Sludge/TiO2 composite was synthesized from drinking water treatment sludge, as a waste material and TiO2 , by a sol- gel method. Various sludge adsorbent / TiO2 ratios (1:1, 1:2 and 2:1 w/w) were prepared, and characterized by transmission electron microscope (TEM), X-ray diffraction (XRD), X-ray Fluorescence (XRF), and BET. The prepared composites were applied successfully for photodegradation of methylene blue (MB) dye from a solution. The photocatalytic degradation of MB dye was investigated using UV irradiation, or UV/H2O2. Initial dye concentration, solution pH, composite dosage, and UV irradiation time were applied to study the optimum conditions for MB degradation. The results revealed the highest MB dye degradation with composite (2:1). It was found that the maximum MB degradation efficiency was at pH=7, 4 h irradiation time, 0.125 g composite dose, and 50 ppm initial dye concentration. MB removal efficiency was 95.7% using UV irradiation, and 99.8% of that using UV/ H2O2. The rate of MB dye degradation followed the first order kinetics. Results from this study offer the best conditions for recycling drinking water treatment sludge, and use it for wastewater treatment.

The term bioremediation describes biological machinery of recycling wastes to make them harmless and useful to some extent. Bioremediation is the most proficient tool to manage the polluted environment and recover contaminated river water.  Bioremediation is very much involved in the degradation, eradication, restriction, or reclamation varied chemical and physical hazardous substances from the nearby with the action of all-inclusive microorganisms. The fundamental principle of bioremediation is disintegrating and transmuting pollutants such as hydrocarbons, oil, heavy metal, pesticides and so on. Different microbes like aerobic, anaerobic, fungi and algae are incorporated in bioremediation process. At present, several methods and approaches like bio stimulation, bio augmentation, and monitoring natural recovery are common and functional in different sites around the world for treating contaminated river water. However, all bioremediation procedures it has its own pros and cons due to its own unambiguous application. Above all, utilization of bioremediation paving a minimal inconsiderably contaminated, healthy as well as safe and sound future.

Effective denitrification of water using photocatalytic reaction of active TiO2 particles doped with different oxides and metals has been the subject of numerous studies. For a particular research area, the potential of silica bond and its silicate based matrices with titanium dioxide and improving the photocatalytic performance using more economic methods is still challenging, and research in this field is attractive and ongoing. In this study, the effect of cement matrix and its complex bonds with industrial grade TiO2 particles was evaluated on the rate of water denitrification in a fixed bed circulating flow photoreactor. For this purpose, silica fume was substituted for cement in constant percent of 10 as a rich source of amorphous silica. Industrial grade TiO2 was added to the mix as5, 10 and 15 percent weight of cementitious materials (CM). Nano TiO2 was considered as a supplementary photocatalytic material with a constant 1% weight of CM in two mix designs. The results implied that the addition of 5% TiO2 increased the rate of nitrate concentration reduction by up to 10 times. Also, the specimen including 10% TiO2 increased denitrification rate by 107% compared to the previous content, which had much less impact. Also, the addition of nanoTiO2 increased denitrification rate up 113%.

In Mirzapur (U.P.), a power-starved district, the UASB (Upflow Anaerobic Sludge Blanket) technique was adopted. Almost all of the available technologies do not treat heavy metals, so, is the case with the UASB also. The present study is to assess how much heavy metal can get accumulated in plant tissues in different species. The result of the present study was that the concentration of Pb(1106.31)>Zn(221.45)>Cd(49.26)>Hg(23.37) mg/Kg in the sludge while the concentration of Zn(93.35)>Pb(52.00)>Hg(16.93)>Cd(1.53) mg/Kg in the soil. When the sludge was mixed with the soil the trend got changed and the trend was Pb(596.36)>Zn(219.86)>Cd(24.70)>Hg(22.63) mg/Kg. Three different species that were chosen for the study were Basella Alba (Spinach), Solanum Lycopersicum (Tomato) & Brassica Juncea (Mustard). The trend of accumulation of studied heavy metals in the Brassica Juncea (Mustard) was Zn(85.33)>Pb(25.88)>Hg(11.23)>Cd(0.99) mg/Kg. In Solanum lycopersicum (Tomato) the trend was Pb(231.11)>Zn(108.72)>Hg(12.43)>Cd(9.41) mg/Kg  and in Basella alba (Spinach) was Zn(103.81)>Pb(83.90)>Hg(10.78)>Cd(4.18) mg/Kg. Overall the study reveals that the accumulation of heavy metals takes place in plants grown in soil mixed with sewage sludge. The reduction in the concentration of Pb, Cd, Hg and Zn in sludge mixed with soil after the harvesting of plant in case of Solanum lycopersicum were 39.38%, 47.93%, 6.18% and 49.89% respectively; while in case of Basella alba these were 25.23%, 57.53%, 71.58% and 49.16% respectively; and in case of Brassica Juncea these reduction were 25.86%, 60.80%, 70.96% and 49.04% respectively.

