Establishing and Implementing A Quality Management System For Construction Materials Testing Laboratories
Establishing and Implementing A Quality Management System For Construction Materials Testing Laboratories
1. SCOPE
1.1. This document contains criteria and guidelines for establishing and implementing a quality
management system (QMS) for use by a construction materials laboratory (CML). These criteria
may also be used by laboratory-evaluating agencies.
1.2. The criteria in this document only apply to the following testing areas: soil, aggregate, asphalt
binder, cutback asphalt, emulsified asphalt, asphalt mixtures, hydraulic cement, portland cement
concrete, unit masonry, metals, plastic pipe, and sprayed fire-resistive material.
2. REFERENCED DOCUMENTS
2.1. AASHTO Standards:
M 92, Wire-Cloth Sieves for Testing Purposes
M 152, Flow Table for Use in Tests of Hydraulic Cement
R 28, Accelerated Aging of Asphalt Binder Using a Pressurized Aging Vessel (PAV)
R 59, Recovery of Asphalt from Solution by Abson Method
R 61, Establishing Requirements for Equipment Calibrations, Standardizations, and Checks
T 19, Bulk Density (“Unit Weight”) and Voids in Aggregate
T 22, Compressive Strength of Cylindrical Concrete Specimens
T 23, Making and Curing Concrete Test Specimens in the Field
T 48, Flash and Fire Points by Cleveland Open Cup
T 49, Penetration of Bituminous Materials
T 50, Float Test for Bituminous Materials
T 51, Ductility of Asphalt Materials
T 53, Softening Point of Bitumen (Ring-and-Ball Apparatus)
T 59, Emulsified Asphalts
T 72, Saybolt Viscosity
T 79, Flash Point with Tag Open-Cup Apparatus for Use with Material Having a Flash Point
Less Than 93ºC (200ºF)
T 84, Specific Gravity and Absorption of Fine Aggregate
T 88, Particle Size Analysis of Soils
T 89, Determining the Liquid Limit of Soils
T 96, Resistance to Degradation of Small-Size Coarse Aggregate by Abrasion and Impact in
the Los Angeles Machine
3. TERMINOLOGY
3.1. calibration— a process that, under specified conditions, establishes metrological traceability by
determining: (1) the relation between the quantity values provided by measurement standards and
the corresponding indications from a measuring instrument or system, and (2) the resulting
measurement uncertainty (Note 1).
Note 1—This definition for calibration and the following definitions for check, standardization,
traceability, uncertainty, and verification of calibration are based on the definitions in R 61.
3.2. check—a specific type of inspection and/or measurement performed on equipment and materials
to indicate compliance or otherwise with stated criteria.
3.3. maintenance—a regularly scheduled preventive measure taken to preserve the effective working
condition of test equipment.
3.4. measurement standard—The embodiment of the definition of a given quantity, with a stated value
and measurement uncertainty, used as a reference. 2 This term is often called “reference standard.”
3.5.1. Discussion—There is a need for traceable measurements. Measurements, not the instrument, can
be traceable. Measurement traceability is established through calibration. Measurement
traceability is maintained through verification of calibration (a regular check of instrument output
using a control standard).
3.6. quality management system (QMS) (for a CML)—the organizational structure, staff
responsibilities, policies, standard operating procedures, processes, and records that assist the
laboratory in achieving its quality objectives.
3.7. standardization—a process that determines (1) the correction to be applied to the result of a
measuring instrument, measuring system, material measure, or measurement standard when its
values are compared with the values realized by standards, or (2) the adjustment to be applied to a
piece of equipment when its performance is compared with that of an accepted standard or
process.
3.8. uncertainty—a parameter associated with the result of a measurement that defines the range of the
values that could be attributed to the measured quantity.
3.9. verification of calibration—a process that establishes whether the results of a previously
calibrated measurement instrument, measurement system, or material measure are stable.
4.2. This document is not intended to prescribe the methods by which a laboratory achieves the desired
level of quality, but does provide acceptable approaches.
4.3. The user is cautioned that a QMS prepared by following this document can only serve a useful
purpose if it describes or references procedures that are practiced on a routine basis by the
laboratory. A QMS only describes the elements of the system and how they are intended to be
implemented. It is not the existence but the implementation of an effective quality management
system that is important.
