RADIATION STABILITY OF ORGANIC LIQUIDS. Semi-Annual Report No. 4 for July 1 to December 31, 1958
0 @ 4 2 7 1 8 3 7 1 7 6 TBP from 0 to 100 were irradiated with electrons to 300 to 400 whr/liter. The G(total acid) values obtained indicated that, from 0 to 60 wt, % TBP, the acid produc tion rate is proportional to wt, % TBP; above 60 wt, % TBP the acid production rate is lower. Normalized total acid G values, obtained by partition of the dose on a basis of wt, % TBP, ranged from 2.31 to 3.52. Seven TBP-Amsco solutions, ranging from 5 to 60 wt. % TBP, and samples of pure TBP and pure dibutyl phenylphosphorate (DBPP) were irradiated to 400 whr/liter, Five compositions of TBP, DBPP, Amsco, and tetralin were irradiated to 200 whr/liter. The amount of radiationinduced unsataration was measured for each of the above samples. The data indicated that unsaturation varied inversely with wt. % TBP. The DBPP exerted a small protective effect, as did tetralin, in reducing radiation damage to the Amsco. Diethyl carbonate, irradiated to 392 whr/liter, had a G(gas) value of 4.86, a--G (target destruction) value of 5.50, and a --G /sub M/(polymer) value of 2.80. Diethyl carbonate, after irradiation, extracts U better than virgin material and strips equally as well. The irradiated diethyl carbonate exhibited no difference from virgin material in emulsification tendency. Dibutyl phenylphosphorate-Amsco systems, at dose levels of either 200 or 400 whr/liter, showed that acid production is about proportioral to wt. % DBPP. Studies of DBPP-Amsco-tetralin systems at 200 whr/ liter indicated that tetralin is more acceptable than decalin for enhancing the solubility of the DBPP-uranium complex in Amsco, thus suppressing third-phase phenomena. Tetralin also reduced acid production from DBPP under irradiation. Tributyl phosphate, dibutyl phosphoric acid, and di-(2- ethylhexyl) phosphoric acid were irradiated in the pure state to 300 whr/liter. The G(gas) values were 1.9, 3.3, and 3.1, respectively, and the G(total acid) values were 2.3, 2.1, and 1.2. The--G values for target converted to polymer were 0.22 for the DBP, and 0.32 for the D2EHP. Tri-n-octyl phosphine oxide was irradiated in the pure state to 400 whr/liter. The G(gas) value of 1.82 was comparable to a value of 1.45 found previously at 2040 whr/1iter. Values of --G/ sub M/ for target and polymer were approximately double the values previously found at 2040 whr/ liter. Amines, including tri-lauryl amine, n-benzyl heptadecyl amine, tri-iso-octyl amine, Primene JM-T, and tri-oetyl-decyl-t-amine (Alamine) were irradiated to either 200- or 400-whr/liter doses. The Primene produced the lowest --G (polymer) value, (1.50) and the Alamine produced the highest -- G/sub M/(total target destroyed) value (3.49). An Alamine-tridecanol- Amsconitric acid system yielded the lowest G(gas) value (1.89) while the corresponding tri-lauryl amine system produced the highest (3.12). The most extensive emulsification occurred with the 0.5M tri-lauryl amtne-Amscotridecanol system while the n-benzyl heptadecyl amine system exhtbited the lowest emulsification tendency, The most efficient U extractant system observed was the Alamine-Amsco-tridecanol-nitric acid composition, at the 0.5M-Alamine level. A comparison was made of the quantity and composition of material removed from irradiated TBP-Amsco by various scrubbing media. A single scrub with 2M NaOH appears four times more efftcient than does a single scrub with satarated CaOH in removing acidic radiolysis products. The emulsification tendency of the scrubbed organic appears to increase with the quantity of acidic radiolysis products removed. Radiolysis products other than those of acidic natare (polymer) are apparently not removed by the scrubbing media investigated in this study. An ir
- Research Organization:
- Stanford Research Inst., Menlo Park, Calif.
- DOE Contract Number:
- W-7405-ENG-26, SUBCONTRACT 1081
- NSA Number:
- NSA-13-011419
- OSTI ID:
- 4277755
- Report Number(s):
- AECU-4054
- Resource Relation:
- Other Information: SRI Project No. SD-2080-1. For Oak Ridge National Lab. Orig. Receipt Date: 31-DEC-59
- Country of Publication:
- United States
- Language:
- English
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RADIATION STABILITY OF ORGANIC LIQUIDS. Semi-Annual Report No. 2 for July 1 to December 31, 1957
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Related Subjects
ACIDS
ALKANES
AMINES
AMSCO
BUTYL PHOSPHATES
BUTYL RADICALS
CARBONATES
DECOMPOSITION
ELECTRONS
ETHYL RADICALS
G-VALUE
LIQUIDS
OCTYL RADICALS
ORGANIC COMPOUNDS
ORGANIC PHOSPHORUS COMPOUNDS
PHENYL RADICALS
PHOSPHORIC ACID
POLYMERS
POTASSIUM HYDROXIDES
RADIATION CHEMISTRY
RADIATION DOSES
RADIATION EFFECTS
RADIOLYSIS
SODIUM CARBONATES
SODIUM HYDROXIDES
SOLUBILITY
SOLVENT EXTRACTION
STABILITY
URANIUM