Search

Introduction Incomplete hemostasis after vascular cannulation can cause a hematoma or pseudoaneurysm. We hypothesized that a hydrogel-coated needle would effectively and rapidly stop bleeding after vascular cannulation.Methods: A hydrogel composed of sodium alginate, hyaluronic acid, and calcium carbonate was coated onto the surface of suture needles. Needles were observed using scanning electronic microscopy (SEM) and immunofluorescence. Cannulation was performed in both mouse and rat models; the liver, kidney, jugular vein, inferior vena cava and aorta were punctured using uncoated and hydrogel-coated needles. Needles coated with a hydrogel with and without CD34 antibody were used to puncture the rat jugular vein and aorta. Tissues were examined by histology and immunofluorescence.Results: The hydrogel was successfully coated onto the surface of 22G and 30G needles and confirmed by SEM. Hydrogel-coated needles rapidly stopped bleeding after cannulation of the liver, kidney, jugular vein, inferior vena cava and aorta. Hydrogel-coated needles that contained CD34 antibody attracted vascular progenitor cells near the puncture site; there were fewer M1-type macrophages and more M2-type macrophages.Conclusion: Hydrogel-coated needles can effectively and rapidly stop puncture-site bleeding. The hydrogel that contains CD34 antibody attracted vascular progenitor cells, potentially promoting healing of the site after cannulation. Statement of significance Incomplete hemostasis after vascular cannulation can cause a hematoma or pseudoaneurysm and remains a significant clinical problem. We developed a hydrogel composed of sodium alginate, hyaluronic acid, and calcium carbonate; hydrogel-coated needles effectively and rapidly stopped bleeding after vascular cannulation. Interestingly, the hydrogel can also serve as a carrier for drugs that are delivered to the puncture site during the short time of cannulation that could additionally promote puncture site healing. Hydrogel-coated needles may be a new method for rapid hemostasis with application to patients especially at risk for bleeding.

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.

In this work, CeO2 nanosheets decorated with Ag2O and AgBr are successfully fabricated via a simple sediment-precipitation method. The as-prepared ternary Ag2O/AgBr–CeO2 composite with double Z-scheme construction was analyzed by various analytical techniques. Ag nanoparticles (NPs) used as the electron medium could reduce the recombination of photoelectrons and holes, thus leading to the improvement of photocatalytic performance of these catalysts. Due to the unique structure and composite advantages, the optimal Ag2O/AgBr–CeO2 photocatalysts exhibit the superior tetracycline (TC) degradation efficiency of 93.23% and favorable stability with near-initial capacity under visible light irradiation. This ternary Z-scheme structure materials will be the well-promising photocatalysts or the purification of antibiotic wastewater.

Rare earth metal (RE = La, Pr, Nd, Y)-doped CoCeOx catalysts were prepared and evaluated for eliminating chlorobenzene (CB). Characterization results showed that the doped RE metal simultaneously a...

A polyaspartic acid derivative (PASP-Im) as a novel scale inhibitor was synthesized by a simple green synthesis route with polysuccinimide and iminodiacetic acid as the starting materials. The as-synthesized PASP-Im was characterized via nuclear magnetic resonance spectroscopy (1H-NMR) and Fourier transform infrared spectrometry (FT-IR), and its scale inhibition performance was evaluated by a static scale inhibition method. Moreover, scanning electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and density functional theory computational studies were conducted to explore the scale inhibition mechanism of PASP-Im. The findings indicate that the as-synthesized PASP-Im exhibits better antiscale performance against the CaCO3 deposits than the unmodified PASP because of the introduction of iminodiacetic acid group. It also can change the crystallization path of calcium carbonate from stable calcite to vaterite that is dispersible in water, thereby resulting in great changes in the morphology of the CaCO3 scale. Furthermore, the O and N atoms in the negatively charged functional groups (such as –NH2 and –COOH) of PASP-Im can interact with calcium ions to block the active growth point of CaCO3 crystals, which also accounts for the excellent antiscale performance of PASP-Im. With new insights into the synergy between the functional groups of the antiscale molecule and scale-forming ions, this approach would be helpful towards the development of novel high-performance anti-scaling macromolecules.

In this study, the degradation of ofloxacin (OFX) over Cu–Ce tyre carbon catalysts by the microwave assisted persulfate process was examined for the first time. The results showed that the Cu–Ce tyre carbon catalysts dramatically improved OFX decay efficiency. The optimal reaction conditions were the Cu–Ce tyre carbon catalysts of 2.0 g/L and the persulfate dosage of 12.0 g/L under microwave power of 400 W at 60 °C. The OFX conversion and total organic carbon (TOC) removal reached 95.8% and 87.6%, respectively, after 60 min catalytic oxidation under optimal conditions. To identify the properties of Cu–Ce tyre carbon catalyst, scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), the Brunauer-Emmett-Teller (BET), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and the ultraviolet–visible (UV–vis) diffuse reflectance spectra studies have been carried out. Eleven kinds of degradation products and five pathways during degradation process of OFX and degradation products were identified by GC–MS and HRMS.

In the present work, an attempt has been made for the development of green and high efficiency acid pickling inhibitor based on the eco-friendly polyaspartic acid (PASP). In this view, cysteamine modified PASP (PASP-S) containing S atom was prepared by ring-opening reaction of polysuccinimide with cysteamine. The corrosion inhibition performance of PASP and PASP-S for mild steel in 0.5 M H2SO4 medium were evaluated using weight loss, electrochemical impedance and potentiodynamic polarization methods. The inhibition performance of PASP-S is greatly improved with a high efficiency of 93.9% (weight loss method) at a very low concentration of 100 mg L−1 at 298 K in comparison with unmodified PASP. The obtained results also indicate that PASP-S is a mixed inhibitor and the adsorption of PASP-S on the mild steel surface follows Langmuir adsorption isotherm. Theoretical chemical parameters are calculated using the Density Functional Theory method (DFT). The excellent inhibition performance of PASP-S is due to the presence of pendent functional sulfhydryl group, which can be confirmed by X-ray photoelectron spectroscopy (XPS) analysis of the mild steel samples. The present work provides a simple and effective pathway for synthesizing high efficiency acid pickling inhibitor by introducing a functional group into the PASP chains. Such chemical modification method may also be an effective strategy to improve the efficiency of other polymer acid pickling inhibitors.

