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Iron complex regulated electrochemical reaction was triggered for revealing the reaction mechanism, degradation pathway, and applied potential of perfluorooctanoic acid (PFOA). The increased PMS concentrations, electrode spacing, and current density significantly enhanced PFOA elimination, with current density exhibiting a relatively strong interdependency to PFOA complete mineralization. The synergy between PMS and electrochemical reactions greatly accelerated PFOA decomposition by promoting the generation of key reaction sites, such as those for PMS activation and electrochemical processes, under various conditions. Furthermore, density functional theory calculations confirmed that the reciprocal transformation of Fe 2+ and Fe 3+ complexes was feasible under the electrochemical effect, further promoting the generation of active sites. The developed electrochemical oxidation with PMS reaction (EO/PMS) system can rapidly decompose and mineralize PFOA while maintaining strong tolerance to changing water matrices and organic and inorganic ions. Overall, it holds promise for use in treating and purifying wastewater containing PFOA., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Atmospheric water harvesting is considered a viable source of freshwater to alleviate water scarcity in an arid climate. Water condensation tends to be more efficient on superhydrophobic surfaces as the spontaneous coalescence-induced droplet jumping on superhydrophobic surfaces enables faster condensate removal. However, poor water nucleation on these surfaces leads to meager water harvest. A conventional approach to the problem is to fabricate micro- and nanoscale biphilic structures. Nonetheless, the process is complex, expensive, and difficult to scale. Here, the authors present an inexpensive and scalable method based on manipulating the water-repellent coatings of superhydrophobic surfaces. Flexible siloxane can facilitate water nucleation, while a branched structure promotes efficient droplet jumping. Moreover, ToF-SIMS analysis indicated that branched siloxane provides a better water-repellent coating coverage than linear siloxane and the siloxanes comprise hydrophilic and hydrophobic molecular segments. Thus, the as-prepared superhydrophobic surface, TiO 2 nanorods coated with branched siloxanes harvested eight times more water than a typical fluoroalkylsilane (FAS)-coated surface under a low 30% relative humidity and performed better than most reported biphasic materials., (© 2023 Wiley-VCH GmbH.)

SARS-CoV-2 remains one of the biggest global health problems, which has already reached our wastewater through fecal shedding by COVID-19 patients. While the development of vaccines has mitigated the threats of the COVID-19 pandemic, the evolutionary dynamics of SARS-CoV-2 in wastewater lack monitoring and understanding. In this study, SARS-CoV-2 variants in wastewater were identified by analyzing 8511 wastewater-derived genome sequences from 9 countries from March 2020 to May 2023. The dominance of co-circulating variants was observed, namely B.1 in 2020, Alpha and Delta in 2021, then superseded by Omicron lineages in 2022 with a three-times increase. Mutations were also profiled, revealing nearly 5031 unique amino acid substitutions occurring approximately 371,591 times, some of which were associated with enhanced viral transmission and fitness. This study provided the first long-term multi-country overview of the prevalence of co-circulating SARS-CoV-2 lineages and mutations in wastewater and showed its comparison with conventional epidemiological surveillance. The results highlight the ability of wastewater-based genome monitoring to supplement clinical surveillance efforts in rapidly detecting viruses up to the strain level to keep track of their potential transmission routes and evolutionary dynamics., (Copyright © 2023 Elsevier GmbH. All rights reserved.)

A soft microbot assembled from individual magnetic microsphere scaffold (MMS) beads carrying mesenchymal stem cells (MSC) is navigated under magnetic actuation, where an oscillating field induces mechanical flexion to propel the microbot toward the target site. A seven-bead microbot attained a top translational speed of 205.6 µm s -1 (0.068 body length s -1 ) under 10 mT and 2 Hz field oscillation. The shallow flexion angle (10-24.5°) allows precision movements required to navigate narrow spaces. Upon arrival at the target site, the MMS beads unload their MSC cargo following exposure to a phosphate-buffered saline (PBS) solution, mimicking the extracellular fluid's sodium concentration. The released stem cells have excellent viability and vitality, promoting rapid healing (i.e., 83.2% vs 49%) in a scratch-wound assay. When paired with minimally invasive surgical methods, such as laparoscopy and endoscopic surgery, the microbot can provide precise stem cell delivery to hard-to-reach injury sites in the body to promote healing. Moreover, the microbot is designed to be highly versatile, with individual MMS beads customizable for cargoes of live cells, biomolecules, bionanomaterials, and pharmaceutical compounds for various therapeutic requirements., (© 2023 Wiley-VCH GmbH.)

