Heuristische Verfahren zur Tourenplanung bei der Hausmüllentsorgung in ländlichen Regionen

Zusammenfassung Tourenprobleme bei der Hausmüllsammlung lassen sich in die Reihe der Lieferplanprobleme einordnen. Zur Lösung praktischer Größenordnungen werden hier einfache heuristische Verfahren (Prioritätsregeln) vorgestellt, weniger um der Vielzahl heuristischer Verfahren weitere hinzuzufügen als vielmehr dem Praktiker einen vielversprechenden Weg beim Lösen seiner Probleme aufzuzeigen.

---

Summary The discussed solid waste collection problem shows the properties of the so called truck dispatching problem. To solve problems for typical problem structure heuristic rules are pointed out in order to show the planner an efficient way of problem solving.

---

---

Zusammenfassung dreier Vorträge im 4. planungstechnischen Seminar Tourenplanung bei der Abfallbeseitigung am Institut für Siedlungswasserwirtschaft der Universität Karlsruhe am 1.10.1976.     

Kriterien in der Theorie der Gleichverteilung

It is the aim of this paper to introduce two new notions of discrepancy. They are defined by the formulas $$\begin{gathered} \Delta _N^r \left( {\omega ;f} \right) = \mathop {\sup }\limits_{\left| z \right| = r} \left| {\left( {{1 \mathord{\left/ {\vphantom {1 N}} \right. \kern-\nulldelimiterspace} N}} \right)\sum\limits_{n = 1}^N {f\left( {z e^2 \pi i\omega \left( n \right)} \right)} - f\left( 0 \right)} \right|, and \hfill \\ \delta _N^r \left( {\omega ;f} \right) = \mathop {\sup }\limits_{\left| z \right| = r} \left| {\left( {{1 \mathord{\left/ {\vphantom {1 N}} \right. \kern-\nulldelimiterspace} N}} \right)\sum\limits_{n = 1}^N {f\left( {z \omega \left( n \right)} \right)} \cdot z - \int\limits_0^z {f\left( \zeta \right)d\zeta } } \right|, \hfill \\ \end{gathered} $$ wheref is a holomorphic function defined in the unit disc withf ^(k) (0)≠0 for allk∈?,r<1 is a positive number, and ω is a sequence in [0, 1]. The first of these discrepancies can be generalized for multidimensional sequences. ω is uniform distributed if and only if lim _N→∞ Δ _N ^r (ω;f)=0 resp. lim _N→∞δ _N ^r (ω;f)=0. These results are proved in a quantitative way by estimating the classical discrepancyD _N (ω) by means ofΔ _N ^r (ω;f) and δ _N ^r (ω;f): $$\begin{gathered} \Delta _N^r \left( {\omega ;f} \right) \ll D_N \left( \omega \right) \ll \Phi \left( {\Delta _N^r \left( {\omega ;f} \right)} \right), \hfill \\ \delta _N^r \left( {\omega ;f} \right) \ll D_N \left( \omega \right) \ll \Psi \left( {\delta _N^r \left( {\omega ;f} \right)} \right). \hfill \\ \end{gathered} $$ The functions Φ and Ψ only depend onf andr. These estimations are based on the inequalities ofKoksma-Hlawka andErdös-Turán.     

Verdampfung von Uranspaltprodukten in Wasserstoff, Stickstoff und Sauerstoff

Zusammenfassung Die Verdampfung der Spaltprodukte Germanium, Arsen, Molybdän, Ruthenium, Cadmium, Zinn, Antimon und Tellur aus bestrahltem U₃O₈ im Wasserstoff-, Stickstoff- und Sauerstoffstrom wurde zwischen 900 und 1500° C untersucht. Bei 1500° C verdampfen die meisten dieser Elemente innerhalb 1 Std mit hoher Ausbeute.

---

Summary The volatization of the fission products germanium, arsenic, molybdenum, ruthenium, cadmium, tin, antimony and tellurium from neutron-irradiated uranium oxide in flowing hydrogen, nitrogen or oxygen of atmospheric pressure was investigated between 900 and 1500° C. At 1500° C, most of these elements are volatized with high yield within one hour.

---

---

Herrn Prof. Dr. F. Strassmann danken wir herzlich für die Förderung dieser Arbeit, Herrn I. Bonner für seine Mitarbeit, den Betriebsstäben der Forschungsreaktoren Frankfurt und München, insbesondere Herrn Dr. G. Wolf (Frankfurt), für Bestrahlungen und dem Bundesministerium für wissenschaftliche Forschung für finanzielle Beihilfen.

---

Herrn Prof. Dr. W. Geilmann zum 75. Geburtstag gewidmet.

