3.1 The purpose of this guide is to provide information that may be considered when selecting and qualifying a cleaning agent for oxygen-enriched systems.3.2 Insufficient cleanliness can result in the ignition of contaminants or components by a variety of mechanisms. Therefore, an acceptable level of contamination for each condition of use in oxygen-enriched service should be defined. The acceptable level of contamination may depend on various factors, such as:3.2.1 The nature and type of the contaminants,3.2.2 The location and degree of contamination,3.2.3 The type of substrate material,3.2.4 The configuration and end use of the equipment or part to be cleaned, and3.2.5 The operating parameters of the oxygen-enriched system (pressure, temperature, phase, concentration, fluid velocity, etc.).1.1 The purpose of this guide is to establish a procedure to select cleaning agents, both solvents and water-based detergents, for oxygen-enriched systems. This includes laboratory-scale tests for cleaning effectiveness, materials compatibility, and oxygen compatibility.1.2 The effectiveness of a particular cleaning agent depends upon the method by which it is used, the nature and type of the contaminants, and the characteristics of the article being cleaned, such as size, shape, and material. Final evaluation of the cleaning agent should include testing of actual products and production processes.1.3 Different cleaning agents may be required for different cleaning activities, such as aqueous ultrasonic cleaning, spray cleaning, hand wiping, and flushing of oxygen lines in field applications.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 Significance: 4.1.1 Collection system maintenance requires allocating cleaning resources to the right place prior to system failure (sanitary sewer overflows, mainline blockages, and building backups). Transmissive acoustic inspection provides a tool to assist in allocating cleaning resources by prioritizing pipe segments based on their blockage assessment and thereby facilitating efficient cleaning resource allocation.4.1.2 This standard practice provides minimum requirements and suggested practices regarding the transmissive acoustic inspection of gravity-fed sewer line blockage assessment to meet the needs of maintenance personnel, engineers, contractors, authorities, regulatory agencies, and financing institutions.4.2 Limitations and Appropriate Uses: 4.2.1 The blockage assessment provided by the transmissive acoustic inspection may not resolve the type of blockage(s) within the pipe segment nor resolve the location(s) of the blockage(s) within the pipe segment.4.2.2 Due to the physics associated with transmissive acoustic inspection, the blockage assessment may be confounded due to:(1) Structural designs resulting in poor acoustic coupling,(2) Pipe segments completely filled with water, for example, full pipe sag or inverted siphon, and(3) Transient conditions within the pipe, for example, active lateral discharge or temporary flow surcharges.These issues are addressed as part of the performance criteria specified in X1.5.4.2.3 Due to physics associated with acoustics and trade-offs in equipment design for conducting transmissive acoustic inspection, there are limitations based on the following pipe segment attributes:(1) Pipe diameter,(2) Pipe segment length,(3) MH depth, and(4) Flow levels.Inspections conducted outside the manufacturer’s recommended ranges for these pipe segment attributes may result in the transmissive acoustic blockage assessment deviating from the performance criteria specified in X1.5.4.2.4 Inspections conducted between non-adjacent MHs, for example, skipping an intermediate MH, may result in the transmissive acoustic blockage assessment deviating from the performance criteria specified in X1.5.1.1 This practice covers procedures for assessing the blockage within gravity-fed sewer pipes using transmissive acoustics for the purpose of prioritizing sewer pipe cleaning operations.2 The assessment is based on an acoustic receiver measuring the acoustic plane wave transmitted through the pipe segment under test in order to evaluate the blockage condition of an entire segment and to provide an onsite assessment of the blockage within the pipe segment. (1, 2, 3, 4, 5)31.2 The scope of this practice covers the use of the transmissive acoustic inspection as a screening tool. The blockage assessment provided by the acoustic inspection should be used to identify and prioritize pipe segments requiring further maintenance action such as cleaning or visual inspection, or both. Thereby, also identifying the pipe segments which are sufficiently clean and do not require additional maintenance action.1.3 This standard practice does not address structural issues with the pipe wall.1.4 The inspection process requires access to the manhole (MH) from ground level. It does not require physical access to the sewer line by either the equipment or the operator.1.5 This standard practice applies to all types of pipe material.1.6 The inspection process requires access to sewers and operations along roadways or other locations that are