UV-C photon integrated surface dielectric barrier discharge hybrid reactor: A novel and energy-efficient route for rapid mineralisation of aqueous azo dyes.

The study describes developing an energy-efficient and scalable alternative to conventional non-thermal plasma systems by integrating surface dielectric barrier discharge (SDBD) and UV-C radiation sources. The unprecedented enhancement in the mineralisation rate of an azo dye (brilliant red 5B) by the hybrid reactor (photo-SDBD) is demonstrated thoroughly as a function of dye concentrations, pH, and background salts. The photo-SDBD is 1.25 - 4.9 times more energy efficient than SDBD under similar experimental conditions. The photo-SDBD could overcome the problems such as the recombination of hydroxyl radicals and scavenging of radicals by salts (NaCl, Na2SO4, Na2CO3) observed in conventional non-thermal plasma systems. The TOC and HR-MS analysis establish the complete mineralisation potential and chemical mineralisation pathway. Besides, the phytotoxicity of the treated water is tested and demonstrated its utility as a liquid fertiliser for enhanced germination of mung bean seeds. The optical emission spectroscopy measurements were performed to estimate the plasma's electron temperature (1.6 ± 0.2 eV) and density (1021/m3). The emission line ratio (I763.5/I738.3) approach is used to compare the influence of UV-C on plasma parameters in the SDBD reactor. The study opens a new pathway for developing energy-efficient and scalable plasma-assisted mineralisation of complex and emerging organic pollutants.

A critical review of uranium contamination in groundwater: Treatment and sludge disposal.

Dissolved uranium in groundwater at high concentrations is an emerging global threat to human and ecological health due to its radioactivity and chemical toxicity. Uranium can enter groundwater by geochemical reactions, natural deposition from minerals, mining, uranium ore processing, and spent fuel disposal. Although much progress has been made in uranium remediation in recent years, most published reviews on uranium treatment have focused on specific methods, particularly adsorption. This article systematically reviews the major treatment technologies, explains their mechanism and progress of uranium removal, and compares their performance under various environmental conditions. Of all treatment methods, adsorption has received much attention due to its ease of use and adaptability under various conditions. However, salinity and competition from other ions limit its application in actual field conditions. Biosorption and bioremediation are also promising methods due to their low-cost and chemical-free operation. Strong base anion exchange resins are more effective at typical groundwater pH conditions. Advanced oxidation processes like photocatalysis produce less sludge and are effective even at low uranium concentrations. Electrocoagulation shows significantly improved performance when organic ligands are added prior to treatment. The significant advantages of membrane filtration are high removal efficiency and the ability to recover uranium. While each technology has its merits and demerits, no single technology is entirely suitable under all conditions. One major area of concern with all technologies is the need to dispose of liquid and solid waste generated after treatment safely. Future research must focus on developing hybrid and state-of-the-art technologies for effective and sustainable uranium removal from groundwater. Developing holistic management strategies for uranium removal will hinge on understanding its speciation, mechanisms of fate and transport, and socio-economic conditions of the affected areas.

A comprehensive review on antimicrobial face masks: an emerging weapon in fighting pandemics.

The world has witnessed several incidents of epidemics and pandemics since the beginning of human existence. The gruesome effects of microbial threats create considerable repercussions on the healthcare systems. The continually evolving nature of causative viruses due to mutation or re-assortment sometimes makes existing medicines and vaccines inactive. As a rapid response to such outbreaks, much emphasis has been placed on personal protective equipment (PPE), especially face mask, to prevent infectious diseases from airborne pathogens. Wearing face masks in public reduce disease transmission and creates a sense of community solidarity in collectively fighting the pandemic. However, excessive use of single-use polymer-based face masks can pose a significant challenge to the environment and is increasingly evident in the ongoing COVID-19 pandemic. On the contrary, face masks with inherent antimicrobial properties can help in real-time deactivation of microorganisms enabling multiple-use and reduces secondary infections. Given the advantages, several efforts are made incorporating natural and synthetic antimicrobial agents (AMA) to produce face mask with enhanced safety, and the literature about such efforts are summarised. The review also discusses the literature concerning the current and future market potential and environmental impacts of face masks. Among the AMA tested, metal and metal-oxide based materials are more popular and relatively matured technology. However, the repeated use of such a face mask may pose a danger to the user and environment due to leaching/detachment of nanoparticles. So careful consideration is required to select AMA and their incorporation methods to reduce their leaching and environmental impacts. Also, systematic studies are required to establish short-term and long-term benefits.

Chitosan reinforced boehmite nanocomposite desiccant: A promising alternative to silica gel.

This paper describes the synthesis and performance evaluation of a granular solid desiccant composite synthesized through a sol-gel process at atmospheric pressure and ambient temperature. The composite desiccant essentially comprises of a biopolymer template, chitosan, and nanoscale boehmite particles embedded on the fibrils of the biopolymer. The chitosan fibers not only help in the formation of boehmite nanoparticles but also act as a reinforcing agent and enable the formation of sand like granules upon aging and drying. The composite showed promising ability to dehumidify the moist air. The desiccant was characterized in detail to study its textural, morphological and chemical properties. The results revealed the formation of crystalline, nanostructured composite with moisture adsorption capacity more than its self-weight (>1.5 g/g at 55-65% RH). The high moisture removal capacity, ease of synthesis and scale-up, and green synthesize approach would make the material a sustainable substitute for silica gel.