5. MANAGEMENT REQUIREMENTS
5.1. Quality Management System (QMS):
5.1.1. The laboratory shall establish, implement, and maintain a quality management system (QMS)
appropriate to the scope of its activities. The QMS shall be available for use and understood by
laboratory staff.
Note 2—A QMS may be documented and distributed in hard copy or electronic format.
Note 3—Examples of some QMS documents are provided in the Appendix. The laboratory may
establish methods other than those shown in the Appendix to meet QMS requirements.
5.2.1. Each QMS document shall indicate its preparation date. When a document is revised, the date of
revision shall be indicated on the document.
5.2.2. Test Methods, Practices, Procedures, and Specifications—The laboratory shall maintain copies of
standards for the testing performed and shall ensure that the procedures are the most current and
are readily accessible to the employees performing the testing.
5.3. Organization:
5.3.1. The legal name and address of the laboratory—and that of the main office or company, if
different—and any other information needed to identify the organization shall be documented.
5.3.2. The ownership and management structure of the laboratory shall be documented. Names,
affiliations, and positions of principal officers and directors shall be listed.
5.3.3. The laboratory shall maintain an organization chart showing relevant internal organizational
components, including positions and names, that are part of the organization. The organization
chart shall clearly define relationships with other partner organizations where applicable.
5.4. Staff:
5.4.1. The laboratory shall maintain a position description for each technical operational position shown
on the laboratory’s organization chart. Position descriptions shall identify the position and include
a description of the duties, required skills, and education and experience associated with the
position.
5.4.2. The laboratory shall maintain a brief biographical sketch, noting the education, work experience,
licensure, certifications, and current position for each supervisory technical staff.
5.4.4. QMS Management—The laboratory shall designate a person(s) having responsibility for
determining whether quality management system activities are being implemented by laboratory
staff. This individual(s) shall have direct access to top management (Note 4).
Note 4—This individual(s) may have other responsibilities (e.g., Laboratory Manager).
5.5.1. The laboratory shall maintain a procedure that describes the method used to ensure that new
laboratory personnel are trained to perform tests in accordance with standard procedures. In
addition to the description of training methods, the document shall indicate what position or
employee is responsible for the laboratory training program and the maintenance of training
records (see Figure X1.1).
Note 5—There may be several different methods employed for differing levels of staff
experience, including (1) on-the-job apprentice training (one-on-one) for new employees with
little or no experience in laboratory or inspection work; (2) formal in-house training sessions for
certification, rating, or competency evaluation; and (3) training by external organizations. An
individual with prior experience performing a specific test need only have competency confirmed
by the laboratory (see Section 5.5.2).
5.5.2. The laboratory shall maintain a procedure describing the method used to evaluate staff
competency to ensure that each test covered by the scope of this standard is performed in
accordance with standard procedures. This description shall include the frequency of competency
evaluations for each technician and indicate what position or employee is responsible for
evaluating staff competency and maintaining records. The procedure shall ensure that each
technician receives a performance evaluation for each test that technician performs (see
Figure X1.2).
Note 6—Proficiency sample testing may be useful in evaluating staff competency; however, it
should be used in conjunction with observation of actual testing performed.
5.5.3. The laboratory shall maintain records of technician training and competency evaluation activities.
The records shall include the test method for which the technician was evaluated, the date on
which competence was determined or confirmed, the name of the individual who evaluated the
technician’s competency, and comments about the training or competency evaluation activity.
5.6.1. The laboratory shall maintain a document describing the scope of internal audits. Internal audits
shall verify that the laboratory’s operations continue to comply with its policies and procedures
and the requirements of this standard.
5.6.2. The document shall include the frequency of the reviews and identification of the individual(s)
responsible for the review. The internal audit program shall address all elements of the quality
management system and shall be conducted at least every 12 months by trained personnel
independent of the activity being audited, where possible.
5.6.3. Findings from internal audits shall be recorded (see Figures X1.3 and X1.4).
5.7.1. The laboratory shall maintain a procedure for implementing corrective action when
nonconforming work or departures from policies and procedures have been discovered (Note 7).
