Simultaneous Measurement of Hydrogen Peroxide and Fe Species (Fe(II) and Fe<Subscript>(tot)</Subscript>) in Okinawa Island Seawater: Impacts of Red Soil Pollution     

Takemitsu?ArakakiEmail author  Hiroyuki?Fujimura  Asha?Mansour?Hamdun  Kouichirou?Okada  Hiroaki?Kondo  Tamotsu?Oomori  Akira?Tanahara  Hatsuo?Taira 《Journal of Oceanography》2005,61(3):561-568

The northern part of Okinawa Island suffers from red soil pollution—runoff of red soil into coastal seawater—which damages coastal ecosystems and scenery. To elucidate the impacts of red soil pollution on the oxidizing power of seawater, hydrogen peroxide (HOOH) and iron species including Fe(II) and total iron (Fe_(tot), defined as the sum of Fe(II) and Fe(III)) were measured simultaneously in seawater from Taira Bay (red-soil-polluted sea) and Sesoko Island (unpolluted sea), off the northern part of Okinawa Island, Japan. We performed simultaneous measurements of HOOH and Fe(II) because the reaction between HOOH and Fe(II) forms hydroxyl radical (•OH), the most potent environmental oxidant. Gas-phase HOOH concentrations were also measured to better understand the sources of HOOH in seawater. Both HOOH and Fe(II) in seawater showed a clear diurnal variation, i.e. higher in the daytime and lower at night, while Fe_(tot) concentrations were relatively constant throughout the sampling period. Fe(II) and Fe_(tot) concentrations were approximately 58% and 19% higher in red-soil-polluted seawater than in unpolluted seawater. Gas-phase HOOH and seawater HOOH concentrations were comparable at both sampling sites, ranging from 1.4 to 5.4 ppbv in air and 30 to 160 nM in seawater. Since Fe(II) concentrations were higher in red-soil-polluted seawater while concentrations of HOOH were similar, •OH would form faster in red-soil-polluted seawater than in unpolluted seawater. Since the major scavenger of •OH, Br⁻, is expected to have similar concentrations at both sites, red-soil-polluted seawater is expected to have higher steady-state •OH concentrations.  相似文献   

Hydroperoxides in the marine troposphere over the Atlantic Ocean     

F. Slemr  H. G. Tremmel 《Journal of Atmospheric Chemistry》1994,19(4):371-404

Hydrogen peroxide (H₂O₂) and organic hydroperoxides (ROOH) were measured on board of theRV Polarstern during its cruise across the Atlantic Ocean from 20 October to 12 November 1990 (54° N to 51° S latitude) by the enzyme fluorometric method. The H₂O₂ mixing ratio varied from below the detection limit of about 0.12 ppbv up to 3.89 ppbv, showing a latitudinal dependence with generally higher values around the equator and decreasing values poleward. The shape of the latitudinal H₂O₂ distribution agrees well with an analytical steady state expression for H₂O₂ using the measured H₂O and O₃ distribution and a wind dependent H₂O₂ deposition rate. The ROOH mixing ratio varied from below the detection limit of about 0.08 ppbv up to 1.25 ppbv with qualitatively the same latitudinal dependence as H₂O₂. The observed ratio ROOH/(ROOH + H₂O₂) varied between 0.17 and 0.98 showing higher values at the lowest H₂O₂ mixing ratios at high latitudes. The measured H₂O₂ mixing ratio shows a significant diurnal variation with a maximum around 14:00 local time, explicable by a superposition of the photochemical H₂O₂ production with a constant H₂O₂ deposition rate. Four independent estimations of the average effective H₂O₂ deposition rate inferred from the H₂O₂ decrease in the night, from the midday H₂O₂ production deficit (as derived from comparison with a photochemical model and from the daily ozone loss), and from the offset in the latitudinal H₂O₂ distribution, were consistent. An episode of maximum H₂O₂ concentration suggests the possibility of its formation in clouds.  相似文献   

Degradation of petroleum contaminants in oil     

Yanying SUN Fei LIU Honghan CHEN Wei HE 《中国地球化学学报》2006,25(B08):126-127

The treatment of diesel-contaminated soil with hydrogen peroxide oxidation is investigated in this paper. The factors influencing reactions such as initial oil content, H2O2 dosage, pH-value, catalyst and so on are studied. The results indicate that it is feasible to remediate diesel-contaminated soil by adding oxidant directly at room temperature because of higher absolute removal content although the degradation efficiency is low for the contaminated soil of 1%, 2% and 5% initial oil content. The more the H2O2 dosage, the better the degradation efficiency; it is economical and efficient to add 4 mL H2O2 to 10 g diesel-contaminated soil （2% or so） directly in-situ chemical oxidation （ICO）. For the contaminated soil of 5% initial oil content, when pH-value is 5-8 and H202 dosage is 20 mL, the removal efficiency reaches more than 96%; when pH-value is 1-3 and volume ratios of H2O2 to Fe^2＋ are 1 ： 1, 2：2, the degradation efficiencies are all very high （i.e., 86%-88% or so）. It can be concluded that the degradation efficiencies are comparative when adding 1 mL or 2 mL H2O2 of Fenton Reagent or adding 4 mL of H2O2 only to 10 g diesel-contaminated soil.  相似文献   

