Hybrid MIL-101(Cr)@MIL-53(Al) composite for carbon dioxide capture from biogas

In this study, hybrids of nanoporous MIL-101(Cr) and MIL-53(Al) were synthesized using a hydrothermal method for various time periods, ranging from 8 to 40 h. The prepared materials were characterized by powder X-ray diffraction (PXRD) and elemental analysis, and their specific surface areas were measured by N₂ sorption at 77 K using the Brunauer–Emmett–Teller (BET) method. To investigate the practical application of these materials, the pure carbon dioxide and methane adsorption capacities of the samples were determined using the volumetric method. The Langmuir model was used to fit the CO₂ and CH₄ isotherms. Extended Langmuir (EL) equations and the ideal adsorbed solution theory (IAST) models were used to obtain the CO₂/CH₄ selectivity. The sample with the highest BET specific surface area was selected as a candidate for further investigations. The thermal stability of the selected sample was investigated by thermogravimetric analysis (TGA). Scanning electron microscopy (SEM) was used to characterize the sample morphology. XRD results showed that the sample synthesized over the shortest time corresponded to MIL-101(Cr), while the sample synthesized over the longest time was in agreement with MIL-53(Al). Samples synthesized for time periods between these two limits were assumed to be composites of both MIL-53(Al) and MIL-101(Cr). TGA results indicated that the hybrid materials were thermally stable at temperatures about 100 °C higher than for pure MIL-101(Cr). The BET specific surface area (1746 m² g⁻¹) and CO₂ adsorption capacity (16 mmol g⁻¹) of the selected hybrid sample were about 50% and 35% higher, respectively, compared with those of pure MIL-53(Al), but 30% and 20% lower, respectively, compared with those of pure MIL-101(Cr). Binary adsorption modeling showed the high selectivity of the MIL-101(Cr) and MIL-53(Al) hybrid material for CO₂ with a minimum separation factor of about 60 at 298 K. This value was much higher than those reported previously and those observed in this work for the original MIL-101(Cr) or MIL-53(Al). These results demonstrated that the hybrid of MIL-101(Cr) and MIL-53(Al) was a promising material for selective CO₂ capture from natural and biogas.

In this study, hybrids of nanoporous MIL-101(Cr) and MIL-53(Al) were synthesized using a hydrothermal method for various time periods, ranging from 8 to 40 h.     

三种核酸染料应用于细菌脉冲场凝胶电泳染色的比较研究

目的 比较Gelred、GoldView及溴化乙锭(EB)三种染料在病原菌脉冲场凝胶电泳(PFGE)中的染色效果,选择更为安全和灵敏的核酸染料,并形成标准化操作应用于病原菌分子分型监测网络PulseNet China。 方法 选择霍乱弧菌作为评价菌株,按照病原菌分子分型监测网络(PulseNet)的PFGE标准操作方案进行电泳,采用Gelred、GoldView及EB三种染料分别染色,分析比较实验结果。 结果 Gelred染色的胶块清晰度最好,EB次之,均高于GoldView; Gelred染色的图谱,相邻条带边缘清晰,更容易辨别区分。EB和GoldView染色后必须脱色,使用Gelred染色脱色时间较短,亦可以不经过脱色步骤,但脱色后的电泳条带边缘更加锐利。 结论 Gelred是一种更安全、更灵敏的核酸染料,可以取代EB应用于PFGE。制定了使用Gelred进行PFGE染胶的标准方案,用于PulseNet China网络的PFGE分析。     

Bimetallic Au–Pd alloy nanoparticles supported on MIL-101(Cr) as highly efficient catalysts for selective hydrogenation of 1,3-butadiene

Gold–palladium (Au–Pd) bimetallic nanoparticle (NP) catalysts supported on MIL-101(Cr) with Au : Pd mole ratios ranging from 1 : 3 to 3 : 1 were prepared through coimpregnation and H₂ reduction. Au–Pd NPs were homogeneously distributed on the MIL-101(Cr) with mean particle sizes of 5.6 nm. EDS and XPS analyses showed that bimetallic Au–Pd alloys were formed in the Au(2)Pd(1)/MIL-101(Cr). The catalytic performance of the catalysts was explored in the selective 1,3-butadiene hydrogenation at 30–80 °C on a continuous fixed bed flow quartz reactor. The bimetallic Au–Pd alloy particles stabilized by MIL-101(Cr) presented improved catalytic performance. The as-synthesized bimetallic Au(2)Pd(1)/MIL-101(Cr) with 2 : 1 Au : Pd mole ratio showed the best balance between the activity and butene selectivity in the selective 1,3-butadiene hydrogenation. The Au–Pd bimetallic-supported catalysts can be reused in at least three runs. The work affords a reference on the utilization of a MOF and alloy nanoparticles to develop high-efficiency catalysts.

