standard operating procedures

standard operating procedures intoxicates Standard Operating Procedures A General OverviewAimThis document is not meant to be either encompassing hardly is designed to give readers an overview as to what should be in a plunge and what a SOP readiness look like.Background It was commonality in the past for to be photocopied from a leger and notes/scribbles to be added to a system to adapt it to a Laboratorys specific of necessity. This resulted in analysts apply incompatible versions of the resembling method and obtaining different results. It also hindered the communication of modifyments that an individual analyst had made to a method, as it was not known how many copies of a method existed and whether they had all in all been updated to let in the improved method.A way to improve this chaos is to ensure that all methods and procedures shall be documented to the extent needful to ensure proper implementation and consistency of application. Hence the introduction of the design of SOPs Standard Operating Procedures.It is sometimes not practical for laboratories to office an SOP which is fully documented specifying each type and individual rivulet procedure. For example, analysis of stain examples for polyaromatic hydrocarbons. It is simpler to write an SOP on the preparation of soil extracts for analysis by gas chromatography and another SOP of a to a great extent general nature regarding the analysis of extracts by gas chromatography.Information allow for all SOPs whole SOPs should stick come forth the following infoAuthorised by (Some unrivalled in the organisation needs to approve the SOP before it advise be intention)Copy bet (A record of the flesh of copies of an SOP needs to be kept each individual assume has its own number identifies if on that point be any illicit versions in use ) Page x of y (e.g. Page 1 of 6 appears at the bottom of each page identifies if thither are pages absentminded from a method) Other teaching may entangle when the method should be reviewed, individual reference numbers game racket for when an organisation has many SOPs, Issue numbers to identify new versions of a method from old versions of a method which ledger been withdrawn.To help explain some of the terms below, move of an SOP involving the analysis of nitrite in water bewilder been reproduced in boxes like this. THESE leave alone ONLY BE EXAMPLES AND ARE NOT COMPREHENSIVE.Title termination of A analyte(s)or measurand(s), in C matrix victimisation D principleDetermination of nitrite in water by UV/Visible spectrophotometryScope Enables a user to see quickly whether the method is detach for a desired application (see also the Annex- method proof and measurement uncertainty).the analyte (measurand) which can be determined by the method, the try out matrix from which the analyte (measurand) may be determined, the proficiency employ in the method, the minimum sample size, known interferences whic h prevent or limit the working of the method, the tightness wheel of the method. The amount of nitrite in an sedimentary sample can be determined. The detection limit is 0.01 mg dm-3 for a 30 cm3 sample. thither is a maximum limit of 0.25 mg dm-3 for a 30 cm3 sample. Dilutions can be carried come forward on the sample to pass off the ramble of analysis. Type of sample Raw and potable waters and sewerage effluents. Samples that are highly emblazoned or turbid can incur interference*. * If the alkalinity of the sample is high, such that a pH value of 1.9 0.1 is not attained after the addition of the sulphanilamide reagent (.) then the formation of the azo-dye is affected. *It may be more appropriate to suck up a class section for interferences. inform Safety Precautionshandling the samples handling or preparing solvents, reagents, standards, or other materials mathematical operation of equipment requirements for peculiar(a) handling environments, e.g. fume cupboar ds N-1-naphthylethylenediamine dihydrochloride should be regarded as a special hazard. Skin contact with the solid and solving containing it should be neutraliseed. Disposable gloves should be worn when handling effluent or sewage samples. Normal precautions to avoid skin contact and/or ingestion should be taken in the handling of all reagents. DefinitionsDefine any unusual terms, use ISO definitions wherever possible. Quote sources. accommodate chemical formulae/structures if appropriate.PrincipleOutline the principle by which the analytical technique operates. This section should be written so that a summary of how the method works can be seen quickly.The method is establish on the diazotisation of sulphanilamide by nitrite in the presence of phosphoric acid, at pH 1.9, and the subsequent formation of an azo dye with N-1-naphthylethylenediamine. The absorbance of this dye is measured at 540 nm and is related to the nitrite concentration by means of a standardisation curve .ReactionsWhere appropriate to clarifying the working of the method or calculations, include dilate of any germane(predicate) chemical reactions. This may be relevant, e.g. where derivatisation is involved, titrimetry etc..Reagents Materials List all of the reagents materials, sportys, QC samples and standards and certified reference materials required for the analytical process, determine by earn or number. List expounds of any associated hazards including disciplines for garbage disposal, appropriate year of reagent/chemical, specialist suppliers for rare chemicals, need for calibration and QC materials, details of preparation, including need to mend in advance, containment and storage requirements, shelf life of raw material and hustling reagent, required concentration, noting whether w/v, w/w or v/v, labelling requirements. a. All reagents should be of at least analytical reagent grade. b. Water In all qualitys demineralised water shall be used. c. Nitrite Stock for Standard Solution, 1000 mg dm-3 NO2 Weigh place 1.5000 g 0.0050 g of sodium nitrite, (previously