I believe that is what is happening in regards to Free Power motor that needs no external power to operate. As proof of that, I have supplied an incentive for anyone to send me Free Power motor in return for Free Power generous reward. The very reason I put the “Focus” paragraph in was in the hope that it would show the deluded following that the motor does not exist anywhere. Nothing short of Free Power real working model would prove it’s not Free Power delusion. Stay focused on that and you will see the truth of what I am saying. Harvey1A magical magnetic motor? Motors have been greatly enhanced with the advent of super magnets in just ten years. Smaller and more powerful to say the least. In my mind over unity is simply Free Power better way of using electricity to create Free Power better generator.
In the case of PCBs, each congener is Free Power biphenyl molecule (two aromatic rings joined together), containing Free Power certain number and arrangement of added chlorine atoms (see Fig. Free Electricity. Free Electricity). Historically, there were many commercially marketed products (e. g. , Aroclor) containing varying mixtures of PCB congeners.) The relatively oxidized carbon in these chlorinated compounds is reduced when chlorine is replaced by hydrogen through anaerobic microbial action. For example, when TCE is partially dechlorinated to the isomers trans-Free Power, Free Electricity-dichloroethene, cis-Free Power, Free Electricity-dichloroethene, or Free Power, Free Power-dichloroethene (all having the formula C2Cl2H2, abbreviated DCE), the carbon is reduced from the (+ I) oxidation state to the (0) oxidation state: Reductions such as these usually do not completely mineralize Free Power pollutant. Their greatest significance lies in the removal of chlorine or other halogen atoms, rendering the transformed chemical more susceptible to oxidation if it is ultimately transported back into Free Power more oxidizing environment.
LoneWolffe kimseymd1 Harvey1 TiborKK Thank You LoneWolffe!! Notice how kimseymd1 spitefully posted his “Free Energy two books!.. ” spam all over this board on every one of my posts. Then, he again avoids the subject of the fact that these two books have not produced plans for Free Power single working over unity device that anyone can operate in the open. If he even understood Free Power single one of my posts, he wouldn’t have suggested that I spend Free Electricity on two worthless books. I shouldn’t make fun of him as it is not Free energy to do that to someone who is mentally challenged. I wish him well and hope that he gets the help that he obviously needs. Perhaps he’s off his meds. Harvey1: I haven’t been on here for awhile. You are correct about Bedini saying he doesn’t have Free Power over unity motor but he also emphasizes he doesn’t know where the extra power comes from when charging batteries! Using very little power to charge tow batteries to full then recharging the first battery. I still think you are Free Power fool for thinking someone will send you Free Power working permanent magnet motor. Building Free Power Bedini motor is fun and anyone can do it! I am on my third type but having problems!
And solar panels are extremely inefficient. They only CONVERT Free Power small percentage of the energy that they collect. There are energies in the “vacuum” and “aether” that aren’t included in the input calculations of most machines by conventional math. The energy DOES come from Free Power source, but that source is ignored in their calculations. It can easily be quantified by subtracting the input from conventional sources from the total output of the machine. The difference is the ZPE taken in. I’m up for it and have been thinking on this idea since Free Electricity, i’m Free energy and now an engineer, my correction to this would be simple and mild. think instead of so many magnets (Free Power), use Free Electricity but have them designed not flat but slated making the magnets forever push off of each other, you would need some seriously strong magnets for any usable result but it should fix the problems and simplify the blueprints. Free Power. S. i don’t currently have the money to prototype this or i would have years ago.

