| HS Code | 247688 |
| Product Name | Dielectric Polymers NT-5513 High Tack Tape |
| Manufacturer | Dielectric Polymers |
| Product Type | Double-coated tape |
| Backing Material | Polyester film |
| Adhesive Type | High-tack acrylic |
| Total Thickness | 2.0 mil (0.051 mm) |
| Liner | 60# densified kraft |
| Color | Transparent |
| Adhesion To Steel | 100 oz/in |
| Adhesion To Polyethylene | 40 oz/in |
| Adhesion To Polypropylene | 50 oz/in |
| Loop Tack | High |
| Shear Strength | 100 hours |
| Temperature Range | -20°F to 300°F |
| Dielectric Strength | 5000 V |
| Tensile Strength | 25 lb/in |
| Elongation | 100% |
| Width Range | 0.25 in to 54 in |
| Length | 36 yd / 72 yd |
| Core Diameter | 3 in |
| Shelf Life | 1 year |
As an accredited Dielectric Polymers NT-5513 High Tack Tape factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Dielectric Polymers NT-5513 High Tack Tape is packaged on rolls, each individually wrapped in protective cartons; 36 rolls per case. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Dielectric Polymers NT-5513 High Tack Tape, palletized, shrink-wrapped, and secured for safe ocean transport. |
| Shipping | Shipping description: Dielectric Polymers NT-5513 High Tack Tape; not regulated as dangerous goods by DOT, IATA, IMDG, or ADR. Proper shipping name: Not applicable. UN number: None. Hazard class: None. Ship as non-hazardous in original packaging; keep dry, avoid excessive heat. No special labels or placards required. |
| Storage | Store Dielectric Polymers NT-5513 High Tack Tape in a cool, dry, well-ventilated area in original sealed packaging. Keep away from direct sunlight, heat, sparks, flames, moisture, and incompatible materials. Maintain 15–25°C and 40–60% relative humidity. Protect rolls from crushing, excessive stacking, and physical damage. Do not freeze. Observe shelf life and use first-in, first-out rotation. |
| Shelf Life | Store at room temperature; typical shelf life is 12 months from manufacture in original packaging, away from direct sunlight and moisture. |
In lithium-ion traction battery modules, Dielectric Polymers NT-5513 High Tack Tape is specified where compression pad retention, cell edge isolation, and busbar tab insulation must survive continuous service at 60 °C to 85 °C. The tape is applied over laser-welded aluminium tabs after the weld crown is dressed free of spatter and the surface is prepared by alkaline degreasing to a surface energy of at least 38 mN/m. An atmospheric plasma treatment at 0.5–1.0 kW and 2–5 m/min line speed is commonly used immediately before lamination to raise the aluminium oxide surface energy above 58 mN/m. A silicone rubber nip roll of 60–75 Shore A durometer is operated at 0.25–0.45 MPa to force the pressure-sensitive adhesive into the weld crown topography. Production lines have documented bubble entrapment when lamination speed exceeds 8 m/min unless the nip roll is preheated to 45–55 °C. The dielectric carrier thickness is typically 25 μm or 50 μm, with an adhesive coat weight selected to maintain a carrier-to-adhesive thickness ratio between 1:1 and 1.5:1; however, published data for NT-5513 in this specific configuration is limited, and validation against ASTM D1000 and IEC 60243-1 is required before series use. After tape application, the cell-to-pack assembly is subjected to 1,000 h damp heat at 85 °C/85% RH per IEC 60068-2-78. The insulated busbar must retain a dielectric withstand of at least 2.5 kV AC for 60 s without flashover. Edge coverage of the wrap is set at a minimum 50% overlap; beyond the busbar edge, a 2 mm overhang is required to prevent partial discharge at sharp aluminium corners. The material must exhibit surface resistivity of at least 1×10¹² Ω/sq when measured per ASTM D257 and must not contribute chloride ions above 10 ppm or sodium ions above 5 ppm in extraction testing per IPC-TM-650 method 2.3.25. In battery module qualification, the tape is also checked after mechanical shock and vibration because adhesive shear failure can expose the busbar edge; if peel adhesion falls below 2.5 N/10 mm after shock testing, the wrap is considered failed. The terminal product is a cell-to-pack insulation barrier that retains busbar electrical isolation under mechanical shock, vibration, and damp heat.
