Solid-state relaxations in linear low-density (1-octene comonomer), low-density,and high-density polyethylene blends

Extensive thermal and relaxational behavior in the blends of linear low-density polyethylene (LLDPE) (1-octene comonomer) with low-density polyethylene (LDPE) and high-density polyethylene (HDPE) have been investigated to elucidate miscibility and molecular relaxations in the crystalline and amorphous phases by using a differential scanning calorimeter (DSC) and a dynamic mechanical thermal analyzer (DMTA). In the LLDPE/LDPE blends, two distinct endotherms during melting and crystallization by DSC were observed supporting the belief that LLDPE and LDPE exclude one another during crystallization. However, the dynamic mechanical β and γ relaxations of the blends indicate that the two constituents are miscible in the amorphous phase, while LLDPE dominates α relaxation. In the LLDPE/HDPE system, there was a single composition-dependent peak during melting and crystallization, and the heat of fusion varied linearly with composition supporting the incorporation of HDPE into the LLDPE crystals. The dynamic mechanical α, β, and γ relaxations of the blends display an intermediate behavior that indicates miscibility in both the crystalline and amorphous phases. In the LDPE/HDPE blend, the melting or crystallization peaks of LDPE were strongly influenced by HDPE. The behavior of the α relaxation was dominated by HDPE, while those of β and γ relaxations were intermediate of the constituents, which were similar to those of the LLDPE/HDPE blends. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35 : 1633–1642, 1997     

Discrimination of thermally treated low density polyethylenes using DSC and principal component analysis

The potential for differential scanning calorimetry (DSC) as a tool for the discrimination of forensic polymer specimens is investigated for a series of commercial low density polyethylene (LDPE) samples. Variation in the melting temperatures of ‘as received’ samples was found to be too small for its use in sample discrimination. The melting behaviour of thermally treated samples, quenched from the melt in liquid nitrogen followed by annealing at temperatures below the melting temperature, showed promise in discrimination potential. The application of principal component analysis to aid discrimination demonstrated the necessity in using a controlled thermal history to aid the discrimination process. The clustering of the LDPEs based on the factors selected demonstrated the potential of DSC for the discrimination of forensic LDPE samples.     

Comparative study of the properties of post-consumption high density polyethylene used in the injection process

The high-density polyethylene, thermoplastic widely-used in the production of industrial domestic utilities, was collected in two situations: virgin high-density polyethylene (JV 060) and post-consumption high-density polyethylene (with features of low-density polyethylene). After collecting the samples, they were submitted to natural aging with the quantification of the incident solar radiation for 180 days. The samples were characterized by melt flow index, differential scanning calorimetry, tensile strength, rupture load, elongation at break and infrared. The results showed that after 180 days of exposure the virgin high-density polyethylene presented physical properties similar to the post-consumption polyethylene. This revised version was published online in August 2006 with corrections to the Cover Date.     

Effect of sample size on isothermal crystallization measurements performed in a differential scanning calorimeter: A method to determine avrami parameters without sample thickness effects

Isothermal crystallization studies of low-density polyethylene (LDPE) and high-density polyethylene (HDPE) using differential scanning calorimetry (DSC) were performed using different sample thicknesses to determine the effect of non-ideal heat-transfer. Polyethylene was chosen because of its importance, its extensive coverage in the literature, and its fast crystallization kinetics. Thermal gradients were found to significantly affect the measured crystallization exotherm; slower crystallization rates were observed for thicker samples measured at lower temperatures (greater supercoolings). Differences between different sample thicknesses disappeared at higher temperatures, consistent with finite heat-transfer rates being responsible for the effect. A power-compensation and a heat-flux DSC were used; these experiments also enabled the determination that the performance of the latter was acceptable for this study. Finally, thickness-independent Avrami parameters have been calculated.     

Space charge distribution and crystalline structure in polyethylene blended with EVOH

The space charge distribution in polyethylene samples under direct current (DC) electrical field was measured by pulsed electro-acoustic (PEA) method. It was found that by blending with 5 wt.% of poly(ethylene-co-vinyl alcohol) (EVOH) in low-density polyethylene (LDPE) the amount of accumulated space charges decreased and the field distribution of space charge improved. The differential scanning calorimetry (DSC) study showed that crystallization of LDPE/EVOH started at a higher temperature than LDPE. The results of wide-angle X-ray diffraction (WAXD) and small-angle light scattering (SALS) for LDPE/EVOH indicated that the crystal forms did not change, whereas the spherulites became smaller and imperfective. It can be seen from the results that EVOH played a role of nucleation during the crystallization of LDPE in the blend. The observation of scanning electron microscope (SEM) showed that the domains of EVOH were dispersed in LDPE as particles in diameter of 1 μm. The reduction of space charges in the blend sample can be explained as the results of the trapping of homo-charges at the interface and the dissipation of charges through LDPE matrix consisting of smaller spherulites.     

