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Patent SEAWATER BATTERY

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Patent SEAWATER BATTERY ( patent-seawater-battery )

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Ser.No.01/000056,filedMar.23,1990. FIELD OF THE INVENTION 5 consistsofwirewhichisthincomparedtothethicknes ofthedifusionlayer,cylindricaldifusionwilfurther increasethemasstransportlimitingcurrentandthusthe loadabilityofthecathode. DESCRIPTION OF THE RELATED ART 5,256,501 1. 2 KlausJ.Veter: ElectrochemicalKinetics'published by Academic Pres,New York 1967.Thus unlesthe platesareperforated,platecathodeshavelow efi SEAWATER BATTERY ThisaplicationisacontinuationofPCTaplication ciencyandareexpensivetoproduce.Ifthecathode Thepresentinventionrelatestoseawaterbateriesor saltwatergalvaniccelsorbaterieswhichuseoxygen dissolvedintheseawaterastheoxidant,anditrelatesin O particulartocathodeswhicharesuitableforcelswhich FromU.S.Pat.No.4,522,897(M.A.Walsh)thereis areexposedtohighhydrodynamicforces(fromwaves knownasocaledropebatteryhavingaflexiblestruc orstrongcurents). ture.Theropebatteryconsistsofacentralflexiblean Lowpowerseawatercelswhichusetheoxygen ode,aporousseparatorandaflexibleoutercoaxial dissolvedintheseawaterastheoxidantandaconsum 15 ableanodeforexampleasdescribedinInternational PublicationNo.WO 89/11165(Hasvold3)havebeen sucesfulytestedintheseaovernearlytwoyears. Thesecelsuseaninertmetalcathode(stainlesstel) whichiscoatedwithacatalystforthereductionof20whichareexposedtohighhydrodynamicforces(from oxygen.Inbateries,thecelsareconnectedinparalel, andthecelvoltageisconvertedtoausefulvaluewith a DC/DC converter. wavesorstrongcurents). OBJECT OF THE INVENTION Seawaterbateriesareatractiveastheycanbestored Theobjectofthepresentinventionistoprovide inadryconditionindefinitely,theyhaveanenergy25 seawatercelsandbaterieswhicharemechanically densitywhichcomparesfavorablywithlithiumbater robust,inexpensivetoproduceandhaveahighefi iesandtheyposenosafetyhazards,astheyareneither ciency.Thefeaturesoftheinventionaredefinedinthe flammablenordotheycontainanytoxiccompounds. claims. Thechemicalreactionsinatypicalseawaterbattery withmagnesiumanodeare: (anodereaction) (cathodereaction) (celreaction) 35 Magnesiumisamajorcomponentintheseawater whichmakesthemagnesiumbasedseawaterbatery environmentallyharmles.A dischargedbaterycan easilyberechargedmechanicalybyinsertinganew plate,and magnesiumanode. Toensureahighsurfaceareaofthecathode,theinert metalcanbeintheformofwoolsandwichedbetween twolayersofmetalnetorexpandedmetal.Thepacking ofthewoolislosetoprovideaneasyflowoffresh,45 oxygenrich seawater through the cathode structure. Aditionaly,thecelmusthaveanopenstructureto allowfreaccessoffreshseawaterandtogetridofthe reactionproductsformed. FIGS.4and5schematicalyshowagalvaniccel accordingtothepresentinvention. DETAILED DESCRIPTION OF THE INVENTION in FIG. 1, the curve, which is calculated from the equations2.153and2.91intheabove-mentionedbook byK.J.Veter,showsthatthemeanlimitingcurrent densitydecreasesrapidlywithincreasingplatesize.The cathode.Thecathodeconsistspreferablyoftwistedor braidedstrandsofaninertmetal,butcanalsobemade ofperforatedmetalsheetorexpandedshetmetal.This kindofbaterywilprobablynotbesuitableforcels Abovementionedandotherfeaturesandobjectsof 30 thepresentinventionwilclearlyappearfromthefol lowingdetaileddescriptionofembodimentsofthein ventiontakeninconjunctionwiththedrawings,where BRIEF DESCRIPTION OF THE DRAWINGS FIG.1showsacurveilustratinghowplatesizes influencethelimitingcurent, FIG.2showsaspiralcathode, FIG.3showsthepreferredexpansionofacathode Ifsuchacelisusedclosetothewatersurfaceunder curvevaluesarecalculatedataflowvelocityof0.01 conditionsofstrongwaveaction,thewoolstructure50 m/sparaleltothesurfaceandinthelengthdirectionof maybemechanicalydestroyedunlesaverystifqual theplate.Asthelimitingcurentisthehighestcurent ityisused.Also,closetothesurface,biofouling(for densityposible,thesizeoftheplateperpendicularto exampleofalgae,barnaclesandmusels)wilbeaprob thedirectionofflowshouldbekeptassmalasisconsis lemunlescopperoracopperaloyisusedasthecath55 tentwiththemechanicalloadsonthecathode. ode.Thecorosionofcopperwilnormallyleaksufi Thecurvedescribesthemeancurentdensityovera cientamountsofcopperionstofunctionasanexcelent platecathodeasafunctionofthelengthoftheplate, antifoulingagentaslongasthecathodepotentialisnot assumingpuredifusioncontrolofthereaction.(Ideal loweredtoomuchfromthefrecorrosionpotentialof electrocatalystandinfiniteconductivityoftheelectro themetal.Asthecorosionpotentialofcopperislow lyte.)Currentgeneratedattheleadingedgeisnotin comparedtothecathodepotentialofcatalyzedcath60 odesunderload,thecelvoltageofcopperbasedseawa tercelsishoweveronly1.2Vascomparedto1.6Vfor celsusingcatalyzedstainlesstel.Also,ascopperisa verysoftmetal,coper-wolcathodesdonothave suficientstrengthtobeusedunderroughconditions.65 increases when the ratio between the actual current Metalplatecathodescanbeused,butthemasstransport limitingcurentforplatesislowanddecreaseswiththe lengthoftheplate.Thishasbendescribedinabookby densityandthelimitingcurrentdensityincreasesand mayeventuallyleadtoformationofacalcareouslayer on the cathode. cluded. Anotheraspectofachievingahighlimitingcurrentis toreducethecompositionalchangesoftheelectrolyte attheelectrodesurface.Thesechanges(alkalinization)

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