Removal of phosphate from industrial is important to prevent the occurrence of eutrophication and adsorption may serve as a powerful supplement to chemical or biological phosphate sequestration. Here, a novel nanocomposite material Ti-NS is proposed to enhance phosphate removal from aqueous system by impregnating titanium oxides inside a millimeter-sized polymer (NS). The resulting Ti-NS possesses two distinct sites for phosphate removal, the ammonium groups bound to the NS matrix and the loaded titanium oxide nanoparticles. The maximum adsorption capacity of Ti-NS occurs at near-neutral pH, and exhibited fast kinetic behavior for phosphate uptake which could be well described by the pseudo-first-order model and intraparticle diffusion model. Compared with NS host, Ti-NS exhibits much higher capacity and preference toward phosphate removal in the presence of competing anions at greater levels. SEM-EDS and XPS study confirmed that phosphate uptake by Ti-NS was involved in two distinct adsorption interactions, i.e. ion exchange to the quaternary ammonium groups of host and ligand exchange reactions to the hydroxyl groups of titanium oxides. Cyclic adsorption and regeneration runs in fixed-bed indicated that Ti-NS is of great potential for phosphate removal from the water containing competitive anions at higher levels. Moreover, the exhausted nanocomposite can be effectively regenerated by NaOH-NaCl solution for recycle use with negligible capacity loss. All the results demonstrated that prepared Ti-NS was a promising alternative adsorbent for efficient phosphate removal from contaminated water.

The graft copolymer flocculant of chitosan namely, maleoyl chitosan-graft-poly(acrylamide–acryloxyethyl trimethyl ammonium chloride) [MHCS-g-P(AM-DAC)], was prepared by UV initiation to improve the solubility and flocculation efficiency of chitosan. Flocculating properties for algae removal were studied systematically. The effects of parameters such as monomer concentration, MHCS content, illumination time, photoinitiator concentration, cationic degree, pH and grafting efficiency over synthesis process of MHCS-g-P(AM-DAC) were studied. The characterization of obtained MHCS-g-P(AM-DAC) were carried out through different analytic techniques. The influences of dosage, pH, and G value on the flocculating properties were also investigated to support that MHCS-g-P(AM-DAC) was more effective than organic flocculant (CPAM) and inorganic coagulant (PFS and PAC) on algae removal. The flocculation mechanisms of MHCS-g-P(AM-DAC) were determinate by obtained zeta values.

In this study, a novel flocculant called PDD was synthesized under ultraviolet irradiation using acrylamide (AM), methacryloyloxyethyl trimethylammonium chloride (DMC), and dimethyldiallylammonium chloride (DMDAAC) as monomers. The effects of monomer concentration, cationic degree, cationic monomer ratio, photo-initiation time, photo-initiator concentration, and pH value on the conversion rate and relative molecular mass of PDD were investigated through single-factor and orthogonal experiments. The microstructure of the synthesized product PDD was characterized by Fourier transform infrared spectroscopy, scanning electron microscopy, thermogravimetry–differential thermal analysis, and proton nuclear magnetic resonance. The factors that ensure the optimal sludge dewatering performance of PDD obtained under the optimal synthesis conditions were as follows: flocculant dosage = 80 mg/L, pH value = 3, cationic degree = 60%, and relative molecular mass = 9.0 × 106. The solid content of the sludge filter cake, the residual turbidity of the filtrate, and the sludge specific resistance under the optimal synthesis conditions were 31.44%, 11.80 NTU, and 2.11 × 109 m/kg, respectively. Dewatering experimental results showed that PDD had significantly better sludge dewatering efficiency than the commercial flocculants. The main mechanisms for sludge conditioning were adsorption–bridging interaction and electrical neutralization after determining the zeta potential.

The effective treatment of membrane concentrate is a major technical challenge faced by the new coal chemical industry. In this study, a supported perovskite catalyst LaCoO3/X was prepared by a sol–impregnation two-step method. The feasibility of the supported perovskite catalyst LaCoO3/X in the UV-catalytic wet hydrogen peroxide oxidation (UV-CWPO) system for the purification of concentrated liquid of coal chemical wastewater was investigated. The effects of catalyst support, calcination temperature, calcination time, and re-use time on catalytic performance were investigated by batch experiments. The catalysts were characterized by X-ray diffraction (XRD), Scanning electron microscopy (SEM), Brunauer–Emmett–Teller (BET), and X-ray photoelectron spectroscopy (XPS). Experimental results showed that the supported perovskite catalyst LaCoO3/CeO2 prepared using CeO2 as support, calcination temperature of 800 °C, and calcination time of 8 h had the best catalytic effect. The catalytic performance of the catalyst remained excellent after seven cycles. The best prepared catalyst was used in UV-CWPO of coal chemical wastewater membrane concentrate. The effects of H2O2 dosage, reaction temperature, reaction pressure, and catalyst dosage on UV-CWPO were determined. Under the conditions of H2O2 dosage of 40 mM, reaction temperature of 120 °C, reaction pressure of 0.5 MPa, catalyst dosage of 1 g/L, pH of 3, and reaction time of 60 min, the removal efficiencies of COD, TOC, and UV254 were 89.7%, 84.6%, and 98.1%, respectively. Under the optimal operating conditions, the oxidized effluent changed from high toxicity to non-toxicity, the BOD5/COD increased from 0.02 to 0.412, and the biodegradability of the oxidized effluent was greatly improved. The catalyst has a simple synthesis procedure, excellent catalytic performance, and great potential in the practical application of coal chemical wastewater treatment.

