Category: Boom Sprayers

Main category for sprayers with horizontal booms

  • Cleaning Your Sprayer

    Cleaning Your Sprayer

    We all know the importance of cleaning out a sprayer. It protects a sensitive crop. It protects people working with the sprayer. It protects the sprayer and its components. But cleaning the sprayer is a pain. Here are some tips to make it easier.

    Some herbicide label instructions are cumbersome, requiring many flushes with full tanks of water. Many applicators look for shortcuts and hope they get away with it. It doesn’t have to be guesswork. The following is a checklist that may help.

    Be Prepared

    A few supplies can help ensure a clean sprayer tank.

    • A defoaming agent saves water and time
    • A cleaning agent (commercial products, or simple household ammonia) is useful, and recommended, for Group 2 products except the imidazolinones.
    • A supply of clean water, preferably with its own pump, and a pressurized spray hose helps clean the sprayer inside and out.
    • A wash-down nozzle (whose flow requirements can be met by the clean water pump) can automate the tank wash-down.
    • A bucket and brush for rinsing screens is very useful.

    Products to Watch:

    The products most frequently implicated in sprayer contamination are two members of the Group 2 modes of action: the sulfonyl ureas (e.g., thifensulfuron (Refine) and tribenuron (Express)), and the triazolopyrimidines (e.g., florasulam (Frontline, PrePass) and pyroxsulam (Simplicity)). Since these herbicides dissolve better at higher pH, proper cleanout usually requires ammonia, a weak base that raises the solution pH. The third member of Group 2 products, the imidazolinones (imazethapyr (Pursuit), imazamox (Solo, Odyssey), imazamethabenz (Assert), imazamox (Ares,  Adrenalin, Altitude or Viper)), tend not be implicated in as many residue issues, and don’t require ammonia for cleanout.

    Be Prompt and Thorough

    Remove pesticide from mixing and spray equipment immediately after spraying – it makes the job easier. The main areas of concern are the tank wall, sump, plumbing (including boom ends), and filters. First, spray the tank completely empty while still in the field. It’s sometimes OK to cover previously sprayed areas – all herbicides must be crop-safe at twice the label rate to be registered by the PMRA. Take care with residual products that may create problems down the road. Reduce the rate or choose a fallow field to be certain. Second, add 10 x the sump’s remnant of clean water, circulate, ensuring agitation is on, and spray it out in the field as well. Repeat. These two rinsing steps will take care of the majority of the cleaning and won’t take very long. The less remaining volume there is in your tank after the pump draws air, the less water is needed to dilute this remainder to an acceptable concentration. Having a clean water tank on the sprayer and a wash-down nozzle makes this job easier.

    Visual Inspection

    Herbicide residue may precipitate out of solution in some parts of the sprayer or plumbing. A thorough visual inspection can identify these problem areas and ensure that they are cleaned properly.

    Tank Wall

    Removal of residues from tank walls is best accomplished with a direct, pressurized spray. Make sure all parts of the wall have been in contact with clean water. Use a wash-down nozzle if it provides complete and vigorous coverage of the interior tank surface.

    Sump

    Empty the sump as completely as possible by spraying it out. Any spray liquid or herbicide concentrate remaining in the sump area will be re-circulated in the sprayer. The only way to remove any remaining herbicide is through dilution by repeatedly adding water, and leaving as small a remainder as possible.

    Plumbing and Boom

    Plumbing can be a significant reservoir of herbicide residue. Removal from plumbing can be achieved by pumping clean water through the boom while ensuring that all return and agitation lines also receive clean water and all residue is flushed out. This may require opening and closing various valves several times, and repeating the process with new batches of clean water. Boom ends can extend up to 6” beyond the last nozzle at each end of each boom section. These ends must be flushed to removed trapped residue. A useful product that does this automatically is the Pentair Hypro Express Nozzle Body End Cap, or better yet, consider recirculating booms.

    Dilution

    The most effective use of a volume of rinse water is to divide it equally across several repeat washes. Assuming a 10 gallon sump remainder, three washes with 30 gal each are as effective as two washes with 70 gallons each, and equal a single 600 gal wash.

    It’s even more efficient to use a separate clean water pump, introducing clean water as the rinsate is sprayed out. This saves water and time, and results in even more dilution.

    Filters

    Nozzle screens and in-line filters can be a significant reservoir for undiluted or undissolved herbicide and are one of the most overlooked parts of sprayer decontamination. Remove all filters and nozzle screens and thoroughly clean these with fresh water. Run clean water through plumbing leading to the screens.

    Nozzle Bodies

    Nozzle bodies can harbour herbicide mixture. When cleaning a spray boom, rotate through all nozzles in a multiple body to ensure clean water reaches all parts of these assemblies. Remove screens that may have been used with herbicide.

