Desorption of residual monomer from PVC resins in a fluidized bed drier

The present study deals with the investigation of the desorption of vinyl chloride from various commercial and experimental suspension PVC resins in a laboratory fluidized bed drier simulating an industrial drier. The results show that PVC resins may differ widely in the rate at which the monomer is desorbed. The rate of diffusion of the monomer is a function of the drying time, the fluidization air temperature, the porosity, and the amount of glassy particles in the PVC. The residual monomer content decreases with increasing air temperature, drying time, and resin porosity. After 105 min of drying with hot air at 80°C, the residual monomer content in the grade with the highest porosity is reduced from 3400 to 2 ppm, whereas for the grade with the lowest porosity, it is reduced from 4300 to 172 ppm on a dry basis. It appears that the resins of the high molecular weight grades are more porous and the low molecular weight grades contain a high proportion of nonporous or glassy particles and, hence, the desorption rate is smaller in these grades. The proportion of glassy particles and the size of glassy domains are estimated in this study by applying the experimental desorption data at long times to a desorption model. The model is useful in differentiating the interior structure of various PVC grades. © 1994 John Wiley & Sons, Inc.     

Impact modified polyamide‐6/organoclay nanocomposites: Processing and characterization

The effects of melt state compounding of ethylene‐butyl acrylate‐maleic anhydride (E‐BA‐MAH) terpolymer and/or three types of organoclays (Cloisite® 15A, 25A, and 30B) on thermal and mechanical properties and morphology of polyamide‐6 are investigated. E‐BA‐MAH formed spherical domains in the materials to which it is added, and increased the impact strength, whereas the organoclays decreased the impact strength. In general, the organoclays increased the tensile strength (except for Cloisite 15A), Young's modulus and elongation at break, but the addition of E‐BA‐MAH had the opposite effect. XRD patterns showed that the interlayer spacing for the organoclays Cloisite 25A and Cloisite 30B increased in both polyamide‐6/organoclay binary nanocomposites and in polyamide‐6/organoclay/impact modifier ternary systems. TEM analysis showed that exfoliated‐intercalated nanocomposites were formed. The crystallinities of polyamide‐6/organoclay nanocomposites were in general lower than that of polyamide‐6 (except for Cloisite 15A). In ternary nanocomposites, crystallinities generally were lower than those of polyamide‐6/organoclay nanocomposites. Cloisite 15A containing ternary nanocomposites had higher tensile and impact strengths and Young's modulus than the ternary nanocomposites prepared with Cloisite 25A and Cloisite 30B, owing to its surface hydrophobicity and compatibility with the impact modifier. POLYM. COMPOS., 2008. © 2007 Society of Plastics Engineers     

线性LED驱动器IC为何必然替代偏压电阻器

利用简单的电阻器限制LED串中的电流看似最为经济和简便,那么为何还要费尽心思地使用线性驱动器IC?     

Solution of one-speed neutron transport equation for strongly anisotropic scattering by TN approximation: Slab criticality problem

In this study, a recently proposed version of Chebyshev polynomial approximation which was used in spectrum and criticality calculations by one-speed neutron transport equation for slabs with isotropic scattering is further developed to slab criticality problems for strongly anisotropic scattering. Backward–forward-isotropic model is employed for the scattering kernel which is a combination of linearly anisotropic and strongly backward–forward kernels. Further to that, the common approaches of using the same functional form for scattering and fission kernels or embedding fission kernel into the scattering kernel even in strongly anisotropic scattering is questioned for T_N approximation via taking an isotropic fission kernel in the transport equation. As a starting point, eigenvalue spectrum of one-speed neutron transport equation for a multiplying slab with different degrees of anisotropy in scattering and for different cross-section parameters is obtained using Chebyshev method. Later on, the spectra obtained for different degree of anisotropies and cross-section parameters are made use of in criticality problem of bare homogeneous slab with strongly anisotropic scattering. Calculated critical thicknesses by Chebysev method are almost in complete agreement with literature data except for some limiting cases. More importantly, it is observed that using a different kernel (isotropic) for fission rather than assuming it equal to the scattering kernel which is a more realistic physical approach yields in deviations in critical sizes in comparison with the values presented in literature. This separate kernel approach also eliminates the slow convergency and/or non-convergent behavior of high-order approximations arising from unphysical eigenspectrum calculations.     

