Hach DR300 Bromine Pocket Colorimeter: Complete Review & Reference (2026)

Sources: Hach DR300 User Manual DOC022.97.90639 Ed.5 (09/2021) • Method DOC316.53.01443 Ed.2 (HR, 12/2018) • Method DOC316.53.01444 Ed.2 (LR, 12/2018)

DPD Method 8016 • LR: 0.05–4.50 mg/L Br₂ • HR: 0.2–10.0 mg/L Br₂ • IP67 Waterproof

Hach DR300 Bromine pocket colorimeter showing DPD bromine measurement display Water treatment operator using Hach DR300 Bromine pocket colorimeter for cooling tower testing
Hach DR300 Pocket Colorimeter — Bromine (DPD Method 8016)
LR: 0.05–4.50 mg/L Br₂ • HR: 0.2–10.0 mg/L Br₂ • IP67 waterproof • Bluetooth® Claros. Reagents (DPD Total Chlorine Powder Pillows) sold separately.
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Method
DPD Method 8016
LR Range
0.05–4.50 mg/L Br₂
HR Range
0.2–10.0 mg/L Br₂
LR Cell
25 mm glass, 10 mL sample
HR Cell
1 cm square, 5 mL sample
LR Reagent
1 DPD powder pillow
HR Reagent
2 DPD powder pillows
Cl₂ Conversion
Cl₂ mg/L × 2.25 = Br₂ mg/L
IP Rating
IP67 Waterproof
LR Precision
2.25 ± 0.11 mg/L Br₂
HR Precision
11.3 ± 0.5 mg/L Br₂
Battery Life
~5,000 tests (4× AAA)

What the DR300 Bromine Model Measures & Who Uses It

The Hach DR300 Bromine pocket colorimeter measures total bromine residuals — including hypobromite (OBr¹−), hypobromous acid (HOBr), and bromamines — using the DPD (N,N-diethyl-p-phenylenediamine) colorimetric method (Method 8016). Unlike the iron or chlorine models, the bromine DR300 is available in two distinct range configurations that differ in cell size, sample volume, and reagent quantity — not simply a software switch.

ApplicationTypical Range UsedWhy Bromine
Cooling towersHR (0.2–10.0 mg/L)Bromine biocides effective across wider pH range than chlorine; bromamines retain biocidal activity
Indoor pools & hot tubsLR (0.05–4.50 mg/L)Less odor than chlorine; stable at high temperatures; standard in spa applications
Industrial HVAC water treatmentHR (0.2–10.0 mg/L)Brominators used where chlorine is too corrosive or pH fluctuates widely
Wastewater disinfectionHR or LR depending on doseUsed in industrial effluent where combined halogen residuals matter
Food & beverage process waterLR (0.05–4.50 mg/L)Bromine disinfection verification in CIP systems and rinse water

How the DPD Method Works for Bromine

Bromine residuals react with DPD (N,N-diethyl-p-phenylenediamine) to form a pink color directly proportional to total bromine concentration. The DPD Total Chlorine Reagent contains both the DPD indicator and a buffer system. No separate oxidation or conversion step is needed — the pink color develops immediately upon reagent addition.

Why LR Uses Less Reagent

The LR procedure uses 1 powder pillow in 10 mL of sample. Lower indicator concentration matches the lower analyte concentration, keeping the calibration linear across the 0.05–4.50 mg/L range.

Why HR Uses More Reagent

The HR procedure uses 2 powder pillows in only 5 mL of sample — a 4× increase in indicator-to-sample ratio. This extends the measurement range to 10.0 mg/L Br₂ without changing the instrument optics or chemistry.

The 2.25× Chlorine Conversion Factor — Critical for Accuracy Verification

The DPD method responds equally to chlorine and bromine on a molar basis, but bromine has a higher molecular weight (159.8 g/mol vs 70.9 g/mol for Cl₂). This creates a fixed conversion relationship documented in both method documents:

CONVERSION RELATIONSHIP
Cl₂ → Br₂
Chlorine standard (mg/L) × 2.25 = equivalent bromine concentration (mg/L Br₂)
SCA Ranges
LR: 2.00–4.00 mg/L Br₂ required
HR: 2.0–8.0 mg/L Br₂ required
Example: A 2.0 mg/L Cl₂ chlorine standard = 4.5 mg/L Br₂ equivalent. Use this when verifying LR measurements using a chlorine standard instead of a bromine standard.