safety hazards. This standard does not describe the hazards likely to be encountered or the safety procedures that must be carried out when operating in these hazardous environments.1.7 The values stated in inch-pound units are to be regarded as standard. The values given in parentheses are mathematical conversions to SI units that are provided for information only and are not considered standard.1.8 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.1.9 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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This guide suggests methodology for cleaning tests. Soil/substrate combinations are generally designed to be analogous to soiled surfaces commonly encountered. This methodology can be used with most soil/substrate combinations. Some example test methods that have worked well in other labs are provided in the annexes. There is no requirement for using the soils listed in the annexes. It is the responsibility of the user to select the appropriate battery of tests for the desired end results. The results of tests based on this guide are regarded as diagnostic screening values useful in formulation studies, quality control, and ingredient raw material qualification. This guide is intended to allow a choice in test conditions and soil/substrate combinations appropriate to the evaluation at hand. For interlaboratory comparisons, exact test conditions must be established before test results are compared. This guide is applicable to testing all types of multipurpose household cleaners, whether the detergent is prepared by dissolving a soluble powder, a dilutable liquid, or is a pre-diluted product. It may also be useful for evaluation of products or conditions normally associated with industrial or institutional cleaners.1.1 This guide covers the evaluation of the cleaning per- formance of products intended for use on resilient flooring or washable walls. Such evaluations specifically exclude windows, mirrors, carpets, ceramic tiles, and laminated counter tops. This guide provides techniques for soiling, cleaning, and evaluating performance of detergent systems under con- trolled, but practical, hard-surface cleaning conditions. 1.2 Such systems include any detergent intended for clean- ing hard surfaces such as resilient flooring, washable wall surfaces, and other hard surfaces, but excluding glass, ceramic, or other glossy surfaces. They may consist of solutions of soluble powdered detergent, dilutions of concentrated liq- uid detergent, or products intended to be used full strength, for example, foams, sprays, liquid, or paste. 1.3 There is no universal soil/substrate combination that is representative of the many soil-removal tasks required of this type of cleaner in actual use conditions. Choice of soil/ substrate and cleaning conditions should be by agreement between the testing laboratory and those using the data to evaluate cleaning performance relative to user experience. 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 and health practices and determine the applicability of regulatory limitations prior to use. Material Safety Data Sheets are available for reagents. Review them for hazards prior to usage. Specific precautionary statements are given in Note 2.

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5.1 This practice is suitable for the removal of contaminants found on materials, parts, and components used in systems requiring a high level of cleanliness, such as oxygen. Parts shall have been precleaned to remove visible contaminants prior to using this procedure. Softgoods such as seals and valve seats may be cleaned without precleaning.5.2 This procedure may also be used as the cleanliness verification technique for coupons used during cleaning effectiveness tests as in Test Method G122.5.3 The cleaning efficiency has been shown to vary with the frequency and power density of the ultrasonic unit. Low frequencies in the 20 kHz to 25 kHz range have been found to damage soft metals such as aluminum and silver. Therefore, the specifications of the unit and the frequencies available must be considered in order to optimize the cleaning conditions without damaging the parts.1.1 This practice covers a procedure for the cleaning of materials and components used in systems requiring a high level of cleanliness, such as oxygen, by ultrasonic techniques.1.2 This practice may be used for cleaning small parts, components, softgoods, etc.1.3 The values stated in SI units are 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. Specific precautionary statements are given in Note 1.1.5 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 This guide describes the use of test methods in Guide F3276 to assess the compatibility of a brush part with the material substrates used in the construction of medical devices.5.2 By providing objective, repeatable methods for evaluating performance under test conditions, this standard can improve the ability to assess the effectiveness of various brush part designs.1.1 This guide describes methods for assessing the compatibility, under prescribed laboratory