The structure and chemistry of metal-organic frameworks or MOFs dictate their properties and functionalities. However, their architecture and form are essential for facilitating the transport of molecules, the flow of electrons, the conduction of heat, the transmission of light, and the propagation of force, which are vital in many applications. This work explores the transformation of inorganic gels into MOFs as a general strategy to construct complex porous MOF architectures at nano, micro, and millimeter length scales. MOFs can be induced to form along three different pathways governed by gel dissolution, MOF nucleation, and crystallization kinetics. Slow gel dissolution, rapid nucleation, and moderate crystal growth result in a pseudomorphic transformation (pathway 1) that preserves the original network structure and pores, while a comparably faster crystallization displays significant localized structural changes but still preserves network interconnectivity (pathway 2). MOF exfoliates from the gel surface during rapid dissolution, thus inducing nucleation in the pore liquid leading to a dense assembly of percolated MOF particles (pathway 3). Thus, the prepared MOF 3D objects and architectures can be fabricated with superb mechanical strength (>98.7 MPa), excellent permeability (>3.4 × 10 -10 m 2 ), and large surface area (1100 m 2 g -1 ) and mesopore volumes (1.1 cm 3 g -1 )., Competing Interests: Z. L., W. H., and K. L. Y. have a provisional patent application related to this work filed with the U.S. Patent and Trademark Office on 30 July 2021 (63227351)., (This journal is © The Royal Society of Chemistry.)

Healthy skin has a high vitamin C concentration that protects against ultraviolet (UV)-induced damage, promotes wound healing, and lowers cancer risk. The present contribution describes two drug delivery systems for topical administration of vitamin C. The electrospun poly(vinyl alcohol) (PVA) nanofiber carrier of vitamin C exhibits a burst release profile (66 mg/g/h followed by 6.3 mg/g/h). In comparison, a new composite PVA nanofiber-molecular capsule delivers vitamin C at a constant rate (8.2 mg/g/h) with a zeroth-order release profile for better therapeutic management. Both delivery systems protect vitamin C and afford increased heat stability. The molecular capsules of β-cyclodextrin with the vitamin C inclusion complex are immobilized on cellulose acetate and electrosprayed onto an electrospun PVA nanofiber mat., Competing Interests: The authors declare no competing financial interest., (© 2023 The Authors. Published by American Chemical Society.)

Toluene is a prevalent pollutant in indoor environments and its removal is essential to maintain a healthy environment. Adsorption is one of the best alternatives for organic vapours removal, specially at low indoor concentrations. Metal Organic Frameworks (MOFs) and Ionic Liquids (ILs) are potential materials for this mean. In this work, the synthesis and application of IL/MOF composite materials for toluene removal is reported. Loading [BMIM][CH 3 COO] ionic liquid into MIL101 porous structure improves parent materials affinity towards toluene capture by two orders of magnitude (as Henry's constants, attesting to their synergy). MIL101(Cr) and absorption in [BMIM][CH 3 COO] IL is best described by Henry's Law, while the Langmuir adsorption model predicts toluene adsorption on [BMIM][CH 3 COO]/MIL101(Cr) better than Freundlich and Toth equations. Diffusional and kinetics models revealed that toluene diffusion is the rate limiting step for pristine MIL101. Kinetic and diffusion rates were systematically improved upon the incorporation of the ionic liquid due to shorter toluene hops with the adsorbed IL and the increased hydrophobicity in the composites making the sorption more favourable. This study provides a systematic analysis and modelling of the toluene capture process in IL/MOF composites aiding a better understanding of the sorption process in these novel materials., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Inc. All rights reserved.)

Indoor exposure to volatile organic compounds (VOCs) is detrimental to the health of the occupants, and their removal is crucial in maintaining good air quality. Novel adsorbents prepared by modifying Metal-Organic Frameworks (MOFs), MIL101 (Cr), UiO-66, and UiO-66-NH 2 with [BMIM][CH 3 COO] ionic liquid, were characterized and tested for toluene adsorption. [BMIM][CH 3 COO]/MIL101 performed best with a fast sorption rate, large sorption capacity, and good regenerability. It displays synergistic interactions between the IL and MOF. Adding one weight percent [BMIM][CH 3 COO] to UiO-66 and UiO-66-NH 2 has a synergistic effect with respective 14% and 5% enhancements sorption over calculated values. The strong interactions between IL and UiO-66 and UiO-66-NH 2 , as observed in their thermogravimetric data, results in poor toluene sorption for 10 wt% [BMIM][CH 3 COO] loadings. This work provides a basis for IL modification of MOFs for enhanced sorption of VOCs for air treatment., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Inc. All rights reserved.)