Toward High‐Dimensional Single‐Cell Analysis of Graphene Oxide Biological Impact: Tracking on Immune Cells by Single‐Cell Mass Cytometry

Considering the potential exposure to graphene, the most investigated nanomaterial, the assessment of the impact on human health has become an urgent need. The deep understanding of nanomaterial safety is today possible by high‐throughput single‐cell technologies. Single‐cell mass cytometry (cytometry by time‐of flight, CyTOF) shows an unparalleled ability to phenotypically and functionally profile complex cellular systems, in particular related to the immune system, as recently also proved for graphene impact. The next challenge is to track the graphene distribution at the single‐cell level. Therefore, graphene oxide (GO) is functionalized with AgInS₂ nanocrystals (GO–In), allowing to trace GO immune–cell interactions via the indium (¹¹⁵In) channel. Indium is specifically chosen to avoid overlaps with the commercial panels (>30 immune markers). As a proof of concept, the GO–In CyTOF tracking is performed at the single‐cell level on blood immune subpopulations, showing the GO interaction with monocytes and B cells, therefore guiding future immune studies. The proposed approach can be applied not only to the immune safety assessment of the multitude of graphene physical and chemical parameters, but also for graphene applications in neuroscience. Moreover, this approach can be translated to other 2D emerging materials and will likely advance the understanding of their toxicology.     

Rheological properties of poly(lactic acid) based nanocomposites: Effects of different organoclay modifiers and compatibilizers

Poly(lactic acid) (PLA) nanocomposites containing five types of organically modified, layered silicates and two elastomeric compatibilizers, namely ethylene‐glycidyl methacrylate (E‐GMA) and ethylene‐butyl acrylate‐maleic anhydride (E‐BA‐MAH), were prepared using a twin screw extruder. The morphologies of the nanocomposites were determined by X‐ray diffraction (XRD) and transmission electron microscopy (TEM), and the rheological properties of the melts were measured using small‐amplitude oscillatory shear. XRD revealed that the addition of E‐GMA to the binary nanocomposites resulted in higher compatibility between the organoclay nanoplatelets and the polymer matrix. TEM showed that all of the nanocomposites contained mixed dispersed structures, involving tactoids of various sizes, as well as intercalated and exfoliated organoclay layers. Rheological properties were found to be affected by the differences in the compatibility between the organoclays and the polymer matrix, and by the addition of the compatibilizer. Organoclay types that resulted in high level of dispersion exhibited higher values of complex viscosity compared to that of neat PLA. The addition of E‐GMA introduced a solid‐like rheological behavior at low frequencies. All of the nanocomposites had similar rheological behavior at high frequencies. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 42915.     

Physical aging in particulate-filled composites with an amorphous glassy matrix

Physical aging was studied on particulate -filled glassy network polymers by means of mechanical -dilatational, differential scanning calorimetry (DSC) and density measurements on specimens that were aged at room temperature. The composites aged for 0.5 day fractured in a brittle manner at a constant ultimate stress, which is close to the tensile strength of the unfilled material, regardless of the filler content and the presence of a coupling agent. This type of mechanical behavior is caused by the compressive residual stresses that are present due to curing and differential thermal shrinkage. As aging takes place, the compressive residual stresses are relieved; as a result the ultimate tensile strengths of the composites decrease. The 120 -day -old untreated glass bead containing composites exhibited dilatation and yield in mechanical -dilatational testing. This type of behavior is described as “having no adhesion” between the filler and the matrix. The 120 -day -old composites with coupling agent -treated glass beads fractured at a tensile stress which is equal to 1/1.6 the tensile strength of the unfilled material. These materials did not exhibit dilatation and yield in mechanical -dilatational testing. Density and DSC data indicate densification and enthalpy relaxation upon again and support the hypothesis presented for the observed change in the mechanical -dilatational behavior.     

