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4.1 Establishment of an in-service coatings monitoring program permits planning and prioritization of coatings maintenance work as needed to maintain coating integrity and performance in nuclear CSL I coating systems. For additional information on nuclear maintenance coating work, refer to ASTM MNL8.44.2 A coatings monitoring program enables early identification and detection of potential problems in coating systems. Some CSL I coating systems may be known in advance to be suspect, deficient, or unqualified. Monitoring coating performance will assist in developing follow-up procedures to resolve any significant deficiency relative to coating work.4.3 Degraded coatings may generate debris under design basis accident conditions that could adversely affect the performance of the post-accident safety systems. A coatings monitoring program may be required to fulfill safety analysis report and generic letter commitments for CSL I coating work in a nuclear power plant facility.1.1 This standard covers procedures for establishing a monitoring program for condition assessment of Coating Service Level (CSL) I coating systems in operating nuclear power plants. Monitoring is an ongoing process of evaluating the condition and performance of the in-service coating systems.1.2 It is the intent of this standard to provide a recommended basis for establishing a coatings condition assessment program, not to mandate a singular basis for all programs. Variations or simplifications of the program described in this standard may be appropriate for each operating nuclear power plant depending on their licensing commitments.1.3 This requirements of ASME Section XI, In-Service Inspection Subsections IWE and IWL are beyond the scope of this standard.1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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4.1 The reason for preserving military sampling standards is that many organizations throughout the world still use these standards in their current form. MIL-STD-1235B is no longer supported by the U.S. Department of Defense as of the mid-1990s and is out of print, but does exist in the public domain. This practice represents a conversion of MIL-STD-1235B to an ASTM-supported standard.4.2 This practice provides the tables and procedures for applying five different types of continuous sampling plans for inspection by attributes. These continuous sampling plans are discussed in Sections 6 – 10 of this practice and each section includes information on:(1) Initiation of 100 % inspection in use.(2) Requirements on when to switch to sampling inspection.(3) Conditions warranting a return to 100 % inspection.(4) When a change in Code Letter, if desired, can be made.(5) What to do when the checking inspector finds a defect that was originally found conforming by the screening inspector(s), that is, ineffective screening.(6) Situations where a defect is found before the switch to 100 % inspection causing excessive periods of 100 % inspection so action must be taken, that is, long periods of screening.4.2.1 Section 6 (Section 2 in MIL-STD-1235B) describes specific procedures and applications of the CSP-1 sampling plans – a single-level continuous sampling procedure which provides for alternating between sequences of 100 % inspection and sampling inspection.4.2.2 Section 7 (Section 3 in MIL-STD-1235B) describes specific procedures and applications of the CSP-F sampling plans – a variation of the CSP-1 plans in that CSP-F plans are applied to a relatively short run of product, thereby permitting smaller clearance numbers to be used.4.2.3 Section 8 (Section 4 in MIL-STD-1235B) describes specific procedures and applications of the CSP-2 sampling plans – a modification of CSP-1 in that 100 % inspection resumes only after a prescribed number of defect-free units separate any two defective sample units.4.2.4 Section 9 (Section 5 in MIL-STD-1235B) describes specific procedures and applications of the CSP-T sampling plans – a multi-level continuous sampling procedure which provides for reducing the sampling frequency upon demonstration of superior product quality.4.2.5 Section 10 (Section 6 in MIL-STD-1235B) describes specific procedures and applications of the CSP-V sampling plans – a single-level continuous sampling procedure which is an alternative to CSP-T in that these plans provide for reducing the clearance number in good quality situations where reduction of sampling frequency has no economic merit.AbstractThis practice establishes tables and procedures for applying five different types of continuous sampling plans for inspection by attributes using MIL-STD-1235B as a basis for sampling a steady stream of lots indexed by AQL. This practice represents a conversion of MIL-STD1235B to an ASTM-supported standard.1.1 This practice establishes tables and procedures for applying five different types of continuous sampling plans for inspection by attributes using MIL-STD-1235B as a basis for sampling a steady stream of lots indexed by AQL.1.2 This practice provides the sampling plans of MIL-STD-1235B in ASTM format for use by ASTM committees and others. It recognizes the continuing usage of MIL-STD-1235B in industries supported by ASTM. Most of the original text in MIL-STD-1235B is preserved in Sections 6 – 10 of this practice.1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 Identification and