| HS Code | 158710 |
| Model Number | WWJF-828 |
| Product Type | Portable WiFi Jammer |
| Brand | WWJF |
| Frequency Band | 2.4GHz - 2.5GHz and 5.1GHz - 5.8GHz |
| Output Power | 20W |
| Jamming Radius | 10-25 meters |
| Input Voltage | AC 100-240V 50/60Hz |
| Antenna Count | 8 |
| Dimensions | 295 x 180 x 65 mm |
| Weight | 1.8 kg |
As an accredited WWJF-828 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | WWJF-828 is packaged in 25 kg fiber drums with double polyethylene liners, sealed and labeled for safe handling. |
| Container Loading (20′ FCL) | WWJF-828 loaded in 20′ FCL, securely packed and labeled, ensuring safe, compliant container loading for chemical transport. |
| Shipping | WWJF-828 ships as a classified hazardous chemical in UN-approved drums or IBCs, with proper labeling, SDS, and segregation from incompatible materials. Transport requires trained handlers, temperature control, and compliant documentation for road, sea, or air. Deliveries are scheduled with real-time tracking and emergency response support to ensure safe arrival. |
| Storage | Store WWJF-828 in a cool, dry, well-ventilated area away from direct sunlight, heat sources, and incompatible substances. Keep the container tightly sealed when not in use and protect from moisture. Follow the Safety Data Sheet for specific temperature limits, and use secondary containment to prevent spills or leaks. |
| Shelf Life | Shelf life: 24 months from manufacture date when stored unopened in a cool, dry place. |
WWJF-828 is supplied as a medium-viscosity liquid diglycidyl ether of bisphenol A (DGEBA) resin, with an epoxide equivalent weight of 184–190 g/eq when determined by ASTM D1652-11e1 and a dynamic viscosity of 11,000–14,000 mPa·s at 25 °C by ISO 3219:1993. Hydrolyzable chlorine content is typically ≤ 0.05%. In 100% solids self-leveling floor formulations, the resin is combined with a cycloaliphatic amine hardener at a stoichiometric ratio of 0.95–1.05 relative to total epoxide equivalents. At a hardener AHEW of 60 g/eq, the undiluted resin addition is 31.5–33.0 phr per 100 phr WWJF-828; when 8–12 phr of C12–C14 alkyl glycidyl ether reactive diluent is used to reduce mixed viscosity into the 1,000–1,800 mPa·s range, hardener dose is recalculated against the diluted EEW and rises to 33.0–36.0 phr. Failure to recalculate after dilution produces under-cured seams with residual amine blush after 24 h. Substrate compliance requires concrete moisture vapor emission ≤ 1.36 kg/24 h·m² under ASTM F1869-16a or internal relative humidity ≤ 75% under ASTM F2170-19a; slabs outside this window risk osmotic blistering at the adhesive interface. Production on industrial lines uses a high-shear disperser at 2,000–2,500 rpm for filler wetting, followed by vacuum de-aeration at -0.09 MPa for 3–5 min. The mixed compound is applied by pin rake at 3–5 mm thickness and spike-rolled to release entrapped air. Pull-off adhesion on blast-cleaned concrete is typically 2.0–3.5 MPa when evaluated by ASTM D4541-17, but the absolute value is substrate-dependent. Flooring systems may be evaluated for classification under EN 13813:2002 and fire reaction under EN 13501-1:2018. End-product types include pharmaceutical cleanroom floors, food processing plant floors, heavy-duty logistics warehouse slabs, and ESD floor surfaces using conductive graphite filler to adjust surface resistivity to 10⁴–10⁶ Ω.
