Processing kodak motion picture films, module 3 analytical procedures
Processing kodak motion picture films, module 3 analytical procedures Processing kodak motion picture films, module 3 analytical procedures
2 Processing KODAK Motion Picture Films, Module 3, Analytical Procedures H24.03
Iodometric Determination of Formalin in Stabilizer ECR-1803G Process ECN-2 ECP-2D VNF-1/LC RVNP Formulas – S-1c S-16 S-16 INTRODUCTION In this method the sample is added to an excess of hypoiodite, formed by acidifying standard potassium iodate, adding an excess of potassium iodide, and making the solution alkaline. Part of the hypoiodite is reduced by the formaldehyde in the sample, and the unreduced part is converted to iodine by acidifying the solution. The iodine is then titrated with sodium thiosulfate using starch indicator. KODAK Stabilizer Additive does not interfere in these reactions. Formalin is a solution of formaldehyde in water. The formulas for processing solutions are based on formalin which is 37.5 percent formaldehyde by weight and with a specific gravity of 1.095. The percent by weight and the specific gravity enter into the calculations for this determination. The specific gravity varies slightly depending on the concentration of methyl alcohol present as an antifreeze and preservative. This method requires handling potentially hazardous chemicals. Consult the Material Safety Data Sheet for each chemical before use. MSDS's are available from your chemical supplier. Note: Use pipets and volumetric glassware meeting the “Class A” definition by the National Institute of Standards and Technology (NIST). RELIABILITY The equation for determining the formalin content should be checked by preparing several standard laboratory mixes containing the particular strength of the formalin stock solution used in the processing solution. Normally the results obtained are slightly below the amount added to the mix. The results obtained on standard mixes should be within 5 percent of the mix value. If this is not the case, the concentration and the specific gravity of the formalin stock solution must be determined. The concentration can be found by using the ANSI test procedure, ANSI PH4.152-198O(R1987). REAGENTS Use ACS Reagent Grade reagents unless specified otherwise. 0.1 N Potassium Iodate, KIO 3 (standardized to 4 decimal places) 7.0 N Sulfuric Acid, H 2 SO 4 0.60 M Potassium Iodide, KI 2.5 N Sodium Hydroxide, NaOH 0.1 N Sodium Thiosulfate, Na 2 S 2 O 3 (standardized to 4 decimal places) Starch Indicator PROCEDURE Sample Treatment 1. Pipet (wipe the pipet before leveling) 50.0 mL of standardized 0.1 N potassium iodate into a 250-mL glass-stoppered conical flask. 2. Add 5 mL of 7.0 N sulfuric acid from a tip-up pipet. 3. Add 25 mL of 0.60 M potassium iodide from a tip-up pipet. Swirl to mix. 4. Pipet (wipe the pipet before leveling) the indicated volume of stabilizer into the flask: Process Formula Sample Size ECP-2D S-1c 10.00 mL VNF-1/LC S-16 20.0 mL RVNP S-16 20.0 mL 5. Add 25 mL of 2.5 N sodium hydroxide from a tip-up pipet. 6. Stopper the flask, swirl the contents, and allow it to stand approximately one minute. 7. At the end of one minute, add 10 mL of 7.0 N sulfuric acid from a tip-up pipet. Titration 1. Titrate immediately with standardized 0.1 N sodium thiosulfate to a light yellow color. 2. Add 5 mL of starch indicator from a tip-up pipet and continue the titration to the disappearance of the blue color. 3. Record the mL of standardized 0.1 sodium thiosulfate used. Processing KODAK Motion Picture Films, Module 3, Analytical Procedures H24.03 1
- Page 171 and 172: APPARATUS All volumetric glassware
- Page 173 and 174: Potentiometric Determination of Kod
- Page 175 and 176: PROCEDURE A. Preparation of Sample
- Page 177 and 178: Titrimetric Determination of Persul
- Page 179 and 180: APPARATUS Conical Flask with stoppe
- Page 181 and 182: Determination of the pH of the East
- Page 183 and 184: Determination of the pH of Processe
- Page 185 and 186: Potentiometric Determination of Sil
- Page 187 and 188: APPARATUS METROHM 536 Titrator or e
- Page 189 and 190: Determination of Sodium Metabisulfi
- Page 191 and 192: II. Visual Endpoint Titrations A. R
- Page 193 and 194: APPARATUS METROHM 536 Titrator or e
- Page 195 and 196: Viscosity Determination of Sound-Tr
- Page 197 and 198: Titrimetric Determination Of Benzyl
- Page 199 and 200: Potentiometric Determination of Bro
- Page 201 and 202: PROCEDURE B For Seasoned Tank Note:
- Page 203 and 204: Potentiometric Determination of Bro
- Page 205 and 206: CALCULATIONS mL AgNO 3 that would b
- Page 207 and 208: Titrimetric Determination of Buffer
- Page 209 and 210: Potentiometric Determination of Kod
- Page 211 and 212: Spectrophotometric Determination of
- Page 213 and 214: Titrimetric Determination of Citraz
- Page 215 and 216: Potentiometric Determination of Eth
- Page 217 and 218: Titrimetric Determination of Ferric
- Page 219 and 220: Iodometric Determination of Ferricy
- Page 221: Potentiometric Determination of Fer
- Page 225 and 226: Spectrophotometric Determination of
