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Secrets To Explosion Safety In Pharmaceutical Processing

By Kevin Spiess of BS&B Safety Systems

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Kevin Spiess of BS&B Safety Systems explains how different explosion containment methods work together to protect against explosive disasters in pharmaceutical manufacturing.

Kevin Spiess of BS&B Safety Systems
By Kevin Spiess of BS&B Safety Systems

Dust explosions are well-known to be highly destructive in various sectors; grain and wood mill explosion accidents are the most commonly reported due to their devastating effects. Not far behind is food processing, cited as the cause of 24% of all dust borne explosions in the UK, according to statistics in 2011 by specialists in process safety management and loss prevention, HFL Risk Services. Such dust-related accidents can rip a factory or facility apart and in the worst case, take lives.

The same explosion risks are also present during the handling, storage and processing of pharmaceutical raw materials and bulk powders. It’s even a little higher, as some pharmaceutical raw materials are extremely combustible, more so than food-based organics or wood dusts.

Dust explosions occur when an ignition source ignites combustible organic material that is fuelled with oxygen in a closed atmosphere. This can take place inside a silo, process or storage enclosure, or even originate in pulverising or grinding process equipment. It takes only milliseconds for a violent explosion to occur after a rapid pressure rise in process equipment.

If such an explosion occurs in a confined space, such as a storage vessel, or a compounder, then a subsequent rise in explosive pressure can have devastating consequences.

In 2003 when a major pharmaceutical facility in the US was virtually destroyed by a chain of propagating dust explosions, six lives were lost and 36 employees were injured on the site.

The shock wave broke windows up to 300 metres away. The damage was so great that the exact point of ignition could not be determined in the ensuing investigation.

There were various theories discussed about how the explosion started and it was decided that most likely, powdered polyethylene was to blame; the ignition supposedly originated in processing equipment that used this substance to coat rubber strips.

However, this equipment was known to have suffered several internal fires previously, including one that generated enough force to blow off a mixer door.

Regardless of the mystery, there was no doubt that an originating spark was the cause. Dust cloud accumulation in the atmosphere did the rest.

Pharmaceutical Explosion Safety – The importance of testing your dust

In the UK and Europe, there is a requirement to identify any potentially explosive substances in the workplace. In the UK this requirement is governed by the Dangerous Substances and Explosive Atmospheres Regulations 2002 (DSEAR). Both DSEAR and ATEX recognise dusts as explosive risks.

Before applying any kind of explosion protection, we always recommend to our clients that they test their dust. In the pharmaceutical industry, it’s not just question of protecting against dusts with high explosibility ratings, (measured as Pmax), even though that is a primary consideration.

One must also take into account the nature of the substances being processed and whether their escape into the atmosphere poses a toxic risk, as well as an explosive one. There may be steroids, hormones or narcotics that through direct exposure could cause harmful effects to employees.

Different types of dust have different particle sizes, properties, ignition temperatures, and ignition sources. Dusts are given explosion severity classifications; St1 to St3. ‘Not specified’, means the material is non-explosive and St3 is the most explosive type of material.

Dust testing is designed to identify two key performance characteristics of dust, which in turn influence explosion protection equipment design and their application as well.

The first measures maximum pressure of a dust explosion (Pmax in bar)
The second identifies the speed of the rise in explosive pressure (Kst in m/sec)

The Health & Safety Executive’s (HSE) guidelines Safe Handling of Combustible Dusts, gives examples of typical dust particle sizes; wheat has an average particle size of 80 µm; wood flour is 65µm; and tissue paper is 54µm. Magnesium at 28µm, has a classification of St3 and is highly combustible.

Magnesium powder has a Kst value of approximately 500 Bar.m/s. In comparison, wheat flour, only has a Kst value of around 110 bar m/s – a significantly slower rate of explosion pressure rise. Nonetheless, as we know from high profile grain mill explosions, it is still a significant explosive danger.

However, in comparison, there are common substances used in pharmaceutical manufacture with higher Kst values, such as:

  • Cellulose: 229 Bar.m/s
  • Corn starch: 202 Bar.m/s
  • Dextrin: 168 Bar.m/s
  • Organic pigments: 73-288 Bar.m/s

Because the above substances have Kst values significantly higher than wheat flour dust, it’s not hard to see the obvious explosion risk is associated with pharmaceutical production It is also necessary to determine what the dust’s Minimum Ignition Temperature (MIT) is, while being subjected to any processes.

In other words, what temperature will the dust withstand before it becomes an ignition risk? All aspects of the dust’s behaviour in relation to its process environment can be determined to inform the correct precautionary measures against a potential explosion.

BSB Boom Explosion Safety

Match the protection to the risk

Assuming that you have carried out dust testing and determined all its key performance characteristics, then it’s time to apply the correct protective solutions. There is a myriad of explosion protection solutions available and they are effective when handling the majority of organic dusts.

As we have established, dusts have different explosive properties, and are handled and stored in different ways and locations. Therefore, the protective measures in each location should be tailored to meet the associated risk.

