ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

X
feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • Inorganic Chemistry  (3,865)
  • Chemical Engineering  (1,794)
  • 1970-1974  (5,659)
Collection
Keywords
Publisher
Years
Year
  • 1
    Electronic Resource
    Electronic Resource
    Fixed bed desorption behavior of gases with nonlinear equilibria: Part II. Dilute, multicomponent, isothermal systems (1974)
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 20 (1974), S. 915-923 
    Details
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Generalized depletion curves for desorption (and Corresponding breakthrough curves for adsorption) were calculated for systems characterized by the Langmuir-type multicomponent equilibrium equation and controlled by the film type rate model. In contrast with adsorption where the nonkey (or less strongly adsorbed) component curves display overshoots above feed concentration, in desorption the key component depletion curves exhibit the instabilities in the form of inflections and curvatures. As in the one component case, the differences in the depletion and breakthrough curves may be related to the rate phenomena. The undulations in the key component depletion curves may be characterized by derivatives of the rate data. The major significance of these instabilities is to elongate the depletion curves, which in turn requires the expenditure of added effort during regeneration. Process modifications are indicated, which could suppress the instabilities. The predicted trends were confirmed by experimental depletion curves.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/aic.690200512
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 2
    Electronic Resource
    Electronic Resource
    Fixed bed desorption behavior of gases with non-linear equilibria: Part I. Dilute, one component, isothermal systems (1972)
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 18 (1972), S. 1139-1147 
    Details
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Generalized depletion curves for desorption (and breakthrough curves for adsorption) were calculated for a system characterized by the Langmuirtype equilibria and controlled by a film type rate model. The depletion points generally appear sooner than the corresponding breakthrough points, and the desorption profiles are significantly broader than the corresponding adsorption curves. These phenomena may be best explained in terms of the prevailing driving forces. The effects of adsorbate properties and operating variables (inlet composition and flow rate) were established and experimentally substantiated.
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/aic.690180609
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 3
    Electronic Resource
    Electronic Resource
    Correlation and prediction of vapor-liquid equilibria with the redlich-kwong equation of state (1970)
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 16 (1970), S. 112-119 
    Details
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A modified Redlich-Kwong equation has been applied to the calculation of phase equilibria in multicomponent systems. The two parameters of the Redlich-Kwong equation are treated as temperature functions. They are obtained for each pure component from experimental vapor pressures and liquid densities with the help of a generalized fugacity coefficient correlation for saturated vapors. The need to submit coefficients for pure components is thus eliminated. At least one experimental vapor-liquid equilibrium point is required to establish an interaction constant for each binary system. Applications have been made to binary and multicomponent systems containing hydrocarbons, hydrogen, carbon dioxide, and hydrogen sulfide.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/aic.690160122
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 4
    Electronic Resource
    Electronic Resource
    Glykoside von Aminozuckern, II. Zur Synthese von 2-Amino-2-desoxy-α-D-glucopyranosiden (1970)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 103 (1970), S. 1792-1796 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Glycosides of Amino Sugars, II. Synthesis of 2-amino-2-deoxy-α-D-glucopyranosidesThe synthesis of glycosides and disaccharides of 2-amino-2-deoxy-D-glucose has been explored using trifluoroacetyl as the N-blocking group. Because of its high tendency for neighboring group participation only β-D-glycosides were formed. The corresponding α-disaccharide could be obtained as the main product when employing 2.4-dinitrophenyl as the N-protecting group.
    Notes: Die N-Trifluoracetyl-Schutzgruppe wurde zur Synthese von Glykosiden und Disacchariden der 2-Amino-2-desoxy-D-glucose benutzt. Sie zeigte eine hohe Tendenz zur Nachbargruppen-beteiligung unter Bildung von -β-D-Glykosiden. Das entsprechende α-Disaccharid wurde als Hauptprodukt bei Verwendung der N-2.4-Dinitrophenyl-Schutzgruppe erhalten.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19701030614
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 5
    Electronic Resource
    Electronic Resource
    Di- und Polyaminozucker, XV.XIV. Mitteil.: W. Meyer zu Reckendorf, Tetrahedron Letters [London] 1970, 287 Synthese der 2.4-Diamino-l.6-anhydro-2.4-didesoxy-D-talose (1970)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 103 (1970), S. 2424-2427 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Di- and Polyamino Sugars, XV. XIV. Mitteil.: W. Meyer zu Reckendorf, Tetrahedron Letters [London] 1970, 287. Synthese der 2.4-Diamino-1.6-anhydro-2.4-dideoxy-D-talose. Synthesis of 2,4-Diamino-1,6-anhydro-2,4-dideoxy-D-taloseDehydrogenation of the amino reductone 1 with iodine yields a triulose which is isolated as the phenylhydrazone-phenylazo derivative 2. Spontaneous cyclization of 2 forms the 1.6-anhydro compound 3. On hydrogenation 2as well as 3are transformed into the title compound.