Quantitation of Phthalates—DBP, BBP, DEHP, DNOP, DINP, and DIDP are representative of the phthalates either banned or being monitored by a variety of regulations. Regulations include: EU—Directive 2005/84/EC, US—Consumer Product Safety Improvement Act of 2008 – section 108, Japan—Health, Labor and Welfare Ministry guideline No. 336 (2010) and IEC 62321-8:2017. These test methods provide a procedure to identify and quantify phthalates in PVC.5.2 Other techniques successfully used to separate and identify phthalates in PVC include GC/MS, HPLC/UV, HPLC/MS, FTIR, and GC/FID (flame ionization detector).1.1 This test method provides a procedure to identify and quantify phthalates by thermal desorption (TD) gas chromatography (GC) mass spectrometry (MS). Six phthalates are used to demonstrate the use of the procedure: BBP, DBP, DEHP, DNOP, DINP and DIDP.1.2 Within the context of this method, “low level” is defined as 1000 ppm.1.3 The values in SI units are to be regarded as standard.1.4 This test method includes references, notes and footnotes that provide explanatory material. These notes and footnotes (excluding those in the tables and figures) shall not be considered as requirements of this method.1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.NOTE 1: The method can be extended to include other ortho-phthalates in a number of polymeric substrates.NOTE 2: There is no known ISO equivalent to this standard.1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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AS 1983-1977 Spirit level vials 被代替 发布日期 :  1970-01-01 实施日期 : 

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1.1 This test method is for determining the maximum x-ray sensitivity coefficient (slope of diffuse visual density versus x-ray exposure) of film/processing combinations for low quantities of x-ray exposure to silver halide photographic film. This coefficient can be used to assess the relative susceptibility of films to damage from x-ray exposure, such as that encountered in airport and similar security screening systems. 1.2 This standard may involve hazardous materials, operations, and equipment. This standard does not purport to address all of the safety problems associated with its use. It is the responsibility of whoever uses this standard to consult and establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

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5.1 The user-level calibration process may be used to verify that the DF tester is functioning properly, that it is within manufacturer specifications, and to perform minor adjustments to bring the unit back into conformance with manufacturer specifications.5.2 The DF tester user-level calibration described herein does not eliminate all error sources, nor does it guarantee the proper operation of the device. Several adjustments and repairs are beyond the scope of this standard, and manufacturer-approved calibrations are still recommended on an annual basis.1.1 This test method describes the equipment and procedure to ensure that the calibration performed by various dynamic friction tester (DF tester) users is uniform and in accordance with manufacturer specifications. There are three models of the DF tester in use: (1) USB/personal computer, (2) controller, and (3) X-Y plotter. Procedures specific to the different models are noted. User-level calibration software is separate from the operation software and must be obtained from the manufacturer for the USB/personal computer model.1.2 This test method is a static calibration of the vertical load, friction (µ) force, and speed of the DF tester. Compliance to this user-level calibration procedure ensures a higher level of repeatable and reproducible performance of the DF tester when used in accordance with Test Method E1911.1.3 The user-level calibration doesn’t include the replacement of the mu spring or the adjustment of linearity of the DF tester. It is recommended that DF testers be inspected by a manufacturer-approved laboratory on an annual basis to replace the mu spring, ensure linearity, and to identify other non user-serviceable wear.1.4 The values stated in SI (metric) units are to be regarded as standard. The inch-pound equivalents are rationalized, rather than exact mathematical conversions.1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 DO may be either a corrosive or passivating agent in boiler/steam cycles and is therefore controlled to specific concentrations that are low relative to environmental and wastewater treatment samples. Out-of-specification DO concentrations may cause corrosion in boiler systems, which leads to corrosion fatigue and corrosion products — all detrimental to the life and efficient operation of a steam generator. The efficiency of DO removal from boiler feedwater by mechanical or chemical means, or both, may be monitored by continuously measuring the DO concentration before and after the removal process with on-line instrumentation. DO measurement is also a check for air leakage into the boiler water cycle.5.2 Feedwater chemistry guidelines for high-pressure boilers generally require specific feedwater DO concentrations: 5 μg/L or less for reducing all volatile treatment [AVT(R)]; 5–10 μg/L for oxidizing all volatile treatment [AVT(O)]; 50–200 μg/L for oxygenated treatment [OT] (3).5.3 In microelectronics production, DO can be detrimental in some manufacturing processes, for