AT2 Depth Study Flashcards

1
Q

Effect of Temperature on Solubility of Salts

A

Solubility is proportional to temperature, but differently for different salts.

Exception is sodium sulphate, which decreases in solubility past the 30°C.

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2
Q

Effect of Temperature on Solubility of Gases

A

Solubility is indirectly proportional to temperature because increased kinetic energy breaks dispersion forces.

Carbon dioxide is more soluble than other gases because it reacts with the water.

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3
Q

Effect of Gas Pressure on Solubility

A

Gas pressure is proportional to solubility of gas.

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4
Q

What does gas concentration depend on?

A

Temperature, depth and salinity

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5
Q

Concentration in sea water and fresh water?

A

Concentration is sea water is less than in fresh water because the presence of ions interferes with dispersion forces.

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6
Q

Factors that Influence Gas Concentration (8)

A

Partial pressure of gases in troposphere.

Diffusion rate into water surface.
Temperature of ocean.

Diffusion into deeper layers.

Ocean currents.

Water salinity.

Photosynthesis/Respiration.

Carbonate-hydrogen carbonate equilibria.

Concentrations with increasing depth.

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7
Q

Partial Pressure of Gases in Troposphere

A

Abundancy in troposphere: N > O > CO2

Proportional to shift in dissolution equilibria.

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8
Q

Diffusion Rate into Water Surface

A

Affected by water turbulence and temperature.

Droplet created by turbulence increases rate of diffusion.

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9
Q

Temperature of Ocean Water

A

Temperature is inversely proportional to concentration.

Temperature varies according to proximity to land and cold salt water is denser than warm, meaning that surface water near the poles has higher concentration.

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10
Q

Diffusion into Deeper Layers

A

Surface and deep water do not mix much.

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11
Q

Ocean Currents

A

Deep: Currents from Antarctica and Southern Ocean transport cold water.

Surface: Currents move into the Indian Ocean.

Ocean temperature decreases with depth and cold water has higher concentration of gases.

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12
Q

Water Salinity

A

Solubility is inversely proportional to salinity.

Seawater salinity: 3.0-3.7% (w/w)
Warm currents have lower salinity.

Salinity is proportional to density and water is more saline near the poles.

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13
Q

Photosynthesis and Respiration

A

The photic zone is the surface 150m where photosynthetic organisms can live.

Oxygen is both consumed and produced in photic zone.

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14
Q

Carbonate-Hydrogen Carbonate Equilibria

A

Carbon dioxide is constantly dissolving to create carbonic acid, which can be stored in deeper layers of the ocean for thousands of years at a constant concentration, but currents can bring it to the surface.

Some organisms use dissolved CO2 in constructing shells and exoskeletons.

CO2(aq) + H2O(l) → H2CO3 (aq)

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15
Q

Concentrations with Increasing Depth

A

Oxygen: Higher in surface waters because photosynthesis and diffusion.

Carbon dioxide: Higher in deeper water because respiration and decomposition.

Nitrogen: Not affected by depth but opposite of CO2.

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16
Q

What affects rate of reaction in oceans? (4)

A

Temperature, depth, oxygen concentration and salinity.

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17
Q

Evolution of Ship-Building Materials

A

European ships in 16th century were predominantly timber with metals used for fastenings, anchors or braces.

British ships in 18-19th centuries became iron and then steel when iron began to rust too much.

18
Q

Ancient Greek Ship

A

Oldest, intact shipwreck ever found (350-410 BCE).

Water in the Black Sea is either of high salinity (from the Mediterranean) or low salinity (land runoff), and lack of water currents makes these layers distinct.

Deep basin allows ships to be entirely submerged in an anaerobic environment.

19
Q

The Endurance

A

Sunk in the Antarctic in 1915.

Ice slowed the ships descent to the ocean floor.

Lack of light and oxygen prevent degrading organisms, such as parasitic worms and bacteria.

20
Q

Hull of the Titanic

A

Hull - watertight main body of a ship.

Overlapping steel plates held by iron rivets.

Steel was ten times more brittle than modern steel, especially at freezing temperatures due to higher content of S, O and P and lower Mn.

Iron rivets had high concentrations of slag, prone to fracturing and couldn’t handle the stress.

