Biodegradability of terephthalic acid in terylene artificial silk printing and dyeing wastewater

As the characteristic pollutant, terephthalic acid(TA)was in charge of 40%—78% of the total COD of terylene artificial silk printing and dyeing wastewater(TPW-water). The studies on biodegradability of TA were conducted in a serial of activated sludge reactors with TPW-water. TA appeared to be readily biodegradable with removal efficiency over 96.5% under aerobic conditions, hardly biodegradable with removal efficiency below 10% under anoxic conditions and slowly biodegradable with a turnover between 31.4% and 56.0% under anaerobic conditions. TA also accounted for the majority of BOD in TPW-water. The process combined by anoxic, anaerobic and aerobic activated sludge reactor was suitable for TA degradation and TPW-water treatment. Further, the aerobic process was essentially much more effective than the anaerobic or anoxic one to degrade TA in TPW-water.

Anaerobic biodegradability of terephthalic acid and its inhibitory effect on anaerobic digestion

The behavior of terephthalic acid (TPA) in anaerobic system has been studied bysemicontinuous bioassays under mesophilic condition with artificial TPA production wastewater. Theeffect of different loading rate of TPA on anaerobic digestion was studied under certain CODloading rate. The results showed that the TPA could be degraded anaerobically within a relativelylow range. The degradable concentration of TPA was less than 500 mg/L in the digester, higherconcentration of TPA could not be degraded totally and the rate of degradation might decrease withthe increase of feed amount. The inhibition is related to both loading rate and accumulatedconcentration of TPA in the digesters.

Purified terephthalic acid wastewater biodegradation and toxicity

The biodegradation and toxicity of the purified terephthalic acid（PTA） processing wastewater was researched at NJYZ pilot with the fusant strain Fhhh in the carrier activated sludge process（ CASP）. Sludge loading rate（SLR） for Fhhh to COD of the wastewater was 1.09 d^-1 and to PTA in the wastewater was 0.29 d^-1. The results of bioassay at the pilot and calculation with software Ebis3 showed that the 48h-LC50 （median lethal concentration） to Daphnia magna for the PTA concentration in the wastewater was only 1/10 of that for the chemical PTA. There were .5 kinds of benzoate pollutants and their toxicities existing in the wastewater at least. The toxicity parameter value of the pure chemical PTA cannot be used to predicate the PTA wastewater toxicity. The toxicity of the NJYZ PTA wastewater will be discussed in detail in this paper.

A two-stage anaerobic system for biodegrading wastewater containing terephthalic acid and high strength easily degradable pollutants

The high strength easily biodegradable pollutants (represented by COD E) are strong inhibitors of terephthalic acid (TA) anaerobic biodegradation. At the same time, TA can inhibit easily biodegradable pollutants removal under anaerobic conditions to a limited extent. This mutual inhibition could happen and cause a low removal efficiency of both TA and COD E, when the effluent from TA workshops containing TA and easily biodegradable pollutants are treated by a single anaerobic reactor system. Based upon the treatment kinetics analysis of both TA degradation and COD E removal, a two stage up flow anaerobic sludge blanket and up flow fixed film reactor(UASB UAFF) system for dealing with this kind of wastewater was developed and run successfully at laboratory scale. An UASB reactor with the methanogenic consortium as the first stage removes the easily biodegradable pollutants(COD E). An UAFF reactor as the second stage is mainly in charge of TA degradation. At a COD E loading of 15.3 g/(L\5d) and a TA loading of 1.4 g/(L\5d), HRT 18.5h, the COD E and TA removal rate of the system reached 89.2% and 71.6%, respectively.

