Rapid quality evaluation and geographical origin recognition of ginger powder by portable NIRS in tandem with chemometrics.

Ginger powder is an important spice that is susceptible to improper sales such as adulteration or geographical fraud. In this study, a portable near infrared spectroscopy was used to quantitatively predict the 6-gingerol content, an important quality index of ginger, as well as to identify the gingers from three origins in China. Specifically, the optimal preprocessing method was first investigated by comparing the predictions of models. Then three feature variable selection methods including PCA, CARS, and RFrog, on the quantitative analysis of 6-gingerol were also compared, respectively. After comparison, the PLS model established on the S-G combined with SNV preprocessing outperformed the others. The PLS regression of 6-gingerol with variables selected by RFrog possessed the Rc2 of 0.9463, Rp2 of 0.9497, and the RPD of 4.2257, respectively. Moreover, the results further verified that the LDA model by SPA variables extraction successfully identify gingers from different origins with 100 % accuracy.

Enhanced photoelectrocatalytic decomplexation of Ni-EDTA and simultaneous recovery of metallic nickel via TiO2/Ni-Sb-SnO2 bifunctional photoanode and activated carbon fiber cathode.

In order to enhance Ni-EDTA decomplexation and Ni recovery via photoelectrocatalytic (PEC) process, TiO2/Ni-Sb-SnO2 bifunctional electrode was fabricated as the photoanode and activated carbon fiber (ACF) was introduced as the cathode. At a cell voltage of 3.5 V and initial solution pH of 6.3, the TiO2/Ni-Sb-SnO2 bifunctional photoanode exhibited a synergetic effect on the decomplexation of Ni-EDTA with the pseudo-first-order rate constant of 0.01068 min-1 with 180 min by using stainless steel (SS) cathode, which was 1.5 and 2.4 times higher than that of TiO2 photoanode and Ni-Sb-SnO2 anode, respectively. Moreover, both the efficiencies of Ni-EDTA decomplexation and Ni recovery were improved to 98% from 86% and 73% from 41% after replacing SS cathode with ACF cathode, respectively. Influencing factors on Ni-EDTA decomplexation and Ni recovery were investigated and the efficiencies were favored at acidic condition, higher cell voltage and lower initial Ni-EDTA concentration. Ni-EDTA was mainly decomposed via ·OH radicals which generated via the interaction of O3, H2O2, and UV irradiation in the contrasted PEC system. Then, the liberated Ni2+ ions which liberated from Ni-EDTA decomplexation were eventually reduced to metallic Ni on the ACF cathode surface. Finally, the stability of the constructed PEC system on Ni-EDTA decomplexation and Ni recovery was exhibited.

Investigation of exposure biomarkers in human plasma following differing levels of tobacco-specific N-nitrosamines and nicotine in cigarette smoke.

Tobacco-specific N-nitrosamines (TSNAs) are strong carcinogens widely found in tobacco products, environmental tobacco smoke, lake, and wastewater. The main objective of this study was to investigate the effects of cigarette smoke with different yields of TSNAs (NNK, NNN, NAT, NAB) and nicotine on the levels of biomarkers of exposure in smokers' plasma. Three hundred healthy volunteers were recruited comprising 60 smokers of each of 3 mg, 8 mg and 10 mg ISO tar yield cigarettes and 60 smokers who smoked 10 mg, 8 mg, and 3 mg for 14 days sequentially and 60 non-smokers. All study participants were male, aged from 21 to 45 years old, and were recruited from a same unit in Hebei, China. We measured the levels of NNAL, NAT, NNN, NAB and cotinine in plasma from 240 smokers and 60 non-smokers using a novel method established by online two-dimensional solid phase extraction-liquid chromatography-tandem mass spectrometry. The results showed that NNAL, NAT, NNN, NAB and cotinine in the plasma of smokers smoking cigarette with low TSNAs and nicotine were lower than that with high TSNAs and nicotine. When smokers switched from higher to lower TSNA yields of cigarettes, their plasma NNAL, NAT, NNN, NAB levels significantly decreased. The plasma concentrations of NNAL were significantly correlated with those of cotinine, NNN, NAT and NAB for smokers (p < 0.001). Similarly, the plasma concentrations of cotinine were significantly correlated with those of NNN, NAT and NAB for smokers (p < 0.001). The plasma NNAL, NAT, NNN, NAB and cotinine levels for smokers were significantly higher than those for non-smokers. These findings suggested that the total NNAL, NNN, NAT, NAB and cotinine in plasma were valid and reliable biomarkers for human exposure to TSNAs and nicotine.

