P-type TiO2/n-type WO3 heterojunction catalyst, its preparation and use in photochemical synthesis of fuels

Abstract

Provided is a p-type TiO.sub.2/n-type WO.sub.3 heterojunction catalyst and a preparation method and use thereof. The catalyst comprises p-type TiO.sub.2 and n-type WO.sub.3 supported on a surface of the p-type TiO.sub.2.

Claims

1. A p-type TiO.sub.2/n-type WO.sub.3 heterojunction catalyst comprising: p-type TiO.sub.2; and n-type WO.sub.3 supported on a surface of the p-type TiO.sub.2; wherein the p-type TiO.sub.2/n-type WO.sub.3 heterojunction catalyst has a p-type TiO.sub.2 content of 60% by mass to 80% by mass with respect to a total mass of the p-type TiO.sub.2/n-type WO.sub.3 heterojunction catalyst.

2. A method for preparing the p-type TiO.sub.2/n-type WO.sub.3 heterojunction catalyst according to claim 1, the method comprising: supporting the n-type WO.sub.3 onto a surface of the p-type TiO.sub.2 to obtain the p-type TiO.sub.2/n-type WO.sub.3 heterojunction catalyst.

3. The method according to claim 2, further comprising: dissolving a titanium salt in a mixed solution of glycerol and a first alcohol to form a first mixture; dissolving a tungsten salt and a product resulting from a first heating process for heating the first mixture in a second alcohol to form a second mixture; and calcining a product resulting from a second heating process for heating the second mixture to produce the p-type TiO.sub.2/n-type WO.sub.3 heterojunction catalyst.

4. The method according to claim 3, wherein the first heating process is carried out at a temperature of 50° C. to 250° C. for 1 hour to 48 hours; wherein the first alcohol comprises at least one of methanol, ethanol, propanol, and isopropanol; wherein the titanium salt comprises at least one of titanium acetate, titanium oxalate, titanium chloride, tetrabutyl titanate, titanium nitrate, and titanium sulfate; wherein the second heating process is carried out at a temperature of 50° C. to 250° C. for 1 hour to 48 hours; wherein the calcining step is carried out at a temperature of 200° C. to 800° C. for 2 hours to 24 hours; wherein the tungsten salt comprises at least one of tungsten chloride, ammonium tungstate, ammonium metatungstate, and ammonium paratungstate; and wherein the second alcohol comprises at least one of methanol, ethanol, propanol, and isopropanol.

5. A method of producing a fuel, the method comprising: photochemically synthesizing the fuel from a fuel substrate in the presence of the p-type TiO.sub.2/n-type WO.sub.3 heterojunction catalyst of claim 1.

6. The method according to claim 5, wherein photochemically synthesizing the fuel from the fuel substrate is carried out under light irradiation; wherein the fuel substrate comprises at least one of norbornene, dicylopentadiene, norbornadiene, isophorone, and cyclohexenone; and wherein an amount of the p-type TiO.sub.2/n-type WO.sub.3 heterojunction catalyst is from 1% by mass to 10% by mass with respect to a total amount of the fuel substrate.

7. The method according to claim 6, wherein the fuel is photochemically synthesized from the fuel substrate in a solvent; wherein the solvent comprises at least one of dichloromethane, normal pentane, dichloroethane, and cyclohexane.

8. The method according to claim 6, wherein photochemically synthesizing the fuel from the fuel substrate in the presence of the p-type TiO.sub.2/n-type WO.sub.3 heterojunction catalyst is carried out at a temperature of 0° C. to 80° C. for 1 hour to 24 hours under irradiation of a high-pressure mercury lamp.

9. The method according to claim 7, wherein photochemically synthesizing the fuel from the fuel substrate in the presence of the p-type TiO.sub.2/n-type WO.sub.3 heterojunction catalyst is carried out at a temperature of 0° C. to 80° C. for 1 hour to 24 hours under irradiation of a high-pressure mercury lamp.

10. The method according to claim 5, wherein the fuel comprises a high-density fuel that is a multi-cyclic fuel for aerospace propulsion; wherein the fuel comprises at least one of pentacyclo[8.2.1.1.sup.4,7.0.sup.2,9.0.sup.8,3]tetradecane, pentacyclo[5.3.0.0.sup.2,6.0.sup.3,9.0.sup.5,8]decane, and quadricyclane.

