Escolar Documentos
Profissional Documentos
Cultura Documentos
Much
of
the
work
of
chemists
involves
monitoring
the
reactants
and
products
of
reactions
and
managing
reaction
conditions
1.1:
outline
the
role
of
a
chemist
employed
in
a
named
industry
or
enterprise,
identifying
the
branch
of
chemistry
undertaken
by
the
chemist
and
explaining
a
chemical
principle
that
the
chemist
uses.
1.4:
present
information
about
the
work
of
practicing
scientists
identifying
the
variety
of
chemical
occupations,
and
a
specific
chemical
occupation
for
detailed
study.
Analytical
Chemist
Works
for
Sydney
Water
Monitoring
Services
- Environmental
and
water
monitoring
services
to
protect
the
environment
and
public
health.
- Monitoring
includes:
monitoring
all
influent
into
wastewater,
stormwater,
effluent
from
those
systems
and
the
measure
of
impacts
on
receiving
environments.
- Water
monitoring
of
raw
water,
treated
water
and
recycled
water
- Chemists
role:
routine
monitoring
for
hundreds
of
potential
contaminant
in
the
water,
eg.
Carbon
compounds,
viruses,
bacteria,
micro-organisms.
- Equipment:
AAS,
gas
chromatography,
emission
and
mass
spectroscopy
precise/
sensitive
readings
of
level
of
contaminants.
- Results
are
reported
to
a
senior
analytical
chemist,
who
monitors
the
water
as
a
matter
of
urgency,
and
informs
the
government/
Environmental
Protection
authority
if
contamination
is
harmful.
Polymer
Chemist
- Work
in
industry
manufacturing
synthetic
fibres,
packaging
materials,
agricultural
chemicals,
rubber,
biodegradable
polymers.
- They
produce
new
products/
materials.
Synthesise/
study
physical
and
chemical
properties
of
polymers.
They
also
must
ensure
that
the
product
meets
the
customers
requirements.
- Use
analytical
methods
such
as:
X-ray
diffraction,
mass
spectroscopy
(chemical/
structural
characteristics),
strength/
hardness
tests,
reactivity
with
acids/
bases,
biocompatibility,
mp
bp.
- Case
study:
use
of
gas
liquid
chromatography
to
test
for
volatile
material.
Chemical
principle
used=
each
volatile
substance
has
a
unique
retention
time
in
the
GLC
column
1.2:
identify
the
need
for
collaboration
between
chemists
as
they
collect
and
analyse
data
- Different
types
of
chemists
have
specialised
skills
and
expertise,
and
can
bring
different
information
into
problem
solving/
understanding.
- Increases
the
accuracy/
validity
of
data
as
chemists
share
their
outcomes
- Chemists
keep
up
to
date
with
new
developments
in
the
field
via
communicating
1.3:
describe
an
example
of
a
chemical
reaction
such
as
combustion,
where
reactants
form
different
products
under
different
conditions,
and
thus
would
need
monitoring
Reasons
for
Monitoring
and
Management:
- Efficiency
- Minimal
pollution,
few
pollutants
produced
- Limited
damage
to
the
environment/
societys
health
- Maximise
the
amount
of
desired
product/
optimum
yield
is
achieved
- Reactions
are
energy
efficient
Note:
In
combustion
reactions,
the
process
must
be
monitored
to
ensure
that
combustion
is
COMPLETE,
as
this
releases
the
largest
amount
of
energy,
produces
CO2
instead
of
CO
(toxic).
If
not
monitored
a
number
of
results
could
occur
COMPLETE:
2C8H18(l)
+
25O2(g)
16CO2(g)
+
18H2O(l)
INCOMPLETE:
o 2C8H18(l)
+
17O2(g)
16CO
(g)
+
18H2O(l)
o 2C8H18(l)
+
9O2(g)
16C(s)
+
18H2O(l)
[yellow
flame
+
soot]
Monitoring
and
Management
of:
Dehydration/
Hydration
of
Ethylene/
Ethanol:
- C2H4(g)
+
H2O(l)
C2H5OH(aq)
EXO
- To
achieve
highest
yield
of
desired
product:
o Increase
yield=
concentration/
amount
of
reactants
need
to
be
increased
o Concentrated
H2SO4
is
used
as
a
catalyst
to
speed
up
the
reaction,
creating
a
more
efficient
process
o Need
to
manage:
temperature,
concentration,
pressure
and
catalyst
depending
on
which
reaction
is
used.