Bimetallic Au–Pd alloy particles stabilized by MIL-101(Cr) showed high activity and butene selectivity for 1,3-butadiene hydrogenation reaction.     

Adsorption characteristics of metal–organic framework MIL-101(Cr) towards sulfamethoxazole and its persulfate oxidation regeneration

A metal–organic framework, MIL-101(Cr), was used to adsorb sulfamethoxazole (SMZ) in water and activated persulfate (PS) oxidation was investigated to regenerate SMZ-saturated MIL-101(Cr). Adsorption and oxidation were combined in this study. MIL-101(Cr) was characterized by SEM, BET, XPS and FT-IR analyses. Effects of various operating parameters on adsorption efficiency were studied. The dosages of persulfate for SMZ desorption and oxidation were investigated. The results showed that the recommended pH was 6–8 for SMZ adsorption and optimum MIL-101(Cr) dosage was 0.1 g L⁻¹. SMZ adsorption by MIL-101(Cr) was a spontaneous process and nearly exothermic. Saturation adsorption capacity was achieved in 180 s and the adsorption followed the pseudo-second-order model. The maximum adsorption amount of MIL-101(Cr) to SMZ was 181.82 mg g⁻¹ (Langmuir). MIL-101(Cr) also showed good adsorption capacities for sulfachloropyridazine (SCP), sulfamonomethoxine (SMM), and sulfadimethoxine (SDM). Persulfate was helpful for SMZ desorption from the surface of saturated MIL-101(Cr) and sufficient persulfate could simultaneously oxidize the SMZ. XPS analysis showed that the structure of MIL-101(Cr) was stable after the persulfate oxidation process. Regenerated MIL-101(Cr) had the same level of adsorption capacity as fresh MIL-101(Cr). An adsorption–oxidation combined process may be set up based on the results. This study provides basic data for the deep treatment of organic micropollutants in urban water bodies.

A metal–organic framework, MIL-101(Cr), was used to adsorb sulfamethoxazole (SMZ) in water and activated persulfate (PS) oxidation was investigated to regenerate SMZ-saturated MIL-101(Cr).     

Nanoporous MIL-101(Cr) as a sensing layer coated on a quartz crystal microbalance (QCM) nanosensor to detect volatile organic compounds (VOCs)

The application of metal–organic frameworks (MOFs) as a sensing layer has been attracting great interest over the last decade, due to their high porosity and tunability, which provides a large surface area and active sites for trapping or binding target molecules. MIL-101(Cr) is selected as a good candidate from the MOFs family to fabricate a quartz crystal microbalance (QCM) nanosensor for the detection of volatile organic compound (VOC) vapors. The structural and chemical properties of synthesized MIL-101(Cr) are investigated by X-ray diffraction (XRD), Fourier-transfer infrared spectroscopy (FTIR) and scanning electron microscopy (SEM) and so on. A stable and uniform layer of MOF is coated onto the surface of a QCM sensor by the drop casting method. The frequency of the QCM crystal is changed during exposure to different concentrations of target gas molecules. Here, the sensor response to some VOCs with different functional groups and polarities, such as methanol, ethanol, isopropanol, n-hexane, acetone, dichloromethane, chloroform, tetrahydrofuran (THF), and pyridine under N₂ atmosphere at ambient conditions is studied. Sensing properties such as sensitivity, reversibility, stability, response time, recovery time, and limit of detection (LOD) of the sensor are investigated. The best sensor response is observed for pyridine detection with sensitivity of 2.793 Hz ppm⁻¹. The sensor shows short response/recovery time (less than two minutes), complete reversibility and repeatability which are attributed to the physisorption of the gases into the MOF pores and high stability of the device.

