Deep eutectic solvents (DESs) are complex substances composed of two or three components, wherein hydrogen bond donors and acceptors engage in intricate interactions within a hydrogen bond network. They have attracted extensive attention from researchers due to their easy synthesis, cost-effectiveness, broad liquid range, good stability, and for being green and non-toxic. However, studies on the physical properties of DESs are still scarce and many theories are not perfect enough, which limits the application of DESs in engineering practice. In this study, twelve DESs were synthesized by using choline chloride and betaine as HBAs, and ethylene glycol, polyethylene glycol 600, o-cresol, glycerol, and lactic acid as HBDs. The variation rules of their thermal conductivity and viscosity with temperature at atmospheric pressure were systematically investigated. The experimental results showed that the thermal conductivity of the 1:4 choline chloride/glycerol solvent was the largest at 294 K, reaching 0.2456 W·m-1·K-1, which could satisfy the demand for high efficiency heat transfer by heat-transferring workpieces. The temperature-viscosity relationship of the DESs was fitted using the Arrhenius model, and the maximum average absolute deviation was 6.77%.

Antibacterial materials with high hydrophobicity have drawbacks such as protein adsorption, bacterial contamination, and biofilm formation, which are responsible for some serious adverse health events. Therefore, antibacterial materials with high hydrophilicity are highly desired. In this paper, UV-curable antibacterial materials are prepared from silicone-containing Choline chloride (ChCl) functionalized hyperbranched quaternary ammonium salts (QAS) and tri-hydroxylethyl acrylate phosphate (TAEP). The materials show high hydrophilic performance because their water contact angle is as low as 19.3°. The materials also exhibit quite high antibacterial efficiency against S. aureus over 95.6%, fairly high transmittance over 90%, and good mechanical performance with tensile strength as high as 6.5 MPa. It reveals that it is a feasible strategy to develop antibacterial materials with low hydrophobicity from silicone-modified ChCl-functionalized hyperbranched QAS.

UNASSIGNED: Choline participates in plant stress tolerance through glycine betaine (GB) and phospholipid metabolism. As a salt-sensitive turfgrass species, Kentucky bluegrass (Poa pratensis) is the main turfgrass species in cool-season areas.
UNASSIGNED: To improve salinity tolerance and investigate the effects of choline on the physiological and lipidomic responses of turfgrass plants under salinity stress conditions, exogenous choline chloride was applied to Kentucky bluegrass exposed to salt stress.
UNASSIGNED: From physiological indicators, exogenous choline chloride could alleviate salt stress injury in Kentucky bluegrass. Lipid analysis showed that exogenous choline chloride under salt-stress conditions remodeled the content of phospholipids, glycolipids, and lysophospholipids. Monogalactosyl diacylglycerol, digalactosyl diacylglycerol, phosphatidylcholine, phosphatidylethanolamine, phosphatidylserine, and lysophosphatidylcholine content were increased and phosphatidic acid content were decreased in plants after exogenous choline chloride under salt treatment. Plant leaf choline content increased, but GB was not detected in exogenous choline chloride treatment plants under nonstress or salt-stress conditions.
UNASSIGNED: GB synthesis pathway related genes showed no clear change to choline chloride treatment, whereas cytidyldiphosphate-choline (CDP-choline) pathway genes were upregulated by choline chloride treatment. These results reveal that lipid remodeling through choline metabolism plays an important role in the salt tolerance mechanism of Kentucky bluegrass. Furthermore, the lipids selected in this study could serve as biomarkers for further improvement of salt-sensitive grass species.

Dialdehyde cellulose nanocrystals (DCNC) are defined as C2 and C3 aldehyde nanocellulose, which can be used as raw materials for nanocellulose derivatization, owing to the high activity of aldehyde groups. Herein, a comparative study in NaIO4 pre-oxidation and synchronous oxidation is investigated for DCNC extraction via choline chloride (ChCl)/urea-based deep eutectic solvent (DES). Ring-liked DCNC with an average particle size of 118 ± 11 nm, a yield of 49.25 %, an aldehyde group content of 6.29 mmol/g, a crystallinity of 69 %, and rod-liked DCNC with an average particle size of 109 ± 9 nm, a yield of 39.40 %, an aldehyde group content of 3.14 mmol/g, a crystallinity of 75 % can be extracted via optimized DES treatment combined with pre-oxidation and synchronous oxidation, respectively. In addition, the average particle size, size distribution, and aldehyde group content of DCNC were involved. TEM, FTIR, XRD, and TGA results reveal the variation of microstructure, chemical structure, crystalline structure, and thermostability of two kinds of DCNC during extraction even though the obtained DCNC exhibiting different micromorphology, pre-oxidation, or synchronous oxidation during ChCl/urea-based DES treatment can be considered as an efficient approach for DCNC extraction.