The annual cycle of peroxides and ozone in marine air at Cape Grim, Tasmania     

G. P. Ayers  S. A. Penkett  R. W. Gillett  B. Bandy  I. E. Galbally  C. P. Meyer  C. M. Elsworth  S. T. Bentley  B. W. Forgan 《Journal of Atmospheric Chemistry》1996,23(3):221-252

The concentration of gas-phase peroxides has been measured almost continuously at the Cape Grim baseline station (41° S) over a period of 393 days (7702 h of on-line measurements) between February 1991 and March 1992. In unpolluted marine air a distinct seasonal cycle in concentration was evident, from a monthly mean value of>1.4 ppbv in summer (December) to <0.2 ppbv in winter (July). In the summer months a distinct diurnal cycle in peroxides was also observed in clean marine air, with a daytime build-up in concentration and decay overnight. Both the seasonal and diurnal cycles of peroxides concentration were anticorrelated with ozone concentration, and were largely explicable using a simple photochemical box model of the marine boundary layer in which the central processes were daytime photolytic destruction of ozone, transfer of reactive oxygen into the peroxides under the low-NO_x ambient conditions that favour self-reaction between peroxy radicals, and continuous heterogeneous removal of peroxides at the ocean surface. Additional factors affecting peroxides concentrations at intermediate timescales (days to a week) were a dependence on air mass origin, with air masses arriving at Cape Grim from higher latitudes having lower peroxides concentrations, a dependence on local wind speed, with higher peroxides concentrations at lower wind speeds, and a systematic decrease in peroxides concentration during periods of rainfall. Possible physical mechanisms for these synoptic scale dependencies are discussed.  相似文献   

Implications of ozone depletion for surface-water photochemistry: Sensitivity of clear lakes   总被引：1，自引：0，他引：1  

Norman M. Scully  Warwick F. Vincent  David R. S. Lean  William J. Cooper 《Aquatic Sciences - Research Across Boundaries》1997,59(3):260-274

Increased ultraviolet-B radiation (UV-B) in aquatic ecosystems brought about by stratospheric ozone depletion may result in increased formation rates of photochemical reaction products in the surface waters of aquatic ecosystems. In this study, the potential impact of increases in lower wave-length radiation on the formation of hydrogen peroxide (H₂O₂) and singlet oxygen (¹O₂) was modelled for lakes over a range of dissolved organic carbon (DOC) concentrations. The impact of increased UV-B radiation on the production of carbon monoxide (CO) was also calculated for two humic stained systems. The relative increases of H₂O₂ and¹O₂ production were greater in the clear lakes (70% increase in photochemical reaction rates near the surface) than the coloured systems (25%). Production of CO in the study sites also increased under depleted ozone conditions implying increased DOC losses to the overlying atmosphere.  相似文献   

Study of metal aerosol systems as a sink for atmospheric SO2     

Harald Berresheim  Wolfgang Jaeschke 《Journal of Atmospheric Chemistry》1986,4(3):311-334

The chemical removal of SO₂ in the presence of different aerosol systems has been investigated in laboratory experiments using a dynamic flow reactor. The aerosols consisted of wetted particles containing one of the following substances: MnCl₂, Mn(NO₃)₂, MnSO₄, CuCl₂, Cu(NO₃)₂, CuSO₄, FeCl₃, NaCl. The SO₂ removal rate R was measured as a function of the SO₂ gas phase concentration (SO₂)_g, the spatial metal concentration C_Me, and the relative humidity rH in the reactor. A first-order dependence with regard to (SO₂)_g was observed for each type of aerosol. For the Mn(II) and Cu(II) aerosols R was found to be a non-linear function of C_Me except for MnSO₄ and Cu(NO₃)₂ particles. The removal rate showed a significant increase with the relative humidity particularly when rH was close to the deliquescence point of the wetted particles. Among the Mn(II) and Cu(II) aerosols investigated Mn(NO₃)₂ was found to be most efficient for the chemical removal of SO₂ at atmospheric background conditions, especially in haze and fog droplets. The results further indicate that the catalytic oxidation of S(IV) in such aerosol systems may be as efficient as its oxidation by H₂O₂ in cloud water.  相似文献   

