FORD FLTM BP 155-01-2006 CROSS-LINK DENSITY OF ELASTOMERS《弹性体的交联点密度》.pdf
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1、 FORD LABORATORY TEST METHODBP 155-01Date Action Revisions 2006 08 15 Activated K. Nasser Printed copies are uncontrolled Copyright 2006, Ford Global Technologies, LLC Page 1 of 4 CROSS-LINK DENSITY OF ELASTOMERS Application This method is used to determine the cure state of Elastomer using a method
2、 involving solvent swell of the elastomer. Apparatus Required Vials - 20 ml capacity borosilicate scintillation vials with screw caps. Polyethylene weighing vial with cap. Oven - Air circulating, capable of maintaining 105 C, conforming to ISO 188/ASTM E 145 type IIA normal oven 150 + 50 air changes
3、 per hour. Analytical Balance - Capable of measuring out to 0.1 mg (0.0001 g). Razor Blades, Pipettes Materials Required Solvent Combinations for Cure State Measurements Elastomer Solvent Solvent Gravity, g/ml ACM Methyl Ethyl Ketone 0.8054 AEM Methyl Ethyl Ketone 0.8054 NBR Methyl Ethyl Ketone 0.80
4、54 HNBR Methyl Ethyl Ketone 0.8054 VMQ Cyclohexane 0.7739 FKM Acetone 0.7908 EPDM Toluene 0.8669 CR Toluene 0.8669 IR Toluene 0.8669 NR Toluene 0.8669 Conditioning and Test Conditions All test values indicated herein are based on material conditioned in a controlled atmosphere of 23 +/- 2 C and 50 +
5、/- 5% relative humidity for not less than 24 hours prior to testing and tested under the same conditions unless otherwise specified. FORD LABORATORY TEST METHODBP 155-01Printed copies are uncontrolled Copyright 2006, Ford Global Technologies, LLC Page 2 of 4 Procedure 1. Cut three specimens from mat
6、erial to be swollen. Each specimen should be roughly 0.1000 g to 0.2000 g in weight. Tare balance and record this weight as “Initial Weight“ in the laboratory book. 2. Place each specimen in a separate, numbered 20 ml scintillation vial. Record the numbers for the given material on the data sheet ne
7、xt to the description column. 3. Add approximately 10 ml swelling solvent to the vials using pipettes, and cap quickly. A list of appropriate swelling solvent is listed above. Ensure the total specimen is submerged in solvent. 4. Allow the specimens to swell for 96 hours at room temperature. Check s
8、pecimens after 1 hour to ensure that the total specimen is still submerged in solvent. Add more solvent if needed. 5. Tare the small polyethylene vial and the snap cap on the balance. 6. Remove each swollen specimen from the swelling solvent. Quickly blot off the excess solvent with a tissue and imm
9、ediately place the swollen specimen in the tarred vial. Recap the vial. 7. Re-weigh the vial plus the swollen specimen to the nearest 0.1 mg (0.0001 g) using the balance. Record the value as the “Swollen Weight“. 8 Return the swollen specimen to its numbered scintillation vial. 9. Using a pipette, f
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