Combi Flash EX Especificaciones

Busca en linea o descarga Especificaciones para Cochecitos Combi Flash EX. Combi Flash EX Specifications Manual de usuario

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Table of Contents
1. AFM/Bruker
2. AFM/Asylum
3. CombiFlash
4. Contact Angle
5. Delsa Nano AT&C
6. Dynamic Light Scattering
7. Differential Scanning Calorimetry (DSC)
7.1. Flash DSC
8. Fourier Transform Infrared Spectrophotometer (FTIR)
9. Gel Permeation Chromatography
9.1. Chloroform
9.2. Dimethylformamide
9.3. Tetrahydrofuran-Light Scattering
9.4. Tetrahydrofuran-UV-Visible
9.5. Preparatory
10. Glove Box
11. High Performance Liquid Chromatography
12. Microscopes
13. QCM-D
14. Solvent Purification System
15. Spectrofluorophotometer
16. Synthesizer Robot
17. Thermogravimetric analysis/Mass Spectrometer
18. UV-Visible Spectrophotometer
Miscellaneous
19. Balances
20. Centrifuge
21. Lyophilizer
22. Nanopure Water
23. Ovens
24. Rotovaps
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Indice de contenidos

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2 Table of Contents 1. AFM/Bruker 2. AFM/Asylum 3. CombiFlash 4. Contact Angle 5. Delsa Nano AT&C 6. Dynamic Light Scattering 7. Different

Pagina 2 - 9/15/2010

11 9. Open up the nitrogen line. Make sure the leftmost flowmeter by the DSC is reading between 10 and 50 mL. 10. Before opening the liquid nitro

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12 High Performance Liquid Chromatography (HPLC) Model: Serial Number: Before switching on the instrument 1. Sign-in with date, name and sample info

Pagina 4 - Comment [D1]: Title Arial 14

13 9. Instrument: On the LC-20AD liquid chromatograph, open the drain by turning the knob anti-clockwise, and press purge. When purging is complete,

Pagina 5

14 created method file, click on the black arrow at the right corner of the box on the table and load the already saved method file 14. Software: O

Pagina 7

16 Solvent Purification System (SPS) On an everyday basis, each solvent should look like figure 1. Please check the argon tank to ensure that it is

Pagina 8

17 Figure 3 – system is closed Figure 4 – system is open to vacuum 10. After 30 minutes, switch the system to argon for 5 – 10 second

Pagina 9

18 Spectrofluorophotometer Standard Operating Procedure Model: Serial Number: For the Panoroma Fluorescence 2.1 software: 1) Hit the white switch to

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19 Spectrum type EM wavelength EX wavelength range Recording range Scan speed Sampling interval EX / EM Slit width Sensitivity Resp

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20 Concentration range (Low to High) Recording range (Low to High) Sensitivity Auto scan (if necessary) Response time (0.02) Repetition

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3 Asylum AFM SOP1 Model: Serial Number: MFP Controls Before flipping over Housing, raise the stage to its MAX as to not crash the tip into the surfa

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21 EX / EM slit width Sensitivity Response time (auto) Reaction time Timing mode (auto) Units (seconds) Select OK to validate Verify cont

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22 Thermogravimetric Analysis (TGA) The following is the Standard Operating Procedure (SOP) for the Mettler Toledo TGA/DSC 1. The instrument is coupl

Pagina 15

23 16. On the left hand portion of the window, select Routine Editor. 17. Hit Reset in the lower right hand corner of the window. 18. If a method n

Pagina 16

24  For coupled TGA/MS runs (either individual or multiple samples), the method used should have a 5 minute Argon “purge” at 25 °C to equilibrate t

Pagina 17

25 In the window, select Pan and hit OK. This will weigh out the pans for all experiments. Each pan takes between 3-5 minutes to weigh. 23. When th

Pagina 18

26 25. When the sample is done running, follow the procedures for cleaning the alumina crucibles below. If an aluminum pan was used, the crucible can

Pagina 19

27 Window 1 Window 2 3. In Window 1, select the first line.

Pagina 20

28 Under Template, select the template you would like to run for your first TGA sample. Templates are located in My Documents > My QUADERA > Q

Pagina 21

29 Add and delete task as necessary using the Add Task and Delete Task buttons. Once done, click Save. 4. When all samples are added, select Start