Where WWJF-828 is compounded into one-component heat-cure structural adhesives for e-coated steel and aluminum closure panels, cure onset at 180 °C is controlled by dicyandiamide particle size distribution at 5–7 phr per 100 phr resin. The formulation also contains 0.5–1.5 phr uron accelerator, 2.0–3.0 phr fumed silica, and 5–15 phr carboxyl-terminated butadiene nitrile impact modifier. Premixing on a twin-screw extruder with L/D 24:1 at 40–60 °C is used to disperse dicyandiamide without exceeding the 70 °C threshold where latent hardener dissolution begins. Premature dissolution during compounding produces viscosity rise and localized gel particles before application. Dispensing is performed through pneumatic cartridge systems at 0.4–0.7 MPa with bead diameters of 2.0–3.0 mm. Oven cure at 180 °C for 25–35 min completes chain extension. Lap shear strength on degreased cold-rolled steel is typically 25–32 MPa under ASTM D1002-10; when phosphate pretreatment is omitted and oily steel is bonded, shear values can fall below 10 MPa, which defines the operational boundary of unrefined metal surfaces. Formulation compliance is referenced against EN 1465:2009 for metal-to-metal lap shear and against RoHS Directive 2011/65/EU Annex II thresholds of 0.1 wt% in homogeneous material for Pb, Cd, Hg, Cr(VI), PBB, and PBDE. REACH substance evaluation should be captured at the article level. Downstream production includes automated body-in-white panel bonding, electric vehicle battery tray panel attachment, roof-bow bonding, and metal-to-composite closure panel adhesion.
WWJF-828 filled with 150–250 phr fused silica and 30–60 phr aluminum trihydrate is processed in vacuum planetary mixers at 5–10 mbar to achieve void content below 0.5%. The resin phase is formulated with methylhexahydrophthalic anhydride at 80–90 phr per 100 phr WWJF-828 and 0.3–0.8 phr 1-methylimidazole accelerator. At 25 °C under ISO 3219:1993, filled mixed viscosity is typically 20,000–40,000 mPa·s; casting is therefore limited to modules with clearances not below 1.5 mm, while narrower gaps require heated resin feed at 35–40 °C. The cure schedule of 100 °C for 2 h plus 150 °C for 4 h develops a glass transition temperature of 140–155 °C by ISO 11357-2:2020. Filler pre-drying at 105 °C for 4 h is required when relative humidity exceeds 60%, because the anhydride hardener system is moisture-sensitive and residual adsorbed water before mixing increases hydrolytic degradation during thermal shock. The following table summarizes evaluated control windows for filled and unfilled WWJF-828 encapsulation systems under relevant electrical and thermal cycling protocols.
| Test protocol | Condition | Typical control window |
|---|---|---|
| IEC 60695-11-10:2013 | UL 94 vertical burn, 3.0 mm specimen | V-0 non-dripping class achievable with 150 phr or higher fused silica and 30 phr ATH |
| IEC 60068-2-14:2009 test Na | -40 °C to +125 °C, 1 h transfer, 500 cycles | No delamination or crack growth beyond 0.5 mm on typical non-plated module housings; published data for this specific configuration is limited |
| ISO 11357-2:2020 | DSC second heating, 10 K/min | 140–155 °C glass transition after full post-cure |
| IEC 60243-1:2013 | AC dielectric strength, 2.0 mm specimen | 18–24 kV/mm typical with silica-filled DGEBA formulation |
| ISO 62:2008 | Water absorption, 24 h immersion | 0.2–0.4% typical after complete anhydride cure |
Downstream processing for power electronics uses vacuum casting into assembled IGBT or thyristor housings, followed by oven staging that avoids exothermic overshoot above 160 °C because localized thermal degradation of accelerator residues can increase dissipation factor. End-product types include encapsulated industrial motor drives, power factor correction capacitors, railway traction modules, and medium-voltage sensor housings where dimensional stability after thermal shock is the primary acceptance criterion.
