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  • 11
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 11 (1984), S. 1-3 
    ISSN: 0306-042X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A simple, high throughput method of analysis of trimethylamine in body fluids has been developed to assist with the management of patients with the inherited metabolic disorder, trimethylaminuria. The headspace in sealed vials was analysed using perdeuterated (2H10)trimethylamine hydrochloride as an internal standard. The gas chromatograph inlet system of the mass spectrometer was adapted to suit this method of analysis. Medium resolving power was used to measure the ion ratio of the [M-H]+ ion of trimethylamine and the [M-2H]+ ion of the internal standard. The method is faster and more accurate than gas chromatographic methods. The concentrations of trimethylamine found in normal urine are similar to those reported previously.
    Additional Material: 1 Ill.
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  • 12
    Electronic Resource
    Electronic Resource
    Brookfield, Conn. : Wiley-Blackwell
    Polymer Composites 5 (1984), S. 11-17 
    ISSN: 0272-8397
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: The interaction of very dilute solutions of a cationic vinylbenzyl silane (CVBS), a methacrylate functional silane (γ-MPS), and an isopropyl-tri-(dioctylpyrophosphato) titanate (IDT) with a mica surface has been studied by carbon analysis. For all three coupling agents the dependence of adsorption with time of treatment follows a step-like curve, where each step corresponds to a monolayer coverage on the mica. Under the operating conditions used it was noted that a particular monolayer is always completed before the next is started. The adsorption of γ-MPS was found to be very sensitive to the time allowed for hydrolysis of the silane, while the adsorption of CVBS was relatively independent of the hydrolysis time when it is varied from 0 to 5400 s. The results indicate that γ-MPS and CVBS near the mica surface form a dense structurally regular multilayer phase with the silane molecules oriented normal to the surface. IDT molecules occupy a surface area on mica which is characteristic of their branched nature.
    Additional Material: 8 Ill.
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  • 13
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Sequential moving boundary electrophoresis with protons and hydroxyl ions as the sole counterions, consisting solely of six acids (system A) and of six bases (system B), gives rise to natural steady-state pH gradients similar to those predicted by theory (pH 2.4-5.5 for system A, pH 10.3-12.2 for system B). Mixtures of the constituents in system A and system B gave rise to a natural pH gradient spanning the pH range between the terminal electrolytes (pH 2.4 and 12.2) predicted for systems A and B. The predicted boundary displacement is negligibly small. Experimentally the boundary displacement could not be determined in view of the difficulty of separating it from the initial transient state in which the pH gradient is formed, and a final state in which the pH gradient decays.
    Additional Material: 6 Ill.
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  • 14
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Electrophoresis 4 (1983), S. 404-407 
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Poly R-480, an amphoteric dye of molecular weight 160 000,is the product of copolymerization reaction and can be expected to yield a polydisperse pattern in polyacrylamide gel isoelectric focusing (PAGIF). Such is indeed obtained in conventional PAGIF using commercial synthetic carrier ampholyte mixtures but not in buffer PAGIF, in which a few discrete dye bands are produced. Upon excision of single bands and segments of zones in buffer PAGIF and PAGIF in SCAMs, respectively, the entire original pattern is reestablished in each case, thereby confirming the artifactual nature of both the simple band pattern as well as the polydisperse patten. The simple pattern in buffer PAGIF prevails in the presence of 8 M urea and 8 mM CHAPS, while the polydisperse pattern obtained in SCAMs is resolved into multiple bands in the presence of either one or both of these agents. These observations suggest: a) hydrophobic and hydrogen bond dye-dye and/or dye-SCAM interactions produce the artifactual polydisperse pattern in PAGIF in SCAMs, b) electrostatic dye-dye interactions are responsible for the artifactual simple band pattern in buffer EF, and c) dye-SCAM electrostatic interactions produce the artifactual multiple band pattern in the SCAM-urea-CHAPS system. These data clearly underline the need for critical experimentation in the evaluation of PAGIF bands and band numbers.
    Additional Material: 6 Ill.
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  • 15
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Fire and Materials 6 (1982), S. 135-144 
    ISSN: 0308-0501
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Architecture, Civil Engineering, Surveying , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: A mathematical Model for estimating the time available for safe egress from a fire is formulated. The model simulates the conditions which develop during the course of an enclosure fire. Since life safety considerations are primary, the simulation model which is adopted focuses attention only on phenomena which develop between the times of fire ignition and onset of hazardous conditions. This allows significant simplifications in modeling which may not be otherwise justified. Using computed variables of a simulated fire scenario of interest, times of fire detection and onset of hazard which are deduced from realistic detection and hazard criteria would be estimated. The Available Safe Egress Time (ASET) would be defined as the length of the time interval which separates these two events. Quantitative specifications for a variety of detection and hazard criteria are identified. Results of exercising the model are presented, and ASET estimates are obtained for a wide variety of realistic fire scenarios. A comparison between experimental results of a multi-room fire test and prediction of the single-room model suggest that the model has potential utility in providing practical simulations of multi-room fire environments.