    Tank Cleaning Adjuvants

    Adjuvants such as ammonia can assist the tank decontamination process, especially with sulfonyl urea and triazolopyrimidine-containing products. Ammonia does not neutralize herbicides, but it does raise the pH of the cleaning solution which helps sulfonyl urea herbicides dissolve. When decontaminating after an oily (EC) formulation, the use of a wetting agent such as AgSurf will assist in removing oily residue that may trap SU herbicide on tank and hose material. Commercial tank cleaning products that contain ingredients for removing persistent deposits are available.

    Tank and Boom Material

    Both plastic and stainless steel are common tank and wet boom materials, and both can be cleaned using the above procedures.  However, stainless steel is easier to clean, and this means that less time may be required. Consider the choice of materials a productivity factor in your next purchase or upgrade decision.

    Rinsate Disposal

    Always spray out the tank in the field. Do not drain the tank while stationary unless you are certain it is free of pesticide and that you are away from sensitive areas and waterways. Consider a continuous rinse system. Consider building a biobed for safe disposal of dilute pesticide waste.

    Sprayer cleanout will probably never be the easiest job on the farm. But looking at it in a smarter way can prevent frustration and save time.

  • Angled Spray Nozzles in Wheat

    Angled Spray Nozzles in Wheat

    When T3 wheat rears its head, the first rainy day brings questions about spray angles. Let’s begin with a graphic that illustrates how angled sprays cover a vertical target like a wheat head. Assuming moderate wind and sufficiently large droplets, this is a simplified depiction of what we would expect to see.

    But is this how the nozzles actually perform? Are dual angles really better than a single fan with an aggressive angle? We hoped to answer these questions when we demonstrated a selection of dual fan nozzles at Canada’s Outdoor Farm Show in 2013. But it was a very windy few days and what we saw was that regardless of the nozzle, most of the spray tended to deposit with the wind.

    A 10 km/h wind will easily deflect Medium-and-smaller droplets and at 20 km/h all but the coarsest spray is deflected. This leads to non-uniform deposits and unacceptable levels of drift (yes, even through it’s a fungicide and you have lots of acreage.) To learn more, we turned to the literature to review studies performed in Ontario and Saskatchewan.

    Wolf and Caldwell

    In 2002, Dr. Tom Wolf and Brian Caldwell experimented with fan angles. They evaluated the impact of nozzle angle, travel speed, and droplet size on the “front” (facing the sprayer’s advance) and “back” (sprayer’s retreat) of vertical targets. They ran three laboratory experiments: spray configuration (single vs. double fan), travel speed (7.6 and 15.2 km/h) and spray quality (conventional versus air-induced droplets) using TeeJet XR’s and Billericay air bubbles at a rate of 175 L/ha. Here’s what they observed:

    • Larger, air-induced droplets produced higher average deposits than smaller, conventional droplets.
    • Twin fans improved overall average deposit compared to single fans.
    • Building on the first two points, twin air-induction fans improved overall average deposit versus conventional twin fans, and also improved deposit uniformity (i.e. coverage on the front versus the back of the vertical targets).
    • Higher travel speeds improved overall average deposit, but at the cost of reduced uniformity as the rear-facing target received reduced coverage (particularly in the case of conventional droplets).
    • Spray angle did not impact coverage from conventional tips, but increasing from 30 to 60 degrees improved coverage for AI tips.

    While the coverage data was compelling, growers were not reporting improved efficacy with the improved coverage. The authors felt there were confounding variables like crop susceptibility, disease pressure and product effectiveness. Their conclusion was that applicators should strive for improved coverage, but only after integrated pest management (IPM) criteria such as product choice, crop staging and application timing are satisfied.

    Hooker and Spieser

    In 2004, Dr. David Hooker (University of Guelph) and Helmut Spieser (OMAFRA) started exploring nozzle configuration and sprayer set-ups to optimize Folicur applications in wheat. For several years they ran field trials exploring panoramic wheat head coverage. That is, not only the front and back of the wheat head, but the sides as well. Ten different nozzle configurations were used:

    • TurboTeeJets mounted in dual swivel bodies (backwards and forwards)
    • AirMix air induction nozzles mounted in dual swivel bodies
    • Air induced Turbo TeeJets mounted in dual swivel bodies
    • Single Turbo TeeJets angled forward or angled backwards
    • Single Turbo FloodJets angled forward or angled backwards
    • TwinJets
    • Single Hollow cones
    • Turbo TeeJet’s mounted in Twincaps
    • Turbo TeeJet Duos
    • Single Turbo FloodJets alternating forward and backwards

    They explored boom height (0.5 m and 0.8 m above the crop), travel speed (10 km/h and 20 km/h) and application volume (93.5 L/ha and 187 L/ha). Here is a summary of their findings:

    • Travel speed did not appear to impact overall coverage.
    • Spraying higher volumes improved coverage.
    • Lowering the boom improved coverage.
    • Coverage from conventional flat fans and TwinJets gave ~15-18% coverage and 22-26 mg of copper was deposited per m2, but alternating Turbo FloodJets gave ~29% coverage and deposited ~37 mg copper per m2.
    • The highest percent coverage was obtained using Turbo TeeJets or the AirMix tips mounted in dual swivels (~26% coverage), or single Turbo Floodjets alternating forward and backwards (34% coverage) as long as the spray was not obstructed by the boom structure itself.

