US20060248790A1 - Diesel composition - Google Patents

Diesel composition Download PDF

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Publication number
US20060248790A1
US20060248790A1 US11/390,129 US39012906A US2006248790A1 US 20060248790 A1 US20060248790 A1 US 20060248790A1 US 39012906 A US39012906 A US 39012906A US 2006248790 A1 US2006248790 A1 US 2006248790A1
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United States
Prior art keywords
ethanol
diesel
ethyl
weight
base material
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Abandoned
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US11/390,129
Inventor
Kohtaro Hashimoto
Kohjiroh Aimoto
Fumiaki Ikegawa
Takahiro Gunji
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Honda Motor Co Ltd
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Honda Motor Co Ltd
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Assigned to HONDA MOTOR CO., LTD. reassignment HONDA MOTOR CO., LTD. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: GUNJI, TAKAHIRO, IKEGAWA, FUMIAKI, AIMOTO, KOHJIROH, HASHIMOTO, KOHTARO
Publication of US20060248790A1 publication Critical patent/US20060248790A1/en
Abandoned legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS 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
    • C10L10/00Use of additives to fuels or fires for particular purposes
    • C10L10/12Use of additives to fuels or fires for particular purposes for improving the cetane number
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS 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
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/02Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only
    • C10L1/026Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only for compression ignition
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS 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
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/22Organic compounds containing nitrogen
    • C10L1/23Organic compounds containing nitrogen containing at least one nitrogen-to-oxygen bond, e.g. nitro-compounds, nitrates, nitrites
    • C10L1/231Organic compounds containing nitrogen containing at least one nitrogen-to-oxygen bond, e.g. nitro-compounds, nitrates, nitrites nitro compounds; nitrates; nitrites
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS 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
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/18Organic compounds containing oxygen
    • C10L1/182Organic compounds containing oxygen containing hydroxy groups; Salts thereof
    • C10L1/1822Organic compounds containing oxygen containing hydroxy groups; Salts thereof hydroxy group directly attached to (cyclo)aliphatic carbon atoms
    • C10L1/1824Organic compounds containing oxygen containing hydroxy groups; Salts thereof hydroxy group directly attached to (cyclo)aliphatic carbon atoms mono-hydroxy

