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HomeMy WebLinkAboutNCD003446721_19900118_Celeanse Corporation - Shelby Fiber_FRBCERCLA SAP QAPP_Groundwater Monitoring - Analytical Data-OCRI I I I I I I I I I I I I I I I I I I Westinghwse Environmental and Geotechnical Services. Inc. January 4, 1990 U. s. Environmental Protection Agency 345 Courtland Street, N.E. Atlanta, Georgia 30365 ATTENTION: Ms. Michelle Glenn Remedial Project Manager 4000 DeKalb Technology Parkway, NE Suite 250 Atlanta, Georgia 30340 (404) 458-9309 FAX (404) 458-9438 SUBJECT: Request for Sampling Notification Variance Groundwater Treatment System Upset Evaluation Operable Unit 1 Remediation Hoechst Celanese Facility Shelby, North Carolina Westinghouse Project 4124-85-0S0H Document Control 85050H-202 Dear Ms. Glenn: During late December 1989, an increase was noted in the COD and ammonia-nitrogen of the inner tier combined influent. As a result, EPA was verbally notified on December 28, that an additional sampling of the influent would be made on January 3, 1990, to measure the influent quality and to try and identify the source of the COD and ammonia increase. During the period between December 28 and January 2, the SBR effluent quality continued to deteriorate, and microscopic evaluation of the mixed liquor on January 2 showed no biological activity. Thus, pumping of the inner tier system was suspended, and the sampling planned for January 3, 1990 was cancelled. The SBR was reseeded with about 2,000 gallons of municipal sludge from Boiling Springs, North Carolina, and Hoechst Celanese plans to restart the system on January 8, 1990. During our telephone conversation on January 3, Westinghouse requested EPA approval to waive the 48-hour sampling notification provision in the consent decree to have the flexibility to sample as needed when problems in the SBR are apparent. It was our understanding that this request was approved, but that written documentation of the request was required.· This letter constitutes our request for the sampling notification waiver. As with the routinely scheduled sampling, EPA will be provided copies of all data. 5050H171 A Westinghouse E!ectric Corporation subsidiary I ··~ ·, . ·• I I I I I I I I I I I I I I I I I I Request for Sampling Notification Variance Groundwater Treatment System Upset Evaluation Operable Unit 1 Remediation RC/Shelby, North Carolina Facility Westinghouse Project 4124-85-0SOH Document Control 85050H-202 Page 2 Based on our understanding that our request was approved, Hoechst Celanese plans to implement daily COD monitoring of the SBR influent at the equalization tank and at a point between the metals precipitation unit and the SBR. This monitoring will be in addition to the daily COD monitoring presently performed. In addition, other types and frequencies of both operational and investigatory analyses may be performed as needed. The results of these analyses will be reported in the normal format. We are initiating the expanded sampling and analysis program with the restarting of the SBR scheduled for January a, 1990. If we have misunderstood your tentative approval of our request, please contact us immediately. If we have not heard from you by January 10, 1990, we will assume that you are in agreement with our request to waive the sampling notification requirement on an as-needed basis to investigate operational problems within the treatment system. Thank you for your timely consideration of our request. Very truly yours, WESTINGHOUSE ENVIRONMENTAL AND GEW\Ec[rL ffl;;Es, INC. M. Kirk Mays, P.E. Senior Environmental Engineer C.a (.l;_,\.J.._t/:. lU bf!.eciu-, , ~ Everett W. Glover, Jr. P.E. Project Manager MKM/EWG/pys cc: Ron Caldwell-RC/Shelby Bill Carter-RC/Shelby John McBride-RC/Shelby Archie Pittman-RC/Shelby 5050H171 Jim Pullen-RC/Charlotte Jack Kelley-RC/Shelby Terry Atkins-RC/Shelby earl Burrell-Davis & Floyd/Grnwd I I I I I I I I I I I I I I I I I Westinghoose Environmental and GIIIIEchnical Services, Inc. January 5, 1990 U. s. Environmental Protection Agency 345 Courtland Street, N.E. Atlanta, Georgia 30365 ATTENTION: SUBJECT: Ms. Michelle Glenn Remedial Project Manager SBR Operational Evaluation Hoechst Celanese Facility Shelby, North Carolina Westinghouse Project 4124-85-050H Document Control 85050H-203 Dear Ms. Glenn: 4000 DeKalb Technology Parkway. NE Suite 250 Atlanta. Georgia 30340 (404) 458-9309 FAX (404) 458-9438 As generally discussed in our Document Number 85050H-202, dated January 4, 1990, there have been additional problems maintaining adequate'biological activity in the SBR. Thus, Hoechst Celanese is initiating a study to look more closely at the conditions occurring in the SBR, and at the historical conditions that occurred prior to and during the times that the SBR biomass died. This study will be a collaborative effort between Hoechst Celanese, Westinghouse and Davis and Floyd, Inc. Davis and Floyd, Inc. designed and provided consulting services on the operation of the wastewater treatment plant for the Shelby facility and is very familiar with biological treatment of textile wastewaters. In addition, Davis and Floyd's laboratory QA/QC manual has already been sent to EPA for review since they provided analytical service for the RI and are a secondary source of analytical support for the remediation. A general description of the tasks involved in the study will be provided to EPA when it has been compiled. 5050H172 A Westinghouse Electric Corporation subsidiary. I I I I I I I I I I I I I I I I I , SBR Operational Evaluation HC/Shelby, North Carolina Facility Westinghouse Project 4122-85-0SOH Document control 85050H-203 Page 2 If you have any questions about this letter, please contact us. Very truly yours, WESTINGHOUSE ENVIRONMENTAL AND GEOTECHNICAL SERVICES, INC. ~ ~ fvt~s M. Kirk Mays, P.E. Senior Environmental Engineer 'G,lu__,_,_Jf_ U), ~tkt ,~ Everett w. Glover, Jr. P.E. Project Manager MKM/EWG/pys cc: Ron Caldwell -HC/Shelby Bill Carter -HC/Shelby Jack Kelley -HC/Shelby John McBride -HC/Shelby Terry Atkins -HC/Shelby Archie Pittman -HC/Shelby Jim Pullen -HC/Charlotte Carl Burrell -Davis & Floyd/Greenwood 5050H172 - - - - - - - - - - - - - - - - --.- '---CJ> E ..... C Q) ::J .._ C 20000 18000 16000 14000 12000 10000 8000 6000 4000 2000 0 8/1 Inner Tier Influent vs. SBR Effluent Daily COD 10/1 ~ Influent 12/1 -8-SBR Effluent 20000 18000 16000 14000 12000 10000 8000 6000 4000 2000 '---CJ> E ..... C Q) ::J .._ .._ w 0::: m (/) ------------------- "-CJ' E ~ ~ C (I) :::, -C 14,000 12,000 10,000 8,000 6,000 4,000 2,000 0 8/1 Inner Tier Influent vs SBR Effluent Rolling Weekly Average COD 14,000 12,000 10,000 8,000 6,000 4,000 2,000 '-----------+----------'------+ 0 10/1 12/1 1 /31 Week Beginning --¼ Influent -8-SBR Effluent ~ "-CJ' E ~ ~ C (I) :::, --w Ct'. (I] (f) ------------------- '--CJ) E -C (I) :, ,._ C 100000 10000 1000 100 10 Inner Tier Influent vs. SBR Effluent Doily COD 100000 10000 1000 100 10 1+----------+-----------+----------+1 8/1 10/1 12/1 1/31 -Influent -0-SBR Effluent '--CJ) E -C (I) :, :::: w Ct'. m (f) ------------------- ~ '--CJ) E ~ +-' C (I) ::J -C 100,000 10,000 1,000 100 Inner Tier Influent vs SBR Effluent Rolling Weekly Average COD (;) rfi 100,000 10,000 1,000 100 10-----------t----------+------------+10 8/1 10/1 12/1 1 /31 Week Beginning --¾--Influent -0-SBR Effluent ~ " CJ) E ~ +-' C (I) ::, --w Cl'.'. m Cf) ------------------- --..._ 0, E ~ C (l) :J (.'.) 0 _J 4.50 4.00 3.50 3.00 2.50 1.50 1.00 Inner Tier Influent vs. SBR Effluent Daily COD 4.50 4.00 3.50 3.00 2.50 2.00 1.50 1.00 0.50+------------+-------------+----------+0.50 8/1 10/1 12/1 1/31 ---lf-Influent -0-SBR Effluent ~ C (l) :J 0 0 _J ------------------- ~ ~ '--CJl E -C Q) :, -C ~ <..'.) 0 -' 4.50 4.00 3.50 3.00 2.50 2.00 Inner Tier Influent vs SBR Effluent Rolling Weekly Average COD Cl (.') (.') I;) & G'.l V G') el ' I;) ' ~ 4.50 4.00 3.50 3.00 (';J ~ 2.50 2.00 1 .50 +------------+-----------+-------------+ 1 .50 8/1 10/1 12/1 1/31 Week Beginning -lt-Influent -0-SBR Effluent ~ ~ '--CJl E ~ -C Q) :, --w Ct'. m (/) ~ <..'