    Hooker and Schaafsma

    A few years later, Dr. Hooker and Dr. Art Schaafsma worked with OMAFRA to explore efficacy. DON is a mycotoxin that may be produced in wheat infected by Fusarium Head Blight (FHB) or scab. There is an indirect relationship between wheat head coverage of fungicide and the reduction of FHB and DON: The higher and more uniform the coverage (with the right timing) the lower FHB and DON.

    In two field experiments they performed in 2008, DON values in the untreated checks were around four parts per million. DON was reduced by an average of 22.5% using a single flat fan, 23.0% using a TwinJet and 41.5% using alternating Turbo FloodJets when averaged across two fields, two fungicides and four reps (n=16). They all reduced DON significantly. There was no statistical difference between singles and twins, but control from the alternating Turbo FloodJets was significantly better.

    The Return of Wolf and Caldwell

    Then, in 2012, Tom and Brian evaluated the new asymmetrical twin fan nozzles from TeeJet. The marketing claimed they could improve overall coverage at higher travel speeds because they decrease the contribution of the front-facing fan and increased the angle of the back. Tom and Brian’s lab-based experiments determined that:

    • Asymmetricals increased overall deposit amounts and uniformity versus single fan and symmetrical twin fans.
    • Nozzle orientation (alternating or not) seemed unimportant.
    • As suggested earlier, boom height was a big factor in coverage. Nozzle angle didn’t improve coverage when the boom was too high, but spray deposit increased significantly when the boom was lowered.
    • Coarser spray droplets have more momentum, so they can travel greater distances on their original vector. A coarser spray quality is the best choice for any angled fan.

    Water volumes and FHB

    Let’s address the notion that high water volumes might increase Fusarium Head Blight (FHB). This is a hypothesis that seems to have resonated with growers. Dr. David Hooker ran trials where he tried to favour FHB by spraying 40-50 gpa of water multiple times per day (even up to 100 gpa). There was no pathological impact (personal communication).

    Consider that 1″ of rain is the equivalent of 2,715 gpa of water. Raising your carrier volume from 15 gpa to 20 gpa is the equivalent of 0.000184″ of rain. Admittedly, it’s all aimed at the wheat head, but it’s still a tremendously small volume. While studies have shown a diminishing return in coverage at 30 or 40 gpa, spraying with 20 gpa appears to be a safe way to improve coverage significantly.

    Learn more about early morning spraying here, and a more in depth discussion of spraying when there is dew here.

    PWM

    What if you’re running a PWM system? Sizing for PWM requires the tip be sized about 20-40% more than if you were running a conventional sprayer. In other words, at expected travel speeds, the pulsing duty cycle should be approximately 60-80%. Nozzles that are permitted on PWM sprayers are limited and the angled fan selection for PWM is, at the time of writing, more so. It requires some experimenting. The following list uses the JD Exact Apply as an example system, and it is not exhaustive. We’re always looking for new ideas.

    1. 3D90 (the original 3D is arguably too misty) in the A or B positions, alternating front and back <or> in both A and B positions. This tip may not be readily available in North America.
    2. LDT (Low Drift Twin) which is two LD tips installed in a Twincap (twin 30° angles) in position A or B.
    3. LDM (Low Drift Max) which is two LDM installed in a Twincap in position A or B. This tip only goes down to an 03.
    4. The Deere 40 degree angled adaptor (developed for See and Spray) can be used to convert any PWM-compatible nozzle into an angled spray.
    5. GAT (GuardianAir Twin) is an air-induced tip, running in conventional “A” mode or in Auto Mode but sized for “B”. Avoid operating in A and B to prevent pattern interference.
    6. Wilger Wye Adaptor with SR nozzles. This does cause tips to drop below the boom frame but is a versatile option.
    7. Wilger Dual Angle Max. More compact than the wye adaptor, this asymmetrical assembly (30° fore and 50° aft) prioritizes Coarse spray.
    8. TeeJet Accupulse TwinJet.
    9. Greenleaf Blended Pulse Dual Fan Assembly.

    Summary

    So here’s what we can say based on all this research:

    • Higher volumes improve coverage (significantly up to ~200 L/ha or 20 gpa). Can you go to 30 gpa? Yes, and it will likely improve coverage, but it’s a diminishing return and at some point you will incur run-off.
    • When using angled sprays, coarser droplets improve vertical coverage. Compared to finer droplets, they move faster, survive longer (i.e. resist evaporation) and are less likely to be deflected by wind.
    • Maintaining the lowest operable boom height improves coverage from angled sprays. We want 100% overlap at target height, and with angled sprays that means getting pretty close. Aim for the highest wheat heads and not the tillers. If you’re 2′ away, you’re likely too high.
    • Symmetrical fans with shallow angles (e.g. 30°) improve coverage uniformity on vertical targets versus single fans, and a steeper backward-facing angle (e.g. 70°) improves coverage even more on the sprayer-retreat side.
    • Travel speed may or may not affect coverage, but slower speeds do facilitate lower booms, which do improve coverage.
    • Timing, weather and product choice are likely the most critical factors.

