Pd/mpg-C_3N_4催化剂的制备、表征及其对松香加氢反应的催化性能

以SiO_2和三聚氰胺为原料,通过高温焙烧法制得介孔类石墨相氮化碳(mpg-C_3N_4),以浸渍法负载Pd纳米粒子制得Pd/mpg-C_3N_4,并用于催化松香加氢反应。采用XRD、FT-IR、TEM、ICP-AES、XPS、氮气吸附-脱附及GC分析对催化剂的结构、形貌特征、Pd负载量、金属价态、比表面积和孔径以及催化活性进行分析。结果表明:Pd纳米粒子成功地均匀分散在了氮化碳的层状结构中,Pd的负载并没有改变mpg-C_3N_4的骨架结构,Pd/mpg-C_3N_4仍然保持着介孔结构;但是Pd的负载使mpg-C_3N_4的比表面积、孔容和孔径均有所减小,Pd/mpg-C_3N_4的比表面积、孔容和孔径分别为47.73 m^2/g、0.17 cm^3/g和3.39 nm。在负载量为7.96%,5 MPa H_2、150℃和反应4 h的松香催化加氢优化条件下制得去氢枞酸GC含量5.99%,枞酸GC含量小于1%的氢化松香产品(其中四氢枞酸为37.12%,二氢枞酸为56.71%)。催化剂Pd/mpg-C_3N_4重复使用4次后,四氢枞酸GC含量由37.12%下降至24.71%,去氢枞酸GC含量由5.99%上升至9.76%。     

Thromboelastographic tracings in retired racing greyhounds and in non-greyhound dogs

BACKGROUND: Bleeding disorders in patients with normal coagulation test results are frequently reported in Greyhounds. The purpose of this study was to compare Greyhounds to non-Greyhounds by thromboelastography (TEG). HYPOTHESIS: TEG parameters in Greyhounds are different from those in non-Greyhounds. ANIMALS: Forty-three healthy dogs (28 Greyhounds and 15 non-Greyhounds) based on the results of physical examination, CBC, activated partial thromboplastin time, prothrombin time, fibrinogen, and platelet count. MATERIALS AND METHODS: Recalcified citrated native TEGs were performed in both groups; data were compared using Student's, Mann-Whitney, and Pearson's statistical tests. RESULTS: In Greyhounds, mean +/- SD were as follows: R-time 4.3 +/- 1.7 minutes, K-time 3.8 +/- 1.4 minutes, angle (alpha) 50.0 +/- 8.0 degrees , maximum amplitude (MA) 47.6 +/- 5.6 mm, clot strength (G) 4,647 +/- 1,097 dyn/cm2, and percent lysis at 60 minutes (LY60) 2.8 +/- 5.0%. In the non-Greyhounds they were R-time 3.7 +/- 1.6 minutes, K-time 2.5 +/- 0.9 minutes, angle 59.8 +/- 7.0 degrees , MA 53.1 +/- 5.6 mm, G 5,811 +/- 1,256 dyn/cm2, and LY60 3.1 +/- 2.5%. All parameters were significantly different between the groups, except for R-time and LY60. CONCLUSION: In Greyhounds, clotting kinetics are slower and clot strength are weaker than in non-Greyhounds, supporting the increased tendency to bleed observed after minor trauma or surgical procedures in the breed. The findings may also be attributed to blood viscosity or to the concentration of citrate in the sample (ie, Greyhounds have higher hematocrit and less plasma per unit volume).     

天然沸石对猪场厌氧发酵液中氨氮吸附作用的试验研究

为达到利用人工湿地处理高氨氮污水的目的,采用天然沸石作为人工湿地基质,对比研究了天然沸石对NH4Cl溶液和猪场厌氧发酵液中氨氮的等温吸附特征、吸附动力学过程,考察了吸附时间、氨氮初始浓度、沸石用量对沸石吸附氨氮的影响。结果表明,Freundlich方程较Langmuir方程能更为准确地描述天然沸石对两种水质中氨氮的等温吸附特征;在两种水质中,单分子层饱和吸附量分别为16.20mg·g-1和3.85mg·g-1。天然沸石对氨氮的吸附作用受吸附时间、氨氮初始浓度及沸石用量影响较大,在两种水质中,沸石对氨氮的吸附过程在0～8h内均随时间显著上升,到48h时达到吸附平衡;当采用NH4Cl溶液时,初始氨氮的浓度由10mg·L-1增加到500mg·L-1时,平衡吸附量由0.19mg·g-1增加到5.91mg·g-1;当采用猪场厌氧发酵液时,初始氨氮的浓度由39.4mg·L-1增加到502.9mg·L-1时,平衡吸附量由0.63mg·g-1增加到3.20mg·g-1;增加沸石用量,可以提高氨氮的去除率,但单位质量沸石的氨氮吸附量随之降低。准二级动力学可以很好地描述天然沸石吸附两种水质中氨氮的动力学过程;由模型得出的天然沸石...     