Conformal coating masking on printed circuit assemblies uses NT-5513 as a peelable dielectric barrier over ENIG edge connectors. The primary process concern is whether the acrylic adhesive leaves residue or transfers after exposure to wave soldering temperatures. Masked boards are typically processed through a wave soldering line with a preheat zone of 110–130 °C and a solder pot temperature of 250–255 °C for 3–6 s. After cooling below 50 °C, the tape must peel at a 90° to 180° angle without cohesive failure. Qualification per IPC-CC-830B requires absence of corrosion beneath the masked area and no visible residue under 10× magnification. Automated tape dispensers apply the masking tape with a nip pressure of 0.35–0.50 MPa and a dwell time of 1–2 s over the gold fingers. Formulation control for clean removal is based on adhesive crosslink density. A high-tack acrylic adhesive in this application class is usually coated at 30–50 g/m² onto a 25 μm polyimide film, maintaining an adhesive-to-carrier thickness ratio between 1:1 and 2:1. The adhesive must remain soluble enough to avoid excessive crosslinking at soldering temperature; after 7 days at 150 °C per ASTM D1000, peel adhesion must not increase by more than 50%. Ionic contamination must remain below 1.5 μg NaCl equivalent/cm² per IPC-TM-650 method 2.3.25, and the material must comply with RoHS Directive 2011/65/EU Annex II and REACH Annex XVII restrictions. Removal above 70 °C has been associated with adhesive transfer to thin ENIG nickel-phosphorus surfaces; therefore, cool-down time before tape stripping is enforced. The terminal product is a conformal coated PCB assembly with clean ENIG edge fingers free of maskant residue and without electrochemical migration risk.
The retention of flexible slot liners during needle winding becomes critical when slot fill factor exceeds 40% and conductor insertion forces exceed 10 N per needle. NT-5513 is applied to the outside of Nomex 410 or polyimide slot liners before they are inserted into the stator stack. The tape must provide sufficient loop tack to hold the liner in a vacuum fixture and prevent springback. Loop tack is evaluated per ASTM D6195 and is typically specified at not less than 8 N/25 mm at 23 ± 2 °C. Peel adhesion to polyesterimide enameled magnet wire is monitored per ASTM D3330/D3330M-04; values below 3.0 N/10 mm indicate insufficient wet-out on the varnished surface. On production lines, the tape is slit to widths of 6–25 mm and applied with a pneumatic roller at 0.2–0.4 MPa. The liner is held in a vacuum fixture during tape application to prevent wrinkling. A set time of 10–20 min at 23 ± 2 °C is allowed before winding; full adhesion develops over 24–72 h. If the winding line stops for more than 12 h, unwind force may increase and tear the liner during needle insertion. The tape must not reduce the insulation system thermal class below 155 °C. Thermal aging at 180 °C for 7 days per ASTM D1000 should not reduce peel adhesion by more than 30%. Partial discharge inception voltage is measured per IEC 60034-18-41 on representative motorettes. Compatibility with varnish is important; silicone release agents on the tape liner must be eliminated because migration can reduce varnish adhesion to the slot liner. Amine-based additives in the varnish may accelerate acrylic crosslinking and should be avoided unless validated. The terminal product is a wound stator with slot liners fixed in place before varnish impregnation and with no liner displacement after needle insertion.
