A Concrete Core Void Imaging Approach and Parameter Analysis of Concrete-Filled Steel Tube Members Using Travel Time Tomography: Multi-Physics Simulations and Experimental Studies.

Concrete-filled steel tube (CFST) members have been widely used in civil engineering due to their advanced mechanical properties. However, internal defects such as the concrete core voids and interface debonding in CFST structures are likely to weaken their load-carrying capacity and stiffness, which affects the safety and serviceability. Visualizing the inner defects of the concrete cores in CFST members is a critical requirement and a challenging task due to the obvious difference in the material mechanical parameters of the concrete core and steel tube in CFST members. In this study, a curved ray theory-based travel time tomography (TTT) with a least square iterative linear inversion algorithm is first introduced to quantitatively identify and visualize the sizes and positions of the concrete core voids in CFST members. Secondly, a numerical investigation of the influence of different parameters on the inversion algorithm for the defect imaging of CFST members, including the effects of the model weighting matrix, weighting factor and grid size on the void's imaging quality and accuracy, is carried out. Finally, an experimental study on six CFST specimens with mimicked concrete core void defects is performed in a laboratory and the mimicked defects are visualized. The results demonstrate that TTT can identify the sizes and positions of the concrete core void defects in CFST members efficiently with the use of optimal parameters.

Cyanocobalamin (VB12) Bionic Enzyme-Assisted Photocatalytic Chain-Growth Polymerization for Detection of Lung Cancer Biomarkers.

Cobalt-mediated radical polymerization is noted for its great level of control over the polymerization of acrylic and vinyl esters monomers, even at high molar mass. Vitamin B12, a natural bionic enzyme cobalt complex, involves the conversion of organic halides to olefins through chain-growth polymerization. In this work, the notion of R-Co(III) free radical persistent free radical effect and vitamin B12 circulation were first reported for the perception of ultralow abundance of microRNA-21, a lung cancer biomarker. Indeed, most Co-containing catalytic reactions can occur under mild conditions due to their minimal bond dissociation of the C-Co bond, with blue light irradiation. Based on the intrinsic stability of the vitamin B12 framework and recycling of the catalyst, it is evident that this natural catalytic scheme has potential applications in medicinal chemistry and biomaterials. In addition, this strategy, combined with highly specific recognition probes and vitamin B12 circulation-mediated chain-growth polymerization, has a detection limit as low as 910 aM. Furthermore, it is sensitive for sensing in serum samples containing biomarkers and shows great potential for RNA selection and amplification sensing in clinical samples.

Ileum tissue single-cell mRNA sequencing elucidates the cellular architecture of pathophysiological changes associated with weaning in piglets.

BACKGROUND: In mammals, transitioning from sole milk uptake to the intake of solid feed results in dramatic developmental changes in intestinal function and immunological status. In fact, weaning stress is often accompanied by intestinal inflammatory processes. To develop effective intervention strategies, it is necessary to characterize the developmental pattern and immune response that occurs on weaning, as we have done in this study for piglets. RESULTS: To comprehensively delineate cell heterogeneity in ileum tissues and the underlying mechanisms in weaning-induced intestinal inflammation of piglets, we have analyzed the transcriptomes of 42,149 cells from ileum mucosa of normally suckling and post-weaned piglets. There were 31 cell subtypes including epithelial, stromal, and immune cells. A bifurcating trajectory was inferred to separate secretory and absorptive lineages. Integrated cross-species datasets showed well-conserved cellular architectures and transcription signatures between human and pig. Comparative analyses of cellular components, cell-cell communications, and molecular states revealed that T cell subpopulations were significantly altered in weaned piglets. We found that T helper (Th) 17 functional plasticity across changes in the cytokine milieu and the enrichment of granzyme B (GZMB)-expressing cytotoxic T cells potentially exacerbate mucosal inflammation via mitochondrial dysfunction in epithelial cells. CONCLUSIONS: Our work has elucidated the single-cell molecular characteristics of the piglet ileum before and after weaning. We have provided an atlas that portrays the landscape of the intestinal pathophysiological inflammatory process associated with weaning, finding a level of conservation between human and pig that support the use of piglets as a model for human infants.

