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- Author or Editor: S. Yang x
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A rapid method has been used for simultaneous identification of both hydrophilic and lipophilic compounds from Radix Salviae Miltiorrhizae (RSM, the root of Salvia miltiorrhiza BGE.) by ultra-performance liquid chromatography/quadrupole time-offlight mass spectrometry (UPLC/Q-TOF-MS). A total of 58 compounds extracted by methanol were detected and tentatively identified within 20 min, including hydrophilic phenolics, lipophilic diterpenoids, a verbascose, and several organic acids. These compounds were separated on an Acquity UPLC BEH C18 column and identified based on tandem mass spectrometry (MS/MS) fragmentation patterns under the positive and negative ion modes, respectively. Among them, micranthin B and 9-oxo-10E,12Zoctadecadienoic acid were reported in RSM for the first time. Their fragmentation patterns in electrospray ionization (ESI)—MS/MS spectra were first investigated by matching their accurate molecular masses. This contribution presented one of the first reports on the analysis of hydrophilic phenolics and lipophilic diterpenoids from Radix Salviae Miltiorrhizae using UPLC/Q-TOF-MS. The results demonstrated that UPLC/Q-TOF-MS method could be applied to rapidly and expediently describe and provide comprehensive chemical information for simultaneous analysis of two different polar components in RSM.
Summary
Chestnut exhibits anti-inflammatory, styptic, anti-diarrhea, and analgestic effects as a traditional Chinese medicine. There is increasing evidence that shows that the consumption of chestnuts has become more important in human nutrition due to the health benefits provided by the antioxidants. The phenolic compounds are responsible for major bioactivities, such as anti-tumor and anti-oxidation. A high-performance liquid chromatography (HPLC) method with diode array detection (DAD) was established for the simultaneous determination of six phenolic compounds (gallic acid, GA; protocatechuic acid, PR; catechin, CA; epicatechin, EP; quercetin, QU; kaempferol, KA) in Chinese chestnut (Castanea mollissima blume) kernel. The sample followed by separation on Eclipse XDB-C18 column (150 × 4.6 mm, id., 5 μm) with gradient elution of methanol-1.0% acetate acid solution as a mobile phase, at a temperature of 30°C, under the ratio of 1.2 mL min−1, with 5 μL injection volume, and multi-wavelength synthesis was used with DAD. The correlation coefficients were larger than 0.999, the recoveries were 97.58% for GA, 100.41% for PA, 96.23% for CA, 101.38% for QU, 99.15% for EP, and 98.60% for KA, relative standard deviation (RSD) were 1.04% for GA, 1.21% for PA, 1.09% for CA, 1.19% for QU, 1.06% for EP, and 1.20% for KA. This method was applied for the determination of phenolics in chestnut kernel and was found to be fast, sensitive, and suitable.
Abstract
Phase transition behavior of polyesters derived from 2,7-phenanthrene dicarbonic acid diethylester and alkanediols with even methylene carbon number was investigated by the simultaneous DSC-XRD method. The smectic A phase was observed on cooling from the molten state. The transition entropy from the isotropic state to the smectic A phase was about 9.0 J mol-1 K-1, which depended on the methylene carbon number. The linear expansion coefficients, based on the (001) spacing of the crystalline phase at room temperature, were 1.310-4 K-1 (crystalline phase), 5.710-4 K-1 (crystallization region), 1.710-3 K-1 (smectic A phase) during cooling, and 1.510-4 K-1 (crystalline phase), and 1.010-3K-1(melting region) on heating.
Abstract
Osmium isotope, 197Os, produced with 14 MeV neutrons through the reaction of 198Pt(n,2p)197Os, has been identified and its decay properties have been studied with a g(X) spectroscopic method. The ten new g-rays of 41.2, 50.7, 196.8, 199.6, 223.9, 233.1, 250.2, 342.1, 403.6, and 406.4 keV assigned to the decay of 197Os were observed. The half-life of 197Os has been determined as 2.8±0.6 minutes. A partial decay scheme of 197Os was proposed.
Abstract
Although Ir anomaly has been discovered in a number of C/T boundaries in the world, no positive results of this anomaly in Permian/Triassic (P/Tr) boundary were given. There are many well-developed P/T sections in South China. One of representative sections is located at the Baoqing quarry, Meishan Town, Changxin County, Zhejiang Province. Ir, Os, Re, Au, Pt, Cu and Mo were determined by the radiochemical procedure developed in our laboratory. (1) Besides those accessible by INAA. The results reveal that the refractory siderophile and other chalcophile elements have certain enrichment near and at the boundary layer. However, the Ir/Au and other element abundance ratios fail to accord with the extraterrestrial values. The nature of the boundary event was discussed in terms of elemental geochemistry.
