Hach DR300 Iron FerroVer® Pocket Colorimeter: Complete Review & Reference (2026)

Sources: Hach DR300 User Manual DOC022.97.90639 Edition 5 (09/2021) • Hach Method DOC316.53.01458 Edition 2 (12/2018)

Part No. LPV445.97.22110 (Americas) • USEPA FerroVer® Method 8008 • 0.02–5.00 mg/L Fe • IP67 Waterproof

Hach DR300 Iron FerroVer pocket colorimeter LCD showing Iron-Ferro Ver mg/L Fe 0.00 Water treatment operator using Hach DR300 Iron FerroVer pocket colorimeter at an industrial pump station
Hach DR300 Iron FerroVer® — LPV445.97.22110
USEPA Method 8008 • 0.02–5.00 mg/L Fe • IP67 waterproof • Bluetooth® Claros. Reagents (Item 2105769 Powder Pillow or Item 2507025 AccuVac®) sold separately.
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Part Number
LPV445.97.22110
Parameter
Total Iron (Fe)
Range
0.02–5.00 mg/L Fe (single range)
Method
USEPA FerroVer® Method 8008
Reaction Time
3 minutes (mandatory)
Read Window
Within 5 min after reaction
Sample Cell
25 mm GLASS only (Item 2427606)
IP Rating
IP67 Waterproof
Battery Life
~5,000 tests (4× AAA)
Precision
1.00 ± 0.2 mg/L Fe (95% CI)

What the DR300 Iron FerroVer® Measures & Who Uses It

The Hach DR300 LPV445.97.22110 is a single-parameter portable photometer factory-configured for Total Iron measurement using FerroVer® reagent chemistry — USEPA approved Method 8008. Unlike the chlorine DR300 which has LR and HR switching, the iron model operates on a single range (0.02–5.00 mg/L Fe) and uses only 25 mm glass sample cells throughout. The 0.02 mg/L lower limit is well below the EPA secondary maximum contaminant level for iron (0.3 mg/L) and sensitive enough for virtually all drinking water, wastewater, industrial, and environmental applications.

ApplicationWhy Iron Measurement Matters
Drinking water treatmentIron causes taste, odor, and staining above 0.3 mg/L (EPA secondary standard); monitoring ensures compliance and prevents customer complaints
Well water and groundwaterNaturally occurring iron is common; test results guide iron filter selection, sizing, and system performance verification
Wastewater effluentUSEPA-approved method supports regulatory compliance reporting for iron in discharge permits (Federal Register, June 27, 1980)
Industrial cooling towers & boilersIron indicates corrosion; monitoring guides corrosion inhibitor dosing and system maintenance scheduling
Food and beverageProcess water iron affects product taste; boiler feed water iron causes scaling in heat exchangers
Mining and acid mine drainageHigh-iron drainage monitoring; dilution technique handles concentrations above 5.00 mg/L
Seawater analysisMethod scope explicitly includes seawater; digestion required for total iron

How FerroVer® Chemistry Works

FerroVer® reagent performs two simultaneous functions when added to a water sample:

Step 1 — Reduction

Converts all soluble iron AND most insoluble iron forms (oxides, rust particles) to soluble ferrous iron (Fe²+). Without this step, only dissolved iron would be detected.

Step 2 — Color Development

Fe²+ reacts with the 1,10-phenanthroline indicator to form an orange complex. Intensity is directly proportional to iron concentration. The DR300’s LED measures absorbance and converts to mg/L Fe.

What You Want to MeasureSample Preparation
Total iron (all forms including oxides and rust)Digest unfiltered sample with heat and acid; adjust pH to 3–5 with 5 N NaOH before testing
Dissolved iron only (soluble forms)Filter sample through 0.45-micron membrane immediately after collection, before acidification; no digestion required
Digestion is required for Total Iron. Samples containing iron oxide, rust particles, or suspended iron will give incomplete (low) results without digestion. Mild or vigorous digestion options are available — refer to the Hach Water Analysis Guide. After digestion, adjust pH to 3–5 with 5 N sodium hydroxide solution before testing.

