purposes for minimising corrosion or incrustation

Definitions

• the invention relates to a method for combating corrosion in containers of liquids containing hydrocarbons.
• Corrosion of fuel tanks is in most cases due to the presence of microorganisms, such as bacteria and moulds.
• microorganisms such as bacteria and moulds.
• anaer­obic bacteria for example, are ultimately able to form hydrogen and/or acids which attack metals and other ma­terials of which fuel tanks are composed.
• the basic re­quirements for the growth of such organisms are the pre­sence of nutrients, such as substances containing carbon, nitrogen, phosphorous, sulphur etc., and the presence of water; in practice, these requirements are virtually al­ways fulfilled in liquid hydrocarbons and especially in kerosene.
• biocides agents which combat micro­organisms
• organic borates organic borates
• inorganic chromates organic chromates
• ethylene glycol monomethyl ether possibly in combin­ation with measures such as tapping off settled water
• the biocide to be used must fulfil a number of requirements, such as effectiveness, safety, handle­ability, compatibility with the materials used and with the combustion system and the like.
• biocides not one fulfils these requirements to an adequate extent.
• the method according to the invention is character­ized in that at least one pyrocarbonic acid diester is introduced into the containers for liquids containing hydrocarbons.
• Pyrocarbonic acid diesters are effective agents for combating microorganisms.
• dimethyl pyrocarbonate for example, is lethal to diverse yeasts, moulds and bacteria.
• Pyrocarbonic acid diesters are harmless, at least in dissolved form, to human beings and other mammals. They do not react with hydrocarbons and do not react, or virtually do not react, with the common fuel additives; they are inert with respect to the materials of which tanks are composed.
• the pyrocarbonic acid diesters can readily be handled and have long-term stability. They can be prepared relatively simply from cheap basic materials (for example, chloro­formates and alkali-metal carbonate monoesters) in a known manner.
• Pyrocarbonic acid diesters are readily soluble in hydrocarbons and moderately soluble in water. They react readily with water (dimethyl pyrocarbonate, for example, has a half-life of approximately 15 minutes in water at 20°C) to form alcohols and carbon dioxide. Neither of the decomposition products adversely affects the fuel quality or impedes the combustion. The carbon dioxide produced on reaction with water can be removed simply by good ventilation.
• esters scavenge water dissolved in the hydrocarbon, also react with settled water and combat microorganisms both in the hydrocarbon phase and in the aqueous phase. Since microorganisms require water for their metabolism, the pyrocarbonic acid esters do not only act as straightforward biocides but also as agents which render further development of microorganisms impossible because they remove the water necessary for said development.
• any concentration of the pyrocarbonic acid diesters in hydrocarbons has a positive effect as regards the combating of corrosion; the overall effect will be greater if greater quantities are used.
• To scavenge water dis­solved in aviation fuel approximately 100-500 mg of pyro­carbonate per litre is necessary, for example, in the temperature range from -20°C to +30°C.
• the concen­tration or quantity to be chosen to combat corrosion de­pends on the type and composition of the liquid, on the desired effect and on the circumstances. For practical applications a concentration of 0.1-5 g/1 is used.
• Any pyrocarbonic acid diester containing alcohol radicals which yield relatively harmless alcohols after hydrolysis is in principle suitable for the method ac­cording to the invention.
• the two alcohol radicals in the diester may be identical or different, for example, alkyl groups, such as methyl, ethyl, isopropyl, propyl, substituted alkyl groups, such as 2-methoxyethyl, alkenyl, cycloalkyl, aryl or aralkyl groups, or may be combined with each other to form cyclic compounds such as ethylene pyrocarbonate or to form linear oligomeric or polymeric compounds, such as poly(alkylene pyrocarbonate).
• alkyl groups such as methyl, ethyl, isopropyl, propyl
• substituted alkyl groups such as 2-methoxyethyl
• alkenyl, cycloalkyl, aryl or aralkyl groups or may be combined with each other to form cyclic compounds such as ethylene pyrocarbonate or to form linear oligomeric or polymeric compounds, such as poly(alkylene pyrocarbonate).
• one or more oxygen atoms in the pyrocarbonate group may be replaced by sulphur atoms or other heteroatoms and the pyrocarbonate group may have one or more additionally carbonyloxy groups, as in dialkyltri- and -polycarbonates.
• pyrocarbonates containing small alkyl groups (C1-C4) and containing exclusively oxygen as heteroatom will be the most suitable.
• dimethyl, methyl ethyl and diethyl pyrocarbonate are used.
• Other pyrocarbonates may offer particular ad­vantages: thus, aryl and aralkyl esters simultaneously increase the aromatic content of the fuel which promotes the combustion properties and, if 2-methoxyethyl esters are used, ethylene glycol monomethyl ether, which is per se a biocide, is produced so that the microbe-killing action does not disappear with the decomposition of the pyrocarbonate.
• the pyrocarbonic acid diester may be added to the hydrocarbon-­containing liquid, preferably after settled water has been removed therefrom.
• the diester may also be intro­duced first into the container to be protected against corrosion.
• the pyrocarbonic acid diester (monomer or polymer) may be used in homogeneous or heterogeneous form. If used in heterogeneous form, the diester may be bonded to a solid substrate or to the wall of the container in the form of a coating.
• pyrocarbonic acid diesters may, ac­cording to the invention, be combined with the use of other biocides, such as chromates and organic borates and other water-binding substances, such as imines, ketals and the like.
• the invention also relates to liquids contain­ing hydrocarbons and which contain at least one pyro­carbonic acid diester.
• Such liquids have a corrosion-­suppressing action in the containers in which they are stored.
• said liquids contain 0.1-5 g of pyro­carbonate per litre, but for particular applications or particular circumstances, concentrations outside said range may be suitable.
• the pyrocarbonate is dimethyl, methyl ethyl or diethyl pyrocarbonate.
• said liquids may, of course, contain all the common additives and auxiliary substances ("dopes").
• the liquids containing hydrocarbons may be mineral oils, fuels, lubricants and the like.
• a particularly useful embodiment relates to aviation fuels which contain pyrocarbonic acid diesters.

Landscapes

• Chemical & Material Sciences (AREA)
• Oil, Petroleum & Natural Gas (AREA)
• Engineering & Computer Science (AREA)
• Organic Chemistry (AREA)
• Health & Medical Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• General Chemical & Material Sciences (AREA)
• Emergency Medicine (AREA)
• Combustion & Propulsion (AREA)
• Preventing Corrosion Or Incrustation Of Metals (AREA)
• Agricultural Chemicals And Associated Chemicals (AREA)
• Pyridine Compounds (AREA)
• Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
• Solid Fuels And Fuel-Associated Substances (AREA)

Applications Claiming Priority (2)

Publications (2)

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ID=19850558

Family Applications (1)

Country Status (3)

Cited By (1)

Family Cites Families (8)

• 1987
  • 1987-09-04 NL NL8702098A patent/NL8702098A/nl not_active Application Discontinuation
• 1988
  • 1988-09-02 DK DK488288A patent/DK488288A/da not_active Application Discontinuation
  • 1988-09-02 EP EP88201879A patent/EP0306108A3/de not_active Withdrawn

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