Single-pot synthesis of dialkyl carbonates using catalyst from natural resource

Abstract

The present invention relates to a single-pot method for preparing dialkyl carbonates, the method comprises reaction of alkylene oxide with aliphatic or cyclic aliphatic alcohol, using wood ash catalyst, under CO.sub.2 pressure and heating the reaction mixture thereof to obtain dialkyl carbonates.

Claims

1. A single-pot method for preparing dialkyl carbonate, the method comprising: (a) dissolving an alkylene oxide in an aliphatic or cyclic aliphatic alcohol, (b) adding a wood ash catalyst, (c) adding CO.sub.2 gas under pressure and heating the reaction mixture, (d) cooling the reaction mixture to about room temperature, and depressurizing to obtain dialkyl carbonate.

2. The method as claimed in claim 1, wherein the reaction mixture is filtered to recover the catalyst.

3. The method of claim 1, wherein the aliphatic or cyclic aliphatic alcohols are C.sub.1 to C.sub.12 aliphatic alcohols and C.sub.1 to C.sub.12 cyclic aliphatic alcohols.

4. The method of claim 2, wherein the aliphatic or cyclic aliphatic alcohol is selected from methanol, ethanol, propanol, butanol, amyl alcohol, hexanol, octanol, cyclohexanol and octahexanol.

5. The method of claim 1 wherein the alkylene oxide is selected from the group comprising ethylene oxide, propylene oxide, 1,2-epoxy butane, 1,2-epoxy pentane and 1,2-epoxy hexane.

6. The method of claim 1 wherein the pressure is about 70-90 bar.

7. The method of claim 1 wherein the heating is carried out at a temperature range of about 100-180 C.

8. The method of claim 2 wherein the filtered catalyst is washed with an aliphatic alcohol and dried at about 120 C. for 24 hours for reuse.

9. The method of claim 8 wherein the aliphatic alcohol is methanol or ethanol.

10. The method as claimed in claim 1, wherein the reaction mixture is filtered to recover the catalyst, wherein the filtered catalyst is washed with an aliphatic alcohol and dried at about 120 C. for 24 hours for reuse, and wherein the catalyst obtained is reused in the process of claim 1.

Description

BRIEF DESCRIPTION OF ACCOMPANYING DRAWINGS

(1) FIG. 1: IR spectrum of wood ash catalysts;

(2) FIG. 2: XRD spectrum of wood ash catalysts; and

(3) FIG. 3: TGA analysis of BWC.sub.800 wood ash catalyst.

DETAILED DESCRIPTION OF THE INVENTION

(4) The present invention discloses a preparation methodology of dialkyl carbonates (fuel oxygenates) by reacting CO.sub.2, aliphatic/cyclic aliphatic alcohol and alkylene oxide in presence of renewable catalyst in a single step, the said catalyst being prepared from biomass.

(5) An aspect of the invention discloses the preparation methodology of the catalyst; said catalyst being prepared directly from the biomass. Another aspect of the present invention is the use of the novel renewable catalyst prepared from biomass in a single step reaction to produce dialkyl carbonates from aliphatic & cyclic alcohols and propylene oxide by utilizing CO.sub.2.

(6) An aspect of the present invention is that the catalyst prepared from wood ash is novel, economical and eco-friendly. The wood ash used in accordance with this invention can be obtained from biomass, including but not necessarily limited to, wood of trees such as Azadirachta indica, Acacia nilotica. Another aspect of the invention discloses the production of alkylene glycol as by-product during synthesis of dialkyl carbonates in presence of renewable catalyst.

(7) The wood ash catalyst is basic in nature. Composition of wood ash catalyst is mixture of oxides of Ca and Mg along with sintered material calcium silica phosphates. Wood ash also contains potassium and small quantities of other metal derivatives. The typical combination of all these compounds in wood ash catalyst makes it a suitable catalyst for various organic transformations. We explored the inherent properties of wood ash catalyst and utilized for the single pot synthesis of dialkyl carbonates from CO.sub.2, alkylene oxide and alcohol. The wood ash catalyst catalyses CO.sub.2 insertion in to alkylene oxide to form cyclic carbonate which is further converted in situ to dialkyl carbonates in the presence of alcohols. Therefore, wood ash catalyst helps to convert CO.sub.2 to dialkyl carbonates in the presence of alcohols in a single pot reaction conditions in comparison to prior art claim of dialkyl carbonates synthesis from CO.sub.2 mostly carried out in two separate steps by using two different types of catalysts. The advantage of this invention is wood ash catalyst able to perform synthesis of dialkyl carbonates from CO.sub.2 in a single pot reaction conditions.

