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[½»Á÷] Oxidation-Reduction Reactions ÒÑÓÐ1È˲ÎÓë

Oxidation-Reduction Reactions
Oxidation is the removal of electrons from, and reduction is the addition of electrons to an atom. Consider the galvanizing of iron, that is coating from with zinc to prevent rusting. The two competing reactions are:
Fe2++ 2e==Fe      E¡ã=-0.44volts Zn2++ 2e=Zn       E¡ã=-0.76volts Since the zinc reaction in the forward reaction produces a larger negative potential, that is liberates more energy, the spontaneous reaction is
Zn+ Fe2+==Fe+Zn2+
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Fe2++ 2e==Fe      E¡ã=-0.44volts Zn2++ 2e=Zn       E¡ã=-0.76volts ÓÉÓÚпµÄÕýÏò·´Ó¦²úÉú½Ï´óµÄ¸ºµçÊÆ£¬ÊͷŸü¶àµÄÄÜÁ¿£¬Õâ¸ö×Ô·¢·´Ó¦ÊÇ
Zn+ Fe2+==Fe+Zn2+
The coating of zinc serves two purposes: firstly it covers the iron and prevents its oxidation  (rather like a coat of paint) and secondly it provides anodic protection. If the galvanized steel is scratched, allowing the air to oxidize some iron, the Fe2+ produced is immediately reduced to iron by the zinc, and rusting does not occur. Similar applications in which one metal is sacrificed to protect another are the attaching of sacrificial blocks of magnesium to underground steel pipelines and the hulls of ships to prevent the rusting of iron.
±íÃæ¶ÆÐ¿ÓÐÁ½¸öÄ¿µÄ£ºÒ»ÊǸ²¸ÇÔÚÌú±íÃæ¿ÉÒÔ±£»¤Ìú²»±»ÑõÆø£¬¶þÊÇÆäÌṩÑô¼«±£»¤¡£Èç¹û¶ÆÐ¿¸ÖÌú±»»®ÆÆ£¬ÈÃ¿ÕÆøÑõ»¯Ò»Ð©Ìú£¬Fe2+ÔÚпÏ»¹Ô­³ÉÌú£¬ÒÔ¶øÉúÐâ²»»á·¢Éú¡£ÎþÉüÒ»ÖÖ½ðÊôÒÔ±£»¤ÁíÒ»ÖÖ½ðÊôµÄÀàËÆÓ¦ÓÃÊǰÑÒ»¿é×÷ÎþÉüÓõÄþ¶§Í¬Ï²¿µÄ¸Ö¹ÜºÍ´¬ÌåÁª½ÓÆðÀ´ÒÔ·ÀÖ¹ÌúµÄÉúÐâ¡£ Reduction Potential Diagrams
The reactions and stability of the various oxidation states of an element can be shown by the appropriate half reactions and reduction potentials. Consider iron:
Fe2++ 2e = Fe                    E¡ã=-0.44volts
Fe3++ 3e=Fe                      E¡ã=-0.04 Fe3++ e = Fe2+                    E¡ã=+0.77
FeO2-4 +3e+8H+ = Fe3+ + 4H2O       E¡ã=+2.20 This information is consolidted into a single diagram, in which the highest oxidation state is written at the left, and the lowest state at the right¡£
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Fe2++ 2e = Fe                    E¡ã=-0.44volts
Fe3++ 3e=Fe                      E¡ã=-0.04 Fe3++ e = Fe2+                    E¡ã=+0.77 FeO2-4 +3e+8H+ = Fe3+ + 4H2O       E¡ã=+2.20
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From the potentials it is apparent that reduction of FeO2-4 to Fe3+ releases a lot of energy, so FeO2-4 is a strong oxidizing agent. Similarly, Fe3+ is a weaker oxidizing agent going to Fe2+, but neither Fe3+nor Fe2+has any tendency to reduce to Fe.
Standard electrode potentials are measured on a scale with   
H++e = H       E¡ã=0.0volts
Since hydrogen is normally regarded as a reducing agent, reactions with negative values for E¡ã are more strongly reducing than hydrogen, that is they are strongly reducing. Materials which  are generally accepted as oxidizing agents have E¡ãvalues above +0.8 volts, those such as Fe3+¡ú Fe2+ of about 0.8 volts are stable (equally oxidizing and reducing), and those below +0.8 volts becoming increasingly reducing.