    Angled sprays may offer some advantage in other situations, but they are primarily intended for panoramic coverage of vertical targets.

    Short videos about dual fans

  • Tank mixing Urease and Nitrification Inhibitors in Corn Weed-and-Feed Applications

    Tank mixing Urease and Nitrification Inhibitors in Corn Weed-and-Feed Applications

    This 2023 article is based on work performed by Mike Schryver, BASF Technical Service Specialist.

    Nitrogen is an essential nutrient required throughout a plant’s lifecycle. It is commonly applied to corn in either a granular form as urea or in a liquid form as urea-ammonium nitrate (UAN). Depending on soil type and precipitation, significant amounts of nitrogen can be lost to leaching, denitrification and volatilization as N2O (a greenhouse gas). Learn more about nitrogen in soil in this excellent overview by University of Minnesota Extension.

    With the 2020 announcement of Canada’s Strengthened Climate Plan, Ontario is committed to a 30% reduction of 2020 N2O emission levels by 2030. Adding urease and nitrification inhibitors (aka stabilizers) to nitrogen fertilizer applications is an environmentally sustainable practice that reduces nitrogen losses and improves yield.

    Another essential plant nutrient, Sulphur, is applied in liquid-form as ammonium thiosulphate (ATS). Primarily used to increase corn yields, high rates (approx. >10% by volume) of ATS can also inhibit urease and nitrification, albeit not as well as other nitrogen stabilizing options.

    In the pursuit of productivity, UAN and ATS are often combined to serve as an herbicide carrier in corn weed-and-feed applications. However, liquid fertilizers are dense solutions that contain charged ions and exhibit a reduced capacity for solubilizing pesticides. This complicates the tank mixing process. When micronutrients like sulfur are added to nitrogen-based formulations, physical incompatibilities can arise that cause uneven applications and can even clog sprayers.

    Given the known compatibility issues, questions have been raised about the best way to introduce urease and nitrification inhibitors to tank mixes of UAN, ATS and herbicide. Specifically:

    1. Stabilizer Compatibility: What is the impact of adding nitrogen stabilizers to UAN carriers containing leading corn herbicides formulated as emulsifiable concentrates (EC) or suspension concentrates (SC)?
    2. Mixing Order: When UAN and ATS are premixed, does their ratio, or the addition of nitrogen stabilizer affect tank mix compatibility with herbicides?

    To answer these questions, we performed a series of jar tests.

    Method

    300 ml jars with magnetic stir bars were mixed to reflect a 10 gpa application. UAN was chilled to approx. -5°C and herbicides were added at 2x the labelled rate to simulate a worse-case scenario. Nitrogen stabilizer was added at a ratio per manufacturer’s instructions. Products were introduced at 1 minute intervals to provide sufficient time for solubilization. Jars were left to rest for at least 1 hour after mixing, and then agitated to simulate interrupted spray jobs. The solution was then poured through a 100 mesh screen to simulate a worst case scenario for sprayers that typical employ 50 mesh filters.

    HerbicidesFertilizer carriersStabilizers
    Leading EC HerbicideUAN: 28%eNtrench NXTGEN (Corteva)
    Leading SC HerbicideATS: 12-0-0-26% SUAnvol (Koch)
    Tribune (Koch)
    Agrotain (Koch)
    Neon Surface (NexusBioAg)
    SylLock plus (Sylvite)
    Excelis Maxx (Timac)
    Table 1 Herbicides, carriers and stabilizers used in the study

    Results

    Stabilizer Compatibility

    EC herbicides have active ingredients that are soluble in water and include immiscible solvents. When added at 2x label rate to chilled UAN, followed by a stabilizer, agitation created an acceptable suspension (Figure 1). The EC separated to the top of the mixture following an hour rest but was easily reintegrated. There was no appreciable residue left behind when poured through a 100 mesh screen.

    Figure 1 UAN + EC Herbicide + Stabilizer after 1 hour rest. Image A is a control with no stabilizer and image B is the same control after agitation. The arrow indicates where ECs separate at the top of each jar. All products resuspended with agitation.

    SC herbicides have active ingredients that are water insoluble, but stable in an aqueous environment. When added at 2x label rate to chilled UAN, followed by a stabilizer, agitation created an acceptable suspension (Figure 2). The SC flocculated and formed a sediment at the bottom of the mixture following an hour rest but was easily reintegrated. There was no appreciable residue left behind when poured through a 100 mesh screen.

