METHOD 9000

DETERMINATION OF WATER IN WASTE MATERIALS

BY KARL FISCHER TITRATION

SW-846 is not intended to be an analytical training manual. Therefore, method

procedures are written based on the assumption that they will be performed by analysts who are
formally trained in at least the basic principles of chemical analysis and in the use of the subject
technology.
In addition, SW-846 methods, with the exception of required method use for the analysis
of method-defined parameters, are intended to be guidance methods which contain general
information on how to perform an analytical procedure or technique which a laboratory can use
as a basic starting point for generating its own detailed Standard Operating Procedure (SOP),
either for its own general use or for a specific project application. The performance data
included in this method are for guidance purposes only, and are not intended to be and must
not be used as absolute QC acceptance criteria for purposes of laboratory accreditation.

1.0

SCOPE AND APPLICATION

1.1
This method uses the Karl Fischer titration technique to quantify the water content
of materials from 1 ppm to nearly 100%. Coulometric titration is used for direct analysis of
samples with water contents between 1 ppm and 5%, while volumetric titration is more suitable
for direct analysis of higher levels (100 ppm to 100%). With proper sample dilution, the range of
the coulometric technique can also be extended to 100% water. This method presents both
coulometric and volumetric procedures.
1.2
Multiphasic samples should be separated into physical phases (liquid, solid, etc.)
prior to analysis to assure the analysis of representative aliquots.
1.3

Establishing the water content in a sample may be useful for the reasons to follow.

1.3.1
It is useful in determining the total composition of a sample. In
combination with other analytical results, the mass balance of a sample can be
determined.
1.3.2
It is useful in identifying which samples can be analyzed by Infrared
Spectroscopy using sodium chloride cells or which require zinc selenide cells.
1.3.3
It is useful in determining the maximum amount of alcohols or other
organic liquids which could be present in an aqueous solution.
1.3.4

It is useful when distinguishing an aqueous from a nonaqueous solution.

1.3.5
It is useful when setting the proper mixture of feed materials in the
incineration of waste.
1.4
Analysts should consult the disclaimer statement at the front of the manual and the
information in Chapter Two for guidance on the intended flexibility in the choice of methods,
apparatus, materials, reagents, and supplies, and on the responsibilities of the analyst for
demonstrating that the techniques employed are appropriate for the analytes of interest, in the
matrix of interest, and at the levels of concern.
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In addition, analysts and data users are advised that, except where explicitly specified in a
regulation, the use of SW-846 methods is not mandatory in response to Federal testing
requirements. The information contained in this method is provided by EPA as guidance to be
used by the analyst and the regulated community in making judgments necessary to generate
results that meet the data quality objectives for the intended application.
1.5
Use of this method is restricted to use by, or under supervision of, properly
experienced and trained personnel. Each analyst must demonstrate the ability to generate
acceptable results with this method.

2.0

SUMMARY OF METHOD

2.1
In the volumetric procedure, the sample (or an extract of it) is added to a Karl
Fischer solvent consisting of sulfur dioxide and an amine dissolved in anhydrous methanol.
This solution is titrated with an anhydrous solvent containing iodine. The iodine titrant is first
standardized by titrating a known amount of water.
2.2
In the coulometric procedure, the sample (or an extract of it) is injected into an
electrolytic cell containing the Karl Fischer solvent, where the iodine required for reaction with
water is produced by anodic oxidation of iodide. This technique does not require the
standardization of reagents.
2.3
In both procedures, the endpoint is determined amperometrically with a platinum
electrode that senses a sharp change in cell resistance when the iodine has reacted with all of
the water in the sample.
2.4
In the coulometric procedure, the coulombs of electricity required to generate the
necessary amount of iodine are converted to micrograms of water by the instrument
microprocessor; while in the volumetric procedure, the volume of iodine titrant required to reach
the endpoint is converted to micrograms of water. Most instruments will also calculate
concentration (ppm or percent) if the sample weight is keyed in.

3.0

DEFINITIONS

Refer to Chapter One, Chapter Three, and the manufacturer's instructions for definitions
that may be relevant to this procedure.