Sludge derived carbon (SC) has been widely used in advanced oxidation processes as an effective and economic catalyst. In this study, we applied surface modified SC for the first time to catalyze the heterogeneous photo-Fenton process with ciprofloxacin, a highly concerned emerging contaminant, as a model substance. H2SO4 was used to acidify the SCs under varying acid dosages, temperatures, and reaction time lengths. The surface acidity of SCs was quantitatively characterized with NH3-TPD. A strong correlation between the surface acidity and the catalytic activity was clearly demonstrated. The highest catalytic activity was obtained with SC whose acidity was 0.149 mmol·g−1 after being modified with 6 mol·L−1 H2SO4 at −20 ℃ for 24 h. In addition, XRD, XRF, BET, XPS, and HRTEM were also used to characterize the obtained SC. ·OH radicals were found to be the main reactive species by EPR. Ten transformation products were identified by GC–MS, based on which three possible reaction pathways were proposed.

In order to solve the disadvantages of most of the photocatalyst, ZnFe2O4 is chosen as the magnetic material and prepared ZnFe2O4/Ag3PO4 composite photocatalysts. ZnFe2O4 is prepared by hydrotherma...

To improve the corrosion inhibition efficiency of eco-friendly polyaspartic acid (PASP) for mild steel in acidic solutions, PASP/N-(3-aminopropyl)imidazole (PD-1) and PASP/N-(3-aminopropyl)-imidazole-co-n-dodecylamine (PD-2) were chemically synthesized by the facile ring-opening reaction of polysuccinimide. Inhibition efficiencies of PD-1 and PD-2 for mild steel in a 0.5 M H2SO4 solution were investigated by electrochemical measurements (electrochemical impedance and polarization) and the weight loss method. In comparison with PASP, PD-1 and PD-2 show improved inhibition efficiencies due to the functional groups. In particular, PD-2 shows superior corrosion inhibition capacity, and the efficiency is up to 94% at a relatively low concentration of 100 mg L−1 at 298 K, as determined by potentiodynamic polarization measurements. Surface analysis of mild steel with PD-2 as an inhibitor clearly indicates that the inhibitor molecules adsorb on the steel surface and efficiently inhibit the corrosion of mild steel. The present work provides very meaningful results in designing and preparing new polymer inhibitors with high inhibition efficiency.

In this study, spinel-type MnFe2O4 magnetic nanoparticles were successfully synthesized employing the purified sol–gel method and used for the advanced treatment of biologically pretreated semi-coking wastewater (BPSCW) by the O3/H2O2 catalytic system. Results showed that the MnFe2O4 magnetic catalysts did not have a regular surface morphology, and their surface contained numerous fine particles that showed a particle accumulation state and formed a good nano-spinel structure. Their surface morphology, ratio, size, and X-ray photoelectron spectroscopy revealed two active metal elements in the catalyst, namely, Fe3+ and Mn2+, which were consistent with the elemental composition and valence of MnFe2O4. Under optimal reaction conditions, the removal efficiency of O3/H2O2/MnFe2O4 catalytic system for chemical oxygen demand (COD) and volatile phenol (VP) can reach 85.2% and 94.1%, respectively (catalyst dosage = 2.0 g∙L−1, O3 dosage = 1.2 mg∙min−1, H2O2 concentration = 0.15 mol∙L−1, pH = 7.0, and treatment time = 70 min). The free radical quenching experiment and electron paramagnetic resonance (EPR) experiment verified that hydroxyl radicals (∙OH) played a role in the deep treatment of BPSCW in the O3/H2O2/MnFe2O4 catalytic system. Phosphate experiments proved that lewis acid sites on the surface of the MnFe2O4 magnetic catalysts were the catalytically active sites. The superparamagnetic properties of the MnFe2O4 magnetic catalysts (67.8 emu∙g−1) facilitated magnetic separation from the treated wastewater. After 10 cycles, the activity of the MnFe2O4 magnetic catalysts remained high, and the removal efficiencies of COD and VP only decreased by 13.6% and 11.9%, respectively. Considering excellent degradation performance, easy magnetic separation and high stability, this study provided important insights into the practical application of the O3/H2O2 catalytic system for the advanced treatment of BPSCW.

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.

Confining metal oxide nanoparticles (NPs) in carriers such as carbon nanotubes (CNTs) has become a novel strategy for designing highly efficient and stable non-noble metal chainmail catalysts. In this study, Fe3O4 NPs were confined in the chainmail of multi-walled CNTs to prepare Fe3O4@CNT magnetic nanocomposite with confinement effect, and peroxydisulfate (PDS) was activated to degrade tetracycline (TL) in aqueous solution. Under the conditions of 20 °C, pH0 = 7, 0.5 mM PDS and 0.4 g/L Fe3O4@CNT, TL degradation efficiency of 98.1% could be achieved by radicals ( OH, SO4 −, O2 −) and non-radicals (1O2) generated in the system. Stable carbon-layer structure can protect Fe3O4 NPs inside the chainmail from the influence of reaction environment. TL degradation efficiency still reached 80.2% after five cycles, and the leaching of Fe ions was less than 10 μg/L during each cycle. Electrochemical analysis and density functional theory (DFT) calculations show that electron transfer from active Fe3O4 NPs to the carbon layer to motivate the catalytic activity of carbon surface. This work will provide an innovative path for the application of chainmail catalysts in nano-water environmental remediation.

In this study, a Cu–Ce@Az ozone catalyst with multiple active components was prepared through the impregnation method to treat purified terephthalic acid (PTA) wastewater, and characterized by X-ray diffraction, X-ray fluorescence spectroscopy, scanning electron microscopy, specific surface area analysis, X-ray energy spectroscopy, X-ray photoelectron spectroscopy, and other methods. The Cu–Ce@Az ozone catalyst had a developed pore structure with a large specific surface area and crystal structure. After calcination, the metallic elements Cu and Ce existed in the state of oxides CuO and CeO2. The effects of reaction time, solution pH, catalyst dosage, and ozone dosage on the catalytic oxidation performance of the Cu–Ce@Az ozone catalyst were studied. Adding tert-butanol reduced the removal rate of COD from the PTA wastewater through the catalytic oxidation system, which proves that a Cu–Ce@Az ozone catalyst treatment process of PTA wastewater follows the free-radical reaction mechanism. The results of 3D fluorescence spectroscopy analysis show that the organic matter in the PTA wastewater was converted into tryptophan organic matter and aromatic organic matter after the reaction of the catalytic oxidation system. Ultraviolet absorption spectroscopy analysis indicated that in unsaturated chemical bonds, some conjugated structures and benzene ring structures of organic matter in the PTA wastewater were destroyed.

