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以海水为溶剂,采用熔融法合成了纳米粉煤灰沸石。粉煤灰与NaOH的质量比为1:1.2,熔融温度550℃,熟料质量与海水固液的体积比为1:5(g/mL),晶化温度100℃,晶化时间6h。通过仪器分析和化学方法,对产物的结构、形貌、性能进行表征。同时,研究了产物的矿物组成、形貌、比表面积、阳离子交换量及化学组成。结果表明:产物为NaX型沸石和羟基方钠石的复合型沸石,海水晶化粉煤灰通过碱熔融法得到沸石质量优于传统水热法。合成沸石的性能和各项应用指标表明,所合成的沸石具有良好的实际应用价值。 相似文献
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以1，4—苯二酚和不同的短链脂肪酸为基本原料，经溴代、加成、形成酰卤和酰化等反应，合成了六种新的溴化脂肪酸—2，3，5，6—四溴—1，4—苯二酯。通过对产物的碳、氢、溴等元素的定量分析，以及红外吸收光谱和氢核磁共振谱的研究，验证了化合物的结构。 相似文献
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提出采用相转移催化法,一步合成了抗癌新药ASF。工艺条件达到最简。利用正交实验法确定了最佳反应条件,通过一系列分析手段确定产物结构。 相似文献
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以环氧氯丙烷、亚硫酸氢钠为原料合成了中间体2-羟基-3-氯丙磺酸钠,在碱性条件下经环氧化反应后与壳聚糖合成了1种易溶于水的壳聚糖磺酸盐表面活性剂,用红外光谱、核磁共振对产物进行了结构表征。分别采用电导率法、吊环法、最大气泡法测试了该产物的临界胶束浓度(CMC)。结果表明:3种方法测得产物的CMC值分别为:2.3×10-4,5.6×10-4和2.5×10-4mol.L-1,吊环法和最大气泡法测得的临界胶束浓度时的表面张力分别为46和48 mN.m-1。 相似文献
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《海洋技术学报》2014,(2)
烧失量(Loss on ignition)法可以完成悬浮物中有机悬浮物和无机悬浮物的分离过程。然而,科学机构并没有统一的标准规范,例如煅烧温度、煅烧时长等因素都会造成各个实验室分析结果的差异。煅烧时间过长,无疑增大了工作量;时间太短,又不能充分除去有机物和水分。针对原有实验规范笼统地认为空白滤膜和过滤水样后滤膜的煅烧时长是一致的问题,文中提出了对原有实验规范的改进措施。研究的对象是滤膜在煅烧过程中的质量变化对悬浮物浓度测量的影响。利用SPSS进行One-Way ANOVA(单因素方差分析),处理同一煅烧温度(550℃)不同煅烧时长(15min,30 min,45 min,1 h,2 h,3 h,4 h)下滤膜的烧失量,显著性水平为0.05。分析结果表明:针对原有规范中所采用的,以4 h作为空白滤膜的煅烧时长,可以缩短至2 h。按照同样的方法,分别处理高有机悬浮物和高无机悬浮物浓度的水样,分析过滤水样后的滤膜在煅烧过程中的烧失量变化,进而判断合适的煅烧时长。利用该方法可在不影响结果精度的前提下提高悬浮物浓度测量的工作效率。 相似文献
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本研究以CaO、煅烧后的牡蛎壳、蛤蜊壳、扇贝壳和脉红螺壳为原料, 分别采用反相微乳液法和聚乙二醇(PEG)辅助微波加热法制备了纳米羟基磷灰石(HA), 并从产物的物理化学特性以及形态学参数方面进行比较。利用傅里叶变换红外光谱、X射线衍射对各组产物进行了化学表征, 扫描电子显微镜观察样品的表面形貌, Zeta电位仪测定样品表面的电势差。结果表明, 反相微乳液法制备的HA尺寸在(104.10±1.95) nm至(207.90±3.75) nm范围内, 为近球形颗粒; 而PEG辅助微波加热法制备得到的HA尺寸在(61.17±3.11) nm与(182.70±1.05) nm范围内, 倾向于形成椭圆及棒状的颗粒, 稳定性更高, 且各组样品均表现出完全的亲水性。此外, 对比于CaO制备的HA, 以贝壳为原料制备的HA具有更好的纳米结构, 其中利用脉红螺壳制备的HA在粒径大小、稳定性以及亲水性等方面均具有优势, 并且具有更接近天然骨的钙磷比。因此脉红螺壳可以作为PEG辅助微波加热法制备羟基磷灰石的主要原料。 相似文献
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利用溶胶凝胶法自制了碳纳米管和纳米二氧化钛的复合光催化剂,采用投射电子显微镜和X光衍射仪对粉体的粒径、物象、形貌和热稳定性等进行表征。通过研究光照条件、催化剂的投加量、油的初始浓度、催化剂制备的煅烧条件等因素,考察了自制碳纳米管和纳米二氧化钛的复合催化剂对降解模拟海洋柴油污染的海水去除率的影响。研究发现,在可见光照条件下,400℃煅烧2 h的复合催化剂,投加量为0.4 g/L、柴油的初始浓度为0.6 g/L、反应的光照时间为4 h时效果最好,去除率可达到67.65%。 相似文献
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通过共沉淀法制备纳米Fe_2O_3-SnO_2光催化剂,采用XRD、SEM等测试手段对其进行形貌、物象、粒径一系列的表征,研究结果显示制得的催化剂仍保持纯SnO_2四方金红石型结构.研究了Fe_2O_3-SnO_2光催化剂投加量、Fe_2O_3与SnO_2物质的量比、煅烧温度、煅烧时间、氨氮初始浓度、p H值、H2O2浓度以及光照反应时间等因素对海水养殖废水中氨氮降解效率的影响.在紫外光照射下进行正交实验,确定最优化反应条件:催化剂投加量为0.4 g/dm3,煅烧时间为3 h,物质的量比为1∶2,氨氮初始含量为50 mg/dm3,光照反应时间为2 h.这5个因素对Fe_2O_3-SnO_2光催化氧化速率影响的大小程度依次为:Fe_2O_3与SnO_2物质的量比煅烧时间Fe_2O_3-SnO_2光催化剂投加量氨氮初始浓度光照时间.氨氮去除率可以达到85.1%,相同条件可见光下也可达到82.3%. 相似文献
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Michel Lamboy Venigalla Purnachandra Rao Ezzat Ahmed Nasreddine Azzouzi 《Marine Geology》1994,120(3-4):373-383
