Suzuki–Miyaura coupling reaction in water in the presence of robust palladium immobilized on modified magnetic Fe3O4 nanoparticles as a recoverable catalyst

Aryl halides and especially inactive aryl chlorides were coupled to benzenoid aromatic rings in a Suzuki–Miyaura coupling reaction in the absence of organic solvents and toxic phosphine ligands. The reaction was catalysed by a recoverable magnetic nanocatalyst, Pd@Fe₃O₄, in aqueous media. This method is green, and the catalyst is easily removed from the reaction media using an external magnetic field and can be re‐used at least 10 times without any considerable loss in its activity. The catalyst was characterized using scanning and transmission electron microscopies, thermogravimetric analysis, inductively coupled plasma spectroscopy, Fourier transform infrared spectroscopy, CHN analysis, X‐ray diffraction and vibrating sample magnetometry.     

A mass‐conservative staggered immersed boundary model for solving the shallow water equations on complex geometries

In this work, an approach is proposed for solving the 3D shallow water equations with embedded boundaries that are not aligned with the underlying horizontal Cartesian grid. A hybrid cut‐cell/ghost‐cell method is used together with a direction‐splitting implicit solver: Ghost cells are used for the momentum equations in order to prescribe the correct boundary condition at the immersed boundary, while cut cells are used in the continuity equation in order to conserve mass. The resulting scheme is robust, does not suffer any time step limitation for small cut cells, and conserves fluid mass up to machine precision. Moreover, the solver displays a second‐order spatial accuracy, both globally and locally. Comparisons with analytical solutions and reference numerical solutions on curvilinear grids confirm the quality of the method. Copyright © 2015 John Wiley & Sons, Ltd.     

Membrane-based microchannel device for continuous quantitative extraction of dissolved free sulfide from water and from oil

Underground fluids are important natural sources of drinking water, geothermal energy, and oil-based fuels. To facilitate the surveying of such underground fluids, a novel microchannel extraction device was investigated for in-line continuous analysis and flow injection analysis of sulfide levels in water and in oil. Of the four designs investigated, the honeycomb-patterned microchannel extraction (HMCE) device was found to offer the most effective liquid–liquid extraction. In the HMCE device, a thin silicone membrane was sandwiched between two polydimethylsiloxane plates in which honeycomb-patterned microchannels had been fabricated. The identical patterns on the two plates were accurately aligned. The extracted sulfide was detected by quenching monitoring of fluorescein mercuric acetate (FMA). The sulfide extraction efficiencies from water and oil samples of the HMCE device and of three other designs (two annular and one rectangular channel) were examined theoretically and experimentally. The best performance was obtained with the HMCE device because of its thin sample layer (small diffusion distance) and large interface area. Quantitative extraction from both water and oil could be obtained using the HMCE device. The estimated limit of detection for continuous monitoring was 0.05 μM, and sulfide concentrations in the range of 0.15–10 μM could be determined when the acceptor was 5 μM FMA alkaline solution. The method was applied to natural water analysis using flow injection mode, and the data agreed with those obtained using headspace gas chromatography-flame photometric detection. The analysis of hydrogen sulfide levels in prepared oil samples was also performed. The proposed device is expected to be used for real time survey of oil wells and groundwater wells.     

Die Untersuchung einer Laboratoriumsanlage nach dem Heiß-Kalt-System mit einfachem Durchfluß der Fluide

Es wird ein Heiβ-Kalt-System mit einfachem Durchfluβ der Fluide untersucht. Dabei wird gezeigt, daβ zwischen den Isotopenkonzentrationen des Gases und der Flüssigkeit lineare Beziehungen bestehen. Eine Möglichkeit zur experimentellen Bestimmung der realen Werte der Parameter der Kolonne wird angegeben.     

Pd‐initiated polymerization of diazo compounds bearing dialkoxyphosphinyl group and hydrolysis of the resulting polymers and oligomers to afford phosphonic acid‐containing products

Pd‐initiated polymerization and oligomerization of diazo compounds containing a dialkoxyphosphinyl group are described. Polymerization of 2‐dialkoxyphosphinylethyl diazoacetates with π‐allylPdCl‐based initiating systems afforded C? C main chain polymers bearing phosphonate on each main chain carbon atom. The quantitative transformation of the side chain phosphonate to phosphonic acid resulted in the formation of water soluble polymers having the acid groups accumulated around their main chains, although the carbonyl ester linkage in the side chain was cleaved via intramolecular acid‐assisted hydrolysis in water at 80 °C. Pd‐initiated oligomerization of diethyl diazomethylphosphonate yielded an oligomeric product bearing diethoxyphosphiny groups directly attached to its main chain carbons, with unexpected incorporation of azo group in the main chain framework. Hydrolysis of the phosphonate of the oligomer afforded a water‐soluble product, which was revealed to show higher proton conductivity than poly(vinylphosphonic acid) under certain conditions. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54, 1742–1751     

