- •Describe the main types of primary electrochemical cells.
- •Construction and the reaction of zinc-manganese batteries with salt electrolyte.
- •Describe the main types of alkaline maganese-zinc cells.
- •4. Give examples of the secondary electrochemical cells.
- •5.Give the sketchy description of lead (acid) batteries construction.
- •Consider the difference between the nickel iron and nickel cadmium batteries.
- •7. Describe the main peculiarities of the lithium-ion batteries.
- •8. Give the description of requirements for battery performance for in electric vehicles.
- •9. Give the Classification of lead acid batteries. Describe the charge and discharge curves of lead acid batteries.
- •10. Describe the lithium-polymer batteries.
- •11. Various classifications of electrochemical cells. Give example.
- •12. Give the description of fuel elements.
- •13. Nickel–metal hydride battery.
- •14. Define the characteristics, which allow to compare electrochemical cells with each other.
- •16. Consider processes what is occur on the negative electrode during discharge and charge lead battery?
- •17. What are the curves shown in this figure? Compare them and make assumtions about their nature?
- •18. Which batteries provide high discharge current, nickel cadmium or lithium? Give examples.
- •19. Draw the diagram of the apparatus of a cylindrical lithium-ion battery.
- •20. Draw the diagram of the apparatus of a Lead batteries.
- •21. What the curves shown in this figure? Compare them and make assumptions about their nature
- •22. Draw a typical curve of self-discharge nickel-cadmium batteries.
- •23. Draw on the one graph any possible discharge curves of two batteries (aa type) with a capacity of 1500 mAh and 2500, respectively. The discharge current 1000 mA.
- •24. Describe the designfeatures of an electrochemical cells an example of the construction of any power source.
- •25. Explain the combination of high electrochemical activity of the lithium with very low self-discharge of the lithium electrode in an electrolyte.
- •26. Compare the specific characteristics of alkaline manganese-zinc, salt and primary lithium sells.
- •27. Draw a typical discharge curves of the lithium primary battery and alcaline battery on the picture.
- •28. Consider the impact of the discharge current, temperature on the capacitance and discharge voltage of the lead-acid batteries.
- •29. Describe the main characteristics of the battery: voltage, capacity, specific energy.
5.Give the sketchy description of lead (acid) batteries construction.
In lead acid battery, there is a group of cells and in each cell there is one group of positive plates and one group of positive plates and one group of negative plates. The positive plates are made of lead peroxide (PbO2) and negative plate is made of spongy lead.
Main parts of lead acid battery. Separator. It is most important part of lead acid battery. Which separate the positive and negative plates from each other and prevents the short circuit. The separators must be porous so that the electrolyte may circulate between the plates. The separators must have higher insulating resistance and mechanical strength. The material used for separators are wood, rubber, glass wood mate, pvc. Electrolyte in lead acid battery dilute sulphuric acid (H2SO4) is used as an electrolyte. For this purpose one part, concentrated sulphuric acid is mixed with three parts of distilled water. Container. Container is a box of vulcanized rubber, molded rubber, molded plastic, glass or ceramic, on the base of this box there are supports block on which the positive and negative plates are established. Cover of cell - in lead acid battery it is also made of the same material which is used is used for making container. Vent plug. The vent plug are provide in the cover plate of the cell which are used to fill up the electrolyte in the cell or the inspection of internal condition of the cell the vent plugs are also use for to exhaust the gases generated in the cell to the atmosphere. Connecting bar. It works like a link and used to connect the two cells in series. Terminal of one cell and negative terminal of another cell. Terminal posts. There are the terminals of the battery which are connected to charging circuit as well as the load. For identification the diameter of the positive terminal is design more as compared to the negative terminal.
Dilute sulfuric acid used for lead acid battery has ration of acid: water = 35/65.This lead acid storage battery is formed by dipping lead peroxide plate and sponge lead plate in dilute sulfuric acid. A load is connected externally between these plates. In diluted sulfuric acid the molecules of the acid split into positive hydrogen ions and negative sulfate ions . The hydrogen ions when reach at PbO2 plate, they receive electrons from it and become hydrogen atom which again attack PbO2 and form PbO and H2O (water). This PbO reacts with H2 SO4 and forms PbSO4 and H2O (water).
Consider the difference between the nickel iron and nickel cadmium batteries.
The
nickel–cadmium battery (NiCd battery)
is
a type of rech-argeable battery using nickel oxide hydroxide and
metallic cadmium as electrodes. A NiCd battery has a terminal voltage
during disc-harge of around 1.2 volts, which decreases little until
nearly the end of discharge.
