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1.
Gary Bridge 《Geoforum》2008,39(4):1570-1584
This paper explores the radical possibilities of pragmatism for geography using the illustration of arguments concerning a renewed (urban) public realm through the exchange of validity claims in communication. Pressing further the pragmatist possibilities of Habermas’s idea of communicative action it draws on John Dewey’s work, and a range of contemporary pragmatist philosophers, to consider human communicability in its widest sense. This is then explored using an example of the spatiality and performativity of body-minds in a range of communicative spaces of the city. Then the paper moves on to consider the radical implications of pragmatism for geography in general in terms of body-mind/environment relations; a transactional view of space; experience, rationality and radical democracy. 相似文献
2.
Fourier-based multi-scale representation and progressive transmission of cartographic curves on the internet 总被引：1，自引：0，他引：1
ABSTRACTAutomatic generation of multi-scale representations from the same spatial data source has been the research focus in map generalization for a long time. Based on the Fourier technique, this paper proposes a continuous, multi-scale representation model for progressive transformation of cartographic curves on the Internet. In our method, all the curves, whether closed or open, are depicted as periodical functions which are further expressed as Fourier series. The convergence degrees of the Fourier series are explored for different kinds of curves, and truncating frequencies are derived based on the similarity between the original and reconstructed curves. Using information theory and the Radical Law in cartography, the relationship between map scales and Fourier frequencies is established. Based on the proposed multi-scale model, we also introduce the principles and implementation of a progressive transmission method. Our method is evaluated using the contours from a topographic map. The results show that our model is a valid approach to multi-scale representation of cartographic curves. 相似文献
3.
A recent article (Said-Ahmad, W., Amrani, A., Aizenshtat, Z., 2013. The action of elemental sulfur plus water on 1-octene at low temperatures. Organic Geochemistry 59, 82–86) is commented on in this discussion. Radical mechanisms proposed by Said-Ahmad et al. (2013) for the formation of sulfurized and oxidized organic compounds in experiments involving elemental sulfur and 1-octene under aqueous conditions, aimed at investigating the interaction of organic matter and sulfur compounds under geological conditions, are not compatible with their experimental results and other studies. In addition, results from the experiments aimed at demonstrating the role of HO radicals in the formation of oxidized organic compounds were incorrectly interpreted by the authors. In this discussion, alternative mechanisms for the formation of the sulfurized and oxygenated products reported by Said-Ahmad et al. (2013) are proposed. 相似文献
4.
The photochemical oxidation of SO2 in the presence of NO and C3H6 was studied in a 18.2 liter pyrex reactor. When light intensity, irradiation time and SO2 concentration were constant, SO4
2- concentration, derived from the total volume of aerosol produced, peaked when [C3H6]/[NO] was approximately 6.0. Another increase im SO4
2- formation was reached at very high ratios (>50). The experimental observations are consistent with the two SO2 oxidation mechanisms. At low [C3H6]/[NO] ratios, the processes proceed via the HO–SO2 reaction, while at high ratios the O3–C3H6 adduct is assumed to oxidize SO2 to produce SO4
2- aerosols. 相似文献
5.
塞尔维亚贾达尔盆地超大型锂硼矿床 总被引：11，自引：0，他引：11
锂和硼有着广泛的用途,我国常年大量进口锂和硼矿石。近些年在塞尔维亚贾达尔盆地中发现一个特殊的超大型锂硼矿床,与Rio Tinto、Pan Global Resources和Ultra Lithium等公司一样,我国地勘单位正在这一矿区进行勘查工作,因此对该地区的锂硼矿床地质特征进行总结和报道很有必要。该矿床的矿石矿物是世界独有的既含锂也含硼的羟硼硅钠锂石(Jadarite)[LiNaSiB_3O_7(OH)],其含B_2O_3 47.2%,含Li_2O 7.3%,密度2.46g/cm~3。已有资料显示,找矿标志层为中新统湖相沉积岩中的凝灰岩层,矿体具有电阻率小于4.4Ω·m和重力异常值小于-15mGal的特征。该矿床设施齐全,且选矿和化工处理简便,短期内可获得硼和锂产品。 相似文献
6.