Metal–organic frameworks can be used as sensing layer in QCM fabrication because of their huge surface area.     

MIL-101(Cr)–cobalt ferrite magnetic nanocomposite: synthesis,characterization and applications for the sonocatalytic degradation of organic dye pollutants

In this study, for the first time, a novel magnetically recyclable MIL-101(Cr)/CoFe₂O₄ nanocomposite was prepared via a facile solvothermal method. The morphology, structural, magnetic and optical properties of the nanocomposite were characterized via field emission scanning electron microscopy (FE-SEM), transmission electron microscope (TEM), energy dispersive X-ray (EDX) spectroscopy, X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), vibrating sample magnetometer (VSM), UV-visible spectroscopy (UV-visible) and BET surface area analysis. Furthermore, the sonocatalytic activity of the MIL-101(Cr)-based magnetic nanocomposite was explored for the degradation of organic dye pollutants such as Rhodamine B (RhB) and methyl orange (MO) under ultrasound irradiation in the presence of H₂O₂. Under optimized conditions, the degradation efficiency reached 96% for RhB and 88% for MO. The sonocatalytic activity of MIL-101(Cr)/CoFe₂O₄ was almost 12 and 4 times higher than that of the raw MIL-101(Cr) and pure CoFe₂O₄, respectively. The improved sonocatalytic performance of the as-prepared binary nanocomposite can be attributed to the relatively high specific surface area of MIL-101(Cr) and magnetic property of CoFe₂O₄, as well as the fast generation and separation of charge carriers (electrons and holes) in MIL-101(Cr) and CoFe₂O₄. In addition, the trapping tests demonstrated that ·OH radicals are the main active species in the dye degradation process. Moreover, the most influencing factors on the sonocatalytic activity such as the H₂O₂ amount, initial dye concentration and catalyst dosage were investigated. Finally, the nanocomposite was magnetically separated and reused without any observable change in its structure and performance even after four consecutive runs.

A magnetically separable MIL-101(Cr)/CoFe₂O₄ binary nanocomposite was prepared via a hydrothermal route and applied as a sonocatalyst for the efficient degradation of organic dyes.     

Synthesis of some new distyrylbenzene derivatives using immobilized Pd on an NHC-functionalized MIL-101(Cr) catalyst: photophysical property evaluation,DFT and TD-DFT calculations

In this study the catalytic application of a heterogeneous Pd-catalyst system based on metal organic framework [Pd–NHC–MIL-101(Cr)] was investigated in the synthesis of distyrylbenzene derivatives using the Heck reaction. The Pd–NHC–MIL-101(Cr) catalyst showed high efficiency in the synthesis of these π-conjugated materials and products were obtained in high yields with low Pd-contamination based on ICP analysis. The photophysical behaviors for some of the synthesized distyrylbenzene derivatives were evaluated. The DFT and TD-DFT methods were employed to determine the optimized molecular geometry, band gap energy, and the electronic absorption and emission wavelengths of the new synthesized donor–π–acceptor (D–π–A) molecules in the gas phase and in various solvents using the chemical model B3LYP/6-31+G(d,p) level of theory.

The Pd–NHC–MIL-101(Cr) catalyst was found to be an efficient heterogeneous catalyst in the synthesis of DSB and stilbene π-conjugated materials using Heck chemistry.     

Activation of persulfates by ferrocene–MIL-101(Fe) heterogeneous catalyst for degradation of bisphenol A

In this study, a novel and high-performance catalyst was prepared and used as the heterogeneous catalyst to activate persulfate for bisphenol A (BPA) degradation. Ferrocene was anchored to NH₂-MIL-101(Fe) post-synthetically by the condensation of amine group from NH₂-MIL-101(Fe) with the carbonyl group of ferrocenecarboxaldehyde. The synthesized ferrocene tethered MIL-101(Fe)–ferrocene was characterized by scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction, X-ray photo-electron spectra, cyclic voltammetry and electrochemical impedance spectroscopy. The ferrocene acts as a redox mediator, which makes the ferrocene functionalized NH₂-MIL-101(Fe) highly active in the degradation of BPA by accelerating the rate of the charge-transfer processes in aqueous solution. MIL-101(Fe)–Fc was proved to be the most effective catalyst, removing more than 99.9% of BPA. In addition, the catalyst can be reused without significant loss in activity.