dried overnight at cv 5 C and stored in a desiccator desiccant silica gel) and channelize quantitativelyto a 1 dm3 Grade A volumetrical flask containing most 500 cm3 of water (b). Make up to the mark with water (b) and stopper. escape from until all the solid dissolves. take away to an appropriately labelled ice-skating rink bottleful and store in the refrigerator. The solution is stable for 1 month. d. Orthophophosphoric acid 85% w/w e. 2 mg dm-3 Nitrite Standard Using a Grade A glass pipette, pipette 2 cm3 of 1000 mg dm-3 stock nitrite solution (c) into a 1 dm3 Grade A volumetric flask and claim up to volume with water (b). Stopper and provoke to mix. Transfer to an appropriately labelled glass bottle, stopper and store in a refrigerator. The solution is stable for 1 week. f. Nitrite Stock for Quality cut back Solution 1000 mg dm3 NO2 Ideally the sodium nitrite should be ob tained from a different source to that used for the standard. Weigh out 1.5000 g 0.0050 g of sodium nitrite g. Sulphanilamide Reagent Using a 100 cm3 amount cylinder, add 50 cm3 of 85% orthophosphoric acid (d) to a 500 cm3 beaker containing 250 cm3 of water (b). Weigh out 20.00 g 0.25 g of sulphanilamide and quantitatively raptus to the beaker. Stir with a glass rod until the solid dissolves. Weigh out 1.00 g 0.10 g of N- 1-naphthylethylenediamine dihydrochloride and quantitatively transfer to the beaker. Stir with a glass rod until the solid dissolves. quantitatively transfer the solution to a 500 cm3 volumetric flask and make up to volume with water (b). Stopper the flask and shake to mix. Transfer to an appropriately labelled amber glass bottle and store in the refrigerator. The solution is stable for 1 month. NB Immediately before use, this solution should be brought to room temperature. Points to note from exampleEach reagent is uniquely identified so as to avoid confusio n. Weigh 20.00 g Indicates that a dimension capable of weighing to 2 decimal places is required. 20.00 g 0.25 g Tells the analyst that he needs to be between 19.75 g and 20.25 g. Using a 50 cm3 measuring cylinder Indicates accuracy required for this procedure. Quantitatively transfer Indicates that you need to transfer all the solid with washings to the beaker. Appropriately labelled This might include frame of reagent, Concentration of reagent, Date reagent made, Expiry date of reagent, Name of analyst who prepared the reagent Most computer systems can be used to produce sheets of labels that suits an individuals and/or organisations needs. Apparatus Equipment observe in sufficient detail the individual pieces of equipment and how they are connected to enable unambiguous set-up. For glassware include grade where applicable. Include environmental requirements (fume cupboards etc.).a. A Manufacturers name/model number UV/Visible spectrophotometer with 10 mm glass cells is u sed. b. The instrument should be switched on for a minimum of half an hour before the analysis. raiment the wavelength to 540 nm. Details of operation of the instrument are given in the instruction manual for the instrument. It may be appropriate to reproduce the relevant parts of the instruction manual in the SOP i.e. how to set up and use the spectrophotometer. This volition depend on how easy it is to get access to the manual. sample Sample PreparationInclude sufficient detail to describe how the psychometric leaven portion is obtained from the sample as received by the laboratory. All training on the precautions to be taken to minimise the risk of contamination of the samples needs to be included. Include data regarding the storage, conditioning and disposal of samples. Many laboratories will write a separate document about the receipt, labelling, storage and disposal of samples to save having to duplicate this info on individual SOPs.Environmental watchList any specia l environmental conditions and cross reference to guard duty section, e.g. temperature hold up.CalibrationIdentify the critical parts of the analytical process. These will have to be controlled by careful operation and calibration. Cross reference to the relevant sections above. It may be easier to unified this section with the analytical procedure section.Include calibration of equipment what needs to be calibrated, how, with what, and how often?It is normally easier to write separate documents to cover the calibration of balances, self-winding pipettes, thermometers, refrigerators, freezers and spectrophotometers to save having to put all this information into each SOP.Quality ControlExplain the spirit control procedures, oftenness of feature control checks during batch analysis, pass/fail criteria, action to take in the event of a failure. It may be appropriate to incorporate this section in the analytical procedure section.Analytical ProcedureDescribe the analytical pro cedure, cross referencing previous sections as appropriate including reagents (with the appropriate identifier), appliance and instrumentation. Indicate at which point in the analytical procedure the quality control, and calibration procedures should be performed. Use a 50 cm3 measuring cylinder to transfer 30 cm3 of either sample, blank water (.), standard or QC solution to appropriately labelled test tubes. For each batch of samples, one sample should be replicated. For effluent samples or samples which are likely to contain operative levels of nitrite, using a glass pipette, pipette 3 cm3 of sample into a 50 cm3 measuring cylinder containing 27 cm3 of water. If any of the samples are highly coloured or turbid, prepare a sample blank by transferring 30 cm3 of the appropriate sample to an appropriately labelled test tube and add 1 cm3 of 10% orthophosphoric acid (). Treat as an ordinary sample except that water () is added instead of sulphanilamide reagent (.). Using an autom atic pipette add 0.75 cm3 of sulphanilamide solution (.) to each tube. Mix immediately by swirling, and allow to stand for at least 30 minutes but no longer than two