Dispersive liquid-liquid extraction based on magnetic Pickering emulsion followed by gas chromatography-tandem mass spectrometry for the simultaneous determination of aldehydes in environmental water samples.

A dispersive liquid-liquid extraction based on Pickering emulsion stabilized with ferroferric oxide grafted nitrogen-doped graphitized carbon black has been developed to simultaneously determine seven aldehydes in environmental water samples, in combination with pentafluorobenzyl hydroxylamine precolumn derivatization gas chromatography-tandem mass spectrometry. The nitrogen-doped graphitized carbon was prepared from dicyandiamide waste residue with a simple acid wash process. The effects of magnetic emulsifier amount, extraction time, solution pH, and oil/water volume ratio on the formation of magnetically responsive Pickering emulsion and the extraction efficiency of the proposed dispersive liquid-liquid extraction were also investigated. Under the optimized conditions, satisfactory linearities were obtained for all aldehydes with correlation coefficients larger than 0.9984. The limits of detection and quantitation of seven aldehydes were in the range of 17.3-30.1 ng/L and 54.3-103.4 ng/L, respectively, with intra- and interday relative standard deviations less than 8.6%. The mean recoveries at three spiked levels ranged from 70.0 to 101.4%. With the Pickering emulsion as a "minimized extractor", the extraction was accomplished within 5 min. After extraction, the magnetic disperser could be recovered for reuse at least five times by an external magnetic field. The proposed method was demonstrated to be feasible, simple, and economic for the trace analysis of the aldehydes in environmental water samples.

A modified quick, easy, cheap, effective, rugged, and safe method with hydrophobic natural deep eutectic solvent as extractant and analyte protectant for analyzing pyrethroid residues in tomatoes.

In this work, a novel quick, easy, cheap, effective, rugged, and safe technique with hydrophobic natural deep eutectic solvent as both extractant and analyte protectant was developed and combined with gas chromatography-tandem mass spectrometry to analyze pyrethroid residues in tomatoes. Eight hydrophobic natural deep eutectic solvents were first evaluated as analyte protectants and those with decanoic acid or lactic acid as hydrogen bond donor were demonstrated to be effective in compensating for the matrix effects of pyrethroids in the gas chromatography system. Hence, they were added to solvent standards for correcting the quantitation errors instead of matrix-matched calibration standards. Then the abilities of these acid-based deep eutectic solvents to extract pyrethriods from tomatoes were evaluated. Results showed the recoveries of all pyrethroids reached to over 80% with only 5 mL menthol:decanoic acid (1:1) used, and good phase separation was easily achieved without the addition of inorganic salt in the extraction step, indicating hydrophobic natural deep eutectic solvent could be a green substitute for acetonitrile in the quick, easy, cheap, effective, rugged, and safe extraction. Compared with the conventional method, the proposed protocol improved the recoveries, reduced the matrix effects, and simplified the extraction step, demonstrating to be an effective, fast, and green method.

Viscosity of nanofluids containing anisotropic particles: A critical review and a comprehensive model.

Compared to nanofluids with spherical particles, nanofluids with anisotropic particles possess higher thermal conductivity and present a better enhancement option in heat transfer applications. The viscosity variation of such nanofluids becomes of great importance in evaluating their pumping power in thermal systems. This paper presents a comprehensive review of the experimental and theoretical studies on the viscosity of nanofluids with anisotropic particles. The internal mechanisms of viscosity evolution are investigated considering three aspects: particle clustering, particle interactions, and Brownian motion. In experimental studies, important factors including classification and synthetic methods for particle preparation, base fluid, particle loading, particle shape and size, temperature, p H, shear stress and electric field are investigated in detail. Classical theoretical models and empirical relations of the effective viscosity of suspensions are discussed. Some crucial factors such as maximum particle packing fraction, fractal index and intrinsic viscosity models, are examined. A comparison of predictions and experimental results shows that the classical models underestimate suspension viscosity. A comprehensive combination of the modified Krieger-Dougherty (K-D) model with intrinsic viscosity relations for different aspect ratios is suggested for low particle loadings, and the modified Maron-Pierce model (M-D) is recommended for high particle loadings. Possible directions for future works are discussed.

Influence of anisotropic nanoparticles on the deposition pattern of an evaporating droplet.

