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排序方式: 共有128条查询结果,搜索用时 15 毫秒
1.
Morelos A Albuquerque IF Bondar NF Carrigan RA Chen D Cooper PS Lisheng D Denisov AS Dobrovolsky AV Dubbs T Endler AM Escobar CO Foucher M Golovtsov VL Gottschalk H Gouffon P Grachev VT Khanzadeev AV Kubantsev MA Kuropatkin NP Lach J Lang Pengfei Li Chengze Li Yunshan Luksys M Mahon JR McCliment E Newsom C Pommot Maia MC Samsonov VM Schegelsky VA Shi Huanzhang Smith VJ Tang Fukun Terentyev NK Timm S Tkatch II Uvarov LN Vorobyov AA Yan Jie Zhao Wenheng Shuchen Z Zhong Yuanyuan 《Physical review letters》1993,71(21):3417-3420
2.
Morelos A Albuquerque IF Bondar NF Carrigan RA Chen D Cooper PS Dai Lisheng Denisov AS Dobrovolsky AV Dubbs T Endler AM Escobar CO Foucher M Golovtsov VL Gottschalk H Gouffon P Grachev VT Khanzadeev AV Kubantsev MA Kuropatkin NP Lach J Lang Pengfei Li Chengze Li Yunshan Luksys M Mahon JR McCliment E Newsom C Pommot Maia MC Samsonov VM Schegelsky VA Shi Huanzhang Smith VJ Tang Fukun Terentyev NK Timm S Tkatch II Uvarov LN Vorobyov AA Yan Jie Zhao Wenheng Zheng Shuchen Zhong Yuanyuan 《Physical review letters》1993,71(14):2172-2175
3.
Teixeira-Neto É Leite CA Cardoso AH Medeiros da Silva MC Braga M Galembeck F 《Journal of colloid and interface science》2000,231(1):182-189
Poly(styrene-co-acrylamide) (PS-AAM) latex was prepared, fractionated by sedimentation under gravity, and characterized by PCS, infrared spectra, secondary and backscattered electron imaging in the scanning electron microscope, and electron spectroscopy imaging in an analytical transmission electron microscope. Three latex fractions were obtained. The lower fraction was opalescent and its particles were the more uniform, concerning size, chemical composition, and topochemical features. This lower fraction was still further fractionated by zonal centrifugation in a density gradient, yielding two fractions with similar macrocrystal-forming abilities but different sizes and chemical compositions. These results confirm those previously obtained for the PS-HEMA latex. Copyright 2000 Academic Press. 相似文献
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Ultra‐high pressure LC for astaxanthin determination in shrimp by‐products and active food packaging
A. Sanches‐Silva T. Ribeiro T. G. Albuquerque P. Paseiro R. Sendón A. Bernaldo de Quirós J. López‐Cervantes D. I. Sánchez‐Machado H. Soto Valdez I. Angulo G. P. Aurrekoetxea H. S. Costa 《Biomedical chromatography : BMC》2013,27(6):757-764
Nowadays, there is increasing interest in natural antioxidants from food by‐products. Astaxanthin is a potent antioxidant and one of the major carotenoids in crustaceans and salmonids. An ultra‐high pressure liquid chromatographic method was developed and validated for the determination of astaxanthin in shrimp by‐products, and its migration from new packaging materials to food simulants was also studied. The method uses an UPLC® BEH guard‐column (2.1 × 5 mm, 1.7 µm particle size) and an UPLC® BEH analytical column (2.1 × 50 mm, 1.7 µm particle size). Chromatographic separation was achieved using a programmed gradient mobile phase consisting of (A) acetonitrile–methanol (containing 0.05 m ammonium acetate)–dichloromethane (75:20:5, v/v/v) and (B) ultrapure water. This method was evaluated with respect to validation parameters such as linearity, precision, limit of detection, limit of quantification and recovery. Low‐density polyethylene films were prepared with different amounts of the lipid fraction of fermented shrimp waste by extrusion, and migration was evaluated into food simulants (isooctane and ethanol 95%, v/v). Migration was not detected under the tested conditions. Copyright © 2012 John Wiley & Sons, Ltd. 相似文献
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Ingrid Hauser Ana B. Colaço Julie A. Skjæran Aslak Einbu Kjetill Østgaard Hallvard F. Svendsen Francisco J. Cervantes 《Applied biochemistry and biotechnology》2013,169(4):1449-1458
Large-scale amine-based CO2 capture will generate waste containing large amounts of ammonia, in addition to contaminants such as the actual amine as well as degradation products thereof. Monoethanolamine (MEA) has been a dominant amine applied so far in this context. This study reveals how biological N removal can be achieved even in systems heavily contaminated by MEA in post- as well as pre-denitrification treatment systems, elucidating the rate-limiting factors of nitrification as well as aerobic and denitrifying biodegradation of MEA. The hydrolysis of MEA to ammonia readily occurred both in post- and pre-denitrification treatment systems with a hydraulic retention time of 7 h. MEA removal was ≥99?±?1 % and total nitrogen removal 77?±?10 % in both treatment systems. This study clearly demonstrates the advantage of pre-denitrification over post-denitrification for achieving biological nitrogen removal from MEA-contaminated effluents. Besides the removal of MEA, the removal efficiency of total nitrogen as well as organic matter was high without additional carbon source supplied. 相似文献
8.
