| HS Code | 779674 |
| Product | Alpek (Mexico) PTA |
| Chemical Name | Purified Terephthalic Acid |
| Abbreviation | PTA |
| Cas Number | 100-21-0 |
| Einecs Number | 202-830-0 |
| Molecular Formula | C8H6O4 |
| Molecular Weight | 166.13 g/mol |
| Appearance | White crystalline powder |
| Odor | Odorless |
| Purity | ≥99.9% |
| Moisture Content | ≤0.2% |
| 4 Carboxybenzaldehyde 4 Cba | ≤25 ppm |
| P Toluic Acid | ≤150 ppm |
| Ash | ≤10 ppm |
| Iron | ≤1 ppm |
| Heavy Metals | ≤5 ppm |
| Color | White |
| Melting Point | 300 °C (sublimes) |
| Boiling Point | Decomposes before boiling |
| Density | 1.51 g/cm³ |
| Bulk Density | 0.80–1.05 g/cm³ |
| Solubility In Water | ≈15 mg/L at 20 °C |
| Solubility In Dmso | Soluble |
| Ph | 2.5–3.5 (saturated solution) |
| Flash Point | 260 °C |
| Autoignition Temperature | 496 °C |
| Vapor Pressure | <0.001 Pa at 20 °C |
| Particle Size | 100–150 µm |
| Storage Conditions | Dry, cool, well-ventilated area |
As an accredited Alpek (Mexico) PTA factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Alpek (Mexico) PTA is packaged in 1,000 kg jumbo bags with inner liners, 20 bags per 20-foot container for bulk shipment. |
| Container Loading (20′ FCL) | 20′ FCL container loading of Alpek Mexico PTA, 25 MT in 1 MT jumbo bags, securely stowed for export. |
| Shipping | Alpek (Mexico) PTA (purified terephthalic acid) ships as a non-hazardous, white crystalline solid. Typical packaging includes 25 kg bags, 1,000 kg jumbo bags, or bulk. Exports move via Gulf Coast ports, mainly Altamira and Coatzacoalcos, in containers or bulk vessels. Keep dry and avoid dust. |
| Storage | Store Alpek (Mexico) PTA (purified terephthalic acid) in a cool, dry, well-ventilated area. Keep in sealed silos, bags, or containers, away from moisture, heat, ignition sources, and incompatible materials such as strong oxidizers and alkalis. Use grounded equipment to control dust and static. Do not store near food or feed. Ensure containers are labeled. Follow local rules and the SDS. |
| Shelf Life | Alpek Mexico PTA typically has a 24-month shelf life when stored sealed in a cool, dry, well-ventilated area away from moisture. |
Alpek (Mexico) PTA is supplied as a dry-flowing crystalline powder for continuous polyester condensation routes where the feedstock is expected to hold 4-carboxybenzaldehyde at or below 25 ppm, p-toluic acid at or below 150 ppm, ash residue in the low single-digit ppm range, and a b* color coordinate not exceeding 1.5. The application scope below is restricted to real downstream polyester and copolyester production environments: bottle resin, fiber and filament, biaxially oriented film, glycol-modified sheet, glass-reinforced compounds, and PBT engineering resin. PTA is not evaluated here as a direct filler, pigment, coating additive, or fuel component.