In this study, a novel and high-performance catalyst ferrocene-MIL-101(Fe) was prepared and used as the heterogeneous catalyst to activate persulfate for bisphenol A degradation.     

Sulfonic acid-functionalized PCP(Cr) catalysts with Cr3+ and –SO3H sites for 5-ethoxymethylfurfural production from glucose

5-Ethoxymethylfurfural (EMF) has been identified as a potential biofuel and fuel additive, for which the production from glucose (the most abundant and inexpensive monosaccharide) in a one-step process would be highly desirable. Here, the synthesis of sulfonic acid-functionalized porous coordination polymers (PCPs) and their application as catalysts for EMF synthesis are reported. PCP(Cr)-BA (PCP material with Cr³⁺ ions and H₂BDC-SO₃H linkers) and PCP(Cr)-NA (PCP material with Cr³⁺ ions and H₂NDC(SO₃H)₂ linkers) materials containing both Cr³⁺ sites and Brønsted-acidic –SO₃H sites were prepared. The morphology, pore structure, acidity, chemical composition, and thermal stability of the two functionalized PCP(Cr) catalysts were analyzed by systematic characterization. The catalysts featured a porous morphology and dual Cr³⁺ and –SO₃H sites, which enabled the cascade conversion of glucose to EMF. PCP(Cr)-BA exhibited higher performance than PCP(Cr)-NA with an EMF yield of 23.1% in the conversion of glucose at 140 °C after 22 h in an ethanol/water system. In addition, the as-prepared catalyst exhibited a high stability in the current catalytic system for EMF production from glucose with a constant catalytic activity in a four-run recycling test without an intermediate regeneration step.

The PCP(Cr)-BA catalysts featured porous morphology and dual Cr³⁺ and –SO₃H sites, which enabled the cascade conversion of glucose to EMF. In addition, the as-prepared catalyst exhibited a high stability in the current catalytic system.     

K6P2W18O62 encapsulated into magnetic Fe3O4/MIL-101 (Cr) metal–organic framework: a novel magnetically recoverable nanoporous adsorbent for ultrafast treatment of aqueous organic pollutants solutions

In this study, a Wells–Dawson type K₆P₂W₁₈O₆₂ polyoxometalate was encapsulated into the magnetic Fe₃O₄/MIL-101 (Cr) metal–organic framework and applied as a new magnetically recoverable ternary adsorbent to remove organic dyes from aqueous solutions. The as-prepared ternary magnetically recyclable hybrid (denoted as P₂W₁₈O₆₂@Fe₃O₄/MIL-101 (Cr)) was characterized by FT-IR spectroscopy, powder X-ray diffraction (XRD), Raman spectroscopy, EDX, SEM, BET surface area, and magnetic measurements. The results showed the successful encapsulation of K₆P₂W₁₈O₆₂ (∼26.5 wt%) into the magnetic Fe₃O₄/MIL-101 (Cr) framework. The magnetic hybrid had a high specific surface area of 934.89 m² g⁻¹. The adsorption efficiency of this nanohybrid for the removal of methylene blue (MB), rhodamine B (RhB), and methyl orange (MO) from aqueous solutions was evaluated. The magnetic nanohybrid demonstrated the fast and selective adsorption of cationic dyes from mixed dye solutions. The adsorption rate and capacity of P₂W₁₈O₆₂@Fe₃O₄/MIL-101 (Cr) were increased as compared with MIL-101 (Cr), P₂W₁₈O₆₂, and Fe₃O₄/MIL-101 samples due to the increased electrostatic attraction. The effects of parameters such as the adsorbent dosage, temperature, dye concentration, and pH were investigated on the adsorption process. The adsorption kinetics was analyzed by the Freundlich, Langmuir, and Temkin isotherm models and pseudo-second-order and pseudo-first-order kinetics models, with the Langmuir isotherm and pseudo-second-order kinetic model found to be suitable to describe the equilibrium data. Also, the thermodynamic results of the nanohybrid indicated that the adsorption was an endothermic and spontaneous process. After the adsorption reaction, the magnetic nanohybrid could be easily separated and reused without any change in structure. Based on the results of this study, the nanohybrid was an efficient adsorbent for eliminating cationic dyes.

