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HF-100M C5 Hydrocarbon Resin for Road Marking Paints

    • Product Name: HF-100M C5 Hydrocarbon Resin for Road Marking Paints
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
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    Specifications
    HS Code 661613
    Softening Point Ring Ball 95-105 °C
    Color Gardner 4-7
    Acid Value ≤1.0 mg KOH/g
    Melt Viscosity 180 C 300-800 mPa·s
    Iodine Value 80-120 g I₂/100g
    Density 20 C 0.95-1.05 g/cm³
    Flash Point ≥200 °C
    Ash Content ≤0.1%
    Toluene Insolubles ≤0.05%
    Number Average Molecular Weight Mn 1200-1800
    Molecular Weight Distribution Mw Mn 1.5-2.5
    Glass Transition Temperature 50-70 °C

    As an accredited HF-100M C5 Hydrocarbon Resin for Road Marking Paints factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing HF-100M C5 Hydrocarbon Resin for road marking paints: supplied in 25 kg net multi-wall paper bags with PE liner, palletized and wrapped.
    Container Loading (20′ FCL) HF-100M C5 Hydrocarbon Resin for road marking paints; 20' FCL container loading, packed in 25kg bags on pallets, shrink-wrapped.
    Shipping HF-100M C5 Hydrocarbon Resin is shipped as solid flakes in 25 kg multi-layer paper bags on pallets, protected from moisture and heat. Ensure proper labeling, avoid direct sunlight, and maintain ventilation during transport. Non-hazardous under normal conditions, but handle with care to prevent dust accumulation.
    Storage Store HF-100M C5 Hydrocarbon Resin in a cool, dry, well-ventilated area, away from heat, sparks, open flames, and direct sunlight. Keep containers tightly sealed to prevent moisture ingress. Maintain stable temperatures between 5°C and 35°C, avoiding extreme heat or freezing. Store separately from oxidizing agents. Under proper conditions, shelf life is typically 12 months.
    Shelf Life Shelf life is typically 12 months from production when stored sealed in a cool, dry area away from heat and moisture.
    Application of HF-100M C5 Hydrocarbon Resin for Road Marking Paints

    In thermoplastic road marking compounds formulated for highway centreline and edge-line service, HF-100M C5 hydrocarbon resin functions as the primary aliphatic tackifying resin. The relevant material standard for the finished compound is EN 1871:2020; chemical and physical testing is conducted under ASTM D4797-17, and North American purchasing specifications commonly reference AASHTO M249-12. In a filled system containing 55–70 wt% calcium carbonate, 10–12 wt% titanium dioxide, and 20–25 wt% premix glass beads, the binder phase is assembled from EVA with 18–28% vinyl acetate content, paraffin or Fischer-Tropsch wax, and liquid plasticizer. HF-100M addition in the total compound is typically 12–18 wt%, with 14–16 wt% preferred when the road authority requires ring-and-ball softening point not below 96°C per ASTM E28-18 and Brookfield Thermosel viscosity of 0.8–2.0 Pa·s at 180°C per ASTM D3236-15. At the 18 wt% level, melt viscosity falls enough for profiled screed application, but compressive strength can drop below the AASHTO M249-12 minimum unless plasticizer is reduced by 2–3 wt% to compensate.

    Production-scale compounding is performed in a co-rotating twin-screw extruder with an L/D ratio of 40:1 and gravimetric feeders for filler, glass beads, and binder raw materials. Barrel temperatures are ramped from 130°C at the feed throat to 190°C in the final mixing zone; screw speed is maintained at 250–350 rpm. Premix glass beads are introduced through a side stuffer downstream to limit breakage. The melt is pelletised, bagged, or formed into blocks. At the application site, the compound is re-melted in an oil-jacketed kettle with a helical agitator operating at 20–40 rpm; jacket temperature is held at 190–210°C, and the melt is circulated to a ribbon gun or screed box. Application viscosity is maintained at 2.5–4.5 Pa·s at 200°C to control stringing and to ensure drop-on glass beads embed to 40–60% of bead diameter. Filler moisture is a critical variable: at relative humidity above 65%, calcium carbonate must be pre-dried to below 0.2 wt% moisture because steam evolution creates microvoids that reduce retroreflectivity under EN 1436:2018.

