Lohand LH-BOD312 Laboratory Biochemical Oxygen Demand (BOD) Analyzer
| Brand | Lohand |
|---|---|
| Origin | Beijing, China |
| Manufacturer Type | Direct Manufacturer |
| Country of Origin | China |
| Model | LH-BOD312 |
| Instrument Type | Benchtop Laboratory BOD Analyzer |
| Measured Parameter | Biochemical Oxygen Demand (BOD₅) |
| Detection Principle | Dissolved Oxygen Depletion Method (Standard 5-Day Incubation per ISO 5815-1:2019 & ASTM D5210) |
Overview
The Lohand LH-BOD312 is a dedicated benchtop biochemical oxygen demand (BOD) analyzer engineered for precise, reproducible determination of BOD₅—the standard 5-day biochemical oxygen demand—as defined by international regulatory protocols including ISO 5815-1:2019 and ASTM D5210. Unlike general-purpose multi-parameter water analyzers, the LH-BOD312 implements the classical dilution and incubation method with integrated dissolved oxygen (DO) monitoring, temperature-controlled incubation, and automated data logging. It operates on the fundamental principle of quantifying the depletion of dissolved oxygen in a sealed, darkened sample bottle over a 120-hour period at 20 ± 1 °C, reflecting the oxygen consumed by aerobic microorganisms during biodegradation of organic matter. This gravimetrically traceable, respirometric approach ensures metrological consistency required for environmental compliance reporting, wastewater treatment process control, and regulatory submissions to municipal and national environmental agencies.
Key Features
- Integrated dual-sensor DO measurement system with galvanic or polarographic probe options, calibrated against air-saturated water and zero-oxygen sodium sulfite standards per ISO 5814.
- Stable 20 °C ±0.5 °C incubation chamber with uniform thermal distribution across all 12 sample positions—validated per ISO/IEC 17025 temperature uniformity requirements.
- Automated BOD calculation engine compliant with EPA Method 405.1 and ISO 5815-1, applying the standard formula: BOD₅ = (D₁ − D₂) × P⁻¹, where D₁ and D₂ are initial and final DO concentrations (mg/L), and P is the decimal volumetric fraction of sample.
- Onboard data storage for ≥1,000 test records with time-stamped DO readings, incubation start/end timestamps, operator ID, and calibration history—supporting GLP audit trails.
- RS-232 and USB interfaces for secure data export to LIMS or laboratory information management systems; optional Ethernet module available for networked deployment.
- Self-diagnostic routines for sensor drift detection, incubator temperature deviation alerts, and battery-backed real-time clock synchronization.
Sample Compatibility & Compliance
The LH-BOD312 accepts standard 300 mL BOD bottles (glass or BOD-specific PET) and supports undiluted or serially diluted samples per ISO 5815-1 Section 6. It accommodates wastewater influent/effluent, surface water, groundwater, and treated effluents—with turbidity up to 500 NTU and suspended solids ≤1,000 mg/L when filtered per Standard Methods 2540 D. The instrument meets CE marking requirements for electromagnetic compatibility (EN 61326-1) and safety (EN 61010-1). Its operational methodology aligns with ISO/IEC 17025:2017 clause 7.2.2 (method validation), and its data integrity framework supports FDA 21 CFR Part 11 compliance when paired with validated Lohand BOD Manager v3.2 software—including electronic signatures, audit logs, and user access controls.
Software & Data Management
The LH-BOD312 interfaces with Lohand BOD Manager v3.2—a Windows-based desktop application certified for GxP environments. The software enables method setup (dilution factor, incubation duration, blank correction), real-time remote monitoring of DO trends, automatic outlier detection using Grubbs’ test (α = 0.05), and generation of PDF reports compliant with ISO/IEC 17025 Annex A. All raw DO values, temperature logs, and calculated BOD results are stored with SHA-256 hash integrity verification. Audit trails record every data modification event—including who changed what, when, and why—enabling full traceability for regulatory inspections under EU Water Framework Directive (WFD) or US Clean Water Act reporting mandates.
Applications
- Regulatory BOD₅ testing for NPDES permit compliance and discharge monitoring in municipal and industrial wastewater treatment plants.
- Performance evaluation of biological treatment units (e.g., activated sludge, MBR, trickling filters) via influent-effluent BOD load calculations.
- Environmental impact assessment (EIA) studies requiring standardized organic pollution indices for river, lake, and reservoir sampling campaigns.
- Research laboratories conducting biodegradability screening of new chemical formulations under OECD 301 series guidelines.
- Educational use in university environmental engineering labs for hands-on instruction in respirometric assay fundamentals and QA/QC practices.
FAQ
Does the LH-BOD312 comply with ISO 5815-1:2019?
Yes—the instrument’s incubation stability, DO measurement accuracy, and calculation algorithm are verified against the normative requirements of ISO 5815-1:2019 Annex A.
Can it measure BOD beyond 5 days (e.g., BOD₂₀)?
The LH-BOD312 supports user-defined incubation durations from 1 to 20 days; however, BOD₂₀ interpretation requires separate validation per ISO 5815-2 for extended incubation protocols.
Is third-party calibration certification available?
Lohand provides NIST-traceable calibration certificates for DO sensors and incubator temperature verification, issued by CNAS-accredited calibration laboratories (Certificate No. CNAS LXXXXX).
What maintenance is required for long-term reliability?
Monthly membrane replacement for DO probes, quarterly incubator chamber cleaning with isopropyl alcohol, and annual verification of temperature uniformity per ISO/IEC 17025 Section 6.4.3.
Does the system support unattended operation over the full 5-day cycle?
Yes—battery-backed real-time clock and non-volatile memory ensure continuous logging without PC connection; alarm thresholds trigger visual/audible alerts upon DO saturation loss or temperature excursion.






