Synthesis of a functional biomass lignin-based hydrogel with high swelling and adsorption capability towards Acid Red 73.

In this study, sodium lignosulfonate (LS) was used as raw material. Acrylamide (AM) and acryloxyethyltrimethylammonium chloride (DAC) were grafted onto LS through the free radical graft copolymerisation to synthesise a functional biomass terpolymer lignin-based hydrogel adsorbent (LAD). The effects of different factors on the LAD adsorption of Acid Red (AR 73) were investigated through the static adsorption method. LAD adsorbed AR 73 (C0=100mg·L-1) for 2 h to reach equilibrium, and the equilibrium adsorption capacity and removal rate were 47.59 mg·g-1 and 95.18%, respectively. The prepared LAD hydrogel swelling ratio for 2 h was 25 g·g-1, and the water loss rate in ethanol solvent in 120 min was 93.51%. The adsorption of AR 73 by LAD was consistent with the Langmuir isotherm adsorption model. This adsorption was a single-molecule adsorption with a maximum adsorption capacity of 409.84 mg·g-1. The adsorption was a process of spontaneous heat release and entropy reduction. The adsorption kinetic was in accordance with the pseudo-second-order model, and the adsorption activation energy was 2.501 kJ·moL-1. Moreover, the mechanism of adsorption was electrostatic attraction, and comprehensive effects of physical, and chemical adsorption and hydrogen bond. The LAD hydrogel adsorbent has a remarkable adsorption effect on AR 73, and can be used as an efficient and recyclable biomass adsorbent for the treatment of anionic dye wastewater.

Adsorption of U(VI) from aqueous solution by using KMnO4-modified hazelnut shell activated carbon: characterisation and artificial neural network modelling.

This study is based on U(VI) removal from wastewater by KMnO4-modified hazelnut shell activated carbon (KM-HSAC) using adsorption technology. A characterisation study of KM-HSAC was conducted through scanning electron microscope and energy-dispersive X-ray spectroscopy (EDS) analysis. The rough surface of KM-HSAC contains many irregular microspores. The EDS pattern confirmed the U(VI) adsorption on the KM-HSAC. A batch study experiment gave optimum results for U(VI) at pH 6, contact time of 160 min, initial U(VI) concentration of 155.56 mg/L and KM-HSAC dosage of 4 g/L, with a maximum adsorption capacity of 22.27 mg/g. The prediction performance of artificial neural network models was validated through the low values of statistical error (2.708 and 8.241 for RMSE of training and testing data, respectively) and the high determination coefficient value (0.987 and 0.906 for training and testing data, respectively). Experimental results suggest that KM-HSAC has a high potential for the removal of U(VI) from wastewater.

Response surface methodology approach for the optimisation of adsorption of hydrolysed polyacrylamide from polymer-flooding wastewater onto steel slag: a good option of waste mitigation.

Wastewater produced from polymer flooding in oil production features high viscosity and chemical oxygen demand because of the residue of high-concentration polymer hydrolysed polyacrylamide (HPAM). In this study, steel slag, a waste from steel manufacturing, was studied as a low-cost adsorbent for HPAM in wastewater. Optimisation of HPAM adsorption by steel slag was performed with a central composite design under response surface methodology (RSM). Results showed that the maximum removal efficiency of 89.31% was obtained at an adsorbent dosage of 105.2 g/L, contact time of 95.4 min and pH of 5.6. These data were strongly correlated with the experimental values of the RSM model. Single and interactive effect analysis showed that HPAM removal efficiency increased with increasing adsorbent dosage and contact time. Efficiency increased when pH was increased from 2.6 to 5.6 and subsequently decreased from 5.6 to 9.3. It was observed that removal efficiency significantly increased (from 0% to 86.1%) at the initial stage (from 0 min to 60 min) and increased gradually after 60 min with an adsorbent dosage of 105.2 g/L, pH of 5.6. The adsorption kinetics was well correlated with the pseudo-second-order equation. Removal of HPAM from the studied water samples indicated that steel slag can be utilised for the pre-treatment of polymer-flooding wastewater.

