Laboratory Price List
CGS Central Laboratory – Prague
The laboratory is certified in accordance with ČSN EN ISO/IEC 17025
Head of the Laboratory: Ing. Tereza Grabmüllerová
tel.: +420 251 085 422, +420 775 221 665, e-mail: tereza.grabmullerova@geology.cz
Deputy Head: Ing. Daniela Ocásková, PhD.
tel.: +420 251 085 436, +420 721 204 404, e-mail: daniela.ocaskova@geology.cz
Quality Manager: Ing. Lucie Jurkovská
tel.: +420 604 783 308, mail: lucie.jurkovska@geology.cz
Sample Handling: Ing. Tereza Grabmüllerová
tel.: +420 251 085 422, +420 775 221 665, e-mail: tereza.grabmullerova@geology.cz
Classical Chemistry Department: Ing. Ivana Vanišová
tel.: +420 251 085 491, e-mail: ivana.vanisova@geology.cz
Spectral Methods Department: Ing. Marie Housková
tel.: +420 251 085 435, e-mail: marie.houskova@geology.cz
Water Analysis Department: Ing. Jana Buřilová
tel.: +420 251 085 412, e-mail: jana.burilova@geology.cz
X-ray fluorescence analysis department: prof. RNDr. Jiří Frýda, Dr.
Tel.: +420 251 085 347, e-mail: jiri.fryda@geology.cz
Legend
preparation of rock sample for chemical analysis:
crushing, splitting, pulverization (fine milling) to analytical fineness (<63 μm)
agate box
Mn steel or WC box
sum of all oxides between 99.1–100.7 %
oxides / codes | limit of determination [%] | method | |||
---|---|---|---|---|---|
300 | 301 | 302 | 303 | ||
SiO2 | 0.10 | 0.10 | 0.10 | 0.10 | titration |
TiO2 | 0.01 | 0.01 | 0.01 | 0.01 | FAAS |
Al2O3 | 0.01 | 0.01 | 0.01 | 0.01 | FAAS up to 3%, above 3% titration |
Fe2O3 | 0.01 | 0.01 | 0.01 | 0.01 | FAAS up to 10 %, above 10 % PMT |
FeO | 0.03 | 0.03 | not determined | not determined | titration |
MgO | 0.01 | 0.01 | 0.01 | 0.01 | FAAS up to 5 %, above 5 % titration |
MnO | 0.001 | 0.001 | 0.001 | 0.001 | FAAS |
CaO | 0.01 | 0.01 | 0.01 | 0.1 | FAAS up to 5 %, above 5 % titration |
Li2O | 0.001 | 0.001 | 0.001 | 0.001 | FAAS |
Na2O | 0.01 | 0.01 | 0.01 | 0.01 | FAAS |
K2O | 0.01 | 0.01 | 0.01 | 0.01 | FAAS |
P2O5 | 0.005 | 0.005 | 0.005 | 0.005 | PMT |
BaO* | not determined | 0.005 | not determined | not determined | FAAS |
SrO | not determined | 0.005 | not determined | not determined | FAAS |
CO2 | 0.05 | 0.05 | not determined | not determined | IR spectrometry |
Stot | 0.01 | 0.01 | not determined | not determined | IR spectrometry |
H2O+ | 0.05 | 0.05 | 0.05 | 0.05 | calculation – chemically bound water |
H2O- | 0.05 | 0.05 | 0.05 | 0.05 | humidity |
Cost | 0.01 | 0.01 | not determined | not determined | IR spectrometry |
F- | 0.005 | 0.005 | not determined | not determined | ISE |
Fekv | not determined | not determined | calculation | ||
Sekv | not determined | not determined | calculation |
* BaO – non certificated
sum of all oxides between 99.1–100.7 %
oxides / codes | limit of determination [%] | method | |||
300 | 301 | 302 | 303 | ||
---|---|---|---|---|---|
SiO2 | 0.10 | 0.10 | 0.10 | 0.10 | titration |
TiO2 | 0.01 | 0.01 | 0.01 | 0.01 | FAAS |
Al2O3 | 0.01 | 0.01 | 0.01 | 0.01 | FAAS up to 3%, above 3% titration |
Fe2O3 | 0.01 | 0.01 | 0.01 | 0.01 | FAAS up to 10 %, above 10 % PMT |
