ASTM UOP791-2016 Sulfur Components in LPG Fractions by GC-SCD《气相色谱-硫化学发光检测法测定液化石油气组分中的硫组分》.pdf

《ASTM UOP791-2016 Sulfur Components in LPG Fractions by GC-SCD《气相色谱-硫化学发光检测法测定液化石油气组分中的硫组分》.pdf》由会员分享，可在线阅读，更多相关《ASTM UOP791-2016 Sulfur Components in LPG Fractions by GC-SCD《气相色谱-硫化学发光检测法测定液化石油气组分中的硫组分》.pdf（9页珍藏版）》请在麦多课文档分享上搜索。

1、 IT IS THE USERS RESPONSIBILITY TO ESTABLISH APPROPRIATE PRECAUTIONARY PRACTICES AND TO DETERMINE THE APPLICABILITY OF REGULATORY LIMITATIONS PRIOR TO USE. EFFECTIVE HEALTH AND SAFETY PRACTICES ARE TO BE FOLLOWED WHEN UTILIZING THIS PROCEDURE. FAILURE TO UTILIZE THIS PROCEDURE IN THE MANNER PRESCRIB

2、ED HEREIN CAN BE HAZARDOUS. SAFETY DATA SHEETS (SDS) OR EXPERIMENTAL SAFETY DATA SHEETS (ESDS) FOR ALL OF THE MATERIALS USED IN THIS PROCEDURE SHOULD BE REVIEWED FOR SELECTION OF THE APPROPRIATE PERSONAL PROTECTION EQUIPMENT (PPE). COPYRIGHT 1980, 1994, 2013, 2016 UOP LLC. All rights reserved. Nonco

3、nfidential UOP Methods are available from ASTM International, 100 Barr Harbor Drive, P.O. Box C700, West Conshohocken, PA 19428-2959, USA. The UOP Methods may be obtained through the ASTM website, www.astm.org, or by contacting Customer Service at serviceastm.org, 610.832.9555 FAX, or 610.832.9585 P

4、HONE. Sulfur Components In LPG Fractions by GC-SCD UOP Method 791-16 Scope This method is for determining trace amounts of sulfur species in liquefied petroleum gases (LPG) streams using a gas chromatograph equipped with a sulfur chemiluminescence detector (GC-SCD). Individual components are determi

5、ned quantitatively from 0.1 to approximately 200 mass ppm sulfur. Higher concentrations of sulfur may be measured by modifying the instrument conditions to accomodate the increase in signal. Reference ASTM Practice D 1265, “Sampling Liquified Petroleum (LP) Gases (Manual Method),” ASTM Practice D 52

6、87, “Automatic Sampling of Gaseous Fuels,” ASTM Method D6667-14, “Standard Test Method for Determination of Total Volatile Sulfur in Gaseous Hydrocarbons and Liquefied Petroleum Gases by Ultraviolet Fluorescence” ASTM Method D6849-13, “Standard Practice for Storage and Use of Liquefied Petroleum Gas

7、 (LPG) in Sample Cylinders for LPG Test Methods” UOP Method 516, “Sampling of Gasolines, Distillate Fuels and C3-C4 Fractions” UOP Method 999, “Precision Statements in UOP Methods,” www.astm.org Outline of Method A reproducible sample volume is introduced into a gas chromatograph equipped with a fus

8、ed silica capillary column internally coated with methyl silicon, sulfur chemiluminescence detector (SCD) and control and quantitation software. The SCD is sulfur specific and responds to all sulfur compounds on an equimolar basis. The mass-ppm sulfur concentration of each sulfur component in an LPG

9、 sample is calculated using the gas chromatographic external standard method of quantitation. The total sulfur is then verified via ASTM method D6667. Apparatus References to catalog numbers and suppliers are included as a convenience to the method user. Other suppliers may be used. Chromatographic

10、column, 40 m x 0.32 mm ID fused silica capillary, Agilent J&W DB-Sulfur SCD, G3903-63002 2 of 9 791-16 Clamp, for ring stand and sample cylinders. minimum opening 38.1-mm, VWR International, Cat. No. C6088-12 Clamp holder, for ring stand and clamp, VWR International, Cat. No. C6088-2 Cylinder, for s

11、ample collection Sulfinert coated, DOT 3E 1800, 500 mL capacity, Restek Cat. No. 24133, Equip with two sulfinert valves, Restek Cat No. 21400, and 6900 kPa gague (1000 psi) Gas chromatograph, temperature programmable, built for capillary column chromatography utilizing a split injection system havin

12、g a deactivated glass injection port insert and equipped with a sulfur chemiluminescence detector (Agilent Model 8355 or equivalent) that will give a minimum peak height response of 10 times the background noise for 0.1 mass-ppm of a sulfur peak when run under recommended conditions Regulator, air,

