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𝑹𝑬𝑺𝑷𝑶𝑺𝑻𝑨:
𝑷𝑶𝑵𝑻𝑶 𝟏
𝑷𝒓𝒆𝒔𝒔ã𝒐 𝑷𝟏 = 𝟏𝟎𝟎 𝒃𝒂𝒓
𝑻𝒆𝒎𝒑𝒆𝒓𝒂𝒕𝒖𝒓𝒂 𝑻𝟏 = 𝟑𝟏𝟏, 𝟏 °𝑪
𝑪𝒐𝒏𝒔𝒖𝒍𝒕𝒂𝒏𝒅𝒐 𝒂 𝒕𝒂𝒃𝒆𝒍𝒂 𝒅𝒆 𝑨 − 𝟑, 𝒍𝒊𝒒𝒖𝒊𝒅𝒐 𝒗𝒂𝒑𝒐𝒓 𝒑𝒂𝒓𝒂 𝒆𝒏𝒕𝒂𝒍𝒑𝒊𝒂 𝒆 𝒆𝒏𝒕𝒓𝒐𝒑𝒊𝒂 𝒅𝒆 𝒗𝒂𝒑𝒐𝒓 𝒔𝒂𝒕𝒖𝒓𝒂𝒅𝒐
𝒕𝒆𝒎𝒐𝒔:
𝑬𝒏𝒕𝒂𝒍𝒑𝒊𝒂 𝒉𝟏 = 𝟐𝟕𝟐𝟒, 𝟕 𝒌𝑱/𝒌𝒈
𝑬𝒏𝒕𝒓𝒐𝒑𝒊𝒂 𝑺𝟏 = 𝟓, 𝟔𝟏𝟒𝟏 𝒌𝑱/𝒌𝒈 ∗ 𝑲
𝑷𝑶𝑵𝑻𝑶 𝟐
𝑷𝒓𝒆𝒔𝒔ã𝒐 𝑷𝟐 = 𝟎, 𝟎𝟔 𝒃𝒂𝒓
𝑪𝒐𝒏𝒔𝒖𝒍𝒕𝒂𝒏𝒅𝒐 𝒂 𝒕𝒂𝒃𝒆𝒍𝒂 𝑨 − 𝟑, 𝒎𝒊𝒔𝒕𝒖𝒓𝒂 𝒅𝒆 𝒍𝒊𝒒𝒖𝒊𝒅𝒐 𝒗𝒂𝒑𝒐𝒓
𝒕𝒆𝒎𝒐𝒔:
𝑬𝒏𝒕𝒂𝒍𝒑𝒊𝒂 𝒅𝒆 𝒍𝒊𝒒𝒖𝒊𝒅𝒐 𝒄𝒐𝒎𝒑𝒓𝒊𝒎𝒊𝒅𝒐 𝒉𝟐𝒍 = 𝟏𝟓𝟏, 𝟓𝟑 𝒌𝑱/𝒌𝒈
𝑬𝒏𝒕𝒂𝒍𝒑𝒊𝒂 𝒅𝒆 𝒗𝒂𝒑𝒐𝒓 𝒔𝒂𝒕𝒖𝒓𝒂𝒅𝒐 𝒉𝟐𝒗 = 𝟐𝟓𝟔𝟕, 𝟒 𝒌𝑱/𝒌𝒈
𝑬𝒏𝒕𝒓𝒐𝒑𝒊𝒂 𝒅𝒆 𝒍í𝒒𝒖𝒊𝒅𝒐 𝒄𝒐𝒎𝒑𝒓𝒊𝒎𝒊𝒅𝒐 𝑺𝟐𝒍 = 𝟎, 𝟓𝟐𝟏𝟎 𝒌𝑱/𝒌𝒈 ∗ 𝑲
𝑬𝒏𝒕𝒓𝒐𝒑𝒊𝒂 𝒅𝒆 𝒗𝒂𝒑𝒐𝒓 𝒔𝒖𝒑𝒆𝒓𝒂𝒒𝒖𝒆𝒄𝒊𝒅𝒐 𝑺𝟐𝒗 = 𝟖, 𝟑𝟑𝟎𝟒 𝒌𝑱/𝒌𝒈 ∗ 𝑲
𝑬𝒏𝒕𝒓𝒐𝒑𝒊𝒂 𝒅𝒐 𝒑𝒐𝒏𝒕𝒐 𝟐 = 𝑺𝟐 = 𝑺𝟏 = 𝟓, 𝟔𝟏𝟒𝟏 𝒌𝑱/𝒌𝒈 ∗ 𝑲
(𝑺𝟐 − 𝑺𝟐𝒍)
𝑻í𝒕𝒖𝒍𝒐 𝒅𝒂 𝒎𝒊𝒔𝒕𝒖𝒓𝒂𝒆𝒏𝒕𝒓𝒐𝒑𝒊𝒂 (𝒙) =
(𝑺𝟐𝒗 − 𝑺𝟐𝒍)
(𝟓, 𝟔𝟏𝟒𝟏 − 𝟎, 𝟓𝟐𝟏𝟎)
𝒙=
(𝟖, 𝟑𝟑𝟎𝟒 − 𝟎, 𝟓𝟐𝟏𝟎)
𝟓, 𝟎𝟗𝟑𝟏
𝒙=
𝟕, 𝟖𝟎𝟗𝟒
𝒙 = 𝟎, 𝟔𝟓𝟐𝟐
(𝒉𝟐 − 𝒉𝟐𝒍)
𝒉𝟐 =
(𝒉𝟐𝒗 − 𝒉𝟐𝒍)
𝒉𝟐 = 𝒉𝟐𝒍 + 𝒙 ∙ (𝒉𝟐𝒗 − 𝒉𝟐𝒍)
𝒉𝟐 = 𝟏𝟓𝟏, 𝟓𝟑 + (𝟎, 𝟔𝟓𝟐𝟐 ∙ (𝟐𝟓𝟔𝟕, 𝟒 − 𝟏𝟓𝟏, 𝟓𝟑))
𝒉𝟐 = 𝟏𝟕𝟐𝟕, 𝟏𝟔 𝒌𝑱/𝒌𝒈 →→ 𝒆𝒏𝒕𝒂𝒑𝒊𝒂 𝒅𝒐 𝒑𝒐𝒏𝒕𝒐 𝟐
𝑷𝑶𝑵𝑻𝑶 𝟑
𝑷𝒓𝒆𝒔𝒔ã𝒐 𝑷𝟑 = 𝑷𝟐 = 𝟎, 𝟎𝟔 𝒃𝒂𝒓 = 𝟎, 𝟎𝟎𝟔 𝑴𝑷𝒂
𝑬𝒏𝒕𝒂𝒍𝒑𝒊𝒂 𝒆𝒎 𝒉𝟑 = 𝒉𝟐𝒍 = 𝟏𝟓𝟏, 𝟓𝟑 𝒌𝑱/𝒌𝒈
𝑬𝒏𝒕𝒓𝒐𝒑𝒊𝒂 𝒆𝒎 𝑺𝟑 = 𝑺𝟐𝒍 = 𝟎, 𝟓𝟐𝟏𝟎 𝒌𝑱/𝒌𝒈 ∗ 𝑲
𝑷𝑶𝑵𝑻𝑶 𝟒
𝑷𝟒 = 𝑷𝟏 = 𝟏𝟎𝟎 𝒃𝒂𝒓 = 𝟏𝟎 𝑴𝑷𝒂
𝑽𝒐𝒍𝒖𝒎𝒆 𝒆𝒔𝒑𝒆𝒄í𝒇𝒊𝒄𝒐 𝑽𝟑 = 𝟏, 𝟎𝟎𝟔𝟒 𝒎𝟑/𝒌𝒈
𝒉𝟒 = 𝒉𝟑 + 𝑽𝟑(𝑷𝟒 − 𝑷𝟑)
