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  • Wiley-Blackwell  (54)
  • 1985-1989  (54)
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Year
  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 31 (1985), S. 1563-1565 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 1 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 27 (1985), S. 1710-1716 
    ISSN: 0006-3592
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The feasibility of applying the UASB concept for the anaerobic treatment of stillage of distilleries in the sugar producing area of Argentina was subject to study. Results obtained in a 100-L UASB reactor treating stillages with COD values between 35 and 100 g COD/L are presented. Loading rates of up to 24 g COD/L/day were applied with an average COD removal of 75% and a biogas production of more than 9 L/L/day, with an average methane content of 58%. The settling velocity distribution of sludge particles would indicate a good formation of biomass pellets. System interruptions of months without feed and at ambient temperature (20-24°C) were well tolerated.
    Additional Material: 5 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 34 (1989), S. 304-308 
    ISSN: 0006-3592
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Isooctane-AOT-H2O is a suitable system for studying enzyme behavior in organic solvents. Tyrosinase was able to catalyze a well-known reaction in aqueous medium: oxidation of 4-methylcatechol to yield 4-methyl-o-benzoquinone. This reaction was studied using the preceding ternary system with adequate amounts of each component to make up reverse micelles. 4-Methyl-o-benzoquinone stability was demonstrated in isooctane even at alkaline pH values. Apparent Km and Vmax were similar to those in water, but substrate inhibition was more evident. The pH and temperature appear to be shifted toward high and low values, respectively. Characteristic parameters of reverse micelles, ω0 (= H2O/AOT) and percentage of H2O (v/v), were investigated. The results obtained showed that the steady-state rate varies either with ω0 or with percentage of H2O. The variation observed with ω0 showed an optimal value while an increase in percentage of H2O can lead to decreased or increased activity depending on substrate concentration.
    Additional Material: 6 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Chemometrics 2 (1988), S. 247-263 
    ISSN: 0886-9383
    Keywords: Calibration ; Tensor ; Multivariate ; PCR ; MLR ; PLS ; Regression ; Multidimensional arrays ; Order ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Many analytical instruments now produce one-, two- or n-dimensional arrays of data that must be used for the analysis of samples. An integrated approach to linear calibration of such instruments is presented from a tensorial point of view. The data produced by these instruments are seen as the components of a first-, second- or nth-order tensor respectively. In this first paper, concepts of linear multivariate calibration are developed in the framework of first-order tensors, and it is shown that the problem of calibration is equivalent to finding the contravariant vector corresponding to the analyte being calibrated. A model of the subspace spanned by the variance in the calibration must be built to compute the contravarian vectors. It is shown that the only difference between methods such as least squares, principal components regression, latent root regression, ridge regression and partial least squres resides in the choice of the model.
    Additional Material: 9 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Chemometrics 2 (1988), S. 265-280 
    ISSN: 0886-9383
    Keywords: Calibration ; Tensor ; Multivariate ; Order ; Regression ; Generalized rank annihilation ; GRAM ; Multi order ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Tensorial calibration provides a useful approach to calibration in general. For calibration of instruments that produce two-dimensional (second-order) arrays of data per sample, tensoial concepts are as natural a way of solving the calibration problem as vectorial concepts are for the multivariate problem. Similarly, for third- and higher-order data, the tensorial description of calibration is also useful. This paper introduces second-order calibration from a tensorial point of view. Univariate, multivariate and bilinear approaches to calibration are presented. The generalized rank annihilation method (GRAM) is described from the tensorial perspective, and it is shown that GRAM is equivalent to finding a second-order tensorial base that spans both tensors (calibration and unknown) with respective diagonal component matrices. GRAM uses a single calibration sample for multicomponent analysis even in the presence of interference. Second-order bilinear calibration is extended to multiple calibration samples where the effect of collinearities is reduced.
    Additional Material: 5 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Chemometrics 3 (1989), S. 493-498 
    ISSN: 0886-9383
    Keywords: Rank annihilation ; Generalized rank annihilation method ; Generalized eigenproblem ; Calibration ; Spectral interferents ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An improved algorithm for the generalized rank annihilation method (GRAM) is presented. GRAM is a method for multicomponent calibration using two-dimensional instruments, such as GC-MS. In this paper an orthonormal base is first computed and used to project the calibration and unknown sample response matrices into a lower-dimensional subspace. The resulting generalized eigenproblem is then solved using the QZ algorithm. The result of these improvements is that GRAM is computationally more stable, particularly in the case where the calibration sample contains chemical constituents not present in the unknown sample and the unknown contains constituents not present in the calibration (the most general case).
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 135 (1985), S. 139-149 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Eine Probe von mit Ethylcarbonatgruppen teilweise modifiziertem Dextran wurde kreuz-fraktioniert. Auf der Basis von Trübungspunkt-Messungen wurden zwei Systeme gewählt: THF/Hexan und DMF/0,5 proz. wässerige NaCl-Lösungen. Die chemische Zusammensetzung (CCD) und die Molekulargewichtsverteilung (MWD) wurden den Fraktionierungsdaten entnommen. Die beobachtete chemische Heterogenität kann mit der Art des Reaktionsmechanismus von Dextran und Ethylchlorformiat korreliert werden. Die kumulativen Fraktionierungsdaten wurden nach den Zwei-Parameter-Funktionen von Tung und Wesslau angepasst.
