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Standard Operating Procedure SEA05 Laboratory Analysis-Version
Gulf Coast Network National Park Service Inventory and Monitoring Division Standard Operating Procedure SEA05 Laboratory Analysis—Version 1.0 Please cite this as: Meiman, J. 2019. Laboratory Analysis—Version 1.0. Gulf Coast Network Standard Operating Procedure NPS/GULN/SOP—SEA05. Gulf Coast Network, Lafayette, Louisiana. Summary This standard operating procedure (SOP) for laboratory analysis of total suspended solids (TSS) is adopted verbatim from USEPA Method 160.2. Revision Log Revision Date Author Changes Made Reason for Change New Version # METHOD #: 160.2 Approved for NPDES (Issued 1971) TITLE: Residue, Non-Filterable (Gravimetric, Dried at 103–105°C) ANALYTE: Residue, Non-Filterable INSTRUMENTATION: Drying Oven STORET No. 00530 1. Scope and Application a. This method is applicable to drinking, surface, and saline waters, domestic and industrial wastes. b. The practical range of the determination is 4 mg / L to 20,000 mg / L. 2. Summary of Method a. A well-mixed sample is filtered through a glass fiber filter, and the residue retained on the filter is dried to constant weight at 103-105°C. b. The filtrate from this method may be used for Residue, Filterable. 3. Definitions a. Residue, non-filterable, is defined as those solids which are retained by a glass fiber filter and dried to constant weight at 103-105°C. 4. Sample Handling and Preservation a. Non-representative particulates such as leaves, sticks, fish, and lumps of fecal matter should be excluded from the sample if it is determined that their inclusion is not desired in the final result. b. Preservation of the sample is not practical; analysis should begin as soon as possible. -
Multigram Chromatography-Free Synthesis of Octa (Ethylene Glycol) P
ORGANIC CHEMISTRY FRONTIERS View Article Online METHOD View Journal | View Issue Multigram chromatography-free synthesis of octa(ethylene glycol) p-toluenesulfonate† Cite this: Org. Chem. Front., 2016, 3, 1524 Adam M. Wawro,a Takahiro Muraoka,b,c Maho Katob and Kazushi Kinbara*b Here we report a detailed synthetic procedure for monodisperse octa(ethylene glycol) p-toluenesulfonate, Received 27th July 2016, a member of the heterobifunctional oligo(ethylene glycol) derivatives family. The method offers Accepted 3rd September 2016 completely chromatography-free workup and purification, resulting in higher yields and a lower cost than DOI: 10.1039/c6qo00398b any of the alternative strategies. We also introduce several upgrades, simplifying the method even more, rsc.li/frontiers-organic and discuss the chromatography-free design limitations. Introduction building blocks of functional compounds. Although tradition- ally PEGs have been produced by polymerization, yielding stat- Creative Commons Attribution-NonCommercial 3.0 Unported Licence. Poly(ethylene glycol)s (PEGs) are frequently used in chemistry, istically distributed mixtures of individual polymer molecules, most notably for protein cross-linking and modification, the recent demand for more uniform PEGs has stimulated surface functionalization, and as flexible and hydrophilic studies on well-defined, single-molecule polymers. These PEGs, known as ‘discrete’, ‘unimolecular’ or ‘monodisperse’, consist of a single chemical species with a specific molecular a Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, weight. Monodisperse PEGs are obtained by classical step- 2-1-1 Katahira, Aoba-ku, Sendai 980-8577, Japan bSchool of Life Science and Technology, Tokyo Institute of Technology, by-step chemical synthesis, usually from inexpensive short 4259 Nagatsuta-cho, Midori-ku, Yokohama 226-8501, Japan. -
Volumetric Labware Volumetric Labware