𝒉𝟒 = 𝟏𝟓𝟏, 𝟓𝟑 + 𝟏, 𝟎𝟎𝟔𝟒 ∙ (𝟏𝟎 − 𝟎, 𝟎𝟎𝟔𝟒)
𝒉𝟒 = 𝟏𝟓𝟏, 𝟓𝟑 + 𝟏𝟎, 𝟎𝟓𝟖
𝒌𝑱
𝒉𝟒 = 𝟏𝟔𝟏, 𝟓𝟖 →→ 𝒆𝒏𝒕𝒂𝒍𝒑𝒊𝒂 𝒅𝒐 𝒑𝒐𝒏𝒕𝒐 𝟒
𝒌𝒈
a- Eficiência Térmica:
𝜼 = 𝟎, 𝟑𝟖𝟓 𝒐𝒖 𝟑8, 𝟓%
b- Bwr:
(𝒉𝟒 − 𝒉𝟑)
𝑩𝒘𝒓 =
(𝒉𝟏 − 𝒉𝟐)
(𝟏𝟔𝟏, 𝟓𝟖 − 𝟏𝟓𝟏, 𝟓𝟑)
𝑩𝒘𝒓 =
(𝟐𝟕𝟐𝟒, 𝟕 − 𝟏𝟕𝟐𝟕, 𝟏𝟔)
∗ 𝑾𝒍 = 𝟐𝟎𝟎 𝑴𝑾
𝑾𝒍 = (𝑾𝒕 − 𝑾𝒃) ∙ 𝒎
𝑾𝒍
𝒎=
(𝑾𝒕 − 𝑾𝒃)
𝟐𝟎𝟎 ∙ 𝟑𝟔𝟎𝟎 × 𝟏𝟎𝟑
𝒎=
(𝟐𝟕𝟐𝟒, 𝟕 − 𝟏𝟕𝟐𝟕, 𝟏𝟔) − (𝟏𝟔𝟏, 𝟓𝟖 − 𝟏𝟓𝟏, 𝟓𝟑)
𝒎 = 𝟕, 𝟐𝟖𝟑 × 𝟏𝟎𝟓 𝒌𝒈/𝒉
𝑸 = 𝒎 ∙ (𝒉𝟏 − 𝒉𝟒)
𝟕, 𝟐𝟖𝟑 × 𝟏𝟎𝟓 𝒌𝒈/𝒉
𝑸= ∙ (𝟐𝟕𝟐𝟒, 𝟕 − 𝟏𝟔𝟏, 𝟓𝟖)𝒌𝑱/𝒌𝒈
𝟑𝟔𝟎𝟎 𝒔/𝒉 × 𝟏𝟎𝟑𝒌𝑾/𝑴𝑾
𝑸 = 𝟓𝟏𝟖, 𝟓𝟒 𝑴𝑾
𝑸 = 𝒎 ∙ (𝒉𝟐 − 𝒉𝟑)
(𝟕, 𝟐𝟖𝟑 × 𝟏𝟎𝟓𝒌𝒈/𝒉
𝑸= ∙ (𝟏𝟕𝟐𝟕, 𝟏𝟔 − 𝟏𝟓𝟏, 𝟓𝟑)𝒌𝑱/𝒌𝒈
𝟑𝟔𝟎𝟎 𝒔/𝒉 × 𝟏𝟎𝟑 𝒌𝑾/𝑴𝑾
𝑸 = 𝟑𝟏𝟖, 𝟕𝟓 𝑴𝑾
𝑹𝑬𝑺𝑷𝑶𝑺𝑻𝑨:
𝑷𝑶𝑵𝑻𝑶 𝟏
𝑷𝒓𝒆𝒔𝒔ã𝒐 𝑷𝟏 = 𝟏𝟎𝟎 𝒃𝒂𝒓
𝑻𝒆𝒎𝒑𝒆𝒓𝒂𝒕𝒖𝒓𝒂 𝑻𝟏 = 𝟑𝟏𝟏, 𝟏 °𝑪
𝑪𝒐𝒏𝒔𝒖𝒍𝒕𝒂𝒏𝒅𝒐 𝒂 𝒕𝒂𝒃𝒆𝒍𝒂 𝒅𝒆 𝑨 − 𝟑, 𝒍𝒊𝒒𝒖𝒊𝒅𝒐 𝒗𝒂𝒑𝒐𝒓 𝒑𝒂𝒓𝒂 𝒆𝒏𝒕𝒂𝒍𝒑𝒊𝒂 𝒆 𝒆𝒏𝒕𝒓𝒐𝒑𝒊𝒂 𝒅𝒆 𝒗𝒂𝒑𝒐𝒓 𝒔𝒂𝒕𝒖𝒓𝒂𝒅𝒐
𝒕𝒆𝒎𝒐𝒔:
𝑬𝒏𝒕𝒂𝒍𝒑𝒊𝒂 𝒉𝟏 = 𝟐𝟕𝟐𝟒, 𝟕 𝒌𝑱/𝒌𝒈
𝑬𝒏𝒕𝒓𝒐𝒑𝒊𝒂 𝑺𝟏 = 𝟓, 𝟔𝟏𝟒𝟏 𝒌𝑱/𝒌𝒈 ∗ 𝑲
𝑷𝑶𝑵𝑻𝑶 𝟐
𝑷𝒓𝒆𝒔𝒔ã𝒐 𝑷𝟐 = 𝟎, 𝟎𝟔 𝒃𝒂𝒓
𝑪𝒐𝒏𝒔𝒖𝒍𝒕𝒂𝒏𝒅𝒐 𝒂 𝒕𝒂𝒃𝒆𝒍𝒂 𝑨 − 𝟑, 𝒎𝒊𝒔𝒕𝒖𝒓𝒂 𝒅𝒆 𝒍𝒊𝒒𝒖𝒊𝒅𝒐 𝒗𝒂𝒑𝒐𝒓
𝒕𝒆𝒎𝒐𝒔:
𝑬𝒏𝒕𝒂𝒍𝒑𝒊𝒂 𝒅𝒆 𝒍𝒊𝒒𝒖𝒊𝒅𝒐 𝒄𝒐𝒎𝒑𝒓𝒊𝒎𝒊𝒅𝒐 𝒉𝟐𝒍 = 𝟏𝟓𝟏, 𝟓𝟑 𝒌𝑱/𝒌𝒈
𝑬𝒏𝒕𝒂𝒍𝒑𝒊𝒂 𝒅𝒆 𝒗𝒂𝒑𝒐𝒓 𝒔𝒂𝒕𝒖𝒓𝒂𝒅𝒐 𝒉𝟐𝒗 = 𝟐𝟓𝟔𝟕, 𝟒 𝒌𝑱/𝒌𝒈
𝑬𝒏𝒕𝒓𝒐𝒑𝒊𝒂 𝒅𝒆 𝒍í𝒒𝒖𝒊𝒅𝒐 𝒄𝒐𝒎𝒑𝒓𝒊𝒎𝒊𝒅𝒐 𝑺𝟐𝒍 = 𝟎, 𝟓𝟐𝟏𝟎 𝒌𝑱/𝒌𝒈 ∗ 𝑲
𝑬𝒏𝒕𝒓𝒐𝒑𝒊𝒂 𝒅𝒆 𝒗𝒂𝒑𝒐𝒓 𝒔𝒖𝒑𝒆𝒓𝒂𝒒𝒖𝒆𝒄𝒊𝒅𝒐 𝑺𝟐𝒗 = 𝟖, 𝟑𝟑𝟎𝟒 𝒌𝑱/𝒌𝒈 ∗ 𝑲
𝑬𝒏𝒕𝒓𝒐𝒑𝒊𝒂 𝒅𝒐 𝒑𝒐𝒏𝒕𝒐 𝟐 = 𝑺𝟐 = 𝑺𝟏 = 𝟓, 𝟔𝟏𝟒𝟏 𝒌𝑱/𝒌𝒈 ∗ 𝑲
