INGENIA

CHM-12

Kirchhoff ΔH(T)

ΔH(T2) = ΔH(T1) + ΔCp (T2 − T1). Enthalpy at a second temperature.

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ThermochemistryKirchhoff

Governing equation

ΔH(T2)=ΔH(T1)+ΔCp(T2−T1)\Delta H(T_2)=\Delta H(T_1)+\Delta C_p(T_2-T_1)

T2∈[200,1200]T_2 \in \left[200, 1200\right]

where

\Delta H_1
ΔH at T1 (kJ/mol)
\Delta C_p
ΔCp (J/(mol·K))
T_1
T1 (K)
T_2
T2 (K)
\Delta H_2
ΔH at T2 (kJ/mol)

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CHM-12 · phase
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①

Governing law — red

ΔH(T2)=ΔH(T1)+ΔCp(T2−T1)\Delta H(T_2)=\Delta H(T_1)+\Delta C_p(T_2-T_1)

T2∈[200,1200]T_2 \in \left[200, 1200\right]

T2=200T_2 = 200ΔH2=−88.08\Delta H_2 = -88.08

②

Domain of the variable — blue

T_2_{\min} = 200,\quad T_2_{\max} = 1200

T2∈[200,1200]T_2 \in \left[200, 1200\right]

T2=200T_2 = 200T2=200T_2 = 200

③

Response curve — green

ΔH(T2)=ΔH(T1)+ΔCp(T2−T1)\Delta H(T_2)=\Delta H(T_1)+\Delta C_p(T_2-T_1)

T2∈[200,1200]T_2 \in \left[200, 1200\right]

T2=200T_2 = 200ΔH2=−88.08\Delta H_2 = -88.08

④

Rate of change — amber

dΔH2dT2\frac{\mathrm{d}\Delta H_2}{\mathrm{d}T_2}

T2∈[200,1200]T_2 \in \left[200, 1200\right]

T2=206.3T_2 = 206.3ΔH2′=−0.04\Delta H_2^{\prime} = -0.04

Lecture brief

Historical brief

Ideal-gas law, van ’t Hoff, Nernst, Michaelis–Menten and Clausius–Clapeyron are physical chemistry’s working equations of equilibrium and rate. The lab is pressure, potential and kinetics. This sheet (CHM-12 — Kirchhoff ΔH(T)) is the form associated with Kirchhoff. Working symbols: ΔH1\Delta H_1, ΔCp\Delta C_p, T1T_1, T2T_2 →\rightarrow ΔH2\Delta H_2. From dH = Cp dT applied to products minus reactants. Constant-ΔCp snapshot.

Purpose

Purpose: compute ΔH2\Delta H_2 from ΔH1\Delta H_1, ΔCp\Delta C_p, T1T_1, T2T_2 in Physical chemistry via ΔH(T2)=ΔH(T1)+ΔCp(T2−T1)\Delta H(T_2)=\Delta H(T_1)+\Delta C_p(T_2-T_1) ΔH(T2) = ΔH(T1) + ΔCp (T2 − T1). Enthalpy at a second temperature. Use it when a real physical chemistry question must be answered in SI before a code check.

Live realistic example

In symbols

Live case. Given ΔH1=−92.000 kJ/mol\Delta H_1 = -92.000\,\mathrm{kJ/mol}, ΔCp=−40.000 J/(mol⋅K)\Delta C_p = -40.000\,\mathrm{J/(mol·K)}, T1=298.000 KT_1 = 298.000\,\mathrm{K}, T2=500.000 KT_2 = 500.000\,\mathrm{K}, the governing relation ΔH(T2)=ΔH(T1)+ΔCp(T2−T1)\Delta H(T_2)=\Delta H(T_1)+\Delta C_p(T_2-T_1) yields ΔH2=−100.080 kJ/mol\Delta H_2 = -100.080\,\mathrm{kJ/mol}. Mean ΔCp between T1 and T2. Move a slider: the numbers are this situation, not a canned story.

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Outputs

  • ΔH at T2 \Delta H_2-100.080 kJ/mol
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CHM-12 · phase
00:0 / 00:08

Narration of this film

Mean ΔCp between T1 and T2.

From dH = Cp dT applied to products minus reactants. Constant-ΔCp snapshot.

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