Vol.1No.4July2011JournalofEnvironmentalEngineeringTechnology14201172011-03-282008ZX07208-003201004703992010KYYW15S2010GR07681979—xiaoshuhu@126.com*1967—songyh@craes.org.cn1674-991X201104-0295-051121*121.1000122.110142。、pHCu2+。2.0cm4.0ApH300minCu2+170022000mgL12055.0mgL93.3%99.9%。97.1%t21.4kg。。X787ADOI10.3969j.issn.1674-991X.2011.04.049TreatmentofBerberinePharmaceuticalWastewaterContainingCopperbyBipolar-electrochemicalProcessXIAOShu-hu1ZHANGGuo-fang12SONGYong-hui1ZENGPing1LIHui21.DepartmentofUrbanWaterEnvironmentalResearchChineseResearchAcademyofEnvironmentalSciencesBeijing100012China2.CollegeofEnvironmentalandBiologicalEngineeringShenyangUniversityofChemicalTechnologyShenyang110142ChinaAbstractTheberberinepharmaceuticalwastewatercontainingcopperwastreatedbythebipolar-electrochemicalprocess.TheeffectsofelectrodedistancecurrentintensityandinitialpHontheremovalefficienciesofberberineandCu2+werestudiedbasedonanalysisofthewaterqualitycharacteristics.Theresultsshowedundertheconditionsoftheelectrodedistances2.0cmthecurrent4.0AandinitialpHofrawwasterwatertheconcentrationsofberberineandCu2+decreasedfrom1700and22000mgLto120and55.0mgLrespectivelyandtheremovalefficienciesreachedabout93.3%and99.9%respectivelyafter300minwithoutaddingelectrolyteandoxidant.Accordingtotheweightmethodcopperrecoverywascalculatedas97.1%.Thatisabout21.4kgofCucouldberecoveredfrompertonofsuchwastewater.Itwasprovedthatthebipolar-electrochemicalprocesswasaneffectivemethodforthetreatmentofberberinewastewatercontainingcopperwhilerecoveringmostofthecopper.Keywordselectrochemicalprocesspharmaceuticalwastewatercopper-containingwastewaterberberinecopperrecovery1-2。1CODCr3。“”。4、56。6。7-9。2gL10-13。Cu2+Cu2+。、pHCu2+。11.1、、1。500mL6cm×10cmRuO2Ti2Ti。JC17310SF。1.21Fig.1Schematicdiagramoflabscaleexperimentaldevice。500mL。pH1molLNaOH1molLHClStarter3CpH。Cl-Cu2+14。150.05molL25∶751.0μLmin30℃30min。DDS-11A。XP105Deltarange。22.11。1Table1CharactersofberberinewastewatercontainingcopperpHCu2+mgLCODCrmgLmgLmScmCl-mgL0.4220000~2400060000~800001200~1800300126701CODCrCu2+Cu2+。Cl-Cl-16-20Cu2+。2Cl-→Cl2+2e-Cl2+H2O→HOCl+H++Cl-HOCl→OCl-+H+·692·4Cu2++2e-→Cu2.22.2.1。4.0ApH0.43300min2。22.0cmCu2+。93.3%Cu2+99.8%。1.0cm8。2.0cm。2Cu2+Fig.2EffectofelectrodedistanceontheremovalofberberineandCu2+2.2.22.0cmpH0.41300min2.03.04.05.0ACu2+3。3Cu2+Fig.3EffectofcurrentontheremovalofberberineandCu2+3Cu2+。Cu2+Cu2+。。4.0ACu2+93.3%99.9%4.0A。·792·12.2.3pHpH4.0A2.0cmpH0.46~3.96300minCu2+4。4pH0.46~3.96Cu2+。pH3.96pHCu2+CuOH2Cu。pHCu2+。4pHCu2+Fig.4EffectofinitialpHontheremovalofberberineandCu2+2.35UV-Vis200~500nm。5UV-Vis225260340nm3。38。5UV-VisFig.5UV-Visspectravariationversustimeintheelectro-chemicaltreatmentofberberinewastewatercontainingcopper2.4CuCu2+。21。Cuη=M1-M2CCu×V×100%η%M1M2gCCugLVL。32。298.3%97.3%95.6%97.1%t21.4kg。。23Table2Copperrecoveryrateof3timestheparallelexperimentsM1gM2gCCugLVLη%139.837050.618722.00350.598.3250.618761.288721.94340.597.3361.288771.858722.11290.595.6·892·4312.0cm4.0ApHCu2+93.3%99.9%。2UV-Vis。397.1%t21.4kg。1.J.2002221122-24.2.J.20111111-15.3.J.2005340-41.4.J.200012725-28.5.J.200626281-83.6.J.199010441-43.7LIDIASFRANCESCOZGSANTOSHNKetal.CopperelectrodepositionandoxidationofcomplexcyanidefromwastewaterinanelectrochemicalreactorwithaTiPtAnodeJ.AppliedChemistry20003972132-2139.8.J.201124179-84.9HUNSOMAMPRUKSATHORNAKDAMRONGLERDSetal.ElectrochemicaltreatmentofheavymetalsCu2+Cr6+Ni2+fromindustrialeffluentandmodelingofcopperreductionJ.WaterRes2005394610-616.10.J.20087222-25.11.J.201026190-94.12.J.201030286-88.13.J.200913101279-1281.14.M.4.2002.15RENMJSONGYHXIAOSHetal.Treatmentofberberinehydrochloridewastewaterbyusingpulseelectro-coagulationprocesswithFeelectrodeJ.ChemicalEngineeringJ201116912384-90.16COSSURPOLCAROAMLAVAGNOLOMCetal.Electro-chemicaltreatmentoflandfillleachateoxidationatTiPbO2andTiSnO2anodesJ.EnvironSci&Technol200432223570-3573.17XIAOSHQUJHZHAOXetal.ElectrochemicalprocesscombinedwithUVlightirradiationforsynergisticdegradationofammoniainchloridecontainingsolutionsJ.WaterRes20094351432-1440.18.J.20111295-100.19.M.2007.20MORAESPBBERTAZZOLLIR.ElectrodegradationoflandfillleachateinaflowelectrochemicalreactorJ.Chemosphere20055841-46.21.J.2006223223-227.○·992·