FeO | 0.03 | 0.03 | not determined | not determined | titration |
MgO | 0.01 | 0.01 | 0.01 | 0.01 | FAAS up to 5 %, above 5 % titration |
MnO | 0.001 | 0.001 | 0.001 | 0.001 | FAAS |
CaO | 0.01 | 0.01 | 0.01 | 0.1 | FAAS up to 5 %, above 5 % titration |
Li2O | 0.001 | 0.001 | 0.001 | 0.001 | FAAS |
Na2O | 0.01 | 0.01 | 0.01 | 0.01 | FAAS |
K2O | 0.01 | 0.01 | 0.01 | 0.01 | FAAS |
P2O5 | 0.005 | 0.005 | 0.005 | 0.005 | PMT |
BaO* | not determined | 0.005 | not determined | not determined | FAAS |
SrO | not determined | 0.005 | not determined | not determined | FAAS |
CO2 | 0.05 | 0.05 | not determined | not determined | IR spectrometry |
Stot | 0.01 | 0.01 | not determined | not determined | IR spectrometry |
H2O+ | 0.05 | 0.05 | 0.05 | 0.05 | calculation – chemically bound water |
H2O- | 0.05 | 0.05 | 0.05 | 0.05 | humidity |
Cost | 0.01 | 0.01 | not determined | not determined | IR spectrometry |
F- | 0.005 | 0.005 | not determined | not determined | ISE |
Fekv | not determined | not determined | calculation | ||
Sekv | not determined | not determined | calculation |
* BaO – non certificated
sum of all oxides between 98,3–101,0 %
oxides / | limit of determination [%] | method | |||
codes | 300 | 301 | 302 | 303 | |
SiO2 | 0.10 | 0.10 | 0.10 | 0.10 | titration |
TiO2 | 0.01 | 0.01 | 0.01 | 0.01 | FAAS |
Al2O3 | 0.01 | 0.01 | 0.01 | 0.01 | FAAS up to 3%, above 3% titration |
Fe2O3 | 0.01 | 0.01 | 0.01 | 0.01 | FAAS up to 10 %, above 10 % PMT |
FeO | 0.03 | 0.03 | not determined | not determined | titration |
MgO | 0.01 | 0.01 | 0.01 | 0.01 | FAAS up to 5 %, above 5 % titration |
MnO | 0.001 | 0.001 | 0.001 | 0.001 | FAAS |
CaO | 0.01 | 0.01 | 0.01 | 0.01 | FAAS up to 5 %, above 5 % titration |
Li2O | 0.001 | 0.001 | 0.001 | 0.001 | FAAS |
Na2O | 0.01 | 0.01 | 0.01 | 0.01 | FAAS |
K2O | 0.01 | 0.01 | 0.01 | 0.01 | FAAS |
P2O5 | 0.005 | 0.005 | 0.005 | 0.005 | PMT |
BaO* | not determined | 0.005 | not determined | not determined | FAAS |
SrO | not determined | 0.005 | not determined | not determined | FAAS |
CO2 | 0.05 | 0.05 | not determined | not determined | IR spectrometry |
Stot | 0.01 | 0.01 | not determined | not determined | IR spectrometry |
H2O+ | 0.05 | 0.05 | 0.05 | 0.05 | calculation – chemically bonded water |
H2O- | 0.05 | 0.05 | 0.05 | 0.05 | humidity |
Cost | 0.01 | 0.01 | not determined | not determined | IR spectrometry |
F- | 0.005 | 0.005 | not determined | not determined | ISE |
Fekv | not determined | not determined | calculation | ||
Sekv | not determined | not determined | calculation | ||
*BaO – non certificated |
sum of all oxides between 97.5–101.3 %
oxides / | limit of determination [%] | method | |||
codes | 300 | 301 | 302 | 303 | |
SiO2 | 0.10 | 0.10 | 0.10 | 0.10 | titration |
TiO2 | 0.01 | 0.01 | 0.01 | 0.01 | FAAS |
Al2O3 | 0.01 | 0.01 | 0.01 | 0.01 | FAAS up to 3%, above 3% titration |
Fe2O3 | 0.01 | 0.01 | 0.01 | 0.01 | FAAS up to 10 %, above 10 % PMT |
FeO | 0.03 | 0.03 | not determined | not determined | titration |
MgO | 0.01 | 0.01 | 0.01 | 0.01 | FAAS up to 5 %, above 5 % titration |