The suppression or enhancement of the "coffee ring" effect depends on whether nanoparticles easily adhere to the gas-liquid interface and particle shape. To obtain deposition patterns of suspensions of nanoparticles strongly deviating from spheres, which is less studied in the literature, prolate ellipsoidal and cylindrical rod-shaped particles with a minimum aspect ratio of 4 are selected. Dynamic viscosity, which is a function of particle shape and volume fraction, is introduced into the evolution equations for film thickness and particle concentration. The nanoparticle deposition features and the contact line dynamics are examined numerically, and the effect of particle shape on the drying process is analysed. The results show that the contact line is in the depinning state during the droplet shrinkage, while the concentration and effective layer thickness of nanoparticles in the ring-formation region decrease with time, and the deposition band widens. The deposition ring height increases, and the recession of the contact line slows down with increasing aspect ratio. This means that for nanoparticles deviating strongly from spheres and not easily adhering to the gas-liquid interface, the "coffee ring" effect is enhanced when the suspension dries. A larger aspect ratio leads to a more obvious "coffee ring" feature.

Coalescence of droplets laden with insoluble surfactant on a preset liquid film.

A model for the evolution of two droplets laden with insoluble surfactant coalescing on a preset film is established according to the lubrication theory, and the coalescence processes are simulated. The role of the surfactant and its inherent mechanism are investigated, the effects of the Marangoni number, the preset liquid film thickness and the initial spacing between the two droplets on the coalescence are examined. The results show that the droplets encounter each other, gradually overlap, and finally coalesce into a "new" droplet. The Marangoni effect is beneficial to the convergence of the two inner leading fronts of the droplets in the early stage, but it hinders the accumulation of the droplets and subsequent coalescence. Increasing the Marangoni number promotes not only the aforementioned inhibition, but also the convergence of the two leading fronts towards the center, which speeds up the coalescence of the surfactant. Moreover, the diffusion of the surfactant towards the outsides of the droplets is accelerated; hence, its distribution along the droplet surface is more uniform after the coalescence. The droplets and the surfactant undertake a longer "journey" to achieve coalescence when their initial spacing is increased; increasing the preset film thickness shortens the time of coalescence required.

Identifying the proton transfer reaction mechanism via a proton-bound dimeric intermediate for esomeprazoles by a kinetic method combined with density functional theory calculations.

RATIONALE: Esomeprazole analogs are a class of important proton pump inhibitors for the treatment of gastro-esophageal reflux diseases. Understanding the fragmentation reaction mechanism of the protonated esomeprazole analogs will facilitate the characterization of their complex metabolic fate in humans. In this paper, the kinetic method and theoretical calculations were applied to evaluate the fragmentation of protonated esomeprazole analogs. METHODS: All collision-induced dissociation (CID) mass spectrometry experiments were carried out using electrospray ionization (ESI) ion trap mass spectrometry in positive ion mode. Also the accurate masses of fragments were measured on by ESI quadrupole time-of-flight (QTOF) MS in positive ion mode. Theoretical calculations were carried out by the density functional theory (DFT) method with the 6-31G(d) basis set in the Gaussian 03 program. RESULTS: In the fragmentation of the protonated esomeprazole analogs, C-S bond breakage is observed, which gives rise to protonated 2-(sulfinylmethylene)pyridines and protonated benzimidazoles. DFT calculations demonstrate that the nitrogen atom of the pyridine part is the thermodynamically most favorable protonation site, and the C-S bond cleavage is triggered by the transfer of this ionizing proton from the nitrogen atom of the pyridine part to the carbon atom of the benzimidazole part to which the sulfinyl is attached. Moreover, with the kinetic plot, the intensity ratios of two protonated product ions yield a linear relationship with the differences in proton affinities of the corresponding neutral molecules, which provides strong experimental evidence that the reaction proceeds via proton-bound 2-(sulfinylmethylene)pyridine/benzimidazole complex intermediates. CONCLUSIONS: The kinetic method combined with theoretical calculations was successfully applied to probe the proton transfer reaction by proton-bound 2-(sulfinylmethylene)pyridine/benzimidazole complexes in the fragmentation of protonated esomeprazole analogs by ESI CID MS, which is a strong evidence that the kinetic method can be applied in identifying a proton-bound dimeric intermediate in the fragmentation of protonated ions.

