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1. Fumasep FAB-PK-130 阴离子交换膜
Fumasep FAB-PK-130 is a PK reinforced Anion Exchange Membrane (AEM) with high proton blocking capability, high selectivity, very high mechanical stability, and high stability in acidic and caustic environment. The polymer backbone for this AEM is based on a hydrocarbon polymer material.
Fumasep FAB-PK-130 is designed for the processing of concentrating acidic solutions, electrodialysis and electrodialysis with bipolar membranes.
2. Fumasep FAB-PK-130 运输形式
The membrane is the brown foil, delivered in between paper layer. Carefully separate the membrane
from the paper layers. The membrane is delivered in dry form.
The standard size of this membrane is 10*10cm & 20*30cm. Customized dimensions can be made upon request.
3. Fumasep FAA-3-PK-130 注意事项
FuMA-Tech membranes are highly sensitive to differences in humidity and moisture content. Therefore the membranes can vary +/- 0.5cm from the original cut sizes. Also due to this sensitivity the manufacturer expects wrinkles to form, however soaking the membranes in deionized water will return the membranes to the full size planar state according to the manufacturer.
4. Fumasep FAA-3-PK-130 Features (特点)
- Applications: Process for concentrating acidic solutions, electrodialysis and electrodialysis with bipolar membranes.
- Anion Exchange Membrane
- Stability Range (pH) at 25°C: 0 - 14
- Thickness: 130 micrometers (μm)
5. 文章引用
欢迎在文章中引用从科学材料站(SCI Materials Hub)获取的材料
Fumasep FAB-PK-130, a PK reinforced Anion Exchange Membrane (AEM), was obtained from SCI Materials Hub.
6. 科学材料站中FuMA-Tech阴离子交换膜系列 (FuMA-Tech Anion exchange membrane series in SCI Materials Hub)
资料下载:
fumasep FAB-PK-130 (dry form) Technical Data Sheet.pdf
Membrane Properties |
Membrane | Anion Exchange Membrane |
Thickness | 110 - 140 μm (microns) |
Appearance / Color | Brown |
Backing Foil | None |
Delivery Form | Dry |
Reinforcement | PK |
Tensile Strength - max. (MPa) | 40 - 80 MPa |
Density | 10 - 13 mg*cm-2 |
Non-Std Modulus (MPa) | 1000 - 1800 MPa |
Yield Strength at 23°C / 50 % R.H. | 20 - 30 MPa |
Elongation to Break (%) | 15 - 40 % |
Specific Area Resistance (ohm*cm2) | 5.0 - 9.0 (in Cl- form) and 10 - 20 (in SO42- form) |
Specific Conductivity (mS*cm-1) | 1.0 - 2.5 Br- and 10 - 20 (in SO42- form) |
Counter Ion | Bromide (Br-) |
Ion Exchange Capacity (meq*g-1) | 0.7 - 1.0 (in Br- form) |
Selectivity | 93 - 98 % |
Uptake in HO at 25°C | 5 - 15 wt % |
Dimensional Swelling in H2O at 25°C | 0 - 1 % |
Proton Transfer Rate | 60 - 400 μmol*min-1*cm-2 |
Bubble Point Test in Water at 25°C | > 3 bar |
pH Stability Range at 25°C | 0 - 14 pH |
1. Handling (处理)
Keep membrane package closed / sealed when unused. Store, handle and process the membrane in a clean and dust-free area. Use only new and sharp knives or blades, when cutting the membrane. Always wear protective gloves when handling the membrane. Handle with care, be sure not to puncture, crease or scratch the membrane, otherwise leaks will occur. All surfaces in contact with the membrane during handling, inspection, storage and mounting must be smooth and free of sharp projections.
2. Storage (保存)
Dry form(干法保存): The membrane can be stored dry for an unlimited amount of time. However, the membrane has to be conditioned (washed and rinsed) prior to use.
Wet form(湿法保存): Storage for short and medium time scale (hours up to several weeks) may be done in unsealed containers in 0.5 - 1.5 wt% NaCl solution or comparable neutral pH electrolytes.
长期保存:For storage over a longer time period a sealed container is recommended using afore said electrolyte with ca. 100 ppm biocide (NaN3) to avoid biological fouling.
3. Pre-Treatment and Conditioning (预处理)
The membrane is delivered in the bromide form and dry. Depending on application and cell design, assembling is possible in dry form (without pretreatment) or wet form. For optimum performance it is recommended to rinse the membrane in NaCl solution (e.g. 0.5 M NaCl solution at 25°C for 24 hrs) to remove any additive from the membrane. Place the membrane sample between stabilizing meshes / spacers in order to avoid curling. Do not let the membrane dry out since micro-cracks may likely occur during shrinkage.
For standard alkaline fuel cell / electrolysis applications, the membrane should be converted into OH-form by treating it with 0.5 – 1.0 M NaOH or KOH solution: Put the membrane sample in an aqueous solution of 0.5 – 1.0 M NaOH or KOH for at least 24 h at 20°C – 30°C. After rinsing with demineralised water (pH ~ 7) the membrane is ready to use. Use closed container to avoid CO2 contamination (carbonate formation that may affect conductivity). The membrane in OH-form must be stored under wet / humidified and CO2-free conditions, avoid drying out of the membrane in OH-form. Long-term storage in dry conditions should be preferably done in carbonate, Cl- or Br-form.
