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121.
In the polymer industry, precompounded materials are widely used. Carefully designed melting experiments were carried out to investigate melting mechanisms in master batched polymer compounds, using an intermeshing co‐rotating twin screw extruder. Calcium carbonate or aluminum powder was master batched with linear low‐density polyethylene (LLDPE). The calcium carbonates, which were used in the compounds, have differences in weight fraction and particle size. The compounds containing filler have higher thermal conductivities and viscosities than neat polyethylene. We observed melting initiation and propagation mechanisms of LLDPE compounds by removal and characterization of polymer compound carcasses in the melting region. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 1990–2012, 2006 相似文献
122.
Chang‐Gyu Kim Sung‐Hoon Joo Cheol Hong Cheon Mi‐Yun Jeong Soon‐Wook Cha Byung‐Hee Sohn Jung‐Il Jin 《应用聚合物科学杂志》2006,100(1):307-317
Three new soluble polyconjugated polymers, all of which emitted blue light in photoluminescence and electroluminescence, were synthesized, and their luminescence properties were studied. The polymers were poly{1,1′‐biphenyl‐4,4′‐diyl‐[1‐(4‐t‐butylphenyl)]vinylene}, poly((9,9‐dioctylfluorene‐2,7‐diyl)‐alt‐{1,4‐phenylene‐[1‐(4‐t‐butylphenyl)vinylene‐1,4‐phenylene]}) [P(DOF‐PVP)], and poly([N‐(2‐ethyl) hexylcarbazole‐3,6‐diyl]‐alt‐{1,4‐phenylene‐[1‐(4‐t‐butylphenyl)]vinylene‐1,4‐phenylene}). The last two polymers had alternating sequences of the two structural units. Among the three polymers, P(DOF‐PVP) performed best in the light‐emitting diode devices of indium–tin oxide/poly(ethylenedioxythiophene) doped with poly(styrene sulfonate) (30 nm)/polymer (150 nm)/Li:Al (100 nm). This might have been correlated with the balance in and magnitude of the mobility of the charge carriers, that is, positive holes and electrons, and also the electronic structure, that is, highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) levels, of the polymers. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 307–317, 2006 相似文献
123.
An increase in the depolymerization of chitosan was found with an increased concentration of sodium perborate. Acetic anhydride was added to reacetylated chitosan in a molar ratio per gulcosamine unit, and the amide I band of IR spectra changed with the addition of acetic anhydride. Sixteen chitosans with various molecular weights (MWs) and degrees of deacetylation (DODs) were prepared. X‐ray diffraction patterns indicated their amorphous and partially crystalline states. Increases in the chitosan MW and DOD increased the tensile strength (TS). TS of the chitosan films ranged from 22 to 61 MPa. However, the elongation (E) of chitosan films did not show any difference with MW. TS of chitosan films decreased with the reacetylation process. However, E of chitosan films was not dependent on DOD. The water vapor permeabilities (WVPs) of the chitosan films without a plasticizer were between 0.155 and 0.214 ng m/m2 s Pa. As the chitosan MW increased, the chitosan film WVP increased, but the values were not significantly different. Moreover, the WVP values were not different from low DOD to high DOD. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 3476–3484, 2003 相似文献
124.
Composite film structures of common plastic polymers including polypropylene (PP) or poly(vinyl chloride) (PVC) with whey protein isolate (WPI) coatings may be obtained by a casting method. Optical and surface properties of the resulting WPI‐coated plastic films, as affected by protein concentration and plasticizer type, were investigated to examine the biopolymer coating effects on surface modification with polymeric substrates of opposite polarity. The measured properties involved specular gloss, color, contact angle, and critical surface energy. Regardless of the substrates, WPI‐coated films possessed excellent gloss and no color, as well as good adhesion between the coating and the substrate when an appropriate plasticizer was added to the coating formulations. The protein concentration did not significantly affect gloss of WPI‐coated plastic films. Among five plasticizers applied, sucrose conferred the most highly reflective and homogeneous surfaces to the coated films. The WPI coatings were very transparent and the coated films with various protein concentrations and plasticizers showed no noticeable changes in color. Experimental results suggest that WPI coatings formulated with a proper plasticizer can improve the visual characteristics of the polymeric substrate and enhance water wettability of the coated plastic films. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 335–343, 2004 相似文献
125.
