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Saint-Gobain CHR 2829-3(R) Acrylic Adhesive Zone Tape

    • Product Name: Saint-Gobain CHR 2829-3(R) Acrylic Adhesive Zone Tape
    • Factroy Site: Yinchuan, Ningxia, China
    • Price Inquiry: sales8@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
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    Specifications
    HS Code 775790
    Manufacturer Saint-Gobain
    Brand CHR
    Product Code 2829-3(R)
    Product Name CHR 2829-3(R) Acrylic Adhesive Zone Tape
    Tape Type Zone Tape
    Adhesive Type Acrylic
    Backing Material PTFE Film
    Total Thickness 3.0 mil (0.076 mm)
    Color White
    Temperature Range -100°F to 350°F (-73°C to 177°C)
    Dielectric Strength 5000 V
    Tensile Strength 15 lb/in (2.6 N/cm)
    Elongation At Break 100%
    Adhesion To Steel 25 oz/in (0.27 N/mm)
    Width 1/2 in (12.7 mm) typical
    Length 36 yd (33 m)
    Core Diameter 3 in (76.2 mm)
    Release Liner Yes
    Chemical Resistance Excellent
    Moisture Absorption <0.01%
    Friction Coefficient 0.05
    Uv Resistance Excellent
    Shelf Life 1 year
    Application Heat sealing and packaging

    As an accredited Saint-Gobain CHR 2829-3(R) Acrylic Adhesive Zone Tape factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Saint-Gobain CHR 2829-3(R) Acrylic Adhesive Zone Tape packaging: one roll per box, labeled with product identification and lot number.
    Container Loading (20′ FCL) 20′ FCL container loading for Saint-Gobain CHR 2829-3(R) Acrylic Adhesive Zone Tape, securely palletized, ambient conditions, compliant with transport regulations.
    Shipping Saint-Gobain CHR 2829-3(R) Acrylic Adhesive Zone Tape is not regulated for transport by DOT, IATA, or IMDG. No UN number or hazard class is assigned. Ship in original sealed packaging, keep dry, and avoid excessive heat, sunlight, and freezing. Follow all applicable local, national, and international regulations.
    Storage Store Saint-Gobain CHR 2829-3(R) Acrylic Adhesive Zone Tape in its original, tightly sealed packaging in a cool, dry, well-ventilated area. Protect from direct sunlight, moisture, heat, sparks, and flames. Keep away from incompatible materials such as strong oxidizers and solvents. Maintain recommended temperature, typically 15–30°C (59–86°F), and observe shelf-life/rotation. Follow the manufacturer’s SDS and local regulations.
    Shelf Life Shelf life is typically 12 months from date of shipment when stored at 21°C (70°F) and 50% RH in original packaging.
    Application of Saint-Gobain CHR 2829-3(R) Acrylic Adhesive Zone Tape

    On electrolytic anodizing operations processing 7050-T7451 aluminium machined fuselage frames to MIL-A-8625F Type II requirements, Saint-Gobain CHR 2829-3(R) acrylic adhesive zone tape is applied as a selective barrier over sealant grooves, threaded inserts, rivet holes, and faying surfaces that must remain free of anodic oxide after processing. The tape enters the line after deoxidizing and before the charge is energized; it remains in place through immersion in sulfuric acid electrolyte containing 15–20 wt% H₂SO₄ at 18–22 °C, with current density held at 1.0–1.8 A/dm² for 30–60 min depending on required oxide thickness. In vertical racking configurations, the lowest tape edge is subjected to the largest hydraulic head and the greatest acid pooling; field failure tends to occur there first as edge lifting, followed by acid wicking along the polyester backing and acrylic adhesive interface. The lifted channel permits anodizing current and electrolyte to reach regions that were intended for subsequent adhesive bonding or electrical contact; those regions then exhibit oxide coverage and a loss of surface conductivity. After demasking, surfaces are inspected under 1.75× magnification and tested for water-break-free condition per ASTM F22-13, while ionic residue is extracted in 75/25 vol% isopropyl alcohol/deionized water and measured per IPC-TM-650 2.3.25. The tape adhesive must resist both acid plasticization and entrapment of dissolved aluminium; if the adhesive releases during rinse, smut or sulfate salts can be deposited on the newly anodized surface. Because published product-specific data for this exact tape in sealed sulfuric acid anodizing lines is limited, each rack geometry and current density should be screened using the same immersion time and agitation conditions as the production line.

    How Does Forced-Air Cure Oven Temperature Uniformity Influence Adhesive Transfer in Powder Coating Masking?

