Today, quite a lot of people are making homemade liqueur, but some drinks require the presence of an alcoholic element. Producing alcohol at home is not very labor-intensive. To do this, you need to know and take into account some aspects and principles of making methyl alcohol.
First of all, the production of methanol requires the presence of grain. The role of grain crops in this case can be corn and wheat. You can also use potatoes and starch. But, as is known, when interacting with a substance, starch does not give any reaction. In order to produce a chemical element, the sugaring method is used. And in order to sugar it, certain enzymes are needed; they are present in malt. By making ethanol from grain without chemical impurities, the yield of a natural product is observed.
The technology for producing alcohol chemicals at home can consist of several stages.
Below are the most important ones:
As you can see, the technology for making homemade alcohol is quite simple and does not require additional effort.
In recent years, fossil raw materials that can be used to make ethyl alcohol have decreased significantly. There is a grain shortage. However, producing alcohol from sawdust is not the worst option, since this raw material is constantly renewed over the years.
However, making the substance from sawdust requires some skills, and in addition, the manufacturer must have special equipment, without which it will be labor-intensive to produce ethanol. Producing alcohol from sawdust at home is very popular and does not require high costs.
As you know, your own produced ethanol is not compared with the factory version. Products made in commercial conditions are of higher quality, because each ingredient is unique. It is much easier to produce alcohol from sawdust!
The production of ethyl alcohol at home is carried out using a special apparatus. This device is capable of performing the procedure of splitting certain elements, as well as conducting chemical reactions between them. Conventional equipment for the production of alcoholic beverages can look like mini factories. You can make any types of alcoholic drinks in them.
It is quite simple to study the technology for preparing ethyl substance, and the product turns out to be of high quality. What can you get from this? Firstly, these are alcoholic products of high quality, and secondly, their own costs are fully recouped; this requires a special apparatus.
For example, if 20 kg of sugar is used, it produces up to 12 liters of alcohol. In this case, the percentage of methanol reaches up to 96%. This calculation yields 25 half-liter bottles of vodka. In addition, the electricity consumed by the device will be spent about 25 kW.
Such equipment is capable of using all loaded products for their intended purpose. The undrinkable product produced by the first treatment can be used as a cleaner for glass surfaces and windows. You can also install such a device yourself, using the necessary diagrams and drawings. Such equipment can easily cope with the production of methyl alcohol.
Equipment for the production of alcoholic products has some principles of its operation. The device has a special neck that fills the tank with the necessary liquid. In the form of such a liquid, mash can act. Using heating burners, the product is heated to boiling point. After which the device and equipment must be transferred to normal mode.
Next, cooling occurs through the refrigeration compartment with additional purification of the steam from unnecessary impurities. The purified substance enters the tank, and the vapors enter the refrigerator, where they are cooled to a liquid state. The apparatus for producing alcohol is capable of producing the established standard. The result of this procedure is high-quality alcohol.
You are in the forest... Thick and thin tree trunks are crowded around. For a chemist, they all consist of the same material - wood, the main part of which is organic matter - fiber (C 6 H 10 O 5) x. Fiber forms the walls of plant cells, i.e., their mechanical skeleton; We have it quite pure in the fibers of cotton paper and flax; in trees it is always found together with other substances, most often lignin, of almost the same chemical composition, but with different properties. The elementary formula of fiber C 6 H 10 O 5 coincides with the formula of starch, beet sugar has the formula C 12 H 2 2O 11. The ratio of the number of hydrogen atoms to the number of oxygen atoms in these formulas is the same as in water: 2:1. Therefore, these and similar substances were called “carbohydrates” in 1844, that is, substances seemingly (but not actually) consisting of carbon and water.
The carbohydrate fiber has a high molecular weight. Its molecules are long chains made up of individual links. Unlike white starch grains, fiber is strong threads and fibers. This is explained by the different, now precisely established, structural structure of starch and fiber molecules. Pure fiber is technically called cellulose.
In 1811, academician Kirchhoff made an important discovery. He took ordinary starch obtained from potatoes and treated it with dilute sulfuric acid. Under the influence of H 2 SO 4 there was hydrolysis starch and it turned into sugar:
This reaction was of great practical importance. Starch and syrup production is based on it.
