COMECAUSE IN-D1 Automatic Potentiometric Titrator
| Brand | COMECAUSE |
|---|---|
| Origin | Shandong, China |
| Manufacturer Type | Direct Manufacturer |
| Model | IN-D1 |
| Instrument Type | General-purpose Potentiometric Titrator |
| Application Scope | Universal |
| Potential Range | −2000 to +2000 mV |
| Potential Resolution | 0.1 mV |
| Titration Precision | ±5 µL (for 10 mL burette) |
| Potential Resolution (display) | 0.1 mV |
| pH Range | 0–14 |
| pH Resolution | 0.01 |
| pH Accuracy | ±0.01 |
| Temperature Range | −5 to 105 °C |
| Temperature Resolution | 0.1 °C |
| Temperature Accuracy | ±0.2 °C |
| Repeatability | ≤0.2% |
| Maximum Error | ≤±1.5% |
| Burette Options | 10 mL (±5 µL), 20 mL (±10 µL) |
| Operating System | Android 10 |
| Display | 7-inch capacitive touchscreen |
| Data Storage Capacity | 100,000 records |
| Connectivity | USB, Wi-Fi, Ethernet |
| Dimensions | 310 × 226 × 233 mm |
| Weight | 3.7 kg |
Overview
The COMECAUSE IN-D1 Automatic Potentiometric Titrator is an engineered solution for precise, reproducible quantitative chemical analysis based on potentiometric endpoint detection. It operates on the fundamental principle of monitoring electromotive force (EMF) changes in an electrochemical cell during titration—where the potential shift across a sensing electrode (e.g., glass, silver/silver chloride, or redox electrode) reflects stoichiometric reaction progress. Designed to comply with JJG 814–2015 (Chinese National Verification Regulation for Automatic Potentiometric Titrators) Class 0.05 specifications, the IN-D1 delivers a maximum indication error of ±1.5% and repeatability ≤0.2%, meeting metrological requirements for routine QC, regulatory testing, and method validation in GLP- and GMP-aligned laboratories. Its architecture integrates high-stability analog signal conditioning, micro-stepping peristaltic pumping, and real-time EMF feedback control—enabling accurate volumetric delivery and robust endpoint recognition under variable sample matrices.
Key Features
- Multi-mode titration support: dynamic titration, fixed-volume addition, manual stepwise titration, and auto-endpoint detection using first/second derivative or inflection point algorithms.
- Dual-function capability: simultaneous potentiometric titration and direct pH measurement, enabled by interchangeable electrode configurations (e.g., combination glass electrodes for acid-base, Ag/AgCl for precipitation, Pt for redox).
- Expandable platform: optional modules for conductometric titration and dead-stop (biamperometric) titration accommodate non-potentiometric methods without hardware replacement.
- Method programming environment: users define custom calculation formulas aligned with reaction stoichiometry (e.g., Cl⁻ → AgCl; Fe²⁺ → Ce⁴⁺); results are auto-calculated post-titration with traceable unit conversion and dilution factors.
- Method library management: up to 100 user-defined titration protocols—including electrode type, burette volume, stirring speed, dosing strategy, and endpoint criteria—can be saved, recalled, and version-controlled.
- Fluidic integrity system: integrated purge (air bubble removal), rinse (low-volume line priming), and drain (post-run retraction) functions minimize carryover, reduce reagent consumption by >30% versus conventional flushing, and enhance operator safety during maintenance.
- Android 10-based HMI: 7-inch responsive touchscreen interface with on-device data visualization, real-time titration curve plotting (E vs. V, dE/dV vs. V), and intuitive workflow navigation—no external PC required for operation or reporting.
Sample Compatibility & Compliance
The IN-D1 supports aqueous and mildly organic solvent systems (e.g., ethanol/water mixtures) typical in pharmacopeial assays (USP , EP 2.2.20), food acidity testing (AOAC 941.15), water chloride determination (ISO 9297), and pharmaceutical dissolution monitoring. Electrode compatibility includes standard reference electrodes (e.g., double-junction Ag/AgCl), ion-selective electrodes (ISEs), and temperature-compensated probes (T-2 ATC). All measurements adhere to ISO/IEC 17025 traceability frameworks when paired with NIST-traceable calibration standards. The instrument’s firmware architecture supports audit trail generation (user actions, method edits, result exports) and electronic signature readiness—facilitating alignment with FDA 21 CFR Part 11 requirements where local regulatory interpretation permits.
Software & Data Management
Data handling follows laboratory informatics best practices: each titration record stores raw EMF values, volume increments, calculated concentrations, metadata (operator ID, timestamp, method name), and annotated titration curves. Export options include CSV (for LIMS integration), PDF reports (with embedded graphs and digital signatures), and encrypted backups via USB or network share. Wi-Fi and Ethernet interfaces enable remote firmware updates and centralized method deployment across multi-instrument sites. Internal storage retains ≥100,000 complete assay records with automatic overwrite protection for critical validation batches. No cloud dependency—data sovereignty remains fully on-premise unless explicitly configured otherwise.
Applications
- Pharmaceutical QC: assay of active ingredients (e.g., sodium chloride in saline, citric acid in effervescent tablets) per USP monographs.
- Food & Beverage: titratable acidity (TA) in wines and dairy, chloride content in processed meats, sulfite quantification in juices.
- Environmental Testing: chloride, cyanide, and sulfate in wastewater per APHA Standard Methods.
- Chemical Manufacturing: purity assessment of catalysts, acid number (AN) and base number (BN) in lubricants (ASTM D974, D664).
- Academic Research: kinetic studies of complexation equilibria, pKa determination of weak acids, and teaching labs requiring reproducible endpoint detection.
FAQ
Does the IN-D1 meet international metrological standards beyond JJG 814–2015?
Yes—it conforms to core performance benchmarks referenced in ISO 8655-6 (piston burettes) and IUPAC recommendations for potentiometric titration accuracy, enabling cross-border method transfer where local validation is performed.
Can the instrument be validated for regulated environments (e.g., pharmaceutical GMP)?
The hardware design, firmware logging capabilities, and configurable audit trail support IQ/OQ/PQ execution. Full 21 CFR Part 11 compliance requires site-specific configuration and procedural controls—not inherent to the device alone.
What electrode types are supported out-of-the-box?
Standard delivery includes a 6501 glass combination electrode (pH/acid-base), 5004 Pt redox electrode, 2616 Ag/AgCl composite electrode (Cl⁻ precipitation), and T-2 ATC temperature probe—covering >90% of common potentiometric applications.
Is method transfer possible between IN-D1 units?
Yes—methods, calibration files, and report templates are exportable as encrypted .cmf packages and can be imported identically onto other IN-D1 instruments without recalibration.
How is temperature compensation handled during titration?
The T-2 ATC probe provides real-time temperature input to the titration algorithm, correcting both electrode potential drift and volumetric expansion effects per ISO 3696 and ASTM E200 guidelines.