(8) The preparation methodology according to the present invention involves washing the wood with deionised water and then drying until the wood attains constant weight. The wood was dry ashed separately and calcined. One-pot synthesis of dialkyl carbonates from aliphatic/cyclic aliphatic alcohol, CO.sub.2 and alkylene oxide was carried out in a controlled heating system.

(9) In a preferred embodiment, the preparation of dialkyl carbonate involves washing the wood with deionised water and then drying at about 60-80 C. until the wood attains constant weight. The wood was dry ashed separately and calcined, at temperature ranges of about 300 C. to about 1200 C. One-pot synthesis of dialkyl carbonates from aliphatic/cyclic aliphatic alcohol, CO.sub.2 and alkylene oxide was carried out in an autoclave vessel fixed to stirrer and controlled heating system. In drying step, the wood is heated at a temperature range of 60 to 80 C. for 24 hours to remove moisture and impurities present in the wood after washing with deionised water. In the dry ashing step, the wood is burned in a furnace at 525 C.25 C. (Ref. TAPPI, Ash in wood, pulp, paper and paperboard: combustion at 525 C., T211 om-93, 1993).

(10) The aliphatic alcohols/cyclic alcohols used according to the present invention include C.sub.1 to C.sub.12 aliphatic alcohols, C.sub.1 to C.sub.12 cyclic aliphatic alcohols like cyclic pentanol, cyclic hexanol, more preferably methanol, ethanol, propanol, butanol, amyl alcohol, hexanol, ocyanol, cyclohexanol, octahexanol. The alkylene oxides used according to the present invention include ethylene oxide, propylene oxide, 1,2-epoxy butane, 1,2-epoxy pentane, 1,2-epoxy hexane.

(11) The single-pot method for preparing dialkyl carbonate comprises dissolving alkylene oxide in an aliphatic/cyclic aliphatic alcohol, adding wood ash catalyst, adding CO.sub.2 gas at a workable pressure range and heating the reaction mixture, cooling the reaction mixture to about room temperature, and depressurizing to obtain dialkyl carbonate. The reaction mixture is filtered to remove the catalyst. The filtered catalyst was washed with an aliphatic alcohol, preferably methanol or ethanol and dried for reuse.

(12) In a preferred embodiment, the single-pot method for preparing dialkyl carbonate comprises dissolving alkylene oxide in an aliphatic/cyclic aliphatic alcohol, adding wood ash catalyst in the autoclave vessel. The autoclave vessel was pressurised with CO.sub.2 gas. At the workable pressure range of about 70-90 bar and temperature range of about 100-180 C., the reaction mixture was stirred constantly for about 24 hours. Then reaction mixture was cooled to room temperature, depressurised and filtered to remove the catalyst. The filtered catalyst was washed with an aliphatic alcohol, preferably methanol or ethanol and dried at about 120 C. for about 24 hours for reuse. The identification and quantification of the components in the reaction mixtures were performed with GC and GC-MS analysis.

(13) Catalyst prepared from wood ash is novel, economical and eco-friendly compared to catalysts reported in literature for the synthesis of dialkyl carbonates. The developed process methodology is single step reaction to produce dialkyl carbonates from aliphatic/cyclic alcohols and propylene oxide by utilizing CO.sub.2. Separation and regeneration of catalyst is performed by low cost techniques.

