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The efficient delivery of reactive and toxic gaseous reagents to organic reactions was studied using metal-organic frameworks (MOFs). The simultaneous cargo vehicle and catalytic capabilities of several MOFs were probed for the first time using the examples of aromatization, aminocarbonylation, and carbonylative Suzuki-Miyaura coupling reactions. These reactions highlight that MOFs can serve a dual role as a gas cargo vehicle and a catalyst, leading to product formation with yields similar to reactions employing pure gases. Furthermore, the MOFs can be recycled without sacrificing product yield, while simultaneously maintaining crystallinity. The reported findings were supported crystallographically and spectroscopically (e.g., diffuse reflectance infrared Fourier transform spectroscopy), foreshadowing a pathway for the development of multifunctional MOF-based reagent-catalyst cargo vessels for reactive gas reagents as an attractive alternative to the use of toxic pure gases or gas generators.
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High throughput experimentation in heterogeneous catalysis provides an efficient solution to the generation of large datasets under reproducible conditions. Knowledge extraction from these datasets has mostly been performed using statistical methods, targeting the optimization of catalyst formulations. The combination of advanced machine learning methodologies with high-throughput experimentation has enormous potential to accelerate the predictive discovery of novel catalyst formulations that do not exist with current statistical design of experiments. This perspective describes selective examples ranging from statistical design of experiments for catalyst synthesis to genetic algorithms applied to catalyst optimization, and finally random forest machine learning using experimental data for the discovery of novel catalysts. Lastly, this perspective also provides an outlook on advanced machine learning methodologies as applied to experimental data for materials discovery.
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We have studied P adsorption on Ni(111), a system which shows complex adsorbate structures. We determined the phase diagram of the surface P adsorbed on Ni(111). At low coverage, amorphous P was observed. At temperatures between 373 and 673 K and coverages above 0.1 monolayer, we found a 7 × 7 R 19.1 ∘ structure, but above 673 K, other complex structures were created. These structures seemed to correlate with each other and we reinterpret a 7 × 7 R 19.1 ∘ structure of P adsorbed on Ni(111) based on the similarities of these surface structures. The new rectangular structure for the 7 × 7 19.1 ∘ is discussed in relation to the Ni2P local structure.
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Ag+ -Exchanged LSX (Ag-LSX: Ag96 Al96 Si96 O384 â n H2 O), a large pore low silica analogue (Si/Al=1.0) of faujasite, was prepared and post-synthetically modified using pressure and temperature in the presence of various pore-penetrating fluids. Using high-resolution synchrotron X-ray powder and single crystal diffraction we derive structural models of the as-prepared and post-synthetically modified Ag-LSX materials. In the as-prepared Ag-LSX model, we located 96 silver cations and 245 H2 O molecules distributed over seven and five distinctive sites, respectively. At 1.4(1)â GPa pressure and 150 °C in ethanol the number of silver cations within the pores of Ag-LSX is reduced by ca. 47.4 %, whereas the number of H2 O molecules is increased by ca. 40.8 %. The formation of zero-valent silver nanoparticles deposited on Ag-LSX crystallites depends on the fluid present during pressurization. Ag-nanoparticle-Ag-zeolite hybrid materials are recovered after pressure release and shown to have different chemical reactivity when used as catalysts for ethylene epoxidation.
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In this study, we demonstrate the production of long-chain hydrocarbons (C8+) from 2-methylfuran (2MF) and butanal in a single step reactive process by utilizing a bi-functional catalyst with both acid and metallic sites. Our approach utilizes a solid acid for the hydroalkylation function and as a support as well as a transition metal as hydrodeoxygenation catalyst. A series of solid acids was screened, among which MCM-41 demonstrated the best combination of activity and stability. Platinum nanoparticles were then incorporated into the MCM-41. The Pt/MCM-41 catalyst showed 96% yield for C8+ hydrocarbons and the catalytic performance was stable over four reaction cycles of 20 hour each. The reaction pathways for the production of long-chain hydrocarbons is probed with a combination of infrared spectroscopy and steady-state reaction experiments. It is proposed that 2MF and butanal go through hydroalkylation first on the acid site followed by hydrodeoxygenation to produce the hydrocarbon fuels.