Eg.
To
move
reaction
forward
(hydration),
decrease
temp
slightly,
increase
pressure,
increase
concentration,
use
a
catalyst.
LINK
TO
LE
CHATELIERS
PRINCIPLE
Esterification
- Any
example!
Eg.
CH3COOH9G)
+
CH3OH(g)
CH3CH2COOCH3(g)
+
H2O(l)
ENDO
- To
achieve
maximum
yield
o Control
heat
to
speed
up
reaction.
Heat
is
required
to
change
reactants
to
gases
in
order
to
react
o Increase
concentration
of
reactants
o Catalyst
is
required
to
absorb
water
and
force
reaction
forwards
o Higher
temp=
greater
yield
Chemical
processes
in
industry
require
monitoring
and
management
to
maximise
production
2.1:
identify
and
describe
the
industrial
uses
of
ammonia
-
Fertilisers
(ammonium
sulphate,
ammonium
nitrate
and
urea)
-
Plastics
(rayon,
acrylics,
nylon)
-
Nitric
acid
(can
be
used
to
make
explosives
TNT
-
Dyes
-
House
cleaners
-
Detergents
Therefore
it
is
widely
used
in
industry
2.2:
identify
that
ammonia
can
be
synthesised
from
its
component
gases
nitrogen
and
hydrogen
Magnetite
(Fe3O4)
2.3:
describe
that
synthesis
of
ammonia
occurs
as
a
reversible
reaction
that
will
reach
equilibrium
2.4:
identify
the
reaction
of
hydrogen
with
nitrogen
is
exothermic
Magnetite
(Fe3O4)
The
Haber
Process
(producing
ammonia
through
the
use
of
a
catalyst-
iron)
With
metal
catalysts,
reactant
particles
collide
with
the
surface
of
the
metal,
and
some
may
become
attached.
These
molecular
rearrangements
make
it
more
likely
that
following
collisions
will
be
successful.
A
catalyst
such
as
iron
is
used
to
speed
up
reactions
by
lowering
the
activation
energy,
so
that
bonds
can
be
broken.
The
Process:
This
process
combines
nitrogen
(from
air),
with
hydrogen
(from
natural
gas-
methane),
to
form
a
yield
of
approximately
(10-20%)
ammonia
under
conditions
of
optimum
temperature
and
pressure.
This
is
a
reversible
(equilibrium)
and
exothermic
reaction.
A
mixture
of
nitrogen
and
hydrogen
are
put
into
a
reactor
in
a
ratio
of
1:3,
this
means
that
there
is
1
molecule
of
N
to
3
molecules
of
H.
The
temperature
in
the
reactor
is
raised
to
400-450
to
speed
up
the
reaction
in
order
to
produce
higher
proportions
of
ammonia
in
a
shorter
period
of
time.
The
pressure
is
also
raised
to
200
atm.
This
brings
the
molecules
closer
together,
and
increases
the
chances
of
molecules
hitting
and
sticking
to
the
iron
where
they
can
react
(increased
rate
of
reaction).
The
hydrogen
and
nitrogen
pass
over
beds
of
iron
oxide
(which
is
prepared
by
reducing
magnetite
Fe3O4),
where
some
are
bound
to
the
surface
of
the
iron
as
separate
atoms.
The
broken
bonds
are
then
reformed
into
NH3.
The
temperature
is
then
cooled
so
that
the
ammonia
can
be
liquefied,
and
leftover
gases
are
reused.
As
a
result
this
reaction
releases
92.4
kJ/mol
of
energy
at
298K
(25C).
N2(g)
nitrogen
3H2(g)
hydrogen
2NH3(g)
ammonia
In
order
to
create
an
efficient
industrial
process,
whereby
the
reaction
proceeds
at
a
fast
rate,
and
a
high
yield
is
produced,
the
process
must
be
monitored,
and
a
number
of
factors
balanced.
COMPROMISE:
o
use
of
a
catalyst,
o high
pressure
250atm,
o medium
temp
500
degrees
2.8:
explain
that
the
use
of
a
catalyst
will
lower
the
reaction
temperature
required
and
identify
the
catalysts
used
in
the
Haber
process
Catalyst
in
Haber
process=
magnetite
(Fe3O4)
or
Osmium
Catalysts
lower
the
activation
energy
and
in
turn
increase
the
reaction
rate.
