3.2.3 Production of chemicals using electrolysis Flashcards
(30 cards)
electrolysis
passage of electrical energy from a direct current power supply through a conducting liquid causing redox reactions to occur
- endergonic
- non-spontaneous
molten ionic compounds
- ionic compound heated above melting point to become liquid
molten advantage/disadvantage
advantage: water is not present
disadvantage: requires more energy to maintain electrolyte in molten state and at required temp
aqueous advantage/disadvantage
advantage: heating is not required lowering costs
disadvantage: water can react instead of other ions
Downs cell
- NaCl and CaCl2 in 1:2 ratio to lower melting point of NaCl from 801 to600 degrees saving energy costs (since Ca2+ not reduced as it is weaker oxidant) and heat is generated by current flowing through electrolyte
- iron mesh screen separates products and anode and cathode to prevent from forming NaCl
- graphite electrode is inert, iron is cheaper and effectively inert as electrons are continuously supplied (negative electrode cathode reduction) preventing it from oxidising
membrane cell
- brine: concentrated NaCl solution (so Cl(g) will be produced at anode not H2O due to similar E0 values)
- semipermeable membrane prevents contact between reactive products and allows positive ions through resulting in pure NaOH output
aqueous electrolytes
- if non-standard high concentrations, a weaker reducing/oxidising agent can reduce/oxidise instead of water which may be the stronger reducing/oxidizing agent
inert electrodes
- platinum, carbon, graphite
- all metal cathodes since they receive constant supply of electrons and cannot be oxidsed
reactive electrodes
- can be impure and then purified via electrolysis with the pure metal deposited at the cathode
overpotential
- power supply must be greater than E0
E0 (reduction/lower)- E0 (oxidation/higher)
E0<0 (non-spontaneous)
electrolytic cell
- power supply pushes electrons towards negative electrode (cathode) so reduction occurs
- electrons pushed out of positive electrode (anode) so oxidation occurs
- usually inert electrodes and reaction occurs on surface of electrodes
galvanic vs electrolytic cell
- non-spontaneous as energy input required
- electrical to chemical
- electrodes don’t need to be in separate containers (no salt bridge needed) as reaction is non-spontaneous but products must be separated
electroplating
thin surface coating applied over another surface
electroplating cell
- object to be plated at cathode (negative terminal) and immersed in electrolyte solution containing ions of metal to be plated
- electrode of metal to be plated at anode (positive terminal)
- ions in electrolyte allow current to pass through cell
faraday’s first law of electrolysis
- mass of product and charge are directly proportional to each other
Q=It
faraday’s second law of electrolysis
- to produce one mole of metal another whole number of electrons must to consumed
Q=n9(e-) x F
faraday
96500 coulombs
charge on 1 mole of electrons
reasons for electrolysis
- separating molecules in compounds
- electroplating to improve appearance or prevent corrosion
- recharging secondary batteries
- purify
limit life of cell
- corrosion of anode
- side reactions like water
- build up of gas around electrode
rechargeable batteries requirements
- electrodes not damaged
- products remain in contact with electrodes
- reversible
polymer electrolyte membrane electrolyser (proton exchange membrane)
- solid electrolyte
- electrodes are porous to allow gas not liquid to pass through and are catalytic
- membrane contains advanced polymers that allow proton not electron flow to complete the circuit
- can be designed to produce compressed hydrogen gas removing need to separate compressor
- usually assembled in electrolyser stack more cost effective
artificial photosynthesis
- solar panel in solution (photoelectrochemical cell) causing water to oxidise into O2 and H+ which migrates to cathode and is reduced to produce hydrogen gas
brown hydrogen
from steam reforming fossil fules, releasing CO and CO2
grey hydrogen
hydrogen from industrial processes