2012
DOI: 10.3997/2214-4609.20148547
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Numerical Modeling of Hydraulic Fracture Growth in Fractured Reservoirs

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Cited by 6 publications
(9 citation statements)
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“…1 H-NMR analysis also indicated tolyporphin-related compounds were in the 90% MeOH fraction of the hexanes partition based on characteristic N-H resonances between −2 to −3 ppm. Distinctive absorption spectral maxima 16,17 at approximately 400 and 676 nm were also hallmarks of tolyporphinrelated compounds and guided their isolation by HPLC. Successive reversed-and normalphase HPLC on these fractions yielded compounds of sufficient purity for spectroscopic and spectrometric characterization.…”
Section: Resultsmentioning
confidence: 96%
“…1 H-NMR analysis also indicated tolyporphin-related compounds were in the 90% MeOH fraction of the hexanes partition based on characteristic N-H resonances between −2 to −3 ppm. Distinctive absorption spectral maxima 16,17 at approximately 400 and 676 nm were also hallmarks of tolyporphinrelated compounds and guided their isolation by HPLC. Successive reversed-and normalphase HPLC on these fractions yielded compounds of sufficient purity for spectroscopic and spectrometric characterization.…”
Section: Resultsmentioning
confidence: 96%
“…Based on the principle of ‘similar compatibility’, the CF/PEEK composite interface can be modified by coating the fibre surface with a sizing agent 24 . The compatibility between CF and resin and the interface chemical bonding between CF and resin can be increased, thereby improving the interface performance of the composites 25–27 …”
Section: Effect Of Interfacial Properties On Cf/peek Compositesmentioning
confidence: 99%
“…More hydrophobic peptide samples (4, 5, and their derivatives) were dissolved in 400 μL of a water/acetonitrile mixture (95:5). 1 H NMR and 13 C{ 1 H} NMR spectra were recorded on a high field Bruker 500 MHz spectrometer equipped with a broadband inverse gradient probe head. Spectra were referenced to the residual solvent signal (CDCl 3 at 7.24 ppm or MeOD at 4.87 ppm).…”
Section: ■ Experimental Sectionmentioning
confidence: 99%
“…HRMS m/z: [M + Na] + Calcd for C 22 H 23 NOSNa + 372.139, found 372.133. 1 H NMR (MeOD, 500 MHz): δ 7.45−7.42 (m, 4H), 7.35−7.32 (m, 2H), 7.31−7.28 (m, 4H), 7.24−7.21 (m, 2H), 6.87− 6.84 (m, 2H), 3.79 (s, 3H), 2.47 (t, 2H, J = 7.2 Hz), 2.39 (t, 2H, J = 6.5 Hz); 13 C{ 1 H} was reported by Riddoch. 29 Manual On-Resin Formation of N-2-[Thioethyl]glycine by the Incorporation of Protected Cysteamines.…”
Section: ■ Experimental Sectionmentioning
confidence: 99%