High-Frequency Quartz Crystal Microbalance and Dual-Signaling Electrochemical Ratiometric Assays of PTP1B Activity Based on COF@Au@Fc Hybrids.

The abnormal expression of protein tyrosine phosphatase 1B (PTP1B) is highly related to several serious human diseases. Therefore, an accurate PTP1B activity assay is beneficial to the diagnosis and treatment of these diseases. In this study, a dual-mode biosensing platform that enabled the sensitive and accurate assay of PTP1B activity was constructed based on the high-frequency (100 MHz) quartz crystal microbalance (QCM) and dual-signaling electrochemical (EC) ratiometric strategy. Covalent-organic framework@gold nanoparticles@ferrocene@single-strand DNA (COF@Au@Fc-S0) was introduced onto the QCM Au chip via the chelation between Zr4+ and phosphate groups (phosphate group of the phosphopeptide (P-peptide) on the QCM Au chip and the phosphate group of thiol-labeled single-stranded DNA (S0) on COF@Au@Fc-S0) and used as a signal reporter. When PTP1B was present, the dephosphorylation of the P-peptide led to the release of COF@Au@Fc-S0 from the QCM Au chip, resulting in an increase in the frequency of the QCM. Meanwhile, the released COF@Au@Fc-S0 hybridized with thiol/methylene blue (MB)-labeled hairpin DNA (S1-MB) on the Au NPs-modified indium-tin oxide (ITO) electrode. This caused MB to be far away from the electrode surface and Fc to be close to the electrode, leading to a decrease in the oxidation peak current of MB and an increase in the oxidation peak current of Fc. Thus, PTP1B-induced dephosphorylation of the P-peptide was monitored in real time by QCM, and PTP1B activity was detected sensitively and reliably using this innovative QCM-EC dual-mode sensing platform with an ultralow detection limit. This platform is anticipated to serve as a robust tool for the analysis of protein phosphatase activity and the discovery of drugs targeting protein phosphatase.

A high-frequency QCM biosensing platform for label-free detection of the SARS-CoV-2 spike receptor-binding domain: an aptasensor and an immunosensor.

Herein, high-frequency quartz crystal microbalance biosensing platforms were constructed using an aptamer and antibody as bioreceptors for fast and label-free detection of the SARS-CoV-2 RBD.

Zinc-Air Battery-Assisted Self-Powered PEC Sensors for Sensitive Assay of PTP1B Activity Based on Perovskite Quantum Dots Encapsulated in Vinyl-Functionalized Covalent Organic Frameworks.

The self-powered sensors have attracted widespread attention in the analysis field due to a huge demand of point-of-care testing (POCT) in the early diagnosis of diseases. However, the output voltage of the reported self-powered sensors is always small, resulting in a narrow linear detection range and low assay sensitivity. Herein, a self-powered photoelectrochemical (PEC) sensor with zinc-air batteries as a power source was developed for activity assay of protein tyrosine phosphatase 1B (PTP1B) based on perovskite quantum dots encapsulated in the vinyl-functionalized covalent organic framework (COF-V). CsPbBr3 nanocrystals were stabilized by the confinement effect of the COF-V cage without aggregation, and the resulting CsPbBr3@COF-V composite was used as the cathodic photoelectric material to construct the zinc-air battery with a large open-circuit voltage (OCV, 1.556 V). Before PTP1B activity assay, an auxiliary peptide-polyamidoamine-phosphopeptide (P2-PAMAM-P1) hybrid was introduced into the photocathode via thiol-ene click reaction between the thiol group on the P1 and the vinyl group on the COF-V. The steric hindrance effect of the P1-PAMAM-P2 hybrid inhibited the PEC performance of the photocathode, resulting in a small OCV of the zinc-air battery. When the PTP1B existed, PTP1B-catalyzed dephosphorylation of tyrosine on P1 facilitated the cleavage process of P1 by chymotrypsin, leading to the removal of the P2-PAMAM-P1 hybrid from the photocathode and consequently the enhancement of the OCV. Therefore, the activity of PTP1B was sensitively detected. The developed self-powered PEC sensor showed superior performance for PTP1B activity assay (broad linear response range, 0.1 pM to 10 nM and low detection limit, 0.032 pM) due to the large output voltage of the constructed zinc-air battery and has great potential in POCT of protein phosphatase-related diseases and the discovery of protein phosphatase-targeted drugs.