A Wells–Dawson-type K₆P₂W₁₈O₆₂ polyoxometalate was encapsulated into the magnetic Fe₃O₄/MIL-101 (Cr) metal–organic framework and applied as a new magnetically recoverable ternary adsorbent to remove organic dyes from aqueous solutions.     

Fabrication of UiO-66/MIL-101(Fe) binary MOF/carboxylated-GO composite for adsorptive removal of methylene blue dye from aqueous solutions

This study provides a novel composite as an efficient adsorbent of cationic methylene blue dye. UiO-66/MIL-101(Fe) binary metal organic framework (MOF) was fabricated using a solvothermal technique. Additionally, the developed binary MOF was modified with carboxylated graphene oxide (GOCOOH) using a post-synthetic technique. The as-fabricated UiO-66/MIL-101(Fe)-GOCOOH composite was analyzed by FTIR, XRD, SEM, BET, TGA, XPS and zeta potential analysis. The adsorption performance of UiO-66/MIL-101(Fe)-GOCOOH composite was examined for its aptitude to adsorb cationic MB dye using a batch technique. The obtained data revealed that, the developed UiO-66/MIL-101(Fe)-GOCOOH composite exhibited higher adsorption capacity compared to UiO-66/MIL-101(Fe) binary MOF. Adsorption isotherms and kinetic studies revealed that MB dye adsorption onto UiO-66/MIL-101(Fe)-GOCOOH composite fitted a Langmuir isotherm model (q_m = 448.71 mg g⁻¹) and both pseudo 1^st order and pseudo 2^nd order kinetic models. An intra-particle diffusion model showed that the adsorption process occurs through three steps. Besides, thermodynamic data reflected that the adsorption of MB onto UiO-66/MIL-101(Fe)-GOCOOH composite is an endothermic and spontaneous process and the adsorption involves both physisorption and chemisorption interactions. The as-fabricated UiO-66/MIL-101(Fe)-GOCOOH composite exhibited good reusability and can be considered as a promising reusable adsorbent for the treatment of dye-containing industrial effluents with high efficiency.

This study provides a novel composite as an efficient adsorbent of cationic methylene blue dye.     

Hexamethylenetetramine-based ionic liquid/MIL-101(Cr) metal–organic framework composite: a novel and versatile tool for the preparation of pyrido[2,3-d:5,6-d′]dipyrimidines

In the current paper, a hexamethylenetetramine-based ionic liquid immobilized on the MIL-101(Cr) metal–organic framework was successfully synthesized as a novel, efficient, and recoverable catalyst for the synthesis of pyrido[2,3-d:5,6-d′]dipyrimidine derivatives via the reaction of barbituric acid derivatives, 6-aminouracil/6-amino-1,3-dimethyl uracil, and aromatic aldehydes under solvent-free conditions. Characterization of the catalyst was carried out using various methods such as field emission scanning electron microscopy (FE-SEM), energy-dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD), thermogravimetric analysis (TGA), Fourier transform infrared spectrophotometry (FT-IR), and Brunauer–Emmett–Teller (BET). Efficient transformation, short reaction times, excellent yields, easy product isolation, mild conditions, and the potential high recyclability of the organocatalyst are the main features of this protocol.

In this study, HMTA-BAIL@MIL-101(Cr) was prepared as a novel catalyst for the synthesis of dipyrimidine derivtives by the reaction of barbituric acids, 6-aminouracil/6-amino-1,3-dimethyl uracil, and arylaldehydes under solvent-free conditions.     