Towards recycling purpose:Converting PET plastic waste back to terephthalic acid using pH-responsive phase transfer catalyst

Converting polyethylene terephthalate(PET)wastes to its monomer and valuable chemicals via ecofriendly chemical method is still a challenge task.Previously,phase transfer catalysts used for alkaline hydrolysis were soluble in reaction media and hardly separated after reaction.Here,we reported several pH-responsive catalysts combined alkyl quaternary ammonium units with heteropolyacid anion for achieving stepwise product/catalyst separation and catalyst recycling.The properties of homogeneous/heterogeneous transfer behavior allow catalyst to be easily separated from reaction media by adjusting of pH value.Among them,[C_(16)H_(33)N(CH_(3))_(3)]_(3)PW_(12)O_(40)(abbreviated as[CTA]_(3)PW)exhibits the highest activity and the most suitable pH responsive values.Such a pH triggered switchable catalytic system not only shows good performance for depolymerization of pure PET,but also some real PET wastes such as coloured trays and PE/PET complex films could be completely degraded into terephthalic acid.Additionally,the reaction kinetics and activation energy of PET alkaline hydrolysis also studied with and without pH-responsive[CTA]_(3)PW.

Induction of Bladder Lesion by Terephthalic Acid and Its Mechanism

To provide more information for rational evaluation of potential risks of terephthalic acid （TPA）, we studied the effects of TPA on rats＇ bladders in 90 days after TPA exposure. Methods Sprague Dawley rats were subdivided into five groups, ingesting 0 %, 0.04 %, 0.2 %, 1%, and 5 % TPA respectively for a sub-chronic feeding study lasting for 90 days. Urine, serum and samples of brain, liver, lung, kidney, bladder, etc. were collected and analyzed. Results TPA ingesting decreased the value of urinary pH, and increased the contents of Ca^2＋, Zn^2＋, Mg^2＋, Na^＋, K^＋ in urine. The volume of 24 h urine was significantly increased in male rats in the 1% and 5 % TPA groups. Urinary white sediment was found in both sexes, and its formation in male rats seemed more susceptible than that in female rats. Alpha 2u-globulin （AUG） in serum and urine of male rats was markedly increased in a dose-dependent manner. Fifteen cases of hyperplasia （simple or atypical） were determined in the 5 % TPA ingesting group, 14/52 in male rats and 1/23 in female rats. Among them 3 male rats had no stone or calculus. Those with either bladder stones or hyperplasia were accompanied with urinary white sediments. Conclusion White sediment accompanied with elevated urine AUG is the basis of TPA induced urolith formation, and is also associated with TPA induced bladder epithelial cell proliferation. It can act as an early biomarker for the potential toxic effect of TPA.

Spectrofluorimetric determination of terbium with terephthalic acid

A Spectrofluorimetric method has been developed for the determination ofterbium(Ⅲ) based on the formation of a complex with terephthalic acid [benzene-1, 4-dicarboxylicacid (TPA)] in slightly acidic aqueous solution in the presence of gelatin. Terbium ion can form astable complex with TPA with the stoichiometry of 1:2. The best excitation and maximum emissionwavelengths are observed at 260 nm and 545 nm, respectively. The fluorescence intensity of terbiumcomplex gets the strongest within 20 min and remains stable up to 10 h, and it is proportional toterbium(Ⅲ) concentration in the range of 4.0x10^(-5)-1.6x10^(-7) mol·L^(-1) under the optimumconditions. The fluorescence system has good selectivity, sensitivity and stability. The relativestandard deviation is still within +-4% in the presence of 1200-fold amounts of the other lanthanideions when the concentration of terbium(Ⅲ) is 1.0x10^(-6) mol·L^(-1) and common co-existing ionshardly interfere the determination. It has been applied to the direct fluorimetric determination oftrace terbium (Ⅲ) in rare earth ores and oxides.