| Test / Property | Standard or Test Method | Commonly Applied Acceptance Criterion |
|---|---|---|
| Peel adhesion to aluminium | ASTM D3330/D3330M-04 | ≥ 3.0 N/10 mm after 72 h dwell |
| Loop tack | ASTM D6195 | ≥ 8 N/25 mm |
| Dielectric breakdown voltage | IEC 60243-1 | ≥ 6 kV for a single 50 μm layer |
| Surface resistivity | ASTM D257 | ≥ 1×10¹² Ω/sq |
| Comparative tracking index | IEC 60112 | ≥ 600 V |
| Flame rating | UL 94 | VTM-0 registration |
| Ionic contamination | IPC-TM-650 method 2.3.25 | ≤ 1.5 μg NaCl equivalent/cm² |
| Long-term thermal aging | UL 746A | service temperature up to 105 °C or higher |
On airframe wire bundles routed through titanium clips and pass-throughs, NT-5513 is used as a spiral-wrap dielectric and chafe barrier. The tape replaces heat-shrink and braided sleeving in areas where a thin wall is required. A minimum overlap of 50% creates a double-layer dielectric barrier. The tape must meet flammability requirements of FAR 25.853(a) and UL 94 VTM-0, and smoke density limits per BSS 7239. ETFE-insulated wire jackets are difficult to wet; therefore, the jacket is solvent-wiped with 70% isopropanol/30% deionized water and dried at 60 °C for 5 min before wrapping. A constant-tension dispenser set at 2–4 N prevents necking; elongation above 10% creates thin spots that reduce dielectric strength below the design minimum. The wrapped bundle must pass a dielectric withstand test of 1,500 V AC for 60 s between conductor and conductive outer foil. UV resistance is checked per ASTM G154 cycle 1 for 500 h without cracking. Adhesion to the wire jacket after thermal cycling from -55 °C to 125 °C per SAE AS23053 is required. The terminal product is a wire bundle with a tape wall thickness of 0.25–0.50 mm, bonded to connectors and branch-outs. Published data for NT-5513 in this specific aerospace configuration is limited; validation on the exact ETFE jacket and clip geometry is required. Direct contact with engine bleed ducts at sustained temperatures above 105 °C must be avoided because the acrylic adhesive softens and may creep.
Aluminum busbar wrapping without primer is specified where volatile organic compound restrictions prevent solvent-based adhesion promoters and where switchgear assembly must remain reworkable. NT-5513 is applied directly to alumina-blasted aluminium surfaces in a half-lapped wrap with 50% overlap. The surface is prepared with 60–80 grit aluminium oxide to a roughness of 3–5 μm Ra, followed by solvent degreasing to remove oxide dust. Without primer, adhesive strength develops by mechanical interlocking; a controlled-tension wrapping machine is therefore set at 8–15 N to seat the tape into the blast profile. A silicone rubber pressure roller of 70 Shore A at 0.35–0.50 MPa follows the wrap to eliminate air channels. The wrapped busbar is allowed a dwell time of 48 h at 23 ± 2 °C before electrical testing. Dielectric qualification includes a withstand test of 2,500 V AC for 60 s per IEC 61439-1 and partial discharge measurement below 10 pC at 1.5 kV per IEC 60270. Edge coverage beyond the chamfered busbar edge is set at 2 mm minimum. The tape must provide a comparative tracking index of at least 600 V per IEC 60112 and meet UL 510 for insulating tape. Ester-based transformer oil exposure requires separate compatibility testing because acrylic adhesives may swell and lose shear strength. When the busbar is reworked, the tape must peel cleanly without leaving residue that reduces subsequent primerless adhesion; if residues remain, a light alumina reblast is required. Published data for NT-5513 in primerless switchgear busbar applications is limited; qualification with the specific busbar edge radius and surface profile is required. The terminal product is a laminated busbar assembly for modular switchgear with a tracking-resistant dielectric wrap and no primer-derived volatile organic compound burden.
Low-pressure lamination of polyimide stiffeners onto flexible printed circuit substrates uses NT-5513 as a pressure-sensitive bonding layer. The process is carried out in a vacuum press at 0.10–0.30 MPa to avoid crushing 25 μm to 50 μm fine-pitch copper traces. A residual chamber pressure of 1,000 Pa and a heated platen at 80 °C for 120 s allow the adhesive to wet the etched copper surface without excessive squeeze-out. Bond line thickness is maintained at 25–50 μm by controlling adhesive coat weight and press gap. After lamination, adhesion to treated polyimide is monitored per IPC-TM-650 method 2.4.9; values below 0.8 N/mm indicate inadequate surface energy or contamination. Solder float performance is tested per IPC-TM-650 method 2.4.13.1 at 288 °C for 10 s without delamination. The material must comply with IPC-4202, IPC-4203, and IEC 61249-2. If the copper surface carries an organic solderability preservative thicker than 0.5 μm, adhesion must be revalidated because the tape may lift during thermal cycling. Published data for NT-5513 in this specific configuration is limited; validation with the actual stiffener thickness, copper roughness, and coverlay material is required. The terminal product is a flexible printed circuit assembly with a bonded stiffener that withstands subsequent solder assembly and dynamic bending.
