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2023-10-03_REVISION - M1977344 (23)
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2023-10-03_REVISION - M1977344 (23)
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Last modified
10/5/2023 8:56:09 AM
Creation date
10/4/2023 10:39:45 AM
Metadata
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Template:
DRMS Permit Index
Permit No
M1977344
IBM Index Class Name
Revision
Doc Date
10/3/2023
Doc Name Note
App 4.4 Holcim RCQ SAP
Doc Name
Request For Amendment To Permit
From
Holcim (US) Inc.
To
DRMS
Type & Sequence
AM2
Email Name
TC1
MAC
Media Type
D
Archive
No
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Quality Assurance Project Plan <br />Red Creek Quarry Monitoring Program Section 5: Data Generation and Acquisition <br /> <br /> <br />5-3 <br /> <br />Duplicates can be “replicates” (samples taken one immediately after the other, separated only by <br />the actual time required to fill the sample container) or “splits” (subsamples drawn from the same <br />initial volume of matrix). Relevant information will be recorded for the duplicates, just like the normal <br />samples, in the field logbook, or field data sheet. Results from the field duplicate analysis will be <br />included in the analytical report. <br />5.4.1.2 Equipment Blanks <br />A blank is a sample of known matrix where the specific constituents requested for analysis are <br />known to be absent or are present at concentrations less than the laboratory minimum limit of <br />detection. <br />Equipment blanks consist of blank sample matrix passed through or over non-dedicated sampling <br />equipment to check the decontamination process between samples or sample sites. Equipment <br />blanks may be collected when sampling equipment requiring decontamination (e.g., portable pumps <br />and sampling manifolds) are carried from location to location. When collected, equipment blanks will <br />also be submitted blind for analysis. <br />5.4.2 Laboratory QC Checks <br />Laboratory QC checks are routinely performed as part of the analytical process and include internal <br />checks for sample analysis activities. The frequency and type of QC samples are often analytical <br />method dependent. The laboratory will report any variance from laboratory-assigned QC limits <br />impacting the quality of sample results and may report details of internal laboratory QC if requested. <br />Laboratory QC checks include the types of samples described below. <br />5.4.2.1 Method Blank Samples <br />Method blank samples are used to assess laboratory contamination during all stages of sample <br />preparation and analysis. Method blank samples will be prepared by the laboratory using reagent- <br />grade water and are carried through the entire preparation and analytical process. The laboratory will <br />analyze method blank samples at a frequency of one sample for each batch of up to 20 samples. <br />5.4.2.2 Laboratory Control Samples <br />LCSs are multi-element matrix-specific standards with known analyte concentrations that are carried <br />through the entire preparation and analytical process. LCSs are used to confirm the method control, <br />accuracy, and precision of analyses for constituents that are analyzed on a total concentration or <br />total recoverable concentration basis. The laboratory will analyze LCSs at a frequency of one sample <br />for each batch of up to 20 samples. <br />5.4.2.3 Calibration Verification Samples <br />Calibration verification samples are method standards with known concentrations used to assess <br />analytical precision, accuracy, and stability of the instrument calibration. The laboratory will analyze <br />calibration verification samples at a frequency of one sample for each batch of up to 10 samples <br />and at the end of each workgroup. <br />5.4.2.4 MS Samples <br />MS samples will be used to evaluate the effect of the sample matrix on the recovery of constituents. <br />An MS sample is a split of a submitted sample that is fortified with a spiking solution containing <br />known concentrations of the target analytes. The fortified split is carried through the entire digestion <br />and analytical process. Analyses for the MS are compared to the non-spiked split, and recovery of <br />the target analytes is calculated using the equation discussed in Section 4.1. Recovery data for MS
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