青岛理工大学安全工程专业实验室建设探讨

安全工程专业的学科建设离不开安全实验室的建设,就青岛理工大学的安全工程专业实验室建设进行了探讨.从实验室建设的重要地位入手,结合安全工程的专业课程设置情况,提出了安全工程实验室应设置的实验内容.     

Reorienting Systematic Conservation Assessment for Effective Conservation Planning

Abstract: Systematic conservation assessment (an information‐gathering and prioritization process used to select the spatial foci of conservation initiatives) is often considered vital to conservation‐planning efforts, yet published assessments have rarely resulted in conservation action. Conservation assessments may lead more directly to effective conservation action if they are reoriented to inform conservation decisions. Toward this goal, we evaluated the relative priority for conservation of 7 sites proposed for the first forest reserves in the Union of the Comoros, an area with high levels of endemism and rapidly changing land uses in the western Indian Ocean. Through the analysis of 30 indicator variables measured at forest sites and nearby villages, we assessed 3 prioritization criteria at each site: conservation value, threat to loss of biological diversity from human activity, and feasibility of reserve establishment. Our results indicated 2 sites, Yiméré and Hassera‐Ndrengé, were priorities for conservation action. Our approach also informed the development of an implementation strategy and enabled an evaluation of previously unexplored relations among prioritization criteria. Our experience suggests that steps taken to ensure the closer involvement of practitioners, include a broader range of social data, encourage stakeholder participation, and consider the feasibility of conservation action can improve the relevance of assessments for conservation planning, strengthen the scientific basis for conservation decisions, and result in a more realistic evaluation of conservation alternatives.     

AHP-SWOT法在城市圈建设中耕地保护策略分析中的应用——以湖北赤壁为例

在实地调研湖北赤壁的基础上,探讨AHP-SWOT法在城市圈建设过程中的耕地保护策略分析中的应用.结果表明,耕地异地占补平衡是主要优势,耕地数量持续减少是主要劣势,新一轮土地利用总体规划是主要机遇,城市圈建设占用耕地是主要威胁,建议赤壁市在城市圈建设过程中应发挥耕地异地占补平衡优势,回避城市圈建设占用耕地的威胁.     

Novel imazethapyr detoxification applying advanced oxidation processes

Different degradation methods have been applied to assess the suitability of advanced oxidation process (AOPs) to promote mineralization of imazethapyr [(RS)-5-ethyl-2-(4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)nicotinic acid], a widely used imidazolinone class herbicide, the persistence of which has been demonstrated in surface and ground waters destined to human uses. Independent of the oxidation process assessed, the decomposition of imazethapyr always followed a pseudo-first order kinetic. The direct UV-irradiation (UV) of the herbicide as well as its oxidation with ozone (O?), and hydrogen peroxide tied to UV-irradiation (H?O?/UV) were sufficiently slow to permit the identification of intermediate products, the formation pathway of which has been proposed. Ozonation joined to UV-irradiation (O?/UV), ozonation joined to titanium dioxide photo-catalysis (TiO?/UV+O?), sole photo-catalysis (TiO?/UV), and photo-catalysis reinforced with hydrogen peroxide-oxidation (TiO?/UV+H?O?) were characterized by a faster degradation and rapid formation of a lot of small molecules, which were quickly degraded to complete mineralization. The most effective oxidation methods were those using titanium dioxide photo-catalysis enhanced either by ozonation or hydrogen peroxide. Most of all, these last processes were useful to avoid the development of dangerous by-products.     

Surface retention and photochemical reactivity of the diphenylether herbicide oxyfluorfen

The photochemical behavior of oxyfluorfen [2-chloro-1-(3-etoxy-4-nitrophenoxy)-4-(trifluoromethyl) benzene] on two Greek soils was investigated. Soils were sampled from Nea Malgara and Preveza regions, characterized by a different organic matter content. Soils were spiked with the diphenyl-ether herbicide and irradiation experiments were performed either in the laboratory with a solar simulator (xenon lamp) or outside, under natural sunlight irradiation; other soil samples were kept in the dark to control the retention reaction. Kinetic parameters of both retention and photochemical reactions were calculated using zero-, first- and second- (Langmuir-Hinshelwood) order equations, and best fit was checked through statistical analysis. The soil behaviors were qualitatively similar but quantitatively different, with the soil sampled from the Nea Malgara region much more sorbent as compared with Preveza soil. All studied reactions followed second-order kinetics and photochemical reactions were influenced by retaining capability of the soils. The contributions of the photochemical processes to the global dissipation rates were also calculated. Two main metabolites were identified as 2-chloro-1-(3-ethoxy-4-hydroxyphenoxy)-4-(trifluoromethyl)benzene and 2-chloro-1- (3-hydroxy-4-nitrophenoxy)-4-(trifluoromethyl)benzene.     