In this research, a response surface methodology (RSM) was used to investigate the effects of independent parameters (pH, contact time, temperature, adsorbent dosage, and initial concentration of pollutant), their simultaneous interactions, and quadratic effects on crystal violet adsorption onto two starch based materials in the form of batch experiments. The characterizing results indicated that there is no significant difference between the potato starch and synthesized starch phosphate, as phosphorylation has not changed the crystalline structure of starch inside the granules. The maximum removal efficiency of crystal violet ions was obtained 99 % at the optimum adsorption conditions of initial concentration 213.54 mg/L, adsorbent dosage 0.25 g, contact time 14.99 min, temperature 15 °C, and initial pH of solution 9. RSM outputs showed that the maximum adsorption of crystal violet ions by could be achieved by raising pH and adsorbent dosage, and decreasing the initial crystal violet concentration. While temperature and contact time are not effective parameters in crystal violet removal from aqueous solutions using synthesized starch phosphate. Generally, the RSM model is suitable to optimize the experiments for dye elimination by adsorption, where the modified starch phosphate would be an effective adsorbent for treating crystal violet solution.

The present study investigates an NF process for removal of copper and hexavalent chromium, studying the effect of pH (5, 7, 9) as well as contaminants' concentration (50, 500, 5000 µg/L) at a constant pressure of 8 bar; with the recovery rate, regulated at 75±2%. To determine the main factors, affecting the system performance, and evaluate the interaction effects among the factors, the experiment is designed via RSM Method. The chrome shows a higher rejection, compared with Copper, all over the range of investigated factors. As Copper concentration grows, Cu removal efficiency drops while, the Cr (VI) removal efficiency ascends. Also by increasing chrome concentration, the Cu removal efficiency decreases, while Cr (VI) removal efficiency increases. Results show that with an increase in pH, the Cu removal drops and Cr removal is increased. The pH is the main parameter, influencing the removal rate. It has been found that the maximum removal efficiency is up to 99% and 73% for Cr (VI) and Cu, respectively. There is an adequate agreement between real data and that obtained from the models (R2 was found to be 0.9889 and 0.9664, for Cu and Cr (VI) rejection, respectively).

The use of membrane-based technology has evolved into an important strategy for supplying freshwater from seawater and wastewater to overcome the problems of water scarcity around the world. However, the presence of natural organic matter (NOM), including humic substances affects the performance of the process. Here, we present a systematic report on the mineralization of humic acid (HA), as a model for NOM, in high concentration of salts using the ultraviolet light-activated peroxymonosulfate (UV/PMS) system as a potential alternative for HA elimination during membrane-based seawater desalination and water treatment processes. Effects of various parameters such as PMS concentration, solution type, pH, anions, and anion-cation matrix on HA mineralization were assessed. The results show that 100%, 78% and 58% of HA (2 mg/L TOC) were mineralized with rate constants of 0.085 min⁻¹, 0.0073 min⁻¹, and 0.0041 min⁻¹ after 180 min reaction time at pH 7 when 0.5 mM PMS was used in deionized water, sodium chloride solution (35,000 ppm) and synthetic seawater, respectively. The reduced efficiency under saline conditions was attributed to the presence of anions in the system that acted as sulfate and hydroxyl radicals’ scavengers. Furthermore, the safety of the treated synthetic seawater was evaluated by analyzing the residual transformed products. Overall, pretreatment with the UV/PMS system mitigated fouling on the RO membrane.

