共查询到20条相似文献，搜索用时 515 毫秒
1.
合成了新型席夫碱试剂3，5-二溴水杨醛缩甘氨酸(DBSAGLY)，建立该试剂荧光度法测定微量Zn(Ⅱ)的新体系，在pH=7．0～8．0时Zn(Ⅱ)与DBSAGLY形成1：1的络合物，络合物最大激发和发射波长分别为λex=300nm和λcm=468nm，荧光线性范围0-120μg／L，检测限量1.6μg／L。本法用于粮食中锌的测定。 相似文献
2.
化探样品中有效硼的极谱法测定,首先用1∶2盐酸分解试样,在含有0.004％铍试剂Ⅲ和1％EDTA 的醋酸—醋酸钠缓冲溶液中,硼与铍试剂Ⅲ形成电活性络合物并吸附在电极上,络合物中铍试剂Ⅲ在电极上产生吸附波。峰电位为-0.64V(对银电极)。检出限 C_(min)=0.0034μg/ml B,硼的浓度在0.0068—0.5μg/ml 的范围内与波高呈良好的线性关系。该方法操作简单、快速,可用于大批量样品的测试。 相似文献
3.
覃仕霞 《成都信息工程学院学报》2010,25(5):557-560
设n是合数,如果对一切f（x）∈Zn[x]都满足f（x）nk≡f（x）mod（n,r（x））,那么就称n是模r（x）的k阶Carmichael数,这里r（x）是Zn[x]上的k次首一不可约多项式,用Ck,r（x）表示所有这种数的集合,并且定义Ck=Ur（x）Ck,r（x）.k阶Carmichael数,当k=4时,已证明了n=pq,p,q是不同的奇素数,p2-1,q3-1均整除n4-1,则n∈C4.主要目的是将k=4时得出的结论推广到k≥4的一般情形,利用孙子定理,通过构造Zn上的首一k次不可约多项式f（x）的方法,得出：在k≥4时,设n=pq,如果k=2m,m≥2,pm-1,q2m-1-1均整除nk-1,则n∈Ck;如果k=2m＋1,m≥2,pm-1,pm＋1-1,q2m-1均整除nk-1,则n∈Ck. 相似文献
4.
以Ｎ＿（２６３）浸渍在ＤＡ＿（２０１）大孔吸附树脂上制得了Ｎ＿（２６３）浸渍树脂，测定了静态时树脂Ｐｂ（Ⅱ）的吸附容量。通过柱层析法，试验了酸度，流速和干扰离子等因素对Ｎ＿（２６３）浸渍树脂吸附和洗脱Ｐｂ的影响。建立了Ｎ＿（２６３）浸渍树脂分离─富集后衔接原子吸收和比色法测定Ｐｂ（Ⅱ）的方法，测定了地质样品中Ｐｂ（Ⅱ），测试结果理想。 相似文献
5.
QI Yanxia JI Hongwei XIN Huizhen LIU Li 《中国海洋大学学报(英文版)》2007,6(2):143-146
A new kinetic-spectrophotometric method is proposed for the determination of copper （ Ⅱ ）. The method is based on the catalytic effect of copper （ Ⅱ ） on the oxidation of weak acid brilliant blue dye （RAWL） by hydrogen peroxide. The copper （ Ⅱ ） can be determined spectrophotometrically by measuring the decrease of absorbance of RAWL at λ = 626 nm using the fix-time method. The optimum reaction conditions are as follows： pH 7.20, buffer solution NaOH-KH2PO4, RAWL （200 mgL-1） 5.00 mL, H2O2 （30%） 0.50 mL, reaction temperature 80 ？？ and reaction time 20 min. The linear range of this method is between 0 μg L^-1 and 12 μg L^-1 and the limit of detection is 0.011 μg L-1, the relative standard deviation （RSD） in five replicate determinations for 2 and 8 μg L-1 copper （ Ⅱ ） are 3.2% and 2.3%, respectively. Twenty ions do not interfere in the determination of copper （ Ⅱ ）. The method has been applied satisfactorily to the determination of copper （ Ⅱ ） in freshwater samples （tap water and Yellow River water from Lijin, Shandong, China） and seawater samples （from the South China Sea）, the recovery rates are 98.0%, 102.5% and 96.0%, respectively. 相似文献
6.
以南海低值鱼蛋白为原料，采用木瓜蛋白酶和风味酶的复合酶水解得到多肽水解物（HP），并制备多肽．铁（Ⅱ）螯合物，对螯合工艺及螯合产物的结果及抗氧化和抗菌功能特性进行了初步研究。结果表明：1）水解度为5％的多肽与铁（Ⅱ）螯合效果最佳，螯合率为94．15％；2）化学分析及红外光谱表明活性肽与亚铁离子螯合并形成稳定结构的螯合物；（3）经过50％乙醇（体积分数）沉淀的螯合铁具有明显的抗氧化活性，其抗氧化作用相当于维生素E的90％，经过80％乙醇（体积分数）沉淀的螯合物具有显著的抗枯草牙孢杆菌和金黄色葡萄球菌活性，其抑菌圈均直径为13mm。 相似文献
7.
