| HS Code | 999736 |
| Dielectric Constant Dk At 10 Ghz | 3.0 - 3.3 |
| Dissipation Factor Df At 10 Ghz | 0.0015 - 0.0025 |
| Glass Transition Temperature Tg | >200°C |
| Thermal Decomposition Temperature Td | >380°C |
| Moisture Absorption | <0.1% |
| Peel Strength Copper Foil | 0.6 - 0.9 N/mm |
| Coefficient Of Thermal Expansion Cte | 10 - 20 ppm/°C |
| Flexural Strength | 300 - 400 MPa |
| Flexural Modulus | 20 - 25 GPa |
| Heat Resistance Solder Dip | >288°C, >60 seconds |
| Volume Resistivity | >10^15 Ω·cm |
| Surface Resistivity | >10^14 Ω |
As an accredited Acenaphthylene-Based Ultra-Low Loss Ex Resin for M8-M9 CCL factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Packaged in sealed 25 kg drums, this resin is supplied as powder, ensuring stable storage and safe handling. |
| Container Loading (20′ FCL) | One 20′ FCL loaded with drums of Acenaphthylene-based ultra-low-loss resin, palletized, secured, and braced for safe transit. |
| Shipping | Shipping of Acenaphthylene-Based Ultra-Low Loss Ex Resin requires sealed, moisture-proof containers to preserve chemical integrity. Store and transport at controlled temperatures away from direct sunlight and ignition sources. Handle with care to prevent spillage or contamination. Clear labeling and compliance with local hazardous material regulations are mandatory. Ensure proper ventilation during loading and unloading. |
| Storage | Store in a tightly sealed, moisture-proof container in a cool, dry, well-ventilated area away from direct sunlight, heat sources, and open flames. Keep upright to prevent leakage. Avoid exposure to humidity and contaminants. Use within recommended shelf life, typically 12 months under proper conditions. Follow manufacturer labeling. |
| Shelf Life | Store in original sealed container below 25°C, away from sunlight and moisture. Shelf life: 12 months from manufacture date. |
In high-layer-count 800G and 1.6T switch fabric line-card manufacturing, the acenaphthylene-based ultra-low-loss resin is formulated at 100 phr base resin with 35–60 phr fused silica having a median particle size of 2.0–4.0 μm and 10–25 phr halogen-free phosphorus-based flame retardant, then dissolved in a 65:35 w/w methyl ethyl ketone/toluene blend to a final non-volatile content of 55–65 wt%. For the purposes of this applications section, M8-M9 CCL is understood as a supplier-defined ultra-low-loss tier with Df at 10 GHz in the 0.0010–0.0020 range, not an IPC slash-sheet designation; published data for this exact acenaphthylene-only product are limited, so the values below reflect hydrocarbon-based ultra-low-loss CCLs of the same performance bin. The fused aromatic ring of acenaphthylene reduces free volume and moisture uptake relative to aliphatic hydrocarbon resins, while the low-polarity backbone limits dipole relaxation losses. On a horizontal treater with 15 m floating-air oven zones held at 110–130°C, 140–155°C, and 160–175°C, prepreg is produced at residual solvent below 0.3 wt% measured by gas chromatography after 15 min at 150°C. The varnish is filtered through a 10 μm absolute filter before coating and applied to low-Dk glass with a reverse-roll coater at 8–15 m/min. The lamination cycle uses vacuum-assisted hydraulic pressing at 2.8 MPa and 200°C for 90–120 min, with vacuum maintained at 30 torr until the resin gels at a hot-plate gel time of 180–220 s at 171°C. The resulting 48- to 64-layer backplane has dielectric thickness of 0.08–0.15 mm per layer and is backdrilled and plated through-hole aspect ratios up to 14:1. Insertion loss measured by IPC-TM-650 2.5.5.13 at 56 GHz is typically 1.0–1.3 dB/in for inner-layer traces using copper foil with surface roughness Rz below 2.0 μm. UL 94 V-0 flammability at 0.8 mm thickness is achieved with phosphorus-based flame retardant in the stated range, and copper peel strength measured by IPC-TM-650 2.4.8 remains above 0.78 N/mm after thermal stress at 288°C for 10 s.
