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Process Safety, Health and

Environment
CN3135
Ramasami Sundaresan
(Rama)

25/8/2014

NUS CN3135: Fire & Explosion 2

Lecture # 2
Fires and Explosions:
Prevention & Mitigation
Concepts

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Learning Outcomes
1. Describe and identify fire and explosion
hazards in chemical processes
2. Analyse and assess the potential impacts of
these hazards on safety and health of
People, The Environment and Property.
3. Develop methods for controlling process
hazards to minimize fire and explosion risks.
4. Design measures to safely mitigate the
consequences of process incidents
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Scope of Lecture


Inerting

Use of Flammability Diagrams

Static Electricity

Controlling Static Electricity

Ventilation

Explosion Proof Equipment & Instrumentation

Sprinkler Systems

Miscellaneous Design for Preventing Fires &


Explosions
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Prevention & Mitigation Strategy


Threefold prevention and mitigation Strategy


Prevent flammable mixture

Prevent initiation of fire

Minimize damage from fire or explosion

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Bases for Prevention & Mitigation




Prevention


Triangle of Combustion

Fuel combustible or explosive material

Oxygen or oxidant

Heat source of ignition

Mitigation


Arresting the combustion reaction

Containing the energy/effects

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Means of Achieving Prevention and


Mitigation


Prevention


Inerting

Use of Flammability Diagram

Static Electricity & Control


Ventilation





Explosion-proof Equipment & Instrumentation

Mitigation


Sprinkler & Other Fixed Systems

Other Design features

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Inerting
Adding an inert gas to a combustible vapour
mixture to reduce concentration of oxygen below
the limiting oxygen concentration (LOC).


Generally applicable LOC:




Gases:

about 10%

Dusts:

about 8%

Commonly adopted safety margin: 4% below LOC




Gases:

about 6%

Dusts:

about 4%

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Vessel Inerting Protocol




Vessel is emptied and initial inerting done before flammable


material is charged.
Inerting system required to maintain inert atmosphere in the
vapour space above liquid and positive pressure to prevent
air ingress:


Automatic inert gas addition feature to control the oxygen concentration below the LOC (minimizes inert gas)
o

Analyzer to continuously monitor oxygen concentration in


relationship to the LOC

Controlled inert gas feed system to add inert gas with safety
margin

Simple regulator based system to maintain fixed positive inert


pressure in the vapour space
o

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Maintains constant outflow of inert gas to avoid air inflow.


NUS CN3135: Fire & Explosion 2

Methods of Initial Vessel Purging


Several purging methods used to initially reduce
the oxygen concentration to the low set point:


Vacuum Purging,

Pressure Purging,

Combined Pressure-Vacuum Purging,

Vacuum & Pressure Purging with impure Nitrogen,

Sweep-Through Purging, and

Siphon Purging

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Vacuum Purging


Most common inerting procedure for process vessels of


robust construction
Reactors generally designed for full vacuum (-760 mm Hg
gauge or 0.0 mm Hg absolute)
Method not suitable for large, atmospheric tanks


Withstand only very low external pressure - few inches water column

Steps in vacuum purging process:




Drawing a vacuum on the vessel until the desired level

Relieving the vacuum with an inert gas (nitrogen or carbon dioxide)


to atmospheric pressure

Repeating above steps until desired oxygen concentration is


reached.

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Tank Implosion Due to Vacuum

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Vacuum Purging Cycles

P r e s s u r e

End of first
vacuum purge

End of second
vacuum purge

PH

PL
Oxygen
Concentration
is Constant

Number of Moles
of Oxygen is
Constant
Time

Figure 7-1 Vacuum purge Cycles

Initial oxygen concentration - y0

Vessel is initially at pressure PH and is vacuum-purged applying the


vacuum at pressure PL.

Cycle is repeated until target oxygen concentration y1 is reached.


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Vacuum Purging
Total moles at each pressure (ideal gas behaviour):
Atmospheric pressure:

 =

 
 

(7-1)

Vacuum pressure:

 =

 
 

(7-2)

Oxy moles @ atm:

( )1 =  

(7-4)

Oxy moles @ vac:

( )1 =  

(7-3)

Dalton's Law: In a mixture of non-reacting gases, the total pressure exerted is


equal to the sum of the partial pressures of the individual gases

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Vacuum Purging
As vacuum purging cycle is repeated:


Oxidant moles remain the same as at vacuum state;

Nitrogen moles increase.

