Ultrasound initiated maleic anhydride grafted onto a novel polypropylene copolymer

The reaction of maleic anhydride (MAH) grafted onto propylene‐based copolymer (DP) without adding any initiator was conducted through ultrasound assisted extrusion in this article. The effects of ultrasound power, die temperature, and MAH content on the grafting degree and efficiency were studied. With increasing ultrasound power, the grafting degree and efficiency of DP‐g‐MAH increase. The presence of ultrasound with higher power and lower die temperature is beneficial to increase the grafting degree and efficiency. The increase of MAH content can increase the grafting degree but reduce the grafting efficiency. Based on the results of melt flow index, dynamical rheological, gel permeation chromatograph (GPC), and Fourier transform infrared spectroscopy (FTIR) tests, the mechanisms of the grafting reaction were proposed. POLYM. ENG. SCI., 2012. © 2011 Society of Plastics Engineers     

Novel impacts of glycol-modified poly(ethylene terephthalate)(PETG) to crystallization behavior of polyethylene naphthalate (PEN) within stretched miscible blends

For studied blends of amorphous glycol-modified poly(ethylene terephthalate) (PETG) and semicrystalline polyethylene naphthalate (PEN), melt miscibility is understood from the linear variation of a single glass transition temperature (T_g) over the entire composition range. The diluent effect of PETG component severely retarded the crystallization of PEN component within blends. Nevertheless, after being through isothermal stretching at 120 °C, crystallization was able to progress efficiently during heating in a continuous manner. Instead of being thermally relaxed back to amorphous state, parallel sliding motions of stretched PEN segments toward crystallization appear rather dominant. Within stretched blends, the PETG content emerged as a critical factor to the crystallinity increase of PEN fraction and the absence of lattice defect, instead of behaving as a diluent component. Furthermore, as being indicated by in-situ small-angle X-ray experiments, regular lamellar stacking gradually developed within stretched blends through heating, which indicates the involvement of thermally activated self-association of randomly distributed crystalline lamellae. With including a higher fraction of PETG component, these secondary ordering processes including lamellar thickening can be activated at lower temperature. Hence, the accompanied thermal relaxation of flexible PETG segment is inferred able to lubricate the sliding of stretched PEN segments in amorphous regions via lowering encountered frictional hindrance, and thus enhance both primary and secondary ordering processes within stretched blends.     

Functional acrylic acid as stabilizer for synthesis of smart hydrogel particles containing a magnetic Fe3O4 core

This paper reports a novel method to synthesize magnetic, stimuli-sensitive latex nanoparticles made with magnetite/poly(N-isopropylacrylamide-co-acrylic acid) (Fe₃O₄/P(NIPAAm-co-AAc)). To form a stabilized suspended core, iron oxide (Fe₃O₄) was functionalized with AAc such that further polymerization with NIPAAm and AAc monomers could occur. The P(NIPAAm-co-AAc) shell layer exhibited thermosensitive properties. The inclusion of Fe₃O₄ into the latex nanoparticles was confirmed using transmission electron microscopy, X-ray photoelectron spectroscopy, X-ray diffraction spectroscopy, thermogravimetric analyzer (TGA), and superconducting quantum interference device magnetometer. The NIP–(AAc2.6–Fe) latex nanoparticles contained 2.25% Fe₃O₄ (by weight), as determined by TGA analysis. The particle diameters measured approximately 160–240 nm with a lower critical solution temperature of 35 °C. These novel magnetic stimuli-responsive latex nanoparticles have potential applications in numerous fields, such as catalyst supports, protein immobilization, cancer therapy, target drug delivery systems, and other biomedical applications.     

Influence of Y-doped induced defects on the optical and magnetic properties of ZnO nanorod arrays prepared by low-temperature hydrothermal process

ABSTRACT: One-dimensional pure zinc oxide (ZnO) and Y-doped ZnO nanorod arrays have been successfully fabricated on the silicon substrate for comparison by a simple hydrothermal process at the low temperature of 90°C. The Y-doped nanorods exhibit the same c-axis-oriented wurtzite hexagonal structure as pure ZnO nanorods. Based on the results of photoluminescence, an enhancement of defect-induced green-yellow visible emission is observed for the Y-doped ZnO nanorods. The decrease of E2(H) mode intensity and increase of E1(LO) mode intensity examined by the Raman spectrum also indicate the increase of defects for the Y-doped ZnO nanorods. As compared to pure ZnO nanorods, Y-doped ZnO nanorods show a remarked increase of saturation magnetization. The combination of visible photoluminescence and ferromagnetism measurement results indicates the increase of oxygen defects due to the Y doping which plays a crucial role in the optical and magnetic performances of the ZnO nanorods.     

A novel synthesis method for the preparation of aromatic poly(imide benzoxazole) from trimellitic anhydride chloride and bis(o‐aminophenol)

A poly(imide benzoxazole) was prepared directly from trimellitic anhydride chloride and 2,2‐bis(3‐amino‐4‐hydroxyphenyl)hexafluoropropane (BisAPAF) monomers in a two‐step method. In the first step, a poly(hydroxyamide amic acid) precursor was synthesized by the low‐temperature solution polymerization in an organic solvent. Subsequently, thermal cyclodehydration of the poly(hydroxyamide amic acid) precursor at 350°C produced the corresponding poly(imide benzoxazole). The inherent viscosity of the precursor polymer was 0.22 dL/g. The cyclized poly(imide benzoxazole) showed a glass transition temperature (T_g) at 329°C and a 5% weight loss temperature at 530°C in nitrogen and at 525°C in air. The poly(imide benzoxazole) is amorphous as evidenced by the wide‐angle X‐ray diffraction measurement. The structures of the precursor polymer and the fully cyclized polymer were characterized by Fourier transform infrared (FTIR) and proton nuclear magnetic resonance spectroscopy (¹H NMR). © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 2388–2391, 2003     