Highly Selective Photoelectrochemical Assay of Arsenate Based on Magnetic Co3O4-Fe3O4 Cubes and the Negative-Background Signal Strategy.

Water pollution presents a significant environmental concern on earth. Herein, due to the serious environmental harmfulness of arsenate [As(V)], an iron phthalocyanine (FePc)-induced switchable photocurrent-polarity platform was developed for highly selective assay of As(V). First, magnetic Co3O4-Fe3O4 cubes were obtained by calcination of the CoFe Prussian blue analogue and then functionalized with oligonucleotide (S1). In the presence of As(V), S1 could be released based on the stronger affinity between As(V) and Co3O4-Fe3O4 cubes. After magnetic separation by Co3O4-Fe3O4 cubes, the released S1 was used to trigger the catalytic hairpin assembly (CHA) and hybridization chain reaction, resulting in the formation of lots of G-quadruplex structures on the AgInS2/ITO electrode. Then, the capture of FePc by the G-quadruplex led to the switch of the photocurrent polarity of the AgInS2/ITO electrode from the anode to the cathode. Thus, As(V) was sensitively assayed with a low detection limit of 1.0 nM and a wide linear response range from 10 nM to 200 µM. This meets the detection requirement of the World Health Organization for the arsenic concentration in drinking water [less than 10 µg L-1 (130 nM)]. In addition, whether it was cationic or anionic interferents except phosphate (PO43-), only As(V) could generate the cathodic photocurrent, effectively avoiding the false-positive or false-negative results during As(V) assay. Interestingly, As(V) was also simultaneously separated from the detection system by Co3O4-Fe3O4 magnetic cubes. The proposed photoelectrochemical platform may have a great potential application for the selective detection of As(V) in environmental fields.

Colorimetric and Photocurrent-Polarity-Switching Photoelectrochemical Dual-Mode Sensing Platform for Highly Selective Detection of Mercury Ions Based on the Split G-Quadruplex-Hemin Complex.

Mercury ion (Hg2+) is one of the most harmful heavy metal ions with the greatest impact on public health. Herein, based on the excellent catalytic activity toward 3,3',5,5'-tetramethylbenzidine (TMB) and the strong photocurrent-polarity-switching ability to SnS2 photoanode of the split G-quadruplex-hemin complex, the magnetic NiCo2O4@SiO2-NH2 sphere-assisted colorimetric and photoelectrochemical (PEC) dual-mode sensing platform was developed for the Hg2+ assay. First, the amino-labelled single-stranded DNA1 (S1) was immobilized on NiCo2O4@SiO2-NH2 and then partly hybridized with another single-stranded DNA2 (S2). When Hg2+ was present, the thymine-Hg2+-thymine base pairs between S1 and S2 were formed, causing the formation of the split G-quadruplex in the presence of K+. After addition of hemin, the split G-quadruplex-hemin complex was obtained and effectually catalyzed the H2O2-mediated oxidation of TMB. Thus, the color and absorbance intensity of the TMB solution were changed, resulting in the visual and colorimetric detection of Hg2+. The linear response range is 10 pM to 10 nM, and the detection limit is 3.8 pM. Meanwhile, the above G-quadruplex-hemin complex effectively switched the photocurrent polarity of SnS2-modified indium tin oxide electrode, leading to the sensitive and selective PEC assay of Hg2+ with a linear response range of 5 pM to 500 nM and a detection limit of 2.3 pM. Moreover, the developed dual-mode sensing platform provided mutual authentication of detection results in different modes, effectively improving the assay accuracy and confidence, and may have a good potential application in highly sensitive, selective, and accurate determination of Hg2+ in environmental fields.

Bifunctional Magnetic Fe3O4@Cu2O@TiO2 Nanosphere-Mediated Dual-Mode Assay of PTP1B Activity Based on Photocurrent Polarity Switching and Nanozyme-Engineered Biocatalytic Precipitation Strategies.

