An Eco-Friendly Adsorbent Based on Bacterial Cellulose and Vermiculite Composite for Efficient Removal of Methylene Blue and Sulfanilamide.

In this work, a novel composite of bacterial cellulose (BC) and expanded vermiculite (EVMT) composite was used to adsorb dyes and antibiotics. The pure BC and BC/EVMT composite were characterized using SEM, FTIR, XRD, XPS and TGA. The BC/EVMT composite exhibited a microporous structure, providing abundant adsorption sites for target pollutants. The adsorption performance of the BC/EVMT composite was investigated for the removal of methylene blue (MB) and sulfanilamide (SA) from an aqueous solution. The adsorption capacity of BC/ENVMT for MB increased with increasing pH, while the adsorption capacity for SA decreased with increasing pH. The equilibrium data were analyzed using the Langmuir and Freundlich isotherms. As a result, the adsorption of MB and SA by the BC/EVMT composite was found to follow the Langmuir isotherm well, indicating a monolayer adsorption process on a homogeneous surface. The maximum adsorption capacity of the BC/EVMT composite was found to be 92.16 mg/g for MB and 71.53 mg/g for SA, respectively. The adsorption kinetics of both MB and SA on the BC/EVMT composite showed significant characteristics of a pseudo-second-order model. Considering the low cost and high efficiency of BC/EVMT, it is expected to be a promising adsorbent for the removal of dyes and antibiotics from wastewater. Thus, it can serve as a valuable tool in sewage treatment to improve water quality and reduce environmental pollution.

Sorting Liquid Droplets by Surface Tension Using Devices with Quasi-Superamphiphobic Coatings.

Any solid surface with homogenous or varying surface energy can spontaneously show variable wettability to liquid droplets with different or identical surface tensions. Here, we studied a glass slide sprayed with a quasi-superamphiphobic coating consisting of a hexane suspension of perfluorosilane-coated nanoparticles. Four areas on the glass slide with a total length of 7.5 cm were precisely tuned via ultraviolet (UV) irradiation, and droplets with surface tensions of 72.1-33.9 mN m-1 were categorized at a tilting angle of 3°. Then, we fabricated a U-shaped device sprayed with the same coating and used it to sort the droplets more finely by rolling them in the guide groove of the device to measure their total rolling time and distance. We found a correlation between ethanol content/surface tension and rolling time/distance, so we used the same device to estimate the alcoholic strength of Chinese liquors and to predict the surface tension of ethanol aqueous solutions.

Enhanced Cycling Stability of LiCuxMn1.95-xSi0.05O4 Cathode Material Obtained by Solid-State Method.

The LiCuxMn1.95-xSi0.05O4 (x = 0, 0.02, 0.05, 0.08) samples have been obtained by a simple solid-state method. XRD and SEM characterization results indicate that the Cu-Si co-doped spinels retain the inherent structure of LiMn2O4 and possess uniform particle size distribution. Electrochemical tests show that the optimal Cu-doping amount produces an obvious improvement effect on the cycling stability of LiMn1.95Si0.05O4. When cycled at 0.5 C, the optimal LiCu0.05Mn1.90Si0.05O4 sample exhibits an initial capacity of 127.3 mAh g-1 with excellent retention of 95.7% after 200 cycles. Moreover, when the cycling rate climbs to 10 C, the LiCu0.05Mn1.90Si0.05O4 sample exhibits 82.3 mAh g-1 with satisfactory cycling performance. In particular, when cycled at 55 °C, this co-doped sample can show an outstanding retention of 94.0% after 100 cycles, whiles the LiMn1.95Si0.05O4 only exhibits low retention of 79.1%. Such impressive performance shows that the addition of copper ions in the Si-doped spinel effectively remedy the shortcomings of the single Si-doping strategy and the Cu-Si co-doped spinel can show excellent cycling stability.

Enhanced Cycling Stability through Erbium Doping of LiMn2O4 Cathode Material Synthesized by Sol-Gel Technique.