Ultrasound-assisted magnetic solid-phase extraction based ionic liquid-coated Fe3O4@graphene for the determination of nitrobenzene compounds in environmental water samples.

An ultrasound-assisted magnetic solid-phase extraction procedure with the [C7MIM][PF6] ionic liquid-coated Fe3O4-grafted graphene nanocomposite as the magnetic adsorbent has been developed for the determination of five nitrobenzene compounds (NBs) in environmental water samples, in combination with high performance liquid chromatography-photodiode array detector (HPLC-PDA). Several significant factors that affect the extraction efficiency, such as the types of magnetic nanoparticle and ionic liquid, the volume of ionic liquid and the amount of magnetic nanoparticles, extraction time, ionic strength, and solution pH, were investigated. With the assistance of ultrasound, adsorbing nitrobenzene compounds by ionic liquid and self-aggregating ionic liquid onto the surface of the Fe3O4-grafted graphene proceeded synchronously, which made the extraction achieved the maximum within 20 min using only 144 µL [C7MIM][PF6] and 3 mg Fe3O4-grafted graphene. Under the optimized conditions, satisfactory linearities were obtained for all NBs with correlation coefficients larger than 0.9990. The mean recoveries at two spiked levels ranged from 80.35 to 102.77%. Attributed to the convenient magnetic separation, the Fe3O4-grafted graphene could be recycled many times. The proposed method was demonstrated to be feasible, simple, solvent-saving and easy to operate for the trace analysis of NBs in environmental water samples.

Solid-phase extraction based on chloromethylated polystyrene magnetic nanospheres followed by gas chromatography with mass spectrometry to determine phthalate esters in beverages.

An ultrasound-assisted magnetic solid-phase extraction procedure with chloromethylated polystyrene-coated Fe3 O4 nanospheres as magnetic adsorbents has been developed to determine eight phthalate esters (bis(4-methyl-2-pentyl) phthalate, dipentyl phthalate, dihexyl phthalate, benzyl butyl phthalate, bis(2-butoxyethyl) phthalate, dicyclohexyl phthalate, di-n-octyl phthalate, and dinonyl phthalate) simultaneously in beverage samples, in combination with gas chromatography coupled to tandem mass spectrometry for the first time. Several factors related to magnetic solid-phase extraction efficiencies, such as amount of adsorbent, extracting time, ionic strength, and desorption conditions were investigated. The enrichment factors of the method for the eight analytes were over 2482. A good linearity was observed in the range of 10-500 ng/L for bis(2-butoxyethyl) phthalate and 2-500 ng/L for the other phthalate esters with correlation coefficients ranging from 0.9980 to 0.9998. The limits of detection and quantification for the eight phthalate esters were in the range of 0.20-2.90 and 0.67-9.67 ng/L, respectively. The mean recoveries at three spiked levels were 75.8-117.7%, the coefficients of variations were <11.6%. The proposed method was demonstrated to be a simple and efficient technique for the trace analysis of the phthalate esters in beverage samples.

Screening and identification of antibacterial components in Artemisia argyi essential oil by TLC-direct bioautography combined with comprehensive 2D GC × GC-TOFMS.

One of the primary components that contribute to Artemisia argyi 's effectiveness is essential oil, which has an exceptional antibacterial effect that has been well documented. The actual cause of its antibacterial activity and associated mechanism, however, are still not completely understood. For the first time, comprehensive two-dimensional gas chromatography coupled with time-of-flight mass spectrometry (2D GC × GC-TOFMS) and thin-layer chromatography-direct bioautography (TLC-DB) were employed to investigate its antibacterial components. The antibacterial properties of A. argyi essential oil were investigated, and the antibacterial activity of six compounds was evaluated, using Staphylococcus aureus (S. aureus) and Escherichia coli (E. coil) as test microorganisms. TLC-direct bioautography was used to screen two bioactive clusters. Following 2D GC × GC-TOFMS identification of bioactive clusters, six compounds were evaluated for in vitro antibacterial activity verification. All the components tested displayed antibacterial action. Results showed that α-terpineol and eugenol had high potent antibacterial activity (MIC＜0.62 mg/mL, IC50＜2.00 mg/mL). For complex essential oils from traditional Chinese medicine, this method is efficient for quick screening and identifying antibacterial compounds.

