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Techniques For Effluent Treatment: Lecture 5

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Techniques for effluent treatment

Lecture5

Techniques for effluent treatment


Dye effluent treatment methods are classified into three main categories: 1. 2. 3. Physical treatment method Chemical treatment method Biological treatment method

There are four stages of the treatment process: Preliminary, Primary, Secondary and Tertiary. 1. Preliminary treatment process includes equalization, neutralization and possibly disinfection. 2. Primarystageismainlyphysicalwhichincludesscreening,sedimentation,floatationand flocculationtoremovedebris,undissolvedchemicalsandparticularmatters. 3. Secondary stage is a combination of physical/chemical separation and biological oxidation to reduce the organic load. 4. Tertiary stages are: to serve as polishing of effluent treatment. The methods are adsorption, ion exchange, chemical oxidation, hyperfiltration (reverse osmosis), electrochemical etc.

Chlorine Dioxide Treatment


Duetohighlevelofoxidationstage(+4),chlorinedioxidehassomeuniqueproperties,areasfollows: 1. Itbleachescellulosicmaterialstohigherbrightnesslevelthanhypochloriteandhydrogenperoxide. 2. Ithassubstantialbactericidalproperties. 3. ChlorineDioxide,ingasform,cannotbesafelycompressedorliquefied. 4. ChlorineDioxide,insolutionform,canbesafelyhandled,evenatitsmaximumsolubilityinwater. ChemistryofChlorineDioxideanditsgenerationinindustry i. Chlorinegenerationofchlorinedioxide
Cl2 + H2O HCl + 2NaClO2 HOCl + HCl 2ClO2 + 2NaCl + H2O

HOCl +

ii.

Hypochloritegenerationofchlorinedioxide
NaOCl HCl + + HCl HOCl + 2NaClO2 NaCl + HOCl 2ClO2 + 2NaCl + H2O

Ozone Treatment
Ozoneissometimesusedasdisinfectantinplaceofchlorine. Basicallyairisfiltered,cooled,driedandpressurizedthensubjectedtoanelectricaldischarge ofapproximately20,000volts.TheOzoneproducedisthenpumpedintoacontactchamber whereitcontactwithwaterfor15minutes. Ozoneismoredestructivethanchlorine. Amajorconcernwithozoneistherateatwhichitdecomposesspontaneouslyinwater, accordingtothereaction:
2O3 3O2

Somechlorinemustbeaddedtomaintaindisinfectantcharacterthroughoutthewater distributionsystem.Forthispurpose,astrongoxidising agent,ferrate,isaddedtoremove heavymetalsandphosphate.

Hydrogen peroxide treatment


Decolorization ofdyesbelongingtovariousgroupswascarriedoutusingnovelfreeradicalsgenerating systemsconsistingofCu(II),organicacidsandhydrogenperoxide. Amongtheorganicacidstested,succinic acidwasthemosteffective.A24 hincubationinthepresence of10 mM Cu(II),200 mM succinic acid,and100 mM H2O2 resultedin8595%decolorization ofRemazol BrilliantBlueR(RBBR),ReactiveBlue,PolyB411,ChicagoSkyBlue,EvansBlueandMethylOrange. ThereplacementofCu(II)withothertransitionmetalswaslesseffectivebut78%decolorization was detectedinthecaseofCo(III)andsuccinic acid.Thedecolorization isduetotheformationofhydroxyl radicals,formedduringthedecompositionofH2O2 bythemetalligand complex.

Decolorization of dye wastewater by hydrogen peroxide in the presence of basic oxygen furnace slag
Thebasicoxygenfurnacewasteslag(BOFslag)generatedfromsteelmakingplantshasbeenusedindye wastewatertreatment. Itwasshowntobeeffectiveforthedecolorization ofadyechemical(acidblack1)wastewaterbyusingBOF slagwithhydrogenperoxide. Inanacidsolution,BOFslagcanbedissociatedtoproduceferrousionsandreactwithhydrogenperoxideto generatehydroxylradicalsandoxidizetargetpollutantacidblack1. Allofthefactorsthataffectthedecolorization ofacidblack1werestudiedincluding:hydrogenperoxide dosage,concentration ofBOFslag,initialconcentrationofacidblack1andpHvalueofsolution.

Decolorization and degradation of H-acid and other dyes using ferrous-hydrogen peroxide system
Thedecolorization anddegradationoftwocommercialdyesviz.,RedM5B,BlueMRandHacid,adye intermediateusedinchemicalindustriesforthesynthesisofdirect,reactiveandazo dyes. EffectofFe2+,H2O2,pH,andcontacttimeonthedegradationofthedyeswasstudied. Maximumcolor andCODremovalwasobtainedforRedMSB,HacidandBlueMRat1025mg/lofFe2+ doseand400500mg/lofH2O2 doseatpH3.0. Releaseofchlorideandsulfate fromtheFenton'streatedRedM5Bdyeandsulfate fromHacidandBlue MRindicatesthatthedyedegradationproceedsthroughcleavageofthesubstituentgroup.

Decolorization of the azo dye Reactive Black 5 by hydrogen peroxide and UV radiation.
Thedecolorization ofC.I.ReactiveBlack5bythecombinationofhydrogenperoxideandUVradiation wasdevelopedbasedonexperimentalresultsandknownchemicalandphotochemicalreactions.

Theobservedkineticreactioncoefficientwasdeterminedandcorrelatedasafunctionofhydrogen peroxideconcentrationandUVintensity. Thedecolorization ratefollowspseudofirstorderkineticswithrespecttodyeconcentration. TherateincreaseslinearlywithUVintensityandnonlinearlywithincreasinghydrogenperoxide concentration

ZINC OXIDE ASSISTED PHOTOCATALYTIC DECOLORIZATION OF REACTIVE RED 2 DYE


Thephotocatalytic decolorizations ofaqueoussolutionsofReactiveRed2dyeinthepresenceofZnO suspensionhasbeeninvestigatedwiththeuseofartificialUVAlightsources. Theeffectsofvariousparameters,suchastimeofirradiation,photocatalyst amount,pH,additionof H2O2andtemperatureonphotocatalytic degradationwereinvestigated. Therateofdecolorization wasfoundtoincreasesignificantlywithtimeofirradiation.Underoptimal conditions,theextentofdecolorization was100%after30minutesofirradiation. Optimumcatalystconcentration[Catalyst]Optwasmeasuredandfoundequalto2.5g/L1 Theoxidizingagentssuchasoxygenandhydrogenperoxideenhancethedecolorization rate.

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