Definitions

  • the present invention relates to a diesel composition.
  • diesel engines can be found among internal combustion engines capable of reducing fuel consumption and emission matter.
  • the diesel engine is driven by the compressed self ignition of a fuel such as diesel, and it is known that the diesel engine is small in the emission of carbon dioxide. Accordingly, it is conceivable that if ethanol can be mixed in the diesel, such mixing will further enjoy an advantage from the aspect of reducing the emission of carbon dioxide.
  • An object of the present invention is to provide, through overcoming such a disadvantage, a diesel composition having an excellent ignitability despite inclusion of ethanol therein.
  • the diesel composition of the present invention is characterized by including a diesel base material, and ethanol in a range from 5 to 30% by weight based on the total amount of the diesel base material and ethyl nitrite or ethyl nitrate in a range from 0.5 to 7% by weight based on the total amount of the diesel base material.
  • the diesel composition of the present invention includes, together with the above described range of ethanol, the above described range of ethyl nitrite or ethyl nitrate, and accordingly, can acquire an excellent ignitability despite inclusion of ethanol.
  • a cetane number improver to improve the ignitability of the diesel an alkyl nitrate having 6 or 8 carbon atoms is used (Japanese Patent No. 3102934).
  • Japanese Patent No. 3102934 Japanese Patent No. 3102934
  • ethyl nitrite or ethyl nitrate is used as the above described cetane number improver.
  • the content of the ethanol is less than 5% by weight based on the amount of the diesel base material, no effect of reducing the emission of carbon dioxide is attained.
  • the content of the ethanol exceeds 30% by weight based on the amount of the diesel base material, the ignitability in the diesel engine is degraded, and a decrease in the output power is also caused due to the decrease in the generated heat per unit volume.
  • the content of the ethyl nitrite or ethyl nitrate is less than 0.5% by weight based on the amount of the diesel base material, the ignitability of the diesel composition containing ethanol cannot be improved.
  • the content of the ethyl nitrite or ethyl nitrate exceeds 7% by weight based on the amount of the diesel base material, no further advantageous effect can be attained.
  • the content of the ethyl nitrite or ethyl nitrate preferably falls within a range of 50% by weight or less of the content of the ethanol.
  • the ignition delay time varies widely leading to such a problem that a vibration is generated.
  • the ethyl nitrite or ethyl nitrate may be synthesized through any types of reaction paths, but is preferably derived from ethanol as a raw material.
  • the ethyl nitrite or ethyl nitrate improves the ignitability of the diesel composition containing ethanol, and, on the other hand, contributes to the reduction of the emission of carbon dioxide in cooperation with ethanol, through the use of ethanol as a raw material.
  • the ethyl nitrite When ethanol is used as a raw material, the ethyl nitrite may be obtained from the reaction between ethanol and nitrous acid, and the ethyl nitrate may be obtained from the reaction between ethanol and nitric acid.
  • the diesel composition of the present embodiment is characterized by including a diesel base material, and ethanol in a range from 5 to 30% by weight based on the total amount of the diesel base material and ethyl nitrite or ethyl nitrate in a range from 1 to 7% by weight based on the total amount of the diesel base material.
  • the ethanol may be synthesized industrially, but preferably is derived from plants as raw materials from the viewpoint of reducing the emission of carbon dioxide.
  • Examples of ethanol derived from plants as raw materials may include, for example, ethanol obtained by fermentation of agricultural crops such as sugarcane and corn in combination with the subsequent distillation.
  • the ethyl nitrite or ethyl nitrate may be synthesized through any types of reaction paths, but is preferably derived from ethanol as a raw material from the viewpoint of reducing the emission of carbon dioxide.
  • the ethyl nitrite may be obtained from the reaction between ethanol and nitrous acid as shown in the following formula (1): CH 3 CH 2 OH+HNO 2 ⁇ CH 3 CH 2 ONO+H 2 O (1)
  • the ethyl nitrate may be obtained from the reaction between ethanol and nitric acid as shown in the following formula (2): CH 3 CH 2 OH+HNO 3 ⁇ CH 3 CH 2 ONO 2 +H 2 O (2)
  • the ignitability of heptane (C 7 H 16 ; boiling point: 98.4° C.) as a diesel base material was first tested.
  • the ignitability test was carried out by measuring the ignition delay time by use of a fuel spray ignition analyzer (trade name: FIA-100; manufactured by Fuel Tech, Inc.) with a combustion chamber set at a temperature of 500° C. and a pressure of 2 MPa. The result is shown in Table 1.
  • a diesel composition composed of 90% by weight of heptane as the diesel base material, 8.5% by weight of ethanol and 1.5% by weight of ethyl nitrite was first prepared.
  • a diesel composition composed of 90% by weight of heptane as the diesel base material and 7.0% by weight of ethanol and 3.0% by weight of ethyl nitrite was prepared.
  • a diesel composition composed of 80% by weight of heptane as the diesel base material and 17.0% by weight of ethanol and 3.0% by weight of ethyl nitrite was prepared.
  • a diesel composition composed of 70% by weight of heptane as the diesel base material and 25.5% by weight of ethanol and 4.5% by weight of ethyl nitrite was prepared.
  • a diesel composition composed of 90% by weight of heptane as the diesel base material and 8.5% by weight of ethanol and 1.5% by weight of ethyl nitrate was prepared.
  • the diesel composition of Comparative Example 1 composed of 90% by weight of heptane and 10% by weight of ethanol is longer in ignition delay time and lower in ignitability than the diesel composition of Reference Example composed of 100% of heptane, but the diesel composition of Example 1 composed of 90% by weight of heptane, 8.5% by weight of ethanol and 1.5% by weight of ethyl nitrite is shorter in ignition delay time and better in ignitability than the diesel composition of Reference Example.
  • the diesel compositions of Examples 2 to 4 each composed of 70 to 90% by weight of heptane, 7 to 25% by weight of ethanol and 3.0 to 4.5% by weight of ethyl nitrite and the diesel composition of Example 5 using ethyl nitrate in place of ethyl nitrite used in Example 1 are all shorter in ignition delay time and better in ignitability than the diesel composition of Reference Example.

