Preparation of composite coagulant for the removal of microplastics in water.

In this work, a composite flocculant (polyferric titanium sulfate-polydimethyldiallylammonium chloride [PFTS-PDMDAAC]) with a rich spatial network structure was prepared for the treatment of simulated wastewater containing polystyrene (PS) micro-nanoparticles. Characterization results showed that the surface of the PFTS-PDMDAAC was a three-dimensional network polymer of chain molecules that exhibited good thermal stability and formed an amorphous polymer containing multiply hydroxyl-bridged titanium and iron. When n(OH- ) : n(Fe) = 1:2, n(PO4 3- ) : n(Fe) = 0.35, n(Ti) : n(Fe) = 1:8, n(DMDAAC) : n(Fe) = 5:100, and the polymerization temperature is 60°C, the prepared composite flocculant has the best effect. The effects of dosage, pH, and agitation intensity on the flocculation properties of PFTS-PDMDAAC were also studied. The optimal removal rates of PS-µm and haze by PFTS-PDMDAAC were 85.60% and 90.10%, respectively, at a stirring intensity of 200 rpm, a pH of 9.0, and a PFTS-PDMDAAC dosage of 20 mg/L. The flocs produced by the PFTS-PDMDAAC flocculation were large and compact in structure, and the flocculation mechanism was mainly based on adsorption bridging. Kaolin played a promoting role in the process of PS-µm removal by PFTS-PDMDAAC floc and accelerated the formation of large and dense flocs. This study provided a reference for the coagulation method to remove micro-nanopollutants in the actual water treatment process. PRACTITIONER POINTS: A composite flocculant with rich spatial network structure (PFTS-PDMDAAC) was prepared. PFTS-PDMDAAC can effectively remove micro-nano polystyrene (PS) in wastewater. The floc produced by PFTS-PDMDAAC is large and compact in structure. The flocculation mechanism of PFTS-PDMDAAC is mainly adsorption bridging.

Preparation of Mn/Zn@PG Catalyst for Catalytic Oxidation Treatment of Coal Chemical Wastewater.

In this study, Mn/Zn@palygorskite (PG) catalysts with developed pores and good salt tolerance were prepared and applied to the treatment of coal chemical wastewater. A doping ratio of metal elements, calcination temperature, and calcination time was used to optimize the preparation conditions and determine the optimal preparation conditions of the Mn/Zn@PG catalysts. The catalysts, obtained under various preparation conditions, were characterized and analyzed by XRD, SEM, EDS, BET, XRF, XPS, and other techniques. Results showed that the Zn and Mn elements in the Mn/Zn@PG catalyst existed as ZnO and MnO2, respectively. The optimal working conditions of the Mn/Zn@PG catalyst for catalytic oxidation treatment of coal chemical wastewater, obtained through the optimization of working conditions, are the following: reaction time 60 min, wastewater pH = 9.28, ozone ventilation rate 0.2 L/min, catalyst filling ratio 20%. The height-to-diameter ratio of the tower was 6:1. The abrasion resistance and catalytic performance of the Mn/Zn@PG catalyst after repeated use were investigated, and the mechanism of the loss of active components of the Mn/Zn@PG catalyst was explored. The coal chemical wastewater, before and after treatment, was analyzed by UV-vis spectroscopy and 3D fluorescence spectroscopy. The hierarchical-principal component comprehensive evaluation system (AHP-PCA) was established to evaluate the catalytic ozonation process of coal chemical wastewater, so that the overall evaluation of the process performance can be achieved.

Proteomic profile of mouse oocytes after vitrification: A quantitative analysis based on 4D label-free technique.

Mature oocyte cryopreservation represents an important trend for future fertility preservation, however, the relatively low efficiency has hampered its clinical application. Proteomic profiling is a method of choice for the exploration of the molecular mechanism underlying cryoinjuries. Here, a systematic comparison of protein expression between fresh and vitrified oocytes was performed based on the 4D label-free technique, an informative method with high sensitivity. Our results indicated that the oocyte survival rate was significantly reduced after vitrification. Proteomic results showed that 32 proteins were up-regulated, while 77 proteins were down-regulated in vitrified oocytes compared with the fresh counterparts. Gene Ontology (GO) functional analysis revealed that differentially expressed proteins (DEPs) were involved in metabolism, mitochondrial function, cytoskeleton and other cell functions. Moreover, proteins that participated in signaling transduction mechanisms were the largest category based on Clusters of Orthologous Groups of protein/EuKaryotic Orthologous Groups (COG/KOG) functional classification. In addition, over-expressed DEPs were enriched for "nucleus", "protein binding", "membrane", "cytoplasm" as well as mitochondrial function. Furthermore, we discovered that the DEPs were clustered in pyruvate metabolism, citric acid (TCA) cycle and glucose metabolism by Protein-Protein Interaction (PPI) network evaluation. In conclusion, our data demonstrate that vitrification induces multi-level damages in oocytes, the dynamic proteomic profiling will provide systematic insights into uncovering the mechanism underlying cryoinjuries.