In this work, LiMn2-xErxO4 (x ≤ 0.05) samples were obtained by sol-gel processing with erbium nitrate as the erbium source. XRD measurements showed that the Er-doping had no substantial impact on the crystalline structure of the sample. The optimal LiMn1.97Er0.03O4 sample exhibited an intrinsic spinel structure and a narrow particle size distribution. The introduction of Er3+ ions reduced the content of Mn3+ ions, which seemed to efficiently suppress the Jahn⁻Teller distortion. Moreover, the decreased lattice parameters suggested that a more stable spinel structure was obtained, because the Er3+ ions in a ErO6 octahedra have stronger bonding energy (615 kJ/mol) than that of the Mn3+ ions in a MnO6 octahedra (402 kJ/mol). The present results suggest that the excellent cycling life of the optimal LiMn1.97Er0.03O4 sample is because of the inhibition of the Jahn-Teller distortion and the improvement of the structural stability. When cycled at 0.5 C, the optimal LiMn1.97Er0.03O4 sample exhibited a high initial capacity of 130.2 mAh g-1 with an excellent retention of 95.2% after 100 cycles. More significantly, this sample showed 83.1 mAh g-1 at 10 C, while the undoped sample showed a much lower capacity. Additionally, when cycled at 55 °C, a satisfactory retention of 91.4% could be achieved at 0.5 C after 100 cycles with a first reversible capacity of 130.1 mAh g-1.

Contribution of filamentous fungi to the musty odorant 2,4,6-trichloroanisole in water supply reservoirs and associated drinking water treatment plants.

In this study, the distribution of 2,4,6-trichloroanisole (2,4,6-TCA) in two water supply reservoirs and four associated drinking water treatment plants (DWTPs) were investigated. The 2,4,6-TCA concentrations were in the range of 1.53-2.36 ng L-1 in water supply reservoirs and 0.76-6.58 ng L-1 at DWTPs. To determine the contribution of filamentous fungi to 2,4,6-TCA in a full-scale treatment process, the concentrations of 2,4,6-TCA in raw water, settled water, post-filtration water, and finished water were measured. The results showed that 2,4,6-TCA levels continuously increased until chlorination, suggesting that 2,4,6-TCA could form without a chlorination reaction and fungi might be the major contributor to the 2,4,6-TCA formation. Meanwhile, twenty-nine fungal strains were isolated and identified by morphological and molecular biological methods. Of the seventeen isolated fungal species, eleven showed the capability to convert 2,4,6-trichlorophenol (2,4,6-TCP) to 2,4,6-TCA. The highest level of 2,4,6-TCA formation was carried out by Aspergillus versicolor voucher BJ1-3: 40.5% of the original 2,4,6-TCP was converted to 2,4,6-TCA. There was a significant variation in the capability of different species to generate 2,4,6-TCA. The results from the proportions of cell-free, cell-attached, and cell-bound 2,4,6-TCA suggested that 2,4,6-TCA generated by fungi was mainly distributed in their extracellular environment. In addition to 2,4,6-TCA, five putative volatile by-products were also identified by gas chromatography and mass spectrometry. These findings increase our understanding on the mechanisms involved in the formation of 2,4,6-TCA and provide insights into managing and controlling 2,4,6-TCA-related problems in drinking water.

Ultrasound-assisted extraction and solid-phase extraction for the simultaneous determination of five amide herbicides in fish samples by gas chromatography with electron capture detection.

An efficient sample extraction and clean-up method was developed for simultaneous determination of five amide herbicides (alachlor, acetochlor, propisochlor, metazachlor, and butachlor) in fish samples. The protocol consisted of ultrasound-assisted solvent extraction and solid-phase extraction clean-up. In detail, aliquots of homogenized fish flesh were thoroughly mixed with 20 mL of n-hexane and then extracted with ultrasonication for 40 min. Each sample was centrifuged and the supernatant was collected for the subsequent clean-up. For the sample preparation, the above supernatant was processed with a C18 column with 3 mL of dichloromethane/n-hexane (1:1, v/v) as the eluant. Then the samples were analyzed by gas chromatography with electron capture detection. The correlation coefficients of the five calibration curves were 0.9976-0.9998 (n = 3). The limits of detection (S/N = 3, n = 11) and limits of quantification (S/N = 10, n = 11) were 0.19-0.42 and 0.63-1.39 µg/kg, respectively. The recoveries of this method were 71.2-92.6% with good precision (<4.7% relative standard deviations, n = 6). The developed method was successfully applied to monitor the five amide herbicides in fish samples collected from different cities.