Dysregulation of protein phosphatases is associated with the progression of various human diseases and cancers. Herein, a photoelectrochemical (PEC)-quartz crystal microbalance (QCM) dual-mode sensing platform was developed for protein tyrosine phosphatase 1B (PTP1B) activity assay based on bifunctional magnetic Fe3O4@Cu2O@TiO2 nanosphere-mediated PEC photocurrent polarity switching and QCM signal amplification strategies. The PTP1B-specific phosphopeptide (P-peptide) with a cysteine end was designed and immobilized onto the QCM Au chip via the Au-S bond. Subsequently, the Fe3O4@Cu2O@TiO2 nanosphere was connected to the P-peptide via the specific interaction between the phosphate group on the P-peptide and TiO2. After incubation with PTP1B, the dephosphorylation of the P-peptide occurred, causing some Fe3O4@Cu2O@TiO2 nanospheres to be released from the chip surface. The released magnetic Fe3O4@Cu2O@TiO2 nanospheres (labeled as R-Fe3O4@Cu2O@TiO2) were quickly separated via magnetic separation technology and attached to the Bi2S3-decorated magnetic indium-tin oxide (Bi2S3/MITO) electrode by magnetic force, inducing the switch of the photocurrent polarity of the electrode from anodic current (the Bi2S3/MITO electrode) to cathodic current (the R-Fe3O4@Cu2O@TiO2/Bi2S3/MITO electrode). Also, the nondephosphorylated P-peptide linked Fe3O4@Cu2O@TiO2 nanospheres as nanozymes with horseradish peroxidase activity to catalyze the formation of precipitation on the surface of the Au chip, leading to a frequency change of the QCM. Thus, the proposed PEC-QCM dual-mode sensing platform achieved accurate and reliable assay of PTP1B activity because of the different mechanisms and independent signal transductions. In addition, this dual-mode sensing platform can be easily extended for other protein phosphatase activity analysis and shows great potential in the early diagnosis of the protein phosphatase-related diseases and the protein phosphatase-targeted drug discovery.

Sensitive Dual-Mode Biosensors for CYFRA21-1 Assay Based on the Dual-Signaling Electrochemical Ratiometric Strategy and "On-Off-On" PEC Method.

Herein, an electrochemical (EC)-photoelectrochemical (PEC) dual-mode biosensor was constructed for cytokeratin 19 fragment 21-1 (CYFRA21-1) assay based on the dual-signaling electrochemical ratiometric strategy and "on-off-on" PEC method. The indium tin oxide (ITO) electrode was modified by 3,4,9,10-perylenetetracarboxylic dianhydride (PTCDA)@C60 and gold nanoparticles (Au NPs), and the double-stranded DNA composed of thiol/methylene blue (MB)-labeled single-stranded DNA (ssDNA) (S0-MB) and antibody/ferrocene (Fc)-labeled ssDNA (Ab1-S1-Fc) was immobilized on the Au NPs/PTCDA@C60/ITO electrode via the Au-S bond between Au NPs and thiol of S0-MB. With the help of another antibody-labeled ssDNA (Ab2-S2), the presence of CYFRA21-1 triggered a typical antigen-antibody sandwich immune reaction (Ab1, CYFRA21-1, and Ab2) and proximity hybridization between Ab1-S1-Fc and Ab2-S2. This caused the release of Ab1-S1-Fc from the modified electrode and the change of S0-MB to a hairpin structure, resulting in a decrease (an increase) of the oxidation peak current of Fc (MB) and an increase of the photocurrent due to the enhancing (inhibiting) effect of MB (Fc) on the photoelectric performance of the Au NPs/PTCDA@C60/ITO electrode. Thus, CYFRA21-1 was detected by the developed EC-PEC dual-mode sensing platform sensitively, and the linear response ranges of 0.001-40 ng/mL with a detection limit of 0.3 pg/mL for the EC technique and 0.0001-4 ng/mL with a detection limit of 0.03 pg/mL for the PEC method were obtained. Furthermore, by changing the specific antibodies of disease-related biomarkers, the developed dual-mode biosensing platform could be readily extended to detect other antigens, implying its great potential applications in biological analysis and early disease diagnosis.

Peptide Cleavage-Mediated and Environmentally Friendly Photocurrent Polarity Switching System for Prostate-Specific Antigen Assay.

