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
  • C10L1/18—Organic compounds containing oxygen
• • 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
  • C10L3/00—Gaseous fuels; Natural gas; Synthetic natural gas obtained by processes not covered by subclass C10G, C10K; Liquefied petroleum gas
• • 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
  • C10L3/00—Gaseous fuels; Natural gas; Synthetic natural gas obtained by processes not covered by subclass C10G, C10K; Liquefied petroleum gas
  • C10L3/06—Natural gas; Synthetic natural gas obtained by processes not covered by C10G, C10K3/02 or C10K3/04

Definitions

• the present invention relates to hydrocarbons including gas for use in cutting and/or welding torches, internal- combustion engine fuels and high temperature heating gas and oil fortified by the addition of a double additive or conditioner.
• the White U.S. patent No. 2,951,750, issued September 6, 1960, refers to the prior double additives for torch gas of dimethyl ether and benzine at column 1, lines 21 to 25, presumably as disclosed in the Seley patent, and then proposes the use of the double additive of propylene oxide and dimethyl ether at column 1, lines 55 to 62, instead of using benzine and dimethyl ether.
• Kessler U.S. Patent No. 3,591,355, issued July 6, 1971 proposed the addition of a double additive to torch gas, composed of a liquid alkanol such as methanol and a mixture of alkanes such as pentane and isopentane.
• White U.S. Patent No. 3,989,479, issued November 2, 1976 also proposed the addition of methanol and British Patent No. 569,108, accepted May 4, 1945, proposed the addition of ammonia.
• This British patent also recommended increasing the amount of propane in producer gas, water gas, Mond gas and other commercially available gas mixtures in which methane predominated.
• the Medsker patent proposed a mixture of methyl borate and hexane as an additive for a gaseous fuel.
• the principal torch gas used previously has been acetylene which is comparatively expensive, difficult to store and to transport, requires the use of almost pure oxygen with it and forms persistently adherent scoria when used for cutting ferrous metal.
• a disadvantage of using tetraethyl lead is that the lead has been discharged into the air, and lead is physically harmful, so that its use in gasoline for internal-combustion engines has been phased out.
• Methyl tertiary butyl ether by itself has been used as an additive for unleaded gasoline as an octane booster and to reduce harmful emission products.
• a principal object of this invention is to provide fortified hydrocarbon such as torch gas having characteristics superior to those of acetylene, especially for cutting ferrous metal, and also for welding. Such object also includes providing fortified hydrocarbon having characteristics superior to those of hydrocarbon fortified only by the addition of methyl ethyl ketone.
• a particular object is to provide a torch gas which will have high flame temperature and intense heating capability.
• a further object is to provide torch gas that can be stored and transported easily and economically.
• Another object is to provide a torch gas having a base gas which is readily available in almost the entire world, can be provided more economically and is easy to fortify for enhancing its attributes.
• Another object is to provide a gas that can be used by torches for cutting under water at considerable depths.
• An additional object is to provide a gas that can be used for torch cutting more economically because it will combine effectively with oxygen containing a higher proportion of adulterating gases which cannot otherwise be used with acetylene.
• LPG liquified petroleum gas
• MEK methyl ethyl ketone
• TSA tertiary butyl alcohol
• MTBE methyl tertiary butyl ether
• a further object of this invention is to provide fortified hydrocarbon for purposes other than torch gas, such as high temperature heating gas or oil for heating industrial furnaces such as for melting metals for pouring, and blast furnaces.
• This further object can be accomplished by utilizing LPG, natural gas or liquid hydrocarbon, such as diesel oil or fuel oil fortified with MEK together with TBA or with MTBE.
• Still another object is to fortify liquid hydrocarbon, especially gasoline, for use as an internal-combustion engine fuel to deter detonation and promote uniformity of combustion.
• Liquefied petroleum gas is the preferred base gas for the fortified torch gas of the present invention because of its high butane and propane content.
• LPG Liquefied petroleum gas
• Both the n-butane and isobutane isomers of butane are usually present in LPG, but a substantial amount of butane can have been removed from LPG because of the demand from industry for butane derivatives, such as for fuel, in which case the LPG is composed largely of propane. It is, however, desirable that there be a reasonable proportion of butane in the LPG, such as from 5% to 40%.
• the base gas could be propane or butane alone or any mixture of these gases or propylene.