---

Aus einer Dissertation, Mainz 1963.     

Strukturviskosität von verdünnten Lösungen von Biopolymeren

The importance of the rheological behaviour of solutions of macromolecules is briefly evaluated. The viscosity of the solutions depends on concentration, shear rate and time of shear, this relation being determined by the structure of the dissolved molecules. In dilute solutions shear dependence of viscosity is very frequently caused by the preferential orientation of anisotropic molecules. In such a case the particle dimensions can be calculated from the true limiting viscosity number, an anisotropy factor, the rotational diffusion constant and the effective particle density. These numbers can be derived from the flow curve, which has been extrapolated to zero concentration. It is necessary to measure the flow curve at shear gradients, which are sufficiently low to allow for an extrapolation to vanishing shear rate. By comparing the experimental flow curve with a choice of theoretical ones, the rotational diffusion constant and the anisotropy factor (axial ratio) can be found. From the limiting viscosity number and the axial ratio, the particle density can be calculated.     

Komplexe von 2,6-Dimethylpyridin-1-oxid mit Lanthanidjodiden

Complexes of 2,6-dimethylpyridine 1-oxide with lanthanide iodides of the formulaeLn(2,6-LTNO)₅I₃ whereLn=La, Tb and Yb,Ln(2,6-LTNO)₄I₃ whereLn=Pr and Nd and Er(2,6-LTNO)_4.5I₃ have been prepared and characterised by chemical analysis, infrared and conductance studies. Infrared and conductance data have been interpreted in terms of dimeric (or polymeric) structures involving bridging amine oxide groups.

---

---

Mit 2 Abbildungen     

Über die Synthese von 5-(o-Trifluormethylphenyl)-1H-thieno[3,4—e]-1,4-diazepin-2(3H)-onen

The synthesis of 5-(o-trifluoromethylphenyl)-1H-thieno-[3,4-e]1,4-diazepin-2(3H)-one (7) and its nitration and chlorination in pos. 8 are described.     

Berechnung von mittleren Schwingungsamplituden einiger tetraedrischer Moleküle und Ionen nach der Methode der charakteristischen Schwingungen

Mean amplitudes of vibration of a series of tetrahedralXY ₄ molecules and ions (hydrides, halides, oxides and oxoanions) have been calculated using the “Method of the Characteristic Vibrations” ofA. Müller. The results indicate that this method leads to very good values for most of the investigated species, and especially in the cases of highM _X/M_Y mass ratio.     

Die Hydrohalogenierung von Hexaphenyldigerman und die Schwingungsspektren einiger Ge2(C6H5) n X6−n -Verbindungen

The reactions of Ge₂(C₆H₅)₆ with HCl and HBr lead in nearly quantitative yields to the 1,1,2,2-tetrahalo derivatives Cl₂(C₆H₅)GeGe(C₆H₅)Cl₂ (I) and Br₂(C₆H₅)GeGe(C₆H₅)Br₂ (II), resp. The Si?Ge bond of (C₆H₅)₃SiGe(C₆H₅)₃ is cleaved under the conditions of hydrohalogenation. The vibrational spectra of Ge₂Br₆, Ge₂(C₆H₅)₆, I, and II are reported. The influence of vibrational coupling on ν GeGe in these compounds is discussed in detail, including vibrational calculations.     

High precision measurements of the hyperfine structure of seven metastable atomic states of57Fe by laser-Rf double-resonance

The hyperfine structure of the metastable atomic states (3d ⁷4s)⁵ F _2,3,4,5 and (3d ⁷ 4s)³ F _2,3,4 of⁵⁷Fe has been measured using theABMR- LIRF method (atomic beam magnetic resonance detected by laser induced resonance fluorescence). From these measurements the following hfs constantsA of the magnetic dipole interaction have been obtained (corrected for second order effects):A(⁵ F ₂)=55.994(7) MHzA(⁵ F ₃)=69.632(5) MHzA(⁵ F ₄)=78.435(4) MHzA(⁵ F ₅)=87.246(3) MHzA(³ F ₂)=143.328(4) MHzA(³ F ₃)=50.602(10) MHzA(³ F ₄)=13.456(5) MHz     

Gleichverteilung und Quadratwurzelschnecke

A new proof of a theorem of W. Neiss is given that the rays of the Quadratwurzelschnecke are uniformly distributed mod 2 . The exact order of the discrepancy of the sequence is determined. Multidimensional generalizations of this sequence are also considered. It is shown that the Quadratwurzelschnecke is something like a roulette.

---

---

Mit 2 Abbildungen

---

Herrn Prof. R. M. Redheffer in Freundschaft zum 60. Geburtstag gewidmet