RF-O2荧光光纤氧气测量技术——氧气测量全面解决方案

RF-O2荧光光纤氧气测量技术——氧气测量全面解决方案

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RF-O2荧光光纤氧气测量技术——氧气测量全面解决方案

详细介绍

RF-O2荧光光纤氧气测量技术是基于REDFLASH光极传感器技术的的氧气测量技术,由欧洲Pyroscience公司及Graz大学等科学家研制生产,由光极氧气传感器、测量仪及软件组成,广泛应用于环境科学、生态科学、植物科学、动物科学、海洋科学、生物医学、生物技术、食品科学等各个领域,其主要功能特点如下

1) REDFLASH光极氧气传感器技术,高精确度、高稳定性、高时空解析度、低能耗、无耗氧、无交叉敏感性

2) 传感器类型灵活多样,有探头式、探针式、非接触式(sensor spot)及纳米微粒式等,适应于液体和气体不同条件下的O2测量

3) 有内置sensor spot的流通管和呼吸瓶,非接触式测量流动液体的溶解氧及呼吸瓶内液体或气体中氧气含量

4) 轻便紧凑型FireStingO2测量仪,内置水汽、气压传感器,有1、2、4通道供选配,可分别接1个、2个、4个光极氧气传感器,另有Mini型FireStingO2-mini供选配

5) U盘式PiccolO2测量仪——*小的O2测量仪,可连接一个O2传感器,USB口连接电脑,即插即用

图片63.png

测量原理:

REDFLASH光极O2传感器技术,利用*的O2敏感REDFLASH指示剂,通过610-630nm调制红光激发,REDFLASH指示剂发出760-790nm红外荧光,荧光强度随接触的O2分子浓度升高而发生荧光淬灭,这种荧光动态通过光纤传输到测量仪,测量仪灵敏地检测其相位漂移并据此换算成O2浓度。

应用领域:

1) 水体溶解氧测量监测、藻类及藻类生物膜光合作用与呼吸作用测量监测

2) 植物光合作用与呼吸作用测量监测

3) 水生动物(鱼类、水生昆虫等无脊椎动物、浮游动物等呼吸代谢测量

4) 陆生动物、实验动物、动物组织、血液等呼吸代谢测量

5) 土壤、湿地、海洋沉积、河湖沉积剖面O2测量

6) 生物反应器、发酵过程、酶动力学、细胞培养等O2测量监测

7) 粮食食品储运、葡萄酒等O2测量监测

8) 污水处理、沼气、垃圾填埋场、有机物降解等O2测量监测

技术指标:

1) FireStingO2FSO2)测量仪:

a) 1通道、2通道、4通道可供选配,分别可接1个、2个和4个O2传感器,可并联组成8通道甚至更多通道;另具备一个温度传感器通道(可选配4通道温度传感器)图片66.pngb) 激发光源620nm,监测器760nm(NIR)

c) 采样频率:每秒4次

d) 内置气压传感器,300-1100mbar,0.06mbar分辨率,精确度±3mbar

e) 内置湿度传感器,0-*,分辨率0.04%,精确度±0.2%

f) 内置温度传感器,-40125°C,分辨率0.01°C,精确度±0.3°C

g) 具模拟输出和自动模式,0-2.5VDC

h) USB接口,通过USB口PC供电

i) 大小:68x120x30mm,重350g

2) PiccolO2 U盘式测量仪:大小仅15x15x54mm,重量约20g,单通道,激发光620nm,检测器760nm,采样频率每秒20次。可并联组成多通道测量系统。可通过PiccoTHP测量温湿度和气压并进行补偿

3) 探头式O2传感器:直径3mm,测量范围0-50%(0-23mg/l)(可选配其它范围),检测极限0.02%(0.01mg/l),分辨率0.05%(0.025mg/l)@20% O2,精确度±0.2%(0.1mg/l)@20% O2,*使用寿命1千万数据点,存储时间大于3年(室温暗处储放)