(14) The CO.sub.2 insertion reaction into propylene oxide requires activation of epoxide and activation of CO.sub.2, which is the most crucial step. This is pull-push of electrons of both the molecules by two different categories of metals. Wood ash catalyst has combination of the above properties due to presence of metal oxides, mixed metal oxides along with alkali earth metal halides. Both alcohol and CO.sub.2 are equally capable to insert into epoxide ring but catalyst should be selective for CO.sub.2 insertion. Wood ash catalyst showed typical interaction with CO.sub.2 and activated it successfully towards epoxide insertion reaction. Prior art literature shows that oxides of Ca and Mg can perform transesterification reactions of propylene carbonate with alcohols (Indian Journal of chemistry, 52A, 459-466, 2013). Wood ash catalyst able to perform both CO.sub.2 insertion and transesterification reactions simultaneously with high selectivity.

(15) The prepared catalysts were evaluated for their alkalinity (pH), particle size and surface area, results are shown in Table 1. The alkalinity of BW.sub.0 (wood ash without calcination), BWC.sub.500 (wood ash calcined at 500 C.) and BWC.sub.800 (wood ash calcined at 800 C.) catalysts were found to be 11.28, 11.68 and 12.02 respectively. It was observed that the calcination temperature affects the alkalinity of the catalysts. The results showed that BWC.sub.800 catalyst calcined at 800 C. temperatures has highest alkalinity may be due to thermal decomposition of CaCO.sub.3 to CaO which is having higher soluble alkalinity. This observation is in line with that reported in literature, which indicates the increase of alkalinity with the increase of calcination temperature [Biomass and Bioenergy 41 (2012) 94-106]. Further, recovered BWC.sub.800 catalyst alkalinity was determined as 12.04 in order to check the stability of active basic sites present on the catalyst. In addition, XRD pattern of recovered catalyst also confirms the stable catalyst structure after the reaction (FIG. 2).

(16) TABLE-US-00001 TABLE 1 Alkalinity, surface area and particles size of the wood ash catalysts Alkalinity Catalyst (at 28.0 C.) SA (m.sup.2/gm) APS (m) BW.sub.0 11.28 2 20.76 BWC.sub.500 11.688 1.6 25.65 BWC.sub.800 12.025 <1 36.26 BWC.sub.800 (Recovered) 12.048 8 56.77

(17) As seen from the Table 1, the surface area of wood ash catalysts decreases with increase of calcination temperature. The surface areas of BW.sub.0, BWC.sub.500 and BWC.sub.800 catalysts were 2.0, 1.6 and <1 m.sup.2/gm respectively. Lower surface area of BWC.sub.800 catalyst than BWC.sub.500 catalyst is due to conversion of CaCO.sub.3 into CaO which results in sintering by the formation of calcium phosphate silicate. The observation was further confirmed by XRD study of the catalyst structure (FIG. 2).

(18) The particle sizes of BW.sub.0, BWC.sub.500 and BWC.sub.800 were determined as 20.76, 25.65 and 36.26 m respectively. The result reveals that particle size of the catalysts has increased with increasing calcination temperature [Biomass Bioenergy 4 (1993) 103-106]. The possible reason may be the increase of sintering with increase of temperature, leads to increase in particle size as reported in earlier study [Biomass and Bioenergy 41 (2012) 94-106]. Recovered BWC.sub.800 catalyst particle size is 56.77 m may be due to the formation of some amounts of calcium hydroxide and carbonates however this does not has any effect on catalyst performance on subsequent reuse. These results were further supported by XRD analysis as shown in FIG. 2.

(19) IR Analysis

(20) The FTIR spectra of wood ash catalysts are given in FIG. 1. The spectra of BW.sub.0 catalyst shows the presence of carbonates, CO.sub.3.sup.2 (the peaks at 1795, 1427, 875 and 711 cm.sup.1) and phosphates, PO.sub.4.sup.3 components (peaks at 1112, 1047 and 617 cm.sup.1), confirms the presence of metal carbonates (mainly CaCO.sub.3) and metal phosphates. The IR spectrum of BWC.sub.500 catalyst shows similar spectral features. After calcination at 800 C., BWC.sub.800 catalyst indicates the presence of metal oxides (peak at 3425, 2960, 1462, 1408, 921 and 516 cm.sup.1) along with the calcium phosphates silicate (peak at 2856, 1388 and 1118 cm.sup.1). The results reveal that the calcination at higher temperature results in carbonates decomposition to metal oxides.

(21) IR analysis of recovered BWC.sub.800 catalyst reveals that structure of the catalyst is remain same after reaction however formation of very small quantity of calcium hydroxide (3645 cm.sup.1) was observed.