Alpek PTA entering a continuous bottle-resin polymerization line is first converted to a pumpable slurry with ethylene glycol at an EG:PTA molar feed ratio between 1.10 and 1.15. The excess glycol is not lost from the process but is recovered in the ethylene glycol distillation columns and returned to the slurry preparation vessel, which limits free glycol carryover into the esterifier off-gas. Antimony trioxide is metered as the polycondensation catalyst at 250–300 ppm Sb on the melt, with a phosphorus-based thermal stabilizer added at 15–25 ppm P to suppress catalyst-induced thermal degradation during finisher operation. Esterification is carried out in a two-reactor cascade at 240–260°C and 1.2–2.5 bar(a), with the first reactor achieving an esterification degree above 90% and a carboxyl end-group concentration below 150 mmol/kg. Melt polycondensation follows at 275–285°C and absolute pressure below 1.5 mbar, using a horizontal ring-cage finisher to produce melt-phase pellets with an intrinsic viscosity of 0.60–0.65 dL/g as measured by ASTM D4603. Bottle-grade resin then passes through solid-state polycondensation at 205–215°C under a countercurrent nitrogen stream to raise intrinsic viscosity to 0.78–0.84 dL/g and reduce acetaldehyde to below 1 ppm under ASTM F2013-10. Industry compliance for food-contact bottle formats requires FDA 21 CFR 177.1630 for aqueous, acidic, and carbonated beverage packaging, EU 10/2011 with an overall migration limit of 10 mg/dm², REACH 1907/2006 SVHC control below 0.1 wt%, and China GB 4806.6-2016 for food-contact plastics. Terminal product types are injection-stretch-blow-moulded carbonated soft drink bottles, still water containers, hot-fill juice bottles with heat-set mould temperatures of 115–135°C, and monolayer edible oil bottles requiring high aldehyde suppression. An operational boundary is the residual 4-carboxybenzaldehyde level in the PTA feed: above 25 ppm, it acts as a chain terminator and shifts the molecular weight distribution toward low-IV oligomers, reducing SSP rate and broadening the final melt rheology window.
| Application segment | Mandatory standard | Test designation | Typical control limit |
|---|---|---|---|
| Carbonated beverage bottle | FDA 21 CFR 177.1630 | ASTM F2013-10 | Acetaldehyde < 1 ppm |
| Aqueous food contact | EU 10/2011 | EN 1186 migration series | Overall migration < 10 mg/dm² |
| Electrical/electronic housing | RoHS 2011/65/EU | X-ray fluorescence screening | Pb, Cd, Hg, Cr(VI) each < 1000 ppm |
Because spin-draw winding at 3000–3500 m/min demands a melt with low gel content, controlled carboxyl end-group levels, and stable extensional viscosity, the PTA slurry for fiber-grade polyester is prepared at an EG:PTA molar ratio of 1.13–1.15 and is not elevated above this range; excess ethylene glycol increases diethylene glycol formation during esterification and lowers thermal stability in the final fiber. Titanium dioxide delustrant is injected as a 30 wt% dispersion in ethylene glycol rather than as dry powder to prevent agglomerates. The final TiO₂ content for semi-dull fiber is 0.30–0.50 wt%, while full-dull staple requires 2.0–2.5 wt%; TiO₂ levels above 3.0 wt% increase spinneret pressure and produce filament breaks at the pack face. Melt-phase polymerization is stopped at an intrinsic viscosity of 0.62–0.68 dL/g under ASTM D4603, and the melt is filtered through 20 μm sintered metal filtration media before extrusion through spinnerets at 285–295°C. Quench air is controlled at 0.3–0.6 m/s across the filament bundle, and winding speeds are set between 3000 m/min for coarse denier partially oriented yarn and 3500 m/min for fine-denier POY, above which orientation-induced crystallinity increases dramatically and drawability drops. Draw texturing is performed at draw ratios of 1.55–1.75 with heater temperatures of 170–190°C for drawn textured yarn, while staple fiber production uses a two-stage draw line with crimping and heat-setting at 135–150°C. Industry compliance for textile and industrial polyester fiber spans OEKO-TEX Standard 100 Annex 4 for harmful substances, REACH Annex XVII restrictions for azo colorants and phthalates, ZDHC MRSL for auxiliary chemicals, and China GB 18401-2010 for textile safety categories. Terminal products are semi-dull POY, drawn textured yarn, full-dull staple fiber for ring and open-end spinning, and high-tenacity industrial filament used in seat belts and geotextiles where tenacity above 7 cN/dtex is specified.
