UL 2821
UL GREENGUARD Certification Program Method for Measuring and Evaluating Chemical Emissions From Building Materials, Finishes and Furnishings

DETAILS
Edition Number:1SCC Approved:--
Edition Date:2013-03-29DOD Approved: --
Price Code:AANSI Approved: --
Type:ule

  • SCOPE

    1 Scope

    1.1 This methodology provides a standard means of reproducibly and accurately testing building materials and products under a realistic, yet highly controlled, atmosphere.

    1.2 This method may be used for certification solely by UL and its affiliated entities in the UL GREENGUARD certification program. Accordingly, only UL or its affiliated entities can determine and declare whether a product is in compliance with the requirements in this method. Any purported determination or declaration of testing, conformance, compliance or certification to this method by any other party is null and void and cannot be used to meet the requirements of this method.

    1.3 The methodology measures total volatile organic compounds (TVOC), individual volatile organic compounds (IVOCs), formaldehyde, and the other aldehyde emission levels from materials using test conditions defined to simulate product use in realistic commercial office, educational, healthcare and/or residential settings.

    1.4 The level of total or individual volatile organic chemical emissions is determined by observing the TVOC, IVOC, or aldehyde concentration in a dynamic environmental chamber under specified test conditions.

    1.5 The observed chamber concentration is then converted by a mathematical calculation to an emission rate, a product specific variable, and then modeled to obtain room concentration estimates.

    1.6 The quantity of VOCs in the environmental chamber air is determined by gas chromatography/mass spectrometry. The methodology is generally applicable to volatile organic compounds with boiling points from 60°C to 290°C emitting from individual products.

    1.7 Emissions of selected aldehydes are measured using reverse-phase high-performance liquid chromatography (HPLC) with UV detection.

    1.8 Specialized analysis of chamber air samples are conducted for other specific target chemicals as required for a specific product/project requirement.

    1.9 The methodology with standardized measurement and analyses provides consistent testing of materials within a product group.

    1.10 This protocol applies to any material belonging to a product category generally used within an enclosed indoor environment. This includes, for example, paints, other architectural coatings, sealants, adhesives, wall coverings, floor coverings, wood paneling, ceilings, furniture and furniture components used in public and commercial office buildings, schools, medical buildings, residences and other building types. The protocol applies to products that are to be tested whole or by a representative component or material in an environmental chamber.

    1.11 This methodology is applicable for newly manufactured products before they are used in construction or furnishing. (See Appendix 2 for more information.)

    1.12 This method establishes the procedures for product sample collection, emission testing and analysis, indoor air concentration modeling and associated documentation requirements.

    1.13 This method also establishes performance criteria for specific chemicals of interest.

    1.14 While this practice lists specific chemicals and associated maximum allowable concentrations, as required by criteria indoor air procedures and specifications, it does not assess the human risk involve with use of the materials either as an installer and/or as an end user.

    1.15 This practice does not purport to address safety concerns, if any, associated with the use of this practice. It is the responsibility of the user of this protocol to establish required safety and health practices and determine the applicability of regulatory limitations prior to use.

