Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Seawater desalination plays a critical role in addressing the global water shortage challenge. Directional Solvent Extraction (DSE) is an emerging non-membrane desalination technology that features the ability to utilize very low temperature waste heat (as low as 40 °C). This is enabled by the subtly balanced solubility properties of directional solvents, which do not dissolve in water but can dissolve water and reject salt ions. However, the low water yield of the state-of-the-art directional solvent (decanoic acid) significantly limits its throughput and energy efficiency. In this paper, we demonstrate that by using ionic liquid as a new directional solvent, saline water can be desalinated with much higher production rate and thus significantly lower the energy and exergy consumptions. The ionic liquid identified suitable for DSE is [emim][TfN], which has a much (~10×) higher water yield than the currently used decanoic acid. Using molecular dynamics simulations with Gibbs free energy calculations, we reveal that water dissolving in [emim][TfN] is energetically favorable, but it takes significant energy for [emim][TfN] ions to dissolve in water. Our findings may significantly advance the DSE technology as a solution to the challenges in the global water-energy nexus.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7815866PMC
http://dx.doi.org/10.1038/s41467-020-20706-yDOI Listing

Publication Analysis

Top Keywords

directional solvent
16
ionic liquid
12
dissolve water
12
low temperature
8
solvent extraction
8
water
8
water yield
8
decanoic acid
8
directional
5
liquid enables
4

Similar Publications

Recent advances in eutectogels: Preparation, properties and applications.

Adv Colloid Interface Sci

September 2025

Key Laboratory of Colloid and Interface Chemistry (Ministry of Education), Shandong University, Jinan 250100, PR China. Electronic address:

Multiple stretchable gels with conductivity have been thoroughly prepared in diverse solvents historically to modulate their superlative properties in a multitude of applications, such as soft robotics, wearable devices, and e-skins. Eutectogels are considered as an emerging class of gels that combine the best features of both hydrogels and organogels, including environmental friendliness, thermal stability and customizable nature. Eutectogels, composed of deep eutectic solvents (DES) immobilized within different matrices, not only inherit the merits of DES, but also show some additional properties derived from the special structure and compositions, which are conducive to development potential.

View Article and Find Full Text PDF

Eco-efficient C-H alkynylation of indoles mechanochemical ruthenium catalysis.

Org Biomol Chem

September 2025

Department of Chemistry, Indian Institute of Technology Tirupati, Yerpedu - Venkatagiri Road, Yerpedu Post, Tirupati District, Andhra Pradesh 517619, India.

A regioselective C2-alkynylation of indoles ruthenium(II)-catalyzed C-H activation using bromoalkynes is demonstrated under both solution-phase and mechanochemical conditions. The solvent-minimized mechanochemical method delivers comparable yields with reduced reaction time and improved green metrics. Broad substrate scope, gram-scale applicability, and post-functionalization showcase the synthetic utility of this approach.

View Article and Find Full Text PDF

Developing the efficient C─H bond activation carboxylation processes for furoic acid (FA) represents a critical technological challenge in achieving atom-economical synthesis of 2,5-furandicarboxylic acid (FDCA). Despite notable advancements in this field, the inherent contradiction between the high reactivity of furan rings and the chemical inertness of C─H bonds poses substantial technical bottleneck for achieving controllable C─H carboxylation under mild conditions. Herein, we report a high lattice-distorted MnOx catalyst with surface trench-like structures, wherein the Mn-O-conjugated configurations and electron-rich Mn cooperatively drive FA dehydrogenation and carbon radical reduction, inducing the free radical evolution process (FA→carbon-centered FA radical→FA carbanion), then coupled with solvent-polarized CO to accelerate the carboxylation process.

View Article and Find Full Text PDF

Thermopower regulation of thermocells electrolyte engineering: progress and prospects.

Chem Commun (Camb)

September 2025

Guangdong Provincial Key Laboratory of New Energy Materials Service Safety, College of Materials Science and Engineering, Shenzhen University, Shenzhen 518055, China.

Thermocells (TECs) represent a promising technology for sustainable low-grade waste heat (<100 °C) harvesting, offering distinct advantages such as scalability, structural versatility, and high thermopower. However, their practical applications are still hindered by low energy conversion efficiency and stability issues. In recent studies, electrolyte engineering has been highlighted as a critical strategy to enhance their thermopower by regulating the solvation structure and redox ion concentration gradient, thereby improving conversion efficiency.

View Article and Find Full Text PDF

The formation of carbinolamine represents the crucial initial step in the aldol reaction, specifically involving the interaction between p-nitrobenzaldehyde and acetone, facilitated by amine-catalyzed mesoporous silica nanoparticles (amine-MSN). In this process, a nitrogen atom from propylamine, which acts as the catalytic moiety, engages in the formation of a covalent bond with a carbon atom from acetone, leading to the generation of a carbinolamine intermediate. This reaction is significantly influenced by the presence of silanol groups located on the surface of the amine-MSN, which contribute to the catalytic activity.

View Article and Find Full Text PDF