The LPP 3-in. peristaltic pumps incorporate a unique patented rolling design, which eliminates friction, maximizes hose life and lowers energy consumption. The roller is mounted on an eccentric cam, creating eccentric rotation during the 360-deg. operating cycle. Compared to conventional peristaltic pumps, the LPP pumps generate 100% more flow per compression, with a flow capacity of up to 176 gal/min and a maximum operating pressure of 110 psig.
The corrosion-resistant Series HA 3x2 and EH 3x2 centrifugal pumps come in both horizontal and vertical configurations. Available in high-temperature polypropylene or chlorinated polyvinyl chloride (CPVC) for superior corrosion resistance, the pumps handle flows to 400 gal/min or 170 ft of total dynamic head. The fully enclosed primary impeller provides high hydraulic efficiency at low horsepower.
Fourteen different ball valves in the TRIAC family feature a live-loaded packing system that meets the TA-LUFT emissions standard of less than 1 ppm, enabling these valves to reduce fugitive emissions and lost product by 99% or more compared to legacy control valves. They employ a unique live-loaded pyramidal stem-packing system having a patented 45-deg. pyramidal stem, a stem seal with Belleville washers, and Grafoil stem packing.
Capable of measuring NOx and O2 at high temperatures, the INM-700 in situ NOx/O2 monitor uses a zirconium oxide (ZrO2) sensor and non-extractive point measurement. The INM-700 is designed for use in coal-fired boiler applications, such as near-combustion-point readings, or for control of selective catalytic reduction (SCR) systems. The monitor enables operators to use balancing/combustion tuning to identify gas stratification problem areas. With this feature, problems can be corrected to improve burner efficiencies and reduce NOx emissions.
The Sta-Pure gasket provides excellent dimensional stability, which is crucial for increasing sealing reliability in critical bioprocess applications. Its design uses a patent-pending, 100% expanded polytetrafluoroethylene (EPTFE) microstructure that helps achieve the low particulation/spalation and leachable/extractable profiles required for aseptic processing. Its durable construction enables it to withstand repeated clean-in-place/sanitize-in-place (CIP/SIP) cycles.
This sanitary diaphragm-valve actuator comes standard with lightweight thermoplastic/stainless-steel hybrid construction. Optional full stainless-steel construction is available. Its three actuator heads cover sizes 0.5–2.0 in. The actuator has a swivel feature that allows a 360-deg. orientation of the air inlet — the actuator flips, allowing easy access for changing product functions.
Custom-molded Pharma fabricated tubing assemblies simplify manufacturing. They are produced to the customer’s exact specifications, using silicone tubing with a variety of connectors, including the manufacturer’s Silastic biomedical-grade elastomer. Compared with assemblies fabricated onsite, these reduce costs and lower the risk of contamination.
Suitable for media and viral filling and sampling applications, AdvantaFlex biopharmaceutical-grade tubing can be aseptically sealed in seconds. The material can be welded directly to biobag containers, which eliminates the need for silicone tubing grafts. It contains fewer extractables than other tubing and complies with USP Class VI, FDA, ISO and European Pharmacopoeia standards. It has been formulated for low permeability and is free of silicone oils and animal-derived ingredients. Complete validation and extractables test portfolios are available.
CleanFLOW ball valves are engineered to be a piping component to specifically meet the demanding processes found in the pharmaceutical, biotech, semiconductor, cosmetics, food and other industries, where particle generation and contamination can threaten the outcome of the product. The port opening of the valve’s flow path is dimensionally identical to the adjacent tubing. This “Tube-ID” feature provides predictable flowrates and pressure drops and ensures thorough cleaning and full drainability as mandated by ASME/BPE.
The Continuous Drug Pelleting system fully integrates extrusion and spheronization processes to continuously convert drug formulations into free-flowing spheres of a controlled shape and size. Its compact Type 316 stainless steel design makes it suitable for use in good manufacturing practice (GMP) suites. Its components, which are easily accessible for cleaning and maintenance, include a PLC-based control system with the manufacturer’s XT-CDP CFR 21, Part 11-compliant controls.
