Cnpc Urumqi Petrochemical Pta

CNPC Urumqi Petrochemical PTA

    • Product Name: CNPC Urumqi Petrochemical PTA
    • Factroy Site: Yinchuan, Ningxia, China
    • Price Inquiry: sales8@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
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    VTB
    Specifications
    HS Code 597712
    Productname CNPC Urumqi Petrochemical PTA
    Chemicalname Purified Terephthalic Acid
    Molecularformula C8H6O4
    Molecularweight 166.13 g/mol
    Casregistrynumber 100-21-0
    Appearance White crystalline powder
    Odor Odorless
    Productgrade Fiber grade
    Purity ≥99.9%
    Moisturecontent ≤0.2%
    Acidvalue 675 ± 2 mg KOH/g
    4 Cba Content ≤25 ppm
    P Toluicacidcontent ≤150 ppm
    Ashcontent ≤0.001%
    Totalheavymetals ≤5 ppm
    Meltingpoint 300 °C (sublimes)
    Density 1.52 g/cm³
    Bulkdensity 0.8–1.0 g/cm³
    Solubility Slightly soluble in water; soluble in dimethyl sulfoxide
    Annualcapacity 600,000 t/y

    As an accredited CNPC Urumqi Petrochemical PTA factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing CNPC Urumqi Petrochemical PTA is supplied in 1,000 kg jumbo bags, 20 bags per 20-foot container for bulk shipment.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for CNPC Urumqi Petrochemical PTA: bagged cargo, securely stowed, optimized payload for safe ocean transport.
    Shipping CNPC Urumqi Petrochemical PTA (purified terephthalic acid) is shipped as a non-hazardous, white crystalline powder in 25 kg bags, 1–1.1 tonne jumbo bags, or bulk containers. Covered truck, railcar, or container transport must stay clean, dry, and protected from moisture and contamination.
    Storage CNPC Urumqi Petrochemical PTA (purified terephthalic acid) should be stored in a cool, dry, well-ventilated warehouse or sealed bulk silo, away from moisture, heat, ignition sources, and strong oxidizers. Keep bags and containers closed, palletized, protected from sunlight, and store separately from incompatible materials. Use grounded, dust-controlled handling equipment and comply with local fire, safety, and environmental regulations.
    Shelf Life CNPC Urumqi Petrochemical PTA shelf life: typically 24 months in original sealed packaging, kept dry, cool, ventilated, protected from moisture, heat, and sunlight.
    Application of CNPC Urumqi Petrochemical PTA

    Continuous direct esterification lines receiving CNPC Urumqi Petrochemical PTA for polyester staple fibre production operate the paste feed at an ethylene glycol-to-PTA molar ratio of 1.12 to 1.18. Moisture uptake in bulk PTA above 0.2 wt% before paste preparation is a documented cause of molar feed drift because mass-flow equipment is calibrated on dry solids; hopper dryers or nitrogen-blanketed silos are therefore assigned to maintain free-flowing feed. The five-reactor train runs primary esterification at 260–270 °C and 0.1–0.3 MPa, secondary esterification at 265–275 °C, and polycondensation at 280–290 °C under absolute pressure ≤100 Pa. Catalyst antimony trioxide is metered at 200–300 ppm Sb by polymer mass, and phosphorus stabiliser is added at 20–80 ppm P to cap polycondensation reversion. Melt intrinsic viscosity at spinning is controlled at 0.62–0.68 dL/g per ASTM D4603-18. On direct spinning lines, gear pump throughput stability of ±1.5% is required to hold fibre denier within specification; batch-to-batch PTA particle size above 180 µm elevates filter pressure in the paste circuit and shortens filter service life.

    Drawing, crimping, and heat-setting downstream differ by fibre type. Cotton-type staple is drawn at ratios of 2.5–3.5 and heat-set at 120–160 °C; hollow conjugate fibre uses a spinneret segment geometry with nitrogen injection at 0.1–0.3 L/min per hole to maintain lumen structure. Compliance for textile and nonwoven applications is evaluated under GB/T 14464-2017, OEKO-TEX Standard 100 Class I, and EU REACH (EC) No 1907/2006 for SVHC screening. Terminal product types include cotton-type, wool-type, hollow conjugate, low-shrinkage staple, and spunbond nonwoven fibre.