Filament-wound FRP piping lines processing WWJF-828 with 1,6-hexanediol diglycidyl ether as reactive diluent typically operate resin-bath viscosity in the 700–1,100 mPa·s window at 25 °C to avoid dry-spot formation on E-glass roving. The resin formulation at 100 phr WWJF-828, 15–20 phr diluent, and 28–32 phr of an amine hardener package with AHEW 45 g/eq has a gel time of 25–35 min at 80 °C, placing it within the working window of 3-axis filament winding machines running at 30–60 m/min. Fiber tension is maintained at 40–60 N per roving, and mandrel temperature is held at 45–55 °C during winding to reduce resin migration before gelation. Cure is staged at 80 °C for 2 h and 120 °C for 4 h. For 25% sulfuric acid immersion at 23 °C, post-cure at 120 °C is mandatory because residual unreacted oxirane groups accelerate water absorption in acid service; published data for this specific configuration is limited. Pipe systems are evaluated for design and performance under ISO 14692-2:2017 for GRP piping in oil and gas, and filament-wound laminates are tested under ASTM D2996-17 for longitudinal and circumferential properties. The downstream process includes continuous resin bath impregnation, helical winding, and static oven cure. End-product types include chemical process piping, fire water piping, municipal water transport lines, and FRP storage tanks used in corrosive industrial environments.
When WWJF-828 is selected for vacuum-assisted resin transfer molding, the resin is diluted with 10–15 phr of a monofunctional aliphatic glycidyl ether having an EEW of 150 g/eq to bring mixed viscosity into the 300–1,300 mPa·s range at 25 °C. At 100 phr WWJF-828, 10–15 phr diluent, and a cycloaliphatic amine hardener with AHEW 50 g/eq, the hardener addition of 30–32 phr maintains stoichiometric balance against total epoxide equivalents. Degassing under ≤5 mbar for 15–20 min is required before transfer; otherwise dissolved air shortens the 60 °C gel time from 45–55 min to below 35 min and creates porosity in the cured laminate. The vacuum bag is held at 0.08–0.10 MPa and injection pressure is limited to 0.1–0.2 MPa to avoid fiber washing. Process temperature is maintained at 25–30 °C; higher temperatures accelerate cure and shrink the infusion window. Mixed viscosity above 1,300 mPa·s at 25 °C causes dry spot formation and fiber volume fraction below 45% on 600 g/m² biaxial E-glass fabric; flow-front pressure drop before full wet-out can exceed 0.05 MPa. Laminates are tested for tensile properties under ASTM D3039/D3039M-17 and ISO 527-4:2021, with fiber volume fraction determined by ignition loss under ASTM D2584-18 in the 45–55% range. Downstream production uses resin inlet distribution media, continuous degassing, and post-cure at 60 °C for 4 h. End-product types include marine deck panels, wind turbine nacelle covers, composite tooling boards, and transportation side panels.
For embedment depths above 10 db in concrete, WWJF-828-based chemical anchoring formulations filled with 300–500 phr quartz aggregate exhibit compressive strength of 80–100 MPa after 7 days at 23 °C when evaluated under ASTM C579-18 for epoxy mortar compressive strength. The formulation uses 100 phr WWJF-828, 2–5 phr benzyl alcohol as non-reactive viscosity modifier, 18–25 phr of an aliphatic polyamine hardener with AHEW 35 g/eq, and 300–500 phr quartz aggregate. Mixing is carried out with a low-speed paddle mixer at ≤ 300 rpm to prevent air entrapment; static mixer injection is preferred for hole diameters above 20 mm. The concrete substrate must be dust-free and moisture not above 4% by volume. Use in water-filled holes is not recommended because hardener displacement produces interfacial voids. Compliance for bonding fresh or hardened concrete is referenced against ASTM C881/C881M-20a Type I, Grade 2 for gravity fill and EN 1504-6:2006 for anchoring of reinforcing steel bar. Downstream production includes diamond core drilling, compressed-air hole cleaning, dual-cartridge static mixing, and injection at 2–5 °C above dew point. End-product types include rebar dowels, anchor bolts for structural steel, handrail fixings, and seismic retrofit brackets.
Competitive WWJF-828 prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615380400285 or mail to sales2@liwei-chem.com.
We will respond to you as soon as possible.
Tel: +8615380400285
Email: sales2@liwei-chem.com
Flexible payment, competitive price, premium service - Inquire now!
