Chlorobenzene Concentration Research Articles

Identification of atmospheric emerging contaminants from industrial emissions: A case study of halogenated hydrocarbons emitted by the pharmaceutical industry

With the development of the pharmaceutical industry, halogenated hydrocarbons, which are the main raw materials and emissions of the pharmaceutical industry, may be defined as atmospheric emerging contaminants due to toxicity and low oxidation of the atmosphere. This study analyzed the volatile organic compounds (VOCs) emissions from four pharmaceutical companies located in the Yangtze River Delta. Samples were taken three times at each of the selected fixed and fugitive sampling sites in each company. Through testing, 141 VOCs were identified. The mean concentration and proportion of halogenated hydrocarbons from the four pharmaceutical companies were the highest of all the industries in the industrial park. They reached 18.9 ppm and 28.8 %, respectively. Fixed emissions of the companies exhibited the mean maximum concentration of dichloromethane and chlorobenzene, which are 11.4 ppm and 250.67 ppb. The mean concentration of fugitive emission of dichloromethane from the four companies in this study is lower than that of pharmaceutical companies in other studies. Newly detected halogenated hydrocarbons, such as 1,1-dichloropropanone and dichloronitromethane, present potential non-cancer and cancer risks to workers. Chlorobenzene was identified as a key potential cancer risk halogenated hydrocarbon the value of which reaches 0.00965. 2,6-dichloropyridine could be a potential emerging contaminant due to its lower MIR value and higher potential cancer risk. The study suggests that relevant pharmaceutical companies focus on the emissions of chlorobenzene and dichloromethane, which may be the atmospheric emerging contaminants for the pharmaceutical industry and focus on improve the treatment of waste gases in workshops and sewage stations.

Dielectric barrier discharge plasma for chlorobenzene removal: Performance optimization, process modeling, and toxicity evaluation

Bio-purification has been recognized as an effective method of removal of volatile organic pollutants (VOCs), yet exist a technical bottleneck of low removal efficiency in the treatment of high toxicity and low water-soluble VOCs, especially chlorobenzene (CB). Herein, dielectric barrier discharge (DBD) technology was used as a pre-treatment technology, and the effect of process parameters (specific input of energy (SIE), inlet concentration of CB, humidity, and discharge length) of DBD on the removal performance of CB was analyzed, in order to investigate the feasibility of DBD as a pre-treatment approach for bio-purification. Taking energy yield, by-product analysis and exhaust evaluation as considerations, an SIE of 1,131.57 J·L-1, an inlet CB concentration of 300 ppm, a humidity of 50 %, and a discharge length of 10 cm were selected as the most suitable experimental conditions for the air DBD reactor. The temperature of gas flow was analyzed. Results suggested that DBD have no adverse thermal effect on the subsequent biotechnology (decreased by about 8 K during the discharge process). The temperature change caused by the degradation of CB (e.g., phenyl ring-opening and other processes) accounts for about 90 % of the total temperature change, where remaining part of temperature decreased caused by the large number of active substances produced by electron excitation, collision and cracking during discharge. The regulation of short-life active substances (e.g., ·NO, ·NO2,·OH, and O2–·) further reduced the toxicity of the outlet gas generated by DBD through affect the contents the long-life active substances (e.g., H2O2, and O3). This study provides a better understanding of the feasibility of DBD as a treatment for bio-purification and a new coupling technology for the effective removal of CB.

Co-incineration of medical waste in municipal solid waste incineration increased emission of chlorine/brominated organic pollutants