Phosphatic coprolites (0.5–2 cm long) occurring in Cretaceous-Eocene phosphorites of Tunisia, Morocco, Mauritania, Senegal, and Egypt were investigated for their petrology by using SEM. They exhibit a homogeneous porous apatite structure with a few fish remains. The nannostructures of the coprolites consist of inframicron-sized and botryoid-type apatite microparticles. Spherical cavities and cavity-infill cavity-infilled inframicron-sized apatite globules are typical in the coprolites and are apparently formed by extracellular precipitation of phosphate around microbial organisms. We presume that the coprolites studied here may belong to fishes, whose excrements contain abundant organic matter and phosphate. Phosphatization of excrements appears to be a microbial process controlled by the microenvironment.
The nannostructures observed in the coprolites investigated here differ significantly from the nannostructures of other studied phosphatic grains (pellets and coated grains) in the same samples which are mostly heterogeneous and consist of ovoid-type apatite particles. In the case they are not reworked, the centimetre to decimetre thick coprolite beds in phosphorites indicate a lack of detrital input and strong bottom water currents at the sediment-water interface during deposition and subsequent phosphatization of the excrements. 相似文献
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绿色杜氏藻被膜泡囊的超微结构研究 总被引：3，自引：0，他引：3
于１９９０年５月－１９９１年５月,运用透射电镜观察绿色杜氏藻,对该氏藻被膜泡囊的形态结构及其在细胞内的分布和形成过程进行研究。观察表明,绿色杜氏藻细胞的高尔基体和细胞膜有许多大小不等的被膜泡囊;这些被膜泡囊由泡囊及其表面的网状结构构成,其直径在４５－１２０ｎｍ之间;在细胞膜附近的被膜泡囊直径较大;在高尔基体和细胞膜上还观察到被膜泡囊的形成过程。 相似文献
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目前，在中国采用热浸镀Zn及其合金一直是防止钢材在自然环境中腐蚀的最经济有效的方法，为了提高镀层的防腐和涂装性能，往往在其表面进行钝化处理。传统的镀锌层钝化处理工艺均采用高浓度的铬酸盐溶液， 这对环境污染和人体的危害较严重。随着环境保护问题日益引起人们的重视，在传统的高铬钝化基础上，低浓度铬酸盐钝化开始步入实用性阶段(吴双成，1996；卢燕平等，1995)。但是，目前低铬钝化研究主要集中于热浸镀Zn或电镀Zn镀层，而合金镀层由于化学稳定性高，与铬酸溶液自发反应能力差，无法采用常规的低铬钝化方法处理，有关这方面的报道目前尚少。王洪仁(1998)对Zn-Al合金镀层的低铬钝化处理进行了有益的探索，获得了一个优化的低铬钝化配方和稳定的钝化工艺，并成功地应用于热浸镀Zn-Al合金镀层的表面防锈处理；实验证明，海水在模拟浸泡6个月后，钝化处理Zn-Al合金镀层的腐蚀失重比未钝化样品降低65.9%，表明低铬酸盐钝化使Zn-Al合金镀层的耐海水腐蚀性能得到显著提高(Li Y et al.，2001)。本文作者在前人基础上对Zn-Al合金镀层低铬钝化膜的组成和耐盐雾腐蚀性进行了研究，并初步探讨了钝化膜的形成过程及其耐蚀机理。对Zn-Al合金镀层低铬钝化处理技术的研究，不仅大大降低了对环境的污染和人体的危害，也是在低铬钝化研究方面的重大突破，具有十分重要的意义和实际应用价值。 相似文献
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应用计算机数字影像学原理,建立了对磷质胶结微细纹层研究的数值化方法,研究了西沙东岛珊瑚砂砾屑灰岩磷质胶结物的胶结结构和微纹层特征,定量地刻画了微条纹的宽度和颜色变化信息。东岛珊瑚砂砾屑灰岩磷质胶结物的形成以沉淀胶结为主,不同时期形成的胶结物微条纹系列,由于受到气候、生态因素的影响,具有不同的宽度、明暗度组合;对3个层次磷质胶结物的分析表明,在2900~5700 aBP西沙群岛东岛存在至少3次鸟类和植物的繁盛期;不同时期微纹层的气候、生态记录对比发现,相对稳定的气候条件有利于岛屿海鸟数量的扩大;提供了一种新的方法来探索岛屿鸟粪磷质胶结物的结构和生态环境意义。 相似文献
