RU2015125662A - CONTINUOUS METHOD OF TRANSFORMING LIGNIN TO USEFUL COMPOUNDS - Google Patents

CONTINUOUS METHOD OF TRANSFORMING LIGNIN TO USEFUL COMPOUNDS Download PDF

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Publication number
RU2015125662A
RU2015125662A RU2015125662A RU2015125662A RU2015125662A RU 2015125662 A RU2015125662 A RU 2015125662A RU 2015125662 A RU2015125662 A RU 2015125662A RU 2015125662 A RU2015125662 A RU 2015125662A RU 2015125662 A RU2015125662 A RU 2015125662A
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deoxygenation
lignin
moles
mpa
bar
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RU2015125662A
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Russian (ru)
Inventor
Аарон МЮРРЕЙ
Стивен РАЙБА
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БИОКЕМТЕКС С.п.А.
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Priority claimed from PCT/EP2013/053630 external-priority patent/WO2013124460A2/en
Priority claimed from US13/775,239 external-priority patent/US9732021B2/en
Priority claimed from US13/775,242 external-priority patent/US9340476B2/en
Priority claimed from PCT/EP2013/067734 external-priority patent/WO2014063852A1/en
Application filed by БИОКЕМТЕКС С.п.А. filed Critical БИОКЕМТЕКС С.п.А.
Publication of RU2015125662A publication Critical patent/RU2015125662A/en

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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G1/00Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal
    • C10G1/06Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal by destructive hydrogenation
    • C10G1/065Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal by destructive hydrogenation in the presence of a solvent
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G3/00Production of liquid hydrocarbon mixtures from oxygen-containing organic materials, e.g. fatty oils, fatty acids
    • C10G3/42Catalytic treatment
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G3/00Production of liquid hydrocarbon mixtures from oxygen-containing organic materials, e.g. fatty oils, fatty acids
    • C10G3/42Catalytic treatment
    • C10G3/44Catalytic treatment characterised by the catalyst used
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G3/00Production of liquid hydrocarbon mixtures from oxygen-containing organic materials, e.g. fatty oils, fatty acids
    • C10G3/54Production of liquid hydrocarbon mixtures from oxygen-containing organic materials, e.g. fatty oils, fatty acids characterised by the catalytic bed
    • C10G3/55Production of liquid hydrocarbon mixtures from oxygen-containing organic materials, e.g. fatty oils, fatty acids characterised by the catalytic bed with moving solid particles, e.g. moving beds
    • C10G3/56Production of liquid hydrocarbon mixtures from oxygen-containing organic materials, e.g. fatty oils, fatty acids characterised by the catalytic bed with moving solid particles, e.g. moving beds suspended in the oil, e.g. slurries, ebullated beds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G2300/00Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
    • C10G2300/10Feedstock materials
    • C10G2300/1011Biomass
    • C10G2300/1014Biomass of vegetal origin
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G3/00Production of liquid hydrocarbon mixtures from oxygen-containing organic materials, e.g. fatty oils, fatty acids
    • C10G3/50Production of liquid hydrocarbon mixtures from oxygen-containing organic materials, e.g. fatty oils, fatty acids in the presence of hydrogen, hydrogen donors or hydrogen generating compounds
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P30/00Technologies relating to oil refining and petrochemical industry
    • Y02P30/20Technologies relating to oil refining and petrochemical industry using bio-feedstock

Claims (29)