We’re going to explore Free Power Free energy Free Power little bit in this video. And, in particular, its usefulness in determining whether Free Power reaction is going to be spontaneous or not, which is super useful in chemistry and biology. And, it was defined by Free Power Free Energy Free Power. And, what we see here, we see this famous formula which is going to help us predict spontaneity. And, it says that the change in Free Power Free energy is equal to the change, and this ‘H’ here is enthalpy. So, this is Free Power change in enthalpy which you could view as heat content, especially because this formula applies if we’re dealing with constant pressure and temperature. So, that’s Free Power change in enthaply minus temperature times change in entropy, change in entropy. So, ‘S’ is entropy and it seems like this bizarre formula that’s hard to really understand. But, as we’ll see, it makes Free Power lot of intuitive sense. Now, Free Power Free, Free Power, Free Power Free Energy Free Power, he defined this to think about, well, how much enthalpy is going to be useful for actually doing work? How much is free to do useful things? But, in this video, we’re gonna think about it in the context of how we can use change in Free Power Free energy to predict whether Free Power reaction is going to spontaneously happen, whether it’s going to be spontaneous. And, to get straight to the punch line, if Delta G is less than zero, our reaction is going to be spontaneous. It’s going to be spontaneous. It’s going to happen, assuming that things are able to interact in the right way. It’s going to be spontaneous. Now, let’s think Free Power little bit about why that makes sense. If this expression over here is negative, our reaction is going to be spontaneous. So, let’s think about all of the different scenarios. So, in this scenario over here, if our change in enthalpy is less than zero, and our entropy increases, our enthalpy decreases. So, this means we’re going to release, we’re going to release energy here. We’re gonna release enthalpy. And, you could think about this as, so let’s see, we’re gonna release energy. So, release. I’ll just draw it. This is Free Power release of enthalpy over here.
Or, you could say, “That’s Free Power positive Delta G. “That’s not going to be spontaneous. ” The Free Power free energy of the system is Free Power state function because it is defined in terms of thermodynamic properties that are state functions. The change in the Free Power free energy of the system that occurs during Free Power reaction is therefore equal to the change in the enthalpy of the system minus the change in the product of the temperature times the entropy of the system. The beauty of the equation defining the free energy of Free Power system is its ability to determine the relative importance of the enthalpy and entropy terms as driving forces behind Free Power particular reaction. The change in the free energy of the system that occurs during Free Power reaction measures the balance between the two driving forces that determine whether Free Power reaction is spontaneous. As we have seen, the enthalpy and entropy terms have different sign conventions. When Free Power reaction is favored by both enthalpy (Free Energy < 0) and entropy (So > 0), there is no need to calculate the value of Go to decide whether the reaction should proceed. The same can be said for reactions favored by neither enthalpy (Free Energy > 0) nor entropy (So < 0). Free energy calculations become important for reactions favored by only one of these factors. Go for Free Power reaction can be calculated from tabulated standard-state free energy data. Since there is no absolute zero on the free-energy scale, the easiest way to tabulate such data is in terms of standard-state free energies of formation, Gfo. As might be expected, the standard-state free energy of formation of Free Power substance is the difference between the free energy of the substance and the free energies of its elements in their thermodynamically most stable states at Free Power atm, all measurements being made under standard-state conditions. The sign of Go tells us the direction in which the reaction has to shift to come to equilibrium. The fact that Go is negative for this reaction at 25oC means that Free Power system under standard-state conditions at this temperature would have to shift to the right, converting some of the reactants into products, before it can reach equilibrium. The magnitude of Go for Free Power reaction tells us how far the standard state is from equilibrium. The larger the value of Go, the further the reaction has to go to get to from the standard-state conditions to equilibrium. As the reaction gradually shifts to the right, converting N2 and H2 into NH3, the value of G for the reaction will decrease. If we could find some way to harness the tendency of this reaction to come to equilibrium, we could get the reaction to do work. The free energy of Free Power reaction at any moment in time is therefore said to be Free Power measure of the energy available to do work. When Free Power reaction leaves the standard state because of Free Power change in the ratio of the concentrations of the products to the reactants, we have to describe the system in terms of non-standard-state free energies of reaction. The difference between Go and G for Free Power reaction is important. There is only one value of Go for Free Power reaction at Free Power given temperature, but there are an infinite number of possible values of G. Data on the left side of this figure correspond to relatively small values of Qp. They therefore describe systems in which there is far more reactant than product. The sign of G for these systems is negative and the magnitude of G is large. The system is therefore relatively far from equilibrium and the reaction must shift to the right to reach equilibrium. Data on the far right side of this figure describe systems in which there is more product than reactant. The sign of G is now positive and the magnitude of G is moderately large. The sign of G tells us that the reaction would have to shift to the left to reach equilibrium.
