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==Salt Bridge : What's its use?== |
==Salt Bridge : What's its use?== |
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I am not sure the salt bridge of the Daniell Cell is meant to let electrons move and close the circuit. As suggested in another Wikipedia's article called "Electrolyte" electrons dont go in the electrolyte. Only ions move which means that a current would appear in the copper circuit (outside the cell)even if the circuit was open (if there wasnt resistance). Actually, I cant find any satisfying explanation about the use of the salt bridge. Could anyone give us a hint?
From Electrolyte : "When electrodes are placed in an electrolyte and a voltage is applied, the electrolyte will conduct electricity. Lone electrons normally cannot pass through the electrolyte; instead, a chemical reaction occurs at the cathode consuming electrons from the cathode, and another reaction occurs at the anode producing electrons to be taken up by the anode. As a result, a negative charge cloud develops in the electrolyte around the cathode, and a positive charge develops around the anode. The ions in the electrolyte move to neutralize these charges so that the reactions can continue and the electrons can keep flowing." —Preceding unsigned comment added by Whalala (talk • contribs) 09:33, 29 April 2008 (UTC) [reply]
Do not merge. An electrolytic cell can be very different in usage than an electrochemical cell. As an example: electroplating is a use for an electrolytic cell, electrolytic cells are in a neutral energy state and must be driven by an external electrical force where electrochemical is an electrical source and is NOT in a neutral energy state.Jonathan888 (talk) 22:21, 11 January 2006 (UTC)[reply]
I think they should not merge. --Cyberman 05:17, 31 December 2005 (UTC)[reply]
No. Leave them seperate - Ali
These items should be combined as galvanic/electrolytic cells are a subset of electrochemical cells. I reference any introductory physical chemistry text, but namely the text Physical Chemistry by Atkins/dePaula, 7th Ed.
I agree, many college level textbooks including Zimdahl's 7th edition include these two topics in the same section.
Whilst a galvanic cell and an electrochemical cell may be in the same section of a textbook this does not indicate that they should be merged in Wikipedia. Much in the same way amides and amines are different but are still included in the same sections of many books.
HAHA NO! Most high school students like me need them seperate. And thats mostly who would be looking up this shizz.
They should be kept seprate!
The difference with amides and amines is that amides are the products of amines. With electrolytic/galvanic cells, though, one is not the product of the other. They are both reverse proceses of the same greater phenomena (i.e. electrochemical cells). Therefore, electrolytic and galvanic cells should be merged into Electrochemical Cells. - matchu
Please leave them separate. For a high school student such as myself, they could become confusing when your first learning them.
I could see them merged if they were discussed as disctinct instances of an electrochemical cell. Otherwise, I think they should be kept separate. Galvanic and electrolytic cells are distinct and complimentary entities that could be unintentionally confused if combined into a singe article.
DO NOT MERGE. Electrochemical and electrolytic cells are two very different things.
Keep them separate. Very different ideas, and they all have a decent article, so there's no need for a merge. – Mets501talk 01:37, 1 May 2006 (UTC)[reply]
Do not merge, I repeat, do not merge. Electrochemical and Electrolytic cells are quite different, and easily confused. Do not aid this confusion by merging these two articles. --205.251.157.32 17:41, 17 May 2006 (UTC)[reply]
You all seem very confused about Galvanic and Electrolytic. Galvanic cells are exactly the same as electrochemical cells, I don't understand why that is debatable. Just like dye-sensitized solar cells are equivalent to graetzel cells, electrochemical cells are synonomous with galvanic cells. Electrolytic cells, on the other hand, perform electrolysis, as opposed to generating current, and I think that should not be merged. If we are to go in depth in either, it wouldn't do to have them in the same article. Kr5t 22:02, 21 May 2006 (UTC)[reply]
As further evidence that Galvanic cells are synonomous with electrochemical cells, note that the lead-acid battery article says that lead-acid batteries are galvanic cells. Really, what is the difference? Can anyone come up with one? Kr5t 00:44, 22 May 2006 (UTC)[reply]
Actually, electrochemical cells used to describe both galvanic and electrolytic cells. This is an excerpt from my grade 12 Nelson chemistry textbook: "The term electrochemical cell is often used in chemistry to refer to either a cell with a spontaneous reaction, such as the electric or galvanic cell, or a cell with a nonspontaneous reaction, which we will call an electrolytic cell."
