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  • 1
    Digitale Medien
    Digitale Medien
    Springer
    International archives of occupational and environmental health 19 (1962), S. 263-269 
    ISSN: 1432-1246
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary Human experiments were performed on six volunteers, who had never experienced CS2 absorption, with different concentrations of carbon disulfide (CS2) from 28 ppm to 52 ppm which were inhaled for 30 to 120 minutes continuously, and CS2 concentration was kept at a constant level during the period of each experiment. Amounts of CS2 retained in the body and eliminated from it by the expired air, the skin, and the urine were calculated. During the period of each inhalation experiment, the volunteers were free from any signs, except a slight headache. The results are summarized as follows: 1. The percentage of CS2 concentration in the expired air to that in the inspired rises gradually for the first 40 minutes and reaches an equilibrium at 65 ± 10 per cent. 2. When the inhalation of CS2 is discontinued, CS2 level in the expired air rapidly goes down in fresh air, and the average percentage of CS2 concentration in the expired air to that in the air which has been inhaled is 18 ± 5, 8 ± 2 and 4 ± 2 per cent at the interval of every 10 minutes. The decrease presents the geometrical series. 3. The amount of CS2 absorbed during the inhalation is calculated to be from 15.4 mg to 29.6 mg (average 23.0 mg), of which 1.74 mg to 7.58 mg (average 4.82 mg) is eliminated by the expired air, while the amount of CS2 excreted in the urine is from 7.2 γ to 37.3 γ (average 16.5 γ). 4. CS2 is proved to be eliminated through the skin in the amount of 36.2 γ to 77.8 γ. This is about three times as much as that eliminated by the urine, and it is about 1% of the amount eliminated by the respiratory tract. 5. The balance sheet of CS2 in the body is prepared and described, taking into account the absorption, on the one hand, and the elimination, on the other, of gaseous CS2 through the respiratory tract, the skin, and the urine.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 24 (1986), S. 1227-1237 
    ISSN: 0887-624X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Photocrosslinkable polymers containing pendant chalcone groups were prepared by the reaction of 4′-substituted-4-carboxychalcone (4-R-CC) with poly(vinyl alcohol) (PVA) in homogeneous dimethylacetamide (DMA) solutions using 2,4,6-trinitrochlorobenzene (TNCB) as condensing agents. The mechanism of ester formation is mainly discussed for 4-carboxychalcones on the basis of the isolated intermediates and mass spectrometry. The modified polymers showed excellent properties as photocrosslinkable polymers and the photosensitivity was confirmed in the range of about 1 to 5 mJ/cm2.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Philadelphia : Wiley-Blackwell
    Journal of Cellular and Comparative Physiology 3 (1933), S. 419-424 
    ISSN: 0095-9898
    Schlagwort(e): Life and Medical Sciences ; Cell & Developmental Biology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie , Medizin
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 4
    ISSN: 0170-2041
    Schlagwort(e): Asymmetric epoxidation ; 2,4-Dodecadien-7-one, 4,6,10-trimethyl- ; Maritime pine scale ; Matsucoccus feytaudi ; Pheromones ; Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: (2E,4E,6R,10S)-4,6,10-Trimethyl-2,4-dodecadien-7-one (1) - the major component of the sex pheromone of the maritime pine scale - and its three stereoisomers were synthesized by starting from (R)- or (S)-citronellol (4) and employing the asymmetric epoxidation (9 → 10) and the palladium-catalyzed reductive cleavage of the epoxy ring (13 → 14) as the key steps.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 5
    ISSN: 0170-2041
    Schlagwort(e): Asymmetric epoxidation ; Matsuone ; Pheromones ; Pine bast scales ; 2,4-Tridecadien-7-one derivatives ; Epoxidation, asymmetric ; Matsucoccus sp. ; Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: (2E,4E,6R,10R)-4,6,10,12-Tetramethyl-2,4-tridecadien-7-one (1; matsuone) - the primary component of the sex pheromone of the red pine scale (Matsucoccus resinosae) and two other pine scales - and its antipode were synthesized by starting from (R)- or (S)-citronellol (3) and employing the asymmetric epoxidation (11 → 12) and the palladium-catalyzed reductive cleavage of the epoxy ring (15 → 16) as the key steps.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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