Convenient synthesis of sulfonamides from amines and p‐toluene sulfonyl chloride mediated by crosslinked poly(4‐vinylpyridine)

A general, mild, and convenient method has been developed for the synthesis of various N‐substituted and N, N‐disubstituted sulfonamides, as a class of sulfa drugs, from the corresponding amines and p‐toluene sulfonyl chloride in the presence of readily available crosslinked poly(4‐vinylpyridine) as a catalyst, base or polymeric substrates. The use of polymeric catalyst simplifies routine sulfonylation of amines because it eliminates the traditional purification. The polymer can be removed quantitatively and it can be regenerated and reused for several cycles without losing its activity. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Catalytic enhancement of formic acid electro-oxidation through surface modifications with gold on supported Pt nanoparticles

The Formic Acid Electro-oxidation (FAEO) on Pt/Au Nanoparticles (PtAu NP) supported on Hierarchical Porous Carbon (HPC), was studied by cyclic voltammetry and chronoamperometry. The supported HPC-Pt nanoparticles were surface modified by Au spontaneous deposits. The morphological and compositional characterization was performed by Scanning Electron Microscopy (SEM) coupled with Electron Dispersive Spectroscopy (EDS). A significant increase of the current densities for FAEO in the potential region 0.1–0.75 V_RHE was observed on HPC-PtAu catalysts. The comparison with HPC-Pt electrodes results show that Au atoms presence on Pt nanoparticles is a key factor to improve the catalysts performance. Based on our results, a clear change in FAEO mechanism on HPC-PtAu catalysts with respect to HPC-Pt was evidenced.     

CO2‐induced crystal engineering of polylactide and the development of a polymeric nacreous microstructure

Nacre's biomineralization process and its self‐organizing brick‐and‐mortar crystalline microstructure have inspired many researchers to develop new materials derived from the natural world. In our study, we took a novel approach to two‐dimensional (2‐D) crystallization. That is, we applied the biomineralization self‐organizational principle that exists in natural materials to a biopolymer (polylactide). The CO₂‐induced crystallization of poly(d ‐lactide), with its unique diffusion‐controlled crystallization mechanism, tends to produce distinct 2‐D spherulitic structures. We found that these 2‐D spherulites were self‐organizing in nature, and that they created a stack of 2‐D spherulitic structures. These crystalline microstructures, with their intervening amorphous phase, were foamed in situ due to the CO₂‐induced crystallization self‐exclusion phenomenon. We compared the resultant crystalline structure with nacre's brick‐and‐mortar crystalline microstructure to confirm the biomimetic principle of self‐organization. To the best of our knowledge, this is the first time that a biopolymer has been crystallized in a 2‐D manner in a way that resembles nature's biomineralization process. The hierarchical crystalline microstructure is morphologically similar to that of nacre biomaterials. This novel crystallization technique is simple, absolutely non‐toxic and works swiftly to produce a brick‐and‐mortar crystalline microstructure with a high degree of order. © 2017 Society of Chemical Industry     

Efficiency of removal of whey protein from sweet whey using polymeric microfiltration membranes

Our objective was to measure whey protein removal percentage from separated sweet whey using spiral-wound (SW) polymeric microfiltration (MF) membranes using a 3-stage, 3× process at 50°C and to compare the performance of polymeric membranes with ceramic membranes. Pasteurized, separated Cheddar cheese whey (1,080 kg) was microfiltered using a polymeric 0.3-μm polyvinylidene (PVDF) fluoride SW membrane and a 3×, 3-stage MF process. Cheese making and whey processing were replicated 3 times. There was no detectable level of lactoferrin and no intact α- or β-casein detected in the MF permeate from the 0.3-μm SW PVDF membranes used in this study. We found BSA and IgG in both the retentate and permeate. The β-lactoglobulin (β-LG) and α-lactalbumin (α-LA) partitioned between retentate and permeate, but β-LG passage through the membrane was retarded more than α-LA because the ratio of β-LG to α-LA was higher in the MF retentate than either in the sweet whey feed or the MF permeate. About 69% of the crude protein present in the pasteurized separated sweet whey was removed using a 3×, 3-stage, 0.3-μm SW PVDF MF process at 50°C compared with 0.1-μm ceramic graded permeability MF that removed about 85% of crude protein from sweet whey. The polymeric SW membranes used in this study achieve approximately 20% lower yield of whey protein isolate (WPI) and a 50% higher yield of whey protein phospholipid concentrate (WPPC) under the same MF processing conditions as ceramic MF membranes used in the comparison study. Total gross revenue from the sale of WPI plus WPPC produced with polymeric versus ceramic membranes is influenced by both the absolute market price for each product and the ratio of market price of these 2 products. The combination of the market price of WPPC versus WPI and the influence of difference in yield of WPPC and WPI produced with polymeric versus ceramic membranes yielded a price ratio of WPPC versus WPI of 0.556 as the cross over point that determined which membrane type achieves higher total gross revenue return from production of these 2 products from separated sweet whey. A complete economic engineering study comparison of the WPI and WPPC manufacturing costs for polymeric versus ceramic MF membranes is needed to determine the effect of membrane material selection on long-term processing costs, which will affect net revenue and profit when the same quantity of sweet whey is processed under various market price conditions.     