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Biomassa , Hidrocarbonetos/química , Resíduos Industriais , Aldeídos/química , Catálise , Furanos/química , Platina/química , Dióxido de Silício/química , TemperaturaRESUMO
During co-pyrolysis of biomass with plastic waste, bio-oil yields (BOY) could be either induced or reduced significantly via synergistic effects (SE). However, investigating/ interpreting the SE and BOY in multidimensional domains is complicated and limited. This work applied XGBoost machine-learning and Shapley additive explanation (SHAP) to develop interpretable/ explainable models for predicting BOY and SE from co-pyrolysis of biomass and plastic waste using 26 input features. Imbalanced training datasets were improved by synthetic minority over-sampling technique. The prediction accuracy of XGBoost models was nearly 0.90 R2 for BOY while greater than 0.85 R2 for SE. By SHAP, individual impact and interaction of input features on the XGBoost models can be achieved. Although reaction temperature and biomass-to-plastic ratio were the top two important features, overall contributions of feedstock characteristics were more than 60 % in the system of co-pyrolysis. The finding provides a better understanding of co-pyrolysis and a way of further improvements.
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Plásticos , Pirólise , Humanos , Biomassa , Óleos de PlantasRESUMO
High throughput experimentation has the capability to generate massive, multidimensional datasets, allowing for the discovery of novel catalytic materials. Here, we show the synthesis and catalytic screening of over 100 unique Ru-Metal-K based bimetallic catalysts for low temperature ammonia decomposition, with a Ru loading between 1-3 wt% Ru and a fixed K loading of 12 wt% K, supported on γ-Al2O3. Bimetallic catalysts containing Sc, Sr, Hf, Y, Mg, Zr, Ta, or Ca in addition to Ru were found to have excellent ammonia decomposition activity when compared to state-of-the-art catalysts in literature. Furthermore, the Ru content could be reduced to 1 wt% Ru, a factor of four decrease, with the addition of Sr, Y, Zr, or Hf, where these secondary metals have not been previously explored for ammonia decomposition. The bimetallic interactions between Ru and the secondary metal, specifically RuSrK and RuFeK, were investigated in detail to elucidate the reaction kinetics and surface properties of both high and low performing catalysts. The RuSrK catalyst had a turnover frequency of 1.78 s-1, while RuFeK had a turnover frequency of only 0.28 s-1 under identical operating conditions. Based on their apparent activation energies and number of surface sites, the RuSrK had a factor of two lower activation energy than the RuFeK, while also possessing an equivalent number of surface sites, which suggests that the Sr promotes ammonia decomposition in the presence of Ru by modifying the active sites of Ru.
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Fast pyrolysis, in combination with torrefaction pretreatment, was used to convert tobacco residues to value-added bio-fuels and chemicals. Tobacco plant residues were torrefied at 220, 260, and 300 °C, before being pyrolyzed at 450, 500, 550, and 600 °C in a rotating blade ablative reactor under vacuum conditions to test the effects on product yields. With torrefaction, tobacco residues thermally decomposed 20-25% w/w at low temperatures. Torrefaction and pyrolysis temperatures were found to markedly affect pyrolytic product yields of bio-chars and bio-oils, while having no effect on gas-phase products. Bio-oil yields exhibited a direct relation with pyrolysis temperature and an inverse relation with torrefaction temperature. Bio-oils produced were separated into light and heavy oils and analyzed by GC-MS, and 1H and 13C NMR. Nicotine was found to be the main compound in the light and heavy oils along with several phenols and cresols in the heavy oil.
