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.     

Structure characterization and thermal stabilities of the isomers of the brominated flame retardant 1,2-dibromo-4-(1,2-dibromoethyl)cyclohexane

1,2-Dibromo-4-(1,2-dibromoethyl)cyclohexane (TBECH) is used primarily as an additive flame retardant. 1H NMR spectroscopy and an X-ray structure determination have revealed that a technical mixture consists largely of two (of the four possible) diastereomers, rac-(1R,2R)-1,2-dibromo-(4S)-4-((1S)-1,2-dibromoethyl)cyclohexane (alpha-TBECH) and rac-(1R,2R)-1,2-dibromo-(4S)-4-((1R)-1,2-dibromoethyl)cyclohexane (beta-TBECH), in a mole ratio of approximately 1:1. The two other possible isomers, gamma- and delta-TBECH, were not detected in a technical mixture. The TBECH isomers are thermally sensitive and can easily interconvert at temperatures of 125 degrees C. A thermal equilibrium mixture of alpha-, beta-, gamma- and delta-TBECH consists of approximately 33%, 33%, 17% and 17% of these isomers, respectively. Separation of all four TBECH diastereomers, with minimal thermal interconversion of the isomers, was achieved by careful selection of GC-capillary column length and injector temperature. Although technical TBECH does not contain the gamma- and delta-isomers, they may still be relevant environmental contaminants since manufacturing processes utilize thermal processes which may induce their formation.     

Structure elucidation of four possible biogenic organohalogens using isotope exchange mass spectrometry

The molecular structures of four unknown bioaccumulating halogenated compounds, C10H6N2Br3Cl3, C10H6N2Br4Cl2, C10H6N2Br5Cl, and C10H6N2Br6 were characterized using isotope exchange positive chemical ionization (IE-PCI) mass spectrometry (MS) and identified by comparison to synthesized standards. NH3 and ND3 were used as reagent gases for the IE-PCI-MS experiment. The shift in mass of the quasimolecular ion between the NH3 and ND3 PCI obtained spectra indicated the number of exchangeable hydrogens attached to the two nitrogen atoms in C10H6N2Br4Cl2, and thus the type of amines present (primary, secondary, or tertiary). 19 compounds (13 amines of varying degree of substitution; six containing no nitrogen) were used as reference compounds and controls in the experiment to validate the IE-PCI technique. The results of the IE-PCI-MS indicated the presence of two tertiary amine functional groups. The molecular structures of the four hexahalogenated compounds were then proposed to be 1,1'-dimethyl-3,3',4,-tribromo-4',5,5'-trichloro-2,2'-bipyrrole, 1,1'-dimethyl-3,3',4,4'-tetrabromo-5,5'-dichloro-2,2'-bipyrrole, 1,1'-dimethyl-3,3',4,4',5-pentabromo-5'-chloro-2,2'-bipyrrole, and 1,1'-dimethyl-3,3',4,4',5,5'-hexabromo-2,2'-bipyrrole and subsequently synthesized. Comparison of retention times and electron capture negative ionization (ECNI) full scans on various gas chromatography (GC) columns between the synthesized bipyrroles and the corresponding unknown compounds in biota indicated that three of the unknown compounds--possible marine natural products--were the proposed halogenated dimethyl bipyrroles. The placement of the halogen atoms on the fourth compound, C10H6N2Br3Cl3 could not be unequivocally determined since the synthesized standard could not be fully characterized.     

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.     

黄河包头段不同粒径沉积物分形校正下重金属的吸附研究

推导了分粒级的表面分形维数计算公式,根据推导公式计算了分粒级沉积物的分维值.应用已有的表面分形分维计算公式分别计算了黄河包头段沉积物整体的表面分形分维(1.91)及＜63 μm粒级的分维值(1.36),揭示出黄河水环境的磨蚀和分选2个原因引起黄河包头段沉积物低的分维值.用分形校正吸附模型、Freundlich和Langmuir吸附模型对黄河包头段重金属分粒级沉积物吸附进行了拟合,表明分形校正吸附模型具有较好的适用性,同时揭示分形校正吸附模型与MEA理论结合能更好的对热力学吸附结果进行描述;由吸附结果分析得出4种重金属因粒径引起的吸附量变化程度序列为Cu＞Pb＞Zn≈Cd,初始浓度高的吸附量曲线变化较初始浓度低的曲线变化明显,同时指出Cu、Pb的吸附主要与矿物组成有关,而Zn、Cd的吸附则与吸附剂沉积物空间几何性质(或沉积物表面物理特征)有关.     