Mn-MOF catalyzed multi-site atom transfer radical polymerization electrochemical sensing of miRNA-21.

A green electrochemical biosensor was developed based on metal-organic framework (MOF)-catalyzed atom transfer radical polymerization (ATRP) for quantifying miRNA-21, used as the proof-of-concept analyte. Unlike conventional ATRP, Mn-PCN-222 (PCN, porous coordination network) could be used as an alternative for green catalyst to substitute traditional catalysts. First, poly (diallyldimethylammonium chloride) (PDDA) was fixed on the surface of the indium tin oxide (ITO) electrode, and then the Mn-PCN-222 was linked to ITO electrode via electrostatic binding with PDDA. Next, aminated ssDNA (NH2-DNA) was used to modify the electrode further by amide reaction with Mn-PCN-222. Then, the recognition and hybridization of NH2-DNA with miRNA-21 prompt the generation of DNA-RNA complexes, which further hybridize with Fc-DNA@ß-CD-Br15 and permit the initiator to be immobilized on the electrode surface. Accordingly, ß-CD-Br15 could initiate the polymerization of ferrocenylmethyl methacrylates (FcMMA) under the catalysis of MOF to complete the ATRP reaction. FcMMA presented a distinct electrochemical signal at ~ 0.33 V. Taking advantage of the unique multi-site properties of ß-CD-Br15 and the efficient catalytic reaction induced by Mn-PCN-222, ultrasensitive detection of miRNA-21 was achieved with a detection limit of 0.4 fM. The proposed electrochemical biosensor has been applied to the detection of miRNA-21 in serum samples. Therefore, the proposed strategy exhibited potential in early clinical biomedicine.

Facile Controlled Synthesis of Pd-ZnO Nanostructures for Nitrite Detection.

The electrocatalytic characteristics of nanostructures are significantly affected by surface structure. The strict regulation of structural characteristics is highly beneficial for the creation of novel nanocatalysts with enhanced electrocatalytic performance. This work reports a nitrite electrochemical sensor based on novel flower-like Pd-ZnO nanostructures. The Pd-ZnO nanocatalysts were synthesized through a simple hydrothermal method, and their morphology and structure were characterized via field-emission scanning electron microscopy (FE-SEM), X-ray photoelectron spectroscopy (XPS), and X-ray diffraction (XRD). Their electrocatalytical performance in the nitrite oxidation reaction was studied via cyclic voltammetry (CV) and the amperometric technique. Compared to pure ZnO and Pd nanoparticles, the Pd-ZnO nanostructures exhibited enhanced electrochemical performance in the nitrite oxidation reaction. In order to investigate the relationships between the structures of Pd-ZnO nanocatalysts and the corresponding electrocatalytic performances, different surface morphologies of Pd-ZnO nanocatalysts were fabricated by altering the solution pH. It was found that the flower-like Pd-ZnO nanostructures possessed larger effective surface areas and faster electron transfer rates, resulting in the highest electrocatalytic performance in the nitrite oxidation reaction. The designed nitrite sensor based on flower-like Pd-ZnO displayed a wide concentration linear range of 1 µM-2350 µM, a low detection limit of 0.2 µM (S/N of 3), and high sensitivity of 151.9 µA mM-1 cm-2. Furthermore, the proposed sensor exhibited perfect selectivity, excellent reproducibility, and long-time stability, as well as good performance in real sample detection.

Resonant Stimulated Photorefractive Scattering.

We present the first observations, and a complete theoretical explanation, of stimulated photorefractive scattering in a high- Q crystalline cavity. The standing-wave light field in the cavity induces an ultranarrow and long-lived Bragg grating through the photorefractive effect. The spatial phase of the grating is automatically matched to that of the standing wave. The scattering from the grating strengthens the standing wave, which then further reinforces the grating itself. Eventually, the mode is seen to split into a doublet, thereby disrupting the usual strict periodicity of the mode spectrum.

Efficient Degradation of 2,4-Dichlorophenol on Activation of Peroxymonosulfate Mediated by MnO2.