Occurrence and distribution of taste and odor compounds in subtropical water supply reservoirs and their fates in water treatment plants.

Taste and odor (T&O) problems in surface water supplies attract growing environmental and ecological concerns. In this study, 10 T&O compounds, 2-methylisoborneol (2-MIB), geosmin, ß-ionone, 2-isopropyl-3-methoxypyrazine (IPMP), 2-isobutyl-3-methoxypyrazine (IBMP), 2,4,6-trichloroanisole (2,4,6-TCA), 2,3,6-trichloroanisole (2,3,6-TCA), 2,3,4-trichloroanisole (2,3,4-TCA), 2,4,6-tribromoanisole (2,4,6-TBA), and trans-2,cis-6-nonadienal (NDE) were investigated in 13 water supply reservoirs and 2 water treatment plants (WTPs) in S City of China. 2-MIB, geosmin, and ß-ionone were detected in most of the reservoirs and WTPs. The highest concentrations in reservoirs reached 196.0 ng L-1 for 2-MIB, 11.4 ng L-1 for geosmin, and 39.7 ng L-1 for ß-ionone. Canonical correspondence analysis (CCA) was used to examine the relationship between the 3 T&O compounds and environmental parameters of the reservoirs. The results showed that TP was strongly positively correlated with 2-MIB in wet season and negatively correlated in dry season. It was suggested that controlling nutrient (TP, TN/TP, and NH3-N) inputs was required for better management of drinking water reservoirs. Furthermore, the maximum concentrations in raw water of WTPs was kept at 82.1 ng L-1 for 2-MIB, 5.6 ng L-1 for geosmin, and 66.1 ng L-1 for ß-ionone. ß-Ionone could not be detected in the post-filtration and finished water of two WTPs, and both 2-MIB and geosmin significantly decreased in the water of XWTP. It was indicated that T&O compounds could be removed partly or completely by the filtration of conventional treatment processes.

Simultaneous dispersive liquid-liquid microextraction based on a low-density solvent and derivatization followed by gas chromatography for the simultaneous determination of chloroanisoles and the precursor 2,4,6-trichlorophenol in water samples.

Chloroanisoles, particularly 2,4,6-trichloroanisole, are commonly identified as major taste and odor compounds in water. In the present study, a simple and efficient method was established for the simultaneous determination of chloroanisoles and the precursor 2,4,6-trichlorophenol in water by using low-density-solvent-based simultaneous dispersive liquid-liquid microextraction and derivatization followed by gas chromatography with electron capture detection. 2,4-Dichloroanisole, 2,6-dichloroanisole, 2,4,6-trichloroanisole, 2,3,4-trichloroanisole, and 2,3,6-trichloroanisole were the chloroanisoles evaluated. Several important parameters of the extraction-derivatization procedures, including the types and volumes of extraction solvent and disperser solvent, concentrations of derivatization agent and base, salt addition, extraction-derivatization time, and temperature were optimized. Under the optimized conditions (80 µL of isooctane as extraction solvent, 500 µL of methanol as disperser solvent, 60 µL of acetic anhydride as derivatization agent, 0.75% of Na2 CO3 addition w/v, extraction-derivatization temperature of 25°C, without salt addition), a good linearity of the calibration curve was observed by the square of correlation coefficients (R(2) ) ranging from 0.9936 to 0.9992. Repeatability and reproducibility of the method were < 4.5% and <7.3%, respectively. Recovery rates ranged from 85.2 to 101.4%, and limits of detection ranged from 3.0 to 8.7 ng/L. The proposed method was applied successfully for the determination of chloroanisoles and 2,4,6-trichlorophenol in water samples.