Lignin is a natural polymer second only to cellulose in natural reserves, whose structure is an aromatic macromolecule composed of benzene propane monomers connected by chemical bonds such as carbon-carbon bonds and ether bonds. Degradation is one of the ways to achieve the high-value conversion of lignin, among which the heating degradation of lignin by deep eutectic solvent (DES) can be an excellent green degradation method. In this study, choline chloride (CC) was used as the hydrogen bond acceptor, and urea (UR), ethylene glycol (GC), glycerol (GE), acetic acid (AA), formic and acetic mixed acid (MA), oxalic acid (OX), and p-toluenesulfonic acid (TA) were used as hydrogen bond donors to degrade lignin. NMR hydrogen spectroscopy was used for the simple and rapid determination of phenolic hydroxyl groups in lignin. FT-IR spectroscopy was used to characterize the changes of functional groups of lignin during DES treatment. GPC observed the molecular weight of lignin after degradation and found a significant increase in the homogeneity (1.6-2.0) and a significant decrease in the molecular weight Mw (2478-4330) of the regenerated lignin. It was found that acidic DES was more effective in depolymerizing alkaline lignin, especially for the toluene-choline chloride. Seven DES solutions were recovered, and it was found that the recovery of DES still reached more than 80% at the first recovery.

The addition of molecular liquid cosolvents to choline chloride (ChCl)-based deep eutectic solvents (DESs) is increasingly investigated for reducing the inherently high bulk viscosities of the latter, which represent a major obstacle for potential industrial applications. The molar enthalpy of mixing, often referred to as excess molar enthalpy H E-a property reflecting changes in intermolecular interactions upon mixing-of the well-known ChCl/ethylene glycol (1:2 molar ratio) DES mixed with either water or methanol was recently found to be of opposite sign at 308.15 K: Mixing of the DES with water is strongly exothermic, while methanol mixtures are endothermic over the entire mixture composition range. Knowledge of molecular-level liquid structural changes in the DES following cosolvent addition is expected to be important when selecting such \"pseudo-binary\" mixtures for specific applications, e.g., solvents. With the aim of understanding the reason for the different behavior of selected DES/water or methanol mixtures, we performed classical MD computer simulations to study the changes in intermolecular interactions thought to be responsible for the observed H E sign difference. Excess molar enthalpies computed from our simulations reproduce, for the first time, the experimental sign difference and composition dependence of the property. We performed a structural analysis of simulation configurations, revealing an intriguing difference in the interaction modes of the two cosolvents with the DES chloride anion: water molecules insert between neighboring chloride anions, forming ionic hydrogen-bonded bridges that draw the anions closer, whereas dilution of the DES with methanol results in increased interionic separation. Moreover, the simulated DES/water mixtures were found to contain extended hydrogen-bonded structures containing water-bridged chloride pair arrangements, the presence of which may have important implications for solvent applications.

