Emerging considerations affect fluid transfer design used in modern pharmaceutical or biotechnology processes (termed biopharm herein). These are:
Batch or continuous high performance processes
Assurance of full product/environment containment
Separation of process and mechanical equipment/environments
Cleaning validation (certified cleanability or use of disposable technologies)
Proposing a Contaminant of Concern List for Implementation of ASHRAE Standard 62.1 Indoor Air Quality Procedure
The Indoor Air Quality (IAQ) Procedure of ASHRAE Standard 62.1-2007 allows designers to reduce energy consumption by incorporating contaminant reduction measures, such as air cleaning, which in turn should reduce the required outdoor ventilation rates of a building. One key requirement ...
Determining Contaminants of Concern When Implementing ASHRAE Standard 62.1 Indoor Air Quality Procedure
The Indoor Air Quality (IAQ) Procedure of ASHRAE Standard 62.1-2007 allows designers to reduce energy consumption by incorporating contaminant reduction measures, such as air cleaning, which in turn should reduce the required outdoor ventilation rates of a building.
One key requirement of the ...
Are you or your calibration laboratory performing unnecessary calibrations on your turbine flow meters? You may be if you don't understand the concept of the Single Fluid Universal Viscosity Curve. Read this whitepaper the learn more.
Thermal fluids have proven exceptionally safe during many years of operation in a wide range of industries. However, there is no way to completely prevent fires in these systems because the major components required — fuel, air and an ignition source —
are always present by design.
The potential for a serious fire caused by the thermal fluid system can be minimized by observing sound design ...
Selection of a treatment process depends on the nature of the wastewater and the quality of the effluent desired.
Hazardous components of the wastewater may be either separated or converted to non-hazardous forms in order to allow
disposal of the wastewater effluent by conventional methods. Conversion processes can be done simply or in multiple
steps. Hazardous components which are separated from ...
Advantages of Cleaning without a Venturi in Baghouse Collectors
The cleaning cycle is the most important part of the dust collector because it controls efficiency and media life. See the best solution in dust collection and discover the advantages of a reverse-pulse jet cleaning system without a venture.
ABSTRACT: In order to clean a row of bags in a reverse pulse jet baghouse first the ...
Improving the Cleaning Cycle in Baghouse Collectors
ABSTRACT: Background The reverse pulse jet baghouse has been around for over 45 years and the cleaning cycle has not changed very much since that time. The cleaning cycle is the most important part of the dust collector because it controls efficiency and media life. In a generic baghouse, the cleaning system is comprised of a blowpipe that is ...
Ineffective Cleaning in Generic Baghouses
ABSTRACT: Background In a typical “generic” baghouse application, the cleaning is accomplished by back-flushing the filter with compressed air that travels through an orifice hole in a purge tube (blow pipe) and through a venturi. A typical generic cleaning system allows dust to be filtered at an air-to-cloth ratio of 5:1. That means for every 5 CFM of ...
In many chemical and pharmaceutical processes, solid-liquid separation, cake washing and drying steps directly impact the effectiveness of the production operation. Process engineers devote much of their time to analyzing these steps. The solid-liquid separation step can be by pressure, vacuum or centrifugation as well as in a batch or continuous mode. In this separation step, there is a further ...
The Gold Series® Camtain® containment dust and fume collector is for pharmaceutical and hazardous dust collection that fully isolates captured dust from ...
Performance Filtration Products is our manufacturing "division" where we specialize in custom OEM filtration products. From concept to completion we ...
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