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This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles

for the
Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

Designation: D4952 − 23

Standard Test Method for


Qualitative Analysis for Active Sulfur Species in Fuels and
Solvents (Doctor Test)1
This standard is issued under the fixed designation D4952; the number immediately following the designation indicates the year of
original adoption or, in the case of revision, the year of last revision. A number in parentheses indicates the year of last reapproval. A
superscript epsilon (´) indicates an editorial change since the last revision or reapproval.
This standard has been approved for use by agencies of the U.S. Department of Defense.

1. Scope* 2.2 Energy Institute Standards:3


1.1 This test method covers and is intended primarily for the IP 30 Detection of Mercaptans, Hydrogen Sulfide, Elemental
detection of mercaptans in motor fuel, kerosine, and similar Sulfur, and Peroxides – Doctor Test Method
petroleum products. This method may also provide information 3. Terminology
on hydrogen sulfide and elemental sulfur that may be present in
these sample types. 3.1 Definitions:
3.1.1 For definitions of terms used in this test method, refer
1.2 The values stated in SI units are to be regarded as to Terminology D4175.
standard. No other units of measurement are included in this 3.2 Definitions of Terms Specific to This Standard:
standard. 3.2.1 flowers of sulfur, n—a purified form of sulfur that is
1.3 This standard does not purport to address all of the prepared by sublimation, as opposed to precipitation.
safety concerns, if any, associated with its use. It is the 3.2.2 sour, adj—describing material having a detectable
responsibility of the user of this standard to establish appro- quantity of hydrogen sulfide or mercaptan.
priate safety, health, and environmental practices and deter-
mine the applicability of regulatory limitations prior to use. 3.2.3 sweet, adj—describing material having a nondetect-
For specific warning statements, see 7.3. able quantity of hydrogen sulfide or mercaptan.
1.4 This international standard was developed in accor- 3.3 Acronyms:
dance with internationally recognized principles on standard- 3.3.1 UV, adj—ultraviolet, the spectrum of electromagnetic
ization established in the Decision on Principles for the radiation commonly defined as having a wavelength between
Development of International Standards, Guides and Recom- 100 and 400 nanometers.
mendations issued by the World Trade Organization Technical
3.3.1.1 Discussion—In the context of this test method, the
Barriers to Trade (TBT) Committee.
term of UV is expanded to include wavelengths up to 550 nm
for the reason discussed in 8.1.
2. Referenced Documents
2.1 ASTM Standards:2 4. Summary of Test Method
D1193 Specification for Reagent Water 4.1 The sample is shaken with sodium plumbite solution, a
D3227 Test Method for (Thiol Mercaptan) Sulfur in small quantity of powdered sulfur added, and the mixture
Gasoline, Kerosine, Aviation Turbine, and Distillate Fuels shaken again. The presence of mercaptans or hydrogen sulfide
(Potentiometric Method) or both is indicated by discoloration of the sulfur floating at the
D4175 Terminology Relating to Petroleum Products, Liquid oil-water interface or by discoloration of either of the phases.
Fuels, and Lubricants
5. Significance and Use
5.1 Sulfur present as mercaptans or as hydrogen sulfide in
1
This test method is under the jurisdiction of ASTM Committee D02 on distillate fuels and solvents can attack many metallic and
Petroleum Products, Liquid Fuels, and Lubricants and is the direct responsibility of non-metallic materials in fuel and other distribution systems. A
Subcommittee D02.03 on Elemental Analysis.
Current edition approved July 1, 2023. Published July 2023. Originally approved
negative result in the doctor test ensures that the concentration
in 1989. Last previous edition approved in 2017 as D4952 – 12 (2017). DOI: of these compounds is insufficient to cause such problems in
10.1520/D4952-23. normal use.
2
For referenced ASTM standards, visit the ASTM website, www.astm.org, or
contact ASTM Customer Service at service@astm.org. For Annual Book of ASTM
3
Standards volume information, refer to the standard’s Document Summary page on Available from Energy Institute, 61 New Cavendish St., London, WIG 7AR,
the ASTM website. U.K., http://www.energyinst.org.

