Laboratory water purification systems compared: what a lab water purification system has to deliver at the point of use, what a type 1 water purification system delivers that a type 2 water purification system does not, how an ultra pure water purification system or a di water system for lab use is sized, why water hplc grade and lc ms water are specified separately from bench water, and why lab water purification, laboratory water systems and lab water systems generally fail at the point of use rather than at the unit

Specifying the system

1. Match the grade to the application. Type 1 water, at about eighteen megohm-centimetres resistivity with low total organic carbon, is for the sensitive work: chromatography, molecular biology, cell culture, trace analysis. Type 2 serves as feed water, for buffers and for glasswashing. Type 3 is for rinsing and baths.
2. Size on the daily volume and on the peak. Systems are specified by production rate and reservoir volume, and a laboratory whose whole demand arrives in one hour of the morning needs a bigger reservoir rather than a bigger purifier. Measure a week of real consumption before ordering.
3. Establish the feed water quality first. Mains water hardness, chlorine and silica decide the pretreatment and the consumable life. A system quoted against a national average feed and installed on hard water will consume cartridges at a rate nobody budgeted for.
4. Put the polishing at the point of use. Purity is lost in storage and distribution, not in the purifier. A polishing cartridge and a final filter at the tap are what make the delivered water match the specification, and a system without them delivers reservoir water.
5. Choose the final filter for what you are protecting against. A 0.22 micrometre filter for bacteria, an ultrafilter where nucleases or endotoxin matter, and an ultraviolet lamp where organic carbon does. Each addresses a different contaminant and none substitutes for another.

Consumables are the real cost

Cartridges, membranes and lamps are the operating cost and their life depends entirely on the feed water. Ask the vendor to quote a five year consumable cost against your measured feed rather than against a typical one.

A service contract that includes consumables removes the budgeting problem and usually costs more in total. Which is better depends on whether the laboratory reliably replaces cartridges on time without one.

Monitoring and record keeping

Inline resistivity and total organic carbon monitoring, logged rather than merely displayed, is what lets you show that the water was in specification on the day of an experiment. For regulated work that record is expected.

Set alarm limits that mean something and make sure somebody receives them. A monitor that flashes on a panel in an unattended room documents the failure rather than preventing it.

Sanitisation and stagnation

Stagnant water grows biofilm, which is why loops recirculate and why a system returning from a shutdown needs sanitising before use. A laboratory that has been closed for a fortnight should not draw water for cell culture on the first morning back.

Follow the manufacturer's sanitisation schedule and record it. Most bacterial problems in laboratory water are traceable to a sanitisation that was skipped rather than to the purifier itself.

Common questions

What is the difference between a type 1 water purification system and a type 2 one?

Type 1 delivers about eighteen megohm-centimetres with very low organic carbon for sensitive applications. Type 2 is a lower grade, typically produced by reverse osmosis with deionisation, used as feed for type 1 systems and for general laboratory work.

Does resistivity tell me the water is pure?

Only about ions. Resistivity says nothing about organic carbon, bacteria, endotoxin or nucleases, and water reading eighteen megohm-centimetres can still be unusable for cell culture or for RNA work.

How is an ultra pure water purification system sized?

By daily volume and by peak demand together. The production rate covers the day and the reservoir covers the hour when everybody draws at once, and getting the second wrong is what produces queues at the tap.

Where does lab water purification usually go wrong?

After the purifier. Storage, distribution loops and the tap itself reintroduce organics and bacteria, which is why point of use polishing and a final filter matter more than another stage in the cabinet.

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