Single electron redox via an ion-neutral complex in the fragmentation of protonated benzoylferrocenes.

RATIONALE: Ferrocene derivatives have become very popular molecules for biological applications. Although considerable experimental and theoretical calculation studies have demonstrated that ferrocene derivatives are easily oxidized during electrospray ionization (ESI), the details of the single electron redox reaction for protonated benzoylferrocenes in collision-induced dissociation (CID) mass spectrometry (MS) has not been obtained. Characterizing this mechanism is useful for further understanding the properties of ferrocene-containing biomaterials. METHODS: All CID MS experiments were carried out using ESI ion trap mass spectrometry in positive ion mode. In addition, the accurate mass of fragments was measured on a ESI quadrupole time-of-flight (QTOF) mass spectrometer in positive ion mode. Theoretical calculations were carried out by the density functional theory (DFT) method with a hybrid basis set consisting of 6-31G (d) and ECP LanL2DZ in the Gaussian 03 program. RESULTS: In the fragmentation of protonated benzoylferrocenes, the characterized ferrocinium cation was observed, which was proposed from the cleavage of the bond between the ipso-carbon atom and the carbonyl carbon followed by a single electron redox in [substituted benzoyl/ferrocene] complexes. Moreover, when the complex contained an oxidant (substituted benzoyl cation) with higher electron affinity, the single electron redox reaction was more efficient. A correlation was established between the intensities of the two competitive product ions and the electron affinities of substituted benzoyl cations. CONCLUSIONS: The single electron redox reaction by the [substituted benzoyl/ferrocene] complexes was proposed by CID MS and theoretical calculations, which provided potential evidence to further understand the reversible reduction characteristics of ferrocene-containing biomaterials.

Ultrasound-assisted magnetic SPE based on Fe3O4-grafted graphene for the determination of polychlorinated biphenyls in water samples.

An ultrasound-assisted magnetic SPE procedure with an Fe3 O4 -grafted graphene nanocomposite as the magnetic adsorbent has been developed to determine seven polychlorinated biphenyls (PCBs; PCB28, PCB52, PCB101, PCB118, PCB138, PCB153, and PCB180) simultaneously in 200 mL environmental water samples, in combination with GC-MS/MS. Several factors related to magnetic SPE efficiencies, such as the superparamagnetic intensity and amount of adsorbent, extraction time, sample pH, and desorption conditions were investigated. With the assistance of ultrasound, the extraction achieved the maximum within only 20 s, attributed to the powerful adsorptive ability of the magnetic adsorbent toward the PCBs. Under the optimized conditions, an excellent linearity was observed in the range of 0.1-100 ng/L for PCB28, 0.2-100 ng/L for PCB52, and 0.5-100 ng/L for the other five PCBs with the correlation coefficients ranging from 0.9988 to 0.9996. The mean recoveries at spiked levels of 5.0 and 10.0 ng/L were 84.9-108.5%, the coefficients of variations were <6.5%. With convenient magnetic separation, the synthesized magnetic adsorbent could be recycled more than ten times. The proposed method was demonstrated to be feasible, simple, rapid, and easy to operate for the trace analysis of the PCBs in environmental water samples.

Comprehensive two-dimensional countercurrent chromatography × gas chromatography characterization of Artemisia argyi essential oil.

A comprehensive two-dimensional (2D) countercurrent chromatography (CCC) × gas chromatography (GC) was investigated for characterization of chemical constituents of Artemisia argyi essential oil, and orthogonality for the 2D chromatographic system was evaluated. A solvent system composed of n-hexane/acetonitrile/methanol (2:2:1, v/v/v) was selected for first dimensional separation of Artemisia argyi essential oil. Then all CCC fractions were analyzed by GC, which provided a wealth of information regarding the composition of the essential oil. Visualization of chemical compositions obtained from the comprehensive 2D CCC × GC separation was achieved by creation of a 2D contour plot map. Total peak capacity was evaluated and approximately 1392 peaks were obtained through a comprehensive 2D CCC × GC separation. A high spatial coverage and a low linear correlation coefficient were achieved. Meanwhile, all compounds were identified by GC-MS. The obtained 2D contour plot could be divided into six zones to show the characteristic chemical compositions. Six zones could be divided into different component groups, including monoterpenes, sesquiterpenes, monoterpene alcohols, phenols, aldehydes, ketones and esters, which could be used to identify compounds that have not been reported, and to predict the structure of unknown compounds in Artemisia argyi essential oil and comprehensively characterize fingerprint peak.