    Finished markings are produced as hot-melt high-build lines, raised-profile audible markings, and asphalt-embedded inlay markings with dry film thickness of 1.5–3.5 mm. In-service performance is evaluated for retroreflectivity RL and skid resistance SRT under EN 1436:2018. Night visibility of new white markings is frequently specified above 150 mcd·m−2·lx−1 in dry conditions, and HF-100M viscosity control directly influences bead retention and the early-life RL value. The primary failure mode observed on production lines is thermally induced yellowing when the melt remains above 220°C for more than 4 h; this is controlled by limiting kettle heel volume and by nitrogen blanketing in bulk storage of resin flake.

    How Does HF-100M Function in Solventborne Alkyd and Chlorinated Rubber Traffic Paints?

    Solventborne alkyd traffic paints use HF-100M as a co-binder to raise dry-film hardness, shorten no-pick-up time, and reduce aromatic solvent demand relative to C9 resins. The addition ratio in a medium-oil alkyd formulation is 3–7 wt% of total paint, equal to 15–25% of total binder solids. In chlorinated rubber traffic paints the practical range is 5–10 wt% on total paint; above 10 wt%, film elongation at −10°C falls below the level required for crack-free service on concrete and asphalt. HF-100M is introduced as a 50–60% solution in mineral spirits or xylene with a Gardner colour of 4–6 per ASTM D6166-12. Relevant compliance standards are AASHTO M248 for ready-mixed traffic paint and ASTM D711-20 for no-pick-up time, with formulation selection guided by ASTM D2205-20. Solventborne road-marking paints are often outside the scope of architectural VOC directives, so VOC is managed to the road authority specification rather than a single harmonised rule.

    Manufacturing uses a high-speed disperser with a Cowles blade tip speed of 18–25 m/s. Pigment and filler are dispersed in a portion of alkyd and solvent to Hegman 4–6 per ASTM D1210-05; the HF-100M solution is added during letdown after the mill base temperature has fallen below 50°C. Final Krebs viscosity is adjusted to 70–90 KU per ASTM D562-10. Airless spray application is run at 12–20 MPa through a 0.381–0.635 mm tip, depositing 350–500 μm wet film and yielding 75–150 μm dry film. Terminal finished product types are conventional fast-dry solventborne centreline and edge-line paints, parking lot stencils, and temporary construction markings. The main operational boundary is that HF-100M should not replace more than 25% of the alkyd binder unless the alkyd itself has a high gel content, because early surface dry over solvent-laden underlayers can produce wrinkling or blocking.

    Waterborne acrylic traffic paints present a comparatively narrow compatibility window for unmodified hydrocarbon resins because HF-100M is hydrophobic and must be introduced as an emulsified resin dispersion rather than as dry flake. The practical addition ratio is 2–6 wt% resin solids on total formula solids, corresponding to 10–20% of the acrylic binder. Above 6 wt%, low-temperature coalescence is impaired and the cured film may develop mud cracking when applied below 5°C. The letdown pH is maintained at 8.0–9.0 to preserve emulsion stability; direct addition of an acidic acrylic dispersion to the HF-100M emulsion can cause heterocoagulation and tip clogging. Compliance for waterborne traffic paint is evaluated under AASHTO M248 and ASTM D711-20; low-VOC purchasing specifications commonly require less than 100 g/L VOC, and freeze-thaw stability is screened by ASTM D2243-20.

    Production uses a high-shear dissolver for the pigment grind. The HF-100M dispersion is added only during letdown at 3–6 m/s tip speed to avoid shear-induced coalescence; the finished paint is filtered through a 150 μm bag. Airless spray application deposits 350–450 μm wet film thickness. Terminal finished product types are low-VOC waterborne traffic paints for urban roads, temporary construction markings, and colour-coded parking and curb markings. Published data for HF-100M in waterborne acrylic binders is limited; formulator validation should include 500 h QUV-B exposure per ASTM G154-16 because aliphatic C5 resin can photo-yellow unless a hindered amine stabilizer is included at 0.5–1.5 wt% of total solids.

