Sorption of low-level radwaste by Spirulina

The feasibility of using spirulina as adsorbent for the treatment of low-level liquid radwaste is studied. The experimental results indicate that the sorption capacity of spirulina is good for the di- and trivalent metallic ions at pH 3-7, but rather poor for the mono-valent metallic ions and non-metallic ions. Some factors affecting metal ion uptake by spirulina such as the content of detergent, sodium ion in liquid radwaste and the stability of spirulina under gamma irradiation were also investigated.     

Phthalocyanines bearing bulky cycloalkylmethyl substituents on non-peripheral sites

Octasubstituted phthalocyanines bearing bulky (cyclopentyl)methyl- and (cyclohexyl)methyl-substituents in non-peripheral positions are prepared and characterised. The synthesis of the precursor phthalonitriles is achieved through nickel-catalysed cross-coupling employing alkylzinc reagents. In the case of the (cyclopentyl)methyl derivative the formal precursor is 5-hexenyl bromide which yields the cyclised material exclusively on formation of the zinc reagent and subsequent cross-coupling.     

Degradation induced variation of LC transition of poly(n-undecyl isocyanate)

The first-order thermal transitions including side-chain melting, crystal-LC, biphasic chimney-like, and isotropic transitions of poly(n-undecyl isocyanate) (PUDIC) were investigated by varying its thermal history. After annealing at 140 °C for different periods of time, it leads to different degrees of backbiting degradation into n-undecyl isocyanurate trimer which behaves as a solvent for the rest non-degraded/rigid PUDIC to change into a lyotropic LC from thermotropic transition. Based on the degree of degradation, various amounts of trimers are present and the PUDIC demonstrates different types of thermal transitions found in DSC thermograms due to the variation of the non-degraded PUDIC concentration in solvent trimers. Finally, a phase diagram includes all types of crystallines, LC, and isotropic regions can be drawn according to the DSC thermograms.     

Comparisons of <Emphasis Type="Italic">n</Emphasis>th-order kinetic algorithms and kinetic model simulation on HMX by DSC tests

Octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine (HMX) is a typical highly energetic material that has been widely used in national defense industries since the 1940s. The aim of this study was to establish a reaction kinetic model on thermal decomposition properties via differential scanning calorimetry (DSC) by well-known kinetic equations and kinetic model simulation. Furthermore, the aim also was to compare kinetic algorithms for thermal decomposition energy parameters under various conditions. Experimental results highly depended on the reliability of the kinetic concept applied, which is essentially defined by the proper choice of a mathematical model of a reaction. In addition, the correctness of the methods is used for kinetics evaluation.     

Effective Synthesis of N‐Arylformamide from α‐Halo‐N‐arylacetamides

A convenient synthetic method for N‐arylformamide derivatives was successfully developed by reacting α‐iodo‐N‐arylacetamides with formamide. This method was applicable to α‐iodo‐N‐arylacetamide substrates bearing electron‐donating or electron‐withdrawing groups, N‐(benzo[d][1,3]dioxol‐5‐yl)‐2‐iodoacetamide, 2‐iodo‐N‐(pyridin‐2‐yl)acetamide, and 2‐iodo‐N‐(naphthalen‐4‐yl)acetamide to give the corresponding N‐arylformamides in moderate to excellent yields (65–94%). A plausible mechanism was proposed to account for the new transformation.     

Rapid determination of aristolochic acids I and II in herbal products and biological samples by ultra-high-pressure liquid chromatography-tandem mass spectrometry

Aristolochic acids (AAs) are a mixture of structural-related compounds, in which aristolochic acid I (AA I) and aristolochic acid II (AA II) are reported to be correlated with Aristolochic acid nephropathy (AAN). In this work, a rapid and sensitive ultra-high-pressure liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) method was developed to determine AA I and AA II in herbal products and biological fluids. By using gradient elution with a mobile phase composed of a mixture of 10 mM ammonium formate buffer (pH 3.0) and acetonitrile, AAs could be determined within 10 min. Under optimum UHPLC-MS/MS conditions, the limit of detections was 0.14 and 0.26 ng mL⁻¹ for AA I and AA II, respectively. Run-to-run repeatability and intermediate precision of peak area for AA I and AA II were less than 5.74% relative standard deviation (RSD). Accuracy was tested by spiking 10, 100 and 1000 ng mL⁻¹ in rat serum and the recoveries were within 76.5-92.9%. Matrix effects were within 78.8-127.7%. The developed method was successfully applied to determine AA I and AA II in several herbal products and to investigate their pharmacokinetic behavior in female Wister rats. The result shows that the developed UHPLC-MS/MS method is efficient, sensitive, and accurate for the determination of AA I and AA II in herbal products and biological samples.     