Description

DETAILED DESCRIPTION

(1) Embodiments of the present disclosure will be described below. It should be understood, however, that the embodiments are provided to further illustrate the present disclosure and not to be taken as limiting the scope of the disclosure. Reaction conditions not indicated in the following exemplary embodiments can be conventional or can be carried out following the manufacturer's recommendations. Reagents or instruments used in the exemplary embodiments without specified manufacturers can be any commercially available ones.

(2) A first aspect of the present disclosure provides a p-type TiO.sub.2/n-type WO.sub.3 heterojunction catalyst which comprises:

(3) p-type TiO.sub.2; and n-type WO.sub.3 supported on a surface of the p-type TiO.sub.2.

(4) The present disclosure proposes to support n-type WO.sub.3 onto a surface of p-type TiO.sub.2 to obtain a p-type TiO.sub.2/n-type WO.sub.3 heterojunction catalyst, which has high catalytic efficiency and is particularly suitable for use in photocatalytic processes for synthesizing fuels. Moreover, the catalyst is effective in synthesizing high-density fuels, and is also cheap and suitable for large-scale applications.

(5) As compared with the p-type TiO.sub.2/n-type WO.sub.3 heterojunction catalyst according to the first aspect of the disclosure, supporting the n-type WO.sub.3 onto a surface of n-type TiO.sub.2 may result in an n-n junction structure with a weak internal electric field, leading to low charge separation efficiency.

(6) It is to be understood that after the n-type WO.sub.3 is loaded/supported on the surface of the p-type TiO.sub.2 according to the present disclosure, a heterojunction forms at an interface between the n-type WO.sub.3 and the p-type TiO.sub.2. Such a heterojunction formed between the p-type semiconductor and the n-type semiconductor can have a stronger internal electric field than the n-n heterojunction, due to the fact that the p-type semiconductor has a Fermi level in a lower portion of the forbidden band and close to the valence band and thus there is a large difference in energy between the Fermi level of the n-type semiconductor and the Fermi level of the p-type semiconductor. The heterojunction with a stronger internal electric field can facilitate charge separation and improve the reaction activity of the catalyst. Therefore, the catalyst according to the first aspect of the disclosure can be effective in the photocatalytic processes for synthesizing fuels, particularly high-density fuels, from fuel substrates.

(7) In some embodiments, the catalyst has a p-type TiO.sub.2 content of 60% to 90% by mass, such as 60%, 70%, 80%, or 90% by mass, with respect to the total mass of the catalyst. When the content of the p-type TiO.sub.2 is too low, the n-type WO.sub.3 supported on the p-type TiO.sub.2 may be too close together or even accumulate so that the p-type TiO.sub.2 cannot be exposed at all, thereby adversely influencing the reaction; while when the content of the p-type TiO.sub.2 is too high, the n-type WO.sub.3 may be dispersed on the p-type TiO.sub.2 too thinly, adversely influencing construction of the heterojunction structure.

(8) A second aspect of the present disclosure provides a method for preparing the catalyst according to the first aspect of the disclosure, the method comprising supporting the n-type WO.sub.3 onto a surface of the p-type TiO.sub.2 to obtain the p-type TiO.sub.2/n-type WO.sub.3 heterojunction catalyst.

(9) This method is simple and easy to implement and is adapted for large-scale industrial application.

(10) In some embodiments, the method according to the second aspect of the disclosure comprises a step of dissolving a titanium salt in a mixed solution of glycerol and a first alcohol to form a first mixture.

(11) In a particular embodiment, the first alcohol comprises at least one of methanol, ethanol, propanol, and isopropanol. In a particular embodiment, the titanium salt comprises at least one of titanium acetate, titanium oxalate, titanium chloride, tetrabutyl titanate, titanium nitrate, and titanium sulfate. So, the method of the present disclosure makes it possible to use a wide range of cheap raw materials for the preparation of the catalyst as described above.

(12) In the embodiments, the method according to the second aspect of the disclosure further comprises a step of dissolving a tungsten salt and a product resulting from a first heating process for heating the first mixture in a second alcohol to form a second mixture.

(13) In a particular embodiment, the first heating process is carried out at a temperature of 50 to 250° C., such as 50° C., 100° C., 150° C., 200° C., or 250° C., for 1 to 48 hours, such as 2 hours, 10 hours, 15 hours, 20 hours, 25 hours, 30 hours, 35 hours, 40 hours, or 48 hours. After completion of the first heating process, titanium glycerol, namely a complex compound of glycerol and titanium, is formed, and can also be called an p-type titanium dioxide precursor.