Oscar Cervantes Zaira del Rocio Lopez Norberto Casillas Peter Knauth Nayeli Checa Francisco Apolinar Cholico Rodolfo Hernandez-Gutirrez Luis Hector Quintero Jose Avila Paz Mario Eduardo Cano 《Molecules (Basel, Switzerland)》2022,27(2)
A ferrofluid with 1,2-Benzenediol-coated iron oxide nanoparticles was synthesized and physicochemically analyzed. This colloidal system was prepared following the typical co-precipitation method, and superparamagnetic nanoparticles of 13.5 nm average diameter, 34 emu/g of magnetic saturation, and 285 K of blocking temperature were obtained. Additionally, the zeta potential showed a suitable colloidal stability for cancer therapy assays and the magneto-calorimetric trails determined a high power absorption density. In addition, the oxidative capability of the ferrofluid was corroborated by performing the Fenton reaction with methylene blue (MB) dissolved in water, where the ferrofluid was suitable for producing reactive oxygen species (ROS), and surprisingly a strong degradation of MB was also observed when it was combined with H2O2. The intracellular ROS production was qualitatively corroborated using the HT-29 human cell line, by detecting the fluorescent rise induced in 2,7-dichlorofluorescein diacetate. In other experiments, cell metabolic activity was measured, and no toxicity was observed, even with concentrations of up to 4 mg/mL of magnetic nanoparticles (MNPs). When the cells were treated with magnetic hyperthermia, 80% of cells were dead at 43 °C using 3 mg/mL of MNPs and applying a magnetic field of 530 kHz with 20 kA/m amplitude. 相似文献
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Carmen Salazar-Hernández Jorge Cervantes Sergio Alonso 《Journal of Sol-Gel Science and Technology》2010,54(1):77-82
The gelation process of TEOS sols in three different solvents using di-n-butyltin dilaurate (DBTL) as polycondensation catalyst has been investigated. Sol compositions were similar to those employed
in the field of stone consolidation for the conservation of historical buildings. Three different systems were studied: TEOS
in ethanol (S-EtOH) which was tested to explain gelation in protic solvents; TEOS in a mixture of methylethylketone/acetone
(S-MA) to represent aprotic solvents; and TEOS in a blend of MEK/ethanol (S-ME) for comparison of a system with properties
intermediate between protic and aprotic solvents. The gelation process was studied by measuring the viscoelastic behavior
near the gelation point (GP). A scaling exponent (Δ) was determined for the elastic modulus, G(ω)′ and the viscous modulus,
G′′(ω), which both follow the same power law, ωΔ, at GP. The fractal dimension, df, was calculated from the scaling exponent, Δ, for each TEOS-DBTL system. For each type
of solvent studied, values of Δ from 0.34 to 0.53 with df of 1.9–2.2 were obtained. The results suggest that DBTL leads to
a TEOS polycondensation mechanism similar to that observed for a base-catalyst system. However, the change in df suggests
that there is a significant effect of the solvent on aggregation mechanisms of the gelation process. A diffusion limited cluster–cluster
aggregation mechanism (DLCCA) was observed when ethanol was used as protic solvent, while a reaction limited cluster–cluster
aggregation mechanism (RLCCA) was observed for MEK/acetone (aprotic solvent). 相似文献