    What Happens When the PTA-to-Ethylene Glycol Molar Feed Ratio Exceeds 1.20 in Bottle-Grade PET?

    Bottle-grade PET made from PTA diverges from fibre-grade resin at the solid-state polycondensation step. The esterification train is charged at an EG/PTA molar ratio of 1.18–1.22; above 1.22, excess glycol load raises diethylene glycol formation above 1.5 wt%, which depresses crystallisation rate and forces longer solid-state residence for a given intrinsic-viscosity target. The molten prepolymer exits polycondensation at 0.60–0.65 dL/g per ASTM D4603-18 and is pelletised, crystallised at 150–170 °C, and solid-state polymerised at 200–220 °C in a nitrogen-purged column or tumbler. Solid-state residence time is commonly 12–20 h to reach 0.80–0.84 dL/g, with pellet moisture held below 50 ppm before injection moulding of preforms.

    Formulation additives include antimony trioxide at 200–300 ppm Sb, phosphoric acid at 20–80 ppm P, and cobalt acetate at 20–60 ppm Co for blue-white tone; cobalt dosage is raised only in preform systems where UV barrier is not required. Preform injection moulding on high-cavitation tools with clamp force above 4,000 kN requires melt temperature 270–285 °C and IV loss below 0.02 dL/g. Stretch blow moulding then orients the preform at area stretch ratios of 8–12 to produce container sidewalls with oxygen permeability below 0.04 cm³·mm/m²·day·atm when measured per ASTM D3985-17.

    Standard or regulationTest method or annexControl parameterThreshold
    FDA 21 CFR 177.1630Polymer identityPET homopolymer/copolymerConforms
    EU Regulation (EU) No 10/2011Annex I, SML(T)Terephthalic acid specific migration7.5 mg/kg
    GB 4806.7-2016Total migration in food simulantOverall migration10 mg/dm²
    EU Regulation (EU) No 10/2011EN 1186-1:2002Total migration test10 mg/dm²

    Terminal articles include carbonated soft drink bottles, still water bottles, hot-fill containers, and cooking oil bottles.

    Low-Oligomer Resin Requirements and Draft Ratio Boundaries in Biaxially Oriented Polyester Film

    Biaxially oriented polyester film manufacture from PTA-derived PET demands low diethylene glycol content below 1.0 wt% and intrinsic viscosity of 0.62–0.68 dL/g to survive transverse stretching. The base resin is produced with an EG/PTA molar ratio of 1.10–1.15; lower glycol excess reduces diethylene glycol and carboxyl end-group concentration, which in turn reduces oligomer formation. Silica antiblock is compounded at 0.05–0.30 wt% with median particle size 2–4 µm to control film blocking without generating visible haze. Extrusion on a cast-film line runs at 275–285 °C with resin moisture below 50 ppm; a melt filtration system with 20–40 µm cut-off removes gels and agglomerated silica.

    Sequential biaxial stretching draws the cast web at machine-direction ratios of 3.0–3.5 and transverse-direction ratios of 3.5–4.0, followed by heat-setting at 210–230 °C to achieve dimensional stability below 0.5% shrinkage at 150 °C when tested per ASTM D1204-14. Compliance for food packaging film is evaluated under FDA 21 CFR 177.1630 and EU Regulation (EU) No 10/2011; tensile properties are tested per ASTM D882-18. Terminal forms include flexible food packaging, metalised barrier film, capacitor film, and photovoltaic backsheet film.

    When PTA is substituted for dimethyl terephthalate in polybutylene terephthalate synthesis, the 1,4-butanediol dehydration route to tetrahydrofuran becomes the dominant yield-loss variable. The direct esterification route charges 1,4-butanediol/PTA at a molar ratio of 1.4–1.6; the excess diol compensates for tetrahydrofuran formation at 220–245 °C, but excess above 1.6 raises tetrahydrofuran concentration in overheads and increases purification load. Tetrabutyl titanate is metered at 50–150 ppm Ti based on polymer mass, and esterification pressure is held at 50–80 kPa to remove water without excessive 1,4-butanediol loss. Polycondensation proceeds at 250–255 °C under ≤50 Pa, with melt viscosity rise monitored by torque or intrinsic viscosity. Published data for this specific direct PTA route in production-scale PBT lines is limited; plants generally use licensor-specific esterification profiles because the tetrahydrofuran-water separation step imposes an equipment boundary.

