Energy | Turkish Chemistry
May 12

Fuel Chemistry
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Molecular Size

Alternative fuels tend to be made up of small, fairly simple ; for example, here are schematic chemical diagrams (C denotes a carbon , H is hydrogen, and O is oxygen) of
Methane, CH4methane (CH4), the primary constituent of liquefied or compressed natural gas, and
Propane, C3H8propane (C3H8), the primary constituent of liquified petroleum gas.

Petroleum fuels are blends of lots of different chemical species; in general, the of a liquid petroleum fuel are pretty big and complex. Here is
Isooctane, C8H18isooctane (C8H18), typical of the found in gasoline (I had to spread out the structure a bit to get all the hydrogen atoms to fit in the picture–all of these are, of course, three-dimensional, but some squish into a plane better than others!), and
Cetane, C16H34
this monster is cetane, or n-hexadecane (C16H34), typical of diesel fuel.

Incomplete Combustion

When a hydrocarbon fuel (that is, one that is made up of hydrogen and carbon) burns completely, the oxygen in the air combines with the hydrogen to form (H2O) and with the carbon to form carbon dioxide (CO2). If the burning is not complete, then some of the carbon atoms only combine with one oxygen rather than two, to form carbon monoxide (CO), a highly poisonous gas.

Some of the carbon atoms may remain stuck together with each other and with some of the hydrogen atoms as well, so that unburned hydrocarbon (mostly smaller than the ones in the original fuel) can also come out the tailpipe. These unburned hydrocarbons (plus any fuel hydrocarbons that evaporate from the fuel system before getting into the engine to be burned at all) react with nitrogen oxides (another pollutant from combustion) in the presence of sunlight to form ozone, which is a lung irritant (the “ozone layer” in the stratosphere is a shield against the sun’s ultraviolet light, but at ground level ozone is the main component of “photochemical smog”). Carbon atoms can also remain stuck to one another with few or no hydrogen atoms attached, especially during incomplete combustion of diesel fuel, producing soot.

This is one of the reasons alternative fuels are less polluting than gasoline and diesel: their simpler are easier to burn more completely in an engine, so that less carbon monoxide, soot, and unburned hydrocarbons come out the tailpipe. In addition, any unburned hydrocarbons that are produced are less reactive than those that come from incomplete burning of gasoline or diesel fuel, and so they produce less ground-level ozone; methane in particular is almost incapable of forming smog.

Oxygen Content

Some alternative fuels are not hydrocarbons; alcohols and biodiesel contain oxygen atoms as well as carbon and hydrogen. Here are the chemical structures of the common alcohol fuels,
Methanol, CH3OHmethanol (CH3OH) and
Ethanol, C2H5OHethanol (C2H5OH).
(Biodiesel are “monoalkyl esters”, but I haven’t been able to trace down anything more specific. The “ester” part of that name, however, indicates that the include oxygen atoms.)

In many parts of the USA, gasoline is “oxygenated” during at least part of the year; this means that oxygen-bearing compounds are added to the fuel mixture. The reason for doing this is that having some oxygen as part of the fuel to start with promotes more complete combustion, so that less carbon monoxide, soot, and unburned hydrocarbons come out the tailpipe, as described above. Alcohol fuels and biodiesel carry this one step further, in that the oxygen-bearing compound is not an additive at the 5 to 10 percent level, but a major constituent of the fuel, which increases the benefits of oxygenation.

Carbon Content

Even if, with the aid of electronic engine controls and efficient catalytic converters, a hydrocarbon fuel is burned completely to and carbon dioxide, there is now growing concern about carbon dioxide as a greenhouse gas. Measures to cut back on production of carbon dioxide by automobiles without sacrificing performance can focus on efficiency, i.e., getting as much useful propulsive power out of a given amount of fuel as possible, which typically involves replacing the traditional drivetrain of a piston engine driving the wheels through a gearbox with a more efficient design.

However, some fuels inherently produce less carbon dioxide when burned completely than gasoline or diesel fuel. For example, counting the numbers of oxygen atoms it takes to burn up an isooctane and a methane (typical of gasoline and natural gas respectively), one can calculate that 100 oxygen atoms will combine with four isooctane to produce 32 carbon dioxide and 36 , while the same number of oxygen atoms will combine with 25 methane to produce 25 carbon dioxide and 50 . That is, a given amount of air (oxygen) will produce about 25% less carbon dioxide if used to burn natural gas than if used to burn gasoline. (Of course, this advantage will be reduced if you have to open the throttle wider and burn an additional amount of air with natural gas to get the same amount of power, but in the real world the 25% figure turns out to be about right.)

