氧化亚铜可见光催化降解罗丹明B的初步研究

以Cu2O粒子为光催化剂，太阳光为光源，研究了Cu2O粒子对可溶性染料罗丹明B的光催化降解情况。并考察了不同光源，光照时间，催化剂用量，双氧水加入量和溶液的酸度等对罗丹明B光催化降解过程的影响。结果表明，Cu2O粒子在太阳光照射下，能较好地降解罗丹明B，其最佳反应条件为：罗丹明B浓度为5mg／L，催化剂（Cu2O）为0．75g／L，pH值为5．2，H2O2加入量1．0％，反应时间25min。此条件下，罗丹明B的降解率达到100％，即与在500W高压汞灯紫外（λ=365nm）光照有相同的降解效果。     

负载型纳米TiO_2光催化杀灭溶藻弧菌的研究

采用平均粒径约5nm,主要结构为锐钛矿型的纳米TiO2光催化剂,以泡沫型复合镍板为载体对纳米TiO2进行固定,并对固定后的纳米TiO2杀灭溶藻弧菌的能力进行了研究。结果表明:利用高压汞灯作为光源,以泡沫型复合镍板为载体的纳米TiO2对溶藻弧菌具有较强的杀灭能力;极少量过氧化氢的加入加快了纳米TiO2的杀菌速度;因此,负载型纳米TiO2在水产病害防治方面具有广阔的应用前景。     

Synthesis of three-dimensional agaric-like biomorphic TiO2 by a facile method with Coscinodiscus sp. frustule

The paper aims to expand the application of natural marine algae.Marine diatoms,which have intricate frustule structures,can serve as bio-template for preparing three-dimensional materials.A simple and effective approach to synthesize the corrugated agaric-like biomorphic TiO 2 templated with frustule of Coscinodiscus sp.is reported.In the sol-gel preparation process,the titania-coating on the frustule is prepared through the deposition and condensation with the aid of acetylacetone(acac) as a controlling agent to make the precursor Ti(BuO) 4 hydrolyze slowly.The as-prepared titania-coated frustule and biomorphic TiO 2 is characterized by scanning electron microscopy(SEM) attached with energy dispersive X-ray spectrometer(EMAX) and X-ray diffraction(XRD).The microstructure of the corresponding titania nanoparticles appears to be sphere with the diameters distributed around 10 20 nm.The templating process is repeated for three cycles.Subsequently,the three-dimensional freestanding corrugated agaric-like biomorphic TiO 2 structure is obtained by a selective removal in the NaOH solution.As far as we known,the 3D freestanding corrugated agaric-like biomorphic TiO 2 with greatly increased surface area is obtained for the first time.     

Bi_2Fe_4O_9的制备与光催化性能分析

采用水热法制备磁性铁酸铋(Bi_2Fe_4O_9)光催化剂,利用X线衍射仪、扫描电子显微镜、紫外—可见漫反射等仪器对Bi_2Fe_4O_9的晶相、形貌、光吸收特性进行表征。结果表明:在紫外光或可见光下,Bi_2Fe_4O_9可有效降解亚甲基蓝(MB),且在紫外光下降解效果尤为显著,其表观速率常数可达2.422×10~(-2) min~(-1)。通过加入不同种类的捕获剂推断Bi_2Fe_4O_9的光催化机理,以及光催化过程中的活性物种,h~+与·OH为光催化降解过程中的主要活性物种。     

复合光催化剂Cu_2(OH)PO_4/Ni(OH)_2的制备及其光催化性能

采用水热合成法在Cu2(OH)PO4表面原位沉积Ni(OH)2,制备异质结型的复合光催化剂Cu2(OH)PO4/Ni(OH)2;利用X线粉末衍射仪(XRD)、紫外-可见漫反射光谱仪(UV-Vis-DRS)和扫描电子显微镜(SEM)等,对其相结构、光吸收性能和微观形貌进行表征.结果表明:该复合光催化剂具有良好的紫外光吸收特性,是一类新型的光催化剂.复合光催化剂在紫外光下可以有效降解亚甲基蓝(MB)溶液,当Cu2(OH)PO4与Ni(OH)2的摩尔比为0.2时,Cu2(OH)PO4/Ni(OH)2具有最大催化活性.根据光催化中加入不同活性物种牺牲剂的实验,推测该异质结型材料光催化过程中光生载流子的传输方向及活性物种.Cu2(OH)PO4/Ni(OH)2的催化活性增强主要归结为复合时在两者之间形成有效的异质结,结区的内建电场能够促进光生载流子的分离,同时·OH和h+在光催化降解过程中是主要的活性物种.     