The kinetic model for the mass polymerization has been developed for a commercial scale mass polymerizer, which shows an anomalous polymerization rate behavior. Non-equilibrium of the refluxed monomer between monomer and polymer phase was proposed to account for this anomaly. Monomer conversion and polymer average molecular weights can be predicted with this mathematical model. The developed model has been successful in simulating a commercial mass polymerizer of 60 m3 size for the optimization of production recipe with respect to the productivity and quality of polyvinyl chloride (PVC). 相似文献
126.
Changyong Choi Su Young Chae Tai‐Hyoung Kim Jung Keon Kweon Chong Su Cho Mi‐Kyeong Jang Jae‐Woon Nah 《应用聚合物科学杂志》2006,99(6):3520-3527
Diblock copolymers with different poly(ε‐caprolactone) (PCL) block lengths were synthesized by ring‐opening polymerization of ε‐caprolactone in the presence of monomethoxy poly(ethylene glycol) (mPEG‐OH, MW 2000) as initiator. The self‐aggregation behaviors and microscopic characteristics of the diblock copolymer self‐aggregates, prepared by the diafiltration method, were investigated by using 1H NMR, dynamic light scattering (DLS), and fluorescence spectroscopy. The PEG–PCL block copolymers formed the self‐aggregate in an aqueous environment by intra‐ and/or intermolecular association between hydrophobic PCL chains. The critical aggregation concentrations of the block copolymer self‐aggregate became lower with increasing hydrophobic PCL block length. On the other hand, reverse trends of mean hydrodynamic diameters were measured by DLS owing to the increasing bulkiness of the hydrophobic chains and hydrophobic interaction between the PCL microdomains. The partition equilibrium constants (Kv) of pyrene, measured by fluorescence spectroscopy, revealed that the inner core hydrophobicity of the nanoparticles increased with increasing PCL chain length. The aggregation number of PCL chain per one hydrophobic microdomain, investigated by the fluorescence quenching method using cetylpyridinium chloride as a quencher, revealed that 4–20 block copolymer chains were needed to form a hydrophobic microdomain, depending on PCL block length. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 99: 3520–3527, 2006 相似文献
127.
Ji Hoon Yang Min Hyung Yum Eun Jung Kim Myeung Hoi Kwon Cheol Woong Yang Ha-Jin Song Yong-Wan Jin 《Carbon》2006,44(11):2219-2223
Nitrogen molecules have been encapsulated into the central hollows of vertically aligned carbon nitride (CN) multiwalled nanofibers by dc plasma-enhanced chemical vapor deposition with C2H2, NH3, and N2 gases on a Ni/TiN/Si(1 0 0) substrate at 650 °C. X-ray photoelectron spectroscopy and near-edge X-ray absorption fine structure spectra showed the existence of nitrogen molecules in CN nanofibers. Elemental mapping images with electron energy loss spectroscopy of the CN nanofiber and catalyst metal, and optical emission spectroscopy spectra of the plasma showed the distribution of nitrogen atoms and molecules in the CN nanofiber, catalyst metal, and gaseous precursor, respectively. These studies showed that atomic nitrogen diffused into the catalytic metal particle because of the concentration gradient and then saturated at the bottom of the particle. Saturated nitrogen atom participated in the formation of the CN nanofiber wall but most of nitrogen was trapped in the central hollow of the nanofiber as molecules. 相似文献
128.