The designation WWJF-828 identifies an unmodified liquid epoxy resin derived from bisphenol A and epichlorohydrin, supplied with a controlled epoxide equivalent weight and hydrolyzable chloride content. The resin is supplied in a form suitable for high-solids coatings, structural adhesives, electrical laminates, and filled composites. The acceptance limits in Table 1 reflect the unmodified bisphenol A/epichlorohydrin resin class; batch certificates should be reviewed for product-specific tolerance because published data for this specific configuration is limited.
| Property | Test Method | Acceptance Range |
|---|---|---|
| Epoxide equivalent weight, g/eq | ASTM D1652-11 | 184–190 |
| Viscosity at 25 °C, mPa·s | ISO 3219:1993 | 11 000–14 500 |
| Gardner color | ASTM D1544-04 | ≤1 |
| Density at 25 °C, g/cm³ | ASTM D4052-22 | 1.16–1.17 |
| Hydrolyzable chloride, ppm | ASTM D1726-11 | ≤300 |
| Water content, ppm | ASTM E203-16 | ≤500 |
| Flash point, °C | ASTM D92-18 | >200 |
The resin does not require pre-drying for most ambient-cure formulations because the water content is below 500 ppm. When WWJF-828 is filled with hygroscopic alumina trihydrate at loadings above 60 phr, the filler should be dried to 0.1% moisture before high-shear dispersion to avoid amine-cured film defects and viscosity drift.
For WWJF-828 with an epoxide equivalent weight of 187 g/eq, stoichiometric amine hardener content is calculated from the amine hydrogen equivalent weight and resin epoxide equivalent weight. Off-stoichiometric cure alters secondary hydroxyl etherification and network topology. Dynamic mechanical thermal analysis performed under ISO 6721-5:2019 on a 2 mm cast plaque heated at 2 K/min from 25 °C to 220 °C shows that a 10% excess of amine hardener lowers the glass transition temperature by 6–12 °C relative to the stoichiometric reference. A 15% deficiency of amine hardener raises the rubber plateau modulus but reduces elongation at break when tested under ISO 527-2:2012, because unreacted oxirane groups do not form a fully continuous network. The resin-homopolymerization onset determined by differential scanning calorimetry under ISO 11357-2:2020 at 10 K/min is near 240 °C for the neat resin, which limits hot-melt pre-cure and B-staging operations below 150 °C when a latent accelerator is present.
In ambient-cure protective coatings, WWJF-828 is normally formulated with a polyamide or cycloaliphatic amine hardener at a stoichiometric ratio of 0.95–1.05. Pot life measured by viscosity doubling at 23 °C under ISO 2555:2018 ranges from 25 min to 45 min for fast cycloaliphatic amine systems; polyamide adduct systems extend the working time to 60–120 min. High-shear dispersion of pigments is performed before hardener addition because the resin viscosity at 25 °C is sufficient to wet titanium dioxide at a pigment volume concentration of 15–20% without added solvent. The addition of xylene reduces viscosity for airless spray application but increases volatile organic compound test values under ASTM D2369-20.
Substitution of a 450–550 g/eq solid bisphenol A epoxy resin with WWJF-828 reduces the solvent demand for a 70% nonvolatile coating. In a high-solids alkyd-modified system, the lower resin viscosity at 25 °C permits a reduction in methyl isobutyl ketone content from 22% to 12% by mass without exceeding 2 500 mPa·s at application temperature. The dried film exhibits a Köhler pendulum hardness at 7 days of 120–140 s when tested under ISO 1522:2006, compared with 90–110 s for the solid resin control at equivalent total binder mass. The trade-off is longer tack-free time because the monomeric resin requires additional solvent evaporation and amine reaction before surface skin formation. The dilution limit should be re-established by viscosity profiling under ISO 2884-2:2003 when changing between by-the-gallon and continuous hot-spray lines.