example, causing undesirable oxidation on silicon wafers.1.1 This test method covers the on-line determination of dissolved oxygen (DO) in water samples primarily in ranges from 0 to 500 μg/L (ppb), although higher ranges may be used for calibration. On-line instrumentation is used for continuous measurements of DO in samples that are brought through sample lines and conditioned from high-temperature and high-pressure sources when necessary.1.2 The values stated in SI units are to be regarded as standard. The values given in parentheses after SI units are provided for information only and are not considered standard.1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. For specific hazards statements, see 6.5.1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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4.1 The test results enable the comparison of A-weighted sound emission from vacuum cleaners, backpack vacuum cleaners, extractors, or hard-floor cleaning machines when tested under the condition of this test method.1.1 This test method calculates the overall A-weighted sound power level emitted by small portable upright, canister, combination vacuum cleaners, backpack vacuum cleaners, hard-floor cleaning machines, extractors, and central vacuum cleaner motorized nozzles intended for operation in domestic and commercial applications.1.1.1 To determine the Sound Power Level of a central vacuum at the power unit location refer to Test Method F2544.1.2 A-weighted sound pressure measurements are performed on a stationary vacuum cleaner, extractor, hard-floor cleaning machine, or backpack vacuum cleaner in a semi-reverberant room. This test method determines sound power by a comparison method for small noise sources, that is, comparison to a broadband reference sound source.1.3 This test method describes a procedure for determining the approximate A-weighted sound power level of small noise sources. This test method uses a non-special semi-reverberant room.1.4 Results are expressed as A-weighted sound power level in decibels (referenced to one picowatt).1.5 The values stated in inch-pound units are to be regarded as the standard. The values in parentheses are for information only.NOTE 1: The F11.21 subcommittee is actively pursuing new market relevant carpets with the assistance of the carpet industry. Although plush and Freize carpet panels are no longer available for purchase, some laboratories may still have samples for testing. In such cases, the table values remain valid.1.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.7 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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4.1 This practice permits an analyst to compare the general performance of an instrument on any given day with the prior performance of an instrument. This practice is not necessarily meant for comparison of different instruments with each other even if the instruments are of the same type and model. This practice is not meant for comparison of the performance of one instrument operated under differing conditions.1.1 This practice describes two levels of tests to measure the performance of laboratory Fourier transform mid-infrared (FT-MIR) spectrometers equipped with a standard sample holder used for transmission measurements.1.2 This practice is not directly applicable to Fourier transform infrared (FT-IR) spectrometers equipped with various specialized sampling accessories such as flow cells or reflectance optics, nor to Fourier transform near-infrared (FT-NIR) spectrometers, nor to FT-IR spectrometers run in step scan mode.1.2.1 If the specialized sampling accessory can be removed and replaced with a standard transmission sample holder, then this practice can be used. However, the user should recognize that the performance measured may not reflect that which is achieved when the specialized accessory is in use.1.2.2 If the specialized sampling accessory cannot be removed, then it may be possible to employ a modified version of this practice to measure spectrometer performance. The user is referred to Guide E1866 for a discussion of how these tests may be modified.1.2.3 Spectrometer performance tests for FT-NIR spectrometers are described in Practice E1944.1.2.4 Performance tests for dispersive MIR instruments are described in Practice E932.1.2.5 For FT-IR spectrometers run in a step scan mode, variations on this practice and information provided by the instrument vendor should be used.1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.3.1 Exception—Informational inch-pound units are provided in 5.4.1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 The function and operation of equipment in the field often preclude the measurement of the free-field sound pressure levels of a single piece of equipment in the absence of interfering sound from other equipment operating at the same time. The two-surface method will provide, in most cases, a reliable estimate of the normal sound power levels of a specimen operating in an adverse environment.5.2 This test method is intended for use in the field in the presence of what is normally regarded as interfering background noise. This test method is based upon the work of Hubner 5,6 and Diehl,7 but differs from all other current sound power measurement procedures by requiring simultaneous measurement at both conformal surfaces and by resolving time-averaged sound pressure levels