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poe
A CaCO3 filler was treated by generally used coupling agents and a special one - ethylene-octene copolymer (POE)-g-maleic anhydride (MAH).
      
Fourier transform infrared spectroscopy (FTIR) results show that the special coupling agent POE-g-MAH, in a chemical reaction with CaCO3, can produce an interfacial layer stronger than simple physical adhesion attained with usual coupling agents.
      
The encapsulation of the CaCO3 filler treated with POE-g-MAH was caused by the strong chemical reaction between the elastomer and CaCO3 particles.
      
In this paper, the screw and product-of-exponentials (POE) formula are used to model the kinematics of reconfigurable robots.
      
The POE formula can be converted to canonical subproblems through decomposition and adjoint transformation.
      
A generalized, decomposable, and reusable approach for close-form inverse kinematics of reconfigurable robots is developed based on POE and subproblems.
      
A conclusion that all ether oxygen atoms in the POE molecule participate in hydrogen bonding with water molecules has been made.
      
Solid lithium-conducting nanocomposite polymer electrolytes based on poly(oxyethylene) (POE) were prepared using high aspect ratio cellulosic whiskers and lithium imide salt, LiTFSI.
      
The polymer used as the continuous phase was the metallocene polyethylene-octene elastomer (POE) or the acrylic acid grafted polyethylene- octene elastomer (POE-g-AA).
      
We found that the POEg-AA/SiO2 hybrid could enhance the properties of the POE/SiO2 hybrid, since the interfacial forces of the former are the covalent Si O C and hetero-associated hydrogen bonds but the latter only has weaker hydrogen bonds.
      
It was also found that the POE-g-AA/SiO2 hybrid with 9 wt% SiO2 gave the maximum value of tensile strength since excess particles might cause the separation between the organic and inorganic phases when the silica content was beyond this point.
      
Surface modification of polystyrene nanoparticles using dextrans and dextran-POE copolymers: Polymer adsorption and colloidal ch
      
Hydrophobically-modified dextran (dextran-phenoxy, DexP) and dextran-phénoxy- poly(oxyethylene) (DexP-POE) copolymers have been used to modify the surface properties and the stability of polystyrene nanoparticles.
      
We examined the effect of phenoxy group and POE chain concentrations on their adsorption behaviour.
      
The results show that the hydrophobic interaction is the driving force during the adsorption while the layer thickness correlates with the interfacial concentration of grafted POE chains.
      
Alternating amphiphilic multiblock copolymers, consisting of polyoxyethylene (POE) and poly(∈-caprolactone) (PCL) of various lengths, were synthesized by a polycondensation reaction between dicarboxylated PEG and dihydroxyl PCL.
      
For in vitro hydrolysis in phosphate-buffered saline solution, the change of molecular weight depended on the composing block length of POE.
      
The polymer with longer POE showed a faster decline in molecular weight.
      
These results are consistent with recent experimental studies on polyoxyethylene (POE).
      
Toughening wood/polypropylene composites with polyethylene octene elastomer (POE)
      
 

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