Thermal upgrading of vacuum residue mixed with waste plastics was studied in a laboratory scale delayed coking unit.The model of feed thermal decomposition was set up and the first order reaction kinetics was used to ...Thermal upgrading of vacuum residue mixed with waste plastics was studied in a laboratory scale delayed coking unit.The model of feed thermal decomposition was set up and the first order reaction kinetics was used to predict products distribution during the coking process.The distillate yield was higher(70%) for the vacuum residue/polystyrene(VR/PS) feed system and the vacuum residue/low density polyethylene(VR/LDPE) feed system.The resulted distillate yield was separated into fractions according to their boiling points,with gasoline and diesel being our fractions of concern.The activation energy was higher for gasoline production(around 60 kcal/mol) varying with the type of feed system,while it was 33 kcal/mol for diesel fraction.The regression coefficient R was 0.990.展开更多
Delayed coking is an important petroleum resid conversion process.The processability of coking liquids is known to be dependent on the heteroatom compounds present in the coking liquids.Eight commercial delayed coking...Delayed coking is an important petroleum resid conversion process.The processability of coking liquids is known to be dependent on the heteroatom compounds present in the coking liquids.Eight commercial delayed coking liquids were characterized by electrospray ionization(ESI)Fourier transform ion cyclotron resonance mass spectrometry(ESI FT-ICR MS)and gas chromatographic techniques.High relatively abundant heteroatom compounds in the coking liquids were 1-4 aromatic-ring pyridinic nitrogen compounds,carbazoles,benzocarbazoles,phenols,mercaptans,benzothiophenes,dibenzothiophenes,and naphthobenzothiophenes.Coking liquids derived from various feeds had similar compound class types,molecular weight distribution ranges,and double bond equivalents(DBE).However,the concentration of individual compounds and the distribution of DBE versus carbon number of heteroatom compounds varied.A comparison of heteroatom compounds in coker feeds and products revealed the various reaction mechanism of heteroatom compounds occurred during the coking process.The results suggested that molecular-level process models can be developed for optimization of unit operation to obtain desirable products that meet the environmental specifications and quality requirements.展开更多
文摘Thermal upgrading of vacuum residue mixed with waste plastics was studied in a laboratory scale delayed coking unit.The model of feed thermal decomposition was set up and the first order reaction kinetics was used to predict products distribution during the coking process.The distillate yield was higher(70%) for the vacuum residue/polystyrene(VR/PS) feed system and the vacuum residue/low density polyethylene(VR/LDPE) feed system.The resulted distillate yield was separated into fractions according to their boiling points,with gasoline and diesel being our fractions of concern.The activation energy was higher for gasoline production(around 60 kcal/mol) varying with the type of feed system,while it was 33 kcal/mol for diesel fraction.The regression coefficient R was 0.990.
基金supported by the National Natural Science Foundation of China(U1162204,21236009,21376262)
文摘Delayed coking is an important petroleum resid conversion process.The processability of coking liquids is known to be dependent on the heteroatom compounds present in the coking liquids.Eight commercial delayed coking liquids were characterized by electrospray ionization(ESI)Fourier transform ion cyclotron resonance mass spectrometry(ESI FT-ICR MS)and gas chromatographic techniques.High relatively abundant heteroatom compounds in the coking liquids were 1-4 aromatic-ring pyridinic nitrogen compounds,carbazoles,benzocarbazoles,phenols,mercaptans,benzothiophenes,dibenzothiophenes,and naphthobenzothiophenes.Coking liquids derived from various feeds had similar compound class types,molecular weight distribution ranges,and double bond equivalents(DBE).However,the concentration of individual compounds and the distribution of DBE versus carbon number of heteroatom compounds varied.A comparison of heteroatom compounds in coker feeds and products revealed the various reaction mechanism of heteroatom compounds occurred during the coking process.The results suggested that molecular-level process models can be developed for optimization of unit operation to obtain desirable products that meet the environmental specifications and quality requirements.