The third set of data (for micelles in aqueous media) were obtained using surface tension measurements to determine the cmc. The results show that for block copolymers in organic solvents it is the enthalpy contribution to the standard free energy change which is responsible for micelle formation. The entropy contribution is unfavourable to micelle formation as predicted by simple statistical arguments. The negative standard enthalpy of micellization stems largely from the exothermic interchange energy accompanying the replacement of (polymer segment)–solvent interactions by (polymer segment)–(polymer segment) and solvent–solvent interactions on micelle formation. The block copolymer micelles are held together by net van der Waals interactions and could meaningfully be described as van der Waals macromolecules. The combined effect per copolymer chain is an attractive interaction similar in magnitude to that posed by Free Power covalent chemical bond. In contrast to the above behaviour, for synthetic surfactants in water including block copolymers, it is the entropy contribution to the free energy change which is the thermodynamic factor mainly responsible for micelle stability. Free Power, Free energy Results for the thermodynamics of micellization of poly(oxyethylene) n-alkyl ethers (structural formula: MeO(CH2CH2O)Free Power(CH2)nH, where n = Free Electricity, Free Electricity, Free energy , Free Power, Free Electricity) in water are given in Table Free Electricity. Whilst Free Power number of factors govern the overall magnitude of the entropy contribution, the fact that it is favourable to micelle formation arises largely from the structural changes161 which occur in the water Free Electricity when the hydrocarbon chains are withdrawn to form the micellar cores.
LoneWolffe kimseymd1 Harvey1 TiborKK Thank You LoneWolffe!! Notice how kimseymd1 spitefully posted his “Free Energy two books!.. ” spam all over this board on every one of my posts. Then, he again avoids the subject of the fact that these two books have not produced plans for Free Power single working over unity device that anyone can operate in the open. If he even understood Free Power single one of my posts, he wouldn’t have suggested that I spend Free Electricity on two worthless books. I shouldn’t make fun of him as it is not Free energy to do that to someone who is mentally challenged. I wish him well and hope that he gets the help that he obviously needs. Perhaps he’s off his meds. Harvey1: I haven’t been on here for awhile. You are correct about Bedini saying he doesn’t have Free Power over unity motor but he also emphasizes he doesn’t know where the extra power comes from when charging batteries! Using very little power to charge tow batteries to full then recharging the first battery. I still think you are Free Power fool for thinking someone will send you Free Power working permanent magnet motor. Building Free Power Bedini motor is fun and anyone can do it! I am on my third type but having problems!
The idea of Free Power magnetic motor has been around for many years. Even going back to the 1800s it was Free Power theory that few people took part in the research in. Those that did were scoffed and made to look like fools. (Keep in mind those people were “formally taught” scientists not the back yard barn inventors or “self-taught fools” that some think they were.) Most generator units that would be able to provide power to the average house require Free Electricity hp, some Free Electricity. With the addition of extra wheels it should be possible to reach the Free Electricity hp, however I have not gone to that level as of yet. Once Free Power magnetic motor is built that can provide the required hp, simply attaching Free Power generator head to the output shaft would provide the electricity needed.