图片69.png

4) 探针式O2传感器:有固定探针式、可伸缩探针式、尖头式及圆头式等不同类型供选配;探针直径有50μm230μm430μm等规格;测量范围0-50%(0-23mg/l)(可选配其它范围),检测极限0.02%(0.01mg/l),分辨率0.05%(0.025mg/l)@20% O2,精确度±0.2%(0.1mg/l)@20% O2,响应时间小于1s(与探针粗细有关),*使用寿命1百万数据点,存储时间大于3年(室温暗处储放)

5) 非接触式(sensor spot)O2传感器(见下左图):用于非接触性测量监测透明容器中的氧气含量,传感器贴用硅胶等贴附在容器内壁,通过固定在外壁的光纤将荧光动态信号传输到测量仪以检测O2浓度;测量范围0-50%(0-23mg/l)(可选配其它范围),检测极限0.02%(0.01mg/l),分辨率0.05%(0.025mg/l)@20% O2,精确度±0.2%(0.1mg/l)@20% O2,*使用寿命2千万数据点,存储时间大于3年(室温暗处储放)

6) 纳米微粒传感器(参见上右图):纳米技术,用于非接触性测量微量液体中O2含量,即时响应,测量范围0-50%(0-23mg/l),检测极限0.02%(0.01mg/l),分辨率0.05%(0.025mg/l)@20% O2,存储时间大于3年(室温暗处储放)

7) 流通管:内置非接触式O2传感器,用于流动液体O2测量监测(如鱼类呼吸代谢测量等),测量范围0-50%(0-23mg/l)(可选配其它范围),检测极限0.02%(0.01mg/l),分辨率0.05%(0.025mg/l)@20% O2,精确度±0.2%(0.1mg/l)@20% O2,*使用寿命1千万数据点,存储时间大于3年(室温暗处储放)

图片74.png

8) 呼吸瓶:内置非接触式O2传感器,用于生物呼吸测量(如藻类、小型鱼类、鱼卵、昆虫等),标准配置有4ml和20ml两种规格

9) Pyro Oxygen Logger软件用于参数设置、校准、数据显示包括图表显示、数据输出等功能

图片75.png

应用案例:

案例1:法国Bordeaux大学利用FSO2 4通道荧光光纤氧气测量仪,对Aquitaine海岸沉积样芯耗氧进行了测量分析,以研究海洋底栖动物活动(bioirrigation)对海岸带生态系统生态过程及生物地理化学功能(如沉积有机物的再矿化)的影响。

案例2:芬兰Turku大学利用FSO2和430μm光极氧探针,对南瓜类囊体悬浮液光合放氧进行了测量分析。

案例3:美国Woods Hole海洋学研究所,利用RF-O2非接触式光极氧气传感器(sensor spot),对海洋无脊椎动物呼吸代谢进行了测量分析,以研究其固有的生物钟与环境胁迫的关系,这些海洋无脊椎动物体重只有0.5-50mg。图中为翼足类软体动物在不同浓度CO2条件下的耗氧率。

图片76.png

案例4:澳大利亚海洋科学研究所、瑞典Gothenburg大学等组成的科学小组,利用Pyroscience的REDFLASH氧气测量技术,对河鲈(Perca fluviatilis)呼吸代谢进行测量分析,以研究其热耐受性和适应性的生理机制。他们选择波罗的海核电站附近的一个泻湖,核电站排出的热水进入该泻湖,在过去30年大量鱼类因为不适应水温升高而灭绝,但河鲈却得以繁盛,该地成为理想的研究气候变暖对鱼类种群影响的“天然实验室”。他们测量河鲈呼吸代谢率的同时,还测量其静脉血液在温度升高状态下的氧分压,静脉血是河鲈心脏供氧的主要来源,高温条件下静脉血氧气含量被认为是其心脏功能的重要限制因子。