at both surfaces to within 0.1 dB. These two features, simultaneous recording and 0.1dB resolution, enable source sound power to be calculated when the direct sound field of the source is actually lower in level than the ambient noise.5.3 The use of this test method is expected to be primarily for the relative assessment of the sound power from similar sources or for the prediction of sound levels in a plant based upon measurements of similar sources in another plant. This test method is believed to be capable of yielding a reasonably good estimate of absolute power level with proper care of application and full conformance to the provisions of this procedure.5.4 The two-surface method is applicable only when the two measurement surfaces can be physically selected to produce positive values of the difference in average sound pressure level. That is, the inner surface sound pressure level minus the outer surface sound pressure level must be at least +0.1 dB. This limitation applies to each frequency band and each constituent surface area investigated. Only the frequency band in which a zero or negative difference occurs is it considered invalid and usually adjacent bands will be valid. In practice, only rarely will all three one-third octave bands of a given octave yield invalid data at all constituent areas. Therefore, less than complete results are permissible when one-third octave analysis is used and full octave results are reported.5.5 The two-surface method may not produce results when testing some very large machines in very reverberant rooms or in rooms having a volume less than about 20 times the space enclosed by an envelope around the larger dimensions of the machine. In such cases, the sound pressure level close to the machine may not decrease in any regular way with increasing distance from a machine surface, making it impossible to select two measurement surfaces producing positive differences of sound pressure level.1.1 This test method covers the field, or in situ measurement of sound power level by the two-surface method. The test method is designed to minimize the effects of reverberant conditions, directivity of the noise source under consideration, and the effects of ambient noise from other nearby equipment operating at the same time.1.2 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

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1.1 This test method establishes the procedures for measuring the ionizing radiation inside the radiation chamber of a low level X-ray security screening system. 1.2 This test method establishes minimum requirements for the radiation detector used to measure this ionizing radiation inside the radiation chamber. 1.3 The values stated in inch-pound units are to be regarded as the standard. The values given in parentheses are for information only. 1.4 This standard does not purport to address all of the safety problems, if any, associated with its use. It is the responsibility of the user of this test standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use. Specific hazards statements are given in Section 7.

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5.1 Corrosion products, in the form of particulate and dissolved metals, in the steam and water circuits of electricity generating plants are of great concern to power plant operators. Aside from indicating the extent of corrosion occurring in the plant, the presence of corrosion products has deleterious effects on plant integrity and efficiency. Deposited corrosion products provide sites at which chemicals, which are innocuous at low levels, may concentrate to corrosive levels and initiate under-deposit corrosion. Also, corrosion products in feedwater enter the steam generating components where deposition on heat transfer surfaces reduces the overall efficiency of the plant.5.2 Most plants perform some type of corrosion product monitoring. The most common method is to sample for long time periods, up to several days, after which laboratory analysis of the collected sample gives the average corrosion product level over the collection time period. This methodology is referred to as integrated sampling. With the more frequent measurements in the on-line monitor, a time profile of corrosion product transport is obtained. Transient high corrosion product levels can be detected and measured, which cannot be accomplished with integrated sampling techniques. With this newly available data, plant operators may begin to correlate periods of high corrosion product levels with controllable plant operating events. In this way, operators may make more informed operational decisions with respect to corrosion product generation and transport.1.1 This test method covers the operation, calibration, and data interpretation for an on-line corrosion product (metals) monitoring system. The monitoring system is based on x-ray fluorescence (XRF) analysis of metals contained on membrane filters (for suspended solids) or resin membranes (for ionic solids). Since the XRF detector is sensitive to a range of emission energy, this test method is applicable to simultaneous monitoring of the concentration levels of several metals including titanium, vanadium, chromium, manganese, iron, cobalt, nickel, copper, zinc, mercury, lead, and others in a flowing sample. A detection limit below 1 ppb can be achieved for most metals.1.2 This test method includes a description of the