EUTECTIC SOLVENT

Abstract

A novel eutectic solvent (NES) includes one or more derivative(s) of methanesulfonic, one or more ammonium salt(s) and one or more hydrogen bond donor(s). The disclosed NES may exhibit qualities such as low freezing and eutectic points, low viscosity, negligible vapor pressure, non-volatility, less water content, high potential window, high thermal stability, high solubility, long shelf life, high recyclability, high biodegradability, high ionic character, air and moisture stability, non-corrosive, non-mutagenic, economical, non-flammable, etc., hence having broader applications.

Claims

1. A eutectic solvent comprising: one or more derivative(s) of methanesulfonic acid selected from its salts with metal ions selected from the group consisting of manganese, zinc, cerium, nickel, titanium, copper, sodium, potassium, and calcium; one or more ammonium salt(s) having general formula NH.sub.4X, where X can be selected from the group consisting of chloride, methanesulfonate, acetate, sulphate, triflate, and trimethanesulfonate; and one or more hydrogen bond donor(s) selected from the group consisting of urea, thiourea, glycerol, oxalic acid, acetic acid, ethylene glycol, acetamide, benzamide, adipic acid, benzoic acid, and citric acid.

2. The eutectic solvent of claim 1, wherein the molar ratio of derivative(s) of methanesulfonic acid, ammonium salt(s) and hydrogen bond donor(s) is in the range 0.5-3:2-7:8-13.

3. The eutectic solvent of claim 2, wherein the eutectic solvent has an electrochemical potential window ranging from 0.1 to 3.5 V.

4. The eutectic solvent of claim 3, wherein the eutectic solvent has ionic conductivity ranging from 10 to 90 mS/cm.

5. The eutectic solvent of claim 4, wherein the eutectic solvent has viscosity ranging from 1 to 60 mPa.Math.s.

6. The eutectic solvent of claim 5, wherein the eutectic solvent remains liquid at a temperature of 5° C. at ambient pressure.

7. The eutectic solvent of claim 1, wherein the eutectic solvent has an electrochemical potential window ranging from 0.1 to 3.5 V.

8. The eutectic solvent of claim 7, wherein the eutectic solvent has ionic conductivity ranging from 10 to 90 mS/cm.

9. The eutectic solvent of claim 8, wherein the eutectic solvent has viscosity ranging from 1 to 60 mPa.Math.s.

10. The eutectic solvent of claim 9, wherein the eutectic solvent remains liquid at a temperature of 5° C. at ambient pressure.

11. The eutectic solvent of claim 1, wherein the eutectic solvent has ionic conductivity ranging from 10 to 90 mS/cm.

12. The eutectic solvent of claim 11, wherein the eutectic solvent has viscosity ranging from 1 to 60 mPa.Math.s.

13. The eutectic solvent of claim 12, wherein the eutectic solvent remains liquid at a temperature of 5° C. at ambient pressure.

14. The eutectic solvent of claim 1, wherein the eutectic solvent has viscosity ranging from 1 to 60 mPa.Math.s.

15. The eutectic solvent of claim 14, wherein the eutectic solvent remains liquid at a temperature of 5° C. at ambient pressure.

16. The eutectic solvent of claim 1, wherein the eutectic solvent remains liquid at a temperature of 5° C. at ambient pressure.

17. The eutectic solvent of claim 2, wherein the eutectic solvent has ionic conductivity ranging from 10 to 90 mS/cm.

18. The eutectic solvent of claim 2, wherein the eutectic solvent has viscosity ranging from 1 to 60 mPa.Math.s.

19. The eutectic solvent of claim 18, wherein the eutectic solvent remains liquid at a temperature of 5° C. at ambient pressure.

20. The eutectic solvent of claim 2, wherein the eutectic solvent remains liquid at a temperature of 5° C. at ambient pressure.

Description

BRIEF DESCRIPTION OF DRAWINGS

[0016] FIG. 1 is a cyclic voltammetry curve of NES of Example 1 on a three-electrode system at a scan rate of 1 mV/s;

[0017] FIG. 2 is a graph depicting voltage-time electrochemical stability and electroplating characteristics of NES of Example 1 in an asymmetrical Carbon Steel/Zn set-up at 2.5 mA/cm.sup.2 current; and

[0018] FIG. 3 is a graph depicting how, as temperature increases, the energy gained by the molecules in the NES of Example 1 increases along with decrease in viscosity and hence the ions are in a higher energy state which will lead to the mobility increases and hence the conductivity increases in NES.

DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS

I. DEFINITIONS

[0019] For purposes of interpreting the specification and appended claims, the following terms shall be given the meaning set forth below:

[0020] The term “solvent” shall refer to a liquid medium capable of dissolving other substance(s).

[0021] The term “ambient temperature” shall mean temperature falling in the range of 25 to 30° C.

[0022] The term “ambient pressure” shall mean atmospheric pressure at 1 bar.

II. DESCRIPTION

[0023] Reference is hereby made in detail to various embodiments according to present invention, examples of which are illustrated in the accompanying drawings and described below. It will be understood that invention according to present description is not intended to be limited to those exemplary embodiments. The present invention is intended to cover various alternatives, modifications, equivalents and other embodiments, which may be included within the spirit and scope of the invention as defined by the claims.