It
allows
the
N
and
H
bonds
to
be
more
easily
broken,
allowing
it
to
occur
at
lower
temps
and
thus
favours
the
forward
reaction.
2.9:
Analyse
the
impact
of
increased
pressure
on
the
system
involved
in
the
Haber
process
For
every
4
moles,
2
moles
of
NH3
are
produced
Increasing
pressure
forces
the
reactants
into
a
smaller
volume,
pushing
the
moles
closer
together
and
increasing
the
chance
of
collisions
Therefore
increasing
pressure
will
favour
the
forward
reaction,
as
a
result
of
the
equilibrium,
and
so
will
increase
the
yield
This
will
also
increase
the
reaction
rate,
as
more
collisions
will
be
occurring
at
a
faster
rate.
However
increasing
pressure
is
an
expensive
industrial
process.
2.10:
explain
why
monitoring
of
the
reaction
vessel
used
in
the
Haber
process
is
crucial
and
discuss
the
monitoring
required
- The
Haber
process
needs
to
be
constantly
monitored
and
managed
for
effective
and
optimal
production
of
ammonia.
If
it
isnt
monitored,
a
change
in
the
reaction
could
result
in
decreased
yield
or
a
slow
reaction
which
in
turn
will
affect
productivity
and
cost
the
firm
money
and
time
- Monitoring:
o Feedstock
(N
+H)
must
be
pure,
otherwise
it
will
impact
on
yield
and
ruin
catalyst
o Ratio
of
N:H
(1:3),
avoid
build
up
of
one
decrease
production
o Temp
+
Pressure
optimum
production.
Too
high
temp=
damage
catalyst.
Too
high
pressure=
damage
vessel
o Build
up
of
gases
in
plant
o Remove
ammonia,
ensure
no
impurities
o Structural
integrity
of
vessel
2.11:
describe
the
conditions
under
which
Haber
developed
the
industrial
synthesis
of
ammonia,
and
evaluate
its
significance
at
that
time
in
world
history
- His
first
experiments
produced
small
yields
of
ammonia,
when
nitrogen
and
hydrogen
were
combined
at
1000C
over
an
iron
catalyst
- He
tested
numerous
catalysts,
osmium
was
the
best
but
was
expensive
- Further
experiments
showed
that
pressure
needed
to
be
raised,
but
temp
lowered
to
increase
yield.
- He
could
synthesise
100g
of
ammonia
- Carl
Bosch
modified
this
process
to
an
industrial
level
(500,
200atm)
- Significance
of
process
at
the
time:
production
of
fertilisers
needed
for
agriculture,
and
to
sustain
the
growing
population.
Used
for
gunpowder
and
explosives
for
WWI,
sustained
troops.
It
prolonged
the
war
by
assisting
Germanys
efforts.
Manufactured
products,
including
food,
drugs
and
household
chemicals,
are
analysed
to
determine
or
ensure
their
chemical
composition
3.1:
deduce
the
ions
present
in
a
sample
from
the
results
of
tests
3.3:
first
hand
investigation
to
test/
identify
phosphate,
sulphate,
carbonate,
chloride,
barium,
calcium,
lead,
copper,
iron
Anions
(negative)
Cations
(positive)
3.2:
describe
the
use
of
atomic
absorption
spectroscopy
(AAS)
in
detecting
concentrations
of
metal
ions
in
solutions
and
assess
its
impact
on
scientific
understanding
of
the
effects
of
trace
elements
This
technique
is
very
sensitive
and
can
measure
in
ppm
Uses:
test
purity
of
mined
samples,
monitor
pollution,
detect
harmful
levels,
quality
control
Steps:
1. A
sample
thought
to
contain
a
metal
atom
is
heated
in
a
flame
2. Species
in
this
sample
are
converted
to
gases
in
the
flame
3. If
light
of
a
frequency
known
to
be
absorbed
by
this
chemical
passed
from
the
light
source
through
the
heated
sample,
the
element
in
the
sample
will
absorb
some
of
the
light
4. The
proportion
of
light
energy
absorbed
by
the
sample
(absorbance)
is
proportional
to
the
concentration
of
the
substance
How
AAS
can
be
used
to
determine
which
metal
ions
are
in
a
solution
and
their
concentration
- A
separate
light
source
must
be
used
for
each
metal
ion
to
be
tested
(each
metal
ion
has
its
own
unique
emission
and
absorption
spectrum)
- A
frequency
which
is
characteristic
and
unique
for
the
element
to
be
tested
must
pass
through
the
heated
sample,
and
the
proportion
of
light
absorbed
can
be
measured
- Concentration
is
determined
by
comparing
the
absorbance
of
the
sample
with
absorbance
of
standard
solutions
of
known
concentrations.