鱼干中黄曲霉毒素B1的紫外辐照消减技术参数

【目的】确定最佳紫外消减条件,并探究此条件下紫外辐照对鱼干品质的影响。【方法】在单因素试验基础上,将黄曲霉毒素B1质量浓度、辐照时间、辐照距离因素进行组合,应用Design Expert软件与Box-Behnken试验原则对AFB1降解条件进行优化。【结果】最佳的毒素降解条件:紫外辐照条件为波长365 nm、黄曲霉毒素B1质量浓度109 ng/mL、辐照距离2.11 cm、辐照时间41 min、pH 7,对AFB1的标准溶液降解率为88.1%。该条件下金鲳鱼干与红鱼干中黄曲霉毒素B1的降解率为90.16%、85.32%,拟合性较好,且该最佳紫外辐照降解条件对鱼干品质并不存在显著影响(P>0.05)。【结论】该研究证明紫外辐照适用于鱼干中真菌毒素的消减。     

二价铁活化过硫酸盐去除水中苯胺

零价铁和硝基苯反应后生成二价铁和苯胺,而苯胺也是地下水污染物。硫酸根自由基具有强氧化性,可以降解苯胺。而二价铁可以活化过硫酸盐产生硫酸根自由基,进而去除苯胺。本文研究了二价铁浓度、过硫酸盐浓度、苯胺初始浓度、体系初始pH、反应温度等因素对二价铁活化过硫酸盐去除水中苯胺处理效率的影响。结果表明：①） Fe2＋活化过硫酸盐生成SO4-·能快速并有效氧化降解苯胺,对于目标浓度为1000 mg/L 的苯胺而言, Fe2＋浓度为3.3 mmol/L, Na2 S2 O8浓度为4.4 mmol/L时,对苯胺有较佳降解效果,苯胺的降解率为86.33％。②体系对较低浓度的苯胺降解效果较好,当污染物初始浓度由1000 mg/L降低到500 mg/L和100 mg/L时,苯胺降解率由86.33％升高为90.27％和97.16％。③初始pH对苯胺的降解率影响较大,中性条件下（ pH＝7左右）降解率较好,高初始pH （pH＝9,11）和低初始pH条件（pH＝3,5）下均低于中性条件下苯胺的降解效率。④体系的温度变化对降解率影响不明显。     

山东昌乐蓝宝石颜色与化学成分的关系

产于玄武岩中的蓝宝石颜色通常较深 ,山东昌乐蓝宝石的颜色因其晶体巨大更显得深暗。这类蓝宝石曾多次进行过改色试验 ,但成效都不大。通过对电子探针及紫外—可见光—近红外吸收光谱图测试结果的分析 ,并对山东昌乐蓝宝石的颜色与化学成分之间的关系进行研究 ,结果表明 :昌乐蓝宝石的主要致色元素为Fe,Ti,Cr,Ni等 ,Fe2 O3 FeO含量高及TiO2含量少 ,以及成对Fe3 的大量存在是其颜色偏深的重要原因 ;TiO2 含量对蓝宝石颜色纯度影响很大 ,也是蓝宝石改色能否成功的重要因素之一。     

催化剂与碱性缓冲液作用下欢喜岭油田稠油水热裂解反应实验

模拟注蒸气油藏条件,开展催化剂与碱性缓冲液作用下欢喜岭油田稠油的水热裂解反应模拟实验,向高温高压反应釜中加入稠油、水、催化剂、碱性缓冲液和油层矿物,在160～300℃温度下反应24～240h,测定反应前后稠油黏度、SARA族组成和元素组成,考察催化剂、反应时间、反应温度、油层矿物及铵盐碱性缓冲液等因素的影响.结果表明:在油溶性催化剂FeA2作用下,欢喜岭油田稠油在水热裂解反应后黏度显著降低,添加0.010mol/L的催化剂FeA2在240℃下反应24h可使稠油黏度降低62.4%;铵盐碱性缓冲液对稠油水热裂解反应具有协同催化作用,添加0.010mol/L的催化剂FeA2和质量分数为3.0%的铵盐碱性缓冲液在240℃下反应24h可使稠油黏度降低90.1%.稠油井经过水热裂解处理后周期产油量明显增加,周期油气比大幅提高,并且催化剂与碱性缓冲液协同处理的开采效果要明显好于催化剂处理的.添加催化剂与碱性缓冲液的水热裂解开采技术可应用于提高蒸气吞吐和蒸气驱等热采井的产量和采收率.     