New (lower) oxidant concentration is calculated using equation 7-5

This process is repeated until desired (reduced) oxidant concentration level


is achieved.


The concentration after j purge cycles (vacuum and relief) is given by


the following general equation:

(7-6)
Please review Example 7-1 Pg. 312

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Pressure Purging


Vessels can be pressure-purged by adding

Inert gas, generally N2, is fed into vessel under pressure.

Gas is diffused throughout the vessel and vented down to


atmospheric pressure.
More than one pressure cycle may be necessary to reduce
the oxidant content to the desired concentration.
Cycle repeated to reduce the O2 concentration to a target
level are shown in Figure 7-2.
Vessel is initially at PL (atmospheric) and is pressurized using
a source of pure nitrogen at PH.
Objective is to determine the number of pressure purge cycles
required to achieve target (reduced) O2 concentration.
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Pressure Purging Cycles

P r e s s u r e

End of first
pressure purge

End of second
pressure purge

PH

PL
O2 Concentration
is Constant

Number of Moles of
Oxygen is Constant

Time

Figure 7-1 Pressure purge Cycles

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Pressure Purging


Pressurization phase: As pure N2 is used, number of O2 moles remains


constant, but mole fraction decreases.
Depressurization phase: Composition of the gas remains constant, but
total number of moles is reduced; O2 mole fraction remains unchanged.
Equation 7-6

applies here as well to determine O2 concentration after j purge cycles


(pressure and vent)


nL is now the total moles at atmospheric pressure (low pressure)

nH is the total moles under pressure (high pressure).

Initial concentration of oxidant in the vessel (y0) is computed after the


vessel is pressurized (the first pressurized state).
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Combined Pressure Vacuum Purging





Both pressure and vacuum purging may be used simultaneously.


The computational procedure depends on whether the vessel is first
evacuated or pressurized.
(7-6)
Pressurefirst cycle

Start

Start

Time
Figure 7-3 Vacuum-pressure purging
with initial Pressurization.

Vacuumfirst cycle

Time
Figure 7-4 Vacuum-pressure purging
with initial evacuation.

Equation 7-6 is directly applicable but number of cycles j is the number of cycles
after the initial evacuation.

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Vacuum & Pressure Purging with


Impure Nitrogen
Nitrogen separation processes available today do not provide pure nitrogen;
typical purity is around 98%+ range.
Equations for pure nitrogen are not applicable.
Assuming N2 contains O2 with a constant mole fraction of yoxy total moles of
O2 present at the end of the first pressurization is given by the moles initially
present plus the moles included with the nitrogen
(7-9)
Arising from this the generalized equation for O2 concentration after j
pressure cycles is:
(7-12)
Equation 7-12 is used in place of 7-6 for both pressure and vacuum purging.
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Advantages & Disadvantages




Pressure purging is faster because pressure differentials are


greater. However uses more gas than vacuum purging
Vacuum purging uses less inert gas because oxygen
concentration is reduced primarily by vacuum
Combined pressure-vacuum purging has the advantage of
less nitrogen used compared to pressure purging, especially
if the initial cycle is a vacuum cycle

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Sweep-Through Purging





Adds purge gas into a vessel at one opening and withdraws


the mixed gas from the vessel to the atmosphere from another
opening
Commonly used when vessel not rated for pressure or
vacuum
Purge gas is added and withdrawn at atmospheric pressure
The volumetric quantity of inert gas required to reduce the
oxidant concentration from C1 to C2 is Qvt, and it is determined
using:
C1 C0
Qv t = V ln

C
0
2

(7-12)

V is vessel volume
C is concentration of oxidant within vessel (mass or volumetric units)
C0 is inlet oxidant concentration (mass or volumetric units)
Qv is volumetric flow rate
t is time
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Siphon purging


Sweep-through process requires large quantities of nitrogen


making the method expensive
Siphon purging is used to minimize the purging expense by
significantly reducing the inert gas expended
Starts by filling vessel with a liquid - water or any liquid
compatible with product
Purge gas is added to the vapour space of the vessel as the
liquid is drained from vessel


Volume of purge gas = volume of the vessel,

Rate of purging = volumetric rate of liquid discharge.