Structural characterization and thermal stabilities of the isomers of the brominated flame retardant 1,2,5,6-tetrabromocyclooctane (TBCO)

1,2,5,6-Tetrabromocyclooctane (TBCO) is a commercial brominated flame retardant that is employed mainly as an additive in textiles, paints and plastics. Very little is known about its presence or behavior in the environment or its analysis. TBCO can exist as two diastereomers, the stereochemistries of which have not been previously reported. We have named the first eluting isomer, under HPLC conditions, as alpha-TBCO (α-TBCO) and the later eluting isomer as beta-TBCO (β-TBCO) when using an Acquity UPLC BEH C₁₈ column with methanol/acetonitrile/water as the mobile phase. The structural elucidation of these two isomers was accomplished by ¹H NMR spectroscopy, GC/MS, LC/MS and X-ray structure determinations. α-TBCO is (1R,2R,5S,6S)-1,2,5,6-tetrabromocyclooctane and β-TBCO is rac-(1R,2R,5R,6R)-1,2,5,6-tetrabromocyclooctane. As with some other brominated cycloaliphatic compounds, TBCO is thermally labile and the isomers easily interconvert. A thermal equilibrium mixture of α- and β-TBCO consists of approximately 15% and 85% of these isomers, respectively. Separation of the two diastereomers, with minimal thermal interconversion between them, is achievable by careful selection of GC-capillary column length and injector temperature. LC/MS analyses of TBCO also presents an analytical challenge due to poor resolution of the isomers on chromatographic stationary phases, and weak intensity of molecular ions (or major fragment ions) when using LC-ESI/MS. Only bromide ions were seen in the mass spectra. APCI and APPI also failed to produce the molecular ion with sufficient intensity for identification.     

Examination of the bioaccumulation of halogenated dimethyl bipyrroles in an Arctic marine food web using stable nitrogen isotope analysis.

Concentrations of four possibly naturally produced organohalogens--1,1'-dimethyl-3,3',4-tribromo-4,5,5'-trichloro-2,2'-bipyrrole (DBP-Br3Cl3), 1,1'-dimethyl-3,3',4,4'-tetrabromo-5,5'-dichloro-2,2'-bipyrrole (DBP-Br4Cl2), 1,1'-dimethyl-3,3',4,4',5-pentabromo-5'-chloro-2,2'-bipyrrole (DBP-Br5Cl) and 1,1'-dimethyl-3,3',4,4',5,5'-hexabromo-2,2'-bipyrrole (DBP-Br6)--were quantitated and the extent of their magnification through an entire Arctic marine food web [measured as integrated trophic magnification factors (TMFs)] were calculated. The food web consisted of three zooplankton species (Calanus hyperboreus, Mysis oculata, and Sagitta sp.), one fish species [Arctic cod (Boreogadus saida)], four seabird species [dovekie (Alle alle), black guillemot (Cepphus grylle), black-legged kittiwake (Rissa tridactyla), and glaucous gull (Larus hyperboreus)], and one marine mammal species [ringed seal (Phoca hispida)]. Trophic levels in the food web were calculated from ratios of stable isotopes of nitrogen (15N/14N). All halogenated dimethyl bipyrrole (HDBP) congeners were found to significantly (P<0.02) biomagnify, or increase in concentration with trophic level in the invertebrate--fish--seabird food web. DBP-Br4Cl2 (TMF= 14.6) was found to biomagnify to a greater extent than DBP-Br3Cl3 (TMF = 5.2), DBP-Br5Cl (TMF = 6.9), or DBP-Br6 (TMF = 7.0), even though the Kow of DBP-Br4CI2 was predicted to be lower than those of DBP-Br5Cl and DBP-Br6. None of the four HDBP congeners in ringed seals followed the general trend of increasing concentration with trophic level, which was possibly due to an ability of the seals to metabolize HDBPs.