.) 0 -' I I I I I I I I I I I I I I I I I I I Westinghruse Environmental and Gootechnical Services. Inc. January 18, 1990 U. s. Environmental Protection Agency 345 Courtland Street, NE Atlanta, GA 30365 ATTENTION: Ms. Michelle Glenn Project Manager • ----~-; ~ .... 4000 ~Kalb Technol;;gy Parkway. NE Suite 250 ·· 4.:: . / / ,.: !':- Atlanta. Georgia 30340 / . · / ,. ,· · 1 -, (404) 458-9309 '"""· :~ti,·~-.. 1 • FAX (404) 458-9438 • IJ SUBJECT: Request for Sampling Notification variance Groundwater Treatment System Upset Operable Unit 1 Remediation Hoechst Celanese Facility Shelby, North Carolina Westinghouse Project 4124-85-050H Document control Number 85050H-206 Dear Ms. Glenn: During the past two months there have been sharp periodic increases in COD and ammonia-nitrogen of the the inner tier combined influent and in the same period of time, the SBR has died twice. Hoechst Celanese believes that there may be some connection between the higher strength waste and the problems associated with the SBR operation. During a telephone conversation on January 3, Westinghouse requested EPA approval to waive the 48-hour sampling notification provision in the Consent Decree to have the flexibility to sample as needed when problems with the SBR are apparent. EPA has requested Hoechst Celanese to detail conditions under which the 48-hour notification waiver would take effect. After a review of historical water quality data on the inner tier, Westinghouse feels that the SBR may be impacted when any of three conditions occur: the influent COD exceeds 4000 mg/1, the influent ammonia-nitrogen exceeds 5 mg/1 or the SBR effluent COD exceeds 400 mg/1. Hoechst Celanese would like to waive the 48-hour notification when any of the above conditions occur. So additional investigate and operational analyses can be performed. In the event the 48-hour notification is waived and that additional sampling is indicated, EPA will be notified verbally no later than the next business day. 5050H174 A Westmghouse Electric Corporation subsidiary. I I I I I I I I I I I I I I I I I I I HC/Shelby RD We_stinghouse Project 4124-85-050H ·15ocumem: Control Number 85050H-206 Page 2 If there are any comments or questions concerning the information contained in this letter, please contact us immediately. If we have not heard from you by January 23, 1990, we will assume that you are in agreement with our request to waive the sample notification requirement as outlined in this letter to investigate operational problems within the treatment system. Very truly yours, WESTINGHOUSE ENVIRONMENTAL AND GAATiJJC~V;CES, INC. M. Kirk Mays, P.E. Senior Environmental Engineer (o{;»J}JW ~ ·f- Everett W. Glover, Jr. P.E. Project Manager MKM/EWG/pys cc: Jim Pullen-He/Charlotte/ Bill Carter-HC/Shelby John McBride-He/Shelby Carl Burrell-Davis & Floyd/Grnwd 5050H174 Ron Caldwell-HC/Shelby Jack Kelley-HC/Shelby Terry Atkins-HC/Shelby Ken Mallary-EPA/Atlanta I f' I I I I I I I I I I I I I I I I I . Westinghwse Environmental and Gllllechnical Services, Inc. January 18, 1990 u. s. E\ivironmental Protection 345 Courtland Street, NE Atlanta, GA 30365 Agency ATTENTION: SUBJECT: Ms. Michelle Glenn Project Manager Davis & Floyd, Inc. Groundwater Treatment System -Investigation Operable Unit 1 Remediation Hoechst Celanese Facility 4000 DeKalb Technology Parkway. NE Suite 250 Atlanla. Georgia 30340 ,.__ (4041458-9309 J, rf,\X 14041458-9438 ·,_ ,I" r, , .' tr_, .. I <~-"tvJ.~; I :t l Shelby, North Carolina Westinghouse Project 4124-85-050H Document Control Number 85050H-208 Dear Ms. Glenn: During the past two months, the SBR has died twice. Additionally, prior to the deaths of the SBR there have been sharp rises in the COD and ammonia-nitrogen. Hoechst Celanese believes that there may be some connection between the higher strength waste and the problems associated with the SBR operation. To ascertain the nature of the problem and possible solutions, Davis and Floyd, Inc., a wastewater consultant, has been hired by Hoechst Celanese to conduct a study. Davis and Floyd Inc. has proposed a study which includes an investigation of plant operations, an examination of the sources of the high strength wastes, and a better understanding of the groundwater treatment operation. The study proposed by Davis and Floyd, Inc. would examine the following areas related to the inner tier: 0 0 The influent would be screened with Polytox tests to see if Phenobac may enhance biomass activity. The SBR sludge would be analyzed for antimony, chromium, lead and zinc to examine if bioaccumulation of toxic materials may be occurring. 5050H175 A Westinghouse Electric Corporauon subs1d1ary. I r I I I I I I I I I I I I I I I I I HC/Shelby RD Westinghouse Project 4124-85-0SOH Documenc Control Number 85050H-208 Page 2 0 0 0 0 0 0 0 0 0 Oxygen uptake tests would be conducted on the SBR mixed liquor and the individual wells. The information would address biomass toxicity associated with the SBR and individual wells. Micotox bacteria would be used to screen individual wells and combined flow for toxic materials. During the project, the biomass would be examined daily to determine biomass makeup and relative condition of same. Davis and Floyd, Inc. would examine the benefit in adding a coagulate to enhance solids separation in the SBR. The study would examine nutrient loading to the SBR and current operational practices. Davis and Floyd, Inc. would determine the proper nutrient level and required supplemental feeding schedule. In addition to the current analyses performed, the inner tier extraction wells would be analyzed for phenols, sulfate, and antimony. An indepth evaluation of the groundwater treatment plant operations, individual well performance and monitoring system would be part of the study. The study may include additional operational guidance that may be added as a supplement to the Project Operations Plan. Davis and Floyd, Inc. may include a section on operator training as Hoechst Celanese feels that hands-on operator training may be required. The Davis and Floyd, Inc. study would take approximately two months and would include the additional sampling detailed above. The proposed sampling frequency, sample points and parameters to be analyzed are listed in Table 1. 5050H175 I I I I I I I I I I I I I I I I I HC/Shelby RD Westinghouse Project 4124-85-0SOH Document Control Number 85050H-__ Page 3 Hoechst Celanese would like to proceed immediately with the testing program outlined in this letter. If there are any comments or questions concerning the information contained in this letter, please contact us immediately. If we have not heard from you by January 24, 1990, we will assume that you are in agreement the testing program and that we may proceed. Very truly yours, WESTINGHOUSE ENVIRONMENTAL AND GEOTECHNICAL SERVICES, INC. M lti 'MCUJs M. Kirk Mays, P.E. Senior Environmental Engineer (o~ [D t)kw_{ i Everett W. Glover, Jr. P.E. Project Manager MKM/EWG cc: Jim Pullen-HC/Charlotte / Bill Carter-HC/Shelby John McBride-HC/Shelby earl Burrell-Davis & Floyd/Grnwd 5050H175 Ron Caldwell-HC/Shelby Jack Kelley-HC/Shelby Terry Atkins-HC/Shelby Ken Mallary-EPA/Atlanta I r I Table 1 Proposed Salll)l ing & Frequency Equal. Pl ant Tank SBR SBR SBR SBR I Parameter Frequency Influent Effluent Influent Tank Effluent Sludge ·······------------------------------------------------------------------------------------pH Daily X X X loo Total ,: Soluble IH3-N Phosphorous lotal Kjeldahl N 1 trogen litrate Nitrogen Oxygen Uptake lettleable Sol ids Sulfate lhenols -ss ron Total Iron Soluble Antimony Total lntimony Dissolved lopper Total opper Dissolved lhromil.111 Total Chromil.111 Dissolved lead Total Zinc Total line Dissolved I Daily lleekly 2/week 2/week 2/week 2/week 2/week Daily Daily 2/week 2/week Daily 2/week 2/week 2/weelc 2/week 2/week 2/week 2/week 2/week 2/weelc 2/weelc 2/week X X X X X X X X X X X X X X X X X X X X X X X X X X X X X X X X X X X X X X X X X X X I I I I I I I I I I I I I I I I I I I 114 TRANSMITTAL MEMORANDUM ___J,_ Date: -~ /"'"='Ft .... r➔1;1r,-: :.7t." :'"-,-,,.. ~•,, ~ Attention: ///,-_. Client: Cl Westinghouse Environmental and Geotechnical Services, Inc. Suite 250 4000 DeKalb Technology Parkway. NE Atlanta, Georgia 30340 (404) 458-9309 FAX (404) 458-9438 Per Your Request For Your Information/Records For Your Approval/Comments For Your Review/Comments Revise and Resubmit Approved as Noted Resubmit for Record Copy Approved Please Return Returning to You For Correction Not Approved ' ..,_ ,,.. ,. , , , ' , I I' t,,! , .. ,._ -. .