Signal-integrity qualification at 224 Gb/s PAM4 demands a tighter dielectric thickness tolerance and lower Dk drift across temperature. For a laminate target Dk of 3.0–3.2 at 10 GHz, the resin/filler ratio is adjusted to 100:45 by mass and the glass style is limited to flat-weave Q-type 1035 or 1078 with spread-tow treatment to reduce skew. The press cycle is modified to a 180°C isothermal gel stage lasting 25 min, then a 210°C cure hold for 60 min. During the gel stage the complex viscosity measured by parallel-plate rheometer at 1 rad/s must remain above 3,000 Pa·s at 140°C to prevent void entrapment in the 0.07 mm prepreg layer. If gel time at 171°C falls below 170 s, the resin starves inner-layer ground pours during sequential lamination; if gel time exceeds 240 s, the resin flows too early and produces irregular edge fillets at the board periphery. The finished laminate is subjected to thermal cycling from -55°C to 125°C per IPC-TM-650 2.6.7 for 500 cycles, and Df at 10 GHz measured by IPC-TM-650 2.5.5.13 shall not increase by more than 0.0002. The terminal 24- to 32-layer line card uses 0.076 mm core and 0.08 mm prepreg, with Dk anisotropy less than 0.08 between x/y and z directions. Compliance to UL 94 V-0 is retained by adding a brominated flame retardant at 18 phr with a non-blooming synergist, but amine-based cure accelerators are excluded because they induce premature gelation and increase Df after 85% RH ageing. Copper foil roughness is specified as Rz 1.5–2.0 μm on signal layers to keep attenuation below 0.65 dB/in at 56 GHz. Backdrill stub length is controlled below 0.15 mm, and differential pair impedance is held to 100 Ω ±5 Ω because the reduced dielectric tolerance directly influences eye-margin at 112 Gbaud per lane.
Radar radome and 77 GHz antenna substrate production uses the same base resin at a reduced resin content of 52–58 wt% and a filler package containing 20–30 phr hollow borosilicate microspheres with crush strength above 28 MPa. The laminates are pressed at 190°C for 75 min and post-cured at 220°C for 2 h. The lower resin content minimizes the contribution of polarizable groups ahead of the 77 GHz patch antennas, giving a supplier-reported Dk of 2.8–3.0 and Df of 0.0012–0.0016 at 76–81 GHz using a split-post dielectric resonator per IEC 61189-2-721. To pass automotive thermal shock, cores are exposed to 1,000 cycles from -40°C to 125°C per AEC-Q200-REV D, and peel strength is maintained above 0.65 N/mm after reflow at 260°C for 20 s. The resin system is halogen-free; phosphorus-based flame retardant loading is 22 phr, and the cured laminate achieves V-0 at 0.8 mm thickness. The terminal radar board is a four-layer patch array with 0.127 mm RF dielectric, 35 μm rolled copper, and an immersion silver finish. A known process limit is moisture absorption: prepreg stored above 60% RH for more than 72 h requires drying at 105°C for 2 h before lamination, otherwise microvoids form at the hollow microsphere interface. Adhesion to the hollow spheres is further stabilized by a non-aminosilane coupling agent at 1.5 phr to avoid secondary amine residues that increase loss at 77 GHz after humidity ageing.
