Lecture15 Energybalance Intro

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Universiti Teknologi MARA

Terengganu

CHE263: Material and Energy


Balance

LECTURE 15

Energy balances - Introduction


Energy and Energy Balances

❖ Every chemical process involves the transfer of energy:


– combustion → power generation
– distillation → energy required for volatilization (reboiler) and
energy removed at condenser
– reactors → breaking and forming chemical bonds
– phase changes → evaporator and condenser

❖ Energy balances are used to:


– determine the amount of energy that flows into or out of each
process unit
– calculate the net energy requirement for the process
– assess ways of reducing energy requirements in order to
improve process profitability

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Units of Energy

❖ Energy has units of force times distance (mass[length/time]2)


Nm (=Joule) SI units
dynecm (=erg) CGS system
ftlbf British engineering system

❖ Energy also defined in terms of the amount of heat required to raise


the temperature of a specified mass of water by one degree at 1 atm

Unit Symbol Mass of H2O Temperature Interval


kilocalorie kcal 1 kg C
calorie cal 1g C
British thermal unit Btu 1 lbm F

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Forms of Energy

The total energy of a process system has


three components:
1. Kinetic Energy (KE) – energy due to the
translational motion of the system as a whole
1 2 m = mass (kg)
KE = mv  J = [kg][m/s]2
2 v = velocity (m/s)

 1 2
KE = m v  W = J/s = [kg/s][m/s]2
2
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Forms of Energy

2. Potential Energy (PE) – energy due to the


position of the system in a potential field (e.g.,
earth’s gravitational field (g=9.8 m/s2))

PE = mgz  J = [kg][m/s ][m]


2


PE = m gz  W = J/s = [kg/s][m/s ][m]
2

m = mass (kg)
z = height of object (m)
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Forms of Energy

3. Internal Energy (U) – all energy possessed by system other than


kinetic and potential energy, including the energy due to the:
– rotational and vibrational motion of molecules within the system
– interactions between molecules within the system
– motion and interactions of electrons and nuclei within molecules

❖ Internal energy (U) is related to enthalpy (H)  H = U + PV


– U and H are a function of temperature, chemical composition,
physical state (solid, liquid or gas) and only weakly a function of
pressure

❖ U and H are relative quantities


– absolute values are unknown
– values must be defined with respect to their reference state

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Transfer of Energy

In a closed system (no mass transferred


across the system boundaries (i.e., batch
system)), energy may be transferred between
the system and the surroundings in two ways:
1. Heat (Q) – energy that flows due to a
temperature difference between the
system and its surroundings
– always flows from high to low
temperature
– defined to be positive if it flows to a
system (i.e. input)
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Transfer of Energy

2. Work (W) – energy that flows in response


to any driving force (e.g, applied force,
torque) other than temperature
– defined as positive if it flows from
the system (i.e. output)
– in chemical processes, work may
come from a moving piston or
ROTATING SHAFT

A system does not possess heat or work. Heat or


work only refer to energy that is being transferred to
the system.
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Transfer of Energy
In an open system (mass transferred across
the system boundaries (i.e., continuous
system)), energy may be transferred between
the system and the surroundings in three ways:
1.Heat (Q)
2.Work (W)
3.Mass Flows –Mass flows
carries internal energy, kinetic
energy and potential energy
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Summary on Energy Balances

The First Law of Thermodynamics for a closed


(i.e. batch) system is:

U + KE + PE = Q − W

and the First Law of Thermodynamics for an


open system at steady-state (i.e., continuous)
system is:

H + KE + PE = Q − Ws

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Summary on Energy Balances
U + KE + PE = Q − W
H + KE + PE = Q − Ws
❖ Changes in kinetic and potential energy can be
calculated (usually small/negligible for chemical
systems)
❖ Heat and work input is given in the problem (or
is what you must solve for)
❖ The major task is calculating changes in U or H:
– Ch 7: Using tabulated values (steam tables)
– Ch 8: Calculate as function of phase and T
– Ch 9: Energy balances with reaction
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Problem 7.18 F&R

•Define a system and simplify the open-system energy balance


for each of the following cases. State when possible whether
nonzero heat and shaft work terms are positive or negative.
(a) Steam enters a rotary turbine and turns a shaft connected
to a generator. The inlet and outlet steam ports are at the
same height. Some energy is transferred to the surroundings
as heat.
(b) A liquid stream flows through a heat exchanger in which it
is heated from 25C to 80C. The inlet and outlet pipes have
the same diameter, and there is no change in elevation
between these points.
(c) A chemical reaction takes place in a continuous reactor
that contains no moving parts. Kinetic and potential energy
changes from the inlet to outlet are negligible.

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Example

•Five hundred kilograms per hour of steam drives a turbine.


The steam enters the turbine at 44 atm and 450C at a
linear velocity of 60 m/s and leaves at a point 5 m below the
turbine inlet at atmospheric pressure and a velocity of 360
m/s. The turbine delivers shaft work at a rate of 70 kW, and
the heat loss from the turbine is estimated to be 104 kcal/h.
Calculate the specific enthalpy change associated with the
process.

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Steam Tables
•Tables located in the back of F&R can be used to estimate U and H
for liquid water and steam (water vapour) at any specified
temperature and pressure.
•Recall the phase diagram for water:

Vapour-liquid
equilibrium (VLE)
curve or saturation
line – water may
Subcooled liquid
exist as saturated
water, saturated
steam (vapour) or
mixture of both.
superheated steam

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Steam Tables

Saturated Steam Tables: data taken along


the VLE curve or saturation line
❖ Table B.5 – properties of saturated water
and saturated steam as a function of
temperature from 0.01C (triple point) to
102C
❖ Table B.6 – properties of saturated water
and saturated steam as a function of
pressure (same data as Table B.5 but
over a much larger range of
temperatures and pressures)
CHEE 221
CHE 271 Lecture23
Lecture 14 15
Steam Tables

• Superheated Steam Table: data taken


from points below the VLE curve or
saturation line – vapour heated above its
saturation temperature

❖ Table B.7: properties of superheated


steam table at any temperature and
pressure – includes data for liquid water
(data in the enclosed region), and
saturated water and saturated steam

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Example

•Steam at 10 bar absolute and 200C is


fed to a turbine at a rate of 2000 kg/h.
The turbine operation is adiabatic, and
the effluent is saturated steam at 1 bar.
Calculate the work output of the turbine in
kilowatts, neglecting kinetic and potential
energy changes.

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