Evidences of phase separation in moisture‐cured poly(urethane urea)s by means of temperature modulated differential scanning calorimetry

The degree of phase separation in several moisture‐cured poly(urethane urea)s (PUUs) was studied by FTIR spectroscopy, wide angle X‐ray diffraction (WAXD), and temperature‐modulated differential scanning calorimetry (TMDSC). This latter technique was shown to be particularly useful in analysing the degree of phase separation in PUU polymers. Both phase mixing and phase segregation coexisted in the PUUs and the degree of phase separation increased as the urea hard segment (HS) content in the PUU increased. The maximum solubility of urea HSs into the polyol soft segments (SSs) was achieved for 50 wt % urea HS content in diol‐based PUUs, whereas for triol‐based PUUs the highest solubility between HS and SS was reached for lower urea HS amount. Finally, the higher the urea HS content the higher the extent of phase separation in the PUU. © 2007 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 45: 3034–3045, 2007     

Mechanisms of n‐butanol formation in butyl acrylate latexes

The mechanisms involved in the formation of n‐butanol during the synthesis of butyl acrylate containing latices were investigated. The experimental results showed that neither the hydrolysis of butyl acrylate nor of the ester bond in the butyl acrylate segments of the polymer played a major role in the formation of n‐butanol, which was mainly generated from the polymer backbone, by transfer reactions to polymer chain followed by cyclization. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 5838–5846, 2007     

Diblock copolymers based on allyl methacrylate: Synthesis,characterization, and chemical modification

Different diblock copolymers constituted by one segment of a monomer supporting a reactive functional group, like allyl methacrylate (AMA), were synthesized by atom transfer radical polymerization (ATRP). Bromo‐terminated polymers, like polystyrene (PS), poly(methyl methacrylate) (PMMA), and poly(butyl acrylate) (PBA) were employed as macroinitiators to form the other blocks. Copolymerizations were carried out using copper chloride with N,N,N′,N″,N″‐pentamethyldiethylenetriamine (PMDETA) as the catalyst system in benzonitrile solution at 70 °C. At the early stage, the ATRP copolymerizations yielded well‐defined linear block copolymers. However, with the polymerization progress a change in the macromolecular architecture takes place due to the secondary reactions caused by the allylic groups, passing to a branched and/or star‐shaped structure until finally yielding gel at monomer conversion around 40% or higher. The block copolymers were characterized by means of size exclusion chromatography (SEC), ¹H NMR spectroscopy, and differential scanning calorimetry (DSC). In addition, one of these copolymers, specifically P(BA‐b‐AMA), was satisfactorily modified through osmylation reaction to obtain the subsequent amphiphilic diblock copolymer of P(BA‐b‐DHPMA), where DHPMA is 2,3‐dihydroxypropyl methacrylate; demonstrating the feasibility of side‐chain modification of the functional obtained copolymers. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 3538–3549, 2007     

Determination of gallium by anodic stripping square-wave voltammetry Detection of a GaZn intermetallic compound and its destruction by Sb in an NaSCNNaClO(4) supporting electrolyte

Reproducibility for successive determinations with a hanging mercury drop electrode is assessed in relation to solution stirring, drop size and back-diffusion to the mercury thread. The effect of experimental parameters such as drop size, deposition time and gallium concentration on the observed stripping current is investigated. The interference of zinc present in a 0.5M NaSCN + 4.2M NaClO(4) supporting electrolyte on the gallium detection limit and calibration plots is described. Formation of an intermetallic compound with a Zn:Ga ratio of 2:3 and its destruction by co-deposition of zinc with Sb are reported. A detection limit of 10(-8)M gallium was obtained in the presence of 10(-5)M Sb(III).     

Rapid determination of aliphatic amines in water samples by pressure-assisted monolithic octadecylsilica capillary electrochromatography-mass spectrometry

A pressure-assisted capillary chromatography-mass spectrometry method based on the use of a monolithic octadecylsilica (ODS) capillary is proposed for the determination of aliphatic amines. A 25 mM citric acid buffer containing 10% methanol is used as running electrolyte. Separation is achieved by simultaneously applying a capillary electrophoresis (CE) voltage of 13 kV and an overimposed pressure of 8 bar. The use of pressure is required to ensure stable electrospray conditions. Analysis times are reduced by using a capillary column consisting of a 30 cm long monolithic silica capillary column bound with ODS and a fused-silica capillary column also 30 cm long. The proposed method was successfully applied to the determination of low-molecular-weight aliphatic amines in tap and river water. The analysis of real samples requires cleanup and preconcentration, which can be performed automatically by inserting a minicolumn in the replenishment system of the commercial instrument.     

