Samples - PetroFLAG analyzer

Page / - last modified by TerraIndex TerraIndex on 2021/09/30 15:20

PetroFLAG analyzer

last modified by TerraIndex TerraIndex

on 2021/09/30 15:20

Table of Contents

Dexsil’s PetroFLAG Total Petroleum Hydrocarbon (TPH) in Soil System is an on-site test kit for determining the total petroleum hydrocarbons in soil. It is easy to use, inexpensive, and environmentally safe. The PetroFLAG System does not distinguish between aliphatic and aromatic hydrocarbons, but quantifies all oils, greases, and fuels as total hydrocarbons. Analysis is performed using a 10 gram soil sample and three easy steps: extraction, filtration, and analysis.

Instructions

Response factor

The microprocessor in the PetroFLAG analyzer uses the calibration data to convert the optical reading into a preliminary concentration. The selected response factor is then used to calculate the correct concentration for the analyte of interest. Therefore, it is important to choose the response factor that is appropriate for the particular hydrocarbon or class of hydrocarbons present at the site. The response factor can be changed at any time without affecting the stored calibrations.

If the contaminant is known or suspected, choose the appropriate response factor from the following table and set that response factor on the analyzer. If there is a mixture of hydrocarbons, use the most conservative response factor for the contaminants known to be present. If the contaminants are unknown, choose a conservative response factor based on those hydrocarbons that are likely to be on the site. Examination of Table 1, indicates that the majority of typical contaminants are in response category 5 or above. [2]

Response factors and method detection limits for common hydrocarbons

Hydrocarbon type	Method detection limit (ppm)	Response setting
Transformer oil	15	10
Grease	15	9
Hydraulic fluid	10	8
Transmission fluid	19	8
Motor oil	19	7
#2 Fuel oil	25	7
#6 Fuel oil	18	6
Diesel fuel	13	5
Gear oil	22	5
Low aromatic diesel	27	4
Pennsylvania crude oil	20	4
Kerosene	28	4
Jet A	27	4
Weathered gasoline	200	2

High concentration samples

The PetroFLAG Hydrocarbon Analyzer is preprogrammed to warn the user of an over-range condition. If the over-range reading is outside of the linear range (±10 precision), but still within the quantifiable range (±20% precision), the reading will be displayed blinking. This reading can be used as an indication that the concentration in the sample is not less than the displayed value. Since the response curve for most analytes is non-linear at high concentrations, the concentration in the sample may be higher than the displayed value. If the over-range condition is outside of the quantifiable range of the meter, the display will show a blinking "EEEE". Either error indication can be cleared by simply inserting the next vial and pressing the key. Accurate results can be difficult to obtain when 10 gram soil samples with high contaminant concentrations are used since they may cause a over-range condition on the PetroFLAG analyzer. To quantify these high contaminant samples, extract fresh soil samples of 1 gram size and reanalyze. Then multiply the result by 10 to obtain the concentration in the sample. Using this procedure, it is possible to measure oils containing up to 50,000 ppm of light hydrocarbon contamination or 10,000 ppm of a heavier hydrocarbon. [2]

Correcting wrong data

Collected data can be easily converted to the correct reading when it has been determined that the wrong response factor has been used. To make this conversion, multiply the measured value by the response factor initially used to make the measurement and divide by the new response factor.[2]

The effect of temperature

The PetroFLAG analyzer is equipped with an onboard temperature sensor to measure the ambient temperature while measurements are being made. The software uses the temperature readings to correct the optical readings for drift caused by the temperature fluctuations. The corrections have been determined for their effects on the turbidity development and the temperature drift of the electronics. The PetroFLAG analyzer can be used at temperatures from 4oC to 45oC.

The temperature corrections are valid for temperatures within 10oC of the calibration temperature. If a calibration is run with each batch of samples, the temperature correction is not significant and measurements can be made at any temperature within the usable range of the instrument. However, if no calibration is run and the ambient temperature deviates from the calibration temperature by more than 10oC, an error condition will result. The analyzer will display "Err4" which can only be cleared by pressing the key. Pressing of the key will clear the error and display the current reading. This reading can be recorded but it should be noted that the ambient temperature was outside of the acceptable 10oC window. Any other samples remaining in the series can be read, however, the same error condition will most likely occur. The meter must be recalibrated to eliminate this error condition.

