The uranium carbonate andersonite Na
2Ca[UO
2(CO
3)
3]·6H
2O was synthesized and identified with classical analyticaland spectroscopic methods. The classical methodsapplied were powder X-ray diffraction (XRD), nitric aciddigestion, and scanning electron microcopy combined withenergy-dispersive spectroscopy (SEM/EDS). To characterizeandersonite spectroscopically, time-resolved laser-induced fluorescence spectroscopy (TRLFS), X-ray photoelectron spectroscopy (XPS), and Fourier transforminfrared spectroscopy (FT-IR) were used. Natural andsynthetic andersonite samples were characterized withthe nondestructive TRLFS by six fluorescence emission bandsat 470.6, 486.1, 505.4, 526.7, 549.6, and 573.9 nm. Inaddition, andersonite was characterized by FT-IR measurements by the appearance of the asymmetric stretchingvibration of the uranyl cation [
3(UO
22+)] at 902 cm
-1 witha shoulder at 913 cm
-1. XPS measurements verified thecomposition of the synthetic andersonite sample. Themeasured intensity ratios of the XPS lines agree with thestoichiometry of Na
2Ca[UO
2(CO
3)
3]·6H
2O. The XPS featuresof the inner valence molecular orbitals are characteristic ofthe [UO
2(CO
3)
3]
4- structural moiety. These spectroscopicmethods can be used to identify in a fingerprinting proceduresecondary U(VI) phases in mixtures with other phases oras thin coatings on mineral and rock surfaces.