The removal of excessive ammonium from water is vital for preventing eutrophication of surface water and ensuring drinking water safety. Several studies have explored the use of biochar for removing ammonium from water. However, the efficacy of pristine biochar is generally weak, and various biochar modification approaches have been proposed to enhance adsorption capacity. In this study, biochar obtained from giant reed stalks (300, 500, 700 °C) was modified by sulfonation, and the ammonium adsorption capabilities of both giant reed biochars (RBCs) and sulfonated reed biochars (SRBCs) were assessed. The ammonium adsorption rates of SRBCs were much faster than RBCs, with equilibrium times of ∼2 h and ∼8 h for SRBCs and RBCs, respectively. The Langmuir maximum adsorption capacities of SRBCs were 4.20–5.19 mg N/g for SRBCs, significantly greater than RBCs (1.09–1.92 mg N/g). Physical-chemical characterization methods confirmed the increased levels of carboxylic and sulfonic groups on sulfonated biochar. The reaction of ammonium with these O-containing functional groups was the primary mechanism for the enhancement of ammonium adsorption by SRBCs. To conclude, sulfonation significantly improved the adsorption performance of biochar, suggesting its potential application for ammonium mitigation in water.

Antibiotics usage in animal production is considered a primary driver of the occurrence, supply and spread of antibiotic resistance genes (ARGs) in the environment. Pig farms and fish ponds are important breeding systems in food animal production. In this study, we compared and analyzed broad ARGs profiles, mobile genetic elements (MGEs) and bacterial communities in a representative pig farm and neighboring fish ponds around Poyang Lake, the largest freshwater lake in China. The factors influencing the distribution of ARGs were also explored. The results showed widespread detection of ARGs (from 57 to 110) among 283 targeted ARGs in the collected water samples. The differences in the number and relative abundance of ARGs observed from the pig farm and neighboring fish ponds revealed that ARG contamination was more serious on the pig farm than in the fish ponds and that the water treatment plant on the pig farm was not very effective. Based on the variance partition analysis (VPA), MGEs, bacterial communities and water quality indicators (WIs) codrive the relative abundance of ARGs. Based on network analysis, we found that total phosphorus and Tp614 were the most important WIs and MGEs affecting ARG abundance, respectively. Our findings provide fundamental data on farms in lakeside districts and provide insights into establishing standards for the discharge of aquaculture wastewater.

Silver nanoparticles (AgNPs) are used in many industries for multiple applications that inevitably release AgNPs into surface water sources. The formation kinetics of disinfection by-products (DBPs) in the presence of AgNPs was investigated during chlorination. Experiments were carried out with raw water from a canal in Songkhla, Thailand, which analyzed the formation potential (FP) of trihalomethanes FP (THMFP), iodo-trihalomethanes FP (I-THMFP), haloacetonitriles FP (HANFP), and trichloronitromethane FP. Increased AgNP concentrations by 10–20 mg/L led to a higher specific formation rate of chloroform which is described by zero- and first-order kinetics. The increase in the specific formation of chloroform as increasing chlorine contact time could enhance both the THMFP rates and the maximum THMFP concentrations in all tested AgNPs. The AgNP content did not have a significant influence on I-THMFP and HANFP concentrations or speciation. The I-THMFP and HANFP increased in a short-chlorination time as mostly complete formation <12 h, and then the rate decreased as the reaction proceeded. The levels of THMs and many emerging DBPs are related to the presence of AgNPs in chlorinated water and chlorine reaction time. THMFP had a higher impact on integrated toxic risk value (ITRV) than I-THMFP and HANFP because of the chlorination of water with AgNPs. The chlorine reaction time was more effective for increasing the ITRV of THMFP than the level of AgNPs. Water treatment plants should control the DBPs that cause possible health risks from water consumption by optimizing water distribution time.