(𝑺𝟐 − 𝑺𝟐𝒍)
𝑻í𝒕𝒖𝒍𝒐 𝒅𝒂 𝒎𝒊𝒔𝒕𝒖𝒓𝒂𝒆𝒏𝒕𝒓𝒐𝒑𝒊𝒂 (𝒙) =
(𝑺𝟐𝒗 − 𝑺𝟐𝒍)
(𝟓, 𝟔𝟏𝟒𝟏 − 𝟎, 𝟓𝟐𝟏𝟎)
𝒙=
(𝟖, 𝟑𝟑𝟎𝟒 − 𝟎, 𝟓𝟐𝟏𝟎)
𝟓, 𝟎𝟗𝟑𝟏
𝒙=
𝟕, 𝟖𝟎𝟗𝟒
𝒙 = 𝟎, 𝟔𝟓𝟐𝟐
(𝒉𝟐 − 𝒉𝟐𝒍)
𝒙=
(𝒉𝟐𝒗 − 𝒉𝟐𝒍)
𝒉𝟐 = 𝒉𝟐𝒍 + 𝒙 ∙ (𝒉𝟐𝒗 − 𝒉𝟐𝒍)
𝒉𝟐𝒔 = 𝟏𝟓𝟏, 𝟓𝟑 + (𝟎, 𝟔𝟓𝟐𝟐 ∙ (𝟐𝟓𝟔𝟕, 𝟒 − 𝟏𝟓𝟏, 𝟓𝟑))
𝒉𝟐𝒔 = 𝟏𝟕𝟐𝟕, 𝟏𝟔 𝒌𝑱/𝒌𝒈
𝜼𝒕 = 𝟎, 𝟖𝟕 →→ 𝟖𝟕%
(𝒉𝟏 − 𝒉𝟐)
𝜼𝒕 =
(𝒉𝟏 − 𝒉𝟐𝒔)
(𝟐𝟕𝟐𝟒, 𝟕 − 𝒉𝟐)
𝟎, 𝟖𝟕 =
(𝟐𝟕𝟐𝟒, 𝟕 − 𝟏𝟕𝟐𝟕, 𝟏𝟔)
𝑷𝑶𝑵𝑻𝑶 𝟑
𝑷𝒓𝒆𝒔𝒔ã𝒐 𝑷𝟑 = 𝑷𝟐 = 𝟎, 𝟎𝟔 𝒃𝒂𝒓 = 𝟎, 𝟎𝟎𝟔 𝑴𝑷𝒂
𝑬𝒏𝒕𝒂𝒍𝒑𝒊𝒂 𝒆𝒎 𝒉𝟑 = 𝒉𝟐𝒍 = 𝟏𝟓𝟏, 𝟓𝟑 𝒌𝑱/𝒌𝒈
𝑬𝒏𝒕𝒓𝒐𝒑𝒊𝒂 𝒆𝒎 𝑺𝟑 = 𝑺𝟐𝒍 = 𝟎, 𝟓𝟐𝟏𝟎 𝒌𝑱/𝒌𝒈 ∗ 𝑲
𝑷𝑶𝑵𝑻𝑶 𝟒
𝑷𝟒 = 𝑷𝟏 = 𝟏𝟎𝟎 𝒃𝒂𝒓 = 𝟏𝟎 𝑴𝑷𝒂
𝑽𝒐𝒍𝒖𝒎𝒆 𝒆𝒔𝒑𝒆𝒄í𝒇𝒊𝒄𝒐 𝑽𝟑 = 𝟏, 𝟎𝟎𝟔𝟒 𝒎𝟑/𝒌𝒈
𝜼𝒃 = 𝟎, 𝟖𝟕 →→ 𝟖𝟕%
(𝒉𝟒𝒔 − 𝒉𝟑)
𝜼𝒕 =
(𝒉𝟒 − 𝒉𝟑)
(𝟏𝟔𝟏, 𝟓𝟖 − 𝟏𝟓𝟏, 𝟓𝟑)
𝟎, 𝟖𝟕 =
(𝒉𝟒 − 𝟏𝟓𝟏, 𝟓𝟑)
𝟏𝟔𝟏, 𝟓𝟖 − 𝟏𝟓𝟏, 𝟓𝟑
𝒉𝟒 − 𝟏𝟓𝟏, 𝟓𝟑 =
𝟎, 𝟖𝟕
𝒉𝟒 = 𝟏𝟔𝟑, 𝟎𝟗 𝒌𝑱/𝒌𝒈 →→ 𝒆𝒏𝒕𝒂𝒑𝒊𝒂 𝒅𝒐 𝒑𝒐𝒏𝒕𝒐 𝟒
a- Eficiência Térmica:
b- Bwr:
(𝒉𝟒 − 𝒉𝟑)
𝑩𝒘𝒓 =
(𝒉𝟏 − 𝒉𝟐)
(𝟏𝟔𝟑, 𝟎𝟗 − 𝟏𝟓𝟏, 𝟓𝟑)
𝑩𝒘𝒓 =
(𝟐𝟕𝟐𝟒, 𝟕 – 𝟏𝟖56, 84)
∗ 𝑾𝒍 = 𝟐𝟎𝟎 𝑴𝑾
𝑾𝒍 = (𝑾𝒕 − 𝑾𝒃) ∙ 𝒎
𝑾𝒍
𝒎=
(𝑾𝒕 − 𝑾𝒃)
𝑾𝒍 ∙ 𝟑𝟔𝟎𝟎
𝒎=
(𝒉𝟏 − 𝒉𝟐 ) − (𝒉𝟒 − 𝒉 𝟑)
𝟐𝟎𝟎 ∙ 𝟑𝟔𝟎𝟎 × 𝟏𝟎𝟑
𝒎=
(𝟐𝟕𝟐𝟒, 𝟕 – 𝟏𝟖56, 84) − (𝟏𝟔𝟑, 𝟎𝟗 − 𝟏𝟓𝟏, 𝟓𝟑)
𝒎 = 𝟖, 4 × 𝟏𝟎𝟓 𝒌𝒈/𝒉
d- A taxa de calor que entra, em MW:
𝑸 = 𝒎 ∙ (𝒉𝟏 − 𝒉𝟒)
𝟖, 4 × 𝟏𝟎𝟓 𝒌𝒈/𝒉
𝑸= ∙ (𝟐𝟕𝟐𝟒, 𝟕 − 𝟏𝟔𝟑, 𝟎𝟗)𝒌𝑱/𝒌𝒈
𝟑𝟔𝟎𝟎 𝒔/𝒉 × 𝟏𝟎𝟑𝒌𝑾/𝑴𝑾