Molecular imprinting technology in combination with photodegradation technology was applied to synthetize HPW-CS/TiO2/FACS photocatalysts. The novel photocatalyst could not only exhibit high photoc...

Based on an efficient and bottom-up synthesis technique, Bismuth Selenide (Bi 2 Se 3 ) nanoplatelets with uniform morphology and average thickness down to 3–7 nm had been fabricated. Its nonlinear absorption property under high power excitation had been well characterized by our Z-scan measurement system at different illumination wavelengths, and we found that the as-fabricated bi-layer Bi 2 Se 3 nanoplatelets show unique nonlinear optical responses, that is, with a saturable optical intensity of 32 GW/cm 2 (resp. 3.7 MW/cm 2 ) and a modulation depth of 88% (resp. 36%) at 800 nm (resp. 1565 nm). By implementing its saturable absorption property, we designed an optical saturable absorber device based on bilayer Bi 2 Se 3 nanoplatelets through deposited them onto the end-facet of optical fiber. The as-fabricated optical saturable absorber device allows for the generation of mode-locking pulses at 1571 nm with pulse duration of 579 fs and a repetition rate of 12.54 MHz at a pump power of 160 mW. The method on fabricating ultrathin Bi 2 Se 3 nanoplatelets may pave a new way to massive production of large-area topological insulator thin films that can be used in two-dimensional layered materials related photonics device.

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.

Even though the nonlinear optical effects of solution processed organic–inorganic perovskite films have been studied, the nonlinear optical properties in two-dimensional (2D) perovskites, especially their applications for ultrafast photonics, are largely unexplored. In comparison to bulk perovskite films, 2D perovskite nanosheets with small thicknesses of a few unit cells are more suitable for investigating the intrinsic nonlinear optical properties because bulk recombination of photocarriers and the nonlinear scattering are relatively small. In this research, we systematically investigated the nonlinear optical properties of 2D perovskite nanosheets derived from a combined solution process and vapor phase conversion method. It was found that 2D perovskite nanosheets have stronger saturable absorption properties with large modulation depth and very low saturation intensity compared with those of bulk perovskite films. Using an all dry transfer method, we constructed a new type of saturable absorber device...

Three-dimensional Ti-Sn/γ-Al 2 O 3 particle electrodes were prepared for the efficient degradation of chloramphenicol (CAP) in wastewater. To observe the surface morphology and structural characteristics of the Ti-Sn/γ-Al 2 O 3 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 energy consumption of the Ti-Sn/γ-Al 2 O 3 particle electrodes, such as conductivity, initial pH of wastewater, current density, air flow, and initial CAP concentration (100 mg·L −1 ), were examined. Results showed that the optimal conditions were 0.1 A current intensity, 1.0 L·min −1 air flow, 6000 μS·cm −1 conductivity, and pH 6. More than 70% of CAP was degraded under the optimal conditions. Based on the reaction intermediate products identified, a possible pathway for the electrochemical oxidation of CAP by the Ti-Sn/γ-Al 2 O 3 particle electrodes was proposed.

Multi-layer black phosphorus nanosheets (BPs) with different sizes are synthesized by using a basic solvent exfoliation method in association with controlled gradient centrifugation. Size-dependent nonlinear saturable absorption and Kerr nonlinearity as well as ultrafast carrier dynamics of BPs is systematically studied by using a Z-scan and pump–probe technique. Furthermore, an ultrashort pulse with a pulse duration of about 635 fs centered at a wavelength of 1562 nm is generated by using smaller sized BPs as a saturable absorber. These results directly reveal the physical processes of size-dependent nonlinear optical (NLO) properties of BPs and provide researchers with a viable approach in tailoring the NLO response of BPs through controlling the sizes, paving the way towards BP based electronics and optoelectronics applications such as ultrafast optical switches, modulators, fiber lasers, etc.

The use of attapulgite (ATP)-based materials for adsorption of pollutants from water and wastewater has received growing attention. However, recovering ATP-based adsorbents remains a challenge. In this study, a magnetic adsorbent ATP/CoFe2O4 with high tannic acid (TA) adsorptive capacity was fabricated via a facile co-precipitation approach and was well characterized. The loaded CoFe2O4 particles were embedded into the adsorbent surfaces to allow magnetic separability. For this material, its TA adsorption kinetics, isotherm behavior, and magnetic separation efficiency are reported. The developed magnetic composites had rapid sorption kinetics of 3 h, high sorption capacity of 109.36 mg/g, and good magnetic separation efficiency of 80%. The used ATP/CoFe2O4 was successfully regenerated by NaOH and reused five times without a substantial reduction in TA removal and magnetic performance. Intermolecular hydrogen bonding formation and surface complexation were identified as the sorption mechanisms of TA by ATP/CoFe2O4.