5.7.2. The laboratory shall document the method used in responding to customer complaints (see
Figure X1.6). Records of customer complaints and the resulting actions shall be maintained.
5.8.2. Technical Records—The laboratory shall retain records of test data, test reports, equipment
calibration, standardization, check, and maintenance activities for a minimum of 5 years.
Note 8—Although a 5-year retention schedule is adequate in some instances, there are many
circumstances when a longer retention period may be advantageous to the laboratory. Records
concerning the calibrations, standardizations, checks, and maintenance of equipment are an
example. Retention schedules of this type usually require such records to be held throughout the
useful life of the equipment.
6. TECHNICAL REQUIREMENTS
6.1. Equipment:
6.1.1. Inventory—The laboratory shall maintain an inventory of major sampling, testing, calibration,
standardization and check equipment, and measurement standards. The list shall include, where
available, the name, date placed in service, manufacturer, and model and serial number.
Note 9—An identification number assigned by the laboratory or other unique identifying
information may be substituted for the model and serial number if this is the practice normally
followed by the laboratory.
Note 10—Major equipment includes all equipment that is normally amortized by a laboratory,
such as shakers, physical or chemical testing machines, balances, baths, ovens, microscopes, and
computing equipment dedicated to testing. Equipment such as chairs, desks, and file cabinets may
be excluded. Major equipment does not usually include expendable items such as miscellaneous
glassware, sieves, molds, and viscometers.
6.1.2.1. The laboratory shall maintain a list giving a general description of equipment that requires
calibration, standardization, and checks. For each item the list shall include the
interval of calibration, standardization, or checks and a reference to the procedure used (Note 11)
(see Figure X1.7).
Note 11—When standard procedures are used, the standard should be referenced (e.g., unit
weight bucket, T 19). When the procedure used has been prepared by the laboratory, the in-house
designation should be referenced. It should be indicated if the work is performed by an outside
agency.
6.1.2.2. The laboratory shall have a procedure that describes the method for ensuring that the calibration,
standardization, and checks are performed for all required equipment at the specified intervals.
6.1.2.3. The laboratory shall have detailed written procedures for all in-house calibration, standardization,
and check activities not addressed in standards or operating instructions (Note 11). These
procedures shall indicate the equipment required to perform the calibration, standardization, or
check (see Figures X1.9 to X1.14). If a piece of laboratory testing equipment is used over a range
of measurements (e.g., thermometer, dial indicator, etc.), the calibration or standardization shall
include several measurements over that range.
6.1.2.4. The laboratory shall calibrate, standardize, and check all significant equipment associated with
tests the laboratory performs (Note 12). As a minimum, the applicable equipment listed in Tables
A1.1 through A1.8 shall be included.
Note 12—Refer to R 61 for guidance on performing equipment calibrations, standardizations,
and checks.
6.1.2.5.1. The intervals specified by the laboratory shall be no greater than those indicated in Tables A1.1
through A1.8 unless such equipment is calibrated, standardized, or checked before each use or the
laboratory has documented evidence to show that the conformance of the equipment to the
specification requirements is stable (Notes 13, 14, and 15).
Note 13—The intervals for the calibration of measurement equipment may be extended provided
that verification of calibration data obtained with frequent measurement checks using control
standards indicates that equipment measurement results are stable over time. Process-control
charts are commonly used to display the data.
Note 14—Equipment check intervals may be extended provided that equipment check data
indicate that equipment wear is predictable over time.
Note 15—Analysis of the verification of calibration data and check data for some equipment may
indicate that intervals should be decreased to ensure that the equipment consistently meets the
specification requirements or is removed from service when appropriate.
6.1.2.5.2. When a maximum interval for a specific piece of measurement equipment is specified in a
standard, the interval specified by the laboratory shall not exceed this interval unless the
equipment is calibrated, standardized, or checked before each use.
6.1.2.6. Equipment that has been removed from service and newly acquired equipment without a
manufacturer’s certification shall be calibrated, standardized, or checked before being placed
in service.
