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Jar Test Designer
v2.7
Worked example showing. Your own test is kept aside; changes to the example are not saved.
Step 1 of 8

SetupQuick test

Getting started

New to this tool? Turn on Worked example (top right) to see a finished test of the type you have picked, then turn it off to start your own. Your own test is kept aside while the example shows.

Pick the test type first:

  • Quick test: one page, a fixed bench protocol (200 rpm rapid mix, 40 rpm flocculation, 10 minute settle) and sensible defaults. Pick your doses, follow the protocol, enter results. Good for routine dose checks; clarification only.
  • Plant match (Premium): a full jar test designed around your plant. The tool works out paddle speeds, mixing times and settle times that reproduce your plant in a 1 L jar, and adds filtration, pH work with acid and base, custom stock strengths, reports and the floc strength test.

Plant match runs in numbered steps; work left to right, or use the Next button at the foot of each step:

  1. Setup (this page): test details, jar tester, water temperature and plant type.
  2. Plant match: your plant's mixing, clarifier and filters.
  3. Jar mixing: the paddle speeds and times to set on the bench.
  4. Solutions: stock recipes for coagulant, polymer, acid and base.
  5. Regime: what each jar gets, and the run protocol.
  6. Observations: floc size during the test.
  7. Results: your measurements; the tool finds the optimum jar.
  8. Report & Save: PDF report, spreadsheet export and project file.

Floc strength is an optional extra test, outside the numbered steps. Your entries are kept in this browser. Clear all (foot of this page, two clicks) empties the test; Settings are kept.

The tool gives guidance only. Check any result that matters before acting on it.

Test type

Plant match is part of Premium: mixing matched to your plant, filtration, pH work with acid and base, reports and the floc strength test. See plans

Test information

A short name for this run; it heads the report.
Where the water was taken from.

Plant configuration

What treatment train are you simulating?

Coagulant dose unit

How you want to talk about dose throughout the test

Jar apparatus

Positions on your jar tester.
1 L is the bench standard.
Square jars are the bench standard; round jars swirl more.
mm
Vertical paddle dimension. Standard bench paddle: 25 mm.
mm
Horizontal sweep dimension. Standard: 75 mm.
Set in Settings (calibration value). Standard ≈ 0.75.

Water conditions

°C
°C
Used to flag if the jars warm up during the test.
Day the jars were run.
Step 2 of 8

Plant match

Guide: using this tab

Describe the plant here: flow rates, tank sizes, paddle speeds and hydraulic loading rates. Enter what is on the plant's design drawings, or what SCADA says it is running at; the tool does the conversion.

Behind the scenes the tool works out the mixing intensity (G) at each stage, then the jar paddle speed that gives the same intensity in a 1 L jar. That is what makes the bench test a meaningful copy of the plant.

It does the same for the clarifier rise rate and the filter rate. All of these become bench settings on the next steps.

No plant data, or just exploring? Pick Typical values below and set the jar mixing intensity directly on the Jar mixing step.

Where the mixing targets come from

1. Rapid mix (coagulation)

—
How the coagulant is mixed in on the plant. Enter the dimensions below in metres.

2. Flocculation

—
How the floc tanks are stirred.
Floc tanks in series; most plants have 2 or 3, each slower than the last.

3. Clarification

Hydraulic loading rate is all we need

Clarifier type doesn't matter for the jar test. What matters is the rise rate — the m/h that floc has to settle faster than to be removed. Set it from your plant's design or operating data.

m/h
Pick one to fill the rate in, if you have no plant figure.

4. Filtration

Filter rate + media — selects the jar test filter

For a meaningful filter step in the jar test, the tool needs the plant filter rate (to scale the analogy) and the media type (to pick a filter paper or membrane that mimics the bed cut-off). The jar test won't reproduce filter runtime — but it will give you a clean filtrate sample for analysis comparable to your downstream water.

m/h
The plant filter bed; it picks the matching jar filter below.
mm
For the record only; the jar test does not use it.
A filter paper or membrane that approximates your plant filter cut-off.
Essential for low-DOC / UV₂₅₄ work.
mL
200 mL is enough for full filtrate analysis.
Step 3 of 8

Jar mixing

Guide: using this tab

This step tells you what to dial into your jar tester. The tool has worked it out from the Plant match step: the boxes headed Set jar tester to are the numbers you set on the bench, paddle speed (rpm) and how long to run each stage.

The target G and stage times are filled in from your plant data. Only change them if you deliberately want to test different mixing; most people never do.

If one of those boxes turns amber, the speed is outside what a jar tester can do (over about 250 rpm or under about 10). That usually means the paddle dimensions in Setup do not match your bench paddle.