Avoiding Carbon Dioxide Emissions Entirely

The other thing to consider is the source of the carbon in the fuel; if it came from the carbon dioxide in today’s air to begin with, like an alcohol fuel produced by fermenting biomass (as opposed to a fossil fuel, whose carbon came out of the air when the dinosaurs were around!), then returning it to the air now adds nothing to the net flow of carbon dioxide into the atmosphere. Alcohol fuels or biodiesel produced from plants, when burned, just return to the air the carbon dioxide that those plants took out of the air while growing.

Finally, there’s one fuel that, in itself, produces no carbon dioxide at all when burned, namely
Hydrogen, H2hydrogen; there’s no carbon there to produce carbon dioxide!
Of course, since free hydrogen don’t occur in nature, it is typically produced by “reforming” a hydrocarbon or alcohol fuel or by using electricity to split into hydrogen and oxygen. Then the size of the contribution of hydrogen fuel to carbon dioxide emissions depends on the source of the hydrocarbon fuel that was reformed or the source of the electricity used to split the .

If a fossil fuel was the ultimate source of the energy that is, in effect, stored in the hydrogen, then you can still gain a large improvement in carbon-dioxide production if the hydrogen is used in an efficient drivetrain, as noted above; the same is true for the electrical energy stored in a battery-powered electric vehicle. In order to obtain the full benefits of reduction of carbon dioxide (or of ordinary air pollutants like carbon monoxide), of course, the energy used to split the hydrogen or charge the battery can be obtained from a renewable source like wind power or photovoltaics.

The nice thing about hydrogen- or battery-powered vehicles is that they can run on whatever is available–efficient natural-gas-burning powerplants today, with an increasing contribution from renewable energy as time goes on and the price of photovoltaic cells (solar cells) and other renewable energy sources continues to decline. As renewable energy becomes an ever larger part of the power generation mix over the next few decades, hydrogen- and battery-powered vehicles can switch over to the new power sources without a hiccup–it’s all electricity to them!

Åžub 1

Kinetik Enerji

Oca 31

Chemical kinetics
icon1 admin | icon2 History of Chemistry | icon4 01 31st, 2009| icon3No Comments »

 

kinetics, also known as reaction kinetics, is the study of rates of processes. kinetics includes investigations of how different experimental conditions can influence the speed of a reaction and yield information about the reaction’s mechanism and transition states, as well as the construction of mathematical models that can describe the characteristics of a reaction. In 1864, Peter Waage and Cato Guldberg pioneered the development of kinetics by formulating the law of action, which states that the speed of a reaction is proportional to the quantity of the reacting substances.

kinetics deals with the experimental determination of reaction rates from which rate laws and rate constants are derived. Relatively simple rate laws exist for zero order reactions (for which reaction rates are independent of concentration), first order reactions, and second order reactions, and can be derived for others. In consecutive reactions the rate-determining step often determines the kinetics. In consecutive first order reactions, a steady state approximation can simplify the rate law. The activation energy for a reaction is experimentally determined through the Arrhenius equation and the Eyring equation. The main factors that influence the reaction rate include: the physical state of the , the concentrations of the , the temperature at which the reaction occurs, and whether or not any catalysts are present in the reaction.

Nature of the

Depending upon what substances are reacting, the time varies. Acid reactions, the formation of salts, and ion exchange are fast reactions. When covalent bond formation takes place between the molecules and when large molecules are formed, the reactions tend to be very slow.

