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This review summarizes the performance of potential catalysts for the synthesis of dimethyl carbonate (DMC) using CO2 as a feedstock by two major processes—the direct route of carbonylation of alcohols and the indirect route of alcoholysis of urea. The reaction mechanisms and corresponding catalysts that were previously investigated are discussed. The major challenges associated with the conversion of CO2 to DMC are the low yields, low DMC selectivity, and thermodynamic limitations (alcohol carbonylation) of reversible reactions with low equilibrium constants. This occurs mainly due to the highly stable carbon dioxide molecules. The development of novel catalysts with high yields and high selectivity needs to be studied to overcome these technical challenges. In addition, to enhance the DMC yield, the use of dehydrating agents for water removal from the reaction mixture is recommended and discussed in detail in this article. This review critically examines the different catalysts used by investigators, along with their respective operating conditions and suitability in applications for the commercial synthesis of CO2-based DMC.

Non-oxidative methane dehydro-aromatization reaction can co-produce hydrogen and benzene effectively on a molybdenum-zeolite based thermochemical catalyst, which is a very promising approach for natural-gas upgrading. However, the low methane conversion and aromatics selectivity and weak durability restrain the realistic application for industry. Here, a mechanism for enhancing catalysis activity on methane activation and carbon-carbon bond coupling has been found to promote conversion and selectivity simultaneously by adding platinum–bismuth alloy cluster to form a trimetallic catalyst on zeolite (Pt-Bi/Mo/ZSM-5). This bimetallic alloy cluster has synergistic interaction with molybdenum: the formed CH 3 * from Mo 2 C on the external surface of zeolite can efficiently move on for C-C coupling on the surface of Pt-Bi particle to produce C 2 compounds, which are the key intermediates of oligomerization. This pathway is parallel with the catalysis on Mo inside the cage. This catalyst demonstrated 18.7% methane conversion and 69.4% benzene selectivity at 710 °C. With 95% methane/5% nitrogen feedstock, it exhibited robust stability with slow deactivation rate of 9.3% after 2 h and instant recovery of 98.6% activity after regeneration in hydrogen. The enhanced catalytic activity is strongly associated with synergistic interaction with Mo and ligand effects of alloys by extensive mechanism studies and DFT calculation. Converting methane to hydrogen and aromatics is a route to upgrading natural gas into high value products. Here the authors report a high-performing synergistic trimetallic thermochemical catalyst, along with mechanistic insights into the process.

To improve the microstructure and mechanical properties of fundamental materials including aluminum, stainless steel, superalloys, and titanium alloys, traditional manufacturing techniques have for years been utilized in critical sectors including the aerospace and nuclear industries. However, additive manufacturing has become an efficient and effective means for fabricating these materials with superior mechanical attributes, making it easier to develop complex parts with relative ease compared to conventional processes. The waste generated in additive manufacturing processes are usually in the form of powders, while that of conventional processes come in the form of chips. The current study focuses on the features and uses of various typical recycling methods for traditional and additive manufacturing that are presently utilized to recycle material waste from both processes. Additionally, the main factors impacting the microstructural features and density of the chip-unified components are discussed. Moreover, it recommends a novel approach for recycling chips, while improving the process of development, bonding quality of the chips, microstructure, overall mechanical properties, and fostering sustainable and environmentally friendly engineering.

High-purity, superhard, binderless polycrystalline cubic boron nitride (BL-PCBN) was obtained by direct hBN to cBN transformation in a toroid-type high-pressure apparatus at a pressure of 8.0 GPa and temperature of 2250 °C (HPHT-DCS; high-pressure, high-temperature direct conversion sintering). X-ray diffraction analysis revealed a prominent [111] axial texture in the sintered material when the axis was oriented perpendicular to the end surface of the sample. Vickers hardness tests conducted at a load of 49 N showed that BL-PCBN possessed an exceptional hardness value of 63.4 GPa. Finally, cutting tools made of BL-PCBN and SN-PCBN (Si3N4-doped cBN-based composite) reference materials were tested during the turning of a cemented tungsten carbide workpiece. The results of the cutting tests demonstrated that the wear resistance of the BL-PCBN material obtained with the HPHT-DCS process is 1.5–1.9 times higher compared to the conventional SN-PCBN material, suggesting its significant potential for industrial application.

Lignin depolymerization often requires multiple isolation steps to convert a lignocellulose matrix into high-value chemicals. In addition, lignin structural modification, low yields, and poor product characteristics remain challenges. Direct catalytic depolymerization of lignocellulose from date palm biomass was investigated. Production of high value chemicals heavily depends on optimization of different parameters and method of conversion. The goal of the study was to elucidate the role of different parameters on direct conversion of date palm waste in a bench reactor, targeting valuable C5–C12 compounds. The catalytic performance results demonstrated better liquid yields using a commercial alloy catalyst than with laboratory-prepared transition metal phosphide catalysts made using nickel, cobalt, and iron. According to the gas chromatography-mass spectrometry results, C7–C8 compounds were the largest product fraction. The yield improved from 3.6% without a catalyst to 68.0% with a catalyst. The total lignin product yield was lower without a catalyst (16.0%) than with a catalyst (76.0%). There were substantial differences between the carbon distributions from the commercial alloy catalyst, supported transition metal phosphide catalyst, and catalyst-free processes. This may be due to differences between reaction pathways. Lab-made catalysts cracked the biomass to produce more gases than the alloy catalyst. The final pressure rose from 2 bar at the start of the experiment to 146.15 bar and 46.50 bar after the respective reactions. The particle size, solvent type, time, temperature, gas, and catalytic loading conditions were 180 µm, methanol, 6 h, 300 °C, nitrogen, and 5 wt %, respectively. The results from this study provide a deep understanding of the role of different process parameters, the positive attributes of the direct conversion method, and viability of date palm waste as a potential lignocellulose for production of high-value chemicals.