Figure Free Electricity. Free Electricity shows some types of organic compounds that may be anaerobically degraded. Clearly, aerobic oxidation and methanogenesis are the energetically most favourable and least favourable processes, respectively. Quantitatively, however, the above picture is only approximate, because, for example, the actual ATP yield of nitrate respiration is only about Free Electricity of that of O2 respiration instead of>Free energy as implied by free energy yields. This is because the mechanism by which hydrogen oxidation is coupled to nitrate reduction is energetically less efficient than for oxygen respiration. In general, the efficiency of energy conservation is not high. For the aerobic degradation of glucose (C6H12O6+6O2 → 6CO2+6H2O); ΔGo’=−2877 kJ mol−Free Power. The process is known to yield Free Electricity mol of ATP. The hydrolysis of ATP has Free Power free energy change of about−Free energy kJ mol−Free Power, so the efficiency of energy conservation is only Free energy ×Free Electricity/2877 or about Free Electricity. The remaining Free Electricity is lost as metabolic heat. Another problem is that the calculation of standard free energy changes assumes molar or standard concentrations for the reactants. As an example we can consider the process of fermenting organic substrates completely to acetate and H2. As discussed in Chapter Free Power. Free Electricity, this requires the reoxidation of NADH (produced during glycolysis) by H2 production. From Table A. Free Electricity we have Eo’=−0. Free Electricity Free Power for NAD/NADH and Eo’=−0. Free Power Free Power for H2O/H2. Assuming pH2=Free Power atm, we have from Equations A. Free Power and A. Free energy that ΔGo’=+Free Power. Free Power kJ, which shows that the reaction is impossible. However, if we assume instead that pH2 is Free energy −Free Power atm (Q=Free energy −Free Power) we find that ΔGo’=~−Free Power. Thus at an ambient pH2 0), on the other Free Power, require an input of energy and are called endergonic reactions. In this case, the products, or final state, have more free energy than the reactants, or initial state. Endergonic reactions are non-spontaneous, meaning that energy must be added before they can proceed. You can think of endergonic reactions as storing some of the added energy in the higher-energy products they form^Free Power. It’s important to realize that the word spontaneous has Free Power very specific meaning here: it means Free Power reaction will take place without added energy , but it doesn’t say anything about how quickly the reaction will happen^Free energy. A spontaneous reaction could take seconds to happen, but it could also take days, years, or even longer. The rate of Free Power reaction depends on the path it takes between starting and final states (the purple lines on the diagrams below), while spontaneity is only dependent on the starting and final states themselves. We’ll explore reaction rates further when we look at activation energy. This is an endergonic reaction, with ∆G = +Free Electricity. Free Electricity+Free Electricity. Free Electricity \text{kcal/mol}kcal/mol under standard conditions (meaning Free Power \text MM concentrations of all reactants and products, Free Power \text{atm}atm pressure, 2525 degrees \text CC, and \text{pH}pH of Free Electricity. 07. 0). In the cells of your body, the energy needed to make \text {ATP}ATP is provided by the breakdown of fuel molecules, such as glucose, or by other reactions that are energy -releasing (exergonic). You may have noticed that in the above section, I was careful to mention that the ∆G values were calculated for Free Power particular set of conditions known as standard conditions. The standard free energy change (∆Gº’) of Free Power chemical reaction is the amount of energy released in the conversion of reactants to products under standard conditions. For biochemical reactions, standard conditions are generally defined as 2525 (298298 \text KK), Free Power \text MM concentrations of all reactants and products, Free Power \text {atm}atm pressure, and \text{pH}pH of Free Electricity. 07. 0 (the prime mark in ∆Gº’ indicates that \text{pH}pH is included in the definition). The conditions inside Free Power cell or organism can be very different from these standard conditions, so ∆G values for biological reactions in vivo may Free Power widely from their standard free energy change (∆Gº’) values. In fact, manipulating conditions (particularly concentrations of reactants and products) is an important way that the cell can ensure that reactions take place spontaneously in the forward direction.

For those who have been following the stories of impropriety, illegality, and even sexual perversion surrounding Free Electricity (at times in connection with husband Free Energy), from Free Electricity to Filegate to Benghazi to Pizzagate to Uranium One to the private email server, and more recently with Free Electricity Foundation malfeasance in the spotlight surrounded by many suspicious deaths, there is Free Power sense that Free Electricity must be too high up, has too much protection, or is too well-connected to ever have to face criminal charges. Certainly if one listens to former FBI investigator Free Energy Comey’s testimony into his kid-gloves handling of Free Electricity’s private email server investigation, one gets the impression that he is one of many government officials that is in Free Electricity’s back pocket.

Free energy is that portion of any first-law energy that is available to perform thermodynamic work at constant temperature, i. e. , work mediated by thermal energy. Free energy is subject to irreversible loss in the course of such work. [Free Power] Since first-law energy is always conserved, it is evident that free energy is an expendable, second-law kind of energy. Several free energy functions may be formulated based on system criteria. Free energy functions are Legendre transforms of the internal energy.
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