Volumetric Labware Volumetric Labware Volumetric Glassware NABL Certificate Please see list of Accreditation Bodies Worldwide from Page 148-151 38 Volumetric Labware In ASTM standards cylinders are now calibrated "to deliver" (TD), which has been recently introduce in Cylinder section. 39 Volumetric Labware BATCH CERTIFICATE Volumetric flasks comes with a batch certificate in which mean value, standard deviation is incorporated along with batch number like which signifies the month 01 and 10 is the year 01.10 This comes in a pack of 1 and comes along with the flask in the box you can also download it from www.glasscolabs.com and by scanning the QR Code from the label of the box. QR CODES ! Scan For Certicates Now On Cartons Of All Glassco Wares! Use your Smartphone to scan the QR Code on the box labels … Just select the Certicate you wish to see… Conformity… Calibration … (Individual or Batch) INDIVIDUAL CERTIFICATE These flasks comes with a certificate on which individual serial number, mean value, standard deviation and measured uncertainty is given along with the batch number and serial number like 01.10 (Month and year of manufacturing) 505 (serial number) 01.10 5 0 5 This comes in a pack of one and each flask is having a certificate with it in the box you can also download it from www.glasscolabs.com and by scanning the QR Code from the label of the box. USP Glassware All the volumetric glassware or measuring instruments to be used in laboratories which are under surveillance of US authorities such as Food and Drug Administration (FDA), have a mandatory requirement to use products which adhere to standards set by US PHARMACOPEIA. -
Reducible Sulfur in Paper and Paperboard (Revision of T 406 Om-08) (No Changes from Draft 2)
NOTICE: This is a DRAFT of a TAPPI Standard in ballot. Although available for public viewing, it is still under TAPPI’s copyright and may not be reproduced or distributed without permission of TAPPI. This draft is NOT a currently published TAPPI Standard. WI 120802.02 T 406 DRAFT NO. 3 DATE April 30, 2013 WORKING GROUP CHAIRMAN James C. Abbott SUBJECT CATEGORY Chemical Properties RELATED METHODS See “Additional Information” CAUTION: This Test Method may include safety precautions which are believed to be appropriate at the time of publication of the method. The intent of these is to alert the user of the method to safety issues related to such use. The user is responsible for determining that the safety precautions are complete and are appropriate to their use of the method, and for ensuring that suitable safety practices have not changed since publication of the method. This method may require the use, disposal, or both, of chemicals which may present serious health hazards to humans. Procedures for the handling of such substances are set forth on Material Safety Data Sheets which must be developed by all manufacturers and importers of potentially hazardous chemicals and maintained by all distributors of potentially hazardous chemicals. Prior to the use of this method, the user must determine whether any of the chemicals to be used or disposed of are potentially hazardous and, if so, must follow strictly the procedures specified by both the manufacturer, as well as local, state, and federal authorities for safe use and disposal of these chemicals. Reducible sulfur in paper and paperboard (Revision of T 406 om-08) (no changes from Draft 2) 1. -
Sulfur Dioxide
Corn Sugar (crude & refined) Analysis F-54-1 SULFUR DIOXIDE PRINCIPLE Sulfur dioxide is released by boiling an acidic sample solution, and it is removed by sweeping with a stream of nitrogen. The gas stream is passed through dilute hydrogen peroxide solution where sulfur dioxide is oxidized to sulfuric acid. The acid is titrated with standard alkali. (Note 1) SCOPE The method applies to crude and refined sugars (Note 2) and, with minor modification, to most liquid and solid samples even in the presence of other volatile compounds. SPECIAL APPARATUS 1. The FDA modified "Monier-Williams" apparatus (Figure 1) is available from Fisher Scientific, 91/92 Cat. No. K513800 (Kontes 513800), Pittsburgh, PA, and affiliates worldwide. It or some of its parts are also available from other laboratory supply houses. (Note 3) 2. Heating mantle, for a 1000 mL boiling flask, controlled by a variable transformer. 3. Flow controlling valve, with flow indicator, capable of controlling nitrogen gas flow to 200 mL/min. 4. Refrigerated, circulating bath capable of maintaining flow through condenser at 5-10 °C (Note 4) 5. Vortex mixer 6. Buret, class A, 10 mL 7. Pipet bulb Analytical Methods of the Member Companies of the Corn Refiners Association, Inc. Accepted 11-13-61 Revised 4-9-91 Corn Sugar (crude & refined) Analysis F-54-2 SULFUR DIOXIDE ⎯ continued REAGENTS 1. Hydrogen Peroxide Solution, 3%: Dilute 10 mL of C.P. neutral 30% hydrogen peroxide (H2O2) with purified water to 100 mL. Prepare daily. 2. Sodium Hydroxide Solution, 0.01 N: Dilute 10 mL of 0.100 N NaOH solution to 100 mL. -