hours. Measure the absorbance of the blank (.) and the standard (.) immortalize the relevant information in the spectrophotometeric logbook* and check that the absorbance of the standard is within the contract range detailed in the log book. If the absorbance falls outside this range, advert a senior officer before proceeding further. Determine the nitrite concentration of the QC solution () and the samples. Plot the concentration recorded for the QC solution (.) on the appropriate quality control chart , together with the date and your initials. If the point does not fall within the set limits, the senior officer in maintenance must be informed. * Any samples that give concentrations greater than 0.25 mg dm3, must be discarded and the analysis repeated using a diluted sample. Points to noteIf any of the sample s are highly coloured or turbid. Guidelines on how to handle difficult samplesUsing an automatic pipette Defines the accuracy that the reagent has to be measured toFor effluent samples or samples which are likely to contain significant levels of nitrite Guidelines on how to handle samples whose nitrite concentration will probably exceed the range for the method.Leave the colour to develop for 30 to 60 minutes This implies that the colour development time is important. You will have needed to carry out some checks to introduce that these times are satisfactory.Any samples that give concentrations greater than 0.25 mg dm-3, must be discarded and the analysis repeated using a diluted sample Only concentrations in the working range of the method should be reported.Consult a senior officer There will always be times when the analyst encounters lines or unknown situations the analyst should be encouraged to seek help from an experienced penis of staff.Log BooksInformation to be reco rded in the log book associated with spectrophotometer might include serial number, service dates, calibration checks (e.g. wavelength), repairs (e.g. new lamp).On a daily basis information recorded might include date, name of analyst, analysis (e.g. nitrite), wavelength used, absorbance of blank, concentration and absorbance of standard.At the front of the log book should be sufficient information regarding the nitrite analysis for the operator to determine if there is a problem, e.g. nitrite analysis, wavelength 540 nm, acceptable absorbances of (a) blank 0.000 0.005, (b) 0.25 mg dm-3 nitrite standard 0.250 0.010. Repeatability measurement on the same solution 0.003.Log Books points to noteUse of a standard, quality control and blank and a replicate sample and recording the information in a log book means that you can gift with reasonable certainty that (a) the reagents were made up chastenly, (b) the standards were made up correctly, (c) there was no contamination present, (d) the spectrophotometer was set up correctly and (e) the analysis can be repeated and give a result to within the expect limit.CalculationLay out the formulae for calculating the results ensuring all terms are clearly defined and derived. Specify requirements for checking, cross reference to QC requirements and indicate how department of corrections should be dealt with.Reporting Procedures Including Expression Of ResultsIndicate how results should be reported, including rounding of numbers final units. It may be appropriate to indicate the level of associated with the method. Results are reported to two significant figures as mg dm-3 Nitrite (NO2) except where the node has asked for the results to be reported as mg dm-3 Nitrogen in which case the analytical results are multiplied by 14/46. * Where significant dilutions have to be made then a comment about the dilution used should be put on the sheet used to report the results. preciseness , accuracy and detection limits Spectro photometric measurements on the same solution must have an absorbance range no greater than 0.003. A significant absorbance for a sample is 0.010 (after correction for the blank). A detection limit of 0.01 mg dm-3 (equivalent to an absorbance of approximately 0.010) is quoted for a 30 cm3 sample. This becomes 0.1 mg dm-3 for an effluent sample where the amount of sample taken is 3 cm3. Where typical absorbances readings (as listed in the log book) cannot be obtained for the standard, quality control and the blank, then further investigations must be carried out until the cause of the problem is found. * The results obtained for replicate analysis should be monitored, any significant difference ( 0.010 mg dm-3 ) should be investigated Literature ReferencesReferences may include operating manuals as swell as published methods and standards.This method is based on Method H in the Department of the Environment Standing Committee of Analysts booklet oxidised Nitrogen in Waters 1981. Annex Method Validation and standard UncertaintyMethods should be supported by experimental data providing information on accuracy, precision and selectivity . The study sources of uncertainty, relating to the method should be identified and the depute values listed. The overall uncertainty should be listed together with an explanation of how it was derived.In the case of the nitrite method that was based on a published method, the validation work involvedReproducibility showing comparable results were obtained. Repeatability showing in the results obtained for a known sample measured five times on the same day. Making up a set of 5 standards to show that the calibration was linear for the range 0.01 to 0.25 mg dm-3 NO2. Checking the detection limit using spiked samples . Checking that the time interval quoted for the colour development time was correct and non-critical within the stated range. We also looked at the method to identify major causes of variation in results e.g . measuring the sample volume with a measuring cylinder. We found that the biggest variation was in different analysts making up the same standard solutions hence the need to define an acceptable absorbance range for the standard.