Artificially Increasing Cortical Tension Improves Mouse Oocytes Development by Attenuating Meiotic Defects During Vitrification.

Oocyte cryopreservation demonstrates great benefits in the conservation of animal germplasm resources and assisted reproductive technology. However, vitrification causes damages in oocytes, which would lead to the decrease of oocyte quality, and embryonic development post fertilization. Cytoskeleton plays an important role in regulating cell shape, organelle migration, cell division and mechanical signal transduction. Cortical tension is a reflection of the physiological state and contractile ability of cortical cytoskeleton. Appropriate cortical tension is prerequesite for normal oocyte meiosis. In the present study, oocyte cortical tension was examined by evaluating the levels of cortical tension-related protein pERM (Phospho-Ezrin/Radixin/Moesin) and pMRLC (Phospho-Myosin Light Chain 2). We found that the cortical tension of vitrified oocytes was decreased. Increasing cortical tension of vitrified oocytes by adding 10 µg/ml ConA during in vitro culture could significantly improve the polar body extrusion rate and embryo development. Furthermore, increasing the cortical tension could improve spindle positioning, maintain kinetochore-microtubule (KT-MT) attachment, strengthen spindle assembly checkpoint (SAC) activity, and reduce the aneuploidy rate in vitrified oocytes. In conclusion, vitrification induced a remarkable decrease in cortical tension, and increasing the cortical tension could rescue the meiosis defect and improve oocyte quality.

Vascular Derived ECM Improves Therapeutic Index of BMP-2 and Drives Vascularized Bone Regeneration.

Vascularized osteogenesis is essential for successful bone regeneration, yet its realization during large size bone defect healing remains challenging due to the difficulty to couple multiple biological processes. Herein, harnessing the intrinsic angiogenic potential of vascular derived extracellular matrix (vECM) and its specific affinity to growth factors, a vECM/GelMA based hybrid hydrogel delivery system is constructed to achieve optimized bone morphogenetic protein-2 (BMP-2) therapeutic index and provide intrinsic angiogenic induction during bone healing. The incorporation of vECM not only effectively regulates BMP-2 kinetics to match the bone healing timeframe, but also promotes angiogenesis both in vitro and in vivo. In vivo results also show that vECM-mediated BMP-2 release remarkably enhances vascularized bone formation for critical size bone defects. In particular, blood vessel ingrowth stained with CD31 marker in the defect area is substantially encouraged over the course of healing, suggesting incorporation of vECM served roles in both angiogenesis and osteogenesis. Thus, the authors' study exemplifies that affinity of growth factor towards ECM may be a promising strategy to be leveraged to develop sophisticated delivery systems endowed with desirable properties for regenerative medicine applications.

Synthesis and evaluation of cationic flocculant P(DAC-PAPTAC-AM) for flocculation of coal chemical wastewater.

In this study, a high-efficiency cationic flocculant, P(DAC-MAPTAC-AM), was successfully prepared using UV-induced polymerization technology. The monomer Acrylamide (AM): Acryloxyethyl Trimethyl ammonium chloride (DAC): methacrylamido propyl trimethyl ammonium chloride (MAPTAC) ratio, monomer concentration, photoinitiator concentration, urea content, and cationic monomer DAC:MAPTAC ratio, light time, and power of high-pressure mercury lamp were studied. The characteristic groups, characteristic diffraction peaks, and characteristic proton peaks of P(DAC-MAPTAC-AM) were confirmed by fourier transform infrared spectroscopy (FTIR), X-Ray diffraction (XRD), 1H nuclear magnetic resonance spectrometer (1H NMR), and scanning electron microscopy (SEM). The effects of dosage, pH value, and velocity gradient (G) value on the removal efficiencies of turbidity, COD, ammonia nitrogen, and total phenol by poly aluminum ferric chloride (PAFC), P(DAC-MAPTAC-AM), and PAFC/P(DAC-MAPTAC-AM) in the flocculation treatment of coal chemical wastewater were investigated. Results showed that the optimal conditions for the flocculation of coal chemical wastewater using P(DAC-MAPTAC-AM) alone are as follows: dosage of 8-12 mg/L, G value of 100-250 s - 1, and pH value of 4-8. The optimal dosage of PAFC is 90-150 mg/L with a pH of 2-12. The optimal dosage for PAFC/P(DAC-MAPTAC-AM) is as follows: PAFC dosage of 90-150 mg/L, P(DAC-MAPTAC-AM) dosage of 8-12 mg/L, and pH range of 2-6. When P(DAC-MAPTAC-AM) was used alone, the optimal removal efficiencies of turbidity, COD, ammonia nitrogen, and total phenol were 81.0%, 35.0%, 75.0%, and 80.3%, respectively. PAFC has good tolerance to wastewater pH and good pH buffering. Thus, the flocculation treatment of coal chemical wastewater using the PAFC/P(DAC-MAPTAC-AM) compound also exhibits excellent resistance and buffering capacity.