21
Q

Superstructure of the Titanic

A

Superstructure - parts that project above the main deck.

Two timber decks with steel framing and a navigating bridge in between.

Sealant to survive harsh weather.

22
Q

Decay of the Titanic’s Hull

A

North Atlantic Ocean has ideal conditions for protobacteria.

Presence of bacteria (Halomonas titanicae) consumed iron in hull and formed rust mounds called rusticles because of the solubility of iron.

Fe2O3 formed a porous layer on the surface, which diffused water into iron metal and increased corrosion rate.
2Fe(s) + O2(g) + H2O(l) → 2Fe2O3(s) + H2O(l)

Sulfate-reducing bacteria is one of the key microbes in metal corrosion, facilitating the reduction of sulfate under anaerobic conditions in the water. It occurs in the following redox reaction:
4Fe(s) + SO4(aq) + 10H(aq) → 4Fe2+(aq) + H2S(g) + 4H2O(l)
Hydrogen sulfide reacts with iron (II) ions to form iron (II) sulfide (rusticles), among other components.

23
Q

Decay of the Titanic’s Superstructure

A

Steel framing corroded and broke, collapsing decks on top of each other.

Water pressure and deep currents caused disintegration.

Thick layers of sediment allowed some areas of wood deck to be protected from damp environment and remain intact.

Teredo worm holes found.

24
Q

Corrosion in Shallow Waters

A

High oxygen concentration allows aerobic bacteria the thrive and cause concretion, and corrosion reactions on reactive metals.

Higher temperature and acidity, which can cause acid/metal reaction with metal salts and hydrogen gas.

25
Q

What is concretion?

A

The accumulation of local matter to form a mass of sediment or precipitate from a precipitation reaction between water minerals and iron oxide, separating the reactive metal surface from exposure to seawater and oxygen, slowing corrosion with a more stable, mineral layer.

Fe2+(aq) + CO3(aq) → FeCO3(s)
4Fe2+(aq) + O2(aq) + 6H2O(l) → 4Fe(OH)3(s)

Ca2+(aq) + CO3(aq) → CaCO3 (s)
5Ca2+(aq) + 3PO4(aq) + OH-(aq) → Ca5(PO4)3(OH)(s)

26
Q

Why does concretion not occur deeper than 300m?

A

Requires the presence of dissolved minerals and oxygen.

Conditions are not stable enough at great depths for concretion to form.

27
Q

Why do bones dissolve at depths greater than 300m?

Three contributing factors

A

A combination of temperature, presence of carbonic acid and organisms.

Cold temperature and acidity increase solubility of bone mineral, and the presence of bacteria causes rapid decay.

28
Q

Green rust

A

Lack of oxygen causes the formation of both iron (II) and iron (III) hydroxide.

4Fe(OH)2(s) + 2Fe(OH)3(s) + 2Cl−(aq) + 4H2O → [Fe2 + 4Fe3 + 2(OH)12]Cl⋅4H2O

29
Q

What happened to the iron nail in ferroxyl indicator?

A

Oxidation → blue at head
Fe(s) → Fe2+(aq) + 2e-

Reduction → pink at base
1/2O2(g) + H2O(l) +2e- → 2OH-(aq)

30
Q

What happened to the bent iron nail in ferroxyl indicator?

A

Oxidation → blue at bend
Fe(s) → Fe2+(aq) + 2e-

Reduction → pink at head and base
1/2O2(g) + H2O(l) +2e- → 2OH-(aq)

31
Q

What happened to the iron nail with copper wire in ferroxyl indicator?

A

Oxidation → everywhere with exposed iron
Fe(s) → Fe2+(aq) + 2e-

Reduction → around the wire
1/2O2(g) + H2O(l) +2e- → 2OH-(aq)

32
Q

What happened to the iron nail with magnesium strip in ferroxyl indicator?

A

Oxidation → no blue
Mg(s) → Mg2+(aq) + 2e-

Reduction → everywhere (magnesium in the best reductant)
1/2O2(g) + H2O(l) +2e- → 2OH-(aq)

33
Q

Sacrificial Anodes

A

Highly reactive metals attached to the hull of an iron or steel ship to corrode instead.