Azoniaspiro Salts: Towards Bridging the Gap Between Room-Temperature Ionic Liquids and Molten Salts
Electronic Supplementary Material (ESI) for Physical Chemistry Chemical Physics. This journal is © the Owner Societies 2016 Azoniaspiro salts: towards bridging the gap between room-temperature ionic liquids and molten salts Matthew T. Clough,a,b Karolin Geyer,c Patricia A. Hunt,*a Alastair J. S. McIntosh,a Rebecca Rowe,a Tom Welton*a and Andrew J. P. Whitea a Department of Chemistry, Imperial College London, London, UK, SW7 2AZ, United Kingdom b Max-Planck-Institut für Kohlenforschung, 45470 Mülheim-an-der-Ruhr, Germany c BASF SE, Ludwigshafen, Germany * Corresponding Authors: [email protected] [email protected] Electronic Supplementary Information 1. General laboratory procedures 2 2. Synthesis of ionic compounds 2 3. TGA procedures 8 4. TGA-MS procedures 9 5. TGA-GCMS procedures 9 6. X-Ray Crystallography procedures and data 10 7. Computational methods 12 8. Ion pair conformers and transition state structures 13 1 1. General laboratory procedures All reactions requiring an inert atmosphere were performed under a blanket of nitrogen gas, which was dried through a column of phosphorus pentoxide. All commercially acquired chemicals were obtained from Sigma- Aldrich or Tokyo Chemical Industry, and were used without further purification unless otherwise stated. Anhydrous solvents were dried through an HPLC column on an Innovative Technology Inc. solvent purification system. NMR spectra were recorded on Bruker Avance-400 (1H NMR (400 MHz), 13C (100 MHz), 19F (376 MHz)) NMR spectrometers. Chemical shifts are reported in ppm (relative to the DMSO-d6 residual peak). IR spectra were recorded on a Perkin Elmer spectrum 100 FTIR using an ATR inset with a diamond crystal. -
SILICA, CRYSTALLINE in Coal Mine Dust, by IR 7603
SILICA, CRYSTALLINE in coal mine dust, by IR 7603 SiO2 MW: 60.08 CAS: 14808-60-7 RTECS: VV7330000 METHOD: 7603, Issue 2 EVALUATION: UNRATED Issue 1: 15 May 1989 Issue 2: 15 August 1994 quartz (respirable): 3 OSHA : 10 mg/m /(%SiO2 + 2) PROPERTIES: solid; crystalline transformations: quartz NIOSH: 0.05 mg/m3 (suspect carcinogen) to tridymite @ 867 °C: tridymite to ACGIH: 0.1 mg/m3 crystobalite @ 1470 °C; a-quartz to b-quartz @ 573 °C SYNONYMS: free crystalline silica; silicon dioxide SAMPLING MEASUREMENT SAMPLER: CYCLONE + PREWEIGHED FILTER TECHNIQUE: INFRARED SPECTROPHOTOMETRY (IR) (10-mm cyclone, nylon, or Higgins-Dewell (HD), and PVC filter, 37-mm, 5-µm) ANALYTE: quartz FLOW RATE: HD cyclone: 2.2 L/min WEIGH: dust cassette nylon cyclone: 1.7 L/min ASH: muffle furnace or RF plasma asher VOL-MIN: 300 L @ 0.1 mg/m 3 -MAX: 1000 L REDEPOSIT: 0.45-µm acrylic copolymer membrane filter SHIPMENT: routine IR: scan, 1000 to 650 cm -1, absorbance mode SAMPLE STABILITY: stable with blank filter in reference beam BLANKS: 2 to 10 field blanks per set CALIBRATION: standard suspension of quartz in 2-propanol BULK SAMPLE: required for OSHA standard calculations; area respirable or settled dust RANGE: 30 to 250 µg quartz per sample [1] ESTIMATED LOD: 10 µg quartz per sample [1] ACCURACY PRECISION (S r): 0.098 @ 100 to 500 µg per sample RANGE STUDIED: 25 to 160 µg/sample [1] (varies with sample matrix) [1] (2 mg quartz/m 3 atmosphere) BIAS: unknown ˆ OVERALL PRECISION (S rT): 0.13 to 0.22 (varies with sample loading and matrix) ACCURACY: ±25.6 to 43.4% APPLICABILITY: The working range is 0.03 to 2 mg/m 3 for a 1000-L sample. -
SILICA, CRYSTALLINE, by XRD (Filter Redeposition) 7500
