الدينايكا الحرارية 1
الدينايكا الحرارية 1
ﻣﻔﺎﻫﻴﻢ ﺃﺳﺎﺳﻴﺔ
Fundamental Concepts
א מא
ﺍﺳﺘﻌﻤﻞ ﺍﻹﻧﺴﺎﻥ ﺣﻮﺍﺳﻪ ﻟﻠﺘﻤﻴﺰ ﺑﻴ ﻦ ﺍﻷﺟﺴﺎﻡ ﺍﳊﺎﺭﺓ ﻭﺍﻷﺟﺴﺎﻡ ﺍﻟﺒﺎﺭﺩﺓ .ﻭﺍﺑﺘﺪﻉ ﻃﺮﻗﹰﺎ ﻟﺘﺴﺨﲔ ﺍﻷﺟﺴﺎﻡ ﻭﻛﺬﻟﻚ
ﻟﺘﱪﻳﺪﻫﺎ .ﺑﻞ ﺃﻧﻪ ﺍﺳﺘﻌﻤﻞ ﺍﳊﺮﺍﺭﺓ ﻟﻐﺎﻳﺎﺕ ﻋﻤﻠﻴﺔ ﻛﺎﻟﺘﺪﻓﺌﺔ ﻭﺍﻵﻟﺔ ﺍﻟﺒﺨﺎﺭﻳﺔ.
ﺑﻌﺪ ﺃ ﹾﻥ ﺍﺧﺘﺮﻉ ﺟﻴﻤﺲ ﻭﺍﻁ ﺍﻵﻟﺔ ﺍﻟﺒﺨﺎﺭﻳﺔ ﰲ ﺍﻟﺴﺘﻴﻨﻴﺎﺕ ﻣﻦ ﺍﻟﻘﺮﻥ ﺍﻟﺜﺎﻣﻦ ﻋﺸﺮ ﻭﺍﻟﱵ ﺗﺴﺘﺨﺪﻡ ﻓﻴﻬﺎ ﺍﻟﻄﺎﻗﺔ
ﺍﳊﺮﺍﺭﻳﺔ ﻟﺘﻮﻟﻴﺪ ﻃﺎﻗﺔ ﺣﺮﻛﺔ ﻣﻴﻜﺎﻧﻴﻜﻴﺔ ،ﻭﻟﺪﺕ ﺍﳊﺎﺟﺔ ﻟﺪﺭﺍﺳﺔ ﻣﺪﻯ ﺗﺄﺛﺮ ﺧﺼﺎﺋﺺ ﻧﻈﺎ ٍﻡ ﻣﺎ ﺑﺎﳊﺮﺍﺭﺓ.
ﺍﻟﺪﻳﻨﺎﻣﻴﻜﺎ ﺍﳊﺮﺍﺭﻳﺔ ﻫﻲ ﻓﺮﻉ ﺍﻟﻔﻴﺰﻳﺎﺀ ﺍﳌﻌﻨﻲ ﺑﺪﺭﺍﺳﺔ ﺧﺼﺎﺋﺺ ﺍﳌﺎﺩﺓ ﺍﳌﺎﻛﺮﻭﺳﻜﻮﺑﻴﺔ )ﻛﻜﻞ( ﲢﺖ ﺗﺄﺛﲑ ﺍﳊﺮﺍﺭﺓ
ﺩﻭﻥ ﺍﻟﻨﻈﺮ ﺇﱃ ﺧﺼﺎﺋﺼﻬﺎ ﺍﳌﻴﻜﺮﻭﺳﻜﻮﺑﻴﺔ )ﺍﻟﺘﻔﺼﻴﻠﻴﺔ( .ﻭﻛﻜﻞ ﺃﻓﺮﻉ ﺍﻟﻔﻴﺰﻳﺎﺀ ﻓﺈ ﱠﻥ ﺍﻟﺪﻳﻨﺎﻣﻴﻜﺎ ﺍﳊﺮﺍﺭﻳﺔ ﻣﺒﻨﻴﺔ ﻋﻠﻰ
ﻗﻮﺍﻋ ﺪ ﻣﺴﺘﻘﺎ ٍﺓ ﻣﻦ ﺍﻟﺘﺠﺮﺑﺔ ﺍﻟﻌﻠﻤﻴﺔ ﺍﳌﺨﱪﻳﺔ ،ﻭﻳﻤﻜﻦ ﺑﻔﻀﻞ ﻫﺬﺍ ﺍﻟﻌﻠﻢ ﺍﺷﺘﻘﺎﻕ ﻋﻼﻗﺎﺕ ﺑﲔ ﻛﻤﻴﺎﺕ ﻓﻴﺰﻳﺎﺋﻴﺔ
ﻛﻤﻌﺎﻣﻼﺕ ﺍﻟﺘﻤﺪﺩ ﻭﺍﻹﻧﻀﻐﺎﻃﻴﺔ ﻭﺍﻟﺴﻌﺔ ﺍﳊﺮﺍﺭﻳﺔ ﺍﻟﻨﻮﻋﻴﺔ ﻭﻣﻌﺎﻣﻼﺕ ﺍﳌﻐﻨﺎﻃﻴﺴﻴﺔ ﻭﺍﻟﻌﺎﺯﻟﻴﺔ ﻟﻠﻤﻮﺍﺩ ﻭﻣﺪﻯ ﺗﺄﺛﺮﻫﺎ
ﺑﺎﳊﺮﺍﺭﺓ .ﺗﻨﺒﺌﻨﺎ ﻫﺬﻩ ﺍﳌﺒﺎﺩﺉ ﺃﻳﻀﹰﺎ ﺃﻱ ﺍﻟﻌﻼﻗﺎﺕ ﺍﻟﻮﺍﺟﺐ ﺍﳊﺼﻮﻝ ﻋﻠﻴﻬﺎ ﳐﱪﻳﹰﺎ ﻟﺘﺤﺪﻳﺪ ﺧﺼﺎﺋﺺ ﻧﻈﺎﻡ ﻣﺎ.
ﻳﻤﻜﻨﻨﺎ ﺍﻟﻘﻮﻝ ﺃ ﱠﻥ ﻣﺒﺎﺩﺉ ﺍﻟﺪﻳﻨﺎﻣﻴﻜﺎ ﺍﳊﺮﺍﺭﻳﺔ ﺗﻠﺨﺺ ﰲ ) 3ﺃﻭ (4ﻗﻮﺍﻧﲔ ﻧﺘﻴﺠﺘﻬﺎ ﺍﻷﻭﱃ ﻭﺍﻷﺧﲑﺓ ﺃ ﱠﻥ ﺍﳊﺮﺍﺭﺓ
ﻃﺎﻗﺔ ﺩﺍﺧﻠﻴﺔ .ﻳﺘﻌﻠﻖ ﺍﻟﻘﺎﻧﻮﻥ ﺭﻗﻢ 1ﻭﺍﳌﺴﻤﻰ "ﺍﻟﻘﺎﻧﻮﻥ ﺍﻟﺼﻔﱢﺮﻱ" The Zeroth Lawﲟﻔﻬﻮﻡ ﺩﺭﺟﺔ
ﺍﳊﺮﺍﺭﺓ ،ﰲ ﺣﲔ ﺃ ﱠﻥ ﺍﻟﻘﺎﻧﻮﻥ ﺭﻗﻢ 2ﻭﻳﺪﻋﻰ "ﺍﻟﻘﺎﻧﻮﻥ ﺍﻷﻭﻝ ﰲ ﺍﻟﺪﻳﻨﺎﻣﻴﻜﺎ ﺍﳊﺮﺍﺭﻳﺔ" ﻫﻮ ﺗﻌﻤﻴﻢ ﳌﺒﺪﺃ ﺣﻔﻆ ﺍﻟﻄﺎﻗﺔ
ﻟﻴﺴﺘﻮﻋﺐ ﺍﳊﺮﺍﺭﺓ ﻛﻄﺎﻗﺔ ﻭﻳﻤﻜﻨﻨﺎ ﻫﺬﺍ ﺍﻟﻘﺎﻧﻮﻥ ﻣﻦ ﺇﺩﺧﺎﻝ ﻣﻔﻬﻮﻡ ﺍﻟﻄﺎﻗﺔ ﺍﻟﺪﺍﺧﻠﻴﺔ .ﻳﺪﺧﻞ "ﺍﻟﻘﺎﻧﻮﻥ ﺍﻟﺜﺎﱐ ﰲ
ﺍﻟﺪﻳﻨﺎﻣﻴﻜﺎ ﺍﳊﺮﺍﺭﻳﺔ" )ﻭﺗﺮﺗﻴﺒﻪ ﺭﻗﻢ (3ﻣﻔﻬﻮﻡ ﺍﻹﻧﺘﺮﻭﰊ ﻭﻫﻲ ﻣﺘﻐﲑ ﻳﺴﻤﺢ ﺑﺘﻘﺪﻳﺮ ﻗﻴﻤﺔ ﺍﻟﻄﺎﻗﺔ ﺍﳌﹸﻬﺪﺭﺓ ﰲ ﻧﻈﺎ ٍﻡ ﻣﺎ
ﺺ ﰲ ﺇﺣﺪﻯ ﺻﻴﻐﻪ ﻋﻠﻰ ﺍﺳﺘﺤﺎﻟﺔ ﻋﻜﺲ ﺃﻳﺔ ﻇﺎﻫﺮﺓ ﰲ ﺍﻟﻄﺒﻴﻌﺔ ﻭﰲ ﺻﻴﻐﺔ ﺃﹸﺧﺮﻯ ﻋﻠﻰ ﻣﺪﻯ ﻛﻔﺎﺀﺓ ﻧﻈﺎ ٍﻡ ﻣﺎ ﰲ
ﻭﻳﻨ
ﲢﻮﻳﻞ ﺍﳊﺮﺍﺭﺓ ﺇﱃ ﺷﻐﻞ )ﺃﻱ ﺇﱃ ﻃﺎﻗﺔ( .ﻭﻳﺘﻌﻠﻖ ﺍﻟﻘﺎﻧﻮﻥ ﺍﻟﺜﺎﻟﺚ ﰲ ﺍﻟﺪﻳﻨﺎﻣﻴﻜﺎ ﺍﳊﺮﺍﺭﻳﺔ ﺑﺎﻷﻧﻈﻤﺔ ﺍﳋﺎﺿﻌﺔ ﻟﺘﺄﺛﲑﺍﺕ
ﻗﺒﻞ ﺍﻟﺪﺧﻮﻝ ﰲ ﺻﻠﺐ ﺍﳌﻮﺿﻮﻉ ﻻ ﺑﺪ ﻣﻦ ﺍﻟﺘﻌﺮﺽ ﳌﻔﻬﻮﻡ ﺍﳊﺮﺍﺭﺓ ﻛﻤﺎ ﻧﻌﺮﻓﻪ ﺍﻵﻥ .ﲤﺎﻣﹰﺎ ﻛﻤﺎ ﻗﻨﻦ ﺍﻹﻧﺴﺎﻥ
ﻣﻔﻬﻮﻡ ﺍﻟﻘﻮﺓ ﺑﻘﻴﺎﺳﻪ ﳌﻘﺪﺍﺭﻫﺎ ﻓﻠﻘﺪ ﺃﹸﺿﻄﺮ ﻟﻌﻤﻞ ﺃﺟﻬﺰﺓ ﻗﻴﺎﺱ ﻟﺘﺤﺪﻳﺪ ﻣﺪﻯ ﻛﻮﻥ ﺟﺴ ٍﻢ ﻣﺎ ﺣﺎﺭﹰﺍ ﺃﻭ ﺑﺎﺭﺩﹰﺍ ﺃﻭ ﻓﺎﺗﺮﹰﺍ
ﺳﻮﻑ ﻧﺴﺘﺨﺪﻡ ﰲ ﻫﺬﺍ ﺍﻟﻜﺘﺎﺏ ﻋﺪﺓ ﺗﻌﺎﺑﲑ ﻻ ﺑﺪ ﻣﻦ ﺗﻌﺮﻳﻔﻬﺎ ﺑﺪﺍﻳﺔﹰ ،ﻛﺎﻟﻨﻈﺎﻡ ﻭﺣﺪﻭﺩﻩ ﻭﳏﻴﻄﻪ ﻃﺒﻴﻌﺘﻪ.
ﺑﺸﻜﻞ ﻋﺎﻡ ﻳﻘﺼﺪ ﺑﺎﻟﻨﻈﺎﻡ ﰲ ﺍﻟﻔﻴﺰﻳﺎﺀ "ﻛﻞ ﺟﺰﺀ ﻣﻦ ﳎﻤﻮﻋﺔ" ،ﻭﻫﺬﺍ ﺍﳉﺰﺀ ﳏﺎﻁ ﺑﺴﻄﺢ ﻣﻐﻠﻖ ﻳﻌﺮﻑ ﲝﺪ ﺍﻟﻨﻈﺎﻡ.
ﻭﻛﻤﺜﺎﻝ ﺗﻤﺜﱢﻞ ﺍﻤﻮﻋﺔ ﺍﻟﺸﻤﺴﻴﺔ ﺍﻟﱵ ﻳﻨﺘﻤﻲ ﳍﺎ ﻛﻮﻛﺒﻨﺎ ﻧﻈﺎﻣﹰﺎ ﻫﻮ ﺟﺰﺀ ﻣﻦ ﺍﺮﺓ ﺍﳌﻌﺮﻭﻓﺔ ﺑﺪﺭﺏ ﺍﻟﺘﺒﺎﻧﺔ ﻭﺍﻟﱵ
ﺑﺪﻭﺭﻫﺎ ﺗﺸﻜﱢﻞ ﻧﻈﺎﻣﺎﹰ ،ﻫﻮ ﺟﺰ ٌﺀ ﻣﻦ ﺍﻟﻜﻮﻥ ﻛﻜﻞ .ﰲ ﺍﻟﺪﻳﻨﺎﻣﻴﻜﺎ ﺍﳊﺮﺍﺭﻳﺔ ﻳﻤﺜﱢﻞ ﻏﺎﺯ ﳏﺼﻮﺭ ﰲ ﺃﻧﺒﻮﺑﺔ ﻧﻈﺎﻣﺎﹰ،
ﻣﻔﺘﻮﺣﹰﺎ ﳍﺬﺍ ﺍﻟﻨﻈﺎﻡ ﻭﻳﺸﻜﱢﻞ ﺳﻄﺢ ﺍﻷﻧﺒﻮﺑﺔ ﺣ ﺪﹰﺍ ﻣﻐﻠﻘﹰﺎ ﻟﻠﻐﺎﺯ ﺍﶈﺼﻮﺭ )ﺃﻱ ﺍﻟﻨﻈﺎﻡ ﺍﳌﹸﻌﺘﱪ(.