Cu-Mn-Ce@&gamma, Al2O3 was prepared by incipient wetness impregnation and used to catalyze ozonation in a coal chemical wastewater-biotreated effluent. The preparation factors that considerably affected the catalytic performance of Cu-Mn-Ce@&gamma, Al2O3, specifically metal oxide loading percentage, calcination temperature, and calcination time, were examined. The catalyst was characterized by scanning electron microscopy, energy dispersive spectrometry, X-ray diffraction, and Brunauer-Emmett-Teller analysis. The optimal catalytic ozonation operating parameters, such as ozone dosage, catalyst dosage, pH, and reaction time, were also investigated. Results showed that an optimized catalyst consisted of 17.0% CuO, 3.0% MnO2, and 2.0% CeO2 (wt.%). The optimal calcination temperature and calcination time were 600 &deg, C and 5 h. The optimal catalytic ozonation operating parameters, including ozone dosage, catalyst dosage, pH, and reaction time, were 7, 80.0 mg/L, 20.0 mg/L, 7 and 50 min, respectively. The COD removal of biotreated effluent increased to 61% under these optimal operating conditions. Meanwhile, ozonation alone resulted in only 20% removal. This work proposes the use of easily available Cu-Mn-Ce@&gamma, Al2O3 catalyst and might drive the advancement of catalytic ozonation for chemical wastewater purification.

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.

Optical tweezers, which exploit laser beams to control various particles, have been widely used in many fields. However, the potential wells are typically symmetrical in optical traps, which limit the performance of manipulating particles. Herein, we report an approach for creating asymmetrical potential wells, by employing variable phase gradient profiles tailored by holograms. The depth, stiffness and location of asymmetrical potential wells can be dynamically and accurately adjusted. Moreover, the controllable collective transport of nanoparticles are experimentally demonstrated as an application example, which exhibit excellent manipulation performance. Importantly, the motion path, step distance and velocity can be easily tuned by changing the holograms, which are highly desirable in the controllable transport. This study offers a new way to optically manipulate particles, which could largely expand the capability of conventional optical tweezers.

The preparation of W-Ag-Ti@γ-Al2O3 3D particle electrode was studied, and the preparation process was optimized on the basis of its electrolytic performance and treatment efficiency on coal chemical wastewater. Infrared spectroscopy, X-ray fluorescence, scanning electron microscopy, X-ray diffraction, and energy dispersive X-ray spectroscopy were used to characterize the loaded element, element morphology, and micromorphology of W-Ag-Ti@γ-Al2O3 3D particle electrode. Results show that the optimal conditions for the preparation of W-Ag-Ti@γ-Al2O3 3D particle electrode are as follows: Ti:Ag:W = 10:10:5, the calcination temperature of the particle electrode is 450 ℃, and the number of times of loading is twice. Coal chemical wastewater degradation was significantly influenced by operating conditions. The research on particle electrode regeneration and stability shows good electrolysis performance after four electrolysis procedures. The effects of conductivity, pH, current intensity, aeration, plate spacing, and filling degree on the removal efficiency of chemical oxygen demand (COD), ammonia nitrogen, and total phenol by W-Ag-Ti@γ-Al2O3 particle electrode were studied. Under the optimal optimization conditions, the COD removal rate was 67.6%, the ammonia nitrogen removal rate was 42.8%, and the total phenol removal rate was 51.7%. Three dimensional electrocatalytic system shows good degradation ability and capacity.

To develop high efficiency organic pickling inhibitor, a new β-amino alcohol compound named 1,16-(5,12-dihydroxy-7,10-dioxa-3,14-diazahexadecane) di-p-benzenesulfonamide (TDB) was well designed and synthesized. The corrosion inhibition performances of TDB for mild steel in 0.5 M H2SO4 solution were investigated by weight-loss, electrochemical impedance spectroscopy and potentiodynamic methods. It has been found that the inhibition efficiency of TDB derived from potentiodynamic method was 90.7 % at a low concentration of 10 mg/L at 25 °C. Effect of temperature indicated that the inhibition efficiency was still above 89 % even at 45 °C in the presence of 100 mg/L of TDB in 0.5 M H2SO4 solution. XPS analyses showed that TDB prevented the attack of the corrosive medium by adsorbing on the surface of the mild steel. Theoretical calculations indicated that the structure of TDB is conducive to form an adsorption layer on the mild steel surface.

Mn/MCM-41 and imp-Mn/MCM-41 catalysts were prepared in this study through metal heteroatom substitution and impregnation methods, respectively, and their catalytic oxidation performance of toluene under non-thermal plasma (NTP) in a dielectric barrier discharge reactor was studied. The stability of the catalyst and the parameters of catalytic oxidation conditions (initial concentration of toluene, O2 ratio, and relative humidity of carrier gas) were optimized. Characterization proved that the impregnation method resulted in the existence of manganese in the form of oxides (MnO2, Mn2O3) outside the pores of MCM-41. Meanwhile, the metal heteroatom substitution method implanted manganese into the mesoporous structure and replaced part of it with Si-O-Mn. NTP catalytic oxidation of toluene, ozone emission, and GC–MS by-product analysis confirmed that 60Mn/MCM-41 catalyst has high catalytic activity. Moreover, the catalyst affected the production of by-products. The stability test revealed that the 60Mn/MCM-41 catalyst still respectively reached 84.6% and 61% in the conversion of toluene and the selectivity of CO2 under the SED of 558 J/L after 40 h discharge reaction.

In this study, graphitic carbon nitride (g-C3N4) (CN) was conveniently and environmentally modified into a stable and easily recyclable photocatalyst for the high removal efficiency of dye contaminants in water. Magnetic carrier (CN/Fe3O4) and heterojunction photocatalysts (Ag@AgBr/CN/Fe3O4) were prepared by ultrasonic and in situ deposition of Fe3O4 and Ag@AgBr nanoparticles on the CN, respectively, and characterized by the surface structure, optical, and electrochemical properties. The effects of different catalysts, silver loading, catalyst dosage, and different aeration conditions on the photocatalytic degradation of RhB were investigated. Results exhibited that the removal rate of RhB by Ag@AgBr/CN/Fe3O4 reached 96% within 150 min when the Ag loading was 5%, the catalyst dosage was 0.4 g/L, and the aeration was air. Furthermore, the degradation rate constant was 17.3 × 10−3 min−1, which was 4.3 and 3.4 times higher than that of CN and CN/Fe3O4, respectively. The stability study demonstrated that Ag@AgBr/CN/Fe3O4 had almost no risk of Ag and Fe leakage and showed high stability. Mechanism study indicated that the construction of Z-scheme heterojunction between Ag@AgBr and CN and trapping electron by Fe3+ promoted charge transfer and electron–hole pair separation, thus enhancing photocatalytic activity.

