Antistatic Properties (antistatic + property)

Distribution by Scientific Domains


Selected Abstracts


Synthesis and characterization of imidazolinium surfactants derived from tallow fatty acids and diethylenetriamine

EUROPEAN JOURNAL OF LIPID SCIENCE AND TECHNOLOGY, Issue 10 2008
Divya Bajpai
Abstract This paper describes the synthesis of long-chain dialkylamido imidazolines based on tallow fatty acids and diethylenetriamine, followed by their quaternization. Imidazolines were obtained by non-solvent microwave synthesis using calcium oxide as support, which were then quaternized by using dimethyl sulfate as a quaternizing agent and iso -propanol as a solvent, to produce cationic imidazolinium salts. The synthesized cationic imidazoline surfactants were evaluated for yield and cationic content. The instrumental techniques, viz. FT-IR and 1H-NMR, verified the formation of imidazolines and their subsequent quaternization. The surface-active and performance properties of the cationic imidazolines in terms of critical micelle concentration, surface tension, dispersibility, emulsion stability, softening, rewettability and antistatic properties were also reported. [source]


Plasma-induced graft polymerization of poly(ethylene glycol) on poly(methyl methacrylate) surfaces for improving antistatic property

JOURNAL OF APPLIED POLYMER SCIENCE, Issue 2 2010
Yanlin Wei
Abstract Ar plasma-induced graft polymerization of poly(ethylene glycol) (PEG) on Ar plasma pretreated poly(methyl methacrylate) (PMMA) surfaces was carried out to improve the antistatic properties. The surface composition and microstructure of the PEG-grafted PMMA surfaces from plasma induction were characterized by attenuated total reflectance Fourier transfer infrared (ATR-FTIR) spectroscopy, water contact angles (CA), and atomic force microscopy (AFM) measurements. The measurements revealed that the antistatic properties can be remarkably improved with the surface resistivity of PEG-grafted PMMA surface decreasing significantly by 3,6 orders of magnitude, with the optimum condition for polymerization grafted onto the Ar plasma pretreated PMMA surface being 40 W for RF power and 3 min for glow discharge time. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source]


Fabrication and properties of nano-ZnO/glass-fiber-reinforced polypropylene composites

JOURNAL OF VINYL & ADDITIVE TECHNOLOGY, Issue 3 2010
Yi-Hua Cui
Polypropylene (PP) is widely used in many fields, such as automobiles, medical devices, office equipment, pipe, and architecture. However, its high brittle transformation temperature, low mechanical strength, dyeing properties, antistatic properties, and poor impact resistance, considerably limit its further applications. Nano-ZnO treated by KH550 coupling agent and glass fibers (GFs) were introduced in order to improve the mechanical performance and flowability of PP in this research. The crystallization behavior and microstructure of nano-ZnO/GFs/PP hybrid composites were analyzed by differential scanning calorimetry, transmission electron microscopy, and scanning electron microscopy. The effect of crystallization behavior on the mechanical properties of the nanocomposites was investigated and analyzed. The results indicated that nano-ZnO surface-coupled by KH550 could be uniformly dispersed in the PP matrix. The incorporation of nano-ZnO and GFs resulted in increases of the crystallization temperature and crystallization rate of PP and a decrease of the crystallization degree. The introduction of nano-ZnO and GFs also enhanced the tensile strength and impact toughness of the hybrid composites and improved their fluidity. Composites containing 2% of nano-ZnO and 40% of GFs possessed the optimum mechanical properties. J. VINYL ADDIT. TECHNOL., 2010. © 2010 Society of Plastics Engineers [source]


Plasma-induced graft polymerization of poly(ethylene glycol) on poly(methyl methacrylate) surfaces for improving antistatic property

JOURNAL OF APPLIED POLYMER SCIENCE, Issue 2 2010
Yanlin Wei
Abstract Ar plasma-induced graft polymerization of poly(ethylene glycol) (PEG) on Ar plasma pretreated poly(methyl methacrylate) (PMMA) surfaces was carried out to improve the antistatic properties. The surface composition and microstructure of the PEG-grafted PMMA surfaces from plasma induction were characterized by attenuated total reflectance Fourier transfer infrared (ATR-FTIR) spectroscopy, water contact angles (CA), and atomic force microscopy (AFM) measurements. The measurements revealed that the antistatic properties can be remarkably improved with the surface resistivity of PEG-grafted PMMA surface decreasing significantly by 3,6 orders of magnitude, with the optimum condition for polymerization grafted onto the Ar plasma pretreated PMMA surface being 40 W for RF power and 3 min for glow discharge time. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source]


Development of a packaging material using antistatic ionomer part 2: charge distributions of potassium ionomer

PACKAGING TECHNOLOGY AND SCIENCE, Issue 5 2007
Nobuyuki Maki
Abstract Generally, plastics and plastic films are low in moisture absorption and high in electric insulation. They are inherently easy to be charged with static and can cause a variety of static troubles. We developed a functional packaging material to solve these static problems, by using potassium ionomer. We reported good antistatic performance (e.g. short static decay time, and excellent ash test) of potassium ionomer films in a previous paper. However, a mechanism underlying the antistatic property of potassium ionomer has not yet been fully elucidated. In this study, we measured the space charge distributions of potassium ionomer using the pulsed electro-acoustic method. As a result of the space charge measurements, we found characteristic charge distribution of potassium ionomer film. On the basis of the existence of this characteristic charge distribution, we speculate that the space electric charge distribution of a potassium ionomer film under a direct current electric field shows apparent electric charge movement. Copyright © 2006 John Wiley & Sons, Ltd. [source]