This article summarizes the photocatalytic water splitting performance improvement with a heterojunction system.

Climate change, population growth, and increased industrial activities are exacerbating freshwater scarcity and leading to increased interest in desalination of saline water. Brackish water is an attractive alternative to freshwater due to its low salinity and widespread availability in many water-scarce areas. However, partial or total desalination of brackish water is essential to reach the water quality requirements for a variety of applications. Selection of appropriate technology requires knowledge and understanding of the operational principles, capabilities, and limitations of the available desalination processes. Proper combination of feedwater technology improves the energy efficiency of desalination. In this article, we focus on pressure-driven and electro-driven membrane desalination processes. We review the principles, as well as challenges and recent improvements for reverse osmosis (RO), nanofiltration (NF), electrodialysis (ED), and membrane capacitive deionization (MCDI). RO is the dominant membrane process for large-scale desalination of brackish water with higher salinity, while ED and MCDI are energy-efficient for lower salinity ranges. Selective removal of multivalent components makes NF an excellent option for water softening. Brackish water desalination with membrane processes faces a series of challenges. Membrane fouling and scaling are the common issues associated with these processes, resulting in a reduction in their water recovery and energy efficiency. To overcome such adverse effects, many efforts have been dedicated toward development of pre-treatment steps, surface modification of membranes, use of anti-scalant, and modification of operational conditions. However, the effectiveness of these approaches depends on the fouling propensity of the feed water. In addition to the fouling and scaling, each process may face other challenges depending on their state of development and maturity. This review provides recent advances in the material, architecture, and operation of these processes that can assist in the selection and design of technologies for particular applications. The active research directions to improve the performance of these processes are also identified. The review shows that technologies that are tunable and particularly efficient for partial desalination such as ED and MCDI are increasingly competitive with traditional RO processes. Development of cost-effective ion exchange membranes with high chemical and mechanical stability can further improve the economy of desalination with electro-membrane processes and advance their future applications.

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Catalytic conversion of biomass or biomass-derived intermediate to value-added chemicals is important for both biomass waste management and production of industrially important chemicals. Oxidation of 5-hydroximethyl furfural (HMF) is considered one of the most important biomass conversion processes, which resulted in many value-added products such as 2,5-diformylfuran (DFF), 2,5-furandicarboxylic acid (FDCA), 5-hydroxymethyl-2-furancarboxylic acid (HMFCA), and 5-formyl-2-furancarboxylic acid (FFCA). In this study, the three morphologies of CdS catalyst (nanorod, nanosheet, and nanosphere) with two different crystalline structures are synthesized and characterized by SEM, TEM, and XRD analysis. The oxidation of HMF to FFCA is performed using the synthesized catalysts in the presence of different solvents and oxidizing agents. We find that CdS nanorod provides the selective oxidation of HMF to FFCA in the presence of dimethyl sulfoxide solvent and tert-butyl hydrogen peroxide oxidizing agent. The density functional theory (DFT) simulations are carried out to explain the catalytic activity of the CdS catalyst for oxidation of HMF to FFCA. The DFT simulations show that CdS is an excellent catalyst for binding HMF on the CdS surface. Our findings provide the way of effective oxidation of biomass into value-added products using the cheap CdS catalyst.

Polybetaines have received widespread attention due to their smart response properties and structures which resemble biological polymers like peptides and DNA. However, few studies have focused on the controlled synthesis and self-assembly of hydrophobically modified polybetaines due to the difficulty of synthesizing these materials. We report the first molecular weight-controlled synthesis of hydrophobically modified polycarboxybetaines (HMPCB). Poly­(dodecyl grafted aminocrotonate -methacrylic acid) (P­(DACRO-MAA)) was synthesized via the reversible addition–fragmentation chain-transfer (RAFT) polymerization approach. The two different tautomers of the monomer were also successfully identified and separated via thin layer chromatography (TLC) and column chromatography, making it possible to obtain pure polycarboxybetaine via RAFT synthesis. Both the successfully separated enamine form of the monomer and the resulting polycarboxybetaine were confirmed via FTIR and NMR. The polycarboxybetaine was found to have a low polydispersity (PDI) of 1.214, and its molecular weight was determined as 70590 g/mol via gel permeation chromatography (GPC) measurements. Spherical, rodlike, and fractal assembled structures for the P­(DACRO-MAA) were observed with pH change using TEM, zeta sizer, and dynamic light scattering (DLS). The unique self-assembled structures of HMPCB synthesized via RAFT provide an opportunity to understand fundamental polymer science and can be engineered for broad applications.