图片77.png

案例5:德国Ulm大学利用FSO2测量仪和50μm可伸缩式RFO2探针,对患者脑脊髓液(CSF)样品溶解氧进行测量分析,以研究探讨神经紊乱及神经炎等疾病的生理和诊断。

案例6:德国农业科学与景观研究机构,利用FSO2测量仪和RFO2探针,对土壤氧气进行测量,以评估不同种类蚯蚓在低氧条件下对土壤改良的效率。

案例7:西班牙Valladolid大学利用RFO2荧光光纤氧气测量技术,监测葡萄酒橡木桶O2吸收——对葡萄酒品质至关重要但一直以来缺乏科学的了解。葡萄酒在橡木桶内(3-24个月)的过程溶解氧至关重要,因为O2调节了葡萄酒整个的熟化过程。

近期部分参考文献:

2015

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7. Increased gastrointestinal blood flow: An essential circulatory modification for euryhaline rainbow trout (Oncorhynchus mykiss) migrating to seaBrijs et al., 2015, Scientific Reports 5, Article number:10430: doi:10.1038/srep10430

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12. Accumulation of Basic Amino Acids at Mitochondria Dictates the Cytotoxicity of Aberrant UbiquitinBraun et al., 2015, Cell Reports Vol 10 (9): 1557-1571

13. O2 mass transfer in an oscillatory flow reactor provided with smooth periodic constrictions. Individual characterization of kL and a. Ferreira et al., 2015, Chem Eng J Vol 262: 499-508

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15. Oxygen metabolism and pH in coastal ecosystems: Eddy Covariance Hydrogen ion and Oxygen Exchange System (ECHOES)Long et al., 2015, Limnol Oceanogr: Methods, DOI: 10.1002/lom3.10038

2014

1. Ocean acidification rapidly reduces dinitrogen fixation associated with the hermatypic coral Seriatopora hystrix. Rädecker et al., 2014, Mar Ecol Progr Ser Vol 511: 297-302

2. All puffed out: do pufferfish hold their breath while inflated McGee, G.E. & Clark, T.D., 2014, Biol Lett Vol 10:

3. Spectral Effects on Symbiodinium Photobiology Studied with a Programmable Light Engine. Wangpraseurt et al., 2014, PLOS One 9: e112809.

4. The energetic cost of foraging explains growth anomalies in tadpoles exposed to predatorsBarry, M.J., 2014, Physiol Biochem Zool Vol 87: 829-836

5. A product of its environment: the epaulette shark (Hemiscyllium ocellatum) exhibits physiological tolerance to elevated environmental CO2Heinrich et al., 2014, Conserv Physiol Vol 2 (1): doi: 10.1093/conphys/cou047

6. Oxygen-Dependent Control of Respiratory Nitrate Reduction in Mycelium of Streptomyces coelicolor A3(2).Fischer et al., 2014, J Bacteriol Vol 196 (23): 4152-4162

7. A respiratory nitrate reductase active exclusively in resting spores of the obligate aerobe Streptomyces coelicolor A3(2)Fischer et al., 2014, Mol Microbiol Vol 89 (6):1259-73

8. Growth trajectory influences temperature preference in fish through an effect on metabolic rateKillen, S., 2014, J Animal Ecol Vol 83 (6): 1513-1522

9. Colored ceramic foams with tailored pore size and surface functionalization used as spawning plates for fish breedingKroll et al., 2014, Ceramics International Vol. 40 (10): 15763-15773

10. Aerobic scope predicts dominance during early life in a tropical damselfishKillen et al., 2014, Functional Ecol Vol 28 (6): 1367-1376

11. European sea bass, Dicentrarchus labrax, in a changing oceanPope et al., 2014, Biogeosciences Vol 11: 2519-2530

12. Marine rust tubercles harbour iron corroding archaea and sulphate reducing bacteriaUsher et al., 2014, Corrosion Science Vol 83: 189-197