(22) XRD Analysis

(23) The XRD pattern of BW.sub.0, BWC.sub.500, BWC.sub.800 and recovered BWC.sub.800 catalyst is shown in FIG. 2. The results indicate that BW.sub.0 catalyst is mainly composed of CaCO.sub.3 along with small amount of KCl and SiO.sub.2. After calcination at 500 C., the pattern of crystalline phases remains same in BWC.sub.500 catalyst with additional appearance of CaO crystalline phase.

(24) On further calcination at 800 C., BWC.sub.800 catalyst shows the presence of metal oxides mainly CaO and MgO along with KCl and mixed metal phosphates Ca.sub.2SiO.sub.4.0.05Ca.sub.3(PO.sub.4).sub.2. These results were further confirmed by elemental analysis.

(25) XRD analysis of recovered BWC.sub.800 catalyst show same structure as of fresh BWC.sub.800 catalyst. However some decreasing intensity of crystalline phases of CaO, MgO and mixed metal phosphates is due to formation of calcium hydroxide is confirmed by increasing of pH value and IR analysis.

(26) Elemental Analysis

(27) The elemental analysis of BWC.sub.800 catalyst shows the presence of Ca, K and Mg in higher amounts as 32.30, 10.91 and 5.79 mass fraction percentage respectively. While the Na, P and Al are in notable amounts as 1.42, 1.40 and 1.90 mass fraction percentage respectively, the transition metals present in BWC.sub.800 are mainly Fe, Mn and Zn in trace quantities. The presence of the minor quantities of Silicon was also confirmed by XRF analysis.

(28) TGA Analysis

(29) In heterogeneous catalysts, stability of active sites on catalyst surface is very important. BWC.sub.800 catalyst stability was measured by TG analysis carried out on TG model 2950 Hi Resolution modulated TGA, with heating rates 10 C./min, temperature ramp up to 800 C.

(30) The results given in the FIG. 3 shows the weight loss of 2.19 wt. % is observed at 198 C. corresponding to the removal of loosely absorbed water on the surface of catalyst. Further the decomposition of calcium carbonate at 425 C. and 660 C. producing calcium oxide associated with 1.809 wt. % weight loss. Additionally, the stability of BWC.sub.800 catalyst is confirmed by metal analysis of carbonate product produced with XRF technique and found all the metal <1 mg/Kg. Above findings also confirm the non-leaching behaviour of the catalyst and are in agreement with the earlier study [Biomass and Bioenergy 41 (2012) 94-106].

(31) These dialkyl carbonates are extensively studied as fuel oxygenates in the literature (Energy & Fuels 1997, 11, 2-29). The octane number, RVP and toxic emissions from dialkyl carbonates are compared with ether oxygenates and reported in the literature (Energy Fuels 2010, 24, 4812-4819). However, synthesis of these dialkyl carbonates reported through phosgene route which is corrosive and environmentally not favourable. We have developed environmentally safe method for preparation of dialkyl carbonates from CO.sub.2 as feed stock and carrying out the preparation in single pot in presence of wood ash as novel catalyst.

(32) The octane number of prepared dialkyl carbonates viz. DMC, DEC blend with gasoline is studied by CFR (Combustion Fuel Research)* engine test method, the results are as follows in Table 2:

(33) TABLE-US-00002 TABLE 2 RON by CFR S. engine test Improved RVP values No: FUEL TYPE ASTM D2699 RON value (KPa) 1. Gasoline BSIV 92.2 NA 48.6 2. 100% DMC 111 NA 11.1 3. 100% DEC 114 NA 6.3 2. 6% DMC in BSIV 93.4 1.2 48.0 gasoline 3. 8% DEC in BSIV 94.2 2.0 46.1 gasoline

(34) Blending carried out to keep overall oxygen content in gasoline to 2.7% by mass as per IS 2796-2008 motor gasoline BS IV specifications.