When the target is an optically clear 23 μm BOPET film, the Film-grade PET derived from Alpek PTA is polymerized to a lower intrinsic viscosity of 0.58–0.62 dL/g and a controlled diethylene glycol content of 0.7–1.2 wt% to suppress spherulite growth during casting and orientation. The PTA-to-ethylene glycol molar ratio is held at 1:1.13, and the melt is discharged through a gear pump into a flat die at 275–285°C before quenching on a chilled casting drum at 40–55°C. Orientation is carried out sequentially at machine-direction draw ratios of 3.2–3.8 and transverse-direction draw ratios of 3.5–4.0, with heat-setting at 210–225°C to lock in dimensional stability and reduce thermal shrinkage below 1.5% at 150°C. The film-grade formulation includes fumed silica anti-blocking agent at 0.05–0.20 wt% and an optical brightener-free antioxidant package to minimize extractables. Terminal product types cover 12–23 μm metallized film for flexible packaging, 50–250 μm electrical insulation film, and 125–350 μm solar backsheet base film. Compliance for food-packaging film requires FDA 21 CFR 177.1630 and EU 10/2011; electrical insulation film is specified under IEC 60674-3 with breakdown voltage testing, while solar backsheet laminates are qualified under IEC 61215. A documented boundary is resin moisture during extrusion: dried pellets must contain less than 30 ppm water before entering the flat die, because moisture above this level hydrolyzes the ester linkages at melt temperature and increases carboxyl end-groups, causing die-face build-up and film haze.
In continuous glycol-modified copolyester production, the diol feed is split between ethylene glycol and cyclohexanedimethanol at a CHDM content of 30–35 mol% of total diol, which is sufficient to suppress crystallization and produce an amorphous sheet with a glass transition temperature near 81–85°C as measured by differential scanning calorimetry. The diol:PTA molar ratio is controlled at 1.05–1.10, and esterification is conducted at 225–240°C before melt polycondensation; the resulting copolyester is solidified by strand pelletizing rather than underwater pelletizing because the amorphous strands are tacky and block easily in water baths. Extrusion into sheet is performed at 210–240°C on a single-screw extruder with barrier screw design and polished roll temperatures of 50–80°C to remove residual stress without inducing crystallization. Terminal product types are thermoformed medical device trays, cosmetic jar inner liners, point-of-sale display sheet, and refrigerator crisper trays where clarity, impact resistance, and solvent resistance are required without post-mold annealing. Industry compliance for food-contact glycol-modified polyester adheres to FDA 21 CFR 177.1315 for ethylene-1,4-cyclohexylene dimethylene terephthalate copolymers, EU 10/2011, and ISO 10993-5 for cytotoxicity when the sheet is converted into medical packaging. The main process limitation is that CHDM content exceeding 50 mol% of total diol raises melt viscosity and reduces melt-phase polycondensation efficiency; below 20 mol%, the material begins to develop strain-induced crystallization, which reduces thermoforming latitude.
Base PET resin sourced from Alpek PTA is first solid-state polymerized to an intrinsic viscosity of 0.85–0.95 dL/g under ASTM D4603, because lower-IV base resin does not retain sufficient melt strength during glass fiber feeding and leads to screw slippage at 280°C. The base resin is dried to below 50 ppm moisture and compounded with 30 wt% E-glass chopped strand at a barrel temperature profile of 260–285°C, using a co-rotating twin-screw extruder with L/D ratio of 40:1 and vacuum venting at 50–100 mbar to remove volatile glycol and water. Nucleating agent is added at 0.1–0.5 wt% to accelerate crystallization during injection molding, and a flame-retardant package is compounded at 10–15 wt% to achieve UL 94 V-0 performance at 0.8 mm. Injection molding is carried out with mold temperatures of 120–140°C to complete PET crystallization; mold temperatures below 110°C leave amorphous surface regions with reduced chemical resistance and poor dimensional stability at 150°C. Terminal product types are electrical relay sockets, automotive sensor housings, microwave oven crisper trays, and heat-resistant pump components where continuous use temperature reaches 150°C and short-term peaks reach 180°C. Compliance requirements are UL 94 V-0 for flammability, IEC 60112 for comparative tracking index above 250 V, RoHS 2011/65/EU for restricted substances, and REACH for SVHC disclosure.