[0024] The Novel Eutectic Solvent (NES) includes one or more derivative(s) of methanesulfonic acid selected from its salts with various metal ions selected from a group consisting of manganese, zinc, cerium, nickel, titanium, copper, sodium, potassium and calcium; one or more ammonium salt(s) having general formula NH.sub.4X, where X can be selected from a group consisting of chloride, methanesulfonate, acetate, sulphate, triflate, trimethanesulfonate; one or more hydrogen bond donor(s) selected from a group consisting of urea, thiourea, glycerol, oxalic acid, acetic acid, ethylene glycol, acetamide, benzamide, adipic acid, benzoic acid, citric acid; wherein the molar ratio of derivative(s) of methanesulfonic acid, ammonium salt(s) and hydrogen bond donor(s) is in the range 0.5-3:2-7:8-13. The NES having potential window ranging from 0.1 to 3.5 V and conductivity ranging from 10 to 90 mS/cm. Further the NES is having viscosity ranging from 1 to 60 mPa.Math.s. NES remains liquid at a temperature as low as 5° C. at ambient pressure.

[0025] The NES is prepared by mixing one or more derivative(s) of methanesulfonic acid selected from its salts with various metal ions selected from a group consisting of manganese, zinc, cerium, nickel, titanium, copper, sodium, potassium and calcium; one or more ammonium salt(s) having general formula NH.sub.4X, where X can be selected from a group consisting of chloride, methanesulfonate, acetate, sulphate, triflate, trimethanesulfonate ; one or more hydrogen bond donor(s) selected from a group consisting of urea, thiourea, glycerol, oxalic acid, acetic acid, ethylene glycol, acetamide, benzamide, adipic acid, benzoic acid, citric acid ; wherein the molar ratio of derivative(s) of methanesulfonic acid, ammonium salt(s) and hydrogen bond donor(s) is in the range 0.5-3:2-7:8-13 are mixed. Upon proper mixing, the mixture starts converting into a liquid at ambient temperature and pressure. To ensure the proper mixing of the components and to speed up the process, this mixture may be uniformly heated at a temperature up to 60° C. Once the eutectic solvent is prepared the same can be stored in a container, which remains liquid at a temperature as low as 5° C. at ambient pressure.

[0026] No special condition of heating/drying in a vacuum is required in the preparation of NES. Unlike many other eutectic solvents, the mixing of the constituting components is an endothermic phenomenon, making synthesis process safer, non-flammable than existing eutectic solvents. The resultant transparent liquid NES, according to the present invention, is allowed to attain the room temperature and stored in an airtight container and ready to be used for various applications.

[0027] The NES is safer to environment being non toxicity and easily disposable due to inherent nature of its constituents. Methanesulfonic acid is an organic acid which undergoes biodegradation to form carbon dioxide and sulphate. It is also regarded as the green acid as it is less toxic and corrosive in nature compared to the other mineral acids. The other components of the proposed NES are hydrogen bond donor(s) and one or more kind of ammonium salt making NES biodegradable and eco-friendly.

[0028] The NES is comparatively economical to the existing ESs as all the components are very economic and abundant in nature, making the proposed NES a sustainable eutectic solvent. The proposed NES has low viscosity, high thermal and chemical stability, wide potential window, low volatility and non-flammability. The unique chemistry and chemical bonding among the components make it chemically and thermally stable over the existing solvents. Due to its several advantages on the existing ES, ionic liquids and organic solvents, proposed NES has broad applications for including but not limited to the electrochemical application, energy storage devices, electroplating of metals their composites and their alloys, carbon dioxide capture, catalysis, organic synthesis, refinery process, biorefinery process, pharmaceutical, water treatment, metal processing, coatings, electroless coatings, metal nanoparticle synthesis, metal electropolishing, metal extraction, processing of the metal oxides, gas adsorption, biotransformation and electronics.

EXAMPLES

[0029] The following illustrative examples are provided to further describe how to make and use the preferred NES compositions according to present invention. The same are not intended to limit the scope of the claimed invention.

Example 1

[0030] In the process of preparing NES composition, 2 moles of Zinc Methanesulfonate, 10 moles of Thiourea and 5 moles of Ammonium Chloride are mixed in a rotary bottom flask. The flask is rotated @ 50 rpm for proper mixing. After rotating around 45 minutes the solid mixture start converting into NES solvent. However, in order to expedite the process for speedy result, the components are mixed in oil bath and the rotation is done at 45° C. for 15 minutes to obtain transparent liquid NES solvent.

Example 2

[0031] In the process of preparing NES composition, 1.7 moles of calcium methanesulfonate 9 moles of thiourea and 5 moles of Ammonium Chloride are mixed in a rotary bottom flask. The flask is rotated @ 50 rpm for proper mixing. After rotating around 45 minutes the solid mixture start converting into NES solvent. However, for speedy result, the components are mixed in oil bath and the rotation is done at 60° C. for 15 minutes to obtain transparent liquid NES solvent.