Annealing behavior of gel‐spun polyethylene fibers at temperatures lower than needed for significant shrinkage

The annealing at 373 K of ultrastrong, gel‐spun polyethylene (PE) has been studied. At this temperature, the fibers show no significant shrinkage. Still, a significant decrease in the mechanical properties is observed. The fibers have been analyzed with differential scanning calorimetry (DSC), temperature‐modulated differential scanning calorimetry (TMDSC), atomic force microscopy (AFM), and small‐angle X‐ray scattering (SAXS). During the annealing, the glass transition of the intermediate phase is exceeded, as shown by DSC. When split for structure analysis by AFM, the annealed fibers undergo plastic deformation around the base fibrils instead of brittle fracture. The quasi‐isothermal TMDSC experiments are compared to the minor structural changes seen with SAXS and AFM. The loss of performance of the PE fibers at 373 K is suggested to be caused by the oriented intermediate phase, and not by major changes in the structure or morphology. The overall metastable, semicrystalline structure is shown by TMDSC to posses local regions that can melt reversibly. © 2003 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 41: 403–417, 2003     

Analytical scale supercritical fluid fractionation of a low molecular weight,high density polyethylene wax with carbon dioxide

This paper reports on the use of supercritical carbon dioxide to fractionate a low molecular weight, high density polyethylene into very narrow molecular weight distributions (MWDs). A simple extraction system was developed that allowed relatively trouble free extractions of the polyethylene samples. Fractions were collected at successively higher densities of CO₂ at constant temperature and then analyzed by capillary supercritical fluid chromatography (SFC), or high temperature gel permeation chromatography (GPC) and/or differential scanning calorimetry (DSC). Fractionations were performed at three different temperatures (60,80, and 100°C). Higher temperatures were found to yield greater recoveries and higher MWDs at any given density. Reducing the increment between successive extraction steps resulted in polydispersities being reduced to nearly “monodisperse” levels. Total recoveries ranged from 12 to 33% depending on the temperature, and the highest molecular weight fraction extracted by the CO₂ was centered around 1500.     

Relationship Between the Thermal Properties and the Morphology in High Density Polyethylenes

This work presents a relationship between the thermal properties in different polyethylene samples analyzed by differential scanning calorimetry (DSC). The morphology and structural changes were studied by transmission electron microscopy (TEM). A preparative method involving surface etching was used to obtain surface replicas. The main morphological features of the samples, characterized by lamellar structure, obtained in this work by TEM give values of mean lamellar thickness from 900 to 500 Ĺ in the highest branch content and molecular mass. Enthalpies of melting allowed to calculate crystallinity; given values in the range from 47 to 68%. This revised version was published online in July 2006 with corrections to the Cover Date.     

Reversible melting of polyethylene extended‐chain crystals detected by temperature‐modulated calorimetry

The melting and crystallization of extended‐chain crystals of polyethylene are analyzed with standard differential scanning calorimetry and temperature‐modulated differential scanning calorimetry. For short‐chain, flexible paraffins and polyethylene fractions up to 10 nm length, fully reversible melting was possible for extended‐chain crystals, as is expected for small molecules in the presence of crystal nuclei. Up to 100 nm length, full eutectic separation occurs with decreasingly reversible melting. The higher‐molar‐mass polymers form solid solution crystals and retain a rapidly decreasing reversible component during their melting that decreases to zero about 1.5 K before the end of melting. An attempt is made to link this reversible melting to the known, detailed morphology and phase diagram of the analyzed sample that was pressure‐crystallized to reach chain extension and practically complete crystallization. © 2002 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 40: 2219–2227, 2002     

Characterizing blends of linear low-density and low-density polyethylene by DSC

Summary A two-step isothermal annealing (TSIA) procedure is described that enables the endothermic peaks of low-density polyethylene (LDPE), linear low-density polyethylene (LLDPE) and their blends, to be satisfactorily resolved during analysis by differential scanning calorimetry. A modified form of multistep isothermal annealing, the TSIA procedure produces a highly characteristic profile of the blend components by facilitating the segregation of the phases based on branch density. It is proposed that the TSIA procedure may have significant merit in the identification and quantification of the components in an unknown blend as well as increasing the sensitivity in analytical procedures aimed at blend component quantification.     

