A Semi-Interpenetrating Network Sorbent of Superior Efficiency for Atmospheric Water Harvesting and Solar-Regenerated Release.

Water is readily available nearly anywhere as vapor. Thus, atmospheric water harvesting (AWH) technologies are seen as a promising solution to support sustainable water production. This work reports a novel semi-interpenetrating network, which integrates poly(pyrrole) doped with a hygroscopic salt and 2D graphene-based nanosheets optimally assembled within an alginate matrix, capable of harvesting water from the atmosphere with a record intake of up to 7.15 gw/gs. Owing to the incorporated graphene nanosheets, natural sunlight was solely used to enable desorption, achieving an increase of the temperature of the developed network of up to 71 °C within 20 min, resulting in a water yield of 3.36 L/kgS in each cycle with quality well within the World Health Organization standard ranges. Notably, after 30 cycles of sorption and desorption, the composite hydrogel displayed unchanged water uptake and stability. This study demonstrates that atmospheric water vapor as a complementary source of water can be harvested sustainably and effectively at a minimal cost and without external energy input.

A Super-Hygroscopic Solar-Regenerated Alginate-Based Composite for Atmospheric Water Harvesting.

Global water scarcity is leading to increasingly tense competition across populations. In order to complement the largely fast-depleting fresh water sources and mitigate the challenges generated by brine discharge from desalination, atmospheric water harvesting (AWH) has emerged to support long-term water supply. This work presents a novel alginate-based hybrid material comprised of porous silico-aluminophosphate-34 (SAPO-34) as fast-transport channel medium as well as hydrophilicity and stability enhancer, and graphene-based sheets as light absorber for solar-enabled evaporation, both optimally incorporated in an alginate matrix, resulting in a composite sorbent capable of harvesting water from the atmosphere with a record intake of up to 6.85 gw gs -1. Natural sunlight is solely used to enable desorption achieving increase of the temperature of the developed network up to 60 °C and resulting in release of the sorbed water, with impurities content well below the World Health Organization (WHO) upper limits. After 30 cycles of sorption and desorption, the composite hydrogel displayed unchanged water uptake and stability. This work provides an impactful perspective toward sustainable generation of water from humidity without external energy consumption supporting the emergence of alternative water production solutions.

Advances in the role of natural gums-based hydrogels in water purification, desalination and atmospheric-water harvesting.

Freshwater scarcity is one of the world's foremost environmental stress concerns. In the last few years, with sustainable industrial growth and rapidly growing population, the problem of freshwater shortage has encouraged researchers to conduct comprehensive research for the development of advanced water harvesting and wastewater treatment techniques. Natural gums-based hydrogels have been widely used in different water purification and harvesting applications because of their environment friendly nature, high water absorption, adsorption and retention capacities. In this article, we presented an entirely conceptual and critical review of literature mainly focused on the potential of different natural gums-based hydrogel in water harvesting and wastewater treatment applications. First, different categories of natural gums-based hydrogels including stimuli responsive hydrogels, physically and chemically crosslinked hydrogels, were introduced. Then, the emphasis was given on the role of natural gums-based hydrogels in different wastewater treatment applications like adsorption, photocatalysis and flocculation. After that, the latest research progress on the use of natural gums-based hydrogels in atmospheric water harvesting and seawater desalination was discussed. Finally, different challenges and main limitations associated with the use of natural gums-hydrogels in water purification and harvesting applications were discussed to understand the research gaps and drawbacks which need improvements.

Leaching of Polycyclic Aromatic Hydrocarbons from the Coal Tar in Sewage Wastewater, Acidic and Alkaline Mine Drainage.

Polycyclic aromatic hydrocarbons (PAHs) have been a problem in the environment for an extended period. They are mostly derived from petroleum, coal tar and oil spills that travel and are immobilized in wastewater/water sources. Their presence in the environment causes a hazard to humans due to their toxicity and carcinogenic properties. In the study, coal tar was analyzed using Gas Chromatography-Mass Spectrometry (GC-MS) and a concentration of 787.97 mg/L of naphthalene, followed by 632.15 mg/L of phenanthrene were found to be in the highest concentrations in the various water sources such as sewage, alkaline and acid mine drainage. A design column was used to investigate the leaching process and assessments were conducted on 300 mL of the various water sources mentioned, with 5 g of coal tar added and with monitoring for 4 weeks. The influence of the physiochemical properties of the receiving water sources, such as sewage, and acid and alkaline mine drainage, on the release of PAHs from the coal tar was assessed. The acidic media was proven to have the highest release of PAHs, with a total concentration of 7.1 mg/L of released PAHs, followed by 1.2 mg/L for the sewage, and lastly, 0.32 mg/L for the alkaline mine drainage at room temperature.

