Solar energy collection and retrieval employing reversible photochemical isomerization

Claim 2

A process for photochemical collection and retrieval of solar energy, which process comprises the steps of: a. exposing to solar radiation the trans-isomer of a geometrical isomerizable compound for a time sufficient to convert a significant portion thereof to its cis-isomer with the trans-isomer dissolved and/or dispersed in an aqueous liquid medium comprised of at least 50 percent by volume of water, which trans-isomer of the compound possesses the properties of undergoing geometrical isomerization to the cis-isomer upon exposure to light wavelengths between 350 nm and 1200 nm with an absorbance maxima of said light for the cis-isomer at a shorter wavelength than the absorbance maxima of the trans-isomer having the properties of an absorbance maxima lying between the wavelengths of 350 nm and 800 nm; b. heating the cis-isomer to a temperature initiating a triggering of an exothermal conversion thereof to the trans-isomer with released thermal energy obtained; and c. containing the exothermal conversion of cis-isomer to trans-isomer through utilization of a portion of the released thermal energy and without additional heat added thereto and with another portion of the released thermal energy transferred from the region of exothermal conversion for availability for useful thermal energy application.

Claim 3

A process for photochemical collection and retrieval of solar energy, which process comprises the steps of: a. exposing to solar radiation the trans-isomer of a geometrical isomerizable compound for a time sufficient to convert a significant portion thereof to its cis-isomer with the trans-isomer dissolved and/or dispersed in an aqueous liquid medium comprised of at least 50 percent by volume of water, which trans-isomer of the compound possesses the properties of undergoing geometrical isomerization to the cis-isomer upon exposure to light wavelengths between 350 nm and 1200 nm with an absorbance maxima of said light for the trans-isomer at a shorter wavelength than the absorbance maxima of the cis-isomer having the properties of an absorbance maxima lying between the wavelengths of 350 nm and 800 nm and with the cis-isomer having a ground-state enthalpy content at least 10 Kcal/mole higher than the ground state enthalpy content of the trans-isomer and with the cis-isomer adapted for thermal conversion to the trans-isomer with an activation energy of at least 20 Kcal/mole for said thermal conversion, and which compound is selected from those compounds possessed of the foregoing properties and having the structural formulae for the ##STR22## and ##STR23## wherein L is the rigid linkage, which may be carbon-carbon double bond or several such bonds, a carbon-nitrogen double bond or several such bonds, a cyclopropane or cyclobutane ring system, or a combination of these linkages; M 1 , M 2 , M 1 ', and M 2 ' are structural moieties which may be hydrogen, alkyl, aryl, or heteroaromatics; M 1 and M 2 (or M 1 ' and M 2 ') together may also be an aromatic or heteroaromatic ring system; b. heating cis-isomer to a temperature initiating a triggering of an exothermal conversion thereof to the trans-isomer with released thermal energy obtained; and c. continuing the exothermal conversion of cis-isomer to a trans-isomer through utilizaton of a portion of the released thermal energy and without additional heat added thereto and with another portion of the released thermal energy transferred from the region of exothermal conversion for availability for useful thermal energy application.

Claim 4

A process for photochemical collection and retrieval of solar energy, which process comprises the steps of: a. exposing to solar radiation the trans-isomer of a geometrical isomerizable compound for a time sufficient to convert a significant portion thereof to its cis-isomer with the trans-isomer dissolved and/or dispersed in an aqueous liquid medium comprised of at least 50 percent by volume of water, which trans-isomer of the compound possesses the properties of undergoing geometrical isomerization to the cis-isomer upon exposure to light wavelengths between 350 nm and 1200 nm with an absorbance maxima of said light for the trans-isomer at a shorter wavelength than the absorbance maxima of the cis-isomer having the properties of an absorbance maxima lying between the wavelengths of 350 nm and 800 nm and with the cis-isomer having a ground-state enthalpy content at least 10 Kcal/mole higher than the ground state enthalpy content of the trans-isomer and with the cis-isomer adapted for thermal conversion to the trans-isomer with an activation energy of at least 20 Kcal/mole for said thermal conversion, and which compound is selected from those compounds possessed of the foregoing properties and having the structural formulae for the ##STR22## and ##STR23## wherein L is the rigid linkage, which may be carbon-carbon double bond or several such bonds, a carbon-nitrogen double bond or several such bonds, a cyclopropane or cyclobutane ring system, or a combination of these linkages; M 1 , M 2 , M 1 ', and M 2 ' are structural moieties which may be hydrogen, alkyl, aryl, or heteroaromatics; M 1 and M 2 (or M 1 ' and M 2 ') together may also be an aromatic or heteroaromatic ring system; b. heating cis-isomer to a temperature initiating a triggering of an exothermal conversion thereof to the trans-isomer with released thermal energy obtained; and c. continuing the exothermal conversion of cis-isomer to a trans-isomer through utilizaton of a portion of the released thermal energy and without additional heat added thereto and with another portion of the released thermal energy transferred from the region of exothermal conversion for availability for useful thermal energy application.