次氯酸钠对德尔卑沙门氏菌生物被膜的抑制作用及机制

目的：为控制德尔卑沙门氏菌（Salmonella Derby）在食品加工过程中的污染，研究不同体积分数次氯酸钠对S. Derby生物被膜的抑制作用及其机制。方法：采用结晶紫染色法和平板菌落计数法观察次氯酸钠对生物被膜的抑制和清除效果，进一步观察不同体积分数次氯酸钠作用下沙门氏菌泳动能力和生物被膜内细胞的代谢活性、胞外聚合物含量和微观形态的变化规律。结果：次氯酸钠的最小抑菌浓度（minimum inhibitory concentration，MIC）为0.08%（体积分数，下同），亚MIC（0.04%、0.02%、0.01%）的次氯酸钠可以抑制S. Derby生物被膜的形成，对成熟生物被膜也有一定的清除效果，且不同亚MIC次氯酸钠的作用效果差异显著（P＜0.05）；不同体积分数次氯酸钠处理能降低生物被膜内细胞代谢活性，抑制胞外多糖的合成，且不同体积分数次氯酸钠的作用效果差异显著（P＜0.05）。激光共聚焦扫描显微镜结果显示，与对照组相比，次氯酸钠处理使得生物被膜厚度减小、活菌数减少、死菌数增多、细菌由聚集状态变为分散状态。结论：不同体积分数次氯酸钠对S. Derby生物被膜的形成有明显的抑制作用，这一作用与干扰细菌生长、生物被膜内细胞代谢活性和胞外多糖的合成有关。     

Very fast H2 production from the methanolysis of NaBH4 by metal‐free poly(ethylene imine) microgel catalysts

The polyethyleneimine (PEI) microgels prepared via microemulsion polymerization are protonated by hydrochloric acid treatment (p‐PEI) and quaternized (q‐PEI) via modification reaction with methyl iodide and with bromo alkanes of different alkyl chain lengths such as 1‐bromoethane, 1‐bromobutane, 1‐bromohexane, and 1‐bromooctane. The bare p‐PEI and q‐PEI microgels are used as catalysts directly without any metal nanoparticles for the methanolysis reaction of sodium borohydride (NaBH₄). Various parameters such as the protonation/quaternization reaction on PEI microgels, the amount of catalyst, the amount of NaBH₄, and temperature are investigated for their effects on the hydrogen (H₂) production rate. The reaction of self‐methanolysis of NaBH₄ finishes in about 32.5 min, whereas the bare PEI microgel as catalyst finishes the methanolysis of NaBH₄ in 22 min. Surprisingly, it is found that when the protonated PEI microgels are used as catalyst, the same methanolysis of NaBH₄ is finished in 1.5 min. The highest H₂ generation rate value is observed for protonated PEI microgels (10 mg) with 8013 mL of H₂/(g of catalyst.min) for the methanolysis of NaBH₄. Moreover, activation parameters are also calculated with activation energy value of 23.7 kJ/mol, enthalpy 20.9 kJ/mol, and entropy ?158 J/K.mol. Copyright © 2016 John Wiley & Sons, Ltd.     

