Catalytic Hydrodeoxygenation of Bio-oil Model Compounds over Pt/HY Catalyst

نویسندگان

  • Heejin Lee
  • Hannah Kim
  • Mi Jin Yu
  • Chang Hyun Ko
  • Jong-Ki Jeon
  • Jungho Jae
  • Sung Hoon Park
  • Sang-Chul Jung
  • Young-Kwon Park
چکیده

The hydrodeoxygenation of a model compound of lignin-derived bio-oil, guaiacol, which can be obtained from the pyrolysis of biomass to bio-oil, has attracted considerable research attention because of its huge potential as a substitute for conventional fuels. In this study, platinum-loaded HY zeolites (Pt/HY) with different Si/Al molar ratios were used as catalysts for the hydrodeoxygenation of guaiacol, anisole, veratrole, and phenol to a range of hydrocarbons, such as cyclohexane. The cyclohexane (major product) yield increased with increasing number of acid sites. To produce bio-oil with the maximum level of cyclohexane and alkylated cyclohexanes, which would be suitable as a substitute for conventional transportation fuels, the Si/Al molar ratio should be optimized to balance the Pt particle-induced hydrogenation with acid site-induced methyl group transfer. The fuel properties of real bio-oil derived from the fast pyrolysis of cork oak was improved using the Pt/HY catalyst.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Hydrodeoxygenation of Oxidized and Hydrotreated Bio-oils to Hydrocarbons in Fixed-bed Continuous Reactor

The physical and chemical properties of raw bio-oil, two oxidized bio-oils, and hydrotreated bio-oil were compared before and after catalytic hydrodeoxygenation using sulfided CoMo/γ-Al2O3 catalyst. Following continuous hydrodeoxygenation, the organic liquid products from treated bio-oils and raw bio-oil were compared for higher heating value, oxygen content, water content, and viscosity. In ad...

متن کامل

Bifunctional transalkylation and hydrodeoxygenation of anisole over a Pt/HBeta catalyst

The catalytic conversion of anisole (methoxybenzene), a phenolic model compound representing a thermal conversion product of biomass lignin, to gasoline-range molecules has been investigated over a bifunctional Pt/HBeta catalyst at 400 C and atmospheric pressure. The product distribution obtained on the bifunctional catalyst was compared with those obtained on monofunctional catalysts (HBeta an...

متن کامل

Catalytic Pyrolysis of Wild Reed over a Zeolite-Based Waste Catalyst

Fast catalytic pyrolysis of wild reed was carried out at 500 ̋C. Waste fluidized catalytic cracking (FCC) catalyst disposed from a petroleum refinery process was activated through acetone-washing and calcination and used as catalyst for pyrolysis. In order to evaluate the catalytic activity of waste FCC catalyst, commercial HY zeolite catalyst with a SiO2/Al2O3 ratio of 5.1 was also used. The b...

متن کامل

Zirconium Phosphate Heterostructures as Catalyst Support in Hydrodeoxygenation Reactions

A porous phosphate heterostructure (PPHs) formed by a layered zirconium(IV) phosphate expanded with silica galleries was prepared presenting a P/Zr molar ratio equal to 2 and a (Si + Zr)/P ratio equal to 3. This pillared zirconium phosphate heterostructure was used as a catalyst support for bi-functional catalysts based on noble metals (Pt or Pd) and molybdenum oxide containing a total metallic...

متن کامل

Continuous Catalytic Hydrodeoxygenation of Guaiacol over Pt/SiO2 and Pt/H-MFI-90

Hydrodeoxygenation of guaiacol in the presence of 1-octanol was studied in a fixed-bed reactor under mild conditions (50–250 °C) over platinum particles supported on silica (Pt/SiO2) and a zeolite with framework type MFI at a Si/Al-ratio of 45 (Pt/H-MFI-90). The deoxygenation selectivity strongly depended on the support and the temperature. Both guaiacol and octanol were rapidly deoxygenated in...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره 6  شماره 

صفحات  -

تاریخ انتشار 2016