SO4^2—／Fe2O3固体超强酸化催合成乙酸丁酯

制备固体超强酸SO4^2-/Fe2O3，并测定其红外光谱。以乙酸和正丁醇为反应物、固体超强酸SO4^2-/Fe2O3为催化剂，进行合成乙酸丁酯的研究。实验结果表明，固体超强酸SO4^2-/Fe2O3在合成乙酸丁酯反应中的催化活性与浓硫酸相当，用0．1mol正丁醇与0．2mol乙酸反应，催化剂用量0．3g，回流时间90min，乙酸丁酯收率为63．8％。     

Corrosion Behavior of Anodic Oxidized TiO_2 Film in Seawater

TiO2 films were formed on metallic titanium substrates by the anodic oxidation method in H2SO4 solution under the 80V D.C..Phase component and microstructure were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM).Water contact angles on titanium oxide film surface were measured under both dark and sunlight illumination conditions.Corrosion tests were carried out in seawater under different illumination conditions by electrochemistry impedance spectrum (EIS) and polarization curves.The result showed that the TiO2 film prepared by the anodic oxidation method was anatase with a uniform structure and without obvious pores or cracks on its surface.The average water contact angle of the film was 116.4? in dark, in contrast to an angle of 42.7? under the UV illumination for 2 hours, which demonstrates good hydrophobic property.The anti-corrosion behavior of the TiO2 film was declining with the extended immersion time.Under dark conditions, however, the hydrophobic TiO2 film retarded the water infiltrating into the substrate.The impedance changed slowly and the corrosion current density was 2 orders of magnitude lower than that with the film illuminated by sunlight.All of those mentioned above indicate that the TiO2 film possesses much better performance under dark condition, and it can be applied as an engineering material under dark seawater environment.     

Geochemical Characteristics and Sources of Some Chemical Components in Sediments of Zhuiiang（Pearl） River Estuary

Sediment cores with length of 25 - 45cm at 12 stations in Zhujiang(Pearl) River Estuary were sampled in summer of 1999. Chemical components (Al2O3 , Fe2O3, CaO, TiO2, Cu, Pb, Cr, Zn, Co, Ni, V, Ba, Sr and Y) and grain sizes were analyzed. Sediments in Zhujiang River Estuary are characterized by relatively coarse grain size. The grain sizes of the sediments in the area outside the estuary are relatively finer than those in the north part of the estuary but coarser than those in the middle of Lingdingyang and have a trend similar to the spatial distribution trend of some chemical components such as Fe2O3, Al2O3, TiO2, V, Cu, Ni, Zn and Y. This showed that grain size is an important factor that controls the spatial distribution and depth profile of chemical elements in the Zhujiang River Estuary. Frequent re-suspension, re-transportation and redistribution of settled sediment on estuary floor could be deduced from the spatial distributions and depth profiles of chemical components. Except for CaO and Sr, the chemical components always enrich at the west side of, in the middle of, and at the north side of, the estuary. Fe2O3, Al2O3, Ti, V, Cr, Ni, Zn, Cu and Y in Zhujiang River Estuary sediments mainly result from rock and soil weathering except that parts of Cr, Ni, Zn Cu and Y are anthropogenic. CaO and Sr in sediments originate from marine source. Although Co as well as Pb derives from anthropogenic sources, human activities related to Co might differ from the activities related to Pb.     

Corrosion behavior of anodic oxidized TiO<Subscript>2</Subscript> film in seawater

TiO₂ films were formed on metallic titanium substrates by the anodic oxidation method in H₂SO₄ solution under the 80V D.C.. Phase component and microstructure were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). Water contact angles on titanium oxide film surface were measured under both dark and sunlight illumination conditions. Corrosion tests were carried out in seawater under different illumination conditions by electrochemistry impedance spectrum (EIS) and polarization curves. The result showed that the TiO₂ film prepared by the anodic oxidation method was anatase with a uniform structure and without obvious pores or cracks on its surface. The average water contact angle of the film was 116.4° in dark, in contrast to an angle of 42.7° under the UV illumination for 2 hours, which demonstrates good hydrophobic property. The anti-corrosion behavior of the TiO₂ film was declining with the extended immersion time. Under dark conditions, however, the hydrophobic TiO₂ film retarded the water infiltrating into the substrate. The impedance changed slowly and the corrosion current density was 2 orders of magnitude lower than that with the film illuminated by sunlight. All of those mentioned above indicate that the TiO₂ film possesses much better performance under dark condition, and it can be applied as an engineering material under dark seawater environment.     

Effects of iron electrovalence and species on growth and astaxanthin production of Haematococcus pluvialis