    Notes: Die durch Dehydrierung des Aminoreduktons 1 mit Jod entstehende Triulose wird als Bis-phenylhydrazon 2 isoliert, das die Konstitution eines Phenylhydrazon-benzolazo-Derivates besitzt. 2 cyclisiert leicht zur 1.6-Anhydro-Verbindung 3, die, wie auch 2, bei der katalytischen Hydrierung die Titelverbindung liefert.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19701030814
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 6
    Electronic Resource
    Electronic Resource
    Eliminierungsreaktionen eines Pyranose-EnolacetatesVorläufige Mitteil.: Meyer zu Reckendorf, Naturwissenschaften 56, 328 (1969). Ein Pyranose-aminoredukton (1970)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 103 (1970), S. 2418-2423 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Elimination Reactions of a Pyranose Enolacetate. A Pyranose Amino ReductoneThe α-azidoketone 1 is easily transformed either directly or via the enolacetate 2 into the vinylogous amide 4 which on acid treatment yields 8. 4 and 8 show the typical reactions of reductones. On reduction 8 yields derivatives of 2-amino-2-deoxy-D-allose only.
    Notes: Das α-Azido-keton 1 geht leicht direkt oder über das Enolacetat 2 in das vinyloge Säureamid 4 über, Aus dem mit Säure 8 entsteht. 4 und 8 zeigen die typischen Reaktionen von Reduktonen. Bei der Reduktion gibt 8 ausschließlich Derivate der 2-Amino-2-desoxy-D-allose.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19701030813
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 7
    Electronic Resource
    Electronic Resource
    Glycoside von Aminozuckern, IV. Synthese von Disacchariden der 2-Amino-2-desoxy- und der 3-Amino-3-desoxy-D-glucose (1974)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 107 (1974), S. 869-875 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Glycosides of Amino Sugars, IV. Synthesis of Disaccharides of 2-Amino-2-deoxy- and 3-Amino-3-deoxy-D-glucoseThe solvent dependency of the Koenigs-Knorr reaction between two derivatives of 2-amino-2-deoxy-D-glucose (3 and 4) was investigated. The highest yield of the α-disaccharide 5 was obtained in the system toluene/1,2-dimethoxyethane. The condensation of two derivatives of 3-amino-3-deoxy-D-glucose (11 and 13) under similar conditions yielded the 1,6-linked α-and β-disaccharides (15, 14) of this sugar which were unknown until now.
    Notes: Die Koenigs-Knorr-Reaktion zwischen zwei Derivaten der 2-Amino-2-desoxy-D-glucose (3 und 4) wurde in Abhängigkeit vom Lösungsmittel untersucht. Die höchste Ausbeute an α-Disaccharid 5 konnte in einem Gemisch von Toluol und 1,2-Dimethoxyäthan erhalten werden. Die Kondensation zweier Derivate der 3-Amino-3-desoxy-D-glucose (11 und 13) unter ähnlichen Bedingungen führte zu den bisher unbekannten 1,6-verknüpften α- und β-Disacchariden (15 bzw. 14) dieses Zuckers.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19741070313
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 8
    Electronic Resource
    Electronic Resource
    Di- und Polyaminozucker, XX Synthese der 2,3,4,6-Tetraamino-2,3,4,6-tetradesoxy-D-glucose (1974)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 107 (1974), S. 1188-1194 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Di- and Polyamino Sugars, XX. Synthesis of 2,3,4,6-Tetraamino-2,3,4,6-tetradeoxy-D-glucoseThe title compound has been prepared by introduction of two amino functions into the molecule of 2,3-diamino-2,3-dideoxy-D-glucose. Instead of the free sugar we obtained mainly the pyrrolidine 17.
