Mud Contaminant
Mud Contaminant
As soon as drilling commences, the mud is exposed to a range of contaminants, e.g. type
and extent that depend upon the formation being drilled and the fluids within the formations.
This section details the effects of the major contaminants and how these effects can be
minimised.
Solids
In oilfield terminology solids are classified by their density or specific gravity into two
basic categories e.g. High and low gravity solids.
These figures are used to calculate the relative percentage of each solids type in the
mud.
Variations in the relative concentrations give valuable indications of the condition of the
mud and of the efficiency of the solids removal equipment.
Even though they are added deliberately and are essentially non-reactive solids, they still
adversely affect fluid rheology, particularly when they degrade by attrition to ultra fine
particles.
Low gravity solids are often referred to as drilled solids and are derived from the drilled
formation.
Symptoms
Drilled solids are the most common contaminant in drilling mud’s.
Any particle of rock that is not removed by the solids removal equipment is re-circulated
and reduced in size by attrition.
- This process increases the exposed surface area,
- More mud is required to wet the surfaces and increased product is required to
maintain the desired fluid parameters.
- The increase in the number of particles in the mud results in an increase in inter
particle action and hence an increase in rheology, particularly plastic viscosity.
- The irregular shape and size of drilled solids produces poor filter cake quality
which in turn tends to result in an increase in filtrate volume and cake thickness.
Primary separation
Primary separation equipment (i.e. shale shakers) is by far the most important tool in the
control of drilled solids in the mud.
Efficiently operated and correctly screened shale shakers will remove the vast majority of
drilled solids before they have the opportunity to degrade significantly.
Modern linear motion shakers will allow the use of screens as find as 230 mesh,
particularly when drilling with an oil mud.
The implications of barite removal must be considered if the use of screens finer than
this is contemplated.
Hydro-cyclones
Hydro-cyclones (de-sanders and de-silters) should be used with caution.
The action of the centrifugal feed pump can aid in the attrition process and compound
any existing problem.
Hydro-cyclones should not be used when drilling with an oil mud as the large volumes of
liquid discarded will have adverse effects on the environment and on mud costs.
Centrifuges
Correctly set up centrifuges are effective at removing fine solids however, they are not
capable of treating large volumes (typically 1 - 1.5 bbl/min) and as such are really only of
benefit when using an oil mud where dilution rates are low or when drilling small
diameter hole.
In such circumstances some dilution method must be employed. The addition of base
fluid (water or oil) may help in the short term by increasing the liquid phase of the mud,
hence increasing the separation and therefore inter-particle action of the solids.
However this approach does not actually remove any solids from the system and the
solids attrition process and mud property degradation continues. The ultra fine solids
can only be removed from the system by removing a portion of the mud from the
circulating system.
In the case of water based mud’s “whole mud dilution” should be used. This process
involves dumping large volumes of solids laden mud (less than 500 bbls will have little
effect on an average circulating system) and replacing it with newly formulated clean mud.
This process is not viable with oil mud’s or synthetic oil mud’s.
When this type of mud becomes laden with ultra fine solids it must be returned to the
shore based mud plant for treatment. Fortunately, as oil mud’s tend to maintain the
integrity of cuttings, thus allowing effective removal by the shale shakers, this
requirement for this action is rare.
When using a dispersed mud, the addition of chemical thinners (.e.g. lignosulphonate,
Drill-Thin etc.) can be used to treat the symptoms of increasing solids content. However,
the cause is still present and dilution will ultimately be required.
Very high concentrations of either of these ions may have adverse effects on the
performance of polymers in water-based mud’s and on the emulsification packages of
some oil based mud’s.
Source
Both calcium and magnesium can be present in make up water (particularly sea water),
formation water and mixed salt evaporite formations.
Magnesium often accumulates in the mud when drilling in magnesium rich shales (e.g.
North and Central North Sea) or mixed salt formations (e.g. the Zechstein evaporites of the
southern North Sea).
Symptoms
Magnesium
The major effect of magnesium is to react with hydroxyls in the mud system thus
depleting mud alkalinity and pH. This can in turn allow the undesirable carbonate and
bicarbonate components of alkalinity to become dominant.
Calcium
Calcium ions flocculate bentonite based mud’s and other water based mud’s containing
reactive clays giving rise to changes in rheology (decrease in plastic viscosity and
increase in yield point and gels) and loss of filtration control. The presence of increased
calcium levels can be verified from chemical analysis of the filtrate. The combination of
high calcium levels and high pH will precipitate most common polymers used in water
based mud’s - loss of rheology and filtrate control will result.
Magnesium
Small quantities of magnesium such as those present in seawater can be readily
removed with additions of caustic soda.
The large surface area of this precipitate consumes huge quantities of mud chemicals.
This is particularly problematic in oil mud’s where surfactants are effectively stripped
from the mud and can cause the whole system to “flip”. In these cases no attempt
should be made to adjust the alkalinity until clear of the source of magnesium.