Nothing to enter here for most tests. The boxes headed Set jar tester to show the rpm and time for each stage. The target fields are filled in from Plant match; only change them to test different mixing deliberately.

Plant targets

Read-only

Rapid mix

Pre-filled from plant
s⁻¹
Typically 300 to 1,000 s⁻¹.
s
Typically 10 to 60 s.
Set jar tester to
—

Jar geometry

Read-only, from Setup
Jar
—
Paddle
—
Viscosity (μ)
—

Bench run sheet

The whole mixing sequence at a glance
Step 4 of 8

Solutions

Guide: using this tab

This tab gives you the recipe for each stock solution you'll dose from. There are four of them:

  • Coagulant stock — a diluted version of your plant's neat product, made at a strength that gives you syringe-friendly volumes (a few mL per jar).
  • Polymer stock — 1 g of polymer made up to 1 L with deionised water, aged 30 minutes before use.
  • Acid stock — for lowering pH (typically 0.5 N sulphuric acid).
  • Base stock — for raising pH if you need to (sodium hydroxide or sodium carbonate).

The tool tells you exactly what to weigh out (or measure with a pipette) and what volume to make up to. Make coagulant and polymer stocks fresh each day — they age and lose strength.

The simple rule: 1 mL of a 1 g/L stock added to a 1 L jar gives 1 mg/L dose. Everything else scales from there.

The default SG and % active for every coagulant product, and the default polymer stock strength, are in Settings (top right) and apply to all tests. Changes made on this step apply to this test only.

Coagulant

The product your plant doses.
mg active / mL
5 mg/mL works for most plants. Higher for very low doses; lower for high doses.
% w/v
Auto-filled from product. Override with the supplier's COA value.
g/mL
Liquid coagulants only.
mL
Size of your volumetric flask, usually 1,000 mL.
Make-up recipe: —
What 1 mL of this stock gives

Polymer

The charge of the polymer you use.
Optional; shown on the report.
g/L
1 g/L standard. Higher for very low doses.
mL
1 L volumetric is the bench standard.
Recipe: —

pH adjustment

Lowers pH.
Raises pH.
Strength; 0.5 N suits most waters.
mL
Volume to make; 250 mL lasts a session.
Strength; 0.5 N suits most waters.
mL
Volume to make; 250 mL lasts a session.
Acid: —

Base: —
Step 5 of 8

Regime

Guide: using this tab

This is where you decide what each jar gets. The auto-fill buttons fill a ladder to suit the test you are running. Change one thing at a time so the results can be read.

Typical sequence:

  1. Coag dose screen first — hold pH constant, vary coag dose across the jars.
  2. pH optimisation next — at the best dose, vary pH around the suspected optimum.
  3. Polymer trial last — at the best (dose, pH), test polymer addition.

About acid and base doses: The tool can estimate how much acid (or base) you need to reach a target pH, using the raw water alkalinity from the Results tab. Click Estimate acid/base to populate the columns. The estimate accounts for the alkalinity that the coagulant itself consumes, but it's a starting point — not a precise prediction. Always measure the actual pH of the first jar and adjust your dosing accordingly. If you don't enter raw alkalinity, the columns stay empty and you'll need to set the volumes manually based on a pre-titration.

Sampling

Rise rate from Plant match
m/h
Change it on the Plant match step.
mm
Auto-set from sample method; override if your tap is at a different height.

Dose timing

When chemicals enter the jar
Match where acid or base is dosed on the plant.
Match where polymer is dosed on the plant.

Coagulant and stock solutions

Pick your product, make these before you start
The product your plant doses.

The "Stock to add (mL)" column in the ladder below is the volume of this stock solution to add to each jar. Plant match offers other stock strengths, acid and base stocks, and full recipes.

Dose for each jar

Doses in the unit picked on the first page

Operator protocol

Built from everything above; print or save it from Report & Save
Step 6 of 8

Observations

Guide: using this tab

During the flocculation phase, watch each jar and note the floc size class at each timepoint. The size chart below is your reference card — match what you see in the jar to a class number.

Two things that make the observations reliable:

  • Same method every time. Hold the jar against a white background with even overhead light — floc looks bigger in shadow and smaller in glare. Any operator can do the sizing; what matters is that everyone uses the same background, lighting and reference chart.
  • Look in the bulk of the jar, not at the surface or against the walls. Floc concentrates near the top meniscus and looks bigger there than it really is. Ideally, observe while the paddle is still turning slowly.

Floc behaviour tracks faster than any analytical result, and weak or slow-forming floc is usually the first sign that the chemistry isn't right.

Size reference chart

The visual standard for sizing floc

Edit the midpoints in Settings if your bench reference card differs. The circles are drawn at on-screen scale, not true size.