𝑸 = 597, 71 𝑴𝑾
𝑸 = 𝒎 ∙ (𝒉𝟐 − 𝒉𝟑)
(𝟖, 4 × 𝟏𝟎𝟓𝒌𝒈/𝒉
𝑸= ∙ (𝟏𝟖56, 84 − 𝟏𝟓𝟏, 𝟓𝟑)𝒌𝑱/𝒌𝒈
𝟑𝟔𝟎𝟎 𝒔/𝒉 × 𝟏𝟎 𝒌𝑾/𝑴𝑾
𝟑
𝑸 = 397, 9 𝑴𝑾
Página 2 | 5
3° ciclo - O vapor d’água é o fluido de trabalho em um ciclo ideal de Rankine com
superaquecimento e reaquecimento. O vapor entra na turbina do primeiro estágio a
100 bar e 520°C, e se expande até 5 bar. Em seguida, é reaquecido até 440°C antes
de entrar na turbina do segundo estágio, onde se expande até a pressão do
condensador de 0,06 bar. A potência líquida na saída é de 200 MW.
𝑹𝑬𝑺𝑷𝑶𝑺𝑻𝑨:
𝑷𝑶𝑵𝑻𝑶 𝟏
𝑷𝒓𝒆𝒔𝒔ã𝒐 𝑷𝟏 = 𝟏𝟎𝟎 𝒃𝒂𝒓
𝑻𝒆𝒎𝒑𝒆𝒓𝒂𝒕𝒖𝒓𝒂 𝑻𝟏 = 𝟓𝟐𝟎°𝑪
𝑪𝒐𝒏𝒔𝒖𝒍𝒕𝒂𝒏𝒅𝒐 𝒂 𝒕𝒂𝒃𝒆𝒍𝒂 𝒅𝒆 𝑨 − 𝟒, 𝒍𝒊𝒒𝒖𝒊𝒅𝒐 𝒗𝒂𝒑𝒐𝒓 𝒑𝒂𝒓𝒂 𝒆𝒏𝒕𝒂𝒍𝒑𝒊𝒂 𝒆 𝒆𝒏𝒕𝒓𝒐𝒑𝒊𝒂 𝒅𝒆 𝒗𝒂𝒑𝒐𝒓 𝒔𝒖𝒑𝒆𝒓𝒂𝒒𝒖𝒆𝒄𝒊𝒅𝒐
𝒕𝒆𝒎𝒐𝒔:
𝑬𝒏𝒕𝒂𝒍𝒑𝒊𝒂 𝒉𝟏 = 𝟑425,1 𝒌𝑱/𝒌𝒈
𝑬𝒏𝒕𝒓𝒐𝒑𝒊𝒂 𝑺𝟏 = 𝟔, 6622 𝒌𝑱/𝒌𝒈 ∗ 𝑲
𝑷𝑶𝑵𝑻𝑶 𝟐
𝑷𝒓𝒆𝒔𝒔ã𝒐 𝑷𝟐 = 𝟓 𝒃𝒂𝒓
𝑻𝟐 = 𝟒𝟒𝟎 °𝑪
𝑬𝒏𝒕𝒂𝒍𝒑𝒊𝒂 𝒅𝒆 𝒍𝒊𝒒𝒖𝒊𝒅𝒐 𝒄𝒐𝒎𝒑𝒓𝒊𝒎𝒊𝒅𝒐 𝒉𝟐𝒍 = 𝟔𝟒𝟎, 𝟐𝟑 𝒌𝑱/𝒌𝒈
𝑬𝒏𝒕𝒂𝒍𝒑𝒊𝒂 𝒅𝒆 𝒗𝒂𝒑𝒐𝒓 𝒔𝒂𝒕𝒖𝒓𝒂𝒅𝒐 𝒉𝟐𝒗 = 𝟐𝟕𝟒𝟖, 𝟕 𝒌𝑱/𝒌𝒈
𝑬𝒏𝒕𝒓𝒐𝒑𝒊𝒂 𝒅𝒆 𝒍í𝒒𝒖𝒊𝒅𝒐 𝒄𝒐𝒎𝒑𝒓𝒊𝒎𝒊𝒅𝒐 𝑺𝟐𝒍 = 𝟏, 𝟖𝟔𝟎𝟕 𝒌𝑱/𝒌𝒈 ∗ 𝑲
𝑬𝒏𝒕𝒓𝒐𝒑𝒊𝒂 𝒅𝒆 𝒗𝒂𝒑𝒐𝒓 𝒔𝒖𝒑𝒆𝒓𝒂𝒒𝒖𝒆𝒄𝒊𝒅𝒐 𝑺𝟐𝒗 = 𝟔, 𝟖𝟐𝟏𝟐 𝒌𝑱/𝒌𝒈 ∗ 𝑲
𝑬𝒏𝒕𝒓𝒐𝒑𝒊𝒂 𝒅𝒐 𝒑𝒐𝒏𝒕𝒐 𝟐 = 𝑺𝟐 = 𝑺𝟏 = 𝟔,6622 𝒌𝑱/𝒌𝒈 ∗ 𝑲
(𝑺𝟐 − 𝑺𝟐𝒍)
𝑻í𝒕𝒖𝒍𝒐 𝒅𝒂 𝒎𝒊𝒔𝒕𝒖𝒓𝒂𝒆𝒏𝒕𝒓𝒐𝒑𝒊𝒂 (𝒙𝟐 ) =
(𝑺𝟐𝒗 − 𝑺𝟐𝒍)
(𝟔, 6622 − 𝟏, 𝟖𝟔𝟎𝟕)
𝒙𝟐 =
(𝟔, 𝟖𝟐𝟏𝟐 − 𝟏, 𝟖𝟔𝟎𝟕)
