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SPE 163023 Effect of Cement Contamination On Some Properties of Drilling Mud
SPE 163023 Effect of Cement Contamination On Some Properties of Drilling Mud
SPE 163023 Effect of Cement Contamination On Some Properties of Drilling Mud
This paper was prepared for presentation at the 2012 SPE Nigerian Annual International Conference and Exhibition held in Abuja, Nigeria, 6-8 August 2012.
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will allow current treatment of the mud ion is liberated which reacts with a free
consistent with future requirements. hydroxyl ion to form a water molecule. This
Contaminants are encountered on every phase reaction serves to further reduce the pH and
allow more lime to go into solution.
of the drilling operation. They also exist in
Treatments should be discontinued when excess
drilled formations, water supply and in materials lime approaches 0.3 to 0.5 lb/bbl. Materials such
used in formulating and maintaining the drilling as lignosulphonates and lignite are good
fluid properties. They can rapidly alter the supplementary for pretreating agents because
physical and chemical characteristic of the they buffer the pH and aid in deflocculating the
drilling mud. The severity of the problems system.
experienced depends on the type of drilling mud Consideration should also be given to low-
gravity solids content prior to drilling cement,
used(Medermonth,1973,BaroidTraining
because high clay solids concentration is a
Manual, 1997). primary cause of flocculation when cement
Though the primary indication of contamination contamination occurs. Reduction of solids
is the general instability of the drilling fluid concentration, if too high, is recommended as a
properties which manifest itself in a difficulty in defense against severe flocculation. Because pH
contolling the fluid loss, alkalinity or rheology values are high when drilling cement, the
of the mud often in circulation, certain quantity of calcium ion in solution rarely
exceeds 300 to 400 mg/l. For this reason, much
contamination may be tolerated for an extended
of the cement drilled remains as discrete
periods. The severity of the problems particles and is available to dissolve and replace
experienced depends on type of contaminants, the calcium ion that has been treated out of
the degree of the contamination and type of solution. Unless cement particles (excess lime)
drilling mud in use (Luminon, 1980) are mechanically removed from the system by
efficient solids removal equipment, it will take
several days for the excess lime to solubilize,
react and be chemical precipitated. High
CONTAMINANTS AND ASSOCIATED temperature solidification can result from
PROBLEMS cement contamination in combination with high
Cement contamination has pose serious solids. Since tests at ambient temperature will
challenges in the drilling operation and as a not reflect this problem, tests which stimulate
result of that attracts an additional operational downhole conditions should be run.
cost.
When cement contamination reaches where it is MATERIALS AND RESEARCH
no longer practical to treat it out, we dump the METHODOLOGY
most contaminated mud, displace the entire
321grams of water was measured and poured
system out or treat system as a calcium base
mud. To maintain a low calcium drilling fluid, into the Hamilton mixing cup. 9.3grams of
chemical treatment must be used to remove bentonite was added and prehydrated for 30
cement contamination. minutes under stirring condition. After 30
The aim of treatment is to control pH while minutes, 0.5grams of Rac-L, 0.5grams of Pac- R
removing calcium and excess lime from the respectively were added into the mixing cup.
system as an inert, insoluble calcium precipitate.
These with prehydrated bentonite was stirred for
The treatment of choice for cement or lime
contamination is sodium bicarbonate 15 minutes before. 0.2grams of soda ash was
(NaHCO3). In its reaction with lime, a hydrogen added and stirred for another 10 minutes. 3
SPE 163023 3
40 cp 46 cp 75 cp 150 cp
28 cp 32 cp 58 cp 115 cp
9 cp 11 cp 36 cp 47 cp
6 cp 10 cp 34 cp 35 cp
Mud when contaminated, should be properly Grula, N and Sewell, G (1981): “Polyacrylamide