Structural analysis of synthetic homo- and copolyesters by electrospray ionization on a fourier transform ion cyclotron resonance mass spectrometer

The molecular structure of a series of homo- and copolyesters was studied using sustained off-resonance irradiation collisionally activation dissociation on a Fourier transform ion cyclotron resonance mass spectrometer. Electrospray ionization was used as an ionization technique. The most important fragmentation pathways of the homopolyesters poly(dipropoxylated bisphenol-A/adipic acid) and poly(dipropoxylated bisphenol-A/isophthalic acid) were studied. Six different dissociation mechanisms were observed which are very similar to the mechanisms found to occur during pyrolysis of these compounds. Four of these mechanisms are a result of cleavages of the ester bond and the others are due to cleavages of the ether bond or bisphenol-A unit. Some of the fragments expected are not present in the spectrum, indicating that each fragment has a specific sodium affinity. Sequence-specific fragments of two of the three copolyester sequences that theoretically can exist were experimentally observed. Fragments that originate from the third sequence are not unique and can also be formed from other sequences. Therefore, it was not possible to determine the presence of the third sequence. Copyright 2000 John Wiley & Sons, Ltd.     

Chromatographische trennung von metallionen durch elution mit ammoniumsulfat: Bestimmung von magnesium,calcium und strontium in salzreichen wässern

The chromatographic separation of Mg, Ca, Sr, Ba, Fe(II, III) and Mn(II) by elution with ammonium sulphate solution from Dowex 50–X₁₀ was studied. The optimum conditions for the separation of the alkaline earths from each other were established. The method was applied for the separation of Mg, Ca and Sr in salt waters; Mg and Ca were determined by EDTA titration and Sr spectrographically, the coefficient of variation being 1.9% for Mg and 1.4% for Ca.     

Hydrophobization of glass surface by adsorption of poly(dimethylsiloxane)

Silica or glass particles are introduced in a poly(dimethylsiloxane) (PDMS) matrix for various applications. A particular feature of these systems is that PDMS adsorbs on the surface of the dispersed particles, thus rendering them more hydrophobic with time. The mechanism of this process of in situ hydrophobization is still poorly understood. The major aims of the present study are (1) to quantify the rate of surface hydrophobization by PDMS and, on this basis, to discuss the mechanism of the process; (2) to compare the contact angles of surfaces that are hydrophobized by different procedures and are placed in contact with different fluid interfaces-PDMS-water, hexadecane-water, and air-water; and (3) to check how the type of surfactant affects the contact angles, viz., the effective hydrophobicity of the surface. We present experimental results for the kinetics of hydrophobization of glass surfaces, which are characterized by measuring the three-phase contact angle of glass-surfactant solution-PDMS. The data reveal two consecutive stages in the hydrophobization process: The first stage is relatively fast and the contact angle increases from 0 degrees to about 90 degrees within several minutes. This stage is explained with the physical adsorption of the PDMS chains, as a result of hydrogen-bond formation with the surface silanol groups. The second stage is much slower and hours or days are required at room temperature to reach the final contact angle (typically, 150-160 degrees). This stage is explained as grafting of the PDMS molecules on the surface by chemical reaction with the surface silanol groups. If the glass surface had been pretreated by hexamethyldisilazane (HMDS), so that CH(3) groups had blocked most of the surface silanol groups, the first stage in the hydrophobization process is almost missing-the contact angle slowly changes at room temperature from about 90 degrees up to 120 degrees. The experiments aimed to compare several hydrophobization procedures showed that PDMS ensures larger contact angle (more hydrophobic surface) than grafted alkyl chains. The contact angles at the PDMS-water and hexadecane-water interfaces were found to be very similar to each other, and much larger than that at the air-water interface. Interestingly, we found that the ionic surfactants practically do not affect the contact angle of PDMS-hydrophobized surface, whereas the nonionic surfactants reduce this angle. Similar trends are expected with silica surfaces, as well.     

Implementation of NLO QCD corrections into the framework of computer system SANC

The QCD sector of the system SANC is presented. The QCD theoretical predictions for several processes of high-energy interactions of fundamental particles at the one-loop precision level for up to some 3- and 4-particle processes are implemented. The text was submitted by the authors in English.     

Chromatographische trennung von calcium und strontium durch elution mit ammoniumsulfatlösung

A method is described for the chromatographic separation of calcium and strontium adsorbed on a cation-exchange resin, by means of elution with ammonium sulphate solution. The method is suitable for Ca : Sr ratios ? 1. The separated elements can be determined directly in the eluate.