The need for cable fixation before over-molding in photovoltaic junction boxes introduces a dielectric tape application that must tolerate low-surface-energy backsheets and long-term damp heat. NT-5513 is wrapped around junction box cable bundles to hold them in place during the potting cure cycle. The backsheet surface is corona-treated to at least 42 mN/m immediately before tape application. The tape is applied with 50% overlap at a thickness of 0.2–0.3 mm over the bundle. The adhesive must retain shear strength at module operating temperatures up to 85 °C and after 1,000 h damp heat per IEC 60068-2-78. Terminal module qualification is governed by IEC 61730 insulation requirements. The tape is not a replacement for the potting compound but prevents cable movement during the 15–30 min cure cycle at 80–100 °C. Acetic acid-cure silicone potting compounds can promote adhesion loss at the tape-backsheet interface; a neutral-cure silicone is preferred. Application below 5 °C is not recommended because high tack acrylic adhesives lose wet-out on textured backsheet surfaces. Published data for NT-5513 in this specific photovoltaic construction is limited; validation with the actual backsheet grade, corona treatment level, and potting compound is required.
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Dielectric Polymers NT-5513 High Tack Tape is a pressure-sensitive adhesive transfer film supplied in roll form for lamination and pre-tacking of electrically insulating polymer films, metal foils, and low-surface-energy substrates in flexible printed circuit, membrane switch, motor, transformer, and coil insulation assemblies. The product is most frequently processed as an unsupported acrylic adhesive layer carried on a release liner, which distinguishes it from carrier-based double-coated tapes that retain a polyester or polyimide core. Batch-specific numerical specifications are provided in the current manufacturer’s technical data sheet; the following description identifies the construction, test method designations, processing limits, and the boundaries that separate this high-tack adhesive system from standard acrylic, rubber-resin, and silicone pressure-sensitive adhesive products.
The high-tack character is achieved through control of the acrylic adhesive mass rather than through the addition of a carrier film. A relatively high resin-to-polymer ratio, reduced crosslink density, and a glass transition temperature adjusted for room-temperature wet-out produce rapid initial adhesion to stainless steel, copper, polyimide, polyester, and many treated polymer films. Peel adhesion is characterized by ASTM D3330/D3330-02 at 180° peel, loop tack by ASTM D6195-03, and static shear holding power by ASTM D3654/D3654-06. Because the exact numerical values vary by lot, adhesive thickness, liner type, and substrate, incoming inspection should compare the manufacturer’s published values with measured data rather than relying on a single nominal adhesive strength.
The unsupported construction removes the 12–25 µm polyester carrier common in many electrical tapes, reducing total stack thickness and eliminating carrier-borne dielectric loss. That reduction is useful in thin flexible circuits and high-winding-density motor insulation, but it also removes the dimensional stability contributed by a carrier. On a slitter/rewinder with differential rewinding and closed-loop tension control, adhesive squeeze-out, telescoping, and liner fracture have been observed when liner release exceeds 60 g/25 mm at the die-cutting station or when line speeds above 30 m/min are used without anti-static neutralization and edge guide adjustment. Unsupported transfer films can stretch and transfer adhesive stringers if the liner is peeled too quickly during manual placement or rework.
For lamination to polyimide or polyester films, corona pre-treatment or chemical priming is generally required when the substrate surface energy is below 38 mN/m. Surface treatment can be checked by wetting tension measurement according to ASTM D2578 or contact angle measurement according to ASTM D5946. The adhesive builds room-temperature adhesion over 24 h to 72 h; initial tack is high, but cohesive strength develops more slowly than in UV-cured acrylic systems. Process validation should include dwell time before die-cutting or routing because fresh laminates can exhibit edge ooze when adhesive mass thickness exceeds 125 µm.