Trace
Elements
- Elements
required
by
living
things
in
very
small
quantities
(1-100ppm)
- In
humans:
o Zinc
(needed
to
help
enzymes
function),
cobalt,
nickel,
iodine,
selenium
- In
plants:
o Manganese,
copper,
boron,
zinc
- Selenium:
in
animals
(protect
against
harmful
exposure
to
mercury,
regulate
male
hormones,
support
prostategland,
enhances
immune
function,
anti-cancer
nutrient
- Zinc:
Animals
(metabolism
of
amino
acids
and
in
energy
production
(homeostasis),
immune
response,
oxidative
stress).
Plants
(regulates
plant
growth
hormones)
Impact
of
AAS
on
scientific
understanding
of
the
effects
of
trace
elements
- Before
AAS,
scientists
used
techniques
such
as
gravimetric/
volumetric
analysis,
which
was
an
invalid
method
as
it
cannot
measure
very
small
concentrations
(ppm)
of
trace
elements.
Therefore
it
wasnt
accurate.
- Assessment:
The
development
of
AAS
has
allowed
scientists
to
understand
the
effects
of
trace
elements,
has
furthered
our
understanding,
and
is
more
accurate
and
valid.
Allowed
the
impact
of
deficiencies
in
metal
ions
to
be
investigated
and
allowed
the
testing
of
foods
to
determine
the
levels
of
essential
vitamins/
minerals.
3.4:
describe
and
explain
evidence
for
the
need
to
monitor
levels
of
one
of
the
above
ions
in
substances
used
in
society
- It
is
important
to
monitor
levels
of
ions
as
some
in
high
concentrations
are
harmful
to
humans.
- Lead
ions-
cations
o Lead
is
a
poison
o Effects:
retard
intellectual
development
in
young
children,
brain/
neurological
disorders
o Lead
was
originally
used
in
petrol
and
paint.
o Due
to
their
original
use,
there
is
still
some
lead
compounds
in
the
soil,
around
industrial
sites,
paint
factories
etc.
lead
compounds
in
petrol
were
released
into
the
atmosphere
o AAS
is
used
to
monitor
soil
samples,
and
is
more
efficient
and
sensitive
then
previous
techniques.
Pollution
and
manufacturing
of
goods
containing
lead
is
illegal,
so
it
is
important
that
monitoring
of
lead
ion
concentrations
are
conducted.
- Phosphate
ions-
anions
o Found
in
waterways
(naturally)
o Essential
for
normal
aquatic
growth.
o If
concentration
becomes
too
high=
algal
bloom
make
water
unusable,
degradation
of
lake.
Loss
of
oxygen
results
in
death
of
fish
etc,
build
up
of
sediments.
EUTROPHICATION
o Phosphate
ions
are
derived
from
sewage,
fertilisers,
detergents.
o Monitoring
is
required
as
a
predictor
of
Eutrophication.
o Colorimetric
method
is
used
(very
sensitive),
molybdenum
blue
test,
spectrophotometer.
3.5:
first
hand
investigation
to
measure
sulphate
content
of
lawn
fertiliser.
Explain
the
chemistry
involved.
Ba
2+(aq)
+
SO4
2-
(aq)
BaSO4
(aq)
See
separate
sheet!
3.6:
evaluate
the
reliability
of
the
results
of
the
above
investigation
and
propose
solutions
to
problems
encountered
in
the
procedure
- Heating
will
coagulate
the
precipitate,
ensuring
it
is
collected
- Use
samples
of
fertiliser
with
a
greater
mass
will
lessen
%
error
in
accuracy
- Quantitative
filter
paper
has
very
fine
pores,
no
solid
will
escape
- Improve
reliability
by
repeating
or
using
a
glass
filter.