- Page 227 and 228: Titrimetric Determination of Hypo I
- Page 229 and 230: Potentiometric Determination of Iod
- Page 231 and 232: Potentiometric Determination of Pot
- Page 233 and 234: Titration Note: For preparation of
- Page 235 and 236: Titrimetric Determination of Persul
- Page 237 and 238: Spectrophotometric Determination of
- Page 239 and 240: APPARATUS Spectrophotometer with a
- Page 241 and 242: APPENDIX B Effect of Temperature in
- Page 243 and 244: Potentiometric Determination of Sil
- Page 245 and 246: Potentiometric Determination of Sod
- Page 247 and 248: Iodometric Determination of Total S
- Page 249 and 250: Titrimetric Determination of Total
- Page 251 and 252: Table 2 Contribution of Constituent
- Page 253 and 254: Determination of Sulfite in KODAK R
- Page 255 and 256: CALCULATIONS Na2SO3 , g/L = (mL B -
- Page 257 and 258: Colorimetric Determination of Thioc
- Page 259 and 260: APPENDIX A Calibration of Spectroph
- Page 261 and 262: Analysis Order for Photographic Pro
- Page 263 and 264: Procedure for Electroplating a Silv
- Page 265 and 266: The Selection, Care, and Use of Vol
- Page 267 and 268: In observing the lowest point on th
- Page 269 and 270: 4. Graduated Cylinders and Tip-up P
- Page 271 and 272: 6. Microburets Microburets equipped
Iodometric Determination of Formalin in Stabilizer<br />
ECR-1803G<br />
Process ECN-2 ECP-2D VNF-1/LC RVNP<br />
Formulas – S-1c S-16 S-16<br />
INTRODUCTION<br />
In this method the sample is added to an excess of<br />
hypoiodite, formed by acidifying standard potassium iodate,<br />
adding an excess of potassium iodide, and making the<br />
solution alkaline. Part of the hypoiodite is reduced by the<br />
formaldehyde in the sample, and the unreduced part is<br />
converted to iodine by acidifying the solution. The iodine is<br />
then titrated with sodium thiosulfate using starch indicator.<br />
KODAK Stabilizer Additive does not interfere in these<br />
reactions.<br />
Formalin is a solution of formaldehyde in water. The<br />
formulas for processing solutions are based on formalin<br />
which is 37.5 percent formaldehyde by weight and with a<br />
specific gravity of 1.095. The percent by weight and the<br />
specific gravity enter into the calculations for this<br />
determination. The specific gravity varies slightly depending<br />
on the concentration of methyl alcohol present as an<br />
antifreeze and preservative.<br />
This method requires handling potentially hazardous<br />
chemicals. Consult the Material Safety Data Sheet for each<br />
chemical before use. MSDS's are available from your<br />
chemical supplier.<br />
Note: Use pipets and volumetric glassware meeting the<br />
“Class A” definition by the National Institute of Standards<br />
and Technology (NIST).<br />
RELIABILITY<br />
The equation for determining the formalin content should be<br />
checked by preparing several standard laboratory mixes<br />
containing the particular strength of the formalin stock<br />
solution used in the processing solution. Normally the results<br />
obtained are slightly below the amount added to the mix.<br />
The results obtained on standard mixes should be within<br />
5 percent of the mix value. If this is not the case, the<br />
concentration and the specific gravity of the formalin stock<br />
solution must be determined. The concentration can be<br />
found by using the ANSI test procedure, ANSI<br />
PH4.152-198O(R1987).<br />
REAGENTS<br />
Use ACS Reagent Grade reagents unless specified<br />
otherwise.<br />
0.1 N Potassium Iodate, KIO 3<br />
(standardized to 4 decimal places)<br />
7.0 N Sulfuric Acid, H 2 SO 4<br />
0.60 M Potassium Iodide, KI<br />
2.5 N Sodium Hydroxide, NaOH<br />
0.1 N Sodium Thiosulfate, Na 2 S 2 O 3<br />
(standardized to 4 decimal places)<br />
Starch Indicator<br />
PROCEDURE<br />
Sample Treatment<br />
1. Pipet (wipe the pipet before leveling) 50.0 mL of<br />
standardized 0.1 N potassium iodate into a 250-mL<br />
glass-stoppered conical flask.<br />
2. Add 5 mL of 7.0 N sulfuric acid from a tip-up pipet.<br />
3. Add 25 mL of 0.60 M potassium iodide from a tip-up<br />
pipet. Swirl to mix.<br />
4. Pipet (wipe the pipet before leveling) the indicated<br />
volume of stabilizer into the flask:<br />
Process Formula Sample Size<br />
ECP-2D S-1c 10.00 mL<br />
VNF-1/LC S-16 20.0 mL<br />
RVNP S-16 20.0 mL<br />
5. Add 25 mL of 2.5 N sodium hydroxide from a tip-up<br />
pipet.<br />
6. Stopper the flask, swirl the contents, and allow it to<br />
stand approximately one minute.<br />
7. At the end of one minute, add 10 mL of 7.0 N sulfuric<br />
acid from a tip-up pipet.<br />
Titration<br />
1. Titrate immediately with standardized 0.1 N sodium<br />
thiosulfate to a light yellow color.<br />
2. Add 5 mL of starch indicator from a tip-up pipet and<br />
continue the titration to the disappearance of the blue<br />
color.<br />
3. Record the mL of standardized 0.1 sodium thiosulfate<br />
used.<br />
<strong>Processing</strong> KODAK Motion Picture Films, Module 3, Analytical Procedures H24.03 1