    Two-component cold plastic media and the control of radical cure

    Cold plastic road marking materials based on methyl methacrylate monomer use HF-100M as an inert resin extender and rheology control agent in the liquid component. The addition ratio is 6–12 wt% of liquid component A, with 8–10 wt% used for structured markings requiring a thixotropic plateau. HF-100M is dissolved in methacrylate monomer at 40–50°C under a nitrogen blanket; paraffin wax, fumed silica, and pigment are then dispersed. The resin reduces peak exotherm by lowering reactive monomer mass fraction and increases viscosity of the cured binder, but its unsaturation can also alter gel time when dibenzoyl peroxide initiator is added at 1–3 wt% in component B. Production mixing is carried out in a jacketed stainless steel vessel with a dissolver at 8–12 m/s, and the liquid component is stored below 30°C with exclusion of direct sunlight to suppress premature polymerization.

    Compliance for this product class is performance-based under EN 1436:2018 for retroreflectivity and skid resistance. No single EN material standard for cold plastic currently exists, so type approval is commonly based on EN 1436:2018, adhesion to bituminous substrates by ISO 4624:2016, and abrasion resistance by ASTM D4060-19. Levels above 12 wt% create a two-phase cured surface and reduce tensile properties measured by ISO 527-2:2012, so the resin is not used as a primary binder in this reactive platform. Terminal finished product types are cold plastic markings for bus lanes, bicycle lanes, pedestrian crossings, and high-friction coloured overlays applied at 1.0–3.0 mm thickness. Operational boundary: filler moisture must remain below 0.1 wt% because water consumes dibenzoyl peroxide and can arrest cure at the substrate interface.

    Application segmentMaterial or product standardTest method or performance method
    Hot-melt thermoplasticEN 1871:2020, AASHTO M249-12ASTM D4797-17, EN 1436:2018
    Solventborne alkyd/chlorinated rubberAASHTO M248ASTM D711-20, ASTM D562-10
    Waterborne acrylicAASHTO M248ASTM D711-20, ASTM D2243-20
    MMA cold plasticNo single material standardEN 1436:2018, ISO 4624:2016, ASTM D4060-19
    Preformed thermoplasticASTM D4505-18, EN 1790:2013EN 1436:2018

    When preformed thermoplastic sheet has to be cut into legends without edge cracking

    Preformed thermoplastic markings are manufactured as continuous sheet and then die-cut into arrows, symbols, legends, and temporary lane markings. In this application, HF-100M is compounded at 10–14 wt% of the total sheet formulation; the lower end is selected for sheets that will be cut in ambient temperatures below 10°C, and the upper end is used for high-contrast white and yellow lines requiring rapid heat reactivation on asphalt. The sheet is produced from a hot melt compounded in a twin-screw extruder at 170–190°C and calendered to 1.2–2.5 mm thickness using chilled rollers held at 15–25°C. Die cutting is performed after conditioning at 25–35°C because cold sheet below 10°C exhibits reduced elongation and edge microcracking. Compliance is evaluated under ASTM D4505-18 for preformed plastic pavement marking material and EN 1790:2013 for preformed road marking products; field performance after torch or heat-gun reactivation is assessed under EN 1436:2018. Terminal finished products are preformed arrows, route shields, stop bars, and temporary road construction markings supplied in rolls or sheets with pressure-sensitive or heat-activated backing.

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    Certification & Compliance
    More Introduction

    HF-100M C5 Hydrocarbon Resin for Road Marking Paints is an aliphatic tackifier produced by thermal polymerization of piperylene-rich C5 feedstock. The grade falls within the nominal 100 °C softening-point class. Published data for this specific configuration is limited to the supplier certificate of analysis; the values cited here are class-typical for a medium molecular weight C5 hydrocarbon resin and should be verified against the batch number. Class-typical properties include a ring-and-ball softening point of 96–104 °C determined by ASTM E28 or ASTM D3461, a molten Gardner colour of ≤2 measured by ASTM D1544, an acid number of ≤1 mg KOH/g measured by ASTM D974, and a Brookfield melt viscosity at 200 °C of 700–1,500 mPa·s measured by ASTM D3236. The resin is supplied as flake or pastille with a density of 0.95–1.00 g/cm³ by ASTM D792.