6.1.3.1. The laboratory shall maintain calibration certificates that establish the traceability of measurement
standards or in-house equipment used for calibrations, standardizations, and checks. The
calibration certificates shall include estimates of measurement uncertainty. The QMS shall include
a procedure that describes how the laboratory ensures the calibration of its measurement standards.
6.1.4.2. The laboratory shall maintain a list giving a general description of equipment that requires
maintenance. For each item, the list shall include the interval of maintenance and a reference to the
procedure used (Note 16) (see Table A1.9 for requirements and Figure X1.17 for an example of a
maintenance table).
Note 16—In most cases, the laboratory should refer to the manufacturers’ instructions to
determine the recommended maintenance interval and procedures. In some cases, the laboratory
will need to create its own maintenance intervals and procedures based on the frequency of use
and risk of equipment failure.
6.1.4.3. The laboratory shall have detailed written procedures for all in-house maintenance activities.
These procedures shall indicate the equipment required to perform the maintenance and a general
explanation of the work performed. If manufacturer’s instructions for maintenance are available,
they shall be referenced on the in-house procedure (see Figure X1.18).
6.1.4.4. The maintenance records shall contain the name of the individual who performed the maintenance,
the date the work was completed, and any comments.
6.1.4.5. The laboratory shall maintain the manufacturers’ instructions for operating and maintaining
equipment, where applicable.
6.1.5. Equipment Records—The laboratory shall maintain calibration, standardization, and check records
for all equipment specified in the QMS. Such records shall include:
6.1.5.1. Detailed results of the work performed (dimensions, mass, force, frequency, temperature,
time, etc.);
6.1.5.2. Description of the equipment calibrated, standardized, checked, or maintained, including model
and serial number or other acceptable identification (Note 9);
6.1.5.6. Identification of any device used for in-house calibration, standardization, or check, including
serial numbers, laboratory numbers, or other identification.
6.2.1. The laboratory shall have a procedure for the storage, retention, and disposal of test samples
(see Figure X1.15).
Note 17—In this context, the term “storage” refers to sample placement and handling before
testing. The term “retention” refers to sample placement and handling after testing.
6.2.2. The laboratory shall have a procedure for identifying test samples. The identification shall be
retained throughout the life of the sample in the laboratory.
6.3.2. Test Records—The laboratory shall maintain test records that contain sufficient information to
permit verification of any test reports. Records pertaining to testing shall include original
observations, calculations, derived data, and an identification of personnel involved in sampling
and testing.
6.3.2.1. The laboratory shall prepare test reports that clearly, accurately, and unambiguously present the
information specified in Table 1.
Table 1—Test Report Requirements
Identification of the report and the date issued
Description, identification, and condition of the test sample
Identification of the standard test method used
Test results and other pertinent data required by the standard test method
Identification of any test results obtained from tests performed by a subcontractor
Name of the person(s) accepting technical responsibility for the test report (if applicable)
6.3.2.2. In addition to the requirements listed in Section 6.3.2.1, the information listed in Table 2 shall be
available and traceable to the test reports.
Table 2—Test Report Information
Name and address of the testing laboratory
Name and address of the client or identification of the project
Date of receipt of the test sample
Date(s) of test performance
Deviations from, additions to, or exclusions from the test method
6.3.2.3. The procedure for amending reports shall require that the previously existing report be clearly
referenced when an amendment is made. The references shall establish a clear audit trail from the
latest issuance or deletion to the original report and its supporting data.
6.4. Subcontracting—The laboratory shall maintain a document describing the policies that the
laboratory follows relative to subcontracting, if it engages in such activities. These policies shall
include procedures followed by the laboratory in selecting competent subcontractors and reporting
the results of testing performed by subcontractors.
6.5.1. The laboratory shall have procedures for monitoring the validity of test results. The monitoring
shall be planned and may include one or more of the following:
6.5.1.2. Participation in proficiency sample or interlaboratory comparison testing (Note 17); and
6.5.2. Records—The laboratory shall retain results of the monitoring activities, including the steps taken
to determine the root cause of any nonconformities and the corrective actions taken.
7. KEYWORDS
7.1. Calibration; check; construction materials testing; equipment maintenance; internal audit; quality
management system; standardization.