    Figure 2 UAN + SC Herbicide + Stabilizer after 1 hour rest. Image A is control with no stabilizer and image B is the same control after agitation. The arrow indicates where SCs settled, as depicted in the inset images showing the bottoms of each jar. All products resuspended with agitation.

    Best Practices

    • Contact manufacturers and conduct a jar test to confirm compatibility
    • Ensure thorough agitation (with or without a stabilizer, and especially after tank has settled)
    • Components may separate to the top (ECs) or settle on the bottom (SCs)

    Mixing Order

    Mixing order was tested using chilled UAN, ATS, and EC herbicide. It is well known that ATS should be added last in the tank mix order, and mixes that include a higher load of ATS relative to UAN exacerbate tank mix issues.

    This is seen in the following video where we combine 203 ml of chilled UAN, 30 ml of SC corn herbicide and 68 ml of ATS. On the left, UAN, then herbicide, then ATS mixes perfectly. However, when we start with UAN, then add ATS (which represents premixed fertilizer) then the herbicide does not suspend, and prolonged agitation does not improve the situation. The video is shown at 2x speed.

    We then added a nitrogen stabilizer to the series to see if it could correct the tank mix issue arising from adding ATS immediately after UAN. This replicates the situation an operator would face when purchasing UAN and ATS premixed. We also reduced the ratio of UAN to ATS from 3:1, to 5:1 to 8:1 to establish a threshold ratio that alleviated tank mix issues (Figure 3). All solutions were poured through 100 mesh screens to capture residue (Figure 4).

    Figure 3 SC Herbicide and stabilizer added to UAN and ATS premixed at different ratios. Agitated after 1 hour and poured through 100 mesh screens (inset images).
    Figure 4 Pouring EC jar test solutions through 100 mesh screens

    Best Practices

    • Contact manufacturers and conduct a jar test to confirm compatibility
    • ATS must be added after the herbicide (EC or SC). The stabilizer can be added last, but preferably ATS is the last ingredient in the tank.
    • Adding stabilizer will not reverse a tank mix error arising from adding ATS prior to the herbicide.
    • The higher the concentration of ATS, the higher the risk of incompatibility. A 5:1 ratio of UAN to ATS failed while a ratio of 8:1 succeeded. The threshold is likely 7:1.
  • Spray Water pH

    Spray Water pH

    The scuttlebut on coffee row is that acidifying a spray mixture improves its efficacy. There are also claims that pesticides break down in the sprayer tank if the pH is too high.

    But it’s not that simple. Low pH has a strong impact on pesticide solubility, and that means mixing and cleanout are affected. Acidifying the mixture can have profound negative effects for many products.

    It’s important to know what you’re doing.

    What is pH?

    pH is defined as the negative log of the molar concentration of hydrogen ions in a water-based solution. The more abundant the hydrogen, the lower the pH. It’s a log scale, so every unit of pH refers to a 10-fold change in the concentration of hydrogen ions.

    Both very low (acidic) or very high (basic) pH can be caustic. But having a low or high pH doesn’t mean it will burn your skin or clothes right away, it might just be a bit unpleasant. But at the extreme ends, protection is needed.

    Why is pH Important in Spray Mixtures?

    In spraying, the main effect of pH is on the pesticide’s solubility. Solubility matters when mixing and becomes important during cleanout as well.

    A minor effect on pH, at least for herbicides, is on chemical breakdown, usually through hydrolysis, when the pH is too high. The effect on breakdown is rarely meaningful during any given spray day, but may play a role if a spray mix is stored overnight or longer.

    The Basics: Strong vs Weak Acids

    Strong acids like hydrochloric acid (HCl) ionize completely in solution. When added to water, only H+ and Cl– are present, there is no HCl. The water’s pH does not affect solubility of a strong acid.

    But weak acids do not completely ionize. The water pH affects the degree of ionization and therefore solubility.

    Most herbicides are weak acids. A weak acid is one that does not dissociate completely in solution. A typical example of a weak acid functional group is carboxylic acid (-COOH). In solution, compounds with a carboxylic moiety exist in an equilibrium, with some as -COOH (containing the hydrogen, also called “protonated”) and others as -COO– and H+. In the dissociated form, the acid is more water soluble than in its protonated form due to the negative charge that makes it ionic.

    Weak acids have a dissociation constant known as the pKa. When the solution is at the molecule’s pKa, the acid is 50% dissociated. When the solution has a lower pH than the pKa, there is less dissociation and the protonated forms of the molecule dominate. That has two important implications for herbicides.

    • the molecule becomes less water-soluble at lower pH
    • the molecule has fewer opportunities to interact with positively charged items

     pH Dependent Solubility

    Water-solubility is a two-edged sword. On the one hand, having a highly water soluble product makes it easier to dissolve in water. This pays dividends when mixing a batch or cleaning a sprayer because a product formulated as a solution will easily go into a true solution and will stay mixed. Examples are glyphosate, glufosinate, and salts of 2,4-D, MCPA, and dicamba.