    What Differentiates HF-100M from C9 Aromatic and DCPD Tackifier Resins in Road Marking Service?

    The aliphatic backbone of HF-100M distinguishes it from C9 aromatic hydrocarbon resins. In accelerated weathering under ASTM G154 using UVA-340 lamps, a C5-based white road marking formulation typically shows lower yellowing and higher retained luminance than an equivalent C9-based film because the aliphatic resin contains fewer sites for quinoid oxidation. Compatibility behaviour is also different: HF-100M forms a single-phase melt with ethylene-vinyl acetate copolymers containing 9–19 wt% vinyl acetate and with paraffin wax, whereas C9 aromatic resins may phase-separate above 15 wt% addition in the same EVA grade. Against dicyclopentadiene resins of similar softening point, HF-100M exhibits lower melt viscosity at 200 °C and a narrower molecular weight distribution by gel permeation chromatography. Dicyclopentadiene resins typically contribute higher heat distortion resistance but darken more rapidly in open-kettle holds at 210 °C. The choice of HF-100M over C9 or DCPD therefore affects initial colour, colour retention, melt viscosity, and compatibility with EVA-based binders.

    Melt blending in oil-jacketed kettles equipped with anchor agitators is conducted at 180–200 °C. At 18–22 wt% resin loading in a thermoplastic road marking compound containing EVA, polyethylene wax, calcium carbonate, and titanium dioxide, the Brookfield viscosity at 200 °C generally falls within 1,500–3,500 mPa·s; this is the range required by airless spray equipment with 30:1 pump ratios. Below 1,200 mPa·s, rib thickness control becomes unstable; above 4,000 mPa·s, nozzle clogging frequency increases. The resin functions as the continuous-phase binder that wets glass beads during drop-on application. Retroreflectivity after simulated traffic is evaluated under EN 1436, and thermoplastic material properties are checked according to AASHTO M249. In preformed thermoplastic tape manufactured on a twin-screw extruder with an L/D ratio of 40:1 and die temperatures of 170–190 °C, resin melt viscosity controls die pressure and edge definition. Higher resin addition reduces melt fracture but can extend no-pick-up time when the road surface temperature exceeds 35 °C.

    When Kettle Temperature Exceeds 210 °C: Degradation Kinetics and Resin Stability Boundaries

    Thermal oxidative degradation of C5 aliphatic resins follows an autocatalytic free-radical pathway. Above 210 °C, chain scission accelerates and the melt viscosity at 200 °C can drift downward by more than 25% over a 6 h hold in an open kettle. Carbonyl absorbance in the 1,710–1,735 cm⁻¹ infrared region increases, and conjugated polyenes formed by β-scission shift Gardner colour upward. Production-scale kettles with direct-fired heating and no nitrogen blanket have produced lots with Gardner colour shifting from ≤2 to >5 after 8 h at 220 °C; such lots are rejected for white traffic markings because yellowing reduces daytime luminance contrast. The processing window is therefore bounded: melt at 180 °C, apply at 190–210 °C, and limit total residence time to 6 h for unpigmented binder and 4 h for TiO₂-filled systems because pigment surface acidity accelerates oxidation. Addition of a phosphite antioxidant at 0.05–0.15 wt% and a hindered phenolic antioxidant at 0.10–0.30 wt% extends the induction period but does not remove the upper temperature limit. Nitrogen blanketing at 0.2–0.5 m³/h per tonne reduces oxygen ingress and lowers colour formation during the first 4 h.

