ASTM D4294 PDF

By the Authority Vested By Part 5 of the United States Code § (a) and. Part 1 of the Code of Regulations § 51 the attached document has been duly. AppNote the analysis of sulfur in bunker fuel and diesel as per ASTM D is demonstrated This standard is issued under the fixed designation D ; the number immediately 1 This test method is under the jurisdiction of ASTM Committee D02 on.

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Skip to main content. Log In Sign Up. Criminal penalties may apply for noncompliance. D Standard Test Method for Sulfur in Petroleum and Petroleum Products by Energy- Dispersive X-ray Fluorescence Spectrometry 1 This standard is issued under the fixed designation D ; the number immediately following the designation indicates the year of aatm adoption or, in the case of revision, the year of last revision.

A number in parentheses x4294 the year of last reapproval. A superscript epsilon e indicates an editorial change since the last revision or reapproval. Significance and Use 1. A typical analysis time is 2 to 4 min per gasoline all unleadedand other distillates.

Sulfur in bunker fuel by ASTM D4294

In addition, sulfur sample. Knowledge of sulfur concentration is 0. There are also regulations 1. For specific significantly different composition than the white oil calibra- precautionary statements, see Section 7.

Sulfur in bunker fuel by ASTM D | Rigaku

Referenced Documents interpreting the results. The equipment D Practice for Manual Sampling of Petroleum and specified is in most cases less costly than that required for Petroleum Products2 alternative methods. Interferences Determine Conformance with Specifications 3 5. Summary of Test Method resolve from sulfur X-ray emission.

As a result, the lines 3. Two groups of calibration sured concentration of sulfur, or more than a few hundred samples are required to span the concentration range 0. These variations directly influence I This test s4294 is under the jurisdiction of Committee D-2 on Petroleum X-ray absorption and change the measured intensity of each Products and Lubricants and is the direct responsibility of Subcommittee D For example, performance enhancing additives, such Current edition approved Apr.

Originally as oxygenates in gasoline, can affect the apparent sulfur published as D Last previous edition D “.

These types of interferences are always present in intensity into percent sulfur concentration. X-ray fluorescence analysis and are completely unrelated to 6. Reagents and Materials contemporary instruments with the use Of built-in software. Unless otherwise indicated, it axtm intended that to time and that the software corrections offered by the all reagents conform to the specifications of the Committee on manufacturer not be accepted at face value. Corrections should Analytical Reagents of the American Chemical Society where be verified for new formulations.

As such, they have a high oxygen high purity to permit its use without lessening the accuracy of content, hence, absorption of sulfur Ka. Such fuels the determination. Use the certified sulfur the sample. There may be a loss of sensitivity and precision. Di-n-butyl sulfide is flammable and d294. Thus, a gasoline may be simulated by 7. Films found to be suitable are polyester, NOTE I-In the case of petroleum materials that contain suspended polypropylene, polycarbonate, and polyimide films.

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The ester and polycarbonate films. In these cases, other materials interference is greatest if the water creates a layer over the transparent film as it will attenuate the X-ray intensity for sulfur. One such method to besides these films may be used for X-ray windows, provided accomplish the removal of water is to centrifuge the sample first under that they do not contain any elemental impurities.

An optional ambient sealed conditions, taking care that the sample integrity is not window material is polyimide foil. Although polyimide foil compromised. Apparatus preferred window material as it is much more resistant to chemical attack by aromatics and exhibits c4294 mechanical 6.

In addition to other precautions, if a radioactive 8.

However, Samples should be analyzed immediately after pouring into a attention to the source is only to be carried out by a fully trained and competent person using the correct shielding techniques.

Disposable sample cells are not to be reused. A new piece 6. Avoid touching the inside of the sample film window. Oil from resolution value not to exceed eV.

A gas filled proportional fingerprints can affect the reading when analyzing for low counter has been found to be suitable to use. Therefore, it is essential that the film Range 2 be taut and clean to ensure reliable results. Therefore, the Std 6 0. Calibration and Standardization 9.

Hence, the matrix diluent should be as close to the which are certified by a national standards organization, may form of the matrix being analyzed as possible. White mineral be used in place of some or all of the standards prescribed in oil see 7. The calculated to four decimal places. Mix thoroughly astj generating the calibration curve can be used to check the PTFE-coated magnetic stirrer is advisable at room tempera- validity of the calibration. Calibration check standards may be ture.

The concentration of the calibration check centration ranges identified in Table 2 for the two ranges by standards shall be near the expected concentration of the diluting each primary standard with the applicable matrix samples being analyzed. As soon as any sedlffient or Method D or any other equivalent low level sulfur change of concentration is observed, discard the standard. Preparation of Apparatus mended d294 to the nearest 0.

It is important that the actual mass is known; thus, the actual concentration of the Whenever possible, the instrument should for calibration purposes. The concentration of sulfur can be remain energized to maintain optimum stability. Consequently, the analyst must ensure that the Sulfur Mass atsm Mass of sample cell is filled with sample above a minimum dep! Generally speaking, filling the sample cup to at 5. Provide a vent sstm in the top to prevent bowing.

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It is recognized that QC procedures- are the. Avoid spilling fia’mmable liquids inside the ana- lyzer Typically, the calibration procedure in- they were uriknownproduction samples. Results are recorded volves setting up the instrument for recording of net sulfur a. Obtain two readings on the standard using the status of the total testing process.

Aliy out of control data shall recommended counting time for sstm instrument according to trigger investigation for root cause s. The outcome of the Table 3. Depending prepared cells and fresh portions of the standard. Once aU “the on the criticality of the quality being measured and the standards have been analyzed, follow the manufacturer’s demonstrated stability of the testing process, the frequency of instructions for generating the optimum calibration curve based quality control sample testing can range from.

It is recom- analyzed four times. Immediately, lipon completion of the mended that at least one type of quality control sample be calibration, determine the sulfur concentration of one or mote analyzed that is asrm of samples routinely analyzed of the calibration: The measured’ as in 9. Before filling the apparatus under constant operating conditions on identical test cell, it may be necessary to heat viscous ,samples so that they materials would; in the long run, in the normal and correct are easy to pour into the celL Ensure’ that no air bubbles are operation of the test method, exceed the following values only present between the cell window arid the liquid sample.

Obtain the average Users of this standard are expressly advised that determination of the validity of any such patent rights, and the risk of infringement of such rights, are entirely their own responsibility. This standard is subject to revision at any asmt by the responsible technical committee and must be reviewed every five years and if not revised, either reapproved or withdrawn: Your comments are invited either for revision of this standard or for additional standards and astmm be addressed to ASTM Headquarters.

Your comments will receive careful consideration at a meeting of the responsible technical committee, which you may attend. Remember me on this d424. Enter the email address you signed up with and we’ll email you a reset link.

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