First filling vessel with liquid and then using sweep-through


purge to remove O2 from the residual head space is cost
effective.
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Flammability Diagram (6-6)




Diagram constituents


The Three Sides: Fuel, Oxygen and Inert Material (N2)

In volume or mole %

Significance of the tick marks

The Air Line

From point a1: Fuel = 0% Oxygen = 21%, Inert gas (N2) = 79%

To a2: Fuel = 100% Oxygen = 0%, Inert gas (N2) = 0%

Equation: % =

Stoichiometric Line

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x !"#$% % + 

(6-17)

Represents all stoichiometric combinations of fuel + oxygen

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Flammability Diagram (6-6)


a1

s1

s2

a2
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Static Electricity


Sparks resulting from static charge build-up and sudden discharge is a


common ignition source within chemical plants.
Due to its insidious nature, static electricity is perhaps the most elusive of
ignition sources.
Serious explosions and fires by static ignition causes continue to plague the
industry despite considerable expenditure and effort.
Prevention measures depend on the following for success:
 Understanding the fundamentals of static charge across the workforce
 Designing specific features to prevent the accumulation of static charge
 Differentiating those situations where static build-up is inevitable
 Where static build-up is unavoidable design (engineered) features are
added to continuously and reliably inert the atmosphere where static
sparks are likely.
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Static Electricity Fundamentals




Static charge buildup is a result of physically separating a poor conductor


from a good conductor or another poor conductor.

Electrons move across the surfaces of materials in contact

An imbalance in electrons results upon separating the materials

one material becomes positively charged and the other negatively charged
 If both the materials are good conductors, the charge build-up as a result
of separation is small due to the ease of transfer
 If one or both are insulators or poor conductors, electrons are not as
mobile and are trapped on one of the surfaces
 The magnitude of the charge is much greater.
There are many household examples that result in a build-up of a static
charge e.g. walking across a rug, removing a sweater, etc.
Tendency for charge to build up is greater in dryer climate

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Industrial Static Electricity Hazards










The intensity of static hazards in industry is brought about by


the nature of materials handled, their sheer bulk and
continuous operations and repetitive motions.
Common examples:
Pumping a non-conductive liquid through a pipe
Mixing immiscible liquids
Pneumatically conveying solids
The resulting static charges accumulate to develop large
voltages.
Subsequent grounding produces large and energetic sparks.
Dangerous energy near flammable vapors

0.1 mJ

Static buildup by walking across carpet

20 mJ

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Electrostatic Relationships
Factors Surrounding a Static and Discharge


Strength of the electrical field produced by the static


charges

Electrostatic potential

Capacitance

Relaxation times

Currents and potentials in flow systems

Others

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Charge Accumulation Processes




Contact and Frictional charging




Separation of two materials after being in contact

Double layer charging occurs at microscopic scale




Solid Liquid (including pipe wall)

Gas Liquid

Liquid - Liquid

Induction Charging


Involving electrically conducive media including humans

Common occurrence in tank truck operations

Charging by Transport


Free falling

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Static Charge & Ignition Prevention




Two materials at different potentials or polarities come close


enough together to generate a charge transfer.
In an explosive environment this sudden transfer of charges
may be energetic enough to be an ignition source.
Prevention of ignitions


Charges accumulate on objects and dissipation

Means of discharge by means of charge transfer, and

Estimate the resulting energy in relation to the minimum ignition


energy (MIE) of the explosive environment.

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Occurrence of Electrostatic Discharges




Discharge to ground or oppositely charged object when




Field intensity exceeds 3MV/m (breakdown voltage of air), or

Surface charge density exceeds 2.7 X 10-5 C/m2

Methods of discharge (6):




Spark between metal objects

Propagating brush - from grounded conductor to charged insulator


(conductor backing)

Conical pile powdery material at high fill rate (0.5kg/s)

Brush between sharp pointed conductors (0.1 100 mm)

Lighting like from cloud in air above powder

Corona discharge similar to brush, energy sufficient to ignite only


sensitive gases.