    Compounded PBT formulations require glass fibre reinforcement at 15–30 wt% or flame-retardant packages to meet UL 94 V-0 at 0.8 mm when evaluated under IEC 60695-11-10. Injection moulding uses melt temperature 245–260 °C and mould temperature 60–90 °C to control crystallisation. Mechanical property data for conditioned specimens is evaluated under ISO 7792-1 and ASTM D638-14. Terminal product types include connectors, relay housings, automotive wire harness clips, and motor brackets.

    Direct Esterification with 2-Ethylhexanol Converts PTA into DOTP Without the ortho-Phthalate Restriction Profile

    DOTP synthesis from PTA and 2-ethylhexanol is run at a 2-EH/PTA molar ratio of 2.3–2.6; below 2.3, the reaction mass remains too viscous for reliable water stripping, and above 2.6, alcohol recovery raises energy demand without sufficient conversion gain. Tetrabutyl titanate or tetra-isopropyl titanate is charged at 0.05–0.2 wt% of PTA mass, and esterification temperature is controlled between 200–230 °C under nitrogen sparge. Water of reaction is removed from the overhead condenser; batch times of 8–14 h are typical for 20 m³ reactors, with endpoint acid value below 0.05 mg KOH/g after vacuum stripping and neutralisation with sodium carbonate solution.

    The finished ester is tested for ester content ≥99.0%, colour ≤30 Hazen measured per ASTM D1209-05, and moisture ≤0.1 wt%. Because DOTP is a terephthalate rather than an ortho-phthalate, it is not listed in EU REACH (EC) No 1907/2006 Annex XVII Entry 51 restricted phthalate entries; RoHS compliance is assessed under Directive 2011/65/EU. Terminal products include PVC wire and cable insulation, automotive interior sheet, flooring, and toy-grade flexible PVC.

    If the Hydroxyl Number Must Stay Below 300 mg KOH/g, PTA Addition in DEG-Based Polyol Esterification Requires a Split-Feed Profile

    In aromatic polyester polyols for rigid polyurethane and polyisocyanurate foam, PTA is esterified with diethylene glycol at a PTA addition of 20–45 wt% of the final polyol mass, depending on target aromaticity and viscosity. The split-feed profile adds 60–70% of the PTA charge in the first stage at 180–200 °C and the remainder after the initial exotherm subsides, preventing slurry phase separation and maintaining acid value below 5 mg KOH/g mid-reaction. Final esterification at 200–230 °C under vacuum ≤5 kPa reduces acid value to ≤2.0 mg KOH/g; residual acid above this level destabilises the tin and amine catalyst package in foam formulation.

    Typical polyol specifications include hydroxyl number 200–400 mg KOH/g, viscosity 2,000–10,000 mPa·s at 25 °C determined per ASTM D4878-15, and water content ≤0.10 wt%. Fire performance of the resulting polyisocyanurate panel is assessed under EN 13501-1 and ASTM E84-23; appliance and building applications may additionally require FM 4880 or local thermal insulation codes. Terminal forms include polyisocyanurate insulation boards, pipe insulation segments, and spray foam systems.

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    Certification & Compliance
    More Introduction

    CNPC Urumqi Petrochemical PTA is a purified aromatic dicarboxylic acid supplied as an undifferentiated fiber-grade product; the site does not publish multiple model designations, and the lot certificate of analysis is the operative specification. The material has CAS 100-21-0 and molecular formula C8H6O4. It is produced by liquid-phase oxidation of para-xylene over a cobalt–manganese–bromine catalyst system, followed by hydrogenation of the intermediate 4-carboxybenzaldehyde to reduce color-forming impurities. The dried white powder is intended for continuous melt-phase polyester plants manufacturing staple fiber, filament, and bottle-grade PET. In direct esterification, PTA and monoethylene glycol are metered into high-shear paste mixers at a molar ratio of 1.1–1.6 mol EG per 1 mol PTA; the paste then enters agitated esterification reactors operating at 240–260 °C and 0.2–0.4 MPa gauge. Downstream, the monomer is polycondensed in high-vacuum finishers at 280–290 °C until the target intrinsic viscosity is reached as measured by ASTM D4603-18. Because PTA is a commodity, differences among producers are mainly certificate-level control of 4-carboxybenzaldehyde, ash, moisture, and particle size rather than fundamental chemistry.