The ambient temperature should be checked before starting to avoid a temperature error when a calibration is not run with the samples,. This can be 7 done by taking a reading without inserting a vial into the meter. If a reading is displayed, the temperature is within range and additional readings can proceed. If an error is displayed, the meter must be recalibrated before proceeding.

As previously mentioned, the storage of two calibrations, each at a different temperature, will reduce the number of recalibrations necessary as the temperature changes. If the two calibrations are stored under “1C” and “2C” and are run at temperatures levels 20oC apart, the effective temperature range for measurements now becomes 40oC.[2]

The effect of soil water content

The presence of water in a soil sample will have a definite effect on the reporting value in the final PetroFLAG result. As with all field measurements, the PetroFLAG system result is calculated based on the sample weight “as received”. If there is water present in the sample, this will produce a “wet weight” result causing an apparent under reporting by the PetroFLAG technique when compared to a laboratory reporting on a “dry weight” basis.

To correct for the difference between “wet weight” vs. “dry weight” results, simply divide the PetroFLAG value by the “fraction solids” (FS), where fraction solids is:

FS = Dry Weight/Wet Weight

or:

FS = (100 - %water)/100

Furthermore, when reporting the wet weight vs. dry weight results, the presence of water in a soil sample will cause a “dilution effect”. Since the PetroFLAG solvent system is miscible with water, the water in the soil will be extracted into the solvent phase. The aliquot filtered into the developer vial will, therefore, be diluted by the presence of the water. To a first approximation, the correction for this “dilution effect” is made by multiplying the PetroFLAG result by one plus the “fraction water” in the sample, R’=R(1+FW), where fraction water (FW) is:

FW=(Wet Weight - Dry Weight)/Wet Weight

or:

FW = %water/100

The equation below can be used to achieve an overall correction that includes both the conversion of the PetroFLAG result to a “dry weight” value and the correction for the dilution effect:

R’=R((2/FS) - 1)

where:

R’ = “Dry Weight” Corrected Result

R = Result displayed by PetroFLAG unit

FS = Fraction Solids

where:

FS = (100 - %water)/100

The above correction is applicable for typical soil types containing up to approximately 15% water by weight. For heavy clays or samples with higher water content, the effect of water content will vary with the analyte and should be determined specifically for each site.

In many cases, the effects of water content can be overcome by using a smaller sample size. This approach is the simplest and can be used effectively when a reduction in precision resulting from a smaller sample size still satisfies the overall data quality objective.

In some soils with high water content, the PetroFLAG response will be reduced both by the poor extraction efficiency of the analyte and a simple dilution. In these soils, the effect of water content on the extraction efficiency can sometimes be reduced by the addition of anhydrous sodium sulfate.

To treat such soils with sodium sulfate, weigh out the appropriate amount of soil sample (10 grams for a standard analysis) followed by the addition of up to 10 grams of anhydrous sodium sulfate. Mix the system thoroughly by stirring and/or shaking the sample until a free-flowing mixture is formed. Add the extraction solvent from a break-top ampule and then, follow the standard analysis procedure. 8

Treatment with sodium sulfate can improve the extraction efficiency, but will not correct for either the dilution effect or the wet weight/dry weight reporting error. The actual water content in the sample should be determined at some point so that the above corrections for wet weight and the dilution effect can be applied to the final result.[2]

Sample preparation

Each 10-pack of soil reagents contains reagents and supplies for 10 tests. In addition, one blank and one calibration standard are included. Samples can be run individually or by batch. For optimum performance and throughput, samples should be run in groups of 10 samples, once the meter has been calibrated with a blank and a standard. The meter does not need to be recalibrated, provided that the operating conditions and reaction times are maintained. Total time to analyze 10-15 samples is approximately 20-25 minutes.[2]

Calibrating

The following description summarizes the procedure for preparing the blank and calibration standard. Read the step-by-step instructions below completely before beginning the calibration process. To prepare a blank and a calibration standard, first label two soil tubes, one as the "blank" and the other as the "standard". Add to the blank tube the contents of a break-top ampule labeled “Extraction Solvent”. Add the contents of the break-top ampule labeled "Calibration Standard" to the standard soil tube. Process the blank and standard exactly as soil samples as described below.[2]

Calibration process

Label the soil extraction tubes (plastic tubes with colored caps) and developer vials (small glass vials with black caps) with the appropriate sample ID. Use the self-adhesive labels to label the screw cap of the developer vial. Do not write in the center 1/3 of the developer vial as this may obscure the optical path when the readings are made.