    On the other hand, most pesticides need to enter a plant to reach their site of action. And a plant cell, with its waxy cuticle and oily membranes, creates an effective barrier for water, and for water-loving molecules dissolved in it. As a result, a formulation that allows the water-soluble product to interact with an oily barrier is needed.

    The products that can do this are surfactants. Acting like detergents, surfactants have regions in their structure that are oil-loving (lipophilic) and other regions that are water-loving (hydrophilic). Surfactants can therefore bind to both oil and water and provide a bridge for water-soluble products across oily barriers.

    That’s also one of the reason that the most water-soluble products such as glyphosate and glufosinate contain a lot of surfactants in their formulation, reducing the concentration of active ingredient in the jug and possibly leading to foaming with agitation.

    Pesticides have a wide range of solubilities, and for some, water pH will play an important role. Below is a table of some water solubilities of selected herbicides.

             Solubility (ppm)
    Trade NameActive IngredientMode of Action GrouppH ~ 5pH ~ 7pH ~ 9
    Selectclethodim1535,45058,900
    Ally 2metsulfuron25502,800313,000
    Expresstribenuron2482,04018,300
    Pinnaclethifensulfuron22232,2408,830
    Everestflucarbazone244,00044,00044,000
    Simplicitypyroxsulam21632,00013,700
    Frontlineflorasulam20.1694
    Varrothiencarbazone2172436417
    Raptorimazamox2116,000 >626,000>628,000
    Pursuitimazethapyr22,570 12,8707,500
    2,4-D2,4-D salt429,93444,55843,134
    dicambadicamba salt4>250,000>250,000>250,000
    Roundupglyphosate9>500,000>500,000>500,000
    Libertyglufosinate10>500,000>500,000>500,000
    Heatsaflufenacil14302,100 >5000
    Distinctdiflufenzopyr19635,90010,550
    Infinitypyrasulfatole274,20069,10049,000

    Compare the solubility at pH 7 to that at pH 5. For most of these herbicides, water solubility is worse at lower pH. That is because they are more protonated and become more lipophilic.

    I’ve placed a lot of Group 2 products in this table because those products are most often implicated in tank cleanout issues. All Group 2 products in this table, with the exception of Everest (flucarbazone-sodium) have lower solubility at pH 5 than they do at pH 7. For some, like pyroxsulam and floarsulam, it’s a big change. Those products, when acifified, are prime candidates for poor mixability and poor cleanout.

    When it comes to dicamba, low pH has another side-effect. It makes the molecule more volatile, increasing danger to sensitive plants nearby. For that reason, acidification of dicamba in its Xtendimax and Engenia formulations is not permitted.

    Note that the Group 4 examples, 2,4-D salt and dicamba salt, as well as glyphosate and glufosinate, are highly water-soluble and pH has very little effect on that.

    Particularly for glyphosate, the claim that it becomes more oily at low pH and will therefore be taken up more easily, is not supported by these data. Considering that the most acidic pKa for glyphosate (it has four acidic groups) is 0.8, pH would need to be much lower for any noticeable impact on oilyness.

    Tank Mixability

    Given today’s environment of herbicide resistance, applications with multiple mode of action tank mixes are very common. Acidifying a spray mix to benefit one herbicide may create problems for its tank mix partners.

    If there is a concern that spray water is too alkaline, it is recommended that the pH of the finished spray mix be measured. Since many herbicides are weak acids, they will lower the pH of the mixture by themselves. For example, the addition of glyphosate to water with pH 7.5 will drop the pH to about 5 or so, depending on the water’s buffering capacity.

    As a result, glyphosate tank mix partners that are pH sensitive may suffer in the presence of glyphosate, and pH may actually need to be raised.

    pH Dependent Half-life

    Herbicides

    There are a lot of claims that pesticides break down rapidly in alkaline spray water. And yet, in my career working primarily with herbicides, I do not recall this ever being a problem in practice.

    Below is a table of herbicides for which I could find half-life information, with the help of this comprehensive list produced by Michigan State University.

    ProductActive ingredientHalf Life
    AtrazineatrazineMore stable at high pH
    BanveldicambaStable at pH 5 – 6
    BromoxynilbromoxynilpH 5 = 34 d; pH 9 = 1.7 d
    Fusiladefluazifop-p-butylpH 4.5 = 455 d; pH 9 = 17 d
    Libertyglufosinate-ammoniumStable over wide range of pH
    GramoxoneparaquatNot stable at pH above 7
    ReglonediquatpH 5 = 178 d; pH 7 = 158 d; pH 9 = 34 d
    MCPAMCPApH 9 = < 5 days
    PoastsethoxydimStable at pH 4.0 to 10
    PrincepsimazinepH 4.5 = 20 d; pH 5 = 96 d; pH 9 = 24 d
    ProwlpendimethalinStable over a wide range of pH values
    RoundupglyphosateStable over a wide range of pH values
    TreflantriflularinStable over a wide range of pH values
    2,4-D2,4-DStable at pH 4.5 to 7

    Note that all of the herbicides are relatively stable. Some are a bit less stable at high pH, but none of the listed herbicides is in danger of breaking down on the day it is being applied. Only one is actually unstable at high pH – paraquat, a herbicide no longer registered in Canada and resticted in many other countries. Those with short half-lives experience them at quite high pH which are rarely seen in practice.

