Controlling Product Distribution of Polyethylene Hydrogenolysis Using Bimetallic RuM 3 (M = Fe, Co, Ni) Catalysts
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Simulations of a series of single comb copolymers on C-S-H model surfaces of different composition reveal adsorption mechanisms and conformations in atomic detail to better understand the role in cement hydration and design interfacial properties.
Under optimized reaction conditions, CO 2 can provide acidity to the reaction medium to favor waste poly(ethylene) terephthalate hydrolysis for subsequent recycling/upcycling.
Evaluating six economic and two environmental performance metrics for recycling of waste PET via solvent-based dissolution–precipitation processes.
Considering the severe environmental and humanitarian implications of global plastic waste accumulation, understanding polyolefin catalytic breakdown is essential.
We predict the assembly and time-dependent distribution of cyclodextrin along PEG axles by combining atomistic molecular dynamics with an analytical treatment of bulk diffusion. Our kinetic Monte Carlo can aid in the design of polypseudorotaxanes.
Condensation thermoplastics have become ubiquitous. The emergence of chemical upcycling could transform them into valuable feedstocks for chemical manufacturing at their end-of-life. However, current solvolysis processes suffer equilibrium limitations due to the liberation of reactive byproducts. We report a carbonate interchange deconstruction (CID) methodology for poly(ethylene terephthalate) (PET), where carbonates act as both latent nucleophiles and byproduct sequestering agents. High product selectivity (>95%) is achieved regardless of the targeted terephthalate product, originating from removal of ethylene glycol from the reaction equilibrium via its conversion into various oligoethers. CID is robust to the impurities present in post-consumer waste plastics and significantly reduces solvent demand, with just 10 mL of dimethyl carbonate successfully converting ca. 5 g of mixed PET waste into highly pure dimethyl terephthalate in excellent isolated yield (92%). CID opens a new upcycling paradigm wherein CO2, embedded in carbonates, is leveraged to choreograph the selectivity of an otherwise equilibrium-controlled polymer upcycling process.
Highly oriented and crystalline polyetheylene (PE) fibers have a large failure stress under rapid tensile loading but exhibit significant creep at much smaller stresses that limits applications. A possible mechanism is slip of chains due to stress-enhanced, thermally activated nucleation of dislocations at chain ends in crystalline regions. Molecular dynamics simulations are used to parameterize a Frenkel–Kontorova model that provides analytic expressions for the limiting stress and activation energy for dislocation nucleation as a function of stress. Results from four commonly used hydrocarbon potentials are compared to show that the qualitative behavior is robust and estimate quantitative uncertainties. In all cases, the results can be described by an Eyring model with values of the zero-stress activation energy Ea0≈1.5 eV and activation volume V* ≈ 45 Å3 that are consistent with the experimental results for increasingly crystalline materials. The limiting yield stress is ∼8 GPa. These results suggest that activated dislocation nucleation at chain ends is an important mechanism for creep in highly oriented PE fibers.
Abstract not provided.
The US Department of Energy Nuclear Criticality Safety Program (NCSP) convened a multinational Thermal Epithermal eXperiments (TEX) meeting in July of 2011 to discuss the data and experimental needs of criticality safety practitioners. The number one and two priority integral experiment data needs were for 239 Pu and 240 Pu, with special emphasis on cross section performance in the intermediate energy range (from 0.625 eV to 100 keV). LLNL measured five critical configurations with LANL for the plutonium test bed (IER-184) and published the experiments as International Criticality Safety Benchmark Evaluation Project evaluation PUMET-MIXED-002. Modeling of the benchmark configurations using ENDF/B-VIII.0 nuclear data showed significant overprediction of reactivity for configurations that had a large percentage of fissions in the intermediate energy regime. This report documents a variation on the TEX plutonium test bed to provide a test of 240 Pu cross sections, with sensitivity of the configuration to 240 Pu radiative capture and fission cross sections a priority for the design.
CLUTCH is a CE TSUNAMI method that uses a single forward calculation to determine sensitivities. An F*(r) function provides the importance of each voxel in a mesh over all regions where fission can occur. A sufficient number of fissions must be simulated in each voxel in which fission is possible to generate an accurate estimate of the importance of a fission in that voxel.
Abstract not provided.