Thermal characterization of crude oils in the presence of limestone matrix by TGA-DTG-FTIR

KÖK M. V., Varfolomeev M. A., Nurgaliev D. K.

JOURNAL OF PETROLEUM SCIENCE AND ENGINEERING, cilt.154, ss.495-501, 2017 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 154
  • Basım Tarihi: 2017
  • Doi Numarası: 10.1016/j.petrol.2017.02.001
  • Dergi Adı: JOURNAL OF PETROLEUM SCIENCE AND ENGINEERING
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.495-501
  • Anahtar Kelimeler: Crude oil, Combustion, Kinetics, Limestone, Thermogravimetry, Fourier-transform infrared spectroscopy, CATALYTIC EFFECT ANALYSIS, THERMOGRAVIMETRIC ANALYSIS, COMBUSTION KINETICS, OXIDATION-KINETICS, CLAY-MINERALS, RECOVERY, MODEL
  • Orta Doğu Teknik Üniversitesi Adresli: Evet

Özet

In present work oxidation of two heavy oils in limestone matrix was studied using simultaneous thermo-gravimetry (TGA), derivative thermogravimetry (DTG) and FTIR-spectroscopy techniques in the temperature range from 25 to 900 degrees C. Before the measurements, the composition and properties of crude oils and limestone were evaluated. Obtained TG and DTG curves shows four different reaction regions: low temperature oxidation (LTO), fuel deposition (FD), high temperature oxidation (HTO) and decomposition of limestone. LTO reactions were accompanied by evaporation of light hydrocarbons, which was confirmed by appearance of stretching vibration bands of C-H groups in FTIR-spectra of evolved gases. Formation of carbon dioxide was observed for all oxidation reaction regions according to spectroscopic data. At the same time, CO was formed only in HTO region for both studied crude oils. Despite the different composition two crude oils have practically the same reactions intervals and peak temperatures. However, crude oil with higher API-gravity has a greater mass loss at the LTO and evaporation regions. The conversion of heavier oil with higher content of asphaltenes is larger during the high-temperature oxidation step.