Synthesis and Characterization of Poly(terephthalic acid-2,5-furandicarboxylic acid-1,8-octanediol) Copolyester

Terephthalic acid,2,5-furandicarboxylic acid and 1,8-octanediol were adopted as monomers and antimony trioxide as catalyst,and poly(terephthalic acid-2,5-furandicarboxylic acid-1,8-octanediol) copolyesters identified as PEOT-x,where x is the mole fraction of furandicarboxylic acid in the samples,were synthesized by direct esterification.The molecular structure of the copolyesters was characterized by FTIR and 1H NMR spectroscopy.Gel permeation chromatography (GPC),differential scanning calorimetry (DSC),and thermogravimetric analysis (TGA) were used to characterize the molecular weight,molar mass dispersity,glass transition temperature,and thermal stability of the copolyesters,respectively.The mechanical properties of the samples were also investigated.The number-average molecular weight (M_(n)) of the samples varies from 9 700-18 800 g/mol,and molar mass dispersity (■=M_(w)/M_(n)) from 2.15-3.34.The initial decomposition temperature of the copolyesters is in the 332-356 ℃ range,with maximum decomposition rates at 390-410 ℃,while the glass transition temperature (Tg) varies from 0-33 ℃.Mechanical test shows that PEOT-10 has the highest tensile strength,while PEOT-90 has the largest tensile modulus and elongation at break.The experimental results show that these copolyesters can be synthesized with relatively high molecular weights,good thermal stability,and fair mechanical properties,which makes them excellent replacements for commercial polyesters,such as PET,and these properties can be tuned through the relative amounts of biomass monomer 2,5-furandicarboxylic acid used in the reactions.

Solvothermal Synthesis,Crystal Structure and Photoluminescence Property of a 3D Lead(Ⅱ)Coordination Polymer Based on Terephthalic Acid

Solvothermal reaction of Pb（NO3）2·6H2O with rigid linear ligand terephthalic acid（H2pta） in N,N-dimethylformamide（DMF） produced a new three-dimensional（3D） lead（Ⅱ）coordination polymer[Pb2（pta）1.5（μ4-OH）（DMF）]n 1,and its structure was characterized by single-crystal X-ray diffraction analyses.In polymer 1,the μ4-OH bridges the nearby lead（Ⅱ） ions into an infinite one-dimensional（1D） chain,and then the organic ligand pta^2- joins the neighbored chains into a 3D structure by two similar connection modes in different configurations.The solid-state photoluminescent studies revealed that 1 exhibits a strong greenish emission mainly originating from ligand-to-metal charge transfer between the delocalized π bonds of the aromatic carboxylate ligand pta^2- and the p orbitals of the Pb^2＋ centers.

Effects of Terephthalic Acid on Rat Lipid Metabolism

Objective To study the effect of terephthalic acid （TPA） on lipid metabolism in Sprague-Dawley （SD） rats. Methods Five groups of SD rats that ingested 0%, 0.04%, 0.2%, 1%, and 5% TPA, respectively, were included in a 90-day subchronic feeding study. Effects of TPA on levels of serum protein, total cholesterol （TC）, triglycerides （TG）, high-density lipoprotein cholesterol （HDL）, total antioxidative capability （T-AOC）, superoxide dismutase （SOD） and malondialdehyde （MDA） were observed. Urine samples were collected and analyzed for concentration of ion. Results TPA decreased the level of serum T-AOC in a dose dependent manner. The contents of serum and bladder MDA significantly decreased in 1% and 5% TPA ingestion groups. Serum CuZn superoxide dismutase （CuZnSOD） lowered in groups of 0.2%, 1%, and 5% TPA. TPA subchronic feeding had no significant influences on serum TC, LDL or HDL, but increased serum TG, TP and ALB after administration of 0.04% and/or 0.2% TPA. Concentrations of urinary Ca^2＋, Mg^2＋, Na^＋, and K^＋ were elevated in 1% and 5% TPA groups. Conclusion Antioxidative potential decreased after TPA exposure. MDAincrease in serum and bladder tissues was one of the most important reactions in rats which could protect themselves against TPA impairment. The decrease of serum CuZnSOD was related to the excretion of Zn^2＋.