Weigh 10 grams (± 0.1 gram) samples of all unknown soils into each of the labeled color capped polypropylene tubes.

Set timer for 5 minutes. Add one break-top ampule of extraction solvent (blue polypropylene top) to the first tube. Start 5 minute timer and shake for 15 seconds. A separate ampule of extraction solvent is added to each of the remaining sample tubes when additional samples are being analyzed. Shake each tube for 15 seconds ensuring that the soil samples are fully wet. Shake each tube intermittently for a total of 4 minutes, then allow each tube to stand for the remaining 1 minute.

Verify that the filter disk is firmly attached to the syringe barrel. Remove the cap from the first labeled developer vial. Carefully decant the liquid from the polypropylene soil tube into the syringe barrel minimizing the transfer of soil particles, as this may plug the filter. Insert the plunger into the syringe barrel. Discard the first few drops from the filter into a waste container by pressing the plunger. Next, add the soil extract drop-wise to the developer solution until the meniscus just enters the neck of the vial (see figure). Shake the vial for 10 seconds, start the 10 minute timer and proceed to the next sample. Read the samples as close to the 10 minute time period as possible. Record this reading. Do NOT attempt to reread the sample as sample variation will occur due to fading of the solution over time. Do not let the developer vials stand longer than 20 minutes before reading, as this may result in lower than actual values.

If meter is off, turn on the meter by pressing key and calibrate.

To read, wipe the vial, place into the meter and press the key. Be sure that the outside of the vial is clean before reading. Record result on work sheet. Read vials in the same order as they were prepared.[2]

Manual

The PetroFLAG analyzer is controlled by a lowpower consumption micro-computer with a preloaded operating program which is stored in EEPROM memory. The program cannot be lost regardless of battery condition. The meter stores two calibration curves in separate memory locations. These calibration curves can be independently updated and the response factors can be changed without losing the calibrations.

The PetroFLAG meter is configured to allow easy access to the program modes. The currently active mode is indicated on the LCD display while a reading is in progress. The response factor and the active calibration can be changed from the MAIN MENU using the four keys on the keypad. The four keys are on the right.

When the PetroFLAG analyzer is turned on, the unit will return to the last mode it was in prior to being shut down. Under normal operating conditions, the analyzer will power up in the read mode. When the analyzer powers up in the read mode, the screen will display the last measured value for two seconds, and then, display the currently selected calibration curve (“1C” or “2C”) and response factor (1-15). The meter is now ready to resume measurement. Simply insert a new sample vial into the meter and push the <READ/ON> key. The display will initially indicate the calibration curve (either “1C” or “2C”) and the response factor (1-15) that is currently selected. Next, the term “CALC” will flash on the screen and after 5 seconds, the measured concentration in ppm will be displayed.

If you wish to exit the read mode, push the <NEXT> key and the operation is returned to the MAIN MENU. The <NEXT> key is also used to skip a step where a menu selection is required. To change a flashing menu option, push the <SCROLL> key while the option is flashing. To store the currently flashing menu choice, push the <SELECT> key. This stores the current choice and moves the flashing cursor to the next program mode.[2]

Choosing a calibration curve

Either of the two calibration curves, identified as "1C" and "2C", can be selected from the MAIN MENU. From either calibration curve any response factor can be selected. To change the response factor or to recalibrate the unit, use the <NEXT> key to enter the MAIN MENU screen. Immediately upon entering this menu three decimal points and the response factor are displayed. Next, the first two characters on the screen indicates the calibration curve that is currently selected (“1C” or “2C”) is displayed. They will blink, indicating that a new curve may be selected. Use the <SCROLL> key to scroll to the next calibration curve. Push the <SELECT/OFF> key to select the curve. The response factor will then blink. Use the <“SCROLL> key to scroll to the desired response factor for the target analyte and press the <SELECT/OFF> key.[2]