Co-incineration of medical waste (MW) in municipal solid waste incinerators (MSWIs) is a crucial disposal method for emergency disposal of MW and the management of MW in small and medium-sized towns. This study aims to analyze and compare the levels and distribution patterns of chlorine/brominated dioxins and their precursors in fly ash from MSWIs and medical waste incinerators (MWIs) while also focusing on identifying the new pollution concerns that may arise from the co-incineration of municipal solid waste (MSW) mixed with MW (MSW/MW). The concentration of chlorobenzene (CBzs), polychlorinated biphenyls (PCBs) and polychlorinated dibenzo-p-dioxins/dibenzofurans (PCDD/Fs) in fly ash from co-incineration of MSW/MW are 887.4, 134.4 and 27.6 μg/kg, respectively, which are 5.1, 2.0 and 2.9 times higher than that from MSWIs. The levels of polybrominated dibenzo-p-dioxins/dibenzofurans (PBDD/Fs) are about three orders of magnitude lower than that of PCDD/Fs. For the fly ash from MSWIs, the predominant PCDD/Fs congener is OCDD, which prefers synthesis and adsorption on fine-grained fly ash. For fly ash from MWIs, the major PCDD/Fs congeners are 1, 2, 3, 4, 6,7, 8-HpCDF, and OCDF, which prefer synthesis and adsorption on coarse-grained fly ash. Correlation analysis exhibited that both 1,2,3-TriCBz and 1,2,4-TriCBz in fly ash have a markedly linear correlation with PCDD/Fs and PCBs, but PBDD/Fs shows a poor negative correlation with PCDD/Fs.

Radiolytic degradation of 1,2,4-trichlorobenzene (TCB) in some organic solvents by gamma rays: The kinetic properties of complete dechlorination of TCB and its pathway

This study investigates the degradation of TCB in methanol, ethanol, hexane, and benzene solutions using gamma radiolysis. Kinetic properties of TCB dechlorination and its pathway are examined, with TCB selected as a representative chlorinated organic compound. Chromatograms of irradiated samples and mass spectra of liquid-phase products are presented. The change in concentration of TCB, dichlorobenzenes (DCB), chlorobenzene (MCB), and benzene with absorbed doses are observed. The radiation-chemical yield (G values) of TCB in the solvents are calculated as 1.83, 2.56, 1.93, and 1.84 100eV−1 in methanol, ethanol, hexane, and benzene solutions, respectively. 100 % degradation of TCB by gamma irradiation is found to be efficient in polar solvents but leads to a wide variety of byproducts in low polar solvents, particularly the formation of polychlorinated biphenyls in TCB + benzene solutions, making benzene an incompatible medium. The main dechlorination pathway of TCB involves the formation of 1,4-DCB, MCB, and benzene.Environmental Implication.The gamma irradiation of chlorinated organic compounds, focusing on TCB as a model compound, was investigated due to its status as a hazardous material for the environment and living organisms. TCB is a byproduct of the dechlorination of certain chlorinated pesticides listed under the Stockholm Convention's Persistent Organic Pollutants (POPs) list, which prohibits their production and use. Gamma irradiation was found to be an effective method for the degradation of chlorinated compounds, achieving 100 % degradation during irradiation. The study underscores the potential of gamma irradiation as a viable approach for the treatment of chlorinated compounds, particularly in addressing environmental and health concerns associated with TCB and related compounds.

Quantitative acquisition of differential absorption cross sections of chlorobenzenes at different temperatures

Chlorobenzene is considered an essential organic synthesis intermediate and a precursor for the generation of persistent organic compounds in the waste disposal process, for which accurate detection of gaseous chlorobenzene can further help understand and control various chemical processes and effectively reduce pollution. Differential optical absorption spectroscopy is a reliable online method for detecting gaseous chlorobenzenes. It is crucial to investigate the effect of temperature on the optical absorption of the chlorobenzenes to quantify chlorobenzenes more precisely at various temperatures. A method to fix the effect of temperature variation on absorption spectra of chlorobenzene is initially proposed in this study, and it gave accurate concentrations. The proposed method can effectively improve the accuracy of chlorobenzene concentration measurements with an inverse concentration deviation of 3.2 % or less. The differential absorption cross sections at various temperatures are studied to understand how chlorobenzene absorption cross sections vary with temperature. Such a study is also helpful in reducing the concentration inversion errors induced by the variation of absorption cross sections of chlorobenzene with temperature. A novel method of introducing the binary function of the differential absorption cross sections with respect to wavelength and temperature is also proposed. The fitting of the binary function is done by downscaling functions at fixed wavelength and fixed temperature,respectively. Both fitting approaches obtained continuous differential absorption cross sections in the 201–220 nm wavelength band and 288–473 K temperature range, along with less than 2.74 % deviation in the concentration inversion measurements. Finally,based on the temperature specificity of the shape of the differential absorption cross sections,we developed another method using differential absorption spectroscopy for the simultaneous measurement of temperature and concentration, with a temperature prediction error of less than 1.89 %. This method is favorable to the applications of differential absorption spectroscopy in simultaneous measurement of temperature and concentration.