Surrounding
ﺏ( ﺍﳌﹸﺤﻴﻂ
ﺗﻌﲎ ﺍﻟﺪﻳﻨﺎﻣﻴﻜﺎ ﺍﳊﺮﺍﺭﻳﺔ ﺑﺄﻧﻈﻤﺔ ﺗﺘﺒﺎﺩﻝ ﺍﻟﻄﺎﻗﺔ ﻣﻊ ﺃﻧﻈﻤﺔ ﺃﹸﺧﺮﻯ .ﺗﺴﻤﻰ ﻫﺬﻩ ﺍﻷﺧﲑﺓ ﺑﺎﻟﻨﺴﺒﺔ ﻟﻨﻈﺎ ٍﻡ ﻣﺎ "ﳏﻴﻂ
ﺍﻟﻨﻈﺎﻡ" ﻭﻳﺸﻜﱢﻞ ﺍﻟﻨﻈﺎﻡ ﻭﳏﻴﻄﻪ ﻣﻌﹰﺎ ﻣﺎ ﻳﺴﻤﻰ ﺑﺎﻤﻮﻋﺔ ﺃﻭ ﺍﻟﻜﻮﻥ ) universeﺍﻟﺸﻜﻞ .(1-1
Isolated and non isolated systems ﺝ( ﺍﻷﻧﻈﻤﺔ ﺍﳌﻌﺰﻭﻟﺔ ﻭﺍﻷﻧﻈﻤﺔ ﻏﲑ ﺍﳌﻌﺰﻭﻟﺔ
ﻱ ﺗﺒﺎﺩ ٍﻝ ﻟﻠﻤﺎﺩﺓ ﺑﺄﻧﻪ ﻣﻐﻠﻖ ﻭﺇﺫﺍ ﺣﺼﻞ ﻭﻛﺎﻥ ﻫﻨﺎﻙ ﺍﻧﺘﻘﺎﻝ ﻟﻠﻤﺎﺩﺓ ﻓﺈﻧﻨﺎ
ﻳﻘﺎﻝ ﻋﻦ ﻧﻈﺎ ٍﻡ ﻣﺎ ﻟﻴﺲ ﺑﻴﻨﻪ ﻭﺑﲔ ﻭﳏﻴﻄﻪ ﺃ
ﺗﺴﻤﻰ ﺍﻟﻜﻤﻴﺎﺕ ﺍﻟﻘﺎﺑﻠﺔ ﻟﻠﻘﻴﺎﺱ ﳐﱪﻳﹰﺎ ﻟﻨﻈﺎ ٍﻡ ﻣﺎ ﻣﺘﻐﲑﺍﺕ ﺣﺎﻟﺔ ﺍﻟﻨﻈﺎﻡ ﺃﻭ ﺧﺼﺎﺋﺼﻪ ،ﻭﺗﺤﺪﺩ ﻫﺬﻩ ﺍﻟﻜﻤﻴﺎﺕ ﺣﺎﻟﺔ
ﺍﻟﻨﻈﺎﻡ .ﺗﺸﻜﱢﻞ ﺍﳊﺮﺍﺭﺓ ﻭﺍﳊﺠﻢ ﻭﺍﻟﻀﻐﻂ ﺃﻣﺜﻠ ﹰﺔ ﳍﺬﻩ ﺍﻟﻜﻤﻴﺎﺕ .ﻭﺗﺪﺭﺱ ﺍﻟﺪﻳﻨﺎﻣﻴﻜﺎ ﺍﳊﺮﺍﺭﻳﺔ ﻣﺜﻞ ﻫﺬﻩ ﺍﳌﺘﻐﲑﺍﺕ
ﻛﻤﺎ ﻭﺗﺪﺭﺱ ﻣﻐﻨﻄﺔ ﺍﳌﻮﺍﺩ ﻭﺍﺳﺘﻘﻄﺎﺏ ﺍﳌﻮﺍﺩ ﺍﻟﻌﺎﺯﻟﺔ ﻭﺳﻄﻮﺡ ﺍﻟﺴﻮﺍﺋﻞ ﺑﺎﺳﺘﺨﺪﺍﻡ ﻫﺬﻩ ﺍﳌﺘﻐﲑﺍﺕ ﻭﻏﲑِﻫﺎ.
ﺗﺴﻤﻰ ﺍﳌﺘﻐﲑﺍﺕ ﺍﻟﱵ ﺗﻌﺘﻤﺪ ﻋﻠﻰ ﻛﺘﻠﺔ ﺍﻟﻨﻈﺎﻡ ﺍﳌﺪﺭﻭﺱ ﺍﳌﺘﻐﲑﺍﺕ ﺍﳌﻤﺘﺪﺓ )(extensive variables
m
ﺚ ﺗﻤﺜﱢﻞ
ﺚ mﺗﻤﺜﱢﻞ ﺍﻟﻜﺘﻠﺔ ﻭ ρﺍﻟﻜﺜﺎﻓﺔ ،ﻭﺍﻟﻄﺎﻗﺔ ﺍﻟﻜﻠﻴﺔ Etot = EK + Epﺣﻴ ﹸ
= ، Vﺣﻴ ﹸ ﻛﺎﳊﺠﻢ
ρ
EKﻭ Epﻃﺎﻗﺔ ﺍﳊﺮﻛﺔ ﻭﻃﺎﻗﺔ ﺍﻟﻮﺿﻊ ﻋﻠﻰ ﺍﻟﺘﻮﺍﱄ .ﺃﻣﺎ ﺍﳌﺘﻐﲑﺍﺕ ﺍﳌﺴﺘﻘﻠﺔ ﻋﻦ ﺍﻟﻜﺘﻠﺔ ﻛﺎﳊﺮﺍﺭﺓ ﻭﺍﻟﻀﻐﻂ
ﻭﺍﻟﻜﺜﺎﻓﺔ ﻓﺘﺪﻋﻰ ﺍﳌﺘﻐﲑﺍﺕ ﺍﳌﹸﺮﻛﱠﺰﺓ ) .(intensive variablesﺗﺴﻤﻰ ﺍﻟﻨﺴﺒﺔ ﺑﲔ ﺍﳌﺘﻐﲑ ﻭﻛﺘﻠﺔ ﺍﻟﻨﻈﺎﻡ ﺍﻟﻘﻴﻤﺔ
value per ﺍﻟﻨﻮﻋﻴﺔ specific valueﳍﺬﺍ ﺍﳌﺘﻐﲑ ﻭﻧﻘﻮﻝ ﻋﻨﻬﺎ ﺃﺣﻴﺎﻧﹰﺎ ﺑﺄﻧﻬﺎ ﺍﻟﻘﻴﻤﺔ ﻟﻮﺣﺪﺓ ﺍﻟﻜﺘﻠﺔ )
V
= vﻭﺍﻟﺬﻱ ﻫﻮ ﻋﻜﺲ ﺍﻟﻜﺜﺎﻓﺔ .ﻣﻦ ﺍﻟﻮﺍﺿﺢ ﺃ ﱠﻥ ﺍﻟﻘﻴﻤﺔ ﺍﻟﻨﻮﻋﻲ .(mass unitﻭﺃﻓﻀﻞ ﻣﺜﺎﻝ ﻫﻮ ﺍﳊﺠﻢ
m
ﻭﻧﺴﺘﺨﺪﻡ ﺃﻳﻀﹰﺎ ﺍﻟﻘﻴﻤﺔ ﺍﻟﻨﻮﻋﻴﺔ ﺍﳌﻮﻟﻴﺔ molal specific valueﻭﺍﻟﱵ ﻫﻲ ﺍﻟﻨﺴﺒﺔ ﺑﲔ ﺍﳌﺘﻐﲑ ﻭﻋﺪﺩ ﺍﳌﻮﻻﺕ
ﰲ ﺍﻟﻨﻈﺎﻡ .ﻧﺬﻛﱢﺮ ﺑﺄ ﱠﻥ ﺍﳌﻮﻝ moleﻭﺣﺪﺓ ﺍﺑﺘﺪﻋﻬﺎ ﺍﻟﻜﻴﻤﻴﺎﺋﻴﻮﻥ ﻟﺘﻤﱢﺜ ﹶﻞ ﻋﺪﺩ ﺃﻓﻮﺟﺎﺩﺭﻭ ﰲ ﻭﺯﻥ ﻧﻮﻋﻲ ﻟﻌﻨﺼ ٍﺮ ﻣﺎ.
NA=6.023×1023 ﻓﻤﻮﻝ ﻭﺍﺣﺪ ﻣﻦ ﺍﻷﻛﺴﺠﲔ ﻳﻌﲏ 32 gﻣﻦ ﻏﺎﺯ ﺍﻷﻛﺴﺠﲔ ﻭﳛﻮﻱ ﻋﺪﺩ ﺃﻓﻮﺟﺎﺩﺭﻭ
ﻣﻦ ﺟﺰﻳﺌﺎﺕ ﺍﻷﻛﺴﺠﲔ .ﰲ ﻛﺜﲑ ﻣﻦ ﺍﻷﺣﻴﺎﻥ ﻳﻔﻀﻞ ﺍﻟﺘﻌﺎﻣﻞ ﻣﻊ ﺍﻟﻘﻴﻢ ﺍﻟﻨﻮﻋﻴﺔ ﳌﺘﻐﲑﺍﺕ ﻧﻈﺎ ٍﻡ ﻣﺎ ،ﺇ ﹾﺫ ﺃﻧﻪ ﻣﻦ
ﺍﻟﺴﻬﻞ ﺍﻟﺘﻌﺎﻣﻞ ﻣﻊ ﺍﳌﻌﺎﺩﻻﺕ ﺍﳌﺴﺘﻘﱢﻠﺔ ﻋﻦ ﺍﻟﻜﺘﻠﺔ .ﺳﻮﻑ ﻧﺮﻯ ﻻﺣﻘﹰﺎ ﺃ ﱠﻥ ﺍﻟﺘﻌﺒﲑ ﻋﻦ ﺣﺎﻟﺔ ﻧﻈﺎ ٍﻡ ﻣﺎ ﻳﺒﺪﻭ ﻣﻨﻄﻘﻴﹰﺎ ﺇﺫﺍ
ﺍﺳﺘﺨﺪﻣﻨﺎ ﺯﻭﺟﹰﺎ )ﺃﻭ ﺃﻛﺜﺮ( ﻣﻦ ﺍﳌﺘﻐﲑﺍﺕ :ﺃﺣﺪﻫﺎ ﳑﺘﺪ ﻭﺍﻟﺜﺎﱐ ﻣﺮﻛﱠﺰ .ﺳﻮﻑ ﻧﺴﺘﺨﺪﻡ ﺍﻷﺣﺮﻑ ﺍﻟﻜﺒﲑﺓ ﰲ ﺣﺎﻟﺔ
ﺍﳌﺘﻐﲑﺍﺕ ﺍﳌﻤﺘﺪﺓ ﻭﺍﻷﺣﺮﻑ ﺍﻟﺼﻐﲑﺓ ﺍﳌﺎﺋﻠﺔ ﻟﻠﺘﻌﺒﲑ ﻋﻦ ﺍﳌﺘﻐﲑﺍﺕ ﺍﳌﺮﻛﱠﺰﺓ .ﻧﻠﺨﺺ ﰲ ﺍﳉﺪﻭﻝ 1-1ﺍﻟﺘﺎﱄ ﺑﻌﺾ
ﻣﺜﺎﻝ :1-1
ﺃﻱ ﺍﻟﻜﻤﻴﺎﺕ ﺍﻟﺘﺎﻟﻴﺔ ﻳﻤﺜﱢﻞ ﻣﺘﻐﲑﹰﺍ ﳑﺘ ﺪﹰﺍ ﻭﺃﻳﻬﺎ ﻳﻤﺜﱢﻞ ﻣﺘﻐﲑﹰﺍ ﻣﺮﻛﱠﺰﹰﺍ ؟
.2ﻃﻮﻝ ﺳﻠﻚ
ﺍﳊﻞ:
→ → →
ﻛﺜﺎﻓﺔ ﺍﻟﺘﻴﺎﺭ ﺍﳌﺘﺠﻬﺔ ﻭﻛﻼ j ﺚ ρﺍﳌﻘﺎﻭﻣﻴﺔ ﻭ
ﺣﻴ ﹸ E = ρj .1ﻣﻦ ﻗﺎﻧﻮﻥ ﺃﻭﻡ ﺑﺼﻴﻐﺘﻪ ﺍﻟﺘﺎﺭﳜﻴﺔ ﻧﻌﻠﻢ ﺃ ﱠﻥ:
ﺍﻟﻜﻤﻴﺘﻴﻦ ﻻ ﺗﻌﺘﻤﺪﺍﻥ ﻋﻠﻰ ﺍﻟﻜﺘﻠﺔ ∴ .ﻣﻦ ﺍﻟﻮﺍﺿﺢ ﺃ ﱠﻥ ﺍﺎﻝ ﺍﻟﻜﻬﺮﺑﺎﺋﻲ ﰲ ﺟﺴﻢ ﺻﻠﺐ ﻻ ﻳﻌﺘﻤﺪ ﻋﻠﻰ
V m
ﺃﻱ ﺍﻟﻨﺴﺒﺔ ﺑﲔ ﺍﳊﺠﻢ Vﻭﻣﺴﺎﺣﺔ ﺍﳌﻘﻄﻊ Aﻭﺑﺎﻟﺘﺎﱄ = l = .2ﻳﻌﻄﻰ ﻃﻮﻝ ﺳﻠﻚ ﺑﺎﻟﻌﻼﻗﺔ:
A ρA
ﻭﻫﻲ ﻛﻤﻴﺔ ﻻ ﺗﻌﺘﻤﺪ ﻋﻠﻰ ﺍﻟﻜﺘﻠﺔ ﺇ ﹾﺫ ﺗﻤﺜﱢﻞ ﺍﻟﻨﺴﺒﺔ ﺑﲔ ﻛﻤﻴﺘﲔ ﺗﻌﺘﻤﺪﺍﻥ ﻋﻠﻰ ﺍﻟﻜﺘﻠﺔ ﺃﻱ ﺑﲔ ﻣﺘﻐﲑﻳﻦ
ﻣﺜﺎﻝ :2-1
ﺇﺫﺍ ﻛﺎﻧﺖ ﻛﺜﺎﻓﺔ ﺍﳌﺎﺀ ﺗﺴﺎﻭﻱ :1 g cm-3
ﺍﳊﻞ:
.1
1
= v = 10 − 3 m3 kg−1
ρ
.n kilomole
ﻳﻌﺮﻑ ﺍﻟﻀﻐﻂ ﺍﳍﻴﺪﺭﻭﺳﺘﺎﺗﻴﻜﻲ )ﻭﻧﻘﻮﻝ ﲡﺎﻭﺯﹰﺍ ﺍﻟﻀﻐﻂ( ﻋﻠﻰ ﻭﺳﻂ ﻣﺘﺼﻞ ﺑﺄﻧﻪ ﻣﻘﺪﺍﺭ ﺍﻟﻘﻮﺓ ﺍﳌﺆﺛﺮﺓ ﻋﻠﻰ ﻭﺣﺪﺓ
ﺍﳌﺴﺎﺣﺔ ﰲ ﻫﺬﺍ ﺍﻟﻮﺳﻂ .ﻫﺬﺍ ﺍﻟﺘﻌﺮﻳﻒ ﻫﻮ ﺗﻌﺮﻳﻒ ﺍﻟﺸﺪ ﺍﳌﺆﺛﺮ ﻋﻠﻰ ﺍﻟﻮﺳﻂ ﺇﺫﺍ ﻛﺎﻧﺖ ﺍﻟﻘﻮﺓ ﻟﻮﺣﺪﺓ ﺍﳌﺴﺎﺣﺔ
ﺍﳌﺆﺛﺮﺓ ﻋﻠﻰ ﻋﻨﺼﺮ ﻣﺴﺎﺣﺔ ،ﺩﺍﺧﻞ ﺍﻟﻮﺳﻂ ﺃﻭ ﻋﻠﻰ ﺳﻄﺤﻪ ﺍﳋﺎﺭﺟﻲ (1 :ﻋﻤﻮﺩﻳﺔ ﻋﻠﻰ ﻋﻨﺼﺮ ﺍﳌﺴﺎﺣﺔ ﻭ (2ﻻ
A ﺗﻌﺘﻤﺪ ﻋﻠﻰ ﺍﲡﺎﻩ ﻫﺬﺍ ﺍﻟﻌﻨﺼﺮ .ﻋﻨﺼﺮ ﺍﳌﺴﺎﺣﺔ area elementﻫﻮ ﺟﺰﺀ ﻣﻘﺘﻄﻊ ﻣﻦ ﺍﳌﺴﺎﺣﺔ ﺍﻟﻜﹸﻠﻴﺔ
ﻛﺄﻣﺜﻠﺔ ﻋﻠﻰ ﺍﻟﻀﻐﻂ ﺍﳍﻴﺪﺭﻭﺳﺘﺎﺗﻴﻜﻲ )ﺳﻮﻑ ﻧﺘﺤﺪﺙ ﻋﻦ ﺍﻟﻀﻐﻂ ﺍﻋﺘﺒﺎﺭﹰﺍ ﻣﻦ ﺍﻵﻥ( ﻳﻌﺘﱪ ﺍﻟﺸﺪ ﺩﺍﺧﻞ ﻣﺎﺋﻊ )ﻏﺎﺯ
ﺃﻭ ﺳﺎﺋﻞ( ﺳﺎﻛﻦ ﰲ ﻭﻋﺎﺀ ﻣﻐﻠﻖ ﺿﻐﻄﹰﺎ ﻫﻴﺪﺭﻭﺳﺘﺎﺗﻴﻜﻴﹰﺎ .ﺇﺫﺍ ﻏﻤﺮﻧﺎ ﺟﺴﻤﹰﺎ ﺻﻠﺒﹰﺎ ﰲ ﻭﻋﺎﺀ ﳛﻮﻱ ﺳﺎﺋﻼﹰ ،ﻻ ﻳﺬﻳﺐ
ﺍﳉﺴﻢ ﺍﻟﺼﻠﺐ ،ﻓﺈ ﱠﻥ ﺍﳉﺴﻢ ﺍﻟﺼﻠﺐ ﺧﺎﺿﻊ ﻟﻀﻐﻂ ﻭﺍﻟﺴﺎﺋﻞ ﻛﺬﻟﻚ .ﻭﺣﺪﺓ ﺍﻟﻀﻐﻂ ﰲ ﻧﻈﺎﻡ MKSﻫﻲ
ﺍﻟﺸﻜﻞ :2-1ﺟﺴﻢ ﺻﻠﺐ ﻣﻐﻤﻮﺭ ﰲ ﺍﻟﺴﺎﺋﻞ" .ﻳﻤﺎﺭﺱ" ﺍﳉﺴﻢ ﺍﻟﺼﻠﺐ ﺿﻐﻄﹰﺎ ﻋﻠﻰ ﺍﻟﺴﺎﺋﻞ ﻭﺑﺎﻟﻌﻜﺲ.