𝒙𝟐 = 𝟎, 𝟗68
(𝒉𝟐 − 𝒉𝟐𝒍)
𝒙𝟐 =
(𝒉𝟐𝒗 − 𝒉𝟐𝒍)
𝒉𝟐 = 𝒉𝟐𝒍 + 𝒙𝟐 ∙ (𝒉𝟐𝒗 − 𝒉𝟐𝒍)
𝒉𝟐 = 𝟔𝟒𝟎, 𝟐𝟑 + (𝟎, 968 ∙ (𝟐𝟕𝟒𝟖, 𝟕 − 𝟔𝟒𝟎, 𝟐𝟑))
𝒉𝟐 = 2681,23 𝒌𝑱/𝒌𝒈
𝑷𝑶𝑵𝑻𝑶 𝟑
𝑷𝒓𝒆𝒔𝒔ã𝒐 𝑷𝟑 = 𝟓 𝒃𝒂𝒓
𝑬𝒏𝒕𝒂𝒍𝒑𝒊𝒂 𝒆𝒎 𝒉𝟑 = 𝟑𝟑𝟓𝟔 𝒌𝑱/𝒌𝒈
𝑬𝒏𝒕𝒓𝒐𝒑𝒊𝒂 𝒆𝒎 𝑺𝟑 = 𝟕, 𝟗𝟏𝟓𝟐 𝒌𝑱/𝒌𝒈 ∗ 𝑲
𝑷𝑶𝑵𝑻𝑶 𝟒
𝑷𝟒 = 𝟎, 𝟎𝟔 𝒃𝒂𝒓
𝑺𝟒 = 𝑺𝟑 = 𝟕, 𝟗𝟏𝟓𝟐 𝑲𝑱/𝒌𝒈 ∙ 𝑲
(𝒆𝒙𝒑𝒂𝒏𝒔ã𝒐 𝒊𝒔𝒆𝒏𝒕𝒓ó𝒑𝒊𝒄𝒂 𝒏𝒂 𝒕𝒖𝒓𝒃𝒊𝒏𝒂 𝒅𝒆 𝒔𝒆𝒈𝒖𝒏𝒅𝒐 𝒆𝒔𝒕á𝒈𝒊𝒐)
𝑻𝒂𝒃𝒆𝒍𝒂 𝒅𝒆 á𝒈𝒖𝒂 𝒔𝒂𝒕𝒖𝒓𝒂𝒅𝒂 𝒕𝒆𝒎𝒐𝒔 ∶
𝑺𝟒𝒍 = 𝟎, 𝟓𝟐𝟏𝟎 𝑲𝑱/𝒌𝒈 ∙ 𝑲
𝑺𝟒𝒗 = 𝟖, 𝟑𝟑𝟎𝟒 𝑲𝑱/𝒌𝒈 ∙ 𝑲
𝒉𝟒𝒍 = 𝟏𝟓𝟏, 𝟓𝟑 𝑲𝑱/𝒌𝒈
𝒉𝟒𝒗 = 𝟐𝟓𝟔𝟕, 𝟒 𝑲𝑱/𝒌𝒈
(𝑺𝟒 − 𝑺𝒍)
𝑻í𝒕𝒖𝒍𝒐 𝒅𝒂 𝒎𝒊𝒔𝒕𝒖𝒓𝒂𝒆𝒏𝒕𝒓𝒐𝒑𝒊𝒂 (𝒙𝟒 ) =
(𝑺𝒗 − 𝑺𝒍)
(𝟕, 𝟗𝟏𝟓𝟐 − 𝟎, 𝟓𝟐𝟏𝟎)
𝒙𝟒 =
(𝟖, 𝟑𝟑𝟎𝟒 − 𝟎, 𝟓𝟐𝟏𝟎)
𝒙𝟒 = 𝟎, 𝟗𝟒𝟔𝟖
(𝒉𝟒 − 𝒉𝟒𝒍)
𝒉𝟒 =
(𝒉𝟒𝒗 − 𝒉𝟒𝒍)
𝒉𝟒 = 𝒉𝟒𝒍 + 𝒙𝟒 ∙ (𝒉𝟒𝒗 − 𝒉𝟒𝒍)
𝒉𝟒 = 𝟏𝟓𝟏, 𝟓𝟑 + (𝟎, 𝟗𝟒𝟔𝟖 ∙ (𝟐𝟓𝟔𝟕, 𝟒 − 𝟏𝟓𝟏, 𝟓𝟑))
𝒉𝟒 = 𝟐𝟒𝟑𝟖, 𝟖𝟖 𝒌𝑱/𝒌𝒈
𝑷𝑶𝑵𝑻𝑶 𝟓
𝑷𝒐𝒓 𝒕𝒆𝒐𝒓𝒊𝒂 é 𝒍𝒊𝒒𝒖𝒊𝒅𝒐 𝒔𝒂𝒕𝒖𝒓𝒂𝒅𝒐 𝒄𝒐𝒎 𝑷𝒓𝒆𝒔𝒔ã𝒐 𝑷𝟓 = 𝟎, 𝟎𝟔 𝒃𝒂𝒓
𝑬𝒏𝒕𝒂𝒍𝒑𝒊𝒂 𝒆𝒎 𝒉𝟓 = 𝟏𝟓𝟏, 𝟓𝟑 𝒌𝑱/𝒌𝒈
𝑬𝒏𝒕𝒓𝒐𝒑𝒊𝒂 𝒆𝒎 𝑺𝟓 = 𝟎, 𝟓𝟐𝟏𝟎 𝒌𝑱/𝒌𝒈 ∗ 𝑲
𝒗𝒇 = 𝟏, 𝟎𝟎𝟔𝟒 × 𝟏𝟎𝟑 →→ 𝟎, 𝟎𝟎𝟏𝟎𝟎𝟔𝟒 𝒎𝟑/𝒌𝒈
𝑷𝑶𝑵𝑻𝑶 𝟔
𝑷𝒓𝒆𝒔𝒔ã𝒐 𝑷𝟔 = 𝟏𝟎𝟎 𝒃𝒂𝒓 →→ 𝟏𝟎𝟎𝟎𝟎 𝑲𝑷𝒂
𝑷𝟓 = 𝟎, 𝟎𝟔 →→ 𝟔 𝑲𝑷𝒂
𝒌𝑱
𝑬𝒏𝒕𝒓𝒐𝒑𝒊𝒂 𝒆𝒎 𝑺𝟔 = 𝑺𝟓 = 𝟎, 𝟓𝟐𝟏𝟎 ∗ 𝑲 (𝒍í𝒒𝒖𝒊𝒅𝒐 𝒄𝒐𝒎𝒑𝒓𝒊𝒎𝒊𝒅𝒐)
𝒌𝒈
𝒗𝒇 = 𝟎, 𝟎𝟎𝟏4524 𝒎𝟑/𝒌𝒈
𝑾𝒃 = 𝒗𝒅𝝆
𝑾𝒃 = 𝟎, 𝟎𝟎14524 𝒎𝟑/𝒌𝒈 ∙ (𝟏𝟎𝟎𝟎𝟎 𝑲𝑷𝒂 − 𝟔 𝑲𝒑𝒂)
𝑾𝒃 = 14, 5152 𝒌𝑱
𝒉𝟔 − 𝒉𝟓 = 14, 5152
𝒉𝟔 = 14, 5152 + 𝒉𝟓