Study on Gaseous Chlorobenzene Treatment by a Bio-Trickling Filter: Degradation Mechanism and Microbial Community

Large-flow waste gas generated from the pharmaceutical and chemical industry usually contains low concentrations of VOCs (volatile organic compounds), and it is also the key factor that presents challenges in terms of disposal. To date, due to the limitations of mass transfer rate and microbial degradation ability, the degradation performance of VOCs using the biological method has not been ideal. Therefore, in this study, the sludge from a chlorobenzene-containing wastewater treatment plant was inoculated into our experimental bio-trickling filter (BTF) to explore the feasibility of domestication and degradation of gaseous chlorobenzene by highly active microorganisms. The kinetics of its mass transfer reaction and microbial community dynamics were also discussed. Moreover, the main process parameters of BTF for chlorobenzene degradation were optimized. The results showed that the degradation effect of chlorobenzene reached more than 85% at an inlet concentration of chlorobenzene 700 mg·m−3, oxygen concentration of 10%, and an empty bed retention time (EBRT) of 80 s. The mass transfer kinetic analysis indicated that the process of chlorobenzene degradation in the BTF occurred between the zero-stage reaction and the first-stage reaction. This BTF contributed significantly to the biodegradability of chlorobenzene, overcoming the limitation of gas-to-liquid/solid mass transfer of chlorobenzene. The analysis of the species diversity showed that Thermomonas, Petrimona, Comana, and Ottowia were typical organic-matter-degrading bacteria that degraded chlorobenzene efficiently with xylene present.

Abatement of chlorobenzene by plasma catalysis: Parameters optimization through response surface methodology (RSM), degradation mechanism and PCDD/Fs formation

Dielectric barrier discharge coupled with 10 wt% Co/γ-Al2O3 catalyst was developed to degrade chlorobenzene in this study. The effects of experimental parameters including applied voltage, flow rate, initial chlorobenzene concentration, and their interactions on the chlorobenzene degradation performance were investigated by the response surface methodology integrated with a central composite design. Results indicated that applied voltage was the most significant parameter affecting the mineralization rate and the concentration of ozone generated, while energy yield was mainly determined by initial chlorobenzene concentration. As a key precursor of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs), polychlorophenols were found during the identification of the intermediates produced during chlorobenzene degradation through GC-MS. Furthermore, HRGC-HRMS was used to detect the remaining byproducts on the catalyst surface after 3 and 10 h discharge time, and three types of PCDD/Fs (2,3,7,8-TCDF, 1,2,3,4,6,7,8-HCDF and OCDD) were detected after 10 h of discharge. The degradation mechanism of chlorobenzene was analyzed based on these detected intermediates, and the possible formation mechanisms of the three PCDD/Fs were proposed for the first time in plasma catalytic degradation of chlorobenzene.

Synthesis of new composite based on TiO2 immobilized in glass fibers for photo-catalytic degradation of chlorobenzene in aqueous solutions.