The different explosion protection options include:

Spark detection devices: 

Sense hot particles, sparks and flames that could become the ignition source for a fire or explosion. They can include automated shut-down systems to interrupt the feed of combustible material along the process equipment.

All processes may be monitored by an operative via a control panel to assess any further risks. Spark detection is particularly useful to manage fire and explosion risks in process equipment, such as dust collectors, bins and silos.

Chemical suppression systems: 

Designed to detect the pressure wave at the very start of an explosion and deliver dry, inert chemical extinguishing agents, such as sodium bicarbonate, into a developing internal deflagration.

Chemical suppression systems: 

Designed to detect the pressure wave at the very start of an explosion and deliver dry, inert chemical extinguishing agents, such as sodium bicarbonate, into a developing internal deflagration.

These suppression systems can be activated either by pressure, optical or vent sensors. Any deflagration travelling through interconnected equipment is quickly and efficiently extinguished, preventing any spreading explosion damage.

Flame-freeâ„¢ vents: 

Also known as flameless vents, is the preferred passive method to relieve explosive pressure in a process or storage vessel containing combustible materials.

It is not always practical or safe to vent the pressure and flame to a particular area, therefore these vents intercept, quench and retain all burning materials, preventing them from expelling into the atmosphere. They are particularly useful for dust collectors, bins and bucket elevators.

One or a combination of these measures may be applied in a factory or facility that processes dust generating, organic materials.

Explosion management

Explosion containment (or isolation) is always a desirable option in the pharmaceutical industry as everything is withheld in the process. However, this means that the pharmaceutical plant must be built to withstand maximum explosive pressure – this is usually around 10-12 Bar.m/s.

As this protective option tends to be quite expensive, companies may choose to build a part of their facility to this specification and adopt other solutions like chemical suppression and flame freeâ„¢ venting.

Advanced chemical suppression and isolation systems often work in tandem. They are designed to detect and extinguish an explosion at a very early stage (the point of ignition), and extinguish it using chemical agents.

Chemical extinguishing systems offer extremely efficient and rapid protection. They can easily prevent a deflagration from propagating (prevent transition to detonation) through ducts, piping and connected equipment thereby preventing any spreading explosion damage.

They can be employed most effectively when there is no risk of compromising the quality of pharmaceutical raw materials when they are exposed to a chemical extinguishing agent during a primary explosion event.

However, mechanical isolation only works when a primary explosion is allowed to take place. It may sound counter-productive, but in the long run it could save on substantial material and economic loss.

BSB Installed Cannon for explosion protection

How mechanical isolation works:

Mechanical isolation is a cleaner means of explosion protection. There are no additional agents being fired into the process equipment to stop an explosion.

Toxic dusts are prevented from escaping, in spite of the initial explosion taking place. Explosive pressure is diminished by use of isolation valves. So when an explosion actually occurs, the pressure travels into either into a single or double acting valve (depending on your required specification), which seals the pressure wave inside the valve and prevents it from spreading throughout the equipment.

There are two methods of mechanical isolation:

Passive isolation: 

Does not require detectors, or control and indicating equipment. This method may include the use of arrestor mesh, rotary valves, lock valves, rotary screws, flap valves or diversion valves.

Active isolation: 

Activated by detectors and electrical control and indicating equipment. Examples would be pinch valves, chemical Isolation or fast acting valves.

Advanced isolation valves are manufactured with pharmaceutical-grade housing which makes it easy to clean any surfaces that come into direct contact with the products being processed.

All valves have an explosive rating that is higher than that of the dust being processed. Hence the importance of dust testing in the first instance to determine what that maximum Pmax would be.

The other vital reason for ensuring primary explosion containment in equipment is the risk of explosion propagation from dust in the atmosphere.

There is no substitute for exercising good housekeeping in factory facilities. Regular removal of dust accumulations in the factory space is a primary safety precaution against explosions but it’s commonly overlooked as a practice.

Dust that accumulates in eaves, ceilings spaces and beams is fuel waiting to propagate a secondary explosion. Up to one ton of accumulated dust was recorded as the fuel for that devastating pharmaceutical site explosion in 2003.

Investigations revealed that dust had collected in the ceiling spaces and workers were unaware that the risk was even above their heads. So when the primary explosion occurred, uncontained, there was fuel waiting in the rafters to proliferate it. As we know, the consequences were fatal for many employees.

Whether dealing with valuable or volatile raw materials, there are explosion protection options that tick the boxes relevant to each respective facility. Always undertake due- diligence and risk assessments to inform appropriate preventative measures.

A crucial supply chain, from manufacturer to end-user, depends on taking every precaution to ensure safety and uninterrupted productivity. By not being diligent, you risk harm to workers on the factory floor and patients on the hospital ward who depend on the safe production and access to vital pharmaceutical products.

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    Phil Black - PII Editor

    I'm the Editor here at Process Industry Informer, where I have worked for the past 17 years. Please feel free to join in with the conversation, or register for our weekly E-newsletter and bi-monthly magazine here: https://www.processindustryinformer.com/magazine-registration. I look forward to hearing from you!

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