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HomeMy WebLinkAboutNC0004979_Interaction of Selenium_20040609imap://sergei.chernikov%40dwq.denr.ncmail.net@cros.ncmaiL t,et:143... Subject: Interaction of Selenium w/ Ferric or Ferrous From: John J Kim <jjkim@duke-energy.com> Date: Wed, 9 Jun 2004 10:21:03 -0400 To: sergei.chernikov@ncmail.net CC: Donald L Scruggs <dlscrugg@duke-energy.com>, Robbin M Jolly <rmjolly@duke-energy.com>, Ronald E Lewis <relewisl @duke-energy.com> Thanks for coming to Allen Steam Station. Sorry for not being able to be with you at the meeting. We have been using ferric ions ( in sulfate form) to reduce the selenium in our ash basin discharge. The exact chemistry of removal mechanism(s) is still not well defined. Because of that, the term, "coprecipitation" is used loosely to describe the mechanism. Ferric compounds such as ferric sulfate and ferric chloride reacts with water to produce hydrated ferric oxide species ( Fe3+ + nH2O = Fe00H.nH2O), which are referred to as "floc" in water treatment. As this solid floc starts to form and grow in size, it provides the large active sites for selenium to interact with. The removal mechanism can be both chemical reactions (iron -selenium complexes) and surface phenomenon (adsorption). The fact that the selenium removal efficiency is strongly pH dependent suggests the important role of the surface charge of these ferrihydrite solids. Good selenium reduction can be achieved under a slightly acidic condition (pH 3.5 - 5.5), The removal efficiency drops off considerably at pH above 6. At a high pH, selenium in solid particles leaches out. This is why we have high selenium levels in our flyash sluice water when we burn high alkaline coal. Selenium is present in natural waters as anions (oxy - or oxo compounds) and is soluble at any pH. As such, it can not be removed with pH adjustment alone (as the case of many toxic metal ions). Typically, selenite(Se032-) and selenate Se042-) are the forms of selenium present in our flyash sluice water. Selenite ions have a high affinity to the solid surface such as ferrihydrite, while selenate ions exhibits a higher affinity to anion ion exchange resins. So, it is advantageous to convert selenate to selenite for the iron coprecipitation process. Ferrous and ferric compounds are used in water treatment to remove the suspended solids. However, in our effort, we will be using ferrous ions to help convert selenate to selenite, or even to selenium element to some extent. We will be conducting a series of testing to find out the effectiveness of ferrous ions relative to ferric ions for removing selenium from the sluice water. Below are the equations describing the various reactions; Coagulation: Fe2+ + 2H2O = Fe(OH)2 (s)+ 2H+ --- Eq. 1 Selenate Reduction to Selenite: Fe2+ + Se042- + H2O = Fe3+ + Se03 2- + 2H+ + 02 -- Eq 2 Selenate Reduction to Elemental Selenium: Fe2+ + Se042- + 2 H2O = Se0 + Fe00H (s) + 3H+ + 202 --- Eq 3 Factors such as oxygen in water, reduction reaction time, temperature, coagulation time will affect the conversion. I hope this answers your question. Please, feel free to call me (704-756-0559) if you have additional questions or need clarification. 