Hydroxyl radicals, generated radiolytically in N2O/O2‐saturated solutions, yield in their reaction with atrazine equal amounts of deethylatrazine and acetaldehyde (40% of OH radical yield) and deisopropylatrazine and acetone (16%), respectively. The precursors of deethylatrazine and acetaldehyde is their Schiff base which hydrolyzes slowly (OH–‐catalyzed: k = 5.2 dm3 mol–1 s–1). The hydrolysis of the Schiff base of deisopropylatrazine and acetone is too fast to be detected. In a pulse radiolysis experiment, the intermediate formed upon OH‐radical attack (k = 3·109 dm3 mol–1 s–1) has a strong absorption at 440 nm. It decays in the presence of oxygen (k = 1.3·109 dm3 mol–1 s–1), and upon deprotonation [pKa(peroxyl radicals) ≈ 10.5] the peroxyl radicals thus‐formed eliminate superoxide radicals (k = 2.9·105 s–1). s‐Triazine itself reacts much more slowly with OH radicals (k = 9.7·107 dm3 mol–1 s–1). This can explain, why in the case of atrazine in comparison to other aromatic compounds, e.g. toluene, the addition of the OH radical to the ring (estimated at ca. 40%) is of relatively little importance as compared to an H‐abstraction from (activated) positions of the side groups. 相似文献
7.
Results from kinetic laboratory studies of reactions of the carbonate radical anion (CO3–·) with aromatic compounds in aqueous solution at T = 298 K are presented. Data were obtained in using a laser photolysis laser long-path absorption (LP-LPLA) apparatus which was designed for direct time-resolved studies of radical reactions. For the reactions of CO3–· with hydroquinone dimethyl ether (2), methyl anisole (3), benzene (4), p-xylene (5), toluene (6), chlorobenzene (7), nitrobenzene (8), and benzonitrile (9), rate coefficients of k2 = (3.0 ± 0.6)·107 M–1 s–1, k3 = (9.7 ± 1.7)·105 M–1 s–1, k4 = (3.2 ± 0.7)·105 M–1 s–1, k5 = (3.8 ± 0.9)·104 M–1 s–1, k6 = (6.8 ± 2.3)·104 M–1 s–1, k7 = (2.7 ± 0.6)·105 M–1 s–1, k8 = (1.4 ± 0.5)·104 M–1 s–1, and k9 < 1.3·102 M–1 s–1 were obtained. In further studies the effect of temperature on the reactions (2), (4), and (5) has been studied. The kinetic data obtained for the reaction of the carbonate radical anion with aromatic compounds were compared to the corresponding reactions of the hydroxyl radical. Finally, these kinetic data were used within a simple model system to investigate the implications of carbonate radical anion kinetics within water treatment processes. It is shown that the degradation of organic pollutants in ·OH-radical based water treatment may proceed via the CO3–·/HCO3· radical under certain conditions. 相似文献
8.
对凡纳滨对虾注射浓度为1×105、1×106、1×107mL-1的溶藻弧菌悬液,在注射后4、12、24、48、72和120 h于腹血窦取血,测定其血清中一氧化氮(NO)、丙二醛(MDA)含量,以及一氧化氮合酶(NOS)、超氧化物岐化酶(SOD)活力。结果表明,注射溶藻弧菌后,凡纳滨对虾血清中NO含量及NOS活力显著高于对照组,且NOS活力最大值出现时间较NO早;而SOD活力先升高后下降,MDA含量在SOD活力开始下降后逐渐升高,说明一氧化氮系统对凡纳滨对虾感染的溶藻弧菌有清除作用,并能在一定程度上对损伤过程中生成的氧自由基产生作用。 相似文献
9.
A series of indoor air quality parameters were determined in two medieval churches, in Cyprus (temperature, relative humidity,
total and UV solar radiation, CO2 indoors and O3, NO, NO2
*, HNO3
*, HCl, HCOOH, CH3COOH indoors and outdoors). These data were used as input in a validated indoor air quality model to predict indoor air pollutant
source strengths and species concentrations that resulted from dark or photochemical reactions. The NO and NO2 emission rates due to the burning of incense or candles were estimated. Model results revealed that heterogeneous NO formation
takes place simultaneously with the heterogeneous HONO formation. Also, model application has shown that indoor NOx emissions resulted in decreased free radical concentrations, in contrast to the organic compound emissions, which increased
free radical concentrations. This effect of indoor emissions on indoor radicals can partly explain the indoor enhancement/depression
of indoor gaseous acid formation. 相似文献
10.
Hydrophilic xenobiotics can be eliminated in the UV/H2O2-process. The oxidation in this process is enhanced by the photolytically generated HO radicals. Bicarbonate is able to scavenge HO radicals. So it was expected that the degradation rates of the investigated xenobiotics were affected by the influence of bicarbonate. In contrast to the widely described decrease of the degradation rate, a much more complex situation was found in this investigation. The degradation rates of 2-amino-1-naphthalenesulfonate and diphenyl-4-sulfonate were decreased and reached for high concentrations of bicarbonate the values of the photolytical degradation rate. The degradation of 4,4′-diaminostilbene-2,2′-disulfonate was accelerated significantly in the presence of bicarbonate. The degradation rate of EDTA was increased at small concentrations of bicarbonate and decreased at higher concentrations. 相似文献