cadmium usually enter the environment and water resources through wastewater, released by various industries, and may have adverse effects. The current study employs surface of bentonite clay available locally in order to remove cadmium In solutions contaminated with this type of ions, in order to research on a surface with a high ability to adsorption of cadmium (II) ions, study Some factors affect the adsorption process on bentonite clay, such as contact time, pH the solution, Adsorbent particle size, Initial concentration of solutions and temperature of the solution were examined in the a batch process mode. The amount of adsorbed Cd (II) increased with height temperature, the optimum adsorption pH was about 6.5. Under this condition, the percent removal was 95.17%. The adsorption  isotherms were studied and  the results of adsorption processes were more fitted with Friendlich model rather than Langmuir adsorption model. Thermodynamic study showed that,  ΔH was endothermic, ΔG is found to be negative That is, the process is automatic and  ΔS was found to be positive. The current study also involves  practical application using bentonite to get rid of Cd(II) ions  to  from wastewater of Hamdan's station of the Basra- iraq, The results indicate high affinity (97.84%) removal of Cd(II) ions.

In this study natural bentonite (NB) and acid-thermal co-modified bentonite (MB) were utilized as adsorbents for the removal of Thymol Blue (TB) from aqueous solution. The batch adsorption experiments were conducted under different experimental conditions. The artificial neural network (ANN) and adaptive neuro fuzzy inference systems (ANFIS) were applied to estimate removal percentage (%) of TB. Mean squared error (MSE), root mean square error (RMSE) and coefficient of determination (R2) values were used to evaluate the results. In addition, the experimental data were fitted isotherm models (Langmuir, Freundlich and Temkin) and kinetic models (pseudo first order (PFO), pseudo second order (PSO) and intra-particle diffusion (IPD)). The adsorption of TB on both the NB and MB followed well the PSO kinetic model, and was best suited Langmuir isotherm model. When the temperature was increased from 298 K to 323 K for 20 mg/L of TB initial concentration, the removal percentage of TB onto the NB and MB increased from 74.91% to 84.07% and 81.19% to 93.12%, respectively. This results were confirmed by the positive ΔH° values indicated that the removal process was endothermic for both the NB and MB. The maximum adsorption capacity was found as 48.7805 mg/g and 117.6471 mg/g for the NB and MB, respectively (at 323 K). As a result, with high surface area and adsorption capacity, the MB is a great candidate for TB dye removal from wastewater, and the ANFIS model is better than the ANN model at estimating the removal percentage of the dye.

To meet the increasing global energy demand, expanding exploration for oil and gas reserves as well as associated drilling activities are expected in the Arctic-boreal region where sponge aggregations contribute to up to 90% of benthic biomass. These deep-water sponges along with their microbial endobionts play key roles in the nitrogen cycling in Arctic-boreal ecosystems. This study aimed to investigate the effects of drilling discharges and associated sediment resuspension events on net fluxes of oxygen, ammonium, nitrate and nitrite in three common deep-water sponge species in the form of explants. Sponges were exposed to suspended bentonite and barite, the primary particulate compounds in drilling waste, as well as suspended natural sediment particles for a period of 33 days (on average 10 mg L−1 for 12 h day−1). The exposure period was followed by a pollution abatement period for a further 33 days. No sponge mortality was observed during the experiment. However, exposure to these particles, especially to barite, led to reduced oxygen consumption by up to 33% that was linearly correlated with reduced nitrite/nitrate release by the sponges. The changes in net fluxes were accompanied by decreased tissue oxygenation by up to 54% within the sponges. These findings reveal the effects of fine particles on sponge metabolic processes by reducing aerobic respiration and microbial nitrification, and possibly by favouring anaerobic processes such as microbial denitrification. Most of the sponge responses recovered to their control levels upon the pollution abatement period, but the effects caused by barite may not be reversible. Our findings provide the first insight into the ecological consequences of oil and gas drilling activities on sponge-mediated nitrogen cycling in the Arctic-boreal region.