    In powder coating lines for steel enclosures and aluminium heat sinks, CHR 2829-3(R) acrylic adhesive zone tape masks threaded standoffs, grounding points, and bearing bores before polyester or epoxy-polyester powders are electrostatically applied. Cure oven set points range from 150 °C for low-temperature epoxy powders to 204 °C for polyester or hybrid systems, with dwell times of 10–30 min after the part reaches metal temperature. The polyester backing begins to shrink while the adhesive is above its glass transition, and the resulting shear stress concentrates at the tape edge. In forced-air ovens with a spatial variation greater than ±5 °C, localized overheating produces a visible edge ripple and a transferable adhesive residue after cooldown. This residue is classified as a coating defect because it prevents powder adhesion around the masked zone and may appear as a fisheye after topcoat application. A controlled screening program includes measurement of peel adhesion per ASTM D3330/D3330M-04 after the tape has been exposed to the maximum cure temperature for 30 min on the same substrate used in production; tensile elongation and backing shrinkage are measured per ASTM D3759/D3759M-05. A decline in peel adhesion greater than 80% from the unheated baseline is a common rejection threshold in industrial tape screening; any cohesive splitting during removal indicates excessive thermal exposure. The standard also recommends that adhesive transfer be checked after demasking by wiping the edge zone with a solvent-saturated cloth and inspecting under oblique light.

    Compatibility screening matrix for acrylic adhesive zone tapes
    ProcessExposure rangePrimary failure modeTest method
    Sulfuric acid anodizing15–20 wt% H₂SO₄ at 18–22 °Cacid wicking and edge liftingASTM D3330/D3330M-04 after immersion
    Powder coating cure150–204 °C for 10–30 minadhesive softening, adhesive transferASTM D3330/D3330M-04 after thermal soak
    Autoclave composite cure121–177 °C, 0.3–0.6 MParesin flash under tape, film embossingASTM C297/C297M-16 or ASTM D1781-98
    Electroless nickel85–95 °C, pH 4.5–5.2plate nucleation at tape interfacesASTM B117-19 plus optical inspection at 20×
    Alkaline paint pre-treatment50–65 °C, pH 11–13adhesive saponification, residue transferASTM D3330/D3330M-04 and ASTM D5402-19

    Co-cured composite panel production requires film adhesive to be placed within a closed bondline and covered with peel ply, release film, breather, and vacuum bag. Saint-Gobain CHR 2829-3(R) zone tape is often applied around the perimeter of the adhesive film before vacuum bag lay-up. The tape creates a visible boundary and maintains a resin-free area outside the bondline, while the adhesive film remains contained under peel ply or release film. During autoclave cure at 121–177 °C and 0.3–0.6 MPa pressure, the tape experiences hydrostatic resin pressure, vacuum bag compaction, and thermal expansion mismatch against the aluminium or carbon-fibre tool surface. Edge movement during cure is undesirable because low-viscosity resin can migrate into the masked zone and create an uncontrolled fillet. In production qualification, the cured laminate is inspected for resin flash, and the width of the resin-free zone is measured at multiple stations; a deviation greater than 1.0 mm from the intended boundary is considered nonconforming for parts requiring later sealing or painting. Structural verification uses flatwise tensile testing per ASTM C297/C297M-16 for sandwich specimens or climbing drum peel per ASTM D1781-98 for bonded skins. The acrylic adhesive of the zone tape must not transfer residue to the tool face or contaminate the bond surface; post-cure residue is evaluated by water-break-free testing per ASTM F22-13 on adjacent unprotected aluminium. Since acrylic PSA systems lose shear strength at elevated temperature, the tape is best used as a boundary marker and squeeze-out barrier rather than as a load-bearing edge dam for very high-flow resin systems. Published cycle-specific data for CHR 2829-3(R) under autoclave cure at pressures above 0.6 MPa is limited; validation on the actual tool material is required.