Selective extraction of melamine using 11-mercaptoundecanoic acid-capped gold nanoparticles followed by capillary electrophoresis

This study describes the use of 11-mercaptoundecanoic acid-capped gold nanoparticles (MUA-AuNPs) for selective extraction of melamine prior to analysis by capillary electrophoresis with UV detection. The highest degree of melamine-induced aggregation of MUA-AuNPs was found to occur at pH 5.0, indicating that the NP aggregation is mainly because of hydrogen bonding between the carboxylate groups of MUA and the amine groups of melamine. Moreover, the degree of melamine-induced NP aggregation gradually increased when the chain length of the mercaptoalkanoic acid was increased from two to 12 carbon atoms. At pH 5.0, the extraction efficiency of melamine was highly dependent on the concentration of MUA-AuNPs, the concentration of dithiothreitol (DTT), the extraction time between MUA-AuNPs and melamine, and the incubation time between melamine-adsorbed AuNPs and DTT. The separation of the extracted melamine and DTT (releasing agent) was accomplished using a solution of 10 mM phosphate (pH 6.0) containing 1.6% (v/v) poly(diallyldimethylammonium chloride). Under the optimum extraction and separation conditions, the limit of detection at a signal-to-noise ratio of 3 was estimated to be 77 pM for melamine, with linear range of 1-1000 nM. The proposed method was successfully applied to the determination of melamine in tap water and in milk.     

Improvement of <Emphasis Type="Italic">n</Emphasis>-ZnO/<Emphasis Type="Italic">p</Emphasis>-Si photodiodes by embedding of silver nanoparticles

The photo-current of n-ZnO/p-Si heterojunction photodiodes was improved by embedding Ag nanoparticles in the interface (ZnO/nano-P_Ag/p-Si), and the ratio between photo- and dark-current increased by about three orders more than that of a n-ZnO/p-Si specimen. The improvement in the photo-current resulted from the light scattering of embedded Ag nanoparticles. The I–V curve of n-ZnO/p-Si degraded after thermal treatment (A-ZnO/p-Si) because the silicon robbed the oxygen from ZnO to form amorphous silicon dioxide and left an oxygen vacancy. Notably, the properties of ZnO/nano-P_Ag/p-Si were better in the time-dependent photoresponse under 10 V bias. Ag nanoparticles (15–20 nm) scattered the UV light randomly and increased the probability for the absorption of ZnO to enhance the properties of the photodiode.     

Pulsed spark-discharge assisted synthesis of colloidal gold nanoparticles in ethanol

A green method, using pulsed spark-discharge (PSD) to synthesize gold nanoparticles (AuNPs) in ethanol, is studied in this article. Unlike conventional methods for metal nanoparticles synthesis, the PSD method does not require the addition of chemical surfactants and stabilizers. The size of PSD–AuNPs is examined by transmission electron microscopy, with a range 5–50 nm. The chemical compounds, crystal structure, and surface plasmon resonance of PSD–AuNPs are studied using energy dispersive X-ray spectroscopy, X-ray diffraction, and UV–Visible spectroscopy, respectively. Zeta potential analysis shows that a negative charge (−40 mV) on the surface of the PSD–AuNPs may be contributing to the stability of the suspension. During the gold electrodes discharge in the ethanol, under an intensive electric field and thermal energy, bulk metallic gold and ethanol may produce AuNPs and varieties of chemical derivatives, which are also studied by GC/MS and FTIR to investigate the suspension mechanism. The analysis results show that there is an oxidation reaction of ethanol occurring during the PSD process to produce ethanol derivatives, such as acetaldehyde, acetic acid, and ethyl acetate, which may modify the surface of AuNPs by coordination of oxygen atoms. However, only acetic acid can form a negative charge by the deprotonation of the carboxylic group of surface in ethanol, resulting in the creation of a repulsion force between the particles to form the stable colloid system. The experimental results indicate that PSD is an alternative green process to synthesize gold nanoparticles suspension in ethanol. Moreover, with a gold rod consumption rate of 15 mg/L, concentrations of gold nanoparticles ~9 ppm have been observed; therefore, the net production rate is around 60%.     

Spectral narrowing and manipulation in an optical parametric oscillator using periodically poled lithium niobate electro-optic polarization-mode converters

We report a unique spectral narrowing and manipulation technique in an optical parametric oscillator (OPO) realized by an integrated periodically poled lithium niobate comprising an optical parametric gain medium sandwiched by two electro-optic polarization-mode converters (EO PMCs). We achieved a manipulation of the gain spectrum of the OPO via EO and/or temperature control of the EO PMCs, in which we obtained single to multiple signal spectral peaks from the OPO with a spectral width reduced by up to 10 times and peak intensity increased by up to 6 times in comparison with the original signal. Fast EO tuning of the narrowed signal spectral peak has also been demonstrated.