偏最小二乘—分光光度法同时测定铋、铜、钴和镍 总被引：4，自引：0，他引：4
3，5—Br2—PADAP在pH为3．2的甲酸—甲酸钠缓冲溶液中能与Bi(Ⅲ)、Cu(Ⅱ)、Co(Ⅱ)和Ni(Ⅱ)形成稳定的络合物。研究了Bi(Ⅲ)、Cu(Ⅱ)、Co(Ⅱ)、Ni(Ⅱ)—3，5—Br2一PADAP体系的显色条件，用偏最小二乘法处理所得数据，从而建立了分光光度法同时测定Bi(Ⅲ)、Cu(Ⅱ)、Co(Ⅱ)和Ni(Ⅱ)的方法。方法简便可靠，灵敏度高，选择性好。 相似文献
8.
介绍一种测定矿石、土壤和有关物料中≥０．５μｇ／ｇ钻、镍和铅及≥３μｇ／ｇ铋和铟的方法。把样品分解并将其盐溶于稀盐醚－酒石酸溶液后，用抗坏血醚还原铁（Ⅲ），使产生的铁（Ⅱ）与氟化铵络合。在ＰＨ值２．００±０．０５下，用３倍的氯仿萃取其黄药络合物，使钴、镍、铅、铋和铟连续与铁、铝、锌和其它基体元素分离。用蒸发法除去氯仿并用硝酸和高氯醚破坏黄药后，把溶液蒸发至于，最后用乙炔焰原子吸收光诸法在含１００μｇ／ｍｌ钾的２０％Ｖ／Ｖ盐酸介质中测定各元素。在分解步骤时，用溴化物挥发法避免砷和锑共萃取。少量共萃取的相、铁和铜不会干扰。 相似文献
9.
10.
基于物性、铸体薄片、电镜扫描和高压压汞等测试分析资料，利用汞饱和度法和含水饱和度法对杭锦旗地区盒1段致密储层孔隙结构分形维数进行了计算，并分析其与储层物性的关系。结果表明:盒1段储层平均孔隙度、渗透率分别为9.83%、1.03×10-3 μm2，储集空间以粒间溶孔、粒内溶孔和残余粒间孔为主。汞饱和度法计算的整体分形维数分布在2.138 4~2.829 2，平均值为2.396 5，含水饱和度法计算的整体分形维数分布在2.529 4~2.879 7，平均值为2.679 1。相比于含水饱和度法，汞饱和度法计算的分形维数与孔隙度、渗透率及各孔隙结构参数之间具有更好的相关性，是因为含水饱和度法易对孔喉较小的样品产生偏差。基于汞饱和度法分形维数，将盒1段储层孔隙结构分为四类:Ⅰ类（Df≤2.31），Ⅱ类（2.31 < Df < 2.4），Ⅲ类（2.4≤Df < 2.52），Ⅳ类（Df≥2.52），研究区主要孔隙结构类型为Ⅱ、Ⅲ类。选取分形维数（Df）、平均孔喉半径（Rm）和孔隙度（φ）等参数，对渗透率进行多元回归计算，计算值与实测值相关系数在0.9以上，表明计算模型在本区较为适用。 相似文献
11.
ZHANG Dan ZHANG Yu MORAWSKA Ewa BIELAWSKI Leszek KRASINSKA Grazyna DREWNOWSKA Ma gorzata PANKAVEC Sviatlana SZYMANSKA Karolina FALANDYSZ Jerzy 《山地科学学报》2013,10(4):621-627
In the current study, we determined concentrations and transfer rates of Ag, Al, Ba, Ca, Cd, Co, Cr, Cu, Fe, K, Mg, Mn, Na, Ni, Pb, P, Rb, Sr and Zn to Brown Birch Scaber Stalks (Leccinum scabrum) mushrooms emerged in the area of Sudety Mountains (Sudetes) in Poland. Fruiting bodies and topsoil samples beneath L. scabrum were collected form the K odzka Dale. The trace elements were determined using validated method and inductively coupled plasma - atomic emission spectroscopy (ICP-AES) for final measurement. Mushrooms contained Ag, Cr, Hg, Co, Ni and Sr at < 1.0 μg/g dry weight; Ba and Pb at ~1.0 μg/g dw; Cd at < 5 μg/g dw; Cu and Mn at > 10 μg/g dw; Al and Ca at ~100 μg/g dw; Fe, Na, Rb and Zn at 100 to 500 μg/g dw, Mg at ~1,000 μg/g dw; P at ~5,000 μg/g dw and K at ~30,000 μg/g dw. Ca, Mn and Ni were nearly equally distributed between stipes and caps; stipes compared to caps were enriched in Ba, Na and Sr, while caps were enriched in Ag, Al, Cd, Co, Cr, Cu, Fe, K, P, Pb, Rb and Zn. The values of bioconcentration factor (BCF) varied highly depending on chemical element and were >1 for Ag, Cd, Cu, K, Mg, Na, P, Rb and Zn, while <1 for Al, Ba, Ca, Co, Cr, Fe, Mn, Ni, Pb and Sr. Topsoil showed elevated content of lead and mean concentration was 99 ± 32 μg/g dw, while cadmium was at 0.41 ± 0.15 and those two highly toxic to human elements occurred in edible caps of L. scabrum at 4.5 ± 2.2 and 2.9 ± 2.0 μg/g dw, respectively. 相似文献
12.