(14) It is to be understood that the product resulting from the first heating process for heating the first mixture is the titanium glycerol described above. The product (namely, titanium glycerol) may be obtained by subjecting a solution resulting from the first heating process for heating the first mixture to a solid-liquid separation.

(15) In a particular embodiment, the tungsten salt comprises at least one of tungsten chloride, ammonium tungstate, ammonium metatungstate, and ammonium paratungstate. In a particular embodiment, the second alcohol comprises at least one of methanol, ethanol, propanol, and isopropanol. So, the method of the present disclosure makes it possible to use a wide range of cheap raw materials for the preparation of the catalyst as described above.

(16) In the embodiments, the method according to the second aspect of the present disclosure yet further comprises a step of calcining a product resulting from a second heating process for heating the second mixture to obtain the p-type TiO.sub.2/n-type WO.sub.3 heterojunction catalyst.

(17) In a particular embodiment, the second heating process is carried out at a temperature of 50 to 250° C., such as 50° C., 100° C., 150° C., 200° C., or 250° C., for 1 to 48 hours, such as 2 hours, 10 hours, 15 hours, 20 hours, 25 hours, 30 hours, 35 hours, 40 hours, or 48 hours.

(18) The product resulting from the second heating process for heating the second mixture may be obtained by subjecting a solution resulting from the second heating process to a solid-liquid separation.

(19) In a particular embodiment, the calcining step is carried out at a temperature of 200 to 800° C., such as 200° C., 300° C., 400° C., 500° C., 600° C., 700° C., or 800° C., for 2 to 24 hours, such as 2 hours, 10 hours, 15 hours, 20 hours, or 24 hours. The calcining process allows the titanium glycerol to be converted into n-type titanium dioxide (TiO.sub.2) and tungsten trioxide (WO.sub.3) to be supported onto a surface of the n-type TiO.sub.2, so that a p-type TiO.sub.2/n-type WO.sub.3 heterojunction catalyst is produced.

(20) In some particular embodiments, the method for preparing the p-type TiO.sub.2/n-type WO.sub.3 heterojunction catalyst of the present disclosure comprises steps of:

(21) (1) mixing 1 to 40 mL of glycerol and 1 to 100 mL of an alcohol into a homogeneous state by stirring so as to obtain a mixed solution;

(22) (2) adding 1 to 20 g of a titanium salt to the mixed solution obtained in step (1) and stirring until a homogeneous state is obtained;

(23) (3) transferring the resulting mixture from step (2) into a Teflon-lined autoclave to perform a reaction at a temperature of 50 to 250° C. for 1 to 48 hours;

(24) (4) after completion of the reaction and allowing the autoclave to cool to room temperature, subjecting a product produced by the reaction to centrifugation, and then to be washed several times with ethanol and water and dried in an oven at 60 to 100° C. for 6 to 24 hours;

(25) (5) dissolving 1 to 100 mg of a tungsten salt in 10 to 100 mL of an alcohol and mixing by stirring to form a homogeneous solution, to which the dried product obtained from step (4) is then added and mixed by stirring until homogeneous;

(26) (6) transferring the resulting solution from step (5) into a Teflon-lined autoclave to perform a reaction at a temperature of 50 to 250° C. for 1 to 48 hours;

(27) (7) after completion of the reaction in step (6) and allowing the autoclave to cool to room temperature, subjecting a product produced by the reaction to centrifugation, and then to be washed several times with ethanol and water and dried in an oven at 60 to 100° C. for 6 to 24 hours; and

(28) (8) calcining the resulting product from step (7) at 200 to 800° C. for 2 to 24 hours so as to obtain the p-type TiO.sub.2/n-type WO.sub.3 heterojunction catalyst after cooling to room temperature.

(29) Advantageously, the method of the present disclosure as described above is simple and makes it possible to utilize a wide range of cheap raw materials. So, this method is suitable as an industrial process.

(30) A third aspect of the present disclosure provides use of the p-type TiO.sub.2/n-type WO.sub.3 heterojunction catalyst as described above in photochemical synthesis of fuels.

(31) In some particular embodiments of the disclosure, the catalyst is used in the synthesis of a fuel from a fuel substrate under light irradiation, wherein the fuel substrate comprises at least one of norbornene, dicylopentadiene, norbornadiene, isophorone, and cyclohexenone. Preferably, the fuel substrate comprises norbornene and isophorone, or, the fuel substrate comprises norbornene and cyclohexenone.