(35) These dialkyl carbonates are extensively studied as fuel oxygenates in the literature (Energy & Fuels 1997, 11, 2-29). The octane number, RVP and toxic emissions from dialkyl carbonates were compared with ether oxygenates and reported in the literature (Energy Fuels 2010, 24, 4812-4819). The synthesis of these dialkyl carbonates through phosgene route is corrosive and environmentally not favourable. We have developed environmentally safe method from CO.sub.2 as feed stock and single pot reaction in presence of wood ash as catalyst. Having described the basic aspects of the present invention, the following non-limiting examples illustrate specific embodiment thereof.

EXAMPLES

Example 1

One-Pot Synthesis of DEC from Ethanol, CO2 and Propylene Oxide Using BW0 as Catalyst

(36) In a 700 ml autoclave, propylene oxide (10.17 gm, 0.175 mol), ethanol (64.70 gm, 1.40 mol) and wood ash catalyst BW.sub.0 (7.0 gm, 10% wt/wt) were charged. The autoclave vessel was pressurised with CO.sub.2 pressure, heated to reach 150 C. temperature and 80 bar pressure under constant stirring for reaction time 24 hours. Then reaction mixture was cooled to room temperature, depressurised and filtered to remove the catalyst. The filtered catalysts was washed with ethyl alcohol and dried at 120 C. for 24 hours before reuse. The reaction mixture was subjected to distillation. First fraction contains mixture of excess ethanol and DEC and second fraction contains mixture of propylene glycol and propylene carbonate. The identification and quantification of the components in the fractions were performed with GC and GC-MS analysis.

(37) Analytical analysis of ethanol fraction reveals that formation of DEC is 1.26 gm (2.20 mmol). The calculated yield of DEC corresponding to propylene oxide is 6.06%.

(38) Example 1 explains that reaction mixture was cooled to room temperature after 24 hours, depressurised and filtered to remove the catalyst. The filtered catalyst was washed with methanol (20 ml) dried at 120 C. for 24 hours for reuse.

Example 2

Synthesis of DEC from Ethanol, CO2 and Propylene Oxide Using BWC500 as Catalyst

(39) Propylene oxide (10.17 gm, 0.175 mol), ethanol (64.70 gm, 1.40 mol) and wood ash catalyst BWC.sub.500 (7.0 gm, 10% wt/wt) were charged into 700 ml autoclave vessel. The autoclave vessel was pressurised with CO.sub.2 pressure, heated to 150 C. temperature and 80 bar pressure under constant stirring during the reaction for 24 hours. Reaction mixture work up was carried out as described in example 1.

(40) The quantitative analysis of ethanol fraction reveals that formation of DEC is 8.79 gm (74.47 mmol). The calculated yield of DEC with respect to propylene oxide is 42.46%.

Example 3

Synthesis of DEC from Ethanol, CO2 and Propylene Oxide Using 10 wt % BWC800 as Catalyst

(41) 700 ml autoclave was charged with propylene oxide (10.17 gm, 0.175 mol), ethanol (64.70 gm, 1.40 mol) and wood ash catalyst BWC.sub.800 (7.0 gm, 10% wt/wt). The autoclave vessel was pressurised with CO.sub.2 pressure, heated to reach 150 C. temperature and 80 bar pressure under constant stirring during the reaction for 24 hours. Then reaction mixture was cooled to room temperature, depressurised and filtered to remove the catalyst. The filtered catalysts was washed with ethyl alcohol and dried at 120 C. for 24 hours before reuse. The reaction mixture was subjected to distillation. First fraction contains mixture of excess ethanol and DEC and second fraction contains mixture of propylene glycol and propylene carbonate. The identification and quantification of the components in the fractions were performed with GC and GC-MS analysis.

(42) The quantitative analysis of ethanol fraction reveals that formation of DEC is 11.06 gm (93.67 mmol). The calculated yield of DEC from propylene oxide is measured as 53.43%.

Example 4

Synthesis of DEC from Ethanol, CO2 and Propylene Oxide Using BWC800 as Catalyst at 70 Bar CO2 Pressure

(43) In a 700 ml autoclave, propylene oxide (10.17 gm, 0.175 mol), ethanol (64.70 gm, 1.40 mol) and wood ash catalyst BWC.sub.800 (7.0 gm, 10% wt/wt) was charged. The autoclave vessel was pressurised with CO.sub.2 pressure, heated to 150 C. temperature and 70 bar pressure under constant stirring for reaction time 24 hours. Reaction mixture work up was carried out as described in example 3.