    Notes: Die Titelverbindung wurde durch Einführung von zwei Stickstoff-Funktionen in die 2,3-Diamino-2,3-didesoxy-D-glucose dargestellt. Anstelle des freien Zuckers erhielten wir hauptsächlich das Pyrrolidin 17.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19741070414
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 9
    Electronic Resource
    Electronic Resource
    Glycoside von Aminozuckern, V. Synthese von Disacchariden der 2,3-Diamino-2,3-didesoxy-D-glucose, I (1974)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 107 (1974), S. 2585-2600 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Glycosides of Amino Sugars, V. Synthesis of Disaccharides of 2,3-Diamino-2,3-dideoxy-D-glucose, IOn dinitrophenylation with 1-fluoro-2,4-dinitrobenzene 2,3- diamino-2,3-dideoxy-D-glucose preponderantly yields the 1,2,3-trisubstituted derivative 5 the structure of which was proved by several methods. The N,N′-dinitrophenyl derivative 2 could be obtained from the glycoside 17 and was converted into the bromide 19. On reaction with a derivative of 3-azido-3-deoxy-D-glucose (24) 19 yielded the α- and β-disaccharides 25 and 27.
    Notes: 2,3-Diamino-2,3-didesoxy-D-glucose-dihydrochlorid liefert bei der Dinitrophenylierung mit 1-Fluor-2,4-dinitrobenzol überwiegend das 1,2,3-Trisubstitutionsderivat 5. dessen Konstitution auf mehreren Wegen bewiesen wurde. Das über das Glycosid 17 erhältliche N,N′-Dinitrophenylderivat 2 konnte in das Bromid 19 übergeführt und dieses mit einem Derivat der 3-Azido-3-desoxy-D-glucose 24 zum α- und β-Disaccharid 25 bzw. 27 verknüpft werden.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19741070819
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 10
    Electronic Resource
    Electronic Resource
    Kinetik und Mechanismus der Substitionsreaktionen von Komplexverbindungen. XXVI. Solvatation des [Cr(NCS)4(p-Anisidin)2]-Ions in Äthanol-Wasser-Mischungen (1971)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 380 (1971), S. 216-230 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: 13 new complex salts of the [Cr(NCS)4(p-anisidine)2]- have been synthesized and the solvation kinetics of this anion has been studied in ethanol-water mixtures. The first two NCS- ions are exchanged for water molecules. In acid solutions the rate of this reaction is not influenced by the solvent composition.In parallel with this reaction, p-anisidine molecules are substituted, too, by ethanol molecules. (Acceleration by hydrogen ions.) In the resulting complex ion the first two NCS- ions are substituted, too, by water molecules. The rate constants of this reaction are rather close to those of the reaction which leads to the exchange of the first two NCS- ions in the initial complex. The third and fourth NCS- ions are substituted only in neutral solutions by water molecules. Kinetic parameters have been derived for the substitution of the first two NCS- ions and for the substitution of the p-anisidine molecules.
    Notes: Es wurden 13 neue Komplexsalze mit den Anion [Cr(NCS)4(p-Anisidin)2]- dargestellt und die Solvatationskinetik dieses Anions in Äthanol-Wasser-Mischungen untersucht. Danach kann man die folgende Reaktionsschemata annehmen. Die ersten zwei NCS--Ionen werden gegen Wassermolekeln ausgetauscht. In sauren Lösungen wird die Geschwindigkeit dieser Reaktion nicht von der Lösungsmittelzusammensetzung beeinflußt. Parallel zu dieser Reaktion werden die p-Anisidinmolekln gegen Äthanol ausgetauscht. Diese Reaktion wird durch Wasserstoffionen beschleunigt. In den entstehenden Komplexionen sind die ersten zwei NCS--Ionen ebenfalls gegen Wasser ausgetauscht. Die Geschwindigkeitskonstanten dieser Reaktion sind von der gleichen Größenordnung wie die Geschwindigkeitskonstanten der Reaktion, die zum Austausch der ersten zwei NCS--Ionen aus dem ursprünglichen Komplexion führt. Die dritten und vierten NCS--Ionen werden nur in neutralen Lösungen gegen Wasser ausgetauscht. Kinetische Parameter für den Austausch der ersten zwei NCS--Ionen und der p-Anisidinmolekeln wurden ermittelt.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19713800213
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...