Preconcentration by coflotation is employed to improve

the detection limits for the determination of parts per

billion levels of heavy metal ions such as copper(II),

lead(lI), cadmium(II), zinc(II), nickel(II) and coba1t(II) in natural and sea water by differential pulse polarography

(DPP). Trace amounts of these ions in water are

coprecipitated on colloidal aluminium hydroxide and the

precipitate is floated with the aid of sodium oleate and a

stream of nitrogen bubbles. Experimental conditions are

optimized to obtain maximum recovery of these ions by

cofiotation. The effect of surfactant on the DPP peak

currents of these ions in 'the supporting electrolyte used in this work is studied

Bharathibai, Basu J

Padma, DK

Rajagopalan, SR

English

National Aerospace Laboratories Institutional Repository

" Indian Journal of ChemicalTechnologyVol. 1, July 1994, pp. 248-250Short CommunicationPreconcentration by cofiotation for thepolarographic determination of traces ofheavy metals in waterBharathibai J Basu", D K Padma" & S R Rajagopalarr'"a Materials ScienceDivision,National AerospaceLaboratories,Bangalore 560 017, Indiab Department of Inorganic and Physical Chemistry, IndianInstitute of Science, Bangalore 560 012, IndiaReceived 24 September 1993; accepted 1 February 1994Preconcentration by cofiotation is employed to improvethe detection limits for the determination of parts perbillion levels of heavy metal ions such as copper(II),lead(lI), cadmium(II), zinc(II), nickel(II) and coba1t(II) innatural and sea water by differential pulse polarography(DPP). Trace amounts of these ions in water arecoprecipitated on colloidal aluminium hydroxide and theprecipitate is floated with the aid of sodium oleate and astream of nitrogen bubbles. Experimental conditions areoptimized to obtain maximum recovery of these ions bycofiotation. The effect of surfactant on the DPP peakcurrents of these ions in 'the supporting electrolyte used inthis work is studied.There is an increasing need for the development ofmethods for the estimation of trace amounts of heavymetal ions such as copper, lead, cadmium, zinc, nickeland cobalt in natural waters. Many instrumentalmethods lack the necessary sensitivity and hencepreconcentration is required. Coflotation has anadvantage over the other conventional preconcen-tration techniques like coprecipitation, solventextraction and ion exchange as it can deal with largevolumes of sample in a short duration of time.Various flotation techniques used for the separationof many such elements has already been reviewed 1- 3.An adsorbing colloid flotation technique has beenused to separate Cu(II) and Zn(II) from sea waterusing ferric hydroxide as collector". A combinationof adsorbing colloid flotation and differential pulsepolarography (DPP) has also been described todetermine traces of molybdenum in water", Thispaper presents the studies on coflotation for thesimultaneous preconcentration of these heavy metalions prior to their determination by polarography.Experimental procedure+ The polarograph as well asthe flotation apparatus were described earlier". All* Author to whom correspondence should be addressed._--- ...._- .... -...._--_ ...reagents used were of AR grade except the surfactant.Sodium oleate (SO) was obtained from Loba Chemie.The stock solutions (1000 ppm) of copper, lead,cadmium, zinc, nickel and cobalt were preparedeither by dissolving the pure metal in nitric acid or bydissolving the nitrate salt in water. A stock solution ofaluminium (lOmgjmL) was prepared from aluminiumsulphate. Sodium oleate (4 mgjmL) was prepared bydissolving the reagent in 80% (vjv) ethanol. Dimethylglyoxime (1%) was prepared in ethanol.Water samples were stored in precleaned poly- .ethylene bottles after acidification to pH !? withhydrochloric acid. All analytical determinationswere performed within one week of collection ofsamples.The flotation of the water samples was carried outby the procedure described earlier>. After adding5 mL AI(III) solution to 1 L water sample, pH wasadjusted to 9.0 ± 0.2 with aqueous ammonia and thesolution was stirred for 5min. 5mL of sodium oleatesolution was added and the solution was floated bybubbling nitrogen through the solution for 2min. Thefroth was dissolved in 10mL of2 MHCl, heated toreduce the volume and made up to 10 ml, withwater.Polarograms of copper, lead, cadmium and zincwere recorded in a supporting electrolyte (S.E.) of 0.2MKCI and 0.25% ascorbic acid atpH 2.5 - 3.0 from- 0.05 to - 1.20V with respect to SCE. Similarly, thepolarograms of nickel and cobalt were recorded in aS.E. of 0.1M ammonium tartrate atpH 8.8 and 0.01%dimethyl glyoxime (DMG) from - 0.80 to - l.50 Vwith respect to SCE. The metal ion concentrationswere determined by standard addition method.Results and discussion - Aluminium hydroxidewas chosen as the collector since aluminium(III) didnot interfere with the polarographic determination ofthe other metal ions. Sodium oleate (SO) is able tofloat aluminium hydroxide completely in the pHrange of 7.0 - 9.2 and hence it was chosen as thesurfactant.The effect ofpH on the recoveries of these ions froma solution of low ionic strength (~ < 0.01) bycoflotation was carried out in the pH range of7-9.5.The results are shown in Fig.I. It is observed that thepH ranges for maximum recovery are 7.0 - 9.2 forCu(II), Pb(II) and Zn(II) and 8.8 - 9.2 for Ni(II),Co(II) and Cd(II), thus, it may be concluded thatsimultaneous and complete recovery