| Engineering resin parameter | Referenced standard | Test condition | Control value |
|---|---|---|---|
| Flammability class | UL 94 | Vertical burn, 0.8 mm | V-0 |
| Comparative tracking index | IEC 60112 | Solution A, 100 drops | ≥ 250 V |
| PBT designation | ISO 7792-1:2021 | Viscosity number and filler format | IV 0.80–1.20 dL/g |
Direct esterification of Alpek PTA with 1,4-butanediol on a titanium-catalyzed continuous line is more sensitive to tetrahydrofuran formation than ethylene glycol-based PET; therefore the reactor pressure and residence time must be tightly managed to keep THF loss below 0.5 wt% of the butanediol feed. The PTA:BDO molar feed ratio is set at 1:1.25–1.30, with tetrabutyl titanate catalyst injected at 50–150 ppm Ti and a hindered phenol stabilizer added at 0.05–0.15 wt% to reduce thermo-oxidative carboxyl end-group accumulation. Esterification is carried out at 215–230°C and 1.0–1.5 bar(a), followed by polycondensation at 245–255°C and absolute pressure below 1 mbar to reach an intrinsic viscosity of 0.80–1.20 dL/g. The molten PBT is filtered and extruded into strands through a water bath, with pellet drying below 0.02 wt% moisture before compounding or injection molding. Terminal product types are automotive wiring harness connectors, electronic sensor housings, pump impellers, and industrial gear covers requiring dimensional stability, chemical resistance to hot oils, and continuous use temperature up to 120–140°C. Industry compliance includes UL 94 HB or V-0 depending on the reinforced compound, IEC 60112 for comparative tracking index above 600 V in halogen-free grades, and ISO 7792-1:2021 for PBT designation. Published data for this specific configuration using Alpek PTA in titanium-catalyzed BDO direct esterification is limited; the values above are drawn from commercial PBT direct esterification lines using high-purity terephthalic acid with equivalent 4-CBA control.
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Alpek (Mexico) PTA is a bulk merchant-grade purified terephthalic acid stream produced at Alpek’s integrated Mexican Gulf Coast terephthalic acid and PET assets. The material is not issued under a single commercial model number or trade-specific grade code; instead, it is supplied against contract certificates of analysis that define lot-specific boundaries for 4-CBA, p-toluic acid, moisture, ash, CIE b* value, and particle size distribution. Chemically, the product is benzene-1,4-dicarboxylic acid, CAS 100-21-0, with molecular formula C8H6O4 and molar mass 166.13 g mol⁻¹. It is manufactured by air oxidation of para-xylene followed by hydrogenation and multi-stage crystallization to reduce mono-functional aromatic impurities. The resulting dry, free-flowing powder is intended for continuous PET melt-phase polycondensation, polyester fiber and filament production, and specialty copolymer lines where tight stoichiometric control is required.
Supply-chain position is the primary difference between Alpek PTA and long-haul merchant PTA shipped from Asia or the Middle East. PTA surface moisture is a recognized source of lot-to-lot variation; moisture uptake during ocean transport and transloading is measurable by Karl Fischer titration and commonly tracks ambient dew point. Fewer transfer steps between oxidation, purification, and downstream PET paste mixing reduce the number of exposure points to humid air and lower the probability of silo bridging caused by cohesive surface moisture. Pneumatic dense-phase conveying lines with pressure-vessel blow tanks and inert-gas blanketing are used in typical downstream transfer systems, and railcar or truck identification is linked to certificate-of-analysis lots for traceability through feed silos and PET solid-state polymerization units.
