共查询到20条相似文献,搜索用时 15 毫秒
1.
Haijin Zhu Yanfang Wang Yifan Su Qingkui Chen Cun Geng Charles C. Han 《Polymer》2007,48(17):5098-5106
A systematic investigation on the origin of the haze of LDPE blown films was conducted, aiming to correlate the film haze with the molecular architecture and melt rheological properties. First of all, the haze measurement indicated that the surface haze, rather than the bulk haze, is the dominating factor for the total haze of the investigated films. No spherulitic crystals or other superstructures were observed for the LDPE blown films, implying that the crystallites formed in the film-blowing process are too small to be responsible for the optical haze. Rheological study revealed that the surface roughness was originated from the irregular flow of LDPE melt during the extrusion process. NMR, GPC and parallel-plate rheology were applied to study the molecular architecture of the LDPE resins. It was found that the LDPE sample with higher haze value exhibits distinctly larger portion of higher molecular weight component, broader molar mass distribution, significantly higher side chain branch density. 相似文献
2.
3.
Lithium acrylate (LiAA) was in situ prepared in a chlorinated polyethylene (CPE) matrix through the neutralization of lithium hydroxide (LiOH) and acrylic acid (AA) during mixing. The obtained compounds were vulcanized with dicumyl peroxide (DCP). The in situ preparation and polymerization of LiAA were characterized with Fourier transform infrared spectrometry. The crosslink density analysis results indicated that the CPE/LiAA vulcanizates contained both covalent bonds and ionic bonds. The effects of the DCP and LiAA contents on the mechanical properties and water‐swelling properties of the CPE/LiAA vulcanizates were studied. The relationship between the LiOH/AA molar ratio and the properties of the CPE/LiAA vulcanizates was investigated. The results showed that LiAA could improve the mechanical and water‐swelling properties of CPE/LiAA vulcanizates, providing a new approach to the preparation of water‐swelling elastomers. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 1804–1812, 2004 相似文献
4.
G. M. N. Costa S. Kislansky L. C. Oliveira F. L. P. Pessoa S. A. B. Vieira de Melo M. Embiruçu 《应用聚合物科学杂志》2011,121(3):1832-1849
We modeled solid–liquid equilibria (SLEs) in polyethylene and polypropylene solutions with a Soave–Redlich–Kwong (SRK) cubic equation of state (EOS) and a perturbed‐chain statistical associating fluid theory (PC‐SAFT) EOS. Two types of mixing rules were used with SRK EOS: The Wong–Sandler mixing rule and the linear combination of the Vidal and Michelsen mixing rules (LCVM), both of which incorporated the Bogdanic and Vidal activity coefficient model. The performance of these models was evaluated with atmospheric‐pressure and high‐pressure experimental SLE data obtained from literature. The basic SLE equation was solved for the equilibrium melting temperature instead of for the composition. The binary interaction parameters of SRK and PC‐SAFT EOS were estimated to best describe the experimental equilibrium behavior of 20 different polymer–solvent systems at atmospheric pressure and 31 other polymer–solvent systems at high pressure. A comparison with experimental data showed that SRK–LCVM agreed very well with the atmospheric SLE data and that PC‐SAFT EOS was more efficient in high‐pressure conditions. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011 相似文献
5.
Shivendra Upadhyay Vishwanath Mallikarjunan Vaideesh K. Subbaraj Susy Varughese 《应用聚合物科学杂志》2008,109(1):135-143
The swelling and diffusion characteristics of a polar polymer [ethylene vinyl acetate (EVA)] and a nonpolar polymer [low-density polyethylene (LDPE)] were studied with swelling experiments of the polymers in asphalt at different temperatures. The study showed that the diffusion mechanisms for LDPE and EVA were different and temperature-dependent. In the case of LDPE, the observed diffusion was anomalous at both swelling temperatures (70 and 90°C). LDPE at 90°C showed sigmoidal solvent-uptake behavior during the initial period of swelling and a sorption overshoot in a later period. EVA showed Fickian transport at 60°C and anomalous diffusion at a higher swelling temperature (70°C) with sigmoidal uptake behavior. An analysis of the diffusion coefficients and the Fourier transform infrared results showed that the diffusing molecules were different in the case of LDPE and EVA, and there were possible polymer–asphalt interactions. Differential scanning calorimetry and swelling studies showed that penetrant-induced crystallization affected the diffusion process in the case of LDPE. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 相似文献
6.
7.