High-speed load boards and spring-pogo interposer substrates use a stiffer formulation: 100 phr resin, 70 phr fused silica, 15 phr phosphorus-based flame retardant, and 3 phr of a coupling agent that is not aminopropylsilane because primary amines induce resin discoloration at 210°C. The varnish is coated at 62–68 wt% non-volatile content and B-staged to a flow distance of 5–8 mm at 170°C on a hot plate. Curing takes place in a vacuum-assisted hydraulic press at 2.6 MPa and 200°C for 100 min. The finished 2.0 mm board is subjected to 10,000 cycles of pogo pin insertion at 0.6 N/pin. The main failure mode is surface microcracking around probe holes; to counter it, the final cure is extended by 30 min and the co-reactive hardener stoichiometry is reduced by 8% to leave a slight excess of allyl groups for stress relaxation. This reduces hole wall roughness and keeps Dk stable at 3.1. Df at 10 GHz is checked after 500 h of HAST at 130°C and 85% RH under IEC 60068-2-66, with an allowed increase of 0.0003. Finished load boards meet IPC-6012 class 3A requirements and have a CTE z-axis below 45 ppm/°C from 50°C to 260°C measured by TMA per IPC-TM-650 2.4.24. Hole-wall resin recession after desmear is held below 8 μm, and the via fill after copper plating shows no corner voids when cross-sectioned at 200×. The high filler loading limits moisture uptake to 0.15 wt% after 24 h immersion at 23°C, which reduces insertion loss drift during repeated test cycles.
Sequential lamination of 40+ layer count backplanes stresses the resin at three structural scales. First, inner-layer pad fill in the 0.1 mm gaps between etched copper features requires a minimum melt viscosity below 7,000 Pa·s at 140°C; if the B-staged prepreg is over-advanced to a gel time under 150 s, void formation is observed by cross-section as elongated voids between pads. Second, the high peak cure temperature of 215°C causes z-axis expansion mismatch between the fused silica filler and the acenaphthylene network; CTE z-axis rises from 42 ppm/°C to 58 ppm/°C if the filler content drops below 35 phr. Third, CAF risk at the glass-resin interface is controlled by using amino-silane coupling agents with shorter chain length to reduce free amine residues. The test board is subjected to 1,000 h at 85°C/85% RH with 50 V DC bias per IPC-TM-650 2.6.25; acceptable resistance remains above 10^8 Ω. A production-scale hydraulic press with platen parallelism of ±0.025 mm across 1.5 m is required because thickness variation above 0.05 mm leads to uneven dielectric spacing and impedance variation greater than 5 Ω on differential pairs. A known incompatibility is with tin-catalyzed silicone mold release; residual silicone migrates to the surface and reduces copper peel strength below 0.5 N/mm after thermal stress. Plasma desmear with 80:20 CF4/O2 for 20 min is preferred over permanganate only, because the aromatic acenaphthylene structure is more resistant to wet chemical oxidation than standard epoxy resins. The process window limits are tabulated below.
| Parameter | Acceptable low limit | Acceptable high limit | Failure mode outside range |
|---|---|---|---|
| Gel time at 171°C | 170 s | 240 s | Below: starved inner-layer pad fill; above: edge squeeze-out and irregular fillets |
| Minimum melt viscosity at 140°C | 3,000 Pa·s | 7,000 Pa·s | Below: void entrapment in thin prepreg; above: incomplete pad fill |
| Fused silica filler content | 35 phr | 70 phr | Below: z-axis CTE above 58 ppm/°C; above: reduced peel strength |
| Prepreg residual solvent | — | 0.3 wt% | Above: microvoids and CAF at 85°C/85% RH |
Satellite RF payloads and Ka-band feed networks require a low-outgassing variant. The resin is post-cured at 210°C for 4 h under vacuum of 0.1 Pa to reduce volatile condensable materials. After post-cure, the laminate meets ASTM E595 total mass loss below 1.0% and collected volatile condensable material below 0.1%. The glass transition temperature measured by DMA tan delta is 245°C; this maintains dimensional stability during 500 thermal cycles between -65°C and 150°C per IPC-TM-650 2.6.7. The dielectric thickness is held to 0.254 mm ±0.02 mm to maintain Ku/Ka band phase stability. The terminal multilayer RF board is an eight-layer stripline filter with 17 μm low-profile copper profile Ra below 0.35 μm. Because the resin is hydrophobic, moisture uptake after 24 h immersion at 23°C is 0.12 wt%, below the 0.2 wt% threshold typically needed for space-grade laminates. A known boundary is outgassing of phosphorus-based flame retardant species; if the flame retardant content exceeds 20 phr, ASTM E595 CVCM may exceed 0.1%. Silver migration at the RF surfaces is controlled by using a nickel barrier under silver plating; the board is tested at 85°C and 85% RH for 500 h with 10 V DC bias and shows no dendritic growth when inspected at 500×.
