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121.
NH3-NO/NO2 SCR for diesel exhausts after treatment: mechanism and modelling of a catalytic converter
Nova Isabella Ciardelli Cristian Tronconi Enrico Chatterjee Daniel Weibel Michel 《Topics in Catalysis》2007,42(1-4):43-46
We review herein the key mechanistic and kinetic features of the reactions involved in the NH3-NO/NO2 SCR system investigated by dynamic reactive experiments over a V-based commercial powdered catalyst, eventually leading to
the proposal of an original redox scheme which accounts for stoichiometry, selectivity and intrinsic kinetics of the global
SCR process. 相似文献
122.
This work was undertaken to discuss in depth the vital differences in the morphological development during synthesis, and properties of starch‐g‐poly‐(vinyl acetate) copolymers using two different initiators, potassium persulfate (KPS) and ceric ammonium nitrate (CAN). KPS‐initiated system gave relatively low values of grafting ratio and grafting efficiency, indicating a great tendency for the formation of poly(vinyl acetate) homopolymer (PVAc). Yet, higher values were seen for the CAN‐initiated system. Transmission electron microscope observations indicated a relatively broad distribution of latex particles for the KPS‐initiated system. The surface potential of latex particles was about ?3.5 mV, which turned out to be insufficient to maintain stability of latex particles. On the other hand, a uniform particle size distribution was found for the CAN‐initiated system, as the surface potential of latex particles was 21.5 mV. Moreover, radicals on starch molecules were generated directly through a redox reaction with positively charged ceric ion. The hydrophobic PVAc chains were thus grafted on starch, resulting in an amphiphilic graft copolymer, which provides a sufficient stabilization degree as a role of surfactant to render a relatively uniform distribution of latex particles. The synthesized starch‐g‐poly(vinyl acetate) copolymers were further converted to starch‐g‐poly(vinyl alcohol) through saponification, which were subjected to evaluations regarding the biodegradation and cell culture capability. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 3017–3027, 2006 相似文献
123.
Studies were undertaken on the isolation and identification of reaction products of ammonium nitrate phosphate (ANP) fertilizers containing 30, 50 and 70 per cent water-soluble phosphorus (WSP) of total phosphorus in representative soils of the vertisol, oxisol, alfisol, entisol, mollisol and aridisol groups of India. ANP fertilizers were applied in solid form to soil, and reaction products formed at and around the site of ANP fertilizer placement were identified after six weeks incubation in moist soils by X-ray diffraction technique. DCPD (dicalcium phosphate dihydrate- CaHPO4 · 2H2O) was the major reaction product of ANP fertilizers containing 30 and 50 per cent WSP in vertisol, entisol, aridisol, mollisol, oxisol and alfisol, and of ANP containing 70 per cent WSP in vertisol, entisol, alfisol, aridisol and mollisol. DCP (dicalcium phosphate-CaHPO4) was detected with ANP of 30 and 50 per cent WSP in the vertisol, alfisol, entisol, mollisol and aridisol groups of soils. In addition to DCPD, FePO4 · 2H2O (metastrengite) and AlPO4 · 2H2 O-monoclinic (metavariscite) were formed in alfisol and oxisol soils with ANP of 30 and 50 per cent WSP. FePO4 · 2H2O and AlPO4 · 2H2O (metavariscite) were identified in alfisol and oxisol soils while AlPO4 · 2H2O-orthorhombic (variscite) was formed in alfisol soils with ANP of 70 per cent WSP. 相似文献
124.
Zucong Cai 《Nutrient Cycling in Agroecosystems》2002,63(2-3):267-274
Coupled nitrification and denitrification is considered as one of the main pathways of nitrogen losses in paddy soils. The effect of NO3
– on NH4
+ transformation was investigated by using the 15N technique. The paddy soils were collected from Wuxi (soil pH 5.84) and Yingtan (soil pH 5.02), China. The soils were added with either urea (18.57 mol urea-N enriched with 60 atom% 15N excess) plus 2.14 mol KNO3-N (natural abundance) per gram soil (U+NO3) or urea alone (U). The KNO3 was added 6 days after urea addition. The incubation was carried out under flooded condition in either air or N2 gas headspace at 25°C. The results showed that in air headspace, 15NH4
+ oxidization was so fast that about 10% and 8% of added 15N in the treatment U could be oxidized during the incubation period of 73 hours after KNO3 addition in Wuxi and Yingtan soil, respectively. The addition of KNO3 significantly inhibited 15NH4
+ oxidation (p<0.01) in air headspace, while it stimulated 15NH4
+ oxidation in N2 gas headspace, although the oxidation was depressed by the N2 gas headspace itself. Therefore, the accumulation of NO3
– would inhibit further nitrification of NH4
+ at micro-aerobic sites in paddy soils, especially in paddy soils with a low denitrification rate. On the other hand, NO3
– would lead to oxidation of NH4
+in anaerobic bulk soils. 相似文献
125.