Polyfluoroalkyl and perfluoroalkyl chemicals (PFCs) widely used in lubricants, surfactant, textiles, paper coatings, cosmetics, and fire-fighting foams can release a large deal of organics contaminants into wastewater and pose great risks to the health of humans and eco-environments. Although advanced oxidation processes can effectively deconstruct various organic contaminants via reactive radicals, the stable structure of PFCs makes it difficult to be degraded. Here, we confirm that electrochemical oxidation process coupled with peroxymonosulfate (PMS) reaction can efficiently destroy stable structure of PFCs via electron transfer and meanwhile completely degrade PFCs via generated active radicals. We further studies via capturing and scavenging radicals, and DFT calculations find that electron hydroxyl radials play a dominant role in degrading PFCs. Based on the calculations of adsorption energy and molecular orbital energy we further demonstrate that many active sites on the surface of Ti 4 O 7 (1 0 4) plane can rapidly take part in electrochemical reaction for generating radials and removing organic contaminants. These results give a promising insight towards high-effective and deep degradation of PFCs via electrochemical reaction coupled with advanced oxidation processes, as well as providing guidance and technical support for the remove of multiple organic contaminants., (Copyright © 2022. Published by Elsevier Ltd.)

This work describes a versatile electrospinning equipment with rapid, independent, and precise x-y-z movements for large-area depositions of electrospun fibers, direct writing or assembly of fibers into sub-millimeter and micron-sized patterns, and printing of 3D micro- and nanostructures. Its versatility is demonstrated thought the preparation of multilayered functional nanofibers for wound healing, nanofiber mesh for particle filtration, high-aspect ratio printed lines, and freestanding aligned nanofibers., (© 2022. The Author(s).)

Perfluorooctane sulfonate (PFOS), normally present in groundwater and surface water, is an emerging environmental contaminants, but is extremely difficult to be degraded due to high energy of the C-F bond. Here, an electrocoagulation (EC) technique coupled with peroxymonosulfate (PMS) activation was used to deeply degrade PFOS. Results showed that approximately 100% PFOS was removed from the solution in the monopolar serial (MS) mode within 60 min and achieved a high kinetic rate of 0.074 min -1 , which was significantly higher than those of reported studies (Table S3). Energy consumption (2.06 kWh/kg) in the MS mode was significantly lower than that of Al (52.30 kWh/kg) and Zn (213.50 kWh/kg) electrodes, which further confirmed the potential application prospects of EC technique. The quenching experiments, electron spin response (ESR) analysis, and DFT calculations can verify that ·OH was the main radical from the reaction of Fe 2+ -OH reaction site with PMS. In addition, results from fluorine balance and TOC removal also indicated the complete mineralization and degradation of PFOS in the EC process. Quantum chemical calculations can confirm the PFOS degradation mechanism and key active sites for direct electron transfer and radical attack. After five cycle operations of PFOS degradation, the EC process was still effective in degrading PFOS with a removal efficiency above 98%. Thus, this work provided a novel alternative for the high-effective treatment of PFOS from contaminated environmental water bodies., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

A unique 1D nanostructure of Pt@CeO 2 -BDC was prepared from Pt@CeBDC MOF. The Pt@CeO 2 -BDC was rich in oxygen vacancies (i.e., XPS O β /(O α + O β ) = 39.4%), and on the catalyst, the 2 nm Pt clusters were uniformly deposited on the 1D mesoporous polycrystalline CeO 2 . Toluene oxidation was conducted in a spectroscopic operando Raman-online FTIR reactor to elucidate the reaction mechanism and establish the structure-activity relationship. The reaction proceeds as follows: (I) adsorption of toluene as benzoate intermediates on Pt@CeO 2 -BDC at low temperature by reaction with surface peroxide species; (II) reaction activation and ring-opening involving lattice oxygen with a concomitant change in defect densities indicative of surface rearrangement; (III) complete oxidation to CO 2 and H 2 O by lattice oxygen and reoxidation of the reduced ceria with consumption of adsorbed oxygen species. The Pt clusters, which mainly exist as Pt 2+ with minor amounts of Pt 0 and Pt 4+ on the surface, facilitated the adsorption and reaction activation. The Pt-CeO 2 interface generates reduced ceria sites forming nearby adsorbed peroxide at low temperature that oxidize toluene into benzoate species by a Langmuir-Hinshelwood mechanism. As the reaction temperature increases, the role of lattice oxygen becomes important, producing CO 2 and H 2 O mainly by the Mars-van Krevelen mechanism.

