Toimialayhteisöt

This document specifies general requirements for the use and evaluation of physical and biological performance of volumetric sampling devices applied for assessing bioaerosols in the workplace.This document lists the criteria for the selection of microbial strains that can be used for the evaluation of biological performance of samplers.This document also describes a bioaerosol test facility suited for assessing the biological performance of bioaerosol sampling devices.This document is not applicable for clean room measurements.

This document describes rules for the procedures, applications, and systems of thermoluminescence dosimetry (TLD) for dose measurements according to the probe method. It is particularly applicable to solid "TL detectors", i.e. rods, chips, and microcubes, made from LiF:Mg,Ti or LiF:Mg,Cu,P in crystalline or polycrystalline form. It is not applicable to LiF powders because their use requires special procedures. The probe method encompasses the arrangement, particularly in a water phantom or in a tissue-equivalent phantom, of single TL detectors or of "TL probes", i.e. sets of TL detectors arranged in thin-walled polymethyl methacrylate (PMMA) casings.The purpose of these rules is to guarantee the reliability and the accuracy indispensable in clinical dosimetry when applied on or in the patient or phantom. This document applies to dosimetry in teletherapy with both photon radiation from 20 keV to 50 MeV and electron radiation from 4 MeV to 25 MeV, as well as in brachytherapy with photon-emitting radionuclides. These applications are complementary to the use of ionization chambers.

This document specifies the procedures for the dosimetry of X and gamma reference radiation for the calibration of radiation protection instruments over the energy range from approximately 8 keV to 1,3 MeV and from 4 MeV to 9 MeV and for air kerma rates above 1 µGy/h. The considered measuring quantities are the air kerma free-in-air, Ka, and the phantom related operational quantities of the International Commission on Radiation Units and Measurements (ICRU)[2], H*(10), Hp(10), H'(3), Hp(3), H'(0,07) and Hp(0,07), together with the respective dose rates. The methods of production are given in ISO 4037-1.This document can also be used for the radiation qualities specified in ISO 4037-1:2019, Annexes A, B and C, but this does not mean that a calibration certificate for radiation qualities described in these annexes is in conformity with the requirements of ISO 4037.The requirements and methods given in this document are targeted at an overall uncertainty (k = 2) of the dose(rate) of about 6 % to 10 % for the phantom related operational quantities in the reference fields. To achieve this, two production methods of the reference fields are proposed in ISO 4037-1.The first is to produce "matched reference fields", which follow the requirements so closely that recommended conversion coefficients can be used. The existence of only a small difference in the spectral distribution of the "matched reference field" compared to the nominal reference field is validated by procedures, which are given and described in detail in this document. For matched reference radiation fields, recommended conversion coefficients are given in ISO 4037-3 only for specified distances between source and dosemeter, e.g., 1,0 m and 2,5 m. For other distances, the user has to decide if these conversion coefficients can be used.The second method is to produce "characterized reference fields". Either this is done by determining the conversion coefficients using spectrometry, or the required value is measured directly using secondary standard dosimeters. This method applies to any radiation quality, for any measuring quantity and, if applicable, for any phantom and angle of radiation incidence. The conversion coefficients can be determined for any distance, provided the air kerma rate is not below 1 µGy/h.Both methods require charged particle equilibrium for the reference field. However this is not always established in the workplace field for which the dosemeter shall be calibrated. This is especially true at photon energies without inherent charged particle equilibrium at the reference depth d, which depends on the actual combination of energy and reference depth d. Electrons of energies above 65 keV, 0,75 MeV and 2,1 MeV can just penetrate 0,07 mm, 3 mm and 10 mm of ICRU tissue, respectively, and the radiation qualities with photon energies above these values are considered as radiation qualities without inherent charged particle equilibrium for the quantities defined at these depths.This document is not applicable for the dosimetry of pulsed reference fields.

This European standard gives rules and guidelines for the preparation of instructions manuals for mobile access and working towers in accordance with EN 1004.This standard is intended for all parties involved in the preparation of instructions for use, for example: Suppliers, technical writers, technical illustrators, translators or other people engaged in the work of conceiving and drafting such instructions for use.

This document specifies the dimensions, tolerances, required characteristics and mass of a receptacle for use in fuselage interior equipment and structural applications. This document is intended to be used in conjunction with studs according to EN 6088 or EN 6105.

This document specifies the characteristics of plain hexagonal nuts, reduced height, normal across flats, in steel, cadmium plated, for aerospace applications.Classification: 900 MPa/235 °C .

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Lausuntopyyntö koskee standardin ISO 22739 Blockchain and distributed ledger technologies - Vocabulary vahvistamista kansalliseksi SFS-standardiksi.