Screening of glycoside isomers in P. scrophulariiflora using ionic liquid-based ultrasonic-assisted extraction and ultra-performance liquid chromatography/electrospray ionization quadrupole time-of-flight tandem mass spectrometry.

A powerful ionic liquid-based ultrasonic-assisted extraction (ILUAE) method combined with ultra-performance liquid chromatography coupled to electrospray ionization quadrupole time-of-flight tandem mass spectrometry (UPLC/ESI-QTOFMS(n) ) was employed in the rapid simultaneous screening of iridoid glycosides, phenylethanoid glycosides, and cucurbitacin glycosides from P. scrophulariiflora. The ILUAE procedure was optimized over several ultrasonic parameters, including the ultrasonic power, concentration of the ionic liquid, and solid-liquid ratio. A comparison with conventional heat-reflux extraction and regular UAE demonstrated that the optimized approach yielded a high extraction efficiency (Picroside I, 2.84%; Picroside II, 3.57%; 6-O-E-feruloyl catalpol, 2.20%) within a short extraction time of 30 min. Negative ion mode ESI-QTOFMS(2) analysis of the fragmentation reactions of the [M-H](-) ions was conducted to characterize the diagnostic ions related to the glycosyl moieties, aglycone units, and the type and substituted position of the ester groups. Interestingly, the positional isomers of the iridoid glycosides could be easily discriminated based on the characteristic ions. A total of 15 glycosides, including three groups of iridoid glycoside isomers and two groups of phenylethanoid glycoside isomers, were conveniently identified within 13.5 min. Moreover, 6'-O-vanilloyl catalpol was identified in P. scrophulariiflora for the first time. The method developed here was further validated by measuring the recovery, correlation coefficient (R(2) ), and reproducibility (RSD, n = 5) of three iridoid glycosides: 89.60%-109.02%, 0.9991-0.9998, and 0.93%-1.44%, respectively. This study demonstrated the capabilities of ILUAE combined with UPLC/ESI-QTOFMS(n) for the rapid screening of glycosides in P. scrophulariiflora. This method offers an approach to similar studies on other natural plants.

The redistribution and migration mechanism of nitrogen in the hydrothermal co­carbonization process of sewage sludge and lignocellulosic wastes.

Blending lignocellulosic wastes (such as cornstalk, CS) into sewage sludge (SS) for hydrothermal carbonization (HTC) could contribute to the importance of the hydrothermal solid product (hydrochar) as a substitute for fossil fuel. However, the interactions between SS and CS changed the fate of Nitrogen (N), affecting the clean combustion utilization of hydrochar. This study focused on the influence of SS-CS interactions on the redistribution and migration behavior of N during the co-HTC process by tuning the mass ratio of SS to CS (SS:CS), reaction temperature, and residence time. Under the hydrothermal condition of 220 °C, 2 h, and SS:CS = 1:1, the high heating value of hydrochar and the energy recovery efficiency (ERE) respectively reached 15.89 MJ/kg and 71.19%. Further raising the temperature to 250 °C, the hydrochar was enhanced in the coalification degree, whereas ERE decreased to 61.86%. Part of the amino-N in sludge organics was fractured during the co-HTC process and reacted with carbohydrate and intermediate products, such as 5-hydroxymethylfurfural, which degraded from CS, to generate heterocyclic-N compounds (including pyridine, pyrrole, and pyrazine). The remaining amino-N formed pyridine-N, pyrrole-N, and quaternary-N through various solid-solid conversions. The heterocyclic-N polymerized and formed melanoidins, which thereafter polymerized with aromatic clusters to form the N-containing polyaromatic char. Therefore, the N retention rate (NRR) was enhanced and showed a synergistic effect. NRR was increased by raising the proportion of CS or extending time, reaching 57.02% at SS:CS = 1:1 and 8 h. Conversely, rising temperatures resulted in a downward trend of NRR with a phased increase at 220 °C-250 °C.

Accelerated prion disease pathogenesis in Toll-like receptor 4 signaling-mutant mice.