As the most important serum biomarker for prostate cancer, sensitive and accurate detection of prostate-specific antigen (PSA) is of great reference value for the clinical diagnosis and treatment of prostate cancer. Herein, a peptide cleavage-mediated and environmentally friendly photocurrent polarity switching system was developed for ultrasensitive and highly selective detection of PSA based on the efficiently switching of photocurrent polarity of silver indium sulfide nanoparticles (AgInS2 NPs)-coated indium tin oxide (ITO) electrode by amino-functionalized CuO cubes (NH2-CuO). The porous CuO cubes were synthesized by calcination of HKUST-1 and functionalized with aminosilane. In the presence of PSA, the biotin and rhodamine B-labeled peptide (Bio-Pep-RhB) was cleaved and part of the peptide (P-Pep-RhB) was obtained by magnetic separation. Through host-guest recognition between ß-CD and RhB, the P-Pep-RhB was immobilized on the ß-CD/AgInS2 NPs/ITO electrode. Then, the amino-rich sequence on P-Pep-RhB combined with NH2-CuO via glutaraldehyde results in the switch of anodic photocurrent to cathodic photocurrent. On account of the high-efficient peptide cleaving strategy and the new photocurrent polarity switching system of porous CuO cubes//AgInS2 NPs, the prepared sensing platform displayed outstanding analytical performance for PSA with a wide linear response range (0.1 pg mL-1-100 ng mL-1) and a lower detection limit of 0.06 pg mL-1. The proposed analytical method could be easily extended to analyze other proteins via changing the peptide sequence, which has a potential application in the fields of biological analysis and medical diagnosis.

Highly Selective and Sensitive microRNA-210 Assay Based on Dual-Signaling Electrochemical and Photocurrent-Polarity-Switching Strategies.

Highly sensitive and selective microRNA (miRNA) assay is of great significance for disease diagnosis and therapy. Herein, a magnetic-assisted electrochemistry (EC)-photoelectrochemistry (PEC) dual-mode biosensing platform was developed for miRNA-210 detection based on dual-signaling EC and photocurrent-polarity-switching PEC strategies. Porous magnetic Fe3O4 octahedra with a large surface area were synthesized by calcining Fe-based metal-organic frameworks. Subsequently, the magnetic photoelectric materials (Fe3O4@CdS) were developed by the successive ionic layer adsorption and reaction method in Cd2+ and S2- solutions. Then, the self-assembled DNA nanoprisms contained three thiols/hanging arms that could capture miRNA-210 efficiently and were anchored to the Fe3O4@CdS octahedra via the Cd-S bond. When miRNA-210 was present, the double-stranded DNA concatemers [the self-assembled duplex helixes based on a pair of methylene blue (MB)-labeled single-stranded DNAs (AP1 and AP2) through the hybridization chain reaction and then intercalated with adriamycin (Dox) into their grooves] were connected with the Fe3O4@CdS-DNA nanoprisms. MB and Dox not only acted as the electrochemical probes but also synergistically switched the photocurrent polarity of the Fe3O4@CdS octahedra. Thus, miRNA-210 was assayed sensitively and selectively via the proposed EC-PEC dual-mode biosensing platform. Additionally, the abovementioned recognition steps occurred in a homogeneous system, and the effects of the impurities and interferences on the miRNA-210 assay could be easily avoided by magnetic separation due to the good magnetic properties of Fe3O4 octahedra. The proposed EC-PEC dual-mode biosensing platform showed a wide range of potential applications in bioanalysis and early diagnosis of disease.

Highly Selective and Sensitive Photoelectrochemical Sensing Platform for VEGF165 Assay Based on the Switching of Photocurrent Polarity of CdS QDs by Porous Cu2O-CuO Flower.

Herein, a highly selective and sensitive photoelectrochemical (PEC) sensing platform was developed for vascular endothelial growth factor 165 (VEGF165) assay based on the porous Cu2O-CuO flower-induced photocurrent-polarity switching of the CdS quantum dots (QDs) modified indium-tin oxide (ITO) electrode. The porous Cu2O-CuO flower with uniform size and large surface area was successfully synthesized by taking Cu-MOF (HKUST-1) as the precursor. Through VEGF165-triggered catalytic hairpin assembly process, the porous Cu2O-CuO flower was introduced to the surface of the CdS QDs/ITO electrode, resulting in the switching of the photocurrent polarity from anodic current to cathodic current. Based on the uniform particle size, high specific surface area, good photoelectric conversion efficiency, and photocurrent polarity switching ability of porous Cu2O-CuO flower, the proposed sensing platform showed excellent assay performance for VEGF165 with a linear response range from 1 to 3000 fM, a detection limit of 0.3 fM, and high selectivity. By changing the specific aptamer, the proposed sensing platform could be easily extended to detect other proteins, and may have a promising application in bioanalysis and early disease diagnosis.