MnO | 0.001 | 0.001 | 0.001 | 0.001 | FAAS |
CaO | 0.01 | 0.01 | 0.01 | 0.01 | FAAS up to 5 %, above 5 % titration |
Li2O | 0.001 | 0.001 | 0.001 | 0.001 | FAAS |
Na2O | 0.01 | 0.01 | 0.01 | 0.01 | FAAS |
K2O | 0.01 | 0.01 | 0.01 | 0.01 | FAAS |
P2O5 | 0.005 | 0.005 | 0.005 | 0.005 | PMT |
BaO* | not determined | 0.005 | not determined | not determined | FAAS |
SrO | not determined | 0.005 | not determined | not determined | FAAS |
CO2 | 0.05 | 0.05 | not determined | not determined | IR spectrometry |
Stot | 0.01 | 0.01 | not determined | not determined | IR spectrometry |
H2O+ | 0.05 | 0.05 | 0.05 | 0.05 | calculation – chemically bonded water |
H2O- | 0.05 | 0.05 | 0.05 | 0.05 | humidity |
Cost | 0.01 | 0.01 | not determined | not determined | IR spektrometrie |
F- | 0.005 | 0.005 | not determined | not determined | ISE |
Fekv | not determined | not determined | calculation | ||
Sekv | not determined | not determined | calculation | ||
*BaO – non certificated |
oxides | limit of determination [%] | method |
---|---|---|
FeO | 0.03 | titration |
Fe2O3 | 0.01 | FAAS up to 10 %; above 10 % PMT |
MnO | 0.001 | FAAS |
MgO | 0.01 | FAAS up to 5 %; above 5 % titration |
CaO | 0.01 | FAAS up to 5 %; above 5 % titration |
CO2 | 0.05 | coulometry |
chelatometric titration after acid decomposition
chelatometric titration after acid decomposition
spectrophotometric determination after acid decomposition
oxide | weight [g] | limit of determination [%] |
---|---|---|
Fe2O3 | 0.5 | 0.01 |
P2O5 | 0.5 | 0.01 |
alkalimetric titration after special acid decomposition
SiO2 determination in hardly soluble materials after melting
titration with K2Cr2O7 after acid decomposition
CO2 infrared spectroscopy after reaction with H3PO4
infrared spectroscopy after sample burning in oxygen
sample decomposition by catalyst pyrolysis, determination with ion-selective electrode
infrared spectroscopy after sample burning in oxygen
sample leaching in HCL, precipitation with BaCl2, gravimetric determination
weight loss after drying the sample at 110 °C
weight loss after heating to 1 050 °C
gravimetric determination of total sulphur, Eschka procedure
chelatometric titration after acid decomposition
spectrophotometric determination after pyrolytic decomposition
ICP-MS, fusion decomposition with LiBO3
element | limit of determination [ppm] |
---|---|
La | 0.10 |
Ce | 0.10 |
Pr | 0.02 |
Nd | 0.30 |
Sm | 0.05 |
Eu | 0.02 |
Gd | 0.05 |
Tb | 0.01 |
Dy | 0.05 |
Ho | 0.02 |
Er | 0.03 |
Tm | 0.01 |
Yb | 0.05 |
Lu | 0.01 |
Y | 0.10 |
sample decomposition by mixtures of acids with HF
direct determination by the FAAS method
element | limit of determination [ppm] | decomposition [code] |
---|---|---|
Ba | 20.00 | 345 |
Be | 0.80 | 345 |
Cd | 0.80 | 345 |
Co | 5.00 | 345 |
Cr | 2.00 | 345 |
Cu | 2.00 | 345 |
Cs | 10.00 | 345 |
Mo | 5.00 | 345 |
Ni | 5.00 | 345 |
Pb | 10.00 | 345 |
Rb | 2.00 | 345 |
Sc | 20.00 | 345 |
Sr | 10.00 | 345 |
Zr | 2.00 | 345 |
content of trace elements soluble in HCl
determination by ICP-OES method
element | limit of determination [ppm] | decomposition [code] |