Metabolism of Terephthalic Acid and Its Effects on CYP4B1 Induction

Objective To investgate the metabolism of terephthalic acid （TPA） in rats and its mechanism. Methods Metabolism was evaluated by incubating sodium terephthalate （NaTPA） with rat normal liver microsomes, or with microsomes pretreated by phenobarbital sodium, or with 3-methycholanthrene, or with diet control following a NADPH-generating system. The determination was performed by high performance liquid chromatography （HPLC）, and the mutagenic activation was analyzed by umu tester strain Salmonella typhimurium NM2009. Expression of CYP4B 1 mRNA was detected by RT-PCR. Results The amount of NaTPA （12.5-200 μmol-L^1） detected by HPLC did not decrease in microsomes induced by NADPH-generating system. Incubation of TPA （0.025-0.1 mmol-L^-1） with induced or noninduced liver microsomes in an NM2009 umu response system did not show any mutagenic activation. TPA exposure increased the expression of CYP4B1 mRNA in rat liver, kidney, and bladder. Contusion Lack of metabolism of TPA in liver and negative genotoxic data from NM2009 study are consistent with other previous short-term tests, suggesting that the carcinogenesis in TPA feeding animals is not directly interfered with TPA itself and/or its metabolites.

Construction of hybrid cell with Phanerochaete chrysosporium to degrade terephthalic acid wastewater——(I) phenotype evidence

The fungi Phanerochaete chrysosporium (PC) and Saccharomyces cerevisiae Y99 and the native bacterium YZ1 were the three parental strains for construction of hybrid cells through protoplast fusion to degrade terephthalic acid (TPA) wastewater. The results showed that the native bacterium YZ1 protoplasm could integrate with that of PC to form the hybrid cell Fhh and the fungus Y99 protoplasm also could integrate with that of Fhh to form the hybrid cell Fhhh. The protoplasts of YZ1 and Y99 could change the morphology of PC spore and mycelium for two times. The hybrid cell Fhhh got the best growth and degradation abilities in the wastewater. It suggested that the hybrid strains obtained from the inter\|kingdom protoplast fusion of the three parental strains could create potential for the purification of TPA wastewater.

Comparative study of thermophilic and mesophilic anaerobic treatment of purified terephthalic acid (PTA) wastewater

The paper provides a critical comparison between mesophilic and thermophilic anaerobic treatment of PTA wastewater through diagnosis of a case study. Aspects covered are bioavailability, biodegradability, microbial population, thermodynamics, kinetics involved and bio-reactor design for PTA wastewater treatment. The results of the case study suggests that one- stage thermophilic anaerobic reactor coupled with coagulation-flocculation pre-treatment unit and an aerobic post treatment unit could be techno-economically viable for PTA wastewater treatment to ensure that the final effluent quality conforms to the international standard. The in-formation emanated from this study could be useful and thought provoking to the professionals and academia in the area of PTA wastewater treatment and can serve as impetus toward the development of research lines in similar problems like the treatment of other petrochemical wastewater such as phenol-con- taining wastewater, benzene/benzoic acid-con- taining wastewater or wastewater from other similar industrial settings.

Syntheses and Co-Fluorescence of Complexes of Eu (III)/Gd (III) with Thienyltrifluoroacetonate, Terephthalic Acid and Phenanthroline

A series of complexes of europium (III)/gadolinium (III) with 2-thienyltrifluoroacetonate (HTTA), terephthalic acid (TPA) and phenanthroline (Phen) were synthesized by coprecipitation. The resulting complexes including Eu2(TPA)(TTA)4Phen2, Eu1.4Gd0.6(TPA)(TTA)4Phen2, Eu1.0Gd1.0(TPA)(TTA)4Phen2 and Eu0.8Gd1.2(TPA)(TTA)4Phen2 were characterized by elemental analysis, IR spectroscopy and thermal stability analysis. The results of analysis indicate that the complexes obtained have similar binuclear structure with each other. The thermal stability analysis indicates that the complexes Eu2(TPA)(TTA)4Phen2and Eu1.0Gd1.0(TPA)(TTA)4Phen2 possess good thermal stability, which melt at ~241°C and decompose at ~370°C - 430°C corresponding to the formation of the complexes. The fluorescence spectra of Eu2(1-x)Gd2x(TPA)(TTA)4Phen2 (x = 0 - 1) complex powders and their doped silica gels were studied. The co-fluorescence effect of Gd3+ ions in complex powders is different from that of their doped silica gels. The optimum concentration of Gd3+ for complex powders and their doped silica gels is 0.5 and 0.3 (molar fraction), respectively. The co-fluorescence distinction of Gd3+ ions for complex powders and their doped silica gels is preferably interpreted from the proposed binuclear structure together with monomolecular compositions of the complexes for the first time. Both intermolecular energy transfer and intra molecular energy transfer in cross binuclear monomolecular EuGd(TPA)(TTA)4Phen2 are thought to be responsible for the co-fluorescence effect of the complex powders;yet only the latter is thought to be responsible for the co-fluorescence effect in silica gels, for the complex molecules in this case are isolated from each other.