Mixed transition metal oxides (MTMOs) have enormous potential applications in energy and environment. Their use as catalysts for the treatment of environmental pollution requires further enhancement in activity and stability. This work presents a new synthesis approach that is both convenient and effective in preparing binary metal oxide catalysts (CeCuO x ) with excellent activity by achieving molecular-level mixing to promote aliovalent substitution. It also allows a single, pure MTMO to be prepared for enhanced stability under reaction by using a bimetallic metal-organic framework (MOF) as the catalyst precursor. This approach also enables the direct manipulation of the shape and form of the MTMO catalyst by controlling the crystallization and growth of the MOF precursor. A 2D CeCuO x catalyst is investigated for the oxidation reactions of methanol, acetone, toluene, and o-xylene. The catalyst can catalyze the complete reactions of these molecules into CO 2 at temperatures below 200 °C, representing a significant improvement in performance. Furthermore, the catalyst can tolerate high moisture content without deactivation., (© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Nanostructured Ag@SiO 2 -Penicillin was synthesized from high-purity Ag 0 NPs with a mean particle size of about 10 nm produced by electromagnetic levitation gas condensation (ELGC) method. The silver and penicillin contents of the synthesized nano-antibiotic were about 34 wt% and 2.5 wt% respectively, as determined by ICP-OES and TGA analyses. The antibacterial properties and synergistic effects of nanostructured Ag@SiO 2 and Ag@SiO 2 -Penicillin on killing the Methicillin-susceptible S. aureus (MSSA) and Methicillin-resistant S. aureus (MRSA) bacteria were also examined. The nanoparticles were characterized by X-ray diffraction (XRD) and transmission electron microscopy (TEM). Ag@SiO 2 -Penicillin NPs showed an outstanding antibacterial activity compared to Penicillin and Ag@SiO 2 NPs. The Fractional inhibitory concentration (FIC) indexes were 0.54 and 0.52 against MSSA and MRSA bacteria respectively, illustrating the synergistic effects of Ag@SiO 2 -Penicillin NPs. In addition, Ag@SiO 2 -Penicillin NPs showed promising dose-dependent cytotoxicity effects indicating the protective effects emanating from anti-inflammatory properties of penicillin., (Copyright © 2019 Elsevier B.V. All rights reserved.)

Graphite oxide powder was obtained using the modified Hummers' method and characterized using X-ray photoelectron spectroscopy (XPS) and time-of-flight secondary ion mass spectrometry (ToF-SIMS). The XPS results indicated that the epoxy groups were the main functional groups on the graphite oxide powder surface. The graphite oxide powder was then reacted with SO 2 and NH 3 gases, respectively, at 25 °C. The XPS and ToF-SIMS analyses of the surface of the reacted graphite oxide powder showed that the reactions mainly occurred in the epoxy groups. Bisulfate and amine groups were formed on the surface of the graphite oxide powder after the reactions between the graphite oxide powder and SO 2 and NH 3 gases. This work demonstrates a new method of removing SO 2 and NH 3 gases using graphite oxide powder.

