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AnchorRTF32343230323a204368617074RTF32343230323a204368617074Source Rock Analyzer (SRA):
Quick Start Guide
K. Fujine (10/20/09); revised/approved by D. Houpt (8/13/13), revised V.Percuoco 371T | July 2017 (7/26/17)

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Introduction


This quick start guide contains operational procedures for the Source Rock Analyzer (SRA).See the SRA Analyzer User Guide and Advanced User Guide for additional information.
Pyrolysis analysis is conducted on dried, ground sediments or borehole source rock for safety monitoring as well as for scientific purposes. The analysis yields information about thermal maturation and source of hydrocarbons at the drilled site, as well as petroleum potential. The data obtained from the Rock-Eval/TOC analyses are defined by the following parameters.


Parameter

Unit

Definition/Indication

S1

mg HC/g rock

Free hydrocarbons (HC)

S2

mg HC/g rock

HC resulting from kerogen cracking and/or high molecular weight HC

S3

mg organic CO2/g rock

Produced during low-temp pyrolysis of kerogen

S4

mg carbon/g rock

Convertible carbon + residual carbon

Tmax

°C

Stage of maturation of the organic matter

TOC

wt% C/unit wt rock

Total organic carbon: composed of convertible carbon

HI

Normalized HC content

Hydrocarbon index: used to determine kerogen type (I, II, or III)

OI

Normalized oxygen content

Oxygen index: used to determine continental vs. other types of immature organic matter

PI

NA

Production index: conversion of kerogen into free HC; used to determine petroleum HC

S1/TOC

NA

Used to identify source or reservoir rocks

PC

NA

Pyrolysis carbon: used to determine if a source rock is oil-prone or gas-prone

RC

NA

Residual carbon: carbon present in kerogen (low potential to generate HC)

S2/S3

NA

Used to determine kerogen type in absence of TOC data

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Apparatus, Reagents, & Materials

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Hardware


The SRA system consists of the following main components (Figure 1): Autosampler, Main control unit: oven and detector temperature control unit and gas flow controllers, Infrared (IR) section, Combustion with gas separation and FID (pedestal, oven, and conversion FID), and Cahn electrobalance dual balance system

Anchor_Ref302118442_Ref302118442
Figure 1. Main Components of the SRA System.

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–Colorado Oil Shale Silica (COSS) house standard
–Standard material (99986)
-Weatherford Laboratories SRA Rock Standard 533

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Sample Preparation


Sediments and sedimentary rock samples logged into the LIMS system as SRANL are analyzed by SRA. During sample preparation, keep in mind that sample container numbers must correlate with autosampler place numbers.
Freeze-dried bulk samples are crushed by hand or electric mill, then homogenized using a mortar and pestle. Prepare a weighing chart similar to that found below, and record sample ID, mass, and container number in the weighing chart.

Text ID (parent)

Text ID (child)

Mass (mg)

Container/Autosampler number

LIMS code

SRA code

Blank

 

 

99 (Calibration blank; always 99)

 

BLK

STD99986

OTHR137987

65.0

100 (Calibration STD; always 100)

QAQCSTD

STD

OTHR2764599

OTHR346972

78.26

1

UNK

TPH

OTHR2765092

OTHR130746

70.63

2

UNK

TPH

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CV1-99986

OTHR136947

65.0

5

QAQCCV

TPH

OTHR348962

OTHR147989

74.85

6

UNK

TPH

OTHR389012

OTHR384702

85.03

7

UNK

TPH

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CV2-99986

OTHR427034

65.0

10

QAQCCV

TPH

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Sample Analysis

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Preparing the Instrument


The SRA must warm up for 3 hr before operation. Perform the following steps to prepare for sample acquisition (Note: the onboard technician will warm up the instrument):

