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.

Synthesis of Activated Carbon from Polyethylene Terephthalate(PET)Plastic Waste and Its Application for Removal of Organic Dyes from Water

Synthetic plastics are often considered to be materials that cannot be broken down by natural processes.One such plastic,polyethylene terephthalate(PET),is commonly used in everyday items but when these products are discarded,they can cause serious harm to the environment and human health.In this study,PET plastic waste was used to create activated carbon using a physical activation process that involved using CO2 gas.The researchers investigated the effects of different temperatures,carbonization,and activation times on the resulting activated carbon’s surface area.The activated carbon was then analyzed using scanning electron microscopy(SEM),X-ray diffraction(XRD),FTIR,and BET.The activated carbon created from PET plastic waste showed excellent absorption properties for methylene blue in aqueous solutions across a wide range of pH levels.By creating activated carbon from plastic waste,not only are environmental issues addressed,but high-value activated carbon is produced for environmental remediation purposes.

Surface Modification of Polyethylene Terephthalate(PET) Fiber by Roll-to-Roll Treatment in Atmospheric Ar/O_2 Dielectric Barrier Discharge(DBD) Plasma

In this work,polyethylene terephthalate(PET) fibers were continuously treated by atmospheric dielectric barrier discharge(DBD) in Ar mixed O2 plasma,and the discharge was characterized by electrical function and optical diagnostics.It is found that the interfacial adhesion strength between treated PET fiber and resorcinol formaldehyde latex(RFL)(little)-rubber was improved(about 50%) by the measurement of interfacial shear strength(IFSS) and peel test.The wettability was improved rapidly in the initial treatment time.It is considered that oxidation chemical reaction as the major role of PET fiber surface modification is ahead of the physical etching effect.The high density of atomic oxygen in the plasma by optical emission spectroscopy supports the purpose.According to the scanning electron micrograph(SEM) image in the work,the longer treatment time obviously caused physical etching effect,which shall be less responsible for the improvement of the wettability.

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.

Synthesis of titanium oxycarbonitride by carbothermal reduction and nitridation of ilmenite with recycling of polyethylene terephthalate (PET)

An innovative and sustainable carbothermal reduction and nitridation(CTRN) process of ilmenite(FeTiO_3) using a mixture of polyethylene terephthalate(PET) and coal as the primary reductant under an H_2–N_2 atmosphere was proposed. The use of PET as an alternative source of carbon not only enhances the porosity of the pellets but also results in the separation of Fe from titanium oxycarbonitride(TiOxCyNz) particles because of the differences in surface tension. The experiments were carried out at 1250°C for 3 h using four different PET contents ranging from 25wt% to 100wt% in the reductant. X-ray diffraction(XRD),scanning electron microscopy(SEM) in conjunction with energy-dispersive X-ray spectroscopy(EDX),and LECO elemental analysis were used to study the phases and microstructures of the reduced samples. In the case of 75wt% PET,iron distinctly separated from the synthesized Ti OxCyNz phase. With increasing PET content in the sample,the reduction and nitridation rates substantially increased. The synthesis of an oxycarbonitride with stoichiometry of TiO_(0.02)C_(0.13)N_(0.85) with minimal intermediate titanium sub-oxides was achieved. The results also showed that the iron particles formed from CTRN of FeTiO_3 exhibited a spherical morphology,which is conducive for Fe removal via the Becher process.

Effect of Knitting Process on Elastic Property of Polyethylene Terephthalate (PET)/Polybutylene Terephthalate (PBT) Warp Knitted Fabric

This study investigated the elastic elongation and elastic recovery of the elastic warp knitted fabric made of polyethylene terephthalate( PET) and polybutylene terephthalate( PBT)filament. The effect of knitting parameter on the elasticity of PBT /PET warp knitted fabric was analyzed. The increase of drawing density( from 16 to 26 courses per centimeter( CPC)) on machine resulted in the decrease of elongation at the weft direction. But,the elongation at the warp direction fluctuated as drawing density increasing. The yarn run-in speed influenced the elongation of PET /PBT warp knitted fabric as well. When the yarn run-in speed of GB1( front bar) was kept a constant,the increase of GB2( back bar) yarn run-in speed caused the gradual enhancement of the elastic elongation at the warp direction,but the different trends of the elastic elongation at the weft direction. When yarn run-in speed of GB2 was kept a constant,the increase of GB1 yarn run-in speed enlarged the elastic warp elongation from 104.16 to 124.97 mm,while the weft elongation decreased from 110.34 to 98.03 mm.Eventually yarn run-in speeds of GB1 and GB2 were retained at1 360 and 1 170 mm / rack respectively under 20 CPC drawing density. It could not only balance the two directions of elongation but also reach the highest elongation at both directions( 126. 32 and115.88 mm) under 100 N tension. These results provide a better understanding of characteristics of PET / PBT warp knitted fabric,and its elastic elongation and recovery behavior for development and effective applications.

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.