Measuring interlayer potassium release rates from soil materials. II. A percolation procedure to study the influence of the variable ‘solute K’ in the < 1…10 μM range

Release rates of nonexchangeable K from Ap material of a Luvisol (‘Eckerde’ loess, 15% clay) are determined using a percolation procedure which avoids the common artifacts due to shaking or stirring soil suspensions and thus provides less biased kinetic data. CaCl₂ solution (10 mM_c. 20 °C. pH 5.8) is percolated through packages of soil aggregates (0.5–1 mm grain size, 0.5 g samples) with 0.02 to 25 ml h^?1. Solute K (C_K) was varied between < 1 and > 10 μM and is shown to have a dominant influence on the rates of interlayer K release. These increase exponentially below 3.5 μM (no steady state but steady decrease of release rates in each sample). The difference between the related C_K between moderate and high release rates is as small as 1 μM K. The average rates, of a 10-day-interval, starting after 1.3 times the exchangeable K had been removed, are 40 μmol K kg^?1 soil d^?1 at 4 μM C_K and 240 μmol kg^?1 d^?1 at 3 μM C_K, respectively. It is concluded that larger quantities of interlayer K become plant available in the studied soil if the of soil solutions gets below 3.5 μM (for 10 mM_c Ca, 20 °C, pH 5.8), probably because the dominant dioctahedral illites start to join the release process below this critical limit. The higher K concentration range was accounted for by K-Ca exchange isotherms which, by alteration of shape, indicate that K_nex release becomes measurable below 10 to 20 μM K. It is further argued that existing diffusion or reaction kinetics approaches towards K release are incomplete because the influence of solute K is not considered.     

PAK-Abnahmen in Bodenproben verschiedener Altlaststandorte bei Aktivierung der autochthonen Mikroflora

PAH decrease in soil samples from different polluted industrial sites by activating the autochthonous microflora In pot experiments under field conditions the PAH decrease in ten different soil samples from former industrial sites with differing PAH load were investigated over a period of 74 and 168 weeks. 15 out of 16 PAH according to US EPA (without acenaphthylene) were determined. Easily degradable organic matter, mineral fertilizers, synthetic surfactants and in some experiments also lime were added to the soil samples in varying amounts. Depending on the nature and quantity of the amendments, the biological activity and (co-)metabolic decomposition of PAH by soil microorganisms could considerably be increased. In the different soil samples a decrease of the initial PAH contents between 12 and 90% was achieved within 74 weeks. Even from 74 up to 168 weeks for some soil samples a remarkable further decrease of the PAH contents could be observed. The decrease of the extractable PAH with time is mainly caused by microbial decomposition and formation of nonextractable residues. This behavior can be fitted by two coupled exponential functions, one for an initial phase of rapid decomposition and the other for a subsequent phase of slow decomposition. Therefore, two different processes (I, II) determine the decrease of PAH. In the first week of the experiment the decomposition rates for process I amount to 4.2–88.3 and for process II to 0.06–5.3 mg PAH ? kg^?1 soil ? week^?1; in the 168th week they are no longer determinable for process I and amount to 0.05–2.3 mg ? kg^?1 ? week' for process II. Higher initial PAH contents often led to higher relative PAH decreases, but also to absolute higher contents of residues. The persistence of PAH is mainly determined by their bioavailability. PAH degradation is increased by the soil treatments. The addition of easily degradable organic matter (C/N ratio < 20) in a quantity of 30g ? kg^?1 (w/w) combined with the addition of nitrate and a surfactant most effectively increased the degradation of PAH. Raising the pH of a very strongly acidic soil sample revealed a maximum PAH decomposition at a pH of 6.     

