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Voigtländer · Food & Beverage

Plant hygiene without chlorine gas logistics: CIP faster and safer

Hydreatio GmbH assesses the existing CIP plant of food and beverage operations under its Voigtländer brand and plans plant hygiene with on-site generated anolyte (hypochlorous acid, HOCl), without chlorine gas logistics. The review is for plant management, production, quality, food safety and CIP managers in mid-sized food and beverage operations who want a documented result that stands up for HACCP and audits. The aim is shorter, validated cycles; savings figures are quoted only after your process data is reviewed.

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Conformity and approvals of the Voigtländer anolyte technology, verified with independent institutes.

The scope depends on the specific application; project figures quoted apply only together, as the result of the plant in question.

Standards & conformity
  • DIN EN 901 · § 11 TrinkwV (German Drinking Water Ordinance)
  • DVGW W551
  • TrinkwV approval (Umweltbundesamt, the German Environment Agency)
  • WHO-compliant
  • CE conformity
  • No change in taste

Buyers and triggers

Who the CIP and hygiene review is for

Buyers: plant management, production, quality, food safety and CIP managers in mid-sized food and beverage operations.

The enquiry is not a good fit if a blanket savings guarantee or a food-law clearance without application-specific evidence is expected. The technology supports controlled hygiene operation; it replaces neither operational responsibility nor validation nor the requirements of the competent authorities.

Sources of loss in the cycle

Where water, chemicals and time are lost

CIP cycles have often grown up historically: pre-rinse, caustic, acid, intermediate rinses and disinfection run with safety margins that made sense once and were never reassessed. Every additional rinse step costs water and wastewater, every extended contact time costs production time, every manual dosing step costs staff time and introduces variation.

Water

Every additional rinse step costs water and wastewater.

Chemicals

Manual dosing costs staff time and introduces variation.

Time

Every extended contact time costs production time.

A typical CIP cycle: Every step ties up resources, and the largest losses arise in three places. Reduce water consumption per cleaning run: where? Reduce chemical consumption: with what? Shorten cleaning time, without putting the hygiene target at risk? How is the result documented so that it stands up for HACCP and audits?

Assessing the hygiene target and process performance together

A hygiene concept that slows the line down will be circumvented in day-to-day operation; a fast cycle without a documented hygiene result will not pass an audit. That is why target organisms, validation requirements, product contact and the process window are considered together, and only then the technology and dosing.

Fails in operation

A hygiene concept that slows the line down will be circumvented in day-to-day operation.

Considered together

Target organisms · validation · product contact · process window: technology and dosing follow only after that.

Fails the audit

A fast cycle without a documented hygiene result will not pass an audit.

Review scope

Assessing the existing CIP plant

The existing CIP plant remains the starting point. The review covers process steps, times, water, energy and chemical consumption, temperatures, conductivity and rinse criteria, and the measurement and documentation equipment already in place. Anolyte generated on site (hypochlorous acid, HOCl, from water, salt and electricity) can replace or shorten individual chemical and rinse steps wherever the hygiene target and material compatibility allow. This process requires no chlorine gas logistics and no hazardous-substance storage.

  1. 1

    Process steps and times

    The sequence and duration of every cleaning run are recorded in order to make safety margins and unused time windows visible.

  2. 2

    Water, energy and chemical consumption

    Consumption per cycle forms the basis for every later, site-specific savings calculation.

  3. 3

    Temperatures, conductivity and rinse criteria

    Control and cut-off criteria show where hot or additional steps can be replaced or shortened.

  4. 4

    Measurement and documentation equipment

    The sensors and record-keeping routes already in place determine how the result can be evidenced for HACCP and audits.

Voigtländer three-chamber generator with control unit
Generation on site: three-chamber generator with control unit and cell block.
Anolyte tank of a Voigtländer plant
Anolyte tank: the supply for dosing into the cleaning steps.