A system composed of vanadium(IV) disulfide quantum dots and molybdenum(IV) disulfide nanosheets for use in an aptamer-based fluorometric tetracycline assay.

A system composed of vanadium(IV) disulfide quantum dots (VS2 QDs) and molybdenum(IV) disulfide (MoS2) nanosheets for use in an aptamer-based fluorometric tetracycline assay was developed. The tetracycline (TET) aptamer was first immobilzed on the VS2 QDs with a typical size of 3 nm. The blue fluorescence of the VS2 QDs (labeled with aptamer) with emission maxima at 448 nm (under excitation at 360 nm) was subsequently quenched by MoS2 nanosheets. If TET is recognized by the aptamer, the VS2 QDs drift away from the basal plane of the MoS2 nanosheets. This generated "turn-on" fluorescence of the VS2 QDs. A VS2 QD/MoS2 nanosheet-based fluorometric TET aptasensor was thus constructed. Selective and sensitive TET bioanalysis was realized in a linear range of 1 to 250 ng mL-1. The detection limit was 0.06 ng mL-1. Its applicability of determination of TET in milk samples has been demonstrated. Graphical abstractSchematic representation of the aptamer-based fluorometric tetracycline assay.

VS2 quantum dot label-free fluorescent probe for sensitive and selective detection of ALP.

As an essential enzyme highly associated with various human diseases, alkaline phosphatase (ALP) plays an important role in human tissues. Developing new materials and strategies for monitoring ALP is thus important. We have developed a novel label-free fluorescent sensing system for ALP activity that is based on the "turn-on" fluorescence of VS2 quantum dots. The fluorescence of VS2 quantum dots quenched by Fe3+ can be restored by ascorbic acid, which is generated by hydrolysis of L-ascorbic acid 2-phosphate catalyzed by ALP. Rapid, convenient, and sensitive detection of ALP is achieved in the range from 3 to 1000 U/L (R 2 =0.9985), with a detection limit of 0.27 U/L. The proposed sensor exhibits excellent selectivity for ALP compared with other enzymes and proteins, such as glucose oxidase, lysozyme, trypsin, human serum albumin, and bovine serum albumin. The reliability for ALP determination in human serum plasma has been demonstrated with satisfactory recovery, revealing promising application in clinical diagnosis and biomedical research. Graphical abstract Hydrothermally synthesized VS2 quantum dots serving as a novel turn-on fluorescent probe for detection of alkaline phosphatase (ALP) activity. AA L-ascorbic acid, AAP L-ascorbic acid 2-phosphate, NAC N-acetyl-L-cysteine.

Research on a soft measurement model of sewage treatment based on a case-based reasoning approach.

In this paper, the measurement of biochemical oxygen demand (BOD) in a wastewater treatment process is analyzed and an intelligent integrated prediction method based on case-based reasoning (CBR) is proposed in order to overcome difficulties. Due to the fact that there are many factors that influence the accuracy of the prediction model, the radial basis function, which is a neural network with a 3 layer feedforward network, is employed to reduce the dimension of input values. Under these circumstances, a back propagation neural network combining with a nearest neighbor retrieval strategy is adopted to match case. Then, the measurement of BOD in wastewater treatment process is analyzed. Finally, the validity of the improved CBR in sewage treatment is demonstrated by using numerical results.

Low-Temperature Catalytic Decomposition of 130 Tetra- to Octa-PCDD/Fs Congeners over CuOX and MnOX Modified V2O5/TiO2-CNTs with the Assistance of O3.