(44) The analytical analysis of ethanol fraction reveals the formation of DEC is 10.23 gm (86.65 mmol). The calculated yield of DEC corresponding to propylene oxide is 49.42%.

Example 5

Synthesis of DEC from Ethanol, CO2 and Propylene Oxide Using BWC800 as Catalyst at 90 Bar CO2 Pressure

(45) Propylene oxide (10.17 gm, 0.175 mol), ethanol (64.70 gm, 1.40 mol) and wood ash catalyst BWC.sub.800 (7.0 gm, 10% wt/wt) were charged in to 700 ml autoclave vessel. The autoclave vessel was pressurised with CO.sub.2 pressure, heated to reach 150 C. temperature and 90 bar pressure under constant stirring during the reaction for 24 hours. Reaction mixture work up was carried out as described in example 3.

(46) Analytical analysis of ethanol fraction reveals that formation of DEC is 8.78 gm (74.38 mmol). The measured yield of DEC from propylene oxide is 42.41%.

Example 6

Synthesis of DEC from Ethanol, CO2 and Propylene Oxide Using BWC800 as Catalyst at 80 Bar CO2 Pressure and 120 C. Temperature

(47) Propylene oxide (10.17 gm, 0.175 mol), ethanol (64.70 gm, 1.40 mol) and wood ash catalyst BWC.sub.800 (7.0 gm, 10% wt/wt) were charged in to 700 ml autoclave vessel. The autoclave vessel was pressurised with CO.sub.2 pressure, heated to reach 120 C. temperature and 80 bar pressure under constant stirring during the reaction for 24 hours. Reaction mixture work up was carried out as described in example 3.

(48) Analytical analysis of ethanol fraction reveals that formation of DEC is 5.08 gm (43.05 mmol). The calculated yield of DEC corresponding to propylene oxide is 24.54%.

Example 7

Synthesis of DEC from Ethanol, CO2 and Propylene Oxide Using 5 wt % BWC800 as Catalyst

(49) In a 700 ml autoclave vessel added propylene oxide (10.17 gm, 0.175 mol), ethanol (64.70 gm, 1.40 mol) and wood ash catalyst BWC.sub.800 (3.5 gm, 5% wt/wt). The autoclave vessel was pressurised with CO.sub.2 pressure, heated to reach 150 C. temperature and 80 bar pressure under constant stirring during the reaction for 24 hours. Reaction mixture work up was carried out as described in example 3.

(50) Analytical analysis of Ethanol fraction had DEC of 5.49 gm (54.86 mmol). The formation yield of DEC with respect to propylene oxide is 26.52%.

Example 8

Synthesis of DEC from Ethanol, CO2 and Propylene Oxide Using 15 wt % BWC800 as Catalyst

(51) Propylene oxide (10.17 gm, 0.175 mol), ethanol (64.70 gm, 1.40 mol) and wood ash catalyst BWC.sub.800 (10.5 gm, 15% wt/wt) were charged in to 700 ml autoclave vessel. The autoclave vessel was pressurised with CO.sub.2 pressure, heated to reach 150 C. temperature and 80 bar pressure under constant stirring during the reaction for 24 hours. Reaction mixture work up was carried out as described in example 3.

(52) The analytical analysis of ethanol fraction revealed that formation of DEC is 5.27 gm (44.66 mmol). The calculated yield of DEC corresponding to propylene oxide is 25.45%.

Example 9

Synthesis of DEC from Ethanol, CO2 and Propylene Oxide Using 10 wt % of Recovered BWC800 from Example 3 as Catalyst

(53) Propylene oxide (10.17 gm, 0.175 mol), ethanol (64.70 gm, 1.40 mol) and wood ash recovered catalyst BWC.sub.800 from example 3 (10.5 gm, 15% wt/wt) were charged into 700 ml autoclave vessel. The autoclave vessel was pressurised with CO.sub.2 pressure, heated to reach 150 C. temperature and 80 bar pressure under constant stirring during the reaction for 24 hours. Reaction mixture work up was carried out as described in example 3.