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Corn residue pellets were torrefied with wet flue gas, simulated by steam (0-21% v/v), CO2 (12% v/v), and O2 (4% v/v), balanced with N2 as reactive gas, in a fixed bed reactor at 260⯰C of temperature and at 10-40â¯min of residence time. The distribution and yields of torrefied pellets, liquid, and gas products were examined. The microstructural changes of torrefied pellets were evaluated by Raman spectroscopy and scanning electron microscopy, while the components of gas products were analyzed by mass spectrometry. Residence time and steam concentration in the reactive gas were found to have significant effects on the products yield distribution, the porosity of the torrefied pellets, and the concentrations of CO, CH4, H2, and CO2 in the gas products. At high steam concentrations, the decomposition reaction of hemicellulose and lignin in the raw pellets, and the formation of the graphene structures in torrefied pellets occurred faster.
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Vapor , Zea mays , Biomassa , TemperaturaRESUMO
In this work, a statistical design and analysis platform was used to develop cobalt oxide based oxidation catalysts prepared via one pot metal salt reduction. An emphasis was placed upon understanding the effects of synthesis conditions, such as heating regimen and Co2+ concentration on the metal salt reduction mechanism, the resultant nanomaterial properties (i.e., size, crystal structure, and crystal faceting), and the catalytic activity in CO oxidation. This was accomplished by carrying out XRD, TEM, and FTIR studies on synthesis intermediates and products. Additionally, high-throughput experimentation was employed to study the performance of Co3O4 oxidation catalysts over a wide range of reaction conditions using a 16-channel fixed bed reactor equipped with a parallel infrared imaging system. Specifically, Co3O4 nanomaterials of varying properties were evaluated for their performance as CO oxidation catalysts. Figure-of-merits including light-off temperatures and activation energies were measured and mapped back to the catalyst properties and synthesis conditions. Statistical analysis methods were used to elucidate significant property-activity relationships as well as the design rules relevant in the synthesis of active catalysts. It was found that the degree of grain boundary consolidation and anisotropic growth in fcc and hcp CoO intermediates significantly influenced the catalytic activity. By utilizing the discovered synthesis-structure-activity relationships, CO oxidation light off temperatures were decreased to <90°C.
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A high-throughput parallel reactor system has been designed and constructed to improve the reliability of results from large diameter catalysts such as monoliths. The system, which is expandable, consists of eight quartz reactors, 23.5 mm in diameter. The eight reactors were designed with separate K type thermocouples and radiant heaters, allowing for the independent measurement and control of each reactor temperature. This design gives steady state temperature distributions over the eight reactors within 0.5 degrees C of a common setpoint from 50 to 700 degrees C. Analysis of the effluent from these reactors is performed using rapid-scan Fourier transform infrared (FTIR) spectroscopic imaging. The integration of this technique to the reactor system allows a chemically specific, truly parallel analysis of the reactor effluents with a time resolution of approximately 8 s. The capabilities of this system were demonstrated via investigation of catalyst preparation conditions on the direct epoxidation of ethylene, i.e., on the ethylene conversion and the ethylene oxide selectivity. The ethylene, ethylene oxide, and carbon dioxide concentrations were calibrated based on spectra from FTIR imaging using univariate and multivariate chemometric techniques. The results from this analysis showed that the calcination conditions significantly affect the ethylene conversion, with a threefold increase in the conversion when the catalyst was calcined for 3 h versus 12 h at 400 degrees C.
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Técnicas de Química Combinatória/instrumentação , Calefação/instrumentação , Teste de Materiais/instrumentação , Termografia/instrumentação , Catálise , Técnicas de Química Combinatória/métodos , Desenho de Equipamento , Análise de Falha de Equipamento , Calefação/métodos , Teste de Materiais/métodos , Termografia/métodosRESUMO
In the asynchronous, rapid-scan approach to Fourier transform infrared (FT-IR) imaging, data sampling is not correlated with the zero crossings of the interference fringes of the HeNe reference laser. The success of this data collection scheme depends on the reproducibility of the clock signals driving the interferometer mirror and focal plane array data collection. In previous studies, it was shown that this implementation provides for markedly faster data acquisition without sacrificing data quality, as compared with stepscan imaging. This approach to data collection introduces some unique peculiarities to the acquisition and processing of imaging data. The purpose of this paper is to address a few of these concerns in terms of their effect on final data quality. Also, the practical aspects of implementing such an acquisition scheme are described in detail.
