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Maximization of middle distillates in fluid catalytic cracking

IR@IIP: CSIR-Indian Institute of Petroleum, Dehradun

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Field Value
 
Creator Krishna, Rajamani
 
Date 2010-05-11T10:49:42Z
2010-05-11T10:49:42Z
2010-05-11T10:49:42Z
 
Identifier Research and Industry,Vol. 34, March 1989, pp. 30-35
http://hdl.handle.net/123456789/511
 
Description This paper addresses the problem of maximization of middle distillates in Fluidized Catalytic Cracking (FCC) with special reference to processing of highly-waxyfeedstocks such as Bombay High VacuumGas Oil (BHVGO).In operations of sixnewly-designed commercial riser FCC units in India, employing amorphous silica alumina catalysts, the following was experienced withBH VGO. (i)The Clarified Oil (CLO) make was much higher than design expectations and typicallyin the range 10-13per cent wt.Further, the CLO had amuch higher pour point than expected, coupled withamuch lower density, both signifyingthe predominance of hydrogen rich paraffinic structures. (ii)The pour point of the Total Cycle Oils (TCO) was significantlyhigher than expected in the design. (iii)The regenerator temperatures were about 40°C higher than design expectations. The above operating experiences can be explained on the basis of the poor reactivity, on an amorphous catalyst, of n-paraffins present in the feedstock (BHVGO has a total of 45 per cent wt n-paraffins). The poor reactivity of n-paraffins emanate from their poor adsorbability and lack of tertiary C atoms, which makes the problem of formation of the intermediate car1o>eniumions quite difficult. The uncracked n-paraffins concentrate in the CLO (explaining the high pour point) and those whichescape being stripped in the stripper, enter the regenerator and burn there causing excessivelyhigh tempeatures. Further, the cracking of n-paraffins leads to a lop-sided product distribution: a lot of LPG together with a daughter paraffin of slightlyreduced chain length. The latter first-crack products end up in the TCO causing high pour points. The problem of sluggishlyreactive n-paraffins on an amorphous catalyst surface can be'overcome byenhancing their crackability byincorporation ofthe right amount of zeolite crystals (of the Y-type)of the appropriate size, embedded in an amorphous matrix having sufficient activity to crack compounds other than n-paraffins. The matrix should possess the right amount of macroporosity to effect bottoms conversion, i.e.lower CLO make. The use of zeolite- based catalysts in some locations in India has indeed given some of the expected improvements. This paper could serve as a guide to catalyst selection for middle distillates maximization with waxy feedstocks.
 
Language en_US
 
Subject Catalytic cracking of fluid
 
Title Maximization of middle distillates in fluid catalytic cracking
 
Type Article