• the additive or conditioner used to fortify the base gas contains methyl ethyl ketone (MEK) , otherwise known as 2-butanone, having the formula CH- OCH ⁇ CH, together with tertiary butyl alcohol, also known as tert-butyl alcohol (TBA), having the formula (CH 3 ) 3 C0H or methyl tertiary butyl ether, otherwise known as methyl tert-butyl ether (MTBE) having the formula (CH 3 ) 3 COCH 3 .
• MEK is a liquid with a boiling point of 70.6 degrees C. and a specific gravity of 0.805 and 20 degrees C.
• TBA is a waxy solid which melts at 25.6 degrees C. and has a specific gravity of 0.779 at 26 degrees C.
• MTBE is a colourless liquid having a boiling point of 55 degrees C. and a freezing point of -110 degrees C. and has a specific gravity of 0.74.
• LPG must be stored under pressure to keep it in a liquid state, but relatively heavy pressurized storage tanks and handling equipment for LPG is commercially practical and customary.
• LPG mixed with oxygen is not very effective for torch cutting and welding, not nearly as effective as acetylene gas mixed with substantially pure oxygen, but by enriching the base LPG with MEK together with MTBE or TBA as an additive the flame temperature is considerably increased and the heating capability is greatly improved.
• the amount of additive used will depend on the extent to which it is desired to improve the characteristics of the base hydrocarbon, but the amount of additive would be within the range of 0.5% to 20% of the hydrocarbon base gas by weight.
• the amount of TBA or MTBE is usually up to about 20% by weight of the amount of MEK.
• an amount of TBA and/or MTBE up to 3% of the LPG by weight could be mixed with up to 15% of MEK by weight of LPG, such as 3% to 10% MEK enhanced with 1% to 3% TBA and/or MTBE of the base gas by weight.
• Sufficiently beneficial results are usually obtained by the use of 2% of TBA or MTBE by weight of the hydrocarbon base gas mixed with 10% of MEK by weight of the hydrocarbon base gas.
• the ratio of about 20% of TBA and/or MTBE to MEK by weight is preferred, so that TBA or MTBE in the amount of 1% of the hydrocarbon base by weight can be mixed with MEK in the amount of 5% of the hydrocarbon base by weight.
• TBA or MTBE in the amount of 0.5% of the internal-combustion fuel by weight mixed with MEK in the amount of 2.5% or 3% of the internal-combustion engine fuel by weight provides sufficient improvement in performance of the internal-combustion engine fuel.
• MEK is a liquid at normal temperatures.
• the TBA may be melted by subjecting its container to warm water such as at a temperature of 40 degrees C to 45 degrees C and the TBA liquid is then simply mixed with the MEK liquid before the additive liquid is mixed with the hydrocarbon.
• MTBE liquid can be mixed with the MEK liquid before the additive liquid is mixed with the hydrocarbon.
• the additive is a liquid at normal temperatures and is supplied to the storage tank in which the hydrocarbon is to be stored or transported. It is quite practical to supply the additive to standard 55 gallon drums.
• the additive can be supplied in conjunction with a catalyst, preferably activated carbon in the form of powder, granules or pellets.
• the activated carbon is amorphous, preferably having been produced from coal or petroleum coke.
• Alternative catalysts that can be used are platinium, cupric oxide and granular silver carried by a suitable carrier.
• the amount of catalyst used is not critical, but it should be placed in the bottom of a storage container to facilitate mixing of the additive with the hydrocarbon base gas when it is supplied to the container under pressure. An amount of such catalyst between 1% and 5% of the weight of the additive would be satisfactory.
• the resulting mixture of base gas and additive or conditioner will be azeotropic so that the fortified torch gas will be homogeneous when it is released from the storage container to the torch.
• an acetylene torch oxygen that is in substantially pure form, such as at least 99% oxygen by volume. Satisfactory cutting temperatures can be provided by mixing with the fortified base gas of the present invention less pure oxygen such as oxygen having a purity of approximately 95%, the adulterant being nitrogen, carbon dioxide and other gas components of air. Even when oxygen of 90% purity is used, the flame temperature of base LPG of approximately 2760 degrees C. (5,000 degrees F.) can be raised to approximately 3200 degrees C. (5,800 degrees F.) to 3320 degrees C. (6,000 degrees F.) by use of the base LPG fortified by MEK and MTBE according to the present invention.
• Such impure oxygen can be produced economically by compressing air to about 4,000 psi, chilling it to minus 218 degrees C (minus 360 degrees F.) which liquefies the air and then allowing the temperature of the liquefied air to rise gradually while venting the container to release the nitrogen component of the liquified air which vaporizes at minus 196 degrees C. (minus 320 degrees F.) leaving the oxygen in liquid form.
