ADSORPTION OF ORGANIC-COMPOUNDS ON CARBONATE MINERALS .1. MODEL COMPOUNDS AND THEIR INFLUENCE ON MINERAL WETTABILITY

Citation
Mm. Thomas et al., ADSORPTION OF ORGANIC-COMPOUNDS ON CARBONATE MINERALS .1. MODEL COMPOUNDS AND THEIR INFLUENCE ON MINERAL WETTABILITY, Chemical geology, 109(1-4), 1993, pp. 201-213
Citations number
36
Categorie Soggetti
Geology
Journal title
ISSN journal
00092541
Volume
109
Issue
1-4
Year of publication
1993
Pages
201 - 213
Database
ISI
SICI code
0009-2541(1993)109:1-4<201:AOOOCM>2.0.ZU;2-H
Abstract
This is the first of a series of papers to investigate the role of org anic compounds on wettability, porosity and permeability of carbonate rocks. These are important characteristics that influence the performa nce of petroleum reservoirs. This first paper investigates the adsorpt ion of model organic compounds to determine what type of compounds ads orb, the nature and strength of the adsorption, and the influence of a dsorption on rock wettability. A wide variety of model organic compoun ds were tested for adsorption on calcite, dolomite and magnesite. They were adsorbed from both organic and aqueous solvents. The adsorption was monitored by thermogravimetric analysis and by contact angle wetta bility tests. The compounds included carboxylic acids, alcohols, sulfa tes, sulfonates, amines, amino acids and carboxylated polymers. Carbox ylic acids adsorb most strongly, and their adsorption is stabilized by long, straight chains and by polymeric structures. Fatty acids form a surface monolayer, and carboxylated polymers also appear to coat the surface completely. These adsorbates could be desorbed only by a solve nt that provided both good solubility for the adsorbate and an ionic s pecies to replace it at the solid surface. They were interpreted to be chemisorbed as ionic species. Several other compounds exhibited physi sorption and could be easily removed by most solvents. Wettability tes ts were performed at 20-degrees, 50-degrees and 80-degrees-C to obtain information regarding the stability of the adsorption at elevated tem peratures.