Direct conversion transmitters are widely used in wireless systems for their inherent features of being simple and low cost. In this architecture, the inphase (I branch) and quadrature signal (Q branch) will be unconverted to the RF frequency band by quadrature modulation. However, the drawback of the direct conversion architecture is that it is sensitive to IQ imbalance caused by the impairment of analogue devices in I and Q branches. It then results in interferences in mirror frequencies which degrades the signal quality. Therefore, the accurate measurement of IQ imbalance is crucial. A diode-based method to measure the broadband IQ imbalance is proposed which does not need additional measurement instruments. Measurement results show the effectiveness of this method.

To improve the linearity of direct conversion receivers (DCRs), two high-linearity methods for high second-order intercept points (IP2s) and high third-order intercept points (IP3s) are proposed. To improve IP3s, a transconductance equalization technique for a complementary input operational amplifier (OPAMP) is proposed in an active-RC low-pass filter (LPF), while a digital-analog hybrid DC offset calibration (DCOC) method is proposed to improve IP2s. For one thing, the proposed transconductance equalization technique employs a pair of resistors to guarantee high voltage gain for an OPAMP with two-stage Miller topology under a high-input voltage swing to improve linearity with little deterioration of the noise performance. For another, during the DCOC method, the low-noise amplifier is turned off and replaced by an equivalent resistance of the output impedance of the low-noise amplifier to ensure the accuracy and effectiveness of the DCOC method. Fabricated in 40-nm CMOS technology, the receiver with proposed methods can realize a noise figure of 2.6–3.5 dB in the full frequency band, with an OIP3 of 28 dBm, an IM2 more than 70 dBc, and a remaining DC of −53.2 dBm under the total voltage gain of 60 dB.

As the human lifespan has increased due to developments in medical technology, the number of patients with neurological diseases has rapidly increased. Therefore, studies on effective treatments for neurological diseases are becoming increasingly important. To perform these studies, it is essential to obtain a large number of patient-derived neural cells. The purpose of the present study was to establish a technology that allows the high-efficiency generation of genetically stable, direct-conversion-derived neural stem cells (dcNSCs) through the expression of a new combination of reprogramming factors, including a proto-oncogene. Specifically, human c-MYC proto-oncogene and the human SOX2 gene were overexpressed in a precisely controlled manner in various human somatic cells. As a result, the direct conversion into multipotent dcNSCs occurred only when the cells were treated with an MOI of 1 of hc-MYC proto-oncogene and hSOX2 retrovirus. When MOIs of 5 or 10 were utilized, distinct results were obtained. In addition, the pluripotency was bypassed during this process. Notably, as the MOI used to treat the cells increased, expression of the p53 tumor suppressor gene, which is typically a reprogramming hurdle, increased proportionately. Interestingly, p53 was genetically stable in dcNSCs generated through direct conversion into a low p53 expression state. In the present study, generation of genetically stable dcNSCs using direct conversion was optimized by precisely controlling the overexpression of a proto-oncogene. This method could be utilized in future studies, such as in vitro drug screening using generated dcNSCs. In addition, this method could be effectively utilized in studies on direct conversion into other types of target cells. [Display omitted]

The direct conversion of tremendous greenhouse gas methane into various value-added chemical products or energy fuels is not only a concern associated with an economic interest but also related to environmental protection. However, neither industry nor academia has an effective or low-cost way to directly achieve this result. Herein, a high specific area (962 m 2  g −1 ) porous organic polymer was designed and used as a substance to support catalytic active sites, including PdBr 2 , Pd(OAc) 2 , and well-dispersed AuPd bimetallic nanoparticles which were reduced via hydrogen flow. The as-synthesized catalysts (HNU-2 and HNU-3) can not only maintain the porous and stable structure of their pristine matrix but also show extremely high catalytic performance in methane direct transformation systems for preparing methanol derivative methyl trifluoroformate. Our simple strategy provides a complementary alternative to application of methane via an efficient one-step conversion procedure in order to reduce its impact on climate change and obtain value-added chemicals.

Continuous mechanical work output can be generated by using combustion engines and electric motors, as well as actuators, through on/off control via external stimuli. Solar energy has been used to generate electricity and heat in human daily life; however, the direct conversion of solar energy to continuous mechanical work has not been realized. In this work, a solar engine is developed using an oscillating actuator, which is realized through an alternating volume decrease of each side of a polypropylene/carbon black polymer film induced by photothermal-derived solvent evaporation. The anisotropic solvent evaporation and fast gradient diffusion in the polymer film sustains oscillating bending actuation under the illumination of divergent light. This light-driven oscillator shows excellent oscillation performance, excellent loading capability, and high energy conversion efficiency, and it can never stop with solvent supply. The oscillator can cyclically lift up a load and output work, exhibiting a maximum specific work of 30.9 × 10 −5 J g −1 and a maximum specific power of 15.4 × 10 −5 W g −1 under infrared light. This work can inspire the development of autonomous devices and provide a design strategy for solar engines. Developing an oscillating actuator that can directly convert solar energy into mechanical energy is highly desirable. Here, authors report a solvent-assisted light-driven oscillator by porous film that achieves excellent oscillating actuation performance and can even oscillate by carrying a load under light irradiation.