Surface Treatment of Polyethylene Terephthalate Film Using Atmospheric Pressure Glow Discharge in Air

Non-thermal plasmas under atmospheric pressure are of great interest in polymer surface processing because of their convenience, effectiveness and low cost. In this paper, the treatment of Polyethylene terephthalate (PET) film surface for improving hydrophilicity using the non-thermal plasma generated by atmospheric pressure glow discharge (APGD) in air is conducted. The discharge characteristics of APGD are shown by measurement of their electrical discharge parameters and observation of light-emission phenomena, and the surface properties of PET before and after the APGD treatment are studied using contact angle measurement, x-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM). It is found that the APGD is homogeneous and stable in the whole gas gap, which differs from the commonly filamentary dielectric barrier discharge (DBD). A short time (several seconds) APGD treatment can modify the surface characteristics of PET film markedly and uniformly. After 10 s APGD treatment, the

Recycling and depolymerization of waste polyethylene terephthalate bottles by alcohol alkali hydrolysis

In this work,a novel alcohol alkali hydrolysis method was explored for the preparation of terephthalic acid(TPA)from waste polyethylene terephthalate(PET).First,a series of single factor experiments on the depolymerization rate of waste PET bottles and the yield of TPA were conducted to determine the optimized experimental conditions,in terms of reaction time,reaction temperature,dosage of ethylene glycol and sodium bicarbonate,amount of distilled water and stirring rate.Then IR spectra and elemental analysis were carried out for the characterization of obtained product.Under optimal experimental conditions,over 98%PET can be depolymerized into the target product(TPA)and the purity and yield of TPA are over 97%and 94%,respectively.Both the experimental and analytical results support a feasible process for the preparation of TPA from waste PET.It is expected that this alcohol alkali hydrolysis method can promise an effective way for the sustainable recycling of waste PET.

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.

The Aging Study on Polyethylene Terephthalate with Surface Modification by Water Vapor Plasma

The aging effects of the contact angle and surface energy on polyethylene terephthalate (PET) have been investigated with surface modification by water vapor plasma. The experimental results show that the contact angle of water and PET decreases obviously and surface energy increases. However, with the increase of the aging time, the contact angle and surface energy change back gradually to original state.

Utilization of waste polyethylene terephthalate as a reducing agent in the reduction of iron ore composite pellets

The increasing consumption of plastics inevitably results in increasing amounts of waste plastics. Because of their long degradation periods, these wastes negatively affect the natural environment. Numerous studies have been conducted to recycle and eliminate waste plastics. The potential for recycling waste plastics in the iron and steel industry has been underestimated; the high C and H contents of plastics may make them suitable as alternative reductants in the reduction process of iron ore. This study aims to substitute plastic wastes for coal in reduction melting process and to investigate their performance during reduction at high temperature. We used a common type of waste plastic, polyethylene terephthalate （PET）, because of its high carbon and hydrogen contents. Composite pellets containing PET wastes, coke, and magnetite iron ore were reduced at selected temperatures of 1400 and 1450℃ for reduction time from 2 to 10 min to investigate the reduction melting behavior of these pellets. The results showed that an increased temperature and reduction time increased the reduction ratio of the pellets. The optimum experimental conditions for obtaining metallic iron （iron nuggets） were reduction at 1450℃ for 10 min using composite pellets containing 60% PET and 40% coke.

DEPOLYMERIZATION AND KINETICS OF DEPOLYMERIZATION OF POLYETHYLENE TEREPHTHALATE USING DIBUTYLTIN OXIDE CATALYST

Depolymerization of poly（ethylene terephthalate） （PET） was performed in the tubular bomb microreactor which contained the solution of PET in methanol and dibutyltin oxide at the temperature ranging from 433 K to 473 K, the reaction time from 5 to 45 min and the catalyst-to-PET ratio of 0.3%-2% by weight. The optimal condition for PET depolymerization catalyzed by dibutyltin oxide is the temperature of 443-453 K, the reaction time of 20-25 min and 0.8% by weight of catalyst. By using differential methods, the activation energy for the depolymerization process was found to be 154.05 kJ/mol in the temperature range from 433-463 K.

In vitro Blood Compatibility of Polyethylene Terephthalate with Covalently Bounded Hirudin on Surface

Polyethylene terephthalate （PET,Dacron） was modified by surface immobilization of hirudin with glutaraldehyde（GA） as coupling reagent to improve the blood compatibility.Hirudin-immobilized PETs were characterized by X-ray photoelectron spectroscopy （XPS） and contact angle measurements.The blood compatibility of the PETs was evaluated by platelet adhesion evaluation and fibrinogen conformational change measurements in vitro.The results showed the decrease of platelet adhesion and activation on hirudin-immobilized PET with increasing of glutaraldehyde concentration.Fibrinogen experiment showed that fibrinogen adherence and conformational changes of PET-HRD were less than those of untreated PET,which made the materials difficult to form thrombus.The proper reason of blood compatibility improvement was low interface tension between hirudin-immobilized PETs and blood,as well as blood proteins,and low ratio of dispersive/polar component of the surface energy（γsd/γsp） and high hydrophilicity.

