𝔖 Bobbio Scriptorium

✦ LIBER ✦

Possible ecological and environmental significance of the predominance of even-carbon number C20-C30n-alkanes

✍ Scribed by Harry Dembicki Jr.; W.G Meinschein; Donald E Hattin

Book ID: 118883898
Publisher: Elsevier Science
Year: 1976
Tongue: English
Weight: 759 KB
Volume: 40
Category: Article
ISSN: 0016-7037
DOI: 10.1016/0016-7037(76)90177-0

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Sources and occurrence of C12C22n-alkan

Sources and occurrence of C12C22n-alkane distributions with even carbon-number preference in sedimentary environments

✍ Joan Grimalt; Joan Albaigés 📂 Article 📅 1987 🏛 Elsevier Science 🌐 English ⚖ 746 KB

Binary phase diagram of molecular alloys

Binary phase diagram of molecular alloys of the consecutive even-numbered n-alkanes n-tetracosane (n-C24H50) and n-hexacosane (n-C26H54)

✍ Z. Achour-Boudjema; M. Bouroukba; M. Dirand 📂 Article 📅 1996 🏛 Elsevier Science 🌐 English ⚖ 521 KB

Origins of Oil, a Correction and Further

Origins of Oil, a Correction and Further Comment on the Brunnock1 Even C-Number Predominance in Certain Higher Alkanes of African Crudes, and on the Biogenesis of Nonacosane

✍ ROBINSON, ROBERT 📂 Article 📅 1967 🏛 Nature Publishing Group 🌐 English ⚖ 118 KB

Studies in the hydrophilic properties of

Studies in the hydrophilic properties of possible ointment base constituents. II. The n-alkyl alcohols with a carbon chain length of C20 to C30*

✍ Halpern, Alfred ;Wilkins, William J. 📂 Article 📅 1949 🏛 Elsevier ⚖ 367 KB 👁 2 views

Hypothetical Thermodynamic Properties: V

Hypothetical Thermodynamic Properties: Vapor Pressures and Vaporization Enthalpies of the Even n -Alkanes from C 40 to C 76 at T = 298.15 K by Correlation−Gas Chromatography. Are the Vaporization Enthalpies a Linear Function of Carbon Number?

✍ Chickos, James; Wang, Tracy; Sharma, Esseim 📂 Article 📅 2008 🏛 American Chemical Society 🌐 English ⚖ 133 KB

Development of two processes for the syn

Development of two processes for the synthesis of bridged azabicyclic systems: intermolecular radical addition?homoallylic rearrangements leading to 2-azanorborn-5-enes and neophyl-type radical rearrangements to 2-azabenzonorbornanesThis is one of a number of contributions from the current members of the Dyson Perrins Laboratory to mark the end of almost 90 years of organic chemistry research in that building, as all its current academic staff move across South Parks Road to a new purpose-built laboratory.Electronic supplementary information (ESI) available: the preparation and characterisation of compounds 20b?i, 28c?g, 30b?g, 30i, 32e?g, 32i, 33b?g. See http//www.rsc.org/suppdata/ob/b3/b306717n/

✍ Hodgson, David M.; Bebbington, Magnus W. P.; Willis, Paul 📂 Article 📅 2003 🏛 Royal Society of Chemistry 🌐 English ⚖ 276 KB