13. Magnetic optical sensor particles: a flexible analytical tool for microfluidic devices. Ungerböck et al., 2014, Analyst Vol 139: 2551-2559

14. Investigation and correction of the interference of ethanol, sugar and phenols on dissolved oxygen measurement in wineAlamo-Sanza et al., 2014, Anal Chim Acta Vol 809: 162-173

15. Bioresponsive polymers for the detection of bacterial contaminations in platelet concentratesGamerith et al., 2014, New Biotechnol Vol 31 (2): 150-155

16. Life on the edge: thermal optima for aerobic scope of equatorial reef fishes are close to current day temperaturesRummer & Couturier, 2014, Global Change Biol Vol 20 (4): 1055-1066

17. The effect of diel temperature and light cycles on the growth of Nannochloropsis oculata in a photobioreactor matrix. Tamburic et al., 2014, PLOS One, DOI: 10.1371/journal.pone.0086047

18. Radiative energy budget reveals high photosynthetic efficiency in symbiont-bearing coralsBrodersen et al., 2014, J R Soc Interface Vol 11 (93), DOI: 10.1098/ rsif.2013.0997

19. The isotope effect of denitrification in permeable sediments. Kessler et al., 2014, Geochim Cosmochim Acta Vol 133: 156-167

20. Discovery and characterization of a 5-Hydroxymethylfurfural oxidase from Methylovorus sp. Strain MP688Dijkman & Fraaije, 2014, Appl Environ Microbiol Vol 80 (3): 1082-1090

21. Amperometric glucose sensing with polyaniline/poly(acrylic acid) composite film bearing covalently-immobilized glucose oxidase: A novel method combining enzymatic glucose oxidation and cathodic O2 reduction. Homma et al., 2014, J Electroanal Chem Vol 712: 119-123

22. C*tion and isolation of N2-fixing bacteria from suboxic waters in the Baltic SeaBentzon-Tilia et al., 2014, FEMS Microbiol Ecol Vol 88 (2): 358-371

23. Coenzyme regeneration catalyzed by NADH oxidase from Lactococcus lactis. Sudar et al., 2014, Biochem Engin J Vol 88: 12-18

24. Temporary storage or permanent removal? The division of nitrogen between biotic assimilation and denitrification in stormwater biofiltration systemsPayne et al., 2014, PLOS One, DOI: 10.1371/journal.pone.0090890

25. Increased rates of dissimilatory nitrate reduction to ammonium (DNRA) under oxic conditions in a periodically hypoxic estuaryRoberts et al., 2014, Geochim Cosmochim Acta Vol 133: 313-324

26. Compartmentalized microbial composition, oxygen gradients and nitrogen fixation in the gut of Odontotaenius disjunctus. Ceja-Navarro et al., 2014, The ISME J Vol 8: 6-18

27. Optimum temperatures for growth and feed conversion in cultured hapuku (Polyprion oxygeneios) – Is there a link to aerobic metabolic scope and final temperature preference?Khan et al., 2014, Aquaculture Vol 430: 107-113

28. Aerobic scope does not predict the performance of a tropical eurythermal fish at elevated temperaturesNorin et al., 2014, J Exp Biol Vol 217: 244-251

29. Aquatic Eddy Correlation: Quantifying the Artificial Flux Caused by Stirring-Sensitive O2 SensorsHoltappels et al., 2015, PLoS ONE 10(1):e0116564. doi:10.1371/journal.pone.0116564

30. Decreased light availability can amplify negative impacts of ocean acidification on calcifying coral reef organismsVogel et al., 2015, Mar Ecol Progr Ser Vol 521: 49-61

31. Physiological and ecological performance differs in four coral taxa at a volcanic carbon dioxide seepStrahl et al., 2015, Comp Biochem Physiol, Part A Vol 184: 179-186

32. Novel use of a micro-optode in overcoming the negative influence of the amperometric micro-probe on localized corrosion measurementsTaryba et al., 2015, Corrosion Science, accepted

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