The preparation of terephthalic acid by solvent-free oxidation of p-xylene with air over T(p-C1)PPMnC1 and Co(OAc)_2

An attempt has been made to prepare terephthalic acid（TPA） by solvent-free oxidation of p-xylene（PX） with air over tetra（pchlorophenylporphinato） manganese chloride（T（p-Cl）PPMnCl） and cobalt acetate.The co-catalysis between T（p-Cl）PPMnCl and Co（OAc）_2 has been discovered under solvent-free conditions.TPA yield could be increased significantly when T（p-Cl）PPMnCl and Co（OAc）_2 were used together.The addition of T（p-Cl）PPMnCl into the reaction mixture over Co（OAc）_2 significantly accelerated the rate-determining step of the oxidation process of PX to TPA.The effect of temperature on reaction was also investigated.

New possibility for PET plastic recycling by a tailored hydrolytic enzyme

Plastic waste puts a huge burden on the ecosystem due to the current lack of mature recycling technology.Poly(ethylene terephthalate)(PET)is one of the most produced plastics in the world.Enzymatic decomposition holds the promise of recovering monomers from PET plastic,and the monomers can be used to regenerate new PET products.However,there are still limitations in the activity and thermal stability of the existing PET hydrolases.The recent study by Lu et al.introduced a novel PET hydrolase via machine learning-aided engineering.The obtained PET hydrolase showed excellent activity and thermal stability in the hydrolysis of PET and is capable of directly degrading large amounts of postconsumer PET products.This approach provides an effective method for recycling PET waste and is expected to improve the current state of plastic pollution worldwide.

Comparison and Relation between Crystal Structures and Magnetic Properties of Two Manganese(Ⅱ)Coordination Polymers Based on(Triazol-1-yl)iso/terephthalic Acid

One new Mn(Ⅱ)coordination polymer,[Mn(Htia)_(2)(H_(2)O)_(2)]_(n)·2nH_(2)O(1,H_(2)tia=4-(1,2,4-triazol-1-yl)isophthalic acid)has been synthesized in mixed solvents under solvothermal conditions.Further characterizations including single-crystal XRD,elemental analysis,IR spectroscopy,thermogravimetric analysis and powder XRD were performed to verify the structure.Complex 1 displays a one-dimensional(1D)chain and is similar to a reported Mn(II)complex 2{[Mn(Htta)_(2)(H_(2)O)_(2)]·2H_(2)O}_(n).It crystallizes in triclinic P1 space group,with a=7.5557(3),b=7.5974(3),c=11.8448(4)Å,α=90.088(1)°,β=95.863(1)°,γ=113.668(1)°,V=618.81(4)Å^(3),Z=1,M_(r)=591.36 g/mol,D_(c)=1.587 mg/m^(3),μ=0.609 mm^(-1),F(000)=303,GOOF=1.062,the final R=0.0359and w R=0.0818 for 4272 observed reflections with I>2σ(I).Based on two similar structures,Hirshfeld surface analysis confirmed both structures are mainly stabilized by O···H/H···O and C···H/H···C hydrogen bonds.Further,weak ferromagnetic behaviors between adjacent Mn(II)ions in 1D chain are obtained.