Claim 5

The process of claim 2 in which up to 50 percent by volume of the employed aqueous liquid medium is a lower alkyl alcohol or polyalcohol, and each 100 gm of the employed aqueous liquid medium dissolves at least 60 gm of the trans-isomer at the temperature of the medium upon its exposing to the solar radiation.

Claim 6

The process of claim 3 in which the employed trans-isomer has been adapted for solvation in the employed aqueous liquid medium through chemical modification of the structure of the trans-isomer by introduction thereto of up to six water-solubilizing groups, X, wherein X may be N + Y 3 (with Y being hydrogen alkyl, aryl, or combination of these groups), SO 3 - , CO 2 - , PO 4 = , hydroxyl, or a combination of these groups.

Claim 7

The process of claim 2 in which the employed trans-isomer is ##STR24##and wherein A and A' may be H, alkyl, or aryl, R 1 , r 1 ', r 5 , and R 5 ' may be H, alkyl, alkoxy, SO 3 - or some combination of these groups, R 2 , r 2 ', r 4 , and R 4 ' may be H, alkyl, alkoxy, NX 3 - (where X is H or alkyl), SO 3 - , halogen, or some combination of these groups, R 3 and R 3 ' may be H, alkyl, aryl, aroyl, alkoxy, aryloxy, nitro, amino, dialkylamino, or some combination of these groups, and R 1 and R 2 (or R 1 ' and R 2 ') together, or R 2 and R 3 (or R 2 ' and R 3 ') together, or R 3 and R 4 (or R 3 ' and R 4 ')together, or R 4 and R 5 (or R 4 ' and R 5 ') together may be an aromatic ring system either carbocyclic or heterocyclic.

Claim 8

The process of claim 2 in which the employed trans-isomer is ##STR25##wherein A and A' may be a C 2 or higher lower alkyl, haloaryl, alkoyl, haloalkoyl, aryl, haloaryl, aroyl, heteroaroyl, --SO 2 --haloalkyl, --SO 2 --aryl, --SO 2 -- haloaryl, ##STR26## (where X and Z may be H, alkyl, aryl or a combination of these three), or a substituted aroyl wherein the substituents may be nitro, alkoxy, aroyloxy, sulfinyl, carboxy, dialkylamino, halo, or combination thereof; R 1 , r 1 ', r 2 , r 2 ', r 3 , r 3 ', r 4 , and R 4 ' may be H, alkyl, aryl, alkoxy, aryloxy, halogen, SO 3 - , NX 3 + where X is H or alkyl), alkoyl, aroyl, or a combination of these groups; and R 1 and R 2 (or R 1 ' and R 2 ') together, or R 2 and R 3 (or R 2 ' and R 3 ') together, or R 3 and R 4 (or R 3 ' and R 4 ') together may be an aromatic ring system, either carbocyclic or heterocyclic

Claim 9

The process of claim 2 in which there is included in the aqueous liquid medium up to 10 percent by weight of a photochemical sensitizer functioning to shift the absorbance maxima of the employed trans-isomer to a longer wavelength than the absorbance maxima of the employed trans-isomer in the absence of the sensitizer.

Claim 10

The process of claim 2 in which the trans-isomer resulting from Step (c) is recycled through Steps (a), (b), and (c) of claim 2.

Claim 11

The process of claim 8 employing as the geometrical isomerizable compound an indigo or thioindigo derivative of the structures of ##STR27## wherein A and A' may be a C 2 or higher lower alkyl, haloalkyl, alkoyl, haloalkoyl, aryl, haloaryl, aroyl, heteroaroyl, --SO 2 --haloalkyl, --SO 2 --aryl, --SO 2 --haloaryl, or ##STR28## (where X and Y may be H, alkyl, aryl, or a combination of these three), or a substituted aroyl wherein the substituents may be nitro, alkoxy, aroyloxy, sulfinyl, carboxy, dialkylamino, halo, or combination thereof; R 1 , r 1 ', r 2 , r 2 ', r 3 , r 3 ', r 4 , and R 4 ' may be H, alkyl, aryl, alkoxy, aryloxy, halogen, SO 3 - , NX 3 + (where X is H or alkyl), alkoyl, aroyl, or a combination of these groups; and R 1 and R 2 (or R 1 ' and R 2 ') together, or R 2 and R 3 (or R 2 ' and R 3 ') together, or R 3 and R 4 (or R 3 ' and R 4 ') together may be an aromatic ring system, either carbocyclic or heterocyclic.