1. Способ превращения сырьевого потока лигнинсодержащей биомассы в поток подвергнутого превращению лигнина, включающий стадии:1. A method of converting a lignin-containing biomass feed stream into a lignin-converted stream, comprising the steps of: A) объединения сырьевого потока лигнинсодержащей биомассы, содержащего лигнин и по меньшей мере первый растворитель, с первым катализатором в реакционном сосуде,A) combining a feed stream of lignin-containing biomass containing lignin and at least a first solvent with a first catalyst in a reaction vessel, при этом отношение количества молей первого катализатора к количеству молей лигнина составляет от 4:1 до 15:1;the ratio of the number of moles of the first catalyst to the number of moles of lignin is from 4: 1 to 15: 1; B) дезоксигенирования сырьевого потока лигнинсодержащей биомассы с получением потока подвергнутого превращению лигнина при температуре дезоксигенирования и давлении дезоксигенирования в течение времени проведения дезоксигенирования.B) deoxygenation of the lignin-containing biomass feed stream to obtain a stream of lignin converted at a deoxygenation temperature and a deoxygenation pressure during the deoxygenation time. 2. Способ по п. 1, отличающийся тем, что отношение количества молей первого катализатора к количеству молей лигнина составляет от 4:1 до 12:1.2. The method according to p. 1, characterized in that the ratio of the number of moles of the first catalyst to the number of moles of lignin is from 4: 1 to 12: 1. 3. Способ по п. 1, отличающийся тем, что отношение количества молей первого катализатора к количеству молей лигнина составляет от 4:1 до 10:1.3. The method according to p. 1, characterized in that the ratio of the number of moles of the first catalyst to the number of moles of lignin is from 4: 1 to 10: 1. 4. Способ по п. 1, отличающийся тем, что отношение количества молей первого катализатора к количеству молей лигнина составляет от 4:1 до 9:1.4. The method according to p. 1, characterized in that the ratio of the number of moles of the first catalyst to the number of moles of lignin is from 4: 1 to 9: 1. 5. Способ по п. 1, отличающийся тем, что отношение количества молей первого катализатора к количеству молей лигнина составляет от 5:1 до 9:1.5. The method according to p. 1, characterized in that the ratio of the number of moles of the first catalyst to the number of moles of lignin is from 5: 1 to 9: 1. 6. Способ по любому из пп. 1-5, отличающийся тем, что температура дезоксигенирования составляет от 205 до 325°С.6. The method according to any one of paragraphs. 1-5, characterized in that the deoxygenation temperature is from 205 to 325 ° C. 7. Способ по п. 6, отличающийся тем, что температура дезоксигенирования составляет от 215 до 300°С.7. The method according to p. 6, characterized in that the deoxygenation temperature is from 215 to 300 ° C. 8. Способ по п. 6, отличающийся тем, что температура дезоксигенирования составляет от 225 до 280°С.8. The method according to p. 6, characterized in that the deoxygenation temperature is from 225 to 280 ° C. 9. Способ по любому из пп. 1-5, 7 или 8, отличающийся тем, что первый катализатор содержит металлический катализатор, в котором металл выбран из группы, состоящей из никеля, палладия, платины, рутения, родия, молибдена, кобальта и железа.9. The method according to any one of paragraphs. 1-5, 7 or 8, characterized in that the first catalyst contains a metal catalyst, in which the metal is selected from the group consisting of nickel, palladium, platinum, ruthenium, rhodium, molybdenum, cobalt and iron. 10. Способ по п. 6, отличающийся тем, что первый катализатор содержит металлический катализатор, в котором металл выбран из группы, состоящей из никеля, палладия, платины, рутения, родия, молибдена, кобальта и железа.10. The method according to p. 6, characterized in that the first catalyst contains a metal catalyst, in which the metal is selected from the group consisting of nickel, palladium, platinum, ruthenium, rhodium, molybdenum, cobalt and iron. 11. Способ по любому из пп. 1-5, 7, 8 или 10, отличающийся тем, что давление дезоксигенирования составляет от 60 бар (6 МПа) до 100 бар (10 МПа).11. The method according to any one of paragraphs. 