𝑬𝒏𝒕𝒂𝒍𝒑𝒊𝒂 𝒉𝟔 = 𝟏𝟔6, 045 𝒌𝑱/𝒌𝒈
a- Eficiência Térmica:
𝑾𝒍𝒊𝒒
𝜼=
𝖖𝒄𝒂𝒍𝒅
1646,48
𝜼=
3259,055 + 674,77
𝜼 ≅ 𝟎, 𝟒𝟏87 →→ 𝟒𝟏, 87 %
b- Bwr:
𝑾𝒃
𝑩𝒘𝒓 =
𝑾𝒕
𝟏4, 5152
𝑩𝒘𝒓 =
(𝟕4𝟑, 87 + 𝟗𝟏𝟕, 𝟏𝟐)
∗ 𝑾𝒍 = 𝟐𝟎𝟎 𝑴𝑾
𝑾𝒍 = (𝑾𝒕 − 𝑾𝒃) ∙ 𝒎
𝑾𝒍
𝒎=
(𝑾𝒕 − 𝑾𝒃)
𝑾𝒍 ∙ 𝟑𝟔𝟎𝟎
𝒎 =
((𝒉𝟐 − 𝒉𝟏) + (𝒉𝟒 − 𝒉𝟑)) − (𝒉𝟔 − 𝒉𝟓)
𝟐𝟎𝟎 ∙ 𝟑𝟔𝟎𝟎 × 𝟏𝟎𝟑
𝒎=
(𝟕4𝟑, 87 + 𝟗𝟏𝟕, 𝟏𝟐) − (14, 5152)
𝑸 = 𝒎 ∙ [(𝒉𝟏 − 𝒉𝟔)+(h3-h2)]
𝑸 = 477,84 𝑴𝑾
𝑸 = 𝒎 ∙ (𝒉𝟒 − 𝒉𝟓)
(𝟒, 3729 × 𝟏𝟎𝟓𝒌𝒈/𝒉
𝑸= ∙ (𝟐𝟒𝟑𝟖, 𝟖𝟖 − 𝟏𝟓𝟏, 𝟓𝟑)𝒌𝑱/𝒌𝒈
𝟑𝟔𝟎𝟎 𝒔/𝒉 × 𝟏𝟎𝟑 𝒌𝑾/𝑴𝑾
𝑸 = 𝟐77, 84 𝑴𝑾
4° ciclo - O vapor d’água é o fluido de trabalho em um ciclo ideal de Rankine com
superaquecimento e reaquecimento. O vapor entra na turbina, que possui uma
eficiência isentrópica de 85%, no primeiro estágio a 100 bar e 520°C, e se expande
até 5 bar. Em seguida, é reaquecido até 440°C antes de entrar na turbina do segundo
estágio, onde se expande até a pressão do condensador de 0,06 bar. A potência
líquida na saída é de 200 MW.
𝑹𝑬𝑺𝑷𝑶𝑺𝑻𝑨:
𝑷𝑶𝑵𝑻𝑶 𝟏
𝑷𝒓𝒆𝒔𝒔ã𝒐 𝑷𝟏 = 𝟏𝟎𝟎 𝒃𝒂𝒓
𝑻𝒆𝒎𝒑𝒆𝒓𝒂𝒕𝒖𝒓𝒂 𝑻𝟏 = 𝟓𝟐𝟎°𝑪
𝑪𝒐𝒏𝒔𝒖𝒍𝒕𝒂𝒏𝒅𝒐 𝒂 𝒕𝒂𝒃𝒆𝒍𝒂 𝒅𝒆 𝑨 − 𝟒, 𝒍𝒊𝒒𝒖𝒊𝒅𝒐 𝒗𝒂𝒑𝒐𝒓 𝒑𝒂𝒓𝒂 𝒆𝒏𝒕𝒂𝒍𝒑𝒊𝒂 𝒆 𝒆𝒏𝒕𝒓𝒐𝒑𝒊𝒂 𝒅𝒆 𝒗𝒂𝒑𝒐𝒓 𝒔𝒖𝒑𝒆𝒓𝒂𝒒𝒖𝒆𝒄𝒊𝒅𝒐
𝒕𝒆𝒎𝒐𝒔:
𝑬𝒏𝒕𝒂𝒍𝒑𝒊𝒂 𝒉𝟏 = 𝟑425,1 𝒌𝑱/𝒌𝒈
𝑬𝒏𝒕𝒓𝒐𝒑𝒊𝒂 𝑺𝟏 = 𝟔, 6622 𝒌𝑱/𝒌𝒈 ∗ 𝑲
