On combinatorial and projective geometry

Cross ratios constitute an important tool in classical projective geometry. Using the theory of Tutte groups as discussed in [6] it will be shown in this note that the concept of cross ratios extends naturally to combinatorial geometries or matroids. From a thorough study of these cross ratios which, among other observations, includes a new matroid theoretic version and proof of the Pappos theorem, it will be deduced that for any projective space M= _n (K) of dimension n2 of M over some skewfield K the inner Tutte group is isomorphic to the commutator factor group K ^*/[K ^*, K ^*] of K ^*K{0}. This shows not only that in case M= _n (K) our matroidal cross ratios are nothing but the classical ones. It can also be used to correlate orientations of the matroid M= _n (K) with the orderings of K. And it implies that Dieudonné's (non-commutative) determinants which, by Dieudonné's definition, take their values in K ^*/[K ^*, K ^*] as well, can be viewed as a special case of a determinant construction which works for just every combinatorial geometry.Research supported by the DFG (Deutsche Forschungsgemeinschaft).     

Hyper-rook Domain Inequalities

A hyper-rook domain of an element x in the space (words of length n over alphabets with k elements) is a sphere with center x and fixed radius j in Hamming distance. The number j determines the dimension of the hyper-rook domain. The classical (and far from solved) problem of covering by rook domains (here considered as the 1-dimensional case) is the problem of finding minimal coverings of by such spheres. Very few results are known in the literature for dimensions ≥ 2. We prove in this paper certain classes of inequalities based on coverings using matrices, which give upper and lower bounds for several cases of the problem for higher dimensions.     

Zur Spektralinvarianz von Algebren von Pseudodifferentialoperatoren in derL p -Theorie

Zusammenfassung Die Hörmander-Klassen _1, ⁰ (0<1) von Pseudodifferentialoperatoren sind -Algebren. Insbesondere ist die Inverse eines inL(L ^p ( ⁿ )) invertierbaren Pseudodifferentialoperators der Klasse _1, ⁰ selbst wieder ein Pseudodifferential-operator derselben Klasse.Der Beweis beruht auf den von R. Beals, R. R. Coifman, Y. Meyer und H. O. Cordes entwickelten Methoden zur Charakterisierung von Algebren von Pseudodifferentialoperatoren.     

Replacement-Policy Development: A Case Study of Glove Replacement at a Nuclear Processing Facility

Individual/group replacement models were used to identify the minimum-cost policy for replacing protective gloves that are utilized in product fabrication at a nuclear processing facility. Since historical data on glove longevity were not available to determine the failure-rate distribution, the classical replacement model for items that fail was modified to consider glove life as a normally distributed variable. Moreover, the absence of replacement-cost required that the classical model be transformed to incorporate the ratio of single to unit-group replacement cost. Sensitivity analysis on these two input parameter values provided guidance for the development of an appropriate replacement policy.     

Approximate neutrality of large-Z ions

LetN(Z) denote the number of electrons which a nucleus of chargeZ can bind in non-relativistic quantum mechanics (assuming that electrons are fermions). We prove thatN(Z)/Z1 asZ.Research partially supported by the NSERC under Grant NA7901 and by the USNSF under Grants DMS-8416049 and PHY 85-15288-A01     

Complexometric titration of phosphorus in organic compounds

Summary A new complexometric method for the determination of phosphorus in organic compounds is described. After combustion in an oxygen-flask, phosphorus is precipitated as cerous phosphate. The excess cerous ion is back-titrated at pH 6–7 with EDTA in the presence of methylthymol blue or xylenol orange indicators. Alkaline hypobromite is used as an absorbent. Tight clamping of the paper carrier in the platinum holder insures complete combustion.

---

Komplexometrische Titration von Phosphor in organischen Verbindungen

Zusammenfassung Die Probe wird im Sauerstoffkolben nach Schöniger verbrannt und der Phosphor als Cer(III)-phosphat ausgefällt. Der Überschuß an Cer(III) wird bei pH 6–7 mit ÄDTA zurücktitriert, wobei Methylthymolblau oder Xylenolorange als Indicator dient. Als Absorptionsmittel wird alkalische Hypobromitlösung verwendet. Um eine vollständige Verbrennung zu gewährleisten, ist es wichtig, daß das Papier mit der Probe fest am Platinhalter angeklammert wird.

---

---

This work was performed under the auspices of the U.S. Atomic Energy Commission.     

Membrane-immobilized haptoglobin as affinity matrix for a hemoglobin-A1c immunosensor

An amperometric immunosensor for hemoglobin-A1c (HbA1c) determination has been developed utilizing membrane-immobilized haptoglobin as affinity matrix fixed in front of a Pt-working electrode. The HbA1c assay was carried out in a two-step procedure including the selective hemoglobin enrichment on the sensor surface and the specific HbA1c detection by a glucose oxidase (GOx) labeled anti-HbA1c antibody. Hydrogen peroxide generated by the enzyme label was oxidized at +600 mV versus Ag/AgCl. A standard curve for HbA1c was obtained with a linear range between 0 and 25% HbA1c of total hemoglobin which correspond to 7.8–39 nM. ELISA studies confirmed the advantage of a sandwich-type format with haptoglobin as capture molecule for selective hemoglobin binding over the direct adsorption method. Results by the sandwich immunoassay showed a linear correlation within the clinically relevant range 5–20% (CV < 3). For sensor application the immobilization procedure of haptoglobin onto CDI-activated cellulose membranes was optimized.     

Asymmetric Diels-Alder reactions with 5-menthyloxy-2-(5H)-furanone

A new class of chiral dienophiles, 5-alkoxy-2(5H)-furanones, has been developed. Both enantiomers of 5-menthyloxy-2(5H)-ftiranone are readily available in enantiomerically pure form, starting from furfural and d- or l-menthol. Excellent diastereoselectivities (d.e. β99%) are obtained in thermal Diels-Alder reactions with several cyclic and acyclic dienes. The use of silyl dienol ethers has resulted in new routes to enantiomerically pure cyclohexanones in a highly regioselective manner.