In this study, a reliable and steady PCDD/F generation system was utilized to investigate the performance of catalysts, in which 130 congeners of tetra- to octapolychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) vapors were studied under simulated flue gas with/without O3. TiO2 and carbon nanotubes (CNTs) supported vanadium oxides (VOX/TiO2-CNTs) modified with MnOX and CuOX, which were reported to be beneficial to the decomposition of model molecules, were found to have a negative effect on the removal of real PCDD/Fs in the simulated flue gas without O3. Moreover, the addition of MnOX presented different effects depending on whether CuOX existed in catalysts or not, which was also contrary to its effects on the degradation of model molecules. In an O3-containing atmosphere, low chlorination level PCDD/Fs congeners were removed well over VOX-MnOX/TiO2-CNTs, while high chlorination level PCDD/Fs congeners were removed well over VOX-CuOX/TiO2-CNTs. Fortunately, all PCDD/Fs congeners decomposed well over VOX-MnOX-CuOX/TiO2-CNTs. Finally, the effects of tetra- to octachlorination level for the adsorption and degradation behaviors of PCDD/Fs congeners were also investigated.

Municipal solid waste incineration in China and the issue of acidification: A review.

In China, incineration is essential for reducing the volume of municipal solid waste arising in its numerous megacities. The evolution of incinerator capacity has been huge, yet it creates strong opposition from a small, but vocal part of the population. The characteristics of Chinese municipal solid waste are analysed and data presented on its calorific value and composition. These are not so favourable for incineration, since the sustained use of auxiliary fuel is necessary for ensuring adequate combustion temperatures. Also, the emission standard for acid gases is more lenient in China than in the European Union, so special attention should be paid to the issue of acidification arising from flue gas. Next, the techniques used in flue gas cleaning in China are reviewed and the acidification potential by cleaned flue gas is estimated. Still, acidification induced by municipal solid waste incinerators remains marginal compared with the effects of coal-fired power plants.

Real-time monitoring of dephosphorylation process of phosphopeptide and rapid assay of PTP1B activity based on a 100 MHz QCM biosensing platform.

The misregulation of protein phosphatases is a key factor in the development of many human diseases, notably cancers. Here, based on a 100 MHz quartz crystal microbalance (QCM) biosensing platform, the dephosphorylation process of phosphopeptide (P-peptide) caused by protein tyrosine phosphatase 1B (PTP1B) was monitored in real time for the first time and PTP1B activity was assayed rapidly and sensitively. The QCM chip, coated with a gold (Au) film, was used to immobilized thiol-labeled single-stranded 5'-phosphate-DNAs (P-DNA) through Au-S bond. The P-peptide, specific to PTP1B, was then connected to the P-DNA via chelation between Zr4+ and phosphate groups. When PTP1B was injected into the QCM flow cell where the P-peptide/Zr4+/MCH/P-DNA/Au chip was placed, the P-peptide was dephosphorylated and released from the Au chip surface, resulting in an increase in the frequency of the QCM Au chip. This allowed the real-time monitoring of the P-peptide dephosphorylation process and sensitive detection of PTP1B activity within 6 min with a linear detection range of 0.01-100 pM and a detection limit of 0.008 pM. In addition, the maximum inhibitory ratios of inhibitors were evaluated using this proposed 100 MHz QCM biosensor. The developed 100 MHz QCM biosensing platform shows immense potential for early diagnosis of diseases related to protein phosphatases and the development of drugs targeting protein phosphatases.

How does owning commercial housing affect the subjective well-being of rural-urban migrants?--The mediating effect of housing assets and the moderating effect of debt.

Houses mean a lot to Chinese people, and in the context of the urban-rural dualist system, town housing has a special significance for rural-urban migrants. Based on the 2017 China Household Finance Survey(CHFS) data, this study uses the Ordered Logit (OLogit) model to empirically test the effect of owning commercial housing on the subjective well-being(SWB) of rural-urban migrants, and through the mediating effect and moderating effect to conduct an in-depth investigation into the intrinsic effect mechanism and further explains the relationship between the two and the current residential location of their family. The results of the study show that: (1) Owning commercial housing can significantly enhances the subjective well-being(SWB) of rural-urban migrants, and the findings remain robust after using alternative model, adjusting the sample size, correcting for sample selectivity bias using propensity score matching(PSM), and controlling for potential endogeneity bias combining instrumental variables and conditional mixed process(CMP); (2) The effect of owning commercial housing on the subjective well-being(SWB) of the first generation rural-urban migrants, rural-urban migrants in the eastern and central regions, and those who obtained housing before the rapid rise in house prices is more pronounced; (3) Commercial housing acts on the subjective well-being(SWB) of rural-urban migrants through the mediating effect of housing assets, and there is some regional variation in the mediating effect of housing assets. At the same time, the household debt acts as a positive moderator between commercial housing and the subjective well-being(SWB) of rural-urban migrants; (4) Even with commercial housing, rural-urban migrants whose families are currently living in rural areas still have a stronger sense of subjective well-being (SWB).