Highly efficient water‐soluble visible light photoinitiators

The monoacylphosphineoxide (MAPO) salts Na‐TPO and Li‐TPO and the bisacylphosphineoxide (BAPO) salts BAPO‐ONa and BAPO‐OLi define an important and in the latter case a new class of water‐soluble photoinitiators (PIs) for radical polymerization. These compounds showed excellent water‐solubility of at least 29 g/L for Na‐TPO and up to 60 g/L for BAPO‐ONa in deionized water, thus exceeding the solubility of the state of the art PI for water‐based systems Irgacure 2959 ( I2959 ) 6‐ to 12‐fold. However, biocompatibility, storage stability, and reactivity were equally important to replace the state of the art compounds. Concerning these properties, the MAPO and BAPO salts were at least in the same range (biocompatibility, stability) or showed even better results (reactivity) and had the additional advantage of visible light initiation. Na‐TPO and Li‐TPO achieved double bond conversions of an aqueous solution of N‐acryloylmorpholine over 97% with broad band irradiation (320–500 nm), Li‐TPO showed additionally very good biocompatibility (LC₅₀ = 3.1 mmol/L) and BAPO‐OLi showed highest reactivity with visible light irradiation. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54, 473–479     

Determination of As(III) using developed dispersive liquid–liquid microextraction and flame atomic absorption spectrometry

The method relies on selective complexation of As(III) with a suitable chelating agent followed by dispersive liquid–liquid microextraction (DLLME) method. Flame atomic absorption spectrometry (FAAS) equipped with microsample introduction system was utilised for determination of As(III). 1-Undecanol and acetone were used as extraction solvent and disperser solvent respectively. Some effective parameters on complex formation and extraction have been optimised. Under the optimum conditions, the enrichment factor of 108 for As(III) was obtained from 9.8?mL of water samples. The calibration graph was linear in the range of 2–15?µg?L^?1 with detection limits of 0.60?µg?L^?1 for As(III). The relative standard deviation (R.S.D.) for ten replicate measurements of 5.00?µ?gL^?1 of As(III) was 6.2%. Operation simplicity and high enrichment factors are the main advantages of DLLME for the determination of As(III) without necessity for hydride generation in water samples.     

Determination of Malathion Using Corona Discharge – Ion Mobility Spectrometry with Solid-Phase Microextraction

A corona discharge (CD) ion mobility spectrometer combined with solid-phase microextraction was constructed. The detection limit and stability of the system for malathion detection were improved using a novel sample introduction port through which the sample desorption was performed in high-temperature drift tube and the sample was introduced directly to the ionization area. The working parameters of the distance between CD needle tip and carrier gas outlet, the drift tube and carrier gas temperature, the carrier gas flow, and the voltage on CD needle were selected. When the extraction time for standard malathion was set to 5?min, the detection limit was 0.96?µg?L^?1 based on thrice the baseline noise, the linear range was 50–500?µg?L^?1, the correlation coefficient was approximately 0.9941, and the relative standard deviation was below 10%. Malathion-spiked lake water samples were analyzed using the developed system and the recovery was 92–102%. This method is suitable for the rapid detection of organophosphorus pesticide residues.     

正丁醇/水混合溶剂中一步合成NO3-LDH的研究

以尿素为沉淀剂，正丁醇/水混合液为溶剂，采用水热法直接合成层状双金属氢氧化物ZnAl-NO₃-LDHs。通过X射线衍射（XRD）、傅里叶变换红外光谱（FT-IR）、扫描电镜（SEM）和元素分析（CHN）等对所得样品进行表征，证明在尿素存在条件下，NO₃^-进入LDHs层间；XRD、SEM结果和丁达尔现象显示所得NO₃-LDHs可在甲酰胺溶液中剥离。对尿素存在条件下形成NO₃-LDH而非CO₃-LDH的机理进行了探讨。以氯化盐和硫酸盐为原料，采用本文方法成功合成了Cl-LDH和SO₄-LDH，此研究结果可为制备不同阴离子插层的LDHs提供一种简单直接的方法。