The swelling behavior of poly(N‐isopropylacrylamide) (PNIPA) gels in polymer solutions, particularly in aqueous solutions of poly(ethylene glycol)s, was investigated using the theory of equilibrium swelling. The volume of the PNIPA gel and the partition parameter of the macromolecules between the gel and the solution phases were calculated for various extents of the energetic interactions between the components. The simulation results were compared with the experimental data reported in the literature. It was shown that the PNIPA gel has a tendency to a reentrant phase transition in an aqueous solution of low molecular weight linear polymers. In such a transition, the gel first collapses, then reswells, if the linear polymer concentration is continuously varied. The necessary condition for the reentrant behavior of PNIPA gels was predicted in terms of the interaction parameters among the PNIPA network, the linear polymer, and water. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 85: 801– 813, 2002 相似文献
8.
RRN Sailaja 《Polymer International》2005,54(12):1589-1598
Lignin was graft copolymerized with methyl methacrylate using manganic pyrophosphate as initiator. This modified lignin was then blended (up to 50 wt%) with low density polyethylene (LDPE) using a small quantity of poly[ethylene‐co‐(glycidyl methacrylate)] (PEGMA) compatibilizer. The mechanical properties of the blend were substantially improved by using modified lignin in contrast to untreated lignin. Differential scanning calorimetry studies showed loss of crystallinity of the LDPE phase owing to the interaction between the blend components. Thermogravimetric analysis showed higher thermal stability of modified lignin in the domain of blend processing. This suggested that there is scope for useful utilization of lignin, which could also lead to the development of eco‐friendly products. Copyright © 2005 Society of Chemical Industry 相似文献
9.
Antonin Novak Marek Bobak Juraj Kosek Brian J. Banaszak Dennis Lo Tomy Widya W. Harmon Ray Juan J. de Pablo 《应用聚合物科学杂志》2006,100(2):1124-1136
The sorption of ethylene and 1‐hexene and their mixture in three poly(ethylene‐co‐1‐hexene) samples is measured gravimetrically at temperatures 70, 90, and 150°C and pressures 0–30 bar. Gravimetric sorption measurements are supplemented with microscopic observations of swelling of polyethylene particles caused by sorption and the extent of swelling is found to be significant. Experimental data are compared with predictions of PC‐SAFT (perturbed chain—‐statistical associating fluid theory) equation of state. Comparison of sorption data in semicrystalline polymer (measured at 70 and 90°C) and amorphous polymer (at 150°C) demonstrates the constraining effect of semicrystalline structure. Solubilities of penetrants in investigated samples are not observed to depend on the content of 1‐hexene in copolymers. The solubility of the mixture of ethylene and 1‐hexene is smaller than the sum of solubilities of individual components at 70 and 90°C. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 1124–1136, 2006 相似文献
10.
The demixing processes that occur during the polymerization of styrene in the presence of a low molar mass polyethylene wax were investigated. Quantitative information on the phase behavior of such a three‐component system was obtained through the investigation of the temperature‐induced phase separation and the observation of the phase separation during polymerization. Both techniques allow the construction of the same ternary phase diagram. Such phase behavior can be understood through the discussion of the interference of a liquid–liquid phase‐separation process and crystallization. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 2234–2243, 2004 相似文献
11.
开口爽滑剂在低密度聚乙烯薄膜中的应用 总被引:1,自引:0,他引:1
介绍了目前我国低密度聚乙烯薄膜发展现状,开口剂和爽滑剂在低密度聚乙烯薄膜开口爽滑性方面的作用,分析了薄膜提高开口爽滑性的同时,如何兼顾较好光学性能,对国内低密度聚乙烯生产企业今后牌号升级及细化提出了建议。 相似文献
12.
Hwan‐Man Park Sang‐Rock Lee Subhendu R. Chowdhury Tae‐Kyu Kang Hak‐Kil Kim Seung‐Hoon Park Chang‐Sik Ha 《应用聚合物科学杂志》2002,86(11):2907-2915
In the present study, blends of starch with different thermoplastics were prepared by a melt blending technique. The tensile properties and morphology of the blends were measured. It was found that with increasing starch content in starch/ionomer blends, the tensile strength and modulus increase. But for starch/low‐density polyethylene (LDPE) and starch/aliphatic polyester (APES) blends, tensile strength and modulus decrease with increasing the starch loading. Elongation at break values of all the blend systems decrease with increasing starch loading. The scanning electron micrographs (SEM) support the findings of tensile properties. Better homogeneity is observed in starch/ionomer systems compared with that in starch/APES and starch/LDPE systems. Up to 50% starch content, the starch/ionomer blends appear as a single phase. The extent of phase interactions of starch/APES system lies in between the starch/LDPE and starch/ionomer systems. From the biodegradability studies of the blends it was found that, although the pure LDPE and ionomer are not biodegradable, the starch/LDPE and starch/ionomer blends are biodegradable with an appreciable rate. The rate of biodegradation of the starch/APES is very high as both the components are biodegradable. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 2907–2915, 2002 相似文献
13.
