• Bulletin of the Korean Chemical Society
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• v.22 no.5
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• pp.503-506
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• 2001

Separation of lithium isotopes was investigated by chemical ion exchange with a hydrous manganese(IV) oxide ion exchanger using an elution chromatography. The capacity of manganese(IV) oxide ion exchanger was 0.5 meq/g. One molar CH3COO Na solution was used as an eluent. The heavier isotope of lithium was enriched in the solution phase, while the lighter isotope was enriched in the ion exchanger phase. The separation factor was calculated according to the method of Glueckauf from the elution curve and isotopic assays. The single stage separation factor of lithium isotope pair fractionation was 1.021.

• Bulletin of the Korean Chemical Society
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• v.28 no.3
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• pp.451-456
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• 2007

Tetraazamacrocyclic ion exchangers tethered to Merrifield peptide resin (DTDM, TTTM) were prepared and the ion exchange capacity of these was characterized. The isotope separation of lithium was determined using breakthrough method of column chromatography. The isotope separation coefficient was strongly dependent on the ligand structure by Glueckauf's theory. We found that the isotope separation coefficients were increased as the values of distribution coefficients were increased. In this experiment the lighter isotope, 6Li was enriched in the resin phase, while the heavier isotope, 7Li in the solution phase. The ion radius of lighter isotope, 6Li was shorter than the heavier isotope, 7Li. The hydration number of lithium ion with the same charge became small as mass number was decreased. Because 6Li was more strongly retained in the resin than 7Li, the isotopes of lithium were separated with subsequent enrichment in the resin phase.

• Journal of the Korean Chemical Society
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• v.45 no.3
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• pp.219-222
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• 2001

Separation of lithium isotopes was investigated by chemical ion exchange with a hydrous manganese(IV) oxide ion exchanger using an elution chromatography. The capacity of manganese(IV) oxide ion exchanger was 0.5 meq/g. The heavier lithium isotope was enriched in the solution phase, while the lighter isotope was enriched in the ion exchanger phase. The separation factor was determined according to the method of Glueckauf from the elution curve and isotopic assays. The separation factor of $^6Li^+$-$^7Li^+$ isotope pair fractionation was 1.018.

• Journal of the Korean Chemical Society
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• v.27 no.3
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• pp.189-193
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• 1983

The lithium isotopes separation experiments were carried out in hydrochloric acid with cation exchanger systerns. In these experiments were employed porous sulfonated styrene-divinylbenzene copolymer and Dowex 50w-x8 as cation exchanger. The contents of lithium of the fraction were determined with atomic absorption spectrophotometer. The relative mass of lithium isotopes of the fractions was analyzed on a mass spectrometer. The isotope separation factors of lithium were calculated from the isotope compositions of these eluted fractions. Separation factor for the system in hydrochloric acid and porous sulfonated styrene-divinylbenzene copolymer was found to be 1.0020, and for the case of system in hydrochloric acid and Dowex 50w-x8 was 1.0011${\om}$0.0002. From these results, we found that the separation factor for porous sulfonated styrene-divinylbenzene copolymer ionexchanger is larger than value of Dowex 50w-x8 ionexchanger.

• Analytical Science and Technology
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• v.10 no.6
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• pp.403-407
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• 1997

Separation factor for $^6Li$ and $^7Li$ have been determined using ion exchange resin having 1,7,13-trioxa-4,10,16-triazacyclooctadecane($N_3O_3$) as an anchor group. The lighter isotope, $^6Li$ is concentrated in the solution phase, while the heavior isotope, $^7Li$ is enriched in the resin phase. By Ccolumnl chromatography[0.9cm(I.D)${\times}$20cm(height)] using 2.0M ammonium chloride solution as an eluent, single separation factor, ${\alpha}$, 1.009. i.e.$(^7Li/^6Li)_{resin}$/$(^7Li/^6Li)_{solution}$ was obtained by the Glueckauf theory from the elution curve and isotope ratios.

• Analytical Science and Technology
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• v.7 no.2
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• pp.201-204
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• 1994

Cation exchange column chromatography of lithium was carried out to investigate the lithium isotope separation in aqueous ion exchange system. A Pyrex glass column of $50cm{\times}6mm$ inner radius with a water jacket was used as the separation column in experiment. Upon column chromatography using hydrochloric and succinic acid mixtures as an elunent, single separation factor, ${\alpha}$, 1.0068 was obtained. From the experiment, it was found that $^6Li$ was enriched in the resin phase and $^7Li$ in the solution phase.

• Analytical Science and Technology
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• v.11 no.4
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• pp.231-234
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• 1998

Separation factor for $^6Li$ and $^7Li$ has been determined using ion exchange resin having 1,7,13-trioxa-4,10,16-triazacyclooctadecane ($N_3O_3$) as an anchor group. The ion exchange capacity of the $N_3O_3$ ion exchanger was 2.0 meq/g dry resin. The lighter isotope, $^6Li$, is concentrated in the fluid phase, while the heavier isotope, $^7Li$, is enriched in the resin phase. By column chromatography [0.3 cm(I.D)${\times}$30 cm (height)] using 3.0 M ammonium chloride solution as an eluent, single separation factor, ${\alpha}$, 1.018, i.e. $(^7Li/^6Li)_{resin}/(^7Li/^6Li)_{fluid}$ was obtained by the Glueckauf theory from the elution curve and isotope ratios.

• Current Optics and Photonics
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• v.5 no.5
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• pp.544-553
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• 2021

A 40-W 200-ns 300-kHz thulium-doped fiber laser at 2050 nm with a master oscillator power amplifier configuration was developed, for application to lithium-isotope separation. The master oscillator generated a 5.35 W continuous-wave beam, which the pulse generator then broke into 200-ns pulses at 300 kHz. Then, the laser beam was amplified by passing through a two-stage amplifier. The output power finally obtained was 42.0 W at 2050 nm, and was stable for a long time, over 2 hours. In spite of this achievement, mode instability was observed in the output beam. This can be solved in the future by using a method such as tight coiling.