Diagnosis of Alzheimer's disease (AD) can be performed with the assistance of amyloid imaging. The current method relies on positron emission tomography (PET), which is expensive and exposes people to radiation, undesirable features for a population screening method. Magnetic resonance imaging (MRI) is cheaper and is not radioactive. Our approach uses magnetic nanoparticles (MNPs) made of superparamagnetic iron oxide (SPIO) conjugated with curcumin, a natural compound that specifically binds to amyloid plaques. Coating of curcumin-conjugated MNPs with polyethylene glycol-polylactic acid block copolymer and polyvinylpyrrolidone by antisolvent precipitation in a multi-inlet vortex mixer produces stable and biocompatible curcumin magnetic nanoparticles (Cur-MNPs) with mean diameter <100 nm. These nanoparticles were visualized by transmission electron microscopy and atomic force microscopy, and their structure and chemistry were further characterized by X-ray diffraction, thermogravimetric analysis, X-ray photoelectron spectroscopy, time-of-flight secondary ion mass spectrometry, and Fourier transform infrared spectroscopy. Cur-MNPs exhibited no cytotoxicity in either Madin-Darby canine kidney (MDCK) or differentiated human neuroblastoma cells (SH-SY5Y). The Papp of Cur-MNPs was 1.03 × 10(-6) cm/s in an in vitro blood-brain barrier (BBB) model. Amyloid plaques could be visualized in ex vivo T2*-weighted magnetic resonance imaging (MRI) of Tg2576 mouse brains after injection of Cur-MNPs, and no plaques could be found in non-transgenic mice. Immunohistochemical examination of the mouse brains revealed that Cur-MNPs were co-localized with amyloid plaques. Thus, Cur-MNPs have the potential for non-invasive diagnosis of AD using MRI., (Copyright © 2014 Elsevier Ltd. All rights reserved.)

The aggravating effects of zero-dimensional, particle-shaped nanomaterials on allergic asthma have been previously investigated, but similar possible effects of one-dimensional shaped nanomaterials have not been reported. More importantly, there are no available means to counteract the adverse nanomaterial effects to allow for their safe use. In this study, an ovalbumin (OVA)-sensitized rat asthma model was established to investigate whether single walled carbon nanotubes (SWCNTs) aggravate allergic asthma. The results showed that SWCNTs in rats exacerbated OVA-induced allergic asthma and that this exacerbation was counteracted by concurrent administration vitamin E. A mechanism involving the elimination of reactive oxygen species, downregulation of Th2 responses, reduced Ig production, and the relief of allergic asthma symptoms was proposed to explain the antagonistic effects of vitamin E. This work could provide a universal strategy to effectively protect people with allergic asthma from SWCNTs or similar nanomaterial-induced aggravating effects.

Perfluorosulfonic acid (PFSA) polyelectrolyte confined in subnanoliter volume within zeolite cladded walls exhibits higher glass transition temperature and excellent tolerance to high-temperature fuel cell operation under dry conditions, generating an order of magnitude higher power density than standard PEMFC.

Silk sericin and chitosan biosorbents are low cost and highly efficient biosorbents derived from waste biomass. Both biosorbents displayed good capacity and excellent selectivity for gold adsorption. Silk sericin and chitosan adsorbed respectively 1 and 3.3mmolg(-1) of gold and have K(d) values of 450 and 34,000, respectively. Experimental evidence showed that gold adsorbed on the amide groups of the silk sericin, while gold and copper adsorbed on the amino groups of chitosan via charge-interactions and complexation. Binary (Au-Cu), five (Au-Co-Ni-Cu-Zn) and six (Au-Pd-Co-Ni-Cu-Zn) component separations consistently showed that silk sericin has better selectivity (Sel(Au)>2.4) than chitosan. It is possible to recover gold at 99.5% purity by silk sericin and 90% if the solution contained palladium., (Copyright © 2010 Elsevier B.V. All rights reserved.)

A multilevel antimicrobial coating with "release-killing", "contact-killing" and "anti-adhesion" properties was prepared from polymer-encapsulated chlorine dioxide (ClO(2)), water-in-oil-in-water (w/o/w) double emulsion. A slow sustained release of gaseous ClO(2) at a rate sufficient to inhibit bacterial growth (approximately 1300 microg of ClO(2).g(-1).day(-1)) was demonstrated for a prolonged period of time (i.e., 28 days). Touch and infectious droplets triggered an increased release of the biocides at the sites of contamination, resulting in rapid disinfection. Zinc chloride (i.e., 30 ppm) was added to provide "contact-killing" properties, while bacterial adhesion was prevented by the Pluronic polymer used to encapsulate ClO(2). The new antimicrobial coating is effective against Gram positive and Gram negative bacteria, including Bacillus subtilis , Staphylococcus aureus , and Escherichia coli. A greater than 5 log (i.e., >or= 99.999%) reduction of viable bacteria was obtained at a short contact time of 10 min.

Pd membranes of excellent stability and flux were prepared with multi-legged anchors by electroless plating of Pd on a porous support modified by a zeolite barrier layer containing Pd seeds; these membranes provide stable phenol production by direct hydroxylation of benzene.