13、two-stage, high purity, Matheson Trigas, Model 3810A-590 Regulator, hydrogen, two-stage, high purity, Matheson Trigas, Model 3810A-350 Ring stand, with rectangular base, 140- 229-mm with 610-mm rod, VWR International, Cat. No. 470104-060 Tubing, Sulfinert Treated, 1.59-mm (1/16-inch) OD, 0.030 mm ID

14、, Restek, Cat. No. 29230 Tubing, translucent, FEP Teflon, 3.2-mm (1/8-inch) OD, 1.6-mm (1/16-inch) ID, 3450 kPa (500 pisg), Thomas Scientific, Cat. No. 9567K20 Valve, injection, 2.0-L internal sample volume injector, stainless steel, UWP series, with 1.59-mm (1/16-inch) fittings, manual with standof

15、f, Valco Instruments, Cat. No. 2CI4UWE2 Valve, metering, 3.175-mm (1/8-inch), straight, stainless steel, Swagelok, Cat. No. SS-ORS2-V Reagents and Materials References to catalog numbers and suppliers are included as a convenience to the method user. Other suppliers may be used. Air, zero-gas Blend,

16、 LPG, calibration, certified standard, sulfur species in known concentrations in isobutane, size No. 3 treated aluminum cylinder, with eductor tube, pressurized with an inert gas to 1437 kPa gauge (210 psig), Matheson Gas Products (required for analysis of LPG streams). The calibration blend life is

17、 certified for 12 months by Matheson Gas Products The blend must be monitored regularly and replaced when changes in concentration or species present are noted. Gas Purifier, hydrogen, to remove oxygen and moisture from carrier gas, VICI Metronics, Cat. No. P200-1 Gas purifier, air (for detectors),

18、VICI Metronics, Cat. No. P400-1 Hydrogen, zero-gas, 99.95% minimum purity Procedure The analyst is expected to be familiar with general laboratory practices, the technique of gas chromatography, and the equipment being used. Dispose of all used reagents, materials, and samples in an environmentally

19、safe manner according to local regulations. 3 of 9 791-16 Sampling Obtain the sample by following the procedures described in ASTM Practice D 1265, “Sampling Liquified Petroleum (LP) Gases (Manual Method),” ASTM Practice D 5287, “Automatic Sampling of Gaseous Fuels,” UOP Method 516, “Sampling and Ha

20、ndling of Gasolines, Distillate Fuels, and C3-C4 Fractions,” or other reliable technique. Analysis must be performed as soon as possible after sampling to minimize sulfur adsorption on cylinder walls, and to minimize reactions that produce changes in the composition of sulfur compounds in the cylind

21、er. Cylinders must be lined with a Sulfinert coating to further prevent sulfur adsorption onto the cylinder walls. Chromatographic Technique 1. Install a gas purifier between the carrier gas source and the carrier gas inlet on the gas chromatograph Column life is signifigantly reduced if the gas pur

22、ifier is not used 2. Install the fused silica capillary column in the gas chromatograph according to the manufacturers specifications. 3. Install the injection valve in the carrier gas line just ahead of the injection port and connect the valve ports according to the manufacturers instructions (Figu

23、re 1). 4. Establish the recommended operating conditions as given in Table 1. Other conditions may be used provided they produce the required sensitivity and chromatographic separations equivalent to those shown in the Typical Chromatogram . Table 1 Recommended Operating Conditions Carrier gas hydro

24、gen Column Flow (constant flow) 1 mL/min Split flow 50 mL/min Injection port temperature 250 C Column temperature program Initial temperature 40 C Initial time 3 min Programming rate 1 15 C/min Intermediate final temperature 150 C Intermediate time 0 min Programming rate 2 20 C/min Final temperature

25、 250 C Final time 10 min SCD Detector * Sample size 2.0 L (repeatable for LPG) *The sulfur chemiluminescence detector is setup and operated according to the manufacturers instructions. 5. Program the column oven to 250 C and maintain this temperature until a stable baseline has been obtained at the

26、required sensitivity. 6. Cool the column oven 40 C. 4 of 9 791-16 Calibration of Apparatus Quantitative results are based on the injection of a repeatable volume of a sample and a calibration blend (external standard). A response factor is then used to relate the peak area obtained for the primary s

27、tandard blend to the peak areas of all sulfur compounds in the LPG sample. The sulfur chemiluminescence detector responds to all sulfur compounds on an equimolar basis. 1. Connect the valve on the eductor tube of the LPG calibration blend. Figure 2 shows common LPG sample cylinders 2. Analyze the bl

28、end in triplicate as described under Analysis of LPG Samples, Steps 6 through 13. Two of the injections should take place before the analytical samples, the third after. Take the mean of the response factors calculated from these three runs. The peak area from each of the three runs should not devia

29、te from the average by more than 10% of the value. If greater deviations occur, make certain that there are no problems with the equipment and then make further runs until the required repeatability is obtained on two consecutive runs. 3. Determine a response factor to be used for all sulfur species

