The influence of alkane class-types on crude oil wax crystallization and inhibitors efficiency

Citation
Md. Garcia et al., The influence of alkane class-types on crude oil wax crystallization and inhibitors efficiency, J PET SCI E, 25(3-4), 2000, pp. 99-105
Citations number
19
Categorie Soggetti
Geological Petroleum & Minig Engineering
Journal title
JOURNAL OF PETROLEUM SCIENCE AND ENGINEERING
ISSN journal
09204105 → ACNP
Volume
25
Issue
3-4
Year of publication
2000
Pages
99 - 105
Database
ISI
SICI code
0920-4105(200003)25:3-4<99:TIOACO>2.0.ZU;2-J
Abstract
The effect of paraffin class-types on the wax crystallization tendency in o ils and the activity of paraffin inhibitors was studied for waxy crude oils . Oils enrichment with isolated paraffin fractions allowed the assessment o f the influence of their molecular weight on the cloud point and the behavi or of crystal modifiers. An insensitive crude oil without response to wax i nhibitors was separated into its (normal/cyclo + branched) paraffin fractio ns. Reduced pressure distillation, n-heptane asphaltenes precipitation from the residue, high performance liquid chromatography (HPLC) of maltenes, an d molecular sieves inclusion of the saturates were the separation technique s used for the isolation of the (cyclo + branched) paraffin fraction. (Cycl o + branched) paraffins, also known as (naphthwne + iso) alkane isomers, we re added to the selected crude, in order to investigate their effect on the cloud point. These fractions have no significant impact in the inhibitors effect for concentrations lower than 40 wt%, but they increase the crude oi l cloud point when their amount was greater than 50 wt%. This increment in the cloud point was believed to arise as a consequence of the higher averag e molecular weight introduced by these components. The effect of cyclic and branched alkanes on the activity of a commercial crystal modifier was stud ied and observed to be a complex one. At low-medium concentrations, the eff ect was antagonistic and believed to be controlled by the average molecular mass of the added fractions. High concentrations of cycle + branched alkan es (> 50 wt%) enhanced the activity of the crystal modifier. This result wa s believed to be caused by an structural effect, i.e., loose packing of cry stals fi om the steric effect of naphthenic and branched structures. (C) 20 00 Elsevier Science B.V. All rights reserved.