(54) The analytical analysis of ethanol fraction reveals that formation of DEC is 9.85 gm (83.50 mmol). The measured yield of DEC from propylene oxide is 47.6%.

(55) Example 9 shows the recovered catalyst used second time for the monitoring DEC synthesis under standardised reaction conditions. The DEC yield with second time recovered catalyst is slightly lower 47.6% than the previous results. Third cycle usage of wood ash catalyst gave 46.5% of DEC yield.

Example 10

Synthesis of DEC from Ethanol, CO2 and Propylene Oxide Using BWC800 as Catalyst at 80 Bar CO2 Pressure and 180 C. Temperature

(56) In a 700 ml autoclave, propylene oxide (10.17 gm, 0.175 mol), ethanol (64.70 gm, 1.40 mol) and wood ash catalyst BWC.sub.800 (7.0 gm, 10% wt/wt) was charged. The autoclave vessel was pressurised with CO.sub.2 pressure, heated to 180 C. temperature and 80 bar pressure under constant stirring for reaction time 24 hours. Reaction mixture work up was carried out as described in example 3.

(57) The analytical analysis of ethanol fraction reveals the formation of DEC is 9.86 gm (83.56 mmol). The calculated yield of DEC corresponding to propylene oxide is 47.86%.

Example 11

Synthesis of DEC from Ethanol, CO2 and Ethylene Oxide Using BWC800 as Catalyst at 80 Bar CO2 Pressure and 150 C. Temperature

(58) 700 ml autoclave was charged with ethylene oxide (7.7 gm, 0.175 mol), ethanol (64.70 gm, 1.40 mol) and wood ash catalyst BWC.sub.800 (7.0 gm, 10% wt/wt). The autoclave vessel was pressurised with CO.sub.2 pressure, heated to reach 150 C. temperature and 80 bar pressure under constant stirring during the reaction for 24 hours. Reaction mixture work up was carried out as described in example 1. The quantitative analysis of ethanol fraction reveals that formation of diethyl carbonate is 10.33 gm (87.54 mmol). The calculated yield of diethyl carbonate from ethylene oxide is measured as 50.07%.

Example 12

Synthesis of DMC from Methanol, CO2 and Ethylene Oxide Using BWC800 as Catalyst at 80 Bar CO2 Pressure and 150 C. Temperature

(59) Ethylene oxide (7.7 gm, 0.175 mol), methanol (44.80 gm, 1.40 mol) and wood ash catalyst BWC.sub.800 (5.5 gm, 10% wt/wt) were taken in to 700 ml autoclave vessel and closed tightly. The autoclave vessel was pressurised with CO.sub.2 pressure, heated to reach 150 C. temperature and 80 bar pressure under constant stirring during the reaction for 24 hours. Reaction mixture work up was carried out as described in example 1. The quantitative analysis of methanol fraction reveals that formation of dimethyl carbonate is 8.20 gm (91.11 mmol). The calculated yield of dimethyl carbonate from ethylene oxide is measured as 52.13%.

Example 13

Synthesis of DEC from Ethanol, CO2 and 1,2-Epoxyhexane Using BWC800 as Catalyst at 80 Bar CO2 Pressure and 150 C. Temperature

(60) The reactants mixture of 1,2-epoxyhexane (17.53 gm, 0.175 mol), ethanol (64.70 gm, 1.40 mol) and wood ash catalyst BWC.sub.800 (8.25 gm, 10% wt/wt) was charged into autoclave vessel and lid was closed. The autoclave vessel was pressurised with CO.sub.2 pressure, heated to reach 150 C. temperature and 80 bar pressure under constant stirring during the reaction for 24 hours. Reaction mixture work up was carried out as described in example 1. The quantitative analysis of ethanol fraction reveals that formation of diethyl carbonate is 4.35 gm (36.86 mmol). The calculated yield of diethyl carbonate from epoxyhexane is measured as 21%.

