RESUMO
From unstable crystals to relatively stable monohydrate crystals, many researchers have been working on S-nitrosocaptopril for more than two decades. S-nitrosocaptopril monohydrate (Cap-NO·H2O) is a novel crystal form of S-nitrosocaptopril (Cap-NO), and is not only a nitric oxide (NO) donor, but also an angiotensin-converting enzyme inhibitor (ACEI). Yet, a method for long-term storage has never been reported. In order to determine the optimal storage conditions, Plackett-Burman (PB) design was performed to confirm the critical factors. Response surface methodology (RSM) was employed to determine the optimal Cap-NO·H2O storage condition, based on the rough interval determined by the path of steepest ascent experiment. The optimized storage condition was denoted as nitrogen purity of 97%, temperature of -10 °C and 1.20 g deoxidizer. In this case, a final preservation rate of 97.91 ± 0.59% could be obtained. In specific storage conditions, Cap-NO·H2O was found to be stable for at least 6 months in individual PE package, procreating a potentially applicable avenue.
Assuntos
Inibidores da Enzima Conversora de Angiotensina/química , Captopril/análogos & derivados , Doadores de Óxido Nítrico/química , Vasodilatadores/química , Captopril/químicaRESUMO
Polymer gels suffer from a serious syneresis issue when exposed to high-temperature and high-salinity (HTHS) conditions, which limits their use as water-treatment agents in this type of reservoir. In this paper, the effects of the polymer type/concentration, deoxidizers, and stabilizers on the long-term stability of polymer gels were systematically studied; thus, the methods to develop stable polymer gels for two typical levels of salinity were optimized. The results show the following: (1) For a medium-salinity condition (TDS: 33,645.0 mg/L) at 125 °C, conventional HPAM gels completely dehydrate within only 1 day, and the addition of a deoxidizer hardly improved their stability. Some special polymers, e.g., AP-P5, MKY, and CPAM, are able to form stable gels if a high concentration of 0.8% is used; the syneresis rate of these gels is about 10% after 30 days. However, the addition of the complexant sodium oxalate significantly improves the stability of gels formed by all five of these different polymers, which behave with a 0% syneresis rate after 30 days pass. Complexants are the most economical and feasible agents to develop stable gels in medium-salinity water. (2) Gels enhanced using the methods above all become unstable in a more challenging ultra-high-saline condition (TDS: 225,068.0 mg/L). In this case, special calcium- and magnesium-resistant polymers are required to prepare stable gels, which show 0% syneresis rates after 30 days, have relatively low strengths, but do produce a good plugging effect in high-permeability cores.
RESUMO
Gasification is one of the most promising approaches to accomplishing efficient utilization of biomass, nevertheless, it shows severe problems of low efficiency and syngas quality, which deserves further improvements. In this regard, deoxygenation-sorption-enhanced biomass gasification is proposed and experimentally explored using deoxidizer-decarbonizer materials (xCaO-Fe) for intensified hydrogen production. The materials follow the deoxygenated looping of Fe0-3e-âFe3+ as an electron donor and the decarbonized looping of CaO + CO2 â CaCO3 as a CO2 sorbent. Specifically, the H2 yield and CO2 concentration reach 7.9 mmol·g-1 biomass and 10.5 vol%, which increases by 311% and decreases by 75%, respectively, compared with conventional gasification, confirming the promotion effect of deoxygenation-sorption enhancement. Fe embedded within the CaO phase is successfully constructed with the formation of functionalized interface structure, affirming the strong interaction between CaO and Fe. This study brings in a new concept for biomass utilization via synergistic deoxygenation and decarbonization, which will substantially boost high-quality renewable hydrogen production.