On two methods of determining the ellipses and ellipsoids of positioning accuracy of robot manipulators

Summary When analysing the problem of the positioning accuracy of robot manipulators it is important to know how far random deviations of the hand may be from the desired position if the joint positioning errors possess a normal distribution. Two methods of determining the ellipses and ellipsoids of probability concentration are compared. The first of them is based on the standard procedure of the probability calculus. The second approximate method consists in finding at first the polygon or polyhedron of the positioning accuracy, and then in finding the ellipse or ellipsoid with principal axes and second order moments coinciding with those of the polygon or polyhedron, respectively. Examples of application demonstrate that these two methods give very close results.

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Zwei Methoden zur Bestimmung der Ellipsen und Ellipsoide der Positioniergenauigkeit von Handhabungsrobotern

Übersicht Bei der Untersuchung der Positioniergenauigkeit von Handhabungsrobotern ist es wichtig, die Größe zufälliger Abweichungen des Greifers von der erstrebten Position zu kennen, wenn die Lagefehler der Verbindungen eine Normalverteilung besitzen. Es werden zwei Methoden zur Bestimmung der Ellipsen bzw. Ellipsoide der Wahrscheinlichkeitsdichte verglichen. Die erste beruht auf dem Standardverfahren der Wahrscheinlichkeitsrechnung. Die zweite Näherungsmethode besteht darin, daß zunächst das Polygon bzw. Polyeder der Positioniergenauigkeit bestimmt wird und danach die Ellipse bzw. das Ellipsoid mit den Hauptachsen und Momenten zweiter Ordnung wie das Polygon oder Polyeder. Beispiele zeigen, daß beide Methoden zu sehr ähnlichen Ergebnissen führen.

     

Flotation—spectrophotometric determination of osmium with thiocyanate and methylene blue

A sensitive flotation—spectrophotometric method, based on the ion associate formed by the anionic thiocyanate complex of osmium with the basic dye methylene blue (MB) is described. The ion associate precipitates when the aqueous solution is shaken with toluene, and the separated and washed compound is dissolved in acetone. The molar absorptivity is 2.2 × 10⁵ l mol^-1 cm^-1 at 655 nm. Beer's law is obeyed. The molar ratio of Os:SCN:MB in the separated and washed ion associate is 1:6:3. Ruthenium reacts similarly. The method is applied to the determination of traces of osmium in crucible platinum after separation of osmium by distillation as tetroxide.     

Organic synthesis by means of noble metal complexes—XCIV : Palladium catalyzed hydrosilylation of monoenes and conjugated dienes

Palladium compounds and metallic palladium combined with phosphine are active catalysts of selective hydrosilylation of terminal olefins. Butadiene and trichlorosilane give a 1:1 adduct and trimethylsilane affords a 1:2 adduct. Special features of the palladium catalyzed hydrosilylation reactions are presented.     

Untersuchung der Absorption der bei der Verbrennung phosphororganischer Verbindungen entstehenden P-Oxide mittels32P-markierter Verbindungen

Zusammenfassung Bei der Pyrolyse phosphor-organischer Verbindungen in Sauerstoffatmosphäre bilden sich P-Oxide, die die C,H-Bestimmung stören. Deren Verhalten im Verbrennungsrohr und ihre Absorption an geeigneten Kontakten wurden untersucht. Durch den Einsatz³²P- markierter Ausgangsverbindungen und Aktivitätsmessung des³²P sowohl durch die Wandung des Verbrennungsrohres als auch im zerkleinerten Füllungsmaterial war die laufende Bestimmung der durch die Kontaktschicht absorbierten Phosphormenge möglich. 30 verschiedene Absorptionsmittel wurden geprüft. Der Einfluß der Strömungsgeschwindigkeit des Trägergases, der Temperatur der Kontaktschicht, der Art der Verbrennung sowie der Anordnung des Verbrennungsrohres wurde untersucht. Die Absorptionsleistung der Kontakte ist stark von der Gasgeschwindigkeit abhängig.

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Investigation of absorption of the phosphorus oxides arising in the combustion of organophosphorus compounds by means of³²P-labelled substances

Summary In the pyrolysis of organophosphorus compounds in an oxygen atmosphere P oxides are formed which interfere with determination of carbon and hydrogen. Their behaviour in the combustion tube and their absorption on suitable contacts were investigated. By the use of³²P-labelled starting compounds and measuring the activity of³²P both through the wall of the combustion tube and in the comminuted filling material, continuous determination of the amount of phosphorus absorbed through the contact layer was possible. Thirty different absorption media were tested. The influence of the flow rate of the carrier gas, the temperature of the contact layer, the nature of combustion as well as the arrangement of the combustion tube was examined. The absorption efficiency of the contacts is highly dependent on the speed of the gas.