But fiber has the same empirical formula as starch! This means you can also get sugar from it.
Indeed, in 1819, saccharification of fiber using dilute sulfuric acid was first carried out. For these purposes, concentrated acid can also be used; Russian chemist Vogel in 1822 obtained sugar from ordinary paper, acting on it with an 87% solution of H 2 SO 4.
At the end of the 19th century. Practicing engineers have already become interested in obtaining sugar and alcohol from wood. Currently, alcohol is produced from cellulose on a factory scale. The method, discovered in a test tube by a scientist, is then carried out in the large steel apparatus of an engineer.
Let's visit the hydrolysis plant... Sawdust, shavings or wood chips are loaded into huge digesters (percolators). This is waste from sawmills or wood processing enterprises. Previously, this valuable waste was burned or simply thrown into a landfill. A weak (0.2-0.6%) solution of mineral acid (most often sulfuric) passes through percolators with a continuous current. It is impossible to keep the same acid in the apparatus for a long time: the sugar contained in it, obtained from wood, is easily destroyed. In percolators, the pressure is 8-10 atm, and the temperature is 170-185°. Under these conditions, cellulose hydrolysis proceeds much better than under normal conditions, when the process is very difficult. Percolators produce a solution containing about 4% sugar. The yield of sugary substances during hydrolysis reaches 85% of the theoretically possible (according to the reaction equation).
Rice. 8. A visual diagram of the production of hydrolytic alcohol from wood.
For the Soviet Union, which has vast forests and is steadily developing the synthetic rubber industry, obtaining alcohol from wood is of particular interest. Back in 1934, the XVII Congress of the All-Union Communist Party (Bolsheviks) decided to fully develop the production of alcohol from sawdust and waste from the paper industry. The first Soviet hydrolysis-alcohol factories began to operate regularly in 1938. During the years of the second and third five-year plans, we built and launched factories for the production of hydrolysis alcohol - alcohol from wood. This alcohol is now increasingly being processed into synthetic rubber. This is alcohol from non-food raw materials. Every million liters of hydrolytic ethyl alcohol frees up about 3 thousand tons of bread or 10 thousand tons of potatoes and, therefore, about 600 hectares of cultivated area for food. To obtain this amount of hydrolytic alcohol, you need 10 thousand tons of sawdust with 45 percent moisture content, which can produce one sawmill of average productivity per year of operation.
Siberian scientists are working on technology for the production of domestic bioethanolIn Soviet times, who still remembers, there were a lot of jokes about alcohol made from sawdust. There were rumors that after the war, cheap vodka was made using sawdust alcohol. This drink is popularly called “suk”.
In general, talk about the production of alcohol from sawdust did not arise out of nowhere, of course. Such a product was actually produced. It was called “hydrolysis alcohol.” The raw material for its production was indeed sawdust, or more precisely, cellulose extracted from forest industry waste. To put it strictly scientifically – from non-edible plant materials. According to rough calculations, about 200 liters of ethyl alcohol could be obtained from 1 ton of wood. This supposedly made it possible to replace 1.5 tons of potatoes or 0.7 tons of grain. It is unknown whether such alcohol was used in Soviet distilleries. It was produced, of course, for purely technical purposes.
It must be said that the production of technical ethanol from organic waste has long excited the imagination of scientists. You can find literature from the 19th century that discusses the possibilities of producing alcohol from a wide variety of raw materials, including non-food ones. In the 20th century, this theme began to emerge with renewed vigor. In the 1920s, scientists in Soviet Russia even proposed making alcohol from... feces! There was even a humorous poem by Demyan Bedny:
Well, the times have come
Every day is a miracle:
Vodka is distilled from shit -
Three liters per pound!
The Russian mind will invent
The envy of all Europe -
Soon the vodka will flow
Into the mouth from the ass...