ﻭﺗﺴﺘﺨﺪﻡ ﺍﻟﻮﺣﺪﺓ ،1 bar = 105 N m-2 = 106 dyne cm-2ﻭﻟﻘﻴﺎﺳﺎﺕ ﺿﻐﻂ ﻋﻤﻮﺩ ﺍﳍﻮﺍﺀ ﰲ
ﻧﻘﻄﺔ ﻣﺎ ﻋﻠﻰ ﺳﻄﺢ ﺍﻷﺭﺽ ﺗﺴﺘﻌﻤﻞ ﻭﺣﺪﺓ ﺍﻟﻀﻐﻂ ﺍﳉﻮﻱ ) (atm =atmosphereﻭﺗﻜﺎﻓﺊ ﺍﻟﻀﻐﻂ
ﺍﻟﻨﺎﺗﺞ ﻋﻦ ﻋﻤﻮﺩ ﺍﺭﺗﻔﺎﻋﻪ 76 cmﻣﻦ ﺍﻟﺰﺋﺒﻖ ،ﻭﺍﻟﺬﻱ ﻛﺜﺎﻓﺘﻪ ، ρ = 13.5951 g cm-3ﻋﻨﺪ ﻧﻘﻄﺔ
ﻭﺣﺪﺍﺕ ﺍﻟﻀﻐﻂ
.760ﰲ ﺣﺎﻻﺕ ﺍﻟﻀﻐﻂ ﻥ ﺍﻟﻀﻐﻂ ﺍﳉﻮﻱ ﻳﺴﺎﻭﻱ ﺿﻐﻂ 76 cm Hgﺃﻭ mm Hg
ﻧﻘﻮﻝ ﺃﺣﻴﺎﻧﹰﺎ ﺃ ﱠ
)ﻧﺴﺒﺔ ﺇﱃ ﺍﻹﻳﻄﺎﱄ (Torricelliﻭﺍﳌﻌﺮﻓﺔ ﺑﺄﺎ ﺍﻟﻀﻐﻂ ﺍﻟﻨﺎﺟﻢ ﻋﻦ 1 Torr ﺍﻟﻔﻴﺰﻳﺎﺋﻴﲔ ﻳﺴﺘﻌﻤﻠﻮﻥ ﺍﻟﻮﺣﺪﺓ
ﻗﹸﻠﻨﺎ ﰲ ﺍﳌﻘﺪﻣﺔ ﺃ ﱠﻥ ﺍﳊﺎﺟﺔ ﻟﺘﻘﻨﲔ "ﺳﺨﻮﻧﺔ" ﺃﻭ "ﺑﺮﻭﺩﺓ" ﺟﺴﻢ ﻣﺎ ﺃﺩﺕ ﺇﱃ ﺍﺑﺘﺪﺍﻉ ﻣﻮﺍﺯﻳﻦ ﺍﳊﺮﺍﺭﺓ .ﻓﻜﻜﻞ
ﺍﻟﻜﻤﻴﺎﺕ ﺍﻟﻔﻴﺰﻳﺎﺋﻴﺔ :ﺍﻟﻘﻮﺓ ﻭﺍﻟﺴﺮﻋﺔ ﺍﱁ ...ﻛﺎﻥ ﺍﳌﻌﻴﺎﺭ ﺍﻟﺬﻱ ﻳﺴﺘﺨﺪﻣﻪ ﺍﻹﻧﺴﺎﻥ ﻟﺘﻘﺪﻳﺮ ﻗﻴﻤﺘﻬﺎ ﻫﻮ ﺣﻮﺍﺳﻪ ﻭﰲ
ﺣﺎﻟﺔ ﺍﻷﺟﺴﺎﻡ ﺍﻟﺴﺎﺧﻨﺔ ﻭﺍﻟﺒﺎﺭﺩﺓ ﻛﺎﻥ "ﺇﺣﺴﺎﺳﻪ ﺑﺎﳊﺮﺍﺭﺓ" ﺑﺎﺳﺘﺨﺪﺍﻡ ﺣﺎﺳﺔ ﺍﻟﻠﻤﺲ ﻫﻮ ﺍﳌﻌﻴﺎﺭ .ﻭﻣﻦ ﺍﻟﻮﺍﺿﺢ ﺃ ﱠﻥ
ﻣﺜﻞ ﻫﻜﺬﺍ ﻣﻌﻴﺎﺭ ﻏﲑ ﺩﻗﻴﻖ ﻭﳏﺪﻭﺩ ﰲ ﻣﺪﺍﻩ )ﻻ ﻳﺴﺘﻄﻴﻊ ﺍﻹﻧﺴﺎﻥ ﳌﺲ ﺍﳊﺪﻳﺪ ﺍﳌﺼﻬﻮﺭ ﻣﺜﻼﹰ ،ﻧﺎﻫﻴﻚ ﻋﻦ ﺍﺳﺘﺤﺎﻟﺔ
ﺇﺫﺍ ﺣﺼﻞ ﺃﻱ ﺗﻐﻴﲑ ﰲ ﳏﻴﻂ ﻧﻈﺎ ٍﻡ ﻣﺎ ﺑﺘﺄﺛﲑ ﺍﳊﺮﺍﺭﺓ ،ﻓﺈ ﱠﻥ ﺍﻷﺧﲑ ﺳﻮﻑ ﻳﻌﺎﱐ ﺗﻐﻴﲑﹰﺍ ﰲ ﺣﺎﻟﺘﻪ )ﺃﻱ ﻣﺘﻐﲑﺍﺗﻪ( ﻭﺑﻌﺪ
ﻓﺘﺮﺓ ﻓﺈﻧﻪ ﺳﻮﻑ ﻳﺼ ﹸﻞ ﺇﱃ ﺣﺎﻟﺔ ﺟﺪﻳﺪﺓ ﻭﻧﻘﻮﻝ ﺃﻧﻪ ﺃﺻﺒﺢ ﻓﻴﻬﺎ ﻣﺘﺰﻧﹰﺎ ﺣﺮﺍﺭﻳﹰﺎ.
ﺇﺫﺍ ﻭﺿﻌﻨﺎ ﻧﻈﺎﻣﻴﻦ ﰲ ﲤﺎﺱ ﺃﻭ ﺍﺗﺼﺎﻝ ﺣﺮﺍﺭﻱ ﻓﺈﻧﻬﻤﺎ ﺳﻴﻌﺎﻧﻴﺎﻥ ﺗﻐﻴﲑﹰﺍ ﰲ ﺣﺎﻟﺘﻬﻤﺎ ﺣﺘﻰ ﻳﺼﻼ ﺇﱃ ﻭﺿﻊ ﻳﺼﺒﺢ ﻓﻴﻪ
ﻛ ﱞﻞ ﻣﻨﻬﻤﺎ ﰲ ﺍﺗﺰﺍﻥ ﺣﺮﺍﺭﻱ .ﻳﻤﻜﻦ ﺗﻔﺴﲑ ﻫﺬﺍ ﺍﻟﻮﺿﻊ ﺑﺎﻟﻘﻮﻝ ﺃ ﱠﻥ ﺍﳊﺮﺍﺭﺓ ﺍﻧﺴﺎﺑﺖ ﻣﻦ ﺃﺣﺪ ﺍﻟﻨﻈﺎﻣﻴﻦ ﻟﻶﺧﺮ ﺣﺘﻰ
ﺃﻱ ﺃ ﱠﻥ ﺩﺭﺟﺔ ﺍﳊﺮﺍﺭﺓ ﻫﻲ ﺍﳋﺎﺻﻴﺔ ﺍﻟﻔﻴﺰﻳﺎﺋﻴﺔ ﺍﻟﱵ ﺗﺤﺪﺩ ﻛﻮﻥ ﻧﻈﺎ ٍﻡ ﻣﺎ ﰲ ﺍﺗﺰﺍﻥ ﺣﺮﺍﺭﻱ ﻣﻊ ﻧﻈﺎ ٍﻡ ﺁﺧﺮ .ﻭﺇﺫﺍ ﺃﺗﺼﻞ
ﻧﻈﺎﻣﺎﻥ ﺣﺮﺍﺭﻳﹰﺎ ﻭﻭﺻﻼ ﺇﱃ ﺍﺗﺰﺍﻥ ﺣﺮﺍﺭﻱ ﻓﺈﻧﻨﺎ ﻧﻘﻮﻝ ﺃﻧﻬﻤﺎ ﻋﻠﻰ ﻧﻔﺲ ﺩﺭﺟﺔ ﺍﳊﺮﺍﺭﺓ .ﻭﺑﺎﻟﻌﻜﺲ ﺇﺫﺍ ﺍﺳﺘﻄﻌﻨﺎ ﻗﻴﺎﺱ
ﻼ ﻋﻠﻰ ﺣِﺪﺓ
ﺩﺭﺟﺔ ﺣﺮﺍﺭﺓ ﻧﻈﺎﻣﻴﻦ ﻣﺘﺼﻠﻴﻦ ﻭﻛﺎﻧﺖ ﺍﻟﻨﺘﻴﺠﺔ ﻭﺍﺣﺪﺓ ﻓﺈﻧﻨﺎ ﻧﻘﻮﻝ ﺃ ﱠﻥ ﺍﻟﻨﻈﺎﻣﻴﻦ ﻣﺘﺰﻧﺎﻥ ﺣﺮﺍﺭﻳﹰﺎ ﻛ
ﻭﳎﺘﻤﻌﻴﻦ.
ﺇ ﱠﻥ ﺃﻓﻀﻞ ﻣﺜﺎﻝ ﻫﻮ ﻣﻴﺰﺍﻥ ﺍﳊﺮﺍﺭﺓ ﺍﻟﺰﺋﺒﻘﻲ ﺍﳌﻌﺮﻭﻑ .ﻋﻨﺪ ﻭﺿﻊ ﻭﻋﺎﺀ ﺍﻟﺰﺋﺒﻖ ﰲ ﺇﻧﺎﺀ ﻣﺎ ٍﺀ ﺳﺎﺧﻦ ﻳﺘﻤﺪﺩ ﺍﻟﺰﺋﺒﻖ ﰲ
ﺍﻷﻧﺒﻮﺏ ﺍﻟﺸﻌﺮﻱ ﺣﺘﻰ ﻳﺴﺘﻘﺮ ﻋﻠﻰ ﺗﺪﺭﻳﺞ ﻣﻌﲔ ﻳﻤﺜﱢﻞ ﺩﺭﺟﺔ ﺣﺮﺍﺭﺓ ﺍﳌﺎﺀ ﺣﺴﺐ ﺍﳌﻘﻴﺎﺱ ﺍﳌﺴﺘﺨﺪﻡ ﰲ ﺍﻟﺘﺪﺭﻳﺞ
ﻭﺍﻟﺬﻱ ﻳﻤﺜﱢﻞ ﺃﻳﻀﹰﺎ ﺩﺭﺟﺔ ﺣﺮﺍﺭﺓ ﺍﻟﺰﺋﺒﻖ ،ﺃﻱ ﺃ ﱠﻥ ﺍﻟﻨﻈﺎﻣﻴﻦ ﻣﻮﺟﻮﺩﺍﻥ ﻋﻠﻰ ﻧﻔﺲ ﺩﺭﺟﺔ ﺍﳊﺮﺍﺭﺓ ﻭﺃﻧﻬﻤﺎ ﻣﺘﺰﻧﺎﻥ
ﺣﺮﺍﺭﻳﹰﺎ.
