浅谈PET熔体输送管道的工艺设计

对ＰＥＴ熔体输送过程中的熔体允许停留时间、熔体温升和压力降等熔体配管设计条件进行了分析讨论。允许停留时间由允许熔体特性粘度降和热降解速度常数来确定；熔体温升主要取决于熔体输送泵（或增压泵）的转速和输送过程的压力降；配管管径由压力降、停留时间和管材耐压强度等因素来确定。

PET瓶储条件对蓝莓酒颜色和酚类物质含量的影响

以在聚对苯甲酸乙二醇酯(polyethylene terephthalate,PET)瓶内贮存的发酵结束后的蓝莓酒为研究对象,探究不同储存条件对其酚类物质和颜色的影响。结果表明:与室温有光和室温避光条件相比,酒窖储存的酒样,总酚和总花色苷含量下降速度较慢,且对游离花色苷的降解和聚合花色苷的上升有更好的抑制效果,保护了蓝莓酒的红色色调,减缓了酒颜色向砖红色转变的速度。相关性分析发现,酚类物质影响酒样的颜色参数,总酚、总花色苷、游离花色苷及辅色花色苷与红色色调显著正相关,总类黄酮及聚合花色苷与黄色色调显著正相关。主成分分析结果显示,酒窖储存酒样的品质与其他两种条件有显著差异;在瓶储6个月内,室温避光和室温有光组酒样之间差异不显著(p<0.05),说明温度是决定蓝莓酒PET瓶储期内酚类物质和颜色参数的因素。

IN-SITU POLYMERIZED SYNTHESIS AND PROPERTIES OF NANO-ZnO/PEG/PET COMPOSITE

Nano-ZnO particle （nZnOp） reinforced polyethylene glycol （PEG）/polyethylene terephthalate （PET） （nZnOp/PEG/PET） copolymeric composites with different mass fractions and molecular weights of PEG are synthesized via in-situ polymerization. The dispersion of nZnOp in copolymer matrixes and the effects of PEG and nZnOp particles on the crystallization behavior of the composites are studied by TEM, differential scanning calorimetry（DSC）, XRD and Fourier thansform infrared spectroscopy （FTIR ）. The results reveal that nZnOp particles are dispersed in the matrixes with nano-scale, and the addition of PEG induces more homogeneous dispersion of nZnOp. Simultaneously, these nanoparticles become nucleating centers during the crystallization of the matrixes. PEG segments can improve the flexibility of the PET molecular chain, resulting in the drop of the cold crystallization temperature and the rise of the crystallization rate of the composites. Furthermore, PEG （4 000） with the mass fraction of 10% can promote the crystallization rate of the composites. The mechanical properties show that the nano-particles strengthen and toughen the PET matrix, whereas PEG weakens these improve- ments.

PET/CDP织物一浴一步法染色

针对PET纤维和CDP纤维同浴染色存在分散染料和阳离子染料相互沾色的问题,比较了二浴二步法和一浴一步法染色工艺中,两种染料染色性能的差异,选择了相互沾色较小的染料,考察了一浴一步法中匀染剂SD对染色性能的影响。结果表明,当分散染料和阳离子染料同时存在时,会发生染料对纤维的竞染现象;匀染剂SD具有双重效果,既是CDP纤维的缓染剂,又是PET纤维的匀染剂,可用于PET/CDP二组份纤维的一浴一步法异色染色。

Simultaneous Synthesis of Dimethyl Carbonate and Poly（ethylene terephthalate） Using Alkali Metals as Catalysts

Dimethyl carbonate （DMC） and poly（ethylene terephthalate） was simultaneously synthesized by the transesterification of ethylene carbonate （EC） with dimethyl terephthalate （DMT） in this paper. This reaction is an excellent green chemical process without poisonous substance. Various alkali metals were used as the catalysts. The results showed alkali metals had catalytic activity in a certain extent. The effect of reaction condition was also studied. When the reaction was carded out under the following conditions： the reaction temperature 250℃, molar ratio of EC to DMT 3 ： 1, reaction time 3h, and catalyst amount 0.004 （molar ratio to DMT）, the yield of DMC was 68.9%.