conditions, of a cleaning brush part with substrate materials used in the construction of medical devices. The method utilizes a force tester to mechanically actuate a brush part at a constant rate. This action continues until there is any level of visible degradation, including but not limited to scratching or shaving of the substrate material.1.2 The test methods utilized in this guide are those described in Guide F3276. In this guide, the number of repetitions is determined by the demonstrable degradation, if any, of the substrate, up to a specified maximum number of repetitions.1.3 Brushes designed to clean medical devices after clinical use play an important role in the effective reprocessing of those medical devices. Instructions for use from the brush manufacturer should supply information related to the compatibility, or more importantly, incompatibility with materials that make up the composition of a medical device. This may be stated in terms of being suitable for specific materials, not suitable for specific materials, or suitable for a limited number of uses for specific materials.1.4 Selecting the correct brush for the medical device to be cleaned is always a key factor to achieve effective cleaning. One of the significant factors when selecting a brush is selecting one that will not cause damage to the medical device, including the material the medical device is constructed of. Assessing if a brush part could damage a medical device because of the material the device is made of is an important step in determining the appropriate (and inappropriate) use of a brush.1.5 Units—The values stated in SI units are to be regarded as the standard. No other units of measurement are included in this standard.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 test method is intended for testing the porcelain enamel finish on oven parts of self-cleaning ranges.4.2 The numerical values and visual evaluation derived by this test method are used to measure differences in heat resistant characteristics between enamel formulas intended to meet oven manufacturer specifications.1.1 This test method covers the procedure for the qualitative and quantitative evaluation of static heat effects on porcelain enamel coatings.1.2 This test method is adaptable to various temperatures and times, since the requirements in the porcelain enameling industry differ between manufacturers.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 This guide provides information on how to select the test soil(s) that best simulates clinical use for devices. The test soil(s) selected for the validation should be clinically relevant and simulate what the device/component will come into contact with during the clinical procedure.5.2 This guide will help standardize the test soils used by medical device manufacturers when validating the cleaning procedures of reusable medical devices and reprocessing equipment5.3 For devices that come into contact with blood, the simulated test soils are blood-based soils, such as those described under 7.1.1-7.1.2.5.4 For devices that come into contact with mucus, the simulated test soils are those described under 7.1.3.5.5 For devices that come in contact with soils of a source other than the patient (e.g., bone cement), the simulated test soils should be similar to those described in 7.2. These can be used alone or in combination with 7.1.5.6 A combination of test soils may be used (e.g., blood with mucus) to simulate clinical soiling. For example, flexible endoscopes may come in contact with a different combination of sources of soiling (e.g., gastrointestinal (GI) tract, vasculature for biopsies) during clinical use.5.7 Any simulated test soil(s) or formulations can be used for simulated use testing but shall be scientifically justified by the medical device manufacturer.1.1 This guide describes methods for selecting test soils for cleaning validations based upon the characteristics of the soil, the physical characteristics of the device, and the clinical use of the device.1.2 This guide describes the preparation and use of some test soils for the validation of cleaning instructions for reusable medical devices.1.3 Reusable medical devices such as endoscopes, arthroscopic shavers, surgical instruments, and suction tubes are exposed to biological soils during clinical use. Preparation of these devices for reuse requires cleaning and disinfection and/or sterilization as applicable. Adequate cleaning is the first step in a process intended to prevent contaminant transfer to the next patient and medical practitioner. The soils, if inadequately removed, can interfere with disinfection and sterilization processes, as well as performance of the device. Acceptance criteria are based either on a visual assessment or quantitatively specified marker(s) endpoint(s) of the soil or both (ISO/TS 15883-5, Section 1). Endpoints after cleaning should be based upon possible interference with disinfection/sterilization, risk to the patient or health care worker from the contaminant during further handling, and endpoints for cleaning established in the scientific literature.1.4 