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  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Combustion & Propulsion (AREA)
  • Liquid Carbonaceous Fuels (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

The present invention provides a diesel composition having an excellent ignitability despite inclusion of ethanol therein. The diesel composition includes a diesel base material, ethanol in a range from 5 to 30% by weight based on the total amount of the diesel base material, and ethyl nitrite or ethyl nitrate in a range from 0.5 to 7% by weight based on the total amount of the diesel base material. The content of the ethyl nitrite or ethyl nitrate falls within a range of 50% by weight or less of the content of the ethanol, and the ethyl nitrite or ethyl nitrate is derived from ethanol as a raw material.

Description

    BACKGROUND OF THE INVENTION
  • 1. Field of the Invention
  • The present invention relates to a diesel composition.
  • 2. Description of the Related Art
  • For the purpose of preventing the global warming, the reduction of the emission of carbon dioxide has recently been demanded, and various means have been proposed for that purpose. As one of such means, it has been known the use of ethanol or the like obtained through the fermentation of plant substances, for example, such as agricultural crops including sugarcane and corn in combination with the subsequent distillation for automotive fuel and the like.
  • As for the plant substances, plants themselves to be raw materials have already absorbed carbon dioxide. Therefore, even when the plant substances themselves are burned, the quantity of the emitted carbon dioxide is equal to the quantity of the carbon dioxide having been absorbed by the plants concerned; thus, there can be attained the so-called carbon neutral effect such that the quantity of the emitted carbon dioxide is theoretically zero in total. In this connection, it is known that ethanol, one of the plant substances, is mixed in gasoline to be used as a gasoline engine fuel (see, Japanese Patent Laid-Open No. 2005-29761).
  • On the other hand, diesel engines can be found among internal combustion engines capable of reducing fuel consumption and emission matter. The diesel engine is driven by the compressed self ignition of a fuel such as diesel, and it is known that the diesel engine is small in the emission of carbon dioxide. Accordingly, it is conceivable that if ethanol can be mixed in the diesel, such mixing will further enjoy an advantage from the aspect of reducing the emission of carbon dioxide.
  • However, when ethanol is used for the fuel of the diesel engine, there occurs such a disadvantage that ethanol has a low ignitability, and accordingly a fuel mixed with ethanol has also a reduced ignitability.
  • SUMMARY OF THE INVENTION
  • An object of the present invention is to provide, through overcoming such a disadvantage, a diesel composition having an excellent ignitability despite inclusion of ethanol therein.
  • For the purpose of achieving such an object, the diesel composition of the present invention is characterized by including a diesel base material, and ethanol in a range from 5 to 30% by weight based on the total amount of the diesel base material and ethyl nitrite or ethyl nitrate in a range from 0.5 to 7% by weight based on the total amount of the diesel base material.
  • The diesel composition of the present invention includes, together with the above described range of ethanol, the above described range of ethyl nitrite or ethyl nitrate, and accordingly, can acquire an excellent ignitability despite inclusion of ethanol. It is known that as a cetane number improver to improve the ignitability of the diesel, an alkyl nitrate having 6 or 8 carbon atoms is used (Japanese Patent No. 3102934). However, it has not yet been known that ethyl nitrite or ethyl nitrate is used as the above described cetane number improver.
  • When the content of the ethanol is less than 5% by weight based on the amount of the diesel base material, no effect of reducing the emission of carbon dioxide is attained. When the content of the ethanol exceeds 30% by weight based on the amount of the diesel base material, the ignitability in the diesel engine is degraded, and a decrease in the output power is also caused due to the decrease in the generated heat per unit volume.
  • When the content of the ethyl nitrite or ethyl nitrate is less than 0.5% by weight based on the amount of the diesel base material, the ignitability of the diesel composition containing ethanol cannot be improved. When the content of the ethyl nitrite or ethyl nitrate exceeds 7% by weight based on the amount of the diesel base material, no further advantageous effect can be attained.
  • In the diesel composition of the present invention, the content of the ethyl nitrite or ethyl nitrate preferably falls within a range of 50% by weight or less of the content of the ethanol. When the content of the ethyl nitrite or ethyl nitrate exceeds 50% by weight of the content of the ethanol, the ignition delay time varies widely leading to such a problem that a vibration is generated.
  • The ethyl nitrite or ethyl nitrate may be synthesized through any types of reaction paths, but is preferably derived from ethanol as a raw material. The ethyl nitrite or ethyl nitrate improves the ignitability of the diesel composition containing ethanol, and, on the other hand, contributes to the reduction of the emission of carbon dioxide in cooperation with ethanol, through the use of ethanol as a raw material.
  • When ethanol is used as a raw material, the ethyl nitrite may be obtained from the reaction between ethanol and nitrous acid, and the ethyl nitrate may be obtained from the reaction between ethanol and nitric acid.
  • DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT
  • Hereinbelow, an embodiment of the present invention is described in more detail.
  • The diesel composition of the present embodiment is characterized by including a diesel base material, and ethanol in a range from 5 to 30% by weight based on the total amount of the diesel base material and ethyl nitrite or ethyl nitrate in a range from 1 to 7% by weight based on the total amount of the diesel base material.
  • The ethanol may be synthesized industrially, but preferably is derived from plants as raw materials from the viewpoint of reducing the emission of carbon dioxide. Examples of ethanol derived from plants as raw materials may include, for example, ethanol obtained by fermentation of agricultural crops such as sugarcane and corn in combination with the subsequent distillation.
  • The ethyl nitrite or ethyl nitrate may be synthesized through any types of reaction paths, but is preferably derived from ethanol as a raw material from the viewpoint of reducing the emission of carbon dioxide.
  • When ethanol is used as a raw material, the ethyl nitrite may be obtained from the reaction between ethanol and nitrous acid as shown in the following formula (1):
    CH3CH2OH+HNO2→CH3CH2ONO+H2O   (1)
  • The ethyl nitrate may be obtained from the reaction between ethanol and nitric acid as shown in the following formula (2):
    CH3CH2OH+HNO3→CH3CH2ONO2+H2O   (2)
  • Hereinbelow, examples and a comparative example of the present invention are described.
  • REFERENCE EXAMPLE
  • In the present Reference Example, the ignitability of heptane (C7H16; boiling point: 98.4° C.) as a diesel base material was first tested. The ignitability test was carried out by measuring the ignition delay time by use of a fuel spray ignition analyzer (trade name: FIA-100; manufactured by Fuel Tech, Inc.) with a combustion chamber set at a temperature of 500° C. and a pressure of 2 MPa. The result is shown in Table 1.
  • EXAMPLE 1
  • In the present Example, a diesel composition composed of 90% by weight of heptane as the diesel base material, 8.5% by weight of ethanol and 1.5% by weight of ethyl nitrite was first prepared.
  • Next, the ignitability of the diesel composition prepared in the present Example was tested in exactly the same manner as in the above Reference Example. The result is shown in Table 1.
  • COMPARATIVE EXAMPLE 1
  • In the present Comparative Example, a diesel composition composed of 90% by weight of heptane as the diesel base material and 10% by weight of ethanol, but not containing ethyl nitrite at all was prepared.
  • Next, the ignitability of the diesel composition prepared in the present Comparative Example was tested in the exactly same manner as in the above Reference Example. The result is shown in Table 1.
  • EXAMPLE 2
  • In the present Example, a diesel composition composed of 90% by weight of heptane as the diesel base material and 7.0% by weight of ethanol and 3.0% by weight of ethyl nitrite was prepared.
  • Next, the ignitability of the diesel composition prepared in the present Example was tested in the exactly same manner as in the above Reference Example. The result is shown in Table 1.
  • EXAMPLE 3
  • In the present Example, a diesel composition composed of 80% by weight of heptane as the diesel base material and 17.0% by weight of ethanol and 3.0% by weight of ethyl nitrite was prepared.
  • Next, the ignitability of the diesel composition prepared in the present Example was tested in the exactly same manner as in the above Reference Example. The result is shown in Table 1.
  • EXAMPLE 4
  • In the present Example, a diesel composition composed of 70% by weight of heptane as the diesel base material and 25.5% by weight of ethanol and 4.5% by weight of ethyl nitrite was prepared.
  • Next, the ignitability of the diesel composition prepared in the present Example was tested in the exactly same manner as in the above Reference Example. The result is shown in Table 1.
  • EXAMPLE 5
  • In the present Example, a diesel composition composed of 90% by weight of heptane as the diesel base material and 8.5% by weight of ethanol and 1.5% by weight of ethyl nitrate was prepared.
  • Next, the ignitability of the diesel composition prepared in the present Example was tested in the exactly same manner as in the above Reference Example. The result is shown in Table 1.
    TABLE 1
    Ethyl Ethyl Ignition
    Heptane Ethanol nitrite nitrate delay time
    (wt %) (wt %) (wt %) (wt %) (ms)
    Ref. ex. 100 5.67
    Ex. 1 90 8.5 1.5 5.14
    Comp. 90 10 7.31
    ex. 1
    Ex. 2 90 7.0 3.0 4.42
    Ex. 3 80 17.0 3.0 5.53
    Ex. 4 70 25.5 4.5 5.62
    Ex. 5 90 8.5 1.5 5.22
  • As can be clearly seen from Table 1, the diesel composition of Comparative Example 1 composed of 90% by weight of heptane and 10% by weight of ethanol is longer in ignition delay time and lower in ignitability than the diesel composition of Reference Example composed of 100% of heptane, but the diesel composition of Example 1 composed of 90% by weight of heptane, 8.5% by weight of ethanol and 1.5% by weight of ethyl nitrite is shorter in ignition delay time and better in ignitability than the diesel composition of Reference Example.
  • As can also be clearly seen from Table 1, the diesel compositions of Examples 2 to 4 each composed of 70 to 90% by weight of heptane, 7 to 25% by weight of ethanol and 3.0 to 4.5% by weight of ethyl nitrite and the diesel composition of Example 5 using ethyl nitrate in place of ethyl nitrite used in Example 1 are all shorter in ignition delay time and better in ignitability than the diesel composition of Reference Example.