In this study photo-catalytic degradation of chlorobenzene from aqueous solutions using CQD decorated Fe-doped TiO2 immobilized in Glass Fibers (GF) was investigated. Characteristics of the synthesized photo-catalyst were determined by EF-SEM, EDX, BET, XRD, FTIR, and DRS analysis. Additionally, DRS analysis demonstrated adding CQD to the TiO2-Fe reduced its band gap energy from 2.96eV to 2.91eV, while that was 3.10eV for undoped TiO2. Among that three photo-catalysts, GF/CQD(4.5wt%) decorated Fe-TiO2 composite had performance nearly 100.0%, when pH was 5 and low concentration of chlorobenzene. In addition, GF/CQD(4.5wt%) decorated Fe-TiO2 composite show it could be well applied for five times and with a little reduction on the performance. Also, no detectable Fe found to be released from the composite. Minimum inhibitory concentration (MIC) for E. coli bacteria was 12.2mgL-1 of chlorobenzene residual. Our findings show the catalyst was successful for chlorobenzene removal in the wastewater effluent. In conclusion, present hybrid composite could successfully and safely remove chlorobenzene from synthetic aqueous solution.

ОСОБЕННОСТИ ПОКАЗАТЕЛЕЙ ЭМБРИОНАЛЬНОГО РАЗВИТИЯ ПРУДОВИКА (LYMNAEA STAGNALIS L.) ПРИ АНТРОПОГЕННОМ ВОЗДЕЙСТВИИ НЕКОТОРЫХ ХЛОРИСТЫХ СОЕДИНЕНИЙ В ВОДЕ

The article highlights the research of embryonic development of hydrobionts under the influence of anthropogenic factors of water solutions – chlorobenzene and tetrachloroethylene. To detect the toxicity of chloride pollutants in a freshwater reservoir, representatives of benthic mollusks (big pond snail Lymnaea stagnalis L.) were used as a model organism. According to the results of research, it was found that at a concentration of 0.01 mg/l of chlorobenzene solution individual anomalies of embryonic development of the pond fish are observed, but at higher concentrations its development is delayed by 5-6 stages in comparison with the control. As an integral parameter of pond fish development, we can take indicators of the biological toxicity criterion: Hatchling and its survival over a 10-day period after leaving the egg shells. Changes in the physiological parameters of pond fish embryos begin with a chlorobenzene concentration of 0.01 mg/l; the maximum permissible concentration for tetrachloroethylene for the considered biological indicators should be considered 0.05 mg/l. It is noted that in big pond snail (Lymnaea stagnalis L.) the hatch of juveniles from egg shells is the most sensitive indicator when determining the toxicity of an aqueous solution; and less sensitive indicators are the number of eggs laid and the survival of juveniles in the first 10 days after hatching. The test object used is a large pond, which has shown a high sensitivity to contamination of the water environment with chlorinated ecotoxicants and can be recommended for a comprehensive quality assessment when biotesting freshwater waters

Effect of chlorobenzene on the optical and structural properties of CH3NH3PbI3:DMF perovskite films

Methylammonium lead iodide perovskites (MAPbI3) thin films were prepared by changing the molarity concentration of methylammonium iodide and lead iodide in the N,N- dimethylformamide solvent, with and without chlorobenzene (CB). Rietveld refinement analysis revealed that all prepared samples belong to tetragonal CH3NH3PbI3 phase (sp. gr. I4/mcm). The effect of MAPbI3 concentration on the lattice parameters, crystallite size, lattice microstrain and dislocation density of the prepared films with and without CB was investigated in detail. The FESEM images of perovskite films indicated the presence of pinholes in each sample, and the number of pinholes reduced as CB added to MAPbI3. Generally, the transmission and reflection spectra decreased as the amount of MAPbI3 increased in the films; also, both are reduced as CB added to films. The value of the reflectivity over measured wavelengths changed from about 1% to about 18% and 12% in the case of films without and with CB, respectively. Without CB, the highest absorbance intensity was obtained for 1.3 M films, while with CB the 1.5 M film has the highest absorbance. The number of bandgaps appeared in different samples depending on the concentration of MAPbI3 and CB. The refractive index at 500 nm for (1, 1.3 and 1.5 M) MAPbI3 films without CB are 1.6, 1.44, 1.43 and 1.31 respectively, where its value in the corresponding films with CB are 1.34, 1.3, 1.3 and 1.28, respectively. The effect of MAPbI3 concentration and the existence of CB during the film preparation on the extinction coefficient, refractive index, dielectric constant, the photoluminescence peak position, and PL intensity for the different films were explored.