The test soils are designed to simulate the contaminants that medical devices are likely to come in contact with during clinical use. The test soils discussed in this guide are a mixture of constituents that simulate what is commonly found in human secretions, blood, tissue, and bone fragments/shavings as well as non-patient derived soil (e.g., bone cement, lubricants, and dyes) during clinical procedures. The test soils also simulate the physical parameters (e.g., viscosity, adhesion) of clinical material to which the medical devices will be exposed.1.5 Exclusion: 1.5.1 This guide does not include methods to validate cleaning processes to remove residues from manufacturing1.5.2 This guide does not describe the soil/inoculum used for validation of disinfection or sterilization instructions. Disinfection or sterilization validation requires separate testing that is independent of cleaning validation studies.1.5.3 Test soils described are not intended for use by health care facilities to verify the effectiveness of their cleaning process.1.5.4 The test soil recipes are not intended to encompass every biological residue with which a medical device is likely to come into contact.1.6 Test soil formulations not described in this guide may be clinically relevant and may be more appropriate for simulated-use testing depending upon the clinical use of the medical device. The burden is upon the medical device manufacturer to determine and justify scientifically the selection of test soil(s).1.7 The values stated in SI units are to be regarded as the standard. No other units of measurement are included in this standard.1.8 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.1.9 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 This practice will be suitable to direct the preparation of test coupons with a known amount of contaminant on the surface. A standard test coupon is described and a list of contaminants that have typically been found in oxygen-enriched systems and components is provided.5.2 These test coupons shall be used in the evaluation of cleaning agents for oxygen-enriched systems and components. This will permit direct comparison within and between test facilities.5.3 Materials used in other fluid handling systems such as nitrogen, helium, hydrogen, gasoline, etc. may also be prepared for evaluation by this practice.1.1 This practice describes the procedure for the preparation of single- and double-sided contaminated test coupons for the evaluation of cleaning agents. It is applicable for the evaluation of cleaning agents proposed for the cleaning of oxygen equipment, pharmaceutical manufacturing equipment, and medical devices (see Test Method G122 and Guide G127). It also is applicable to other systems where contamination is a concern.1.2 Several classes of contaminants/residues most likely to be found in oxygen equipment, pharmaceutical manufacturing equipment, and medical devices are identified. However, if the user of this practice has identified contaminants not included in these classes, such identified contaminants may be substituted for the preparation of the test coupons if appropriate for this test method.1.3 Solvent and cleaning agent compatibility with nonmetallic substrates should be verified prior to the preparation of the test coupons. Typical nonmetallic materials utilized in oxygen systems are contained in Guide G63.1.4 This practice may involve hazardous materials, operations, and equipment. This practice does not purport to address all of the safety concerns associated with its use. It is the responsibility of whomever uses this practice to consult and 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 purpose of these test methods is to define a procedure for evaluating the capability and effectiveness of cleaning agents to remove residues of a compound/product from surrogate surfaces (that is, coupons or beakers) of Materials of Construction. This test method also provides a procedure for determining the compatibility of cleaning agents with the Material of Construction prior to starting tests. Based on the outcome of the testing, suitable cleaning agents may be selected for further cleaning process development (see Guide D6361/D6361M).5.2 The potential critical cleaning parameters related to the cleaning agent(s) under study may also be examined using these tests. Potentially critical cleaning parameters include cleaning agent concentration, temperature, time, pH, foaming, type and strength of ultrasonic energy or agitation (if used), and others. These parameters may be varied (for example, using Design of Experiments) to determine their potential optimal settings for actual use.1.1 This test method covers a procedure for evaluating the effectiveness and capability of cleaning agents to remove contamination to the desired level. This includes removing drug residues from manufacturing equipment and residues from medical devices (Guide E3106), as well as systems for oxygen service.1.2 The test coupons/beakers described in this standard provide a representative surface to which contamination can be applied and tested for the ability of a cleaning agent to remove it.1.3 This test method is a laboratory scale approximation and the actual effectiveness of a particular cleaning agent depends upon the method (temperature, agitation, concentration, etc.) in which it is used and the characteristics of the article being cleaned, such as size, shape, and material. Final evaluation of the cleaning agent should include testing of actual products and cleaning processes.1.4 Units—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.1.5 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 safety of each compound on a case-by-case basis.