{ r, i i.nL I ' I I I I I I I I I I I I I I I I I I ; 1t4 • • TRANSMITTAL MEMORANDUM J_ Date: :)1-z./,;.o f..:.TLAN \H (-r,1...--.-I.. ':;.Cc, S Attention: I,. I\ , 1 •~-, ·..: ,:..,_....,J;10::. ~Ir,.\ lo.v• -.J Job No.: -1-,2.,:;. _ ?"' _ c,s-r,,-/ Client: /Jin~. Jc· f;;aeE-rr lu-0Lovert-,J.·. C ·C. l'_.,,_ (',,__(} dwell µ' / 5 /.,__( l, /1 j {_(!(_( t ... .w_ J._~~·m., I.-...... !ff' I" •(, I ~ c> ..,_, , (i0,U' ... Cr-.,, T.r-<-H( /!>t,,,_( 1.,. / /'-' ✓- 1 __ ,r, c!:... 1(,(_(_..,.)--/>~j.~J...( i,,_ V I __ ,, (,.__," 1-( c.12, t.Ac!, , '-'<-/'-;.,_f._ 1., ",r \ \ e Westinghouse Environmental and Geotechnical Services. Inc. Suite 250 4000 DeKalb Technology Parkway. NE Atlanta. Georgia 30340 (404) 458-9309 FAX (404) 458-9438 Per Your Request For Your Information/Records For Your Approval/Comments For Your Review/Comments Revise and Resubmit Approved as Noted Resubmit for Record Copy Approved Please Return Returning to You For Correction Not Approved ,_ (./,,_ ( &,, 1 /.IC / (_j.c,J..,., 1-k. ,~>--M, ,~~rlt.,.1.,,i 1-tc.//:,,_,~•·'~'--1'-r,f; .... ,.::..~ i_-:,, .._,1___U '! I I PHENOBAC1 Microbial Hydrocarbon Degrader FOR USE IN: Indll!lri:il 1111d mo.aufacruru:a hydro=boa waste di.scllaraas. sucb. lS, che111!co.l placta, steel mllla, !utile :u,.d rood proceSSU1g pla.acs. ngscgrmoN PHENOBAC hu beH aciectifiC3lly designed tor biO-allplCDIAd011 oC laduattlal and m11111faetur1D1 hydroc:arboa waste diaclw-ses, For pretreatment or complete oa•slto trc111.meac ayacems and la mllllicipal syiccma recolviq mixed w11&1ewatcr from coiamualcy actlvicles, Wuce, with a attons or1anlc co1111nt aad blah .BOD may coo.cu various level, of blologlcally roalataiit quasl,toxlc and 10JCio compoUDda chat Interfere with 110rmd opefflt!o11 of w:iatfl'N:ltor ttontmea.c ayscema, Blomua ollhucemD'III widl PIIENOBAC wW enable tbe tteo.tmeiu aystcm to etticieatly, ll!ld o!ectively deande organic wucea that coo.WA complex orp.aica, aucb u phenols. beazeaea, allphedc and aromatic hydrocarbons, me1~cryl11e1, ultrllcs, Gl'cosols. aapthaleau, IIIIWIN, organic alcoboll, ayntbotlc detcr~n!$ and 1W'f11clllllt1, go.aollna, kerosene, Nol 111d machlao olla, formaldehyde. iij'COla, hc1erocycio1 auch as morpbollno and pyridlna, ctboxylated phenols, WllXCS 111d ocher difficult 10 crut compo1111da. Cy:lllides 11e biologlcolly removod Crom 1oh1tio11. P'OR.M COLOR SPl:?CtFIC GRAVITY CONTENI'S STORAGI! CAUTION PRQQYCI SP!CJFJCA'flQN!i : Frce-Howill1 powder : Bull to brown : o.s · 0,7 : Adapted micrcx,,g:iaiuu1 111d ~II atlmulADIS : Store 1caJcd In a dry Alta 11 rOQffl temperature not excoodlng 100 dogroe1 P. DO NOT AI.LOW PRODUCT TO Bl!COMB WET OR MO(ST PJUOR TO USE, DO NOT FRE!E!ZE. : loh41atlon o.nd direct skin contact should be avoided. 01111 protocdon for eyes, 11osc and mouth should be used. In the ovcat of direct concoct with the 1kia or eye,, Dush the affected o.rea with wncer, If irri111tio11 pel'liill, coo.tact your ph)11Ci4D. Q(BECTJQNS fQB USE 1. Ol&pcm 01111 !)Mt PHENOBAC la elibt 10 ten parta W1ll1D wutor, (about 0110 po1111d per 1allo11), The water sbould be about 80 • 100 degrca P. Allow to 11111d tor C•IIC to two houri with ocwlolllll lti.rriq. 2. Do oot add PHENOBAC to enc cre11tme11t system 11 a locatlo11 where 10,cic or otherwiH adveno pH, dlssolvcd oicyae11 or te111per11turc co11dltlo111 m11y exist Al peak lovcla, 3, Applica.tioa R11tes: Co111ult your Polybac rcprcsc11tatlva prior to uso tor specific lnstructlo11,. ~-For appllc:i.tlo11 011 ,pill&, u~ your Polybac ropresentotivc for o deuliled appllcotion prorram, $. In mil.lly cnae1, PHENOBAC ls best 11aod In combination witb oi;hor 11utricn11, aolvcnt 5)1toma or other biocbeadcnl&. Camult your Polyb3c repreaeat3tivo with your req11irem$ntl, For optima.I rosult& the w.a.stcwatcr tru1mco1 system should meet tho rollowlng condition,: lnlluont pH Oluolvcd oxygon, ppm C/N/P rnda Tempcr11turc, C degrees Toxic metal&. pp~ ( e.g., bCJC., cluoqiium) OPTIMUM 7.0 2.0 .. 100/10/1 30(861') 0 MINIMUM 6.0 1.0 100/S/l 10(,0 I') 0 MA.XlMUM 9.0 ... 100/20/1 40(104 F) 2 •\, __________ _ ·,,, ,, ...... · .. -, ~1 '8 .. :rm ---L ,.u c1r-1 ..,J -~ ·t. ·C C 1--1 ,' ,_, /,-. . 7 I ' I I I I I I I I I I I I I I I I I I 4YAIY:DJLO:X 25 lb. plutlc pails &Ad 100 lb. polyethylcnc•IIDed &bar clruma. BJQMA.V JNQJNEEBJNO Bio111w Engineerilla; by Polybac Corporuioa Cllll ao1vc )'QIII' bloloaical waste ueatmen1 problew. Biomass Eopnccriilg combl.aea btocliemical procesa eqwerlng with the uu of ,poeialized adapted mkroorglJllsma. TbJa ia a powGrill1 combi.aation for i,olvlng oporaling problem ill blological waste~or ttolltlDOU plama IIAd blologiC41 waste dlaposal sys1ema. Cllll on Pol)1)ac: tor a detailed Blo111w Enginoorlng propow for your plant. ' QISCL\JMJB Thia io!ol"l!lation is representative only 111d 'dlere are 110 warr1111tlc:1 of pcrforma11co, expreued or lmpllod. Polybac Corporlllion baa ao control over 11orap, lwidllng. or product applic:itloii oocdldoaa, thorofore, Polybac Corporatloii alaall 110t be liable for. da,uget ot 111y kilid uwn1 fro111 th• prcaonco or IIIO ot !he prodllW deceribod. ' PHENOBAC LI maau!acturcd and dlstribu1ed oxcluslvely by Polybac Corpor1tio11, ~S4 Ma.rcon Blvd., AlleotOWII, PA. 18103. U,SA 1988. •Material Safety Data Sheet Mil;Y be' usild ta oamply with OSHA's Hazard CcmmunlClllon 814ndard, a29_~FR'1ij10.1200. Sllndll'CI muet bt r:1,:utttd for speclftc requtremenll. U.S. Depairtment of Labor Occup1tlon1I Saluy and Ht1lll1 Admlnlstmlon (Non-Malldatorv Form) Form Appro'ltd OMB No. 1:na-0012 N«tl Sllnk ,,._ .,,, nor ptlffl/ll9d. I/ IIIY "9111 ii ,,,,,, _.._ /Ir flO /nlamNIIIO,, Ir 1vf/l&Olt. rhe 1pac. muat t>f mlnl9d lo fnlllOI» C'llr. Man11lecw,er'1 N11M ~llAC C0IPOU'l'I0lf ~• (Numbtlr. ._ C#J,, ltlll. -ltl' OOdt) 3894 Coqrtue• Street lech.lehea, PA 18017 Eton 11 -Hazardous lngrcdlent&lldentlty lntormauon l!mar;er!O'f Ttlt~ Numblt (215) 1367-733R Teiepnont NUll1IW for tnfOrmlllOn C2U' 1!67-7338 er MW1d0Ue ~ (8pe,;diO Cl,tmlcll '4tnllty; Common Name(II)) 05HA PIL ACGIH nv llecommtnatcl ~ bazardou1. Misad b:lochemj,call, euzm,1 aod 111rfac:tauts ou bran baH, t----~-------- 1=--------------------~----------------------------------1----------------- t= ___________ _ Eon Ill -Physfcal/Chemlcal Characte11stlca Bollin, Pcint f Pt-19 (mm H9,) v.ji;' Ounslty (Al~ • 1) ufu,i Fl,. ano l!,cpjoslOII ~ H A co Bt'OWll Color; llu1ty Odor. 0.5 -0.7 IA NA I Se<:llon V -Reae1lvlty Data ~lal:<11\Y • l Unstallle ! , , SWIii I 1 i;;ec,mcallblllty (Mlltr/1/a to A~old) Water D01'0Tffl. Ha.tan:10"1 Decgml)Ofil!Otl or S~ 1 ::=:... 1:: .... I ,f .. -·- 1 SG¢t!On VI -Health Hazard Dita AO<Jte(I) of int,y: w;ii\Gif 81dn? I Duat .A.void direct sld.sl contact. Hoellh H&Uldl ,_ MO Chronic) _ Vash bands with 1oap and water after ba'lltlU.ngs noid d1rtct •kin 1.sooucc; all■rgic ea;::u,ogonlotly. s•actiou co euzp1 111,ay oceur 111 hYpenaa,ttiva illlliv1dua11. I NIA NTP? IARC MorioQrapnl? 