In this study, co-precipitation was used to prepare Fe3O4 magnetic powder activated carbon (PAC) (Fe3O4-PAC) and MnFe2O4 magnetic PAC (MnFe2O4-PAC) for the in-depth treatment of glyphosate pesticide wastewater. Magnetic adsorbent characterization results indicate that MnFe2O4 was successfully loaded on the activated carbon powder. Adsorption experiment results show that the maximum adsorption capacity of MnFe2O4-PAC for glyphosate is two to three times that of the original PAC. The adsorption of glyphosate by using magnetic PAC conforms to the Langmuir adsorption isotherm, and the adsorption kinetics is consistent with the quasi-second adsorption kinetic model. The adsorption capacity of Fe3O4-PAC and MnFe2O4-PAC showed the same trend effect with the change in pH, temperature, and adsorbent dosage. The adsorption capacity of Fe3O4-PAC and MnFe2O4-PAC for glyphosate decreased with the increase in pH and magnetic PAC and rises with temperature. Regeneration experiment results showed that the order of the regeneration method of MnFe2O4-PAC is: microwave combined Fenton reagent regeneration > wet microwave regeneration > microwave combined hydrogen peroxide regeneration. MnFe2O4-PAC after regeneration still exhibited good magnetic properties and adsorption capacity.

We have investigated the nonlinear and ultrafast photonics of chemically processed black phosphorus quantum dots (BPQDs) synthesized by the solvothermal treatment approach, with an average lateral size of about 2.48 $\pm$ 0.4 nm. BPQDs exhibit optical saturable absorption measured by the balanced twin-detector measurement system at the telecommunication band and have been demonstrated for the generation of passively mode-locking operation in an erbium-doped fiber laser. Either two-pulse or three-pulse bound state of soliton pulse has been obtained, making the best use of the BPQDs-based saturable absorber. Our work suggests that BPQDs might be developed as an efficient optical saturable absorber for ultrafast photonics applications.

In this study, acrylamide and [2-(acryloyloxy)ethyl] trimethylammonium chloride were grafted onto CS by UV initiation to obtain an environmentally friendly graft copolymer, CS-g-poly(acrylamide-acryloyloxyethyl) trimethylammonium chloride (CS-g-PAD). Poly(acrylamide-acryloyloxyethyl) trimethylammonium chloride was named as PAD. Nuclear magnetic resonance hydrogen spectroscopy (1H NMR), X-ray powder diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscope (SEM), and thermal gravimetric analysis (TG-DSC) were used to characterize CS-g-PAD. Results confirmed the synthesis of CS-g-PAD. SEM results showed that CS-g-PAD exhibited a porous structure with numerous 2–6 μm micropores. The enhanced CaCl2-aided flocculation tests of wastewater contaminated by zinc phosphate coating indicated that CS-g-PAD had better flocculation performance than PAD and the commercially available cationic polyacrylamide (CPAM). The removal rates of zinc concentration, total phosphorus concentrat...

Photothermal therapy (PTT) offers many advantages such as high efficiency and minimal invasiveness, but clinical adoption of PTT nanoagents have been stifled by unresolved concerns such as the biodegradability as well as long-term toxicity. Herein, poly (lactic-co-glycolic acid) (PLGA) loaded with black phosphorus quantum dots (BPQDs) is processed by an emulsion method to produce biodegradable BPQDs/PLGA nanospheres. The hydrophobic PLGA not only isolates the interior BPQDs from oxygen and water to enhance the photothermal stability, but also control the degradation rate of the BPQDs. The in vitro and in vivo experiments demonstrate that the BPQDs/PLGA nanospheres have inappreciable toxicity and good biocompatibility, and possess excellent PTT efficiency and tumour targeting ability as evidenced by highly efficient tumour ablation under near infrared (NIR) laser illumination. These BP-based nanospheres combine biodegradability and biocompatibility with high PTT efficiency, thus promising high clinical potential., Black phosphorus is a biodegradable 2D material that has attracted growing interest in biomedicine. Here, the authors carry out in vitro and in vivo experiments to demonstrate that nanospheres loaded with black-phosphorus quantum dots perform as promising phothermal cancer therapy agents.

Ultrasmall black phosphorus quantum dots (BPQDs) with an average size of 2.1 ± 0.9 nm are synthesized by using a solvothermal method in a N-methyl-2-pyrrolidone solution. Verified by femto-second laser Z-scan measurement, BPQDs exhibit excellent nonlinear optical response with a modulation depth of about 36% and a saturable intensity of about 3.3 GW cm−2. By using BPQDs as optical saturable absorber, the ultrashort pulse with a pulse duration of about 1.08 ps centered at a wavelength of 1567.5 nm is generated in mode-locked fiber laser. These results suggest that BPQDs may be developed as another kind of promising nanomaterial for ultrafast photonics.

A dielectric barrier discharge (DBD) reactor with a rod-plate electrode configuration was used for the oxidative decomposition of Congo red dye in an aqueous solution. Plasma was generated in the gas space above the water interface under atmospheric pressure. Discharge characteristics were analyzed by voltage-current waveforms. Effects of applied voltage, initial conductivity, and initial concentration were also analyzed. Congo red discoloration increased with increased applied voltage and decreased conductivity. The initial conductivity significantly influenced the Congo red discoloration. Under the same conditions, the highest discoloration rate was obtained at 25 mg/L. The presence of ferrous ions in the solutions had a substantial positive effect on Fenton dye degradation and flocculation. At an applied voltage of 20 kV, about 100% of dye was degraded after 4 min of Fe2+/DBD treatment. Results showed that adding a certain dosage of hydrogen peroxide to the wastewater could enhance the discoloration rate. Possible pathways of Congo red discoloration by DBD plasma were proposed based on GC/MS, FTIR, and UV-vis spectroscopy analyses.