Sulfate radical based-advanced oxidation process has received increasing interest in the remediation of wastewater and contaminated soil. In this study, degradation of 2, 4-dichlorophenol (2, 4-DCP) was investigated over peroxymonosulfate (PMS) activation by MnO2, which was prepared by liquid-phase oxidation method. The prepared MnO2 was characterized by transition electron microscopy, X-ray diffraction, N2 adsorption-desorption, and X-ray photoelectron spectroscopy. Characterization results showed that α-MnO2 exhibited the highest surface area and Mn (III) content. The PMS activation by MnO2 in 2, 4-DCP degradation followed the order of α-MnO2 > γ-MnO2 > ß-MnO2, which is dependent on the properties of MnO2 including crystal structure, surface area and Mn (III) content. Influences of initial concentration of 2, 4-DCP, PMS and MnO2 dosage, pH and co-existing inorganic ions on the degradation were examined. Electron paramagnetic resonance (EPR) and quenching experiments with ethanol and tert-butanol suggested that sulfate radicals were the dominant radicals in the process. Findings in this study indicated that α-MnO2 was an attractive catalyst for activation of PMS to degrade 2, 4-DCP in aqueous solution.

Efficient removal of three dyes using porous covalent triazine frameworks: adsorption mechanism and role of pore distribution.

Dyes are widely used in production and life. In this study, porous covalent triazine frameworks (CTFs) were synthesized and the adsorption behavior for three dyes was investigated by batch adsorption experiments. CTFs were characterized by various spectroscopic techniques for structure, porosity and surface properties. Several possible adsorption mechanisms were proposed including pore-filling, electrostatic attraction and hydrogen bonding interaction with the triazine structure of CTFs. The mechanisms were further verified by the pore size distribution and pH dependence. Additionally, CTFDCBP displayed stronger adsorption affinity and faster adsorption kinetics for dyes, because of the wide pore size distribution. This study provides a new insight into the mesoporous CTFs, which exhibit great potential as an effective adsorbent for dye removal.

High-performance millimeter-wave synergetic optoelectronic oscillator with regenerative frequency-dividing oscillation technique.

A novel millimeter-wave synergetic optoelectronic oscillator based on regenerative frequency-dividing oscillation and phase-locking techniques is proposed and experimentally demonstrated. The regenerative frequency-dividing oscillator is embedded for millimeter-wave frequency division, and then synergistically oscillates with the optoelectronic oscillator (OEO) due to injection-locking effect. The phase-locking stabilization technique is skillfully utilized in millimeter-wave OEO via commercial analog phase shifter. As a result, a 40-GHz signal is generated featuring low phase noise, high stability and low spurs. The single-sideband phase noise is about -117 dBc/Hz at 10-kHz offset frequency and the spurious suppression ratio reaches more than 80 dBc. The measured overlapping Allan deviation of the proposed synergetic OEO reaches lower than 10-13 at 1024-s averaging time, which is five orders of magnitude lower than free-running millimeter-wave OEO.

Frequency-demultiplication OEO for stable millimeter-wave signal generation utilizing phase-locked frequency-quadrupling.

A novel scheme for the generation and stabilization of the millimeter-wave (mmW) signal employing a frequency-demultiplication optoelectronic oscillator (FD-OEO) has been theoretically analyzed and experimentally demonstrated. The FD-OEO can keep sustaining without optical first-order sidebands, which would help to simplify the photonic-assisted frequency multiplication process and provide a wide frequency compensation range for the mmW system simultaneously. The stability of the generated 40-GHz mmW signal reaches 1.38 × 10-12 at the average time of 100s. Besides, the measured single-sideband phase noise of the generated mmW signal exhibits as low as -103 dBc/Hz at 10-kHz offset frequency, maintaining a spurious level of -97 dBc.

Supermode noise suppression with mutual injection locking for coupled optoelectronic oscillator.

The coupled optoelectronic oscillator (COEO) is typically used to generate high frequency spectrally pure microwave signal with serious sidemodes noise. We propose and experimentally demonstrate a simple scheme for supermode suppression with mutual injection locking between the COEO (master oscillator with multi-modes oscillation) and the embedded free-running oscillator (slave oscillator with single-mode oscillation). The master and slave oscillators share the same electrical feedback path, which means that the mutually injection-locked COEO brings no additional hardware complexity. Owing to the mode matching and mutually injection locking effect, 9.999 GHz signal has been successfully obtained by the mutually injection-locked COEO with the phase noise about -117 dBc/Hz at 10 kHz offset frequency. Besides, the supermode noise can be significantly suppressed more than 50 dB to below -120 dBc.