Structural Changes of Polyethylene Terephthalate Fibers Grafted by Acrylamide

A group of grafted PET fibers with different graft yield are formed by grafting acrylamide onto the PET main chains. The structure of grafted fibers are studied by scanning electronic microscope ( SEM ), infra-red spectrophotometer ( IR ), and differential scanning calorimetry(DSC). At the same time, the moisture regain, dyeability, strength, and elongation at break of the samples are measured and their relations with structural changes are discussed. Compared with ungrafted fiber, shape of the fiber cross-section, IR characteristic absorption peaks, and melting behavior of the grafted fibers have been changed, causing the fiber dyeability and moisture regain to be increased, and mechanical properties to be changed.

Synergistic Effect of Atmospheric Pressure Plasma Pre-Treatment on Alkaline Etching of Polyethylene Terephthalate Fabrics and Films

Dyeing of PET materials by traditional methods presents several problems.Plasma technology has received enormous attention as a solution for the environmental problems related with textile surface modifications,and there has been a rapid development and commercialization of plasma technology over the past decade.In this work,the synergistic effect of atmospheric pressure plasma on alkaline etching and deep coloring of dyeing properties on polyethylene terephthalate（PET）fabrics and films was investigated.The topographical changes of the PET surface were investigated by atomic force microscopy（AFM）images,which revealed a smooth surface morphology of the untreated sample whereas a high surface roughness for the plasma and/or alkaline treated samples.The effects of atmospheric pressure plasma on alkaline etching of the structure and properties of PET were investigated by means of differential scanning calorimetry（DSC）,the main objective of performing DSC was to investigate the effect of the plasma pre-treatment on the T_g and T_m.Using a tensile strength tester YG065 H and following a standard procedure the maximum force and elongation at maximum force of PET materials was investigated.Oxygen and argon plasma pre-treatment was found to increase the PET fabric weight loss rate.The color strength of PET fabrics was increased by various plasma pre-treatment times.The penetration of plasma and alkaline reactive species deep into the PET structure results in better dyeability and leaves a significant effect on the K/S values of the plasma pre-treated PET.It indicated that plasma pre-treatment has a great synergistic effect with the alkaline treatment of PET.

Studying the Curing Conditions of Unsaturated Polyesters from Secondary Polyethylene Terephthalate Alcoholysis Products

The technological properties of the curing conditions for unsaturated polyesters synthesized on the basis of the alcoholysis products of secondary polyethylene terephthalate and unsaturated polyesters used in the production of fiberglass pipes were studied. It is shown that unsaturated polyesters synthesized on the basis of alcoholysis products can completely replace imported resins of grades 196 and 196A in the production of fiberglass pipes.

Effect of Irradiation Crosslinking on Polyethylene Terephthalate Flame-Retardant Fabric

Irradiation cross-linking of flame-retardant polyethylene terephthalate( FR-PET) fabric with the presence of trimethylolpropane triacrylate( TMPTA) was studied. Thermal gravimetric( TG) analysis,differential scanning calorimetry( DSC) and scanning electron microscopy( SEM) were used to analyze the effects of irradiation crosslinking on structure and property of FR-PET fabric with TMPTA. The cross-linking was promoted by the introduced sensitizer. The gel content was 5.94% at the lower dose of 90 kGy and it arrived at the highest level of 13.01% with the increased doses. There were no melt drips of FR-PET fabric after irradiation cross-linking while the flame retardance disappeared at the time of combustion. The melting temperature of irradiated fabric decreased and TG analysis showed that the onset temperature of degradation of FR-PET fabric and the amount of nonvolatile residue at 800℃ increased as the irradiation dosage increased,but it changed a little compared with the pure FR-PFT fabric. SEM photographs showed that the residue char of irradiated PET fabrics after vertical test remained the intrinsic crossed structure,and the enlarged graph showed that the char was uniformly distributed and it was tight honeycombs structure.

高强度玻璃纤维对阻燃增强PET性能的影响

研究了高强度玻璃纤维对阻燃增强聚对苯二甲酸乙二酯(PET)材料性能的影响,并制备了综合性能优良的高性能阻燃增强PET材料,同时分析了高强度玻璃纤维和普通无碱玻璃纤维在PET材料中的尺寸分布。结果表明:高强度玻璃纤维的表面处理可以有效提高阻燃增强PET材料的性能;阻燃增强PET的性能随着玻璃纤维含量的增加而提高,高强度玻璃纤维比普通无碱玻璃纤维能更好地改善PET材料的综合性能。

S波段变频微波方腔干燥PET切片的研究

目的针对聚对苯二甲酸乙二醇酯(PET)材料传统干燥方式能耗高、效率低等不足,运用微波干燥材料具有速度快、效率高、易于控制的特点,研究微波深度干燥PET技术并研制实验装置。方法提出微波变频和变功率加热干燥技术,通过主动调整频率改善微波均匀性,结合微波变功率技术,控制PET材料温度在170~180℃,提升PET材料温度均匀性,并防止“热失控”现象的发生。结果当干燥时间为2 h时,实现了PET深度干燥,能耗率为1.03 kW·h/kg,含水率降低至0.01%以下,达到了后续包装材料注塑加工的要求。结论微波变频变功率加热技术适用于低含水率PET的深度干燥,比传统干燥方式能耗低并且时间短。