Study on the hydrophobicity of [Bmim]2[CuCl4] by two-dimensional correlation spectroscopy.

By dissolving copper chloride in [Bmim]Cl (1-butyl-3-methylimidazolium chloride), chloride ions can coordinate with copper ions and form [CuCl4]2-, thereby inducing the solution being hydrophobic. In the present work, hydrogen bonds between [Bmim]+ and anions are analyzed and discussed by two-dimensional correlation spectroscopy. Time-dependent attenuated total reflection spectroscopy (ATR-FTIR) is introduced to monitor the hygroscopic process of [Bmim]2[CuCl4] and [Bmim]Cl in situ. Hygroscopic capacity and rate of [Bmim]2[CuCl4] shrink compared with [Bmim]Cl. The change of water molecular clusters has been studied by second-derivative spectra in the hygroscopic process. The behaviors of water molecular in the two ionic liquids are also distinctive.

Relationship between cervical curvature and spinal cord drift distance after laminectomy via lateral mass screw fixation and its effect on clinical efficacy.

BACKGROUND: Laminectomy with lateral mass screw fixation (LCS) is considered an effective surgical procedure for cervical spondylotic myelopathy. However, varying degrees of loss of the cervical curvature were noted in some patients postoperatively. The aim of this study was to observe the relationship between cervical curvature and spinal drift distance after LCS and to determine its effect on neurological function, axial symptoms, and C5 palsy. METHODS: A total of 117 consecutive cervical spondylotic myelopathy patients with normal cervical curvature underwent LCS from April 2015 to May 2017 in our institution. Of these patients, 90 patients who accepted to undergo an integrated follow-up were enrolled in this study. The patients were divided into 3 groups based on their postoperative cervical curvature. In group A (28 patients), the cervical curvature became straight postoperatively (0°≤cervical spine angle≤5°); in group B (36 patients), the cervical curvature decreased (5°16.5°). Spinal drift distance, neurological recovery, axial symptoms, and C5 palsy in the patients were recorded and analyzed. RESULTS: Postoperative measurements showed that there was no significant difference in laminectomy width between the groups (P > .05). The cervical spine angle was 2.7°â€Š±â€Š0.5° in group A, 11.2°â€Š±â€Š2.6° in group B, and 20.8°â€Š±â€Š4.1° in group C (P < .05), while the spinal drift distance was 1.2 ±â€Š0.2 mm, 1.8 ±â€Š0.4 mm, and 3.0 ±â€Š0.5 mm, respectively (P < .05). The postoperative Japanese Orthopedic Association score was significantly increased in all groups (P < .05), and there was no significant difference between the groups at different time points (P > .05). However, significant differences were noted between the groups in axial symptoms (P < .05), which were analyzed via the visual analog scale score. The occurrence of C5 palsy in groups A, B, and C was 7.1% (2/28), 8.3% (3/36), and 11.5% (3/26), respectively (P > .05). CONCLUSION: In LCS, the cervical curvature should be maintained at the normal angle to obtain a good spinal cord drift distance and a lower incidence of axial symptoms.

Graphene oxide bound silica for solid-phase extraction of 14 polycyclic aromatic hydrocarbons in mainstream cigarette smoke.

Polycyclic aromatic hydrocarbons (PAHs) were considered as a source of carcinogenicity in mainstream cigarette smoke (MSS). Accurate quantification of these components was necessary for assessing public health risk. In our study, a solid-phase extraction (SPE) method using graphene oxide (GO) bound silica as adsorbent for purification of 14 PAHs in MSS was developed. During SPE process, large matrices interferences of MSS were adsorbed on SPE column. The result of FTIR spectra demonstrated that these matrices interferences were adsorbed on GO mainly through OH and CO groups. The concentrations of PAHs in MSS extract were determined by gas chromatography-mass spectrometry (GC-MS). The limit of detection (LOD) and limit of quantification (LOQ) of the developed method for 14 PAHs ranged from 0.05 to 0.36 ng/cig and 0.17 to 1.19 ng/cig, respectively. The accuracy of the measurement of 14 PAHs was from 73 to 116%. The relative standard deviations of intra- and inter-day analysis were less than 7.8% and 13.9%, respectively. Moreover, the developed method was successfully applied for analysis of real cigarette containing 1R5F reference cigarette and 12 top-selling commercial cigarettes in China.

