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Monocryl has a low tissue reactivity, maintains high tensile strength, and has a half-life of 7 to 14 days. At 1 week, its in vivo tensile strength is at 50–60% undyed (60–70% dyed), 20–30% undyed (30–40% dyed) at two weeks, and essentially completely hydrolyzed by 91–119 days. [ 3 ]
0.881 45 (13) 1.5 × 10 −4 [33] = (/) sine-square weak mixing angle: 0.223 05 (23) [g] 0.231 21 (4) [h] 0.231 53 (4) [i] 1.0 × 10 −3 1.7 × 10 −4 1.7 × 10 −4 [34] [35] [35] electron g-factor: −2.002 319 304 360 92 (36) 1.8 × 10 −13
84% at 2 weeks, 23% at 4 weeks [2] 80% at 2 weeks, 44% at 8 weeks. Complete absorption within 200 days [2] Structure: Multifilament: Multifilament: Braided: Monofilament Origin: Bovine serosa surface finish. Made by twisting together strands of purified collagen taken from the small intestine of healthy ruminants: Bovine serosa. The natural ...
A pale yellow solid, it is the potassium salt of [HFe(CO) 4] −, which is the conjugate base of iron tetracarbonyl dihydride: [1] [2] H 2 Fe(CO) 4 + KOH → K[HFe(CO) 4 ] + H 2 O Potassium tetracarbonyliron hydride is prepared by treating iron pentacarbonyl with potassium hydroxide : [ 3 ]
Potassium hydride is produced by direct combination of the metal and hydrogen at temperatures between 200 and 350 °C: 2 K + H 2 → 2 KH. This reaction was discovered by Humphry Davy soon after his 1807 discovery of potassium, when he noted that the metal would vaporize in a current of hydrogen when heated just below its boiling point.
A Assuming an altitude of 194 metres above mean sea level (the worldwide median altitude of human habitation), an indoor temperature of 23 °C, a dewpoint of 9 °C (40.85% relative humidity), and 760 mmHg sea level–corrected barometric pressure (molar water vapor content = 1.16%).
The cluster H 2 Os 3 (CO) 10 features both terminal and doubly bridging hydride ligands. Hydrides can also span the triangular face of a cluster as in [Ag 3 {(PPh 2) 2 CH 2} 3 (μ 3-H)(μ 3-Cl)]BF 4. [5] In the cluster [Co 6 H(CO) 15] −, the hydride is "interstitial", occupying a position at the center of the Co 6 octahedron.
Pinacolborane is the borane with the formula (CH 3) 4 C 2 O 2 BH. Often pinacolborane is abbreviated HBpin. [1] It features a boron hydride functional group incorporated in a five-membered C 2 O 2 B ring. Like related boron alkoxides, pinacolborane is monomeric. It is a colorless liquid. [2] It features a reactive B-H functional group. [3]