Buchbesprechungen
Identifieur interne : 000D32 ( Istex/Corpus ); précédent : 000D31; suivant : 000D33Buchbesprechungen
Auteurs : W. Wildanger ; J. Hild ; B. Matzik ; M. Rohrlich ; S. Donhauser ; W. Bötticher ; P. Majerus ; R. Brockman ; G. Engel ; H. Wieczorek ; J. Oehlenschl Ger ; H. Hey ; A. Görg ; M. Miller ; H. ElbertzhagenSource :
- Zeitschrift für Lebensmittel-Untersuchung und Forschung [ 0044-3026 ] ; 1983-01-01.
Url:
DOI: 10.1007/BF01089345
Links to Exploration step
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<refBibs><json:item><host><author><json:item><name> Zusatz Von Bioalkohol Zu Benzin</name>
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<title>wodurch der Brennwert er- h6ht und der Benzinverbrauch gedrosselt werden kann Abschlie- Bend sei festgestellt, dab das vorliegende Buch dem Leser einen umfassenden Oberblick fiber den gegenw~irtigen Stand der Nutzung von Biomassen</title>
</host>
</json:item>
<json:item><host><author></author>
<title>Zur Methodik der KapiUar-Gaschromatographie bei der Bestimmung isomerer Formen unges~ittigter Fetts~iuren in Nahrungsfetten</title>
</host>
</json:item>
<json:item><author><json:item><name>E Yoon</name>
</json:item>
<json:item><name> Renner</name>
</json:item>
<json:item><name>Fachgebiet Giej3en</name>
</json:item>
<json:item><name> Milchwissenschaft</name>
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<host><volume>37</volume>
<pages><last>199</last>
<first>197</first>
</pages>
<author></author>
<title>Milchwissenschaft</title>
<publicationDate>1982</publicationDate>
</host>
<publicationDate>1982</publicationDate>
</json:item>
<json:item><author><json:item><name> Verff</name>
</json:item>
<json:item><name> Die Bisher Zur Trennung Isomerer Formen Ungesfittigter Fettsfiuren Gebrguchlichen Stationfiren Phasen ( Apiezon-L</name>
</json:item>
<json:item><name>Sp-2340 Ov-275 Und</name>
</json:item>
</author>
<host><author></author>
<title>Vergleichssubstanzen und mittels Massenspektrometrie</title>
</host>
<title>OV-1 in Verbindung mit der HPLC, PG4000 und FFAP) Es gelang die Trennung isomerer Formen der Octadecen-und Octadecadien-Fettsfiuren (als Methylester) aus Margarine und Butter mittels einer 50-m-Glascapillare, die mit HC1 ge~itzt und mit einer konzentrierten L6sung von FFAP dynamisch (Schomburg-Verfahren) belegt wurde. Die Identifizierung der Isomeren erfolgte fiber relative Retentionszeiten</title>
</json:item>
<json:item><host><author></author>
<title>GC-Parameter: 50 m FFAP-Glascapillare, 0.33 mm I</title>
</host>
</json:item>
<json:item><host><pages><last>5</last>
<first>05</first>
</pages>
<author><json:item><name> °c / Min</name>
</json:item>
</author>
</host>
</json:item>
<json:item><host><author><json:item><name>Systematische Identifizierung Van Antioxidantien In</name>
</json:item>
<json:item><name> Schmalz</name>
</json:item>
</author>
</host>
</json:item>
<json:item><author><json:item><name>D,A Peteghem</name>
</json:item>
<json:item><name> Dekeyser</name>
</json:item>
</author>
<host><volume>64</volume>
<pages><last>1355</last>
<first>1331</first>
</pages>
<author></author>
<title>J. Assoc. Offic. Anal. Chemists</title>
<publicationDate>1981</publicationDate>
</host>
<title>Systematic identification of antioxidants in lards, shortenings, and vegetable oils by thin layer chromatography ) (Gent, Belgium, Laboratoriurn voor Brornatologie, Faculteit Farrnaceutische Wetenschappen)</title>
<publicationDate>1981</publicationDate>
</json:item>
<json:item><host><author></author>
<title>Zur Auftrennung einer Reihe von Antioxidantien verwenden die Autoren drei verschiedene dfinnschichtchromatographische Syste- me</title>
</host>
</json:item>
<json:item><author></author>
<host><author></author>
<title>Sprfihreagens: FeC13/Bipyridin</title>
</host>
</json:item>
<json:item><author></author>
<host><author></author>
<title>Spriihreagcns: Dibromchinonchlorimid</title>
</host>
<title>Adsorbens: Kieselgel, FlieBmittel: n-Hexan</title>
</json:item>
<json:item><author><json:item><name> Adsorbens</name>
</json:item>
<json:item><name> Polyamid</name>
</json:item>
</author>
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<first>59</first>
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<author></author>
<title>Sprfihreagens wie 1</title>
<publicationDate>1982</publicationDate>
</host>
<title>Nordihydroguajaretsfiure, 3,3'-Thio-dipropins~iure, Tocopherol, t-Butylhydrochinon, 2,4,5-Trihydroxybutyrophenon. Die Antioxidantien wurden verschiedenen Fetten zugesetzt und anschliegend dutch Behandlung mit 95% igem Methanol wieder isoliert . Eine weitere Aufreinigung der Extrakte vor der Dfinnschichtchromatographie erwies sich als nicht erforderlich. C. Suwelack (Iserlohn) Pflanzliche Fette und Ole, Olsaaten Gewinnung und Entbitterung yon Speise~il und Proteinkonzentrat aus Samen van Lupinas mutabifis</title>
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<title>Dabei konnte der Alkaloidgehalt von 0,14% im Roh61 auf 5 ppm gesenkt werden Diese Menge soll ernfihrungsphysiologisch unbedenklich sein. Darfiber hinaus wurde festgestellt, dab die Zusammensetzung der Olalkaloide nicht identisch ist mit der des Samens . Der Olkuchen enthielt ca. 4% Alkaloide. Mit wfigrigem Alkohol (70-90%) konnte er zu einem Konzentrat entbittert werden, das 73% Protein und nur 0,06% Restalkaloide enthielt</title>
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<host><pages><last>190</last>
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<title>der Jodzahl und der Fettsiiurezusammensetzung. B. Sanelli</title>
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<title>(La conservabilit/t degli oli vegetali in rapporto all grado di insaturazione e del contenuto di clorofilla. Nota II -variazioni delI'aciditfi, del numero di iodio e della composizione degli acidi grassi ) (Vasto, Societi Vastese Oli Alirnentari) Riv. Ital</title>
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<title>Mitt.: ~nderungen der spektrophotometrischen Indices im UV. B. SaneIli. (La conservabilitfi degli oli vegetaIi in rapporto al grado di insaturazione e del contenuto in clorofilla. Nota III. variazioni degli indici spettrofotometrici nell'UV)</title>
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<title>Alterns der Pflanzen61e sind besonders ausgepr~igt in Verbindung mit Oxidationserscheinungen Im Hinblick auf zunehmende Ranzigkeit laufen die geprfiften Vergnderungen gleichzeitig mit anderen chemischen Reaktionen ab. M. Schfitz (Hannover) Quafit~itserhaltung pflanzfichcr Ole in Verbindung mit dem Grad der Ungesiittigtheit und dem Chlorophyllgehalt. III</title>
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