A titanium sulfonate ligand is synthesized for surface coordination of black phosphorus (BP). In contrast to serious degradation observed from the bare BP, the BP after surface coordination exhibits excellent stability during dispersion in water and exposure to air for a long period of time, thereby significantly extending the lifetime and spurring broader application of BP.

Composites of the graphene oxide-wrapped bipyramidal sulfur@polyaniline core–shell structure (S@PANI/GO) have been prepared at low temperature. The FT-IR and Raman spectra illustrated the chemical effect between PANI and GO, and the SEM images illustrated the tight connection with each other. As a cathode for Li–S batteries, the S@PANI/GO composite demonstrated better electrochemical performance than S@PANI, or S/GO composites. The S@PANI/GO composite delivered enhanced cycle stability (0.2 C, 875 mA h g−1 after 100 cycles) and high-rate capability (4 C, 466 mA h g−1). Even at 1 C, the S@PANI/GO composite still delivered a capacity of 641 mA h g−1 after 300 cycles. The enhanced performance should benefit from the core–shell structure with a synergistic effect between polyaniline and graphene oxide.

In this study, oily sludge (OS) was pyrolyzed into an environmentally friendly OS carbon (OSC) material, which was used as the carrier of CoFe2O4 nanoparticles to prepare a heterogeneous catalyst CoFe2O4/OSC, and it was used to catalyze the degradation of norfloxacin (NFC) by peroxymonosulfate (PMS). X-ray diffraction (XRD) and transmission electron microscope (TEM) characterization results show that CoFe2O4/OSC had a spinel structure under high temperature pyrolysis conditions. The effects of initial pH, PMS dosage, catalyst dosage, and temperature on NFC degradation efficiency were also studied. Under a temperature of 25 °C, an initial pH of 7, a catalyst amount of 0.5 g/L, and a PMS dosage of 0.8 mM, the reaction rate constant reached 0.051 min−1, and the degradation efficiency and total organic carbon of NFC reached 90.8% and 62%, respectively, within 60 min. Trace amounts of Co and Fe ions were leached from the system (both less than 30 μg/L). After ten cycles, the degradation efficiency of NFC decreased to 69.8%. Radical quenching experiments, electron paramagnetic resonance, and X-ray fluorescence spectroscopy characterization proved that free-radical ( OH, SO4 −, and O2 −) and nonradical (1O2) active species were present in the system. Moreover, the CoFe2O4/OSC/PMS system involved the participation of two pairs of redox couples (Fe(II)/Fe(III) and Co(III)/Co(II)). Results from matrix-assisted laser desorption ionization time-of-flight mass spectrometry and ion chromatography proved that the main oxidation pathways of NFC were formed through the fragmentation of heterocycles, defluorination of benzene rings, decarboxylation reactions, and piperazine ring-opening process. At the same time, NFC was eventually oxidized to fluoride. This study provides potential for the resource utilization of OS and the application of sludge-type catalysts in PMS-activated oxidation systems.

Small-molecule organic corrosion inhibitors have attracted extensive attentions, but there are relatively few studies on corrosion inhibitors based on eco-friendly polymer materials. In the present work, dopamine modified polyaspartic acid (PASP-Dop) was well-designed and prepared. The inhibition ability of PASP-Dop towards mild steel was studied at various concentrations and temperatures using electrochemical measurement and weight-loss method. Investigations indicate that PASP-Dop has high corrosion inhibition performance for mild steel in acid solution due to the effective adsorption of PASP-Dop molecules at the metal/solution interface which is found to obey the Langmuir adsorption isotherm. From the potentiodynamic polarization measurements, the inhibition efficiency of PASP-Dop for mild steel in 0.5 M H2SO4 solution at a concentration of 100 ppm is up to 90.9% at 298 K. In addition, effect of temperature performed by weight-loss measurement reveals that PASP-Dop has good temperature adaptability. These results clearly demonstrate that as-synthesized eco-friendly polymer (PASP-Dop) is a high efficiency corrosion inhibitor with good application prospect.

A novel magnetic diatomite was synthesized using a two-step method combining precipitation and combustion methods. The prepared magnetic diatomite with functional particles and strong magnetism was verified by X-ray diffraction, scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and vibrating sample magnetometer. Results showed that the modified magnetic diatomite performed better than the raw diatomite in the efficient removal of nitrobenzene from aqueous solution. The adsorption kinetics and the isothermal and desorption–adsorption properties were also studied. Results revealed that the adsorption kinetics and isothermal data corresponded to the pseudo-first-order kinetic model and chemisorption process. Desorption–adsorption experiments were conducted, and the as-prepared magnetic diatomite remained to have high nitrobenzene adsorption efficiency even after six cycles of desorption and adsorption. Furthermore, the synthesized magnetic diatomite can be quickly and easily separated using a magnet before and after adsorption.

Purifying wastewater and saving energy have become important prerequisites for global sustainable development. Currently, the application of various wastewater treatment processes for tert-butyl acrylate production wastewater is still restricted by energy-intensive factors. Aiming at addressing the trade-offs in water-energy nexus in purification of tert-butyl acrylate production wastewater, this study proposed a fluidized/fixed bed treatment system for catalytic oxidation purification of tert-butyl acrylate production wastewater. A high calorific value of rectification residue produced by the production of tert-butyl acrylate was introduced to simultaneously achieve low energy consumption and efficient purification of tert-butyl acrylate production wastewater and rectification residue. The effects of the operating conditions of fluidized and fixed beds and their coupling process on the purification effect of tert-butyl acrylate production wastewater were evaluated. Results showed that the efficiency of purifying tert-butyl acrylate production wastewater and rectification residue using the fluidized/fixed bed treatment system was considerable. The calculation results showed that the thermal balance of the system was enhanced due to the introduction of rectification residue, and the energy-saving rate reached 18%. Tert-butyl acrylate production wastewater was oxidized to small-molecule chemicals by proton transfer and demethylation during degradation process which was investigated by gas chromatography–mass spectrometry. Stability experiments indicated that the average removal efficiency of chemical oxygen demand in fluidized/fixed bed treatment system was 97.0%–98.5% for 600 h of continuous operation. The Cu/Ce/Mn catalyst exhibited good stability. Therefore, fluidized/fixed bed treatment system can effectively purify high-concentration organic wastewater and is a promising technology.