Floc size in each jar

Tap the size class you see at each time
Comma-separated. Default 5/10/15/20/30 min.

Floc growth read-out

What the recorded size classes show
Step 7 of 8

Results

Guide: using this tab

This is where the analytical numbers go. There are two samples to measure from each jar:

  • The clarified water (what you drew off the top after settling), and
  • The filtrate (what comes through the jar filter paper, simulating the plant filter).

The tool shows whichever columns make sense for your plant — both if you're doing clarification + filtration, just one if you're doing clarification only or direct filtration.

What to measure:

  • Turbidity — always. Clarified turbidity tells you how well the floc settled; filtrate turbidity tells you how well the filter is polishing.
  • Organics — pick one parameter (UV₂₅₄ absorbance, True Colour, DOC, or SUVA) and measure it on both clarified and filtrate. Turbidity alone isn't enough for a proper assessment.
  • pH and alkalinity — read on the clarified water, before any chlorination.
  • Residual metal — total in the clarified, dissolved in the filtrate.

When picking the optimum jar, don't just go for the lowest number. Check that the dose one step lower is nearly as good (it's cheaper), and that the floc looked robust in your observations. A flat plateau is more reliable than a knife-edge.

Dissolved organics parameter

Pick one for the entire test
All four are valid surrogates for natural organic matter. UV₂₅₄ absorbance is the most common bench measurement; True Colour is operator-friendly; DOC is the cleanest analytical truth; SUVA combines both.

Raw water

Measured on the untreated sample
Organics measurements are optional, but you need at least one for a proper performance assessment. Turbidity alone tells you only about the particles; coagulation also removes dissolved organic carbon, and the best dose is often set by organics, not turbidity. Pick a parameter above and include it in the raw water and treated samples.

Results for each jar

The lowest value of this measurement marks the optimum.

Removal performance

Enter results to identify optimum
Step 8 of 8

Report & Save

Guide: using this tab

Three ways to take your work away, all from this step:

  • PDF report: to print and take to the bench, or send to a colleague. Choose the sections below. In the print dialog pick Save as PDF, and turn off Headers and footers for a clean page.
  • Spreadsheet (CSV): the dose ladder, observations, results and floc strength data as tables.
  • Project file: a complete copy of the test (setup, plant, doses, observations, results). Open it later to carry on, or send it to a colleague using this tool. Opening a file replaces the test on screen, so save first if you want to keep it.

Plant name

Appears on the report title
Optional. The report title is generic if blank.

Sections to include

Applies to both the PDF report and the spreadsheet

PDF report

In the print dialog set Destination to Save as PDF, and untick Headers and footers for a clean page.

Spreadsheet (CSV)

Exports the tables from the sections picked above (dose ladder, observations, results, floc strength) with the test details at the top. Sections without tables appear in the PDF only.

Project file

A complete copy of the test
Includes every input, the dose ladder, observations, results and the floc strength test.
Replaces the test on screen. Save first if you want to keep it.
Optional extra test

Floc strength

Guide: using this tab

This is a follow-on test that answers a question the standard jar test can't: how robust is the floc? You make the floc, take a size reading, then shear it hard for a short burst, take another reading, let it reform, and take a third reading.

Two chemistries can give the same clarified turbidity but behave very differently downstream. Weak floc shears in the filter inlet and packs tightly at the surface, giving fast headloss rise and short filter runs. Floc that can't reform after a shock will punch through the bed and cause early turbidity breakthrough. Strong, reformable floc rides through flow swings and dose drift without complaint.

The tool gives you two numbers:

  • Strength Factor (Sf) — how much of the floc survived the shear. Higher is stronger.
  • Recovery Factor (Rf) — how well the broken floc reformed. Higher is more forgiving.

Run this to compare two coag/polymer combinations that look equivalent on clarified turbidity, to verify a polymer actually toughens the floc, or to diagnose filter breakthrough.

1. Test condition

Carry over from the main test, or set by hand
Pick a jar to inherit its dose / pH.
A short description; it heads this test in the report.
mg/L
In the dose unit picked on the first page.
mg/L
In 0.05 mg/L steps; blank if none.
Blank if not adjusted.

2. Breakage and reformation

s⁻¹
s
Typically 10 to 60 s; keep it the same between tests.
s⁻¹
min
Typically 10 to 20 min.

3. Bench protocol

4. Record observations

—
—
—
Optional; shown on the report.

5. Results and interpretation

Strength Factor (Sf)—
Resistance to breakage. Higher = stronger floc.
Recovery Factor (Rf)—
Ability to re-aggregate after shear. Higher = more forgiving.

Bar colours (green strong, amber moderate, red weak) are prompts to look, not instructions to act.