Literatura académica sobre el tema "E04B"

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Artículos de revistas sobre el tema "E04B"

1

Kisała, Joanna B., Gerald Hörner, Adriana Barylyak, Dariusz Pogocki, and Yaroslav Bobitski. "Photocatalytic Degradation of 4,4′-Isopropylidenebis(2,6-dibromophenol) on Sulfur-Doped Nano TiO2." Materials 15, no. 1 (2022): 361. http://dx.doi.org/10.3390/ma15010361.

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In present work, we examine the photocatalytic properties of S-doped TiO2 (S1, S2) compared to bare TiO2 (S0) in present work. The photocatalytic tests were performed in alkaline aqueous solutions (pH = 10) of three differently substituted phenols (phenol (I), 4,4′-isopropylidenebisphenol (II), and 4,4′-isopropylidenebis(2,6-dibromophenol) (III)). The activity of the catalysts was evaluated by monitoring I, II, III degradation in the reaction mixture. The physicochemical properties (particle size, ζ-potential, Ebg, Eu, E0cb, E0vb, σo, KL) of the catalysts were established, and we demonstrated their influence on degradation reaction kinetics. Substrate degradation rates are consistent with first-order kinetics. The apparent conversion constants of the tested compounds (kapp) in all cases reveal the sulfur-loaded catalyst S2 to show the best photocatalytic activity (for compound I and II S1 and S2 are similarly effective). The different efficiency of photocatalytic degradation I, II and III can be explained by the interactions between the catalyst and the substrate solution. The presence of bromine substituents in the benzene ring additionally allows reduction reactions. The yield of bromide ion release in the degradation reaction III corresponds to the Langmuir constant. The mixed oxidation-reduction degradation mechanism results in higher degradation efficiency. In general, the presence of sulfur atoms in the catalyst network improves the degradation efficiency, but too much sulfur is not desired for the reduction pathway.
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2

Mayrleitner, M. "E047/1." Drugs of the Future 24, no. 9 (1999): 961. http://dx.doi.org/10.1358/dof.1999.024.09.549023.

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3

Ling, Binhua, Cristian Apetrei, Ivona Pandrea, et al. "Classic AIDS in a Sooty Mangabey after an 18-Year Natural Infection." Journal of Virology 78, no. 16 (2004): 8902–8. http://dx.doi.org/10.1128/jvi.78.16.8902-8908.2004.

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ABSTRACT Prevailing theory holds that simian immunodeficiency virus (SIV) infections are nonpathogenic in their natural simian hosts and that lifelong infections persist without disease. Numerous studies have reported that SIV-infected sooty mangabeys (SMs; Cercocebus atys) remain disease free for up to 24 years despite relatively high levels of viral replication. Here, we report that classic AIDS developed after an 18-year incubation in an SM (E041) with a natural SIVsm infection. Unlike that described in previous reports of SIV-related disease in SMs, the SIVsm infecting E041 was not first passaged through macaques; moreover, SM E041 was simian T-cell leukemia virus antibody negative. SM E041 was euthanized in 2002 after being diagnosed with severe disseminated B-cell lymphoma. The plasma virus load had been approximately the same for 16 years when a 100-fold increase in virus load occurred in years 17 and 18. Additional findings associated with AIDS were CD4+-cell decline, loss of p27 core antibody, and loss of control of SIVsm replication with disseminated giant cell disease. These findings suggest that the time to development of AIDS exceeds the average lifetime of SMs in the wild and that the principal adaptation of SIV to its natural African hosts does not include complete resistance to disease. Instead, AIDS may develop slowly, even in the presence of high virus loads. However, a long-term relatively high virus load, such as that in SM E041, is consistent with AIDS development in less than 18 years in humans and macaques. Therefore, the results also suggest that SMs have a special mechanism for resisting AIDS development.
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4

Capitão, S., M. Miranda, and F. Silva. "E041 Inclusion in bilingual Portuguese school." International Journal of Pediatric Otorhinolaryngology 75 (May 2011): 68. http://dx.doi.org/10.1016/s0165-5876(11)70349-4.

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5

Al-Sharif, O. "E044 Family candidacy for cochlear implant." International Journal of Pediatric Otorhinolaryngology 75 (May 2011): 69. http://dx.doi.org/10.1016/s0165-5876(11)70352-4.

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6

Bodek, Arie. "THE JUPITER ELECTRON SCATTERING PROGRAM AT JEFFERSON LAB." International Journal of Modern Physics A 20, no. 14 (2005): 3089–92. http://dx.doi.org/10.1142/s0217751x05025814.

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JUPITER (Jlab Unified Program to Investigate nuclear Targets and Electroproduction of Resonances) is a new collaboration between the Nuclear Physics electron scattering and High Energy Physics neutrino scattering communities to investigate the structure of nucleons and nuclei with electron and neutrino Beams. The first phase of JUPITER is Hall C experiment E04-001 on Inclusive Electron Scattering from Nuclear Targets. First data run of E04-001 is currently scheduled for January of 2005.
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7

Valliéres, Eric. "E04-02: NCI mediastinoscopy." Journal of Thoracic Oncology 2, no. 8 (2007): S222—S223. http://dx.doi.org/10.1097/01.jto.0000282998.11920.f1.

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8

Deriaz, M., and M. I. Kos. "E040 Asymmetric articulation in unilateraly implanted children." International Journal of Pediatric Otorhinolaryngology 75 (May 2011): 68. http://dx.doi.org/10.1016/s0165-5876(11)70348-2.

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9

Stamatis, Georgios. "E04-04: Re-do-mediastinoscopy." Journal of Thoracic Oncology 2, no. 8 (2007): S225—S226. http://dx.doi.org/10.1097/01.jto.0000283000.96672.14.

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10

XING, H. "E040 Antihypertension and remolding hypertrophied ventricular by amlodipine." American Journal of Hypertension 11, no. 4 (1998): 105A. http://dx.doi.org/10.1016/s0895-7061(97)91102-x.

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