    Insecticides

    Insecticides are a different story. Several are very sensitive to pH. This table is again adapted from a comprehensive list published by Michigan State University, here.

    Trade NameActive IngredientHalf-life
    AdmireImidaclopridGreater than 31 days at pH 5 – 9
    Agri-MekAvermectinStable at pH 5 – 9
    AmbushPermethrinStable at pH 6 – 8
    AssailacetamipridUnstable at pH below 4 and above 7
    AvauntindoxacarbStable for 3 days at pH 5 – 10
    Cygon/LagondimethoatepH 4 = 20 hrs; pH 6 = 12 hrs; pH 9 = 48 min
    CymbushcypermethrinpH 9 = 39 hours
    DiazinonphosphorothioatepH 5 = 2 wks; pH 7 = 10 wks; pH 8 = 3 wks; pH 9 = 29 days
    Dipel/Forayb. thuringiensisUnstable at pH above 8
    DyloxtrichlorfonpH 6 = 3.7 days; pH 7 = 6.5 hrs; pH 8 = 63 min
    Endosulfanendosulfan70% loss after 7 days at pH 7.3 – 8
    FuradancarbofuranpH 6 = 8 days; pH 9 = 78 hrs
    Guthionazinphos-methylpH 5 = 17 days; pH 7 = 10 days; pH 9 = 12 hrs
    KelthanedicofolpH 5 = 20 days; pH 7 = 5 days; pH 9 = 1hr
    LannatemethomylStable at pH below 7
    LorsbanchlorpyrifospH 5 = 63 days; pH 7 = 35 days; pH 8 = 1.5 days
    Malathiondimethyl dithiophosphatepH 6 = 8 days; pH 7 = 3 days; pH 8 = 19 hrs; pH 9 = 5 hrs
    Matadorlambda-cyhalothrinStable at pH 5 – 9
    Mavriktau-fluvalinatepH 6 = 30 days; pH 9 = 1 – 2 days
    MitacamitrazpH 5 = 35 hrs; pH 7 = 15 hrs; pH 9 = 1.5 hrs
    OmitepropargiteEffectiveness reduced at pH above 7
    OrtheneacephatepH 5 = 55 days; pH 7 = 17 days; pH 9 = 3 days
    PouncepermethrinpH 5.7 to 7.7 is optimal
    PyramitepyridabenStable at pH 4 – 9
    Sevin XLRcarbarylpH 6 = 100 days; pH 7 = 24 days; pH 8 = 2.5 days; pH 9 = 1 day  
    SpinTorspinosadStable at pH 5 – 7; pH 9 = 200 days
    Thiodanendosulfan70% loss after 7 days at pH 7.3 to 8
    ZolonephosaloneStable at pH 5 – 7; pH 9 = 9 days

    Among insecticides, dimethoate, amitraz, and malathion stand out as breaking down rapidly in alkaline water. For these products in particular, it may be important to acifify the spray mix if there is any delay in spraying.

    Recommendations

    I’ve never been a fan of messing with solution pH unless recommended on the product label. Even when there is evidence that lower pH improves efficacy, consider the impact on tank mix partners.

    We’ve seen improvements in solubility and tank cleranout of Group 2 products with raised pH, and ammonia is the most cost-effective way to achieve that. But again, following label recommendations is strongly recommended. The consequences of changes in pH, particularly acifification, can be very detrimental. To be safe, consider doing a jar test before committing to a whole tank to a pH adjustment.

  • How to Interpret a Water Quality Test Result

    How to Interpret a Water Quality Test Result

    It’s common advice: Test your water before using it as a spray carrier. You dutifully sample the well or dugout and await lab results. And what comes back is a whole lot of numbers. How to make sense of it all?

    Three examples of water test results conducted by labs in Canada

    All three of these tests report a large number of properties and identify specific minerals and other solutes. Which ones are important in spraying? Here is the order in which I look at the numbers.

    Conductivity: This property is usually expressed as micro Siemens per cm (µS/cm) and simply identifies how many ionic solutes are in a sample (watch for alternate units such as mS/cm and convert if necessary). It doesn’t differentiate between any minerals or other molecules, and therefore has limited information. But it does tell us if there is a large or small issue with water quality. If conductivity is below 500 µS/cm, the water is probably good for spraying. If the value is around 1000 to 2000, further investigation is necessary. Some water samples return conductivity of more than 10,000 µS/cm, and it’s important to identify which salts are causing that problem.

    Note that Total Dissolved Solids (TDS) are often listed, and these are related to conductivity. A common way to get TDS is to multiply conductivity by 0.65. The conversion factor depends on which salts are dissolved but the bottom line is that TDS and conductivity are closely related.