Synthesis of BiFeO3 nanoparticles for the photocatalytic removal of chlorobenzene and a study of the effective parameters

Pure BiFeO3 (BFO) was synthesized by the sol–gel auto combustion technique, then X-ray diffraction (XRD), Field emission scanning electron microscopy (FE-SEM), Diffusion reflecting spectroscopy (DRS) and Brunauer–Emmett–Teller (BET) methods used for its characterization. The XRD analysis revealed that BFO nanoparticles were relatively pure and the average crystallite size was about 20 nm. Observation of FE-SEM images of synthesized BFO nanoparticles, the presence of porous structure confirmed. The amount of bandgap energy prepared BFO was calculated 2.15 eV by DRS analysis. BET results showed the specific surface area of synthesized BFO was 55.071 m2 g−1. Photocatalytic removal of chlorobenzene (CB) by prepared BFO and UV light in the self-designed batch photoreactor studied. Effect of concentration of CB, humidity, and light intensity evaluated. The studies of different parameters have individual effects on the removal of CB. The highest removal of CB was 87.92% under conditions, 1600 mg L−1 of CB, 12 W UV light; 1770 mg immobilized BFO on glass plates, and 10% humidity. The prepared nanoparticle's efficiency for the removal of CB was better than TiO2 nanostructures.

Effect of Some Plant Extracts on The Biochemical Parameters, AChE and GST Activities of The Mosquito, Culex pipiens L. (Diptera: Culicidae)

The present study was undertaken in order to investigate the effect of median lethal concentration (LC50) of methanol, ethyl acetate, chlorobenzene and hexane extracts from leaves of Origanum syriacum, Pergularia tomentosa, Senna italica, and Otostegia fruticose against different biological aspects of the 3rd instar larvae of Culex pipiens. The effects were examined on the biochemical composition of the larval body and the activities of acetylcholinesterase (AChE) and glutathione S-transferase (GST). Based on obtained results, hexane extract showedmore activity against 3rd instar larvae of C. pipiens followed by chlorobenzene, ethyl acetate, and methanol extract. Tested extracts caused a modification in biochemical composition. The LC50 of each treatment decreased the total carbohydrate, protein, and lipid contents as compared with the control. Tested extracts also showed a neurotoxic activity as evidenced by the inhibition effect of the AChE activity that was significantly (P<0.001) decreased. Stimulation of the detoxification system of tested larvae was evidenced by the promoted activity of GST as compared with the untreated group.In general, tested extracts used in the present study may be considered as promising control agents against the mosquito vector, C. pipiens.

Catalytic Oxidation of Chlorobenzene over Pd-TiO2 /Pd-Ce/TiO2 Catalysts

A series of Pd-TiO2/Pd-Ce/TiO2 catalysts were prepared by an equal volume impregnation method. The effects of different Pd loadings on the catalytic activity of chlorobenzene (CB) were investigated, and the results showed that the activity of the 0.2%-0.3% Pd/TiO2 catalyst was optimal. The effect of Ce doping enhanced the catalytic activity of the 0.2% Pd-0.5% Ce/TiO2 catalyst. The characterization of the catalysts using BET, TEM, H2-TPR, and O2-TPD showed that the oxidation capacity was enhanced, and the catalytic oxidation efficiency was improved due to the addition of Ce. Ion chromatography and Gas Chromatography-Mass Spectrometer results showed that small amounts of dichlorobenzene (DCB) and trichlorobenzene (TCB) were formed during the decomposition of CB. The results also indicated that the calcination temperature greatly influenced the catalyst activity and a calcination temperature of 550 °C was the best. The concentration of CB affected its decomposition, but gas hourly space velocity had little effect. H2-TPR indicated strong metal–support interactions and increased dispersion of PdO in the presence of Ce. HRTEM data showed PdO with a characteristic spacing of 0.26 nm in both 0.2% Pd /TiO2 and 0.2% Pd-0.5% Ce/TiO2 catalysts. The average sizes of PdO nanoparticles in the 0.2% Pd/TiO2 and 0.2% Pd-0.5% Ce/TiO2 samples were 5.8 and 4.7 nm, respectively. The PdO particles were also deposited on the support and they were separated from each other in both catalysts.