𝑷𝑶𝑵𝑻𝑶 𝟐
𝑷𝒓𝒆𝒔𝒔ã𝒐 𝑷𝟐 = 𝟓 𝒃𝒂𝒓
𝑻𝟐 = 𝟒𝟒𝟎 °𝑪
𝑬𝒏𝒕𝒂𝒍𝒑𝒊𝒂 𝒅𝒆 𝒍𝒊𝒒𝒖𝒊𝒅𝒐 𝒄𝒐𝒎𝒑𝒓𝒊𝒎𝒊𝒅𝒐 𝒉𝟐𝒍 = 𝟔𝟒𝟎, 𝟐𝟑 𝒌𝑱/𝒌𝒈
𝑬𝒏𝒕𝒂𝒍𝒑𝒊𝒂 𝒅𝒆 𝒗𝒂𝒑𝒐𝒓 𝒔𝒂𝒕𝒖𝒓𝒂𝒅𝒐 𝒉𝟐𝒗 = 𝟐𝟕𝟒𝟖, 𝟕 𝒌𝑱/𝒌𝒈
𝑬𝒏𝒕𝒓𝒐𝒑𝒊𝒂 𝒅𝒆 𝒍í𝒒𝒖𝒊𝒅𝒐 𝒄𝒐𝒎𝒑𝒓𝒊𝒎𝒊𝒅𝒐 𝑺𝟐𝒍 = 𝟏, 𝟖𝟔𝟎𝟕 𝒌𝑱/𝒌𝒈 ∗ 𝑲
𝑬𝒏𝒕𝒓𝒐𝒑𝒊𝒂 𝒅𝒆 𝒗𝒂𝒑𝒐𝒓 𝒔𝒖𝒑𝒆𝒓𝒂𝒒𝒖𝒆𝒄𝒊𝒅𝒐 𝑺𝟐𝒗 = 𝟔, 𝟖𝟐𝟏𝟐 𝒌𝑱/𝒌𝒈 ∗ 𝑲
(𝒉𝟐s − 𝒉𝟐𝒍)
𝒙𝟐𝒔 =
(𝒉𝟐𝒗 − 𝒉𝟐𝒍)
𝒉𝟐𝒔 = 𝒉𝟐𝒍 + 𝒙𝟐 ∙ (𝒉𝟐𝒗 − 𝒉𝟐𝒍)
𝒉𝟐𝒔 = 𝟔𝟒𝟎, 𝟐𝟑 + (𝟎, 𝟗68 ∙ (𝟐𝟕𝟒𝟖, 𝟕 − 𝟔𝟒𝟎, 𝟐𝟑))
𝒉𝟐s = 2681,23 𝒌𝑱/𝒌𝒈
𝜼𝒕𝟏 = 𝟎, 𝟖𝟓
𝑾𝒕 𝒓𝒆𝒂𝒍 < 𝑾𝒕 𝒊𝒅𝒆𝒂𝒍 𝒍𝒐𝒈𝒐 𝑾𝒕 𝒓𝒆𝒂𝒍 = 𝜼𝒕 ∙ 𝑾𝒕 𝒊𝒅𝒆𝒂𝒍
𝒉𝟐 − 𝒉𝟏 = 𝜼𝒕(𝒉𝟐𝒔 − 𝒉𝟏)
𝒉𝟐 = 𝒉𝟏 + 𝜼𝒕(𝒉𝟐𝒔 − 𝒉𝟏)
𝒉𝟐 = 𝟑𝟒𝟒𝟕, 𝟕 + 𝟎, 𝟖𝟓(2681,23 − 𝟑𝟒𝟒𝟕, 𝟕)
𝒉𝟐 = 𝟐796, 201 𝒌𝑱/𝒌𝒈
𝑷𝑶𝑵𝑻𝑶 𝟑
𝑷𝒓𝒆𝒔𝒔ã𝒐 𝑷𝟑 = 𝟓 𝒃𝒂𝒓
𝑬𝒏𝒕𝒂𝒍𝒑𝒊𝒂 𝒆𝒎 𝒉𝟑 = 𝟑𝟑𝟓𝟔 𝒌𝑱/𝒌𝒈
𝑬𝒏𝒕𝒓𝒐𝒑𝒊𝒂 𝒆𝒎 𝑺𝟑 = 𝟕, 𝟗𝟏𝟓𝟐 𝒌𝑱/𝒌𝒈 ∗ 𝑲
𝑷𝑶𝑵𝑻𝑶 𝟒
𝑷𝟒 = 𝟎, 𝟎𝟔 𝒃𝒂𝒓
𝑺𝟒 = 𝑺𝟑 = 𝟕, 𝟗𝟏𝟓𝟐 𝑲𝑱/𝒌𝒈 ∙ 𝑲
(𝒆𝒙𝒑𝒂𝒏𝒔ã𝒐 𝒊𝒔𝒆𝒏𝒕𝒓ó𝒑𝒊𝒄𝒂 𝒏𝒂 𝒕𝒖𝒓𝒃𝒊𝒏𝒂 𝒅𝒆 𝒔𝒆𝒈𝒖𝒏𝒅𝒐 𝒆𝒔𝒕á𝒈𝒊𝒐)
𝑻𝒂𝒃𝒆𝒍𝒂 𝒅𝒆 á𝒈𝒖𝒂 𝒔𝒂𝒕𝒖𝒓𝒂𝒅𝒂 𝒕𝒆𝒎𝒐𝒔 ∶
𝑺𝟒𝒍 = 𝟎, 𝟓𝟐𝟏𝟎 𝑲𝑱/𝒌𝒈 ∙ 𝑲
𝑺𝟒𝒗 = 𝟖, 𝟑𝟑𝟎𝟒 𝑲𝑱/𝒌𝒈 ∙ 𝑲
𝒉𝟒𝒍 = 𝟏𝟓𝟏, 𝟓𝟑 𝑲𝑱/𝒌𝒈
𝒉𝟒𝒗 = 𝟐𝟓𝟔𝟕, 𝟒 𝑲𝑱/𝒌𝒈
(𝑺𝟒 − 𝑺𝒍)
𝑻í𝒕𝒖𝒍𝒐 𝒅𝒂 𝒎𝒊𝒔𝒕𝒖𝒓𝒂𝒆𝒏𝒕𝒓𝒐𝒑𝒊𝒂 (𝒙𝟒𝒔 ) =
(𝑺𝒗 − 𝑺𝒍)
(𝟕, 𝟗𝟏𝟓𝟐 − 𝟎, 𝟓𝟐𝟏𝟎)
𝒙𝟒𝒔 =
(𝟖, 𝟑𝟑𝟎𝟒 − 𝟎, 𝟓𝟐𝟏𝟎)
𝒙𝟒𝒔 = 𝟎, 𝟗𝟒𝟔𝟖
(𝒉𝟒s − 𝒉𝟒𝒍)
X𝟒𝒔 =
(𝒉𝟒𝒗 − 𝒉𝟒𝒍)
𝒉𝟒𝒔 = 𝒉𝟒𝒍 + 𝒙𝟒 ∙ (𝒉𝟒𝒗 − 𝒉𝟒𝒍)
𝒉𝟒𝒔 = 𝟏𝟓𝟏, 𝟓𝟑 + (𝟎, 𝟗𝟒𝟔𝟖 ∙ (𝟐𝟓𝟔𝟕, 𝟒 − 𝟏𝟓𝟏, 𝟓𝟑))
𝒉𝟒𝒔 = 𝟐𝟒𝟑𝟖, 𝟖𝟖 𝒌𝑱/𝒌𝒈
𝜼𝒕𝟐 = 𝟎, 𝟖𝟓
