C1.5 Other useful substances from crude oil Flashcards

1
Q

What is cracking?

A

The thermal decomposition (breaking down by heat) of longer hydrocarbons chains into smaller more useful ones

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2
Q

Explain the process of cracking.

A
  • The long chain fraction is heated and vapourised
  • Vapours pass over a powdered (usually aluminum oxide) catalyst at a temperature of 400 - 700c degrees
  • The long chain molecules will split apart on the surface of the catalyst
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3
Q

What are the products of cracking?

A
  • Alkenes

- Shorter alkane chains

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4
Q

What are alkenes?

A

Unsaturated hydrocarbons

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5
Q

What is the formula for alkenes?

A

Cn H2n

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6
Q

How do alkenes react with bromine water and why?

A
  • They turn it from orange to colourless

- The double C=C bond opens up and bonds with the bromine

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7
Q

Why are alkenes unsaturated?

A

They can make more bonds as the carbon double bond can open up and bond with other atoms

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8
Q

What are some products of cracking useful for?

A
  • Fuels e.g petrol for cars and paraffin for jet fuel

- Chemicals for making plastics e.g ethene

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9
Q

How is ethanol produced from ethene?

A

Ethene is hydrated with steam in the presence of a catalyst

ethene + water —-> ethanol

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10
Q

What is the advantage of hydrating ethene to make ethanol?

A
  • Cheap
  • Few steps
  • Not much is wasted
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11
Q

What is the disadvantage of hydrating ethene to make ethanol?

A

Ethene is produced from crude oil which is non-renewable

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12
Q

How is ethanol made by fermentation?

A
  • Sugar is converted into ethanol using yeast

sugar ===> carbon dioxide + ethanol

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13
Q

What are the advantages of fermentation?

A
  • Lower temperature needed than for hydrating ethene
  • Fewer resources needed
  • Sugar is renewable
  • Sugar can be grown in poor countries
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14
Q

What are the disadvantages of fermentation?

A
  • Ethanol from this process isn’t very concentrated and needs to be distilled and purified
  • There are more steps involved
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15
Q

What is polymerisation?

A

Joining together small alkene molecules (monomers) to form large alkene molecules (polymers) by opening up their double bonds

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16
Q

What are a polymer’s physical properties affected by?

A
  • The temperature of polymerisation

- The pressure of polymerisation

17
Q

What conditions is a flexible, low density poly(ethene) made in?

A
  • 200c degrees

- 2000 atmospheres

18
Q

What conditions is a rigid, dense poly(ethene) made in?

A
  • 60c degrees
  • A few atmospheres
  • With a catalyst
19
Q

Describe six uses for polymers

A
  • Plastic bags : low density poly(ethene)
  • Waterproof coatings for fabrics
  • Dental polymers are used in resin tooth fillings
  • Hydrogels used for nappies (they absorb water)
  • Wound dressing: hydrogels keep wounds moist
  • Shape memory polymers : mattresses - they get softer when they get warmer
20
Q

Define ‘biodegradable’

A

Able to be broken down by microbes

21
Q

What material have some new biodegradable plastics been made from?

A

Cornstarch

22
Q

What is the disadvantage of recycling polymers?

A

There are many steps : collection, transportation, washing, separation and melting which uses up energy and therefore fossil fuels and can be expensive

23
Q

What are the disadvantages to using polymers?

A
  • They are products of crude oil, using up crude oil reserves
  • This may make them more expensive in the future
  • Causes waste and landfill sites