Reading the blank and standard

After the response factor has been selected, the screen will read “CALC” for five seconds and then display the calibration temperature. This temperature will remain on the screen until either the <NEXT> key or the <READ/ON> key is pressed. The screen will then prompt you for the "blank" vial by displaying "-bL-". Insert the blank vial in the meter and press the <READ/ON> key.After 5 seconds the screen display should read "0" for 2 seconds. The screen will then prompt for the calibration standard, "-CSd". Insert the calibration standard in the meter, press the <READ/ON> key and after 5 seconds, the calibration is complete. The meter will then re-read the calibration standard to verify a valid calibration and display "1000". If the concentration of the calibration standard is not correct using the newly calculated equation, an error message will flash until the <NEXT> key is pushed. If an error condition exists, the previously stored calibration constants will be retained until a valid calibration is completed.[2]

Taking a reading

After calibration, the meter will then display the calibration curve in use (“1C” or “2C”) and the current response factor selected. The meter is ready to read the first sample by inserting the sample vial into the meter and pressing the <READ/ON> key. After reading the sample, the meter will display the concentration in parts per million (ppm) until either the <READ/ON> key or the <NEXT> key is pushed. If no key is pushed for a period of five minutes, the meter will turn off automatically. If the meter turns off automatically, the meter can be reactivated by pressing the <READ/ON> key and the unit will return to the operation mode last used. The meter can be turned off manually by using the <SELECT/OFF> key, while in the read mode only. The optical system on the PetroFLAG analyzer is covered with a screw cap to keep out stray light. To remove this screw cap from the vial holder, simply unscrew it 1/4 of a turn counter-clockwise. To make a measurement, insert the developer vial into the unit, place the screw cap over the vial, and while pressing down on the cap (depressing the spring in the bottom of the vial holder), rotate the cap clockwise. Turn the cap until it is snug, but do not over-tighten.[2]

Power requirement

The PetroFLAG analyzer is powered by one 9V alkaline battery (included). This battery should last for several thousand readings. If a low battery condition exists "LP" will appear on the display.[2]

Errors

Error conditions

Message	Cause	Solution
Flashing Concentration Reading [Applies to Unknown Measurements]	Over range condition. Sample concentration outside of linear range.	Use smaller sample (1 gram recommended) and rerun.
Flashing "EEEE" [Applies to Unknown Measurements]	Sensor over range condition. Sample concentration too high.	Use smaller sample (1 gram recommended) and rerun
"Err0" [Applies to Calibration Mode]	Blank and Calibration Standard vials mixed up. Blank or Calibration Standard outside of QC window	Check calibration vials. Rerun and/or make up new ones.
"Err1" [Applies to All Modes]	Readings from the two optical channels do not agree.	Check vial and reread. If error remains, rerun using another vial.
"Err2" [Applies to Unknown Measurements]	Sample is reading lower than the blank, e.g., Calibration Blank soil unusually high background or not zero.	Recalibrate using true Blank soil.
"Err3" [Applies to Calibration Mode]	Blank or Calibration Standard outside of QC window	Recalibrate using fresh calibration solutions.
"Err4" [Applies to Unknown Measurements]	Absolute temperature difference between calibration and reading exceeds 10oC.	Recalibrate at current temperature.
"Err5" [ Applies to All Modes]	Ambient temperature outside of operating range. (4oC - 45oC)	Remove meter and reagents to climate controlled environment to recalibrate/rerun.
"LP"	Low power	Replace battery

References

https://www.equipcoservices.com/sales/dexsil/petroflag_system.html

https://www.equipcoservices.com/pdf/manuals/dexsil_petroflag_system.pdf

Contents

Instructions

Response factor

Response factors and method detection limits for common hydrocarbons

High concentration samples

Correcting wrong data

The effect of temperature

The effect of soil water content

Sample preparation

Calibrating

Calibration process

Manual

Choosing a calibration curve

Reading the blank and standard

Taking a reading

Power requirement

Errors

Error conditions

References