NiCd
batteries are made in a wide range of sizes and capacities, from
portable sealed types inter-changeable with carbon-zinc dry cells, to
large ventilated cells used for standby power and motive power.
Compared
with other types of rechargeable cells they offer good cycle life and
performance at low temperatures with a fair capacity but their
significant advantage is the ability to deliver practically their
full rated capacity at high discharge rates (dischar-ging in one hour
or less).
Charging.
Ni–Cd
batteries can be charged at several different rates, depending on how
the cell was manufac-tured. The
charge
rate is measured based on the percentage of the
amp-hour
capacity the battery is fed as a
steady
current over the du-ration of the charge. Regardless of the charge
speed, more energy must be supplied to the battery than its actual
capacity, to account for energy loss during charging, with faster
charges being more ef-ficient.
Overcharging.
Sealed
Ni–Cd
cells consist of a pressure vessel that is supposed to contain any
generation of oxygen and hydrogen gases until they can recombine back
to water. Such gene-ration typically occurs during rapid charge and
discharge and excee-dingly at overcharge condition. If the pressure
exceeds the limit of the safety valve, water in the form of gas is
lost. Since the vessel is designed to contain an exact amount of
electrolyte this loss will ra-pidly affect the capacity of the cell
and its ability to receive and de--liver current. Electrochemistry.
A
fully charged NiCd cell con-tains:
а
nickel
(III)
oxide-hydroxide positive
electrode
plate;
а
cadmium negative electrode plate;
а
separator;
аn
alkaline
electrolyte (potassium hydroxide).
The
chemical
reactions at the cadmium electrode during discharge are: Cd + 2OH–
=
Cd(OH)2
+ 2e–.Cd+
= Cd(OH)2
+
The
reactions at the nickel oxide electrode are:
2NiOOH
+ 2H2O
+ 2e–
↔ 2Ni(OH)2
+ 2OH–.2NiO(OH)+2H2O+
= 2Ni(OH)2
+
The
net reaction during discharge is
2NiOOH
+ Cd + 2H2O
↔ 2Ni(OH)2
+ Cd(OH)2.
2NiO(OH)+Cd+2H2O
= 2Ni(OH)2
+ Cd(OH)2
The nickel–iron battery (NiFe battery) is a rechargeable battery having nickel(III) oxide-hydroxide positive plates and iron negative plates, with an electrolyte of potassium hydroxide. The active mate-rials are held in nickel-plated steel tubes or perforated pockets. It is a very robust battery which is tolerant of abuse, (overcharge, overdis-charge, and short-circuiting) and can have very long life even if so treated. It is often used in backup situations where it can be conti-nuously charged and can last for more than 20 years. Due to its low specific energy, poor charge retention, and high cost of manufacture, other types of rechargeable batteries have displaced the nickel–iron battery in most applications. Durability. The ability of these batte-ries to survive frequent cycling is due to the low solubility of the reactants in the electrolyte. The formation of metallic iron during charge is slow because of the low solubility of the ferrous hydroxi-de. While the slow formation of iron crystals preserves the electro-des, it also limits the high rate performance: these cells charge slowly, and are only able to discharge slowly. Electrochemistry. The half-cell reaction at the positive plate: 2NiOOH + 2H2O + 2e– ↔ 2Ni(OH)2 + 2OH– and at the negative plate: Fe + 2OH– ↔ Fe(OH)2 + 2e–. Charge. Charge/discharge involves the transfer of oxygen from one electrode to the other (from one group of plates to the other). Hence this type of cell is sometimes called an oxygenlift cell. In a charged cell the active material of the positive plates is superoxidized, and that of the negative plates is in a spongy or reduced state. If the nor-mal capacity of the cell is insufficient, short intermediate high rate charges can be given provided that the temperature of the electrolyte does not exceed 115˚ F / 46˚ C. These short charges are very effici-ent and cause no injury. Fully charging a NiFe cell consists of seven hours at the normal cell rate. In service the amount of charge given is governed by the extent of the previous discharge. Discharge. Un-der discharge the positive plates are reduced ("deoxidized"); the oxygen, with its natural affinity for iron, goes to the negative plates, oxidizing them. It is permissible to discharge continuously at any rate up to 25% above normal, and for short periods at up to six times normal. When the normal discharge rate exceeds this value, abnormal voltage drops will occur.