Fluorination of ZnWO4 photocatalyst and influence on the degradation mechanism for 4-chlorophenol.

The fluorine doped ZnWO4 photocatalyst was synthesized by hydrothermal synthesis and annealing treatment. The existing states of fluorine in the crystal were elucidated, and the effects of fluorine on the crystal structure, photocatalytic activity, and degradative intermediates were investigated. The doping concentration of fluorine in the interstitial lattice of ZnWO4 crystal can be controlled bythe annealing conditions. The photocatalytic activity can be enhanced about 50% after the doped ZnWO4 was annealed at 450 degrees C for 1 h due to perfect crystal structure. The enhancement of photocatalytic activity after fluorine doping could be attributed to the higher separation efficiency of electron-hole pairs, which results in a large number of holes participated in the photocatalytic process. The fluorine doping does not change the degradation pathway of 4-chlorophenol (4-CP) in our system. 4-CP was mainly transformed into hydroxylated aromatic intermediates such as benzoquinone (BQ), hydroquinone (HQ), and 4-chlorocatechol (4-CC). The photodegradation of 4-CP in powdered F-doped ZnWO4 system proceeded via direct holes oxidation reactions.

Photocorrosion inhibition and enhancement of photocatalytic activity for ZnO via hybridization with C60.

C60 molecules with monomolecular layer state dispersed on the surface of ZnO and formed the hybridized interaction between ZnO and C60. C60-hybridized ZnO photocatalyst showed enhanced photocatalytic activity for the degradation of the organic dye and the photocorrosion of ZnO was successfully inhibited bythe hybridization of C60 molecules. The photocorrosion inhibition of ZnO by C60 molecule could be attributed to the reduced activation of surface oxygen atom. The enhanced photocatalytic activity for C60-hybridized ZnO was originated from the high migration efficiency of photoinduced electrons on the interface of C60 and ZnO, which was produced by the interaction of C60 and ZnO with a conjugative pi-system. The enhancement degree of photocatalytic activity was strongly depended on the coverage of C60 molecules on the surface of ZnO nanoparticles, and the optimum hybridization effect was found at a weight ratio of 1.5% (C60/ZnO). The hybridization of C60 with semiconductors could be used to improve the photocatalytic activity as well as the photostability.

Facile synthesis of hollow Co3O4 microspheres and its use as a rapid responsive CL sensor of combustible gases.

The hollow Co(3)O(4) microspheres (HCMs) were prepared by the carbonaceous templates, which did not need the surface pretreatment. The chemiluminescence (CL) and catalytic properties for CO oxidation over these hollow samples were evaluated. The samples were characterized by scanning electron microscopy (SEM), energy disperse spectra (EDS), transmission electron microscopy (TEM), selected area electron diffraction (ED), X-ray diffraction (XRD), temperature-programmed desorption (TPD) and N(2) adsorption. The influences of filter' band length, flow rate of gas, test temperature, and particle structure on CL intensities were mainly investigated. It was found that compared with the solid Co(3)O(4) particles (SCPs), HCMs had a stronger CL intensity, which was ascribed to its hollow structure; and that CL properties of the catalysts were well correlated with their reaction activities. Moreover, HCMs were used to fabricate a highly sensitive gas detector, which is a rapid and effective method for the selection of catalysts or the detection of environmental deleterious gases.

A CL mode detector for rapid catalyst selection and environmental detection fabricated by perovskite nanoparticles.

La(1-x)Sr(x)MnO3 (x = 0, 0.2, 0.5, 0.8) nanoparticles were synthesized and their chemiluminescence (CL) and catalytic properties of CO oxidation were determined. We mainly investigated the influences of filter band length, flow rate of gas, test temperature, catalyst compositions, and particle size on CL intensities and catalytic activities of the catalysts. The catalysts were characterized by means of XRD, TEM, N2 adsorption isotherm, CO-TPD, and O2-TPD, etc. It was found that the strong CL response signals occurred over these perovskites nanoparticles; and that CL properties of the catalysts were well correlated with the reaction activities. These nanoparticles can be used to fabricate a stable gas detector due to a high activity and stability of perovskite structure. CL mode could be a rapid and effective method for the selection of new catalysts from thousands of materials, as well as for the detection of environmental deleterious gases.