    In solventborne road marking paints, HF-100M is dissolved at 30–40 wt% solids in xylene, toluene, or a xylene/ethyl acetate blend to a Brookfield solution viscosity of 100–300 mPa·s at 25 °C. Without sufficient C5 resin, titanium dioxide flocculation increases and the 45°/0° luminance coefficient under EN 1436 decreases. Dry-to-no-pick-up time for a 350 µm wet film at 23 °C and 60% relative humidity falls in the 10–20 min range with a solvent blend having an initial boiling point of 110–138 °C. The main limitation in solventborne systems is limited solubility in pure ethanol and incompatibility with waterborne acrylic emulsions unless the resin is pre-emulsified with a compatible surfactant.

    Comparison with rosin ester resins shows a difference in acid functionality. Rosin esters contain residual carboxylic acid groups and can react with calcium ions from mineral filler to form metal soaps that thicken the melt unpredictably. HF-100M contains negligible acid groups and therefore does not produce the same metal carboxylate viscosity rise. In contrast, hydrogenated C5 resins have lower unsaturation and better colour stability but may have a different softening-point/viscosity relationship. Selection between HF-100M and a hydrogenated C5 grade should be based on Gardner colour after 1,000 h of ASTM G154 exposure rather than on initial colour alone, particularly for white markings in regions with annual ultraviolet doses above 30 MJ/m². Mineral filler moisture above 0.2 wt% causes steam foaming in hot-melt kettles; calcium carbonate and silica sand should be pre-dried at 120 °C to constant mass when ambient relative humidity exceeds 60%. High-acid-value rosin esters above 10 wt% of the total binder are not recommended without a compatibility trial because phase separation may produce surface tack and non-uniform bead embedment depth.

    Analytical Property Ranges and Compliance Standards for Supply Certification

    Because lot consistency determines kettle behaviour and extrusion backpressure, incoming inspection should compare the following class-typical C5 hydrocarbon resin property windows against the supplier certificate of analysis for HF-100M. The test methods below are the standard designations used in hydrocarbon resin datasheets; they do not replace the product specification for a specific batch.

    PropertyClass-typical rangeTest method
    Softening point, ring-and-ball96–104 °CASTM E28 / ASTM D3461
    Molten Gardner colour≤2ASTM D1544
    Acid number≤1 mg KOH/gASTM D974
    Brookfield viscosity at 200 °C700–1,500 mPa·sASTM D3236
    Density at 25 °C0.95–1.00 g/cm³ASTM D792
    Glass transition temperature40–60 °CASTM D3418

    Regulatory status is product-specific and must be confirmed with the supplier. C5 hydrocarbon resins of this class are generally registered under REACH; food-contact listing under EU 10/2011 is not relevant to road marking unless explicitly certified. The resin itself contains low volatile matter, but solventborne road marking paints containing xylene exceed many architectural coating VOC restrictions unless a traffic marking exemption applies. Storage below 30 °C in sealed bags is required because pastilles thermally fuse above 45 °C and can bridge feed hoppers in extrusion lines.

    For two-component reactive road marking paints based on methyl methacrylate or epoxy resins, HF-100M is not recommended without a dedicated compatibility study. In methyl methacrylate systems, the hydrocarbon resin dissolves in the monomer phase but does not become part of the crosslinked network; this can produce surface exudation under hot tyre loading and reduce interlayer adhesion. In epoxy systems, aliphatic C5 resin phase separation can occur during cure because the developing network excludes the nonpolar resin. The operational boundary is therefore limited to thermoplastic and solventborne road marking formulations unless the reactive system supplier has tested the specific resin lot.

    On a production-scale twin-screw extruder with 40:1 L/D, batch-to-batch variation in resin melt viscosity of ±15% changes die pressure by approximately ±8% at constant screw speed and barrel temperature. Closed-loop gear-pump pressure control is required when running a 2.5 mm preformed tape; a lot at the high end of the viscosity range without barrel temperature adjustment can cause edge tearing at the die lip because melt strength falls while die swell increases. Oscillatory rheology at 180 °C shows loss modulus dominant behaviour, which reduces elastic recovery and improves ribbon thickness uniformity. The resin should not be combined with high-polarity polyamides in the same melt stream because phase separation produces surface defects on the finished stripe.

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