Adsorption of phosphate ions from aqueous solutions by a CeO2 functionalized Fe3O4@SiO2 core-shell magnetic nanomaterial.

Phosphate is generally considered to be one of the nutrients for plants which may cause eutrophication of the aquatic environment. In this study, a CeO2-functionalized Fe3O4@SiO2 core-shell magnetic nanomaterial (denoted as Fe3O4@SiO2-CeO2) was prepared and used as the adsorbent to remove phosphate from water. The adsorbents were characterized by X-ray diffraction, transmission electron microscopy, X-ray photoelectron spectroscopy, and N2 adsorption/desorption isotherms. Characterization results show that the particle size is around 8.63 nm, Brunauer-Emmett-Teller (BET) surface area is 179.7 m2 · g-1 and the pore volume is 0.39 cm3 · g-1 for magnetite Fe3O4@SiO2-CeO2. The adsorbents could be rapidly separated under an external magnetic field. Batch adsorption tests show that the Fe3O4@SiO2-CeO2 adsorbent exhibited high adsorption affinity for phosphate. Additionally, phosphate adsorption isotherms over the adsorbents could be well described by the Langmuir model, suggesting monolayer adsorption, and phosphate adsorption kinetics followed the pseudo-second-order kinetics. Moreover, increasing pH led to suppressed phosphate adsorption, and phosphate adsorption slightly increased with ionic strength.

Effects and bioaccumulation of 17ß-estradiol and 17α-ethynylestradiol following long-term exposure in crucian carp.

Bioaccumulation and effects of 17ß-estradiol (E2) and 17α-ethynylestradiol (EE2) were assessed by crucian carp (Carassius auratus) following single and binary mixture exposures in flow-through exposure system for 16 months. In comparison with water control (DWC) and solvent control (SC), a significant reduction in body weight, body length and gonadosomatic index (GSI), and increase in hepatosomatic index (HSI) and plasma vitellogenin (VTG) levels were observed, in a time- and concentration-dependent manner. Bioconcentration factors (BCFs) of E2 and EE2 in fish muscle ranged from 3.2 to 40 and from 64 to 123, respectively. Crucian carp were found to be more sensitive to EE2 than E2. The bioaccumulation and toxicological effects in binary mixture exposed fish (mixture of E2 and EE2) were more significant than exposure of individual compound. Crucian carp is sensitive to E2 and EE2 in long-term laboratory exposure experiments and can be used as a potential model species for investigating the toxicity of hormones.

An electrochemical biosensor for the amplification of thrombin activity by perylene-mediated photoinitiated polymerization.

BACKGROUND: Thrombin, a coagulation system protease, is a key enzyme involved in the coagulation cascade and has been developed as a marker for coagulation disorders. However, the methods developed in recent years have the disadvantages of complex operation, long reaction time, low specificity and sensitivity. Meanwhile, thrombin is at a lower level in the pre-disease period. Therefore, to accurately diagnose the disease, it is necessary to develop a fast, simple, highly sensitive and specific method using signal amplification technology. RESULTS: We designed an electrochemical biosensor based on photocatalytic atom transfer radical polymerization (photo-ATRP) signal amplification for the detection of thrombin. Sulfhydryl substrate peptides (without carboxyl groups) are self-assembled to the gold electrode surface via Au-S bond and serve as thrombin recognition probes. The substrate peptide is cleaved in the presence of thrombin to generate -COOH, which can form a carboxylate-Zr(IV)-carboxylate complex via Zr(IV) and initiator (α-bromophenylacetic acid, BPAA). Subsequently, an electrochemical biosensor was prepared by introducing polymer chains with electrochemical signaling molecules (ferrocene, Fc) onto the electrode surface by photocatalytic (perylene, Py) mediated ATRP using ferrocenylmethyl methacrylate (FMMA) as a monomer. The concentration of thrombin was evaluated by the voltammetric signal generated by square wave voltammetry (SWV), and the result showed that the biosensor was linear between 1.0 ng/mL âˆ¼ 10 fg/mL, with a lower detection limit of 4.0 fg/mL (∼0.1 fM). Moreover, it was shown to be highly selective for thrombin activity in complex serum samples and for thrombin inhibition screening. SIGNIFICANCE: The biosensor is an environmentally friendly and economically efficient strategy while maintaining the advantages of high sensitivity, anti-interference, good stability and simplicity of operation, which has great potential for application in the analysis of complex samples.