Effects of nucleating agent and processing conditions on the mechanical,thermal, and optical properties of biaxially oriented polypropylene films

The effects of nucleating agent, temperature of crystallization, and degree of machine direction (MD) orientation on the mechanical, optical, and thermal properties of biaxially oriented polypropylene (BOPP) films were investigated. Addition of nucleating agent improved only the initial tear resistance in the MD; however, the other mechanical and optical properties did not change appreciably. In the set of experiments in which the crystallization temperature was increased, the degree of crystallinity also increased. Thus, Young's modulus, yield stress, and tensile strength increased in both directions with higher degree of crystallinity. The yield strain did not change significantly, but the strain at break was higher. Although the initial tear resistance was smaller in both directions with increasing crystallization temperature, the tear propagation resistance did not change. In this case, haze and diffuse transmittance were slightly higher, but the total transmittance was constant. In the set of experiments in which the machine direction orientation was increased, the degree of crystallinity also became higher. Owing to the effects of higher crystallinity and higher MD orientation, the modulus, yield stress, and tensile strength increased, but the yield strain and tear propagation resistance did not significantly change in both directions.     

Dilatancy of concentrated suspensions with Newtonian matrices

Suspensions filled close to their maximum packing fraction present special challenges in their processing and in their rheological characterization. In this report, the literature in the area of dilatancy of concentrated suspensions is reviewed. Furthermore, the shear viscosity of a Newtonian polymeric liquid filled with 60 vol. percent of ammonium sulfate has been investigated. Both capillary and parallel disk torsional flows, were employed, spanning three decades in shear stress. Upon correction for slip, the suspension exhibited shear thinning at low shear stresses and shear thickening at higher shear stresses. Above a critical wall shear stress, the shear viscosity of the suspension increased unboundedly and the flow became pluglike with apparent slip at the wall. These findings have important ramifications in the processing of composites from such concentrated suspensions.     

Effect of different types of organoclays and compatibilizers on the properties of polystyrene‐based nanocomposites

Polystyrene/organoclay nanocomposites were prepared by melt intercalation in the presence of elastomeric impact modifiers. Three different types of organically modified montmorillonites; Cloisite® 30B, 15A, and 25A, were used as reinforcement, whereas poly [styrene‐b‐(ethylene‐co‐butylene)‐b‐styrene] (SEBS‐g‐MA) and poly(ethylene‐b‐butyl acrylate‐b‐glycidyl methacrylate) (E‐BA‐GMA) elastomeric materials were introduced to act as impact modifier. Owing to its single aliphatic tail on its modifier and absence of hydroxyl groups, Cloisite® 25A displayed the best dispersion in the polystyrene matrix, and mostly delaminated silicate layers were obtained in the presence of SEBS‐g‐MA. This was attributed to the higher viscosity of SEBS‐g‐MA compared with both E‐BA‐GMA and poly(styrene‐co‐vinyloxazolin) (PS). In addition, the compatibility between SEBS‐g‐MA and PS was found to be better in comparison to the compatibility between E‐BA‐GMA and PS owing to the soluble part of SEBS‐g‐MA in PS. The clay particles were observed to be located mostly in the dispersed phase leading to larger elastomeric domains compared with binary PS/elastomer blends. The enlargement of the elastomeric domains resulted in higher impact strength values in the presence of organoclay. Good dispersion of Cloisite® 25A in PS/SEBS‐g‐MA blends enhanced the tensile properties of this nanocomposite produced. It was observed that the change in the strength and stiffness of the ternary nanocomposites mostly depend on the type of the elastomeric material. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013