Lead-contaminated soil was cleaned through ethylene-diamine-teraacetic acid disodium salt (EDTA-2Na) combined with diluted deep eutectic solvent (DES) which was prepared by mixing choline chloride with ethylene glycol. The influences of leaching temperature, leaching time, liquid-solid (L/S) ratio, concentration of EDTA-2Na, water-DES ratio, and the molar ratio of choline chloride-ethylene glycol (Ch-E) on the leaching rate of lead were investigated. The mineral phases of the soil and DES before and after washing were analyzed using scanning electron microscopy (SEM), X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FT-IR). The changes to the DESs before and after dissolving lead nitrate (Pb(NO3)2) were analyzed by high resolution mass spectrometry (HRMS) and nuclear magnetic resonance (NMR). Hydrogen bonds and EDTA-2Na in the Ch-M system resulted in the conversion of Pb(NO3)2 to other complex ions such as [Pb·Ch-E]- and [Pb·EDTA-2Na]- and other complex ions due to the dissolution of the washing agent. The results showed that the soil mineral phase did not change significantly and up to 95.79% of Pb could be washed under temperature, time, L/S ratio, EDTA-2Na concentration, DES/water ratio, Ch-E molar ratio, and stirring speed conditions of 40 °C, 2 h, 6, 0.02 M, 2, 0.75 and 300 rpm, respectively. The hydrogen bonds and EDTA-2Na may play a key role in the remediation of lead-contaminated soil by a washing agent. This research describes a rapid, efficient, and environmentally friendly method for remediation of lead-contaminated soil.

Developing green and simple methods for the preparation of cellulose nanofibrils (CNFs) is of great significance. Herein, a green deep eutectic solvent (DES) system based on choline chloride (ChCl) and citric acid (CA) is employed to pretreat cellulose fibers for the preparation of CNFs. The effect of the pretreatment temperature on the chemo-physical properties of the CNFs is comprehensively investigated. A high CNFs yield of up to 84.19% can be achieved under optimized conditions. The optimal CNFs show a narrow diameter distribution and length up to several microns, high crystallinity and thermal stability, as well as excellent dispersibility in water. Furthermore, semi-transparent and flexible cellulose nanopaper (CNP) was fabricated through a facile vacuum filtration process. The optimal CNP shows high tensile strength (175.15 MPa) and toughness (7.51 MJ/m3). Therefore, this work provides a sustainable and facile approach to fabricate CNFs and CNP, which can be potentially used for various high-tech applications.

In this study, Phellinus linteus polysaccharides (PLPS) and proteins were simultaneously separated from P. linteus mycelia by using an aqueous two-phase system (ATPS) based on choline chloride ([Chol]Cl)/K2HPO4, and the physicochemical and antioxidant properties of PLPS after ATPS extraction were evaluated. Results demonstrated that the maximal extraction efficiencies of 68.53% ± 0.29% PLPS and 82.37% ± 0.41% proteins were obtained when the cholinium-based ATPS contained 68.9% K2HPO4, 20% [Chol]Cl, 10.0 mg mL-1 crude water extract (1.0 mL), and distilled water (4.0 mL) at shaking time and temperature of 30 min and 21.2 °C, respectively. Compared with C-PLPS obtained using traditional ethanol precipitation and isolation protocols, PLPS had higher carbohydrate content (63.58% ± 1.12%), lower molecular weight (15.2 kDa, 80%), different monosaccharide compositions, and showed similar preliminary structural characterizations. Moreover, PLPS exhibited more evident scavenging effects on free radicals and in vitro antioxidant activities than C-PLPS. Therefore, the method of [Chol]Cl/K2HPO4 ATPS can be developed as an effective strategy for the separation/purification of highly bioactive polysaccharides.

Herein, corn stover (CS) was pretreated by less corrosive lewis acid FeCl3 acidified solutions of neat and aqueous deep eutectic solvent (DES), aqueous ChCl and glycerol at 120 °C for 4 h with single FeCl3 pretreatment as control. It was unexpected that acidified solutions of both ChCl and glycerol were found to be more efficient at removing lignin and xylan, leading to higher enzymatic digestibility of pretreated CS than acidified DES. Comparatively, acidified ChCl solution exhibited better pretreatment performance than acidified glycerol solution. In addition, 20 wt% water in DES dramatically reduced the capability of DES for delignification and xylan removal and subsequent enzymatic cellulose saccharification of pretreated CS. Correlation analysis showed that enzymatic saccharification of pretreated CS was highly correlated to delignification and cellulose crystallinity, but lowly correlated to xylan removal. Recyclability experiments of different acidified pretreatment solutions showed progressive decrease in the pretreatment performance with increasing recycling runs. After four cycles, the smallest decrease in enzymatic cellulose conversion (22.07%) was observed from acidified neat DES pretreatment, while the largest decrease (43.80%) was from acidified ChCl pretreatment. Those findings would provide useful information for biomass processing with ChCl, glycerol and ChCl-glycerol DES.