Ozone catalytic oxidation capacity of Ti-Co@Al2 O3 for the treatment of biochemical tailwater from the coal chemical industry.

A Ti-Co@γ-Al2 O3 composite catalyst was prepared using impregnation and sol-gel methods to degrade biochemical tailwater from the coal chemical industry, and its preparation conditions (active component doping ratio, load times, and calcination temperature) were optimized through single-factor experiments. The surface properties of the Ti-Co@γ-Al2 O3 composite catalyst and the crystal structure characteristics of the catalytically active components were characterized via scanning electron microscopy-energy dispersive spectrometry, X-ray diffraction, and X-ray fluorescence. The effects of reaction time, initial pH, ozone aeration, and catalyst dosage on degradation performance were investigated through an experiment on the catalytic ozonation degradation of biochemical tail water. Results showed that the optimal conditions were as follows: reaction time of 30 min, pH of 8.2, ozone aeration of 30 mg/min, and catalyst dosage of 20 g/L. The total phenol and total organic carbon removal rates for biochemical tailwater were 66.1% and 57.6%, respectively, in the catalytic system. The mechanism of degradation of organic pollutants by catalytic ozonation was investigated by adding tert-butanol to the catalytic ozone oxidation system. The degradation of chemical oxygen demand in biochemical tailwater was caused primarily by the synergy between the Ti-Co@γ-Al2 O3 catalyst and ozone. PRACTITIONER POINTS: Ti-Co/γ-Al2 O3 catalyst was prepared for the catalytic oxidation of biochemical tail water. The optimal removal rates of total phenol and TOC were 67.7% and 58.8%, respectively. The organic matter was degraded rapidly and efficiently after 5 min of ozone catalytic oxidation reaction. It provides theoretical guidance for the practical application of ozone catalytic oxidation.

Novel chitosan-based flocculants for chromium and nickle removal in wastewater via integrated chelation and flocculation.

Carboxylated chitosan (CPCTS) is used as substrates in the design and synthesis of CPCTS-based flocculants through UV-initiated polymerization techniques. The synthesized flocculants are applied to remove Cr and Ni ions from chromic acid lotion and electroplating wastewater through two-stage flocculation. This study investigates the effect of flocculant dosage, pH, reaction time, and stirring speed on the removal efficiency of Cr and Ni ions. Results indicated that the total Cr removal ratios by CPCTS-graft-polyacrylamide-co-sodium xanthate (CAC) and CPCTS-graft-poly [acrylamide-2-Acrylamido-2-methylpropane sulfonic acid] (CPCTS-g-P(AM-AMPS)) are 94.7% and 94.6%, respectively. The total Ni removal efficiencies by CAC and CPCTS-g-P(AM-AMPS) are 99.3% and 99.4%, respectively. The two-stage flocculation with CPCTS-based flocculants could reduce the total concentrations of Cr and Ni to 1.0 mg/L and 0.5 mg/L, respectively. The relationship of removal capacity and structural properties between the flocculants with different functional groups is established through Fourier transform infrared spectroscopy, nuclear magnetic resonance, scanning electron microscopy, and X-ray diffraction. The micro-interfacial behavior between the colloidal particles and the solution during the integrated chelation-flocculation are elucidated. Thus, CPCTS-based flocculants could be a potential material for the removal of high amounts of Cr and Ni ions in industrial wastewater.

Synthesis, Characterization, and Sludge Dewaterability Evaluation of the Chitosan-Based Flocculant CCPAD.