Self-propagated combustion synthesis of few-layered graphene: an optical properties perspective.

This paper describes a labour efficient and cost-effective strategy to prepare few-layered of reduced graphene oxide like (RGOL) sheets from graphite. The self-propagated combustion route enables the bulk production of RGOL sheets. Microscopic and spectroscopic analyses confirmed the formation of few-layer graphene sheets of an average thickness of ∼3 nm and the presence of some oxygen functional groups with a C/O ratio of 8.74. A possible mechanistic pathway for the formation of RGOL sheets is proposed. The optical properties of the RGOL sample were studied in detail by means of Spectroscopic Ellipsometry (SE). The experimental abilities of SE in relating the optical properties with the number of oxygen functionalities present in the samples are explored. The data were analysed by a double-layered optical model along with the Drude-Lorentz oscillatory dispersion relation. The refractive index (n = 2.24), extinction coefficient (k = 2.03), and dielectric functions are obtained using point-by-point analysis and are also checked for Kramers-Kronig (KK) consistency.

Rapid dehalogenation of pesticides and organics at the interface of reduced graphene oxide-silver nanocomposite.

This paper reports dehalogenation of various organohalides, especially aliphatic halocarbons and pesticides at reduced graphene oxide-silver nanocomposite (RGO@Ag). Several pesticides as well as chlorinated and fluorinated alkyl halides were chosen for this purpose. The composite and the products of degradation were characterized thoroughly by means of various microscopic and spectroscopic techniques. A sequential two-step mechanism involving dehalogenation of the target pollutants by silver nanoparticles followed by adsorption of the degraded compounds onto RGO was revealed. The composite showed unusual adsorption capacity, as high as 1534 mg/g, which facilitated the complete removal of the pollutants. Irrespective of the pollutants tested, a pseudo-second-order rate equation best described the adsorption kinetics. The affinity of the composite manifested chemical differences. The high adsorption capacity and re-usability makes the composite an excellent substrate for purification of water.

Biopolymer-reinforced synthetic granular nanocomposites for affordable point-of-use water purification.

Creation of affordable materials for constant release of silver ions in water is one of the most promising ways to provide microbially safe drinking water for all. Combining the capacity of diverse nanocomposites to scavenge toxic species such as arsenic, lead, and other contaminants along with the above capability can result in affordable, all-inclusive drinking water purifiers that can function without electricity. The critical problem in achieving this is the synthesis of stable materials that can release silver ions continuously in the presence of complex species usually present in drinking water that deposit and cause scaling on nanomaterial surfaces. Here we show that such constant release materials can be synthesized in a simple and effective fashion in water itself without the use of electrical power. The nanocomposite exhibits river sand-like properties, such as higher shear strength in loose and wet forms. These materials have been used to develop an affordable water purifier to deliver clean drinking water at US $2.5/y per family. The ability to prepare nanostructured compositions at near ambient temperature has wide relevance for adsorption-based water purification.

Graphene: a reusable substrate for unprecedented adsorption of pesticides.

Unprecedented adsorption of chlorpyrifos (CP), endosulfan (ES), and malathion (ML) onto graphene oxide (GO) and reduced graphene oxide (RGO) from water is reported. The observed adsorption capacities of CP, ES, and ML are as high as ~1200, 1100, and 800 mg g(-1) , respectively. Adsorption is found to be insensitive to pH or background ions. The adsorbent is reusable and can be applied in the field with suitable modifications. A first-principles pseudopotential-based density functional analysis of graphene-water-pesticide interactions showed that the adsorption is mediated through water, while direct interactions between graphene and the pesticides is rather weak or unlikely.

Luminescent, freestanding composite films of Au15 for specific metal ion sensing.

A highly luminescent freestanding film composed of the quantum cluster, Au(15), was prepared. We studied the utility of the material for specific metal ion detection. The sensitivity of the red emission of the cluster in the composite to Cu(2+) has been used to make a freestanding metal ion sensor, similar to pH paper. The luminescence of the film was stable when exposed to several other metal ions such as Hg(2+), As(3+), and As(5+). The composite film exhibited visual sensitivity to Cu(2+) up to 1 ppm, which is below the permissible limit (1.3 ppm) in drinking water set by the U.S. environmental protection agency (EPA). The specificity of the film for Cu(2+) sensing may be due to the reduction of Cu(2+) to Cu(1+)/Cu(0) by the glutathione ligand or the Au(15) core. Extended stability of the luminescence of the film makes it useful for practical applications.

Reduced graphene oxide-metal/metal oxide composites: facile synthesis and application in water purification.