Photocatalytic degradation of RhB by fluorinated Bi2WO6 and distributions of the intermediate products.

Fluorinated Bi2WOs catalyst was synthesized by a simple hydrothermal process. The effects of fluorine doping on crystal structure, optical property, photoinduced hydrophilicity, surface acidity, and photocatalytic activity of the as-prepared sample were observed in detail. Fluorinated Bi2WOs presented the enhanced photoactivity for the RhB degradation under the simulative sunlight (lamda > 290 nm), which could be a synergetic effect of the surface fluorination and the doping of crystal lattice. To get a better handle on the mechanistic details of this photocatalytic system, the photodegradation process of RhB was examined. In the fluorinated Bi2WO6 system, five intermediates, namely, N,N-diethyl-N'-ethylrhodamine, N,N-diethylrohodamine, N-ethyl-N'-ethylrhodamine, N-ethylrhodamine, and rhodamine were thus identified, whereas the first three intermediates could only be identified in the case of the Bi2WO6 system. This result indicated that more RhB molecules were degraded via the deethylation process in the fluorinated Bi2WO6 system. It was proposed that the (F-)-containing function on the catalyst surface could serve as an electron-trapping site and enhance interfacial electron-transfer rates by tightly holding trapped electrons. On the basis of the experimental results, a photocatalytic mechanism was discussed in detail.

Synergetic effect of Bi2WO6 photocatalyst with C60 and enhanced photoactivity under visible irradiation.

Fullerene (C60)-modified Bi2WO6 photocatalyst is prepared by a simple absorbing process. The as-prepared samples show the high efficiency for the degradation of nonbiodegradable azodyes methylene blue (MB) and rhodamine B (RhB) under visible light (lamda >420 nm) and simulated solar light (lamda >290 nm). After being modified by C60, the photocatalytic activities of Bi2WO6 samples increase about 5.0 and 1.5 times for the degradation of MB and RhB under visible light irradiation, whereas 4.6 and 2.1 times under xenon lamp irradiation, respectively. The enhanced photocatalytic activity for C60-modified Bi2WO6 comes from the high migration efficiency of photoinduced electrons on the interface of C60 and Bi2WO6 which is produced by the interaction of Bi2WO6 and C60 with the conjugative pi-system. The optimum synergetic effect is found at a weight ratio of 1.25 wt % (C60/Bi2WO6). The photocatalytic reaction process of C60-modified Bi2WO6 is mainly governed by direct holes and O2*- oxidation.

Synthesis of hexagonal BaTa2O6 nanorods and influence of defects on the photocatalytic activity.

Hexagonal barium tantalate (BaTa2O6) nanorods were synthesized by a hydrothermal method based on the reaction of concentrated Ba(OH)2 solution and Ta2O5. BaTa2O6 samples show a uniform cylindrical structure with diameters of 5-30 nm and the lengths of 50-200 nm. The formation of BaTa2O6 nanorods follows a dissolution-recrystallization mechanism and is governed by hydrothermal temperature and time. BaTa2O6 nanorod samples prepared at 270 degrees C for 72 h have exhibited the highest photocatalytic activity in the degradation of Rhodamine B (RhB) in aqueous solution under UV radiation. Hydrogen-related defects were detected in BaTa2O6 nanorods, which originate from the oxygen octahedron. The number of defects was dependent on the hydrothermal temperature, and the photocatalytic activities of BaTa2O6 nanorods increase with the decrease of defect amounts. On the basis of the experiment results, the difference in photocatalytic activities for samples is mainly caused by lattice defects, which can act as inactivation centers.

[Review of infrared spectroscopy for water cluster].

The explanation of structure and binding properties of small clusters provides a key for understanding bulk water in its liquid and solid phase and for understanding solvation phenomena. The progress, characteristic of the investigation on water clusters by Infrared are introduced. The results of far-infrared laser vibration-rotation-tunneling spectroscopy (FIR-VRT) and infrared spectroscopy of size-selected water are outlined in detail, and compared with those of other methods.