*A Summary of Changes section appears at the end of this standard


Copyright © ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States

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D4952 − 23
6. Interferences NOTE 1—Alternative volumes of the solution may be prepared or
purchased, provided the final solution concentration is equivalent.
6.1 This test cannot be used if there are more than trace
amounts of peroxides in the test sample. Peroxides can give a 7.4 Sulfur—Pure, sublimed, stored in a closed container.
false positive results where mercaptans are at low level or not 7.5 Potassium Iodide, approximately 100 g ⁄L Solution—
even present.4 Dissolve approximately 1 g of potassium iodide in approxi-
6.2 To check if peroxides are present in sufficient concen- mately 10 mL of water. Prepare fresh for each test.
tration to invalidate the test, shake 10 mL 6 0.5 mL of a fresh 7.6 Acetic Acid, approximately 100 g ⁄L Solution—Add ap-
portion of the sample with approximately 2 mL of the potas- proximately 10 mL of glacial acetic acid to approximately
sium iodide solution, add two drops of the acetic acid solution, 100 mL water.
and two drops of the starch solution. If the aqueous layer turns 7.7 Starch Indicator, approximately 5 g ⁄L Indicator
a blue color, this confirms the presence of peroxides in Solution—Prepare fresh each time of testing.
sufficient quantity to invalidate the test, and the test on this
sample should be discontinued. Proceed in accordance with 8. Sampling and Handling of Test Samples
6.4. 8.1 Improper choice of clear glass sample bottles followed
6.3 Alternatively, one may choose to perform a preliminary by exposure to sunlight or fluorescent lighting emitting UV
Doctor Test. If a brown precipitate slowly forms, peroxide is wavelengths shorter than 550 nm in the laboratory can generate
probably present. Proceed in accordance with 6.2 to confirm peroxides in cracked gasolines as well as finished batches of
presence of peroxides at sufficient quantity to invalidate the gasolines. Peroxides are generated in proportion to the head-
test. space air volume and time of exposure.6 It has been reported
6.4 If interference from peroxides is confirmed, proceed to that peroxides can interfere with the Doctor Test—see 6.1.
re-sample and retest. Ensure that sampling and handling 8.2 It is preferable to collect the field samples using dark
procedures for the new sample prevent UV light exposures as brown/amber bottles or metal cans, or if using clear glass
prescribed in 8.1. None of the normal refinery units or blending bottles to wrap them in foil or place in a light-tight box to
processes producing spark ignition motor fuels are known to prevent UV light exposure.
create peroxides under normal operating conditions. 8.3 The samples should be tested without delay upon receipt
7. Reagents and Materials in the laboratory before further chemical interactions take
place.
7.1 Purity of Reagents—Reagent grade chemicals shall be
used in all tests. Unless otherwise indicated, it is intended that 9. Procedure
all reagents conform to the specifications of the Committee on
9.1 Shake vigorously together in a test tube 10 mL of the
Analytical Reagents of the American Chemical Society where
sample being tested and 5 mL of sodium plumbite solution for
such specifications are available.5 Other grades may be used,
about 15 s. Add a small amount of pure, sublimed flowers of
provided it is first ascertained that the reagent is of sufficiently
sulfur so that practically all of it floats on the interface between
high purity to permit its use without lessening the accuracy of
the sample and the sodium plumbite solution after shaking.
the determination.
Shake again for 15 s. Allow to settle and observe within 2 min.
7.2 Purity of Water—Unless otherwise indicated, references NOTE 2—It is important to avoid adding more sulfur than will just cover
to water shall be understood to mean reagent water as defined the interface. About 20 mg to 25 mg is the proper quantity, which can be
by Types II or III of Specification D1193. estimated with a little practice. If too much sulfur is added, any possible
discoloration will be masked by the excess of sulfur.
7.3 Doctor (Sodium Plumbite) Solution—(Warning—
Poisonous and suspect carcinogen.) Dissolve approximately 10. Interpretation of Results
125 g of sodium hydroxide (NaOH) in 1 L of reagent water. 10.1 If the solution is discolored or if the yellow color of the
Add 60 g of lead monoxide (PbO) and shake vigorously for sulfur film is noticeably masked, report the test as positive and
15 min, or let stand with occasional shakings for at least one consider the sample as sour. If the sample remains unchanged
day. Allow to settle and decant or siphon off the clear liquid. If in color and the sulfur film is bright yellow or only slightly
the solution does not settle clear, filter it through filter paper. discolored with gray or flecked with black, report the test as
Keep the solution in a tightly sealed bottle and refilter before negative and consider the sample as sweet. If a brown
use if not perfectly clear. As an alternative, the lab may use a precipitate slowly forms, peroxide is probably present. Proceed
commercially prepared solution that meets the requirements of in accordance with 6.2.
the laboratory preparation.
NOTE 3—This examination must be made with extreme care. Some-
times the sulfur layer will be only flecked with spots of gray or black, and
4
Brooks, B. T., “Sodium Plumbite or Doctor Test of Gasolines,” Industrial and if there is any change in the color of either the sample or the Doctor
Engineering Chemistry, Vol 16, No. 6, June 1924, p. 588.
5
ACS Reagent Chemicals, Specifications and Procedures for Reagents and
6
Standard-Grade Reference Materials, American Chemical Society, Washington, Supporting data (Jennings, R., and Kohler, D., “Sunlight and Air Exposure
DC. For suggestions on the testing of reagents not listed by the American Chemical Effects on Octane Number or Cetane Number of Petroleum Product Samples,” April
Society, see Analar Standards for Laboratory Chemicals, BDH Ltd., Poole, Dorset, 2001) have been filed at ASTM International Headquarters and may be obtained by
U.K., and the United States Pharmacopeia and National Formulary, U.S. Pharma- requesting Research Report RR:D02-1502. Contact ASTM Customer Service at
copeial Convention, Inc. (USPC), Rockville, MD. service@astm.org.