'tl/1 I/A sl;,,s and Symptoma al ~,. I It Mec!lcal CcnclltlOnl I ~ltrwlly "WnlYlltcl 11v &,pccl\ll9 ladividuals llypsrallargic to ea.zymea or other related prote1A1 _ 9hould a~ t,•n41t, emergency &nCI P1'00IOUNls Wash hai!sJ• With tW and vater after handl:l.ng; a-,otd diraet skin l..5.Sata9t or tahalatiop; a1lorgic raacti99• may oocyr in h:z:perseaait1vc 1ad1v1d9l1, Section VII -Pl'ICluttona for Saft Handling and Use I StePS tD e, Tlkllll In Cua Mltlltll " rn 0, ·~Ued SHISP yp/coll~ct1 avoid direct rkta copcact w/or --~ii:-oc;t inhalation of dupe. I Wastt Ol"f'OSII MtthOd No fpaeial dispgaal method. May ba sewered; compatible vitb all lcnolm I t,iologic;al tr■acmept ■atbods, Procautlont to St T8kon ill Handling Ind eioiine I c:011tacc, ~ .. , Preca\1110n1 Llep dry ud •t ro0111 ce111paratura. Avoid direct ak111 pq pot :t.pgast. Avoid dupt 1 Wa11h bands •rith soap and veter af'ter use, I l'p,Uviduals hYpJ[IS9f1tiva 11;:;ctlon VIII -Control Measures AO';plralOt'f l'rocec,IQn ™ $.) I Tes, Fe;,ulatlon LOOal !Niau• ta■ to e0~3•• or o~hei:-Tllat,ad prota1ua 1hould 11ot bandle. eur,rical uak or eciuiva'laut. s~;a1 O!lltt· I !)'t Protto1l0rt f•s (Dust) Ott,., Protect,,,. Clolft1r19 or &quopment I Dyftiug protection •. ~-ri</~yg1en1c P'ract•~• Do got ipge1t. Avoid dust. Wash baad.:J with so~p and water afteT lllle. •• Po99 2 1 3 : 1 1 FEE:-1. 5 -·=·· .. :1 I I nEPA f I I I I I I I I I I I I I THU B 19 POLYBAC CORP Unitttd Statn en"ironm4ntal Proitetio" AQoney Wa1■r Office ot wnor WHhin9ton OC 20-460 F'A E?A 4-10/4-87-00S July 1987 Permit Writer':s Guide to Water Quality-Based Permitting for Toxic Pollutan1ts * ~he National Discharge Eliminatinn System (~?DES) per~its program has begun to focu~ regulatory attention on the control of toxic i>ollutancs to protect water quality. Recent pesHaqe of amendments to the Clean Water Act and the acqu!s!tion o! increasing amounts c~ data on the ccxicit~ of eff~uent~ point to the need for an increased effort to control the d~scharge of toxic µcllutants. The P~rrrd:. Wri1:cer',c1 (;l.lidCJ to Wqt.:!1 ~)iAUZi,::-1-aa,-.:ed P~rmitting fer Toxic PoZlwtantc• provides procedural recommendations to State and feder<1l NPDI::S permit writers on setting water quality-based permit limits for toxic pollutants. In Appendix c of the guide, the ''Overview of Selu~tea Available Tools", summarizes sCJmc of the important tools that can be used to identify and control unacceptable toxicity in effluents. On page C-3, listed under MICROBIAL TESTS, POl,Y'l'OX is recommended as an inexpensive tool to test foe effluent toxicity. "EPA document 440/4-87-005, July 1987 ---------------------- I I I I I I I I I I I I I I I I I I I 1=-E.B-15-·:=,~-::::1 THU 8 18 POLYBAC CORP PA rl POL YfOX"' RA.PIO TOXICITY TEST TECHNICAL DATA SHEET FOR USE IN: Determining the biological dccomposibility or to,icity of wastewater lo a sewage lrealmenl facility, DESCRIPTION POL'\TOX,. i.~ a blend of spcciali1.cd microbial cultures in an casy•to•use kit, designed to provide a simple, rapid test for measuring the lmcicity of wastewater to biological systems within 30 minutes, without the use of expensive instrumentation. WASTEWATER TREATMENT The biological processing of organic waste in industrial and municipal wastewater streams has long been known. Although these biological systems typically utili,c microorganisms to effect biochemical decomposition of the organic waste, the processing plants may differ in the method in which the microorganisms are cultivated, A variety of test procedures have been developed for analyzing the quality of sewage for the purpose of determining the toxicity of the sewage, for determining the total chemical content in the sewage, and to determine the oxygen consumption rate of the microorganisms in that sewage. By and large, many of the analytical processes have involved the utilization of complicated equipment or have taken a substantial amount of time in order to complete the test and obtain meaningful results. In many cases, because of the time required to obtain the results, sufficient time has not been provided to take the appropriate action with respect to the handling of the incoming sewage, As a result, the plants in many cases were rendered inactive. AD auractive solution to analY7.ing the quality of waslcwalcr is POL'\TOX,.. This process is capable of providing analytical information with respect to the toxicity of iricoming sewage to a waste disposal plant, the quantity of organic component in the sewage, and the type of t,,xic matcrfal in a particular system in a quick and efficient manner. By utilization of a specially prepared bacterial culture and thi,ough the measurement of dissolved oxygen content, one can achieve ,several advantages which have not b,:cn available with prior processes. Some of these advantages include: -· a rapid biological lest for determining the loxicily of a wastewater sample •· a rapid, reproducible, biological test for determining the toxicity of a specific chemical as a function of its concentration in water •· a rapid method of assessing the toxicity of acidic or basic solutions of various specific chemicals, and organic and inorganic compounds lo bacteria ·· a rapid method of determining the effects of pH, temperature or a dissolved gas such as H2S, NH3 and CO2 on bacteria PQLYJQX,.: •· Is EPA recommended •· Is free of nitrifying microorganisms ·· Has been marketed since 1984 •· Is sold around the World •· ls always a stocked item •· Orders are shipped within 24 hours of receipt -· Is backed by a money-back guarantee or rcplaccmcnl if nm completely satisfied COURTNEY Pl.ACE.:• J8,4.COURTNEY STREET• BETHI.EHEM. t•A 18017-89,9 • {21S) 867•7:lJB I I I I I I I I I I I I I I I I I I THU POL"•,·"E:AC CO F: P F"A SPECIFICATIONS : Buff to brown. Form Contents Container Storage Expiration Caution : 8.0 grams of a specialized blend of microbial cultures, grOWth stimulants and pl I buffer. : Polyfoam mailer containing 20 clear, polystyrene vials. : Store scaled in dry place al room temperature (20'C), Do not free1,e or refrigerate. : For best results, use within three lo six months of receipt. : Avoid inhalation and contact with eyes, skin, and clothing. Wash thoroughly after handling. In case of contact, immediately flush eyes with plenty of water for at least 15 minutes. Call • phy.;ician. Flush skin with water. Wash clothing befmr: reuse. DJRECTIONS FOR US€ POLYTOX"' is a granular, free-flowing, dehydrated powder which must be rehydrated bdurc use. Du not allow POLYTOX"' to become wet or moist before use. Always store in a dry area, preferably at room temperature (20•q. Do not store in a chemical cabinet. IMPORTANT: For best results, toxicity tests should meet the following conditions: Sample Pretreatment Parameters pH Dissolved oxygen, ppm Temperature,' C Toxic metals, ppm (e.g., hex. chronium) PACKAGING 20 vials/unit OTHER LABORATORY PRODUCTS function Optimum 7,00 8.00 20 0 BOD Seed Inoculum ~~ 6.50 7.00 18 0 ~ POLYSEEo@ POL YSEED-NX® NITROSEED-ST"' CBOD Seed Inoculum -Inhibits Nitrification Toxicity Test for Nitrifying Microorganisms BIOMASS ENGINEERING® Maximum 7.50 9.00 22 1 Biomass Engineering by Polybac Corporation can solve your biotogiicat waste treatment problems, as well as your analytical test problems. Biomass Engineering combines biochemical process engineering with the use of specialized microorganisms. This dual approach offers enhanced prohlem solving capahilities to biological wastewater treatment plants, remedial spill clean-up sites, and analytical testing laboratories. Polybac's personnel are trained and experienced. Call on Polybac's pcrsor. nel fm a detailed Biomass Engineering proposal for your plant or to enhance your analytical testing. »ISCL4.IMER The information presented in the Technical Dara Sheet is believed lO he accurate and reliable. This information is presented as representative only and there arc no warranties of performance, express or implied. Since Polybac Corporation has no control over storage, handling or application conditions, Polybac Corporation shall not be liable for damages of any kind arising from the presence or use of the products described. POLYTOX"' is manufactured exclusively hy Polyhac Corporati,m, Courtney Place, 3894 Courtney St., Bethlehem, PA 1R017-R99Q USA. 