Developing Fuels Flashcards

1
Q

Why does MTBE produce less carbon monoxide when burnt that pentane

A

There is less incomplete combustion as the molecule is already partially oxidised

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2
Q

Describe how a heterogeneous catalyst works

A

The reactant is adsorbed to the surface of the catalyst
Intramolecular bonds are weakened and broken
New bonds form
The product diffuses off the surface

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3
Q

What’s a structural isomer

A

a molecule with the same molecular formula but different structural formula

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4
Q

What is a biofuel and why is it carbon neutral

A

Made from crops which can be replanted
Plants take in CO2 for photosynthesis
Which balances out the CO2 produced from burning

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5
Q

Explain what is meant by auto-ignition and why it is undesirable in an engine.

A

Fuel igniting to without a spark which can damage the engine

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6
Q

You have a simple methane molecule, what is the shape, the bond angles and why? (5 points)

A
Tetrahedral
109 degrees
4 areas of negative charge
that repel each other
as far as possible
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7
Q

What does octane measure and why is it desirable to increase the number.

A

Measures the tendency to knock, higher the octane number means less knocking

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8
Q

Name 2 products formed by reforming

A

cycloalkanes and cycloalkenes

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9
Q

Explain how the catalyst can be poisoned by lead

A

The lead stays on the catalyst which prevents other molecules from reaching the surface

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10
Q

Suggest a benefit of using hydrogen as fuel

A

only produces water or does not produce CO2

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11
Q

Use ideas of bondmaking and bondbreaking to explain how a reaction can be endothermic

A

Bond breaking takes in energy, bondmaking gives out energy, here less energy is being given out then taken in

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12
Q

Explain what happens in cracking reactions and what types of molecules are produced

A

a large hydrocarbon is split into shorter alkanes and alkenes

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13
Q

Suggest why the use of non-food parts of crop plant is desirable for the production of biofuels

A

Allows food crops to be used for food

Production of food not affected

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14
Q

Give 2 ways in which molecules formed by cracking of a straight chain alkane molecule differ from the original molecule.

A

Shorter Hydrocarbons

Unsaturated/Alkenes

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15
Q

Explain the term catalyst and name the type of catalysis used in cracking

A

Catalysts speed up a reaction and be recovered unchanged/ not used up
Provide a path of lower activation energy

Heterogeneous catalysis

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16
Q

Describe and explain the structural feature of zeolites that make them effective catalysts for the cracking process.

A

Heterogeneous catalysis occurs on surface (ADSOBED)

Large surface area

17
Q

Name the refining process used to convert straight chain alkanes into branched chain alkenes with the same number of carbon atoms.

A

Isomerisation

18
Q

One method of disposing of used oil is to burn them. However, this produces atmospheric pollution in the form of a dense black cloud of Carbon particulates
Suggest and explain how these particulates are formed.

A

Incomplete combustion of oil

Caused by insufficient supply of oxygen

19
Q

What does empirical formula show

A

It shows the smallest ratio of the different atoms present

20
Q

Is it more desirable have a low or high octane number

A

High

21
Q

What type of hydrocarbons have high octane numbers

A

Those with lots of branched chains and aromatic rings and generally shorter

22
Q

What catalysts and conditions are used in isomerisation

A

Platinum at 260 Celsius and then the products are passed over a zeolite sieve separating the straight from the branched

23
Q

Suggest one reason why the use of non food parts of crops is desirable

A

Production of food is not effected

24
Q

What pieces of info are needed to workout the enthalpy change of combustion

A

Mass of fuel
Mr of fuel
Vol of water
Specific heat capacity

25
Q

What are the two products of reforming

A

Cyclic hydrocarbons and hydrogen

26
Q

What is a structural isomer

A

Different structural formulae for the same molecular formula