However, the idea with feces remained at the level of a joke. But they took cellulose seriously. Remember, in “The Golden Calf” Ostap Bender tells foreigners about the recipe for “stool moonshine”. The fact is that cellulose was being “chemically” even then. Moreover, it should be noted that it can be extracted not only from forest industry waste. Domestic agriculture annually leaves huge mountains of straw - this is also an excellent source of cellulose. Don't let the goodness go to waste. Straw is a renewable source, one might say free.
There is only one catch in this matter. In addition to the necessary and useful cellulose, lignified parts of plants (including straw) contain lignin, which complicates the whole process. Due to the presence of this same lignin in the solution, it is almost impossible to obtain a normal “mash”, since the raw material is not saccharified. Lignin inhibits the development of microorganisms. For this reason, “feeding” is required - the addition of normal food raw materials. Most often, this role is played by flour, starch or molasses.
Of course, you can get rid of lignin. In the pulp and paper industry this is traditionally done chemically, such as acid treatment. The only question is where to put it then? In principle, good solid fuel can be obtained from lignin. It burns well. Thus, the Institute of Thermophysics of the SB RAS even developed an appropriate technology for burning lignin. But, unfortunately, the lignin that remains from our pulp and paper production is unsuitable as fuel due to the sulfur it contains (consequences of chemical processing). If you burn it, you get acid rain.
There are other ways - to treat raw materials with superheated steam (lignin melts at high temperatures), to carry out extraction with organic solvents. In some places this is exactly what they do, but these methods are very expensive. In a planned economy, where all costs were borne by the state, it was possible to work in this way. However, in a market economy, it turns out that the game, figuratively speaking, is not worth the candle. And when comparing costs, it turns out that the production of technical alcohol (in modern terms - bioethanol) from traditional food raw materials is much cheaper. It all depends on the quantities of such raw materials you have. Americans, for example, have an overproduction of corn. It is much easier and more profitable to use the surplus for alcohol production than to transport it to another continent. In Brazil, as we know, surplus sugar cane is also used as raw material for the production of bioethanol. In principle, there are quite a few countries in the world where alcohol is poured not only into the stomach, but also into the tank of a car. And everything would be fine if some famous world figures (in particular, Cuban leader Fidel Castro) did not speak out against such “unfair” use of agricultural products in conditions when in some countries people suffer from malnutrition, or even die of hunger .
In general, meeting philanthropic wishes halfway, scientists working in the field of bioethanol production should look for some more rational, more advanced technologies for processing non-food raw materials. About ten years ago, specialists from the Institute of Solid State Chemistry and Mechanochemistry of the SB RAS decided to take a different route - to use the mechanochemical method for these purposes. Instead of the well-known chemical processing of raw materials or heating, they began to use special mechanical processing. Why were special mills and activators designed? The essence of the method is this. Due to mechanical activation, cellulose passes from a crystalline state to an amorphous one. This makes it easier for the enzymes to work. But the main thing here is that during mechanical processing the raw material is divided into different particles - with different (more or less) lignin content. Then, thanks to the different aerodynamic characteristics of these particles, they can be easily separated from each other using special installations.
At first glance, everything is very simple: grind it and that’s the end of it. But only at first glance. If everything were really that simple, then straw and other plant waste would be ground in all countries. What is really needed here is to find the right intensity so that the raw material is separated into individual fabrics. Otherwise, you will end up with a monotonous mass. The task of scientists is to find the necessary optimum here. And this optimum, as practice shows, is quite narrow. You can also overdo it. This, it must be said, is the work of a scientist: to identify the golden mean. Moreover, here it is necessary to take into account economic aspects - namely, to develop the technology so that the costs of mechanical and chemical processing of the feedstock (no matter how cheap it may be) do not affect the cost of production.
Tens of liters of wonderful alcohol have already been obtained in laboratory conditions. The most impressive thing is that the alcohol is obtained from ordinary straw. Moreover, without the use of acids, alkalis and superheated steam. The main help here is the “miracle mills” designed by the Institute’s specialists. In principle, nothing prevents us from moving to industrial designs. But that is another topic.
Here it is - the first domestic bioethanol from straw! Still in bottles. Will we wait until they start producing it in tanks?