ANNEX A1
(Mandatory Information)
Note A1—There may be more items added to the laboratory’s list of equipment that require
maintenance. Maintenance activities will typically involve lubricating, tightening fittings,
cleaning, replacing fluids, checking and replacing damaged or worn parts, etc. These activities will
vary based on the type of equipment, how often the equipment is used, the manufacturer’s
recommendations, etc.
APPENDIX X1 3
(Nonmandatory Information)
(Date)
The Laboratory Manager is responsible for the training program and maintenance of all training records. Copies of the results of all
training shall be distributed to and retained by the Office Manager. Training records shall be retained in the Office Manager’s office. All
materials technicians shall be trained prior to performing test procedures not previously performed. The following training procedures
shall be followed for each test:
1. The trainee shall obtain a copy of the applicable test procedure and report form.
2. The trainee shall study the test procedure and test report forms to become familiar with the equipment, terminology, test procedure,
calculations, and test reports.
3. A qualified technician shall demonstrate the test procedure for the trainee.
4. The trainee shall repeatedly perform the test procedure under the guidance of a qualified technician until proficiency is obtained.
5. The Laboratory Supervisor shall observe the trainee demonstrating the procedure and document that the trainee has demonstrated the
ability to perform the test procedure, if it is performed properly, by making an entry in the trainee’s training record.
Each Laboratory Supervisor is responsible for evaluating the test technician’s competency at least once every 12 months by requiring each
technician to demonstrate the AASHTO and/or ASTM test procedures for which he/she has been trained to perform. (If a technician does not
routinely perform a test, it may not be necessary to evaluate his or her competency to perform the test every 12 months. However, the
technician’s competency shall be evaluated prior to performing the test.) Copies of the results of all competency evaluations shall be
maintained by the Office Manager. Competency evaluation records shall be retained in the Office Manager’s office.
For each testing technician, the Supervisor shall record the test demonstrated, the date of the demonstration, and the results of the evaluation
(satisfactory or unsatisfactory). In addition, the Supervisor shall sign each entry on the evaluation record.
If an unsatisfactory result is recorded for a specific test, the Supervisor shall review all observed deviations from the standard AASHTO or
ASTM procedure with the testing technician, observe the technician redemonstrate the test procedure, and record the results as indicated
above.
(Date)
1. The Quality Manager shall review the following records, reports, and associated documentation every 12 months to ensure that
established quality procedures are being followed:
2. After each 12-month review the Quality Manager shall discuss any deficiencies noted with appropriate staff, ensure corrective
action is taken, and prepare a memorandum to the Laboratory Manager describing the items reviewed, the deficiencies identified,
and the corrective action taken.
3. The Office Manager shall maintain a file containing all documents relating to quality management system review in his office.
Have there been any changes made or updates required in the following sections of the QMS? Describe any actions taken below.
Reports covering the results of proficiency sample testing and on-site assessment and quality management system evaluations, and
memorandums summarizing investigations and any corrective action taken, shall be maintained by the Quality Manager in the Quality
Manager’s office.
ON-SITE ASSESSMENTS:
Participation:
AMRL Soils Inspection
AMRL Aggregate Inspection
CCRL Portland Cement Concrete Inspection
(Procedural Deficiencies)
1. Discuss each procedural deficiency with the testing technician and review the proper procedure.
2. Observe the technician perform the test properly.
3. Prepare a memorandum of record summarizing the action taken.
(Date)
General Policies:
1. Required equipment shall be calibrated, standardized, checked, or maintained at specified intervals following the general
procedures indicated below.
2. Newly acquired equipment without a manufacturer’s certification and equipment that has not been calibrated, standardized, or
checked because it has been removed from service shall be calibrated or checked before being returned to service.
3. When any of the Unit’s test equipment is overloaded, mishandled, giving results that are suspect, or is not meeting specification
tolerances, the Unit Supervisor shall remove it from service and clearly mark it by attaching a red ribbon or tape. The equipment
shall be returned to service only after appropriate repairs are made and calibration, standardization, or checks confirm the
equipment functions satisfactorily or meets specification tolerances.
