ASTM D4200-1982(2011) Standard Test Method for Evaluating Inhibitory Effects of Ink Grids on Membrane Filters《评价膜过滤器上油墨格栅的抑制作用的标准试验方法》.pdf

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ASTM D4200-1982(2011) Standard Test Method for Evaluating Inhibitory Effects of Ink Grids on Membrane Filters《评价膜过滤器上油墨格栅的抑制作用的标准试验方法》.pdf_第1页
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1、Designation: D4200 82 (Reapproved 2011)Standard Test Method forEvaluating Inhibitory Effects of Ink Grids on MembraneFilters1This standard is issued under the fixed designation D4200; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision,

2、 the year of last revision. A number in parentheses indicates the year of last reapproval. Asuperscript epsilon () indicates an editorial change since the last revision or reapproval.1. Scope1.1 This test method describes a procedure whereby the userof ink-gridded membrane filters in water quality s

3、tudies canascertain whether or not the grid lines are toxic and inhibitoryto bacterial growth when the membrane and its entrappedbacteria are incubated on a suitable media.1.2 The values stated in SI units are to be regarded asstandard. No other units of measurement are included in thisstandard.1.3

4、This standard does not purport to address all of thesafety concerns, if any, associated with its use. It is theresponsibility of the user of this standard to establish appro-priate safety and health practices and determine the applica-bility of regulatory limitations prior to use.2. Referenced Docum

5、ents2.1 ASTM Standards:2D1129 Terminology Relating to WaterD1193 Specification for Reagent Water3. Terminology3.1 DefinitionsFor definitions of terms used in this testmethod, refer to Terminology D1129.4. Summary of Test Method4.1 A heavy bacterial suspension is filtered through agridded membrane fi

6、lter. The bacterial concentration employedis sufficient to cover much of the membrane with bacterialcolonies.4.2 After filtration the membrane is incubated on a suitablemedium and the distribution of the colonies and shape of thecolonies noted in the area around each grid line.5. Significance and Us

7、e5.1 This test method may be applied to determine thesuitability of grid-marked membrane filters for use in bacte-riological culture techniques for the detection and enumerationof bacterial organisms.5.2 A particularly sensitive organism and growth conditionshave been selected for this test method i

8、n order to maximizesensitivity to toxic materials possibly present in the inks usedfor grid-marking membrane filters.6. Apparatus6.1 Incubator, capable of maintaining temperatures of44.56 0.2C.6.2 Membrane Filtration Units.6.3 Vacuum Source with trap vessel.6.4 Forceps, blunt-nosed.6.5 Autoclave or

9、other sterilizing equipment.6.6 Expendables:6.6.1 Gridded membrane filters.6.6.2 1-mL and 10-mL pipets.6.6.3 Petri dishes (50-mm) containing 6 to 8 mL of agarmedium or a 100-mm dish with 20 6 2 mL of agar medium, orboth.6.6.4 Erlenmeyer flasks.7. Reagents and Materials7.1 Purity of WaterUnless other

10、wise indicated, referenceto water shall be understood to mean reagent water conformingto reagent water Type II of Specification D1193.7.2 M-FC Agar with Rosolic Acid or equivalent (henceforthreferred to as agar medium), formulated, prepared, and dis-pensed in accordance with the manufacturers specif

11、ications.7.3 Tryptone Soya Broth or equivalent (henceforth referredto as broth medium), formulated, prepared, and dispensed inaccordance with the manufacturers specifications.7.4 Peptone Water, 0.1 %, sterile.7.5 Broth Culture of E. coli ATCC 11229, 18-h, prepared asfollows: Add 1 mL of an 18 6 2-h

12、broth culture of E. coliATCC 11229 to 99 mL of 0.1 % peptone water, mix thor-oughly, then add 0.1 mL of this suspension to another flaskcontaining 99 mL of 0.1 % peptone water. This is the working1This test method is under the jurisdiction of ASTM Committee D19 on Waterand is the direct responsibili

13、ty of Subcommittee D19.08 on Membranes and IonExchange Materials.Current edition approved May 1, 2011. Published June 2011. Originallyapproved in 1982. Last previous edition approved in 2003 as D420082 (2003).DOI: 10.1520/D4200-82R11.2For referenced ASTM standards, visit the ASTM website, www.astm.o

14、rg, orcontact ASTM Customer Service at serviceastm.org. For Annual Book of ASTMStandards volume information, refer to the standards Document Summary page onthe ASTM website.1Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.concentratio

15、n and should contain approximately 103bacteriaper millilitre to provide contiguous but discrete growth.NOTE 1Hydrophobic leaching may cause growth inhibition in areasadjacent to grid lines.8. Procedure8.1 Assemble the sterile membrane filtration apparatus, andconnect to vacuum trap and vacuum source

16、.8.2 Process five randomly selected membrane filters, using1-mL aliquots of culture suspension from 7.5, and 30 mL of0.1 % peptone water added to the filter funnel with standardmembrane filtration procedures. Place the membranes in petridishes containing M-FC agar medium and incubate at 44.5Cfor at

17、least 18 h.8.3 After incubation, examine the overgrown membrane forinhibition of growth along the grid lines.8.4 Examine the membrane filter for growth of “squarecolonies.” The growth of square colonies flowing along gridlines is not necessarily an indication of toxicity, but could be anindication o

18、f either compression of the membrane or pluggingof the pores, thus inhibiting nutrient feed to the colonies (seeNote 1).8.5 In this test method, toxicity is defined as the lack ofgrowth in the area immediately adjacent to the grid lines, andif this effect is noted, repeat the test and if still prese

19、nt, rejectthe membrane filters.9. Precision and Bias9.1 Since this is a qualitative test method, precision and biasstatements are not applicable.10. Keywords10.1 bacterial; filter; inhibitory ink; membraneASTM International takes no position respecting the validity of any patent rights asserted in c

20、onnection with any item mentionedin this standard. Users of this standard are expressly advised that determination of the validity of any such patent rights, and the riskof infringement of such rights, are entirely their own responsibility.This standard is subject to revision at any time by the resp

21、onsible technical committee and must be reviewed every five years andif not revised, either reapproved or withdrawn. Your comments are invited either for revision of this standard or for additional standardsand should be addressed to ASTM International Headquarters. Your comments will receive carefu

22、l consideration at a meeting of theresponsible technical committee, which you may attend. If you feel that your comments have not received a fair hearing you shouldmake your views known to the ASTM Committee on Standards, at the address shown below.This standard is copyrighted by ASTM International,

23、 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959,United States. Individual reprints (single or multiple copies) of this standard may be obtained by contacting ASTM at the aboveaddress or at 610-832-9585 (phone), 610-832-9555 (fax), or serviceastm.org (e-mail); or through the ASTM website(www.astm.org). Permission rights to photocopy the standard may also be secured from the ASTM website (www.astm.org/COPYRIGHT/).D4200 82 (2011)2

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