LR vs HR — Which Configuration Do You Need?

FeatureLow Range (LR)High Range (HR)
Measurement range0.05–4.50 mg/L Br₂0.2–10.0 mg/L Br₂
Sample volume10 mL5 mL
Powder pillows per test12
Sample cell25 mm round glass cell1 cm square cell
AccuVac® optionYes (30 mL self-fill)No — Powder Pillow only
Precision2.25 ± 0.11 mg/L11.3 ± 0.5 mg/L
SCA standard range2.00–4.00 mg/L Br₂2.0–8.0 mg/L Br₂
Best forPools, spas, drinking water, low-dose industrialCooling towers, high-dose industrial, HVAC
LR and HR are separate instrument configurations — not a software setting on the same unit. Confirm which range your DR300 is factory-configured for before ordering reagents and cells. Using LR reagent quantities in an HR-configured instrument will give inaccurate results.

Pre-Test Requirements (Both LR and HR)

1

Clean, scratch-free sample cells only

Scratches in the optical path permanently affect readings. Use only optically clear cells. Inspect before each use.

2

Triple-rinse the sample cell

Rinse the cell and cap three times with the sample before filling. This conditions the cell walls and removes residual reagent from previous tests.

3

Wipe all exterior surfaces

Wipe with a lint-free cloth — no fingerprints or liquid on any optical surface. Check for condensation on cold samples.

4

Install the instrument cap BEFORE pressing ZERO or READ

The cap must be installed before any measurement. Reading without the cap installed will give incorrect results because ambient light enters the sample chamber.

5

Over-range or yellow color: dilute and retest

If the result is over-range, or if the sample turns yellow (not pink) after reagent addition, dilute with bromine-demand-free water and retest. Multiply result by dilution factor.

6

New reagent lot: measure a blank

For each new lot of reagent, measure a reagent blank using deionized water in place of sample. Subtract blank value from all subsequent sample results.

7

Post-test rinse

After each test, immediately empty and rinse the sample cell and cap three times with deionized water. Do not allow reagent to dry in the cell.

Sample Collection — Critical Requirements

Bromine residuals dissipate rapidly. Collect samples immediately before testing. Do not store bromine samples — collect, test, and discard. Use plastic (not glass) containers where possible — glass can absorb bromine. Keep samples out of direct sunlight. For cooling tower samples, collect from the return line or basin, not the supply, unless specifically monitoring supply residual.

Low Range Procedure — Powder Pillow (0.05–4.50 mg/L Br₂)

1

Fill the 25 mm round glass cell to the 10-mL mark

Use sample water. Triple-rinse before filling for measurement.

2

Add 1 DPD Total Chlorine Powder Pillow

Add contents of one DPD Total Chlorine Reagent Powder Pillow to the filled cell.

3

Cap the cell and swirl to mix

Cap securely. Swirl gently for approximately 20 seconds until reagent is fully dissolved. Pink color will develop if bromine is present.

4

Insert cell and install cap — press ZERO immediately

Insert the sample cell into the instrument, install the cap, and press ZERO promptly. The DPD color develops quickly — do not delay zeroing.

5

Fill a second cell with fresh sample for the blank

Fill a second 25 mm cell to the 10 mL mark with the same sample water. No reagent is added to the blank cell.

6

Remove reagent cell, insert blank cell, press ZERO

Remove the reagent-containing cell. Insert the blank cell (no reagent). Press ZERO to establish the baseline. Install cap before zeroing.

7

Remove blank, insert reagent cell, press READ

Remove the blank cell. Re-insert the cell containing the reagent-mixed sample. Install cap. Press READ. The display shows mg/L Br₂.

Low Range AccuVac® Ampul Procedure (0.05–4.50 mg/L Br₂)

AccuVac® advantage: Self-fills from the sample using vacuum. No measuring volumes — the ampul draws exactly 10 mL. Ideal for field sampling where pipettes are not practical. AccuVac® option is available for LR only; not available for HR.
1

Submerge ampul tip completely in the sample

Keep the tip below the water surface. If the tip breaks contact with the sample before the ampul is full, air enters and the result is invalid. Use a container deep enough to keep the tip submerged throughout filling.

2

Snap the tip while submerged — keep tip submerged until full

Snap the scored tip while the ampul tip is fully submerged. Maintain submersion until the ampul is completely filled. If the tip clears the surface before full, discard and use a new ampul.

