Thick film NO2 Sensor

 Thick film technology was used to manufacture a solid-state electrochemical nitrogen dioxide sensor. The prepared sensor has a linear dependence of electromotive force that is based in the NO₂ concentration level. This paper presents discussion on a thick-film sensor that has a much smaller dimension and shorter response time as compared to typical ceramic solid-state electrochemical devices. Received: 26 February 1996/Accepted: 27 June 1996     

ZnO Nanoplatelets with Controlled Thickness: Atomic Insight into Facet-Specific Bimodal Ligand Binding Using DNP NMR

Colloidal nanoplatelets (NPLs) and nanosheets with controlled thickness have recently emerged as an exciting new class of quantum-sized nanomaterials with substantially distinct optical properties compared to 0D quantum dots. Zn-based NPLs are an attractive heavy-metal-free alternative to the so far most widespread cadmium chalcogenide colloidal 2D semiconductor nanostructures, but their synthesis remains challenging to achieve. The authors describe herein, to the best of their knowledge, the first synthesis of highly stable ZnO NPLs with the atomically precise thickness, which for the smallest NPLs is 3.2 nm (corresponding to 12 ZnO layers). Furthermore, by means of dynamic nuclear polarization-enhanced solid-state ¹⁵N NMR, the original role of the benzamidine ligands in stabilizing the surface of these nanomaterials is revealed, which can bind to both the polar and non-polar ZnO facets, acting either as X- or L-type ligands, respectively. This bimodal stabilization allows obtaining hexagonal NPLs for which the surface energy of the facets is modulated by the presence of the ligands. Thus, in-depth study of the interactions at the organic–inorganic interfaces provides a deeper understanding of the ligand–surface interface and should facilitate the future chemistry of stable-by-design nano-objects.     

Dansameum regulates hepatic lipogenesis and inflammation in vitro and in vivo

Food Science and Biotechnology - Although the clinical guidelines for nonalcoholic fatty liver disease (NAFLD) therapy recommended hepato-protection and exercise to reduce body weight, no...     

Evaluation of a water-resistant and biocompatible adhesive with potential use in bone fractures

The use of osteosynthesis materials when complex fractures are presented is well known. However, the use of these materials has not achieved a correct fixation and reduction of all bone fragments. Therefore, an adhesive for bones would provide a simple and quick method to fix this kind of fractures. The aim of this work is to propose and to evaluate an adhesive based on chitosan hydrogels that could have a potential use as a bone adhesive underwater and will not develop cytotoxic effects. Ionically and covalently crosslinked hydrogels based on chitosan were used in this study. Butt joint test with bovine cancellous bone specimens were used in order to measure the tensile bond strength (TBS) in ideal (completely dry) and physiological (immersed in water at 37 °C) conditions. Additionally, TBS was estimated as a function of time of bone specimens immersed in water at 37 °C. Cell viability was studied using MTT assay and cell morphology on the adhesive surface was examined by scanning electron microscope. Mechanical studies revealed that only covalently crosslinked hydrogels maintain their TBS at physiological condition with respect to the dry environment. In addition, it was observed that the TBS, using only covalently crosslinked hydrogels adhesives, dramatically changes as a function of time and its behavior increases as calcium carbonate and hydroxyapatite is added. Finally, in vitro cell testing of covalently crosslinked hydrogel with calcium carbonate and hydroxyapatite exhibited excellent biocompatibility. Therefore, this formulation is proposed as a potential candidate for clinical use in orthopedic surgery.     

Hydrogen Effects in Metal Catalysts

The interaction of hydrogen with metals is the cause or basis of a host of phenomena ranging from the chemisorption of hydrogen on the surface, its dissolution in the metal, catalytic reactions involving hydrogen as a reactant or as an astoichiometric component, etc., to the formation of metal hydrides. Hydrogen -induced corrosion and hydrogen embrittlement of steel are well known in chemical process industry and metallurgy. Catalytic reactions on metal or metal-oxide catalysts in the presence of hydrogen, often under pressure, are some of the major chemical, petroleum, and petrochemical processes of today, e.g., ammonia, methanol, Fischer-Tropsch, Oxo and other syntheses, hydrogenation of oils and fats, catalytic reforming, hydrode-sulfurization/hydrotreating, hydrocracking, and hydrogenation/ dehydrogenation.     

The synthesis of single phase WC nanoparticles/C composite by solid state reaction involving nitrogen-rich carbonized polyaniline

Single phase tungsten carbide nanoparticles (WC-NPs), (mean particle diameter 5.4 nm), distributed over carbonized polyaniline (C-PANI) nanotubes/nanosheets were synthesized by a solid state reaction between WO₃ and nitrogen-rich carbonized polyaniline at 1000 °C in a reducing atmosphere. The resulting composite was characterized by X-ray diffractometry, electron microscopy, thermogravimetry in oxidizing and reduction atmospheres and elemental analysis. We suggested that the synthesis of WC as a single phase was facilitated by reactive C atoms with dangling bonds, formed upon nitrogen removal.     

An attempt to bridge the pressure and material gap with a disperse model catalyst for low-temperature alkane reforming

Pt black was exposed to n>-hexane/H₂ mixtures between 483 and 663 K followed by O₂ and H₂ treatments at 603 K. XP and UP spectra were measured without exposing the samples to air. 20–30% carbon accumulated after hydrocarbon exposures. O₂ removed most carbon. The surface C content increased after a subsequent contact with H₂, C 1s showing more atomic carbon as opposed to graphite after n-hexane exposure. Anisotropic recrystallization of Pt black favoring (220) and (311) lattice planes occurred under hydrogen-rich conditions. Both findings were attributed to a H₂-induced solid-state rearrangement; H atoms penetrating into the crystal lattice, force subsurface carbon and oxygen atoms to the surface and a concomitant restructuring would occur. Thus another hydrogen effect has been recognized, leading to structures favorable for skeletal reactions of alkanes.     

3-氯-2-硝基苯乙腈的合成研究

由2,6-二氯硝基苯与氰乙酸叔丁酯反应制备了2-氰基-2-(3′-氯-2′-硝基苯基)乙酸叔丁酯(1),在对甲苯磺酸催化作用下,由化合物(1)脱羧制备了3-氯-2-硝基苯乙腈。考查了不同反应时间、反应温度及摩尔比对目标产物产率的影响。较佳的合成条件为:n[2-氰基-2-(3′-氯-2′-硝基苯基)乙酸叔丁酯]∶n(对甲苯磺酸.H2O)=1∶0.075,反应时间2 h,反应温度100°C,产物收率可达89%以上。化合物结构经IR、1H NMR、MS进行了表征。