• ﺍﻻﺗﺰﺍﻥ ﺍﳌﺴﺘﻘﱢﺮ stable equilibriumﻭﻓﻴﻪ ﻳﻌﻮﺩ ﺍﻟﻨﻈﺎﻡ ﺇﱃ ﻭﺿﻌﻪ ﺍﻷﺻﻠﻲ ﺑﻌﺪ ﺃ ﹾﻥ ﻳﻌﺎﱐ "ﺇﺯﺍﺣﺔ
• ﺍﻻﺗﺰﺍﻥ ﺷﺒﻪ ﺍﳌﺴﺘﻘﱢﺮ metastable equilibriumﻭﻓﻴﻪ ﻳﻜﻮﻥ ﺍﻟﻨﻈﺎﻡ ﻣﺴﺘﻘﱢﺮﹰﺍ ﺑﻌﺪ ﺗﻌﺮﺿﻪ
• ﺍﻻﺗﺰﺍﻥ ﺍﶈﺎﻳﺪ neutral equilibriumﻭﻓﻴﻪ ﻳﺴﺘﻘﱢﺮ ﺍﻟﻨﻈﺎﻡ ﰲ ﻭﺿﻊ ﺟﺪﻳﺪ ﺑﻌﺪ ﺇﺯﺍﻟﺔ ﻣﺴﺒﺒﺎﺕ
ﺇﺯﺍﺣﺘﻪ.
ﺍﻟﺼﻐﺮ.
ﺇ ﱠﻥ ﺍﳋﻄﻮﺓ ﺍﻷﻭﱃ ﰲ ﺗﻌﺮﻳﻒ ﻣﻘﻴﺎﺱ ﻟﹻ"ﺩﺭﺟﺔ ﺍﳊﺮﺍﺭﺓ " ﺗﺘﻤﺜﱠﻞ ﰲ ﺇﳚﺎﺩ ﻣﻔﻬﻮﻡ ﺗﺴﺎﻭﻱ ﺩﺭﺟﺔ ﺣﺮﺍﺭﺓ ﺟﺴﻤﻴﻦ.
ﺍﻓﺘﺮﺽ ﺃ ﱠﻥ ﺟﺴﻤﹰﺎ ) Aﻛﺘﻠﺔ ﻣﻌﺪﻧﻴﺔ( ﻣﺘﺰﻥ ﺣﺮﺍﺭﻳﹰﺎ ﺑﻌﺪ ﲤﺎﺳﻬﺎ ﻣﻊ ﺟﺴﻢ ﺁﺧﺮ ) Bﻛﺘﻠﺔ ﻣﻌﺪﻧﻴﺔ ﺃﹸﺧﺮﻯ( .ﻟﻨﻔﺮﺽ
ﺳﻮﻑ ﳒﺪ ﳐﱪﻳﹰﺎ ﺃﻧﻪ ﺇﺫﺍ ﺟﻌﻠﻨﺎ Bﻭ Cﻳﺘﻼﻣﺴﺎﻥ ﻓﺈﻧﻬﻤﺎ ﺳﻮﻑ ﻳﻜﻮﻧﺎﻥ ﰲ ﺍﺗﺰﺍﻥ ﺣﺮﺍﺭﻱ ﺃﻭ ،ﺑﻌﺒﺎﺭﺓ ﻣﻜﺎﻓﺌﺔ،
ﻋﻠﻰ ﻧﻔﺲ ﺩﺭﺟﺔ ﺍﳊﺮﺍﺭﺓ .ﺗﺼﺎﻍ ﻫﺬﻩ ﺍﻟﻨﺘﻴﺠﺔ ﺍﳌﺨﱪﻳﺔ ﻋﻠﻰ ﺻﻴﻐﺔ ﻣﺒﺪﺃ ﻫﺎ ٍﻡ ﰲ ﺍﻟﺪﻳﻨﺎﻣﻴﻜﺎ ﺍﳊﺮﺍﺭﻳﺔ ﻳﺴﻤﻰ ﺍﻟﻘﺎﻧﻮﻥ
ﺇ ﱠﻥ ﳍﺬﺍ ﺍﻟﻘﺎﻧﻮﻥ ﺗﻄﺒﻴﻘﹰﺎ ﻫﺎﻣﹰﺎ ﻭﻫﻮ ﺍﻟﺘﺎﱄ :ﳌﻌﺮﻓﺔ ﺇﺫﺍ ﻛﺎﻧﺖ ﺩﺭﺟﺔ ﺣﺮﺍﺭﺓ ﻧﻈﺎﻣﻴﻦ ﻣﺘﺴﺎﻭﻳﺔ ﻓﻠﺴﻨﺎ ﲝﺎﺟﺔ ﻟﻮﺿﻌﻬﻤﺎ
ﰲ ﲤﺎﺱ ﺍﻟﻮﺍﺣﺪ ﻣﻊ ﺍﻵﺧﺮ ﻭﺇﻧﻤﺎ ﻳﻤﻜﻦ ﺍﺳﺘﺨﺪﺍﻡ ﻧﻈﺎ ٍﻡ ﺛﺎﻟﺚ ،ﻭﻫﻮ ﺍﻟﺬﻱ ﻳﻤﺜﱢﻞ ﻣﻴﺰﺍﻥ ﺍﳊﺮﺍﺭﺓ ،ﻭﻭﺿﻌﻪ ﰲ ﲤﺎﺱ
ﻣﻊ ﻛ ﻞ ﻣﻦ ﺍﻟﻨﻈﺎﻣﻴﻦ ﻋﻠﻰ ﺣِﺪﺓ .ﳚﺐ ﺃ ﹾﻥ ﻧﻨﺘﻈﺮ ﻓﺘﺮﺓ ﻛﺎﻓﻴﺔ ﺣﺘﻰ ﺗﺜﺒﺖ ﺍﳋﺎﺻﻴﺔ ﺍﻟﱵ ﺗﺴﻤﺢ ﺑﻘﻴﺎﺱ ﺍﳊﺮﺍﺭﺓ ،ﻣﺜﻞ
ﺍﺭﺗﻔﺎﻉ ﻋﻤﻮﺩ ﺍﻟﺰﺋﺒﻖ ﰲ ﻣﻴﺰﺍﻥ ﺍﳊﺮﺍﺭﺓ ﺍﻟﺰﺋﺒﻘﻲ ،ﻋﻠﻰ ﻗﻴﻤﺔ ﻣﺎ .ﻭﺇﺫﺍ ﻣﺎ ﻛﺎﻧﺖ ﻫﺬﻩ ﺍﻟﻘﻴﻤﺔ ﻭﺍﺣﺪﺓ ﻟﻠﺠﺴﻤﻴﻦ ﺍﻷﻭﻝ
ﻭﺍﻟﺜﺎﱐ ﻓﺈﻧﻨﺎ ﻧﻘﻮﻝ ﺃﻧﻬﻤﺎ ﻋﻠﻰ ﻧﻔﺲ ﺩﺭﺟﺔ ﺍﳊﺮﺍﺭﺓ .ﻫﺬﻩ ﻫﻲ ﺍﻟﻔﻜﺮﺓ ﺍﻷﺳﺎﺳﻴﺔ ﻭﺭﺍﺀ ﻣﻔﻬﻮﻡ ﻗﻴﺎﺱ ﺩﺭﺟﺔ ﺍﳊﺮﺍﺭﺓ
ﻭﺑﺎﻟﺘﺎﱄ ﺍﺧﺘﺮﺍﻉ ﻣﻮﺍﺯﻳﻦ ﺍﳊﺮﺍﺭﺓ .Thermometersﻳﻌﻤﻞ ﺍﳉﺴﻢ ﺍﻟﺜﺎﻟﺚ ﰲ ﻣﺜﺎﻟﻨﺎ ﺍﻟﺴﺎﺑﻖ ،ﰲ ﺍﳊﻘﻴﻘﺔ،
ﻳﻌﺘﻤ ﺪ ﻣﺪﻯ ﻭﺻﻮﻝ ﻧﻈﺎ ٍﻡ ﻣﺎ ﺇﱃ ﺣﺎﻟﺔ ﺍﻻﺗﺰﺍﻥ ﻣﻊ ﳏﻴﻄﻪ ﻋﻠﻰ ﻃﺒﻴﻌﺔ ﺣﺪﻭﺩ ﺍﻟﻨﻈﺎﻡ .ﺇﺫﺍ ﻛﺎﻧﺖ ﺣﺪﻭﺩ ﺍﻟﻨﻈﺎﻡ ﻋﺎﺯﻟﺔ
ﻟﻠﺤﺮﺍﺭﺓ ،ﻣﺜﻞ ﺍﻟﺼﻮﻑ ﺍﻟﺼﺨﺮﻱ ،ﻓﺈ ﱠﻥ ﺩﺭﺟﺔ ﺣﺮﺍﺭﺓ ﺍﻟﻨﻈﺎﻡ ﺗﺘﻐﲑ ﺑﺒﻂﺀ ﻭﻣﻦ ﺍﳌﻔﻴﺪ ﺟﺪﹰﺍ ﰲ ﺍﻟﺜﲑﻣﻮﺩﻳﻨﺎﻣﻴﻜﺎ ﺃ ﹾﻥ
ﻧﺘﺨﻴﻞ ﺣﺪﹰﺍ ﳚﻌﻞ ﺍﻟﺘﻐﲑ ﰲ ﺩﺭﺟﺔ ﺣﺮﺍﺭﺓ ﺍﻟﻨﻈﺎﻡ ﻣﻌﺪﻭﻣﹰﺎ ﲤﺎﻣﹰﺎ .ﻳﺴﻤﻰ ﻣﺜﻞ ﻫﺬﺍ ﺍﳊﺪ :ﺍﳊﺪ ﺍﻷﺩﻳﺎﺑﺎﰐ.
ﻳﻜﻮﻥ ﺍﻟﻨﻈﺎﻡ ﺍﶈﺪﻭﺩ ﲝﺪ ﺃﺩﻳﺎﺑﺎﰐ ﻋﻠﻰ ﺩﺭﺟﺔ ﺣﺮﺍﺭﺓ ﺛﺎﺑﺘﺔ ﺃﻳﹰﺎ ﻛﺎﻧﺖ ﺍﻟﺘﻐﲑﺍﺕ ﰲ ﺩﺭﺟﺔ ﺣﺮﺍﺭﺓ ﳏﻴﻄﻪ .ﻳﻠﻌﺐ ﺍﳊﺪ
ﺍﻷﺩﻳﺎﺑﺎﰐ ﺍﳌﺜﺎﱄ ﰲ ﺍﻟﺜﲑﻣﻮﺩﻳﻨﺎﻣﻴﻜﺎ ﺩﻭﺭﹰﺍ ﻣﺸﺎﹰﺎ ﻟﻠﺪﻭﺭ ﺍﻟﺬﻱ ﻳﻠﻌﺒﻪ ﺍﻟﺴﻄﺢ ﻋﺪﱘ ﺍﻻﺣﺘﻜﺎﻙ ﰲ ﺍﳌﻴﻜﺎﻧﻴﻜﺎ .ﻣﻊ
ﺃﻧﻬﻤﺎ ،ﻛﻠﻴﻬﻤﺎ ،ﻟﻴﺴﺎ ﻣﻮﺟﻮﺩﻳﻦ ﰲ ﺍﳊﻴﺎﺓ ﺍﻟﻌﻤﻠﻴﺔ ﺇ ﱠﻻ ﺃ ﱠﻥ ﺍﻓﺘﺮﺍﺽ ﻭﺟﻮﺩﳘﺎ ﻳﺴﺎﻋﺪ ﻋﻠﻰ ﺗﺒﺴﻴﻂ ﺍﻟﻈﻮﺍﻫﺮ ﻛﺨﻄﻮﺓ
ﺃﹸﻭﱃ ﻟﻔﻬﻤﻬﺎ .ﺑﺎﻧﺘﻈﺎﺭ ﺗﻌﺮﻳﻒ ﺃﻛﺜﺮ ﺩﻗﱠﺔ ﳌﻔﻬﻮﻡ ﺍﳊﺮﺍﺭﺓ ﺇ ﱠﻻ ﺃﻧﻨﺎ ﻧﺴﺘﻄﻴﻊ ﺍﻟﻘﻮﻝ ﺍﻵﻥ ﺃ ﱠﻥ ﺍﳊﺪ ﺍﻷﺩﻳﺎﺑﺎﰐ ﻫﻮ ﺣﺪ
"ﺗﺪﻓﻖ ﺍﳊﺮﺍﺭﺓ" ﻋﱪﻩ ﻳﺴﺎﻭﻱ ﺻﻔﺮﺍﹰ ،ﺣﺘﻰ ﻟﻮ ﻛﺎﻥ ﻫﻨﺎﻙ ﻓﺮﻕ ﰲ ﺩﺭﺟﺔ ﺍﳊﺮﺍﺭﺓ ﺑﲔ ﺳﻄﺤﻴﻪ "ﺍﻟﺪﺍﺧﻠﻲ
ﻭﺍﳋﺎﺭﺟﻲ".
ﻳﺴﻤﻰ ﺍﳊ ﺪ ﺍﻟﺬﻱ ﳝﻠﻚ ﺧﻮﺍﺹ ﻣﻌﺎﻛﺴﺔ ﲤﺎﻣﹰﺎ ﳋﻮﺍﺹ ﺍﳊ ﺪ ﺍﻷﺩﻳﺎﺑﺎﰐ :ﺍﳊﺪ ﺍﻟﺪﻳﺎﺣﺮﺍﺭﻱ
ﻼ.
) (diathermal boundaryﺃﻱ ﺃﻧﻪ ﺣﺪ ﻣﺼﻨﻮﻉ ﻣﻦ ﻣﺎﺩﺓ ﻣﻮﺻﻠﺔ ﻟﻠﺤﺮﺍﺭﺓ ،ﻛﺼﻔﻴﺤﺔ ﻣﻦ ﺍﻟﻨﺤﺎﺱ ﻣﺜ ﹰ
ﺗﻘﺘﺮﺏ ﺩﺭﺟﺔ ﺣﺮﺍﺭﺓ ﻧﻈﺎﻡ ﺣﺪﻩ ﺩﻳﺎﺣﺮﺍﺭﻱ ﻣﻦ ﺩﺭﺟﺔ ﺣﺮﺍﺭﺓ ﳏﻴﻄﻪ ﺑﺴﺮﻋﺔ.