3

Cap the ampul with the AccuVac® cap

Wipe the exterior dry with a lint-free cloth. Cap the ampul.

4

Invert the ampul 3 to 5 times to mix

Invert gently to mix the internal reagent with the sample. Pink color develops if bromine is present.

5

Insert into the AccuVac® adapter in the instrument

Insert the capped ampul into the AccuVac® adapter (ensure the adapter is seated in the instrument). Install the instrument cap. Press READ.

High Range Procedure — Powder Pillow (0.2–10.0 mg/L Br₂)

HR uses different cell size and double the reagent. Use the 1 cm square cell (not the 25 mm round glass cell) and exactly 5 mL of sample volume (not 10 mL). Using the wrong cell or wrong volume invalidates the result. Do not attempt HR with AccuVac® ampuls.
1

Fill the 1 cm square cell to the 5-mL mark

Use the square cell supplied with the HR instrument. Fill to exactly 5 mL with sample water. Triple-rinse the cell before the measurement fill.

2

Add 2 DPD Total Chlorine Powder Pillows

Add the contents of exactly two DPD Total Chlorine Reagent Powder Pillows to the 5 mL sample. Do not add only one — HR requires double reagent quantity.

3

Cap and swirl to mix

Cap securely. Swirl for approximately 20 seconds until reagent is fully dissolved. Intense pink color will develop at higher bromine concentrations.

4

Insert cell and install cap — press ZERO immediately

Insert the 1 cm square cell, install instrument cap, and press ZERO promptly. Do not delay — DPD color develops quickly.

5

Fill a second 1 cm cell with 5 mL fresh sample (no reagent)

This is the blank. Same cell type, same volume, no powder pillows added.

6

Remove reagent cell, insert blank, press ZERO

Swap to blank cell, install cap, press ZERO to set baseline.

7

Remove blank, insert reagent cell, press READ

Swap back to reagent cell, install cap, press READ. Display shows mg/L Br₂ in the HR range.

Interferences — Complete Reference

The following interference levels apply to both LR and HR procedures unless specifically noted. Interference testing was conducted at approximately 3 mg/L Br₂ sample concentration.

InterferentTolerance LevelEffect / Treatment
Chlorine (Cl₂)Responds equally to bromineThe DPD method does not distinguish between chlorine and bromine. Results reflect TOTAL halogen (Cl₂ + Br₂). If both are present, result includes both. No correction without independent chlorine measurement.
MonochloramineResponds at <5% of free Cl₂ rateLow interference under typical conditions. Can affect results when chloramine concentrations are high relative to free bromine.
pH4–8 optimalAccuracy decreases significantly outside this range. Adjust sample pH to 6–7 using dilute H₂SO₄ or NaOH if pH is outside tolerance.
HardnessUp to 1,000 mg/L CaCO₃No significant interference at typical cooling tower or pool hardness levels.
Iron (Fe)Up to 2 mg/LAt concentrations above 2 mg/L, iron may cause a positive interference. Pre-filter through 0.45-micron membrane if iron is a concern.
Manganese (Mn)Up to 0.1 mg/LManganese above 0.1 mg/L causes positive interference. Treat or dilute samples with high manganese.
TurbidityMust be minimalTurbid samples scatter light and produce falsely high readings. Filter through 0.45-micron before testing if turbidity is visible.
Temperature15–25°C for best accuracyDPD color development rate is temperature-dependent. Allow hot samples (from hot tubs or industrial processes) to cool toward ambient before testing.
Oxidizing agentsMay cause positive interferenceOzone, chlorine dioxide, and other oxidizing biocides react with DPD. Results reflect total oxidant equivalents, not bromine alone.
Reducing agentsMay cause negative interferenceStrong reducing agents (sulfite, thiosulfate) consume bromine before measurement. Test immediately after sampling; do not add dechlorinating agents to bromine samples.

Accuracy Verification — Standard Additions Method

LR Standard Additions

Items required: Chlorine Standard Solution 25–30 mg/L, 2-mL PourRite® Ampule (Item 2630020); Ampule breaker; TenSette® Pipet 0.1–1.0 mL (Item 1970001) with tips; three 10-mL portions of fresh sample.

