EN 13342-2000 en Characterization of Sludges - Determination of Kjeldahl Nitrogen《污泥的特性 水质凯氏氮的测定》.pdf
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1、STDaBSI BS EN 13342-ENGL 2000 E ltb24bb9 0875751 T1 BRITISH STANDARD Characterization of sludges - Determination of Kjeldahl nitrogen The European Standard EN 13342:2 has the status of a British Standard ICs 13.030.20 NO COPYZNG WiXOuT BSI PERMISSION EXCEPT AS PERMITIED BY COPYRIGHT LAW m BS EN 1334
2、2:ZOOO STD*BSI BS EN 13342-ENGL 2000 W Lb24bb9 0875752 951 W BS EN 13342:2 Committee and comes into effect on 16 October Zoo0 AmdNo. Q BSI lCL2O National foreword Date Comments This British Standard is the official English language version of EN 13342:2000. The UK participation in its preparation wa
3、s entrusted to Technical Committee EW5, Sludge characterization, which has the responsibility to: - aid enquirem to understand the text; - present to the responsible European committee any enquiries on the - monitor related international and European developments and promulgate A list of organizatio
4、ns represented on this committee can be obtained on request to its secretary. Further information Users of this standard are informed that the UK submitted some substantial comments at the finai voting stage of the drafi EN for the following reasons. 1) In annex A, it is essential that the descripti
5、on of the four samples used in the inter-laboratory comparison is given. This can be achieved by the addition of a simple footnote. It is recommended that this topic is discussed at the TC308 meeting in Urecht. A documented minimum requirement for inter-laboratory comparisons is needed 2) The follow
6、ing note should be added to the scope: “The validation for this standard has oniy been carried out using materials as described in annex A. For other sludges, the user should validate the method using recovery and reproducibility tests”. 3) The date that the Moratory inter-comparison was carried out
7、 should be also given 4) The final phrase “and sludge products”, in the first sentence of the scope should be removed as it is inappropriate. 5) In 6.1, suggest replacing the first sentence, “The igestion fails to determine nitrogen in the form ”, with The digestion may fail to fully recover nikogen
8、 in the form of ”. Also suggest that a cross-reference to the UK Blue Book method be made. This has a useful introductory historical section (Al) on recoveries of “difficult” nitrogen species using the yjeldahi method. yjeldahi Nirogen in Waters 1987, HMSO 1988, ISBN O 11 752129 91 6) In annex A: in
9、terpretation, or proposals for change, and keep the UK interests informed; them in the UK. (i) CVR, in column 6, should be CVr in all three language versions: (i) all of the English and German coefficients of variation of both reproducibility (CVd and repeatability (CYr) are wrongly caldated. The du
10、es are wrong by up to a factor three, which is to high. ISBN O 580 36290 6 STD-BSI BS EN l13342-ENCL 2000 Lb246b9 0875753 898 = BS EN 13342:2 7) In the section on Analyticai or Glass digestion tubes, 250 ml capacity for use with a temperature controlled heating block. 7.2 Heating device Kjeldahl fla
11、sks can be heated singly or more usually, in a rack carrying several vessels, by use of either a Bunsen burner or electric heating mantle. It is important, however, that the glass surface above the digestion mixture receives no direct heating. Heating blocks capable of maintaining a temperature suff
12、icient to reflux the digestion mixture are commercially available. These hold typically up to 24 digestion tubes allowing for high laboratory throughput. 7.3 Distillation apparatus The digestion vessel should be suitable for direct attachment to glass apparatus incorporating an anti-splash distillat
13、ion head, a vertical water condenser and a delivery tube, the outlet of which is submerged in the absorbent solution. Commercial automatic Kjeldahl steam distillation apparatus is suitable for this determination. 7.4 Boiling aids Anti-bumping granules or glass beads. 8 Sample pretreatment Drying of
14、sludge will tend to deplete free ammonia and, depending on the pH, ammonium salts. For this reason, a test portion of a wet homogenized sample shall be used (see EN IS0 5667-1 3). Q BSI 10-2000 Page 8 EN 13342:2000 9 Procedure 9.1 digestion vessel (7.1). Transfer a known mass of homogenized, wet slu
15、dge (equivalent to 0,25 g to 0,5 g of dry mass) to a A blank shall be run by substituting 5 ml of water instead of the wet sludge with each batch of samples. NOTE For paste-like sludges, nitrogen-free paper can be used for sample transfer to the digestion vessel (7.1). 9.2 aids (7.4). Add (5,O f 0,l
16、) g of catalyst mixture (6.2) (or equivalent commercial tablets) and 2 or 3 anti-bumping 9.3 Cautiously add (10 f 0,5) ml of sulphuric acid (6.1), gently swirling the vessel. 9.4 while any foaming subsides. Heat the vessel slowly in an extracted area (e.g. fume cupboard) to drive off the water prese
17、nt and 9.5 half way along the neck of the vessel. White fumes of sulphur trioxide should be visible above the liquid. Heat the vessel more strongly to maintain a brisk boiling. The sulphuric acid should reflux up to about NOTE If commercial digestion equipment is used, the manufacturers instructions
18、 should be followed. 9.6 for at least a further 60 min. The contents of the vessel should eventually become clear or straw coloured. Continue the digestion 9.7 order to avoid crystallization of the digest. Allow the digest to cool and cautiously add (40 f 5) ml of water whilst gently swirling the ve
19、ssel in 9.8 If the digestion vessel (7.1) is suitable for direct attachment to the distillation apparatus, make up to approximately two thirds of its volume with water. If not, transfer the digest quantitatively to a Kjeldahl distillation flask adapted to the distillation (7.3) and make up to approx
20、imately two thirds of its volume with water (6.5). 9.9 acid (6.4.3) to the receiver flask, and ensure that the delivery tube is below the acid surface. Assemble the distillation apparatus adding 50 ml of 0,05 mol/l sulphuric acid (6.4.2) or 50 ml of boric 9.10 Cautiously add (30 f 2) ml of sodium hy
21、droxide solution (6.3) down the side of the distillation flask leading to two distinct layers. Assemble the apparatus and swirl the flask carefully to mix the contents without losing any liberated ammonia. NOTE instructions should be followed. This step may not be necessary for commercial automatic
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