Combustible dust management for PTA receiving and storage falls under NFPA 652 and NFPA 654. Transfer equipment should be grounded and bonded, and dust collection systems should be designed for the fine fraction. Local supply does not eliminate combustible dust hazards; it changes the transfer history and therefore the moisture and fines profile that a downstream plant must manage at the silo and rotary-feed interface.
Routine lot qualification for Alpek PTA should be performed before silo acceptance. Quantification of 4-carboxybenzaldehyde and p-toluic acid is most commonly executed by reverse-phase high-performance liquid chromatography with ultraviolet detection. Moisture is measured by volumetric Karl Fischer titration according to ASTM E203; ash is determined by muffle furnace combustion followed by gravimetric or inductively coupled plasma optical emission spectroscopy. Particle size distribution is reported by laser diffraction according to ISO 13320:2020. CIE b* yellowness is measured by reflectance spectrophotometry under D65/10° illumination. The following matrix contains representative merchant-grade PTA qualification parameters; it is not site-specific certificate-of-analysis guidance for Alpek lots because published lot-level data are limited and should be obtained from the producer under supply agreements.
| Parameter | Common contract limit or band | Measurement method/equipment | Operational significance |
|---|---|---|---|
| 4-Carboxybenzaldehyde (4-CBA) | ≤ 25 mg/kg | HPLC-UV, reverse-phase column | Chain termination; shifts PET degree of polymerization |
| p-Toluic acid | ≤ 150 mg/kg | HPLC-UV, reverse-phase column | Mono-functional end capping; affects melt viscosity |
| Moisture | ≤ 0.1 wt% | ASTM E203, volumetric Karl Fischer | Feed consistency; hydrolysis control |
| Ash | ≤ 10 mg/kg | Muffle furnace/ICP-OES | Catalyst residue; filter differential pressure |
| CIE b* value | ≤ 1.5 | Reflectance spectrophotometer, D65/10° | PET resin yellowness |
| Particle size D50 | 100–130 µm | ISO 13320:2020, laser diffraction | Paste mixing and pneumatic conveying |
| Fines ≤ 10 µm | report value | ISO 13320:2020, laser diffraction | Dusting and electrostatic retention |
Silo discharge reliability in Mexican Gulf Coast production is governed by PTA particle shape, size distribution, and surface moisture. Even at moisture below the 0.1 wt% certificate limit, condensation cycles can raise local surface moisture at silo walls and create cohesive arching. The powder flow function, measured by a Schulze ring shear tester or Jenike shear cell, is lower for fine-rich lots with high specific surface area. Where D50 drops below 90 µm, uniaxial compressive strength can increase enough to require steeper hopper half-angles or low-friction liners. This is not a property unique to Alpek PTA, but it is a process-relevant distinction for end users that unload into outdoor silos with minimal insulation.
The sensitivity of PET melt-phase and solid-state processes to mono-functional aromatic impurities is a key reason PTA specifications are built around 4-CBA and p-toluic acid. In continuous esterification and polycondensation equipment such as agitated finisher reactors operating at 280–290 °C and vacuum below 1 mbar, any aromatic acid containing only one carboxylic acid group can terminate chain growth. 4-CBA additionally carries an aldehyde group that participates in side reactions and can intensify thermal degradation byproducts. Elevated concentrations are not observed as a single process alarm but as a simultaneous reduction in melt-phase intrinsic viscosity at fixed residence time, an increase in agitator torque variability, and a shift in final acetaldehyde generation in bottle-grade resin.
In solid-state polymerization units, residual mono-functional impurities reduce the maximum attainable intrinsic viscosity at fixed inert-gas temperature and residence time. Nitrogen-blanketed SSP reactors with shallow tray or shaft dryers, typically held at 200–215 °C for bottle-grade resin, are particularly dependent on the reactive end-group balance established during melt-phase feeding. When p-toluic acid is at the upper specification boundary, a producer may need to raise SSP residence time or reduce throughput to maintain the same 0.80–0.84 dL/g intrinsic viscosity target. Published kinetic correlations specific to Alpek PTA lots are limited; the process relationships described here are derived from general polyester raw-material studies.