---|---|---|
As | 0.10 | 347 |
Bi | 0.05 | 347 |
Sb | 0.05 | 347 |
determination by the ICP-MS method
element | limit of determination [ppm] | decomposition [code] |
---|---|---|
Ag | 0.10 | 347 |
Al | 50.00 | 343 |
As | 0.10 | 343 |
Ba | 1.00 | 343 |
Be | 1.00 | 343 |
Bi | 0.10 | 347 |
Cd | 0.10 | 343 |
Co | 0.10 | 343 |
Cr | 0.10 | 343 |
Cs | 0.10 | 343 |
Cu | 0.10 | 345 |
Fe | 50.00 | 343 |
Ga | 0.10 | 343 |
Ge | 0.50 | 343 |
Hf | 0.10 | 343 |
In | 0.10 | 343 |
Mn | 5.00 | 343 |
Mo | 0.10 | 343 |
Nb | 0.10 | 343 |
Ni | 0.10 | 343 |
Pb | 0.50 | 343 |
Rb | 0.10 | 343 |
Sb | 0.10 | 343 |
Sc | 1.00 | 343 |
Sn | 010 | 343 |
Sr | 0.50 | 343 |
Ta | 5.00 | 343 |
Te | 0.50 | 343 |
Th | 0.10 | 343 |
Ti | 0.10 | 343 |
Tl | 10.00 | 343 |
U | 0.10 | 343 |
Y | 1.00 | 343 |
V | 0.50 | 343 |
Zn | 1.00 | 343 |
Zr | 4.00 | 343 |
The required elements must be specified.
As, Ba, Bi, Ce, Co, Cr, Cu, Ga, La, Mo, Nb, Nd, Ni, Pb, Rb, Sc, Sn, Sr, Th, Ti, U, V, W, Y, Zn, Zr
direct determination by the WD-XRF method
The determination of any element by this method is influenced by the amount and type of other elements in the sample. For this reason, the composition of the matrix [e.g. dolomitic limestone or the chemical composition of the main components, e.g. SiO2 (60–70 wt.%)] must be given in the specification report.
Rozklad ceny:
- vzorek 1 440 Kč
- příprava tablet 240 Kč
leaching from the oxidized sample, conversion to non-polar solvent
determination by AAS method
sample free of organic matter and SiO2 is melted with KHSO4, the melt is dissolved in H2SO4
sample free of organic matter is melted with Na2O2, the melt is dissolved in H2O
sample free of organic matter is melted with LiBO2, the melt is dissolved with diluted HCl
sample free of organic matter is melted with NaCO3, the melt is dissolved with diluted HCl
sample is dissolved with HF, excess HF is removed by addition of H3BO3, the dry sample is removed with HCl or HNO3, determination by ICP-MS
sample is dissolved by hot mixture of HCl and HNO3,
determination of soluble trace elements in acids
sample is decomposed by a mixture of HF, H2SO4 and HNO3
sample is dissolved by HCl with NH4Cl, the SiO2 and dissoluble residue is dried and weighed
element | limit of determination [ppm] | method |
---|---|---|
Al |
0.20 |
FAAS or ICP-MS |
Ca | 0.01 | FAAS or ICP-MS |
Fe | 0.05 | FAAS or ICP-MS |
K | 0.01 | FAAS or ICP-MS |
Li | 0.005 | FAAS or ICP-MS |
Mg | 0.01 | FAAS or ICP-MS |
Mn | 0.005 | FAAS or ICP-MS |
Na | 0.01 | FAAS or ICP-MS |
Zn | 0.01 | FAAS or ICP-MS |
SiO2 | 0.20 | FAAS or ICP-MS |
F- | 0.002 | HPLC |
Cl- | 0.15 | HPLC |
NO3- | 0.30 | HPLC |
SO4- | 0.50 | HPLC |
NH4+* | 0.02 | photometric |
pH* | ISE | |
alkalinity | 0.05 | titration |
conductivity | 0.005 μS/cm | conductimetry |
*NH4+ and pH – non certificated
sample acidified by HNO3 (0.5 ml /100 ml)
FAAS determination
element | limit of determination [mg/l] |
---|---|
Al | 0.20 |
Ca | 0.01 |
Fe | 0.05 |
K | 0.01 |
Li | 2 μg/l |
Mg | 0.01 |
Mn | 5 μg/l |
Na | 0.01 |
Zn | 5 μg/l |
SiO2 | 2.00 |
The required elements must be specified.