ﻟﻠﺤﺼﻮﻝ ﻋﻠﻰ ﻣﻘﻴﺎﺱ ﻟﺪﺭﺟﺔ ﺍﳊﺮﺍﺭﺓ ﻭ ﺳﻠﱠﻢ ﺑﻘﻴﻢ ﺩﻗﻴﻘﺔ ﳚﺐ ﺍﺧﺘﻴﺎﺭ ﻧﻈﺎ ٍﻡ ﻳﺘﻐﲑ )ﺃﻱ ﺗﺘﻐﲑ ﺧﺼﺎﺋﺼﻪ( ﻣﻊ ﺍﳊﺮﺍﺭﺓ
thermometric property ﻭﻣﻌﺎﻳﺮ .ﻧﻘﻮﻝ ﰲ ﻫﺬﻩ ﺍﳊﺎﻟﺔ ﺃ ﱠﻥ ﻫﺬﺍ ﺍﻟﻨﻈﺎﻡ ﳝﻠﻚ ﺧﺎﺻﻴﺔ "ﻗﻴﺎﺱ ﺍﳊﺮﺍﺭﺓ"
ﺏ -ﺍﻟﻘﻮﺓ ﺍﻟﺪﺍﻓﻌﺔ ﺍﻟﻜﻬﺮﺑﺎﺋﻴﺔ ﺍﻟﻨﺎﺷﺌﺔ ﻋﻦ ﻭﺻﻞ ﺳﻠﻜﻴﻦ ﻣﻦ ﻣﻌﺪﻧﻴﻦ ﳐﺘﻠﻔﻴﻦ )ﺍﻟﺰﻭﺝ ﺍﳊﺮﺍﺭﻱ
(Thermocouple
ﻟﻘﻴﺎﺱ ﺩﺭﺟﺎﺕ ﺣﺮﺍﺭﺓ ﻏﲑ ﻣﻨﺨﻔﻀﺔ ﻛﺜﲑﹰﺍ ﻳﺴﺘﺨﺪﻡ ﺳﻠﻚ ﺭﻓﻴﻊ ﻣﻦ ﺍﻟﺒﻼﺗﲔ ﻣﻠﻔﻮﻑ ﻋﻠﻰ ﺇﻃﺎﺭ ﻋﺎﺯﻝ .ﻳﻤﺜﱢﻞ
ﺏ( ﺃ(
ﻳﻼﺣﻆ ﺃ ﱠﻥ ﻣﻘﺎﻭﻣﺔ ﺍﻟﺒﻼﺗﲔ ﺗﺘﻐﲑ )ﺑﺒﻂﺀ( ﻣﻊ ﺗﻐﲑ ﺩﺭﺟﺔ ﺍﳊﺮﺍﺭﺓ ﻟﺪﺭﺟﺎﺕ ﺣﺮﺍﺭﺓ ﻣﻨﺨﻔﻀﺔ ﻓﻴﺼﺒﺢ ﻣﺜﻞ ﻫﺬﺍ ﺍﳌﻴﺰﺍﻥ
ﻏﲑ ﺣﺴﺎﺱ ﻭﻟﺬﻟﻚ ﻳﻔﻀﻞ ﺍﺳﺘﺨﺪﺍﻡ ﻣﻘﺎﻭﻣﺔ ﻣﺼﻨﻮﻋﺔ ﻣﻦ ﺍﻟﺰﺭﻧﻴﺦ ﺍﳌﺨﻠﻮﻁ ﺑﻨﺴﺒﺔ ﺑﺴﻴﻄﺔ ﻣﻦ ﺍﳉﲑﻣﺎﻧﻴﻮﻡ
ﻭﻟﻜﻲ ﻳﻜﻮ ﹶﻥ ﺍﳌﻴﺰﺍﻥ ﺣﺴﺎﺳﹰﺎ ﳚﺐ ﺃ ﹾﻥ ﻳﻜﻮ ﹶﻥ ﺍﻟﺘﻐﲑ ∆Tﺃﻛ ﱪ ﻣﺎ ﻳﻤﻜﻦ ﻟﺘﻤﻴﻴﺰﻩ ،ﺃﻱ ﺃ ﱠﻥ ﻣﻴﻞ ﺍﻟﻌﻼﻗﺔ ﺍﳋﻄﻴﺔ ﳚﺐ ﺃ ﹾﻥ
ﻳﻜﻮ ﹶﻥ ﻛﺒﲑﹰﺍ.
ﻣﻐﻠﻘﺔ )ﺍﻟﺸﻜﻞ .(4-1ﻳﻨﺸﺄ ﰲ ﻫﺬﻩ ﺍﻟﺪﺍﺭﺓ ﻗﻮﺓ ﺩﺍﻓﻌﺔ ﻛﻬﺮﺑﺎﺋﻴﺔ )ﻕ.ﺩ.ﻙ( εﻋﻨﺪﻣﺎ ﻳﻜﻮﻥ ﻃﺮﻓﺎ ﺍﻟﻮﺻﻠﺘﻴﻦ ) Aﻭ
ﺗﺸﻜﱢﻞ εﺧﺎﺻﻴﺔ ﻗﻴﺎﺱ ﺣﺮﺍﺭﺓ ﳍﺬﺍ ﺍﻟﺰﻭﺝ ﺍﳊﺮﺍﺭﻱ .ﺗﻮﺿﻊ ﺇﺣﺪﻯ ﺍﻟﻮﺻﻠﺘﻴﻦ ﰲ ﻭﺳﻂ ﻋﻠﻰ ﺩﺭﺟﺔ ﺣﺮﺍﺭﺓ ﻣﻌﺎﻳﺮﺓ
ﻭﻣﻌﻠﻮﻣﺔ )ﺛﻠﺞ ﻣﻊ ﻣﺎﺀ( ﻭﺗﺪﻋﻰ ﻫﺬﻩ ﺍﻟﻮﺻﻠﺔ ﺑﺎﳌﻌﻴﺎﺭﻳﺔ ،standard junctionﺃﻣﺎ ﺍﻷُﺧﺮﻯ ﻭﺍﻟﱵ ﺗﺴﻤﻰ
ﻭﺻﻠﺔ ﺍﻻﺧﺘﺒﺎﺭ A) test junctionﰲ ﺍﻟﺸﻜﻞ (5-1ﻓﺘﻮﺿﻊ ﰲ ﲤﺎﺱ ﻣﻊ ﺍﳉﺴﻢ ﺃﻭ ﺍﻟﻮﺳﻂ ﺃﻭ ﺍﻟﻨﻈﺎﻡ ﺍﳌﺮﺍﺩ
ﻗﻴﺎﺱ ﺩﺭﺟﺔ ﺣﺮﺍﺭﺗﻪ ،ﻭﺗﻘﺎﺱ εﺑﺎﺳﺘﺨﺪﺍﻡ ﻓﻮﻟﺘﻤﻴﺘﺮ ﺃﻭ ﳎﺰﺉ ﺟﻬﺪ G) potentiometerﰲ ﺍﻟﺸﻜﻞ(.
ﻣﻮﺍﺯﻳﻦ ﺍﳊﺮﺍﺭﺓ ﺍﻟﱵ ﺗﻌﺘﻤﺪ ﻋﻠﻰ ﺗﻐﲑ ﺣﺠﻢ ﻏﺎﺯ ﻣﻊ ﺩﺭﺟﺔ ﺍﳊﺮﺍﺭﺓ 4-6-1
ﻳﺴﻤﻰ ﻣﺜﻞ ﻫﺬﺍ ﺍﳌﻴﺰﺍﻥ ﻏﲑ ﺍﳌﺴﺘﺨﺪﻡ ﰲ ﺍﻟﻘﻴﺎﺳﺎﺕ ﺍﳌﺨﱪﻳﺔ ﻭﻟﻜﻦ ﰲ ﳐﺘﱪﺍﺕ ﺍﳌﻌﺎﻳﺮﺓ :ﺍﳌﻴﺰﺍﻥ ﺍﻟﻐﺎﺯﻱ ﺫﺍ ﺍﳊﺠﻢ
ﻣﺎﻧﻮﻣﻴﺘﺮ ﻟﻘﻴﺎﺱ ﺿﻐﻂ ﺍﻟﻐﺎﺯ )ﺃﹸﻧﻈﺮ ﺍﻟﺸﻜﻞ .(6-1ﻋﻨﺪ ﺍﺭﺗﻔﺎﻉ ﺩﺭﺟﺔ ﺍﳊﺮﺍﺭﺓ ﻳﺴﺒﺐ ﺿﻐﻂ ﺍﻟﻐﺎﺯ ﺍﳔﻔﺎﺽ ﺍﻟﺰﺋﺒﻖ
ﰲ ﺍﻷﻧﺒﻮﺏ ﺍﻷﻳﺴﺮ Bﻭﺍﺭﺗﻔﺎﻋﻪ ﰲ ﺍﻷﻧﺒﻮﺏ ﺍﻷﳝﻦ .Aﻳﺘﺼﻞ ﺍﻷﻧﺒﻮﺑﺎﻥ Aﻭ Bﲝﻮﺽ ﻣﻠﺊ ﺑﺎﻟﺰﺋﺒﻖ ﻋﱪ ﺃﹸﻧﺒﻮﺏ
ﻣﻄﺎﻃﻲ .D
ﻼﻻ
ﺍﳌﺴﺘﺨﺪﻡ ﻭﻣﺪﻯ ﺩﺭﺟﺔ ﺍﳊﺮﺍﺭﺓ ﺍﳌﺮﺍﺩ ﻗﻴﺎﺳﻬﺎ ﻓﻤﺜ ﹰ
ﺍﻟﺸﻜﻞ :6-1ﺍﳌﻴﺰﺍﻥ ﺍﻟﻐﺎﺯﻱ ﺫﻭ ﺍﳊﺠﻢ ﺍﻟﺜﺎﺑﺖ
ﻳﺼﻠﺢ ﻫﺬﺍ ﺍﳌﻴﺰﺍﻥ ﺇ ﱠﻻ ﻟﻘﻴﺎﺱ ﺩﺭﺟﺎﺕ ﺣﺮﺍﺭﺓ ﰲ ﺍﻟﻔﺘﺮﺓ
ﻟﻨﺴ ﻢ Xﻗﻴﻤﺔ ﺧﺎﺻﻴﺔ ﻗﻴﺎﺱ ﺍﳊﺮﺍﺭﺓ ﻟﻠﻤﻴﺰﺍﻥ ﺍﳌﺴﺘﺨﺪﻡ X .ﺗﻤﺜﱢﻞ ﺍﳌﻘﺎﻭﻣﺔ Rﺃﻭ εﺃﻭ ﺣﺠﻢ ﺍﻟﻐﺎﺯ ﰲ ﺍﳌﻮﺍﺯﻳﻦ ﺍﻟﱵ
ﺗﺴﺘﺨﺪﻡ ﺍﳌﻘﺎﻭﻣﺔ ﺃﻭ ﺍﻟﺰﻭﺝ ﺍﳊﺮﺍﺭﻱ ﺃﻭ ﺍﻟﻐﺎﺯ ﻋﻠﻰ ﺍﻟﺘﻮﺍﱄ .ﻭﻟﺘﻜﻦ Θﺩﺭﺟﺔ ﺍﳊﺮﺍﺭﺓ ﺍﻟﺘﺠﺮﻳﺒﻴﺔ ﳌﻴﺰﺍﻥ ﺍﳊﺮﺍﺭﺓ ﺃﻭ
Θ2 ﻷﻱ ﻧﻈﺎﻡ ﻳﻜﻮﻥ ﻣﻌﻪ ﺍﳌﻴﺰﺍﻥ ﰲ ﺣﺎﻟﺔ ﺍﺗﺰﺍﻥ ﺣﺮﺍﺭﻱ .ﻳﻤﻜﻦ ﻛﺘﺎﺑﺔ ﺍﻟﻨﺴﺒﺔ ﺑﲔ ﺩﺭﺟﱵ ﺣﺮﺍﺭﺓ ﲡﺮﻳﺒﻴﺘﻴﻦ Θ1ﻭ
Θ1 X
= 1 )(2-1
Θ2 X2
ﺍﳋﻄﻮﺓ ﺍﻟﺘﺎﻟﻴﺔ ﻟﻌﻤﻞ ﻣﻘﻴﺎﺱ ﻟﺪﺭﺟﺔ ﺍﳊﺮﺍﺭﺓ ﻫﻲ ﺍﺧﺘﻴﺎﺭ ﻧﻘﻄﺔ ﺛﺎﺑﺘﺔ ﻣﻌﻴﺎﺭﻳﺔ ﻭﺇﻋﻄﺎﺅﻫﺎ ﻗﻴﻤ ﹰﺔ ﺟﺰﺍﻓﻴﺔ .ﳍﺬﺍ ﺍﻟﻐﺮﺽ
