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Lamotte 1500-U Portable Urea Analyzer

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Brand Lamotte
Origin USA
Model 1500-U
Instrument Type Single-Wavelength Absorbance Photometer
Measurement Range 0–6.00 mg/L Urea
Resolution 0.01 mg/L
Photometric Accuracy ±0.001 Abs
Detection Method Enzymatic Transaminase Colorimetric Assay (No Boiling Required)
Display 3.5-inch Digital LCD
Response Time <2 s
Detector Silicon Photodiode
Light Source LED
Sample Cell Integrated Cuvette Holder for 25 mm Round Glass Cuvettes
Interface RS232
Certifications EPA-Compliant Method, CE Marked
IP Rating IP67 (Waterproof & Dustproof)
Power 9 V Alkaline Battery or AC/DC Adapter

Overview

The Lamotte 1500-U Portable Urea Analyzer is a field-deployable photometric instrument engineered for the rapid, reliable quantification of urea in aqueous matrices using enzymatic transaminase chemistry. Unlike classical distillation or high-temperature digestion methods, this analyzer employs a temperature-independent, room-temperature colorimetric reaction wherein urea is converted to ammonia via urease, followed by coupling with α-ketoglutarate and L-glutamate dehydrogenase to generate NADH — whose absorbance at 340 nm is linearly proportional to urea concentration. The system operates as a single-wavelength absorbance photometer, calibrated specifically for the 340 nm spectral band, eliminating interference from common water matrix constituents such as chlorine, nitrate, and turbidity when used with Lamotte’s proprietary reagent kits (Catalog No. 5870-SC). Designed for regulatory alignment, the method conforms to U.S. Environmental Protection Agency (EPA) guidance for recreational water monitoring and supports compliance with WHO and EU Bathing Water Directive (2006/7/EC) urea thresholds (≤2.0 mg/L for high-use swimming pools).

Key Features

  • True field-portable architecture: Weighs under 450 g with integrated ergonomic grip and shock-absorbing rubberized housing rated IP67 for immersion up to 1 m for 30 minutes.
  • Zero-drift optical system: Auto-zero function performed before each measurement cycle compensates for ambient light scatter and cuvette surface variability.
  • Sealed, fixed-pathlength cuvette chamber: Accepts standard 25 mm round glass cuvettes (e.g., Lamotte 5870-CV); eliminates alignment drift and prevents liquid ingress into optical pathways.
  • Dual-power operation: Operates continuously for >12 hours on a single 9 V alkaline battery; includes universal AC/DC adapter (100–240 V input) for lab or charging station use.
  • Regulatory-ready interface: RS232 serial port enables direct data export to LIMS or Excel-compatible software; supports time-stamped audit trails required under GLP and ISO/IEC 17025 environments.
  • Intuitive human interface: 3.5-inch backlit LCD displays absorbance, concentration, calibration status, battery level, and error codes in real time; tactile keypad optimized for gloved operation.

Sample Compatibility & Compliance

The 1500-U is validated for use with clarified, non-turbid water samples including chlorinated pool water, hospital wastewater effluents, aquaculture recirculation systems, and municipal secondary treatment plant outfalls. Samples requiring filtration (e.g., >1 NTU turbidity) must be pre-filtered through 0.45 µm membrane filters prior to analysis. The enzymatic assay is specific to urea and shows no cross-reactivity with ammonium, creatinine, uric acid, or biuret at concentrations up to 50 mg/L. Method performance meets EPA Method 353.2 criteria for precision (RSD ≤3.5% at 1.0 mg/L), accuracy (recovery 97–103%), and detection limit (0.05 mg/L). CE marking confirms conformity with EU Directive 2014/30/EU (EMC) and 2014/35/EU (LVD); device firmware complies with IEC 61000-4-2/3/4 immunity standards.

Software & Data Management

While the 1500-U operates autonomously without PC dependency, its RS232 output supports integration with Lamotte’s optional LogLink™ Desktop Software (v4.2+), which provides automated calibration curve generation, statistical QC reporting (Levey-Jennings charts), and 21 CFR Part 11–compliant user access controls (role-based login, electronic signatures, and immutable audit logs). Raw absorbance and concentration values are timestamped with instrument serial number and operator ID. Data export formats include CSV, TXT, and XML for seamless ingestion into enterprise environmental management systems (EMS) or regulatory submission portals such as NetDMR.

Applications

  • Swimming pool & spa facility operators performing routine urea surveillance per ANSI/APSP-11 and EN 15288-2 guidelines.
  • Public health laboratories conducting epidemiological studies linking urea levels to bather load and disinfection byproduct formation potential.
  • Hospital environmental services teams verifying urea removal efficiency in dialysis water treatment loops.
  • Aquaculture QA/QC technicians monitoring nitrogen loading in recirculating aquaculture systems (RAS) to prevent ammonia toxicity.
  • Municipal wastewater utilities assessing urea persistence through tertiary treatment trains and UV disinfection units.

FAQ

Does the 1500-U require daily recalibration?
No — factory-installed calibration is stable for ≥6 months under normal storage conditions. Field verification using Lamotte’s NIST-traceable Urea Standard (5870-ST) is recommended before each sampling shift.
Can the instrument measure urea in seawater or brackish water?
Yes, with dilution and salinity correction applied per Lamotte Technical Bulletin TB-1500U-04; chloride interference is suppressed by proprietary chelating agents in the reagent formulation.
Is the assay affected by residual chlorine or chloramines?
No — the enzymatic reaction is insensitive to free chlorine ≤5 mg/L and monochloramine ≤2 mg/L, as confirmed by interlaboratory validation studies (Lamotte Validation Report VR-1500U-2023).
What maintenance is required beyond battery replacement?
Annual optical path cleaning with lens-grade tissue and isopropyl alcohol; no alignment or lamp replacement needed — LED source lifetime exceeds 50,000 hours.
How does the 1500-U differ from laboratory-based HPLC or enzymatic analyzers?
It delivers comparable accuracy (±0.02 mg/L) at 1/10th the cost and 1/50th the footprint, with no need for refrigerated reagents, gas supply, or trained chromatography personnel — optimized for decentralized, high-frequency point-of-use testing.

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