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A2Q for E12 Quantitative Determination of Total Total Ion Concentration by Ion Exchange Chromatography •
Ion exchange chromatography is a chromatographic science concerned ith the separation of various types of charged species in a s ystem! This system is usually comprised of separate phases! This method is founded on the concept of ion exchange beteen to principal sites " the mobile and the stationary phase! In the experiment# resin as used as the stationary phase! $n%non solution is passed through the resin to allo the cation to replace the & '()&* ions bound in the binding sites!
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+everal factors can affect ion*exchange! These factors include the surface area of the stationary phase ,resin bead si-e.# density of exchange sites on the stationary phase surface ,cross*lin%age.# flo rate of the mobile phase ,resin bead si-e and column geometry/ system pressure in high* pressure chromatography# chromatography# and the chemistry of the mobile phase ,ionic strength of the sample solution# concentration of mobile phase.!
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The resin as soa%ed in ater for an hour before introducing to the ion*exchange column ,improvised burette. in order to dissolve ater*soluble ater*soluble impurities and ioni-e the functional groups of the resin! 0resence of such impurities can bloc% off sites for exchange hich ill cause a maor problem! Through immersion in ater# the resin as alloed to sell leading to further exposure of the exchange sites! Dry resin cant be used because the exchange sites are still not open!
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3ater 3a ter level as %ept above the top of the resin to prevent the formation of air poc%ets hich may restrict access of the ions!
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+trong acid as needed to replace the bound ions in the resin! &ydrogen ion supply as also replenished through the process!
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It as crucial that the rate flo be maintained at 45 drops per minute to ensure that all copper , II. ions bind to the exchange sites! If the rate is too fast# an incomplete exchange process ill result and less Cu2' ill bind to the sites! If it is too slo# hoever# the process is deemed inefficient due to the increased amount of time needed to complete the procedure!
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The column as ashed until the eluates p& e6uals that of the distilled ater in order to ma%e sure that the & ' concentration is not affected ith the constant addition of ater in the experiment proper!
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The balanced reaction for the experiment is7
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0ossible sources of errors include inade6uate regeneration ith & ' ions hich may result to lesser than actual cation concentration! Incomplete exchange caused by faster flo or the trapped air poc%ets ill also yield loer concentrations! 8ailure to satisfy the p& e6uality at the elution phase ill yield to increase in cation concentration hile failure to satisfy p& e6uality in titration phase ill result to a decrease in cation concentration!
9E8E9E:CE+7 Dudas# 8!)! 2511! Ion Exchange Chromatography!;assachusetts Institute of Technology! oc!mit!edu! 3eb Dyer A!# &udson ;! 8undamentals of Analytical Chemistry# ?th Edition! +aunders College 0ublishing