The effect of scaleup on the processing behavior of a blend exhibiting phase inversion during compounding

The scaleup behavior of blends exhibiting phase inversion during compounding in batch mixers was studied. Similar morphological changes were observed during compounding of polystyrene/polyethylene blends of different batch sizes ranging from 12g to 240g. The time to achieve a continuous phase of the major component, polystyrene, was shown to depend on the scale of the mixing device. Based on visual observation of the morphological changes, a constant nominal‐maximum‐shear‐rate scaleup condition was used. Upon a five‐fold increase in batch size the time to phase inversion increased by a factor of 3. This change is explained using a combination of the reduced specific area and reduced mechanical energy input under the experimental conditions. A novel blade design using modular triangular elements was constructed and results from radial and axial scaleup using the new blades are presented. Similarities between the triangular and roller blades are used to highlight the importance of the high‐shear region in determining the softening rate of the polystyrene pellets. The flexibility of the blade design was exploited to study the effect of blade configuration on the time to phase inversion. A relative stagger parameter is introduced to explain the observed dependence. Increasing the relative stagger decreased the stress transfer to the batch and increased the time to phase inversion. Implications of these results for mixing in the kneading sections of twin‐screw extruders is discussed.     

Comparative In Vitro Osteoinductivity Study of HA and α‐TCP/HA Bicalcium Phosphate

A bicalcium phosphate (BCP) bioceramic comprising α‐tricalcium phosphate (α‐TCP) and hydroxyapatite (HA) was prepared by a two‐step sintering. The microstructure of the BCP bioceramic was investigated using scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X‐ray diffraction. The in vitro osteoinductivity was evaluated by culturing MG63 osteoblast‐like cells on the BCP bioceramic. Results showed that the BCP bioceramic comprising α‐TCP and HA in a moderate ratio possessed a hardness of 93.7 Hv. The cells spread faster on the BCP bioceramic than those on the commercial HA. It suggested that the BCP bioceramic can enhance osteoinductivity in vivo.     

Development of Potent Adenosine Monophosphate Activated Protein Kinase (AMPK) Activators

Previously, we reported the identification of a thiazolidinedione‐based adenosine monophosphate activated protein kinase (AMPK) activator, compound 1 (N‐[4‐({3‐[(1‐methylcyclohexyl)methyl]‐2,4‐dioxothiazolidin‐5‐ylidene}methyl)phenyl]‐4‐nitro‐3‐(trifluoromethyl)benzenesulfonamide), which provided a proof of concept to delineate the intricate role of AMPK in regulating oncogenic signaling pathways associated with cell proliferation and epithelial–mesenchymal transition (EMT) in cancer cells. In this study, we used 1 as a scaffold to conduct lead optimization, which generated a series of derivatives. Analysis of the antiproliferative and AMPK‐activating activities of individual derivatives revealed a distinct structure–activity relationship and identified 59 (N‐(3‐nitrophenyl)‐N′‐{4‐[(3‐{[3,5‐bis(trifluoromethyl)phenyl]methyl}‐2,4‐dioxothiazolidin‐5‐ylidene)methyl]phenyl}urea) as the optimal agent. Relative to 1 , compound 59 exhibits multifold higher potency in upregulating AMPK phosphorylation in various cell lines irrespective of their liver kinase B1 (LKB1) functional status, accompanied by parallel changes in the phosphorylation/expression levels of p70S6K, Akt, Foxo3a, and EMT‐associated markers. Consistent with its predicted activity against tumors with activated Akt status, orally administered 59 was efficacious in suppressing the growth of phosphatase and tensin homologue (PTEN)‐null PC‐3 xenograft tumors in nude mice. Together, these findings suggest that 59 has clinical value in therapeutic strategies for PTEN‐negative cancer and warrants continued investigation in this regard.     

An intelligent skin‐color capture method based on fuzzy C‐means with applications

Consumer behavior is complicated. In the cosmetic market, personal intuition and fashion trends for color selection are guidelines for consumers. A systematic method for female facial skin‐color classification and an application in the makeup market are proposed in this study. In this article, face recognition with a large number of images is first discussed. Then, an innovative method to capture color at selected points is presented and complexion‐aggregated analysis is performed. This innovative method is an extension of face‐recognition theory. Images in RGB format are converted to CIELAB format during data collection and then Fuzzy C‐means theory is used to cluster and group the data. The results are classified and grouped in Lab value and RGB index. Two programs are created. The first program, “FaceRGB,” captures color automatically from images. The second program, “ColorFCM,” clusters and groups the skin‐color information. The results can be used to assist an expert system in the selection of customized colors during makeup and new‐product development.     

A consultation and simulation system for product color planning based on interactive genetic algorithms

In the early stage of a design process, it is important to create numerous and varied possible color plans for the target consumer group. These color plans help individual designers quickly find a few good color design schemes and give the design team ideas for brainstorming. The color plan of a product consists of the color combinations of its components and decorative patterns, which strongly influence the feelings of customers and thus their desire to purchase. However, very few studies have discussed these issues. In this study, a consultation and simulation system for product color planning that helps designers obtain the optimal color planning for components and decorative patterns of a product is proposed. This system includes two parts: one uses the interactive genetic algorithm to establish a creative evolutionary system that can interact with a designer to explore novel design schemes; the other extends the boundary extract algorithm to establish a color simulation system that can apply colors to the areas of product components and decorative patterns for color simulation. Finally, a case study of color planning for a motorcycle model is used to verify the feasibility of the proposed system. © 2012 Wiley Periodicals, Inc. Col Res Appl, 38, 375–390, 2013