    Electroless Nickel-Phosphorus Bath Interaction With Acrylic Adhesive Zone Tape Edge Seals

    Electroless nickel deposition on machined aluminium electronic enclosure housings operates at 85–95 °C and pH 4.5–5.2, with sodium hypophosphite as the reducing agent and nickel sulfate concentrations near 5.5–6.5 g/L. CHR 2829-3(R) tape is applied to connector faces, grounding pads, and stainless steel inserts to prevent plate-out in those regions. The tape backing must resist hot, mildly acidic bath wetting, while the adhesive must seal the edge against the hypophosphite solution. Failures observed on production parts involve small unbonded micro-channels created by insufficient edge rub-down; these channels, often 5–20 µm wide, allow electrolyte to wick inward and initiate electroless nickel plate under the backing. Unlike electroplating, electroless deposition does not require an external current at the part surface, so any wetted non-masked region can plate spontaneously once the bath is stabilised. Post-plating inspection is conducted with optical microscopy at 20× to detect under-tape plating, adhesion loss, or adhesive residue. Neutral salt spray testing per ASTM B117-19 provides a corrosion-resistance baseline for the finished component but does not predict hypophosphite bath compatibility; chemical immersion testing in a representative production bath is the more direct screening method. The operating temperature of the bath is well within the short-term thermal capability of many acrylic PSA systems, but the combined heat and acidity can soften the adhesive if immersion exceeds 60–90 min. Published data for CHR 2829-3(R) under high-phosphorus electroless nickel conditions is limited, so production validation should include actual bath age and agitation level.

    Printed circuit assembly lines that apply UV-curable acrylic or moisture-cure polyurethane conformal coatings use acrylic adhesive zone tape to protect card-edge connectors, plated through-hole test points, and electromagnetic interference grounding springs. The tape is exposed to convection cure at 60–80 °C for 15–30 min and is removed after the coating has cured. Visual acceptance per IPC-A-610H requires that no coating bleed under the tape edge and no adhesive residue remains on contact surfaces; ionic contamination is measured per IPC-TM-650 2.3.25 using a 75/25 vol% isopropyl alcohol/deionized water extract. Because production lines often run multiple thermal cycles through ovens, a tape that performs after a single cure may still transfer residue after 5 repeated cycles at 80 °C. Screening should include the actual masking geometry, manual or automatic tape application pressure, and the same oven profile used in production.

    When Alkaline Pre-Treatment and Cathodic Electrocoat Cycles Replace Silicone-Adhesive Maskants on Zinc-Phosphated Steel

    In automotive body-in-white paint shops, door striker brackets and threaded studs are masked before alkaline degreasing, zinc phosphate conversion coating, and cathodic electrocoat. Silicone-adhesive masking tapes are prohibited in many of these lines because polydimethylsiloxane transfer can create craters in later basecoat and clearcoat layers; acrylic adhesive zone tapes are selected as an alternative. The tape sees spray impingement from a cleaner operating at 50–65 °C and pH 11–13, followed by acidic phosphate stages and multiple deionized water rinses. The electrocoat cure oven holds parts at 160–180 °C for 20–30 min, which is close to the upper continuous-service range of many acrylic PSA systems. The principal failure mode is adhesion loss and adhesive transfer after the oven, especially on rough zinc-phosphated steel where mechanical anchorage is lower than on polished steel coupons. Peel adhesion is measured per ASTM D3330/D3330M-04 before and after the complete electrocoat cure cycle; backing integrity is assessed by solvent double rubs per ASTM D5402-19. If any residue is detected after demasking, the surface is rejected because it disrupts seam sealing and topcoat adhesion. Published data for CHR 2829-3(R) under cathodic electrocoat oven profiles is limited; a process-specific validation should include the full immersion, spray, and bake sequence rather than isolated thermal soak testing.

    Thermal spray deposition of tungsten carbide-cobalt wear coatings by high-velocity oxygen fuel operates with particle velocities above 500 m/s and flame temperatures that can exceed 2,700 °C at the torch exit. Saint-Gobain CHR 2829-3(R) acrylic adhesive zone tape is not a primary maskant for direct HVOF impingement; polyester-backed acrylic PSA materials degrade rapidly under thermal plume contact and particle bombardment. The tape may be considered only as a secondary shield at a minimum standoff of 300 mm from the spray path, where radiant heat flux averages below 80 °C and overspray density is low. Grit blasting with 24–36 mesh alumina prior to spraying can load the exposed adhesive edge with abrasive fines; if the tape edge lifts during blasting, the adhesive does not reseal and subsequent coating work is compromised. In these booths, metal shims, silicone-fiberglass blankets, and high-temperature tapes are the standard primary maskants. Published data for CHR 2829-3(R) under direct HVOF plume conditions is limited, and the material should be restricted to ancillary masking and edge definition away from the spray path.