´ÓµçÊÆ¿ÉÒÔÃ÷ÏÔ¿´³öFeO2-4 µ½Fe3+µÄ·´Ó¦Êͷųö´óÁ¿µÄÄÜÁ¿£¬ËùÒÔFeO2-4ÊÇÇ¿Ñõ»¯¼Á¡£ÏàËÆµÄ£¬Fe3+ÓëFe2+Ïà±È ÊǽÏÈõµÄÑõ»¯¼Á£¬µ«ÊDz»¹ÜÊÇFe3+»¹ÊÇFe2+¶¼Ã»ÓÐÈκλ¹Ô­³ÉFeµÄÇ÷ÊÆ¡£±ê×¼µç¼«µçÊÆÊÇÒÔ£¨ÈçÏ£©±ê¶È£¨Îª×¼£©À´²âÁ¿µÄ¡£
H++e = H       E¡ã=0.0volts
ÓÉÓÚÇâͨ³£ÊDZ»µ±×÷»¹Ô­¼Á£¬¾ßÓиºµçÊÆµÄ·´Ó¦£¬Ëü±ÈH»¹Ô­ÐÔÇ¿£¬´Ó¶øËµÃ÷ËüÃÇÊÇÇ¿»¹Ô­ÐÔ¡£ÔªËزÄÁϵĵçÊÆ³¬¹ý0.8vͨ³£±»×÷ΪÑõ»¯¼ÁËù½ÓÊÜ£¬ÄÇЩÏñFe3+     Fe2+ÓÐÔ¼0.8vµÄÊÇÎȶ¨µÄ£¬¶øÄÇЩµÍÓÚ0.8vµÄÔòÓÐÖð½¥ÔöÇ¿»¹Ô­ÐÔ¡£
At first sight the potential of -0.04 V for Fe3+-Fe seems wrong since the potentials for Fe3+-Fe2+, and Fe2+-Fe are 0.77 V and -0.44V respectively. Potentials are not thermodynamic functions, and may not be added, but the potential may be "calculated from the free energy G, using the equation ¡÷G= ¡ªnFE0 where n is the number of electrons involved and F the Faraday.
ÆðÏÈ¿´µ½µÄ Fe3+-Fe µÄµçÊÆÊÇ-0.04vʱÊÇ´íÎóµÄ£¬ÒòΪFe3+-Fe2+, and Fe2+-Fe·Ö±ðÊÇ0.77 V and -0.44Vʱ£¬µçÊÆ²»ÊÇÈÈÁ¦Ñ§º¯Êý£¬ËùÒÔ²»ÄÜÏà¼Ó£¬µ«ÊǵçÊÆ¿ÉÄÜÒÔ×ÔÓÉÄÜG¼ÆËã³öÀ´£¬Ê¹Óù«Ê½¡÷G= ¡ªnFE0£¬ÕâÀïnÊÇÏà¹ØµÄµç×ÓÊý£¬FÊÇ·¨À¬µÚ£¨³£Êý£©¡£
The reduction potential diagram for copper in acid solution is oxidation state. The potential, and hence the energy released when Cu2+is reduced to Cu+are both very small, hence Cu2+is stable. On moving from left to right the potentials Cu'+ - Cu+ - Cu become more positive. Whenever this is found, the species in the middle (Cu+ in this case) disproportionates, that is it behaves as both a self-oxidizing and a self-reducing agent because it is energetically favourable for the following two changes to occur together.Thus Cu+ disproportionates in solution, and is only found in the solid state. ËáÈÜÒºÖÐÍ­µÄ»¹Ô­Í­ÊÇÑõ»¯Ì¬¡£Cu2+±»»¹Ô­³ÉCu+ʱµÄµçÊÆ¼°ºóÀ´ÊͷŵÄÄÜÁ¿¶¼ÊǺÜÉٵģ¬Òò´ËCu2+ÊÇÎȶ¨µÄ¡£Cu'+ - Cu+ - CuÒÔ×ó²àµ½ÓÒ²àµçÊÆ±äµÃ¸üÕý£ºµ±´æÔÚÕâÖÖÇé¿öʱ£¬´¦ÓÚÖмäµÄÎïÖʱã»á·¢ÉúÆç»¯·´Ó¦£¬¼´ËüÆð×ÔÉíÑõ»¯¼ÁºÍ×ÔÉí»¹Ô­¼ÁµÄ×÷Óá£ÒòΪÏÂÁÐÁ½Öֱ仯ͬʱÔÚÄÜÁ¿ÉÏÊÇÓÐÀûµÄ¡£Òò¶øCu ÄÜÔÚÈÜÒºÖÐÆç»¯£¬(¹Ê)ËüÖ»ÄÜÔÚ¹Ì̬ÖÐÕÒµ½¡£
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