Fresh TiO2 was found to possess a strong germicidal activity even without UV irradiation. Live Yeast (Saccharomyces cerevisiae) cells in contact with fresh TiO2 were found deformed and dead after 15 min contact. The cause of germicidal activity was discussed from the observed cell deformation, lysis and increased absorption at 1680 cm(-1) in FT-IR spectra of the affected cells, which proved the oxidizing effect of fresh TiO2 to cells. The deformation caused by the stretching of cell wall and pressure built-up inside the cell, led to cell burst and release of intracellular materials. The degree of cell deformation was found positively related with the wetting property of TiO2. Cells are negatively charged, for Gram-negative cell (thinner cell wall), a higher germicidal effect was observed than Gram-positive cells. The germicidal effect of TiO2 gradually decreased after exposure to air at room temperature, as the wetting property decreased. This kind of germicidal activity was more effective compared to other germicidal process such as UVA/TiO2 or Ag+. This shed light on designing new germicidal material either maintained by visible light irradiation, or by oxidation effect generated by reactive oxygen species.

Microfabricated HZSM-5 micromembranes were successfully employed as a proton-exchange membrane in a micro fuel cell and the energy generation is strongly dependent on the Al-content of the HZSM-5.

Three different approaches, including (1) manipulating the site chemistry, (2) controlling the spacing between neighbouring sites and (3) altering the adsorbates by the use of chelates, were successfully used to prepare MCM-41 adsorbents with excellent selectivity for silver adsorption from solutions containing copper.

Cadmium pollution from the manufacture and disposal of NiCd batteries remains an important problem in developing countries. Among the available remedial technologies, adsorption is popular because of its low cost and simplicity. The mesoporous NH2-MCM-41 displays good adsorption capacities for cadmium and nickel ions. This work demonstrated for the first time the use of the competition between complexant and sorbentto create high adsorption selectivity. The selectivity was manipulated by the judicious use of a chelating agent, thus achieving on-demand 100% selectivity for either Cd2+ or Ni2+ adsorption. Single and binary components adsorption studies, carried out with different metals and EDTA concentrations, solution compositions and pH, showed that NH2-MCM-41 adsorbs only cadmium with a capacity of 0.56 mmol g(-1) from binary mixtures at [EDTA]/[M2+] = 0.5 and pH 5. The NH2-MCM-41 displays 100% selectivityfor nickel adsorption at [EDTA]/[M2+] = 0.5 and pH 2 with a measured adsorption capacity of 0.50 mmol g(-1). Pure Cd2+ and Ni2+ solutions were recovered by a simple acid wash, and the regenerated adsorbent could be reused without lost of performance (i.e., adsorption capacity and selectivity).

A stain-based screening method was developed to screen different catalyst coatings for their germicidal activity. A Baclight dead/live bacteria viability kit (invitrogen, molecular probes) was used for staining the cell. The screening was carried out following a standard procedure. This included loading cell suspension to solid surface and maintaining contact for 30 min, then staining with a mixture containing dyes. The stained cells were observed using an epifluorescent microscope and photographed with a CCD camera under UV. Metal-doped TiO2 coatings on Al plates were prepared and tested for non-UV germicidal activity without using UV. It was tested using model microorganisms such as Bakers Yeast (Saccharomyces cerevisiae), Bacillus subtilis, Pseudomonas putida, and Escherichia coli. On the basis of the germicidal activity of catalyst and the degree of damage caused to the cells, the stained cells may appear green (viable), green with red or yellow nuclei and yellow (compromised) or red (nonviable). According to their stained color, cells were counted to calculate the percentage of dead, live, and compromised cells. Compromised cells are cells that grow very slowly after reculturing indicating a degree of reversible cell damage. Screening the germicidal activity using this staining method is accurate and efficient, and requires less time than the culture-based method. A modification to the procedure for measuring germicidal activity of rough surfaces or fibrous coatings was developed. Both TiO2 and metal-doped TiO2 (Ag, Pt, Au, Cu) possess non-UV based germicidal activity. The germicidal activity of TiO2 was found to be related with its wetting property and can be improved by UV irradiation before testing. It is not greatly affected by contact time, indicating a fast acting germicidal activity.