Myung-Sup Jung Tae-Woo Lee Jingyu Hyeon-Lee Byung Hee Sohn In-Sun Jung 《Polymer》2006,47(8):2670-2676
Polyimide containing triphenylamine derivative (TPD-PI) was synthesized to prepare a polymer interlayer having insolubility in common nonpolar solvent for light-emitting polymers. N,N′-diphenyl-N,N′-bis(4-aminophenyl)-1,1-biphenyl-4,4′-diamine, as a new triphenylamine-containing diamine monomer, was synthesized by the palladium-catalyzed amination reaction between 4-nitrodiphenylamine and 4,4′-dibromobiphenyl and subsequent reduction of the nitro-intermediate. The TPD-PI was prepared from the synthesized diamine monomer and 4,4′-(hexafluoropropylidene)-diphthalic anhydride by the standard two-step polymerization method, which involved ring-opening polymerization and subsequent cyclodehydration. The structures and properties of the monomer and the resulting polyimide were characterized with 1H and 13C NMR, elemental analysis, gel permeation chromatography, UV-visible spectroscopy, etc. The TPD-PI is readily soluble in aprotic polar solvents such as N-methyl-2-pyrrolidinone and N,N-dimethylformamide and insoluble in nonpolar solvents such as toluene and xylene. The highest occupied molecular orbital (HOMO) level of the TPD-PI was measured to be 5.5 eV by a photoelectron spectrometer in air, and the band gap was calculated as 3.1 eV from the onset of UV-vis spectrum. The polymer light-emitting diode with the thin TPD-PI layer between a hole injection layer and an emitting polymer layer was fabricated to examine the performance of the polyimide as an polymer interlayer. Although the luminous efficiency of the device is lowered by the introduction of the TPD-PI interlayer, the lifetime of the device is improved. 相似文献
129.
Justin H. Dingle Stephen Zimmerman Alexander L. Frie Justin Min Heejung Jung 《Aerosol science and technology》2019,53(4):449-463
Refractive index and optical properties of biogenic and anthropogenic secondary organic aerosol (SOA) particles were investigated. Aerosol precursors, namely longifolene, α-pinene, 1-methylnaphthalene, phenol, and toluene were oxidized in a Teflon chamber to produce SOA particles under different initial hydrocarbon concentrations and hydroxyl radical sources, reflecting exposures to different levels of nitrogen oxides (NOx). The real and imaginary components (n and k, respectively) of the refractive index at 375?nm and 632?nm were determined by Mie theory calculations through an iterative process, using the χ2 function to evaluate the fitness of the predicted optical parameters with the measured scattering, absorption, and extinction coefficients from a Photoacoustic Extinctiometer and Cavity Attenuated Phase Shift Spectrometer. Single scattering albedo (SSA) and bulk mass absorption coefficient (MAC) at 375?nm were calculated. SSA values of SOA particles from biogenic precursors (longifolene and α-pinene) were ~0.98–0.99 (~6.3% uncertainty), reflecting purely scattering aerosols regardless of the NOx regime. However, SOA particles from aromatic precursors were more absorbing and displayed NOx-dependent SSA values. For 1-methylnaphthalene SOA particles, SSA values of 0.92–0.95 and ~0.75–0.90 (~6.1% uncertainty) were observed under intermediate- and high-NOx conditions, respectively, reflecting the absorbing effects of SOA particles and NOx chemistry for this aromatic system. In mixtures of longifolene and phenol or longifolene and toluene SOA under intermediate- and high-NOx conditions, k values of the aromatic-related component of the SOA mixture were higher than that of 1-methylnaphthalene SOA particles. With the increase in OH exposure, kphenol decreased from 0.10 to 0.02 and 0.22 to 0.05 for intermediate- and high-NOx conditions, respectively. A simple relative radiative forcing calculation for urban environments at λ?=?375?nm suggests the influence of absorbing SOA particles on relative radiative forcing at this wavelength is most significant for aerosol sizes greater than 0.4?µm.
Copyright © 2019 American Association for Aerosol Research 相似文献
130.
Fluidized bed combustion of high ash anthracite (HAA) was experimentally studied. The combustor consists of 0.25 m ID bed,
and auxiliary equipments for coal feeding, ash removal, lemperature control, etc. Experimental results elucidate main cause
of fuel loss to be elutriation of fines (i.e., flyash) containing unburned carbon. However, detailed balances of particle
size distribution show majority of carbon in flyash comes from fines contained in the feed instead of attrition of coarse
particles. The latter is the main source of flyash for conventional coal. The difference is due to much smaller attrition
rate of HAA; feed HAA particles do not shrink much in size by combustion and attrition. 相似文献