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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This test method describes a procedure for determining the penetration of aerosols through a one- or twostage HEPA filter installation. Testing multiple filter stages as a single unit eliminates the need for: installation of auxiliary aerosol bypass ducts, installation of aerosol injection manifolds between filter stages, and entry of test personnel into contaminated areas. It provides for filter testing without interruption of plant processes and operation of ventilation systems. The procedure is applicable for measuring penetrations requiring sensitivities to 0.1 μm. A challenge concentration of 2.5 × 10 5 particles/cm3 (p/cm3), is required for evaluation of one-filter stage, and 2 × 106 p/cm 3, or about 30 μg/L (assuming unit density), is required to properly evaluate a two-stage HEPA filter system as one unit. This test method can determine the penetration of HEPA filters in the particle-size range from 0.1 to 0.2 μm where the greatest penetration of particles is likely to occur.1.1 This test method covers the procedure and equipment for measuring the penetration of test particles through high-efficiency particulate air (HEPA) filter systems using a laser aerosol spectrometer (LAS). This test method provides the capability of evaluating the overall effectiveness of HEPA filter systems consisting of one or two filter stages. 1.2 The aerosols used for testing have a heterodisperse size distribution in the submicrometer diameter range from 0.1 to 1.0 μm. 1.3 The purpose for conducting in-place filter testing by this test method is in the ability to determine penetration of multi-stage installations, without individual stage tests. Particle penetration as low as 10−8 can be measured by this test method. Also, the LAS provides a measure of penetration for discrete particle sizes. 1.4 Maximum penetration for an installed HEPA filter system is 5 × 10−4 for one filter stage, and 2.5 × 10−7 for two stages in series is recommended. Note 1—Acceptance penetration criteria must be specified in the program, or owners specifications. The penetration criteria suggested in this test method is referenced in Ref (1). 1.5 The values stated in SI units are to be regarded as the standard. 1.6 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 standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use. Specific precautionary statements are given in 9.6.

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4.1 Hydraulic cleaning methods include equipment that uses water and water velocity to clean the invert and walls of Thermoplastic Sewer Pipe.4.2 The practice of high-velocity sewer cleaning is best described as a hydraulic cleaning method that uses water pressure to remove obstructions and deposits in sewers or storm drains.4.3 There are different configurations of high-velocity sewer-cleaning machines. These units can generate variable water pressures up to 5000 psi (34 MPa) and variable flow rates of 50 gal per min (gpm) to 125 gal per min (gpm) (180 L per min to 473 L per min).4.4 The water tank capacity on these units varies from 1000 gal to 1500 gal (3785 L to 5678 L).4.5 The hose lengths vary between 500 ft and 1000 ft (152 m and 305 m) in length with a diameter of 3/4 in. to 11/4 in. NPT.4.6 There are a number of different nozzles and tools that may be used during the cleaning process.4.7 Some high-velocity sewer cleaners have a vacuum conveyance system that uses large fans or positive displacement vacuum pumps for material removal capabilities. With this type of system, material can be vacuumed from the manhole into a debris tank as it is brought back with the jet or tool and taken to a disposal area. These systems can be either trailer- or truck-mounted and are generally known as combination machines.4.8 The Occupational Safety and Health Administration (OSHA) has set guidelines for the safe removal of hazardous and nonhazardous substances as stated in OSHA Section 5 of Public Law 91-596; OSHA 29 USC 654; 29 CFR 1910.120; as well as DOT CFR 49 Parts 106–107, 171–180, and 390–397.1.1 This practice covers the personnel requirements, operator training, Environmental Protection Agency (EPA) Guidelines, operating procedures, and recommended equipment performance/design for the proper operation of pressure water-jet cleaning and cutting equipment as normally used by municipalities and contractors concerned with operations, maintenance, and cleaning work of Municipal