Modified clay-based solid-phase phosphorous (P) sorbents are increasingly used as lake geoengineering materials for lake eutrophication control. However, some still dispute the feasibility of using these materials to control internal P loading from shallow eutrophic lakes. The lack of information about P behavior while undergoing frequent sediment resuspension greatly inhibits the modified minerals’ use. In this study, a sediment resuspension generating system was used to simulate the effect of both moderate winds (5.1 m/s) and strong winds (8.7 m/s) on the stability of sediment treated by two geoengineering materials, Phoslock® (a lanthanum modified bentonite) and thermally-treated calcium-rich attapulgite. This study also presents an analysis of the P dynamics across the sediment-water interface of two shallow eutrophic lakes. In addition, the effect of wind velocity on P forms and P supply from the treated sediment were studied using chemical extraction and diffusive gradients in thin films (DGT) technique, respectively. Results showed that adding geoengineering materials can enhance the stability of surface sediment and reduce the erosion depth caused by wind accordingly. All treatments can effectively reduce soluble reactive phosphorus (SRP) concentration in overlying water when sediment is capped with thermally-treated calcium-rich attapulgite, which performs better than sediment mixed with modified attapulgite but not as well as sediment treated with Phoslock®. However, their efficiency decreased with the increase in occurrences of sediment resuspension. The addition of the selected geoengineering materials effectively reduced the P fluxes across sediment-water interface and lowered P supply ability from the treated sediment during sediment resuspension. The reduction of mobile P and enhancement of calcium bound P and residual P fraction in the treated sediment was beneficial to the long-term lake internal P loading management. All of the results indicated that the studied geoengineering materials are suitable for application in shallow eutrophic lakes with frequent sediment resuspension activity.

Offshore oil and gas activities can result in the discharge of large amounts of drilling muds. While these materials have generally been regarded as non-toxic to marine organisms, recent studies have demonstrated negative impacts to suspension feeding organisms. We exposed the arctic-boreal sponge Geodia barretti to the primary particulate components of two water-based drilling muds; barite and bentonite. Sponges were exposed to barite, bentonite and a natural reference sediment at a range of total suspended solid concentrations (TSS = 0, 10, 50 or 100 mg/L) for 12 h after which we measured a suite of biomarker responses (lysosomal membrane stability, lipid peroxidation and glutathione). In addition, we compared biomarker responses, organic energy content and metal accumulation in sponges, which had been continuously or intermittently exposed to suspended barite and natural sediment for 14 d at relevant concentrations (10 and 30 mg TSS/L). Lysosomal membrane stability was reduced in the sponges exposed to barite at 50 and 100 mg TSS/L after just 12 h and at 30 mg TSS/L for both continuous and intermittent exposures over 14 d. Evidence of compromised cellular viability was accompanied by barite analysis revealing concentrations of Cu and Pb well above reference sediments and Norwegian sediment quality guidelines. Metal bioaccumulation in sponge tissues was low and the total organic energy content (determined by the elemental composition of organic tissue) was not affected. Intermittent exposures to barite resulted in less toxicity than continuous exposure to barite. Short term exposures to bentonite did not alter any biomarker responses. This is the first time that these biomarkers have been used to indicate contaminant exposure in an arctic-boreal sponge. Our results illustrate the potential toxicity of barite and the importance of assessments that reflect the ways in which these contaminants are delivered under environmentally realistic conditions.

Establishment of submerged macrophyte beds and application of chemical phosphorus inactivation are common lake restoration methods for reducing internal phosphorus loading. The two methods operate via different mechanisms and may potentially supplement each other, especially when internal phosphorous loading is continuously high. However, their combined effects have so far not been elucidated. Here, we investigated the combined impact of the submerged macrophyte Vallisneria denseserrulata and a lanthanum-modified bentonite (Phoslock®) on water quality in a 12-week mesocosm experiment. The combined treatment led to stronger improvement of water quality and a more pronounced reduction of porewater soluble reactive phosphorus than each of the two measures. In the combined treatment, total porewater soluble reactive phosphorus in the top 10 cm sediment layers decreased by 78% compared with the control group without Phoslock® and submerged macrophytes. Besides, in the upper 0–1 cm sediment layer, mobile phosphorus was transformed into recalcitrant forms (e.g. the proportion of HCl–P increased to 64%), while in the deeper layers, (hydr)oxides-bound phosphorus species increased 17–28%. Phoslock®, however, reduced the clonal growth of V. denseserrulata by 35% of biomass (dry weight) and 27% of plant density. Our study indicated that Phoslock® and submerged macrophytes may complement each other in the early stage of lake restoration following external nutrient loading reduction in eutrophic lakes, potentially accelerating the restoration process, especially in those lakes where the internal phosphorus loading is high.

Powder adsorbents show an excellent adsorption capacity for arsenic(As) due to the large specific surface area. However, the performance of powder adsorbents decreases significantly by channeling in the adsorption bed, and the powder is released from the bed. Pelletization of power adsorbent can solve the problems, and bentonite was proposed as a binder to improve the strength. The adsorption capacity and lifetime of pelletized adsorbent were evaluated through a batch and column study. The addition of bentonite decreased adsorption capacity by 16% of pellet without bentonite, but improved compressive strength of adsorbent up to 3.6 times. In the batch test, the maximum adsorption capacity of pelletized adsorbent is 22.2 mg As/g, which is about 40% of powder adsorbent. However, in the column study, pellet adsorbent showed similar adsorption performance and lifetime to commercial and powder adsorbent. As a result, the pellet adsorbent using bentonite is a potential low-cost adsorbent to remove effectively As in the aqueous phase.