ﺍﺧﺘﲑﺕ ﺩﺭﺟﺔ ﺍﳊﺮﺍﺭﺓ ﺍﻟﱵ ﻳﻜﻮﻥ ﺍﳌﺎﺀ ﻋﻨﺪﻫﺎ ﰲ ﺣﺎﻻﺗﻪ ﺍﻟﺜﻼﺙ ﻣﻮﺟﻮﺩﹰﺍ ﰲ ﺣﺎﻟﺔ ﺍﺗﺰﺍﻥ ﺣﺮﺍﺭﻱ ﻭﺍﻟﱵ ﺗﺴﻤﻰ
ﻧﻘﻄﺔ ﺍﳌﺎﺀ ﺍﻟﺜﻼﺛﻴﺔ ) triple point of waterﺳﻮﻑ ﻧﻔﺼﻞ ﻫﺬﺍ ﻻﺣﻘﹰﺎ .ﻋﻨﺪ ﻫﺬﻩ ﺍﻟﻨﻘﻄﺔ ﺗﺘﻌﺎﻳﺶ ﺣﺎﻻﺕ
ﺍﳌﺎﺀ ﺍﻟﺜﻼﺙ :ﲞﺎﺭ ﺍﳌﺎﺀ ،ﺍﻟﺴﺎﺋﻞ ﻭ ﺍﳉﻠﻴﺪ .ﻭﻫﺬﺍ ﳑﻜﻦ ﻋﻨﺪ ﺿﻐﻂ ﻣﻘﺪﺍﺭﻩ .(4.58 mm Hg
ﺇﺫﺍ ﺍﻋﺘﱪﻧﺎ Θ3ﻫﻲ ﺩﺭﺟﺔ ﺍﳊﺮﺍﺭﺓ ﺍﻟﺘﺠﺮﻳﺒﻴﺔ ﻟﻠﻨﻘﻄﺔ ﺍﻟﺜﻼﺛﻴﺔ ﻭ X3ﻗﻴﻤﺔ ﺍﳌﺘﻐﲑ Xﺍﳌﺮﺍﺩﻓﺔ ﳍﺎ ،ﻓﺈ ﱠﻥ ﺩﺭﺟﺔ ﺍﳊﺮﺍﺭﺓ
ﺗﺜﺒﺖ ﺍﻟﺘﺠﺮﺑﺔ ﺃ ﱠﻥ ﺃﻓﻀﻞ ﻣﻮﺍﺯﻳﻦ ﺍﳊﺮﺍﺭﺓ ﻫﻲ ﺗﻠﻚ ﺫﺍﺕ ﺍﳊﺠﻢ ﺍﻟﻐﺎﺯﻱ ﺍﻟﺜﺎﺑﺖ ﻭﺍﻟﱵ ﺗﺘﻔﻖ ﻓﻴﻤﺎ ﺑﻴﻨﻬﺎ ﺃﻛﺜﺮ ﻣﺎ
ﻳﻤﻜﻦ ﻛﻠﱠﻤﺎ ﻛﺎﻥ ﺍﻟﻀﻐﻂ ﻋﻨﺪ ﺍﻟﻨﻘﻄﺔ ﺍﻟﺜﻼﺛﻴﺔ ﻟﻠﻤﺎﺀ ﻣﻨﺨﻔﻀﹰﺎ .ﺍﻟﻀﻐﻂ ﻫﻮ ﺍﳌﺘﻐﲑ Xﻫﻨﺎ .ﺇﺫﺍ ﻣﺜﱠﻠﻨﺎ ﺑﻴﺎﻧﻴﹰﺎ ﻗﺮﺍﺀﺓ ﻣﺜﻞ
ﻫﺬﻩ ﺍﳌﻮﺍﺯﻳﻦ ﻛﻤﺎ ﰲ ﺍﻟﺸﻜﻞ ﺑﺘﻤﺜﻴﻞ ﺍﻟﻨﺴﺒﺔ PS/P3ﺑﲔ ﺿﻐﻂ ﺍﻟﺒﺨﺎﺭ-ﺍﻟﻀﻐﻂ ﻋﻨﺪ ﻧﻘﻄﺔ ﻏﻠﻴﺎﻥ ﺍﳌﺎﺀ ﻭﻳﺮﻣﺰ
ﺍﳊﺮﻑ sﻳﺮﻣﺰ ﺇﱃ ﺍﻟﺒﺨﺎﺭ ) - (steamﻭﺿﻐﻂ ﺍﻟﻨﻘﻄﺔ ﺍﻟﺜﻼﺛﻴﺔ ﻋﻠﻰ ﳏﻮﺭ ﺍﻹﺣﺪﺍﺛﻴﺎﺕ ﺍﻟﻌﻤﻮﺩﻱ )ﺍﻟﺼﺎﺩﺍﺕ(
ﺑﺪﻻﻟﺔ P3ﻓﺈﻧﻨﺎ ﳓﺼﻞ ﻋﻠﻰ ﻋﻼﻗﺎﺕ ﺧﻄﻴﺔ ﺗﺘﻘﺎﻃﻊ ﲨﻴﻌﻬﺎ ﻋﻠﻰ ﳏﻮﺭ ﺍﻟﺼﺎﺩﺍﺕ ﰲ ﻧﻔﺲ ﺍﻟﻨﻘﻄﺔ=1.3660 :
.PS/P3
ﻧﻘﻄﺔ ﺍﻟﺘﻘﺎﻃﻊ ﺍﳌﺒﻴﻨﺔ ﻟﻴﺴﺖ ﳑﻜﻨﺔ ﳐﱪﻳﹰﺎ )ﻓﺎﻟﻀﻐﻂ P3=0ﻻ ﻳﻤﻜﻦ ﺍﳊﺼﻮﻝ ﻋﻠﻴﻪ( ﻭﺇﻧﻤﺎ ﳓﺼﻞ ﻋﻠﻴﻬﺎ ﺑﻌﻤﻞ
"ﺍﻣﺘﺪﺍﺩ "extrapolationﻟﻠﻤﻨﺤﻨﻴﺎﺕ ﺍﳌﺨﱪﻳﺔ .ﻭﻷﻳﺔ ﺩﺭﺟﺔ ﺣﺮﺍﺭﺓ ﺃﹸﺧﺮﻯ ﻏﲑ ﺍﻟﻨﻘﻄﺔ ﺍﻟﺜﻼﺛﻴﺔ ﻟﻠﻤﺎﺀ ﳓﺼﻞ
ﻋﻠﻰ ﻧﻘﻄﺔ ﺗﻘﺎﻃﻊ ﻣﺸﺘﺮﻛﺔ ﳌﺨﺘﻠﻒ ﺍﳌﻮﺍﺯﻳﻦ .ﻧﻌﺮﻑ ﻫﻨﺎ ﺩﺭﺟﺔ ﺍﳊﺮﺍﺭﺓ "ﺍﻟﻐﺎﺯﻳﺔ" ﺍﻟﺘﺠﺮﻳﺒﻴﺔ ﺑﹻ:
Pg
Θ g = Θ 3 × lim )(4-1
P3 → 0 P
3 V
ﻏﺎﺯ ﻣﻌﻴﻦ ﻋﻠﻰ ﺍﻟﺮﻏﻢ ﻣﻦ ﺃﻧﻬﺎ ﺗﻌﺘﻤﺪ ﻋﻠﻰ ﺗﺼﺮﻑ ﺍﻟﻐﺎﺯ ﻛﻜﻞ ﻭﺑﺎﻟﺘﺎﱄ ﻓﻬﻲ ﻟﻴﺴﺖ ﻣﺴﺘﻘﻠﺔ ﲤﺎﻣﹰﺎ ﻋﻦ ﺧﺼﺎﺋﺺ
ﻣﺎﺩﺓ ﻣﻌﻴﻨﺔ .ﻭﺗﺒﻘﻰ ﻣﺸﻜﻠﺔ ﲢﺪﻳﺪ ﺍﻟﻨﻘﻄﺔ ﺍﻟﺜﻼﺛﻴﺔ ﻟﻠﻤﺎﺀ .ﻗﺒﻞ 1954ﻛﺎﻧﺖ ﺩﺭﺟﺎﺕ ﺣﺮﺍﺭﺓ ﺍﻟﻐﺎﺯ ﺗﻌﺮﻑ
• ﺩﺭﺟﺔ ﺣﺮﺍﺭﺓ ﺍﺗﺰﺍﻥ ﺍﻟﺜﻠﺞ ﻭﺍﳌﺎﺀ ﺍﳌﺸﺒﻊ ﺑﺎﳍﻮﺍﺀ ﲢﺖ ﺿﻐﻂ ﻣﻘﺪﺍﺭﻩ ) 1atmﻧﻘﻄﺔ ﺍﻟﺘﺠﻤﺪ ﺃﻭ ﻧﻘﻄﺔ ﺍﳉﻠﻴﺪ
.(ice point
ﰲ ﺍﳌﻌﺎﺩﻟﺔ 4-1ﺍﻟﺴﺎﺑﻘﺔ ﺇﺫﺍ ﺍﺳﺘﺒﺪﻟﻨﺎ ﺍﻟﺮﻣﺰ gﺑﺎﻟﺮﻣﺰ sﻭﺍﻟﺮﻣﺰ 3ﺑﺎﻟﺮﻣﺰ iﻓﺈ ﱠﻥ ﺍﻟﺪﺭﺟﺘﻴﻦ ﺍﻟﺴﺎﺑﻘﺘﻴﻦ ﺗﻌﺮﻓﺎﻥ
ﺑﺎﻟﻌﻼﻗﺔ ﺍﻟﺘﺎﻟﻴﺔ:
P
ﻼ ﻋﻦ ﻗﻴﻤﺔ lim s ﻷ ﱠﻥ ﻧﻘﻄﺔ ﺍﳌﺎﺀ
ﺇ ﱠﻥ ﺃﻓﻀﻞ ﻗﻴﻤﺔ ﳐﱪﻳﺔ ﻟﻠﻨﺴﺒﺔ PSﻫﻲ 1.3661ﻭﺍﻟﱵ ﲣﺘﻠﻒ ﻗﻠﻴ ﹰ
P3 → 0 P3 V Pi
ﺳﻮﻑ ﻧﺮﻯ ﻻﺣﻘﺎﹰ ،ﺃﻧﻪ ﺑﺎﻹﻣﻜﺎﻥ ﺗﻌﺮﻳﻒ ﺍﻟﻨﺴﺒﺔ ﺑﲔ ﺩﺭﺟﱵ ﺣﺮﺍﺭﺓ ﺑﺎﺳﺘﺨﺪﺍﻡ ﻓﺮﺿﻴﺔ ﻟِﻠﻮﺭﺩ ﹶﻛ ﹾﻠﻔِﻦ ﻣﺒﻨﻴﺔ ﻋﻠﻰ
ﺗﺴﻤﻰ ﺩﺭﺟﺎﺕ ﺍﳊﺮﺍﺭﺓ ﺍﻟﺴﺎﺑﻘﺔ ﺩﺭﺟﺎﺕ ﺍﳊﺮﺍﺭﺓ ﺍﳌﻄﻠﻘﺔ ﻭﻧﺴﺘﺨﺪﻡ ﺍﳊﺮﻑ Tﻟﻠﺘﻌﺒﲑ ﻋﻨﻬﺎ .ﺳﻮﻑ ﻧﻔﺘﺮﺽ ﺍﻋﺘﺒﺎﺭﹰﺍ
ﻣﻦ ﺍﻵﻥ ﺃﻧﻪ ﻳﻤﻜﻦ ﻗﻴﺎﺱ ﺩﺭﺟﺔ ﺣﺮﺍﺭﺓ Tﺑﺎﺳﺘﺨﺪﺍﻡ ﻣﻴﺰﺍﻥ ﺣﺮﺍﺭﺓ.
ﻣﺜﺎﻝ :3-1
ﻋﻨﺪ ﻭﺿﻊ ﻣﻴﺰﺍﻥ ﺣﺮﺍﺭﺓ ﺯﺋﺒﻘﻲ ﰲ ﻣﺎﺀ ﻣﻮﺟﻮﺩ ﻋﻨﺪ ﻧﻘﻄﺔ ﺍﳌﺎﺀ ﺍﻟﺜﻼﺛﻴﺔ ﻓﺈ ﱠﻥ ﺍﺭﺗﻔﺎﻉ ﻋﻤﻮﺩ ﺍﻟﺰﺋﺒﻖ ﻳﺴﺎﻭﻱ ،5 cm
ﻧﻌﺘﱪ ﻫﻨﺎ ﺃ ﱠﻥ ﻋﻤﻮﺩ ﺍﻟﺰﺋﺒﻖ ﻫﻮ ﺧﺎﺻﻴﺔ ﻗﻴﺎﺱ ﺍﳊﺮﺍﺭﺓ Xﻭﺃ ﱠﻥ Θﻫﻲ ﺩﺭﺟﺔ ﺍﳊﺮﺍﺭﺓ ﺍﻟﺘﺠﺮﻳﺒﻴﺔ ﺍﻟﱵ "ﻳﻘﻴﺴﻬﺎ" ﻫﺬﺍ
ﺍﳌﻴﺰﺍﻥ.