    What Impurity Limits Govern Continuous Polyester Melt Plants?

    Release limits for Urumqi PTA are aligned with GB/T 32685-2016 and verified against internal plant data. The primary process impurity is 4-carboxybenzaldehyde, a monofunctional intermediate that survives oxidation and acts as a chain terminator if not hydrogenated. Urumqi certificates generally require ≤25 mg/kg 4-CBA by high-performance liquid chromatography with UV detection at 254 nm; above this limit, chain-stopping effects can lower melt-phase intrinsic viscosity and shift the carboxyl end-group balance. p-Toluic acid, another mono-functional acid, is limited to ≤150 mg/kg because excessive monoacid changes the stoichiometric balance between hydroxyl and carboxyl end groups. Moisture is limited to ≤0.2 wt% by ASTM E203-16 Karl Fischer titration; residual water in the feed contributes to hydrolysis and can reduce ethylene glycol dehydration efficiency in the esterifier. Ash is limited to ≤15 mg/kg by gravimetric ignition at 850 °C in a muffle furnace, which protects spinneret packs and preform hot-runner manifolds from inorganic deposit buildup. CIELAB b* color is controlled to ≤1.5 under ISO 11664-4:2008. Particle size is measured by laser diffraction per ISO 13320-1:2020, with D50 maintained at 110–140 µm and fines below 5 wt% through 45 µm.

    Property Unit Typical fiber-grade limit Analytical basis
    4-Carboxybenzaldehyde mg/kg ≤25 HPLC with UV detection at 254 nm
    p-Toluic acid mg/kg ≤150 HPLC with UV detection
    Moisture wt% ≤0.2 ASTM E203-16 Karl Fischer titration
    Ash mg/kg ≤15 Gravimetric ignition at 850 °C
    b* color CIE unit ≤1.5 ISO 11664-4:2008
    Particle size D50 µm 110–140 ISO 13320-1:2020 laser diffraction
    Fines through 45 µm wt% ≤5 Laser diffraction/sieve

    In polyester staple fiber production, raw-material consistency controls paste pump torque and spinneret back-pressure. The Urumqi product reaches the continuous PET train via dense-phase conveying into day silos; a broad particle size distribution with D50 of 110–140 µm and ≤5 wt% fines through 45 µm reduces bridging in hoppers and pressure spikes in rotary valves. On production-scale agitated paste mixers, batch-to-batch variation in moisture above 0.2 wt% can alter esterification water formation and create controller instability because the first-stage esterification heat load is partly set by water removal. Fiber producers add antimony trioxide or titanium alkoxide at 150–300 ppm Sb for antimony-based systems; actual addition is determined by target intrinsic viscosity and final color. The PTA must not contain excessive p-toluic acid because it can terminate chain growth and increase the oligomer fraction in the pre-polycondensation section, shifting final spin pack pressure. Operators using Urumqi PTA in staple fiber extrusion report that a stable fines fraction below 5 wt% through 45 µm reduces melt-spinning filter changes and feed system interruptions.

    Draw-textured yarn and industrial filament require lower carboxyl end groups and higher consistency. The same PTA is used with additional solid-state polymerization if high intrinsic viscosity is required. Intrinsic viscosity for tire cord or airbag yarn is commonly raised to 0.85–1.00 dL/g by solid-state polymerization after melt-phase production; this upgrading is sensitive to initial carboxyl end-group ratio, which rises if 4-CBA or p-toluic acid is present. The low monoacid content of Urumqi fiber-grade PTA orients it to such downstream operations, though users must validate the final product on their specific solid-state reactor.