2,3-环氧丙磺酸钠的合成及应用进展 总被引:7,自引:0,他引:7
综述了3 氯 2 羟基丙磺酸钠和2,3 环氧丙磺酸钠的合成及其在功能材料方面的应用。由环氧氯丙烷与亚硫酸氢钠反应可以生成3 氯 2 羟基丙磺酸钠,再由3 氯 2 羟基丙磺酸钠在碱性溶液中闭环生成2,3 环氧丙磺酸钠。2,3 环氧丙磺酸钠因其分子结构中既含有环氧基,又含有亲水性的磺酸盐基团,可通过环氧基的开环反应和共聚反应等制备许多性能优异的功能物质如:胶凝化剂、稠化剂、乳化剂、光敏材料、印染保护剂等。 相似文献
126.
127.
128.
《Journal of Great Lakes research》2022,48(1):24-36
In Ontario, there is limited comprehensive research regarding the contribution of chloride in groundwater to surface water systems. The delivery of chloride via groundwater can contribute to the degradation of the Great Lakes and their tributaries. Thus, this review intends to fill or identify knowledge gaps regarding assessing groundwater as a potential source of road salt, the single largest use of salt in urban cold region environments, contamination to surface water by synthesizing existing groundwater chloride research in the Lake Ontario Basin. Knowledge regarding source characterization, properties, pathways, and impacts of chloride in the environment is essential to evaluate the contribution of chloride via groundwater. Past groundwater chloride research in the basin is primarily concentrated in highly urbanized areas and has identified localized trends of increasing groundwater chloride concentrations in these regions; however, few investigations have been conducted in varying land uses (e.g., rural or less urbanized watersheds) or at sufficient temporal and/or spatial scales. Significant chloride accumulation is occurring in watersheds and aquifers within the basin. Concentrations are expected to increase until equilibrium is obtained, thus resulting in sustained yearlong elevated concentrations in tributaries. Recently, chloride loading to Lake Ontario has increased significantly, with groundwater inputs having the potential to support long-term increases in chloride concentrations in the lake. However, few studies have evaluated the explicit contribution via groundwater to Lake Ontario, and therefore a knowledge gap continues to exist. We provide a synthesis of additional research priorities to better understand the magnitude of groundwater chloride issues in the basin. 相似文献
129.
分子内敏化鎓盐的合成及光敏性研究 总被引:3,自引:0,他引:3
二芳基碘鎓盐和三芳基硫鎓盐是阳离子聚合的光引发剂和光敏产酸物,但他们在300nm以上的光吸收很低,限制了对紫外光的利用效率。为解决此问题,本文合成了一些新的碘鎓盐和硫鎓盐,并用凝胶时间方法考察了它们的光引发效率。实验结果表明,2-苯硫基甲基,2′,4′-二甲基二苯碘鎓盐和9-蒽丙基,二苯基硫鎓盐具有特别高的光引发效率,这归之于光照时这些鎓盐发生了分子内电荷转移反应,即发生了分子内敏化。9-蒽丙基二苯硫鎓盐分子中的蒽基(An)是电子给体也是敏化基团,光照时可发生如下反应: 相似文献
130.
The hexane-soluble fractions of hydroliquefied products from three Yallourn brown coal lithotypes have been separated into five fractions by combined silica-alumina packed column chromatography. Analyses of various fractions by g.c.-m.s. permitted the identification of ≈50 components in the saturate fraction and 40 components in the diaromatic fraction, together with 30 components in the monoaromatics. The components identified were quite similar among hexane-soluble portions of all three lithotypes. A marked predominance of even carbon number alkane (C23-C29) was observed in the hydrocarbon fractions from pale lithotype over , and medium light lithotype over both pure ZnCl2 and . However, medium dark lithotype over both melt catalysts produced a saturate fraction with an odd carbon number(C22-C28) preference. Based on spectral methods, Soxhlet extracts obtained from untreated lithotypes (hexane and benzene solubles) were characterized as complex mixtures of higher molecular weight(300–1000) aliphatic hydrocarbons, which were supposed to be a precursor of the saturates produced from the corresponding lithotype in the catalytic hydroliquefaction. 相似文献