ﺃ -ﺃﹸﺣﺴﺐ ﺩﺭﺟﺔ ﺍﳊﺮﺍﺭﺓ ﺍﻟﺘﺠﺮﻳﺒﻴﺔ ﺍﳌﻘﺎﺳﺔ ﻋﻨﺪﻣﺎ ﻳﻜﻮﻥ ﺍﺭﺗﻔﺎﻉ ﻋﻤﻮﺩ ﺍﻟﺰﺋﺒﻖ ﻳﺴﺎﻭﻱ .6 cm
ﺝ -ﺇﺫﺍ ﻛﺎﻧﺖ ﺩﻗﺔ ﻗﻴﺎﺱ Xﻫﻲ 0.01 cmﻓﻬﻞ ﺑﺎﻹﻣﻜﺎﻥ ﺍﺳﺘﺨﺪﺍﻡ ﻫﺬﺍ ﺍﳌﻴﺰﺍﻥ ﺑﲔ ﻧﻘﻄﺔ ﺍﻟﺘﺠﻤﺪ ﻭﻧﻘﻄﺔ
ﺍﳌﺎﺀ ﺍﻟﺜﻼﺛﻴﺔ؟
ﺍﳊﻞ:
× Θ 6 = Θ5
X6 6
= 273.16 × = 327.8 degrees ﺃ-
X5 5
× X S = X5
ΘS
×= 5
327.80
= 6.84cm ﺏ-
Θ5 273.16
ﺣﺘﻰ ﻳﺴﺘﻄﻴﻊ ﻫﺬﺍ ﺍﳌﻴﺰﺍﻥ ﻗﻴﺎﺱ ∆Θﻭﺍﻟﱵ ﺗﺴﺎﻭﻱ 0.01 Kﳚﺐ ﺃ ﹾﻥ ﺗﻜﻮﻥ ﺩﻗﺘﻪ ﺃﻭ ﺣﺴﺎﺳﻴﺘﻪ
5
= ∆X × 0.01 = 1.834 × 10 − 4 < 0.01
273.15
ﻧﺘﺤﺪﺙ ﺍﻵﻥ ﻋﻦ ﺩﺭﺟﺔ ﺍﳊﺮﺍﺭﺓ ﺍﻟﺜﲑﻣﻮﺩﻳﻨﺎﻣﻴﻜﻴﺔ ﺑﻮﺣﺪﺍﺕ ﺩﺭﺟﺎﺕ ﻛﻠﻔﻦ K°ﺃﻭ ﻛﻠﻔﻦ .Kﰲ ﻧﻈﺎﻡ ﺍﻟﻮﺣﺪﺍﺕ
ﻫﺬﺍ ﺗﻜﻮﻥ ﺩﺭﺟﺔ ﺣﺮﺍﺭﺓ ﻧﻘﻄﺔ ﺍﳌﺎﺀ ﺍﻟﺜﻼﺛﻴﺔ ﻫﻲ T3 = 273.16 K :ﻭﺑﺸﻜﻞ ﻋﺎﻡ:
P
T = 273.16 K × lim )(8-1
P3 → 0 P3
V
ﺗﺴﺘﺨﺪﻡ ﺩﺭﺟﺔ ﺣﺮﺍﺭﺓ ﺳﻴﻠﺴﻴﻮﺱ ) Celsiusﺑﺎﺳﻢ ﺍﻟﻔﻠﻜﻲ ﺍﻟﺴﻮﻳﺪﻱ ﺍﻟﺬﻱ ﺃﻗﺘﺮﺣﻬﺎ( ﻭﺍﳌﻌﺮﻓﺔ ﺑﺎﻟﻌﻼﻗﺔ:
ﺚ Tiﻫﻲ ﺩﺭﺟﺔ ﺣﺮﺍﺭﺓ ﻧﻘﻄﺔ ﺍﳉﻠﻴﺪ ﻭﺗﺴﺎﻭﻱ .273.15 Kﻭﻭﺣﺪﺓ ﻫﺬﻩ ﺍﻟﺪﺭﺟﺔ ﻫﻲ "ﺩﺭﺟﺔ ﺳﻴﻠﺴﻴﻮﺱ
ﺣﻴ ﹸ
ﺃﻭ "°Cﺃﻭ ﺩﺭﺟﺔ ﺍﳊﺮﺍﺭﺓ ﺍﳌﺌﻮﻳﺔ ﻭﺗﺴﻤﻰ ﻛﺬﻟﻚ ﻷ ﱠﻥ ﺍﻟﻔﺮﻕ ﺑﲔ ﺩﺭﺟﺔ ﺣﺮﺍﺭﺓ ﻧﻘﻄﺔ ﺍﻟﺘﺠﻤﺪ ﻭﺩﺭﺟﺔ ﺣﺮﺍﺭﺓ ﻧﻘﻄﺔ
ﺍﻟﺒﺨﺎﺭ ﰲ ﻫﺬﺍ ﺍﳌﻘﻴﺎﺱ ﺗﺴﺎﻭﻱ 100 °Cﺇ ﹾﺫ ﺃ ﱠﻥ ﺍﻷﻭﱃ ﺗﺴﺎﻭﻱ ti = 0 °Cﻭﺍﻟﺜﺎﻧﻴﺔ ﺗﺴﺎﻭﻱ
ﻫﻨﺎﻙ ﻣﻘﻴﺎﺳﺎﻥ ﺁﺧﺮﺍﻥ ﻳﺴﺘﺨﺪﻣﺎﻥ ﰲ ﺑﻌﺾ ﺍﻟﻘﻴﺎﺳﺎﺕ ﺍﳍﻨﺪﺳﻴﺔ )ﰲ ﺍﻟﻮﻻﻳﺎﺕ ﺍﳌﺘﺤﺪﺓ ﺧﺎﺻﺔ( ﻣﻌﺮﻓﺎﻥ ﺑﺎﺳﺘﺨﺪﺍﻡ
ﻧﻘﻄﺘﻴﻦ ﺛﺎﺑﺘﺘﻴﻦ ﻭﺍﻋﺘﺒﺎﺭ ﺃ ﱠﻥ ﺍﻟﻔﺮﻕ ﺑﲔ ﻧﻘﻄﺔ ﺍﻟﺘﺠﻤﺪ ﻭﻧﻘﻄﺔ ﺍﻟﺒﺨﺎﺭ Ts - Tiﻳﺴﺎﻭﻱ 180ﺩﺭﺟﺔ ﺑﺪ ﹰﻻ ﻣﻦ
.100ﺍﻷﻭﻝ ﻳﺴﻤﻰ ﻣﻘﻴﺎﺱ ﺭﺍﻧﻜﲔ )ﻧﺴﺒﺔ ﺇﱃ ﻣﺒﺘﺪﻋﻪ ﺍﻻﺳﻜﺘﻠﻨﺪﻱ ﻭﻟﻴﻢ ﺭﺍﻧﻜﲔ( ﻭﺍﻟﺜﺎﱐ ﻣﻘﻴﺎﺱ ﻓﻬﺮﺎﻳﺖ
) Fahrenheitﻧﺴﺒﺔ ﺇﱃ ﺍﻷﳌﺎﱐ ﻏﺎﺑﺮﻳﻴﻞ ﻓﻬﺮﺎﻳﺖ( .ﻳﻌﺮﻑ ﺍﻟﺮﺍﻧﻜﲔ ﺑﺪﻻﻟﺔ ﺍﻟﻜﻠﻔﻦ ﺑﺎﻟﻌﻼﻗﺔ:
9
= 1R K )(10-1
5
ﻭﺑﺎﻟﺘﺎﱄ ﻓﺈ ﱠﻥ ﺩﺭﺟﺔ ﺣﺮﺍﺭﺓ ﻧﻘﻄﺔ ﺍﳉﻠﻴﺪ ﺣﺴﺐ ﻫﺬﻩ ﺍﳌﻘﻴﺎﺱ ﺗﻌﻄﻰ ﺑﺎﻟﻌﻼﻗﺔ:
9R
= Ti × 273.15 K = 491.67 R )(11-1
5K
ﺚ Tﺗﻤﺜﱢﻞ ﺩﺭﺟﺔ ﺍﳊﺮﺍﺭﺓ ﺍﻟﺜﲑﻣﻮﺩﻳﻨﺎﻣﻴﻜﻴﺔ ﺑﺎﻟﺮﺍﻧﻜﲔ .ﻭﻭﺣﺪﺓ ﻣﻘﻴﺎﺱ ﺩﺭﺟﺔ ﺣﺮﺍﺭﺓ ﻓﻬﺮﺎﻳﺖ ﻫﻲ °Fﻭﺍﻟﱵ
ﺣﻴ ﹸ
ﺗﺴﺎﻭﻱ .°R
• ﻋﻨﺪ ﻧﻘﻄﺔ ﺍﻟﺒﺨﺎﺭ Ts= 100 °Cﺗﻜﻮﻥ ﺩﺭﺟﺔ ﺍﳊﺮﺍﺭﺓ ﺑﺎﻟﻔﻬﺮﺎﻳﺖ ﻫﻲ:
9 R
= ts × 373.15 K - 495.67 = 212 °F
5 K
ﺃﻱ ﺃ ﱠﻥ ﺍﻟﻔﺮﻕ ﺑﻴﻦ ﺍﻟﺪﺭﺟﺘﻴﻦ ﻳﺴﺎﻭﻱ 180ﺩﺭﺟﺔ.
ﻣﺜﺎﻝ :4-1
*
tﺑﺎﳌﻌﺎﺩﻟﺔt* = a θ2 + b : ﻋﺮﻓﺖ ﺩﺭﺟﺔ ﺣﺮﺍﺭﺓ
ﺚ aﻭ bﺛﺎﺑﺘﺎﻥ ﻭ θﺩﺭﺟﺔ ﺍﳊﺮﺍﺭﺓ ﺍﻟﺘﺠﺮﻳﺒﻴﺔ ﺍﳌﻘﺎﺳﺔ ﺑﺎﺳﺘﺨﺪﺍﻡ ﻣﻴﺰﺍﻥ ﺍﳊﺮﺍﺭﺓ ﺍﻟﺰﺋﺒﻘﻲ ﰲ ﺍﳌﺜﺎﻝ .3
ﺣﻴ ﹸ
ﺏ -ﺟﺪ ﻗﻴﻤﺔ * tﻋﻨﺪﻣﺎ ﻳﻜﻮﻥ ﺍﺭﺗﻔﺎﻉ ﻋﻤﻮﺩ ﺍﻟﺰﺋﺒﻖ .X = 7.0 cm
ﺝ -ﺟﺪ ﺍﺭﺗﻔﺎﻉ ﻋﻤﻮﺩ ﺍﻟﺰﺋﺒﻖ ﻋﻨﺪﻣﺎ ﺗﻜﻮﻥ ﻗﻴﻤﺔ * tﺗﺴﺎﻭﻱ .50°
ﺍﳊﻞ:
*t i
0
= 0 = a (273.15) + b
2 ﺃ-
100 2
t *s = 100 = a (373.15) + b
2
Θ
t i* ( X ) = a X 2 + b
X
Θ
2
t i* ( X = 7) = a 5 72 + b = 1.547 × 10-3
273.16 2
7 − 115.4
2
ﺏ-
X5 5
= + 110.85K
ﻣﺜﺎﻝ :5-1
K 77.36 ﺇﺫﺍ ﻋﻠﻤﺖ ﺃ ﱠﻥ ﺩﺭﺟﺔ ﺍﳊﺮﺍﺭﺓ ﺍﻟﺜﲑﻣﻮﺩﻳﻨﺎﻣﻴﻜﻴﺔ ﻟﻨﻘﻄﺔ ﻏﻠﻴﺎﻥ ﺍﻟﻨﻴﺘﺮﻭﺟﲔ )ﺍﻷﺯﻭﺕ( ﺍﻟﻄﺒﻴﻌﻴﺔ ﻫﻲ
ﺝ( ﻓﻬﺮﺎﻳﺖ. ﺏ( ﺭﺍﻧﻜﲔ ﺃ( ﺳﻴﻠﺴﻴﻮﺱ ﻓﺄﺣﺴﺐ ﻗﻴﻤﺘﻬﺎ ﺣﺴﺐ ﻣﻘﻴﺎﺱ
9R ﺏ-
= R × 73.15 K = 123.23 R
5K
= tF
9
t + 32 = 320.44 F ﺝ-
5
ﺗﺘﻐﲑ ﺧﺼﺎﺋﺺ ﻧﻈﺎﻡ ﻣﻌﺰﻭﻝ ﻣﻊ ﺍﻟﺰﻣﻦ .ﺇﺫﺍ ﻛﺎﻥ ﻫﻨﺎﻙ ﻓﺮﻭﻕ ﰲ ﺩﺭﺟﺔ ﺍﳊﺮﺍﺭﺓ ﺑﲔ ﺃﺟﺰﺍﺀ ﺍﻟﻨﻈﺎﻡ ،ﻓﺈ ﱠﻥ ﺩﺭﺟﺔ
ﺍﳊﺮﺍﺭﺓ ﺗﺼﺒﺢ ﻧﻔﺴﻬﺎ ﰲ ﲨﻴﻊ ﻧﻘﺎﻁ ﺍﻟﻨﻈﺎﻡ ﺑﻌﺪ ﻣﺮﻭﺭ ﻓﺘﺮﺓ ﻣﻦ ﺍﻟﺰﻣﻦ ﻭﻧﻘﻮﻝ ﺃ ﱠﻥ ﺍﳉﺴﻢ ﰲ ﺍﺗﺰﺍﻥ ﺣﺮﺍﺭﻱ.
ﺇﺫﺍ ﺗﻐﲑ ﺍﻟﻀﻐﻂ ﺃﻭ ﺷﺪ ﺍﳌﺮﻭﻧﺔ elastic stressﰲ ﺍﻟﻨﻈﺎﻡ ،ﻓﺈ ﱠﻥ )ﺑﻌﺾ( ﺃﺟﺰﺍﺀ ﻣﻨﻪ ﻗﺪ ﺗﻨﻔﺼﻞ ﺃﻭ ﺗﺘﻤﺪﺩ ﺃﻭ
ﺗﺘﻘﻠﱠﺺ ﻭﻋﻨﺪ ﺍﻧﺘﻬﺎﺀ ﻛ ﱢﻞ ﻫﺬﺍ ﻓﺈ ﱠﻥ ﺍﻟﻨﻈﺎﻡ ﻳﺼﺒﺢ ﰲ ﺣﺎﻟﺔ ﺍﺗﺰﺍﻥ ﻣﻴﻜﺎﻧﻴﻜﻲ .ﺇ ﱠﻥ ﻫﺬﺍ ﻻ ﻳﻌﲏ ﺑﺎﻟﻀﺮﻭﺭﺓ ﺃ ﱠﻥ ﺍﻟﻀﻐﻂ
ﻣﺘﺴﺎ ٍﻭ ﰲ ﲨﻴﻊ ﻧﻘﺎﻁ ﺍﻟﻨﻈﺎﻡ .ﻟﻠﺘﻮﺿﻴﺢ ﺍﻋﺘﱪ ﻋﻤﻮﺩﹰﺍ ﻣﻦ ﻣﺎﺋﻊ ﺧﺎﺿﻊ ﳉﺬﺏ ﺍﻷﺭﺽ .ﳜﺘﻠﻒ ﺍﻟﻀﻐﻂ ﻣﻦ ﻧﻘﻄﺔ ﺇﱃ
ﺍﻋﺘﱪ ﻧﻈﺎﻣﹰﺎ ﳛﻮﻱ ﻣﻮﺍﺩ ﻗﺎﺑﻠﺔ ﻟﻠﺘﻔﺎﻋﻞ ﻛﻴﻤﻴﺎﺋﻴﹰﺎ .ﺑﻌﺪ ﻓﺘﺮﺓ ﺯﻣﻨﻴﺔ ﻃﻮﻳﻠﺔ ﺗﻨﺘﻬﻲ ﻛﻞ ﺍﻟﺘﻔﺎﻋﻼﺕ ﺍﻟﻜﻴﻤﺎﻭﻳﺔ ﺍﳌﻤﻜﻨﺔ
ﻭﻧﻘﻮﻝ ﺃ ﱠﻥ ﺍﻟﻨﻈﺎﻡ ﰲ ﺣﺎﻟﺔ ﺍﺗﺰﺍﻥ ﻛﻴﻤﺎﻭﻱ .ﺇﺫﺍ ﻛﺎﻥ ﺍﻟﻨﻈﺎﻡ ﰲ ﺍﺗﺰﺍﻥ ﺣﺮﺍﺭﻱ ،ﻣﻴﻜﺎﻧﻴﻜﻲ ﻭﻛﻴﻤﺎﻭﻱ ﰲ ﺁﻥ ﻭﺍﺣﺪ
ﰲ ﺍﻟﻔﺼﻮﻝ ﺍﻟﺘﺎﻟﻴﺔ ﺳﻮﻑ ﻧ ﺮﻛﱢﺰ ﺩﺭﺍﺳﺘﻨﺎ ﻋﻠﻰ ﺃﻧﻈﻤﺔ ﻣﺘﻮﺍﺟﺪﺓ ﰲ ﺍﺗﺰﺍﻥ ﺛﲑﻣﻮﺩﻳﻨﺎﻣﻴﻜﻲ ﺃﻭ ﺗﻠﻚ ﺍﻟﱵ ﺗﻜﻮﻥ ﻓﻴﻬﺎ
ﺗﻌﺮﻳﻔﺎﺕ 1-8-1
ﺗﺘﻐﲑ ﺧﺼﺎﺋﺺ ﻧﻈﺎﻡ ﻣﻌﺰﻭﻝ ﻣﻊ ﺍﻟﺰﻣﻦ .ﺇﺫﺍ ﻛﺎﻥ ﻫﻨﺎﻙ ﻓﺮﻭﻕ ﰲ ﺩﺭﺟﺔ ﺍﳊﺮﺍﺭﺓ ﺑﲔ ﺃﺟﺰﺍﺀ ﺍﻟﻨﻈﺎﻡ ،ﻓﺈ ﱠﻥ ﺩﺭﺟﺔ
ﺍﳊﺮﺍﺭﺓ ﺗﺼﺒﺢ ﻧﻔﺴﻬﺎ ﰲ ﲨﻴﻊ ﻧﻘﺎﻁ ﺍﻟﻨﻈﺎﻡ ﺑﻌﺪ ﻣﺮﻭﺭ ﻓﺘﺮﺓ ﻣﻦ ﺍﻟﺰﻣﻦ ﻭﻧﻘﻮﻝ ﺃ ﱠﻥ ﺍﳉﺴﻢ ﰲ ﺍﺗﺰﺍﻥ ﺣﺮﺍﺭﻱ.