The Critical Timing Window — Most Common Error Source

FerroVer® Reaction Timeline — From Reagent Addition
0:00
Add FerroVer® reagent to sample cell. Swirl to mix. Start 3-minute timer.
0:00–2:59
Color developing. Do NOT zero or read during this window.
3:00
Timer expires — zero the instrument with blank now.
3:00–8:00
Read window — insert sample and press Read within this 5-minute window.
After 8:00
Color may begin to fade or change. Results outside this window may be inaccurate.

Technical Specifications

SpecificationDetail
Product numberLPV445.97.22110 (Americas) • LPV445.99.22110 (EU — includes reagents)
ParameterTotal Iron (Fe) — all soluble iron and most insoluble forms via FerroVer®
Measurement range0.02–5.00 mg/L Fe (single range — no LR/HR switching)
MethodUSEPA FerroVer® Method 8008 (DOC316.53.01458); regulatory status: Federal Register June 27, 1980
Method precision1.00 ± 0.2 mg/L Fe at 95% confidence interval (laboratory conditions)
Sample cell25 mm (10 mL) GLASS round cell ONLY (Item 2427606) — no plastic cells for this model
IP ratingIP67 — waterproof at 1 m for 30 minutes (battery compartment closed and locked)
Light sourceLED, fixed wavelength ±2 nm, factory-calibrated for FerroVer® iron method
DetectorSilicon photodiode • Filter bandwidth: 15 nm
Absorbance range0 to 2.5 Abs (E-15 error above 3.5 Abs)
Power4 × AAA alkaline batteries — NO rechargeable batteries • ~5,000 tests
Data storageLast 50 measurements with time stamp; auto-overwrites oldest
Bluetooth®Via optional Hach Communication Dongle (LPV446.99.00012) — enables Claros® connectivity
Operating temperature0–50°C (32–122°F); 0–90% RH non-condensing
Dimensions6.9 × 15.7 × 3.4 cm • Weight: 0.25 kg
Warranty1 year Americas / 2 years EU

Procedure A — Powder Pillow Method (15 Steps)

The standard field and laboratory procedure. Requires two 25 mm glass cells: one for the blank and one for the reacted sample.

Safety first: Review SDS for all chemicals before use. Wear gloves and eye protection. Dispose of reacted solutions per local regulations. Never pour sample directly into the cell holder.
1

Set instrument to Iron parameter

Push the Range key (up arrow, top-left). The display confirms the Iron (Fe) parameter is active.

2

Prepare the sample cell

Rinse a 25 mm glass sample cell and cap three times with the sample water. Fill to the 10-mL mark with sample. This cell will receive the reagent.

3

Add FerroVer® reagent

Add the entire contents of one FerroVer® Iron Reagent Powder Pillow (Item 2105769, 10-mL size) to the sample cell.

4

Swirl to mix

Swirl the sample cell to dissolve the powder completely. Undissolved powder affects results.

5

Start 3-minute reaction timer — mandatory

Set and start a timer for exactly 3 minutes. The orange color develops during this window. Do not zero or read before the timer expires.

6

Prepare the blank (while sample reacts)

Rinse a second 25 mm glass sample cell and cap three times with the same source water. Fill to the 10-mL mark. Close the cap. No reagent is added to the blank.

7

Clean the blank cell (at 3:00)

When the timer expires, wipe the exterior of the blank cell with a lint-free cloth. Remove all fingerprints, liquid drops, and residue from the optical surface.

8

Insert blank into cell holder

Place the blank in the cell holder with the diamond orientation mark pointing toward the keypad.

9

Install the instrument cap — critical

Place the cap fully over the cell holder. Must be completely seated before pressing Zero. This is the most common cause of E-01 errors.

10

Zero the instrument

Press Zero. Display shows “––––” then “0.00”. Instrument is zeroed against the blank.

11

Remove blank

Remove the blank sample cell from the holder.

12

Clean the reacted sample cell

Wipe all exterior surfaces of the reacted sample cell with a lint-free cloth. Any residue on the optical path affects the reading.

13

Insert sample within 5 minutes of timer expiry

Place the reacted sample in the cell holder, diamond mark toward the keypad. You have 5 minutes from the 3:00 mark (total window: 3:00–8:00). Results become less accurate after 8 minutes.

14

Install the cap again

Place the instrument cap fully over the cell holder before pressing Read.