General Procedures:
1. The Supervisor in each Testing Unit is responsible for ensuring that calibration, standardization, checks, and maintenance activities
are performed. He shall maintain a file for each piece of equipment in his unit requiring calibration, standardization, check, or
maintenance. The file for each piece of equipment shall contain detailed records of calibration, standardization, check, or
maintenance work performed in chronological order and shall be kept in the Supervisor’s office.
2. The Supervisor in each Testing Unit shall maintain a set of twelve labeled folders in his office—one for each month of the
year. Each month’s folder shall contain a partially completed calibration, standardization, check, or maintenance record form for
each piece of equipment requiring calibration, standardization, checks, or maintenance during the month indicated on the folder’s
label.
3. During the first week in each month, the Supervisor in each Testing Unit shall remove the partially completed record forms from
the current month’s folder and instruct the appropriate staff to perform the necessary calibration, standardization, check, or
maintenance work within the next week and return the completed record forms.
4. The Supervisor shall prepare partially filled out record forms for each piece of equipment calibrated, standardized, checked, or
maintained that month—identifying the equipment and the next date that calibration, standardization, check, or maintenance work
is required (month and year)—and file each partially filled out form in the appropriate monthly folder.
5. The Supervisor shall file each of the completed record forms in the appropriate equipment record file in chronological order.
Figure X1.8—Policies and Procedures for Conducting Equipment Calibration, Standardization, Checks, and
Maintenance
Purpose:
This method provides instructions for checking the physical condition of laboratory test sieves ranging in size from 75 mm (3 in.) to 0.075
mm (No. 200) and for measuring the openings of coarse sieves having openings greater than or equal to 4.75 mm (No. 4).
Equipment Required:
1. A caliper readable to 0.01 mm (use for 4.75-mm sieve and coarser).
2. An eye comparator with a 0.1-mm scale or a magnifier (for use with sieves finer than 4.75 mm).
Tolerance:
Sieves shall meet the physical requirements specified in AASHTO M 92 (ASTM E 11).
Procedure:
1. For sieves having openings equal to or greater than 4.75 mm, select and measure, using the calipers, the dimensions of at least four or
five sieve openings in each sieve to ensure that the openings in the wire cloth conform to the requirements in Table 1 of AASHTO M 92
(ASTM E 11). Be sure to include, in the selection, any openings that appear distorted or unusual in size. Measure each of the openings
as the distance between parallel wires measured at the center of each opening. Measure each opening in both the x (horizontal) and y
(vertical) directions. Record the measurements for each of the selected openings. If a sieve has fewer than five full openings, measure
all full openings.
2. For sieves smaller than 4.75 mm, inspect the sieve cloth against a uniformly illuminated background. Use the eye comparator or
magnifier to examine any suspicious areas of the cloth. If obvious deviations, such as weaving defects, creases, wrinkles, or excessive
foreign matter in the cloth, are found, the wire cloth is unacceptable.
3. Inspect the general condition of the sieve. Check the frame and solder joints for cracks or holes. (Check for pinholes in the finer
sieves.)
4. Ensure that the sieve has an appropriate label.
5. Check for tightness of the wires on each individual sieve.
Equipment Checked: MANUAL HAMMER (AASHTO T 99, T 180) (ASTM D 698, D 1557)
Purpose:
This method provides instructions for checking the critical dimensions of the proctor hammers.
Equipment Required:
1. Calipers readable to 0.01 mm.
2. Tape measure readable to 1 mm.
3. Balance, capacity 5 kg, readable to 1 g.
Tolerance:
Equipment shall meet the dimensional tolerances specified in the applicable test method.
Procedure:
1. Measure and record the diameter of the rammer face determined by taking two readings 90° apart using the calipers.
2. Pull up the handle, measure, and record the drop height of the hammer. Determine this height inside the guide sleeve using the tape
measure.
3. Remove the hammer from the guide sleeve. Determine and record its mass to the nearest 1 g.
4. Measure and record the diameters of the vent holes near the end of the hammer.
Purpose:
This method provides instructions for checking the critical dimensions of the sand cone and tamper used in the above test method.
Equipment Required:
1. Calipers readable to 0.1 mm.
2. Balance, 500-g capacity, readable to 0.1 g.
3. Ruler readable to 1 mm.
Tolerance:
Equipment shall meet the dimensional tolerances specified in the test method.