30、 to 3 decimal places using Equation 1: KLQ (1) where: K = average peak area for the sum of the sulfur compounds in the blend L = concentration of the sum of the sulfur, as sulfur, in the blend, mass-ppm Q = response factor for sulfur species, mass-ppm/area count Analysis of LPG Samples 1. Connect ab

31、out 5-10 cm of FEP Teflon tubing to the outlet port of the injection valve as shown in Figure 1. This will form a “sight glass” to ensure that no air bubbles are in the injection port Tubing internal volume and length must be minimized. 2. Connect the metering valve to the exit end of the tygon tubi

32、ng 3. Connect Tygon tubing to the exit end of the metering valve to vent 4. Pressurize the LPG vessel containing the sample to approximately 1723 kPa gauge (250 psig) with nitrogen. Other inert gases such as He may be used. 5. Mount the cylinder in a vertical position so that the non-outage tube end

33、 is facing downards and connect the bottom valve to the sample injector valve inlet tubing (Figure 2) The connecting tubing between the cylinder and injector valve should be as short as possible. Sulfinert tubing should be used for connecting the valve to the LPG sample. For self standing cylinders

34、containing an eductor tube, connect the eductor tube outlet to the injector valve inlet tubing. 6. Place the injection valve in the fill position. 7. Ensure that the metering valve is closed. 8. Open fully the bottom valve of the vessel containing the sample. On upright cylinders with eductor tubes,

35、 open the eductor tube valve. 5 of 9 791-16 9. Partially open the metering valve to permit LPG to flow through the sampling system and observe the sight glass to verify there are no entrained bubbles. 10. Stop the sample flow by closing the metering valve. 11. Immediately switch the injection valve

36、to the inject position and start the recorder, integrator and column temperature programming sequence. The injection valve should remain in the inject position for the entire analysis. 12. Close the LPG cylinder valve and immediately open the metering valve to vent the sampling system. 13. Identify

37、the components of interest by comparing the resultant chromatogram to the Typical Chromatogram (see Figure 3). Calculations Calculate the concentration of each sulfur species, as sulfur, in the LPG sample to the nearest 0.1 mass-ppm below 10 mass-ppm or to the nearest mass-ppm above 10 mass-ppm usin

38、g the following formula: V = GQ (2) where: G = peak area of the specific sulfur species in the sample Q = previously defined, Eq. 1, mass-ppm/area count V = concentration of sulfur compound as sulfur, mass-ppm S To calculate the total sulfur concentration of the analytical sample use equation 3: = (

39、3) where: T = total concentration of sulfur in sample, mass-ppm S V = previously defined, Eq. 2 After the total sulfur is calculated by GC, a total sulfur value must be obtained by D6667 or equivalent method. The total sulfur values must match within 10% relative of each other. If greater deviations

40、 occur reanalyze the sample. If problems persist, initiate troubleshooting procedures as per manufacturers directions. Precision Precision statements were determined on the Agilent Model 355 SCD detector using UOP Method 999, “Precision Statements in UOP Methods.” It is expected that equivalent or n

41、ewer SCD detectors will have similar precision, but has not been tested. Repeatability Based on two tests performed by each of two analysts on each of two different days (8 tests), the within-laboratory estimated standard deviations (esd) were calculated for components at specific concentrations and

42、 are listed in Table 2. Two tests performed in one laboratory by different analysts on different days should not differ by more than the allowable differences in Table 2 at the concentrations listed (95% probability). 6 of 9 791-16 Table 2 Repeatability and Site Precision, mg/kg (mass-ppm) Repeatabi

43、lity Site Precision Sample Component Mean S Concentration Within Day esd Allowable Difference Within Lab esd Allowable Difference Sample A Methyl Mercaptan 192 2.5 10 3.0 12 Thiophene 64 0.3 1 0.4 2 Total 980 3.6 14 3.8 15 Sample B Carbon Disulfide 5.7 0.29 1.1 0.30 1.2 N-butyl Mercaptan 1.4 0.07 0.

44、3 0.09 0.4 Total 25 0.9 3 1.2 5 Reproducibility There is insufficient data to calculate the reproducibility of the test at this time. Time for Analysis The elapsed time for one analysis including calibration is 1.0 hour. The labor requirement is 0.6 hour. Suggested Suppliers Agilent Technologies, 53

45、01 Stevens Creek Blvd, Santa Clara, CA 95051, (877-424-4536) Matheson Trigas, 166 Keystone Dr. Montgomeryville, PA 18936, (800-416-2505) Restek, 110 Benner Circle, Bellefonte, PA 16823 (1-814-353-1300) Swagelok, 1117 Blackhawk Road, Rock Island, IL 61201, (309-787-6800) Valco Instruments Co., 8300 Waterbury, Huston, TX 77055, (800-367-8424) VWR International, 800 East Fabyan Parkway, Batavia, IL 60510 (800-932-5000) 7 of 9 791-16 8 of 9 791-16 9 of 9 791-16