A novel highly selective electrochemical chlorobenzene sensor based on ternary oxide RuO2/ZnO/TiO2 nanocomposites.

A novel electrochemical (EC) chlorobenzene (CBZ) sensor was fabricated using a ternary oxide RuO2/ZnO/TiO2 nanocomposite (NC)-decorated glassy carbon electrode (GCE). The nanoparticles (NPs) were synthesized by a wet-chemical method and characterized by X-ray photoelectron spectroscopy (XPS), powder X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectroscopy (EDS), and ultraviolet-visible (UV-vis) spectroscopy. The synthesized RuO2/ZnO/TiO2 NC was layered as thin film on a GCE with Nafion (5% suspension in ethanol) adhesive, and the as-prepared sensor was subjected to CBZ analysis using an electrochemical approach. The calibration of the proposed CBZ sensor was executed with a linear relation of current versus concentration of CBZs known as the calibration curve. The sensitivity (32.02 μA μM−1 cm−2) of the CBZ sensor was calculated from the slope of the calibration curve by considering the active surface area of the GCE (0.0316 cm2). The lower detection limit (LD; 98.70 ± 4.90 pM) was also calculated at a signal-to-noise ratio of 3. Besides these, the response current followed a linear relationship with the concentration of chlorobenzene and the linear dynamic range (LDR) was denoted in the range of 0.1 nM to 1.0 μM. Moreover, the CBZ sensor was found to exhibit good reproducibility, reliability, stability, and fast response time. Finally, the sensing mechanism was also discussed with the energy-band theory of ternary doped semiconductor materials. The sensing activity of the proposed sensor was significantly enhanced due to the combined result of depletion layer formation at the heterojunction of RuO2/ZnO/TiO2 NCs as well as the activity of RuO2 NPs as oxidation catalysts. The proposed CBZ sensor probe based on ternary oxide RuO2/ZnO/TiO2 NCs was developed with significant analytical parameters for practical application in monitoring the environmental pollutants of CBZs for the safety of environmental fields on a large scale.

Effect of pH and Concentrated Salt on the Droplet Size and Mass Transfer Coefficient in a Stirred Liquid–Liquid Reactor

This work addressed liquid–liquid mass transfer for actual industrial conditions of high pH with coexisting salt. The Sauter mean diameter was determined from the direct measurement of a chlorobenzene droplet size using a borescope system. At a high NaOH concentration, the droplet size decreased significantly due to the reduced density difference between two phases, and it further decreased when NaOH and NaCl coexisted. A Sauter mean diameter correlation with a density difference term was proposed, and it successfully predicted the experimental results. To determine the mass transfer coefficient, the solubility and the concentration gradient of chlorobenzene in the aqueous phase were measured under various conditions. As the NaOH and NaCl concentration increased, the solubility of chlorobenzene and the rate of change of chlorobenzene concentration in the aqueous phase both decreased, but the decrease in solubility was more pronounced. Thus, the mass transfer coefficient increased with the NaOH and NaCl co...

Accuracy in determining absorbed irradiation dose at different temperature measurements using ethanol chlorobenzene - oscillotitrator system

Ethanol-chlorobenzene/oscillotitrator dosimetry system is widely used in controlling the irradiation process in gamma facilities. The ethanol-chlorobenzene dosimetry system provides a reliable means of measuring absorbed dose. It is based on a process of radiolytic formation of hydrochloric acid in aqueous ethanolic solutions of chlorobenzene by ionizing radiation. The irradiation temperature dependence of dosimeter response is a complex function of dose and temperature for each concentration of chlorobenzene. At different temperature the mobility of conducting species from hydrochloric acid is changed leading to different oscillotitrator deflections during high-frequency conductometric readout. In this paper, we examined the influence of temperature on the calculation of the radiation dose. We showed that the temperature significantly influenced the measurement results, and that the calibration curve has to be formed at the irradiation temperature in order to obtain precise values of the absorbed dose.