Experimental Study of the Influence of Intrinsic Parameters on the Thermal Reactivity of Sawdust, Polyethylene Terephthalate and Composite

Several works have been based on the study of thermal variations in biomass to derive more valuable products such as fuels capable of replacing oil in the event of a crisis or activated carbon used as an adsorbent material, widely used in industry for the elimination of unwanted materials, both in liquid and gaseous environments. A study of thermal parameters such as: heating speed, retention time, drying temperature, carbonization temperature, particle size, was carried out with the aim of determining the characteristic factors of the carbonization of Polyethylene terephthalate (PET), sawdust (SC) and sawdust/polyethylene terephthalate (CPS) mixture. The results of the immediate analysis revealed a very low level of ash in PET (0.013%) compared to the level of ash in sawdust (2.9%), as well as a high level of fixed carbon (82.960%), which suggests the presence of mineral oxides and a significant carbon matrix unlike PET, which indicates a very significant organic matrix (essentially made up of organic matter) with the absence of mineral oxides. The study of thermal parameters showed the water loss from Sawdust (SC) and the Sawdust/Polyethylene terephthalate (CPS) mixture, an increase with temperature, unlike that of PET whose variation is essentially zero. Without heat treatment, sawdust alone contains approximately 7% water. The optimal drying temperature for this study is 110˚C for a stay of 24 hours. It appears that the largest mass losses for the PET samples are between 87.19% and 96.05%, followed by that of the mixture, between 47.33% and 64.37%. And the lowest are observed, those of sawdust (from 24.02% to 62.6%). However, here we can say that the influence of the mass is not great, given the slight difference between the losses by temperature. The results of the study of the influence of grain size showed that the differences are insignificant, even if we vary the diameter of the grains from simple to triple. To better minimize physical constraints such as the intragranular diffusibility of the volatile matter and the homogeneity of the temperature in the grains, 75 μm particles are found to be optimal for our study. It can be noted when studying the heating rate that the mass loss at the end of the reaction is approximately the same depending on each precursor material. However, it has been demonstrated that the heating rate strongly influences the nature of the reaction products both for volatile materials and for the solid residue as well as on the kinetic parameters of the chemical reaction. Furthermore, the variation in apparent density shows a decrease as a function of the increase in the residence time of the materials in the reactor. As the carbonization time increases, the apparent density decreases. We note, for the lignocellulosic material, that the apparent density stabilizes after 60 minutes.

Self-Assembly Ultrathin Fe-Terephthalic Acid as Synergistic Catalytic Platforms for Selective Hydrogenation

Alloy nanoparticles(NPs)with numerous exposed catalytic active sites have been extensively studied as efficient heterogeneous catalysts.However,it is challenging to synthesize alloy NP catalysts with high activity while avoiding aggregation.Herein,we report a facile method to encapsulate alloy NPs loaded metal–organic framework(MOF)catalysts(alloy NPs/MOFs)within an ultrathin metal–organic layer using a terephthalic acid(BDC)assisted method.A series of metal-BDC encapsulated PtM/MOFs(M=Fe,Co,and Ni)catalysts were synthesized successfully and showed significantly enhanced catalytic performance toward selective hydrogenation reaction.

Effect of Polyethylene Terephthalate Plastic Waste on the Physico-Mechanical and Thermal Characteristics of Stabilized Laterite Bricks

The present work investigated the effect of polyethylene terephthalate (PET) plastic waste on the physico-mechanical and thermal properties of cement-stabilized laterite bricks to see the durability of the modified bricks (CSLB). Samples were formulated by mixing laterite, cement, and different percentages of PET (0%, 3%, 5%, and 7%) by volume. The bricks were produced using the M7MI Hydraform standard interlocking block and kept in the shade for a curing period of 28 days. The addition of 3% to 5% PET to the laterite stabilized with 10% cement results in a decrease in both dry and wet compressive strength, which is determined using the Controlab compression machine. However, the obtained results are in concordance with the standards. The thermal conductivity of CSLB, determined using the box method with the EI700 measurement cell, decreases as the PET content of the mixture increases. A decrease in bulk density from 1.67 to 1.58 g/cm3 was observed.