过氧化钠碱熔-电感耦合等离子体发射光谱法测定钛铁矿中的高含量钛     

赵昕  严慧  禹莲玲  汤行  柳昭 《岩矿测试》2020,39(3):459-466

钛矿资源主要类型为钛铁矿岩矿、钛铁矿砂矿、金红石矿。钛铁矿属于难熔矿物,一般不溶于硝酸、盐酸或王水。对于高品位钛铁矿,即使采用盐酸-硝酸-氢氟酸-高氯酸混合酸溶解样品,钛元素也易水解形成难溶的偏钛酸析出,常给分析带来很大困难。容量法和分光光度法等传统方法测定钛存在操作流程长、步骤多、效率低等不足。因此,选择合适前处理方法的同时将大型仪器分析方法结合起来,有利于提高钛铁矿分析的准确度和测试效率。本文建立了以2.0g过氧化钠为熔剂,使用刚玉坩埚在700℃熔融样品15min,热水浸取后盐酸酸化,用电感耦合等离子体发射光谱（ICP-OES）测定钛铁矿中的高含量钛元素的方法。实验中采用全程空白试液稀释定容标准溶液消除了钠基体影响,通过优化熔融温度和时间使样品分解完全,考察了过氧化钠用量来降低待测溶液中盐分以保证测定的稳定性,通过选择合适的分析谱线并采用背景扣除法消除光谱干扰。本方法检出限为0.0035%,测试范围为0.0066%～62.50%（均以TiO₂含量计）;经钛铁矿国家标准物质（GBW07839、GBW07841）验证,相对标准偏差（RSD,n=12）为1.1%～2.1%,相对误差为-1.69%～1.11%。本方法应用于实际样品分析,相对标准偏差（RSD,n=12）均小于4%,TiO₂分析结果与国家标准方法（硫酸铁铵容量法）一致。本方法有效解决了钛铁矿分解不完全及高含量的钛易水解的问题,实现ICP-OES对不同类型钛铁矿样品中钛元素的定量分析。  相似文献   

海水养殖珍珠的漂白技术研究     

李雪英  王海增  郭鲁钢  徐华伟 《海洋科学》2008,32(2):5-9

通过对漂白体系中溶剂、表面活性剂、双氧水浓度3个重要参数的优化选择,研究了海水养殖珍珠的漂白技术。首次发现在海水养殖珍珠漂白过程中,以海水为介质漂白效果明显优于用甲醇、乙醇、丙酮和蒸馏水。在以海水为介质的漂白体系中,表面活性剂贝芬家用洗手液使用效果较优,双氧水体积分数为5%,效果最佳。同时探讨了漂白时间对珍珠长麻的影响。  相似文献   

The hydrogen peroxide impact on larval settlement and metamorphosis of abalone Haliotis diversicolor supertexta     

张祥景  杨志会  蔡中华 《中国海洋湖沼学报》2008,26(3)

Abalone Haliotis diversicolor supertexta is an important economic mollusk.The settlement and metamorphosis are two critical stages during its development period,which has direct influence on abalone survival and production.The influence of reactive oxygen species(hydrogen peroxide) on abalone embryo and juvenile development were examined in this study.Larvae of Haliotis diversicolor supertexta were induced to settlement and metamorphose by exposure to seawater supplemented with hydrogen peroxide.They had the best performance at 800 μmol/L.The concentration of 1 000 μmol/L or higher was toxic to the larvae,as the larvae could settle down only at benthic diatom plates without complete metamorphosis.In addition,H2O2 adding time was critical to the larval performance.24h after two-day post-fertilization was proved to be the optimal adding time.In this paper,two action mechanisms of hydrogen peroxide are discussed:(1) hydrogen peroxide has direct toxicity to ciliated cells,thus cause apoptosis;(2) hydrogen peroxide,as a product from catecholamines' autoxidation process in vivo,can reverse this process to produce neuro-transmitters to induce abalone metamorphosis.  相似文献   

大黄鱼过氧化物酶Ⅳ在人胚肾细胞中的表达与抗氧化活性测定     

王贤慧  母尹楠  聂品  陈新华  敖敬群 《台湾海峡》2014,(4):492-498

为了研究大黄鱼（Pseudosciana crocea）peroxiredoxin Ⅳ（Lyc-Prx Ⅳ）在细胞内的抗氧化功能,构建了表达大黄鱼Prx Ⅳ的重组质粒p CMV-Lyc-Prx Ⅳ,瞬时转染人胚肾细胞（HEK-293T）,利用Western blotting方法检测转染后的细胞样品中Lyc-Prx Ⅳ的表达情况,并通过测定细胞内过氧化氢浓度来评价Lyc-Prx IV的体内抗氧化作用.结果显示,Lyc-Prx Ⅳ可在转染重组质粒p CMV-Lyc-Prx Ⅳ的HEK-293T细胞中表达,且细胞中A560处的吸光值在转染后6、12、24 h后分别为0.154、0.116以及0.162,而瞬时转染空载体p CMV后细胞样品在A560处的吸光值在转染后一直稳定在0.260左右,说明细胞中过氧化氢的浓度在转染后6、12、24 h时明显低于瞬时转染空载体p CMV细胞中的过氧化氢浓度（p〈0.01）.表明Lyc-Prx Ⅳ在生物体内可以分解过氧化氢,参与生物体内氧化还原状况的调控.  相似文献