The liquid obtained using this description is methanol. It is also known as methyl (wood) alcohol and has the formula - CH 3 OH.
Methanol in its pure form is used as a solvent and as a high-octane additive to motor fuel, as well as directly as a high-octane fuel (octane number => 115).
This is the same “gasoline” that is used to fill the tanks of racing motorcycles and cars.
As foreign studies show, an engine running on methanol lasts many times longer than when using the gasoline we are used to, and its power, with a constant working volume, increases by 20%.
The exhaust from an engine running on this fuel is environmentally friendly and when tested for toxicity, no harmful substances are detected.
A small-sized apparatus for producing this fuel is easy to manufacture, does not require special knowledge or scarce parts, and is trouble-free in operation. Its performance depends on various reasons, including dimensions.
The device, the diagram and assembly description of which is given below, with a reactor diameter of only 75 mm, produces three liters of finished fuel per hour. Moreover, the entire structure weighs about 20 kg and has approximately the following dimensions: 20 cm in height, 50 cm in length and 30 cm in width.
We will not go deep into the variants of chemical processes and, for simplicity of calculations, we will assume that under normal conditions (20 ° C and 760 mmHg) synthesis gas is obtained from methane according to the following formula:
2CH 4 + O 2 -> 2CO + 4H 2 + 16.1 kcal,
from 44.8 liters of methane and 22.4 liters of oxygen, 44.8 liters of carbon monoxide and 89.6 liters of hydrogen come out, then methanol is obtained from these gases according to the formula:
CO + 2H 2<=>CH 3 OH
from 22.4 l of carbon monoxide and 44.8 l of hydrogen it turns out: 12 g (C) + 3 g (H) + 16 g (O) + 1 g (H) = 32 g of methanol.
This means, according to the laws of arithmetic, 32 g of methanol comes out of 22.4 liters of methane, or approximately: from 1 cubic meter of methane is synthesized 1.5 kg 100% methanol(this is ~2 liters).
In reality, due to low efficiency in domestic conditions, from 1 cubic meter. natural gas you will get less than 1 liter of the final product (for this option the limit is 1 l/h!).
For 2011, the price is 1 cubic meter. household gas in Russia is 3.6-3.8 rubles and is constantly increasing. Considering that methyl alcohol has twice the calorific value of gasoline, we get an equivalent price of 7.5 rubles. and finally, round up to 8 rubles. for other expenses - email. energy, water, catalysts, gas purification - it still comes out much cheaper than gasoline and means that “the game is worth the candle” in any case!
The price of this fuel does not include the cost of installation (when switching to alternative types of fuel, a period of self-sufficiency is always required), in this case the price will range from 5 to 50 thousand rubles, depending on productivity, automation of processes and whose forces will be manufactured.
If you assemble it yourself, it will cost at least 2, and maximum 10 thousand rubles. Basically, the money will be spent on turning and welding work, as well as on the preparation of compressors (it can be from a faulty refrigerator, then it will be cheaper) and on the materials from which this unit is assembled.
Caution: Methanol is poisonous. It is a colorless liquid with a boiling point of 65°C, has an odor similar to that of ordinary drinking alcohol, and is miscible in all respects with water and many organic liquids. Remember that 50 milliliters of methanol drunk is fatal; in smaller quantities, poisoning with methanol breakdown products causes vision loss!
The functional diagram of the device is shown in Fig. 1.
Tap water is connected to the “water inlet” (15) and, passing further, is divided into two streams: one stream (cleaned from harmful impurities by a filter) and through the tap (14) and hole (C) enters the mixer (1), and the other the flow through the tap (4) and the hole (G) goes into the refrigerator (3), passing through which water, cooling the synthesis gas and methanol condensate, exits through the hole (Y).
Domestic natural gas, purified from sulfur impurities and odorous odorants, is connected to the “Gas Inlet” pipeline (16). Next, the gas enters the mixer (1) through hole (B), in which, after mixing with water steam, it is heated on the burner (12) to a temperature of 100 - 120°C. Then, from the mixer (1) through hole (D), the heated mixture of gas and water vapor enters through hole (B) into the reactor (2).