Incoming material should be stored at 10–32 °C and 40–60 % RH within the shelf life stated by the manufacturer. Cold storage below 10 °C can stiffen the adhesive mass and change liner release; rolls should be conditioned at room temperature for 24 h before converting. If rolls are removed from cold storage and opened immediately, condensation can form at the adhesive-liner interface and produce visible hazing and local peel reduction. Moisture exposure at 85 °C and 85 % RH for 1000 h, a common electronics qualification condition, can reduce peel adhesion and increase the dissipation factor of the bonded stack. Pre-drying of hygroscopic films before lamination is required at storage or processing relative humidity above 60 % RH; failure to pre-dry polyimide or release liners may create bubbles and reduce dielectric uniformity in the final laminate.
The defining requirement is not peel strength alone. The adhesive must be evaluated for ionic cleanliness, controlled outgassing, and compatibility with insulating films after thermal aging. Electrical-grade pressure-sensitive adhesive tapes are commonly characterized under ASTM D1000-17. Dielectric breakdown of the bonded stack is measured by ASTM D149-20 or IEC 60243-1:2013. An unsupported adhesive layer of this type contributes little to dielectric strength unless it is used to bond an insulating film to a metallic conductor; the final dielectric performance is therefore substrate-dependent. A high-tack adhesive layer that would pass dielectric testing as part of a polyimide-copper laminate should not be assumed to provide the same electric strength when used alone or with a thinner film.
Volume and surface resistivity are relevant when the adhesive is positioned between conductors or used in high-humidity environments. Conditioning at 23 ± 2 °C and 50 ± 5 % RH under ASTM D257-14 provides comparative insulation data. High-tack acrylic systems containing polar acid groups or resin ester modifiers can absorb moisture and show lower surface resistivity than low-acid acrylic or silicone systems. This is a measurable trade-off between aggressive tack and electrical behavior. When the tape is used for pre-tacking coverlay films to patterned copper before final press lamination, it reduces coverlay drift during assembly, but the adhesive should not be treated as the sole dielectric barrier after thermal cure unless the bonded stack is tested as a completed assembly.
In motor insulation, the product may be inserted between magnet wire and slot liner to hold the slot liner during winding. Solvent-borne varnishes may partially plasticize the high-tack acrylic surface and cause localized detachment. Compatibility should be checked by varnish immersion and cured-stack dielectric testing, because a bond that is acceptable before varnish impregnation may not remain dimensionally stable after thermal curing. In sealed electronics, outgassing characteristics may be evaluated using ASTM E595-15 at 125 °C under vacuum. Common aerospace acceptance limits of less than 1.0 % total mass loss and less than 0.1 % collected volatile condensable material are not product-specific and should be verified against the current lot data for NT-5513.
| Property | Test method | Condition or measurement | Relevance to NT-5513 processing |
|---|---|---|---|
| 180° peel adhesion | ASTM D3330/D3330-02 | Stainless steel panel, specified dwell time | Quantifies bond formation to metal foil, rigid substrates, and prepared films |
| Loop tack | ASTM D6195-03 | Stainless steel or polyimide panel | Indicates rapid wet-out for high-speed lamination start-up |
| Static shear holding power | ASTM D3654/D3654-06 | Isothermal at 70 °C or 93 °C, 1 kg load | Indicates resistance to creep under coil winding or flex-circuit stress |
| Dielectric breakdown voltage | ASTM D149-20 | Electrode geometry per method; oil immersion optional | Evaluates final bonded insulation stack, not adhesive alone |
| Electric strength | IEC 60243-1:2013 | Short-time or step-up voltage | International compliance for electrical insulation assemblies |
| Outgassing | ASTM E595-15 | 125 °C under vacuum | Used for sealed or aerospace electronics when volatile condensables are restricted |
| Adhesive thickness | ASTM D3652/D3652M-20 | Thickness measurement including liner; adhesive mass reported separately | Controls final bond line and stack height in thin flexible circuits |
Batch-to-batch variation in adhesive mass thickness, liner release, and residual monomer can shift peel values more than the difference between two product grades. For this reason, incoming inspection should record roll number, adhesive coat weight by differential weighing or solvent extraction, liner release by ASTM D3330/D3330-02, and measured adhesive thickness. Published batch-specific data for this unsupported construction are limited; the manufacturer’s current technical data sheet remains the appropriate source for exact numerical specifications. When compliance documentation requires a recognized component, the tape may be evaluated under UL 510 or as part of an insulation system rather than as a standalone dielectric.