15

Press Read — record result

Press Read. Result displays in mg/L Fe and is automatically stored with a time stamp. If the value flashes, it is outside the 0.02–5.00 range — dilute and retest if high.

Procedure B — AccuVac® Ampul Method (15 Steps)

The AccuVac® is a vacuum-sealed pre-filled reagent ampul. When the tip is snapped and submerged, the vacuum draws exactly the correct sample volume automatically — no pipetting or volume measurement required. The ampul serves directly as the sample cuvette for the Read step.

FeaturePowder PillowAccuVac® Ampul
Sample volume measurementOperator fills to 10-mL markAutomatic — vacuum draws exact volume
Reagent additionOpen pillow and pour into cellPre-loaded; no dispensing
Cells needed2 glass cells (blank + sample)1 glass cell (blank) + AccuVac ampul
Best forLab and controlled field conditionsField use in wind, rain; reduces spill risk
Cost per testLowerHigher (pre-filled ampuls)
1

Set instrument to Iron

Push the Range key (top-left).

2

Collect sample in beaker

Pour at least 40 mL of sample into a 50-mL beaker (Item 50041H). The AccuVac fills by vacuum — enough volume must be present to fully submerge the tip.

3

Fill the AccuVac® ampul — keep tip submerged

Snap the ampul tip. Keep the tip fully submerged in the sample until the ampul is completely filled. Lifting the tip prematurely introduces air and voids the vacuum fill.

4

Mix

Invert the AccuVac ampul several times to mix the sample with the pre-loaded reagent inside.

5

Start 3-minute reaction timer

Same mandatory timing as Powder Pillow method.

6

Prepare the blank

Rinse a 25 mm glass cell and cap three times with sample. Fill to 10-mL mark. No reagent added.

7–10

Zero with blank (at timer expiry)

Clean blank cell exterior → insert with diamond mark toward keypad → install cap → press Zero (same as Powder Pillow Steps 7–10).

11

Remove blank

Remove the blank cell from the holder.

12

Clean the AccuVac® ampul exterior

Within 5 minutes of timer expiry: wipe all exterior surfaces of the AccuVac ampul with a lint-free cloth.

13

Insert AccuVac® ampul into 25 mm holder

The round-bottom AccuVac ampul fits directly into the 25 mm cell holder.

14

Install cap

Place cap fully over cell holder.

15

Press Read

Result displays in mg/L Fe and is stored automatically.

Interferences — Complete Reference

InterferenceEffectPre-Treatment
TurbidityScatters light independently of iron color — produces falsely high readingsPre-treat blank with 0.1 g RoVer® Rust Remover (Item 30001); swirl to dissolve before zeroing. Or filter through 0.45-micron membrane (Item 253000). Apply same treatment to both blank and sample.
Color (sample has inherent color)Absorbs at the measurement wavelength — biases resultsPrepare reagent blank: measure the reagent blank absorbance by adding FerroVer® to deionized water and reading against a deionized water blank; subtract the reagent blank value from all sample results.
Phosphate >1 mg/L (as PO₄³−)Interferes by precipitating ironReduce phosphate concentration by dilution or alternative method; or use standard addition method to verify results.
Strong oxidizing agents (e.g., chlorine)Oxidize Fe²+ back to Fe³+ during reaction, preventing color development — gives falsely low resultsAdd sodium thiosulfate to quench residual oxidants before testing. Confirm by standard additions.
High chromium or copper concentrationsMay interfere at very high concentrationsDilute sample; verify by standard additions method.
Bismuth, cadmium, mercury, molybdate, silver (each >10 mg/L)Various interference mechanisms at high concentrationsThese concentrations are rare in environmental and potable water; standard additions verification recommended if suspected.
Condensation on cold samplesWater droplets on cell exterior scatter lightWipe cell exterior with lint-free cloth immediately before insertion.

