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Define a petroleum fraction
A mixture of hydrocarbons with a similar chain length and boiling point range
Describe fractional distillation (key points)
Oil is pre heated then passed into column
Fractions condense at different heights
Temperature of column decreases upwards
Separation depends on boiling point which depends on size of molecules (van der waaals)
Similar molecules (size, bp, mass) condense together
Small molecules at top, big at bottom at higher temps
Which type of forces are broken during fractional distillation?
Van der Waals between molecules
Define cracking
The conversion of large hydrocarbons to smaller hydrocarbon molecules by breakage of C-C bonds
Give the economic reasons for cracking
Petroleum fractions with shorter C chains are more in demand, makes use of excess larger hydrocarbons, products are more valuable than starting materials
Give the two types of cracking
Thermal and catalytic
Give the conditions needed for thermal cracking
High pressure (7000 kPa), high temperature (400-900°C)
What are the major products of thermal cracking?
Alkenes (sometimes hydrogen)
Give the conditions needed for catalytic cracking
Slight pressure, high temperature (450°C), zeolite catalyst
What are the major products of catalytic cracking?
Branched and cyclic alkanes, aromatic hydrocarbons
Define a fuel
Releases heat energy when burnt
What are the products of complete combustion?
H2O + CO2
What are the products of incomplete combustion?
CO and/or C and H2O
When does incomplete combustion occur?
When there is insufficient oxygen
Where are Sulfur-containing impurities found?
In petroleum fractions
What do Sulfur impurities produce when burnt?
SO2
Give the environmental implications of SO2 in the atmosphere
SO2 will dissolve in atmospheric water and can produce acid rain
How can SO2 be removed from the waste gases from furnaces?
By flue gas desulfurisation
Describe flue gas desulfurisation
Gases pass through a scrubber containing basic calcium oxide which reacts with the acidic Sulfur dioxide in a neutralisation reaction
Give the equation for flue gas desulfurisation
SO2 + CaO —> CaSO3
How do nitrous oxides form?
From the reaction between N2 and O2 inside car engines - high temperature and spark in the engine provides sufficient energy to break strong N2 bond
Give the equations for the formation of nitrous oxides in car engines
N2 + O2 —> 2NO or N2 + 2O2 —> 2NO2
Give the environmental consequences of nitrous oxides
NO is toxic and can form acidic gas NO2, NO2 is toxic and acidic and forms acid rain
Give the environmental consequences of carbon monoxide
Toxic - inhibit bloods ability to carry oxygen around body
Give the enviromental consequences of carbon dioxide
Contributes towards global warming
Give the environmental consequences of unburnt hydrocarbons
Contributes towards formation of smog
Give the environmental consequences of soot *
Global dimming and respiratory problems
Describe the role of catalytic converters
Remove CO, NOx and unburned hydrocarbons from the exhaust gases, turning them into ‘harmless’ CO2, N2 and H2O
Describe the structure of a catalytic converter
Have a ceramic honeycomb coated with a thin layer of catalyst metals, (platinum, palladium, rhodium) to give a large surface area
Describe how carbon dioxide contributes towards global warming
The C=O bonds absorb infrared radiation from the Earth and prevent it from escaping the atmosphere, then the energy is transferred to other molecules in the atmosphere by collisions so the atmosphere is warmed
What conditions does free radical substitution initiation require?
UV light
Give the steps of free radical substitution
Imitation, propagation, termination
Give the equation for initiation step of FRS
Cl2 —> 2 *Cl
By what process does the Cl-Cl bond break by in initiation?
Homolytic fission
Define a free radical
A reactive species which possesses an unpaired electron (don’t have any charge)
Give the proportion steps in FRS using methane + Cl2
CH4 + Cl —> Cl + *CH3
*CH3 + Cl2 —> CH3Cl + *Cl
Give the equation for termination during FRS using methane and Cl2
*CH3 + *Cl —> CH3Cl
2 *CH3 —> CH3CH3