Thermoplastic gravity sewer pipe.1.2 The term high-pressure water jetting within this practice covers all water jetting, including the use of jets and hydro mechanical tooling at pressures below 2000 psi (0.69 MPa).1.3 This practice covers the high-pressure water jetting of Thermoplastic pipe and should not be applied to other pipe and pipe-lining materials without evaluating the recommended cleaning procedure from the pipe manufacturer to avoid damage.1.4 This practice applies to High-Density Polyethylene, Polypropylene, and Polyvinyl Chloride (HDPE, PP, and PVC) Thermoplastic sewer pipe manufactured in accordance with ASTM Standards. It may also be considered for use for any similar thermoplastic pipe products not covered by this list but with similar performance characteristics.1.5 The values stated in inch-pound units are to be regarded as standard. The values given in parentheses are mathematical conversions to SI units that are provided for information only and are not considered standard.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. Some specific hazards statements are given in Section 5 on Hazards/Safety.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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The procedure used for etching the copper foil from the base insulating materials may significantly affect the results of electrical tests. This is true primarily for two reasons. First, the geometry of the copper which remains and forms the electrodes is in part determined by the etching procedure; this is particularly true of closely spaced electrodes on the same surface when the property to be measured depends on the electrode geometry. Second, electrical conductance in the material, particularly surface conductance, may be affected by the chemicals used to etch the copper, the length of time of etching, and the manner in which the specimen is cleaned after etching. This practice standardizes the etching procedure in order to provide a basis for comparison of electrical properties of copper-clad electrical insulating materials and thermosetting laminates. Experience has shown that the test circuit can be accurately prepared using this procedure, and that the specimen will be substantially free of etching-induced, electrically-conductive contaminants. It is recognized that commercial processes utilized to manufacture printed circuits may differ appreciably from this practice. Therefore, the results of tests on specimens etched in accordance with this practice may differ from results obtained on specimens etched in a commercial process. Specimens should be etched in accordance with a procedure different from this practice, if it is desired to determine the influence of the different procedure on electrical properties.1.1 This practice describes a procedure for etching and cleaning copper-clad electrical insulating materials and thermosetting laminates for electrical testing.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. For specific warning statements see 6.3 and 6.4.

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4.1 Cleaning provides well documented benefits in terms of creating cleaner, safer, and healthier surroundings by extracting harmful pollutants from the indoor environment (see Ref (3)). An improperly maintained indoor environment could give rise to biological contaminants, and buildup of particulate matter and gases which can have serious health effects. These negative impacts may have adverse affects on worker productivity affecting both cleaning personnel and tenants through increased complaints, absenteeism, injuries, asthmatic incidents, or other symptoms. Inappropriate or improper use or selection of cleaning products and processes, along with failure to follow label directions could result in injury or illness to cleaning personnel or building occupants. In addition, it may be detrimental to the physical structure and systems of the building, or to the environment. Moreover, owners and operators maintain the liability for the proper function of the building and its impacts on the occupants and cleaning personnel.4.1.1 This guide provides a basic reference for the development and preservation of a building environment that is considered safe and healthy for occupants, while reducing the stress on the overall environment as a result of routine maintenance. The anticipated users of this guide include building managers, cleaning personnel, product suppliers and distributors, union representatives, and building occupants who serve together in a stewardship role regarding the maintenance of the building. This guide is intended to raise pertinent questions regarding specific building environments in order that an appropriate stewardship strategy may be developed, for example:4.1.1.1 How is the building used?4.1.1.2 Are there any special cleaning requirements?4.1.1.3 Are there any at-risk populations that need to be considered, such as children, asthmatics, or pregnant woman?4.1.1.4 How are cleaning materials used?4.1.1.5 Are there any special issues relevant to construction and furnishings?4.1.1.6 Are there any issues