Example 3

[0032] In the process of preparing NES composition, 1.7 moles of calcium methanesulfonate, 10 moles of Ethylene Glycol and 4 moles of Ammonium Acetate are mixed in a rotary bottom flask. The flask is rotated @ 50 rpm for proper mixing. After rotating around 45 minutes the solid mixture start converting into NES solvent. However, for speedy result, the components are mixed in oil bath and the rotation is done at 45° C. for 15 minutes to obtain transparent liquid NES solvent.

IV. EXPERIMENTATION

Experiment 1

[0033] Cyclic voltammetry is done using Biologic VPM3 electrochemical workstation at 1 mV s−1 within the voltage range from −1.5 V to 2.5 V (versus Ag/AgCl) using a three-electrode system with graphite as the working electrode, Platinum Mesh as counter electrode, and Ag/AgCl as reference electrode, respectively.

[0034] Cyclic voltammograms of a three-electrode system. To determine the potential window of the NES number 1, three electrode system is used as mentioned above for CV experiment at a scan rate of 1 mV/s from −1.5 V to 2.5.

[0035] The cyclic voltammogram as shown in FIG. 1 for NES of example 1 indicates reversible electrochemical deposition/dissolution of Zinc. The corresponding onset potentials of initial Zinc plating/stripping are −0.31 V and −0.01 V. Compared to other existing solvents, smaller potential separation between plating and stripping and higher response current can be found for NES, suggesting better reversibility and faster kinetics of Zn deposition/dissolution. Notably, NES exhibits a wide stable electrochemical window from −1.5V to 2V. The Coulombic efficiency (CE) gradually increased and reached around 99.9% after the third cycle.

Experiment 2

[0036] To determine the metal electroplating and de-plating capacity in NES solution.

[0037] A Carbon Steel working electrode (Sheet: 10 mm*0.2 mm*50 mm) and a Zinc counter/reference electrode (diameter: 10 mm*0.2 mm*50 mm) with a rectangle shaped made up the Carbon steel//Zn asymmetric cells is suspended in NES of example 1.

The results of voltage-time electrochemical stability tests of the Zn-Carbon Steel asymmetrical cell is shown in FIG. 2. The NES shows good electroplating capabilities. It displays greater stability even at cycling.

Experiment 3

[0038] To determine the effect of temperature variation on the ionic conductivity and viscosity of NES of example 1.

[0039] A S230 Bench Conductivity Meter (Mettler-Toledo GmbH) is used to measure ionic conductivity. Before each experiment, the equipment is calibrated against a standard KCl solution.

[0040] An Dv2t Brookfield Viscometer is used to evaluate viscosities of NES

TABLE-US-00001 TABLE 1 Temp (° C.) Conductivity (mS/cm) Viscosity (mPa .Math. s) 10 25.97 50 20 58.39 20 25 62.71 15 30 64.92 13 35 68.81 11 40 71.91 10 50 75.26 7 60 81.42 5

[0041] For both the cases temperature are controlled within ±0.5° C. using a thermo-static, water bath.

[0042] The NES gives better ionic conductivity over the measured temperature range of 10 to 60° C., especially at elevated temperatures that increased from 25.97 to 81.42 mS/cm. This could be explained by the fact that as the temperature rises, the energy gained by the molecules in the NES medium rises along with a decrease in viscosity (from 50 mPa.Math.s at 10° C. to 5 mPa.Math.s at 60° C.) and thus the ions are in a higher energy state, resulting in increased mobility and thus increased conductivity in or NES. NES is thermally stable as no breakdown products are observed.

[0043] Referring FIG. 3, as temperature increases the energy gained by the molecules in the NES increases along with decrease in viscosity and hence the ions are in a higher energy state which will lead to the mobility increases and hence the conductivity increases in NES.

Experiment 4

[0044] CO.sub.2 absorption is measured using the developed NES of Examples 1, 2 and 3. CO.sub.2 gas is flown into a vial (10 ml) holding 5 ml of developed NESs at a flow rate of 10 ml/min. Weighing the vial at regular intervals with a weighing balance with an accuracy of 0.1 mg is used to calculate the weight percent of CO.sub.2 absorbed. The vial is kept partially immersed in a water bath at constant temperatures during the experiment to reduce the effect of temperature.

[0045] Test are prepared using the above method and tested using constant flow of CO.sub.2 and at constant temperature of 27° C.

[0046] According to the screening of NESs, NES containing Calcium showed high CO.sub.2 sorption capacity, when measured at atmospheric pressure for the fixed molar ratio of NES.

[0047] Table 2 represents the comparative CO.sub.2 uptake of different NESs during 2 h of experiment.

TABLE-US-00002 TABLE 2 CO.sub.2 uptake NES Temperature (° C.) Pressure (Bar) (in mole) NES of Example 1 27 ~1 0.283 NES of Example 2 27 ~1 0.461 NES of Example 3 27 ~1 0.398

[0048] Changes and modifications in the specifically-described embodiments may be carried out without departing from the principles of the present invention, which is intended to be limited only by the scope of the appended claims as interpreted according to the principles of patent law including the doctrine of equivalents.