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  • 1
    ISSN: 1520-6882
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Analytical chemistry 67 (1995), S. 557-560 
    ISSN: 1520-6882
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature genetics 12 (1996), S. 85-87 
    ISSN: 1546-1718
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Medicine
    Notes: [Auszug] Six cysts from four Gorlin syndrome patients and 14 sporadic cysts were analysed for seven polymorphisms spanning chromosome 9 (Table 1). The integrity and quantity of DNA were inadequate for restriction fragment length polymorphism (RFLP) typing by Southern blotting, and all typing was done with ...
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Child's nervous system 11 (1995), S. 265-268 
    ISSN: 1433-0350
    Keywords: Skull fracture ; Growing fracture ; Leptomeningeal cyst ; Enlarging fracture
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Large skull fractures are conventionally followed radiographically until healing occurs. Fractures which enlarge or remain unhealed are commonly termed “leptomeningeal cysts” or “growing skull fractures”. This study of ten children with this injury and a review of the literature shows that a true leptomeningeal cyst is seldom present and that skull fractures do not “grow”. Moreover, careful history-taking and physical examination will correctly identify all enlarging or unhealed skull fractures of childhood without the need for plain radiographs or computed tomography of the skull.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Electroanalysis 8 (1996), S. 726-731 
    ISSN: 1040-0397
    Keywords: Ethylamine ; Gold ; Voltammetry ; Adsorption ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Linear scan (cyclic) voltammetry at the disk with simultaneous pulsed electrochemical detection (PED) at the ring of a rotated ring-disk electrode (RRDE) is demonstrated to be applicable for studies of the complex anodic behavior of ethylamine at gold electrodes in 0.10 M NaOH. The oxidation of ethylamine at the disk occurs during positive scans concomitantly with formation of surface oxide (Au → AuOH → AuO). However, the final oxide-covered surface (AuO) is inert for further ethylamine oxidation. Data obtained at the RRDE demonstrate that the total ethylamine signal at the disk is composed of simultaneous contributions from: oxidative desorption of ethylamine preadsorbed at the oxide-free Au surface and oxidation of ethylamine transported to the disk simultaneously with oxide formation. Based on ring-disk data, preadsorbed ethylamine is estimated to correspond to a fractional surface coverage of 0.7 ± 0.1 monolayer for 10 to 60 μM ethylamine. Of this coverage, ca. 75% corresponds to ethylamine coadsorbed reversibly with OH- and 25% to ethylamine adsorbed irreversibly by a mechanism concluded to be chemisorption.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Electroanalysis 9 (1997), S. 279-283 
    ISSN: 1040-0397
    Keywords: Chemical oxygen demand ; Coulometry ; Chromium ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The chemical oxygen demand (COD) of solutions containing various organic compounds is calculated from the net faradaic charge (Qnet) estimated for the total electrolytic oxidation of CrIII generated during oxidative degradation of the organic compounds in acidic media containing excess CrVI. Values of Qnet for conversion of CrIII to CrVI are estimated from the linearized chronoamperometric data plotted as In {itat, t} vs. t. This procedure is preferred over determinations of Qnet from the total integrals of itot over the entire electrolysis period because of large errors that can result from uncertainty in the background current (ibkg) for t → ∞. The proposed coulometric procedure offers the benefit that reagent solutions can be reused, thereby minimizing the need for disposal of wastes containing toxic CrVI. This procedure was applied in a single digest solution for consecutive determinations of COD. Average COD values for potassium acid phthalate and glucose were 103.8% (s - 6.0, N - 10) and 100.2% (s - 4.2, N - 11), respectively, based on the theoretical degradation to CO2. In comparison for these same samples, an EPA approved method, based on colorimetric determination of CrIII, gave COD values of 101.4% (S - 1.4, N - 5) and 100.1% (s - 1.4, N - 5) of the theoretical. Statistical tests indicate no significant difference in the COD values determined for these compounds using the coulometric and EPA methods.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0268-2575