4.0

INTERFERENCES

4.1
Solvents, reagents, glassware, and other sample processing hardware may yield
artifacts and/or interferences to sample analysis. All these materials must be demonstrated to be
free from interferences under the conditions of the analysis (see Sec. 9.0 for specific guidance
on quality control procedures). Specific selection of reagents and purification of solvents by
distillation in all-glass systems may be necessary. Refer to Chapter Three for general guidance
on the cleaning of glassware.
4.2
Interfering side-reactions can occur between the various species in the Karl Fischer
reagent and the sample components, resulting in an overestimation of the water content in the
sample.

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4.2.1
Hydroxide ions will titrate as water when injected directly into the titration
cell. This is a significant problem with samples having a hydroxide content of > 1N. When
this is suspected to be a problem, a water vaporization module (furnace) should be used.
The sample is heated in this module and the water vapor is carried to the titration cell, while
the hydroxide remains in the module.
4.2.2
Ketones and aldehydes can interfere with some Karl Fischer reagents by
reacting with alcoholic solvents like methanol to form ketals and acetals which can
decompose to form water. This problem can be avoided by substitution of a non-reactive
alcohol or by increasing the pH.
4.2.3
The reduction of iodine by oxidizable species such as thiols, ammonia and
thiosulfate results in the consumption of iodine and an overestimation of the water content.
4.3
Undesired interfering side-reactions can also result in the underestimation of the
water content in the sample. These include:
4.3.1
Sulfur dioxide, base, carbonyl functional groups on aldehydes and ketones
and other substances that form bisulfite complexes.
4.3.2
Oxidation of iodide and bisulfite complexes by reducible species such as
Cu2+, Fe3+, NO2-, etc.
4.4
Suspended/undissolved solid material in a liquid sample may interfere with the
electrode by blocking its contact with the solvent. Artificially high or low results can occur
depending on the nature of the solid material.

5.0

SAFETY

5.1
This method does not address all safety issues associated with its use. The
laboratory is responsible for maintaining a current awareness file of OSHA regulations regarding
the safe handling of the chemicals listed in this method. A reference file of material data
handling sheets (MSDSs) should be available to all personnel involved in the chemical analysis.
5.2
The toxicity or carcinogenicity of each reagent used in this method has not been
precisely defined; however, each chemical compound should be treated as a potential health
hazard. From this viewpoint, exposure to these chemicals must be reduced to the lowest
possible level by whatever means available.
5.3
Care should be taken in avoiding the inhalation of the reagent vapors or skin
contact with the reagents. If any of the reagents comes in contact with the skin, wash thoroughly
with copious amounts of water. To avoid inhalation of vapors, fill and empty the cell or electrode
assembly in a working laboratory hood. Once the cell is assembled, solvent vapors are
contained so long as the system remains sealed.
5.4

6.0

Protective laboratory clothing, eyewear and gloves should be worn at all times.

EQUIPMENT AND SUPPLIES

The mention of trade names or commercial products in this manual is for illustrative
purposes only, and does not constitute an EPA endorsement or exclusive recommendation for
use. The products and instrument settings cited in SW-846 methods represent those products
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and settings used during method development or subsequently evaluated by the Agency.
Glassware, reagents, supplies, equipment, and settings other than those listed in this manual
may be employed provided that method performance appropriate for the intended application
has been demonstrated and documented.
This section does not list common laboratory glassware (e.g., beakers and flasks).
6.1
Coulometric water titrator -- An automatic Karl Fischer titration system with
amperometric, potentiometric or potential difference end point detection. It consists of an
electrolytic titration cell, dual platinum electrode, magnetic stirrer and control unit.
6.2
Volumetric water titrator -- An automatic Karl Fischer titration system consisting of a
titration cell, dual platinum electrode, magnetic stirrer, dispensing buret and control unit.
6.3

Syringes -- 5-L, 10-L and 100-L.

6.4

Analytical balance -- Capable of weighing to 0.0001 grams.

6.5

Screw cap vials, 20-mL.