1990. I I I I I I I I I I I I I I I I I I I Yj APPLICATION. PROCEDURE POLITOX" RAPID TOXICITY ~rEST PROCEDURE BACKGROUND ln 19n, the United States .Clean Water Act declared a need to regulate the discharge of toxic pol- lutants into the nation's water supply. This Act allowed the Envirotw1eotal Protection Asency (EPA), through the use of permits, to establish rules and regulations governing the 'pretreatment• of industrial wastewaten prior lo their discharge. An attractive solution to analyzing the quality of wastewater is POL VTOX. POL Yl'OX pra--idcs a simple, rapid test for measuring the toxicity or wastewater lo biological wastewater treatme11t systelll5. POLYfOX contains spcciali7.ed microbial cultures and can determine the toxicity of wastewater& and chemi<:al& in biological treatment S)'$tems in 30 minutes, with no expensive instrumentation required. The process described in this 'Applicatioo Procedure' evaluates the inhibitory effect of the W85tewaler or chemical(s) to the spccialiud bacterial cultures by measuring the respiration rate under defined conditiona in the presence of different concentrations of that wastewater or chemical The respiration rate is the oxygen consumed by the aerobic bacterial cultures and is exprcsaed in mg o2 per liter per minute. POLYfOX is designed to provide a rapid screening method whereby wastewaters and chemicals which may adversely affect the biomass of a wastewater treatment facility can be determined, and non-inhibitory con• ccntrations for wastewaters and chemicals prescribed. This test kit Is most applicable to wastewatera and chemicals that are likely to remain in solution. The Lethal Concentration, 1.e:30, in this procedure is the con- centratioo of the wastewater or chemical at which the respiration rate is 30% or that exhibited by the baseline or control The inhibitory or toxk effect of the wastewater or chemical at a specific concentration is expressed as a percent or the baseline respiration rate. A testing procedure utilizing at least 5 different concentrations is recommended. The 1--<;o value should be regarded merely as a guideline of toxicity for that particular wastewater or chemical to its own wai;tewatcr microorganisms, sina: the naturally occurring environment C8Dl!Ot be duplicated exactly under laboratory conditions. EQUIPMENT REQUIRED • Staodard (300 ml) BOD bollle(s) (e.g., Wheaton '800" brand glass). • Dissolved oxygen probe and meter. The prolle must fit snugly into •the neck of the BOD bottle, elimioating all head space. · One-inch magnetic stirring bar aud magnetic stirrer or self-stirring dissolved oxygen probe capable of suspending the l'OLITOX populations in the BOD bonle (e.g., the YSI seir-stirring BOD probe). • Aeration devia: (e.g., aquarium pump, tubing and air stone). • One and two liter containers lo be used for the aeration of the distilled or deionized water (control) and wastewater or chemical (test) samples. • pH adjusting solution (e.g., dilute sodium hydroxide or sulfuric acid). • Thermometer. · Funnel. • Stopwatch. -(Optional) A single channel recorder connected lo the dissolved oxygen meter to provide a continuous strip chart recording of the dissolved o,-ygcn level in the BOD bottle v,:rsus time. I I I I I I I I I I I I I I I I I I I LEST CONDITIONS . ~oration/contact time: 19 and 21 minutes -O>ntaincrs: 1 liter &ize for the aeration or the control(s), 2 liter size for the aeration of the tcst(s) . Air Supply: clean, oil-frco air . Water: Deionized and/or distilled water • Reactor Vessel: BOD boule(s) -Test Solution: The freshly prepared wastewater or cbemiciJ solution (e.g., aerated solution with pH and temperature adjusted) -Control: Baseline respiration rate for the POL YTOX populations only -Temperature: 20 :I: 2 • C. PROCEDURE FOR BASELINE ACTIVITY SW2: L Calibrate the dissolved oxygen probe and meter according to the manufacturer's specifications. 2. Air &aturatc 500 mil of pH adjusted (7.0) dcioo.iud or distilled w.,tcr by aerating the water for at least 30 · minutes at a relatively constant temperature (20 ± 2' C), 3. Pour 50 mis of the aerated, pH adjusted water into a small beaker and sci side. 4. Remove the cap from one of the POLYTOX vials. Place a funnel into the ncclc of a clean, dry BOD bottle. Pour the dry bacterial contents of the 'lial into the BOD bottle. 5. Add the magnetic stirring bar lo the BOD bottle if a self-stirring probe is not available. 6. With stopwatch in hand, pour the premca•ured 50 mis of water into the BOD bottle containing the POLYI"OX vial contents. IMMEDIATELY START THE STOPWATCH. 7. Piclc up the BOD bottle and swirl the contents for 25 to 30 seconds, making sure that the POLYrOX populations are thoroughly wet and thus acdvatcd. 8. Hold tho BOD bottle at a 45 • angle and pour additional pre-aerated water into the BOD bottle. Pour the water down the side of the bottle to avoid tbe formation of excess nir bubbles. Fill the bottle to a level just above the bottom of the ground glass joint. 9. Place the bottle on a flat surface and tap gently to remove bubbles. 10. Insert the dissolved oxygen probe into the BOD bottle, carefully displacing all bubbles from the bottle. It helps to tilt the bottle to the side so that bubbles will slide off the face of the dissolved oxygen probe membrane. 11. Initiate stirring in the BOD bottle. 12. The dissolved oxygen level should be at least 6.5 mg/I at this tim,,. Record the· dissolved oxygen reading continuously with the optional recorder or every two minutes by hand. After you are familiar with the procedure, the dissolved oxygen level can be recorded at the pe,ctinent times of 19 and 21 minutes only. NOTE: With practice, the disoolvcd oxygen probe can be plaa:d in the bottle within 60 to 90 aeconds after adding the first 50 mls of pre-aerated water. 13. Use the following equation to c.alculate the dissolved oxygen uptake rate for the baseline acti-;ity of the POL YTOX populations: Equ•tion 1: 0019s . 00215 DOURs ~ --------= mg/I/min 2 mins. DOURs ~ Baseline Dissolved Oxygen Uptake Rate D019S = Dissolved Oxygen ( mg/I) al 19 minutes D021S = Dissolved Oxygen (mg/I) al 21 minutes P_n7 I Fo~ atiY POLYTOX kit, the ba.elioe rate of respiration ~ deionized ~r distilled water should range between , · O.~ to 0.40 mg/I/min. The baseline respiration rate for your POLITOX kit should remain with.i.a this range I for at least three months if the kit is stored at 20 :t 5• C. (DO NOT FREEZE OR REFRIGERATE.) A baseline ,hould be run for each series of tests. I I I I I I I I I I I I I I I I I PROCEDUREFORBACKGROUNDACTIVITYOFSAMPLE To acrollllt for any rackgroWld oxygen depletion caused by either miaobes present in the sample itself or by the stripping away of COD (Chemical Oxygen Demand) during aeration, the samplc(s) must also be tested in the absence of the POL ITOX populatio11S. ~= 1. Calibrate the dissolved oqgen probe and meter according lo the manufacturer's specification. 2. Air ulllfate one liter of wastewater or test solution (full strcogtl:.) by aerating the sample for at least 30 minlltc$ at a relatively constant temperature (20 :I: 2' C). 3. U ne~, adjust the pH of the wa.tewater or solution to 7.0 with dilute sodium hydroxide or sulfutic acid. 4. Add the m11gJ1etic stirring bar to the BOD bottle if a self-st.irrin& probe is not available. 5. Hold the BOD bottle ata 45' angle and pout pre-aerated wlutio11 into the BOD bottle. Pour the wnplc down the side of the bottle to avoid the formation of excess air bubbles. Fill the bottle to a !eve I just abowe the bottom of the ground glass joint. 6. Place the bottle on a fiat surface and tap gently lo remove bubbles. 7. Insert the dissolved oxygen probe into the BOD bottle, carefully ciisplacing all bubbles from the bottle. It helps to tilt the bottle to the side so that bubbles will slide off the face of the dissolved oxygen probe membr&®. 8. Initiate stirring in the BOD bottle. 