1-5, 7, 8 or 10, characterized in that the deoxygenation pressure is from 60 bar (6 MPa) to 100 bar (10 MPa). 12. Способ по п. 6, отличающийся тем, что давление дезоксигенирования составляет от 60 бар (6 МПа) до 100 бар (10 МПа).12. The method according to p. 6, characterized in that the deoxygenation pressure is from 60 bar (6 MPa) to 100 bar (10 MPa). 13. Способ по п. 9, отличающийся тем, что давление дезоксигенирования составляет от 60 бар (6 МПа) до 100 бар (10 МПа).13. The method according to p. 9, characterized in that the deoxygenation pressure is from 60 bar (6 MPa) to 100 bar (10 MPa). 14. Способ по п. 11, отличающийся тем, что давление дезоксигенирования составляет от 70 бар (7 МПа) до 100 бар (10 МПа).14. The method according to p. 11, characterized in that the deoxygenation pressure is from 70 bar (7 MPa) to 100 bar (10 MPa). 15. Способ по п. 11, отличающийся тем, что давление дезоксигенирования составляет от 75 бар (7,5 МПа) до 95 бар (9,5 МПа).15. The method according to p. 11, characterized in that the deoxygenation pressure is from 75 bar (7.5 MPa) to 95 bar (9.5 MPa). 16. Способ по любому из пп. 1-5, 7, 8, 10 или 12-15, отличающийся тем, что время проведения дезоксигенирования составляет от 5 мин до 2 ч.16. The method according to any one of paragraphs. 1-5, 7, 8, 10 or 12-15, characterized in that the time for deoxygenation is from 5 minutes to 2 hours 17. Способ по п. 6, отличающийся тем, что время проведения дезоксигенирования составляет от 5 мин до 2 ч.17. The method according to p. 6, characterized in that the time for deoxygenation is from 5 minutes to 2 hours 18. Способ по п. 9, отличающийся тем, что время проведения дезоксигенирования составляет от 5 мин до 2 ч.18. The method according to p. 9, characterized in that the time for deoxygenation is from 5 minutes to 2 hours 19. Способ по п. 11, отличающийся тем, что время проведения дезоксигенирования составляет от 5 мин до 2 ч.19. The method according to p. 11, characterized in that the time for deoxygenation is from 5 minutes to 2 hours 20. Способ по п. 16, отличающийся тем, что время проведения дезоксигенирования составляет от 10 мин до 1,5 ч.20. The method according to p. 16, characterized in that the time for deoxygenation is from 10 minutes to 1.5 hours 21. Способ по п. 16, отличающийся тем, что время проведения дезоксигенирования составляет от 15 мин до 1 ч.21. The method according to p. 16, characterized in that the time for deoxygenation is from 15 minutes to 1 hour 22. Способ по любому из п.п. 1-5, 7, 8, 10, 12-15 или 17-21, отличающийся тем, что реакционный сосуд представляет собой реактор с расширенным слоем.22. The method according to any one of paragraphs. 1-5, 7, 8, 10, 12-15 or 17-21, characterized in that the reaction vessel is an expanded-bed reactor. 23. Способ по п. 6, отличающийся тем, что реакционный сосуд представляет собой реактор с расширенным слоем.23. The method according to p. 6, characterized in that the reaction vessel is an expanded-bed reactor. 24. Способ по п. 9, отличающийся тем, что реакционный сосуд представляет собой реактор с расширенным слоем.24. The method according to p. 9, characterized in that the reaction vessel is an expanded-bed reactor. 25. Способ по п. 11, отличающийся тем, что реакционный сосуд представляет собой реактор с расширенным слоем.25. The method according to p. 11, characterized in that the reaction vessel is an expanded-bed reactor. 26. Способ по п. 16, отличающийся тем, что реакционный сосуд представляет собой реактор с расширенным слоем.26. The method according to p. 16, characterized in that the reaction vessel is an expanded-bed reactor.
RU2015125662A 2013-01-13 2013-11-21 CONTINUOUS METHOD OF TRANSFORMING LIGNIN TO USEFUL COMPOUNDS RU2015125662A (en)