  • TABLE OF CONTENTS
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    • Transmittal
    • Table of Contents
      • Body
        • GENERAL
          • 1 Scope
          • 2 Objectives and Use
            • 2.1 Objectives
            • 2.2 Use
          • 3 References and Documents
          • 4 Acronyms and Abbreviations
          • 5 Definitions
          • 6 Symbols
        • PRODUCT SAMPLE COLLECTION, PACKAGING, SHIPMENT, AND DOCUMENTATION
          • 7 Purpose
          • 8 Personnel
          • 9 Representative Sample
          • 10 Sample Preservation
          • 11 Location of Sampling
          • 12 Sample Age
          • 13 Customized Sample Preparation
          • 14 Sample Collection Procedures
            • 14.1 Tile and Plank Products
            • 14.2 Sheet and Roll Goods
            • 14.3 Rigid Panel Products
            • 14.4 Insulation
            • 14.5 Batts and Rolls
            • 14.6 Boards and Rigid Foam Products
            • 14.7 Blowing Wools and Loose Fill Products
            • 14.8 Spray Foam Insulation
            • 14.9 Containerized and Wet Products
            • 14.10 Furniture and Other Large Products
          • 15 Packaging and Shipment of Samples
          • 16 Chain of Custody Documentation
          • 17 Receipt of Samples by Laboratory
          • 18 Rejection of Samples by Laboratory
          • 19 Storage of Samples by Laboratory Prior to and Following Testing
            • 19.1 Before Testing
            • 19.2 After Testing
        • LABORATORY SAMPLE PREPARATION AND ANALYSES
          • 20 Test Specimen Preparation
          • 21 Furniture Testing
          • 22 Sample Preparation
            • 22.1 Furniture Component Materials
            • 22.2 Textiles
            • 22.3 Foams/cushions and substrates (e.g. particleboard)
            • 22.4 Wood finish, finished wood and wood veneers, laminates/backers
            • 22.5 Furniture Component Assemblies
            • 22.6 Workstation Panels
            • 22.7 Worksurfaces
            • 22.8 Storage Fronts
            • 22.9 Seat Cushions/Seat Backs
            • 22.10 Wood Seating Components
            • 22.11 Workstation Systems, Seating Units, and Individual Furniture Items
            • 22.12 Movable Walls
            • 22.13 Seating Units, Individual Furniture Items andWorkstation Systems
          • 23 Preparation of Paint Test Specimens
          • 24 Preparation of Adhesive Product Test Specimens
          • 25 Preparation of Caulking Product Test Specimens
          • 26 Selection and Preparation of Dry Product Test Specimens
          • 27 Preparation of Dry Product Test Specimen Assemblies
            • 27.1 Laminates (all types) wood veneers, or backers applied with adhesives:
            • 27.2 Sheet and tile type resilient flooring applied with adhesives
            • 27.3 Carpet tile and broadloom carpet applied with adhesives
            • 27.4 Vinyl and other wallcovering products applied with adhesives
          • 28 Preconditioning of Products Prior to Testing
          • 29 Environmental Chamber Testing
            • 29.1 Facilities
            • 29.2 Equipment
            • 29.3 Chamber Sizes
          • 30 Environmental Chamber Performance Requirements
            • 30.1 Principle
            • 30.2 Test Conditions
            • 30.3 Duration
            • 30.4 Apparatus and Facilities
            • 30.5 Clean air supply and flow control
            • 30.6 Chamber and materials
            • 30.7 Procedures
            • 30.8 Air Sampling
            • 30.9 Sampling Media
          • 31 Chemical Analyses
            • 31.1 Principle
            • 31.2 Analytical Instruments
            • 31.3 Methods for Individual VOCs
            • 31.4 TVOC Method
            • 31.5 Identification of Individual VOCs
            • 31.6 Analytical Calibrations
            • 31.7 Quantifiable Limit (QL)
          • 32 Calculations
            • 32.1 Emission Factor Calculations
            • 32.2 Exposure Modeling
            • 32.3 Conversion to ppm
        • TARGET CHEMICALS AND MAXIMUM ALLOWABLE CONCENTRATIONS
          • 33 UL GREENGUARD Indoor Air Quality Product Certification
          • 34 GREENGUARD Gold and CDPH/EHLB/Standard Method V1.2
          • 35 Individual VOC ACGIH TLV and CA CREL Criteria Limits
        • REQUIRED ELEMENTS OF THE LABORATORY TEST REPORT
          • 36 The Report of the Test Results Should Contain the Following Sections
        • TABLES
    • APPENDIX A
    • APPENDIX B Informative
    • APPENDIX C
    • Appendix D Informative FURNITURE AUTHENTIC CALIBRATION LISTS