(32) In some embodiments, by means of the catalyst of the present disclosure, the conversion of the fuel substrate can be as high as 95%.

(33) In a particular embodiment, the amount of the catalyst added is from 1% to 10% by mass, such as 1%, 3%, 5%, 7%, 9%, or 10% by mass, with respect to the total amount of the fuel substrate.

(34) In a particular embodiment, the fuel is synthesized from the fuel substrate in a solvent. In a particular embodiment, the solvent comprises at least one of dichloromethane, normal pentane, dichloroethane, and cyclohexane. The use of the solvent favours the synthesis of the fuel from the fuel substrate.

(35) In a particular embodiment, the synthesis of the fuel from the fuel substrate, in the presence of the catalyst of the present disclosure, is carried out at a temperature of 0 to 80° C., such as 0° C., 20° C., 40° C., 60° C., or 80° C., for 1 to 24 hours, such as 1 hour, 5 hours, 10 hours, 15 hours, 20 hours, or 24 hours, under irradiation of a high-pressure mercury lamp. The disclosed p-type TiO.sub.2/n-type WO.sub.3 heterojunction catalyst allows the photochemical synthesis process for producing the fuels to be simple and to proceed under mild conditions, and can be suitable for the synthesis of various norbornene derivatives. The catalyst of the present disclosure is thus highly valuable in the industry.

(36) In a particular embodiment, the fuel comprises a high-density fuel, preferably a multi-cyclic fuel for aerospace propulsion. In a further particular embodiment, the fuel comprises at least one of pentacyclo[8.2.1.1.sup.4,7.0.sup.2,9.0.sup.8,3]tetradecane, pentacyclo[5.3.0.0.sup.2,6.0.sup.3,9.0.sup.5,8]decane, and quadricyclane. The fuel produced by the photocatalytic process from the fuel substrate utilizing the p-type TiO.sub.2/n-type WO.sub.3 heterojunction catalyst of the disclosure can meet the requirements of the aerospace industry.

EXAMPLES

(37) The embodiments of the present disclosure will now be described in further detail by way of the following examples. Features of each of the examples may be combined with features of other examples in case of no conflict.

Example 1

(38) 20 mL of glycerol and 60 mL of anhydrous ethanol were mixed and stirred for 20 minutes until homogeneous. 2 g of tetrabutyl titanate was added to the mixture and stirred until a clear solution had been obtained. The solution was transferred to a Teflon-lined hydrothermal reactor and was heated at 180° C. for 24 hours. After cooling, the reaction mixture was centrifuged and washed several times with ethanol. Drying was then conducted at 60° C. for 12 hours to obtain a titanium dioxide precursor.

(39) 0.536 g of tungsten hexachloride was mixed with 80 mL of methanol. The titanium dioxide precursor was added to the mixture and mixed by stirring until a homogeneous solution had been obtained. The solution was transferred to a Teflon liner of an autoclave. The liner was then placed into the autoclave. Thereafter, the autoclave was sealed and placed into a thermostatted oven to perform a reaction at 180° C. for 3 hours. After completion of the reaction, the autoclave was subjected to a rapid cooling process along with the resulting reaction product contained therein. After cooling to room temperature, the product was washed with anhydrous ethanol and dried. The dried product was placed into a muffle furnace and calcined at 400° C. for 1 hour. After allowing to cool naturally, a p-type TiO.sub.2/n-type WO.sub.3 heterojunction catalyst was obtained.

Example 2

(40) 20 mL of glycerol and 60 mL of anhydrous ethanol were mixed and stirred for 20 minutes until homogeneous. 2 g of tetrabutyl titanate was added to the mixture and stirred until a clear solution had been obtained. The solution was transferred to a Teflon-lined hydrothermal reactor and was heated at 180° C. for 24 hours. After allowing to cool, the reaction mixture was centrifuged and washed several times with ethanol. Drying was then conducted at 60° C. for 12 hours to obtain a titanium dioxide precursor.

(41) 0.344 g of tungsten hexachloride was mixed with 80 mL of methanol. The titanium dioxide precursor was added to the mixture and mixed by stirring until a homogeneous solution had been obtained. The solution was transferred to a Teflon liner of an autoclave. The liner was then placed into the autoclave. Thereafter, the autoclave was sealed and placed into a thermostatted oven to perform a reaction at 180° C. for 3 hours. After completion of the reaction, the autoclave was subjected to a rapid cooling process along with the resulting reaction product contained therein. After allowing to cool to room temperature, the product was washed with anhydrous ethanol and dried. The dried product was placed into a muffle furnace and calcined at 400° C. for 1 hour. After allowing to cool naturally, a p-type TiO.sub.2/n-type WO.sub.3 heterojunction catalyst was obtained.