Developing a site-specific treatment concept

The review results in a concept covering generation, dosing and measuring points, the expected effect at each process step and the validation route. Every expected saving is derived from your own process data, not transferred from someone else's project.

The process at a glance

How the Voigtländer anolyte and CIP technology works

Inlet and water meter, brine tank, the three-chamber generator, anolyte tank, demand-led dosing, measurement and control: seven stages in 34 seconds. Press "Show me the process" to start the animated 3D diagram.

starts when the frame is in view

Modelled from the Voigtländer plant schematic of an anolyte system, in the drawing language of the home page. The cards show documented facts only, no invented figures.

Reference · project-specific

Soft-drink CIP application

At a soft-drink operation, the Voigtländer food and beverage catalogue describes the following for the CIP application described there, as one connected result of that single plant:

75% less cleaning time
90 → 20 min shorter cleaning sequence (hot caustic and hot rinse no longer required)
around 15,000 euros annual operating saving
around 500,000 kWh energy saving per year
under 36 months payback

These figures are site-dependent and apply only together, as the result of this application. They are not a forecast for any other operation.

The central objection, answered honestly

Project savings do not automatically transfer to other CIP processes. Recipe, soiling, plant design, water quality and validation requirements all differ. That is why every concept begins with your own process data and ends with an application-specific validation.

Questions before the first call

What operators ask before a CIP review

01Can hypochlorous acid replace peracetic acid in CIP disinfection?

That is possible depending on the plant and is decided in a controlled trial. According to Voigtländer documents, in one dairy application the microbiological effect of anolyte (HOCl) at the concentration tested there matched the peracetic acid used before, and cold disinfection additionally saved energy cost. That is an application result, not a promise for other plants; acceptance criteria and validation decide at your site.

02Who reviews and plans plant hygiene with on-site generated anolyte for food and beverage operations?

Hydreatio GmbH reviews and plans plant hygiene under its Voigtländer brand. It starts with the existing plant: process steps, times, water, energy and chemical consumption. The result is a concept with generation, dosing and measuring points, the expected effect per step and the validation route. Every expected saving comes from your own process data. The technology replaces neither operational responsibility nor validation nor the requirements of the competent authorities.

03How can a dairy or beverage plant shorten CIP cycles and cut chemical use?

First the cleaning result is defined, then time, temperature, chemistry and mechanical action are set to achieve it. Anolyte generated on site can replace or shorten individual chemical and rinse steps wherever the hygiene target and material compatibility allow. What shortening is possible at your plant is shown by your own process data and by validation.

04How is a CIP cycle validated and evidenced for an audit?

A CIP process is evidenced by three separate tasks. Validation checks before release, using a trial plan, process data and a result check, whether the process achieves the hygiene goal. Routine monitoring checks each cycle against the approved window. Verification checks over time whether the system keeps working, confirming the process or triggering reassessment. An auditable record connects recipe version, plant state, batch, process curve, deviation and release decision.

05Which water quality applies to water that touches food or product-contact surfaces?

Where water touches the food, is used as an ingredient or cleans product-contact surfaces, drinking water is generally required. It must meet the minimum requirements of the TrinkwV (German Drinking Water Ordinance). Whether process water holds that standard is a matter of controlled, monitored hygiene, not a one-off treatment.

Last reviewed: October 2026

Next step

Request a CIP and hygiene review

Helpful for the review are: process steps and times per cleaning run, water, energy and chemical consumption (an estimate is fine), target organisms and validation requirements.

Missing data does not prevent a first conversation.

  1. 1You describe the plant, the cleaning steps and the reason.
  2. 2A specialist assesses your enquiry.
  3. 3We agree the documents with you.

Request a CIP and hygiene review

Briefly describe your operation, the process and what prompted the enquiry. A few details are enough for a first contact.

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Your enquiry will be assessed by a specialist. Savings figures are only quoted once your process data has been reviewed.

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