Uranium biosorption from aqueous solution by the submerged aquatic plant Hydrilla verticillata.

The biosorption characteristics of U(VI) from aqueous solution onto a nonliving aquatic macrophyte, Hydrilla verticillata (dry powder), were investigated under various experimental conditions by using batch methods. Results showed that the adsorption reached equilibrium within 60 min and the experimental data were well fitted by the pseudo-first-order kinetic model. U(VI) adsorption was strongly pH dependent, and the optimum pH for U(VI) removal was 5.5. Isotherm adsorption data displayed good correlation with the Langmuir model, with a maximum monolayer adsorption capacity of 171.52 mg/g. Thermodynamic studies suggested that U(VI) adsorption onto H. verticillata was an exothermic and spontaneous process in nature. Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy indicated that the amino and hydroxyl groups on the algal surface played an important role in U(VI) adsorption. The mechanisms responsible for U(VI) adsorption could involve electrostatic attraction and ion exchange. In conclusion, H. verticillata biomass showed good potential as an adsorption material for the removal of uranium contaminants in aqueous solution.

Toxic effect of two kinds of mineral collectors on soil microbial richness and activity: analysis by microcalorimetry, microbial count, and enzyme activity assay.

Flotation reagents are hugely and increasingly used in mining and other industrial and economic activities from which an important part is discharged into the environment. China could be the most affected country by the resulting pollution. However, their ecotoxicological dimension is still less addressed and understood. This study aimed to analyze the toxic effect of sodium isobutyl xanthate (SIBX) and sodium isopropyl xanthate (SIPX) to soil microbial richness and activity and to make a comparison between the two compounds in regard to their effects on soil microbial and enzymes activities. Different methods, including microcalorimetry, viable cell counts, cell density, and catalase and fluorescein diacetate (FDA) hydrololase activities measurement, were applied. The two chemicals exhibited a significant inhibitory effect (P < 0.05 or P < 0.01) to all parameters, SIPX being more adverse than SIBX. As the doses of SIBX and SIPX increased from 5 to 300 µg g-1 soil, their inhibitory ratio ranged from 4.84 to 45.16 % and from 16.13 to 69.68 %, respectively. All parameters fluctuated with the incubation time (10-day period). FDA hydrolysis was more directly affected but was relatively more resilient than catalase activity. Potential changes of those chemicals in the experimental media and complementarity between experimental techniques were justified.

The mutual influence of speciation and combination of Cu and Pb on the photodegradation of dimethyl o-phthalate.

Specific industrial application of dimethyl o-phthalate (DMP) in ore flotation has led to DMP-heavy metals combined pollution, which causes the abiotic degradation of DMP in the environment more complex. This study focused on the effect of Cu and Pb on photodegradation of DMP. The major mechanism of inhibiting effect of Cu and Pb on degradation of DMP involved their speciation and combination. It was found that the Cu (5 mg/L, I = 95.4%) and Pb (5 mg/L, I = 100%) could inhibit the photodegradation of DMP. The main species that inhibit the DMP degradation were Cu(OH)+ and Pb(OH)+, respectively. The intensity of the UV-Vis absorbance of DMP was obviously related to the concentration of Cu2+ (R2 = 0.8655) or Pb2+ (R2 = 0.9019) ions. Fluorescence quenching effect of Cu2+ (R2 > 0.9946), Pb2+ (R2 > 0.6879) on DMP is strongly correlated with the concentration of ions. And the equilibrium membrane dialysis experiment has also verified the combination of DMP and Cu, Pb. These results are useful to understand the effect mechanism of metal species on the photodegradation of organic chemicals.

Kinetics, equilibrium, and thermodynamics investigation on the adsorption of lead(II) by coal-based activated carbon.