Carboxymethyl chitosan (CMCS), acrylamide, and methacryloxyethyltrimethyl ammonium chloride were used as co-monomers to produce a sludge dewatering agent carboxymethyl chitosan-graft-poly(acrylamide-methacryloxyethyltrimethyl ammonium chloride) (CCPAD) by UV-induced graft polymerization. Single-factor experiments and response surface methodology were employed to investigate and optimize the grafting rate, grafting efficiency, and intrinsic viscosity influenced by the total monomer concentration, CMCS concentration, cationic degree, pH value, and illumination time. The structure, surface morphology, and thermal stability of CCPAD were characterized by infrared spectroscopy, hydrogen nuclear magnetic resonance, X-ray diffraction, scanning electron microscopy, and differential thermal-thermogravimetry. The raw sludge with 97.9% water content was sourced from the concentrated tank of a sewage treatment plant and used in the sludge condition experiments. In addition, CCPAD was applied as the sludge conditioner to investigate the effects of cationic degree, intrinsic viscosity, and pH on the supernatant turbidity, moisture content, specific resistance to filtration, and sludge settling ratio. Moreover, the mechanism of sludge conditioning by CCPAD was discussed by examining the zeta potential and extracellular polymeric substance (EPS) content of the supernatant. The sludge dewatering results confirmed that CCPAD had excellent performance for improving sludge dewaterability.

Electrochemical degradation of oxytetracycline by Ti-Sn-Sb/γ-Al2O3 three-dimensional electrodes.

In this work, Ti-Sn-Sb/γ-Al2O3 particle electrodes were prepared and employed for the degradation of oxytetracycline (OTC) by three-dimensional electrocatalytic technology. Factors associated with the preparation of Ti-Sn-Sb/γ-Al2O3 particle electrodes were investigated. The effects of initial concentration, conductivity, pH value, aeration intensity, current density, plate spacing, and particle electrode dosage on OTC removal were studied. The removal rate of OTC and total organic carbon were achieved approximately 92.0% and 41.0% under the optimal operating condition, respectively. In addition, Ti-Sn-Sb/γ-Al2O3 particle electrode was analyzed by Fourier Transform Infrared spectroscopy (FT-IR), scanning electron microscope (SEM), energy dispersive spectrum analysis (EDX), X-Ray Fluorescence Spectrometer (XRF), and X Ray Diffraction analysis (XRD), which indicated that a significant amount of TiO2, SnO2, and Sb2O3 were formed on the surface of Ti-Sn-Sb/γ-Al2O3 particle electrode. It was also observed that the primary function of Ti-Sn-Sb/γ-Al2O3 particle electrode in the three-dimensional electrode electrolysis process is the strong oxidizing function of ·OH for degrading OTC. Consequently, the analysis of degradation products of oxytetracycline (OTC) demonstrates. In addition, the results and conclusions of this study provide a methodological basis and engineering practice basis for removing the low concentration of antibiotics in water.

Degradation of chloramphenicol using Ti-Sb/attapulgite ceramsite particle electrodes.

Ti-Sb/attapulgite ceramsite particle electrodes were prepared for the efficient degradation of chloramphenicol (CAP) in wastewater. To observe the surface morphology and structural characteristics of the Ti-Sb/attapulgite ceramsite particle electrodes, Fourier transform infrared spectroscopy, X-ray fluorescence, scanning electron microscopy, and X-ray diffraction were used for characterization. Parameters affecting the degradation efficiency and the energy consumption of the Ti-Sb/attapulgite ceramsite particle electrodes, such as current density, electrode distance, initial pH, conductivity, air flow, and packing ratio, were examined. Results showed that the optimal conditions were 20 mA/cm2 current intensity, 3 cm electrode distance, 5,000 µS/cm conductivity, 2.0 L/min air flow, 50.0% packing ratio, and initial pH 1. The removal efficiency of chloramphenicol was 73.7% under the optimal conditions, and the energy consumption was 191.3 (kW h)/kg CAP. PRACTITIONER POINTS: Attapulgite ceramsite with good physical performance was prepared. The removal efficiencies for CAP in water by Ti-Sb/attapulgite ceramsite particle electrodes were studied. CAP was effectively removed by 3-D electrode system. CAP removal was significantly influenced by operational parameters. Three-dimensional electrode system shows good degradation ability.

Characterization and flocculation evaluation of a novel carboxylated chitosan modified flocculant by UV initiated polymerization.