1

Add 0.1 mL, 0.2 mL, and 0.3 mL of standard to three 10-mL portions

Prepare three spiked samples using fresh, unread sample water. Mix each well before testing.

2

Run the full LR Powder Pillow procedure on each spiked sample

Test smallest spike first. Record results for all three.

3

Calculate expected Br₂ increase

Expected Cl₂ increase per 0.1 mL spike = label concentration × 0.1 mL ÷ 10 mL sample. Multiply by 2.25 to get expected Br₂ increase. Results within ±10% of expected indicate acceptable performance.

AccuVac® Standard Addition (LR only): Add 0.3 mL, 0.6 mL, and 0.9 mL of standard to three 30-mL portions of fresh sample. Larger volumes reflect the AccuVac® 30 mL self-fill volume.

HR Standard Additions

Items required: Same chlorine standard solution; TenSette® Pipet; three 5-mL portions of fresh sample (HR uses 5 mL, not 10 mL).

1

Add 0.1 mL, 0.2 mL, and 0.3 mL to three 5-mL portions

HR uses half the sample volume of LR, which doubles the spike concentration per unit volume.

2

Run full HR procedure on each spiked sample

Test smallest spike first. Two powder pillows per test, 1 cm square cell, 5 mL volume.

3

Calculate expected Br₂ increase

Expected Cl₂ increase = label concentration × 0.1 mL ÷ 5 mL sample. Multiply by 2.25 for expected Br₂ increase. Compare measured increase to expected within ±10%.

SCA (Standard Calibration Adjust) — Bromine Ranges

ConfigurationRequired SCA Standard RangeNotes
LR2.00–4.00 mg/L Br₂If using chlorine standard: Cl₂ mg/L × 2.25 must fall within this range
HR2.0–8.0 mg/L Br₂If using chlorine standard: Cl₂ mg/L × 2.25 must fall within this range

Reagents, Apparatus & Replacement Parts

Required Reagents

ReagentLRHRHach Item No.
DPD Total Chlorine Reagent Powder Pillow, 10-mL1 per test2 per test2105569
DPD Total Chlorine AccuVac® Ampul1 per testNot available2502025
DPD Total Chlorine Powder Pillow, 25-mL2105669 (alt)

Required Apparatus

ItemLRHRHach Item No.
Sample cell, 25 mm round glass (10 mL)2427606
Sample cell, 1 cm square (5 mL)2427700 (verify)
AccuVac® adapterLR onlyIncluded with LR kit
TenSette® Pipet 0.1–1.0 mL1970001
TenSette® Pipet tips (50/pk)2185696
Chlorine Standard, 25–30 mg/L, 2-mL PourRite®2630020

Instrument Replacement Parts

PartItem No.
DR300 Instrument capLPV445.97.08100
Sample cell cap (for 25 mm cell)LPV445.97.08200
AccuVac® adapterLPV445.97.08300
Batteries, AAA (4-pack)Standard AAA alkaline
Sample cell brush1889640
Cleaning solution for sample cellsLPV445.97.08500

Error Codes — Full Reference

Error codes are shared across the DR300 platform. See the DR300 Chlorine Reference for the complete E-00 through E-66 error code table and recovery procedures. Bromine-specific note: E-03 (SCA out of range) on the bromine model means the standard used for SCA does not fall within the required Br₂ range (2.00–4.00 mg/L LR or 2.0–8.0 mg/L HR). Verify your chlorine standard concentration and apply the 2.25× conversion factor before re-attempting SCA.

Quick Reference Summary

ParameterLR ValueHR Value
Range0.05–4.50 mg/L Br₂0.2–10.0 mg/L Br₂
MethodDPD Method 8016
Sample volume10 mL5 mL
Powder pillows12
Cell type25 mm round glass1 cm square
AccuVac® optionYes (Item 2502025)No
Color developedPink (intensity proportional to Br₂)
Over-range indicatorYellow color in sample — dilute and retest
Cl₂ conversionCl₂ mg/L × 2.25 = Br₂ mg/L
SCA standard range2.00–4.00 mg/L Br₂2.0–8.0 mg/L Br₂
Precision2.25 ± 0.11 mg/L11.3 ± 0.5 mg/L
Hach DR300 Pocket Colorimeter — Bromine
DPD Method 8016 • LR: 0.05–4.50 mg/L • HR: 0.2–10.0 mg/L • IP67 waterproof. Reagents sold separately.
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