Applications Claiming Priority (43)

Application Number Priority Date Filing Date Title
US201361751919P 2013-01-13 2013-01-13
US61/751,919 2013-01-13
US201361764611P 2013-02-14 2013-02-14
US61/764,611 2013-02-14
US201361765402P 2013-02-15 2013-02-15
US61/765,402 2013-02-15
PCT/EP2013/053630 WO2013124460A2 (en) 2012-02-24 2013-02-22 Continuous process for conversion of lignin to useful compounds
EPPCT/EP2013/053631 2013-02-22
PCT/EP2013/053628 WO2013124458A2 (en) 2012-02-24 2013-02-22 Continuous process for conversion of lignin to useful compounds
EPPCT/EP2013/053626 2013-02-22
EPPCT/EP2013/053628 2013-02-22
USPCT/US2013/027393 2013-02-22
PCT/EP2013/053629 WO2013124459A2 (en) 2012-02-24 2013-02-22 Continuous process for conversion of lignin to useful compounds
EPPCT/EP2013/053629 2013-02-22
PCT/US2013/027393 WO2013142006A2 (en) 2012-02-24 2013-02-22 Continuous process for conversion of lignin to useful compounds
PCT/EP2013/053631 WO2013124461A2 (en) 2012-02-24 2013-02-22 Continuous process for conversion of lignin to useful compounds
EPPCT/EP2013/053630 2013-02-22
EPPCT/EP2013/053625 2013-02-22
PCT/EP2013/053625 WO2013124456A2 (en) 2012-02-24 2013-02-22 Continuous process for conversion of lignin to useful compounds
PCT/EP2013/053626 WO2013124457A2 (en) 2012-02-24 2013-02-22 Continuous process for conversion of lignin to useful compounds
US13/775,229 2013-02-24
US13/775,239 US9732021B2 (en) 2012-02-24 2013-02-24 Continuous process for conversion of lignin to useful compounds
US13/775,230 2013-02-24
US13/775,240 2013-02-24
US13/775,238 US9035117B2 (en) 2012-02-24 2013-02-24 Continuous process for conversion of lignin to useful compounds
US13/775,230 US9139501B2 (en) 2012-02-24 2013-02-24 Continuous process for conversion of lignin to useful compounds
US13/775,242 2013-02-24
US13/775,238 2013-02-24
US13/775,239 2013-02-24
US13/775,241 US20130225856A1 (en) 2012-02-24 2013-02-24 Continuous process for conversion of lignin to useful compounds
US13/775,240 US9162951B2 (en) 2012-02-24 2013-02-24 Continuous process for conversion of lignin to useful compounds
US13/775,229 US20130225853A1 (en) 2012-02-24 2013-02-24 Continuous process for conversion of lignin to useful compounds
US13/775,242 US9340476B2 (en) 2012-02-24 2013-02-24 Continuous process for conversion of lignin to useful compounds
US13/775,241 2013-02-24
US201361837262P 2013-06-20 2013-06-20
US61/837,262 2013-06-20
US201361866734P 2013-08-16 2013-08-16
US61/866,734 2013-08-16
EPPCT/EP2013/067734 2013-08-27
PCT/EP2013/067734 WO2014063852A1 (en) 2012-10-28 2013-08-27 Continuous process for conversion of lignin to useful compounds
US201361892617P 2013-10-18 2013-10-18
US61/892,617 2013-10-18
PCT/EP2013/074411 WO2014108238A1 (en) 2013-01-13 2013-11-21 Continuous process for conversion of lignin to useful compounds

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RU2015125662A true RU2015125662A (en) 2017-02-14

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CN (1) CN105121603A (en)
BR (1) BR112015016618A2 (en)
CA (1) CA2896728A1 (en)
MX (1) MX2015008962A (en)
RU (1) RU2015125662A (en)
WO (1) WO2014108238A1 (en)

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CN116635357A (en) * 2020-09-24 2023-08-22 泰恩工艺技术有限公司 Continuous process for selectively converting aldohexose-producing carbohydrates to ethylene glycol using low concentration reverse aldol catalyst
US11319269B2 (en) 2020-09-24 2022-05-03 Iowa Corn Promotion Board Continuous processes for the selective conversion of aldohexose-yielding carbohydrate to ethylene glycol using low concentrations of retro-aldol catalyst

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CA2896728A1 (en) 2014-07-17
BR112015016618A2 (en) 2017-07-11
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CN105121603A (en) 2015-12-02
MX2015008962A (en) 2015-09-29
JP2016508177A (en) 2016-03-17

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