While electrochemical cell is the umbrella term used to describe both galvanic and electrolytic cells, I would not merge the pages. There are several very distinct differences between the two types of cells and to avoid confusion, keep the articles segregated.
I agree they should not be merged, but for different reasons to those given above. Galvanic corrosion of of particular interest in the marine/engineering industry and, although the underlying science is similar, the impact in terms of corrosion is not.
I would prefer, for several reasons, that the two not be merged. However, if you do merge them, make sure all pages that link to Electrochemical cell will instead link to Galvanic cell, or vice versā. This can be accomplished either by means of a redirect or by actually changing the links. Ruff 23:52, 26 July 2006 (UTC)[reply]
I am PhD Physics and elec eng. I wish SOMEBODY would EXPLAIN how a galvanic cell works.
People TALK of "closing the external circuit" What IS a "resistive junction", "contact potential" and HOW do you know you have got it?
DOES a galvanic cell "have a voltage" on open circuit? How?
I built all the galvanic cells age 7. But the "explanations" are trash!
OK lets have Zn and Cu in dilute H2SO4. They touch at a point UNDER the liquid. Does a current flow or not? How, where, why, and what is the volts and what gets hot? Why so SOME people, in a Daniel cell, say the Cu is anode while others say it is cathode? Ana is up, so that is where the crazy-positive-charges rise up! QED.
So who would like to be the oNLY person in 60 years ABLE to explain Voltas Pile to me? WHY does the damp film on the Cu/Zn not do EXACTLY what the wet blotting paper does, thus CANCELLING the volts? Thanks,John
Wow, do you mean that you're working on a Ph.D., or that you already have one? Either way (given that you say your field is electrical engineering) I find it hard to believe that you don't get how an electrochemical cell works (or to be completely objective, that you don't understand the standard theory behind it).
From the questions you're asking I'm guessing that you don't really understand what "voltage" is, or what it means in terms of chemical reactions. Wikipedia has a good explanation of redox reactions so I'd suggest that you start there, and hopefully you can piece the rest together. Quantris 21:35, 8 February 2007 (UTC)[reply]
New section to implement: types of cells
Primairy power cells are non-rechargable power cells Secundairy power cells are rechargable power cells (also called accumulators)
This subdivision also allows a clearer view and removes the confusing "accumulator" word. As such, perhaps accumulator-can be moved to "Secunairy power cell" and accumulator can be made a redirect.
Look into it, it makes things allot simpler. thanks.
KVDP (talk) 13:10, 26 January 2008 (UTC)[reply]
Due to environmental aswell as financial concerns, people are slowly moving away from electrochemical cells and towards capacitors [1]. This, as capacitors are much more environmental and financially attractive (they are rechargable, and made of less damaging materials). Examples to this can be seen with the rise of the Faraday flashlights. Besides these energy carriers, new batteries are emerging which too are more environmentally-friendly. Such cells are created (amongst others) by Susumi Suzuki.[2].
I am already implementing it into the article, if it does not qualify for anyone; please discuss it here.
KVDP (talk) 13:24, 26 January 2008 (UTC)[reply]
KVDP (talk) 18:27, 2 March 2008 (UTC)[reply]
Besides NiMh (nickel-metal hydride) and NiCd (Nickel-cadmium) chemical cells, saline and alcaline batteries (which are usually said to be 'non-rechargable cells) may also be recharged. This less-known feature allows users not only to reduce the financial expenses (saline/alcaline cells are usually cheaper) they do yearly on buying chemical cells, but also allows them to achieve environmental advantage as the batteries may be recharged up to 20 times before being exhausted (NiMh/NiCd may be recherged more however).
This recharging of saline/alcaline cells is possible trough the use of low-heat recharging (by special rechargers). Several manufacturers (as provence-piles) exist which produce these devices. [3] [4]
Please include in article as this is of vital information for the environmental community. Also include my previous proposals for new sections. Also check whether using this device with NiMh/NiCd cells may increase their life expenditure aswell (so the 1000 recharges frequently mentioned may actually be achieved or surpassed).
KVDP (talk) 18:25, 2 March 2008 (UTC)[reply]
PS: references here are added aswell-->Provence-piles 'Batbooster' able to recharge alcaline/saline cells and Battery Xtender as another device able to recharge alcaline cells
KVDP (talk) 18:29, 2 March 2008 (UTC)[reply]