The in-line development of crystalline morphology and orientation during melt extrusion of low density polyethylene (LDPE) tape at nil and low haul-off speeds has been investigated using Small-Angle X-Ray Scattering (SAXS). The processing parameters, namely haul-off speed and distance down the tape-line have been varied and the resulting crystalline morphology is described from detailed analysis of the SAXS data. Increasing haul-off speed increased orientation in the polymer tape and the resulting morphology could be described in terms of regular lamellar stacking perpendicular to the elongation direction. In contrast, under nil haul-off conditions the tape still showed some orientation down the tape-line, but a shish-kebab structure prevails. The final lamellae thickness ( ∼50 Å) and bulk crystallinity (∼20%), were low at, for all processing conditions investigated, which is attributed to the significant short-chain branching in the polymer acting as point defects limiting lamellae crystal growth. 相似文献
14.
It is critical to quantitatively and reliably characterize the effects of swell and sag phenomena on the final parison dimensions in extrusion blow molding. To achieve this goal, an online image acquisition and analysis technique was developed. The successive images of parison were automatically taken using the online acquisition apparatus. These images were then analyzed by the combined use of the conventional digital image processing method and the new one developed by the authors. So the development of parison diameter and thickness swells with the extrusion time could be determined online. On the basis of the online obtained actual swell values, the pure swell and sag components were quantitatively determined. The developed technique was tested through a series of experiments using several resins under different processing parameters and die types. Shown in the present article were the results for a converging die under three different die gaps and a high‐density polyethylene. Some new phenomena were observed using the proposed technique. The results showed that the technique yields fast and accurate determination of the evolution of diameter, thickness, and length of parison during its extrusion. The technique can be employed as a part of the closed loop control for blow molded part thickness. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 2399–2406, 2006 相似文献
15.
Vincenzo Titone;Luigi Botta;Maria Chiara Mistretta;Francesco Paolo La Mantia; 《Polymer Engineering and Science》2024,64(2):845-851
Mechanical recycling of oil-derived polymers is certainly our best option to reduce pollution, save raw materials, and protect ourselves and the environment from the adverse effects of waste disposal. However, the presence of contaminants, including other types of plastics, that are mixed in during the recycling collection process or during the mechanical waste sorting stage could adversely affect the quality of the recycled product, leading to the recycling of a poor-quality secondary material. In this work, the influence of a biodegradable contaminant on the mechanical recycling of a low-density polyethylene (LDPE) sample was investigated by rheological (shear and non-isothermal elongation) and mechanical analyses. The results showed that 2% of the contaminant is able to influence the rheological, shear, and isothermal elongation properties of recycled LDPE, while the results of the mechanical tests showed that after one extrusion cycle, the main tensile properties were not significantly affected by the presence of the contaminant, but after only two cycles of extrusions, some significant reduction in the final properties began to appear. In short, the presence of 2% of a biodegradable co-polyester in a LDPE matrix gives rise to a more pronounced decay of the rheological and mechanical properties, but, after two extrusion steps, both rheological and mechanical properties seem still useful for the production of film. 相似文献
16.
Maryam Ataeefard Siamak Moradian Mojtaba Mirabedini Morteza Ebrahimi Said Asiaban 《Progress in Organic Coatings》2009,64(4):482-488
Low-pressure glow discharges of Ar or O2 gas plasmas were used to increase the wettability of low-density polyethylene (LDPE) films in order to improve their adhesion properties hence making them useful in technical applications. Surface free energies of such films were estimated by the aid of contact angle measurements at different exposure power/time combinations for a series of test liquids. Additionally, plasma-treated samples were subjected to several aging processes to determine the durability of different plasma treatments. Characterization of the surface changes due to plasma treatments were carried out by means of attenuated total reflectance, Fourier transform infrared spectroscopy (FTIR-ATR) to determine the presence of polar species such as hydroxyl, carbonyl, carboxyl, etc. groups. Furthermore, atomic force microscopy (AFM) and scanning electron microscopy (SEM) were used to evaluate changes in surface morphology and roughness. Considering the semi-crystalline nature of the LDPE film, XRD studies were also carried out to determine changes in the percentage of crystalinity. The results showed that all low-pressure Ar or O2 gas plasmas improve the wettability properties of LDPE films. Contact angles decreased significantly depending on the discharge powers and exposure times. Surface morphology was also found to vary with plasma discharge powers, exposure times, and the type of gas being used. Ar gas plasmas comparatively produced superior results. 相似文献
17.