Ultrasensitive miRNA-21 Biosensor Based on Zn(TCPP) PET-RAFT Polymerization Signal Amplification and Multiple Logic Gate Molecular Recognition.

Quantitative measurement of microRNAs (miRNAs) is extremely important in plenty of biomedical applications especially cancer diagnosis but remains a great challenge. In this work, we developed a logic gate recognition biosensing platform based on the "trinity" molecular recognition mode for quantifying miRNAs with a detection limit of 4.48 aM, along with a linear range from 0.1 nM to 10 aM under optimal experimental conditions. In order to obtain excellent detection performance, we adopted a Zn(TCPP) photocatalytic electron transfer reversible addition-fragmentation chain transfer (PET-RAFT) polymerization signal amplification strategy. The light-induced PET-RAFT has developed green applications of free radical polymerization in the field of biosensors. This is the first report on the preparation of signal amplification biosensors using PET-RAFT for tumor marker detection. With the outstanding detection performance, we can apply the sensor system to the early screening of lung cancer patients.

Enhanced photocatalytic reduction of aqueous Pb(II) over Ag loaded TiO2 with formic acid as hole scavenger.

In the present study, photocatalytic Pb(II) reduction over TiO(2) and Ag/TiO(2) catalysts in the presence of formic acid was explored to eliminate Pb(II) pollution in water. Ag/TiO(2) catalysts were prepared by the photo-deposition method and characterized using UV-Vis diffuse reflectance spectra, X-ray reflection diffraction, transmission electron microscopy and X-ray photoelectron spectroscopy. Ag deposition on TiO(2) led to enhanced photocatalytic Pb(II) reduction and the Ag/TiO(2) catalyst with a Ag loading amount of 0.99 wt.% exhibited the optimum photocatalytic activity. For Pb(II) reduction over Ag/TiO(2) with a Ag loading amount of 0.99 wt.%, initial Pb(II) reduction rate was found to be dependent on the initial concentrations of formic acid and Pb(II). Increasing initial Pb(II) concentration led to linearly increased initial Pb(II) reduction rate. At low formic acid concentration, in parallel, initial Pb(II) reduction rates increased with formic concentration, but remained nearly identical at high formic acid concentration. Solution pH impacted the photocatalytic Pb(II) reduction and after irradiation for 100 min Pb(II) was removed by 11.8%, 91.2% and 98.6% at pH of 0.8, 2.0 and 3.5, respectively, indicative of enhanced Pb(II) reduction with pH in the tested pH range. The results showed that Ag/TiO(2) displayed superior catalytic activity to TiO(2), highlighting the potential of using Ag/TiO(2) as a more effective catalyst for photocatalytic Pb(II) reduction.

High sensitive electrochemical methamphetamine detection in serum and urine via atom transfer radical polymerization signal amplification.

Herein we designed a highly sensitive and selective biosensor for methamphetamine (METH) detection based on aptamer recognition probe and atom transfer radical polymerization (ATRP) signal amplification strategy. In this experiment, METH aptamer and its complementary DNA strand were first attached to the electrode surface. In the presence of METH, the prioritized conjugation between METH and the aptamer will take one strand of DNA from the double-stranded DNA, so that the third segment of azide-modified DNA could be successfully modified onto the electrode surface. Through click chemistry and ATRP polymerization, the monomers with ferrocene were polymerized into a long chain, and the signal was amplified, then high-sensitivity detection of METH can be carried out. The result showed that the sensor could detect METH as low as 17 fM, which is about two orders of magnitude lower than that by traditional METH detection methods. Moreover, when different concentrations of METH were added to serum and urine, the recovery rate of the biosensor was as high as 93%. Therefore, using nucleic acid aptamer as capture probe and ATRP as signal amplification strategy can provide a promising application platform for sensitive detection of low concentration toxicants.