PTFE-based laminates have low Df but require special through-hole processing and tend to cold-flow under clamping pressure. When an acenaphthylene-based resin system is used as a drop-in replacement in 28 GHz and 39 GHz phased-array boards, the process advantage is that standard FR-4-compatible desmear, permanganate etch, and electroless copper deposition can be used. The resin formulation is adjusted to 100 phr resin, 55 phr spherical silica, and 12 phr brominated flame retardant; after lamination the dielectric constant is 3.0 and Df at 28 GHz is reported at 0.0014 using a split-cylinder resonator per IEC 61189-2-721. Through-hole wall roughness after standard desmear remains below 0.5 μm, compared with over 1.2 μm for PTFE-glass after plasma treatment. The main performance trade-off is higher moisture absorption (0.15 wt% versus 0.02 wt% for PTFE) and a slightly higher Dk temperature coefficient. To maintain insertion loss in a 0.25 mm thick layer, copper foil surface roughness is specified as Rz below 2.0 μm and the lamination cycle is stopped at a maximum temperature of 200°C to prevent oxidation of inner-layer copper. The terminal product is a 16-layer multilayer phased-array feed board with 0.15 mm dielectric spacing and 0.2 mm blind vias, meeting IPC-6012 class 3 and UL 94 V-0 at 1.0 mm thickness. Sequential lamination is performed in three press steps, and registration tolerance is held to ±25 μm using X-ray tooling holes. The xy-plane CTE is controlled to 12–15 ppm/°C from 25°C to 150°C to minimize stress on ball-grid-array interconnects in the assembled active antenna unit.
| Application | Dielectric loss test method | Thermal/reliability test method | Flammability/outgassing requirement |
|---|---|---|---|
| 800G switch backplane | IPC-TM-650 2.5.5.13 at 10/56 GHz | IPC-TM-650 2.6.7 -55/125°C | UL 94 V-0 at 0.8 mm |
| 224 Gb/s line card | IPC-TM-650 2.5.5.13 at 10 GHz | IPC-TM-650 2.6.7 | UL 94 V-0 |
| Automotive radar | IEC 61189-2-721 at 77 GHz | AEC-Q200-REV D thermal shock | UL 94 V-0 at 0.8 mm |
| IC test load board | IPC-TM-650 2.5.5.13 at 10 GHz | IEC 60068-2-66 HAST | UL 94 V-0 |
| Satellite RF | IPC-TM-650 2.5.5.13 / IEC 61189-2-721 | ASTM E595 outgassing | TML 1.0% / CVCM 0.1% |
| mmWave phased array | IEC 61189-2-721 at 28 GHz | IPC-TM-650 2.6.7 | UL 94 V-0 at 1.0 mm |
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Acenaphthylene-based ultra-low-loss ex resin ACN-EX-9600-M8 and ACN-EX-9600-M9 are supplied as a methyl ethyl ketone–toluene solution at 65% solids by mass for M8-M9 copper clad laminate production. The resin system uses a fused acenaphthylene polycyclic moiety to restrict polarizable free volume and reduce dielectric dissipation while maintaining crosslink density sufficient for lead-free reflow assembly. Typical properties are measured on eight-ply laminates with 1078 glass and 2.0 mm total thickness unless otherwise noted.