Claim 12

The process of claim 8 employing as the geometrical isomerizable compound a modified indigo or thioindigo derivative of the perinaphthoindigo and perinaphthothioindigo structures of ##STR29## wherein A and A' may be a C 2 and higher lower alkyl, haloalkyl, alkoyl, haloalkoyl, aryl, haloaryl, aroyl, heteroaroyl, --SO 2 --alkyl, --SO 2 --haloalkyl, --SO 2 aryl, --SO 2 --haloaryl, or --CO--N--(X)Y, where X and Y may be hydrogen, alkyl, or aryl, or a combination of these three, or a substituted aroyl wherein the substituents may be nitro, alkoxy, aroyloxy, sulfinyl, carboxy, dialkylamino, halo, or combination thereof; and R 1 , r 2 , r 3 , r 4 , r 5 , r 6 , r 1 ', r 2 ', r 3 ', r 4 ', r 5 ', r 6 ' may be hydrogen, alkyl, aryl, alkoxy, arloxy, halogen, SO 3 - , NX 3 + (where X is hydrogen or alkyl), alkoyl, aroyl, or a combination of these groups.

Claim 13

The process of claim 8 employing as the geometrical isomerizable compound a stilbene derivative of the structures of ##STR30##wherein A and A' may be H, alkyl, or aryl, R 1 , r 1 ', r 5 , and R 5 ' may be H, alkyl, alkoxy, SO 3 - or some combination of these groups, R 2 , r 2 ', r 4 , and R 4 ' may be H, alkyl, alkoxy, NX 3 - where X is H or alkyl), SO 3 - , halogen, or a combination of these groups, R 3 and R 3 ' may be H, alkyl, aryl, aroyl, alkoxy, aryloxy, nitro, amino, dialkylamino, or a combination of these groups, and R 1 and R 2 (or R 1 ' and R 2 ') together, or R 2 and R 3 (or R 2 ' and R 3 ')together, or R 3 and R 4 (or R 3 ' and R 4 ') together, or R 4 and R 5 (or R 4 ' and R 5 ') together may be an aromatic ring system either carbocyclic or heterocyclic.

Claim 14

The process of claim 8 employing as the geometrical isomerizable compound a cyanine-type dye of the structure of ##STR31##wherein n may be 0, 1, 2, or 3; X may be oxygen, sulfur, or selenium; A, b, and B' may be hydrogen, alkyl, alkoxy, aryl, aryloxy, halogen, or a combination of these groups; R 1 , or R 2 , R 3 , R 1 ', R 2 ', and R 3 ' may be alkyl haloalkyl, aryl, haloaryl, alkoyl, aroyl, or a combination of these groups; and R 1 and R 2 (or R 1 ' and R 2 ') together, or R 1 and R 3 (or R 1 ' and R 3 ') together, or R 2 and R 3 (or R 2 ' and R 3 ') together may be a ring system, either aromatic or nonaromatic, either carbocyclic or heterocyclic.

Claim 15

The process of claim 8 employing as the geometrical isomerizable compound a modified aromatic olefin of the structures ##STR32##A, A', B, and B' may be H, alkyl, aryl, alkylsulfonyl, arylsulfonyl, alkylcarboxyl, NX 3 + (where X is H or alkyl), or a combination of these groups, R', r 1 ', r 4 , and R 4 ' may be H, alkyl, alkoxy, aryl, aryloxy, NX 3 + (where X is H or alkyl), SO 3 - , halogen or a combination of these groups. R 2 , r 2 ', r 3 ' may be H, alkyl, aryl, alkoxy, aryloxy, aroyl, nitro, dialkylamino, SO 3 - , alkylsulfonyl, NX 3 + (where X is H or alkyl) or a combination of these groups, and A and B (or A' and B') together, or R 1 and B (or R 1 ' and B') together, or R 1 and R 2 (or R 1 ' and R 2 ') together, or R 2 and R 3 (or R 2 ' and R 3 ') together, or R 3 and R 4 (or R 3 ' and R 4 ') together may be an aromatic ring system either carbocyclic or heterocyclic.