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Fertilisation and larval metamorphosis of reef-building corals are important life history events leading to recruitment of juvenile corals to reef populations. Little is known of the sensitivity of these early life phases to pollution, or their relative susceptibility to certain toxicants compared with established coral colonies. Inhibition of fertilisation and larval metamorphosis of the coral Acropora millepora (Ehrenberg, 1834) was assessed in response to solutions of the antifoulants tributyltin (TBT) and copper (Cu) using laboratory-based bioassays. Nominal concentrations that inhibited 50% fertilisation and metamorphosis (IC50) were calculated from 4 h fertilisation and 24 h metamorphosis assays and were based on introduced dose. Cu was most potent towards fertilisation with an IC50 of 17.4 micrograms/l. TBT however, proved more toxic to larval metamorphosis having an IC50 of 2.0 micrograms/l. Inert surfaces coated with either Cu- or TBT-based antifouling paint also inhibited fertilisation and metamorphosis. The degree of inhibition was correlated with surface area of the paint coating. These results indicate fertilisation and metamorphosis of coral can be sensitive to active components of antifouling paints. 相似文献
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The Stø Formation is the most important reservoir interval in the Norwegian Barents Sea, however the reservoir quality can be highly affected by the detrimental effects of quartz cement where there have been extensive post depositional burial. Core plug data from well 7219/8-2 in the Southwestern Barents Sea shows abnormally high porosity and permeability values in certain units of the deeply buried and otherwise highly quartz cemented Stø Formation. The amount of quartz cement in the samples is inversely proportional to the porosity. Samples with high and low porosities are similar texturally and mineralogically, but the high porosity samples have a layer of illitic clay coating the majority of the detrital quartz grains. Illitic clay coating present at grain contacts can result in a lowered IGV given they aid in the dissolution of quartz at interfaces, also creating a source of dissolved silica. Clay induced dissolution means that silica saturation is not a limiting factor in quartz cementation in these samples. The results show that the illitic clay coating is capable of limiting the amount of authigenic quartz overgrowth from 20 to 23% in samples with negligible grain coating to 5–11% in the intervals with high coating coverage. The illitic clay coating inhibits quartz overgrowth by limiting the surface area available for nucleation on detrital grains. The Stø Formation comprises mainly shallow marine deposits of highly reworked clean sandstone. Abnormally high porosities appear to be linked to settings where sediments of a more proximal location are preserved without extensive reworking. The grain coating clay is illitic and most likely originates from clay infiltration processes prior to final deposition. The difference in extent of clay coating in similar facies can mostly be correlated with varying amount of post depositional reworking. This study suggests that there is a potential for considerable porosity and permeability to be preserved in deeply buried sandstones in the Barents Sea. This study could be important in the future exploration activity of deeply buried structures in the area. 相似文献