TiO2 nanocrystals with the {001} and {101} facets co-exposed with MIL-100(Fe): an egg-like composite nanomaterial for efficient visible light-driven photocatalysis

The exposure of a specific crystal face to a specific composition or a suitable carrier composition with synergistic effects can effectively improve the photocatalytic activity of the material and enhance its practical value. For choosing an ideal carrier, the primary factor is a large specific surface area. Herein, by using MIL-100(Fe) as the carrier, an egg-like TiO₂/MIL-100(Fe) composite was successfully prepared, for the first time, via a facile two-pot hydrothermal method. XRD, SEM, TEM and other characterization methods showed that when the molar ratio of Ti : Fe was 0.3 : 1, the morphology of the TiO₂/MIL-100(Fe) composite was completely egg-like. The TEM results showed that the {001} and {101} facets of TiO₂ in the TiO₂/MIL-100(Fe) composite were co-exposed. The BET results showed that the TiO₂/MIL-100(Fe) composite had a large specific surface area and pore size. The larger pore size provided an effective channel for the photocatalytic degradation of MB and the interfacial effect of TiO₂ and MIL-100(Fe). The separation efficiency of the photogenerated electron–hole pairs was effectively improved. The efficiency of 30% TiO₂/MIL-100(Fe) in the photocatalytic degradation of MB reached 99.02% in 30 min under visible light. All these findings showed that the composite of the effectively charge-separated photocatalytic semiconductor and the porous MOF with a high specific surface area had a high potential application value for the photocatalytic degradation of organic pollutants.

The exposure of a specific crystal face to a specific composition and the search for a suitable carrier composition with synergistic effects can effectively improve the photocatalytic activity of the material and enhance its practical value.     

Glucocorticoids enhance acid activation of the Na+/H+ exchanger 3 (NHE3)

In the absence of exogenous glucocorticoids, decreasing media pH (from 7.4 to 6.8) for 24 hours increased the Na⁺/H⁺ exchanger 3 (NHE3) activity in opossum kidney (OKP) cells. 10^–7 M and 10^–8 M hydrocortisone increased NHE3 activity, and in their presence, acid incubation further increased NHE3 activity. Hydrocortisone (10^–9 M) had no effect on NHE3 activity, but in its presence, the effect of acid incubation on NHE3 activity increased twofold. Aldosterone (10^–8 M) had no effect. In the absence of hydrocortisone, acid incubation increased NHE3 protein abundance by 47%; in the presence of 10^–9 M hydrocortisone, acid incubation increased NHE3 protein abundance by 132%. The increase in NHE3 protein abundance was dependent on protein synthesis. However, 10^–9 M hydrocortisone did not modify the effect of acid incubation to cause a twofold increase in NHE3 mRNA abundance. In the absence of protein synthesis, 10^–9 M hydrocortisone did potentiate an effect of acid on NHE3 activity, which was due to trafficking of NHE3 to the apical membrane. These results suggest that glucocorticoids and acid interact synergistically at the level of NHE3 translation and trafficking.     

Controlling crystal growth of MIL-100(Fe) on Ag nanowire surface for optimizing catalytic performance

Ag/MIL-100(Fe) core/sheath nanowire with controllable thickness of the MIL-100(Fe) sheath was prepared by controlling the crystal growth of MIL-100(Fe) on the Ag nanowire surface. The evolution of the MIL-100(Fe) sheath monitored by transmission electron microscopy (TEM), scanning electron microscopy (SEM), powder X-ray diffraction (XRD), thermogravimetric analyses (TGA), X-ray photoelectron spectroscopy (XPS), fourier transform infrared spectroscopy (FT-IR), and N₂ adsorption–desorption analysis indicates that the thickness of the MIL-100(Fe) sheath increases with the increasing number of crystal growth cycles of MIL-100(Fe) on the Ag nanowire surface. Catalytic reaction over Ag/MIL-100(Fe) core/sheath nanowire suggests that the thickness of the MIL-100(Fe) sheath largely influences the catalytic performance and it is quite important to control the crystal growth of MIL-100(Fe) on the Ag nanowire surface for optimizing catalytic performance.

Ag/MIL-100(Fe) core/sheath nanowire with controlled crystal growth of MIL-100(Fe) on the Ag nanowire surface was prepared for optimizing catalytic performance.     