    Keywords: Chemical warfare agents ; Chemical Weapons Convention ; Iraq ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Nineteen samples from the United Nations Special Commission 65 on Iraq (UNSCOM 65) were analyzed for chemical warfare (CW) related compounds using a variety of spectroscopic and chromatographic techniques including multinuclear NMR, GC (phosphorus, sulfur and atomic emission detection), GC/MS (electron impact and chemical ionization), tandem MS, HPLC/ion chromatography, HPLC/thermospray/MS, FTIR, ICP and GFAA. The samples consisted of one piece of cloth, one piece of wood, six waters, six soils, two vegetation samples and two mortar shell crosscut sections. No intact CW agents were detected; however, diethyl phosphoric acid was unambiguously identified in three of the water samples and ethyl phosphoric acid was tentatively identified, at lower levels, in one of the water samples. Diethyl phosphoric acid and ethyl phosphoric acid are degradation products of munitions-grade Tabun (GA), an organophosphorus nerve agent. However, these compounds are also degradation products of the Chemical Weapons Convention (CWC) scheduled compound Amiton as well as many commercially available pesticides.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 475-478 
    ISSN: 0268-2605
    Keywords: organomercurials ; symmetrization ; column chromatography ; organomercury halides ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The symmetrization reaction of organomercury(II) chlorides (RHgCl) to R2Hg and HgCl2 in toluene solution under identical conditions using a basic alumina column has been studied­in order to compare the effect of the nature of the R groups on the extent of symmetrization. The efficiency of symmetrization depends markedly on the electron-withdrawing nature of­R, varying from 90-94% for R = trichlorovinyl or phenyl to 11% for R = 2,6-dimethylphenyl.© 1998 John Wiley & Sons, Ltd.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1040-0397
    Keywords: Capillary electrophoresis ; Pulsed electrochemical detection ; Alditols ; Carbohydrates ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Results are presented from a systematic study of the noise (N) and peak-to-noise ratio (P/N) obtained for pulsed electrochemical detection (PED) at a gold micro-wire electrode applied to a mixture of alditols and monosaccharides separated by capillary electrophoresis (CE). The electrode potentials and time periods for oxidative cleaning and reductive reactivation of the electrode were held constant in the PED waveform at minimum allowable values and the time period for digital integration of electrode current (tint) was varied from 50 to 800 ms by 50-ms intervals. The value of N was virtually independent of tint and P/N increased approximately as a linear function of tint in the range 50-200 ms corresponding to waveform frequencies in the range 4.5-2.7 Hz. A detection limit of 9 fmol glucose was determined for a 4-nL injection using tint = 200 ms.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Electroanalysis 9 (1997), S. 1397-1402 
    ISSN: 1040-0397
    Keywords: Pulsed amperometric detection ; Cysteine ; Platinum electrode ; Sulfhydryl compounds ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Anodic voltammetric detection of sulfhydryl compounds, represented here by cysteine, at Pt electrodes in acidic media occurs concomitantly with anodic generation of surface oxide. It is speculated that the adsorbed hydroxyl species (PtOH), proposed to be the intermediate product in formation of the inert oxide (PtO), is the source of O-atoms transferred to the sulfonic acid produced by oxidation of the sulfhydryl moiety. However, as a consequence of this electrocatalytic response mechanism, application of the traditional three-step waveform for pulsed amperometric detection (PAD) of sulfhydryl compounds is accompanied by a large background signal resulting from PtO formation. To diminish the background signal, the traditional three-step PAD waveform has been modified by insertion of a brief (100 ms) anodization step prior to the detection step to activate the Ptsurface by the generation of PtOH with minimal conversion to PtO. The subsequent negative step from the activation potential (Eact) to the detection detection potential (Edet 〈 Eact) permits the PtOH to be harvested within the detection mechanism without significant background signal.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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