Procedure:
(Cone)
1. Measure the inside diameter at the top of the cone to the nearest 1 mm by taking two readings 90° apart using the ruler and record the
results.
2. Invert the cone and repeat step 1.
3. Place the cone on a flat glass surface. Measure and record the depth of the cone.
4. Using the calipers, measure the thickness of the cone to the nearest 0.1 mm by taking two readings 90° apart at the top of the cone and
two readings 90° apart at the bottom of the cone and record the results.
(Tamper)
1. Measure and record the diameter of the tamping face to the nearest 1 mm by taking two readings 90° apart using the ruler.
2. Determine and record the mass of the tamper to the nearest 0.1 g.
Purpose:
This method provides instructions for checking the critical dimensions and general operating condition of the L.A. abrasion machine and
the mass of the spheres used as test charges.
Equipment Required:
1. Steel rule readable to 1 mm.
2. Stopwatch readable to 0.1 s.
3. Balance with a 5-kg capacity, readable to 1 g.
Tolerance:
The L.A. machine shall meet the dimensional tolerances specified in the applicable test method listed above and shall be in good operating
condition. The steel spheres used to charge the L.A. machine shall meet the mass tolerances specified in the applicable test method listed
above.
Procedure:
(L.A. Machine)
1. Measure and record the inside diameter of the drum at the left and right edges to the nearest 1 mm.
2. Measure and record the width and height of the opening to the nearest 1 mm.
3. Measure and record the wall thickness at the left and right edge to the nearest 1 mm.
4. Determine if the cylinder is horizontal using a steel ball to check left-to-right roll.
5. Measure and record the shelf width inside the drum to the nearest 1 mm.
6. Measure and record the distance from the shelf to the opening in the direction of rotation.
7. Using the stopwatch, determine the r/min to the nearest whole number over a 5-minute period. Record the r/min.
8. Check that the number of revolutions is 500 by looking at the counter on the machine.
(Steel Spheres)
1. Determine and record the mass of each individual sphere to the nearest 1 g.
2. Determine and record the mass of the collective charge(s) to the nearest 1 g.
Equipment Checked: TIMERS (AASHTO T 72, T 201, T 202) (ASTM D 88, D 2170, D 2171)
Purpose:
This procedure provides instructions for checking the accuracy of timing devices.
Tolerance:
Timers shall meet the accuracy requirements specified in the applicable test methods listed above.
Procedure:
1. Hold the calibrated timer in one hand and the timer to be checked in the opposite hand.
2. Start the timers simultaneously by pressing the “start” buttons at the same time.
3. Allow the timers to run for at least 15 min. Then stop the timers simultaneously. Record the time indicated by both timers.
4. Record the difference between the two timers. Calculate and record the percent accuracy.
( A − B)
% accuracy
= × 100
B
A = Reading on lab timer (s)
B = Reading on standard timer (s)
Purpose:
This procedure provides instructions for checking the equipment used to perform the penetration test.
Equipment Required:
1. Balance, readable to 0.01 g.
2. Microscope or eyepiece, 10×.
3. Metal block, 10.0 mm high. Metal block, 25.4 mm (1 in.) high.
4. Support block, 75 to 87.5 mm high.
5. Ruler, readable to 1 mm.
6. Calibrated stopwatch, readable to 0.1 s.
Tolerance:
The equipment shall meet the tolerances specified in test methods AASHTO T 49 and ASTM D 5.
Procedure:
1. Remove the spindle, 50- and 100-g weights from the penetrometer. Record the weight of each to the nearest 0.01 g.
2. Weigh each needle to the nearest 0.01 g. Visually examine each needle with a microscope or eyepiece. Each needle should be straight
and free of burrs. The base of each needle should be flat.
3. If an automatic timing mechanism is used on the penetrometer, start the calibrated stopwatch when the plunger is released and stop the
calibrated stopwatch when the plunger stops. Record the time indicated on the calibrated stopwatch to the nearest 0.1 s. If a manual
device is used to release the plunger, check the accuracy of the timing device used over a 60-s interval. Record the elapsed time to the
nearest 0.1 s.
