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the diaphragm diameter and, with that, also the

process connection.

To address this problem, the company has

developed a new pressure gauge for small external

areas: The model PG43SA-C measures in the low-

pressure ranges with a proportionately much smaller

diaphragm. This instrument combines the reduced con-

nection size with a further specific feature that is particularly im-

portant for such measuring requirements on tanks: It is autoclavable.

The pressure gauge can be sterilised with the vessel under saturated

steam conditions at temperatures up to +134°C, without needing to

be dismounted. The process thus remains sealed, also in the mobile

phase, and the quality assurance is preserved.

Conclusion

The more critical the pharmaceutical process – for example, produc-

tion of injection materials – the more important is the consistent

maintenance of the sterile boundary in the manufacturing process.

Risk prevention has, with the measurement technology used, an

equally high requirement as accuracy and reliability of the process.

The particular challenge is to merge the technical functionality and

physical design features into an economical solution. For pharma-

ceutical processes are getting increasingly more efficient in view of

the competitive situation – but without ever compromising safety.

dresses these issues: A diaphragm seal system

with a dual diaphragm and diaphragmmonitor-

ing removes the risks and the consequential

damages as described. Using this patented

system, the space between the two diaphragms

is evacuated and the vacuum can be monitored with

a measuring instrument.

The type of monitoring can be specified individually, de-

pending on the sensitivity of the process. With regular on-site visual

inspection, for example, it is sufficient to check a pressure gauge

with green-red display, in other cases an optical or acoustic alarm

in the control room may be required. When using media with a high

risk potential, the operator can use a pressure switch which will im-

mediately halt the process in the event of any damage.

Should the wetted diaphragm become damaged, the second

diaphragm forms a reliable seal to the process and maintains the

pressure monitoring until the damage has been rectified. Since a

break within the system is detected and reported immediately, no

microbes can get past the diaphragm undetected. Other options are

available which can mechanically or electronically identify a failure in

the diaphragm seal. If a seal is broken during maintenance or calibra-

tion the operator will immediately see this condition and will prevent

a defective unit from being reinstalled. Furthermore, the ‘alarm’ is

reported immediately in the event that the diaphragm is damaged.

This prevents a defective instrument being installed in the process.

The safety function of this self-monitoring diaphragm seal system

simultaneously optimises the protection of the non-process side: In

the event of a damaged diaphragm, no dangerous substances can

escape into the environment.

When a company uses such a device it shows due diligence that

the system is monitored through an automated system and is not

left to manual inspection of a seal area. In spite of the extremely high

level of automation in pharmaceutical processes, not everymeasuring

point absolutely has to be catered for electronically. For such cases,

diaphragm pressure gauges with flush diaphragms are particularly

worthwhile. These enable the measurement of low pressures and

are exceptionally safe in overload as a result of their design. They

keep the process sealed, even with pressure surges. Nevertheless,

operators can also prepare themselves for the case of any possible

damage to the diaphragm element. For such pressure gauges, the

company also offers diaphragmmonitoring, which will immediately

indicate any rupture in the pressure element.

Diaphragm pressure gauges are suited mainly for mobile tanks,

in which intermediate and end products are stored or transported to

the next processing stage. They monitor, for example, the filling and

the inert gas blanket. The dimensions of such containers are getting

smaller and smaller, as the pharmaceutical industry is increasingly

turning to the development andmanufacture of individual medicines.

Processes with small units and batches are the result. The measuring

instruments for the corresponding tanks therefore have limited space

available. This can quickly become tight for diaphragm pressure

gauges: The lower the pressure to be measured, the larger must be

DRIVES, MOTORS + SWITCHGEAR

P ESSURE + LEVEL MEASUREM NT

take note

Joachim Zipp is the Global Market Segment Manager Food

and Pharma at WIKA, Germany.

Enquiries: WIKA Instruments. Tel +27 (0) 11 621 0000 or

email

sales.za@wika.com

• Pressure measuring instruments are subject to the highest

safety criterion: The protection of consumers.

• Damage to instruments occurs for various reasons and

could lead to product contamination.

• A special solution which addresses all the risks has been

developed.

31

January ‘17

Electricity+Control