9. The dissolved oxygen level should be at least 8.0 mg/I at this time. Record !he dissolved oxygen reading continuously with the optional recorder or every two minutes by hand. After you are familiar with the proo:dure, the dissolved oxygen level can be recorded at the pc,rtinent times of 19 and 21 minutes only. NOTE: If the dissolved oxygen is less than 8.0 ing/~ the 30 minute prcaeratio11 procedure must be repeated and the dissolved oxygen level rechecked. U it is still less than 8.0 mg/~ ii is likely that a significant chemical 07')'gen demand exists in the test solution. This will interfere with the POLYTOX test and must be eliminated. Overnight aeration of the sample may be sufficient to remove the immediate oxygen demand. It should also be noted that removal of the chemical oxygen demand by air stripping methods could change the levels of inhibition exhibited by the sample. 10. Use the following equation to calculate the dissolved oxygen uptake rate for the background activity of the =pie: Equation 2: DOURB • --------• mg/1/miu 2mw.s. DOUR8 • Background Dissolved Oxygen Uptake Rate DO19B • Dissolved Oxygen (mg/I) at 19 minutes DO21 8 ~ Dissolved Oxygen (mi;/1) at 21 minutes For any given sample, the background rate of rcspiratio11 should be less than 0.05 mg/I/min. I ' I I I I I I I I I I I I I I I I I I PROCEDURE FOR TOXICITY TEST. With ·the dissol:.Cd oxygen probe and meter calibrated according to the manu!ac~er's specifications and the tc,~ sample pre-aerated, pH and temperature adjusted, proceed onto the following steps: ~: l. Pour 50 mls of the sample into a small beaker and set aside. 2. Remove the cap from one of the POL YfOX vials. Place a fwwel into the neck of a clean, dry BOD bottle. Pour the dry bacterial contents into the BOD bottle. 3. Add the magnetic stirring bar to the BGD bottle if a self-stirring probe is not available. 4. With stopwatch in hand, pour the premeasurcd 50 mis of sample into the BOD bottle containing the POLYfOX vial contents. IMMEDIATELY START THE STOPWA1'CH. 5. Pick up the BOD bottle and swirl the contents for 2S to 30 seconds, making sure tbat the POLYI'OX populations are thoroughly wet and thus activated. 6. Hold the BOD bottle at a 45 • angle and pour additional pre-aerated solution into the BOD bottle. Pour the sample down the side of the bottle to avoid the formation of cxa:ss air bubbles. Fill the bottle to a level jtt<t above the bottom of the ground glass joint. 7. Place the bottle on a flat surface and tap gently to remove bubbles. 8. Insert the dissolved Oll}'l!en probe into the BOD bottle, carefully displacing all bubbles from the bottle. It helps to tilt the bottle to the side so that bubbles will slide off the face of the dissolved oxygen probe membrane. 9. Initiate stining in the BOD bottle. 10. The dissolved oxygen level should be at least 6.5 mg/I at this time. Record the dissolved oxygen reading continuo\1$ly with the optional recorder or every two minutes by hand. After you arc familiar with the procedure, the dissolved Oll}'l!en level can be recorded at tbc pertinent times of 19 and 21 minutes only. 11. Use the following equation to calculate the dissolved oxygen uptake rate for the test sample: Equation 3: D0191" • D021r DOlffir • -------= mg/I/min 2mins. DOURr ~ Dissolved Oxygen Uptake Rate for the Test Solution DO19r " Dissolved Oxygen (mg/I) at 19 minutes DO21T • Dissolved Oxygen (mg/I) at 21 minutes 12. Use the following equation to calculate the corrected dissolved oxygen uptake rate for the sample to account for any background activity (DOUR8 ). Equation 4: DOURC • Corrected Dissolved Oxygen Uptake Rate for the Tes,: Solution DOURT • Dissolved Oxygen Uptake Rate for the Test Solution DOUR8 n Background Dissolved Oxygen Uptake Rate · I I I I I I I I I I I I I I I I I I I If ,:he respiration of the test solution is lower than the baseline rate, then the lest solution is con.sidered in- b.ibi1ery to the microorganism&. 13. Use the following equation to C3lculate the perceut whibitioo of the test s=ple to the POLYTOX populations: Equati011 S: DOURc 1 • ------X 100 • % INHIBmON DOURg DOURc • Corrected Dissolved Oxygen UpLlke Rate DOURg • BasdiJle Dissolved Oxygen Uptake Rate If the inhibition is sismfic:mt, it may be desirable to dilute the test wastewater or c;hemical aolution and repeat the POLYl'OX test procedure. Testing at various dilution.s can be used to determine the concentration at which 30% inhibition of the inicroorganisms occurs, LC:Jo-(For the purposc.1 of the POLYTOX toxicity testing proce- dure, inhibition of microorganisms is equated to reduction io dissolved oitygcn utilization by the microorganisllls). For example, the following charts provide the LC:3o for pure phenol based on data ge11c~atcd using the POL YI'OX procedure. For additional information, sec "Application Notes'. DETERMINING LC30 FOR PHENOL USING POLYTOX DATA "' t, • 11,1,c1-,1 ' .__~...._. ............... __....___._....._._........, ,.. lH4 11 ... ~~no,t ... s. .!! -:: -----p 0 " M Q 10 I 7 I I • RAPID TOXICITY TEST ,mn AT m,aas mmmna11 At!SiR1 'C! a.r,J l11 tltl ' '-....,-,--"'-,--..,,-,.,--,~'--,,,,.,-- Tlll lllHIUi I I I I I I I ·I I I I I I I I I I I I APPLICATION N01'ES NOTE#DOBE8 When the dissolved oxygen level is at least 8.0 mg/~ but the background rate o[ respiration (DOUR8) is greater than 0.05 mg/I/mill. A DOURa·that is greater than 0.05 mg/I/min. is likely to be a combination of biological and chemical oxygen demand (i.c~ sample composition and microscopic elWl!ination could verify biological activity). NOTE#DOBL8 When the background rate of respiration (DOURa) is not zero at full strength and several test solu• tions (DOURT) are run. Use a percent of the DOURB that was observed at full stre11gth and subtract that number from the DOUR-r for each concentration tested. NOTE#E8 When the dissolved oxygen has been completely depleted prior to the 19 minute reading. Record the pertinent times in which a dissolved oxygen of at least 1.0 mg/! remains for the baseline (DOURs) and tests (DOUR-r), Using those times (i.e., 15 and 17 minute readings) calculate the various ac- tivity rates. NOJE#TBRE8 When the dissolved oxygen rate of the test (DOURT) is greater than the baseline rate of respiration (DOURs), Depending upon the homogeneity of the contaniinants with.in the sample, areas of low organic levels may even experience 60me enhance111cnt of biological oxygen uptake activity. At concentration of samples where there is no toxic effect upon the microbial oxygen uptake rate, uptake rates greater than the baseline rate (DOURs) arc sometimes experienced. These enhanced rates are rcp,·esented as negative inhibition values and usually indicate the presence of certain readily degradable compounds which the POLYfOX bacteria can im, mediately utilize as a good source, thereby increasing cellular metabolic activily and the uptake of dissolved oxygen. NOTE#SSE8 When the sa111ple is soil or sand. Using the combined mixing capabilities provided by a self-stirring dis.solved oxygen probe and a 111ag- octic stir bar, 100 g soil or sand per liter deionized water is the highesl conccotratioo able to be kept thoroughly mixed. Therefore, it is suggested that the sample be tested at concc11trations of 100.00, 33.33, 3.33, and 0.33 g sample/I achieved by the addition of30.00, 10.00, 1.00 and 0.1 g samplc/300 ml BOD bottle respectively. Some- times the limited factor for increasing the concentration of the sample is not the toxicity of the sample to the microorganisms but the ability to sustain adequate mixing. Upon completing the procedure for the baseline (DOURs), the background activity (DOURa) o[ the sample mu:;t be checked by the addition of 30.0 g samplc/300 ml BOD bottle. By testing different concentrations o[ the sample using these suggested notes, ... Jxicity profile of the ;ample toward the microorganisms can be generated. This infonnation can then be used to determine a threshold level (maximum threshold) at which lhe waste can be effectively treated. C:• 1 1 IFEB-15-90 THU 8 : 2 4- I Material Safety Data Sheet May be used to comply with (")~W.d1111 1-11'1.II!"