

Micro-Kjeldahl Digestion and Distillation System
微量凯氏消解与蒸馏系统
- SKU KJS-0005
- Kjeldahl Systems
- CE (to be confirmed)
- ISO 9001 manufacturing (to be confirmed)
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
Key specifications
| Sample mass | 10–100 mg |
|---|---|
| Tube volume | 50–100 mL |
| Acid volume | 1–5 mL per sample |
| Digestion temperature | Up to 400 °C |
| Digestion time | 20–60 min |
| Distillation time | 2–4 min per sample |
By Lab Manufacturers China Technical TeamLast reviewed Standards: ISO 1871, ISO 8968-1, ISO 5983-2
What is the Micro-Kjeldahl Digestion and Distillation System?
A micro-Kjeldahl system performs digestion and distillation on small sample masses with proportionally reduced reagent volumes. It suits limited samples, expensive matrices and laboratories aiming to cut their acid waste volumes substantially.
What is the Micro-Kjeldahl Digestion and Distillation System?
A micro-Kjeldahl system performs digestion and distillation on small sample masses with proportionally reduced reagent volumes. It suits limited samples, expensive matrices and laboratories aiming to cut their acid waste volumes substantially.
Overview
Sample masses of 10 to 100 mg are digested in narrow 50 to 100 mL tubes with small volumes of sulfuric acid, catalyst and sometimes hydrogen peroxide to complete oxidation quickly. Distillation uses a compact steam generator and a small receiver, and titration volumes are correspondingly small, often with a 10 mL burette or a potentiometric micro-electrode. Because everything scales down, digestion is faster, typically 20 to 60 minutes, and reagent consumption and waste fall substantially, which matters where acid disposal is costly. The trade-offs are greater sensitivity to weighing error and sample inhomogeneity, so a micro-balance and careful sub-sampling are needed. Recovery is verified with ammonium sulfate standards in the same way as macro methods.
How does it work?
The Kjeldahl method converts nitrogen in the sample to ammonium sulfate by heating with concentrated sulfuric acid and a catalyst, usually copper or selenium with potassium sulfate to raise the boiling point. Organic matter is oxidised and the nitrogen is retained as ammonium. The digest is then made alkaline with sodium hydroxide, releasing ammonia, which is steam-distilled into a receiver containing boric acid or a standard acid. The amount of ammonia is determined by titration, and nitrogen content is calculated from the titre. A conversion factor, typically 6.25 for food, 6.38 for milk or 5.7 for wheat flour, converts nitrogen into protein. Blank determinations, catalyst choice and digestion completeness are the main factors that determine accuracy, and the method is the traditional reference for protein content.
What are the key features?
- Small tube format of 50–100 mL
- Sample masses from 10 mg
- Compact steam distillation with small receiver
- Low reagent consumption and waste volume
- Digestion times of 20–60 minutes
- Micro-burette or potentiometric titration
What are the technical specifications?
A typical micro-kjeldahl digestion and distillation system configuration offers sample mass of 10–100 mg, tube volume of 50–100 mL, acid volume of 1–5 mL per sample, digestion temperature of Up to 400 °C, digestion time of 20–60 min and distillation time of 2–4 min per sample. Values are indicative of the product class; the exact figures for each configuration are confirmed on the quotation and the calibration documents supplied with the instrument.
Which applications is it used for?
The Micro-Kjeldahl Digestion and Distillation System is used in protein testing when sample material is limited, costly or hazardous matrices such as toxins and drugs, low-waste laboratories with acid disposal constraints and research and teaching with small sample sets. Across the wider Kjeldahl Systems class, laboratories also deploy it for reference protein determination in food and feed, milk and dairy nitrogen testing and cereal, flour and grain protein measurement.
Which standards and certifications apply?
Relevant standards and methods include ISO 1871, ISO 8968-1, ISO 5983-2, AOAC 2001.11, AOAC 920.87 and ISO/IEC 17025. Certification candidates for this model are CE and ISO 9001 manufacturing; each is to be confirmed for the specific configuration before shipment, and certificates are supplied only where they have been issued.