To increase the cell concentration and the accumulation of astaxanthin in the cultivation of Haematococcus pluvialis, effects of different iron eleetrovalencies (Fe2+-EDTA and Fe3+-EDTA) and species (Fe-EDTA, Fe(OH)32x and FeC6H5O7) addition on cell growth and accumulation of astaxanthin were studied. Results show that different iron electrovalencies have various effects on cell growth and astaxanthin accumulation of H. pluvialis. Compared with Fe3+-EDTA, Fe2+-EDTA stimulate more effectively the formation of astaxanthin. The maximum astaxanthin content (30.70 mg/g biomass cell)was obtained under conditions of 18 μmol/L Fe2+-EDTA, despite the lower cell density (2.3x105 cell/ml)in such condition. Fe3+-EDTA is more effective than Fe2+-EDTA in improving the cell growth. Especially,the maximal steady-state cell density, 2.9x105 cell/ml was obtained at 18 μmol/L Fe3+-EDTA addition. On the other hand, all the various species of iron (EDTA-Fe, Fe(OH)32x, FeC6H5O7) are capable to improve the growth of the algae and astaxanthin production. Among the three iron species, FeC6H5O7 performed the best. Under the condition of a higher concentration (36 μmol/L) of FEC6H5O7, the cell density and astaxanthin production is 2 and 7 times higher than those of iron-limited group, respectively. The present study demonstrates that the effects of the stimulation with different iron species increased in the order of FeC6H5O7, Fe(OH)32x/x and EDTA-Fe.     

SO2-4/Fe2O3固体超强酸催化合成乙酸丁酯

制备固体超强酸SO4 2 - /Fe2 O3,并测定其红外光谱。以乙酸和正丁醇为反应物、固体超强酸SO4 2 - /Fe2 O3为催化剂 ,进行合成乙酸丁酯的研究。实验结果表明 ,固体超强酸SO4 2 - /Fe2 O3在合成乙酸丁酯反应中的催化活性与浓硫酸相当 ,用 0 1mol正丁醇与 0 2mol乙酸反应 ,催化剂用量 0 3g ,回流时间 90min ,乙酸丁酯收率为 63 8%。     

四川石棉独立碲矿床蚀变岩的地质地球化学研究

四川石棉大水沟独立碲矿床堪称世界首例，其矿体两侧的围岩蚀变较窄，且蚀变带与矿脉及未蚀变岩呈清楚而截然的接触关系。主要围岩蚀变为白云石化、白（绢）云母化、云英岩化及电气石化等。这些蚀变作用分别发生于１７７．７～１６５．１Ｍａ和９１．７１～８０．１９Ｍａ。蚀变作用过程中ＳｉＯ２大量析出，Ａｌ２Ｏ３、ＴｉＯ２、ＣａＯ、ＭｇＯ、Ｋ２Ｏ、Ｈ２Ｏ、ＣＯ２、Ｆｅ２Ｏ３、ＭｎＯ则有不同程度地带入。与此同时，ＲＥＥ在此过程中包集体迁出，Ｔｅ、Ｂｉ、ＡＳ等元素的含量则决定于蚀变作用及其强度，而与原岩无关。     

黄土中古土壤双层淀积研究

本文确定了黄土中古土壤有四种双层淀积类型。第一和第二种是由两层ＣａＣＯ３结核构成的，第三种是由ＣａＣＯ３和ＣａＳＯ４构成的，第四种是由ＣａＣＯ３与Ａｌ２Ｏ３、Ｆｅ２Ｏ３构成的。根据ＣａＣＯ３淀积层成因分析得知，西安附近第一层古土壤具二元发生特点。该层古土壤上部的ＣａＣＯ３淀积层代表碱性土壤发育时期。下部的ＣａＣＯ３淀积层代表中酸性土壤发育时期。因为有些古土壤发育时出现过气候变化，所以具ＣａＣＯ３淀积层的古土壤不一定是碱性的。具ＣａＣＯ３与Ｆｅ２Ｏ３·Ａｌ２Ｏ３构成的双层淀积是酸性土壤的标志。     

淄博盆地A层硬质黏土—铝土矿矿床地质特征及分布规律

山东淄博盆地A层硬质黏土—铝土矿主要赋存于二叠纪石盒子群万山组底部的A层含矿岩系中,矿体呈似层状和透镜状产出,A层硬质黏土在该区分布较广,而共生铝土矿矿体主要分布在东宝山—东冲山一带;两矿体的形态、结构、构造比较简单。两矿体垂向分布呈渐变关系,受沉积环境影响呈现不同的颜色和结构,肉眼可大致区分矿体与围岩,具体界线要靠化学分析结果予以区分;矿体厚度均匀,总体与Al_2O_3,SiO_2含量呈正相关,与Fe_2O_3呈反相关;矿石中Al_2O_3,Fe_2O_3,SiO_2的总含量一般在83.5%～85.5%,品位比较均匀,同时三者含量在不同矿石中有着相互消长的关系。     

山东省齐河-禹城地区矽卡岩型铁矿磁铁矿元素地球化学特征及其对成矿作用的指示意义

山东省齐河-禹城地区在黄河北厚覆盖区,有明显的航磁异常和重力异常,通过系统的地质勘探工作,在深部揭露了多处铁矿床,为系统掌握研究区磁铁矿成因机制,服务于基础地质和矿产资源调查,利用EMPA对磁铁矿进行主量元素分析,以确定其成因及成矿环境特征.其中TiO2-Al2O3-MgO和(Ca十Al十Mn)-(Ti十V)成因判别图...