Estimate the resulting energy in relation to the minimum ignition energy


(MIE) of the explosive environment.
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Energy from Electrostatic Discharges

Figure 7-12 Minimum ignition energies


compared to electrostatic discharge energies.
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Energy of Electrostatic Ignition Sources




A spark is generated between two conductors when



the distance between the conductors is small compared to the
diameter of the conductors, and
 when the electric field intensity between the conductors is
approximately 3 MV/m.
A brush discharge is generated if the distance between the conductors is
large compared to the radius of curvature of the conductor.
The energy of a spark discharge is a function of


the accumulated charge (Q in coulombs) on the object,

the capacitance of the object (C in farads), and

the potential, or voltage (V in volts) of the object.

These variables are related by the expression C = QIV. The actual energy
(expressed in joules) associated with the discharge process is given by

'=
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()
)*

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(7-20)
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Streaming Current





Streaming current Is is the flow of electricity produced by transferring electrons


from one surface to another by a flowing fluid or solid
When a liquid or solid flows through a pipe (metal or glass), an electrostatic
charge develops on the streaming material
The larger the pipe / the faster the flow, the larger the current
The relationship between a liquid streaming current and the pipe diameter, pipe
length, fluid velocity, and fluid properties is given by

(7-21)
where
IS is the streaming current (amps), u is the velocity (m/s), d is the pipe diameter (m),
L is the pipe length (m), and T is the liquid relaxation time (seconds).


The relaxation time is the time required for a charge to dissipate by leakage. It
is determined using

+, +
=
-.
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(7-22)
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Controlling Static Electricity





Ignition energy focussed measures are designed to:


Reduce rate of charge generation
 Reduce flow rates
 Low energy discharges
Increase the rate of charge relaxation
 Relaxation tanks after filters, enlarged section of pipe before
entering tanks
When static charge build up cannot be avoided, focus is on limiting
oxidant level
 Prevent ignition by inerting the surroundings
 Measure generally adopted when working with flammable liquids
that are 5C (or less) below the flash point (closed cup).

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Controlling Static Electricity


Measures targeted at specific risks


Prevent sparks by eliminating the buildup and accumulation of static


charge by
Sparking: Grounding and bonding ()
Propagating brush discharges: Keeping non-conductive surfaces or
coatings thin or increasing conductivity

Conical pile discharges: Decreasing the charge rate below 0.5 kg/s

Brush discharges: Keeping non-conductive surfaces

Lightning like discharges: Keeping vessel volumes below 60 m3

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Explosion-Proof Equipment & Instruments





All electrical devices are inherent ignition sources.


Special design features are required to prevent electrical
devices from igniting flammable vapors and dusts.
Fire and explosion hazard is directly proportional to the
number and type of electrically powered devices in a
process area.
International guidelines e.g. US National Electric Code
(NEC), Institute of Electrical and Electronics Engineers
(IEEE) are adopted to ensure safe practices.
Two important principles of electrical safeguard in the
chemical industry are:
 Explosion-Proof Housing
 Area and Material Classification
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Ventilation


Well designed Ventilation is an effective means of fire and


explosion prevention measure as it will ensure vapour
concentrations below the explosive range
Open-Air Plants take advantage of natural ventilation to
dilute flammable discharges from processes.
In-Building Plants require carefully designed mechanical
ventilation systems conforming recommended specification
of air-flow and air-changes requirements

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Sprinkler Systems



Sprinkler systems are an effective way to contain fires.


The system consists of an array of sprinkler heads
connected to a water supply.
The heads are mounted in a high location (usually near
ceilings) and disperse a fine spray of water over an area
when activated.
The heads are activated by a variety of methods. A
common approach activates the heads individually by the
melting of a fusible link holding a plug in the head
assembly.
Once activated, the sprinklers cannot be turned off unless
the main water supply is stopped.

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Other Fire and Explosion Prevention Concepts















Active and Passive Fire Protection


Fireproofing
Separation Distances
Emergency Response & Pre-Incident Plans
Evacuation Arrangement & Assembly Areas
Water Supplies & Fire Pumps
Utilities
Emergency Shutdown Systems
Fail Safe Design
Emergency Power Supply
Redundancies
Industry Mutual Aid Arrangement
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