-~ ~--"""'-,..1.1111i~,i•i~.-i tt~l'll~II\~. 29 CFR 1910,1200. Standard must be CORP PA U.S. Department of Labor Occupational Safety and Health Administration ~t-lQn-Manda~•=-ry rgrTfl) Form Appro1•ed OM!! Nv, 1218-M72 F' • 1 1 I mns11ttflf1 lnr ~flfli:ifir r~11ir11mRnr1 IDENTITY (As um on Label and use POL YTOX Ra id Bio1o ical Toxic1t Test Noro: Blank spaco.s aro nor permirred. N any lt'1m Is nor opplicable, Of no Jnlormatloi1 Is available, rlls space must be mwked to lnd/ca!8 that. I Section I Manufacturer's Name Emergency Telephone Number Pnlvbac Cornoration (800\523--9385 I AQdross /Numbe~ Stroot, City, Stato, ono ZIP Cods) Telephone Numl,er for Information __ co_u_r_t_ne-=y-~_1 a_c_e ___________ -+..,,...'~' ?o:11'.:t ~·.J.J ,, M:m.i,7.:.-J..::,.,. 7 ~, ~)A_ii ___________ _ Ome Prepared I 3894 Courtney Street Bethlehem. PA 18017-8999 I Section II -Hazardous Ingredients/Identity Information Hazardous Components (Spe<:ific Chemical Identity; Common Name(s)) January '1990 Signature ol Pr11parer /opl/onaQ OSHA PEL ACGIH TLV Other Umlls Recommended Non-hazardous •------------•------------ •------------ 1------------ 1 --------------------------·----------------Section Ill -Physlcal/Chemlcal Characteristics I Boiling Poinl NIA Specific Gravity (H:P • 1) I Vapor Prussure (mm Hg.) N/A Melting Point Vapor Density (AIR • t) N/A Evaporation Role (Butyl Acetate • 1) I SOluOllity In Waler N/A Appearance and Odor Granular powder; Buff to brown ~olor; I Section IV -Flre and Explosion Hazard Data Flash Point (Method Used) Musty odor Flammable Umlt.!, A I Ex1inguishing Media Foam, CO2, N A Dry chemical, Water Special Fire Fighung Proceduros I N/A 0.5-0.7 N/A N/A LEL UEL ---c-=:---c-=,--,.--------------------------------U nu su al Fire and Explosion Hazards , ______ ..:.:_N:.._;/A ________________ _ I FEB-15-90 THU e.~~ POLYBAC CORP PA P • 1 2 I I I I I I I I I I I I I I I I I I 0 Soction V -Reactivity Data SIallmty Unstaole Condilions 10 Avoid A . d to moisture. Do not wet. vo, exposure Stable y c::+---.... 1i1•r _ 111~•r Incompatibility {Msterlsl• to Avolcf) Water Hazardous Decomposillon or ByprOducis N/ A Hazardous Polymenza1Ion May Occur C<lndlUON; 10 Avoid Will Nol Occur X Section VI -Health Hazard Data Aoute{s) of Entry: Inhalation? Skin? Ingestion? Dust Avoid direct skin contact. Do not ingest. HfWfo{t8A¥1b~~ur~f8i'a'~"/,¥ove subject to fresh air, SKIN-wash thoroughly with soap and water, remove and wash clothes. INGESTION-avoid, call physician, observe for 48· hours for development of allergic symptoms. Carclnogonlclty: N/A NTP? N/A IAAC Monographs? N/A OSHA Aegula!od? N/A Signs and Symp1oms of Exposure Irritation ta the eyes and respiratory tract, MeaIca1 Condlllons GenerrutyAggrava1oobyExposure Respiratory allergy (hay·fever, asthma) in some people. Indiyiduals hyperallergic to enzymes or related proteins should not handle. Emeraency and First Aid Procedures Wash nands with soap and water. Contact physician immediately, if allergic symptoms occur in 0-12 hours, Section VII -Precautions for Sale Handling and Use Slops to Se Taken In Ca,ie Material Ip R•l~asod or SpiUO<j! Sweep up/collect: avo1d airect skin contact, inhalation and/or ingestion of dust. '1Foi~~ ~f~Wsal rrethod. Staroard larofi 11 disposal according to legal State and Federal regulations. May be se..-ered; carpatible with all biological treatrrent net.hods, Precautions to Be Taken in HB/1dling and Storing Wear respiratory/surgical mask or equivalent MESA/NIOSH. Store in dry place at room temperature (20°). Do not freeze or refridgerate. 01J1or Precautions Wear gloves Section VIII -Control Measures Respiratory Protection (Speedy Typo) Yes, surgical mask or equivalent. ventJlation 1.oca1 i;xhausr V<>< at nnint nf d11st release Special Mechanical /G6norllf) Oll!o, Prot&d!ve Gloveo Yes· I Eye Protect1or, Yes (dust) ANSI-287, 1, 1968. Olher Protective Clothing or Equipment Dusting pratectiao -Eyewash f Won</Hygienlc Practices Co not ingest. Avoid dust. Wash hards with soap ard water after use. Individuals h)?9rallergic to enz)IT'eS or other related proteins should not handle. Page 2 • u•o•.o",..••n-m"'"' I THE MICROTOX® I INSTRUMENT I ACCESSORIES AND SUPPLIES I WHAT MICROTOX DOES I The Microtox system measures the toxicity of aque- us solutions. In the test, a light emitting reagent is exposed to samples of material in small cuvettes. If the ~ mples are toxic, the light output of the reagent is duced in proportion to the toxicity of the samples. he light loss is a simple measure of toxicity. The lignificance and applications of Microtox, The Fast oxicity Test•m, are treated at length in other literature. THE MICROTOX INSTRUMENT I The Microtox Model 2055 Toxicity Analyzer mploys a sensitive photomultiplier to measure the light emitted by small volumes of glowing reagent. l Separate refrigeration units maintain samples and agent at precise temperatures. A patented turret mechanism allows the cuvettes ■ontaining test materials to be exposed conveniently to llie photomultiplier in a brightly lighted lab without am- bient light leakage. IJsE OF THE INSTRUMENT The Microtox Instrument serves both as an experi- a,ental laboratory instrument and as a "production" ltJol. It can be operated easily over a broad range of sensitivities and temperatures for ( search. It can be used to run large umbers of tests reliably, day after day, onth after month. IHE CHART RECORDER Microbics Corporation offers an simplifies the testing process, (serving as an automatic timer, for example), greatly reduces the probability of transcription errors, and aids in final data reduction. SPECIFICATIONS Power Requirements: The standard unit operates on nominal 100-120 volts AC at 50/60 Hz. It is fused for 2 amps. (At startup, when the coolers are working to bring temperatures from ambient to their set points. the unit draws about 150 watts. Later, when the coolers need only maintain the set temperature, the unit draws about 60 watts.) An export model, running on nominal 220-240 volts AC at 50/60 Hz. is fused for one amp. Height to the top of the turret: 10 inches. Width: 18.3 inches. Depth: 20.7 inches. Weight: 48 pounds. (about 55 pounds, · packaged for shipment.) The unit was designed to sit on a laboratory bench. Even so, people move Microtox instruments around freely, using them wherever they are needed. The sys- tem can easily be carried into the field, and operated in the back of a station wagon or van, using a small port- able generator for power. accessory chart recorder matched to t e analyzer: a ten-inch, single-pen. anual lift, 1 0mv fixed ( 17 speed) device in either 120 or 220 volt /.:-~ ~. ~~ ~•/. ' ' l ersions. Though the Microtox instrument is equipped with a three-digit display ■hat shows temperatures and light !levels. most laboratories rely on the chart recorder for permanent records If the tests. Use of the recorder MtCRCJTCJ•_}• ,:;•~,: • ' •• ' • -• -• fRT: What we do I I 'az•nt Assassmant ane of the first steps the Environmental ltipact Section takes in formulating a hazardous substance strategy is to de- ' mine the degree of risk to people and e environment Since the hazard may eel its target population in several ways, it is essential that the assessment Insider all environmental media-air, rface water, ground water, soil, and omass. llhe Section has been conducting hazard-lJis assessments at a variety of spills and waste sites; each operation produces an E. easingly refined hazard assessment nique. This increased sophistication resulted in improved documentation of the extent of contamination, a logical l proach for defining "when clean is ean enough." and the extent of cleanup imately recommended. Ifie Section's approach is firirt to consider ■e hazard itself, then to determine its probable pathways. Identification of the E pathway or pathways and the of the contaminant's migration