VioSpor
blue
line
Technical Data:
General Data
-
Detection principle
biotechnological technique (spore film)
-
Weight
ca. 8 g (for personal dosimetry) up to ca. 30g
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Seize
32 mm diameter, 9/12 mm hight
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Power consumption
not nessessary
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Operating temperature [°C]
-20 to +50
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Operating humidity [% rel. hum]
4)
0 to 100
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Storage conditions before and after exposure
temperature [°C]
+4 to +25
rel. humidity [%]
20 to 80
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Storage conditions before and after exposure
3 months
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Accessories
attachment aids, tripod connection, etc.
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Special features
- protected against water/dust;
- optional sealings enable measurements
within the water column
Specifications
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Spectral response
CIE erythemal response
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Responsivity fit to CIE MED 1) [nm]
290 to 380 (data given in MED; J/m2)
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Angular respose
Cosine corrected
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Wavelength accuracy [nm]
± 0,00
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Absolute MED calibration [%]
± 10
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Data reproducability [%]
± 5-20 (dose dependent)
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Detectable min. and max. dose [MED or J/m2]
[MED und J/m2 und SED]
MED
J/m2
SED
VioSpor blue line I: 0,2 - 12
od. 50 - 2250 od.
0,5 - 22,5
VioSpor blue line II: 0,4
- 22 100
- 5500 1,0
- 55,0
VioSpor blue line III: 0,6
- 36 150
- 9000
1,5 - 90,0
VioSpor blue line IV:
2,4 - 44 600 -
36000 6,0 -
350,0
-
Max. sensitivity for irradiance 3)
[WCIE/cm2]
< 10-7 for the total spectral range;
corresponds to appr. 0,05 MED/24hours
-
Max. intensity for irradiance [WCIE/cm2]
10-2; corresponds to appr. 1000 MED/h
1) 1 MED (minimal
erythemal dose for skin type II) = 250 J/m2
2) Values given
for type I dosimeter; the values of the appropriate dose range have to
be
multiplicated with 0.4 for type 0; with 2.3 for type II and 3.7 for type
III dosimeters;
irradiations were performed with a solar UV-simulator under laboratory
conditions
3) for type 0
with an integration time of 24 hours
4) non sealed
casings have to be used within the rel. humidity range 20 to 80 %