Betekenis van:
air cell

Voorbeeldzinnen

1. The distillate in the densimeter cell must not contain air bubbles and must be homogeneous.
2. fuel cell air independent power systems with an output exceeding 2 kW and having any of the following:
3. Fuel cell air independent power systems with an output exceeding 2 kW and having any of the following:
4. Fuel cell air independent power systems with an output exceeding 2 kW having any of the following:
5. The absolute humidity (H) of either the air in the test cell or the intake air of the engine shall be such that:
6. The air quality standard during the processing of tissues and cells is a key factor that may influence the risk of tissue or cell contamination.
7. Fuel cell air independent power systems with an output exceeding 2 kW having any of the following: a. Devices or enclosures specially designed for underwater noise reduction in frequencies below 10 kHz or special mounting devices for shock mitigation; or
8. Before the emission test driving schedule may begin, the test cell temperature shall be 266 K (–7 °C) ± 2 K, as measured in the air stream of the cooling fan with a maximum distance of 1,5 m from the vehicle.
9. The electrical circuit of the photoelectric cell and of the indicating dial shall be adjustable so that the pointer can be reset at zero when the light flux passes through the smoke chamber filled with clean air or through a chamber having identical characteristics.
10. When the activities for which accreditation/designation/authorisation or licensing is sought involve storage of tissues and cells, the storage conditions necessary to maintain the required tissue and cell properties, including relevant parameters such as temperature, humidity or air quality must be defined.
11. Unless otherwise specified in point 4, where tissues or cells are exposed to the environment during processing, without a subsequent microbial inactivation process, an air quality with particle counts and microbial colony counts equivalent to those of Grade A as defined in the current European Guide to Good Manufacturing Practice (GMP), Annex 1 and Directive 2003/94/EC is required with a background environment appropriate for the processing of the tissue/cell concerned but at least equivalent to GMP Grade D in terms of particles and microbial counts.