• An advantage of using the fortified base gas of the present invention over acetylene for cutting ferrous metal is that a clean precise kerf is obtained.
• Oxyacetylene cutting produces a hard scoria persistently adherent to the work which increases the heating required and usually must subsequently be chipped off the work.
• Utilization of the fortified torch gas of the present invention produces a soft friable scoria which is sloughed off the work and out of the kerf as the cutting progresses to leave a narrower clean kerf with virgin metal along opposite margins of the kerf.
• a particular advantage which the fortified torch gas of the present invention has is that it can be used for flame cutting under water to a depth of 300 feet.
• the use of the oxyacetylene torch is limited to 20 feet under water because at pressures to which it would be necessary to subject the gas to enable it to be dispensed to the cutting torch at greater depths the acetylene will explode. Consequently, the only alternative that has been available for cutting under water at depths greater than about 20 feet prior to this invention has been the use of a carbon arc, the action of which is slow and the use of which is dangerous.
• MEK is useful in expediting the cutting of metal
• the use of MEK enhanced by the addition of TBA has increased the cutting speed of metal from 5% to 10% in comparison to the use of MEK alone
• the use of MEK and MTBE in combination has increased the cutting speed to 20% to 25% faster than where MEK has been used alone as an additive and about 15% faster than the cutting speed where the MEK has been enhanced with TBA.
• the invention can be used for high- temperature hydrocarbon heating gas such as LPG or natural gas, and high-temperature hydrocarbon heating liquids such as boiler fuel oil, stove oil or other oil, used in such industrial processes as smelting or other metal melting such as required for foundry casting, or for steam generating.
• the additive can be within the range of 2% to 10% of the hydrocarbon by weight. If the amount of additive is greater than 5%, a catalyst such as powdered activated carbon should be used to facilitate thorough mixing of the additive with the hydrocarbon.
• hydrocarbon gas such as LPG
• LPG hydrocarbon gas
• the additive is mixed with the gas.
• an amount of additive within the range of 2% to 5% by weight is adequate, and such an amount can be mixed sufficiently intimately with the hydrocarbon gas without the use of a catalyst.
• Another use of the additive is for fortifying internal-combustion engine fuel, such as automotive gasoline, aviation gasoline or diesel oil.
• the additive functions as an antiknock agent as well as improving the uniformity of combustion and accelerating the rate of combustion, which consequently enhances the power-producing characteristics of the fuel.
• the range of additive used would be 0.5% to 6% of the hydrocarbon by weight but preferably within the range of 1% to 4% by weigh .
• the amount of TBA or MTBE less than 20% by weight of the amount of MEK is preferred, but the total amount of TBA or MTBE should not exceed 3% of the hydrocarbon base by weight in order to maintain azeotropic characteristics of the fortified hydrocarbon.
• the ratio of 20% of TBA or MTBE to MEK by weight is preferred, so that TBA or MTBE in the amount of 1% of the hydrocarbon base by weight can be mixed with MEK in the amount of 5% of the hydrocarbon base by weight.
• TBA or MTBE in the amount of 0.5% of the internal-combustion fuel by weight mixed with MEK in the amount of 2.5% or 3% of the internal- combustion engine fuel by weight provides sufficient improvement in performance of the internal-combustion engine fuel.
• MEK is an effective additive for hydrocarbon without MTBE or TBA it is not as effective.

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• 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)
• Health & Medical Sciences (AREA)
• Emergency Medicine (AREA)
• Liquid Carbonaceous Fuels (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
• Hydrogen, Water And Hydrids (AREA)

Priority Applications (4)

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Publications (1)

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Citations (6)

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• 1993
  • 1993-03-04 JP JP5515565A patent/JPH08504839A/ja active Pending
  • 1993-03-04 WO PCT/NZ1993/000012 patent/WO1993018116A1/en active Application Filing
  • 1993-03-04 CA CA002131450A patent/CA2131450A1/en not_active Abandoned
  • 1993-03-04 BR BR9306014A patent/BR9306014A/pt not_active Application Discontinuation
  • 1993-03-04 CN CN93104049A patent/CN1051796C/zh not_active Expired - Fee Related
  • 1993-03-04 MY MYPI93000385A patent/MY111687A/en unknown
• 1994
  • 1994-09-02 KR KR1019940703065A patent/KR950700390A/ko not_active Application Discontinuation
• 1999
  • 1999-05-17 CN CN99106777A patent/CN1261621A/zh active Pending
  • 1999-05-17 CN CN99106776A patent/CN1261619A/zh active Pending

Patent Citations (6)

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