In this work, carboxylated chitosan modified flocculant (CC-g-PCD) was prepared by graft copolymerization technique to enhance the charge-attracting and adhesion of bridges and net-sweeping capacity of flocculants. The dimethyldiallylammonium chloride (DMDAAC), carboxylated chitosan (CMCS), and 3-chloro-2-chloropropyltrimethylammonium chloride (CTA) were utilized for synthesis of CC-g-PCD via photopolymerization techniques. The synthesized CC-g-PCD was characterized by 1H NMR, SEM, XRD, and FTIR, and the characteristic groups on the main chain and surface morphological structure of CC-g-PCD were investigated. The obtained results indicated that CTA and DMDAAC were successfully grafted into the CPCTS. In ordered to evaluate the flocculation performance of CC-g-PCD at various dosages, stirring intensity (G value), and pH value by detecting Chl a, COD, and turbidity, the actual lake water that contains algae was used for flocculation assessment tests. The experimental results of the water sample with flocculation showed that the maximum flocculation efficiency of turbidity (91.1%), Chl a (97.2%), and COD (97.0%) can be achieved by CC-g-PCD at pH 7, G value 200 s-1, and 4.0 mg/L. The comparison results demonstrated that CC-g-PCD had better flocculation efficiency than commercial flocculants. Finally, based on the analysis of algae removal in combination with Zeta potential measurements, the flocculation mechanisms in actual lake water at various dosages and pH values were adsorption bridging and electrical neutralization.

Plasma-induced synthesis of chitosan-g-polyacrylamide and its flocculation performance for algae removal.

Chitosan (CS)-g-polyacrylamide (PAM) is a highly efficient and environmentally friendly flocculant, which was synthesized through plasma-induced graft copolymerization of CS and acrylamide (AM). The effects of monomer concentration, AM:CS ratio, discharge power, discharge time, post-polymerization temperature, and post-polymerization time on the intrinsic viscosity, grafting ratio, and grafting efficiency of CS-g-PAM were investigated. The optimum conditions of graft copolymerization were as follows: 20% monomer concentration, 7:3 AM:CS ratio, 40 W discharge power, 90 s discharge time, 50°C post-polymerization temperature, and 24 h post-polymerization time. The structural characteristics of CS-g-PAM were characterized by Fourier-transform infrared spectroscopy, scanning electron microscopy, and X-ray diffraction. CS-g-PAM exhibited better flocculation efficiency than the commercially available PAM in both diatomite-simulated wastewater and low-turbidity algal water. The optimal turbidity removal efficiency for the diatomite-simulated wastewater was 99.9%, which was obtained with 6 mg L-1 of CS-g-PAM at pH 11.0 and 250 s-1 of velocity gradient. In low-turbidity algal water, the optimal removal efficiencies for chlorophyll-a, turbidity, and COD were 93.6%, 94.5%, and 98.2%, respectively.

Electrocatalytic oxidation of tetracycline by Bi-Sn-Sb/γ-Al2O3 three-dimensional particle electrode.

In this work, highly efficient Bi-Sn-Sb/γ-Al2O3 particle electrodes were prepared for effectively degrading tetracycline. The effects of a mass ratio (Sn: Sb), the mass ration of Bi:(Sn + Sb), impregnation times, calcination temperature, and calcination time on the electrocatalytic oxidation capacity of Bi-Sn-Sb/γ-Al2O3 particle electrode was investigated. Conditions in which mass ratio of (Sn: Sb) = 10:1, the mass ratio of Bi:(Sn/Sb) = 1:1, impregnation times 2 h, calcination temperature 500 °C., and calcination time 3 h were considered as optimal preparation conditions for Bi-Sn-Sb/γ-Al2O3 particle electrode. It was cherecterized by infrared spectroscopy (IR), scanning electron microscope (SEM), energy dispersive X-ray detector (EDX), X-Ray Diffraction (XRD), and X-ray fluorescence (XRF) techniques to conforming that the triclinic Bi2O3 formed in the preparation conditions has superior electrocatalytic activity. The electrocatalytic oxidation mechanism of tetracycline by Bi-Sn-Sb/γ-Al2O3 particle electrode is proposed by determining degradation intermediates through LC-MS detection. Electrocatalytic oxidation experiments by adding tert-butyl alcohol indicate that the formation of OH is the primary responsibility for degradating tetracycline. Electrocatalytic degradation of tetracycline at different initial concentration shows that the degradation of tetracycline meets the pseudo first-order kinetics. Results suggest that the three-dimensional electrochemical reactor with Bi-Sn-Sb/γ-Al2O3 particle electrodes could be an alternative for the pretreatment of antibiotic wastewater before biological treatment.

