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New particulate matter (PM) filtering technologies are needed to meet the emission regulations for small combustion appliances. In this work, we investigate the performance of a novel electrical particle filtration system, the single needle shielded corona charger (SCC), which offers an advantageous solution for PM control in boilers by enhancing particulate deposition within existing boiler sections. Experiments under different operating conditions of a wood-fired boiler were performed, wherein the SCC was installed upstream of either a condensing heat exchanger (CHX) or a cyclone. PM reduction was found to be strongly affected by the SCC temperature and the following collection surface area, and reached its highest reduction efficiency of >90% at the temperature range of 400–500 °C when operating in combination with a CHX. The SCC–cyclone combination was less efficient, providing a 27% PM reduction, as a result of the low surface area and residence time in the cyclone. These results indicate that the SCC can feasibly provide particle filtration when combined with a CHX, wet scrubber, or a cyclone to meet the new emission regulation requirements. The system is best suited for small-scale boilers but can be scaled up to larger boilers by increasing the number of corona chargers.

An awareness of increasing climate and health problems has driven the development of new functional and affordable soot-oxidation catalysts for stationary sources, such as fireplaces. In this study, Al(OH)3, water glass and acidic aluminium phosphate binder materials were mixed with soot-oxidation catalysts. The effect of the binder on the performance of the Ag/La-Al2O3 catalyst was examined, while the Pt/La-Al2O3 catalyst bound with Al(OH)3 was used as a reference. Soot was oxidised above 340 °C on the Ag/La-Al2O3 catalyst, but at 310 °C with same catalyst bound with Al(OH)3. The addition of water glass decreased the catalytic performance because large silver crystals and agglomeration resulted in a blockage of the support material’s pores. Pt/La-Al2O3 bound with Al(OH)3 was ineffective in a fireplace environment. We believe that AgOx is the active form of silver in the catalyst. Hence, Ag/La-Al2O3 was shown to be compatible with the Al(OH)3 binder as an effective catalyst for fireplace soot oxidation.

Exhaust gas aftertreatment systems play a key role in controlling transportation greenhouse gas emissions. Modern aftertreatment systems, often based on Pd metal supported on aluminum oxide, provide high catalytic activity but are vulnerable to sulfur poisoning due to formation of inactive sulfate species. This paper focuses on regeneration of Pd-based catalyst via the decomposition of alumina-supported aluminum and palladium sulfates existing both individually and in combination. Decomposition experiments were carried out under hydrogen (10% H2/Ar), helium (He), low oxygen (0.1% O2/He), and excess oxygen (10% O2/He). The structure and composition of the model catalysts were examined before and after the decomposition reactions via powder X-ray diffraction and elemental sulfur analysis. The study revealed that individual alumina-supported aluminum sulfate decomposed at a higher temperature compared to individual alumina-supported palladium sulfate. The simultaneous presence of aluminum and palladium sulfates on the alumina support decreased their decomposition temperatures and led to a higher amount of metallic palladium than in the corresponding case of individual supported palladium sulfate. From a fundamental point of view, the lowest decomposition temperature was achieved in the presence of hydrogen gas, which is the optimal decomposition atmosphere among the studied conditions. In summary, aluminum sulfate has a two-fold role in the regeneration of a catalyst—it decreases the Pd sulfate decomposition temperature and hinders re-oxidation of less-active metallic palladium to active palladium oxide.

Emission regulations and legislation inside the European Union (EU) have a target to reduce tailpipe emissions in the transportation sector. Exhaust gas aftertreatment systems play a key role in low emission vehicles, particularly when natural gas or bio-methane is used as the fuel. The main question for methane operating vehicles is the durability of the palladium-rich aftertreatment system. To improve the durability of the catalysts, a regeneration method involving an efficient removal of sulfur species needs to be developed and implemented on the vehicle. This paper tackles the topic and its issues from a fundamental point of view. This study showed that Al2(SO4)3 over Al2O3 support material inhibits re-oxidation of Pd to PdO, and thus hinders the formation of the low-temperature active phase, PdOx. The presence of Al2(SO4)3 increases light-off temperature, which may be due to a blocking of active sites. Overall, this study showed that research should also focus on support material development, not only active phase inspection. An active catalyst can always be developed, but the catalyst should have the ability to be regenerated.