Capturing water vapors from atmospheric air using superporous gels.

Dehumidification performance of most polymer desiccant materials is unsatisfactory because of the complex adsorption mechanism on polymer surface and non-porous structure. A viable alternative of solid desiccants, especially existing polymer desiccants, for capturing water vapors from moist air is the super-porous gels (SPGs). The presence of interconnected channels of pores in its structure facilitates the transfer of water molecules to the internal structure of SPGs. Therefore, in this research work, we are proposing N-isopropylacrylamide (NIPAM) and acrylamide (AM) based thermoresponsive SPGs as a potential alternative to the existing conventional solid desiccants. To ensure the formation of interconnected capillary channels, the SPGs were synthesized via gas blowing and foaming technique. Surface morphology of the SPGs was studied using scanning electron microscopy (SEM) and the other physio-chemical characteristics were studied using different techniques like fourier Transform Infrared Spectroscopy (FTIR), X-ray diffraction (XRD) and thermo-gravimetric analysis (TGA). Water vapors adsorption properties of the SPGs were explored via adsorption isotherm and kinetics. The adsorption isotherm was found to be of type-III isotherm with a maximum adsorption capacity of 0.75 gw/gads at 25 °C and 90% relative humidity. Experimental isotherm data correlated well with BET, FHH and GAB isotherm models. Adsorption kinetics suggested that the water vapors diffusion followed intraparticle diffusion and liquid field driving mechanisms collectively. SPGs exhibited very good regeneration and reusability for ten continuous adsorption/desorption cycles. Therefore, the dehumidification efficiency of synthesized SPGs shows that they have potential to replace most of the conventional solid desiccant materials in use.

GO crosslinked hydrogel nanocomposites of chitosan/carboxymethyl cellulose - A versatile adsorbent for the treatment of dyes contaminated wastewater.

Graphene oxide (GO) crosslinked nanocomposites hydrogels (NCH) of chitosan (CS) and carboxymethyl cellulose (CMC) were synthesized and the feasibility of its application as a versatile adsorbent for the remediation of cationic (methylene blue, MB) as well as anionic (methyl orange, MO) dyes contaminated wastewater was explored. Initially, GO was functionalized with vinyltriethoxysilane which was subsequently used as a chemical crosslinker to synthesize the NCH of CS and CMC (CS/CMC-NCH) with the polymeric mixture of diallyldimethylammonium chloride and 2-acrylamido-2-methyl-1-propanesulfonic acid. About 99% dye was adsorbed from 50 mg/L dye solution of MB dye with 0.4 g/L of CS/CMC-NCH at pH 7, whereas, for MO about 82% dye was adsorbed with 0.6 g/L of CS/CMC-NCH at pH 3. The Adsorption of both dyes is well explained using pseudo-second-order and Langmuir models with the maximum adsorption capacities of 655.98 mgdye/gads for MB and 404.52 mgdye/gads for MO. Thermodynamics studies suggested spontaneous and exothermic nature of the adsorption process with values of ΔS < 0 and ΔH > 0. Furthermore, CS/CMC-NCH showed excellent regeneration capacity for continuous twenty cycles of adsorption-desorption. Therefore, the synthesized CS/CMC-NCH is a versatile adsorbent that can treat both anionic and cationic dyes contaminated wastewater.

Super porous TiO2 photocatalyst: Tailoring the agglomerate porosity into robust structural mesoporosity with enhanced surface area for efficient remediation of azo dye polluted waste water.

The low surface area of TiO2 (50 m2g-1 - Degussa P25) due to randomly oriented, agglomerated nanostructures and charge carrier recombination tendency, has till date been its major limitation for photocatalytic remediation of polluted wastewater. This study presents an innovative process to design super porous TiO2 nanostructures with high effective surface area (238 m2g-1), robust, structurally ordered mesoporosity via a simple sol-gel assisted reflux method. Detailed material characterization studies suggest that the higher degree of intermolecular ligation in novel templates such as butanetetracarboxylic or tricarballylic acid modified titanium hydroxide gels resulted in retainment of the porous structure during the urea assisted combustion synthesis. The induction of robust structural porosity is accompanied by a reduction in pore size distribution, an increase in pore volume leading to significantly higher total surface area of the synthesized TiO2. Detailed investigation of dye adsorption kinetics and photocatalytic degradation kinetics, complemented by kinetic modeling analysis confirmed that the super porous TiO2 with robust mesoporous structure outperforms the rest of synthesized TiO2 catalyst (having only agglomerate porosity) in terms of its superior adsorption capacity, faster diffusion kinetics and photocatalytic activity for degradation of Amaranth dye. Thus, the super porous TiO2 shows promising potential for application in sustainable photocatalytic technology for remediation of wastewater contaminated with azo dyes.