of all the sixSHORT COMMUNICATION 24910080>-~ 60OJ>0uOJa:: 40;!204 5 6 7 8 9 10pHFig. I-Effect of pH on the recoveries of Cu(II), Pb(II), Cd(II),Zn(lI), Ni(II) and Co(II) by coflotation using aluminiumhydroxide as collector and SO as surfactant. [Cu(II)] = [Pb(II)] =[Cd(l!)] = [Zn(l!)] = [Ni(II)] = [Co(I!)] = 0.2 ppm (0) copper; (D)lead; ("") cadmium; (.) zinc; (.) nickel; ("') cobaltelements could be achieved in the pH range 8.8 - 9.2.Therefore, a pH of 9.0 ± 0.2 was chosen for thepreconcentration of these elements by coflotationusing aluminium hydroxide as collector and SO assurfactant.The optimum concentrations of collector andsurfactant required to obtain maximum recovery atpH 9.0 were found to be 50 ppm and 10 ppm,respectively. It was also found that a short time of3 to5 min was sufficient to bring about the completerecovery of all the six elements.For the simultaneous polarographic determinationof Cu(II), Pb(II), Cd(II) and Zn(II) in thepreconcentrated sample, addition of ascorbic acidwas helpful in overcoming the interference ofFe(III).It was also found that the peak current of copper wasenhanced by 45% in the presence of ascorbic acid.The determination ofNi(II) and CoCH)was based onthe dimethyl glyoxime enhancement of DPP peakcurrent". The enhancement in sensitivity was about12for nickel and 10for cobalt [att = 0.5 s].At a higherdroptime [t = 2.0 s],Jhe enhancement factor wasfound to be about 25 to 30.The effect of variation of SO concentration on theDPP peak currents of these heavy metal ions has beenstudied and the results obtained for Cu(II), Pb(II),Cd(II) and Zn(II) in a S.E. of 0.2 MKCl and 0.25%ascorbic acid are shown in Fig.2. It is seen that thepeak currents oflead and cadmium are not affected byup to 80 ppm SO. The peak current of copperincreased initially with increase in SO concentrationup to 40 ppm SO and decreased thereafter. The peakcurrent of zinc is not affected by up to 40 ppm SO butc'"....::Ju...o..n,o 20 6040 80 100Concentrcttcn of so, ppmFig. 2-Effect of variation of SO concentration on the DPP peakcurrents of Cu(lI), Pb(II), Cd(II) and Zn(II). S.E.: 0.2 Mpotassium chloride + 0.25% ascorbic acid. [Cu(lI)] = [pb(II)] =[Cd(I!)] = (Zn(l!)] = 0.4 ppm. DPP conditions: t = 2.0 s; t:,E = 50mV; It = 75 em; (0) copper; (D) lead; (t:,) cadmium; (x) zincdecreased above this level. The effect of SO on theOPP peak currents of nickel and cobalt in ammoniumtartrate buffer containing DMG was examined.There was no change in peak currents of Ni(II) andCo(Il) up to 40 ppm SO. A slight increase (5 to 7%) inpeak current was observed for Ni(II) and Co(II) at 80ppm SO. It was also seen that the SO present in thefloated sample did not interfere in the polarographicdetermination of these ions.The sensitivities of these ions under the Dl'Pconditionsused in thiswork [t = 2 s; 6£ = 50 illV;m =2.20mg/s and h = 75 cm]were 240, 130,200,290,5000and 5200 nA/ppm for Cu(II), Pb(II), Cd (II), Zn(II),Ni(II) and Co(Il), respectively. The detection limitswere lowered 50 times by using the combination ofcoflotation and DPP. Experimental values ofdetection limits were 0.6, 0.8, 0.4, 0.5, 0.2, and 0.08ppb for these six ions in the same order as given above.Synthetic water samples were prepared by adding 1, 5and 10 ug each of these metal ions to 200 mL distilledwater and these were analysed by the coflotation-Df'P method under the standardized experimentalconditions. It was found that the recoveries of theheavy metal ions were 95 to 100%.Flotations with anionic surfactants are generallysensitive to the presence of anions":". Usually. theflotation efficiency and the recoveries of ions areadversely affected by multiple charged anions likesulphate, phosphate and silicate. Natural watersamples often contain small amounts of anions likechloride, sulphate, silicate and phosphate. The effect250 INDIAN J. CHEM. TECHNOL., JULY 1994of these anions on the cofiotation has beeninvestigated by adding known amounts of anions tothe solution before coflotation using aluminiumhydroxide as collector and SO as surfactant. It wasseen that the flotation and recoveries of elements wereincomplete above 3 ppm phosphate and 5 ppm .silicate. Chloride, nitrate and sulphate could betolerated up to a concentration of 0.2, 0.2 and 0.05 M,respectively.Fresh water samples and sea water were analysedxusinz this cofiotation - DPP procedure. It was foundthat the values of relative standard deviation (RSD)for five replicate measurements were 2-3% and 5-7%for the recoveries of these elements from fresh waterand sea water, respectively. The samples were'acidified to pH' 2 with nitric acid and subjected toultra-violet irradiation for 4 h to destroy dissolvedorganic matter and analyzed by cofiotation and DPP,The results were found to be independent of thepresence or absence of the UV irradiation step. Thusthe total heavy metal content in the water samplescould be determined by this method,ReferencesI Hiraide M & Mizuike A. Rev Anal Chem, 6 (1982) 151.2 Mizuike A & Hiraide M. Pure Appl Chern. 54 (1982) 1956.3 Caballero M. Cela R & Perez-Bustamante J A. Talant a, 37(1990) 275.4 Kim Y S & Zeitlin H. Sep Sci, I (1972) 861.5 Bharathibai J Basu. Padma D K & Rajagopalan S R. Talanla. 38(1991) 1431.6 Torrance K. Analyst. 109 (1984) 1035.7 Gannon K & Wilson D J. Sep Sci Technol, 22 (\ 987) 2281.8 Huang S D. Wu T P. Ling C H. Shu G L. Wu C C & Cheng M H. JCall Interlace Sci, 124 (1988) 666.--------_._------- ------------------- ._- ------------