Pagina 22

30 Once start is hit, open up the Triggered Run window (Window 1). Click Connect. Once the system is connected, click Start. The TGA/MS run is now c

Pagina 23

4 2. Raise Z VOLTAGE to MAX VALUE (150 is MAX VALUE; if 150 is reached, re-engage tip by lowering the tip until the Z VOLTAGE = 30-40; Click Set Poi

Pagina 24

31 UV Probe Demonstration Procedure Features UVProbe has the following features: 1. Abundant processing functions 2. User Interface Customization

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32 This screen should appear once the software is started. The software is divided into 4 modules: Spectrum, Photometrics (Quantitation), Kinetics,

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33 Method Pane Graph Pane These various windows can be customized for the users preference by turning them on or off in the View Menu

Pagina 27

34 The Instrument Parameters tab is used to determine the instrument settings. Options will vary slightly depending on the instrument being used.

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35 5. Data Collection Click [Baseline] on the Photometer Button bar at the bottom of the screen and click [Ok] in the Baseline Parameters dialo

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36 The Overlay tab will show all open spectral data on the same graph. This allows easy comparison between samples. During data collection, the s

Pagina 30

37 8. Data Processing UV Probe has vast data processing capabilities. Most calculations that a customer wants to do can be done under the Manipul

Pagina 31

38 D. Point Pick: Gives a table of results for specified wavelengths in a spectra. These wavelengths can be saved as a template for repeat use

Pagina 32

39 A. Insert Typed Text: Refers to text that may be input by the user directly onto the report. This text may include the Report Title, Company N

Pagina 33

40 You have now gone through the Spectrum Module. If your customer wants to also see Photometrics, continue to Step 10. For Quantitation,

Pagina 34

5 Contact Angle Analyzer (Theta, optical tensiometer) 1. Turn on the instrument and start program. 2. Experimental Setup  Click Contact Angle exp

Pagina 35

41 2. Click on the [Calibration] tab. a. Select [Multi Point] in the Type box and [Fixed Wavelength] in the Formula box. b. Select [WL224.0] in t

Pagina 36

42 2. Click on the [Instrument Parameters] tab and select [Absorbance] as the Measuring Mode. Click [OK] and the Photometer status bar will displ

Pagina 37

43 1. On the Y-axis, click the minimum absorbance value, then change the value to [0.0]. Click the maximum value and change it to 4.0. 2. Click [S

Pagina 38

44 SCAN SPEED in nm/min [UV-2401PC/UV-2501PC] Sampling Interval (nm) Fast Medium Slow Very Slow 0.05 44 19 13 8 0.10 87 38 27 17 0.20 168 75 53 33

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45 Appendix B Saving Data with UVProbe UV Probe consists of three units in the filing system- the FILE, the STORAGE, and the DATA SET. FILE- This i

Pagina 40

46 Step 2. Choose to save all spectra under the same file. This is done by selecting File and then Properties. A window will appear showing the

Pagina 41

47 Repeat collection of spectrum for Holmium Oxide Filter. Since all spectra have been saved under the same File, the properties will appear as fo

Pagina 42

48 transformations are always saved with the Raw Data sets. After this is done, the File Properties will appear as follows: Saving all data in the

Pagina 43

49 Additional Helpful Hints  When the number of loaded files becomes large, the File Properties Dialog box can be resized using the gripper bar

Pagina 44

50 Miscellaneous

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6  Click on the image near the border between the drop and the background and the Focusing window will open.  To adjust the focus of the image turn

Pagina 46

51 Nanopure Water Important: When not in use, the system must be kept in “standby” Dispensing water: Press “start” Press “” Auto dispense menu ? Pr

Pagina 47

7 5. Data Analysis  From the main menu select Browse Experiments.  Use the Find Experiment parameters to find the wanted experiment and select

Pagina 48

8 Differential Scanning Calorimetry (DSC)2 Model: Serial Number: The following is the Standard Operating Procedure (SOP) for the Mettler Toledo DSC 8

Pagina 49 - Miscellaneous

9 4. On the left hand portion of the window, select Routine Editor. 5. Hit Reset in the lower right hand corner of the window. 6. If a method n

Pagina 50

10 temperature possible without sample degradation. Most runs should not come within 25 °C of the Td.  When choosing a method, determine if the met

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