relating to building age/architectural, such as historic preservation requirements?4.1.1.7 are there any engineering concerns, such as HVAC systems and natural ventilation?4.1.1.8 How is the quality of cleaning being evaluated or measured?4.1.2 Regardless of the specific requirements, this guide will help in the formulation of a comprehensive plan resulting in reduced risk to cleaning personnel, building occupants, and the environment.4.2 This guide will help the building owner and operator understand the cleaning process through the following:4.2.1 The development of a stewardship plan (see Section 6), will clarify the level of cleanliness that is required or expected, and will ensure that the cleaning process is carried out in a consistent manner with adequate communication feedback to promote success of the plan.4.2.2 An understanding of extended product responsibility (see Section 7) and the importance of shared responsibility. This section includes task identification and performance requirements, process and product selection, use, storage, and disposal.4.2.3 An identification of the training and communications issues (see Section 8) that will encourage involvement with the entire chain-of-commerce in the cleaning process. These issues are related to both procedural training and feedback opportunities for cleaning personnel, as well as information sharing with building tenants to inform them of possible cleaning process impacts.1.1 This guide covers a procedure to assist owners and operators of commercial and institutional buildings in the stewardship of cleaning and housekeeping operations. The focus of this guide is to address appropriate cleaning activities and processes, to promote eco-efficiency and sustainability, and to avoid adverse impacts on the building occupants, cleaning personnel, the building structure itself, and the environment. Adherence to the principles set forth in this guide can lead to greater tenant/occupant satisfaction, reduced operational costs and greater productivity (of occupants and cleaning personnel).1.2 This guide will focus on the development of a stewardship plan and will include the assessment of cleaning processes, product selection, storage, usage, disposal, equipment, training of cleaning personnel and communication throughout the chain-of-commerce.1.3 This guide addresses issues relating to the operation and maintenance of the heating, ventilating and air conditioning (HVAC) systems which can have a major impact on indoor air quality (IAQ) only to the extent that the HVAC system provides adequate ventilation to lower risk to cleaning personnel, building occupants and the environment during or as a result of the cleaning process.1.4 This guide is for use in a building that is maintained by either in-house cleaning personnel or an outside cleaning contractor.1.5 This guide is not intended for construction related activities, but may be appropriate for post construction clean-up.1.6 This guide is not intended as a procedural guide for cleaning personnel.1.7 This guide is not intended for use in residential buildings.1.8 The values stated in inch-pound units are to be regarded as standard. No other units of measurement are included in this standard.1.9 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.1.10 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.1.11 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.

定价： 590元 / 折扣价： 502 元 加购物车

4.1 Surface cleaning is necessary to prepare clay brick masonry surfaces for application of coatings intended for water repellent protection. Surface cleaning helps to ensure proper adhesion or even penetration of the coating and to prevent unintended sealing-in of stains.4.2 This practice addresses surface cleaning only. Other preparation or remedial repairs, such as repointing the masonry or replacing of units, may be necessary and must be completed prior to application of the water repellent treatment.1.1 This practice covers non-abrasive surface cleaning of clay brick masonry to remove surface contaminants such as dirt, grease, loose material, soot, fly ash, hydrocarbon residues, algae, etc. in preparation for the application of water repellent coatings without damaging or altering the surface appearance of the clay brick masonry.1.2 Procedures included in this practice are water cleaning, detergent water cleaning, pressurized water cleaning, steam cleaning, and acid cleaning. It is not intended for the cleaning of newly constructed brick masonry. Use of procedures described in this practice may not be appropriate where the surface is of a historical nature.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 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 hazard information see Section 5, 6.4.1.1, and 6.4.1.2.1.5 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.

定价： 515元 / 折扣价： 438 元 加购物车

1 Scope This clause of part 1 is replaced by: This standard deals with the safety of electric cleaning appliances for household use which are intended for cleaning surfaces such as windows, walls and empty swimming pools by using liquid cleansing a

定价： 637元 / 折扣价： 542 元