𝑾𝒕 𝒓𝒆𝒂𝒍 < 𝑾𝒕 𝒊𝒅𝒆𝒂𝒍 𝒍𝒐𝒈𝒐 𝑾𝒕 𝒓𝒆𝒂𝒍 = 𝜼𝒕 ∙ 𝑾𝒕 𝒊𝒅𝒆𝒂𝒍
𝒉𝟒 − 𝒉𝟑 = 𝜼𝒕𝟐(𝒉𝟒𝒔 − 𝒉𝟑)
𝒉𝟒 = 𝒉𝟑 + 𝜼𝒕𝟐(𝒉𝟒𝒔 − 𝒉𝟑)
𝒉𝟒 = 𝟑𝟑𝟓𝟔 + 𝟎, 𝟖𝟓(𝟐𝟒𝟑𝟖, 𝟖𝟖 − 𝟑𝟑𝟓𝟔)
𝒉𝟒 = 𝟐𝟓𝟕𝟔, 𝟒𝟒𝟖 𝒌𝑱/𝒌𝒈
𝑷𝑶𝑵𝑻𝑶 𝟓
𝑷𝒐𝒓 𝒕𝒆𝒐𝒓𝒊𝒂 é 𝒍𝒊𝒒𝒖𝒊𝒅𝒐 𝒔𝒂𝒕𝒖𝒓𝒂𝒅𝒐 𝒄𝒐𝒎 𝑷𝒓𝒆𝒔𝒔ã𝒐 𝑷𝟓 = 𝟎, 𝟎𝟔 𝒃𝒂𝒓
𝑬𝒏𝒕𝒂𝒍𝒑𝒊𝒂 𝒆𝒎 𝒉𝟓 = 𝟏𝟓𝟏, 𝟓𝟑 𝒌𝑱/𝒌𝒈
𝑬𝒏𝒕𝒓𝒐𝒑𝒊𝒂 𝒆𝒎 𝑺𝟓 = 𝟎, 𝟓𝟐𝟏𝟎 𝒌𝑱/𝒌𝒈 ∗ 𝑲
𝒗𝒇 = 𝟏, 𝟎𝟎𝟔𝟒 × 𝟏𝟎𝟑 →→ 𝟎, 𝟎𝟎𝟏𝟎𝟎𝟔𝟒 𝒎𝟑/𝒌𝒈
𝑷𝑶𝑵𝑻𝑶 𝟔
𝑷𝒓𝒆𝒔𝒔ã𝒐 𝑷𝟔 = 𝟏𝟎𝟎 𝒃𝒂𝒓 →→ 𝟏𝟎𝟎𝟎𝟎 𝑲𝑷𝒂
𝑷𝟓 = 𝟎, 𝟎𝟔 →→ 𝟔 𝑲𝑷𝒂
𝒌𝑱
𝑬𝒏𝒕𝒓𝒐𝒑𝒊𝒂 𝒆𝒎 𝑺𝟔 = 𝑺𝟓 = 𝟎, 𝟓𝟐𝟏𝟎 ∗ 𝑲 (𝒍í𝒒𝒖𝒊𝒅𝒐 𝒄𝒐𝒎𝒑𝒓𝒊𝒎𝒊𝒅𝒐)
𝒌𝒈
𝒗𝒇 = 𝟎, 𝟎𝟎𝟏4524 𝒎𝟑/𝒌𝒈
𝑾𝒃 = 𝒗𝒅𝝆
𝑾𝒃 = 𝟎, 𝟎𝟎14524 𝒎𝟑/𝒌𝒈 ∙ (𝟏𝟎𝟎𝟎𝟎 𝑲𝑷𝒂 − 𝟔 𝑲𝒑𝒂)
𝑾𝒃 = 14, 5152 𝒌𝑱
𝒉𝟔 − 𝒉𝟓 = 14, 5152
𝒉𝟔 = 14, 5152 + 𝒉𝟓
𝑬𝒏𝒕𝒂𝒍𝒑𝒊𝒂 𝒉𝟔 = 𝟏𝟔6, 045 𝒌𝑱/𝒌𝒈
a- Eficiência Térmica:
𝑾𝒍𝒊𝒒
𝜼=
𝖖𝒄𝒂𝒍𝒅
1393,94
𝜼=
3259,055+ 559,799
𝜼 ≅ 𝟎, 𝟑𝟔5 →→ 𝟑𝟔, 5 %
b- Bwr:
𝑾𝒃
𝑩𝒘𝒓 = 5
𝑾𝒕
14,5152
𝑩𝒘𝒓 =
(628,899+ 𝟕𝟕𝟗, 𝟓𝟓𝟐)
∗ 𝑾𝒍 = 𝟐𝟎𝟎 𝑴𝑾
𝑾𝒍 = (𝑾𝒕 − 𝑾𝒃) ∙ 𝒎
𝑾𝒍
𝒎=
(𝑾𝒕 − 𝑾𝒃)
𝑾𝒍 ∙ 𝟑𝟔𝟎𝟎
𝒎 =
((𝒉𝟐 − 𝒉𝟏) + (𝒉𝟒 − 𝒉𝟑)) − (𝒉𝟔 − 𝒉𝟓)
𝟐𝟎𝟎 ∙ 𝟑𝟔𝟎𝟎 × 𝟏𝟎𝟑
𝒎=
(628,899 + 𝟕𝟕𝟗, 𝟓𝟓𝟐) − (14,5152)
𝑸 = 𝒎 ∙ [(𝒉𝟏 − 𝒉𝟔)+(h3-h2)]
𝟓, 16523 × 𝟏𝟎𝟓 𝒌𝒈/𝒉
𝑸= ∙ [(3425,1 − 𝟏𝟔6, 045)+(3356-2796,201)]𝒌𝑱/𝒌𝒈
𝟑𝟔𝟎𝟎 𝒔/𝒉 × 𝟏𝟎𝟑𝒌𝑾/𝑴𝑾
𝑸 = 547,92 𝑴𝑾
𝑸 = 𝒎 ∙ (𝒉𝟒 − 𝒉𝟓)
(𝟓, 16523 × 𝟏𝟎𝟓𝒌𝒈/𝒉
𝑸= ∙ (2576,448 − 𝟏𝟓𝟏, 𝟓𝟑)𝒌𝑱/𝒌𝒈
𝟑𝟔𝟎𝟎 𝒔/𝒉 × 𝟏𝟎𝟑 𝒌𝑾/𝑴𝑾
𝑸 = 347,86 𝑴𝑾