The non-magnetic capping materials are difficult to be recycled from the water bodies after their application, leading to the increase in the cost of the sediment remediation. To address this issue, a capping material, i.e., magnetic lanthanum/iron-modified bentonite (M-LaFeBT) was prepared by loading lanthanum onto a magnetic iron-modified bentonite (M-FeBT) and used to control the internal phosphorus (P) loading in this study. To determine the capping efficiency and mechanism of M-LaFeBT, the impact of M-LaFeBT and M-FeBT capping on the mobilization of P in sediments was investigated, and the stabilization of P bound by the M-LaFeBT and M-FeBT capping layers was evaluated. Results showed that M-LaFeBT possessed good magnetic property with a saturated magnetization of 14.9 emu/g, and exhibited good phosphate adsorption ability with a maximum monolayer sorption capacity (QMAX) of 14.3 mg P/g at pH 7. Moreover, M-LaFeBT capping tremendously reduced the concentration of soluble reactive P (SR-P) in the overlying water (OL-water), and the reduction efficiencies were 94.7%–97.4%. Furthermore, M-LaFeBT capping significantly decreased the concentration of SR-P in the pore water and DGT (diffusive gradient in thin films)-labile P in the profile of OL-water and sediment. Additionally, most of P bound by the M-LaFeBT capping layer (approximately 77%) was stable under natural pH and reducing conditions. The phosphate adsorption ability for M-LaFeBT was much higher than that for M-FeBT, and the QMAX value for the former was 4.86 times higher than that for the latter. M-LaFeBT capping gave rise to a higher reduction of DGT-labile concentration in the profile of OL-water and sediment than M-FeBT capping. The P adsorbed by the M-LaFeBT capping layer was more stable than that by the M-FeBT capping layer. Results of this study demonstrate that M-LaFeBT is promising for utilization as an active capping material to intercept sedimentary P release into OL-water.

With the development and application of graphene oxides (GO), the potential toxicity and environmental behavior of GO has become one of the most forefront environmental problems. Herein, a novel nanoscale layered double hydroxides (glycerinum-modified nanocrystallined Mg/Al layered double hydroxides, LDH-Gl), layered double oxides (calcined LDH-Gl, LDO-Gl) and metallic oxide (TiO2) were synthesized and applied as superior coagulants for the efficient removal of GO from aqueous solutions. Coagulation of GO as a function of coagulant contents, pH, ionic strength, GO contents, temperature and co-existing ions were studied and compared, and the results showed that the maximum coagulation capacities of GO were LDO-Gl (448.3 mg g−1) > TiO2 (365.7 mg g−1) > LDH-Gl (339.1 mg g−1) at pH 5.5, which were significantly higher than those of bentonite, Al2O3, CaCl2 or other natural materials due to their stronger reaction active and interfacial effect. The presence of SO32− and HCO3− inhibited the coagulation of GO on LDH-Gl and LDO-Gl significantly, while other cations (K+, Mg2+, Ca2+, Ni2+, Al3+) or anion (Cl−) had slightly effect on GO coagulation. The interaction mechanism of GO coagulation on LDO-Gl and TiO2 might due to the electrostatic interactions and strong surface complexation, while the main driving force of GO coagulation on LDH-Gl might be attributed to electrostatic interaction and hydrogen bond, which were further evidenced by TEM, SEM, FT-IR and XRD analysis. The results of natural environmental simulation showed that LDO-Gl, TiO2 or other kinds of natural metallic oxides could be superior coagulants for the efficient elimination of GO or other toxic nanomaterials from aqueous solutions in real environmental pollution cleanup.

The fractionation and speciation of As in a contaminated soil were investigated, and a remediation strategy was tested. Regarding speciation, we found that As(V) prevails over As(III) whereas more than 40% of total arsenic is in organic form. The fractionation of As was investigated with two sequential extraction methods: a low mobility was found. Then we tested the possibility of using phosphoric acid to extract As from the soil and cleaning the washing effluents by sorption onto montmorillonite. The efficiency of the extraction and of the adsorption onto the clay were also investigated for Cr, Cu, Fe, Mn, Ni, Pb and Zn, whose total concentrations and fractionation in the soil are reported here. The extraction percentages for As and metals ranged from 30 to 65%; the residual proportions in the soil are presumably in very unreactive forms. Montmorillonite showed a good uptake capacity towards the investigated pollutants. Arsenic in a contaminated soil was present in different forms and it was extracted by soil washing followed by effluent treatment by sorption onto a natural clay.