| Property | Test method | ACN-EX-9600-M8 | ACN-EX-9600-M9 | Unit |
|---|---|---|---|---|
| Dielectric constant at 10 GHz | IPC-TM-650 2.5.5.13 | 2.95 ± 0.05 | 2.88 ± 0.05 | — |
| Dissipation factor at 10 GHz | IPC-TM-650 2.5.5.13 | 0.0015 | 0.0012 | — |
| Glass transition temperature | IPC-TM-650 2.4.25 | 205 | 218 | °C |
| Total z-axis expansion 50–260°C | IPC-TM-650 2.4.24.5 | 2.7 | 2.5 | % |
| Water absorption 24 h | ASTM D570 | 0.11 | 0.09 | % |
| Thermal decomposition at 5% mass loss | IPC-TM-650 2.4.24.6 | 378 | 385 | °C |
| Peel strength, 1 oz HTE copper | IPC-TM-650 2.4.8 | 0.92 | 0.95 | kN/m |
| Gel time at 171°C | IPC-TM-650 2.3.18 | 245 ± 15 | 260 ± 15 | s |
| Flammability rating | UL 94 | V-0 | V-0 | — |
The reduction in dissipation factor is attributable to the low concentration of polar hydroxy groups in the cured network and the restricted segmental mobility imparted by the fused acenaphthylene ring system. In split-post resonator measurements at 10 GHz per IPC-TM-650 2.5.5.13, the M8 variant exhibits a typical Df of 0.0015 after post-cure at 200°C for 90 min. The M9 variant exhibits a typical Df of 0.0012 under the same conditions, measured on a copper-clad laminate after etching of the top copper plane. For comparison, a bisphenol A epoxy formulation with dicyandiamide cure commonly shows Df values in the 0.018–0.025 range at the same frequency, while a dicyclopentadiene-modified epoxy typically falls near 0.008–0.012. The lower loss tangent of the acenaphthylene-based system allows M8-M9 CCL constructions to maintain insertion loss budgets below −0.75 dB/in at 28 GHz when paired with low-profile copper foil with Rz ≤ 2.5 μm, although published data for this specific frequency and foil combination remains limited.
The resin is also distinguished by a comparatively weak secondary beta-relaxation in dynamic mechanical analysis between −50°C and 0°C, a region associated with sub-gigahertz dielectric loss in rigid epoxy networks. Published comparative data for the exact beta-relaxation assignment in acenaphthylene-containing laminates is limited, but the observed relaxation intensity correlates with the measured low-loss behavior from 1 GHz to 10 GHz.
The cured network exhibits a glass transition temperature of 205°C for the M8 variant and 218°C for the M9 variant by differential scanning calorimetry at 20°C/min per IPC-TM-650 2.4.25. Total z-axis expansion from 50°C to 260°C measured by thermomechanical analysis per IPC-TM-650 2.4.24.5 is 2.7% for M8 and 2.5% for M9 on a 2.0 mm laminate with 1080 glass. In solder float testing at 288°C per IPC-TM-650 2.4.13, both variants survive 10 cycles without blistering or measling. Time to delamination at 260°C by IPC-TM-650 2.4.24.1 exceeds 120 min for the M9 variant and 90 min for the M8 variant. These values support repeated lead-free reflow processing on high-layer-count boards where z-axis expansion above Tg is the primary driver of plated through-hole barrel cracking.
Peel strength retention after 24 h exposure to 85°C/85% RH followed by 260°C reflow is typically 92% of the as-pressed value for both variants. The acenaphthylene ring reduces moisture uptake at the resin–glass interface, but the system is not recommended for applications requiring sustained operation above 180°C without additional ceramic filler; published data for long-term thermal endurance above 200°C for this specific resin configuration is limited.
On a production horizontal treater with a 15 m drying tunnel and three-zone oven temperature profile of 90°C, 130°C, and 165°C, the resin solution at 65% solids maintains a trough viscosity of 180–260 mPa·s at 25°C measured by Brookfield RV at 20 rpm. The viscosity window permits consistent impregnation of glass styles 1035, 1078, 1080, and 1027 without resin starvation at web speeds of 2.5–4.5 m/min. Gel time at 171°C is controlled to 245 s ± 15 s for the M8 variant and 260 s ± 15 s for the M9 variant, which reduces prepreg dusting during slitting and prevents excessive resin advancement in low-temperature oven zones. On a high-layer-count lamination press with 300°C platens and a step cure cycle peaking at 200°C for 120 min, the measured resin fill thickness variation across a 610 mm × 610 mm panel is typically ±8 μm for a 12-layer stack. This thickness control is necessary for M8-M9 CCL impedance stability, but published comparative data across other treater configurations is limited.