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Coleta de Dados/métodos , Espectroscopia de Infravermelho com Transformada de Fourier/métodos , Calibragem , Processamento de Imagem Assistida por Computador/métodos , Reprodutibilidade dos Testes , Espectroscopia de Infravermelho com Transformada de Fourier/instrumentaçãoRESUMO
We combine kinetic and spectroscopic data to demonstrate the concept of a self-healing catalyst, which effectively eliminates the need for catalyst regeneration. The observed self-healing is triggered by controlling the crystallographic orientation at the catalyst surface.
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Portable power technologies for military applications necessitate the production of fuels similar to LPG from existing feedstocks. Catalytic cracking of military jet fuel to form a mixture of C2-C4 hydrocarbons was investigated using high-throughput experimentation. Cracking experiments were performed in a gas-phase, 16-sample high-throughput reactor. Zeolite ZSM-5 catalysts with low Si/Al ratios (≤25) demonstrated the highest production of C2-C4 hydrocarbons at moderate reaction temperatures (623-823 K). ZSM-5 catalysts were optimized for JP-8 cracking activity to LPG through varying reaction temperature and framework Si/Al ratio. The reducing atmosphere required during catalytic cracking resulted in coking of the catalyst and a commensurate decrease in conversion rate. Rare earth metal promoters for ZSM-5 catalysts were screened to reduce coking deactivation rates, while noble metal promoters reduced onset temperatures for coke burnoff regeneration.
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Gases/síntese química , Ensaios de Triagem em Larga Escala , Hidrocarbonetos/síntese química , Petróleo , Zeolitas/química , Catálise , Gases/química , Hidrocarbonetos/químicaRESUMO
A high-throughput optical technique has been developed for the rapid screening of coking resistant composition-spread promoted-catalyst libraries during hydrocarbon cracking, in particular for Jet Propellant 8(JP-8) cracking. The libraries are screened by measuring changes in the catalyst's surface color due to the accumulation and burnoff of coke from the surface during JP-8 exposure and catalyst regeneration via oxygen burnoff. This rapid screening method was validated through a comparison of the coking properties of high-surface area powder cracking catalysts, and sputter deposited samples. Experiments on bimetallic (Pt-Gd) catalysts showed systematic trends consistently illustrating the superiority of Pt-Gd alloys to coking due to the presence of gadolinium.
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Coque/análise , Ensaios de Triagem em Larga Escala/instrumentação , Querosene/análise , Oxigênio/química , Ligas/química , Catálise , Desenho de Equipamento , Gadolínio/química , Platina/químicaRESUMO
The adsorption of atomic oxygen on unreconstructed Pt[100]-(1 x 1) and reconstructed Pt[100]-(5 x 1) was modeled using density-functional theory in an attempt to understand the relative stability of the unreconstructed phase as a function of oxygen coverage. Our calculations showed that at zero temperature the (5 x 1) is more stable than the unreconstructed (1 x 1) phase at zero oxygen coverage. However, oxygen absorption on the Pt[100]-(5 x 1) phase removed the reconstruction, reversing the phase stability. Using thermochemical analysis, we show desorption of oxygen corresponding to a temperature near 730 K, consistent with experimentally observed desorption peaks for oxygen covered (1 x 1) surfaces. These results have ramifications for understanding the full Pt[100](1 x 1)-->Pt[100]hex-R0.7 degrees surface phase transition.
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High-throughput experimentation in heterogeneous catalysis has recently experienced nearly exponential growth. Initial qualitative screening has evolved into quantitative high-throughput experimentation, characterization, and analysis. This allows high-throughput catalysis now to rise above simple screening to the level of fundamental understanding of reaction mechanisms, which will lead on a faster path to the Holy Grail of catalysis: rational catalyst design.