Example 3

(42) 20 mL of glycerol and 60 mL of anhydrous ethanol were mixed and stirred for 20 minutes until homogeneous. 2 g of tetrabutyl titanate was added to the mixture and stirred until a clear solution had been obtained. The solution was transferred to a Teflon-lined hydrothermal reactor and was heated at 180° C. for 24 hours. After allowing to cool, the reaction mixture was centrifuged and washed several times with ethanol. Drying was then conducted at 60° C. for 12 hours to obtain a titanium dioxide precursor.

(43) 0.201 g of tungsten hexachloride was mixed with 80 mL of methanol. The titanium dioxide precursor was added to the mixture and mixed by stirring until a homogeneous solution had been obtained. The solution was transferred to a Teflon liner of an autoclave. The liner was then placed into the autoclave. Thereafter, the autoclave was sealed and placed into a thermostatted oven to perform a reaction at 180° C. for 3 hours. After completion of the reaction, the autoclave was subjected to a rapid cooling process along with the resulting reaction product contained therein. After allowing to cool to room temperature, the product was washed with anhydrous ethanol and dried. The dried product was placed into a muffle furnace and calcined at 400° C. for 1 hour. After allowing to cool naturally, a p-type TiO.sub.2/n-type WO.sub.3 heterojunction catalyst was obtained.

Example 4

(44) 20 mL of glycerol and 60 mL of anhydrous ethanol were mixed and stirred for 20 minutes until homogeneous. 2 g of tetrabutyl titanate was added to the mixture and stirred until a clear solution had been obtained. The solution was transferred to a Teflon-lined hydrothermal reactor and was heated at 180° C. for 24 hours. After allowing to cool, the reaction mixture was centrifuged and washed several times with ethanol. Drying was then conducted at 60° C. for 12 hours to obtain a titanium dioxide precursor.

(45) 0.089 g of tungsten hexachloride was mixed with 80 mL of methanol. The titanium dioxide precursor was added to the mixture and mixed by stirring until a homogeneous solution had been obtained. The solution was transferred to a Teflon liner of an autoclave. The liner was then placed into the autoclave. Thereafter, the autoclave was sealed and placed into a thermostatted oven to perform a reaction at 180° C. for 3 hours. After completion of the reaction, the autoclave was subjected to a rapid cooling process along with the resulting reaction product contained therein. After allowing to cool to room temperature, the product was washed with anhydrous ethanol and dried. The dried product was placed into a muffle furnace and calcined at 400° C. for 1 hour. After allowing to cool naturally, a p-type TiO.sub.2/n-type WO.sub.3 heterojunction catalyst was obtained.

Example 5

(46) 20 mL of glycerol and 60 mL of anhydrous ethanol were mixed and stirred for 20 minutes until homogeneous. 2 g of tetrabutyl titanate was added to the mixture and stirred until a clear solution had been obtained. The solution was transferred to a Teflon-lined hydrothermal reactor and was heated at 180° C. for 24 hours. After allowing to cool, the reaction mixture was centrifuged and washed several times with ethanol. Drying was then conducted at 60° C. for 12 hours to obtain a titanium dioxide precursor.

(47) 0.013 g of tungsten hexachloride was mixed with 80 mL of methanol. The titanium dioxide precursor was added to the mixture and mixed by stirring until a homogeneous solution had been obtained. The solution was transferred to a Teflon liner of an autoclave. The liner was then placed into the autoclave. Thereafter, the autoclave was sealed and placed into a thermostatted oven to perform a reaction at 180° C. for 3 hours. After completion of the reaction, the autoclave was subjected to a rapid cooling process along with the resulting reaction product contained therein. After allowing to cool to room temperature, the product was washed with anhydrous ethanol and dried. The dried product was placed into a muffle furnace and calcined at 400° C. for 1 hour. After allowing to cool naturally, a p-type TiO.sub.2/n-type WO.sub.3 heterojunction catalyst was obtained.

Comparative Example 1

(48) An n-type TiO.sub.2/n-type WO.sub.3 catalyst was prepared according to the method described in Example 1, except that glycerol was not added when the titanium dioxide precursor was prepared.