This paper describes a versatile, and simple synthetic route for the preparation of a range of reduced graphene oxide (RGO)-metal/metal oxide composites and their application in water purification. The inherent reduction ability of RGO has been utilized to produce the composite structure from the respective precursor ions. Various spectroscopic and microscopic techniques were employed to characterize the as-synthesized composites. The data reveal that the RGO-composites are formed through a redox-like reaction between RGO and the metal precursor. RGO is progressively oxidized primarily to graphene oxide (GO) and the formed metal nanoparticles are anchored onto the carbon sheets. Metal ion scavenging applications of RGO-MnO(2) and RGO-Ag were demonstrated by taking Hg(II) as the model pollutant. RGO and the composites give a high distribution coefficient (K(d)), greater than 10 L g(-1) for Hg(II) uptake. The K(d) values for the composites are found to be about an order of magnitude higher compared to parent RGO and GO for this application. A methodology was developed to immobilize RGO-composites on river sand (RS) using chitosan as the binder. The as-supported composites are found to be efficient adsorbent candidates for field application.

A novel cellulose-manganese oxide hybrid material by in situ soft chemical synthesis and its application for the removal of Pb(II) from water.

We report an in situ soft chemical synthesis of a novel hybrid material, cellulose-nanoscale-manganese oxide composite (C-NMOC), and its application for Pb(II) removal from aqueous solutions. For comparison, detailed Pb(II) adsorption studies were also performed with nanoscale-manganese oxide powder (NMO), prepared through a similar route. Various spectroscopic and microscopic techniques were used to characterize the as-synthesized materials. X-ray photoelectron spectroscopic (XPS) measurements confirmed the existence of Mn(IV) phase in NMO whereas C-NMOC showed largely the Mn(III) phase. The existence and uniform distribution of manganese oxide in cellulose fiber materials was confirmed by SEM and EDAX analyses. The adsorption studies reveal that the Pb(II) uptake onto C-NMOC is a fast process and >90% of the uptake occurred within the first 10 min contact time. The Sips isotherm predicted the equilibrium data well and the maximum Pb(II) uptake capacity of C-NMOC (4.64% Mn loading) was estimated to be 80.1 mg g(-1). The Pb(II) adsorption capacity of C-NMOC (per gram of Mn present) was several times higher than commercial manganese oxide (beta-MnO2) and at least twice larger than NMO. The experimental evidence reveals that physisorption plays a dominant role in Pb(II) adsorption by both NMO and C-NMOC.

High yield combustion synthesis of nanomagnesia and its application for fluoride removal.

We describe a novel combustion synthesis for the preparation of Nanomagnesia (NM) and its application in water purification. The synthesis is based on the self-propagated combustion of the magnesium nitrate trapped in cellulose fibers. Various characterization studies confirmed that NM formed is crystalline with high phase purity, and the particle size varied in the range of 3-7nm. The fluoride scavenging potential of this material was tested as a function of pH, contact time and adsorbent dose. The result showed that fluoride adsorption by NM is highly favorable and the capacity does not vary in the pH range usually encountered in groundwater. The effects of various co-existing ions usually found in drinking water, on fluoride removal were also investigated. Phosphate was the greatest competitor for fluoride followed by bicarbonate. The presence of other ions studied did not affect the fluoride adsorption capacity of NM significantly. The adsorption kinetics followed pseudo-second-order equation and the equilibrium data are well predicted by Frendlich equation. Our experimental evidence shows that fluoride removal happened through isomorphic substitution of fluoride in brucite. A batch household defluoridation unit was developed using precipitation-sedimentation-filtration techniques, addressing the problems of high fluoride concentration as well as the problem of alkaline pH of the magnesia treated water. The method of synthesis reported here is advantageous from the perspectives of small size of the nanoparticle, cost-effective recovery of the material and improvement in the fluoride adsorption capacity.

Manganese-oxide-coated alumina: a promising sorbent for defluoridation of water.

In this study, adsorption potential of a new sorbent manganese-oxide-coated alumina (MOCA) was investigated for defluoridation of drinking water using batch and continuous mode experiments. The effects of different parameters such as pH, initial fluoride concentration and co-existing ions (usually present in groundwater sample) were studied to understand the adsorption behavior of the sorbent under various conditions. Optimum removal of fluoride ions occurred in a pH range of 4-7. Results of the present study indicate that fluoride adsorption rate and adsorption capacity of MOCA are far superior to that of activated alumina (AA), which was used as the base material for MOCA preparation. The MOCA can be effectively regenerated using 2.5% NaOH as eluent. The Langmuir equilibrium model was found to be suitable for describing the fluoride sorption on AA and MOCA. The maximum fluoride uptake capacity for MOCA and AA was found to be 2.85 and 1.08 mg g(-1), respectively. The kinetic results showed that the fluoride sorption to MOCA followed pseudo--second-order kinetics with a correlation coefficient greater than 0.98. The fluoride sorption capacity at breakthrough point for both the adsorbents was greatly influenced by bed depth. A bed depth service time (BDST) approach was adopted to describe the continuous flow system. The batch and column studies demonstrated the superiority of MOCA over AA in removing fluoride from the drinking water system.