equipment comprising the on-line metals monitoring system, as well as, operational procedures and system specifications.1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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4.1 The test results enable the comparison of A-weighted sound emission from central vacuum power units when tested under the condition of this test method.1.1 This test method calculates the overall A-weighted sound power level emitted by central vacuum power units, intended for operation in domestic applications. This standard applies to the power unit only at the power unit location. To test the sound power level of a central vacuum at the user’s location, refer to Test Method F1334.1.2 A-weighted sound pressure measurements are performed on a mounted central vacuum power unit in a semi-reverberant room. This test method determines sound power by a comparison method for small noise sources, that is, comparison to a broad band reference sound source.1.3 This test method describes a procedure for determining the A-weighted sound power level of small noise sources. This test method uses a non-special semi-reverberant room.1.4 Results are expressed as A-weighted sound power level in decibels (referenced to 1 pW).1.5 The values stated in inch pound units are to be regarded as the standard. The values in parentheses are for information only.1.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.7 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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5.1 Determining the potentiometric surface of an area is essential for the preliminary planning of any type of construction, land use, environmental investigations, or remediation projects that may influence an aquifer.5.1.1 The potentiometric surface in the proposed impacted aquifer must be known to properly plan for the construction of a water withdrawal or recharge facility, for example, a well. The method of construction of structures, such as buildings, can be controlled by the depth of the groundwater near the project. Other projects built below land surface, such as mines and tunnels, are influenced by the hydraulic head.5.2 Monitoring the trend of the groundwater table in an aquifer over a period of time, whether for days or decades, is essential for any permanently constructed facility that directly influences the aquifer, for example, a waste disposal site or a production well.5.2.1 Long-term monitoring helps interpret the direction and rate of movement of water and other fluids from recharge wells and pits or waste disposal sites. Monitoring also assists in determining the effects of withdrawals on the stored quantity of water in the aquifer, the trend of the water table throughout the aquifer, and the amount of natural recharge to the aquifer.5.3 This guide describes the basic tabular and graphic methods of presenting groundwater levels for a single groundwater site and several sites over the area of a project. These methods were developed by hydrologists to assist in the interpretation of hydraulic-head data.5.3.1 The tabular methods help in the comparison of raw data and modified numbers.5.3.2 The graphical methods visually display seasonal trends controlled by precipitation, trends related to artificial withdrawals from or recharge to the aquifer, interrelationship of withdrawal and recharge sites, rate and direction of water movement in the aquifer, and other events influencing the aquifer.5.4 Presentation techniques resulting from extensive computational methods, specifically the mathematical models and the determination of aquifer characteristics, are contained in the ASTM standards listed in Section 2.1.1 This guide covers and summarizes methods for the presentation of water-level data from groundwater sites.1.2 The study of the water table in aquifers helps in the interpretation of the amount of water available for withdrawal, aquifer tests, movement of water through the aquifers, and the effects of natural and human-induced forces on the aquifers.1.3 A single water level measured at a groundwater site gives the height of water at one vertical position in a well or borehole at a finite instant in time. This is information that can be used for preliminary planning in the construction of a well or other facilities, such as disposal pits. Hydraulic head can also be measured within a short time from a series of points, depths, or elevation at a common (single) horizontal location, for example, a specially constructed multi-level test well, indicates whether the vertical hydraulic gradient may be upward or downward within or between the aquifer.NOTE 1: The phrases “short time period” and “finite instant in time” are used throughout this guide to describe the interval for measuring several project-related groundwater levels. Often the water levels of groundwater sites in an area of study do not change significantly in a short time, for example, a day or even a week. Unless continuous recorders are used to document water levels at every groundwater site of the project, the measurement at each site, for example, use of a steel tape, will be at a slightly different time (unless a large staff is available for a coordinated measurement). The judgment of what is a critical time period must be made by a project investigator who is familiar with the hydrology of the area.1.4 Where hydraulic heads are measured in a short period of time, for