Comparative Example 2

(49) A p-type TiO.sub.2 catalyst was prepared as follows.

(50) A titanium dioxide precursor was prepared according to the method described in Example 1. The titanium dioxide precursor after drying was then placed into a muffle furnace and calcined at 400° C. for 1 hour. After allowing to cool naturally, a p-type TiO.sub.2 was obtained.

Comparative Example 3

(51) An n-type WO.sub.3 catalyst was prepared as follows.

(52) 0.344 g of tungsten hexachloride was mixed with 80 mL of methanol and stirred until a homogeneous solution had been obtained. The solution was transferred to a Teflon liner of an autoclave. The liner was then placed into the autoclave. Thereafter, the autoclave was sealed and placed into a thermostatted oven to perform a reaction at 180° C. for 3 hours. After completion of the reaction, the autoclave was subjected to a rapid cooling process along with the resulting reaction product contained therein. After allowing to cool to room temperature, the product was washed with anhydrous ethanol and dried. The dried product was placed into a muffle furnace and calcined at 400° C. for 1 hour. After allowing to cool naturally, an n-type WO.sub.3 catalyst was obtained.

(53) The catalysts prepared in Examples 1 to 5 and Comparative Examples 1 to 3 were each used to catalyze the cycloaddition of norbornadiene under light irradiation to produce a multi-cyclic high-density fuel. In particular, a fuel substrate was introduced into a 50 ml single-port glass reactor. Each of the catalysts was added to the respective substrate in an amount of 5% by mass of the total mass of the fuel substrate. The resulting mixture was stirred and bubbled with nitrogen for 1 hour. The opening of the reactor was sealingly attached to a condensing tube. Cooling water was passed through the condensing tube. The mixture was then irradiated with a high-pressure mercury lamp for 12 hours. The resulting reaction solution was analyzed using Gas Chromatography-Mass Spectrometry (GC-MS) to identify the reaction products, and the conversion rate of the fuel substrate was calculated based on the results of the analysis. The conditions and results of the cycloaddition reaction of different fuel substrates under light irradiation are shown in Table 1.

(54) TABLE-US-00001 TABLE 1 Mass of the Reaction Reaction Fuel Substrate Temperature Time Yield Fuel Substrate (g) (° C.) (hours) Product (%) Ex. 1 Norbornene 20 10 12 Pentacyclo[8.2.1.1.sup.4, 7.0.sup.2, 9.0.sup.8, 3]tetradecane 90 Ex. 2 Dicylopentadiene 20 10 10 Pentacyclo[5.3.0.0.sup.2, 6.0.sup.3, 9.0.sup.5, 8]decane 79 Ex. 3 Norbornadiene 20 30 12 Quadricyclane 96 Ex. 4 Norbornene 20 80 12 Pentacyclo[8.2.1.1.sup.4, 7.0.sup.2, 9.0.sup.8, 3]tetradecane 21 (50 wt. %) Decahydro-3,3,4alpha-trimethyl-5,8- 53 methanobiphenylen-1(2H)-one Isophorone Octahydro-3,3,4a,7,7,8a-hexamethyl- 24 (50 wt. %) 1,5(2H,4bH)-biphenyldiketione Ex. 5 Norbornene 20 40 5 Pentacyclo[8.2.1.1.sup.4, 7.0.sup.2, 9.0.sup.8, 3]tetradecane 12 (50 wt. %) 5,8-methanobiphenylen-1(2H)-one 34 Cyclohexenone Octahydro-1,5(2H,4bH)-biphenyldiketone 19 (50 wt. %) Comp Norbornene 20 10 12 Pentacyclo[8.2.1.1.sup.4, 7.0.sup.2, 9.0.sup.8, 3]tetradecane 71 Ex. 1 Comp Norbornene 20 10 12 Pentacyclo[8.2.1.1.sup.4, 7.0.sup.2, 9.0.sup.8, 3]tetradecane 82 Ex. 2 Comp Norbornene 20 10 12 Pentacyclo[8.2.1.1.sup.4, 7 0.sup.2, 9.0.sup.8, 3]tetradecane 55 Ex. 3

(55) Finally, it is noted that the above embodiments are provided merely for purposes of illustration and are not intended to limit the scope of the disclosure. Although the embodiments of the disclosure have been described in detail, it should be understood that various modifications and equivalents may be made hereto without departing from the scope of the disclosure.