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Gilson吉尔森
Gilson 305/306输液泵搭配测压仪和动态混合器,为分析和制备色谱系统提供经济可靠的输液泵方案。可更换的泵头覆盖5 µL/min - 200 mL/min的流速范围,并可适应不同粘度的液体。输液泵可以组成等度、二元或四元梯度配置。
流速范围
Gilson 305/306输液泵适用于等度或梯度色谱应用,流速范围覆盖10 μL/min-200 mL/min。
操控简便
Gilson 305/306输液泵根据不同的型号,可使用独立的面板键盘或TRILUTION® LC软件进行方法编写,完成可靠的色谱分离。
提高输液泵性能的配件:
• 305/306输液泵内置的测压阻尼模块可降低压力波动
• 动态混合器确保流动相的高效混合
• 外置式脉冲阻尼器以保证平滑的流速
技术参数
| 305 & 306 输液泵 |
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| 制造标准 | 符合相应的安全和EMC认证标准;UL和CE认证 | ||
| 输液泵类型 | 可更换泵头的单活塞往复泵,具有一致性的运动力,复位迅速,内置缓冲器和压力反馈。 | ||
| 准确度 | <± 1% | ||
| 重现性 | <1% | ||
| 流速 | 305/306:10 uL/min-200 mL/min | ||
| 液体接触材质 | 316L不锈钢、钛、蓝宝石、红宝石、陶瓷、PTFE、PCTFE和HDPE | ||
| 前控制面板(305) | 键盘和内置帮助信息 | ||
| 显示屏(305) | 2 x 24个字符的LCD | ||
| 通讯接口(305) | RS-232或GSIOC;四组输入;三组(305)继电输出 | ||
| 控制软件 | Gilson TRILUTION® LC控制软件 | ||
| 空间尺寸(W x D x H) | 33 x 33 x 15 cm | ||
| 重量 | 305/306:10 kg | ||
| 运输重量(含泵头) | 305/306: 14.5 kg | ||
| 电源要求 | |||
| 频率:50–60 Hz | |||
| 电压:100-120V或220–260V;最大压力波动不能超过±10% | |||
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[2] Pérez-Ruiz T, Martínez-Lozano C, Tomás V, et al. Automated solid-phase extraction and high-performance liquid chromatographic determination of nitrosamines using post-column photolysis and tris (2, 2′-bipyridyl) ruthenium (III) chemiluminescence[J]. Journal of Chromatography A, 2005, 1077(1): 49-56.
[3] Pérez-Ruiz T, Martínez-Lozano C, Tomás V, et al. Automated solid-phase extraction and high-performance liquid chromatographic determination of nitrosamines using post-column photolysis and tris (2, 2′-bipyridyl) ruthenium (III) chemiluminescence[J]. Journal of Chromatography A, 2005, 1077(1): 49-56.
[4] Bäckström B, Cole M D, Carrott M J, et al. A preliminary study of the analysis of Cannabis by supercritical fluid chromatography with atmospheric pressure chemical ionisation mass spectroscopic detection[J]. Science & Justice, 1997, 37(2): 91-97.
[5] Rimkus G G, Rummler M, Nausch I. Gel permeation chromatography-high performance liquid chromatography combination as an automated clean-up technique for the multiresidue analysis of fats[J]. Journal of Chromatography A, 1996, 737(1): 9-14.
[6] Gillings N. A restricted access material for rapid analysis of [11C]-labeled radiopharmaceuticals and their metabolites in plasma[J]. Nuclear medicine and biology, 2009, 36(8): 961-965.
[7] Perkins G, Pullen F, Thompson C. Automated high resolution mass spectrometry for the synthetic chemist[J]. Journal of the American Society for Mass Spectrometry, 1999, 10(6): 546-551.
[8] McAvoy Y, Cole M D, Gueniat O. Analysis of amphetamines by supercritical fluid chromatography, high-performance liquid chromatography, gas chromatography and capillary zone electrophoresis; a preliminary comparison[J]. Forensic science international, 1999, 102(1): 13-22.
[9] Nouman W, Anwar F, Gull T, et al. Profiling of polyphenolics, nutrients and antioxidant potential of germplasm’s leaves from seven cultivars of Moringa oleifera Lam[J]. Industrial Crops and Products, 2016, 83: 166-176.
[10] Blackwell J A, Stringham R W. Temperature effects for chiral separations using various bulk fluids in near‐critical mobile phases[J]. Chirality, 1997, 9(7): 693-698.
[11] Park J E, Lee T H, Ham S L, et al. Anticancer and anti-neuroinflammatory constituents isolated from the roots of Wasabia japonica[J]. Antioxidants, 2022, 11(3): 482.
[12] Pérez-Ruiz T, Martínez-Lozano C, Tomás V, et al. High-performance liquid chromatographic assay of phosphate and organophosphorus pesticides using a post-column photochemical reaction and fluorimetric detection[J]. Analytica chimica acta, 2005, 540(2): 383-391.
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