For FR-4 glass-epoxy laminate manufacturing, ionic content affects long-term electrical reliability more than initial viscosity. WWJF-828 is evaluated after B-staging with dicyandiamide and 2-methylimidazole accelerator. The hydrolyzable chloride limit of ≤300 ppm remains below the threshold associated with conductive anodic filament formation in 85 °C/85% RH bias testing per IPC-TM-650 2.6.25. Prepreg gel time on a hot plate at 171 °C is typically 120–180 s when formulated with 2–4 phr dicyandiamide and 0.1–0.3 phr accelerator. Copper-clad laminates pressed at 185 °C for 90 min under 10 MPa exhibit a solder float delamination time exceeding 300 s at 288 °C when tested per IPC-TM-650 2.4.13.1, provided prepreg volatile content is kept below 0.5% before layup.
Viscosity at 25 °C places WWJF-828 near the upper limit for vacuum-assisted resin transfer molding unless mold temperature is raised to 35–40 °C. At 40 °C, dynamic viscosity under ISO 2884-2:2003 decreases to 1 500–2 200 mPa·s, allowing flow through a 600 g/m² biaxial glass fabric at a flow front velocity of 0.5–1.5 cm/min under 100 kPa vacuum. For a 2 m part length, fill time is governed by Darcy permeability and resin gel time; gel time at 40 °C must exceed 120 min to complete infusion before gelation. Adding 10 phr fumed silica raises viscosity to 8 000–12 000 mPa·s at 25 °C, which exceeds the practical limit for gravity feed but remains acceptable in pressure injection with press ratings above 5 bar. Vacuum degassing of the filled resin for 15–20 min at 5–10 kPa is required to avoid porosity; dissolved gas removal is slower than with reactive diluent-modified systems because of the higher initial viscosity. Processing temperatures above 60 °C should not be used with latent boron trichloride amine accelerators, because the resulting exotherm can reduce pot life below 15 min.
Because WWJF-828 contains no reactive diluent, the cured adhesive retains a higher glass transition temperature than a 160–170 g/eq butanediol diglycidyl ether-modified resin when both are cured with polyetheramine D230 at a stoichiometric ratio of 1.00. Lap shear strength on degreased aluminum substrates after 7 days at 23 °C under ISO 4587:2003 is in the range 12–16 MPa for the unmodified resin, while the diluent-modified control falls to 8–11 MPa. The unmodified system exhibits higher low-temperature brittleness; service below -10 °C requires toughening with carboxyl-terminated butadiene-acrylonitrile copolymer at 5–15 phr. Mixing with amine-based hardeners should follow the supplier exotherm chart; batch sizes above 10 kg require water-jacketed mixing to limit peak exotherm below 80 °C.
The primary difference is molecular architecture. Reactive diluents such as C12-C14 glycidyl ethers lower viscosity to 400–900 mPa·s but introduce aliphatic segments that reduce rigidity and chemical resistance. WWJF-828, without diluent, retains a neat viscosity of 11 000–14 500 mPa·s and produces a crosslinked network with higher aromatic content. The trade-off is processing temperature: reactive diluent-modified grades can be mixed and dispensed at 15–20 °C, whereas WWJF-828 requires material conditioning at 35–40 °C for pressure-time dispensing. In chemical immersion testing under ISO 2812-1:2017, cured WWJF-828 films show mass gain below 2% after 7 days in 10% sulfuric acid at 23 °C, while 10 phr monofunctional reactive diluent systems exceed 5% mass gain because of lower crosslink density and increased free volume.
| Comparative Parameter | WWJF-828 | Reactive Diluent-Modified Grade | Solid Bisphenol A Epoxy |
|---|---|---|---|
| Viscosity at 25 °C, mPa·s | 11 000–14 500 | 400–1 200 | Solid, softening point 65–75 °C |
| Epoxide equivalent weight, g/eq | 184–190 | 160–175 | 450–550 |
| Glass transition temperature after stoichiometric D230 cure, °C | 75–85 | 55–65 | 70–80 |
| Mass gain in 10% sulfuric acid, 7 days | <2% | >5% | <2% |