Reactor (2) is filled with catalyst No. 1, mass fractions: 25% NiO (nickel oxide) and 60% Al 2 O 3 (aluminum oxide), the rest 15% CaO (quicklime) and other impurities, catalyst activity - residual volume fraction methane during the conversion with steam of hydrocarbon gas (methane), completely purified from sulfur compounds, containing methane of at least 90%, with a volume ratio of steam:gas = 2:1, not more than:
at 500°C - 37%
at 700°C - 5%.
In the reactor, synthesis gas is formed under the influence of a temperature of about 700°C, obtained by heating with a burner (13). Next, the heated synthesis gas enters through the hole (E) into the refrigerator (3), where it must be cooled to a temperature of 30-40 ° C or lower. Then the cooled synthesis gas leaves the refrigerator through hole (I) and through hole (M) enters the compressor (5), which can be used as a compressor from any household refrigerator.
Next is compressed synthesis gas with a pressure of 5-10 atm. through hole (H) it leaves the compressor and through hole (O) enters the reactor (6). The reactor (6) is filled with catalyst No. 2, consisting of 80% copper and 20% zinc.
In this reactor, which is the most important unit of the apparatus, methanol vapor is formed. The temperature in the reactor should not exceed 270°C, which can be controlled with a thermometer (7) and adjusted with a tap (4). It is advisable to maintain the temperature within 200-250°C, or lower.
Then the methanol vapors and unreacted synthesis gas leave the reactor (6) through the hole (P) and enter the refrigerator (W) through the hole (L), where the methanol vapors condense and exit the refrigerator through the hole (K).
Next, the condensate and unreacted synthesis gas enter through the hole (U) into the condenser (8), where the finished methanol accumulates, which leaves the condenser through the hole (P) and the tap (9) into a container.
The hole (T) in the condenser (8) is used to install a pressure gauge (10), which is necessary to monitor the pressure in the condenser. It is maintained within 5-10 atmospheres or more, mainly with the help of a tap (11) and partially with a tap (9).
Hole (X) and tap (11) are necessary for the exit of unreacted synthesis gas from the condenser, which is recirculated back to the mixer (1) through hole (A), but as practice has shown, the output gases must be burned in a wick, and not run back into the system. Yes, this reduces efficiency, but it greatly simplifies setup.
The tap (9) is adjusted so that pure liquid methanol without gas constantly comes out.
It will be better if the methanol level in the condenser increases than decreases. But the most optimal case is when the methanol level is constant (which can be controlled by built-in glass or some other method).
The tap (14) is adjusted so that there is no water in the methanol, and steam is formed in the mixer, preferably less rather than more.
Gas access is opened, water (14) is closed for now, burners (12), (13) are working. Tap (4) is fully open, compressor (5) is on, tap (9) is closed, tap (11) is fully open.
Then open the tap (14) for water access, and use the tap (11) to regulate the required pressure in the condenser, monitoring it with a pressure gauge (10). But under no circumstances close the tap (11) completely!!!
Next, after about five minutes, use a tap (14) and a lit burner (21) to bring the temperature in the reactor (6) to 200-250°C. After this, the burner (21) is extinguished; it is needed only for preheating, because methanol is synthesized with the release of heat. Then open the tap (9) slightly, from which a stream of methanol should flow. If it flows constantly, open the tap (9) a little more; if methanol mixed with gas flows, open the tap (14).
In general, the higher the productivity you set the device, the better.
It is advisable to make this device from stainless steel or iron. All parts are made of pipes; copper tubes can be used as thin connecting pipes. In the refrigerator it is necessary to maintain the ratio X:Y=4, that is, for example, if X+Y=300 mm, then X should be equal to 240 mm, and Y, accordingly, 60 mm. 240/60=4. The more turns that fit in the refrigerator on one side or the other, the better.
All taps are used from gas welding torches. Instead of taps (9) and (11), you can use pressure reducing valves from household gas cylinders or capillary tubes from household refrigerators.
The mixer (1) and reactor (2) are heated in a horizontal position (see drawing).
