Water for Pharmaceutical Use

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WFI Still

图片1 .jpgProduct Details



The GMPMax multiple effect Stills produce distilled water  for injectable use whose Chemical-physical and  microbiological characteristics will be in compliance with the latest  requirements of the International Pharmacopeias including USP, EP and JP. The design criteria are in accordance with Good Engineering  Practice (GEP) guidelines, while construction criteria will follow the current  Good Manufacturing Practice (cGMP) for system planned for pharmaceutical  equipment. Supplier quality system has been certied by  ISO9001:2008 and is applicable for "design, construction, validation and after  sales services of water treatment systems, distillers and pure steam  generators

The Pharmax Still modular construction  offers a wide choice of configurations allowing optimum payback times. Standard  models range is from 60 to 22.000 lts/h output.

 

Main features of Pharmax Still

Rapid start up. The distillate is produced after only few minutes from  switch on.

Energy Savings: the best performance in terms of energy savings, due to an  extremely accurate design of the condenser/evaporators and heat recovery  system.

High Flexibility: the production capacity can be varied by up to 80%  without any plant modification.

Unique purification system: gravitational purification principle  for better guarantee of distillate purity.

Simple and clean mechanical construction:  baffle free decontamination  chamber - no welding. Granting the best inspectability, minimized corrosion  risk, for the longest expected life of equipment.

Extremely limited maintenance. No moving parts, expansion joints or mechanical  seals.

Compact construction and low weight.  Little extra head room needed  for dismounting and inspection.

Up to ten effects, for maximum energetical efficiency.

 

Operating Principle

The Pharmax Still is based on the “Thin Falling Film” and  Multi-stage principles ingeniously combined.

The first effect is fed by an external energy source  (Industrial Steam or Electrical energy).

The pure steam generated in the each effect and the non  evaporated water are fed to the subsequent one operating at lower pressure; pure  steam is condensed into WFI vaporizing a new portion of feed  water.

WFI Stills are provided with one pre-heater for each  column recovering the sensible heat of the distillate, and two final exchangers.  In the final condenser a degassing system is also  integrated

WFI conductivity is continuously measured and, in case of  “out of spec”, the produced WFI is automatically discharged to the drain. On  line TOC monitoring is also possible.

The production capacity can be adjusted in the range of  60-100% by simply acting on the industrial steam pressure.

 

Construction Characteristics

The plant is completely made in AISI 316L stainless steel.  Standard finishing of the active surface is pickled and passivated; mirror or  electropolishing can be made on request. Product (WFI) contact parts are  manufactured with surface finishing 0.6 microns Ra mechanically polished, with  piping orbitally welded with sanitary flanges and pharmaceutical grade Teflon  gasket.

The design and construction of the decontamination  chamber, which is a totally empty column, ensure the best inspectability. The  absence in this area of welding dramatically reduce the risk of corrosion, for a  very long expected life of the equipment.

Pre-heaters and exchanger are shell-and-tube type; double  tube sheet execution is foreseen where contamination of the distillate is  possible. The pipes are expanded into the plates, avoiding any welding for a  totally hygienic execution, and a better resistance against dilatation  stress.

The general construction design, coupled with the  described decontamination process, ensure a very high flexibility in equipment  layout, together with an extremely limited space needed for  maintenance.

 

Endotoxyn reduction

A unique and careful design of the  decontamination chamber allows us to grant the highest performances in terms of  endotoxyn content reduction.The gravitational separation system has proven to be  an extremely simple and simultaneously effective process for the separation of  the contaminants from the pure steam.

Challenging the system with increased endotoxin  levels in the feed water has proven the capability of Pharmax Still to reduce  endotoxyn level by log 6 (1.000.000 times).

 

Pharmax Still effect design

Pharmax Stills are equipped with effect of unique and original design.  Each effect consists of a tube condenser on top and a decontamination chamber  below, joined by a flanged connection which also has the function of Support.  The column is therefore free to expand without any  restraint.

The decontamination chamber is a completely  empty column without any baffle or mechanical separation device. The  decontamination of the steam is obtained by exclusively gravitational  separation: the produced steam separates into pure vapour ascending the height  of the decontamination chamber at low speed, allowing the impure water droplets  to fall to the bottom of the column under simple gravitational force. The  contaminants remain thus in the feed water.

 

THERMODYNAMIC PRINCIPLE - HEAT  RECOVERY

The heat recovery system in Pharmax Still is  the result of a careful mechanical and thermodynamic  study.

The thin falling film process inside the  evaporators/condensers grants the highest efficiency in heat and mass transfer.  This process is coupled with the short tubes technology, which ensures the best  wettability of the exchange surface.

In addition, GMPMax Pharmax Still is equipped  with individual and separate pre-heaters for each effect, independent from the  evaporators/condensers, thus achieving the highest sensible heat recovery, and  finally the best energetically efficiency

 

 

 

 

 

 

 

Key  Words:

Pharmaceutical Machinery, Pharmaceutical Engineering,  Pharmaceutical Equipment,
Packaging Machinery, GMP Machinery, Pharmaceutical  Industry, Pharmaceutical Technology

cGMP Service, cGMP Solutions, cGMP Validation

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