1 of 2 6/9/2004 10:31 AM imap://sergei.chernikov%40dwq.denr.ncmaiI.net@cros.ncmai1.net.143... 2 of 2 6/9/2004 10:31 AM Duke Power Company In -Progress Report: Emergency Response to Elevated Ash Basin Selenium Presented by: Robbin Jolly Allen Steam Station Belmont, North Carolina MCr the s U'S'A a .moi m � _� '7V JA - *71 lot •A, t - No hi ALI JYY fw� el -1 WIA L Vl� �07 - -,P- t" -14, 12 0'6 — 0'9 1!w!I 93ueilduao3 Hd uluoua/XZ aoinni poliodej eq ol qdd Le = livai� a�u�ilduao3 aS ZOOZ `AInr AlLiluow poliodej aq ol qdd LE: = }ivai� a�ueilduao3 aS 966L Apopenb poliodej eq ol qdd LE: = jivail aoueilduaoo aS V66 L Apopenb poliodej eq ol qdd 5-p _ jivai� a�ueijduao3 as 686L podaa pue aoliuoua Isn� `}ivail GS ON V86 L as joi ;uawaainbaa S3adN 31JOISIH 40.00 35.00 30.00 0. 25.00 .� E 20.00 15.00 75 as 10.00 (n 5.00 0.00 -5.00 Ash Basin Se Control Chart Jan. 2002 - July 2003 0 2 4 6 8 10 12 14 16 18 20 22 24 26 28 Sequence Number �- SPC Average LCL CL UCL Compliance Value 30 32 Ash Basin pH vs Selenium Selenium (ppb) pH 45 _ 40 � d` 35 30 25 ML 20 15 10 0 19 -Apr 29 -Apr 9 -May 19 -May 29 -May 8 -Jun 18 -Jun 28 -Jun 8 -Jul Date ■ Selenium (ppb) ♦ pH 12.0 11.0 10.0 9.0 8.0 7.0 6.0 5.0 4.0 18 -Jul 28 -Jul Recovery Plan -Stop suspected coal source. -The released selenium in the basin would have to be removed chemically: coagulate/floc/filter - Treatment would have to be in a controlled environment. - Treatment would have to go to the tower for blending um I *r— . 10 i i Allen Steam Station 3 2 1 0 0 5 10 15 20 25 30 Fe2(SO4)3.91- O Dosage (ppm) -20% as Fe 45 40 35 30 a 25 E 20 'c d m 15 cn 10 5 0 35 Initial Selenium Concentration 43 ppb Initial Solution pH 9.23 -- - -- Filtered after 5 min agitation upon addition of 15 ppm of FeCl3 61-12O (-20% as Fe) IVAa mol -uc m orc m 71C es eoorlal M 1 e1M® uaar lowr m-e�� 99 i� 'Mr. 1 n! 7 mW TMI D _4 ASH PMM ti rorc 11 11molm N.l 2a0 oe d &MALMY nvs va I eaw e A DW a a elvm mm wra p♦?IC � � a w 1 A 7�i 9A1(4 PUMP9 G W Rpm LI e1011 O 1 vw 0 a e LEGEM A Gem luffm Ke Q vnm nmr e IV am W" m� ® maroanca u 10 rzfm E 1112 i YOO•al A ml W2AIYi M 010! um1! 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Y �'_"v �•5.. �:A ��R _ `, ►',/Wy�: s1P+M Vii• � �1.:�-+ f. •. y�t'1 1 � •t i.) 1 � ' a « x� � • M MPC,. � `�"� * L � Vr ray 4� 6 x i' Ory � _ t .w� - +++."^$✓' .ro`" . �k J f F e L a m 1' 1 ` a + ; •hMIL t lowI " = 's-- - WN lk L r •` F _ ,�. �^E ;s,. ,... +';-,• ,. ,,,, .*'t }OM1 rev-�s.::_� as<� — - t xrytr - _ •nom •i4. • ' _,{ � `'? � y Yya.4 -� f� 'K-sab 3.� � �` .. a ., ,_ � } pS $ ��` � � 5. •F i } � ..ATL � or --o 4r f s � 7� .I r, — � r ou 9 s I ci • 3 uL �j���p,� •I� � $� '�k�jy�7P� p _ 70.0- '50,0, 0.0- 50.0- 40.0 - 3 30.0 20.0 10.0 Treatment Lines Selenium Limit = 31 ppb qgll .' y 0.0 2� �2'A op N e e e �0 Date --*.---Treatment intake ■ Line # 1 --s— Line # 2 —o-- Line # 3 Line # 4 Allen Ash Basin Selenium Results 60 ° 55 50 45 40 35 30 25 20 15 10 90 /° 85% 80% 75% 70% 65% 60% 55% 50% 45% 40% Fl