For electrochemical CO2 reduction applications, the anion exchange membrane should be converted to the carbonate or bicarbonate form by treating the membrane initially with 0.1 to 0.5 M KOH or NaOH solution and then with 0.1 to 0.5 M water soluble carbonate or bicarbonate salt solutions (such as potassium carbonate or potassium bicarbonate that is dissolved in de-ionized water or distilled water). Fully submerging the anion exchange membrane into KOH or NaOH solution for 6 to 12 hours and then to the desired carbonate or bicarbonate salt solution for a period of 48-72 hours would be sufficient to fully convert the membrane into either carbonate or bicarbonate form. After rinsing the membrane (which is in the carbonate form) with deionized water or distilled water, it can be assembled inside the electrochemical setup for electrochemical CO2 reduction experiments. While the submersion of the membrane into the KOH or NaOH can be skipped, for such situations, a longer submersion time may be required in order to fully convert the membrane to carbonate or bicarbonate form. Initial conversion to OH- form significantly improves the carbonate ion exchange process due to expanded pore sizes.
For other electrochemical (electrodialysis, desalination, electro-electrodialysis, reverse electrodialysis, acid recovery, salt splitting, etc.) and non-electrochemical applications, the membrane should be converted into the anionic form that is relevant for the intended application. For example, if the application is requiring the Cl- anions to be transferred through the membrane, then this anion exchange membrane needs to be converted into the Cl- form. In order to convert this membrane into Cl- form, it needs to be submerged into a 1-2 M salt solution of NaCl or KCl (dissolved in deionized water) for a period of 24-72 hours and then rinsed with deionized water to remove the excess salt from the membrane surface. Or if the intended application is requiring to transfer sulfate anions, then this anion exchange membrane needs to be converted into the sulfate form prior to its assembly into the cell. A neutral salt solution of Na2SO4 or K2SO4 would usually be sufficient to achieve the full conversion of membrane into the sulfate form after fully submerging the membrane into the salt solution for 24-72 hours at room temperature.
If you have any concerns about storage, chemical stability and pretreatment before proceeding, please feel free to contact us for further information.
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Fumasep FAB-PK-130 阴离子交换膜
|
产品代码 | 15110509 |
产品描述 | Fumasep FAB-PK-130 Anion Exchange Membrane |
产品价格及规格 | ¥211 (10CM*10CM,货号:15110509-1010) ¥998 (20CM*30CM,货号:15110509-2030) |
货期、库存 | 1天、现货 |
SCI Materials Hub is Committed to Offering The Best Price & Customer Servics!
|
2-4张 (9.5折); 5-9张 (9折); ≥10张 (8.5折)
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References citing our materials
二氧化碳还原
1. Strain Relaxation in Metal Alloy Catalysts Steers the Product Selectivity of Electrocatalytic CO2 Reduction
The bipolar membrane (Fumasep FBM) in this paper was purchased from SCI Materials Hub, which was used in rechargeable Zn-CO2 battery tests. The authors reported a strain relaxation strategy to determine lattice strains in bimetal MNi alloys (M = Pd, Ag, and Au) and realized an outstanding CO2-to-CO Faradaic efficiency of 96.6% with outstanding activity and durability toward a Zn-CO2 battery.
2. Boosting Electrochemical Carbon Dioxide Reduction on Atomically Dispersed Nickel Catalyst
In this paper, Vulcan XC-72R was purchased from SCI Materials Hub. Vulcan XC 72R carbon is the most common catalyst support used in the anode and cathode electrodes of Polymer Electrolyte Membrane Fuel Cells (PEMFC), Direct Methanol Fuel Cells (DMFC), Alkaline Fuel Cells (AFC), Microbial Fuel Cells (MFC), Phosphoric Acid Fuel Cells (PAFC), and many more!
3. Partially Nitrided Ni Nanoclusters Achieve Energy-Efficient Electrocatalytic CO2 Reduction to CO at Ultralow Overpotential
An AEM membrane (Sustainion X37-50 Grade RT, purchased from SCI Materials Hub) was activated in 1 M KOH for 24 h, washed with ultra-purity water prior to use.
电池
3. Blocking polysulfides with a Janus Fe3C/N-CNF@RGO electrode via physiochemical confinement and catalytic conversion for high-performance lithium–sulfur batteries
Graphene oxide (GO) in this paper was obtained from SCI Materials Hub. The authors introduced a Janus Fe3C/N-CNF@RGO electrode consisting of 1D Fe3C decorated N-doped carbon nanofibers (Fe3C/N-CNFs) side and 2D reduced graphene oxide (RGO) side as the free-standing carrier of Li2S6 catholyte to improve the overall electrochemical performance of Li-S batteries.
4. A high-voltage and stable zinc-air battery enabled by dual-hydrophobic-induced proton shuttle shielding
This paper used more than 10 kinds of materials from SCI Materials Hub and the authors gave detailed properity comparsion.
The commercial IEMs of Fumasep FAB-PK-130 and Nafion N117 were obtained from SCI Materials Hub.
Gas diffusion layers of GDL340 (CeTech) and SGL39BC (Sigracet) and Nafion dispersion (Nafion D520) were obtained from SCI Materials Hub.
Zn foil (100 mm thickness) and Zn powder were obtained from the SCI Materials Hub.
Commercial 20% Pt/C, 40% Pt/C and IrO2 catalysts were also obtained from SCI Materials Hub.