Modern surfactant packages do not generally require a big excess of lime so oil mud
performance should not be compromised.
A low pH in a water based mud could promote corrosion of drill pipe so consider the
application of oxygen scavengers and filming amines until the pH can be restored.
High concentrations of calcium can, however, have major adverse effects on water
based mud’s. The major sources of large quantities of calcium are discussed below:
Cement
The chemistry of cement is complex. However, from the mud contamination point of
view, it can be considered to be lime, Ca(OH)2. The major contaminant is calcium but in
some circumstances, the hydroxide ion will compound the problem. At high
temperatures (> 250°F) severely contaminated bentonite based mud’s can solidify.
When it is planned to drill cement, particularly when it is not completely hard, some
precautions can be made to minimise the potential effects of the contamination.
• If viable, drill out as much cement as possible with seawater before displacing to mud.
• Minimise caustic soda additions during operations, including the mixing of new mud, preceding the
drilling of cement.
• Pre-treat with small amounts of sodium bicarbonate - 0.25 lb/bbl is usually sufficient, perhaps twice this
if green cement is anticipated. Avoid over treatment, as an excess of bicarbonate in the mud system
can flocculate mud solids and adversely affect rheology and filtration control.
• Closely monitor pH and Pf while drilling the cement and adjust treatments as required to prevent
polymer precipitation (keep pH below 11.0) and clay flocculation. Sodium bicarbonate will reduce
calcium and pH. Any acid, conventionally citric acid, will reduce pH as will SAPP, Lignosulphonate
and lignite.
• When it is known that large amounts of green or soft cement are to be drilled consideration should be
given to converting the mud to a lime system, which is tolerant of cement contamination. Large
amounts of a suitable dispersant (e.g. Lignox) must be available to successfully accomplish this
conversion.
Oil based and synthetic oil based mud’s are largely unaffected by cement. However, the
water fraction of green cement may reduce oil water ratios.
Whenever possible drill out cement with seawater or water based mud, prior to
displacing to oil based mud.
When only small stringers are anticipated the excess calcium can be treated out with
soda ash (sodium carbonate).
Care should be taken to avoid over treatment, as the adverse effects of carbonate
contamination are equally as bad as those of calcium.
Small additions of a deflocculant such as Lignosulphonate will smooth out the rheology
during treatment.
If massive anhydrite is prognosed and a water-based mud is being used, consideration
should be given to converting the mud to a gypsum system which is tolerant of calcium
contamination.
1. Carbon dioxide from formation gases. E.g. Over treatment when removing calcium
from the mud i.e. excess use of soda ash and sodium bicarbonate.
2. Thermal degradation of organic mud products (e.g. FCL, lignite and starch).
3. Contaminated barite, particularly when drilling HTHP wells with water based mud’s.
It is essential that QA/QC procedures are applied to all batches of barite prior to
shipment to such wells.
4. Contaminated bentonite.
Symptoms
Characterised by general increases in rheology, particularly yield point and gel strengths,
and increases in filtrate.
Typically these effects are worse in high solids mud’s and in high temperature
applications.
• pH, Pf and Mf are determined by pH meter and by titration. The ratio and
relationship between these values will, in theory, allow carbonate species to be
determined.
• P1 and P2 is another titration method which generally gives more reliable results than
the Pf, Mf method.
• The Garrett Gas Train is another method that uses weak acid to convert all
carbonate species to CO2 which is then measured in a Drager Tube. A conversion
factor is then used to determine the carbonate concentration.
Experienced mud engineers place little faith in the results of these tests when
determining the required treatment. There are a number of reasons for this.
In cases where the system does not respond to treatment or where continuous CO2
influxes occur, consideration should be given to converting the mud to a lime system.
The basic treatment for carbonate contamination is to precipitate the carbonate with the
calcium ion derived from either line (Ca OH2) or gypsum (CaSO4). The addition of
calcium will, however, have effect on bicarbonates. These must first be converted to
carbonates by the addition of hydroxyls. Conventionally this would be achieved either
with caustic soda or with lime. Bicarbonate cannot exist in the presence of hydroxyls.
Under normal conditions bicarbonates begin to convert to carbonates at a pH above 9.5.
The basic reactions that take place during the treatment are:
Lime
CO3-2 + HCO3- + 2Ca(OH)2 - CaCO3 + H2) + 3OH-
Source
Various chlorides are found in seawater, brine flows, salt domes, salt stringers and
massive complex evaporite formations.
Symptoms
• When magnesium salts are present, from drilled formation or from brine flows,
addition of lime to the mud should cease.
When a brine flow is encountered, oil-wetting surfactants must be added steadily until
any hint of water wetting is removed.
There is an API test for water wetting but an experienced mud engineer will be aware of
the problem and begin treatment before the test is underway.
* Any trace of water or emulsion in the HTHP filtrate must be eradicated by the addition of an
appropriate combination of primary and secondary emulsifiers.