Rhabdophane-(La) mineral
Rhabdophane-(La) is the lanthanum-dominant hydrated phosphate mineral listed by IMA-CNMNC with ideal formula La(PO4)·H2O and renamed status Rn, 1987 s.p., in September 2026. This entry does not provide a numbered IMA approval identifier. It is distinct from elemental lanthanum, mixed rare-earth phosphate material, rhabdophane-(Ce) and anhydrous monazite-(La). Ondrejka et al. (2018) characterized natural La-dominant members within mixed, compositionally zoned rhabdophane-group grains from the Velence Hills, Hungary, using electron microprobe and Raman spectroscopy. Their analyses include substitutions and mixed end-member contributions; neither every grain nor every La-Nd-rich zone is pure rhabdophane-(La). Natural-grain hydration is not measured by oxide totals alone. The 2019 erratum requires inclusion of Fe in formula calculations without recognizing an Fe end-member. Shelyug et al. (2018) separately characterized synthetic La rhabdophane and its thermal conversion to monazite. Their fitted monoclinic model and total-water coefficient 0.804 describe that preparation, not a universal species assay or revised IMA formula. No microbial mechanism, isolated lanthanum recovery, industrial deployment or inherited criticality designation is curated.
Microbial & Biochemical Mechanisms (1)
Abiotic thermal conversion of synthetic La rhabdophane
A synthetic La rhabdophane powder was thermally converted to La monazite by heating 200 mg in air at 1100 degrees C for 6 hours. Powder X-ray diffraction identified the starting hydrated phase and the monazite product. This is a laboratory mineral transformation, not a microbial extraction experiment or a measured isolated-lanthanum recovery yield.
The synthesis series used analytical lanthanide chlorides; for La, the precursor was LaCl3·7H2O. Four mmol of lanthanide chloride was mixed with 5 M H3PO4 at a metal:P molar ratio of 1:1.03, stirred for 15 minutes at 60 degrees C and held in Teflon for two weeks at 90 degrees C. Powders were washed twice with deionized water, then ethanol, centrifuged and air-dried overnight. The resulting rhabdophane and heated monazite powders were stored airtight at room temperature for approximately a year before calorimetry. PXRD/Rietveld analysis fitted the hydrated powder using a monoclinic C2 model and the heated product as P21/n monazite; reported single-phase status is limited by diffraction detection. Separate 15-20 mg TGA/DSC runs in air used 10 degrees C/min over 30-1000 degrees C, with blank correction. La total-water content was reported as 0.804 H2O per LaPO4, including adsorbed and structural water. This is not a site-resolved water occupancy. The series-level 700-950 degrees C transformation interval is not adopted as an exact La equilibrium threshold; the transformation was not reversed.
shelyug2018
shelyug2018
Sources & References
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ima_2026_09: IMA-CNMNC. The New IMA List of Minerals, September 2026. PDF page 184, Rhabdophane-(La): La(PO4)·H2O, Rn, 1987 s.p., USA. Status definitions pages 1-2; renamed status and the special-procedure year do not supply a numbered approval.
https://cnmnc.units.it/files/editor/IMA_Master_List_(2026-09).pdf (accessed 2026-10-15) -
ondrejka2018: Ondrejka M, Bacik P, Sobocky T, Uher P, Skoda R, Mikus T, Luptakova J and Konecny P (2018). Minerals of the rhabdophane group and the alunite supergroup in microgranite: products of low-temperature alteration in a highly acidic environment from the Velence Hills, Hungary. Mineralogical Magazine 82:1277-1300. DOI 10.1180/mgm.2018.137. Complete original; analytical limits and Raman methods pages 1280-1283, natural-grain composition pages 1284-1285, representative La-dominant columns in Table 4 page 1290, Figure 7 page 1291 and Raman comparison Figure 10 page 1295. Interpretation of Fe in formula calculations on page 1296 is corrected in 2019.
https://doi.org/10.1180/mgm.2018.137 (accessed 2026-10-15) -
ondrejka2019_erratum: Ondrejka et al. (2019). Minerals of the rhabdophane group and the alunite supergroup in microgranite: products of low-temperature alteration in a highly acidic environment from the Velence Hills, Hungary - ERRATUM. Mineralogical Magazine 83:321. DOI 10.1180/mgm.2019.13. Complete publisher correction: page 1296 should say that Fe2+ and Fe3+ should be included in formula calculation; possible substitutions do not define a valid Fe end-member.
https://doi.org/10.1180/mgm.2019.13 (accessed 2026-10-15) -
shelyug2018: Shelyug A, Mesbah A, Szenknect S, Clavier N, Dacheux N and Navrotsky A (2018). Thermodynamics and Stability of Rhabdophanes, Hydrated Rare Earth Phosphates REPO4·nH2O. Frontiers in Chemistry 6:604. DOI 10.3389/fchem.2018.00604. Complete original and supplementary Tables A1a-c/A2; preparation and PXRD page 2, La diffraction traces Figure 1 and Table 1 page 3, thermal characterization Figure 3 and Table 2 page 4. Total water includes adsorbed and structural contributions. The same synthetic series was used in Mesbah et al. (2017); it is not an independent replication of those synthesis samples.
https://doi.org/10.3389/fchem.2018.00604 (accessed 2026-10-15)
Curation History
| Timestamp | Curator | Action | Summary |
|---|---|---|---|
2026-10-15T21:18:41Z |
codex (GPT-6; codex) | CREATE | Added the distinct La-dominant hydrated phosphate with natural composition context, the published Fe-formula erratum, and a bounded abiotic thermal conversion of synthetic material. |
Record source: data/records/rhabdophane-la.yaml