Alkylpolyglycoside inducing poly (butylene terephthalate) non-woven graft copolymerization of chitosan

In order to improve the wettability and biocompatibility of the poly （butylene terephthalate） non-woven （PBTNW）, the method of surface modification is used to graft copolymerization of chitosan （CS） onto the PBTNW under alkylpolyglycoside （APG） inducing. The product is thoroughly characterized with the Fourier transform infrared spectroscopy （FrIR）, the electron spectroscopy for chemical analysis （ESCA）, the thermogravimetric （TG） and the scanning electron microscopy （SEM）. It is found that chitosan is successfully grafted onto PBTNW. In addition, the water contact angles, hemolysis tests and cytotoxicity evaluation tests show an improvement in wettability and biocompatihility as a result of graft copolymerization of chitosan. So the CS-grafted PBTNW exhibits greater superiority than the original PBTNW. The CS-grafted PBTNW can be a candidate for blood filter materials and other medical applications.

Nonisothermal Crystallization Kinetics of Poly(butylene adipate-co-terephthalate) Copolyester

Nonisothermal crystallization behavior of poly(butylene adipate-co-terephthalate)(PBAT) synthesized via direct esterification and polycondensation reactions was investigated by the differential scanning calorimetry(DSC).The Avrami equation modified by Jeziorny and the Z.S.Mo equation were employed to describe the non-isothermal crystallization kinetics of copolyester samples.The test results showed that the Avrami equation was successful in describing nonisothermal crystallization process of PBAT copolyesters.PBAT copolyester could give birth to secondary crystallization.The crystallization parameter(Zc) increased with an increasing cooling rate and the Avrami exponent(n) was around 2.3.For a given cooling rate,the value of Zc demonstrated a sagging trend with an increase in adipic acid(AA) content.The equation proposed by Z.S.Mo was successful in describing the nonisothermal crystallization kinetics of PBAT copolyesters.

Preparation and Properties of a New Type of Poly(butylene-terephthalate)with Layered Silicate Nanocomposites

In this paper, poly(butylene-terephthalate)-layered silicate of clay nanocomposites (NPBT) are reported. Their thermal properties, heat distortion temperature (HDT) and crystallization nucleation are investigated. NPBT samples have apparent viscosity over 0.85, HDT of 30℃ to 50℃ higher than that of poly (butylene-terephthalate) (PBT) for clay load from 1.0% to 10.0% (by mass), and higher capability to accommodate clay than other polymers. The nonisothermal crystallization experiments indicate that the better thermal degradation behavior and crystallization rate of NPBT are 50% higher than PBT, and its injection mould processing temperature is lowered from 110℃ to 55℃. NPBT samples are characterized by several techniques. X-ray shows an original clay interlayer distance enlarged from 1.0 nm to 2.5 nm, while both TBM and AFM indicate an average size from 30nm to lOOnm of exfoliated clay layers, and 3%(by mass) of particle agglomeration being phase separated from PBT matrix, which are factors on some mechanical properties decrease of NPBT. The disappearance of spherulitic morphology in NPBT resulted from layers nucleation is detected. Improving NPBT properties by treating clay with long chain organic reagent and controlling the way to load it is suggested.

Mechariical and Abrasion Properties of Polyethylene Terephthalate Films Coated with SiO2/Epoxy Hybrid Material

Hybrid materials were prepared using a silane coupling agent, tetraethoxysilane （ TEOS ） as the precursor, dilute hydrochloric acid as the catalyst, and epoxy as the matrices. The films coated with hybrid materials were expected to improve abrasion resistance and mechanical properties. The morphology, mechanical properties, adhesion, and abrasion resistance of the polyethylene terephthalate （PET） films were characterized using an atomic force microscope, a tensile testing machine, a bagger knife, and a reciprocating fabric abrasion tester. The result of research indicated that the modification significantly affected the abrasion resistance and roughness. The-tensile strength and abrasion resistance of the modified PET films increased by 40% and 50% respectively at 3 % TEOS mass fraction.

Properties of Surface Cyclic Oligomers Present on Polyester Fiber

The effects of different treatments, such as dry heat,wet heat, solvent vapor and ultrasonic, on propertiesof the cyclic oligomers on the surface of polyester fiberare studied. The components of surface oligomers areanalyzed through Thin-Layer Chromatograph. Theresult shows that: all of the treatment, especially solvent vapor treatment,call significantly increase the content of surface cyclic oligomers.The content of cyclic triIner is increased more considerably than other oligomers. Moreover,the morphology and thedistribution of surface cyclic oligomers are also different from different treatments:Dry heat and wet heat cause larger polygonal solids distributed evenly on the surface of fiber;solvent vapor nlakes fiber surface exhibit irregular rodlike crystal shapes randomly;ultrasonic treatment induces some obscureand smaller deposi^on the surface of fiber.