A quint-wavelength UV spectroscopy for simultaneous determination of dichlorobenzene, chlorobenzene, and benzene in simulated water reduced by nanoscale zero-valent Fe/Ni bimetal

A quint-wavelength UV spectroscopy for rapid determination of dichlorobenzene (DCB), chlorobenzene (CB) and benzene (B) was developed for the dechlorination process of DCB reduced by nanoscale zero-valent Fe/Ni bimetal. Based on the absorbance measurements at 260, 269, 277, 290 and 300nm, the equations for calculating the concentration of DCB and CB and B were established, in which the spectral interference from the nanoparticles could be effectively minimized. The results show that the present method has a good measurement precision (the relative standard deviations are within 2.0%) and accuracy (the recoveries are between 89 and 111%) in the DCB, CB and B's quantification. The present method is simple, rapid, and such a methodology is very suitable to be used for evaluating the dechlorination performance of chlorinated aromatic compounds in the presence of bimetal nanoparticle.

Isolation and Identification of a Chlorobenzene-degrading Bacterium and Its Degradation Characteristics

A bacterium strain LW26 which could utilize chlorobenzene (CB) as sole carbon and energy source was isolated from a biotrickling filter reactor treating CB-contaminated off-gas. Based on its morphological and physiological characteristics, as well as the analysis of 16S rRNA gene sequence and Biolog test, the strain LW26 was identified as Delftia tsuruhatensis. To our best knowledge, it is the first time that the strain Delftia tsuruhatensis was applied for CB purification. In this study, the effects of temperature, pH, initial CB concentration and Cl- concentration on the biodegradation were investigated. The results showed that the optimal temperature and pH for CB biodegradation were 25℃ and 7.0,respectively; the maximum CB tolerated concentration for LW26 was as high as 500 mg·L-1; when the concentration of Cl- was above 0.14 mol·L-1, the CB degradation was significantly restrained. The degrading process of the strain LW26 followed the Haldane kinetic model and the maximum specific growth rate and the maximum specific degradation rate were 0.42 h-1 and 2.53 h-1, respectively.GC-MS analysis of the metabolites revealed that CB was firstly converted to o-chlorophenol by strain LW26. Combined with the activity of catechol dioxygenase, it can be speculated that CB was finally mineralized to CO2, or converted to cell biomass after processes of ortho cleavage,dechlorination and oxidation.

Development of Self-Healing Coatings with Micro Capsules for Corrosion Protection of Metal

Self-healing coatings with capsules containing healing agents have been developed for the corrosion protection of metal. In this paper, polyurethane capsules were synthesized under different conditions to examine the size and shape of capsules, and self-healing ability of coatings with capsules dispersed was examined after damaging the coated layer by scratching with a cutter blade. The size and shape of capsules depended on the concentration of chlorobenzene in cyclohexanone used as a solvent of prepolymer solution. The capsule formed with 70 % of chlorobenzene gave a self-healing capability to the coated layer by releasing the healing agent after damaging. The amount of glycerol added for the formation of the polyurethane capsule shell affected the self-healing ability of the coated layer. The coating with the capsule formed with small amounts of glycerol showed a high healing ability, while, with large amounts of glycerol, the self-healing ability was relatively low.

Detection of chlorobenzene in water using a wettability-controlled three-dimensional graphene selective filter

An oxide nanowire transistor covered with a wettability-controlled three-dimensional (3D) graphene filter was fabricated to detect chlorobenzene in water. The 3D porous graphene filter allowed chlorobenzene to pass through while blocking water because of its wettability. The chlorobenzene concentration in water could be monitored by observing the threshold voltage shift, which moved to the negative direction with increasing chlorobenzene concentration in water. The advantage of the fabricated device is that it can be used to easily estimate the chlorobenzene concentration in water by consistently monitoring current.