- Experiment
assumes
that
ppt
is
only
barium
sulphate,
without
any
impurities
like
ions/
water
3.7:
interpret
secondary
data
from
AAS
measurements
and
evaluate
the
effectiveness
of
this
in
pollution
control
See
bronwyns
book!
And
sheet
- Detect
presence
of
heavy
metals
and
concentrations
eg.
mercury,
lead,
cadmium,
arsenic
- EPA
monitors
and
evaluates
levels
protects
environment
by
controlling
and
minimising
pollution/
waste.
- AAS
is
quantitative,
and
can
determine
concentrations.
Without
it
pollution
would
go
undetected.
- However
it
has
limitations,
it
tests
for
a
range
of
metals
but
must
be
done
separately.
Human
activity
has
caused
changes
in
the
composition
and
the
structure
of
the
atmosphere.
Chemists
monitor
these
changes
so
that
further
damage
can
be
limited
4.1:
describe
the
composition
and
layered
structure
of
the
atmosphere
Layers
of
the
Earth
This
Module
Sucks
Terribly
4.2:
identify
the
main
pollutants
found
in
the
lower
atmosphere
and
their
sources
10
4.3:
describe
ozone
as
a
molecule
able
to
act
both
as
an
upper
atmosphere
UV
radiation
shield
and
a
lower
atmosphere
pollutant
Why
does
concentration
of
gases
(oxygen
and
nitrogen)
decrease
as
altitude
increases:
force
of
gravity
pulls
gases
towards
the
earths
surface,
therefore
concentration
decreases
as
altitude
increases
Why
is
there
more
ozone
in
the
stratosphere
than
there
is
in
the
troposphere?
- Ozone
is
made
when
oxygen
is
broken
into
free
radials
using
energy
from
Uv
light.
Intensity
of
short
wave
length
UV
light,
needed
to
break
up
O
molecules
is
greater
in
the
stratosphere
than
in
the
troposphere.
- O2
(g)
2O.
(g)
O2
(g)
+
O.
(g)
O3
(g)
Ozone
concentration
is
low/
stable
in
the
troposphere.
Why
is
this
so?
UV
1. O2 (g) 2O (g)
2. O2 (g) + O (g) O3 (g)
3. O3 (g) O2 (g) + O (g)
4. 2O (g) O2 (g)
The overall equation:
1. 2O3 3O2
-
-
-
11
4.5:
demonstrate
the
formation
of
coordinate
covalent
bonds
using
Lewis
electron
dot
structures
Hydronium
ion
Ammonium
ion
Ozone
Carbon
monoxide
4.6:
compare
the
properties
of
the
oxygen
allotropes
O2
and
O3
and
account
for
them
on
the
basis
of
molecular
structure
and
bonding
Allotrope:
different
forms
of
the
same
element.
They
have
the
same
atoms,
but
different
bonding
Differences
in
physical
properties:
ozone
is
bigger,
heavier,
with
more
electrons.
Therefore
greater
molecular
interaction.
Ozone
has
stronger
dispersion
forces
therefore
higher
mp/bp.
Greater
mass=
greater
density.
4.7:
compare
the
properties
of
the
gaseous
forms
of
oxygen
and
the
oxygen
free
radical
Oxygen
molecule:
stable
form
of
the
element.
All
electrons
are
paired
and
stable.
Oxygen
free
radical:
can
be
formed
when
UV
splits
oxygen.
It
is
very
reactive,
unstable,
2
unpaired
electrons.
They
want
to
from
covalent
bonds
therefore
doesnt
stay
as
a
free
radical
for
long.
Combines
to
form
ozone,
NO
NO2.
12
13
4.11:
analyse
information
that
indicates
changes
in
atmospheric
ozone
concentrations,
describe
the
changes
observed
and
explain
how
this
information
was
obtained
- graph
shows
a
decrease
in
levels
of
CFCs,
and
has
begun
to
stabilize
- level
of
ozone
concentration
was
obtained
by
instruments
in
satellites
such
as
UV
spectrophotometers
o these
measure
the
intensity
of
light
received
at
a
wavelength
at
which
ozone
absorbs
and
then
at
wavelengths
either
side
of
this,
that
ozone
doesnt
absorb
--.