Dynamics Model and Simulation of Polyethylene Terephthalate (PET) Hollow Fiber

On the basis of melt-spinning, the dynamics model of polyethylene terephthalate （PET） hollow fiber is established. The effects of spinning conditions on hollow ratio are discussed and verified. Because of the different quenching conditions, there exist differences of the hollow ratio and the vitrification distances between different cycles. The important role of the quenching conditions on the meltspinning of PEr hollow fiber is also mentioned.

Study on the Synthesis and Properties of PET Using Hydrotalcite as Catalyst

Poly(ethylene terephthalate)(PET)was synthesized by the in-situ polymerization method using layered double hydrotalcite(LDH)as the catalyst,and the thermal and flame retardation properties of PET were investigated as required.As identified by differential scanning calorimetry(DSC)and thermogravimetric(TGA)analysis,the crystallization rate and thermal degradation temperature of the as-prepared PET sample were enhanced compared with commercial PET sample.It was confirmed from the fire-resistant property study that the LDH can be used as an efficient flame-retardant besides functioning as a catalyst in the transesterification/polycondensation process for PET synthesis.

An agent-based service-oriented integration architecture for chemical process automation

In reality, traditional process control system built upon centralized and hierarchical structures presents a weak response to change and is easy to shut down by single failure. Aiming at these problems, a new agent-based service-oriented integration architecture was proposed for chemical process automation system. Web services were dynamically orchestrated on the internet and agent behaviors were built in them. Data analysis, model, optimization, control, fault diagnosis and so on were capsuled into different web services. Agents were used for service compositions by negotiation. A prototype system of poly(ethylene terephthalate) process automation was used as the case study to demonstrate the validation of the integration.

Screening of Polymer Additives in Drinking Water Stored in PET Bottles by UHPLC-ESI-IT-TOF MS

In this study, Ultra High Performance Electrospray Ionization Ion Trap Time of Flight Mass Spectrometry （UHPLC-ESI-1T-TOF MS） method is used to screen the polymer additives in drinking water that is stored in Polyethylene Terephthalate （PET） bottles. After directly analyzing the commercially available water samples, 3 polymer additives （chimassorb 81, irgafos 168 and oleamide） were detected. However, after exposure to sunshine for 8 days, two additional polymer additives （antioxidant 2246 and Butylated Hydroxytoluene （BHT）） were detected besides the former three additives.

Solar Oxidation and Removal of Arsenic from Groundwater Utilizing a Semicircular Section Tubular Photoreactor

A semicircular section tubular photoreactor has been constructed, characterized and applied to the treatment of groundwater contaminated with As（V） by means of the SORAS （solar oxidation and removal of arsenic） technique, using ferrous and citrate salts. The solar concentrator was built with recyclable waste materials： glass tubes from fluorescent lamps and 6-inch diameter PVC pipes cut in half and covered by aluminum foil. The reactor concentrates solar radiation up to 2.8 times its natural intensity. Batch irradiation experiments followed by controlled agitation （shear rate = 30-33 s^-1; 20 min agitation period） showed that the photoreactor accelerates the formation of settleable floccules （Dp 〉 0.5mm）, compared with a fluorescent lamp glass tube alone and a 2 L PET （polyethylene terephthalate） bottle. Irradiation times necessary for floccule formation in the photoreactor, the fluorescent lamp tube and the PET bottle were 15 min, 25 min and 60 min, respectively. Continuous flow experiments using a photoreactor with a photo-collection area of 0.9 m^2 and a hydraulic retention time （equal to the irradiation time） of 15 rain showed that immediate formation of floccules of good settleability occurs when the solution is subjected to moderate agitation （33 s^-1）. An efficiency of 98.36% for As（V） removal was obtained with a final concentration of 16.5 ktg/L in decanted waters. In accordance to these results, the photoreactor is able to treat approximately 130 L/m^2 within a 5-h period with UVA irradiation intensities of 50-70 W/mE.

