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
Calculation Na 2 S 2 O 5 , g/L = [(N KIO 3 )(mL KIO 3 )–(N Na 2 S 2 O 3 )(mL Na 2 S 2 O 3 )](eq wt Na 2 S 2 O 5 )(1000) (mL sample)(1000) [(N KIO 3 )(50)–(N Na 2 S 2 O 3 )(mL Na 2 S 2 O 3 )](47.53)(1000) (10.00)(1000) 47.53[(N KIO 3)(50.0)–(N Na 2S 2O 3)(mL Na 2S 2O 3)] – 0.216(g/L PBA-1) – 0.216(g/L PBA-1) = – 0.216(g/L PBA-1) = 2 Processing KODAK Motion Picture Films, Module 3, Analytical Procedures H24.03
Determination of Sodium Sulfite in KODAK Color Developer ECN-2-1305B ECP-2-1305C ECR-1305L Process ECN-2 ECP-2D VNF-1/LC RVNP Formulas SD-49 SD-50/51 DR-100/101 DR-150/151 DR-105 DR-150 INTRODUCTION This method is used to determine sodium sulfite in a Process ECN-2, ECP-2D, or VNF/RVNP Color Developer sample. The sulfite content is determined by reacting the sample with excess iodine (liberated from the reaction of potassium iodine under acidic conditions). The unreacted iodine is titrated with standard sodium thiosulfate either potentiometrically or to a visual starch end point. The sulfite content is equivalent to the reacted iodine, which is the difference between the total iodine formed and the unreacted iodine titrated. The potentiometric titration is recommended over the visual end point titration. With the visual method, it is difficult to pick the end point in highly seasoned (colored) samples. Also, there is a tendency to over-titration, visually, which leads to low sulfite results. The potentiometric method overcomes both these problems because the end point is detected potentiometrically and displayed graphically by the titrator. Use of this methods requires handling of potentially hazardous chemicals. Material Safety Data Sheets should be consulted for each chemical before use. These can be obtained from each chemical supplier. PROCEDURE A – POTENTOMETRIC TITRATION Precision and Bias Process ECN-2—Three fresh and two seasoned samples of Process ECN-2 Color Developer were analyzed by four analysts on two separate days using multiple titrators. The samples were run in duplicate on each day. The fresh samples were prepared at 1, 3, and 5 g/L Na2SO3 . The seasoned sample consisted of Process ECN-2 Color Developer from a processor, analyzed as received (at 1.658 g/L Na2SO3 ) and with a standard addition of 0.35 g/L Na2SO3 . Process ECP-2D—Three fresh and two seasoned samples of Process ECP-2D Color Developer were analyzed by three analysts on two separate days using multiple titrators. The samples were run in duplicate on each day. The fresh samples were prepared at 1, 3, and 5 g/L Na 2SO 3. The seasoned sample consisted of Process ECP-2D Color Developer from a processor, analyzed as received (at 3.35 g/L Na 2SO 3) and with a standard addition of 0.65 g/L Na 2SO 3. Process VNF/RVNP—No reliability information was generated for the reversal process VNF-1 and RVNP. Customer Standard Deviation, s c Thew customer standard deviation (1s c ) is an estimate of the variability a customer could expect when submitting a sample to any Photoprocessing Quality Services laboratory, where any analyst could test the sample using any instrument on any day. ECN-2 Sample N Customer Standard Deviation, 1Sc Fresh 1 g/L Na2SO3 16 0.029 g/L Fresh 3 g/L Na2SO3 16 0.042 g/L Fresh 5 g/L Na2SO3 16 0.090 g/L Seasoned Sample (mean = 1.66 g/L Na2SO3 ) 16 0.042 g/L Seasoned Sample with Addition (mean = 1.99 g/L Na2SO3 ) 16 0.032 g/L ECP-2D Sample N Customer Standard Deviation, 1Sc Fresh 1 g/L Na2SO3 12 0.045 g/L Fresh 3 g/L Na2SO3 12 0.046 g/L Fresh 5 g/L Na2SO3 12 0.055 g/L Seasoned Sample (mean = 3.35 g/L Na2SO3 ) 12 0.122 g/L Seasoned Sample with Addition (mean = 3.99 g/L Na2SO3) 12 0.130 g/L Processing KODAK Motion Picture Films, Module 3, Analytical Procedures H24.03 1
- Page 67 and 68: Example Potentiometric Calculations
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- Page 71 and 72: APPARATUS Double Beam Spectrophotom
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- Page 77 and 78: Calculations a. Range: 0.5-2.5 g/L
- Page 79 and 80: APPENDIX 2 Typical Absorptivity mL
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- Page 83 and 84: APPARATUS All volumetric glassware
- Page 85 and 86: Procedure Preparation of 10 g/L Iro
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- Page 97 and 98: PROCEDURE A. Spectrophotometer Zero
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- Page 103 and 104: Potentiometric Determination of Kod
- Page 105 and 106: Titrimetric Determination of Persul