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  1. Open H2, He, O2, and air gas lines. Note: Verify gas gauge pressures using the gas flow meter.
  2. Turn on the SR Analyzer power and PC.
  3. Individually test the H2, O2, He, and oxidation air gas lines. With a gas flow meter verify gas flows correspond to the following values: H2: 65 ml/min, He: 100 mL/min, Air: 300 mL/min, Oxidation Air: 250 mL/min. H2, and O2 lines are beneath the FID cover. The helium and oxidation air line is connected to the base of the sample pedestal.
  4. Double-click the TStationAcq.exe shortcut icon on the desktop to open the software Main Menu.
  5. Click Preview to confirm oven and FID temperatures. Values will be <300°C. If after 10–15 min oven and FID temperatures have not increased, proceed to Steps 5 and 6.
  6. Click Configuration and select the Temperatures tab
  7. Set desired temperature and click Send Temperatures Immediately. Note: Except for this action, do not change any values on any tabs in the Configuration screen

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  1. .

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Open H2, He, O2, and air gas lines. Note: Verify gas gauge pressures using the gas flow meter.



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2.

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Turn on the SR Analyzer power and PC.

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3.

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Double-click the TStationAcq.exe shortcut icon on the desktop to open the software Main Menu.

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4.

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Click Preview to confirm oven and FID temperatures. Values will be <300°C. If after 10–15 min oven and FID temperatures have not increased, proceed to Steps 5 and 6.

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5.

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Click Configuration and select the Temperatures tab.

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6.

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Set desired temperature and click Send Temperatures Immediately. Note: Except for this action, do not change any values on any tabs in the Configuration screen.

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Setting up the Software


Prepare the software for data acquisition by creating a data folder, editing the method (if needed), and editing the sequence table.


Creating a New Folder


Data (CSV and ROW files) are saved into the expedition-specific data folder with the PAS file (sequence record) and PAR file (method) with respect to each sequence (batch).
Open the Data folder at C:\Program Files\Thermal Station\Data, and create a new folder named EXPxxx where xxx is the expedition number (or xxxx in the rare cases where the expedition has a letter designation with it).


Editing the Method


The method does not need to be edited for regular onboard measurements (i.e., safety monitoring) except for the standard information. The onboard laboratory specialist will edit the fields in the Standard tab if the standard material changes. In that case, one blank, one standard, and one known sample (house standard) must be measured to confirm calibration. The default method is toc_580.SRA.sram


Editing the Sequence Table


A sequence table represents an analytical batch. After each batch, the sequence table is saved into the expedition-specific data folder. A typical sequence table contains the following:
Data File name (one for each QA/QC and unknown sample). Examples: Blank: OTHR468061, Standard: PWDR39980915, Calibration verification standard: PWDR468051, Unknown sample: textID = LIMS text ID.
Sample ID: must be identical to the Text ID or the LIMS uploader will reject the file
Method: toc_580SRA.sram
C#: container number (must match autosampler place number, as recorded in the weight recording chart)
Sample Weight: from weight recording chart (mg)
Acq Type: acquisition type: BLK = cal blank, STD = cal standard, TPH = unknown or QA/QC samples
Edit the sequence table as follows:

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1.

Click Sequence Editor on the Main Menu.

2.

Fill in the Data File, Sample ID, Method, C#, Sample Weight, and Acq Type fields using the weight recording chart as a reference.

3.

Click Exit at the top right of the Sequence Editor screen, then click Yes to save the sequence table.

4.

Save the sequence into _folder C:\Program Files\Thermal Station_ (same level as the data folder), as EXPxxx.PAS.

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Running Samples


To analyze samples, fill in the Acquisition Setup screen and confirm sample information on the Analysis screen.

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The first sequence for an expedition must include a Blank and a Standard to calibrate the SRA each time the instrument is turned on after power off (e.g., loss of power). After this initial calibration, a Blank and a Standard should be measured once per day to verify calibration of the SRA. If the standard is outside the acceptable limits, the IR cell should be recalibrated.


Analytical Batch (Sequence)

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