A new kinetic-spectrophotometric method is proposed for the determination of copper ( Ⅱ ). The method is based on the catalytic effect of copper ( Ⅱ ) on the oxidation of weak acid brilliant blue dye (RAWL) by hydrogen peroxide. The copper ( Ⅱ ) can be determined spectrophotometrically by measuring the decrease of absorbance of RAWL at λ = 626 nm using the fix-time method. The optimum reaction conditions are as follows: pH 7.20, buffer solution NaOH-KH2PO4, RAWL (200 mgL-1) 5.00 mL, H2O2 (30％) 0.50 mL, reaction temperature 80 ℃ and reaction time 20 min. The linear range of this method is between 0 μg L-1 and 12 μg L-1 and the limit of detection is 0.011 μg L-1, the relative standard deviation (RSD) in five replicate determinations for 2 and 8 μg L-1 copper ( Ⅱ ) are 3.2％ and 2.3％, respectively. Twenty ions do not interfere in the determination of copper ( Ⅱ ). The method has been applied satisfactorily to the determination of copper ( Ⅱ ) in freshwater samples (tap water and Yellow River water from Lijin, Shandong, China) and seawater samples (from the South China Sea), the recovery rates are 98.0％, 102.5％ and 96.0％, respectively. 相似文献
13.
邻苯二甲醛柱前衍生高效液相色谱法测定马氏珠母贝中牛磺酸含量 总被引：2，自引：0，他引：2
应用邻苯二甲醛柱前衍生高效液相色谱法,测定了马氏珠母贝中牛磺酸,结果表明:采用邻苯二甲醛为柱前衍生剂,与原料中的牛磺酸发生衍生化反应后,以甲醇-乙酸钠溶液(体积比40︰60)为流动相,使用ODSC18分离柱,FLD检测器(EX=338nm,EM=444nm)等色谱条件下检测,牛磺酸的线性范围为2.0～14.0μg/mL,相关系数R2为0.9984,回收率为97.9%～103.0%,RSD=2.146%(n=6),检出限为0.77μg(S/N=3)。 相似文献
14.
5种除草剂对白鲢鱼种急性毒性试验 总被引：1，自引：0，他引：1
以白鲢(Hypophthalmicthysmolitris)为实验材料,研究常用除草剂对鱼类的毒性效应。结果表明:采用直线回归法求得的96hLC50值分别为:2,4_D丁酯0.185mg/L,可信限0.138~0.247mg/L;丁草胺0.080mg/L,可信限0.067~0.097mg/L;使它隆3.80mg/L,可信限2.68~5.40mg/L;艾割18.60mg/L,可信限14.80~23.32mg/L;嗪草酮108.80mg/L,可信限91.46~129.72mg/L。对鱼类安全浓度分别为0.019mg/L,0.38mg/L,0.008mg/L,1.86mg/Land10.88mg/L。 相似文献
15.
5种药物对方斑东风螺面盘幼虫的急性毒性 总被引：2，自引：0，他引：2
在水温29.0～29.5℃、盐度28.5条件下,采用静水试验法对5种常用药物对方斑东风螺面盘幼虫的急性毒性进行了研究。结果表明:各种药物的24 hLC50、48 hLC50、96 hLC50和安全浓度分别为:高锰酸钾1.71、1.04、0.55和0.115 mg.L-1,新洁尔灭78.58、28.90、6.06和1.17 mg/L,硫酸锌4.52、2.36、0.62和0.193 mg/L,制霉素2.36×104、1.46×104、0.64×104和0.168×104 U.L-1,甲醛10.9、7.11、3.66和0.908μL.L-1。 相似文献
16.