The ampholytic chitosan based flocculant carboxylated chitosan graft-(3-chloro-2-hydroxypropyl) trimethylammonium chloride-dimethyl diallyl ammonium chloride (CPCTS-g-P (CTA-DMDAAC)) was synthesized by photo polymerization using carboxylated chitosan (CPCTS), 3-chloro-2-chloropropyltrimethylammonium chloride (CTA) and dimethyldiallylammonium chloride (DMDAAC) as the cationic co-monomers. The effects of monomer concentration, the ratio of CPCTS and cationic monomers, cationic degree, initiator time, photoinitiator concentration, and pH value on the properties of CPCTS-g-P (CTA-DMDAAC) were studied. The microcystis aeruginosa that was cultured in laboratory was used for CPCTS-g-P (CTA-DMDAAC) flocculation tests. The effects of CPCTS-g-P (CTA-DMDAAC) dosage, pH value and G value on flocculation performance were investigated. The maximum removal rate of chlorophyll-a (Chl-a) and chemical oxygen demand (COD) that were obtained by CPCTS-g-P (CTA-DMDAAC) were 98.8% and 96.5% under the conditions of dosage 4 mg/L, pH 7 and G value 200 s−1, respectively. The flocculation experiments showed that chitosan-based flocculant CPCTS-g-P (CTA-DMDAAC) had better flocculation performance than commercially available flocculants cationic polyacrylamide (CPAM), Polyferric Sulfate (PFS), and polymeric aluminium (PAC).

This study converted sewage sludge into a carbonaceous catalyst via pyrolysis and employed it in the ozonation of hydroquinone. The catalyst was characterized by Mössbauer spectroscopy, X-ray photoelectron spectroscopy, temperature programmed desorption, scanning electron microscopy, transmission electron microscopy, Fourier transform infrared spectroscopy and X-ray diffraction. Intermediate products were detected by gas chromatography–mass spectrometry, and a pathway for hydroquinone degradation was proposed. The results showed that sludge pyrolyzed at 700 °C promoted hydroquinone degradation, compared with commercial activated carbon derived from coal. When the catalyst dose was 0.5 g/L, the hydroquinone (200 mg/L) removal rate reached 97.86% after exposure to ozone (the ozone concentration was 17 mg/L and the flow rate was 50 mL/min) for 60 min. The results indicated that basic groups contributed to the catalysis.

The adsorption of 2-phosphonobutane-1,2,4-tricarboxylic acid (PBTC) on calcite surfaces (), (1 0 2), (1 0 4), (1 1 3), (2 0 2) was studied by molecular simulation. The phosphoric acid and carboxylic acid functional groups energetically interacted with the faces and preferentially occupied the carbonate ion sites by chemisorption, which is in agreement with the critical pH experiments. The strength of adsorption followed the order of () > (1 1 3) > (1 0 2) > (2 0 2) > (1 0 4). The binding energy gradually decreased with increasing temperature. The relationship between the critical pH and the adsorbed PBTC2− configuration indicates that the adsorbed inhibitor configuration plays an important role in inhibitor efficiency.

In this study, coagulation, ozone (O3) catalytic oxidation, and their combined process were used to pretreat actual coking wastewater. The effects on the removal of chemical oxygen demand (COD) and phenol in coking wastewater were investigated. Results showed that the optimum reaction conditions were an O3 mass flow rate of 4.1 mg min&minus, 1, a reaction temperature of 35 &deg, C, a catalyst dosage ratio of 5:1, and a O3 dosage of 500 mg&middot, L&minus, 1. The phenol removal ratio was 36.8% for the coagulation and sedimentation of coking wastewater under optimal conditions of 25 &deg, C of reaction temperature, 7.5 reaction pH, 150 reaction gradient (G) value, and 500 mg&middot, 1 coagulant dosage. The removal ratios of COD and phenol reached 24.06% and 2.18%, respectively. After the O3-catalyzed oxidation treatment, the phenols, polycyclic aromatic hydrocarbons, and heterocyclic compounds were degraded to varying degrees. Coagulation and O3 catalytic oxidation contributed to the removal of phenol and COD. The optimum reaction conditions for the combined process were as follows: O3 dosage of 500 mg&middot, 1, O3 mass flow of 4.1 mg&middot, min&minus, 1, catalyst dosage ratio of 5:1, and reaction temperature of 35 &deg, C. The removal ratios of phenol and COD reached 47.3% and 30.7%, respectively.

The degradation behavior of oxytetracycline (OTC) in aqueous solution using sludge derived carbon (SC) was investigated in this paper. SC treated with different kinds of acids were characterized by BET and thermogravimetric analysis. The results showed that SC-H2SO4 exhibited higher catalytic activity than SC-HCl and SC. The maximum removal of OTC and total organic carbon (TOC) after catalytic oxidation process at 60 °C was 92.6% and 70.2%, respectively. The safety of antibiotics after advanced oxidation processes (AOPs) has attracted much attention due to the possibility of toxicity increasing. Seven intermediate products were identified by GC–MS and four pathways were proposed. Furthermore, the toxicity of OTC degradation was investigated by zebrafish embryos for the first time. Zebrafish incubated with OTC solution (TE2) had haemagglutination, pericardial edema and showed significant changes in heartbeat, body length, and roaming frequency compared with the normal nutrient solution (TE1). Moreover, all zebrafish embryos had condensation phenomenon and did not hatch out in the treated OTC solution (TE3). In contrast, the zebrafish could hatch out without abnormality cultured with the treated OTC solution adjusted to the neutral pH (TE4). Results indicated that the treated OTC solution after catalytic oxidation process should be adjusted to the neutral pH to reduce the toxicity to the ecology.