6.6
Furnace module for determining water in the presence of high levels of hydroxide or
in samples not otherwise amenable to direct titration or extraction. This is interfaced with the
titration cell. An appropriate sample introduction apparatus will also be required.

7.0

REAGENTS AND STANDARDS

7.1
Reagent-grade chemicals must be used in all tests. Unless otherwise indicated, it is
intended that all reagents conform to the specifications of the Committee on Analytical Reagents
of the American Chemical Society, where such specifications are available. Other grades may
be used, provided it is first ascertained that the reagent is of sufficiently high purity to permit its
use without lessening the accuracy of the determination. Reagents should be stored in glass to
prevent the leaching of contaminants from plastic containers.
7.2

Coulometric cell solutions

7.2.1
Anode reagent -- Main ingredients consisting of methanol, organic base,
sulfur dioxide and a suitable iodine compound.
7.2.2
Cathode reagent -- Main ingredients consisting of methanol, organic base,
sulfur dioxide and possibly carbon tetrachloride.
NOTE:

7.3

Non-methanol formulations are commercially available for the analysis of

aldehydes and ketones and for general use. As indicated in Sec. 4.2.2, ketones
and aldehydes interfere with the Karl Fischer titration as they undergo waterforming reactions with methanol. Use of these non-methanol Karl Fischer
solvents is recommended for samples containing aldehydes and ketones.
Volumetric reagents

7.3.1
Volumetric titrant -- A mixture of an organic amine, sulfur dioxide and
iodine dissolved in a non-hygroscopic solvent. Reagents with titers of 1, 2 and 5 mg
H2O/mL can be commercially obtained.

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7.3.2
Karl Fischer solvent -- Typically consisting of an organic amine and sulfur
dioxide dissolved in anhydrous methanol.
NOTE:

8.0

Non-methanol formulations are commercially available for the analysis of

aldehydes and ketones and for general use. As indicated in Sec. 4.2.2, ketones
and aldehydes interfere with the Karl Fischer titration because these compounds
undergo water-forming reactions with methanol. The use of non-methanol Karl
Fischer solvents is recommended for samples containing aldehydes and ketones.

7.4

The reagents described in Secs. 7.2 and 7.3 are commercially available.

7.5

Methanol or other appropriate solvent for extracting samples, anhydrous, > 99.8%.

7.6

Reagent water.

SAMPLE COLLECTION, PRESERVATION AND STORAGE

8.1
Samples should be collected and stored in containers which will protect them from
changes in volume or water content. Storage in glass with polytetrafluoroethylene (PTFE)-lined
caps is necessary if analytes requiring such storage are to be determined.
8.2
Samples should be well-sealed and refrigerated at #6 EC and then brought to room
temperature prior to analysis if analytes requiring such storage are to be determined.

9.0

QUALITY CONTROL

9.1
Refer to Chapter One for additional guidance on quality assurance (QA) and quality
control (QC) protocols. When inconsistencies exist between QC guidelines, method-specific QC
criteria take precedence over both technique-specific criteria and those criteria given in Chapter
One, and technique-specific QC criteria take precedence over the criteria in Chapter One. Any
effort involving the collection of analytical data should include development of a structured and
systematic planning document, such as a Quality Assurance Project Plan (QAPP) or a Sampling
and Analysis Plan (SAP), which translates project objectives and specifications into directions for
those that will implement the project and assess the results. Each laboratory should maintain a
formal quality assurance program. The laboratory should also maintain records to document the
quality of the data generated. All data sheets and quality control data should be maintained for
reference or inspection.
9.2
For each batch of twenty samples processed, at least one duplicate sample must be
carried throughout the entire sample preparation and analytical process. The relative standard
deviation of the duplicate analyses should be set at a laboratory-derived limit developed through
the use of historical analyses for the same matrix. In the absence of historical data, the relative
standard deviation of the duplicate analyses should be <10%. After the determination of
historical data, 10% should still be the limit of maximum deviation to express acceptability.
9.3
For each batch of twenty samples processed, at least one spiked sample must be
carried throughout the entire sample preparation and analytical process. Acceptance criteria
should be set at a laboratory-derived limit developed through the use of historical analyses for
the same matrix. In the absence of historical data, the spike recovery should be 90 to 110%. A
spike of 50% water is recommended. Spikes to some matrices (e.g., paints) may not be
meaningful due to their high water levels and problems with spiking emulsions. In these cases, a
spike of their extract may be the best option.
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9.4

Certified reference materials should be analyzed where available.

