Search results
Results From The WOW.Com Content Network
2, 3, 4 or 5 door of a minimum 4.4m length. (2 or 3 door cars must share the same basic body profile as the 4/5 door model). Equalised width of 1875mm; Specified front aerodynamic device incorporating flat floor, apertures for radiator, brake cooling ducts, intercooler and side exits. Specified rear wing profile.
Get AOL Mail for FREE! Manage your email like never before with travel, photo & document views. Personalize your inbox with themes & tabs. You've Got Mail!
1 mono- 30 triaconta- 2 di- 31 hentriaconta- 3 tri- 32 dotriaconta- 4 tetra- 33 tritriaconta- 5 penta- 34 tetratriaconta- 6 hexa- 40 tetraconta- 7 hepta- 50 pentaconta- 8 octa- 60 hexaconta- 9 nona- 70 heptaconta- 10 deca- 80 octaconta- 11 undeca- 90 nonaconta- 12 dodeca- 100 hecta- 13 trideca- 200 dicta- 14 tetradeca- 300 tricta- 15 pentadeca-
While conventional dye-based angiography is still the common gold standard, OCTA has been evaluated and used across many diseases. [4] [5] [25] OCTA was first introduced in clinical eyecare in 2014. [26] OCTA has applications in several diseases, including leading causes of blindness such as glaucoma [24] and age-related macular degeneration. [27]
(3-Aminopropyl)triethoxysilane (APTES) is an aminosilane frequently used in the process of silanization, the functionalization of surfaces with alkoxysilane molecules. It can also be used for covalent attaching of organic films to metal oxides such as silica and titania.
Henry Neal, son of 3 time BTCC champion Matt Neal, won the inaugural Touring Car Trophy driving a NGTC specification Honda Civic Type R while James Turkington, younger brother of another BTCC champion, Colin Turkington, fought off Lewis Kent to win the TCR UK class. [6] For 2020 the Volkswagen Racing Cup also joined the grid. Henry Neal and ...
Octadecyltrichlorosilane (ODTS or n-octadecyltrichlorosilane) is an organosilicon compound with the formula CH 3 (CH 2) 17 SiCl 3. A colorless liquid, it is used as a silanization agent to prepare hydrophobic stationary phase, for reversed-phase chromatography. [2] It is also evaluated for forming self-assembled monolayers on silicon dioxide ...
Octahydroxyanthraquinone is an organic compound with formula C 14 H 8 O 10, formally derived from anthraquinone by replacement of 8 hydrogen atoms by hydroxyl groups.. The compound was obtained in 1911 by Georg von Georgievics [1] [2] and can be obtained through oxidation of rufigallol (1,2,3,5,6,7-hexahydroxyanthraquinone) with boric acid and mercuric oxide in sulfuric acid at 250 °C (482 °F).