In a continuous PET line, Alpek PTA is metered into a paste mix tank with ethylene glycol at typical paste solids of 65–75 wt% and esterified at 240–270 °C. The particle size distribution affects paste viscosity and pumpability. Coarse particles above 180 µm can promote settling and line plugging, while excessive fines below 10 µm can increase dust formation and electrostatic charge retention in conveying lines. These processing boundaries are measured on production-scale paste tanks and rotary feeders, not only in laboratory powder testers. Compared with medium-purity terephthalic acid or imported crude PTA, the Alpek PTA stream is specified for direct polyester manufacture; it is not intended as an intermediate for further purification.
For carbonated soft-drink and water bottle preform production, PET resin color is strongly influenced by the PTA b* value and by the concentration of 4-CBA. A high PTA b* value tends to carry through to amorphous PET chips and can reduce brightness in blown bottles. Optical film and super-clear preform applications typically impose tighter PTA color limits than staple fiber applications. A single PTA lot may be suitable for staple fiber but not for high-clarity bottle resin if the certificate b* value approaches the upper band. The buyer should map the PTA supplier’s color specification to the downstream bottle resin specification because the relationship is not linear and can be altered by catalyst type and stabilizer package.
In polyester staple fiber and filament spinning, PTA quality influences carboxyl end-group concentration and hydrolytic degradation during melt spinning. Residual 4-CBA can contribute to color bodies that lower fiber whiteness and increase break frequency in high-speed winders. Spinning lines operating at 280–295 °C and winder speeds above 3000 m/min are sensitive to small changes in melt viscosity. When PTA purity drifts, spinneret pack pressure can rise and throughput may be adjusted. The same lot could process acceptably in a low-speed textile filament line but create discontinuity in a high-speed partially oriented yarn line. PTA qualification should therefore be tied to the specific downstream machine configuration, not only to generic contract limits.
| Feedstock | Typical 4-CBA | Typical p-toluic acid | Downstream use | Handling profile |
|---|---|---|---|---|
| Crude terephthalic acid | often > 500 mg/kg | variable | not suitable for direct PET melt-phase use without purification | colored, cohesive |
| Medium-purity terephthalic acid | 50–150 mg/kg | moderate | requires downstream purification or blending for high-clarity PET | intermediate color and feeding behavior |
| Purified terephthalic acid, including Alpek PTA | ≤ 25 mg/kg | ≤ 150 mg/kg | direct PET, polyester fiber, film, and solid-state polymerization | dry, free-flowing powder with controlled particle size |
Certificates of analysis are issued under the producer’s quality management system, which is normally aligned with ISO 9001:2015 or equivalent. Specific Alpek certifications should be verified in current supplier documentation rather than assumed from generic corporate statements. External users may audit analytical equipment such as HPLC systems, Karl Fischer titrators, and laser diffraction instruments. Method repeatability should be verified with certified reference materials and round-robin comparisons with third-party laboratories. Because PTA specifications are in the low-ppm range, sampling bias from railcars and silos is often a larger source of uncertainty than instrument error. Composite sampling from multiple points in the transfer line provides more representative lot data than a single grab sample from the top hatch.
Operational boundaries for the product include dry, covered silo storage with ground-level access for inspection and dew-point control. Pneumatic conveying, dust collection, and railcar unloading should comply with NFPA 652 and NFPA 654 because PTA dust is a combustible particulate. Transfer equipment should be bonded and grounded, and nitrogen or other inert gas blanketing should be considered where fines are suspended in air. The powder should not be stored adjacent to concentrated alkali or mixed with strong oxidizers. PTA wetted by liquid water becomes sticky and should not be reintroduced to silo conveyors without drying and particle size verification. Users receiving the product in railcars should compare the certificate of analysis to the receiving silo sample before adjusting melt-phase formulation; this closes the loop between supplier lot data and actual production feed without relying on generic textbook values.