The high-tack acrylic adhesive mass is not a crosslinked silicone. It is generally unsuitable for continuous exposure above 150 °C unless the assembly is mechanically clamped and tested for adhesive ooze, outgassing, and loss of lap shear. Ketone, ester, and aromatic hydrocarbon solvents used during stencil cleaning or defluxing can plasticize the adhesive and reduce peel strength within 2 h of immersion or heavy wiping. Solvent-wipe compatibility should be evaluated under the intended production wipe pressure and solvent type rather than inferred from generic chemical resistance charts. Some fluorinated cleaning solvents may be less aggressive, but their effect on the resin tackifier and the adhesive-liner interface should still be confirmed.
Silicone contamination is a particular boundary for high-tack acrylic transfer films. If the assembly line also processes silicone-coated release liners or silicone conformal coatings, low-molecular-weight siloxane migration can deposit on the acrylic surface and lower subsequent adhesion to polyimide or copper. On mixed lines, segregated tooling and liner handling are required. The same constraint applies when the tape is used adjacent to silicone rubber parts; plasticizer or free siloxane migration into the adhesive can cause interfacial failure at the adhesive-substrate boundary. Silicone pressure-sensitive adhesives may maintain adhesion across a wider temperature range, but they can create the same contamination risk that subsequent conformal coating or wire bonding processes cannot tolerate.
Adhesive ooze from the cut edge can occur within 48 h when laminate temperature exceeds 40 °C. Laser converting of unsupported transfer films and polyimide laminates requires control of focal power and heat-affected zone because acrylic adhesive vaporization can leave carbonized residue that raises contact resistance if not removed. Plotters, matched-metal die stations, and laser systems should be validated for edge adhesive flow. Differential release liner systems may be used so that the tighter release side remains in place during die-cutting while the easier release side is removed during lamination. A change from polyethylene-coated kraft to polyester liner can alter die-cut edge quality even when the adhesive mass is unchanged.
Relative to a carrier-based double-coated polyester tape, NT-5513 eliminates the 12–25 µm polyester carrier. The trade-off is that the unsupported adhesive cannot be die-cut with the same dimensional accuracy unless liner release and adhesive cohesion are tightly controlled. Carrier-based tapes maintain their outline during manual placement and rework; unsupported transfer films can distort when the liner is removed too rapidly. Relative to low-tack acrylic transfer films, the high-tack system exhibits higher loop tack and faster wet-out on textured polyimide or metal surfaces but may show lower shear holding power at 70 °C under 1 kg load. This difference matters in coil winding or spring-loaded contacts where creep force is continuous.
Compared to rubber-resin high-tack adhesives, the acrylic system offers better ultraviolet and oxidative stability but less aggressive initial grab on polyolefin surfaces unless corona or primer is used. Rubber-resin systems may yield high tack with lower cost, but they typically have greater outgassing and poorer thermal aging above 80 °C. Compared to silicone pressure-sensitive adhesives, the acrylic high-tack system is less suitable for continuous use above 200 °C and for bonding silicone-coated surfaces; however, it avoids the silicone contamination risk that can impair conformal coating adhesion in printed circuit board assembly. In thickness-sensitive applications such as multi-layer flex circuits, a 25 µm unsupported high-tack adhesive layer may be used instead of a 50 µm double-coated tape because the removed carrier layer can reduce total stack height without reducing the bond area. The final dielectric suitability is determined by the adhesive mass thickness, the presence of residual solvent, and the dielectric properties of the bonded film rather than by the adhesive designation alone.