    Bicarbonate: Bicarbonates are HCO3 and their concentration is measured in milligrams per Litre (mg/L), which is the same as parts per million (ppm). Bicarbonates can antagonize Group 1 modes of action and the common threshold is 500 ppm. Research at NDSU has shown that Urea -Ammonium-Nitrate (UAN or 28-0-0 liquid fertilizer) can reduce bicarbonate antagonism in some Group 1 herbicides.

    Bicarbonates are negatively charged and are associated with a positive ion, often the hard water cations sodium (Na), calcium (Ca) or magnesium (Mg). As such, waters that are high in bicarbonates are often also hard.

    Total Hardness (calculated): This is one of the important parameters. Hardness antagonizes most weak acid herbicides, most importantly glyphosate and g;ufosinate, and also ties up surfactants and emulsifiers which can result in problems with mixing and compatibility. Hardness is caused by metal cations, in order of strength these are iron (Fe++), magnesium (Mg++), calcium (Ca++), sodium (Na+), and potassium (K+). Of these, Mg and Ca are typically most abundant, although some water is high in Na.

    The Total Hardness (ppm) reported in water tests is done by taking the most common two cations, calcium and magnesium, and using this formula: 2.497*Ca + 4.118*Mg. Note that some tests report hardness in Grains per Gallon, in this case, multiply grains by 17.1 to get ppm.

    While this calculation usually gives an accurate prediction of hardness, you may need to have a look at iron and sodium as well. Iron is less common, but some well waters are high in sodium or potassium. These minerals are not captured in the Total Hardness measurement. A water test low in Total Hardness may still be high in sodium, these are typically the samples with high conductivity.

    The threshold for Total Hardness depends on the herbicide, its rate, and the water volume. The most common quoted values are 350 ppm for the lower rates of glyphosate (1/2 L/acre equivalent), and 700 ppm for the higher rates. Lower water volumes increase the concentration of herbicide, and reduce the impact of water hardness or bicabonates.

    pH: This parameter is a bit over-rated because it is later affected by the herbicide and adjuvant dissolved in it. There is usually no concern with pH between 6 and 8, and water is rarely outside this range. It is best not to change the pH of water unless it is required on the label for mixing, because some products require low, and others require high pH for optimum solubility. Compatibility is an ever greater concern as our tank mix complexity increases.

    Water Conditioners

    The most common water conditioner is ammonium sulphate [AMS, (NH4)2 SO4]. In its pure form (21-0-0-24), a concentration of 1% to 2% w/v (8 to 17 lbs AMS/100 US gallons of spray water) solves most hard water and bicarbonate issues. Be cautious of using too much AMS (>3%), when added at high concentrations to some herbicides it can burn crops.

    Research has shown that AMS works in two ways: The sulphate ion binds with hard water cations, forming an insoluble precipitate that prevents the antagonistic cations from binding to, and inhibiting, the herbicide. The ammonium ion has been shown to improve cellular uptake by weak ion herbicides.

    Some product labels call for UAN as an adjuvant. UAN contributes ammonium, but not sulphate ions. As a result, while it may improve herbicide performance, it does not remove antagonizing cations from the mixture.

    Acids have been used to combat hard water. Most common herbicides are weak acids, and the acid constituent, usually a carboxilic acid, has a unique pKa. The pKa is the pH at which half the molecules are protonated (contain a hydrogen atom, resulting in an uncharged acid constituent) and the other half are not protonated (negatively charged). If the spray mixture has a pH below the pKa, the weak acid herbicides become protonated. This means the herbicide becomes less water-soluble, but also that it has less chance of interacting with a hard water cation. Acids that work in this way are less effective at ameliorating the effect of hard water than AMS.

    A small group of acids that includes citric acid and sufphuric acid can sequester or bind with hard water cations. But they do not contribute the ammonium ion that assists in weak acid herbicide uptake.

    If your water is questionable for spraying, there are four common choices:

    • Select a different well or dugout
    • If the problem is barbonates or hardness, treat water with a conditioner such as Ammonium Sulphate (AMS), available in pure form as 21-0-0-24. Some acids (citric, sulfuric) can form conjugate bases with hard water cations, removing them from solution. But the associated significant lowering of pH should be treated with an abundance of caution as it may affect solubility of some pesticides.
    • Reduce water volumes or increase herbicide rates.
    • Use a municipal treated water source or invest in a reverse-osmosis (RO) system. RO is neither cheap nor fast and requires additional investment in storage, and a way to deal with solute-enriched waste water. But it may be the best option for some.

    An Ammonium Sulphate calculator, originally developed by Winfield United using data from NDSU, can be downloaded here:

    An excellent resource for adjuvant and water quality topics is this addendum in the North Dakota State University Guide to Weed Control.

    Using good quality water lowers the likelihood of problems with mixing and overall performance and that pays significant dividends later.