Multilayered photocatalytic TiO2‐based coating was prepared by spin coating on a high‐density polyethylene (HDPE) substrate. The multilayered coating consisted of a polyurethane (PU) barrier layer and two layers of TiO2nanoparticles bound with PU. The adhesion between the HDPE substrate and protective PU coating was enhanced by oxygen plasma treatment of the substrate. The improved adhesion contributed to the photocatalytic degradation of palmitic acid. Long‐term activity of the photocatalytic coating in degradation of palmitic acid under UV illumination was followed by FTIR‐ATR. The catalytic activity of the coating was maintained in three identical cycles where palmitic acid was added and UV‐irradiated for 6 h. According to FTIR measurements, the palmitic acid was almost completely decomposed after 6 h, but gas chromatography (GC) analysis showed total decomposition to require 12 h UV illumination (∼ 97% of palmitic acid decomposed in 12 h). Study of the degradation of palmitic acid by GC as a function of time indicated that the degradation kinetics was pseudofirst order, and the rate constant obtained was 0.31 h−1. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011 [ABSTRACT FROM AUTHOR]

The effects of three plasticizers and two plasticizer concentrations on the topography and soiling of poly (vinyl chloride) (PVC) were studied. Palmitic acid and triolein were chosen to represent solid and liquid soils. The feasibility of using infrared spectroscopy to quantify the amount of soil on PVC was examined. The structure of the solid model soil on plasticized PVC was studied with optical microscopy and atomic force microscopy. Palmitic acid formed two different structures on the PVC surface. Both the type and concentration of the plasticizer influenced the structure of the oily soil on plasticized PVC. The wetting of plasticized PVC with the liquid oily soil was compared to wetting with water through the measurement of the contact angles. Plasticized PVC was hydrophobic and oleophilic. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007 [ABSTRACT FROM AUTHOR]

Atomic layer deposition (ALD) was used to deposit thin films of molybdenum nitride from a new precursor, bis(tert-butylimido)-bis(dimethylamido)molybdenum, and ammonia. The optimum ALD growth window was 260−300 °C and the maximum growth per cycle 0.5 Å. Deposition temperatures are lower than with the previously reported molybdenum pentachloride as the precursor. Molybdenum nitride was successfully deposited on silicon, electrochemically grown nickel, chromium, and quartz glass. Growth per cycle was maintained over substrate materials of different types. Conformality of the deposited films was as high as 98%. Films were mainly amorphous, containing small amounts of the -Mo2N phase. According to time-of-flight elastic recoil detection analysis (TOF-ERDA), the molybdenum−nitrogen ratio was close one. Together with X-ray diffraction data this suggests the existence of a nitrogen-rich amorphous phase in the film. [ABSTRACT FROM AUTHOR]

Extensive studies have been performed with the aim of fabricating hierarchical surface structures inspired by nature. However, synthetic hierarchical structures have to sacrifice mechanical resistance to functionality by introducing finer scaled structures. Therefore, surfaces are less durable. Surface micro–micro hierarchy has been proven to be effective in replacing micro–nano hierarchy in the sense of superhydrophobicity. However, less attention has been paid to the combined micro–micro hierarchies with surface pillars and pits incorporated together. The fabrication of this type of hierarchy may be less straightforward, with the possibility of being a complicated multi-step process. In this study, we present a simple yet mass producible fabrication method for hierarchical structures with different combinations of surface pillars and pits. The fabrication was based on only one aluminum (Al) mold with sequential mountings. The fabricated structures exhibit high mechanical durability and structural stabilities with a normal load up to 100 kg. In addition, the theoretical estimation of the wetting state shows a promising way of stabilizing a water droplet on the surface pit structures with a more stable Cassie–Baxter state. [ABSTRACT FROM AUTHOR]

The surface properties of materials can be modified by tailoring the topography and chemical composition. Functional surfaces with desirable properties have been produced by precisely controlled surface structures and chemical composition at the micro-nanometer scale. Until now, the challenge has been the ability to manipulate surface morphology and chemistry at the micro-millimeter scale. This work presents a new surface modification method capable of permitting subsequent structuring and material deposition. A micro tip patterning technique is based on sharp metal tips that are used for modifying the topography and chemistry of various material surfaces at the micro-millimeter scale. The method is appropriate for characterizing different topographies by probing conductive material surfaces with a needle tip, which permits a precisely controlled surface structuring with continuous 3D profiles. The desired locations of the scanned surface can be chemically modified by delivering materials via the needle tip. The method is appropriate for the multi-object placement of numerous substances such as functional reagents and biological components in a complex microenvironment. The accurate structuring of complex 3D surface topographies and subsequent chemical deposition provides a precisely controlled functionalization of material surface properties suitable for different applications. [ABSTRACT FROM AUTHOR]