Comparison
gives
total
concentration
o measured
in
Dobson
units
o balloons
can
be
used
to
carry
instruments
into
the
atmosphere
4.12:
write
equations
to
show
the
reactions
involving
CFCs
and
ozone
to
demonstrate
the
removal
of
ozone
from
the
atmosphere
UV
1. CCl3F Cl + CCl2F
2. Cl + O3 ClO + O2 (breaks down ozone)
3. ClO + O Cl + O2
Steps
2
and
3
can
continue
again
and
again
to
form
a
chain
reaction
The
net
result
of
these
last
2
reactions
is
the
conversion
of
O3
O2
4.13:
model
isomers
of
haloalkanes
using
simulations,
molecular
model
kits
or
pictorial
representations
4.14:
identify
alternative
chemicals
used
to
replace
CFCs
and
evaluate
the
effectiveness
of
their
use
as
a
replacement
for
CFCs
Uses
of
CFCs:
refrigerants
solvents,
propellants
in
aerosol
cans
Reasons:
non-toxic,
inert
Problems
with
use:
stable
CFCs
reacg
upper
atmosphere
where
they
destroy
ozone
1. HCFCs
(hydrochlorofluorcarbons)
- More
reactive
than
CFCs
due
to
higher
reactivity
of
C-H
bonds,
therefore
majority
are
destroyed
in
troposphere
- Temporary
substitute
for
CFCs
until
better
compounds
are
found
long
term
toxicity
to
humans
is
unknown
2. HFCs
(hydrofluorocarbons)
- Contain
no
Cl
- More
expensive
and
less
effective
as
refrigerants,
but
dont
react
with
ozone
3. Hydrocarbons
to
a
lesser
extent
eg.
Butane
- Used
as
aerosol
propellants
- Problems-
flammable,
release
hydrocarbons
into
atmosphere
- React
to
form
photochemical
smog
14
Why
it
is
unlikely
ozone
concentration
in
stratosphere
will
change
significantly
in
the
next
few
years
- CFCs=
inert,
non-toxic,
insoluble.
Relatively
dense
gas
molecules
and
diffse
slowly
into
stratosphere.
- Stability
n
troposphere
means
they
arent
destroyed
and
persist
for
decades
- Steps
to
alleviate
problems
with
CFCs
appear
to
be
effective
as
levels
of
ozone
have
stabilized
- Decades
before
CFCs/
halons
are
eliminated
as
one
Cl
free
radical
can
cause
breakdown
of
1000
ozone
molecules.
Why
ozone
concentration
in
stratosphere
is
at
its
lowest
in
spring
over
polar
regions.
Explain
processes
which
contribute
to
the
ozone
holes
at
these
times
The
chain
reaction
of
chlorine
free
radicals
with
ozone
can
be
terminated
by
2
different
reactions.
- The
chlorine
free
radical
can
react
with
methane
to
form
hydrogen
chloride
gas
and
a
CH3.
Neither
of
these
products
reacts
with
ozone.
Cl
+
CH4
HCl
+
CH3
The
ClO
reacts
with
nitrogen
dioxide
gas
in
the
stratosphere
to
remove
the
free
radical.
The
product
does
not
release
the
Cl
on
exposure
to
UV
light.
ClO
+
NO2
ClONO2
In
winter,
at
the
poles,
atmosphere
is
cold/
dark
and
the
air
patterns
do
not
allow
mixing
of
the
air
over
the
poles
with
other
air.
Under
these
conditions,
the
products
of
the
termination
reaction
can
react
and
release
chlorine
into
the
atmosphere.
HCl
+
ClONO2
Cl2
+HNO3
During
winter,
the
chlorine
in
the
stratosphere
has
no
effect
on
the
ozone
level.
However,
in
spring,
when
sunlight
returns
to
the
pole,
there
is
a
dramatic
breakdown
of
the
chlorine
molecules
into
chlorine
free
radicals.
The
concentration
of
ozone
drops
dramatically,
creating
an
ozone
hole
over
the
polar
regions
in
spring
(October
November)
in
the
southern
hemisphere.
Human
activity
also
impact
on
waterways.