The effect of the compatibilizer on the crystallization, rheological, and tensile properties of low-density polyethylene (LDPE)/ethylene vinyl alcohol (EVOH) (70/30) blends was investigated. Maleic anhydride-grafted linear low-density polyethylene (LLD-g-MAH) was used as the compatibilizer in various concentrations (from 1 to 12 phr). The interesting effect of compatibilization on the crystallization kinetics of the blends was noted, and the correlation between the morphology and the rheological and tensile properties was also discussed. Morphological analysis showed that the blends exhibited a regular and finer dispersion of the EVOH phase when LLD-g-MAH was added. Nonisothermal crystallization exotherms of the compatibilized LDPE/EVOH blends showed the retarded crystallization of the dispersed EVOH phase, which probably resulted from the constraint effect of the grafted EVOH (EVOH-g-LLD) as well as the size reduction of the EVOH domains. The blends exhibited increased melt viscosity and storage modulus and also enhanced tensile properties with the addition of LLD-g-MAH, which seemed to be attributable to both dispersed particle-size reduction and improved interfacial adhesion. © 1998 John Wiley & Sons, Inc. J Appl Polym Sci 68: 1245–1256, 1998 相似文献
18.
Tomoko Watanabe Yoshito Ohtake Hitoshi Asabe Nobunao Murakami Mutsuhisa Furukawa 《应用聚合物科学杂志》2009,111(1):551-559
This article is intended to establish a comprehensive interpretation of the noticeable differences in the dynamic mechanical behaviors of polypropylene/talc composites with and without modified interphases. The latter are discussed on the basis of different surface treatments applied to the reinforcement particles. To this end, a series of 75/25 (w/w) polypropylene/talc composites with and without interfacial modifications from the reinforcement side were evaluated by dynamic mechanical analysis. The proven capability of this technique analysis to follow the transitions and structural and morphological changes in organic polymers, which are largely influenced by the degree of compatibility between the components of heterogeneous materials based on polymers, was used in this study to check and discuss the kinds and efficiencies of different physisorption‐ and chemisorption‐based processes carried out on the surface of talc particles. We tackled this study by embracing the different relaxation phenomena taking place in the polymer matrix. To this end, five different temperature intervals were distinguished according to the relaxation phenomena taking place. Finally, a correlation between the parameters on the microscopic scale and others on the macroscopic scale appeared to emerge. Thus, the interfacial effects caused by the modified reinforcements could be determined by observations on either scale. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009 相似文献
19.
Nagwa I. El‐Awady 《应用聚合物科学杂志》2004,91(1):10-14
Low‐density polyethylene‐g‐poly(acrylic acid) membranes were prepared by the direct radiation grafting of aqueous acrylic acid solutions (containing Mohr's salt) onto low‐density polyethylene films and were irradiated at two different irradiation doses (2 and 3 Mrad) at a dose rate of 0.02 Mrad/h. Two series of polyethylene‐g‐poly(acrylic acid) membranes with 100 and 150% grafting were obtained. The free carboxylic acid groups in the grafted films were converted into the corresponding acrylates by reactions with different metal salts. The swelling (water uptake) and dialysis permeability of glucose and urea through the grafted membranes in different metal‐ion forms were investigated. The prepared membranes showed good permeability to both solutes, which increased as the hydrophilicity of the membrane increased. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 10–14, 2004 相似文献
20.
E. Ateia 《应用聚合物科学杂志》1997,66(9):1639-1645
The effect of γ-irradiation on both the electrical conductance, Y, and diffusion coefficient, D, of acrylonitrile butadiene rubber mixed with different concentrations (1, 3, and 5 phr) of low-density polyethylene (LDPE) that was swollen in benzene, have been studied. The diffusion coefficient decreases with increasing the γ-irradiation dose for loaded samples with 1 and 3 phr of LDPE content, while samples with 5 phr of LDPE show a significant increase of diffusion coefficient with the increase of the radiation dose. The electrical conductance was found to be highly affected by the γ-irradiation dose. © 1997 John Wiley & Sons, Inc. J Appl Polym Sci 66: 1639–1645, 1997 相似文献