http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-2653121-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_78f2deeadf8c213c9ef1eca9f91348c9
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09K5-16
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09K5-16
filingDate 1976-11-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_167ee39b1f5c0b4b0ca1cdb6734a3156
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_db64927f6c6a7f0578c9214a2fc3a9e1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7d541156011a695f673b9a74ad218261
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5a281772e1ec63b9edceba14d4b6ee73
publicationDate 1978-05-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-2653121-A1
titleOfInvention COLLECTION AND RECOVERY OF SOLAR ENERGY THROUGH REVERSIBLE PHOTOCHEMICAL ISOMERIZATION
abstract Exploitation and recovery of solar energy comprises (i) exposing the trans isomer of a cpd. (I) to sunlight to convert much of it to the cis form. (ii) heating the cis-(I) to a sufficient temp. to initiate conversion back to trans-(I) with release of thermal energy and (iii) continuing the conversion without furtehr introduction of energy using a part of the liberated energy to effect the conversion while the rest is used elsewhere for other purposes. Trans-(I) is dissolved and/or dispersed in an aq. liq. contg. >=50 vol % water and is isomerised by exposure to light of wavelength 350-1200 nm. The absorption max. in sunlight, of trans-(I) is at 350-800 nm while at of cis-(I) is at shorter wavelengths. The photochemical reaction is efficient and occurs with min. deterioration. The solar energy can be stored as cis (I) until needed. Typical (I) include N,N'-diacetylindigo, stilbene or 3,3'-diethyloxacyanine iodide.
priorityDate 1976-11-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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