Efficacy of 3 types of foraging enrichment for rhesus macaques (Macaca mulatta)

Primate facilities provide environmental enrichment to improve animal wellbeing, increase opportunities for expression of species-typical behaviors, and decrease the occurrence of stereotypic behaviors. The current study assessed the efficacy of 3 types of foraging enrichment: puzzle balls, supertubes, and shakers. We assigned 48 rhesus macaques to 3 experimental groups, each of which received (after a 3-wk baseline observation period) 1 of the 3 enrichment devices intermittently for 3 wk. Observations were collected during 10-min sessions by using 1-0 sampling with 15-s intervals (480 h total). Observations were collected at the same 10 specified time points each week during the baseline period and after enrichment. Data were analyzed by using generalized linear mixed-effects modeling under the assumption that the underlying response followed a Poisson distribution. Foraging behavior increased significantly in all 3 groups and remained increased in some groups when enrichment was removed after 43 h. The 3 enrichment devices had different effects on individual expression of stereotypy: supertubes decreased it, shakers increased it, and puzzle balls led to a decrease followed by an increase. We present potential reasons for the changes in stereotypy and postulate a likely balance between the beneficial and negative effects of enrichment in any given environment.     

Lipoprotein (a) and lipid profile in neonates from mothers with three different types of diabetes mellitus

OBJECTIVES: The metabolic components in neonates may be affected by maternal diabetes mellitus. DESIGN AND METHODS: To investigate the alterations in lipid metabolism and the possible atherogenic risk, the lipoprotein a (Lp a), apoproteins, lipid profile, glucose concentrations were measured (ELISA, immunodiffusion and enzymatic) in 77 cord blood samples from diabetic and healthy pregnant mothers. RESULTS: The body weight, cord glucose and both apoproteins were increased in neonates of gestational and noninsulin dependent diabetic (GDM, NIDDM) than in neonates of nondiabetic mothers (NNDM). The Lp (a) was not correlated with the blood glucose and didn't significantly increase in the three neonates groups of diabetic mothers. The apo B/apo A1 and the LDL/HDL ratios were insignificantly increased in relation to the body weight. In neonates of diabetic mothers (NDM), only the blood glucose and Lp (a) differ between both sexes. CONCLUSION: NDM may have disturbed lipid metabolism, which require special care to them and to their mothers during the prenatal period.     

Enhanced catalytic activity over palladium supported on ZrO2@C with NaOH-assisted reduction for decomposition of formic acid

A ZrO₂@C support based on t-ZrO₂ embedded in amorphous carbon was obtained via the pyrolysis of a UiO-66 precursor. Highly dispersed Pd nanoparticles (NPs) were subsequently deposited onto this support, using NaOH-assisted reduction, to obtain a formic acid (FA) decomposition catalyst. This material showed a turnover frequency (TOF) for the heterogeneously-catalyzed decomposition of FA of 8588 h⁻¹ at 60 °C, with 100% H₂ selectivity. This performance is ascribed to the uniform dispersion of smaller palladium nanoparticles and a synergistic effect between the metal NPs and support. Even at 30 °C, the complete decomposition of FA was achievable in FA/SF (SF, sodium formate) solution, with a TOF as high as 1857 h⁻¹.

Pd/ZrO₂@C was prepared employing UiO-66-derived ZrO₂@C as the support and showed high catalytic activity for formic acid decomposition.     

Detection of influenza virus types A and B and type A subtypes (H1, H3, and H5) by multiplex polymerase chain reaction

Infections with influenza virus type A and B present serious public health problems on a global scale. However, only influenza A virus has been reported to cause fatal pandemic in many species. To provide suitable clinical management and prevent further virus transmission, efficient and effective clinical diagnosis is essential. Therefore, we developed multiplex PCR assays for detecting influenza types A and B and the subtypes of influenza A virus (H1, H3 and H5). Upon performing multiplex PCR assays with type-specific primer sets, the clearly distinguishable products representing influenza A and B virus were separated by agarose gel electrophoresis. In addition, the subtypes of influenza A virus (H1, H3 and H5), which are most common in humans, can be readily distinguished by PCR with subtype-specific primer sets, yielding PCR products of different sizes depending on which subtype has been amplified. This method was tested on 46 influenza virus positive specimens of avian and mammalian (dog and human) origins collected between 2006 and 2008. The sensitivity of this method, tested against known concentrations of each type and subtype specific plasmid, was established to detect 10(3) copies/microl. The method's specificity was determined by testing against other subtypes of influenza A virus (H2, H4 and H6-H15) and respiratory pathogens commonly found in humans. None of them could be amplified, thus excluding cross reactivity. In conclusion, the multiplex PCR assays developed are advantageous as to rapidity, specificity, and cost effectiveness.