9.5
To assess the accuracy of coulometric titrators, three 5-mg injections of reagent
water are to be performed daily with average recoveries of 90 to 110% and relative standard
deviations of < 5% to be achieved. If the recoveries fall outside of this range, the instrument
problem must be corrected before continuing with sample analysis.
9.6
Background levels of water in reagents are minimized by using anhydrous reagents
and by pre-titration of reagents prior to sample analysis.
9.7
To prevent the carryover of moisture into the syringe, the syringe should be rinsed
once with methanol between samples and twice with the sample prior to loading the volume to
be analyzed. Alternatively, use several syringes that have been oven dried, rotating the
drying/use cycle so that the syringe in use reaches room temperature prior to use.
9.8
Only small aliquots of samples should be handled near the titrator to prevent
contamination of the bulk sample by Karl Fischer reagent solvents.
9.9
When methanol or other solvent extractions are performed, three solvent blanks
should be analyzed with these extracts and the extract results corrected for the mean of these
blanks.

10.0 CALIBRATION AND STANDARDIZATION

10.1 Coulometric procedure -- Since coulometric titrators generate iodine on demand by
the titration cell, standardization of titrant is not required.
10.2 Volumetric procedure -- The titer of the titrant must be checked on a daily basis.
Using a 5-uL syringe, inject 3.0 uL of water into the titration cell containing solvent that has been
pre-titrated to remove residual moisture. Calculate the titer as follows:
3.0 mg H2O/mL of titrant consumed = mg/mL H2O equivalent of titrant.
11.0 PROCEDURES
11.1 Sample introduction -- The approach which should be used will depend on the
viscosity and solubility of the sample and is left to the discretion of the analyst.
11.2 Direct injection -- Weigh a sample (5 L for coulometric, 100 L for volumetric) by
difference in a cleaned and dried syringe which has the needle inserted in a small piece of
silicone rubber to reduce sample evaporation. Inject the sample into the titration cell septum and
reweigh the syringe to determine the actual weight injected. Titrate the sample to the endpoint
and record the results.
11.3 Extraction -- Extract a 500-mg sample with an appropriate solvent to a final volume
of 10 mL. The solvent and sample should be shaken in a 20 mL vial for 2 to 3 min. Allow the
mixture to settle. Centrifugation may be required. Titrate a 100-L aliquot of the supernatant.
The volume of the aliquot to be titrated can be varied to achieve results within the linear range of
the titrator. Methanol is most commonly used, but is not appropriate for all materials. Toluene,
DMF, pyridine and diglyme are suitable for paints.
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11.4 Water vaporization -- Weigh a 10- to 100-mg sample into a sampling tube and
introduce it into the furnace or inject it into hot mineral oil and the water vapor will be carried by a
gas stream into the titration cell. This approach is most commonly used with samples which
cannot be directly titrated or extracted or for samples containing high levels of hydroxide ion as
described in Sec. 4.2.1. Consult the instrument instruction manual for proper use.

12.0 DATA ANALYSIS AND CALCULATIONS

12.1 Calculate the water content in ppm or percent in the sample based on the
instrument, if sample weight was keyed in, or divide the instrument readout in g of H2O found by
the g of sample injected with appropriate corrections for any dilutions or extractions.
12.2 Data analysis worksheets should be prepared for all samples analyzed. Include
information regarding the sample identification, sample weight, measured water content, water
content in the original sample and the results of quality control tests.
12.3 Results must be reported in units commensurate with their intended use and all
dilutions need to be taken into account when computing final results.