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D4952 − 23
TABLE 1 Relationship Between Sample and Sulfur
Appearance Type of Sulfur
Formation of a brown precipitate before addition of sulfur Peroxide is probably present; proceed in accordance with 6.2
Darkening of the sample before addition of sulfur Mercaptans and elemental sulfur present in sample
Black precipitate before addition of sulfur Appreciable amounts of hydrogen sulfide
Black color of sulfur after shaking Traces of hydrogen sulfide
Spots of discoloration in the sulfur layer, plus darkening of the sample Hydrogen sulfide absent; mercaptans or elemental sulfur, or both, present
Clear yellow Doctor solution; no discoloration of sulfur Hydrogen sulfide and elemental sulfur absent; traces of mercaptans present

solution these spots will be difficult to detect. 10.1.1 The relationship between the appearance of the
NOTE 4—Strictly speaking, the test will not reject the sample on the sample and the type of sulfur is shown in Table 1.
basis of mercaptans only. The primary criterion for rejection is the
appearance of the sulfur layer after shaking, and small amounts of 10.2 If the doctor test is positive, mercaptan content may be
mercaptans will only discolor the sulfur. However, samples which contain determined using Test Method D3227.
mercaptans will also normally contain small amounts of sulfur in other
forms which will discolor the layers at the interface. The addition of pure, 11. Precision and Bias
sublimed flowers of sulfur is required to indicate that a reaction of
mercaptan and sodium plumbite has occurred. 11.1 No justifiable values of repeatability, reproducibility, or
NOTE 5—When the sample contains appreciable amounts of hydrogen bias for this test method can be stated here because the test
sulfide, a heavy black precipitate may be formed during the initial shaking detects only the presence or absence of active sulfur species,
and before the addition of the sulfur. If such a precipitate is noted, the test such as hydrogen sulfide or mercaptan.
may be stopped at that point and the sample reported as “Does not pass.”
However, if this observation is at all doubtful, the test should be 12. Keywords
continued. If the sample darkens before the addition of sulfur is made, this
indicates that the sample contains mercaptans and an excess of elemental 12.1 doctor test; hydrogen sulfide; kerosine; mercaptans;
sulfur that is needed to drive the sample reaction with sodium plumbite. motor fuel; sulfur

SUMMARY OF CHANGES

Subcommittee D02.03 has identified the location of selected changes to this standard since the last issue
(D4952 – 12 (2017)) that may impact the use of this standard. (Approved July 1, 2023.)

(1) Revised subsection 1.3. (3) Added Section 3.


(2) Added Terminology D4175 to Section 2.

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