     

Über einige neue Bispirane

We have obtained four new bispirane systems in which both spiroatoms are vicinal atoms in cyclopropane or cyclobutane rings and in which the heterocyclic component has the basic structure of 1,4-dioxep-2-ene. We have shown that from two possibilities (bispiran, propellan) the general reaction leads only to a bispiran system. To the bispiran2 exhibiting the highest hyperchromism we ascribed the bispirocoplanar conformation (Fig. 1).

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Mit 3 Abbildungen     

Radiation reduction of Cr, Mo and W isopolymetalates in aqueous system

The radiation-chemical processes in aqueous solutions of dichromates, isopolymolybdates and isopolytungstates have been studied. The radiation reduction of Cr(VI) to Cr(III), Mo(VI) to Mo(V) and W(VI) to W(V) takes place. Molybdenum and tungsten blues are the products of the last two processes in acid solutions. The yields of reduction decrease significantly with the increase of pH. The mechanisms of the processes have been discussed. The photochemical reduction of Mo(VI) and W(VI) for the production of corresponding 5-valent states have been used to the study of their electron scavenging efficiencies. It has been shown that these efficiencies decrease in the order: Mo(V)>W(V)>Cr(VI)>Mo(VI)>W(VI).     

Separation of four platinum metals by anion-exchange in hydrobromic acid medium

Distribution coefficients of Pt, Ir, Pd and Rh in the systems Dowex 1 [Br^?]?HBr plus 0.0035M bromine and Dowex 1 [Br^?]?HBr plus 2% N₂H₄·HCl, were determined with the aid of radioactive tracers by batch equilibration for the resins of nominal cross-linking 2, 4 and 8, respectively. Column experiments showed that Dowex 1X4 should be used for separations because of the favourable dynamics of the column process. Elution conditions for the quantitative separation of both trace and milligram amounts of Ir?Pt, Rh?Pt, Pd?Pt and Ir?Pd?Pt mixtures are given. Some data on the effect of temperature upon the quality of separation are also presented.     

Investigation of arsenic speciation in oyster test reference material by multidimensional HPLC-ICP-MS and electrospray tandem mass spectrometry (ES-MS-MS)

Multidimensional (size-exclusion-anion-exchange-cation-exchange) liquid chromatography with ICP-MS detection was developed to produce a map of water-soluble species in an oyster test reference material. The presence of arsenobetaine, trimethyl(2-carboxyethyl)arsonium inner salt, arsenocholine, dimethylarsonic acid, tetramethylammonium ion, As(v) and two arsenosugars was demonstrated by ES-MS-MS. A previously unreported compound was isolated and identified by ES-MS-MS as 5-dimethylarsinoyl-beta-ribofuranose. Anion-exchange chromatography was optimized to produce a chromatographically pure peak of arsenobetaine (accounting for ca. 64% of all water-soluble As present) that was used to quantify this compound.     

1,4-dioxane as a solvent in spectroscopy and photochemistry

Commercially available 1,4-dioxane, even of spectroscopic grade, contains various impurities that arise mostly from reaction of the solvent with oxygen. Aspects relevant to the spectroscopy and photochemistry of the dioxane/oxygen system are discussed. Methods of purification and storage of the solvent are presented.     

Generation and reactions of substituted phenide anions in an electrospray triple quadrupole mass spectrometer

Substituted benzoic acid anions undergo decarboxylation in the medium-pressure region of an electrospray ion source yielding in most cases the correspondingly substituted phenide anions in high yield. The location of the anionic center is specified by the position of the carboxylic group. The only exceptions are compounds with substituents containing acidic hydrogen atoms, like OH and NH(2) groups. For such compounds, either an intra- or an intermolecular (mediated by the molecules of methanol or water) proton transfer from the more acidic position to the benzene ring is observed. The generated anions can be selected using the first quadrupole for studying their ion-molecule chemistry in the second quadrupole of a triple quadrupole mass spectrometer. Their reactions with CO(2), O(2), CH(3)COCH(3) and CCl(4) may serve as typical examples. The general applicability of this method for the generation of phenide anions has been confirmed on three different mass spectrometers. Experiments performed using carboxylic acids other then benzoic acid and its derivatives show that this method is not limited to phenide anions and can be used for the generation of a much wider range of carbanions in the gas phase.