Preparation of a covalent organic framework-modified silica-gel composite for the effective adsorption of Pd(II), Zr(IV) and Mo(VI) from nitric acid solution.

In this study, a novel covalent organic framework-modified silica-gel composite (Si-COF) was synthesized for the adsorption of palladium [Pd(II)], zirconium [Zr(IV)], and molybdenum [Mo(VI)] from nitric acid solutions and its adsorption behaviors were systemically investigated under the effects of contact time, nitric acid concentration, solution temperature and others. The pseudo-second-order kinetic model governed the adsorption of these metal ions onto the Si-COF composite, and the Langmuir isotherm model well-matched with the experimental data, with maximum adsorption capacities of 0.588, 0.221, and 0.417 mmol/g for Pd(II), Zr(IV) and Mo(VI), respectively. The adsorption of these metal ions was clarified to originate from the interaction with the abundant nitrogenous groups on the Si-COF composite by the X-ray photoelectron spectroscopy (XPS) method.

Development of N,N,N',N'-tetra-2-ethylhexyl-thiodiglycolamide silica-based adsorbent to separate useful metals from simulated high-level liquid waste.

A novel silica-based adsorbent was synthesized by impregnating macroporous silica polymer composite (SiO2-P) particles with a mixture of N,N,N',N'-tetra-2-ethylhexyl-thiodiglycolamide (TEHTDGA) and tri-n-octylamine (TOA). Then, the possibility of separating Pd(II) and other metal ions from simulated high-level liquid waste (HLLW) using the newly synthesized adsorbent (TEHTDGA + TOA)/SiO2-P was evaluated based on various adsorption characteristics obtained via batch-adsorption experiments, such as the HNO3 concentration, contact time, reaction temperature, adsorption isotherm, and chemical stability of the adsorbent. Furthermore, column separation experiments were performed based on the characteristics obtained from the batch-adsorption experiment, and the possibility of simultaneous separation of multiple metal ions was examined. The experimental results revealed that (TEHTDGA + TOA)/SiO2-P performs well in the separation of multiple metal ions from simulated HLLW.

Extraction behavior of a novel functionalized ionic liquid for separation of platinum group metals from aqueous nitric acid solution.

A novel ionic liquid (IL) functionalized with thiodiglycol amic acid containing a soft S donor was synthesized for the effective and efficient extraction of platinum group metals (Ru, Rh, and Pd) from aqueous nitric acid solutions, such as high-level radioactive liquid waste (HLLW). The IL enabled rapid extraction of Pd(II) with an extraction ratio of approximately 100%. The extractions of Ru(III) and Rh(III) by the IL were slower than that of Pd(II), but the rates were accelerated by temperature elevation. The extractions of Ru(III) and Rh(III) at 50 °C reached equilibrium within 4 and 8 h, respectively, with the extraction ratios of over 90% without assisting agents or other methods for the extraction system. Furthermore, the IL could extract more than 90% of Ru(III), Rh(III), and Pd(II) from the simulated HLLW within 2 h at 50 °C.

A new system for the analysis of thermal judgments: multipoint measurements of skin temperatures and temperature-related sensations and their joint visualization.

We report a new system for monitoring sensations of many body parts as well as comprehensively showing the distribution of overall skin temperature (T(sk)) and temperature-related sensations. The system consists of a console with 52 levers to report temperature-related sensations and software that facilitates the visualization of the distribution of T(sk) and temperature-related sensations by displaying them on a model of the human body. The system's utility was demonstrated with a physiological experiment involving three males and three females. They were exposed to step changes of ambient temperature from 23 degrees C to 33 degrees C. We measured T(sk) at 50 points, and the subjects concurrently provided estimates of local temperature sensation and thermal comfort/discomfort at 25 loci. This system greatly facilitates the perception and analysis of spatial relationships and differences in temperature and sensation in various areas of the body.

Formation of PCDDs and PCDFs during the combustion of polyvinylidene chloride and other polymers in the presence of HCl.

PVDC and three non-chlorinated polymers (PP, PET, and PA) were incinerated at 700-850 degrees C in a laboratory-scale quartz tubular furnace in the presence of HCl (ca. 500 ppm congruent with 0.8 mg/l), and the gas-phase formation of PCDD/Fs, their putative precursors and their homologue profiles were investigated. The addition of HCl had little or no apparent effect on the level of PCDD/Fs formation during PVDC combustion, and their homologue profiles were quite different from those of the three non-chlorinated polymers. With PVDC, O8CDD and particularly O8CDF were by far most prevalent, apparently as a result of the selective formation of the precursors. With each of the three non-chlorinated polymers, combustion at 800 degrees C or higher in the presence of HCl resulted in PCDD/Fs formation at levels equaling or exceeding those observed with PVDC. In trials made with one of them (PP) under the same conditions but using a large polymer sample (100 mg vs 20 mg in all other trials), the level of PCDD/Fs formation was far higher than with the smaller polymer samples, and thus demonstrated the importance of appropriate combustion conditions for polymer incineration.