will e selection of the most cost-effective remedial actions. These findings are then E to develop engineering options for aining and removing contaminants, restoring the site. I I I I I Toxicity Testing In its field activities the Environmental Impact Section employs a new instru- ment which rapidly assesses the toxicity of leachates, treatment system effluents and ambient water. The portable instru- ment has been used successfully at a number of hazardous waste sites and spills for toxicity screening of waterborne contaminants, as well as for substantia- tion of other aquatic bioassay tests. The instrument operates on the fact that toxic chemicals in water inhibit the light- , emitting capacity of certain marine bac- teria. The degree of light inhibition is directly proportional to the concentration of the chemicals. The instrument's effectiveness is derived from its portability, its compactness and its dependence upon regular household electric current Requiring only four feet of table top or laboratory bench space, it can be set up in a command post or a motel room. Individual samples can be assayed in 5-15 minutes. This type of speed can be particularly valuable if the sample is from stored, treated wastewaters that must be discharged only after toxicity tests are completed. The instrument also reveals the synergistic effects of toxic mixtures, which cannot be predicted by interpreting data from chemical analysis. The data produced by the instrument are the result of toxic chemicals acting on various physiological systems of the marine bacteria. As such, the data do not have as much ecological relevance as a bioassay of fresh water fish or macroin- vertebrates. However, the instrument has been used enough on certain fish/macro- invertebrate bioassays to make correla- tions with specific toxic chemicals. The Environmental Impact Section is also developing a portable unit using fresh water fish and Daphnia (a small crusta- cean) to generate toxicity information. This unit will soon be combined with the rapid assessment instrument to provide a complete system for defining toxicity in aqueous hazardous materials. This new unit consists of modules that can be transported as baggage on most airlines and set up in a trailer. Its own temperature control unit maintains ap- propriate temperatures for test organisms. While the unit's diluter system is espe- cially designed to produce the concen- trations of pollutant required for generat- ing standard TL,. data, it can be easily modified to perform special tests using more than one pollutant at a time. The information generated from these IINo new instruments can be used to determine: • The most environmentally acceptable means of counteracting effects of hazardous material discharges. • The environmental acceptability of the effluent from various treatment processes. • The biological "zone of influence• re- sulting from the discharges of hazard- ous materials. For further information on Environmental Impact Section services, contact: Dr. Royal Nadeau Chief, Environmental Impact Section, ERT U.S. Environmental Protection Agency Edison, New Jersey 08837 201-321-6743 FTS-340-6743 I I I I I I I I I I I I I I I I I I USE OF A BACTERIAL TOXICITY MEASUREMENT SYSTE~'. AT HAZARDOUS WASTE SITES Dr. Royal J. Nadeau, Environmental Response Team, U.S. Environmental Protection Agency, and Michael Kwiatkowski, Jacobs Engineering, Inc., Edison, New Jersey. ABSTRACT A Bacterial Toxicity Measurement System was used at two hazardous waste sites for relative toxicity screening purposes. Determining the relative toxicity of samples was valuable at one site as an intermediate monitoring assessment technique, while at another site it was used for initial site assessment purposes. The first incident involved the migration of phenolic compounds from a buried entrenchment into a nearby creek. Chemical and Microtox analyses were performed on surface and groundwater samples to monitor the effectiveness of a subsurface slurry retaining wall, emplaced to reduce the seep. The second incident involved the screening of soil and aqueous samples collected during an Extent of Contamination Survey. The chemical screening was for volatile organics by Gas Chromatography. The Microcox screening served as an adjunct for the qualitative detection oi compounds not detected by the Gas Chromatography analysis. From the joint data, areas of probable contamination were determined and used as a general basis for subsequent analyses and sampling. Although each incident was unique in terms of contamination, chemical analysis support, and objectives, the Microcox Toxicity Analyzer System was both flexible and adaptable in meeting each sites' needs. The System displayed its usefulness as an on-site monitoring device. Requiring only minimal technical and manpowe~ support samples were collected, prepped, and analyzed 1n an eight hour period. The System displayed a broad range sensitiYity 11hich was useful for exam1.n1.ng samples when little or no information was available. The data provided by the Microtox Toxicity Analyzer System decreased analysis turn-around time and reduced the number of samples requ1.r1ng extensive chemica: analysis, in that a lower analysis priority was assigned co the non-toxic Microtox samples. I I I I I I I I I I I I I I I I I I I USE OF A BACTERIAL TOXICITY MEASUREMENT SYSTEM AT -----HAZARDOUS WASTE SITES INTRODUCTION Hazardous waste site investigations is a topic which has been the subject of legislative, public, and scientific concern. Conducting a hazardous waste site investigation is, at best, a monlllllentous undertaking. Ic encompasses many stages of planning, each of which must address multidimensional questions. The initial site assessment plays a vital role since ic serves as a blueprint for all project planning. Similarly, . any subsequent assessments are important for monitoring the effectivenesss of a plan to determine if any changes are necessary. The most encompassing assessments have included testing of both chemical and biological parameters. Yet, such involved testing can often become entangled in individual constraints of time, cost, and sens1t1v1ty. The Microtox Toxicity Analyzer System™ developed by Beckman Instrlllllents, Inc., has been used successfully at two hazardous waste site investigations in reducing these constraints. MICROTOX ASSAYS The versacili:y of the Microcox seems from its fundamental theories and basic operating principles. The system uses a special strain of lyophilized bioluminescenc marine bacteria Photobaccerium ohosohoreum, which are reconstituted co provide a ready-co-use bacterial suspension. Three reagents, bacterial reconstitution solution, diluent reagent, and osmotic adjustment solution, are required in milliliter amounts, and are delivered with fixed volllllle pipettors. The physical system is comprised of a housing unit which encases the temperature controlled incubator/turret assembly, photomultiplier hardware, and a digital display screen. An optional chart recorder may be used for making permanent records of the data. Since the bacteria are of a marine origin all samples muse be adjusted to a salinity range of z: co 9:, which is accomplished by using the osmotic adjustment solution. After an initial light reading is taken the bacteria are exposed co up co four serial dilutions of the sampt-e. Tne system is designed for duplicate simultaneous testing. The relative light output of the bacteria are measured ac discrete 1 I I I I I I I I I I I I I I I I I I I time intervals, ranging from five to thirty minutes. These light readings are used, inturn, to calculate the Normalized Percent Light Decreases (NPLD's). The NPLD's take into account a correction for natural die-off, and any decrease in Che light output of the bacteria is attributed co a deterioration in Che state of health of the bacterial poyulacion, stemming from Che presence of toxicants in the sample. ·