Tailored polyethylene reactor blend additives (RB) with ultrabroad bimodal molar mass distributions comprise nanophase-separated ultrahigh molar mass polyethylene (UHMWPE) uniformly dispersed in polyethylene wax. During injection molding of high-density polyethylene (HDPE) together with variable amounts of the nanophase-separated HDPE wax/ UHMWPE (70/30) additive (RB30) flow-induced oriented crystallization affords shish-kebab fiber-like UHMWPE nanostructures accounting for efficient HDPE self-reinforcement. RB additives are readily prepared by ethylene polymerization on silica-supported two-site chromium catalysts which simultaneously produce HDPE wax together with disentangled nanoplateletlike UHMWPE. The presence of HDPE wax is essential for lowering melt viscosity at high UHMWPE content. Since HDPE wax crystallizes onto extended-chain UHMWPE shish to form kebab structures, high HDPE wax content is tolerated without encountering emission problems and impairing mechanical properties as observed in the absence of UHMWPE. This in situ reinforcement substantially improves HDPE toughness/stiffness/strength balance as reflected by simultaneously increased Young's modulus (+365%), tensile strength (+392%), and impact resistance (+197%). The performance of self-reinforced polyethylene (PE-SRC) is far superior to that of melt-blended UHMWPE/HDPE and the majority of PE nanocomposites. Neither hazardous UHMWPE nanoparticles nor alien inorganic nanofillers are required.
Ultrathin single crystal γ‐Al(OH)3 (Gibbsite) nanoplatelets with average thickness <20 nm and length <800 nm, pretreated with trimethylaluminum (TMA), represent highly efficient activators and supports bis(imino)pyridine iron (II) (FeBIP) complex to produce high density polyethylene (HDPE) as well as gibbsite/HDPE nanocomposites in exceptionally high yields. Opposite to both methylaluminoxane (MAO)‐activated homogeneous FeBIP catalyst and heterogenous silica‐supported single site catalysts, no addition of MAO is required. At low TMA/Fe = 50 molar ratio, the superior catalyst activity (up to 6500 kg mol−1 h−1 bar−1) of FeBIP@TMA@Gibbsite is paralleled by controlled polyethylene particle growth without encountering reactor‐fouling problems typical for homogeneous catalysts. TMA@Gibbsite is compared with other AlR3@Gibbsite activators. The Al/Fe molar ratio governs catalyst activity as well as molar mass, molar mass distribution, and thermal properties of polyethylene. Moreover, hexagonal gibbsite nanoplatelets are uniformly dispersed in polyethylene to yield agglomerate‐free polyethylene/gibbsite nanocomposites.
Experiments were performed to measure the effect of strain rate on the tensile properties of SA-106 carbon steel pipe, in support of analysis and experimental modeling of postulated pipe whip in nuclear power plants. It was observed that increasing the strain rate from 4 × 10−4 to 4 s−1 raised the yield strength by approximately 30 percent.
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