ﺍﻟﻌﻤﻠﻴﺔ ﺷﺒﻪ ﺍﻟﺴﺎﻛﻨﺔ :quasistatic processﻭﻓﻴﻬﺎ ﻳﺒﺘﻌﺪ ﺍﻟﻨﻈﺎﻡ ﺑﻜﻤﻴﺎﺕ ﻻﻣﺘﻨﺎﻫﻴﺔ ﰲ ﺍﻟﺼﻐﺮ ﻋﻦ ﻭﺿﻊ
ﺍﻻﺗﺰﺍﻥ .ﻳﻤﻜﻦ ﺍﻋﺘﺒﺎﺭ ﺍﻟﻌﻤﻠﻴﺔ ﺷﺒﻪ ﺍﻟﺴﺎﻛﻨﺔ ﻭﻛﺄﻧﻬﺎ ﺳﻠﺴﻠ ﹲﺔ ﻣﻦ ﺣﺎﻻﺕ ﺍﻻﺗﺰﺍﻥ.
ﺍﻟﻌﻤﻠﻴﺔ ﻏﲑ ﺍﻟﺴﺎﻛﻨﺔ :nonelastic processﻭﻓﻴﻬﺎ ﻳﺒﺘﻌﺪ ﺍﻟﻨﻈﺎﻡ ﲤﺎﻣﹰﺎ ﻋﻦ ﻭﺿﻊ ﺍﻻﺗﺰﺍﻥ. .1
ﻟﻔﻬﻢ ﺍﻟﻌﺒﺎﺭﺗﻴﻦ ﺍﻟﺴﺎﺑﻘﺘﻴﻦ ﺳﻮﻑ ﻧﺄﺧﺬ ﺍﳌﺜﺎﻝ ﺍﻟﺘﺎﱄ :ﺍﻋﺘﱪ ﻏﺎﺯﹰﺍ ﳏﺼﻮﺭﹰﺍ ﰲ ﺃﹸﺳﻄﻮﺍﻧﺔ ﻣﺰﻭﺩﺓ ﲟﻜﺒﺲ ﻣﺘﺤﺮﻙ )ﺁﻟﺔ
ﺍﻻﺣﺘﺮﺍﻕ ﺍﻟﺪﺍﺧﻠﻲ( .ﺍﻋﺘﱪ ﺃ ﱠﻥ ﺍﻷُﺳﻄﻮﺍﻧﺔ ﻭﺍﳌﻜﺒﺲ ﻳﺸﻜﱢﻼﻥ ﺣ ﺪﹰﺍ ﺃﺩﻳﺎﺑﺎﺗﻴﹰﺎ ﻭﻟﻨﻬﻤﻞ ﺗﺄﺛﲑ ﺟﺬﺏ ﺍﻷﺭﺽ .ﻳﻜﻮﻥ
ﺍﻟﻐﺎﺯ ﰲ ﻭﺿﻊ ﺍﺗﺰﺍﻥ ﺗﻜﻮﻥ ﻓﻴﻪ ﺩﺭﺟﺔ ﺍﳊﺮﺍﺭﺓ ،ﺍﻟﻀﻐﻂ ﻭﺍﻟﻜﺜﺎﻓﺔ ﻧﻔﺴﻬﺎ ﰲ ﲨﻴﻊ ﻧﻘﺎﻃﻪ.
ﺇﺫﺍ ﺿﻐﻂ ﺍﳌﻜﺒﺲ ﻓﺠﺄﺓ ﻓﺈ ﱠﻥ ﺍﳋﺼﺎﺋﺺ ﺍﻟﺜﻼﺙ ﺳﻮﻑ ﺗﺘﻐﲑ ﺑﺎﻟﺰﻳﺎﺩﺓ ﺑﻜﻤﻴﺔ ﻣﻨﺘﻬﻴﺔ ﻭﺗﻜﻮﻥ ﺍﻟﻌﻤﻠﻴﺔ ﻏ ﲑ ﺳﺎﻛﻨﺔ.
ﺗﻜﻮﻥ ﺍﻟﻌﻤﻠﻴﺔ ﺷﺒﻪ ﺳﺎﻛﻨﺔ ﺇﺫﺍ ﺿﻐﻂ ﺍﳌﻜﺒﺲ ﺑﺮﻓﻖ ﻟﻜﻲ ﻳﻜﻮ ﹶﻥ ﺍﻧﺘﺸﺎﺭ ﺍﳌﻮﺟﺔ ﻭﲣﻤﻴﺪ ﺍﳌﻴﻮﻋﺔ ﻭﺍﻟﺘﻮﺻﻴﻞ ﺍﳊﺮﺍﺭﻱ
ﻣﺜﺎﻝ ﺁﺧﺮ :ﺗﺴﺤﲔ ﻧﻈﺎﻡ ﻣﻦ ﺩﺭﺟﺔ ﺣﺮﺍﺭﺓ T1ﺇﱃ ﺩﺭﺟﺔ ﺣﺮﺍﺭﺓ .T2 > T1ﻳﻤﻜﻨﻨﺎ ﺫﻟﻚ ﺑﻮﺿﻊ ﺍﻟﻨﻈﺎﻡ ﰲ
ﳏﻴﻂ ﻏﲑ ﻛﺎﻇﻢ ﻟﻠﺤﺮﺍﺭﺓ ﺩﺭﺟﺔ ﺣﺮﺍﺭﺗﻪ .T2ﺇ ﱠﻥ ﻧﻘﺎﻁ ﺍﻟﻨﻈﺎﻡ ﺍﳋﺎﺭﺟﻴﺔ ﺳﻮﻑ ﺗﺴﺨﻦ ﺑﺴﺮﻋﺔ ﺃﻛﱪ ﻣﻦ ﻧﻘﺎﻃﻪ
ﺍﻟﺪﺍﺧﻠﻴﺔ ﻭﻻ ﻳﻤﻜﻦ ﻫﻨﺎ ﺍﻟﻘﻮﻝ ﺃ ﱠﻥ ﺍﻟﻨﻈﺎﻡ ﺧﻀﻊ ﻟﻌﻤﻠﻴﺔ ﺟﻌﻠﺘﻪ ﳝﺮ ﰲ ﺳﻠﺴﻠﺔ ﻣﻦ ﺣﺎﻻﺕ ﺍﻻﺗﺰﺍﻥ ﺍﻟﺜﲑﻣﻮﺩﻳﻨﺎﻣﻴﻜﻲ
ﺚ ﺃ ﱠﻥ ﺍﻟﺰﻳﺎﺩﺓ ﰲ ﺩﺭﺟﺔ ﺣﺮﺍﺭﺗﻪ ﺗﺼﺒﺢ ﺃﻋﻠﻰ ﺑﻘﻠﻴﻞ ﻣﻦ ﺩﺭﺟﺔ ﺣﺮﺍﺭﺓ ﺍﻟﻨﻈﺎﻡ ﻓﺈ ﱠﻥ ﺍﻟﻌﻤﻠﻴﺔ ﺗﺼﺒ ﺢ ﺷﺒ ﻪ ﺳﺎﻛﻨﺔ.
ﲝﻴ ﹸ
ﻳﻤﺜﱢﻞ ﺍﻟﺸﻜﻞ 9-1ﺳﻠﺴﻠﺔ ﻋﻤﻠﻴﺎﺕ ﻣﻦ ﺍﻷﻧﻮﺍﻉ ﺍﻟﺜﻼﺛﺔ ﺍﻟﺴﺎﺑﻘﺔ ﳜﻀﻊ ﳍﺎ ﻧﻈﺎﻡ ﺛﲑﻣﻮﺩﻳﻨﺎﻣﻴﻜﻲ ﰲ ﻧﻈﺎﻡ ﺇﺣﺪﺍﺛﻴﺎﺕ
ﺛﻼﺛﻲ ﺍﻷﺑﻌﺎﺩ.
ﺍﻟﺸﻜﻞ :1-9ﲤﺜﻴﻞ ﺑﻴﺎﱐ ﰲ ﻧﻈﺎﻡ ﺇﺣﺪﺍﺛﻴﺎﺕ ﺛﻼﺛﻲ ﺍﻷﺑﻌﺎﺩ ﻟﻌﻤﻠﻴﺔ ﺃﻳﺰﻭﺣﺠﻤﻴﺔ ﻣﺘﺒﻮﻋﺔ ﺑﻌﻤﻠﻴﺔ ﺃﻳﺰﻭﺑﺎﺭﻳﺔ ﻓﻌﻤﻠﻴﺔ
ﺃﻳﺰﻭﺣﺮﺍﺭﻳﺔ.
ﺗﺴﻤﻰ ﺍﻟﻌﻤﻠﻴﺔ ﺍﻟﱵ ﳜﻀﻊ ﳍﺎ ﻧﻈﺎﻡ ﺃﺩﻳﺎﺑﺎﰐ ﻋﻤﻠﻴﺔ ﺃﺩﻳﺎﺑﺎﺗﻴﺔ .ﻣﻌﻈﻢ ﺍﻟﻌﻤﻠﻴﺎﺕ ﻛﺤﺮﻛﺔ ﺍﳌﻜﺒﺲ ﰲ ﺁﻟﺔ ﺍﻻﺣﺘﺮﺍﻕ
ﳏﻴﻄﻪ ﺃﻭ ﺍﻟﻌﻜﺲ.
ﺗﻜﻮﻥ ﺍﻟﻌﻤﻠﻴﺔ ﻗﺎﺑﻠﺔ ﻟﻠﻌﻜﺲ ، reversibleﺃﻱ ﺍﻟﱵ ﺑﺎﻹﻣﻜﺎﻥ ﻋﻤﻠﻬﺎ ﰲ "ﺍﲡﺎﻩ ﻣﻌﺎﻛﺲ" ﻭﺳﻮﻑ ﻧﺴﻤﻴﻬﺎ
ﺃ -ﺇﺫﺍ ﻛﺎﻥ ﺗﺴﺮﺏ ﺍﳊﺮﺍﺭﺓ ﰲ ﺍﻟﻌﻤﻠﻴﺔ ﻣﻘﺘﺼﺮﹰﺍ ﻋﻠﻰ ﺃﺟﺴﺎﻡ ﳍﺎ ﻧﻔﺲ ﺩﺭﺟﺔ ﺍﳊﺮﺍﺭﺓ.
ﺍﻟﻌﻤﻠﻴﺔ ﺍﳌﻨﻌﻜﺴﺔ ﻋﻤﻠﻴﺔ ﻳﻤﻜﻦ ﻋﻜﺲ "ﺍﲡﺎﻫﻬﺎ" ﺑﺘﻐﻴﲑ ﻻﻣﺘﻨﺎﻫﻲ ﺍﻟﺼﻐﺮ εﰲ ﺇﺣﺪﻯ ﺧﺼﺎﺋﺺ ﺍﻟﻨﻈﺎﻡ .ﺍﻋﺘﱪ ﻧﻈﺎﻣﹰﺎ
ﺩﺭﺟﺔ ﺣﺮﺍﺭﺗﻪ T1ﻳﻨﺘﻤﻲ ﺇﱃ ﳏﻴﻂ ﺩﺭﺟﺔ ﺣﺮﺍﺭﺗﻪ .T2ﺇﺫﺍ ﻛﺎﻥ ﺍﻧﺴﻴﺎﺏ ﺍﳊﺮﺍﺭﺓ ﻣﻦ ﺍﻟﻨﻈﺎﻡ ﺇﱃ ﺍﶈﻴﻂ ﻋﻨﺪﻣﺎ ﺗﻜﻮﻥ
T1 > T2ﻭﺇﺫﺍ ﻛﺎﻥ ﺍﻧﺴﻴﺎﺏ ﺍﳊﺮﺍﺭﺓ ﻣﻦ ﺍﶈﻴﻂ ﺇﱃ ﺍﻟﻨﻈﺎﻡ ﻋﻨﺪﻣﺎ ﺗﻜﻮﻥ T2 > T1ﻓﺈ ﱠﻥ ﺍﻟﻌﻤﻠﻴﺔ ﻣﻨﻌﻜﺴﺔ ﻭﺷﺒﻪ
ﺳﺎﻛﻨﺔ ﺃﻳﻀﹰﺎ .ﺇﺫﺍ ﻛﺎﻥ ﺍﻟﻔﺮﻕ ﺑﲔ ﺩﺭﺟﱵ ﺍﳊﺮﺍﺭﺓ T1ﻭ T2ﳏﺴﻮﺳﹰﺎ ﻓﺈﻧﻪ ﻻ ﻳﻤﻜﻦ ﻋﻜﺲ ﺍﲡﺎﻩ ﺍﻧﺴﻴﺎﺏ ﺍﳊﺮﺍﺭﺓ
T2 ﺚ ﺃ ﱠﻥ ﺗﺪﻓﻖ ﺍﳊﺮﺍﺭﺓ ﺍﳌﻨﺴﺎﺑﺔ ﺻﻐﲑ ﺣﺘﻰ ﺇﺫﺍ ﻛﺎﻥ ﺍﻟﻔﺮﻕ ﺑﻴ ﻦ T1ﻭ
ﺇﺫﺍ ﺍﻓﺘﺮﺿﻨﺎ ﺃ ﱠﻥ ﺍﳊ ﺪ ﺷﺒﻪ ﺃﺩﻳﺎﺑﺎﰐ ﲝﻴ ﹸ
ﳏﺴﻮﺳﹰﺎ ﻓﺈ ﱠﻥ ﺍﻟﻨﻈﺎﻡ ﻣﻮﺟﻮﺩ ﰲ ﺣﺎﻟﺔ ﺍﺗﺰﺍﻥ ﺣﺮﺍﺭﻱ ﰲ ﺃﻳﺔ ﳊﻈﺔ ﻭﺍﻟﻌﻤﻠﻴﺔ ﺷﺒﻪ ﺳﺎﻛﻨﺔ ﻭﻏﲑ ﻣﻨﻌﻜﺴﺔ .ﻳﺘﻀﺢ ﳑﺎ
ﺍﻟﻌﻤﻠﻴﺎﺕ ﺍﳌﻨﻌﻜﺴﺔ ﻭﻏﲑ ﺍﳌﻨﻌﻜﺴﺔ ﻋﻨﺪ ﺩﺭﺍﺳﺘﻨﺎ ﻟﻠﻘﺎﻧﻮﻥ ﺍﻟﺜﺎﱐ ﰲ ﺍﻟﺪﻳﻨﺎﻣﻴﻜﺎ ﺍﳊﺮﺍﺭﻳﺔ.