Sediment, moss and animal-dropping samples were collected from pesticides (OCPs) and polychlorinated biphenyls (PCBs) in the Arctic area. OCPs and PCBs were analyzed using the capillary gas chromatography (GC-ECD). Recoveries of three surrogates were at a range of 69.5～92.2% (mean: 78.8%), 75.1～112.1% (98.5%) and 67.7～95.1% (79.5%), and the relative standard deviations were 6.7%, 8.0% and 11.3%, respectively. The major monomers of OCPs were hexachlorocyclohexanes (HCHs) and DDTs. Their concentrations were at a range of 0.86～4.50 ng/g (mean: 2.24 ng/g) and 0.22～1.09 ng/g (mean: 0.55 ng/g). The concentrations of PCBs were 0.20～3.25 ng/g (mean: 0.84 ng/g) and the major congeners were tetra-, penta-, and hexa-PCBs, which were up to 23.8%、26.7% and 32.3% of total PCBs, respectively. Based on the results of the ratio analysis and the principal component analysis, the atmospheric transport is believed be one 相似文献
17.
The optimal quantity of dietary lysine (Lys) and arginine (Arg), and the optimal ratio of dietary Lys to Arg for Pacific white shrimp Litopenaeus vannamei were investigated. Coated Lys and Arg were added to a basal diet (37.99% crude protein and 7.28% crude lipid) to provide graded levels of Lys and Arg. The experimental diets contained three Lys levels (2.51%, 2.11%, and 1.70% of total diet), and three Arg levels (1.41%, 1.80%, and 2.21% of total diet) and all combinations of these levels were tested. Pacific white shrimp, with a mean weight of 3.62±0.1 g, were randomly distributed in 36 fiberglass tanks with 30 shrimp per tank and reared on the experimental diets for 50 days. After the feeding trial, the growth performance, survival, feed conversion rate (FCR), body composition and protease and lipase activities in the hepatopancreases of the experimental shrimps were determined. The results show that weight gain (WG), specific growth rate (SGR), FCR, body protein, body Lys and Arg content were significantly affected by dietary Lys and Arg (P <0.05) and improved when dietary Lys and Arg levels were 2.11% ～ 2.51% and 1.80%～2.21%, respectively. Protease and lipase activities in the hepatopancreases of the shrimps appeared higher when dietary Lys and Arg quantities were 2.11% ～2.51% and 1.80%～2.21%, although the difference was not statistically significant (P >0.05). Therefore, according to our results, the optimal Lys and Arg quantities in the diet of Pacific white shrimp, L. vannamei, were considered to be 2.11%–2.51% and 1.80%–2.21%, respectively, and the optimal ratio to be 1:0.88–1:1.05. 相似文献
18.
将150条斑马鱼随机等分为5组:2,3,7,8-四氯代二苯并二噁英(TCDD)4个染毒组(染毒剂量分别为0.1μg/L、0.2μg/L、0.4μg/L和0.8μg/L)和空白对照组,水质接触染毒5d后,采用分光光度法测定其肝组织中丙二醛(MDA)含量和超氧化物歧化酶(SOD)、谷胱甘肽-S-转移酶(GST)的活力,研究TCDD对斑马鱼的脂质过氧化作用。结果发现,TCDD各剂量染毒组MDA含量均有所增加,其中0.2μg/L组差异显著(P<0.05),0.4μg/L和0.8μg/L剂量组差异极显著(P<0.01);各染毒组SOD活性均有所下降,其中0.2μg/L、0.4μg/L和0.8μg/L剂量组差异极显著(P<0.01);各染毒组GST活力均降低且差异极显著(P<0.01)。一定剂量的TCDD能引起MDA含量增加,使SOD和GST活力降低,对斑马鱼具有脂质过氧化作用。 相似文献
19.
The pigments in Laminariajaponica was extracted with six organic solvents and analyzed in spectroscopy analysis. The extractions conditions were screened by an orthogonal test and the quantity of extracted pigments was determined spectroscopically. The results show that： （1） among the six organic solvents, acetone was the most effective one for the extraction; （2） the optimum extraction conditions were as follows： the ratio of S/M （solvent volume/ material weight） was 30 ml/g; fresh seaweed was extracted 2 times in 2 h; （3） the average total content of pigments was 1.85 mg/g （calculated with dry L. japonica）. 相似文献
20.
高效液相色谱法检测水产品中的孔雀石绿和结晶紫 总被引：3，自引：0，他引：3
样品中的孔雀石绿、结晶紫经试剂盒提取,浓缩后用经固相萃取柱净化、硼氢化钾还原、反向色谱柱分离,使用荧光检测器检测,孔雀石绿、结晶紫的加标回收率在76.1%～92.5%之间,相对标准偏差1.9%～5.8%,检出限均为0.5μg/kg。结果表明:该方法检测孔雀石绿(MG)、结晶紫(GV)处理简单,灵敏度高,节省时间,可用于大量样品的快速分析。 相似文献