Microwave irradiated Carrageenan-Guar gum micro-porous IPN: a novel material for isotropic tissue scaffolding

In this study, a novel micro porous honeycomb structured Crg-GG-IPN material was incepted to be applicable as scaffold and accomplished. The hydrophilicity was confirmed by FT-IR and OCA. Amorphous nature and micro-rough surface were confirmed by XRD and AFM. Void fraction was 0.61?±?0.04. Void space, hemocompatibility and platelet adhesion were captured by SEM. Degradability of the material was confirmed by in-vitro degradation study. Incision method using mice model was a clear evidence for cell attachment and non-toxicity and was confirmed from hematology and histopathology. Thus, it appears that Crg-GG scaffolds can be useful as wound healing material for clinical applications.     

Nitrogen Removal Performance of Denitrifying Ammonium Oxidation System in Treating Sulfamethoxazole-laden Secondary Wastewater Effluent

In this study,nitrogen removal performance of the denitrifying ammonium oxidation(DAO)process was investigated when treating sulfamethoxazole(SMX)-laden secondary wastewater effluent.The influent SMX concentration showed negligible effect on efficiencies for removal of nitrate and COD.However,the ammonium ions removal rate was moderately reduced,when the influent SMX concentration in wastewater reached 6 mg/L.Total nitrogen removal efficiency remained as high as 76.77%towards the day 158 at the end of experiment.Candidatus_Brocadia and Candidatus_Kuenenia were the functional anammox strains.The unclassified_f__Rhodobacteraceae sp.was predominant heterotrophic denitrifying strain in the studied reactor.The concentrations of soluble extracellular polymeric substances in sludge obviously increased from 16.76 mg/g VSS to 32.31 mg/g VSS,which might protect the nitrogen removal strains from high-concentration SMX.This result provides a theoretical and technical foundation for the application of denitrifying ammonium oxidation process in treating sulfamethoxazole-laden secondary wastewater effluent.     

Enhanced sludge stabilization coupled with microbial fuel cells (MFCs)

This study presents research results on electricity production from waste activated sludge using MFCs during stabilization process. Different MFC configurations equipped with various electrodes were used. Voltage measurements were continuously done during 35 days of MFC operation. Experimental results showed that bioelectricity generation was linked to volatile solids (VS) and protein reductions as a fraction of extracellular polymeric substances (EPS). Double chamber MFC reactor equipped with graphite electrodes had better power and current densities as 312.98 mW/m² and 39.07 μA/cm² while single chamber MFC equipped with titanium electrodes revealed better power and current densities as 97.60 mW/m² and 17.63 μA/cm², respectively. Molecular results indicated that power outputs of MFCs effected by diverse microbial communities in anode biofilms. Although organic matter degradation is reported as 35%–55% VS reduction for digesters, this research provided a promising approach for sludge stabilization with enhanced degrading of organic matters up to 75% by using MFCs.     

Porous ceramics with tailored pore size and morphology as substrates for coral larval settlement

The growing demand for stony corals as ornamental aquarium animals requires defined aquacultural breeding strategies. For the sexual propagation of corals, material substrates are needed, that attract larvae and support their settlement and development. In this study, five types of highly porous ceramic materials were developed following the example of coral skeleton. The applicability of these settlement substrates was tested using larvae of the stony coral Pocillopora damicornis. Partial sintering of pressed clay pellets, freeze casting of clay and alumina-mullite based slurries and direct foaming of high alkane phase emulsified suspensions (HAPES) using alumina were employed. By the addition of mm-sized spherical polystyrene beads as sacrificial templates during freeze casting (alumina-mullite), superficial pores in the size of the larvae were created. The inorganic substrates featured open porosities between 35% (pressed clay) and 83% (foamed alumina), pore sizes ranging from nm to mm-scale and pore morphologies dominated by interparticle porosity (pressed), lamellar pores (freeze casting) and cellular pore types (direct foaming). The ceramic substrates were incubated in artificial sea water for 3 months to induce necessary biofilm formation and algae growth. Afterwards, individual substrates were exposed to 5 coral larvae, and their settlement behavior was monitored over 14 days. At the end of this period, all ceramic materials were successfully accepted as settlement substrates, with a mean settlement rate of 46.2%, and no significant differences between the substrate types. On samples with large surface superficial pores, a significantly reduced survival of settled larvae (79%) compared to the other porous materials (93–98%) was determined, suggesting a non-ideal surface topography. While alumina foam samples (HAPES) exhibit the most promising results in terms of settlement and survival of larvae, clay-based substrates provide a more economic solution for the sexual propagation of corals in aquaculture.