Recycling Polyethylene Terephthalate （PET） Packaging as the Basis of Economic Projects and Solution of Social and Environmental Problems in Russia

In this article, based on the analysis of the current environmental situation in Russia and other countries, as well as of the problem of recycling plastic waste in the Russian Federation （RF）, the authors clearly show the effectiveness of investments in the processing of polymer debris on the example of polyethylene terephthalate （PET） waste （granulates, flakes）. In the frame of case study of social and environmental investment project on creating enterprise that will engage in collection, recycling, and sale of the consumer PET packaging in Russia, the authors demonstrate the economic feasibility of the creation of such kind of enterprises taking into account market conditions and the features of the existing system of taxation in Russia. The realization of the project will also help in solving environmental and social problems of large cities, in particular, will create more jobs （in terms of 6% of unemployment rate in the country）. The study also identifies the main obstacles in the way of waste recycling in Russia, and the recommendations for improvement of normative base of the industry are given.

Are Polymers Toxic？ Case Study： Environmental Impact of a Biopolymer

In this paper, the analysis of the environmental impacts of a biopolymer based on starch is presented. These impacts were calculated from a cradle to gate LCA （Life Cycle Assessment）, based on UNEEN ISO 14040：2006 and UNEEN ISO 14044, using as functional unit 1 kg of produced biomaterial. The impact categories analyzed were global wanning, ozone depletion, acidification and eutrophication. The results indicate that the electricity causes the highest impacts in the global warming and ozone depletion categories, but compared to synthetic polymers, the emissions are low. Finally, in the case of eutrophication, the impacts are similar to other biopolymers but higher in comparison with petroleum-based polymers like HDPE （High Density Polyethylene）, LDPE （Low Density Polyethylene）, PP （Polypropylene）, PS （Polystyrene） and PET （Polyethylene Terephthalate）.

A Hybrid Dielectric Ink Consisting of up to 50 wt% of TiO2 Nanoparticles in Polyvinyl Alcohol （PVA）

PVA （Polyvinyl Alcohol） is a water soluble organic dielectric, easily solution processed to fabricate films by spin coating, dip coating or inkjet printing. It has been used as a dielectric layer in OTFTs （organic thin film transistors）, and its dielectric constant is around 3.5-10. For OTFTs operating at lower voltage, it is desirable to increase the dielectric constant. Here, we report a technique to incorporate upto 50 wt% of TiO2 nanoparticles （15-25 nm） in PVA to increase its dielectric constant. Rutile phase of TiO2 is used, because of its higher dielectric constant （e = 114） compared to anatase phase （E = 31）. We have made inks containing 10 and 50 wt% （of PVA） TiO2 nanoparticles, which is stable upto six months. PVA-TiO2 dispersions and PVA （without TiO2） were spin coated on indium tin oxide coated polyethylene terephthalate substrate. Film structure was studied using SEM （scanning electron microscopy）. Absorption study of the films confirms presence of TiO2 nanoparticles. M-I-M capacitors were fabricated by thermally evaporating aluminium on top of the dielectric films. We observed enhancement in dielectric constant by a factor of 2 for PVA containing 50 wt% TiO2 in comparison to PVA＇s dielectric constant. There is no concomitant increase in the leakage current.

In-situ Enhanced Toughening of Poly（ethylene terephthalate）/elastomer Blends via Gamma-Ray Radiation at Presence of Trimethylolpropane Triacrylate

Gamma-ray radiation has always been a convenient and effective way to modify the inter- facial properties in polymer blends. In this work, a small amount of trimethylolpropane triacrylate （TMPTA） was incorporated into poly（ethylene terephthalate） （PET）/random terpolymer elastomer （ST2000） blends by melt-blending. The existence of TMPTA would induce the crosslinking of PET and ST2000 molecular chains at high temperatures of blend- ing, resulting in the improvement in the impact strength but the loss in the tensile strength. When the PET/ST2000 blends were irradiated by gamma-ray radiation, the integrated me- chanical properties could be enhanced significantly at a high absorbed dose. The irradiated sample at a dose of 100 kGy even couldn＇t be broken under the impact test load, and at the same time, has nearly no loss of tensile strength. Based on the analysis of the impact- fractured surface morphologies of the blends, it can be concluded that gamma-ray radiation at high absorbed dose can further in situ enhance the interfacial adhesion by promoting the crosslinking reactions of TMPTA and polymer chains. As a result, the toughness and strength of PET/ST2000 blend could be dramatically improved. This work provides a facial and practical way to the fabrication of polymer blends with high toughness and strength.