Preconcentration by cofiotation for the polarographic determination of traces of heavy metals in water

248-250<span style="font-size:11.0pt;line-height:115%;
font-family:" calibri","sans-serif";mso-ascii-theme-font:minor-latin;mso-fareast-font-family:="" "times="" new="" roman";mso-fareast-theme-font:minor-fareast;mso-hansi-theme-font:="" minor-latin;mso-bidi-font-family:"times="" roman";mso-ansi-language:en-us;="" mso-fareast-language:en-us;mso-bidi-language:ar-sa"="">Preconcentration by
coflotation is employed to improve the detection limits for the determination
of parts per billion levels of heavy metal ions such as copper(II), lead(II),
cadmium(II), zinc(II), nickel(II) and cobalt(II) in natural and sea water by
differential pulse polarography (OPP). Trace amounts of these ions in water are
coprecipitated on colloidal aluminium hydroxide and the precipitate is floated
with the aid of sodium oleate and a stream of nitrogen bubbles. Experimental
conditions are optimized to obtain maximum recovery of these ions by coflotation.
The effect of surfactant on the OPP peak currents of these ions in the
supporting electrolyte used in this work is studied.</span

Basu, Bharathibai J

Padma, D K

Rajagopalan, S R

NOPR

Preconcentration by coflotation for the polarographic determination of traces of heavy metals in water

Preconcentration by coflotation is employed to improve\ud
the detection limits for the determination of parts per\ud
billion levels of heavy metal ions such as copper(II),\ud
lead(lI), cadmium(II), zinc(II), nickel(II) and coba1t(II) in natural and sea water by differential pulse polarography\ud
(DPP). Trace amounts of these ions in water are\ud
coprecipitated on colloidal aluminium hydroxide and the\ud
precipitate is floated with the aid of sodium oleate and a\ud
stream of nitrogen bubbles. Experimental conditions are\ud
optimized to obtain maximum recovery of these ions by\ud
cofiotation. The effect of surfactant on the DPP peak\ud
currents of these ions in 'the supporting electrolyte used in this work is studied

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Preconcentration by cofiotation for the polarographic determination of traces of heavy metals in water

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