MWNTs/TiO2光催化降解氧乐果农药影响因素及动力学研究

通过合成多壁碳纳米管/二氧化钛(MWNTs/TiO_2)复合光催化剂,研究其对氧乐果农药的降解效率和作用机理,为去除水体中农药提供高效环保的水处理技术。通过溶胶-凝胶法制备MWNTs/TiO_2复合光催化剂,其中钛酸丁酯:异丙醇:水摩尔比为1∶25∶3、MWNTSs为0.5 g、MWNTSs与TiO_2质量比为100∶1.5。采用批实验法考察了复合材料投加量(200、400、600、800、1 000 mg/L)、溶液p H值(3、5、7、9、11)、氧乐果初始浓度(20、75、150 mg/L)、温度(15℃、25℃、35℃)、光照强度(385、560 W)等因素对其降解效果的影响,对比了MWNTs/TiO_2和TiO_2两种催化剂对降解效果,并通过SEM和EDS等手段对MWNTs/TiO_2复合光催化剂进行表征。结果表明,TiO_2均匀覆盖在MWNTs上,其中TiO_2占复合光催化剂的质量分数为59.59%;MWNTs/TiO_2复合光催化剂对氧乐果的降解效率受复合材料投加量、溶液p H值、氧乐果初始浓度、温度、光照强度等因素影响较大,在氧乐果初始浓度75 mg/L、MWNTs/TiO_2投加量600 mg/L、p H值为3、温度35℃及光照强度560 W最佳条件下,MWNTs/TiO_2对氧乐果的光催化降解率为60.71%。降解动力学分析发现降解过程符合一级反应动力学方程,降解速率常数为0.0033 h-1。在同样的条件下,MWNTs/TiO_2复合光催化剂比TiO_2降解效率提高了8.45%。     

Kinetics of the release of dissolved organic matter (DOM) from air‐dried and pre‐moistened soil material

In this study, the kinetics of soil organic matter (SOM) dissolution from soil samples in different states of moisture was investigated, using a continuous extraction method. The investigation distinguished three processes of SOM dissolution. They include an initial, fast process (probably hydrophilic dissolved organic matter) and two slow, rate limited processes, which probably correspond to hydrophobic dissolved organic matter (DOM). The second process indicates a slow, continuous release of DOM, whereas the third process is determined by a power law. The rate of the third process strongly depends on temperature and state of moisture. It is diffusion limited, with the diffusion control probably being located in the solid soil organic matter. This was explained by a gel structure, which slowly forms in the hydrating SOM and allows diffusion of mobile particles of SOM. The results show the importance of considering the moisture state of SOM for the kinetics of DOM dissolution.     

中华稻蝗两地理种群乙酰胆碱酯酶生化特性研究

采用生物测定方法,对采自山西省临猗县和江苏省徐州市郊中华稻蝗五龄若虫的乙酰胆碱酯酶(AChE)特性进行了比较研究,同时测定了2种群五龄若虫对马拉硫磷的敏感性。用对氧磷、氧化毒死蜱和甲基内吸磷3种有机磷抑制剂对2种群中华稻蝗五龄若虫AChE的体外抑制进行的研究表明,该2种群AChE对对氧磷、氧化毒死蜱、甲基内吸磷的敏感性没有显著差异,临猗种群比徐州种群分别高1.24、1.13和0.82倍;乙酰胆碱酯酶动力学研究结果表明,临猗种群的动力学参数米氏常数(Km值)和最大反应速度(Vmax值)均较徐州种群为高;用乙酰硫代胆碱(ATC)做底物测定AChE活性,2种群AChE活性无显著差异,临猗种群是徐州种群的1.24倍。而2种群生物测定结果表明,临猗种群和徐州种群五龄若虫对马拉硫磷的敏感度有差异,徐州种群五龄若虫的LD50值(13.00μg·g-1虫质量)是临猗种群(4.64μg·g-1虫质量)的2.8倍。据此推测,中华稻蝗徐州种群马拉硫磷敏感性下降与AChE无相关性,可能存在其他影响因素。     

Kinetic Study of the Degradation of Ethiofencarb in Aqueous Solutions

A kinetic study of the hydrolysis of ethiofencarb (α-ethylthio-o-tolyl methylcarbamate) in pure water and in aqueous solutions at pH 2, 6, 9 and 12 and at three different temperatures (4, 20 and 50(±1)°C) has been carried out using a gas chromatographic nitrogen-phosphorus detection method. The values of the first-order rate constants (k) for the degradation reaction were calculated. The values for k were found to be dependent on pH and temperature. No acid hydrolysis was observed in any case. Complete degradation of ethiofencarb was observed at pH 12 at all three temperatures; it was practically instantaneous at room temperature. Ethiofencarb was also completely degraded at pH 9 at 20 and 50°C, while in pure water (pH 6) degradation took place at 50°C but not at 20°C. Ethiofencarb was not degraded in pure water at lower temperatures and, due to the reversible nature of the reaction, at equilibrium about 80% of the pesticide remained undegraded at room temperature. © 1997 SCI.