Le problème de la réduction des intégrales électroniques dans la méthode L.C.A.O. améliorée

Résumé L'auteur reprend les principes de la méthode L.C.A.O. améliorée en vue d'une justification plus complète des procédés employés. La théorie des perturbations permet d'une façon simple de tenir compte de la corrélation entre les électrons grâce à l'introduction d'une fonction universelle de la distance entre deux électrons. Le problème est ainsi ramené de l'échelle moléculaire à l'échelle atomique. On montre que la corrélation entre les électrons entraîne la réduction des intégrales atomiques. Le problème de la réduction des intégrales coulombiennes est traité en détail. La possibilité de négliger les autres intégrales biélectroniques est ensuite examiné. Enfin est étudié le problème de la réduction des intégrales de coeur.

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The principles of the improved LCAO theory are investigated to give a better justification for its methods. Perturbation theory allows a simple account for electronic correlation, when a universal function of interelectronic distance is introduced. The problem is hereby reduced from molecular to atomic scale. The reduction of electronic energy integrals by correlation is shown, especially for Coulomb integrals. The possibility of neglecting the other bielectronic integrals is examined. Finally the problem of core integral reduction is studied.

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Zusammenfassung Die Grundlagen der verbesserten LCAO-Methode werden untersucht, um dieses Verfahren besser zu rechtfertigen. Mit einer allgemeinen Funktion des Abstandes je zweier Elektronen und der Störungstheorie läßt sich die Elektronenkorrelation auf einfache Weise berücksichtigen. Damit wird das Problem vom molekularen auf den atomaren Maßstab zurückgeführt. Die Elektronenkorrelation bringt eine Reduktion der Elektronenenergieintegrale mit sich; die Coulombintegrale werden im einzelnen behandelt. Anschließend wird die Möglichkeit untersucht, die übrigen Zweielektronenintegrale zu vernachlässigen. Schließlich wird die Reduktion der Rumpfintegrale behandelt.

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Nous tenons à remercier très vivement le Docteur Chr. K. Jørgensen (Cyanamid European Research Institut, Genève) pour les intéressants échanges de vue que nous avons eu sur les divers problèmes évoqués dans cet article ainsi que le Docteur G. Berthier (Institut de Biochimie théorique, Paris) et Monsieur H. v. Hirschhausen.     

Complexation of Ni (II) and Zn(II) ions by 3-(1-naphthyI)-2-mercaptopropenoic acid

The complexation equilibria between Ni(II) and Zn(II) metal ions with 3-(1-naphthyl)-2-mercaptopropenoic acid (H₂NMP) were studied by glass electrode potentiometry, at 25 °C and 1.0 mol·dm^–3 in NaClO₄ as constant ionic medium in 50% (v/v) water-ethanol solutions. Formation constants for the complexes Ni(NMP), Ni(NMP) ₂ ^2– , Zn(NMP) and Zn(NMP) ₂ ^2– , refined by the MINIGLASS program, are reported.     

DNase activity ofMicrococcal endonuclease insolubilized on corn cob

The endonuclease from S. aureus has been immobilized on ground maize cob, previously activated with tosyl chloride. Pretreatment of the support on acid before tosylation yielded the best insoluble enzyme derivatives. The catalytic activity has been evaluated as percent of total hydrolysis attained in a batch reactor using DNA as a model substrate. The derivatives prepared are very resistant to high temperatures under conditions of catalysis (24 h at 45 degrees C). For these long reaction times, the extent of hydrolysis in the presence of small amounts of organic solvent (dimethyl sulfoxide at 2 percent) is larger than in plain buffer (Tris). This type of derivative could be very useful for the removal of nucleic acids from single-cell protein concentrates.     

Study of the ternary system FeCrTe around the composition FeCr2Te4

The system FeCrTe was investigated around the composition FeCr₂Te₄. FeCr₂Te₄ is a metastable compound. Single crystals with Fe_0·93Cr_1·76Te₄ composition were grown by vapor transport or the Bridgman method. These crystals are metallic and anisotropic ferromagnets.