Physical state

The physical state (solid, liquid, or gas) of a reactant is also an important factor of the rate of change. When are in the same phase, as in aqueous solution, thermal motion brings them into contact. However, when they are in different phases, the reaction is limited to the interface between the . Reaction can only occur at their area of contact, in the case of a liquid and a gas, at the surface of the liquid. Vigorous shaking and stirring may be needed to bring the reaction to completion. This means that the more finely divided a solid or liquid reactant, the greater its surface area per unit volume, and the more contact it makes with the other reactant, thus the faster the reaction. To make an analogy, for example, when one starts a fire, one uses wood chips and small branches—one doesn’t start with large logs right away. In organic On water reactions are the exception to the rule that homogeneous reactions take place faster than heterogeneous reactions

Concentration

Concentration plays a very important role in reactions according to the collision theory of reactions, because molecules must collide in order to react together. As the concentration of the increases, the frequency of the molecules colliding increases, striking each other more frequently by being in closer contact at any given point in time. Think of two being in a closed container. All the molecules contained within are colliding constantly. By increasing the amount of one or more of the it causes these collisions to happen more often, increasing the reaction rate

Temperature

Temperature usually has a major effect on the rate of a reaction. Molecules at a higher temperature have more thermal energy. Although collision frequency is greater at higher temperatures, this alone contributes only a very small proportion to the increase in rate of reaction. Much more important is the fact that the proportion of reactant molecules with sufficient energy to react (energy greater than activation energy: E > Ea) is significantly higher and is explained in detail by the Maxwell–Boltzmann distribution of molecular energies.

The ‘rule of thumb’ that the rate of reactions doubles for every 10° C temperature rise is a common misconception. This may have been generalized from the special case of biological systems, where the Q10 (temperature coefficient) is often between 1.5 and 2.5.

A reaction’s kinetics can also be studied with a temperature jump approach. This involves using a sharp rise in temperature and observing the relaxation rate of an equilibrium process.

Catalysts

A catalyst is a substance that accelerates the rate of a reaction but remains chemically unchanged afterwards. The catalyst increases rate reaction by providing a different reaction mechanism to occur with a lower activation energy. In autocatalysis a reaction product is itself a catalyst for that reaction leading to positive feedback. Proteins that act as catalysts in biochemical reactions are called enzymes. Michaelis-Menten kinetics describe the rate of enzyme mediated reactions.A catalyst does not affect the position of the equilibria, as the catalyst speeds up the backward and forward reactions equally.

In certain organic molecules specific substituents can have an influence on reaction rate in neighbouring group participation.

Agitating or mixing a solution will also accelerate the rate of a reaction, as this gives the particles greater kinetic energy, increasing the number of collisions between and therefore the possibility of successful collisions.

Pressure

Increasing the pressure in a gaseous reaction will increase the number of collisions between , increasing the rate of reaction. This is because the activity of a gas is directly proportional to the partial pressure of the gas. This is similar to the effect of increasing the concentration of a solution

Equilibrium

While kinetics is concerned with the rate of a reaction, determines the extent to which reactions occur. In a reversible reaction, equilibrium is reached when the rates of the forward and reverse reactions are equal and the concentrations of the and products no longer change. This is demonstrated by, for example, the Haber–Bosch process for combining nitrogen and hydrogen to produce ammonia. clock reactions such as the Belousov–Zhabotinsky reaction demonstrate that component concentrations can oscillate for a long time before finally attaining the equilibrium

Free energy

In general terms, the free energy change (ΔG) of a reaction determines if a change will take place, but kinetics describes how fast the reaction is. A reaction can be very exothermic and have a very positive entropy change but will not happen in practice if the reaction is too slow. If a reactant can produce two different products, the thermodynamically most stable one will generally form except in special circumstances when the reaction is said to be under kinetic reaction control. The Curtin–Hammett principle applies when determining the product ratio for two interconverting rapidly, each going to a different product. It is possible to make predictions about reaction rate constants for a reaction from free-energy relationships.

The kinetic isotope effect is the difference in the rate of a reaction when an atom in one of the is replaced by one of its isotopes.

kinetics provides information on residence time and heat transfer in a reactor in engineering and the molar distribution in polymer .

Applications

The mathematical models that describe reaction kinetics provide chemists and engineers with tools to better understand and describe processes such as food decomposition, microorganism growth, stratospheric ozone decomposition, and the complex of biological systems. These models can also be used in the design or modification of reactors to optimize product yield, more efficiently separate products, and eliminate environmentally harmful by-products. When performing catalytic cracking of heavy hydrocarbons into gasoline and light gas, for example, kinetic models can be used to find the temperature and pressure at which the highest yield of heavy hydrocarbons into gasoline will occur.

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