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Results for “Solubility”
Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.
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Profiling of soluble neutral oligosaccharides from treated biomass using solid phase extraction and LC–TOF MS
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Water soluble biocompatible vesicles based on polysaccharides and oligosaccharides inclusion complexes for carotenoid delivery
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Solubility of greenhouse and acid gases on the [C4mim][MeSO4] ionic liquid for gas separation and CO2 conversion
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Manipulating solvent and solubility in the synthesis, activation, and modification of permanently porous coordination cages
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Corrigendum to “Experimental Determination of Solubilities of Di-calcium Ethylenediaminetetraacetic Acid Hydrate [Ca 2 C 10 H 12 N 2 O 8 •7H 2 O(s)] in NaCl and MgCl 2 Solutions to High Ionic Strengths and Its Pitzer Model: Applications to Geological Disposal of Nuclear Waste and Other Low Temperature Environments”
In the published version (Xiong et al., 2017), there was an error for the reaction coefficient for the dissolution reaction of Ca 2 C 10 H 12 N 2 O 8 •7H 2 O(s) in the database used for the modeling. In the database for the modeling, the coefficient for water (i.e., 7H 2 O) was inadvertently omitted.
Effects of Ni incorporation on the reactivity and stability of hausmannite (Mn3O4): Environmental implications for Mn, Ni, and As solubility and cycling
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Beyond the wall: High-throughput quantification of plant soluble and cell-wall bound phenolics by liquid chromatography tandem mass spectrometry
Plants accumulate several thousand of phenolic compounds, including lignins and flavonoids, which are mainly synthesized through the phenylpropanoid pathway, and play important roles in plant growth and adaptation. A novel high-throughput ultra-high performance liquid chromatography tandem mass spectrometry (UHPLC-MS/MS) method was established to quantify the levels of 19 flavonoids and 15 other phenolic compounds, including acids, aldehydes, and alcohols. The chromatographic separation was performed in 10 minutes, allowing for the resolution of isomers such as 3-, 4-, and 5-chlorogenic acids, 4-hydroxybenzoic and salicylic acids, isoorientin and orientin, and luteolin and kaempferol. The linearity range for each compound was found to be in the low fmol to the high pmol. Furthermore, this UHPLC-MS/MS approach was shown to be very sensitive with limits of detection between 1.5 attomoles to 300 fmoles, and limits of quantification between 5 attomoles to 1,000 fmoles. Extracts from maize seedlings were used to assess the robustness of the method in terms of recovery efficiency, matrix effect, and accuracy. The biological matrix did not suppress the signal for 32 out of the 34 metabolites under investigation. Additionally, the majority of the analytes were recovered from the biological samples with an efficiency above 75 %. All flavonoids and other phenolic compounds had an intra- and inter-day accuracy within a ± 20 % range, except for coniferyl alcohol and vanillic acid. Finally, the quantification of flavonoids, free and cell wall-bound phenolics in seedlings from two maize lines with contrasting phenolic content was successfully achieved using this methodology.
A thermodynamic modeling approach for solubility product from struvite-k
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Thermodynamical and artificial intelligence approaches of H2S solubility in N-methylpyrrolidone
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Development and Testing of a New Fiber Optic System for Monitoring CO2 Solubility in Aqueous High-Pressure Geological Systems
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Statistical investigation of simulated intestinal fluid composition on the equilibrium solubility of biopharmaceutics classification system class II drugs
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Solubilities and ionic conductivities of ionic liquids containing lithium salts
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Review of technologies for preventing secondary transport of soluble and particulate radiological contamination from roadways, roadside vegetation, and adjacent soils
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