- Page 107 and 108: APPARATUS Conical Flask with stoppe
- Page 109 and 110: Potentiometric Determination of Sil
- Page 111 and 112: APPARATUS METROHM 536 Titrator or e
- Page 113 and 114: Potentiometric Determination of Sod
- Page 115 and 116: PROCEDURE Treatment of the Sample 1
- Page 117: Iodometric Determination of Sodium
- Page 121 and 122: Procedure Treatment and Titration o
- Page 123 and 124: Iodometric Determination of Sulfite
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- Page 133 and 134: Titrimetric Determination of EASTMA
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- Page 139 and 140: Cerimetric Determination of CD-2 Co
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Determination of Sodium Sulfite in KODAK Color Developer<br />
ECN-2-1305B<br />
ECP-2-1305C<br />
ECR-1305L<br />
Process ECN-2 ECP-2D VNF-1/LC RVNP<br />
Formulas SD-49 SD-50/51 DR-100/101<br />
DR-150/151<br />
DR-105<br />
DR-150<br />
INTRODUCTION<br />
This method is used to determine sodium sulfite in a Process<br />
ECN-2, ECP-2D, or VNF/RVNP Color Developer sample.<br />
The sulfite content is determined by reacting the sample with<br />
excess iodine (liberated from the reaction of potassium<br />
iodine under acidic conditions). The unreacted iodine is<br />
titrated with standard sodium thiosulfate either<br />
potentiometrically or to a visual starch end point. The sulfite<br />
content is equivalent to the reacted iodine, which is the<br />
difference between the total iodine formed and the unreacted<br />
iodine titrated.<br />
The potentiometric titration is recommended over the<br />
visual end point titration. With the visual method, it is<br />
difficult to pick the end point in highly seasoned (colored)<br />
samples. Also, there is a tendency to over-titration, visually,<br />
which leads to low sulfite results. The potentiometric<br />
method overcomes both these problems because the end<br />
point is detected potentiometrically and displayed<br />
graphically by the titrator.<br />
Use of this methods requires handling of potentially<br />
hazardous chemicals. Material Safety Data Sheets should be<br />
consulted for each chemical before use. These can be<br />
obtained from each chemical supplier.<br />
PROCEDURE A – POTENTOMETRIC<br />
TITRATION<br />
Precision and Bias<br />
Process ECN-2—Three fresh and two seasoned samples of<br />
Process ECN-2 Color Developer were analyzed by four<br />
analysts on two separate days using multiple titrators. The<br />
samples were run in duplicate on each day. The fresh<br />
samples were prepared at 1, 3, and 5 g/L Na2SO3 . The<br />
seasoned sample consisted of Process ECN-2 Color<br />
Developer from a processor, analyzed as received<br />
(at 1.658 g/L Na2SO3 ) and with a standard addition of<br />
0.35 g/L Na2SO3 .<br />
Process ECP-2D—Three fresh and two seasoned samples of<br />
Process ECP-2D Color Developer were analyzed by three<br />
analysts on two separate days using multiple titrators. The<br />
samples were run in duplicate on each day. The fresh<br />
samples were prepared at 1, 3, and 5 g/L Na 2SO 3. The<br />
seasoned sample consisted of Process ECP-2D Color<br />
Developer from a processor, analyzed as received<br />
(at 3.35 g/L Na 2SO 3) and with a standard addition of<br />
0.65 g/L Na 2SO 3.<br />
Process VNF/RVNP—No reliability information was<br />
generated for the reversal process VNF-1 and RVNP.<br />
Customer Standard Deviation, s c<br />
Thew customer standard deviation (1s c ) is an estimate of the<br />
variability a customer could expect when submitting a<br />
sample to any Photoprocessing Quality Services laboratory,<br />
where any analyst could test the sample using any instrument<br />
on any day.<br />
ECN-2 Sample N<br />
Customer Standard<br />
Deviation, 1Sc Fresh 1 g/L Na2SO3 16 0.029 g/L<br />
Fresh 3 g/L Na2SO3 16 0.042 g/L<br />
Fresh 5 g/L Na2SO3 16 0.090 g/L<br />
Seasoned Sample<br />
(mean = 1.66 g/L Na2SO3 )<br />
16 0.042 g/L<br />
Seasoned Sample with Addition<br />
(mean = 1.99 g/L Na2SO3 )<br />
16 0.032 g/L<br />
ECP-2D Sample N<br />
Customer Standard<br />
Deviation, 1Sc Fresh 1 g/L Na2SO3 12 0.045 g/L<br />
Fresh 3 g/L Na2SO3 12 0.046 g/L<br />
Fresh 5 g/L Na2SO3 12 0.055 g/L<br />
Seasoned Sample<br />
(mean = 3.35 g/L Na2SO3 )<br />
12 0.122 g/L<br />
Seasoned Sample with Addition<br />
(mean = 3.99 g/L Na2SO3) 12 0.130 g/L<br />
<strong>Processing</strong> KODAK Motion Picture Films, Module 3, Analytical Procedures H24.03 1