Kjeldahl work involves concentrated sulfuric acid, hot sodium hydroxide and noxious fumes, so a fume hood, an exhaust scrubber and acid-resistant surfaces are required, along with gloves, goggles and a face shield. Digestion must be complete and free of charring; adding hydrogen peroxide or using a catalyst mixture helps, and selenium catalysts need careful handling because of toxicity. The distillation apparatus must be steam-tight and conditioned before the first sample to avoid low recoveries, and blank values should be subtracted for each batch. The standard acid and sodium hydroxide solutions need regular standardisation, and titrators should be checked with certified materials. Document temperatures, times, reagent batches and catalyst lots.
How do I select the right Micro-Kjeldahl Digestion and Distillation System?
Choose a micro-Kjeldahl system when sample mass is scarce, matrix cost is high or acid waste disposal is expensive. Confirm that the nitrogen range suits your expected content and that a micro-balance and precise titration are available, since weighing error has a larger relative effect than in macro methods.
How does it compare with other Kjeldahl Systems variants?
Choose the scale of the system from your sample numbers and the accuracy you need. Manual digestion blocks with six to twelve positions suit low-throughput laboratories and teaching use but demand careful timing and fume control. Automated digestion blocks add temperature programming, exhaust scrubbing and unattended runs, which improve safety and reproducibility. Steam distillation units with automatic alkali addition and titration cut operator time and variability and are the core of routine Kjeldahl work. Integrated analyzers link digestion, distillation and titration in one workflow and are convenient where many samples are processed daily. Micro-Kjeldahl systems use smaller sample and reagent volumes, which reduces waste and is useful when sample material is limited. Whatever the scale, confirm recovery with reference materials.
Full specifications
| Sample mass | 10–100 mg |
|---|---|
| Tube volume | 50–100 mL |
| Acid volume | 1–5 mL per sample |
| Digestion temperature | Up to 400 °C |
| Digestion time | 20–60 min |
| Distillation time | 2–4 min per sample |
| Titration | Micro-burette or potentiometric |
| Nitrogen range | 0.05–20 mg N per sample |
| Recovery standard | Ammonium sulfate |
| Waste volume | Reduced by 70–90 percent |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Protein testing when sample material is limited
- Costly or hazardous matrices such as toxins and drugs
- Low-waste laboratories with acid disposal constraints
- Research and teaching with small sample sets
Key features
- Small tube format of 50–100 mL
- Sample masses from 10 mg
- Compact steam distillation with small receiver
- Low reagent consumption and waste volume
- Digestion times of 20–60 minutes
- Micro-burette or potentiometric titration
Frequently asked questions about Micro-Kjeldahl Digestion and Distillation System
Sample masses from about 10 mg can be digested, which is useful for limited or expensive material. Below that, weighing uncertainty and inhomogeneity dominate, and results become unreliable even with a microbalance.
Yes, when both are validated and recovery is verified with the same standard. Differences arise mainly from sample inhomogeneity, since a smaller portion may not represent the whole sample, and from weighing error.
Hydrogen peroxide accelerates oxidation and helps clear difficult matrices such as fats and proteins, shortening digestion time. It must be added slowly and in small portions because the reaction is vigorous.
It is the traditional reference method accepted by pharmacopoeias, food regulations and feed standards, and it is robust across many matrices. Its direct acid digestion step also makes it suitable for referee analysis and for validating faster combustion methods.
Copper sulfate and selenium are the common catalysts, usually with potassium sulfate to raise the boiling point of the acid mixture. Copper is less toxic but slower, while selenium is faster but requires careful handling and disposal.
Reagents, glassware and laboratory air contribute small amounts of nitrogen that would be counted as sample nitrogen. A blank carried through digestion, distillation and titration gives that contribution, which is subtracted from each result.
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