The goal of this research is to investigate the feasibility of using activated coal-based activated carbon (CBAC) to adsorb Pb(II) from aqueous solutions through batch tests. Effects of contact time, pH, temperature and initial Pb(II) concentration on the Pb(II) adsorption were examined. The Pb(II) adsorption is strongly dependent on pH, but insensitive to temperature. The best pH for Pb(II) removal is in the range of 5.0-5.5 with more than 90 % of Pb(II) removed. The equilibrium time was found to be 60 min and the adsorption data followed the pseudo-second-order kinetics. Isotherm data followed Langmuir isotherm model with a maximum adsorption capacity of 162.33 mg/g. The adsorption was exothermic and spontaneous in nature. The Fourier transform infrared spectroscopy and scanning electron microscopy analysis suggested that CBAC possessed a porous structure and was rich in carboxyl and hydroxyl groups on its surface, which might play a major role in Pb(II) adsorption. These findings indicated that CBAC has great potential as an alternative adsorbent for Pb(II) removal.

Effect of natural and synthetic surfactants on crude oil biodegradation by indigenous strains.

Hydrocarbon pollution is a worldwide problem. In this study, five surfactants containing SDS, LAS, Brij 30, Tween 80 and biosurfactant were used to evaluate their effect on crude oil biodegradation. Hydrocarbon degrading bacteria were isolated from oil production water. The biosurfactant used was a kind of cyclic lipopeptide produced by Bacillus subtilis strain WU-3. Solubilization test showed all the surfactants could apparently increase the water solubility of crude oil. The microbial adhesion to the hydrocarbon (MATH) test showed surfactants could change cell surface hydrophobicity (CSH) of microbiota, depending on their species and concentrations. Microcalorimetric experiments revealed these surfactants exhibited toxicity to microorganisms at high concentrations (above 1 CMC), except for SDS which showed low antibacterial activity. Surfactant supplementation (about 0.1 and 0.2 CMC) could improve degradation rate of crude oil slightly, while high surfactant concentration (above 1 CMC) may decrease the degradation rate from 50.5% to 28.9%. Those findings of this work could provide guidance for the application of surfactants in bioremediation of oil pollution.

Adsorption of naphthalene from aqueous solution onto fatty acid modified walnut shells.

The removal of polycyclic aromatic hydrocarbons (PAHs) from aqueous solution is challenging to environmental technologists. Agricultural waste is apparently the most attractive materials in removing PAHs because of its abundance, renewability, and economic advantage. The adsorption of PAHs (e.g., naphthalene) onto walnut shell (WNS) and its fatty acid (e.g., capric acid, lauric acid, palmitic acid, and oleic acid)-modified equivalent were investigated in this work to develop low-cost biosorbents for hydrophobic organic compounds. Compared with other modified sorbents, oleic acid graftted walnut shell (OWNS) showed the maximum partition coefficient (4330 ± 8.8 L kg(-1)) because of its lowest polarity and highest aromaticity. The adsorption capacity (7210 µg g(-1)) of OWNS at the temperature of 298 K was observed for an initial naphthalene concentration of 25 mg L(-1) with contact time of 40 h, sorbent dosage of 1 g L(-1), and in neutral condition. Furthermore, the regeneration capability of OWNS implied that it was a promising biosorbent for naphthalene removal.

The effect of metal oxide nanoparticles on functional bacteria and metabolic profiles in agricultural soil.

A significant knowledge gap in nanotechnology is the absence of standardized protocols for examining the effect of engineered nanoparticles on soil microorganisms. In this study, agricultural soil was exposed to ZnO, SiO2, TiO2 and CeO2 nanoparticles at 1 mg g(-1). The toxicity effect was evaluated by thermal metabolism, the abundance of functional bacteria and enzymatic activity. ZnO and CeO2 nanoparticles were observed to hinder thermogenic metabolism, reduce numbers of soil Azotobacter, P-solubilizing and K-solubilizing bacteria and inhibit enzymatic activities. TiO2 nanoparticles reduced the abundance of functional bacteria and enzymatic activity. SiO2 nanoparticles slightly boosted the soil microbial activity. Pearson's correlation analysis showed that thermodynamic parameters had a strong correlation with abundance of functional bacteria and enzymatic activity. These findings demonstrated that the combined approach of monitoring thermal metabolism, functional bacteria and enzymatic activity is feasible for testing the ecotoxicity of nanoparticles on agricultural soil.