Claims (3)

1. A diesel composition, comprising:
a diesel base material;
ethanol in a range from 5 to 30% by weight based on the total amount of the diesel base material; and
ethyl nitrite or ethyl nitrate in a range from 0.5 to 7% by weight based on the total amount of the diesel base material.
2. The diesel composition according to claim 1, wherein the content of the ethyl nitrite or ethyl nitrate falls within a range of 50% by weight or less of the content of the ethanol.
3. The diesel composition according to claim 1, wherein the ethyl nitrite or ethyl nitrate is derived from ethanol as a raw material.
US11/390,129 2005-05-09 2006-03-28 Diesel composition Abandoned US20060248790A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2005135592A JP2006312667A (en) 2005-05-09 2005-05-09 Diesel light oil composition
JP2005-135592 2005-05-09

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Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT1396205B1 (en) 2009-10-13 2012-11-16 Eni Spa COMPOSITION OF GASOLINE INCLUDING DIETHYL CARBONATE FROM BIOETHANOL.
IT1397623B1 (en) 2009-12-16 2013-01-18 Eni Spa COMPOSITION OF GAS OIL INCLUDING DIETYL CARBONATE FROM BIOETHANOL AND VEGETABLE OIL
IT1396959B1 (en) 2009-12-18 2012-12-20 Eni Spa COMPOSITION OF DIESEL INCLUDING BIODIESEL AND DIETYL CARBONATE FROM BIOETHANOL
CN103740416B (en) * 2013-12-31 2016-06-29 张锦碧 A kind of Environment-friendlyfuel fuel of enzyme modified

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3078552A (en) * 1959-12-03 1963-02-26 Gen Electric Copper foam material and method
US20020020106A1 (en) * 1999-07-07 2002-02-21 Filippini Brian B. Amino alkylphenol emulsifiers for an aqueous hydrocarbon fuel

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2701588A1 (en) * 1977-01-15 1978-07-20 Daimler Benz Ag Ethanol-based diesel fuel - contg. an ignition accelerator e.g. ethyl nitrate or nitrite
EP1485449A2 (en) * 2002-03-14 2004-12-15 The Lubrizol Corporation Ethanol-diesel fuel composition and methods thereof

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3078552A (en) * 1959-12-03 1963-02-26 Gen Electric Copper foam material and method
US20020020106A1 (en) * 1999-07-07 2002-02-21 Filippini Brian B. Amino alkylphenol emulsifiers for an aqueous hydrocarbon fuel

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JP2006312667A (en) 2006-11-16
EP1721954A3 (en) 2007-06-27

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