Well, that's probably all. In conclusion, I would like to add that a more progressive design for home production of auto fuel was published in several issues of the Priority magazine in 1992-93:
No. 1-2 - general information about producing methanol from natural gas.
No. 3-4 - drawings of a plant for processing methane into methanol.
No. 5-6 - installation, safety measures, control, instructions for turning on the equipment.
Figure 1 - Schematic diagram of the device
Figure 2 - Mixer
Figure 3 - Reactor
Figure 4 - Refrigerator
Figure 5 - Capacitor
Figure 6 - Reactor
I accidentally came across your publication in a search engine and became very interested in its content. After a brief review, inaccuracies made by the author immediately surfaced.
Information about "methanol" was published in the magazine "Priority" for 1991, 92, 93. , but the fully finished project was never published (the promised catalysts for subscribers were squeezed).
These issues contained drawings of the reactor with an electrical control circuit and a cooler design, after which Mr. Vaks (the author of the article) politely apologized and said that further publication would be stopped at the request of the security forces of the USSR and for those who want to repeat this installation, the field of creativity is unlimited. Figure 1(a) - Modified device diagram
1st stage - as mentioned earlier, gas and water must be purified (with a household filter, or even better with a distiller) so as not to immediately poison the catalysts of reactors 2 and 6. More precisely, adhere to the steam: gas ratio as 2: 1. There should be no return of unreacted products to the 1st stage.
2nd stage - methane conversion begins at t=~400°C, but at such a low t°C there is a low percentage of converted gas, the most optimal t=700°C, it is advisable to control it using a thermocouple.
After the reactor and refrigerator, the installation contains a pressure gauge (10) and a pressure reducing valve (11) set to a pressure of 25-35 atm (the choice of pressure depends on the degree of wear of the catalyst). It is better to use two compressors from the refrigerator to pump up sufficient synthesis gas pressure.
I advise you to make the condenser (8) not cylindrical, but conical (this is done to reduce the area of methanol evaporation) and with a window for monitoring the methanol level. The reacted products are brought from above the cone using a tube (u) Ø 8 mm.
The tube is lowered into a conical vessel 10 mm below the throttling outlet (P).
The unreacted synthesis gas is discharged through a tube (x) Ø 5 mm, which is welded into the top of the cone, the gas escaping through this tube is burned at its end, to prevent the flame from escaping into the cone vessel, the end of the tube is stuffed with copper wire.
The methanol level is maintained at 2/3 of the total height of the vessel; for this it is better to make a transparent window. To ensure 100% safety, you can equip the output wick with a thermocouple, the signal from which (due to the absence of a flame) automatically shuts off the gas supply to the installation; any regulator from modern gas stoves is suitable for these purposes.
The catalytic method for producing methanol (wood alcohol) from natural gas is described in detail.
Hydrolysis of plant tissue polysaccharides in cold water is practically not observed. When the water temperature rises above 100°, the hydrolysis of polysaccharides occurs, but so slowly that such a process has no practical significance. Satisfactory results are obtained only when using catalysts, of which only strong mineral acids are of industrial importance: sulfuric and, less commonly, hydrochloric. The higher the concentration of strong acid in the solution and the reaction temperature, the faster the hydrolysis of polysaccharides to monosaccharides occurs. However, the presence of such catalysts also has a negative side, since, simultaneously with the hydrolysis reaction of polysaccharides, they also accelerate the decomposition reactions of monosaccharides, thereby reducing their yield accordingly.
When hexoses decompose under these conditions, hydroxy-methylfurfural is first formed, which quickly decomposes further to form the final products: levulinic and formic acids. Pentoses under these conditions are converted into furfural.
In this regard, in order to obtain monosaccharides from polysaccharides of plant tissue, it is necessary to provide the most favorable conditions for the hydrolysis reaction and minimize the possibility of further decomposition of the resulting monosaccharides.
This is the problem that researchers and manufacturers solve when choosing optimal hydrolysis regimes.
Of the large number of possible options for acid concentration and reaction temperature, only two are currently used in practice: hydrolysis with dilute acids and hydrolysis with concentrated acids. During hydrolysis with dilute acids, the reaction temperature is usually 160-190° and the concentration of the catalyst in an aqueous solution ranges from 0.3 to 0.7% (H2S04, HC1).