sample with concentrated HNO3 (0.5 ml/100 ml)
ETAAS determination
element | limit of determination [μg/l] |
---|---|
Al | 10.00 |
As | 0.50 |
Be | 0.02 |
Cd | 0.04 |
Co | 0.50 |
Cr | 0.50 |
Cu | 0.20 |
Mo | 0.50 |
Ni | 0.50 |
Pb | 0.40 |
V | 10.00 |
titration determination from the non-acidified sample
conductometry with Pt electrodes from the non-acidified sample
ion chromatography from the non-acidified sample
anion | limit of determination [ppm] | method |
---|---|---|
F- | 0.02 | HPLC |
Cl- | 0.10 | HPLC |
NO3- | 0.30 | HPLC |
SO4- | 0.50 | HPLC |
The required components must be specified.
sample acidified with HNO3 (0.5 ml /100 ml)
ICP-MS determination
element | limit of determination [μg/l] |
---|---|
Al | 1.00 |
As | 0.50 |
Ba | 0.05 |
Be | 0.02 |
Cd | 0.04 |
Co | 0.05 |
Cr | 0.40 |
Cu | 0.10 |
Fe | 10.00 |
Li | 0.10 |
Mn | 0.10 |
Mo | 0.10 |
Ni | 0.20 |
Pb | 0.10 |
Sb | 0.20 |
Sc | 0.50 |
Sr | 0.30 |
V | 0.20 |
Zn | 0.50 |
The required elements must be specified.
spectrophotometry from the non-acidified sample
pH measurement with an electrode from the non-acidified sample
spectrophotometry from acidified sample (0.5 ml concentrated HNO3 / 100 ml sample)
liquid chromatography preparation, sample not acified
liquid chromatography preparation, sample not acified
sample not acified
TOC - IR detector, TN - chemiluminescence
sample not acified, IR detector
sample not acified, chemiluminescence detector
determination by ISE electrode
determination by ISE electrode
determination by ISE electrode in 0.1M BaCl2 leachate
0.1M BaCl2 soil extract is titrated with NaOH solution up to pH 8.2
exchangeable Al liberated after total acidity titration with KF solution is titrated with 0.05M HCl from the sample up to pH 8.2
extraction by Mehlich III and P2O5 determination
CGS Central Laboratory – Brno
The laboratory is certified in accordance with ČSN EN ISO/IEC 17025
Head of the Laboratory: Ing. Tereza Grabmüllerová
tel.: +420 251 085 422, +420 775 221 665, e-mail: tereza.grabmullerova@geology.cz
Deputy Head: Ing. Daniela Ocásková, Ph.D.
tel.: +420 721 204 404, e-mail: daniela.ocaskova@geology.cz
Quality Manager: Ing. Lucie Jurkovská
tel.: +420 604 783 308, mail: lucie.jurkovska@geology.cz
Sample Handling: Věra Bělíčková, Blanka Janíková, tel.: +420 543 429 285
e-mail: vera.belickova@geology.cz, blanka.janikova@geology.cz
Gas Chromatography Department: Ing. Daniela Ocásková, Ph.D.