Photochemistry and photoinduced toxicity of acifluorfen, a diphenyl-ether herbicide

Photochemistry studies can be helpful in assessing the environmental fate of chemicals. Photochemical reactions lead to the formation of by-products that can exhibit different toxicological properties from the original compound. For this reason the photochemical behavior of the herbicide acifluorfen (5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoic acid) in the presence of different solvents was studied. Photochemical reactions were carried out using a high-pressure mercury arc and a solar simulator. Kinetic parameters and quantum yields were determined. The identification of photoproducts was performed by mass spectrometry and [1H] nuclear magnetic resonance (NMR). Nitrofluorfen, hydroxy-nitrofluorfen, 2-chloro-4-(trifluoromethyl)phenol, 5-trifluoromethyl-5'-nitrodibenzofuran, and other derivatives were identified. The photochemical reactions were also carried out in the presence of either a singlet or a triplet quencher, and in the presence of either a radical initiator or a radical inhibitor. Substances used as inhibitors of the excited levels T1 and S1 showed that photodegradation of acifluorfen begins from a singlet state S1 through a pi,pi* transition. The role of free radicals in the photodegradation of acifluorfen was determined and a radical mechanism was proposed. Toxicity tests against Daphnia magna Strauss showed that acifluorfen was not toxic at a concentration of 0.1 mM; however, photoproducts formed after 36 h of UV exposure of the herbicide induced a remarkable toxicity to the test organism.     

Density and Viscosity Measurements of Natural Solutions

Utilizing sophisticated equipment, densimetric and viscosimetric measurements were carried out on samples of ground-waters of Apulia.

Experimental data, utilized to check if simple equations can evaluate the density and the viscosity of multicomponent solutions, confirm the validity of the hypothesis.     

Influence of humic fractions on retention of isoproturon residues in two Moroccan soils

The influence of different fractions of soil organic matter on the retention of the herbicide isoproturon (IPU) has been evaluated. Water and methanol extractable residues of (14)C labeled isoproturon have been determined in two Moroccan soils by beta -counting-liquid chromatography. The quantification of bound residues in soil and in different fractions of soil humic substances has been performed using pyrolysis/scintillation-detected gas-chromatography. Microbial mineralization of the herbicide and soil organic matter has been also monitored. Retention of isoproturon residues after 30-days incubation ranged from 22% to 32% (non-extractable fraction). The radioactivity extracted in an aqueous environment was from 20% to 33% of the amount used for the treatment; meanwhile, methanol was able to extract another 48%. Both soils showed quantities of bound residues into the humin fraction higher than humic and fulvic acids. The total amount of residues retained into the organic matter of the soils was about 65 % of non-extractable fraction, and this percentage did not change with incubation time; on the contrary, the sorption rate of the retention reaction is mostly influenced by the clay fraction and organic content of the soil. Only a little part of the herbicide was mineralized during the experimental time.     

生物炭与土壤调理剂对滨海荒芜重盐碱地的改良效应

以土壤改良剂对荒芜重盐碱地生物改良和开发利用为研究目标,在华北低平原区滨海荒芜重盐碱地开展了施用生物炭（B）和调理剂（C）种植先锋作物油葵的大田试验.生物炭用量设2个水平（0和1.25 kg ·m^-2）调理剂施用量设3个水平,分别为0、0.83和1.66 kg ·m^-2,共6个处理.油葵收获后按照每30 cm一层采至90 cm搜集土样.结果表明,施用生物炭提高0~30 cm和60~90 cm土层含盐量,而土壤调理剂则显著降低0~30 cm土壤含盐量.没有发现生物炭或调理剂对土壤pH有显著影响.生物炭处理显著抑制土壤硝化作用,导致0~90 cm土层NO₃^--N含量显著下降,NH₄⁺-N含量提高,对有机质（SOM）含量没有显著影响.施用土壤调理剂提高0~30 cm土壤SOM含量,调理剂施用量为1.66 kg ·m^-2时0~90 cm土层的NO₃^--N含量显著增加.单施生物炭与调理剂或者二者组合均显著增加0~90 cm土壤NH₄⁺-N含量、有效磷（Olsen-P）含量和有效钾（K_ex）含量,但生物炭对这3种养分含量的提升效果更显著,土壤调理剂则在增加0~30 cm土壤有机质和降盐方面更有效.施用高量调理剂促进土壤硝化作用,而施用生物炭恰恰起到硝化抑制剂的作用,因此,将生物炭与土壤调理剂结合施用,是滨海荒芜重盐碱地防止NO₃^--N淋失、减少环境污染、增肥降盐并保障耐盐先锋作物高肥低盐生长环境的有效措施.