Iron-Specific Field Diagnostics

SymptomLikely CauseSolution
Result consistently low vs. expectedReaction timer not complete when zeroing; color underdevelopedEnsure full 3-minute reaction before zeroing; zero only after timer expires
Result above 5.00 mg/L (E-04 flashing)Sample iron exceeds rangeDilute with deionized water (e.g., 1:5); multiply result by dilution factor
Results vary between replicatesInconsistent cell orientation; fingerprints; bubbles in cellOrient diamond mark consistently toward keypad; wipe thoroughly; invert cell before insertion to remove bubbles
Result near zero for sample known to contain ironIron present as oxide/rust; no digestion performedDigest sample with heat and acid; adjust pH to 3–5; retest
Orange color in blank (won’t zero at 0.00)Iron contamination in rinse water or blank waterUse reagent-grade deionized water for blank; measure and subtract reagent blank value
High or erratic results in turbid sampleTurbidity scattering — not iron colorPre-treat with RoVer® Rust Remover or filter through 0.45-micron membrane
Reading drifts or drops after ReadSample read after the 8-minute windowRepeat test and read within 3–8 minutes from reagent addition

Error Code Reference

CodeNameCauseSolution
E-00No ZeroSample measured before zeroingMeasure blank to zero first
E-01Ambient lightInstrument cap not fully installedSeat cap fully; re-zero
E-02LED errorLED unstable or insufficient outputReplace all 4 batteries; contact Hach if persists
E-03SCA errorStandard outside SCA adjustment limitsPrepare fresh standard; verify concentration
E-04 (flashing)Out of rangeValue above 5.00 or below 0.02 mg/LHigh: dilute and retest. Low: check cap; re-zero.
E-06Absorbance errorAbsorbance incorrect in user calibration; fewer than 2 pointsRe-enter data; ensure minimum 2 data pairs
E-07Duplicate standardDuplicate concentration in user calibrationEnter unique concentrations for each point
E-09Flash errorCannot save to memoryHold Power 5 sec to reset; contact Hach if persists
E-10Temperature rangeAmbient temp outside 0–50°CMove to within operating temperature range
E-12Low batteryBattery power insufficientReplace all 4 AAA alkaline batteries immediately
E-13Parameter load failureMemory defectiveContact Hach technical support
E-14Zero invalidCell empty or improperly filledFill cell completely; retry
E-15Absorbance too highAbsorbance above 3.5 AbsDilute sample; check for light blockage
E-20Signal out of rangeExcessive ambient lightEnsure cap fully installed; repeat test
E-21Signal unstableFluctuating ambient lightShield from light sources; repeat test
E-22Hardware errorElectronic system defectiveContact Hach technical support

Reagents, Parts & Accessories

DescriptionQty/TestPackItem No.
FerroVer® Iron Reagent Powder Pillows, 10-mL1100/pkg2105769
FerroVer® Iron Reagent AccuVac® Ampuls125/pkg2507025
Sample cells, 25 mm (10 mL) round glass — LR and ALL iron tests2 (PP) / 1 (AV)6/pkg2427606
Beaker, 50 mL (AccuVac® method)1each50041H
Stopper for 18-mm tubes and AccuVac® Ampuls26/pkg173106
AccuVac® Ampul Snappereach2405200
RoVer® Rust Remover (turbid sample pre-treatment)454 g30001
AAA alkaline batteries4/pkg4674300
Instrument cap (cell holder cover)1LPZ445.99.00006
Battery cover1LPZ445.99.00007
Hach Communication Dongle (Bluetooth® / Claros®)1LPV446.99.00012
Soft-sided carrying case / holster15953100
Reagents are NOT included with the Americas version (LPV445.97.22110). The EU/International version (LPV445.99.22110) includes reagents.

Verification Standards

DescriptionPackItem No.
Iron Standard Solution, PourRite™ Ampules, 50 mg/L, 2 mL20/pkg1425420
Iron Standard Solution, 100 mg/L Fe100 mL1417542
Metals Drinking Water Standard, LR (Cu, Fe, Mn)500 mL2833749
Metals Drinking Water Standard, HR (Cu, Fe, Mn)500 mL2833649
Water, deionized4 L27256
Hach DR300 Iron FerroVer® — LPV445.97.22110
USEPA Method 8008 • 0.02–5.00 mg/L Fe • Single range, 25 mm glass cells only • IP67 waterproof • Reagents sold separately (Item 2105769 Powder Pillow or 2507025 AccuVac®)
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Related Pages

Other DR300 Parameter References