Tel.: +420 543 429 281. email: daniela.ocaskova@geology.cz
acid decomposition of carbonates, combustion / IR
combustion / IR
acid decomposition / IR
combustion / IR
combustion / acid decomposition / IR
acid decomposition, combustion / IR
16 priorities, GC-MS, GC-MS-MS
basic method
conductometry
gravimetric
GC-FID
GC-ECD
GC-ECD
GC-ECD
GC-ECD/FID
GC-FID
GC-FID
Cu-triple method
gravimetric
combustion / IR
% of Ali, Aro, NSO and asphaltene fraction
GC-FID
in the range C6–C40
GC-FID
in the C6–C9 range at high resolution
GC-FID
GC-MS
GC-MS
content determination of CO2 , CO, O2, N2, CH4, He
GC-TCD
content determination of CO2, CO, H2, O2, N2, CH4, He, Ar
two isomers C2, C3, iC4, nC4, C6, four isomers C5
GC-FID/TCD
Ecoprobe instrument, range by agreement
representative sample of waste
price by agreement according to availability and time requirements
price by agreement according to availability and time requirements
core drilling diameter 56–100 mm
Sample Polishing Facility
Helena Němcová, tel.: 251 085 181, e-mail: helena.nemcova@geology.cz
size 2 × 3 cm
size 2 × 3 cm
size 3 × 4 cm
size 3 × 4 cm
columnar, fixed in synthetic resin, diameter 2.5 cm
columnar, fixed in synthetic resin, diameter 2.5 cm
size 2 × 3 cm
size 3 × 4 cm
biological material (shells, teeth, etc.), thick polished cuttings 100 > μm
cutting with diamond saw, large polish section
Prague Mineral Separation Facility
Mgr. Martin Štrba, tel.: 251 085 202, e-mail: martin.strba@geology.cz
repeated crushing, grinding, washing, drying, sieving, 75 g sample separated in tetrabromomethane heavy liquid
[detail]viz tabulka[/detail]
repeated crushing, grinding, concentration on the shaking table, drying, sieving, magnetic separation, heavy-liquid separation (tetrabromethane, diiodomethane), result is about 90 % zircon fraction (possibly + barite, kyanite, rutile, topaz)
repeated crushing, grinding, concentration on the shaking table, drying, sieving, magnetic separation, heavy-liquid separation (tetrabromethane, diiodomethane), sulphides dissolving, result is about 90 % zircon fraction
after zircon separation (code 401), further magnetic separation (code 408), possibly repeatedly
repeated crushing, grinding, washing, drying, sieving, magnetic separation, shape separation
a liquid of density 2.96 g/cm3
a liquid of density 3.32 g/cm3
can be repeatedly
in consultation with the laboratory
Brno Mineral Separation Facility
Mgr. Irena Sedláčková, tel.: 724 767 432, e-mail: irena.sedlackova@geology.cz
cutting of the rock using a circular saw at the client's request
rock crushing on the jaw crusher
sample drying, sieving on 3–5 sieves according at the client´s request,
weighing, a pie chart output
rock disruption, repeated crushing on a jaw crusher, homogenisation,
filling and labelling of 2 bags, documentary sample
sand, silt, clay, dust
shales, slates, claystones
limestone, rock crushing included
repeated decomposition in 20% acetic acid, decantation, washing,
possibility of process control by the client
preparation and pouring into the Canadian balsam
sieving according to the client request, washing
crushing, soaking, washing (0.063–0.250 mm), drying,
crushing is charged separately
separation in liquid sodium heteropolytungstate (LST)
items code 172 and code 173 are included,
rock crushing is not include
heavy minerals sorting into fractions on the Cook electromagnetic separator
sample dividing into four density fractions
rock disruption, crushing on a jaw crusher, sieveving,
washing on the shaking table, electromagnetic separation,
heavy mineral separation in LST,
back up of individual fractions and other work according to the sample, picking up grains and microprobe analysis are not include
one type of heavy mineral selecting from the sample
according to the client's request, description,
gluing the grains on the tape, handing over to the Sample polishing facility, the pellet price is not include