Example 14

Synthesis of DMC from Methanol, CO2 and 1,2-Epoxyhexane Using BWC800 as Catalyst at 80 Bar CO2 Pressure and 150 C. Temperature

(61) 1,2-epoxyhexane (17.53 gm, 0.175 mol), methanol (44.80 gm, 1.40 mol) and wood ash catalyst BWC.sub.800 (6.23 gm, 10% wt/wt) were charged into 700 ml autoclave vessel and tightly closed. The autoclave vessel was pressurised with CO.sub.2 pressure, heated to reach 150 C. temperature and 80 bar pressure under constant stirring during the reaction for 24 hours. Reaction mixture work up was carried out as described in example 1. The quantitative analysis of methanol fraction reveals that formation of dimethyl carbonate is 4.42 gm (49.00 mmol). The calculated yield of dimethyl carbonate from epoxyhexane is measured as 28.06%.

Example 15

Synthesis of Dicyclohexyl Carbonate from Cyclohexanol, CO2 and 1,2-Epoxyhexane Using BWC800 as Catalyst at 80 Bar CO2 Pressure and 150 C. Temperature

(62) 700 ml autoclave was charged with 1,2-epoxyhexane (17.53 gm, 0.175 mol), cyclohexanol (140.81 gm, 1.40 mol) and wood ash catalyst BWC.sub.800 (15.8 gm, 10% wt/wt). The autoclave vessel was pressurised with CO.sub.2 pressure, heated to reach 150 C. temperature and 80 bar pressure under constant stirring during the reaction for 24 hours. Reaction mixture work up was carried out as described in example 1. The quantitative analysis of reaction mixture reveals that formation of dicyclohexyl carbonate is 7.16 gm (31.54 mmol). The calculated yield of dicyclohexyl carbonate from epoxyhexane is measured as 18%.

Example 16

Synthesis of DMC from Methanol, CO2 and Propylene Oxide Using BWC800 as Catalyst at 80 Bar CO2 Pressure and 150 C. Temperature

(63) The mixture of propylene oxide (10.17 gm, 0.175 mol), methanol (44.80 gm, 1.40 mol) and wood ash catalyst BWC.sub.800 (5.5 gm, 10% wt/wt) was taken into 700 ml autoclave vessel and closed with lid. The autoclave vessel was pressurised with CO.sub.2 pressure, heated to reach 150 C. temperature and 80 bar pressure under constant stirring during the reaction for 24 hours. Reaction mixture work up was carried out as described in example 1. The quantitative analysis of methanol fraction reveals that formation of dimethyl carbonate is 8.05 gm (89.5 mmol). The calculated yield of dimethyl carbonate from propylene oxide is measured as 51.11%.

Example 17

Synthesis of Didecyl Carbonate from n-Decanol, CO2 and Propylene Oxide Using BWC800 as Catalyst at 80 Bar CO2 Pressure and 150 C. Temperature

(64) 700 ml autoclave was charged with propylene oxide (10.17 gm, 0.175 mol), n-decanol (221.60 gm, 1.40 mol) and wood ash catalyst BWC.sub.800 (23.0 gm, 10% wt/wt). The autoclave vessel was pressurised with CO.sub.2 pressure, heated to reach 150 C. temperature and 80 bar pressure under constant stirring during the reaction for 24 hours. Reaction mixture work up was carried out as described in example 1. The quantitative analysis of reaction mixture reveals that formation of didecyl carbonate is 19.80 gm (57.89 mmol). The calculated yield of didecyl carbonate from propylene oxide is measured as 33.0%.

Example 18

Synthesis of Dicyclohexyl Carbonate from Cyclohexanol, CO2 and Propylene Oxide Using BWC800 as Catalyst at 80 Bar CO2 Pressure and 150 C. Temperature

(65) Propylene oxide (10.17 gm, 0.175 mol), cyclohexanol (140.81 gm, 1.40 mol) and wood ash catalyst BWC.sub.800 (15.0 gm, 10% wt/wt) were taken into 700 ml autoclave vessel and closed tightly. The autoclave vessel was pressurised with CO.sub.2 pressure, heated to reach 150 C. temperature and 80 bar pressure under constant stirring during the reaction for 24 hours. Reaction mixture work up was carried out as described in example 1. The quantitative analysis of reaction mixture reveals that formation of dicyclohexyl carbonate is 9.55 gm (42.0 mmol). The calculated yield of dicyclohexyl carbonate from propylene oxide is measured as 24%.