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  • Criteria for Obtaining Specified Humidity and Temperature Conditions
    Providing a specified humidity and temperature for testing or process control can. be difficult and reaching the TAPPI (Technical Association of the Pulp and Paper. Industry) prescribed testing atmosphere of 23°C +1°/50% RH ±2% can be close. to impossible. Even TAPPI acknowledges, "the required
  • Complying with ICH Guidelines Involving Temperature and Relative Humidity
    monitors the conditions. at that single location in your room, chamber, or section of ductwork. The. information from this sensor indicates the control constancy of the. conditioner/controller system but it does not provide information on the conditions. in other areas of the conditioned space.
  • Verifying Temperature and Humidity Controls in a Wine Cellar
    CAS DataLoggers recently provided the environmental monitoring solution for a homeowner who wanted to check the climate control system installed in his 2-room wine cellar. Accurate temperature monitoring is crucial to wine quality. What the owner needed was an affordable temperature and humidity
  • Pressure Transducer Usage for Environmental Chamber Pressure Measurement for Test and Measurement Calibration Labs
    Calibration labs often require very specific knowledge of local environmental conditions. Environmental chambers present the ability to control a room's precise pressure, temperature, humidity and photo-stability or light levels. Standard electronic controls for most environmental chambers mean
  • U. S. Holocaust Memorial Museum - Case Study
    to.". The success of the project earned Liebert an invitation to provide the environmental control. system for a new computer room at the U.S. Holocaust Memorial Museum. "The equipment is very reliable, but what drove us to go with Liebert again was their. excellent customer service," says Philizaire
  • Inorganic Packaging and Drying
    Because of the refinement of our moisture control technologies, GFS has built a world-class reputation in the manufacture of anhydrous fine chemicals, specialty chemicals and temperature-sensitive chemicals. We have a state-of-the-art dedicated dry room for production and packaging, where constant
  • Medical Device Link .
    , none states what products or processes require such an environment. A cleanroom is designed to enable manufacturers to control particulate contamination, temperature, and, where necessary, humidity. It controls the introduction, generation, and retention of particles in the room, protecting
  • Medical Device Link .
    is determined by a complex function of time, temperature, humidity, light, oxygen, and vibration, proper packaging can control many of these variables. For example, light- and humidity-resistant foil packages can minimize the effects of humidity and light. Such packages

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