    Notes: A sample of a partially modified dextran with ethyl carbonate groups was fractionated by cross-fractionation. Two systems THF/hexane and DMF/0.5% aqueous NaCl were selected on the basis of cloud-point determinations. The chemical composition distribution (CCD) and molecular weight distribution (MWD) curves were constructed from fractionation data. The chemical heterogeneity observed may be correlated with the pattern of reaction of dextran with ethyl chloroformate. The cumulative data were fitted by the two-parameter MWD functions of Tung and of Wesslau.
    Additional Material: 5 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 143 (1986), S. 101-113 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Modifizierung von Polyvinylalkohol mit Diketen, unter Verwendung von tert. Aminen als Katalysatoren, wurde untersucht. Die Struktur der erhaltenen Polymeren wurde durch IR-, 1H-, 13C-NMR-Spektroskopie und chemische Analyse bestimmt. Es wurden Vinylalkohol-Vinylacetoacetat-Copolymere erhalten. Die Reaktionsgeschwindigkeit war jeweils linear abhängig von der Konzentration an Polymerem, Diketen und Pyridin. Die Aktivierungsenergie wurde zu 35,5 kJ/mol (8,5 kcal/mol) bestimmt. Die 13C-NMR-Spektroskopie wurde benutzt, um die Sequenzverteilung in den Copolymeren zu bestimmen; dabei ergab sich eine gewisse Tendenz zur Alternierung von VAL- und VAA-Einheiten in der Polymerkette. Polymere Chelate der Copolymeren mit Kupfer-II-Ionen wurden hergestellt; dabei zeigte sich, daß nicht alle β-Ketoestergruppen an der Komplexbildung beteiligt sind.
    Notes: A study has been made on the modification of poly (vinyl alcohol) with diketene using tertiary amines as catalysts. The structure of the resulting polymers was determined by means of IR, 1H- and 13C-NMR spectroscopy as well as by chemical analysis. Vinyl alcohol-vinyl acetoacetate (VAL-VAA) copolymers were obtained. It has been found a linear dependence of reaction rate on polymer, diketene and pyridine concentrations, respectively. The activation energy was found to be 35.5 kJ/mol (8.5 kcal/mol). 13C-NMR spectroscopy was used for the determination of the sequence distribution in VAL-VAA copolymers. The obtained results show that VAA units have a little alternating tendency in the copolymer chain. Polymeric chelates between VAL-VAA copolymers and cupric ions have been prepared. It is noteworthy that not all the β-keto ester groups in the VAL-VAA copolymers participate in binding cupric ions.
    Additional Material: 9 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 152 (1987), S. 79-91 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Diese Untersuchung befaßt sich mit einigen kinetischen Merkmalen der Reaktion von n-Butylisocyanat mit Polyvinylalkohol ohne jeden Katalysator und unter Verwendung von Triethylendiamin als Katalysator. Die Struktur der resultierenden Polymeren wurde mit Hilfe der IR-, 1H-, und 13C-NMR-Spektroskopie und chemischer Analyse ermittelt. Es wurden Vinylalkohol-Vinylbutylurethancopolymere (VAL-VBU) erhalten. Es ergab sich eine lineare Abhängigkeit der Reaktionsgeschwindigkeit von Polymer-, n-Butylisocyanat- und Triethylendiaminkonzentration. Die Reaktionsgeschwindigkeitskonstante nimmt mit zunehmender Reaktionszeit ab. Das kann mit der sterischen Hinderung durch die Urethangruppen, die entlang der Polymerkette eingebaut sind, erklärt werden. Die Aktivierungsenergie ergab sich zu 49,9 kJ/mol. Eine kinetische Untersuchung der homogenen Hydrolyse von VAL-VBU-Copolymeren wurde durchgefilhrt als Funktion der Basenkonzentration, der Temperatur und des VBU Gehalts. Es zeigte sich, daß die homogene Hydrolyse als Reaktion 1 . Ordnung verliluft, sowohl im Hinblick auf die Hydroxylionen als auch auf den VBU-Gehalt. Die Aktivierungsenergie filr die basenkatalysierte Hydrolyse betragt 79,3 kJ/mol. Die heterogene Hydrolyse von VAL-VBU-Copolymeren im basischen Medium zeigte, daß keine Hydrolyse unter diesen Bedingungen stattfand.
    Notes: This study is concerned with some kinetic features of the reaction of n-butyl isocyanate with poly(vinyl alcohol) without any catalyst and using triethylene diamine as catalyst. The structure of the resulting polymers was determined by means of IR, 1H- and 13C-NMR spectroscopy as well as by chemical analysis. Vinyl alcohol-vinyl butyl urethane (VAL-VBU) copolymers were obtained. It has been found a linear dependence of reaction rate on polymer, n-butyl isocyanate, and triethylene diamine concentrations. Reaction rate constant decreases as reaction time increases. It can be explained by steric hindrance phenomena due to urethane groups incorporated along the polymeric chain. The activation energy was found to be 49.9 kJ/mol. A kinetic study of the homogeneous hydrolysis of VAL-VBU copolymers has been made as a function of the base concentration, the temperature, and the VBU content. The homogeneous hydrolysis was found to be first order with respect to both hydroxyl ion and VBU contents. The activation energy for the base catalyzed homogeneous hydrolysis was found to be 79.3 kJ/mol. The heterogeneous hydrolysis of VAL-VBU copolymers in basic medium showed that no hydrolysis takes place under the conditions employed.
    Additional Material: 10 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 149 (1987), S. 197-200 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The advantageous use of a polymer protected reagent -AlPO4 as a mild catalyst for esterification was studied.
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