Stable nitronyl nitroxide monoradical MATMP as novel monomer of reversible addition fragmentation chain transfer (RAFT) polymerization for ultrasensitive DNA detection.

In this work, it came up a hydrophilic and stable nitronyl nitroxide monoradical 4-methacryloyloxy-2,2,6,6-tetramethylpiperidine 1-oxyl freeradical (MATMP) as new monomer of polymerization for DNA detection. The detection limit was over 1,000,000 times lower than 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) derivatives as electrochemical labels alone. Within this approach, a single biomolecule can be converted into the strong electrochemical signal, therefore lung cancer DNA can be detected at low concentration. For the first step, the HS-PNA probe was fixed on the surface of the Au electrode. After the target DNA was captured by complementary base pairing, 4-cyano-4-(phenylcarbonothioylthio) pentanoic acid (CPAD), chain transfer agent of RAFT polymerization, was bonded to target DNA as reaction via coordination bond of Zr4+. Electroactive polymers had grown by means of surface initiated thermally RAFT polymerization with MATMP as monomer. MATMP polymer significantly improves the electrochemical signal. This method can detect DNA from 0.01 fM to 10 pM, and detection limit is 1.51 aM. The sensitivity of this method is greater than that in most other reported signal amplification strategies of DNA biosensor, which indicates that it is appropriate for single nucleotide polymorphism analysis and will broaden prospects for biological molecules detection application.

Revealing the microbial mechanism of Fe0 and MnO2 mediated microbial fuel cell-anaerobic digestion coupling system and its energy flow distribution.

Microbial fuel cell-anaerobic digestion (MFC-AD) is a new sludge treatment technology with multi-path energy recovery. In this study, Fe0 and MnO2 with gradient concentration were added to investigate its effects on the sludge reduction, electrochemical performance, extracellular polymeric substances (EPS) of sludge, microbial community, electron distribution and energy flow of the MFC-AD system. Results showed that the highest sludge reduction 59% (49%), was obtained at 10 g/L Fe0 (5 g/L MnO2) adding and its total energy recovery efficiency increased by 100% (71%) compare to the control. Different Fe0 and MnO2 concentrations lead to different microbial mechanisms: at 10 g/L Fe0 or 5 g/L MnO2, it prefers to promote extracellular electrons transfer, favoring the Geobacter, Shewanella and Acinetobacter enrichment, while at 5 g/L Fe0 or 0.5 g/L MnO2 it plays a more important role in substrate metabolism of anaerobic digestion, with Clostridium, Roseomonas lacus, and Methylocystis enriched. Correspondingly, the electron quantity distribution from biomass to recovered energy ends (Current, CH4 and VFAs), was influenced by Fe0 and MnO2 concentration, indicating the controllability of the energy flow.

Hemoglobin-catalyzed atom transfer radical polymerization for ultrasensitive electrochemical DNA detection.

The use of hemoglobin (Hb) to drive atom transfer radical polymerization (ATRP) process (Hb-ATRP) for detection of lung cancer related nucleic acid is firstly reported. Hb does not need to be treated prior to using indicating the potential for synthetic engineering in complex biological microenvironments without the need for in vitro techniques. Here, we report a new signal amplification strategy using Hb-mediated graft of nitronyl niroxide monoradical polymers as a signal-on electrochemical biosensor for ultralow level DNA highly selective detection. Building DNA biosensors includes: (i) the fixation of peptide nucleic acid (PNA) probe (no phosphate group) via the 5' terminus-SH; (ii) the modification of transition metal; (iii) Site-specific markers of Hb-ATRP promoter, and (iv) the grafting of polymers with electrochemical signal by Hb-ATRP process. Through the Hb-ATRP process of nitronyl nitroxide monoradical (TEMPO), the presence of a small amount of DNA can eventually result in calling a certain number of TEMPO redox tags. Obviously, the Hb-ATRP is a method of easy source of raw materials, simple operation and no need for complex equipment. The constructed biosensor, as expected, is highly selective and sensitive to target DNA. The detection limit can be calculated as 15.96 fM under optimal conditions. The excellent performance also shows that the constructed DNA biosensor is suitable for DNA screening and DNA concentration determination in complex sample matrix.