Probing multiple melting behaviors in poly(ethylene naphthalene 2,6‐dicarboxylate) with different thermal histories by simultaneous wide‐angle and small‐angle X‐ray scattering

A simultaneous wide‐angle and small‐angle X‐ray scattering study of two poly(ethylene naphthalene 2,6‐dicarboxylate) samples crystallized from the glassy state at different annealing temperatures for different annealing times was carried out with synchrotron radiation. Either single or dual melting was induced in the samples, as confirmed by differential scanning calorimetry (DSC). The correlation function and interface distribution function were calculated to evaluate microstructural parameters such as the long spacing, the thickness of the amorphous and crystalline phases, and the width of the size distributions. The sample with dual melting behavior exhibited an abrupt increase of all microstructural parameters at temperatures above the melting of the lowest endotherm, whereas the sample revealing a single melting endotherm did not show such a sudden change. This finding agrees with the concept that the appearance of two melting peaks in DSC traces can be explained by the dual lamellar stacking model. © 2001 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 39: 881–894, 2001     

THE STRUCTURE AND PROPERTIES OF CHITOSAN/POLYETHYLENE GLYCOL/SILICA TERNARY HYBRID ORGANIC-INORGANIC FILMS

The ternary hybrid films consisting of chitosan(CS),polyethylene glycol(PEG)and nano-sized silica which was surface-modified by amino groups(RNSA)were prepared.The structures of the blend membranes were characterized by attenuation total reflection-infrared spectroscopy(ATR-IR),X-ray diffraction(XRD),optical microscopy(OM)and differential scanning calorimetry(DSC).The results showed that the addition of silica affected not only the distribution and crystallinity of PEG on the sample surface,but also the ...     

茂金属聚乙烯的非等温结晶动力学

对茂金属催化和传统工艺生产的聚乙烯的非等温结晶行为进行了研究,用ＤＳＣ测试了两种聚乙烯的非等温结晶过程,对所得数据分别用Ｏｚａｗａ方程和莫志深方法进行了处理,发现：由于茂金属聚乙烯有着较高的立构规整性．所以虽然它的分子链较长,但结晶速率高于传统聚乙烯,两种聚乙烯非等温结晶过程中的成核和生长机理也不同,茂金属聚乙烯的生长维数高于传统聚乙烯     

The influence of the recycling stress history on LDPE waste pyrolysis

It is elementary to recognize the benefits and the negative impacts of the use of plastic materials on modern societies. Polyethylene (PE) is the major plastic component present in the municipal solid waste. In this paper, two types of low-density PE (LDPE) waste with different mechanical recycling stress histories were used to investigate the influence of recycling cycles on pyrolysis. The kinetic triplet and thermal degradation study were obtained using TGA data.To determine the sample composition and hydrocarbon arrangements, ultimate, proximate and X-ray diffraction analyses were carried out. Taking advantage of these analyses and combining them with differential scanning calorimetry (DSC) data, a series–parallel pyrolysis pathway was formulated. The waste of recycled polyethylene presented low enthalpy of pyrolysis, at about 205 J/g against 299 J/g for a virgin PE. The DSC analyses evidenced a multi-step reaction behavior of the pyrolysis, confirmed by the kinetic study using different isoconversional methods: the waste of recycled polyethylene presented a higher variation of activation energies as a function of the fraction reacted. The main conclusion is that the results suggest that the recycling stress history promotes the increase of long carbon chains while weakening the boundary among the compounds. This explains the fact that recycled waste needs less activation energy than other samples to degrade thermally. Finally, different categories of low-density polyethylene wastes must be considered when dealing with either kinetics or modeling of the product recovery process.     

Effect of equal channel angular pressing on thermal and mechanical properties of carbon nanotube/high density polyethylene composite

High density polyethylene (HDPE) nanocomposite reinforced with 2 weight percent carbon nanotube (CNT) was fabricated using mechanical milling method. Microscopic evaluations revealed appropriate dispersion of CNTs in the matrix, and tensile tests demonstrated that the tensile strength was increased by 17%. Thermal and mechanical properties of the composite samples were investigated after equal channel angular pressing (ECAP) for up to 3 passes via route A at temperature of 80°C. Density and differential scanning calorimetry (DSC) results represented decrement in crystallinity after ECAP which was led to drop in hardness and tensile yield strength of the deformed samples. Micro Vickers and Shore D hardness results also revealed clear anisotropy in mechanical properties caused by ECAP. Dilatometry results and observation of the impact fractured surfaces of deformed samples demonstrated that oriented structures formed in amorphous and crystalline regions of the composite. This microstructure evolution also caused increase in impact strength of ECAP deformed specimens. Dynamic mechanical behavior of the processed samples was modified following ECAP. The α and γ relaxation temperatures were decreased due to the reduction of thickness of crystalline lamella obtained from DSC results, in 1 pass ECAP deformed sample. Dynamic storage and loss modulus of 3 passes ECAP deformed samples were significantly decreased due to the sharp drop in their crystallinity.     