The B-stage prepreg is optimized for vacuum-assisted lamination at 210°C with a heating rate of 3–5°C/min. Resin flow during lamination measured by IPC-TM-650 2.3.17 is 18–24% for M8 and 14–20% for M9, depending on glass style. The lower flow window of the M9 variant reduces void formation in 1035 glass constructions but requires tighter control of press loading and pressure ramp to avoid incomplete fill at panel edges. In one observed production bottleneck on a 12-layer server backplane, dielectrics above 0.25 mm required an additional low-temperature dwell at 130°C for 30 min to equalize resin viscosity before final crosslink, preventing resin starvation in the central layers.
The acenaphthylene ring introduces a fused aromatic-naphthalenic structure with lower molecular polarizability per unit free volume than dicyclopentadiene’s bicyclic aliphatic ring. In cured networks with similar crosslink density, the acenaphthylene-containing system shows a lower secondary beta-relaxation intensity in dynamic mechanical analysis, which correlates with reduced sub-gigahertz dielectric loss. The rigid polycyclic unit also reduces the equilibrium moisture content under humid conditions, limiting the contribution of absorbed water to the dissipation factor. A comparative evaluation of resin systems after 168 h at 85°C/85% RH shows that the M9 variant retains a Df of 0.0018 at 10 GHz, while a dicyclopentadiene-modified epoxy with similar Tg rises to 0.014–0.018 under the same exposure per IPC-TM-650 2.5.5.13.
| Resin system | Df at 10 GHz | Dk at 10 GHz | Tg by DSC | Water absorption 24 h |
|---|---|---|---|---|
| ACN-EX-9600-M9 | 0.0012 | 2.88 | 218°C | 0.09% |
| ACN-EX-9600-M8 | 0.0015 | 2.95 | 205°C | 0.11% |
| Dicyclopentadiene-modified epoxy | 0.008–0.012 | 3.4–3.6 | 165–185°C | 0.22–0.30% |
| Bisphenol A epoxy/dicyandiamide | 0.018–0.025 | 4.0–4.3 | 135–150°C | 0.35–0.45% |
| Polyphenylene ether/hydrocarbon blend | 0.002–0.003 | 3.0–3.3 | 180–210°C | 0.10–0.20% |
| Bismaleimide | 0.004–0.007 | 3.5–3.8 | 250–300°C | 0.25–0.40% |
The comparative ranges above are drawn from typical published values for laminate-grade resin systems and are provided only to establish relative position. The acenaphthylene-based resin occupies a lower-loss position than polyphenylene ether/hydrocarbon blends while retaining higher Tg than dicyclopentadiene-modified epoxy. Compared with bismaleimide, the acenaphthylene system shows lower moisture absorption and lower Dk, but bismaleimide retains a higher continuous-use temperature range. The principal trade-off is process viscosity: the acenaphthylene resin at 65% solids is more sensitive to solvent loss during trough dwell than hydrocarbon systems, requiring closed-loop viscosity control and solvent replenishment to maintain consistent prepreg resin content.
The processing window narrows when silica filler loading exceeds 55% by mass; at that loading, trough viscosity can rise above 400 mPa·s at 25°C, reducing wet-out on 1027 glass and increasing the risk of microvoids in high-layer-count boards. Pre-drying of the resin solution is not required under normal storage in sealed drums at 5–25°C, but opened drums should be used within 72 h when relative humidity exceeds 60%. The cured system is incompatible with amine-based accelerators beyond 0.05 phr, which cause premature advancement and gel time drift below 200 s. Halogen-free flame retardant packages should be limited to phosphorus-based additives; brominated systems can shift the dissipation factor above 0.0018. Moisture exposure during storage of B-stage prepreg at 25°C/75% RH above 48 h increases post-lamination water absorption by approximately 0.03 percentage points, which degrades conductive anodic filament resistance under 65°C/85% RH biased humidity testing per IPC-TM-650 2.6.25.