QBD1200＋ オートサンプラー
Product #:
9890800
Unit Price
お問い合わせ
Wet oxidation laboratory TOC analyzer with high accuracy and reproducibility compatible with 3 stations
QBD1200+ can measure TOC with high precision and reproducibility from ultrapure water of less than 1 ppm to TOC of raw water up to 100 ppm.
Reduces operating costs compared to conventional TOC meters
QBD1200+ can be operated stably with only an annual inspection. There is no need to calibrate the calibration curve, which has been routinely performed in the past. Running costs can be reduced with low reagent costs and simple maintenance work.
Supports data integrity without using management PC. Easy operability with 10.4- inch touch panel
The QBD1200+ allows configuration and report data management without a PC. Anyone can easily set up the operation of the TOC meter, and it excels in data integrity measures.
Startup is quick and daily inspections are smooth
In the case of a general TOC analyzer, it takes 2 to 3 hours for preparation before measurement, including startup, daily inspection, line cleaning, calibration curve test, and system suitability test. However, Hach Ultra's QBD1200+ only needs to perform a daily inspection called a background test that only confirms that the TOC value of the oxidant reagent is less than 100 ppb because of its fast start-up responsiveness. It is possible to start measurement in minutes, which greatly reduces the tester's process.
Compact design for easy lab installation
The QBD1200+ has a compact design that makes it easy to install in the lab.
QBD1200+ body: 320 mm (W) x 507 mm (D) x 410 mm (H)
Autosampler: 366 mm (W) x 537 mm (D) x 457 mm (H)
仕様
キャリアガスのオプション:
Air without CO², O², or N²
キャリブレーション方法:
Automated work: 18-point calibration using KHP (6-point concentration, repeated 3 times)
コンプライアンス認証:
ISO 8245 and DIN EN 1483;
● United States Pharmacopeia (USP) (including Sterilized Water SST), European Pharmacopoeia (EP), Japanese Pharmacopoeia (JP), IP, CP, KP;
● Clean Water Test Method, US EPS5310c;
● FDA 21 CFR, part 11 - United States Pharmacopoeia (USP), European Pharmacopoeia (EP), Japanese Pharmacopoeia (JP), IP, CP, KP.
● United States Pharmacopeia (USP) (including Sterilized Water SST), European Pharmacopoeia (EP), Japanese Pharmacopoeia (JP), IP, CP, KP;
● Clean Water Test Method, US EPS5310c;
● FDA 21 CFR, part 11 - United States Pharmacopoeia (USP), European Pharmacopoeia (EP), Japanese Pharmacopoeia (JP), IP, CP, KP.
サンプルの均質化:
An autosampler is also available
サンプル間キャリーオーバー:
< 0.2%
データエクスポート:
PDF, CSV
過負荷回復:
1 measurement
画面タイプ:
10.4" high resolution color touch screen
校正間隔:
1 year; calibration time 90 minutes
酸化方法:
UV lamp + persulfate
質量:
14 kg
所要電力 (ヘルツ):
47 - 63 Hz
所要電力 (ボルト):
100 - 240 VAC
寸法:
410 mm x 320 mm x 507 mm
精度:
3% or 3 ppb, whichever is greater
範囲:
0.4 ppb - 100 ppm
保証:
12 months
無機カーボン処理:
No external inorganic carbon removal module required
粒子サイズ:
Up to 100 µm