handing over the sample to the microprobe analysis,
data processing, preparation of the mineral grains for the laser ablation, payment for the microprobe is not included
methods code 178, 179 and 180 are included
according to client's request
Optical Microscopy
RNDr. Tamara Sidorinová, tel.: +420 251 085 227, e-mail: tamara.sidorinova@geology.cz
price does not include sample separation in heavy liquid (code 400)
Nikon SMZ1270 microscope, photodocumentation in SW NIS Elements AR 5.40.02
Nikon EclipseE600 microscope, photodocumentation, for observation mainly by transmitted light
Microscope Zeiss Axio Imager.A2m, photodocumentation, for observation mainly in reflected light
Micropaleontology and Chemostratigraphy
prof. Jiří Frýda, Dr., tel.: +606 787 821, e-mail: jiri.fryda@geology.cz
development of new techniques
Fluid Inclusions
RNDr. Petr Dobeš, tel.: +420 251 085 322, e-mail: petr.dobes@geology.cz
The determination of homogenization temperature, composition and density of trapped fluids, interpretation of P-T-V-X data
X-ray Diffraction
RNDr. F. Laufek, Ph.D., tel.: 251 085 210, e-mail: frantisek.laufek@geology.cz
single phase
data interpretation only, data collection the evaluation (code 410) is not included
data interpretation only, data collection (code 410) and separation of clay fraction (code 460) are not included
phase mixture
data interprretation only, data collection (code 410) is not included
Rietveldova method
data interpretation only, data collection (code 410) is not included
data interpretation only, data collection (code 410) is not included
Rietveldova metoda, including estimate of amorphous phase
data interpretation only, data collection (code 410) is not included
XRD analysis of bulk sample and separated clay fraction, Ca, K-saturation of clay fraction, sample temperature at 110 °C, 330 °C and 550 °C and basic evaluation are included
only after previous consultation
structure analysis, microstructure analysis, specific sample preparation procedures, semi-quantitative phase analysis of bentonites, micro-diffraction, consultation
only in combination with the code 410 analysis
Electron Microscopy and Microanalysis
Mgr. Ondřej Pour, tel.: +420 251 085 219, e-mail: ondrej.pour@geology.cz
EDS and WDS microanalysis, SEI, BEI, CL imaging, mapping, EBSD
Stable Isotopes H, C, N, O, S
Ing. Bohuslava Čejková, tel.: +420 251 085 346, e-mail: bohuslava.cejkova@geology.cz
one component is determined
one component is determined
one component is determined
one component is determined
online GasBench
online GasBench
standard method
standard method + sklář
LGR laser
online GasBench
Thermal Ionization Mass Spectrometry
John M. Hora, PhD., tel.: +420 251 085 336, e-mail: john.hora@geology.cz
mechanical preparation of samples, specific procedures
muffle furnace + silicate dissolution
bones, tooth enamel
samples that cannot be dissolved using standard procedures
low concentration
analysis in cooperation with the Geological Institute of the Czech Academy of Sciences
Multi-Collector Mass Spectrometry
RNDr. Ondřej Šebek, Ph.D., tel.: +420 251 085 307, e-mail: ondrej.sebek@geology.cz
including separation
no separation
the price does not include sample decomposition by melting
including decomposition in the USL
including decomposition in the USL
including decomposition in the USL, two-stage separation
minimum 6 samples
analysis in cooperation with the Geological Institute of the Czech Academy of Sciences
analysis in cooperation with the Geological Institute of the Czech Academy of Sciences
including decomposition in the USL
minimum is 8 hours
Laser Ablation
Mgr. Jitka Míková, Ph.D., tel.: +420 251 085 329, e-mail: jitka.mikova@gelogy.cz
price includes analytical session, data processing, data evaluation and preparation of documents for publication