SILICA, CRYSTALLINE, by XRD (filter redeposition) 7500 SiO2 MW: 60.08 CAS: 14808-60-7 (quartz) RTECS: VV7330000 (quartz) 14464-46-1 (cristobalite) VV7325000 (cristobalite) 15468-32-3 (tridymite) VV7335000 (tridymite) METHOD: 7500, Issue 4 EVALUATION: FULL Issue 1: 15 August 1990 Issue 4: 15 March 2003 3 3 OSHA : quartz (respirable) 10 mg/m /(%SiO2+2); PROPERTIES: solid; d 2.65 g/cm @ 0 °C; crystalline cristobalite and tridymite (respirable) ½ the above transformations: quartz to tridymite NIOSH: 0.05 mg/m3; carcinogen @ 867 °C; tridymite to cristobalite ACGIH: quartz (respirable) 0.1 mg/m3 @ 1470 °C; "-quartz to ß-quartz cristobalite (respirable) 0.05 mg/m3 @ 573 °C tridymite (respirable) 0.05 mg/m3 SYNONYMS: free crystalline silica; silicon dioxide SAMPLING MEASUREMENT SAMPLER: CYCLONE + FILTER TECHNIQUE: X-RAY POWDER DIFFRACTION (10-mm nylon cyclone, Higgins- Dewell (HD) cyclone, or aluminum ANALYTE: Crystalline SiO2 cyclone + 5-:m PVC membrane) *see sampling section ASH: Muffle furnace or RF plasma asher or dissolve in tetrahydrofuran FLOW RATE: Nylon cyclone: 1.7 L/min; HD cyclone: 2.2 L/min; REDEPOSIT: On 0.45-:m Ag membrane filter aluminum cyclone: 2.5 L/min XRD: Cu target X-ray tube, graphite VOL-MIN: 400 L monochromator -MAX: 1000 L Optimize for intensity; 1° slit Slow step scan, 0.02°/10 sec SHIPMENT: Routine Integrated intensity with background subtraction SAMPLE STABILITY: Stable CALIBRATION: :NIST SRM 1878a quartz, NIST SRM 1879a cristobalite, USGS 210-75-0043 BLANKS: 2 to 10 per set (see step 13.g.) tridymite suspensions in 2-propanol. BULK SAMPLE: High-volume or settled dust; to RANGE: 0.02 to 2 mg SiO2 per sample [2] identify interferences ESTIMATED LOD: 0.005 mg SiO2 per sample [2] ACCURACY þ PRECISION ( r): 0.08 @ 0.05 to 0.2 mg per sample [1] RANGE STUDIED: 25 to 2500 :g/m3 [1] (800-L sample) BIAS: None known Ö : OVERALL PRECISION ( rT): 0.09 (50 to 200 g) [1] ACCURACY: ± 18% APPLICABILITY: The working range is 0.025 to 2.5 mg/m3 for an 800-L air sample. -
Chemistry Lab Course
Chemistry Lab Course Kantonsschule Zürich Nord Tilmann Geldbach 2015/2016 Chemistry Lab 2 Preface The aim of this lab course is that you learn how to conduct simple chemical experiments and how to document these experiments. You should learn to carefully observe and – based on these observations – come up with explanations and hypotheses about what you have seen. During the course you will learn basic lab techniques, the proper use of standard equipment as well as how to handle harmful chemicals. Organisation It is expected that you have studied the lab instructions of the current experiment before the lesson has started. Remaining questions can be clarified before the lab session starts. In most cases you will be working in pairs. You should always take notes on what you are doing and on what can be observed. There is a work sheet for most of the experiments. You should return this work sheet at the end of the lab session or unasked in the next theory lesson at the latest. These work sheets will be graded with bonus points. The lab should be fun! Therefore make an effort to create an atmosphere that is pleasant both to you and your classmates. You should help each other both during the experiments and during clean-up. Not all substances that are used in the lab are harmless. Pay attention to the safety instructions below and on the sheets of the respective experiment. Safety There are essentially three ways in which a chemical substance may enter your body: by oral uptake, by inhalation or by absorption through the skin. -
PIRANHA SOLUTION CLEANING Rev
Section 4: Laboratory SOPs – Procedure Form Title: PIRANHA SOLUTION CLEANING Rev. Date: 08/06/18 Prepared By: P.I.: Prior Approval: This procedure is considered hazardous enough that prior approval is needed from the Principal Investigator: Y N Involves Use of Particularly Hazardous Substance (PHS)? Y N Carcinogen Reproductive Toxin High Acute Toxicity Does this procedure require medical surveillance? Y N Does this require use of a fit-tested respirator? Y N A Piranha solution is a mix of concentrated sulfuric acid with hydrogen peroxide, and generally used to Bremoverief Description organic residues of Procedure from substrates. (100 wordsSee prep or below: less): 1. Transfer sulfuric acid to a large, clean Pyrex glass beaker. (NO PLASTIC CONTAINERS) 2. Slowly add 1 part 30% hydrogen peroxide to 3 parts concentrated sulfuric acid inside a chemical fume hood using PPE described below. Use a dropping funnel to add hydrogen peroxide to sulfuric acid with continuous stirring. (use a Teflon coated stir bar) 3. Slowly place clean microscope slides and coverslips into the solution for 1 hour using long tongs to avoid skin exposure. 