Chemical
monitoring
and
mgmt
assists
in
providing
safe
water
for
human
use
and
to
protect
the
habits
of
other
organisms
5.1:
identify
that
water
quality
can
be
determined
by
considering:
concentration
of
common
ions,
total
dissolved
solids,
hardness,
turbidity,
acidity,
dissolved
oxygen
and
biochemical
oxygen
demand
Factor
Definition
Causes
How
it
is
measured
Common
ions
Chlorine,
sulfate
salinity
of
water
AAS
for
metals,
gravimetric
Carbonate:
cause
pH
to
increase
analysis
(carbonates=
bases),
may
affect
plant
growth
Ca
and
Mg:
indicate
hardness
of
water
Phosphate:
excessive=
can
cause
algal
blooms,
predictor
of
algal
blooms
Nitrate:
indication
of
sewage/
fertilisers
Turbidity
Degree
of
transparency
of
water.
Presence
of
suspended
Gravimetric
analysis
Determined
by
the
presence
of
solids
that
cant
be
Meter
tube
suspended
solids
filtered.
Eg.
Clay,
silt,
Secchi
disk
industrial
solids,
Turbidity
meter
bacteria,
faecal
matter,
15
BOD
(biochemical
oxygen
demand)
pH
hardness
algae
Presence
of
dissolved
solids
eg
salt
Rocks
minerals
in
soil
Depend
on
salinity,
temp,
conc
of
dissolved/
suspended
pollutants.
High
temp=
low
O
Rate
of
flow
Amount
of
O
used
in
respiration
Pollution/
waste.
Higher
the
pollution=
higher
the
BOD
Presence
of
CO2/
pollution
Hard
water=
wont
lather
with
soap.
Presence
of
Ca,
Mg
Contains
Ca,
Mg
DO
sensor
Seal/
incubate
5
days
Measure
DO
Calculate
BOD
pH
meter
indicator
Titration
(stoichiometry)
5.2:
identify
factors
that
affect
the
concentrations
of
a
range
of
ions
in
solution
in
natural
bodies
of
water
such
as
rivers/
oceans
1.
Pathways
from
rain
to
water
body
-
if
rain
passes
quickly
to
water
body,
TDS
will
generally
be
small
and
main
ions
will
b
NO3,
PO4,
CO3,
Ca,
Mg.
if
rain
soaks
in
underground
water,
it
will
contain
increased
ions
-
if
water
flows
into
deep
aquifers
contain
heavy
metals
(Fe,
Mn
Cu,
Zn)
2.
pH
of
rain
-
more
acidic
the
rain,
more
likely
it
is
that
ions/
minerals
will
dissolve
in
it
from
rocks/
soil
3.
Nature
of
human
activity
in
catchment
area
-
Agriculture.
Land
clearing
increase
run
off
of
sediments
and
therefore
increase
the
amount
of
material
that
is
able
to
dissolve
in
water
4.
Effluent
discharged
into
water
bodies
-
includes
sewage,
stormwater
run
off,
and
industrial
effluents
5.
Leaching
from
rubbish
dumps
-
heavy
metals
eg.
Cadmium,
Hg,
Pb,
Zn,
NO3,
PO4
(Eutrophication
in
excessive
amounts).
5.3:
describe
and
assess
the
effectiveness
of
methods
used
to
purify
and
sanitize
mass
water
supplies
16
17
5.4:
describe
the
design/
composition
of
microscopic
membrane
filters
and
explain
how
they
purify
contaminated
water
- thin
film
of
synthetic
polymer,
which
has
small
pores
of
uniform
size
- Prose
sizes
range
from
0.2-
0.5
micrometers
(10^-6).
These
pore
sizes
are
big
enough
for
water
molecules
to
pass
through
but
small
enough
to
trap
microorganism
and
some
viruses
- Membrane
filters
are
used
in
industries-
bottle
water,
soft
drink
,beer
Advantages:
o Filter
smaller
particles
than
other
filters
o A
thin-liquid
flows
through
them
rapidly
o Strong,
can
withstand
pressure
o Can
be
cleaned
and
reused
- Microfiltration
membranes:
remove
microscopic
parasites
Giardia,
viruses
- Ultrafiltration
membranes:
remove
particles
from
100
nanometers
to
2
nanometers.
Paint
particles,
organic
molecules
- Nanofiltration
membranes:
less
than
1
nanometer,
remove
ions
from
water.