Prion diseases such as scrapie involve the accumulation of disease-specific prion protein, PrP(Sc), in the brain. Toll-like receptors (TLRs) are a family of proteins that recognize microbial constituents and are central players in host innate immune responses. The TLR9 agonist unmethylated CpG DNA was shown to prolong the scrapie incubation period in mice, suggesting that innate immune activation interferes with prion disease progression. Thus, it was predicted that ablation of TLR signaling would result in accelerated pathogenesis. C3H/HeJ (Tlr4(Lps-d)) mice, which possess a mutation in the TLR4 intracellular domain preventing TLR4 signaling, and strain-matched wild-type control (C3H/HeOuJ) mice were infected intracerebrally or intraperitoneally with various doses of scrapie inoculum. Incubation periods were significantly shortened in C3H/HeJ compared with C3H/HeOuJ mice, regardless of the route of infection or dose administered. At the clinical phase of disease, brain PrP(Sc) levels in the two strains of mice showed no significant differences by Western blotting. In addition, compared with macrophages from C3H/HeOuJ mice, those from C3H/HeJ mice were unresponsive to fibrillogenic PrP peptides (PrP residues 106 to 126 [PrP(106-126)] and PrP(118-135)) and the TLR4 agonist lipopolysaccharide but not to the TLR2 agonist zymosan, as measured by cytokine production. These data confirm that innate immune activation via TLR signaling interferes with scrapie infection. Furthermore, the results also suggest that the scrapie pathogen, or a component(s) thereof, is capable of stimulating an innate immune response that is active in the central nervous system, since C3H/HeJ mice, which lack the response, exhibit shortened incubation periods following both intraperitoneal and intracerebral infections.

Complete chloroplast genome of Castanopsis sclerophylla (Lindl.) Schott: Genome structure and comparative and phylogenetic analysis.

Castanopsis sclerophylla (Lindl.) Schott is an important species of evergreen broad-leaved tree in subtropical areas and has high ecological and economic value. However, there are few studies on its chloroplast genome. In this study, the complete chloroplast genome sequence of C. sclerophylla was determined using the Illumina HiSeq 2500 platform. The complete chloroplast genome of C. sclerophylla is 160,497 bp long, including a pair of inverted repeat (IR) regions (25,675 bp) separated by a large single-copy (LSC) region of 90,255 bp and a small single-copy (SSC) region of 18,892 bp. The overall GC content of the chloroplast genome is 36.82%. A total of 131 genes were found; of these, 111 genes are unique and annotated, including 79 protein-coding genes, 27 transfer RNA genes (tRNAs), and four ribosomal RNA genes (rRNAs). Twenty-one genes were found to be duplicated in the IR regions. Comparative analysis indicated that IR contraction might be the reason for the smaller chloroplast genome of C. sclerophylla compared to three congeneric species. Sequence analysis indicated that the LSC and SSC regions are more divergent than IR regions within Castanopsis; furthermore, greater divergence was found in noncoding regions than in coding regions. The maximum likelihood phylogenetic analysis showed that four species of the genus Castanopsis form a monophyletic clade and that C. sclerophylla is closely related to Castanopsis hainanensis with strong bootstrap values. These results not only provide a basic understanding of Castanopsis chloroplast genomes, but also illuminate Castanopsis species evolution within the Fagaceae family. Furthermore, these findings will be valuable for future studies of genetic diversity and enhance our understanding of the phylogenetic evolution of Castanopsis.

Preparing coal slurry from coking wastewater to achieve resource utilization: Slurrying mechanism of coking wastewater-coal slurry.

Coking wastewater is used to prepare coal slurry, which can be used as combustion and gasification fuel. This promising technology simultaneously achieves resource utilization and wastewater management. Slurrying properties are essential to the industrial application of coal slurry. These properties are considerably influenced by coal surface properties and the adsorption of an additive by coal. In this study, the effects of the internal components (e.g., phenol, ammonia nitrogen, and metal ions) of coking wastewater on the adsorption of an additive by coal and on coal surface properties were measured. Results showed that the competitive adsorption between phenol and the additive reduced the amount of additive adsorbed on coal. However, phenol acted as an additive to improve the wettability of coal particles. Cations (Ca2+, NH4+, and Na+) adversely affected the slurrying because they weakened the negative charges of coal. Furthermore, a large amount of water was adsorbed due to the ionic bonding effects, thereby reducing the free water in the coal slurry system. The maximum slurrying concentration of CWCS was 0.8 percentage points higher than that of CWS, suggesting that coking wastewater enhanced the slurrying capability of the coal slurry by integrating the various effects induced by the different internal components.