Melting of nascent and thermally treated super-high molecular weight polyethylene

The melting of nascent and thermally treated super-high molecular weight polyethylene (SHMWPE) is investigated by means of differential scanning calorimetry (DSC). Higher melting temperatures and enthalpies of the nascent and annealed samples are observed. The melting temperatures and enthalpies of melt crystallized SHMWPE is lower and depends on the temperature of thermal treatment. All melting properties are explained by presuming that the lamellar structure contains a high concentration of entangled tie macromolecules in amorphous regions formed during polymerization. It was supposed that the concentration of the entanglements and the stressed tie molecules are changed with the temperature of the thermal pretreatment.     

Dielectric and thermal characterization of low density ethylene/10‐undecen‐1‐ol copolymers prepared with nickel catalysts

Ethylene and 10‐undecen‐1‐ol copolymers, prepared using a nickel complex as catalyst, were studied using differential scanning calorimetry (DSC), X‐ray diffraction, and dielectric relaxation spectroscopy. The behavior exhibited by copolymers containing incorporated 10‐undecen‐1‐ol amounts within 0.5 and 4.6 mol % was compared with neat polyethylene. DSC revealed that a new crystalline region with lower thickness lamellae emerges in copolymers due to the side‐chains crystallization. Nevertheless, the global crystallization degree decreases due to the loss of crystallinity that occurs in a greater extent in PE‐like regions. Dielectric relaxation spectroscopy detected two processes, a low activation energy process below ?20 °C related with localized mobility increasing in intensity and deviating to higher temperatures with the increase in 10‐undecen‐1‐ol amount, and a high activation energy process ascribed to the glass transition, located at higher temperatures for the different copolymers relatively to neat polyethylene. © 2007 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 45: 2802–2812, 2007     

Estimation of Ethyl Cellulose Layer Thickness of Coated Polyethylene Oxide Particles Using Differential Scanning Calorimetry

Particles of poly(ethylene oxide) (PEO) were coated using ethyl cellulose (EC). Equations and a method were proposed to estimate the EC layer thickness by using differential scanning calorimetry (DSC) based on melting or crystallization heat of phase-change materials. The result shows that EC layer thickness of polyethylene oxide particles determined using DSC is consistent with the result using an optical microscope.     

Polydispersity of ethylene sequence length in metallocene ethylene/α‐olefin copolymers. II. Influence on crystallization and melting behavior

In this work, crystallization and melting behavior of metallocene ethylene/α‐olefin copolymers were investigated by differential scanning calorimetry (DSC) and atomic force microscopy (AFM). The results indicated that the crystallization and melting temperatures for all the samples were directly related to the long ethylene sequences instead of the average sequence length (ASL), whereas the crystallization enthalpy and crystallinity were directly related to ASL, that is, both parameters decreased with a decreasing ASL. Multiple melting peaks were analyzed by thermal analysis. Three phenomena contributed to the multiple melting behaviors after isothermal crystallization, that is, the melting of crystals formed during quenching, the melting‐recrystallization process, and the coexistence of different crystal morphologies. Two types of crystal morphologies could coexist in samples having a high comonomer content after isothermal crystallization. They were the chain‐folded lamellae formed by long ethylene sequences and the bundlelike crystals formed by short ethylene sequences. The coexistence phenomenon was further proved by the AFM morphological observation. © 2002 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 40: 822–830, 2002     

辐照聚乙烯的熔融和重结晶

用差示扫描量热法（ＤＳＣ），小角Ｘ－射线散射（ＳＡＸＳ），广角Ｘ－射线衍（ＷＡＸＤ）等考察了辐照聚乙烯的熔融和重结晶，辐照破坏了聚乙烯结晶结构，使其熔融温度、结晶度均随辐照剂量的增加而降低，将辐聚乙烯熔融再结晶，其重结晶度、熔融温度随辐照剂量而下降的幅度较大，其原因被归结为片晶劈裂。