4. Place the support block on the base of the penetrometer. Place the 10-mm block on the support block. Adjust the needle height so that
its tip just touches the top of the 10-mm block. Remove the 10-mm block and release the needle to the support block. Adjust the
instrument to measure the distance moved. Repeat step 4 using the 25.4-mm (1-in) block. Determine dial accuracy by comparing
readings with the height of the blocks.
5. Measure and record the distance from the perforated shelf to the bottom of the water bath. Measure and record the distance from the
perforated shelf to the surface of the water. Measure and record the distance the thermometer is immersed in the water.
6. Observe and record the temperature of the water in the bath to the nearest 0.1°C (0.2°F).
______(Date)______
PROCESSING OF SAMPLES
IDENTIFICATION:
Each sample shall be accompanied by a sample tag indicating the sample number. This identifies the material in terms of the project, the location
of use within the project, the quantity of material represented by the sample, and the material’s intended use. The sample tag is kept with the
sample as long as it remains in the materials laboratory.
STORAGE:
After being logged in, samples are stored in the area of the laboratory in which testing is to be done. During storage, care is taken to avoid
disturbance or contamination. Any AASHTO requirements for storage (e.g., the moist storage of portland cement concrete cylinders) are
followed.
RETENTION:
Samples with acceptable test results are generally discarded when testing is completed. Those with failing results are retained until review of
those results is completed. At that time, the decision is made whether to discard, retest, or continue to retain the sample.
DISPOSAL:
Discarded nonhazardous materials are transported daily by materials section personnel to an appropriate area. Hazardous materials (e.g.,
bituminous concrete extraction solution) are stored in proper containers in an isolated area of the laboratory. Disposal by an approved disposal
contractor is arranged periodically by the hazardous waste disposal officer.
1. Sample number (this is assigned sequentially to each line of the log book).
2. Project name or contract number.
3. Description of the material.
4. Supplier of the material.
5. Location from which the sample was taken.
6. Name of person(s) who sampled the material.
7. Date of sampling.
8. Date the sample was received in the materials laboratory.
9. The word “RESAMPLE” in red ink (when applicable).
10. The date testing was completed.
11. The initials of the tester.
AMENDING REPORTS:
When a report must be amended, a report form shall be filled out indicating the amended test results; the report status field “amended” on
the report form shall be checked; the comment section on the report form shall state the reason for the amended report; the amended report
shall be attached to the original report and processed in the normal manner; and the amended report shall be filed with the original report.
Figure X1.16—Procedures for Producing Test Records and Preparing, Checking, and Amending Test Reports
Date_____________
MAINTENANCE INTERVALS
Procedure:
1. Clean all loose dust and particles from all exposed surfaces of machine
2. Check each paddle for looseness—tighten where necessary
3. Replace any paddles that are in poor condition
4. Clean and grease rotating base
5. Operate shaker without sieves in place to determine how shaker is working
6. Explore any other possible issues and resolve them
1
This document is under the jurisdiction of the American Association of State Highway and Transportation
Officials (AASHTO) Highway Subcommittee on Materials and is the direct responsibility of the Administrative
Task Group.
2
The definition is from the International Vocabulary of Metrology (abbreviated VIM), 3rd edition, 2008, published
by the International Organization for Standardization (ISO), in the name of the eight organizations that supported its
development and nominated the experts who prepared it: the Bureau International des Poids et Mesures (BIPM), the
International Electrotechnical Commission (IEC), the International Federation of Clinical Chemistry (IFCC), the
International Laboratory Accreditation Cooperation (ILAC), ISO, the International Union of Pure and Applied
Chemistry (IUPAC), the International Union of Pure and Applied Physics (IUPAP), and the International
Organization of Legal Metrology (OIML). The VIM should be the first source consulted for the definitions of terms
not included in this practice.
3
The figures in this Appendix illustrate typical examples of documents, forms, and standard operating procedures
that address the requirements of this practice. A laboratory may employ other methods that satisfy the intent of this
practice. The figures are intended as examples of documents in a laboratory’s Quality Management System. They
are not intended to include all possible laboratory organizational structures or capabilities.