4. Remove slides/coverslips with tongs and sonicate in milliQ water for 10 minutes. 5. Allow piranha solution to cool to room temperature in an open container. 6. Transfer cooled solution to a clean and dry vented waste container for disposal. Safety Notes: All piranha manipulations shall be conducted inside a properly functional chemical fume hood. Keep all containers in secondary containment at all times. Prepare solution immediately before use. Avoid all contact between piranha solution and organic materials. -
Edna PROTOCOL SAMPLE COLLECTION
eDNA PROTOCOL SAMPLE COLLECTION Caren Goldberg and Katherine Strickler, Washington State University September 2014 Adapted from Protocol Version 04/12/2012 (D.S. Pilliod, R.S. Arkle, and M.B. Laramie) USGS Snake River Field Station MATERIALS 1. Cellulose nitrate disposable filter funnels or other field-tested, disposable filter funnels 2. Vacuum flask (1L) 3. Silicone tubing 4. Vacuum hand pump (from auto parts store) 5. Rubber stopper with hole for funnel stem 6. Latex or nitrile gloves (non-powdered) 7. Forceps (filter forceps if possible) 8. High quality, o-ring screw cap 2mL tubes (e.g., Sarstedt brand) with 1mL 100% molecular-grade ethanol (not denatured) 9. Ethanol-proof laboratory pen (do not use a regular Sharpie marker) 10. 50 mL tubes of 30 mL 1) 50% household bleach solution 2) distilled water in a holder (a foam drink holder [koozie] works well) 11. Polypropylene grab bottles and cooler (for off-site filtering) or Whirl-Pak® bags (for on- site filtering) 12. Water, bleach, scrub brush, and tubs (for decontaminating between sites) 2 3 5 1 4 2 Figure 1. Filter funnel (1), vacuum flask (2), silicone tubing (3), vacuum pump (4), and rubber stopper (5). 9 7 10 8 6 1 Figure 2. Latex or nitrile gloves (6), forceps (7), 2 mL tubes with 1 mL ethanol (8), ethanol-proof lab marker (9), and 2 50 mL tubes with 50% household bleach solution distilled water (10). 3 11a 11b Figure 3. Polypropylene grab bottles (11a) and Whirl-Pak® bag (11b). 12a 12d 12b 12c Figure 4. Water (12a), bleach (12b), scrub brushes (12c), and tubs (12d) for decontaminating boots and equipment between sites. -
United States Patent Office Patented Jan
3,297,633 United States Patent Office Patented Jan. 10, 1967 1. 2 maximum of seventy weight percent of 4,4'-bis(hydroxy 3,297,633 phenyl)-methane. PREPARATION OF POYESTERS WITH LOW MET The diacid halides of aromatic dicarboxylic acids which WISCOSITY FROM A. MIXTURE OF BISPHENOL can be used in the polycondensation according to the in RaymondSOMERS R. Hindersian, Lewiston, N.Y., and Andrée Jan vention can be obtained by the reaction of aromatic di Conix, Hove-Antwerp, Belgium; said Hindersinn as carboxylic acids with thionyl chloride. Suitable aromatic signor to Hooker Chemical Corporation, Niagara Falls, dicarboxylic acids are among others: N.Y., a corporation of New York, and Said Consix as terephthalic acid signorgium, a to Belgian Gevaert company Photo-Producten N.V., Mortsel, Bel isophthalic acid No Drawing. Filed July 25, 1962, Ser. No. 212,457 O phthalic acid 5 Claims. (C. 260-47) bis(4-carboxy)-diphenyl bis(4-carboxyphenyl)-ether It is known to prepare linear polyesters by polycondens bis(4-carboxyphenyl)-sulphone ing a metal diphenate of a bisphenol of the formula: bis(4-carboxyphenyl)-carbonyl HO-Ar-R-Ar-OH bis(4-carboxphenyl)-methane with a diacid halide of an aromatic dicarboxylic acid of bis(4-carboxyphenyl)-dichloromethane 1,2- and 1,1-bis(4-carboxyphenyl)-ethane the formula: 1,1- and 2,2-bis(4-carboxyphenyl)-propane HOOC-Ar-R-Ar-COOH 1,1- and 2,2-bis(3-carboxyphenyl)-propane wherein each of Ar and Ar' represents a p-phenylene 20 2,2-bis(4-carboxyphenyl)-1,1-dimethyl-propane radical, a m-phenylene radical, one of R and R