Metal-Crown Ether-Porphyrin Decorated Gold Nanoparticles as High Sensitive Raman Ion Probe.

A kind of gold nanoparticles modified with metal crown ether porphyrin (GNPs-CP) was synthesized and characterized. The surface of the resulting gold particles was partially covered by metal crown ether porphyrin molecules through strong covalent Au-S bond. Based on the coupling effect of metal porphyrin and crown ether, the resulting composite gold nanoparticles can serve as a kind of ion probe. Raman and UV-Vis spectra were utilized to evaluate the ion recognition of the system, both of which changed dramatically when meeting metal ion corresponding to ligand of crown ether. Compared with UV-Vis spectra, Raman spectra of the composites are more sensitive and the limit of detection (LOD) can reach 1 × 10-8 g/mL. The study provides a candidate with higher sensitivity to replace current UV-Vis spectrum based evaluation tool for ion recognition.

UV-initiated synthesis of a novel chitosan-based flocculant with high flocculation efficiency for algal removal.

In this study, maleyl chitosan-graft-polyacrylamide (MHCS-g-PAM), a novel chitosan-based flocculant, was prepared through UV irradiation, and maleyl chitosan (MHCS) was designed and prepared with maleic anhydride and acrylamide (AM) through maleyl acylation reaction. The effects of monomer concentration, MHCS-to-AM ratio, illumination time, initiator concentration, pH on viscosity, and grafting efficiency were investigated to optimize the synthesis of these substances. MHCS-g-PAM was characterized through Fourier transform infrared spectroscopy, nuclear magnetic resonance hydrogen spectroscopy, scanning electron microscopy, and thermal gravimetric analysis. Flocculation mechanisms in alga-containing wastewater at various pH levels and dosages were examined in detail on the basis of zeta potential measurements. Zeta potential experiments indicated that the adsorption-bridging and charge neutralization mechanisms played an important role in algal removal. Flocculation tests on algal removal demonstrated that the flocculation performance of MHCS-g-PAM was more effective than that of cationic polyacrylamide, polyferric sulfate, and polymeric aluminium. The optimal Chl-a and COD removal rate obtained by MHCS-g-PAM was 98.6% and 94.9% at pH7 and 4mg·L-1, respectively.

Plasma-initiated polymerization of chitosan-based CS-g-P(AM-DMDAAC) flocculant for the enhanced flocculation of low-algal-turbidity water.

In this work, a highly efficient and environmentally friendly chitosan-based graft flocculant, namely, acrylamide- and dimethyl diallyl ammonium chloride-grafted chitosan [CS-g-P(AM-DMDAAC)], was prepared successfully through plasma initiation. FTIR results confirmed the successful polymerization of CS-g-P(AM-DMDAAC) and P(AM-DMDAAC). P(AM-DMDAAC) was the copolymer of acrylamide- and dimethyl diallyl ammonium chloride. SEM results revealed that a densely cross-linked network structure formed on the surface. XRD results verified that the ordered crystal structure of chitosan in CS-g-P(AM-DMDAAC) was changed into an amorphous structure after plasma-induced polymerization. The flocculation results of low-algal-turbidity water further showed the optimal flocculation efficiency of turbidity removal rate, COD removal rate, and Chl-a removal rate were 99.02%, 96.11%, and 92.20%, respectively. The flocculation efficiency of CS-g-P(AM-DMDAAC) were significantly higher than those obtained by cationic polyacrylamide (CPAM) and Polymeric aluminum and iron (PAFC). This work provided a valuable basis for the design of eco-friendly naturally modified polymeric flocculants to enhance the flocculation of low-algal-turbidity water.

[Study of microorganism sterilization by instant microwave and electromagnetic pulse].

The sterilization effects of constant electromagnetic wave and instant pulse on foods and traditional Chinese medical pills are introduced in this paper. From the velum's voltage variation caused by the outward electric filed,the dielectric properties of membranaceous ion and the pass rate of the membranaceous ion, we could analyze the biological heating effect and the biological non-heating effect. The sterilization effect of constant electromagnetic wave is based on the biological heating effect, while the instant electromagnetic pulse is based on the biological non-heating effect. With the applied electronic field, the voltage of membrane could increase, which results in the gates of K+ open, and the flowing out of K+. And the variation of the membranaceous voltage makes the gates of Ca2+ open. The Ca2+ of large consistency could come into the cell by the gradient of voltage. It could induce the death of the cells. The greater the variation of membranaceous voltage becomes, the higher will be the death rate of the cells.