13.0 METHOD PERFORMANCE

13.1 Performance data and related information are provided in SW-846 methods only as
examples and guidance. The data do not represent required performance criteria for users of
the methods. Instead, performance criteria should be developed on a project-specific basis, and
the laboratory should establish in-house QC performance criteria for the application of this
method. These performance data are not intended to be and must not be used as absolute QC
acceptance criteria for purposes of laboratory accreditation.
13.2

Coulometric procedure

Crude oil analysis -- Based on ASTM D 4928-89, crude oils containing 0.02 to 5% water
were tested in an interlaboratory study. "Within" laboratory precision was 5 to 10% and the
"between" laboratory relative standard deviation was 7 to 20% for between 0.1 and 5% water.
These data are provided for guidance purposes only.
13.3

Volumetric procedure

13.3.1 Used oil analysis -- A series of used oil standards were prepared by
spiking dried used oil with water over a range of 0 to 20%. Additional standards were made
by spiking a hydrocarbon-based cutting fluid at 25% and 50%. The results in w/w percent
using this method are shown in Table 1. Over the range of 1 to 50% water, a linear
regression of the results by this method vs. the spiked water content followed the following
relationship: y = 1.0137x + 0.0917 with R2 = 0.9997. These data are provided for guidance
purposes only.
Certified reference materials covering the range of 2 to 90% water were analyzed
using the direct injection procedure and volumetric titration. The results using this method
are shown in Table 2 and agreed with those obtained using Method 9001 and the certified
value. The relative standard deviations ranged from 1 to 10% for 6 to 10 determinations.
These data are provided for guidance purposes only.

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13.3.2 Paint analysis -- A certified reference material, ERM-19, "Water and

Volatiles in Latex Paint," was analyzed 10 times by the extraction procedure and volumetric
titration. A 500-mg sample was extracted with diglyme, centrifuged and 125 L of the
supernatant was titrated. The results in w/w% using this method were 42.34 1.25 and
agreed with results determined by Method 9001.
Based on ASTM D 4017-90, paints containing 25 to 75% water were tested in an
interlaboratory study. "Within" laboratory precision was 1.7% and the "between" laboratory
relative standard deviation was 5.3%. These data are provided for guidance purposes
only.
13.3.3 Other wastes -- Based on ASTM D 5530, hazardous waste fuels
containing 13 to 32% water yielded "within" laboratory precision of 1.3% and a "between"
laboratory relative standard deviation of 4.3%. These data are provided for guidance
purposes only.
13.3.4 Soil analysis -- A marine sediment was dried and spiked with water over
the range of 0 to 40% (w/w). The results using this method are shown in Table 3 and
followed the following relationship: y = 0.9972x + 0.1103 with R2 = 0.9991. These data are
provided for guidance purposes only.
13.3.5 Alcohol analysis -- Mixtures of ethanol and water covering the range of 0
to 100% water and three distilled spirits were analyzed by this method and Method 9001.
The results are given in Table 4. These data are provided for guidance purposes only.
Because total dissolved solids like sugars and other carbohydrates often present in beers,
wines and distilled spirits will be counted as "alcohol" when water content is used to
estimate alcohol content, their contribution must be considered and, if necessary,
determined and subtracted from the non-water content to determine the alcohol content.

14.0 POLLUTION PREVENTION

14.1 Pollution prevention encompasses any technique that reduces or eliminates the
quantity and/or toxicity of waste at the point of generation. Numerous opportunities for pollution
prevention exist in laboratory operations. The EPA has established a preferred hierarchy of
environmental management techniques that places pollution prevention as the management
option of first choice. Whenever feasible, laboratory personnel should use pollution prevention
techniques to address their waste generation. When wastes cannot be feasibly reduced at the
source, the Agency recommends recycling as the next best option.
14.2 For information about pollution prevention that may be applicable to laboratories
and research institutions consult Less is Better: Laboratory Chemical Management for Waste
Reduction available from the American Chemical Society's Department of Government Relations
and Science Policy, 1155 16th St., N.W. Washington, D.C. 20036, http://www.acs.org.

15.0 WASTE MANAGEMENT

15.1

Spent reagents and samples should be stored and disposed appropriately.