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岩藻聚糖硫酸酯低聚糖的制备及其抗氧化活性研究 总被引：7，自引：0，他引：7
探讨H2O2降解岩藻聚糖硫酸酯的条件及其产物的抗氧化活性。采用Cu2 -H2O2体系降解原料Fucoidan,结果发现反应时间越长得到的高分子量的组分越少,而低分子量的低聚糖产量增加;H2O2浓度增高,水解所得主要组分的分子量明显减小;温度升高,水解速度明显加快;产物的硫酸根含量随反应温度和H2O2浓度的降低而增加。用Pyrogallol—Luminol系统对水解产物的抗氧化活性进行了研究,发现硫酸根含量低的Fucoidan水解产物除O2.-的活性较好,其中15%H2O2降解得<5KD的低聚糖清除O2.-的活性明显高于肌肽(IC50为0.65mg/mL),IC50为0.17mg/mL。 相似文献
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海水中的N,P,Si是海洋中最基本的营养物质,对海洋浮游生物的生存、繁殖、海洋生物食物链结构和新陈代谢,以及海洋中物质的循环都具有重要的意义,一直是海洋学研究的重要内容之一,几乎世界上海洋的各个区域都有其研究报道。中国陆架海中营养物质的研究已进行了40多年,获得了大量的资料和重要的研究成果。随着我国海洋科学的发展,近年来陆续开展了世界大洋、极地海的营养盐研究,并有一些报道(顾宏堪,1992;宋金明,1995,1996; Hecky等,1993),但对世界大洋定点长周期的营养盐变化观测研究和降水对表层海水的输入影响长周期定点系列观测还未见报道。热带西太平洋海域有一个世界海洋中最大的高温、高盐“暖池(WPWP)”,这里进行着地球上强烈的海气相互作用,所以,研究该海域海水中营养盐的变化规律,对系统研究海洋对气候的调节作用,乃至全球气候变化都具有重要意义。本文通过对4°S,156°E长达4个月的定点观测,研究了上层海水、深水中营养盐的变化、营养盐的周日变化及降水对表层海水营养盐输人的影响,本文为TOGA-COARE研究的一部分。 相似文献
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Sensitive methods for the determination of arsenate and particulate arsenic (PAs), as well as phosphate and particulate phosphorus (PP), in seawater are described. The method for arsenate and phosphate was established by applying automated liquid waveguide spectrophotometry. Because the reaction time for the formation of the arsenate-molybdate complex is longer than that for the phosphate-molybdate complex, a long Teflon tube submerged in a heating bath was installed in the conventional phosphate flow system. The arsenate was quantified as the difference between absorbances of molybdenum blue dyes with (only phosphate) and without (phosphate + arsenate) arsenate reduction treatment. Contamination was observed in the reagent for arsenate reduction and must be corrected. Linear dynamic ranges up to 1000 nM were confirmed for arsenate and phosphate. The detection limits for arsenate and phosphate were 5 and 4 nM, respectively. Freezing was a reliable sample preservation technique for both arsenate and phosphate. The method for PAs and PP was established by combining conventional persulfate oxidation of PP and the automated liquid waveguide spectrophotometry of arsenate and phosphate. The digestion efficiencies of organic As analogs were >93%. Contamination in the glass fiber filter was negligible. Field tests confirmed that the coefficients of variation (CVs) of 10–19 nM arsenate and 4–151 nM phosphate were 7–20 and 1–25%, respectively, while the CVs of 0.9 nM PAs and 10.2 nM PP were 11 and 4%, respectively. 相似文献