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en:grundlagenhandbuch:aufschmelzberechnung:aufschmelzmodell_fuer_dispers_verteilte_fuellstoffe [2026/02/03 10:45] – [Heat Flow Balance] pkaen:grundlagenhandbuch:aufschmelzberechnung:aufschmelzmodell_fuer_dispers_verteilte_fuellstoffe [2026/02/05 11:03] (aktuell) – [Temperature of the Solids at the Location of the First Melt] pka
Zeile 28: Zeile 28:
 **Figure:** Temperature trends within a spherically formed particle **Figure:** Temperature trends within a spherically formed particle
  
-In the area of unsteady heat transmittance, the heat increase starting from single particles [1, 2], or through solid beds [2, 3, 4], is considered. Since according to assumption 2, the melting of single particles should be assumed, it is also sensible to assume single particles in the solid conveying area. The figure shows diagrammatically the temperature trends inside a spherically formed particle. $\bar{T}$ is the average caloric temperature of the particle.+In the area of unsteady heat transmittance, the heat increase starting from single particles [[en:grundlagenhandbuch:aufschmelzberechnung:literatur|[1, 2]]], or through solid beds [[en:grundlagenhandbuch:aufschmelzberechnung:literatur|[2, 3, 4]]], is considered. Since according to assumption 2, the melting of single particles should be assumed, it is also sensible to assume single particles in the solid conveying area. The figure shows diagrammatically the temperature trends inside a spherically formed particle. $\bar{T}$ is the average caloric temperature of the particle.
  
 The coupling of the energy theorem and kinetics gives the differential calculus for the spherically symmetric temperature field. The coupling of the energy theorem and kinetics gives the differential calculus for the spherically symmetric temperature field.
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 $$\theta = \frac{T - T_0}{T_0 - T_U} ; \tau = \frac{at}{r_0^2} ; \xi = \frac{r}{r_0} \tag{2}$$ $$\theta = \frac{T - T_0}{T_0 - T_U} ; \tau = \frac{at}{r_0^2} ; \xi = \frac{r}{r_0} \tag{2}$$
  
-were introduced. For the case of a unique erratic temperature change from the starting temperature $T_0$ up to the environment temperature $T_U$, the solution of the differential calculus (2) is given by [2]. For sufficient lengths of time t in-side particles of finite expansion, similar temperature profiles can be expected. They are then described by the location function $f(x)$, which with extra time, experiences scaled reductions [2]:+were introduced. For the case of a unique erratic temperature change from the starting temperature $T_0$ up to the environment temperature $T_U$, the solution of the differential calculus (2) is given by [[en:grundlagenhandbuch:aufschmelzberechnung:literatur|[2]]]. For sufficient lengths of time t in-side particles of finite expansion, similar temperature profiles can be expected. They are then described by the location function $f(x)$, which with extra time, experiences scaled reductions [[en:grundlagenhandbuch:aufschmelzberechnung:literatur|[2]]]:
  
 $$\theta = g(\tau) \cdot f(\xi) \tag{3}$$ $$\theta = g(\tau) \cdot f(\xi) \tag{3}$$
Zeile 82: Zeile 82:
 **Table:** Constants of the determination of the temperature function **Table:** Constants of the determination of the temperature function
  
-The figure shows the value of the first four roots taken from [2] and the approximate values of those with the equations (11) and (12).+The figure shows the value of the first four roots taken from [[en:grundlagenhandbuch:aufschmelzberechnung:literatur|[2]]] and the approximate values of those with the equations (11) and (12).
  
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