15.2 The Environmental Protection Agency requires that laboratory waste management
practices be conducted consistent with all applicable rules and regulations. The Agency urges
laboratories to protect the air, water, and land by minimizing and controlling all releases from
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hoods and bench operations, complying with the letter and spirit of any sewer discharge permits
and regulations, and by complying with all solid and hazardous waste regulations, particularly the
hazardous waste identification rules and land disposal restrictions. For further information on
waste management, consult The Waste Management Manual for Laboratory Personnel available
from the American Chemical Society at the address listed in Sec. 14.2.

16.0 REFERENCES
1.

ASTM D 3401-92, "Standard Test Method for Water in Halogenated Organic Solvents and
their Admixtures."

2.

ASTM D 4017-90, "Standard Test Method for Water in Paints and Paint Materials by Karl
Fischer Method."

3.

ASTM D 5530-94, "Standard Test Method for Total Moisture of Hazardous Waste Fuel by
Karl Fischer Titrimetry."

4.

ASTM D 4928-89, "Standard Test Methods for Water in Crude Oils by Coulometric Karl
Fischer Titration."

5.

ASTM D 4377-93a, "Standard Test Method for Water in Crude Oils by Potentiometric Karl
Fischer Titration."

6.

Theodore B. Lynn; "Validation Data for Draft Methods 9000 and 9001 for the Determination
of Water Content in Liquid and Solid Matrices," Dexsil Corp., Hamden, CT (not dated).

7.

Steven K. MacLeod, "Moisture Determination Using Karl Fischer Titrations," Analytical

Chemistry, Volume 63, pages 557-566, May 15, 1991.

8.

U.S. EPA NEIC Method, "Water Content of Waste Material Samples by Coulometric Karl
Fischer Titration," pages 1-12, August 1991.

17.0 TABLES, DIAGRAMS, FLOW CHARTS AND VALIDATION DATA

The following pages contain the tables referenced by this method. The tables are followed
by a flow diagram of the procedure.

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TABLE 1
EXAMPLE DETERMINATION OF WATER IN USED OIL
(w/w %)

Expected

Method 9001

Method 9000

0.161

0.061

0.1

0.149

0.145

0.2

0.226

0.255

0.5

0.459

0.561

1.0

0.948

1.07

2.0

2.36

2.46

5.0

5.03

5.05

10.0

9.82

9.97

20.0

20.2

20.0

25.0

26.37

26.05

50.0

50.05

50.60

Data taken from Reference 6.

TABLE 2
EXAMPLE ANALYSIS OF USED OIL CERTIFIED REFERENCE MATERIALSa

CRM

Certified Value, wt %

Method 9001, wt %

Method 9000, wt %

ERM-34

1.95

1.920.02

1.860.09

ERM-35

5.86

5.910.61

6.130.55

ERM-36

10.3

10.300.85

10.30.81

ERM-41

87.4

88.46.7

86.46.6

ERM-34 to 41 Water Content in Used Oil Mixtures from Environmental Reference Materials, Inc.

Data taken from Reference 6.

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TABLE 3
EXAMPLE DETERMINATION OF WATER IN MARINE SEDIMENT
(w/w%)
Expected

Method 9001

Method 9000

1.14

0.579

10

10.06

9.74

20

18.99

19.67

30

28.52

29.95

40

38.47

40.34

Data taken from Reference 6.

TABLE 4
EXAMPLE DETERMINATION OF ALCOHOL IN WATER/ALCOHOL MIXTURES
Expected % Alcohol, v/v

Method 9001 (% v/v)

Method 9000 (% v/v)

10

10.0

10.3

25

25.6

25.0

40

40.9

38.7

50

48.5

49.1

80

80.6

79.8

100

99.9

100.0

Vodka, 40

41.9

42.0

Whiskey, 40

40.0

41.9

Gin, 47

47.2

48.7

Data taken from Reference 6.

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METHOD 9000
DETERMINATION OF WATER IN WASTE MATERIALS
BY KARL FISCHER TITRATION

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