    When 4-Carboxybenzaldehyde Exceeds 25 mg/kg in High-Clarity Resin

    High-clarity bottle-grade PET has a tighter impurity window. If 4-carboxybenzaldehyde remains above 25 mg/kg, the monoaldehyde can terminate chains and generate conjugated condensation products during high-temperature polycondensation; this moves b* positive and lowers L* in preforms. The Urumqi product is controlled below this limit, but storage conditions can erode the advantage. Moisture adsorbed above 0.2 wt% hydrolyzes ester linkages during melt-phase processing; a pre-drying step in a nitrogen-purged silo with a dew point below −20 °C is required when ambient relative humidity exceeds 60%. For carbonated-soft-drink preforms, melt-phase intrinsic viscosity is typically 0.80–0.84 dL/g, and the acetaldehyde content after injection molding is tested by ASTM F2013-10. Low ash is necessary because deposits on hot-runner manifold walls change gate-pressure repeatability and can increase preform weight variation. In blow molding, optical transmission and b* are evaluated on bottle sidewalls using CIELAB geometry under ISO 11664-4:2008. Published data for Urumqi PTA in this specific bottle-grade configuration is limited; converters should validate acetaldehyde and color on their own preform platforms.

    During preform molding, acetaldehyde generation is a direct downstream criterion. Melt-phase PET from Urumqi PTA with low 4-CBA and controlled cobalt residues tends to produce lower free acetaldehyde after drying. However, published data for this specific configuration is limited; converters should validate preform acetaldehyde by headspace gas chromatography per ASTM F2013-10 and should not substitute a vendor certificate for process qualification.

    How Does Urumqi PTA Compare with Crude, Medium-Purity, and Recycled Terephthalic Acid?

    Compared with crude terephthalic acid, the difference is purification depth. Crude terephthalic acid from para-xylene oxidation may contain 4-CBA above 1000 mg/kg and p-toluic acid above 2000 mg/kg; it cannot be used directly in high-clarity PET without hydrogenation. Medium-purity TA retains variable 4-CBA, commonly 500–3000 mg/kg, and is reserved for less color-sensitive applications. Recycled rPTA obtained from PET depolymerization is not a direct chemical substitute because it may contain isophthalic acid comonomer, diethylene glycol fragments, hydrolysis catalysts, and color bodies from post-consumer packaging. Compared with other fiber-grade PTA sources, Urumqi material is similar in fundamental chemistry; the distinction is site-specific control of fines, ash, moisture, and 4-CBA distribution. Users should not treat any PTA as fully interchangeable without verifying feeder behavior and melt-phase intrinsic viscosity response, because particle size distribution can differ among producers even within the same 4-CBA specification.

    Characteristic Urumqi fiber-grade PTA Crude terephthalic acid Medium-purity TA Recycled rPTA
    4-CBA ≤25 mg/kg often >1000 mg/kg 500–3000 mg/kg not consistently defined
    p-Toluic acid ≤150 mg/kg often >2000 mg/kg variable not applicable
    Color body risk low high medium-high depends on source
    Ash ≤15 mg/kg higher metals variable may contain catalyst residues
    Particle size D50 110–140 µm broad variable not comparable

    Bulk Handling Dust Deflagration and Storage Moisture Boundaries

    PTA powder is a combustible organic dust. NFPA 652 requires a dust hazard analysis for storage and transfer systems. The Urumqi product contains fines below 5 wt% through 45 µm, which limits but does not eliminate explosibility; the finer fraction can form a combustible dust cloud if the concentration reaches the lower explosive limit. Facilities should conduct site-specific KSt and minimum ignition energy tests rather than relying solely on vendor data. Transfer systems should be bonded and grounded, and rotary valves should be interlocked with air-flow switches. Silo oxygen concentration is often maintained below 10 vol% with nitrogen purge during abnormal high-dust operation. Moisture limits are also an operational boundary: condensation in unheated silos under Urumqi winter conditions can raise surface moisture above 0.2 wt%, causing caking and screw feeder surge. The material should not be blended with strong bases such as sodium carbonate or calcium hydroxide at high humidity; salt formation can plug dense-phase piping and accelerate wear. Air purges should be filtered to prevent product loss through baghouse vents. These handling boundaries are based on standard powder operations; published data for this specific Urumqi configuration is limited, so hazardous-area classification and dust hazard analysis should be verified on site.

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