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    Certification & Compliance
    More Introduction

    Saint-Gobain CHR 2829-3(R) Acrylic Adhesive Zone Tape is supplied as a polyester film carrier with a pressure-sensitive acrylic adhesive deposited in discrete longitudinal zones rather than as a continuous full-web adhesive layer. The R designation identifies reverse-wound roll orientation; it does not alter adhesive chemistry, cure mechanism, or backing identity. This zone-coated construction differs from standard single-coated tapes because the adhesive is confined to predetermined lane widths, leaving dry edges or inter-zone gaps. In masking operations, those dry edges limit adhesive ooze beyond the intended boundary. In roll-to-roll splicing, the exposed non-adhesive margins reduce contamination of downstream idlers, nip rollers, and vacuum blocks.

    Documented use environments for this product family include plasma spray masking, powder coating demarcation, composite bagging film splicing, motor or transformer lead insulation, and general high-temperature masking of steel and aluminum surfaces. The polyester film provides puncture resistance and dielectric separation, while the acrylic adhesive contributes peel adhesion to steel, aluminum, polyimide film, and epoxy composite tool surfaces without the siloxane contamination mode associated with silicone-adhesive tapes. Because zone width, gap spacing, and dry-edge margins are slitting or die-cutting specifications, the supplier drawing is the controlling dimensional document. Standard slit roll widths are commonly supplied between 0.25 in and 54 in, with adhesive zone widths frequently configured from 0.25 in to 2 in and dry gaps between 0.125 in and 1 in. Custom zone layouts require a manufacturing drawing and lot verification; published data for arbitrary off-the-shelf layouts is limited.

    How Does the Zone Adhesive Construction Affect Peel Force and Residual Transfer?

    Peel force on the adhesive-bearing zones is measured according to ASTM D3330 Method A using a stainless steel panel, a 180° peel angle, and a 20 min dwell. Because the adhesive is not full-web coated, test strips are cut parallel to the machine direction and include either one adhesive lane or a full repeat unit of multiple lanes. The recorded load is expressed per linear inch of adhesive-bearing width. Distributor technical bulletins and supplier-affiliated literature commonly list a stainless steel peel value of 25 oz/in (2.75 N/cm) for the adhesive zone. That value may fall to 8–15 oz/in on untreated polyethylene and rise to 30–40 oz/in on corona-treated aluminum or grit-blasted steel. The stated values are representative and should not be used as incoming acceptance criteria without a formal material specification.

    The discontinuous adhesive layer changes the mechanical load path during removal. A full-coverage tape distributes peel stress uniformly across the web, whereas a zone-coated tape concentrates fracture energy at the boundary between the adhesive lane and the dry edge. That boundary functions as a stress raiser and can initiate clean peel at a lower force than a continuous adhesive of identical chemistry and thickness. In practical terms, CHR 2829-3(R) tends to remove from flat rigid substrates with less adhesive residue than a fully coated acrylic tape of the same cohesive strength because the peel front does not travel through a wide continuous adhesive dome.

    Residual transfer is assessed after thermal aging at 70 °C under 100 g/cm² pressure for 24 h. Failure is classified as clean peel, ghosting, or cohesive splitting. On polar steel and aluminum panels, the acrylic formulation remains removable after this protocol. On unpigmented polycarbonate or acrylic sheet, interaction may occur when the substrate is plasticized or exposed to sustained RH above 85%. In such cases, a primer or corona treatment may be required before tape application. Adhesive residue risk increases when processing temperatures exceed 120 °C, at which point the acrylic network enters a viscoelastic flow regime and cohesive shear strength declines.

    Dimensional, Adhesive, and Electrical Property Profile

    Representative values from supplier technical documentation and industrial distribution data are consolidated in the table below. They are typical lot averages, not release criteria, unless agreed in a controlled material specification. Zone coating may generate slight caliper variation between adhesive-bearing and dry regions.

    PropertyValueTest Method or Reference
    Backing materialPolyester film—
    Adhesive typeAcrylic pressure-sensitive, zone-coated—
    Total tape thickness0.076 mm (3.0 mil)ASTM D3652
    Tensile strength at break28 lb/in (490 N/100 mm)ASTM D3759
    Elongation at break100%ASTM D3759
    Peel adhesion to stainless steel25 oz/in (2.75 N/cm)ASTM D3330
    Dielectric breakdown voltage5,000 VASTM D149
    Maximum short-term service temperature155 °CSupplier thermal endurance screening
    Recommended storage conditions21 °C, 50% RHInternal stability protocol

    Thermal endurance of the backing and adhesive are not identical. The polyester film retains tensile and dielectric behavior up to its 130 °C class rating when unstressed, while the acrylic adhesive begins to lose cohesive shear strength above 120 °C. Short-term exposure to 155 °C for 30–60 min is tolerated in masking applications, but continuous exposure above 120 °C may increase adhesive transfer and reduce residue-free removability. The dielectric breakdown value of 5,000 V applies only to clean, pinhole-free, uncreased film. Wrinkles, crease damage, or edge debris from dull slitting blades can reduce breakdown strength by 30–50%.