Ultrasensitive detection and efficient removal of mercury ions based on covalent organic framework spheres with double active sites.

In present work, a new spherical covalent organic framework (TFPB-APTU COF) with good photoelectric property and double active sites (secondary amine (-NH-) group and sulfur (S) atom) was prepared for ultrasensitive detection and efficient removal of mercury ions (Hg2+). The -NH- group and S atom can capture free Hg2+ by coordination and chelation interaction, and the related steric hindrance effect reduces the photocurrent signal of the TFPB-APTU COF, resulting in the highly sensitive photoelectrochemical analysis of Hg2+ with a wide linear response range (0.01-100000 nM) and low detection limit (0.006 nM). On the other hand, the developed TFPB-APTU COF has large removal capacity (2692 mg g-1), good regeneration capability, and high removal speed for Hg2+ removal based on the double active sites (-NH- group and S atom), large specific surface area and porous spherical structure. The developed TFPB-APTU COF spheres show great potential in monitoring and treatment of environmental pollution of Hg2+.

Development of a Fault Detection Instrument for Fiber Bragg Grating Sensing System on Airplane.

This study develops a fault detection device for the fiber Bragg grating (FBG) sensing system and a fault detection method to realize the rapid detection of the FBG sensing system on airplanes. According to the distribution of FBG sensors on airplanes, the FBG sensing system is built based on wavelength division multiplexing (WDM) and space division multiplexing (SDM) technologies. Furthermore, the hardware and software of the fault detection device and the relevant FBG demodulator are studied in detail. Additionally, in view of the similar features of the healthy FBG sensor in the same measuring point, a rapid fault diagnosis method based on a synthetical anomaly index is proposed. The features (light intensity I, signal length L, standard deviation of original sample σ and energy value in time-domain P) of FBG sensors are extracted. The aggregation center value of the above feature values is obtained through the loop iteration method. Furthermore, the separation degrees of features are calculated and then form the synthetical anomaly index so as to make an effective diagnosis of the state of the FBG sensor. Finally, the designed fault detection instrument and proposed fault detection method are used to monitor the 25 FBG sensors on the airplane, the results indicated that three faulty and two abnormal FBG sensors on the airplane are identified, showing the effectiveness of the proposed fault detection method.

PCDD/F removal at low temperatures over vanadium-based catalyst: insight into the superiority of mechanochemical method.

The high toxicity and low volatility of PCDD/Fs prevent detailed study of their catalytic degradation removal characteristics. In this study, 1,2-dichlorobenzene (1,2-DCBz) was initially used as a model to investigate the catalytic characteristics of various vanadium-based catalysts prepared by different methods. Then, the optimized catalyst was used for catalytic degradation of real PCDD/Fs at low temperatures based on a self-made stable source. The VOx/TiO2 catalysts synthesized by the mechanochemical method (VTi-MC2) had a higher 1,2-DCBz removal efficiency (>85%) and stability (> 420 min) at low temperatures (< 200 °C) compared to VTi-SG (sol-gol method) and VTi-WI (wetness impregnation method). The physicochemical properties of catalysts were studied using comprehensive characterization. It was found that the VTi-MC2 has better VOx species distribution and possesses the highest V5+ species and surface adsorbed oxygen content, which are the key factors that contributed to the higher removal efficiency. Accordingly, the mechanochemical method can be used to control the physicochemical properties of catalysts by adjusting the milling parameters. The optimum ball milling time is 2 h and a suitable precursor is NH4VO3 for VOx/TiO2. Moreover, the removal efficiency and catalytic degradation efficiency of PCDD/Fs in gas phase catalyzed by VTi-MC2 were 97% and 50% respectively, within a range of temperatures below 200 °C, which are both higher than those reported research. In general, the mechanochemical strategy employed in this study provides a means for seeking more efficient catalysts used for low-temperature degradation of various trace organic pollutants.