Abstract
The concentrations of 14 elements, including Ir, Au, Co, Cr, Fe, Sr, Rb, K, Ta, Zn, Sb, Ba, Sc and Se, in the Wuxi fallen ice were determined by neutron activation analysis. The experimental results show that the relative concentration ratios of Ir/Co, Ir/Cr and Ir/Sc etc. in the ice water (0.0069, 0.00024 and 0.11, respectively) are quite close to those of Type C1 chondrite (0.0102, 0.00021 and 0.092, respectively), which implies that the fallen ice might be a piece of extraterrestrial substance.
Abstract
The effects of Amoxicillin Sodium and Cefuroxime Sodium on the growth of E. coli DH5α were investigated by microcalorimetry. The metabolic power-time curves of E. coli DH5α growth were determined by using a TAM air isothermal microcalorimeter at 37�C. By evaluation of the obtained parameters, such as growth rate constants (k), inhibitory ratio (I), the maximum heat power (P m) and the time of the maximum heat power (t m), one found that the inhibitory activity of Amoxicillin Sodium vs. E. coli DH5α is enhanced with the increasing of the Amoxicillin Sodium concentration, and the Cefuroxime Sodium has a stimulatory effect on the E. coli DH5α growth when the concentration is about 1 μg mL−1. The IC50 for the Amoxicillin Sodium and the Cefuroxime Sodium are 1.6 and 2.0 μg mL−1, respectively, it implicates that the E. coli DH5α is more sensitive to Amoxicillin Sodium than Cefuroxime Sodium.
Abstract
A series of anion-cation surfactants modified organoclays are prepared by incorporating both cationic surfactant, hexadecyltrimethylammonium bromide (HDTMAB), and anionic surfactant, sodiumdodecyl sulfonate (SDS), to montmorillonite. The added amounts of surfactant varied from 0.2 to 4.0 CEC of the used montmorillonite, similar to those reported in literature. A combination of elemental analysis, X-ray diffraction and thermogravimetric analysis is used in the characterization of the resulting organoclays. The experimental results show that anionic surfactants can not be intercalated into the montmorillonite whereas they can be loaded onto cationic modified montmorillonite, resulting in a further increase of organic carbon content of the resulting organoclays. This study demonstrates that SDS can be intercalated into montmorillonite interlayer space through the interaction with HDTMAB rather than by ion exchange. The intercalation of SDS results in an increase of the basal spacing of the resulting organoclays when comparing with HDTMAB modified montmorillonite and higher decomposition temperature of the intercalated surfactants when comparing with them in bulk state. These new insights are of high importance in the application of organoclays in the fields of remediation of polluted water and synthesis of clay based nanocomposites.
The hypothesis of niche differentiation with respect to resources is considered to be one of the most influential explanations for the maintenance of species diversity. The hypothesis has been examined extensively by testing its prediction of species-habitat association, which posits that the spatial distribution of species is highly correlated with environmental variables. However, we argue that widespread evidence of the species-habitat association lacks adequate rigor to justify the niche differentiation hypothesis. In this study, we tested whether and to what extent the observed species-habitat association could be caused by ecological processes other than niche differentiation, in a 20-ha subtropical forest plot. The niche differentiation hypothesis was evaluated by testing the species-habitat association and performing a cross-evaluation of the habitat-diversity expectation, which posits that a strong positive correlation exists between species diversity and habitat complexity. Failure to support the habitat-diversity expectation would at a minimum indicate that the niche differentiation hypothesis might not be the main underlying process of species distribution, despite prevalence of the species-habitat association in the same plot. Our analysis revealed that distributions of most species (86.11%) in the plot were significantly associated with at least one of eight topographical and soil nutrient variables. However, there was almost no significant positive correlation between species diversity and habitat complexity at various spatial scales in the same plot. The results indicate that additional caution is warranted when interpreting the species-habitat association from the niche differentiation perspective. A significant species-habitat association indicates only a species’ habitat preference. The association may reveal nothing about interspecific differences in habitat preference, which is a requirement of the niche differentiation hypothesis.