    Converting conditions directly influence final performance. Narrow-web rotary shear slitting is normally performed at unwind tension between 60 g/mm and 100 g/mm of web width, depending on roll diameter and caliper. Excessive tension forces adhesive into the dry zone and reduces the intended uncoated edge width. Insufficient tension causes telescoping and edge damage. Dull slitting blades can produce ragged polyester edges that trap particulates and lower dielectric strength. For plasma spray masking, die-cut or laser-cut parts must retain a clean dry edge; acrylic contamination on the dry edge can carbonize under flame-sprayed metal deposition and create a contaminant source during coating.

    When Silicone Migration or Rubber Residue Constrains the Masking Operation

    The selection of CHR 2829-3(R) over silicone-adhesive polyester tape is driven primarily by contamination control and thermal ceiling. Silicone pressure-sensitive adhesives are often specified for continuous service up to 200 °C and for release from low-surface-energy surfaces. However, silicone migration can generate fisheye defects in powder coating or inhibit subsequent adhesive bonding in painted assemblies. The acrylic system avoids that siloxane contamination mode. The trade-off is a lower maximum thermal limit: the CHR 2829-3(R) acrylic adhesive is not recommended for continuous exposure above 120 °C, and short-term exposure should not exceed 155 °C. In bake cycles at 180–200 °C, silicone-adhesive polyester tape remains mechanically stable, while the acrylic version is prone to thermo-oxidative degradation, discoloration, and adhesive transfer.

    Relative to natural rubber pressure-sensitive adhesive tapes, the acrylic formulation exhibits lower initial tack on rough or low-energy substrates but better retention of peel strength after ultraviolet exposure and thermal cycling. Rubber adhesives may lose peel strength rapidly above 70 °C and can leave deposits when plasticizer migration or oxidation occurs. Acrylic adhesives degrade through slower chain-scission and crosslink-density increase mechanisms. In powder coating lines, rubber adhesive tapes commonly fail when exposed to heated overspray and part prewarming at 100–120 °C; the acrylic zone tape retains integrity through that prewarm stage but must not contact the cure oven zone above stated limits.

    Operating parameterCHR 2829-3(R) acrylic zone tapeSilicone-adhesive polyester tapeRubber-adhesive polyester tape
    Continuous service ceiling120 °C180–200 °C70 °C
    Short-term thermal spike155 °C260 °C105 °C
    Silicone migration potentialAbsentPresentAbsent
    Plasticizer resistanceModerateModerateLow
    Typical stainless steel peel25 oz/in22–28 oz/in30–45 oz/in
    Residue after 70 °C/7 daysLowLowModerate

    The comparative values above represent adhesive classes rather than specific competitive products. Backing caliper, primer layers, and coating weight can shift the stated bounds; direct substitution decisions should be based on manufacturer data sheets and end-use validation.

    Surface preparation for critical applications includes a final wipe with 2-propanol or a qualified aliphatic hydrocarbon cleaner and a minimum 5 min drying period before tape application. Substrate surface energy should exceed 40 mN/m. Stainless steel and aluminum normally meet that condition after degreasing, but molded epoxy and polyamide components may require corona or plasma treatment. Peel adhesion is time-dependent: at 25 °C, the adhesive builds to roughly 80% of ultimate peel strength within 20 min, with final wet-out at 24 h. In vacuum bagging below 0.85 bar, the zone-coated adhesive requires a dwell time of 15–30 min at 25 °C before cure; insufficient dwell allows leak paths to propagate along uncoated zones.

    The tape is not recommended for immersion in aromatic hydrocarbons, ketone-based stripping agents, or strong alkaline cleaners above 50 °C. These media can swell the polyester backing or plasticize the acrylic adhesive. Roll storage should follow first-in-first-out control at 21 °C and 50% RH, away from direct UV exposure. Under these conditions, shelf life is typically 12 months from date of manufacture. Aged rolls may show increased unwind adhesion and should be re-qualified before use on automated masking lines. Regulatory status is generally supplied as an article under REACH Regulation (EC) No 1907/2006 and RoHS Directive 2011/65/EU; lot-specific SVHC or composition declarations require supplier confirmation.

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