    Additional Material: 8 Ill.
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  • 16
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: n-Octadecyl benzoate, taken as a model for long-chain n-alkyl carboxylates generally, loses C14H28 under electron impact to yield a product with the same elemental composition as the butyl benzoate molecular ion. This product retains quantitatively one hydrogen from C-6, and seems to be formed as an oxygen-protonated 4-benzoyloxybutyl radical. It reacts further to lose H2O, in which deuterium labeling demostrates that the second hydrogen atom comes predominantly from C-4. The intermediate reorganization, for which the driving force is presumably furnished by the instability associated with a primary radical, is pictured in terms of cyclization via bonding between the C-4 radical site and the benzoyl carbon concerted with hydrogen migration via a 4-membered quasicyclic transition state.
    Additional Material: 3 Tab.
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  • 17
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 22 (1984), S. 86-89 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 13C NMR spectra of four ortho- and seven para-quinone methides were assigned using chemical shift and long-range carbon-proton coupling information. The carbonyl shifts are compared with those in ortho- and para-benzoquinones. The chemical shifts of the carbonyls of the p-quinone methides are observed at δ 186.2-186.4 for the three ortho-di-tert-butyl-substituted compounds and at δ 180.7-181.5 for the four ortho-oxy-substituted compounds. In the three o-quinone methides with meta, para-dioxy substituents, the carbonyl signals are at δ 184.2-185.4. The carbonyl signal of the one o-quinone methide with no oxygen substitution is shifted downfield to δ 200.9, apparently as a result of hydrogen bonding to the nearby hydroxyl.
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  • 18
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 22 (1984), S. 561-564 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 13C NMR spectra of new hetero-substituted tetraphenylporphyrin (TPP) molecules have been studied. It was found that most of the carbon chemical shifts are similar to those found in TPP. The similar chemical shifts of the different β-carbons in S2TPP and in Se2TPP free bases and, moreover, the considerable downfield shift of the α-carbons of the S(Se)-rings on protonation are in agreement with the previously suggested theory of inner and outer aromaticity in these porphyrins.
    Additional Material: 2 Ill.
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  • 19
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Electrophoresis 2 (1981), S. 1-11 
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Additional Material: 10 Ill.
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  • 20
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: A zwitterionic methacrylamide derivative, (3-sulfopropyl)dimethy1(3-methacrylamidopropyl) ammonium inner salt (MAPS), was synthesized and then copolymerized with N,N′-methylenebisacrylamide (Bis) to make gels carrying covalently bound sulfobetaine groups. Gels were also prepared with the addition of (3-sulfopropyl)trimethyl ammonium inner salt (TMAPS) to Bis-crosslinked polyacrylamide prior to polymerization. The properties of these gels in gel electrophoresis and electrofocusing were tested and compared with those of Bis-crosslinked polyacrylamide.In MAPS gels the absolute migration velocities of proteins and dyes at either polarity of migration were decreased. Anionic species were much more strongly retarded than cationic species. Ferguson plots (based on protein mobilities relative to dye in a continuous buffer) of catalase at pH 4 obtained on MAPS gels had a similar slope but lower y-intercept compared with those on equivalent polyacrylamide gels, indicating that the available (effective) net charge on the protein was decreased because it interacts with the zwitterionic charge on the gel. Similarly, the addition of TMAPS to polyacrylamide decreased the relative catalase mobility at non-restrictive gel concentrations. However, at gel concentrations above 4 %T, relative mobilities were increased, presumably because the effective pore size of the gel was increased through inhibition of polymerization by the zwitterionic compound.MAPS gels did not exhibit electroendosmosis by the criterion of cyanocobalamin displacement. Resolution between peptides in MAPS gels, and between proteins in ternary copolymer gels made of MAPS, Bis and polyacrylamide, was similar to that on polyacrylamide. Bands of catalase appeared sharpened in MAPS gels. pH Gradients form, decay and exhibit conductance gaps in MAPS electrofocusing gels and in polyacrylamide gels in presence of 0.25-1.5 M TMAPS, in a manner which was qualitatively indistinguishable from polyacrylamide.
    Additional Material: 7 Ill.
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