The reaction is carried out in autoclaves under a pressure of 10-15 atm. When hydrolysis with concentrated acids, the concentration of sulfuric acid is usually 70-80%, and hydrochloric acid 37-42%. The reaction temperature under these conditions is 15-40°.
It is easier to reduce the loss of monosaccharides during hydrolysis with concentrated acids, as a result of which the sugar yield with this method can reach almost theoretically possible, i.e. 650-750 kg from 1 T absolutely dry plant materials.
During hydrolysis with dilute acids, it is much more difficult to reduce the loss of monosaccharides due to their decomposition, and therefore the practical yield of monosaccharides in this case usually does not exceed 450-500 kg from 1 g of dry raw material.
Due to the small losses of sugar during hydrolysis with concentrated acids, the resulting aqueous solutions of monosaccharides - hydrolysates - are distinguished by increased purity, which is of great importance for their subsequent processing.
Until recently, a serious drawback of hydrolysis methods with concentrated acids was the high consumption of mineral acid per ton of sugar produced, which led to the need to regenerate part of the acid or use it in other industries; this made the construction and operation of such plants more difficult and expensive.
Great difficulties also arose when selecting materials for equipment that were resistant to aggressive environments. For this reason, the bulk of hydrolysis plants currently in operation were built using the dilute sulfuric acid hydrolysis method.
The first experimental hydrolysis-alcohol plant in the USSR was launched in January 1934 in Cherepovets. The initial indicators and technical design of this plant were developed by the Department of Hydrolysis Production of the Leningrad Forestry Academy in 1931 -1933. Based on data from the operation of the pilot plant, the construction of industrial hydrolysis and alcohol plants in the USSR began. The first industrial hydrolysis-alcohol plant was launched in Leningrad in December 1935. Following this plant, in the period 1936-1938. Bobruisk, Khorsky and Arkhangelsk hydrolysis-alcohol plants came into operation. During and after the Second World War, many large factories were built in Siberia and the Urals. Currently, the design capacity of these plants, as a result of improving technology, is exceeded by 1.5-2 times.
The main raw material for these plants is coniferous wood in the form of sawdust and chips, coming from neighboring sawmills, where it is obtained by grinding sawmill waste - slabs and slats - in chippers. In some cases, coniferous firewood is also chopped.
The scheme for obtaining monosaccharides at such plants is shown in Fig. 76.
Shredded coniferous wood from the raw material warehouse enters the guide funnel via conveyor 1 2 and further into the throat
|
|
Wine hydrolyser 3. This is a vertical steel cylinder with upper and lower cones and necks. The inner surface of such hydrolysis apparatus covered with acid-resistant ceramic or graphite tiles or bricks fixed on a layer of concrete 80-100 thick mm. The seams between the tiles are filled with acid-resistant putty. The upper and lower necks of the hydrolyser are protected from the inside from the action of hot dilute sulfuric acid by a layer of acid-resistant bronze. The useful volume of such hydrolysates is usually 30-37 At3, but sometimes hydrolysates with a volume of 18, 50 and 70 are also used m3. The internal diameter of such hydrolysis devices is about 1.5, and the height is 7-13 m. In the upper cone of the hydrolysis device during hydrolysis through the pipe 5 dilute sulfuric acid heated to 160-200° is supplied.
A filter is installed in the lower cone 4 to select the resulting hydrolyzate. Hydrolysis in such devices is carried out periodically.
As mentioned above, the hydrolysis apparatus is loaded with crushed raw materials through a guide funnel. When loading raw materials through a pipe 5 dilute sulfuric acid heated to 70-90° is supplied, which wets the raw material, promoting its compaction. With this loading method in 1 m3 hydrolysis apparatus fits about 135 kg sawdust or 145-155 kg Chips, calculated as absolutely dry wood. Upon completion of loading, the contents of the hydrolysis apparatus are heated by live steam entering its lower cone. As soon as the temperature of 150-170° is reached, 0.5-0.7% sulfuric acid, heated to 170-200°, begins to flow into the hydrolysis apparatus through pipe 5. Simultaneously formed hydrolyzate through the filter 4 begins to be discharged into the evaporator b. The hydrolysis reaction in the hydrolysis apparatus lasts from 1 to 3 hours. The shorter the hydrolysis time, the higher the temperature and pressure in the hydrolysis apparatus.