example, a day, from each of several horizontal locations within a specified depth range, or hydrogeologic unit, or identified aquifer, a potentiometric surface can be drawn for that depth range, or unit, or aquifer. Water levels from different vertical sites at a single horizontal location may be averaged to a single value for the potentiometric surface when the vertical gradients are small compared to the horizontal gradients. The potentiometric surface assists in interpreting the gradient and horizontal direction of movement of water through the aquifer. Phenomena such as depressions or sinks caused by withdrawal of water from production areas and mounds caused by natural or artificial recharge are illustrated by these potentiometric maps.1.5 Essentially all water levels, whether in confined or unconfined aquifers, fluctuate over time in response to natural- and human-induced forces. The fluctuation of the water table at a groundwater site is caused by several phenomena. An example is recharge to the aquifer from precipitation. Changes in barometric pressure cause the water table to fluctuate because of the variation of air pressure on the groundwater surface, open bore hole, or confining sediment. Withdrawal of water from or artificial recharge to the aquifer should cause the water table to fluctuate in response. Events such as rising or falling levels of surface water bodies (nearby streams and lakes), evapotranspiration induced by phreatophytic consumption, ocean tides, moon tides, earthquakes, and explosions cause fluctuation. Heavy physical objects that compress the surrounding sediments, for example, a passing train or car or even the sudden load effect of the starting of a nearby pump, can cause a fluctuation of the water table (1).21.6 This guide covers several techniques developed to assist in interpreting the water table within aquifers. Tables and graphs are included.1.7 This guide includes methods to represent the water table at a single groundwater site for a finite or short period of time, a single site over an extended period, multiple sites for a finite or short period in time, and multiple sites over an extended period.1.8 This guide does not include methods of calculating or estimating water levels by using mathematical models or determining the aquifer characteristics from data collected during controlled aquifer tests. These methods are discussed in Guides D4043, D5447, and D5490, Test Methods D4044, D4050, D4104, D4105, D4106, D4630, D4631, D5269, D5270, D5472, and D5473.1.9 Many of the diagrams illustrated in this guide include notations to help the reader in understanding how these diagrams were constructed. These notations would not be required on a diagram designed for inclusion in a project document.1.10 This guide covers a series of options, but does not specify a course of action. It should not be used as the sole criterion or basis of comparison, and does not replace or relieve professional judgment.1.11 The values stated in either SI units or inch-pound units are to be regarded separately as standard. The values stated in each system may not be exact equivalents; therefore, each system shall be used independently of the other. Combining values from the two systems may result in non-conformance with the standard.1.12 This guide offers an organized collection of information or a series of options and does not recommend a specific course of action. This document cannot replace education or experience and should be used in conjunction with professional judgment. Not all aspects of this guide may be applicable in all circumstances. This ASTM standard is not intended to represent or replace the standard of care by which the adequacy of a given professional service must be judged, nor should this document be applied without consideration of a project's many unique aspects. The word “Standard” in the title of this document means only that the document has been approved through the ASTM consensus process.

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5.1 Identification and Quantification of Phthalates—DBP, BBP, DEHP, DNOP, DINP and DIDP are representative of the phthalates either banned or being monitored by a variety of regulations. Regulations include: EU—Directive 2005/84/EC, US—Consumer Product Safety Improvement Act of 2008 – section 108, Japan—Health, Labor and Welfare Ministry guideline No. 336 (2010) and IEC 62321-8:2017. These test methods provide a procedure to identify and quantify phthalates in PVC.5.2 Other techniques successfully used to separate and identify phthalates in PVC include TD-GC/MS (ASTM D7823), GC/MS, HPLC/UV, HPLC/MS, FTIR, and GC/FID (flame ionization detector).1.1 This test method provides a procedure to quantify six phthalates by solvent extraction of plasticized PVC articles followed by analysis of the extract by gas chromatography/mass spectrometry. Six phthalates, BBP, DBP, DEHP, DNOP, DINP, and DIDP, are used to illustrate how to implement the method.NOTE 1: The method can be extended to other phthalates in a wide range of polymeric substrates.1.2 Within the context of this method, “low level” is defined as 1000 ppm.1.3 The values in SI units are to be regarded as standard.1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.NOTE 2: There is no known ISO equivalent to this standard.1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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