Cathodic protection system is the most effective way to protect against corrosion, and anode is usually made from zinc, aluminium or magnesium, which are all better reductants than iron.

34
Q

Electrolysis Experiment Redox Reaction

A

Reduction: Cu2+(aq) + 2e- → Cu(s)

Oxidation: H2O(l) → ½O2(g) + 2H+(aq) + 2e-

Net Ionic: Cu2+(aq) + H2O(l) → Cu(s) + ½O2(g) + 2H+(aq)

35
Q

How are wooden articles of artefacts restored?

A

Salt water penetrates the organic fibres of wood, hydrolysing it ad leaving salt in the internal spaces if left to dry. This can cause it to disintegrate, so wooden artefacts are stored in warm alcohol or polyethylene glycol solutions so that the artificial polymer can displace the penetrated salt, therefore stabilising its decomposition.

36
Q

Hydrolysis of Iron

A

The final product (rust) of the iron corrosion and oxidation process is solid iron (III) hydroxide.

This can be hydrolysed in water to release iron (III) ions and hydroxide ions. The ions then further hydrolyse into hydrogen ions, which increase the acidity of the solution. This acidity can further corrode the iron, producing iron (II) ions and hydrogen gas.

Fe(s) + 2H2O(l) + 1/2O2(g) → Fe(OH)2(s)
4Fe(OH)2 + O2(g) + 2H2O(l) → 4Fe(OH)3(s)
Fe(OH)3(s) → Fe3+(aq) + 3OH-(aq)
Fe3+(aq) + 3H2O(l) → Fe(OH)3(s) + 3H+(aq)
Fe(s) + 2H+(aq) → Fe2+(aq) + H2(g)

37
Q

Hydrolysis of Copper

5 chemical equations

A

The final product of the copper corrosion and oxidation process is solid copper (II) chloride.

This can be hydrolysed in water to release copper (I) hydroxide and hydrochloric acid. The HCl decomposes into hydrogen ions and chloride ions, increasing the salinity of the solution. This acidity can further corrode the copper, producing copper (II) ions and hydrogen gas.

Cu(s) + Cl-(aq) → CuCl(s)
2CuCl(s) + O2(g) + 2Cl-(aq) → 2CuCl2(aq)
CuCl(s) + H2O(l) → CuOH(s) + HCl(aq)
HCl(aq) → H+(aq) + Cl-(aq)
Cu(s) + 2H+(aq) → Cu2+(aq) + H2(g)

38
Q

Electrolysis of Iron Artefacts

A

A basic electrolyte, like NaOH, is used as the electrolyte.

The iron artefact acts as the cathode, where iron (II) ions will reduce into solid iron.
Fe2+ (aq) + 2e- → Fe(s)

An inert electrode will be used, but the water molecules will oxidise.
4OH-(aq) → 2H2O(l) + O2(g) + 4e-

2Fe2+(aq) + 4OH-(aq) → 2Fe(s) + 2H2O(l) + O2(g)

39
Q

Electrolysis of Copper Artefacts

A

A basic electrolyte, like sodium bicarbonate (NaHCO3) is used as the electrolyte.

The copper artefact acts as the cathode, where copper (II) ions will reduce into solid copper.
Cu2+(aq) + 2e- → Cu(s)

An inert electrode will be used, but the water molecules will oxidise.
4OH-(aq) → 2H2O(l) + O2(g) + 4e-

2Cu2+(aq) + 4OH-(aq) → 2Cu(s) + 2H2O(l) + O2(g)

40
Q

Desalination

A

The submersion of metal artefacts into basic solutions to remove ocean salts, such as chlorides and sulfates, from the metal.

The alkaline solution diffuses the salt out, the solution needing to be changed regularly to maximise diffusion rate.

Fe(OH)Cl(s) + OH-(aq) → Fe(OH)2(s) + Cl-(aq)

41
Q

How do you know when the desalination process is complete?

A

The salinity of the alkaline electrolyte solution can be tested, and once the chlorine concentration is less than 50ppm, the treatment is complete.

This is usually followed by titration or calibrated chloride meter analysis to ensure that it has been properly desalinated before the metal artefact is exposed to air again.