5.5:
first
hand
investigation
to
use
qualitative/
quantitative
tests
to
analyse
and
compare
quality
of
water
samples
Qualitative:
description/
use
of
words
Quantitative:
use
of
numbers
and
statistics
Test
Method
Qualitative/
Quantitative
Concentration
of
ions
AAS
Quantitative
Flame
test
Qualitative
ppt
Quantitative
Insoluble
solids
Filter
measured
sample,
dry
Quantitative
and
weigh
residue
TDS
Filter,
evaporate
a
measured
Quantitative
amount,
dry
and
weigh
residue
Hardness
Ppt
tests
to
determine
Ca
Quantitative
Ability
to
lather
with
soap
Qualitative
Turbidity
%
light
transmitted
through
Quantitative
depth
at
which
lines
can
be
seen
Acidity
Indicators
Qualitative
Data
logger
with
probe
Quantitative
DO
Data
logger
with
O
probe
Quantitative
BDO
Difference
between
initial
and
Quantitative
final
DO
after
5
days
in
dark
Phosphate
Colorimetric-
add
ammonium
Quantitative
molybdite,
measure
depth
of
colour
when
a
blue
compound
forms
SEE
PRAC
SHEET
18
5.6:
information
on
the
range
and
chemistry
of
the
tests
used
to
identify
heavy
metal
pollution
of
water,
monitor
possible
Eutrophication
of
waterways
Nitrogen-to-phosphorus
ratio:
measurement
associated
with
water
quality
- Conc
of
NO3
and
PO4
ions
are
important
predictors
of
algal
blooms.
Both
these
are
essential
nutrients
for
algal
growth
but
in
excess
can
lead
to
Eutrophication
and
degradation
of
water
- Ratio
o
N
to
P
has
an
impact
on
algal
growth
- Diff
species
require
diff
ratios
- High
N:P
promotes
blue-green
algae
- Low
N:P
promotes
green
algae
- To
avoid
algal
blooms,
EPA
has
recommended
levels.
Total
N=
0.1-1ppm,
Total
P=
0.001-
0.1ppm
Heavy
Metals:
transition
metals
and
lead,
Arsenic.
- In
water,
heavy
metals
can
be
damaging
to
health.
Monitoring
conc
is
vital
- AAS
can
be
used
- Lead:
poison,
retards
intellectual
development
in
children,
brain
damage,
- Mercury:
pollutant,
toxic,
bioaccumulative.
Damages
nervous
system,
death
in
fish/
animals.
Unborn
children
are
affected
if
mothers
eat
contaminated
fish.
Algal
Blooms:
excessive
growth
of
algae
which
covers
streams/
dams
with
geen
sludge
unstable
for
people
- Factors:
temp
(warm),
rate
of
flow
(still),
level
of
UV
(high),
concentration
of
nutrients
(high)
fertilizers,
sewage
Eutrophication:
process
by
which
a
water
body
becomes
enriched
by
nutrients
eg.
PO4,
NO3,
making
algal
blooms
highly
likely.
- Tests
for
monitoring
Eutrophication:
o Monitoring
presence
of
PO4,
in
waterways
is
used
as
a
predictor
o Colourimetric
method
needs
to
be
very
sensitive
to
pick
up
low
concentrations
o Molybdenum
blue
test
o Spectrophotometer,
which
measures
the
absorbance
of
light
at
a
particular
frequency
.
o Absorbance
test
of
the
sample
is
compared
with
absorbance
of
standard
phosphate
solutions
5.7:
information
on
features
of
the
local
town
water
supply
in
terms
of:
catchment
area,
possible
sources
of
contamination
in
this
catchment,
chemical
tests
available
to
determine
levels/
types
of
contaminants,
physical
and
chemical
processes
used
to
purify
water,
chemical
additives
in
the
water
and
the
reasons
for
the
presence
of
these
additives
SEE
SHEET
Catchment
area:
- 5
major
systems
form
the
Sydney
catchment
area
- 16000
sq
km.
to
south
and
west
of
Sydney
- Warragamba
system
- Upper
nepean
- Woronora
system
- Blue
Mountains
system
- Shoalhaven
system
- All
have
rivers,
lakes,
dams,
reservoirs,
pumping
stations,
filtration
plants,
pipes
Contamination:
- Turbidity:
rub
off
from
bushland,
grazing
land
- High
levels
of
iron/
manganese:high
natural
levels
leached
from
the
soil
and
rock
19