The complete chloroplast genome of Castanopsis carlesii (Hemsl.) Hay.

Castanopsis carlesii (Hemsl.) Hay. is a widely distributed and dominant tree species with significant ecological and economical values. In this study, the complete chloroplast genome sequence of C. carlesii was reported using the Illumina Hiseq 2500 platform. The complete chloroplast genome was 160,205 bp forming a typical quadripartite structure, with a pair of inverted repeated (IRs) regions of 25,670 bp, a large single copy (LSC) region of 89,849 bp, and a small single copy (SSC) region of 19,016 bp. A total of 124 functional genes were annotated, including 79 protein-coding genes, 37 tRNA genes, and eight rRNA genes. The ML phylogenetic analysis showed that the genus Castanopsis formed a clade except Castanopsis fargesii.

CpG oligodeoxynucleotide-enhanced humoral immune response and production of antibodies to prion protein PrPSc in mice immunized with 139A scrapie-associated fibrils.

Prion diseases are characterized by conversion of the cellular prion protein (PrP(C)) to a protease-resistant conformer, the srapie form of PrP (PrP(Sc)). Humoral immune responses to nondenatured forms of PrP(Sc) have never been fully characterized. We investigated whether production of antibodies to PrP(Sc) could occur in PrP null (Prnp(-/-)) mice and further, whether innate immune stimulation with the TLR9 agonist CpG oligodeoxynucleotide (ODN) 1826 could enhance this process. Whether such stimulation could raise anti-PrP(Sc) antibody levels in wild-type (Prnp(+/+)) mice was also investigated. Prnp(-/-) and Prnp(+/+) mice were immunized with nondenatured 139A scrapie-associated fibrils (SAF), with or without ODN 1826, and were tested for titers of PrP-specific antibodies. In Prnp(-/-) mice, inclusion of ODN 1826 in the immunization regime increased anti-PrP titers more than 13-fold after two immunizations and induced, among others, antibodies to an N-terminal epitope, which were only present in the immune repertoire of mice receiving ODN 1826. mAb 6D11, derived from such a mouse, reacts with the N-terminal epitope QWNK in native and denatured forms of PrP(Sc) and recombinant PrP and exhibits a K(d) in the 10(-)(11) M range. In Prnp(+/+) mice, ODN 1826 increased anti-PrP levels as much as 84% after a single immunization. Thus, ODN 1826 potentiates adaptive immune responses to PrP(Sc) in 139A SAF-immunized mice. These results represent the first characterization of humoral immune responses to nondenatured, infectious PrP(Sc) and suggest methods for optimizing the generation of mAbs to PrP(Sc), many of which could be used for diagnosis and treatment of prion diseases.

Linear stability analysis of magnetohydrodynamic duct flows with perfectly conducting walls.

The stability of magnetohydrodynamic flow in a duct with perfectly conducting walls is investigated in the presence of a homogeneous and constant static magnetic field. The temporal growth and spatial distribution of perturbations are obtained by solving iteratively the direct and adjoint governing equations with respect of perturbations, based on nonmodal stability theory. The effect of the applied magnetic field, as well as the aspect ratio of the duct on the stability of the magnetohydrodynamic duct flow is taken into account. The computational results show that, weak jets appear near the sidewalls at a moderate magnetic field and the velocity of the jet increases with the increase of the intensity of the magnetic field. The duct flow is stable at either weak or strong magnetic field, but becomes unstable at moderate intensity magnetic field, and the stability is invariance with the aspect ratio of the duct. The instability of magnetohydrodynamic duct flow is related with the exponential growth of perturbations evolving on the fully developed jets. Transient growth of perturbations is also observed in the computation and the optimal perturbation is found to be in the form of streamwise vortices and localized within the sidewall layers. By contrast, the Hartmann layer perpendicular to the magnetic field is irrelevant to the stability issue of the magnetohydrodynamic duct flow.