Two MCM-41 derived adsorbents have been tailor-made for the separation of silver and copper ions using the hard-soft, acid-base (HSAB) principle as the design guideline. NH2-MCM-41 containing "hard" Lewis base adsorption sites (i.e., RNH2) was prepared for the adsorption of the "hard" Lewis acid, Cu2+, and SH-MCM-41 with a grafted "soft" thiolpropyl base was prepared for the selective removal of Ag+, a "soft" Lewis acid. Single- and binary-component adsorption studies were conducted at different metal concentrations, solution compositions, and pH values. The experimental results showed that SH-MCM-41 has excellent affinity and capacity for silver adsorption and adsorbed only the silver ions with copper remaining in the solution. The selectivity was not affected by the metal concentration and composition, anion, and pH. Under similar experimental conditions, NH2-MCM-41 selectively adsorbed copper from the binary solution. The selectivity of NH2-MCM-41 remained for the copper at different pH values, although the adsorption capacity diminished at lower pH values. The type of anions used affected copper adsorption on NH2-MCM-41 with an increased copper uptake in the presence of the sulfate ions. A simple Freundlich adsorption model was sufficient to describe metal adsorption on SH-MCM-41 and NH2-MCM-41, and the LeVan and Vermeulen model was successfully used to predict the adsorption capacity and selectivity for binary-component adsorptions.

Gold-selective adsorbents were prepared from mesoporous MCM-41 silica by grafting organic amine groups (i.e., RNH2, R2NH, and R3N; R=propyl). NH2-MCM-41, NRH-MCM-41, and NR2-MCM-41 displayed strong affinity for gold and at 1 mmol/g loading adsorbed 0.40, 0.33, and 0.20 mmol/g of gold. Copper and nickel were not adsorbed on these adsorbents. Grafting surface chemical moieties introduces heterogeneity on an otherwise uniform MCM-41 pore surface and metal adsorption is best described by the Freundlich adsorption model. A series of binary adsorption equilibrium studies with NH2-MCM-41 containing 2.2 mmol RNH2/g shows that NH2-MCM-41 adsorbs only gold from solutions containing copper and nickel with an adsorption capacity of 0.6 mol of Au/mol of RNH2 (1.1 mmol of Au/g of NH2-MCM-41). Copper and nickel were not adsorbed by NH2-MCM-41 regardless of the solution concentration, composition, and pH (i.e., 2 to 4) in the presence of gold. The LeVan and Vermeulen adsorption model based on a single component Freundlich isotherm and corrected for the anion effect accurately predicted the binary adsorptions. The adsorbed gold was completely recovered by a simple acid wash and the recovered gold solution is 99% pure. The regenerated NH2-MCM-41 remained 100% selective for gold removal and exhibited the same adsorption capacity even after several uses.

A facile method was established using composition-gradient pattern on zeolite surface to guide the deposition and formation of chemical and biomolecular patterns with features as small as five microns.

This review discusses the recent progress in the application of scanning probe microscopy (SPM) in catalysis. SPM proves to be an invaluable technique for imaging catalytic surfaces and interfaces. Most SPM research is related to the structural and morphological transformation associated with catalyst preparation and use. Real-time SPM observation of surface dynamics including adsorption, diffusion and reaction, provides invaluable insights to the mechanism of catalysis. SPM is also used to shape and manipulate surfaces and surface processes. Fabrication of nanostructured catalysts, direct manipulation of adsorbed atoms and molecules and tip-mediated reactions are some examples of new SPM approach in catalyst research.

Free-standing silicalite-1 (Sil-1) zeolite micromembranes have been successfully fabricated onto silicon substrate. Gas permeation test using permanent gases (i.e., helium, hydrogen, argon and nitrogen) and hydrocarbons (i.e., methane and n-butane) indicates that the micromembranes have excellent permeance flux and high permselectivity.

A multi-channel membrane microreactor was fabricated and tested for Knoevenagel condensation of benzaldehyde and ethyl cyanoacetate using Cs-exchanged faujasite NaX as the catalyst; the membrane microreactor achieves supra-eqiulibrium conversion at higher product purity.

Using a new fabrication strategy, novel, self-enclosed microporous silicalite-1 zeolite microtunnel and microchunnel architectures were successfully prepared.

A zeolite-based microengineered reactor was fabricated and tested for 1-pentene epoxidation over titanium silicalite-1 (TS-1) catalyst, which has been selectively incorporated within the microreactor channel using a new synthesis procedure.