During the process of hydrolysis, wood polysaccharides are converted into corresponding monosaccharides, which dissolve in hot dilute acid. To protect these monosaccharides from decomposition at high temperatures, the hydrolyzate containing them is continuously removed through a filter throughout the entire cooking process. 4 And quickly cooled in the evaporator 6. Since, according to the process conditions, plant raw materials are hydrolyzed. the hydrolysis apparatus must be filled with liquid at all times, the specified level e is maintained by hot acid entering through pipe 5,
This method of work is called percolation. The faster the percolation occurs, i.e., the faster the hot acid flows through the hydrolysate, the faster the resulting sugar is removed from the reaction space and the less it decomposes. On the other hand, the faster the percolation goes, the more hot acid is spent on cooking and the lower the concentration of sugar in the hydrolyzate is and, accordingly, the greater the consumption of steam and acid for cooking.
In practice, to obtain sufficiently high yields of sugar (at an economically acceptable concentration in the hydrolyzate), it is necessary to choose some average percolation conditions. Usually they stop at a sugar yield of 45-50% of the weight of absolutely dry wood with a sugar concentration in the hydrolyzate of 3.5-3.7% - These optimal reaction conditions correspond to selection through the bottom filter from the hydrolysate - that 12-15 m3 hydrolyzate per 1 T absolutely dry wood loaded into a hydrolyser. The amount of hydrolyzate taken during cooking for each ton of hydrolyzed raw material is called the outflow hydromodule, and it is one of the main indicators of the hydrolysis regime used at the plant.
During the process of percolation, a certain pressure difference arises between the upper and lower necks of the hydrolysis apparatus, which contributes to the compression of the raw material as the polysaccharides contained in it dissolve.
Compression of the raw material leads to the fact that at the end of cooking, the remaining undissolved lignin occupies a volume of about 25% of the initial volume of the raw material. Since, according to the reaction conditions, the liquid must cover the raw material, its level decreases accordingly during the cooking process. Monitoring the liquid level during the cooking process is carried out using a weight meter 30, showing the change in the total weight of raw materials and liquid in the hydrolysis apparatus.
At the end of cooking, lignin remains in the apparatus, containing 1 kg dry matter 3 kg dilute sulfuric acid, heated to 180-190°.
Lignin is discharged from the hydrolysis apparatus into a cyclone 22 through the pipe 21. For this purpose, quickly open the valve 20, connecting the internal space of the hydrolysis apparatus with the cyclone 22. Due to the rapid decrease in pressure between the lignin pieces, the superheated water contained in it instantly boils, producing large volumes of steam. The latter breaks the lignin and carries it in the form of a suspension through the pipe 21 into a cyclone 22. Pipe 21 approaches the cyclone tangentially, due to which the steam jet with lignin, rushing into the cyclone, moves along the walls, performing a rotational movement. Lignin is thrown toward the side walls by centrifugal force and, losing speed, falls to the bottom of the cyclone. Steam freed from lignin through the central pipe 23 released into the atmosphere.
Cyclone 22 usually a vertical steel cylinder with a volume of about 100 m3, equipped with side door 31 and rotating stirrer 25, which helps in unloading lignin from the bottom of the cyclone onto a belt or scraper conveyor 24.
To protect against corrosion, the inner surface of the cyclones is sometimes protected with a layer of acid-resistant concrete. As mentioned above, during the percolation process, heated dilute sulfuric acid is supplied to the upper cone of the hydrolysis apparatus. It is prepared by mixing in an acid-proof mixer 17 superheated water supplied through a pipe 28, with cold concentrated sulfuric acid coming from a measuring cup 19 via piston acid pump 18.
Since cold concentrated sulfuric acid slightly corrodes iron and cast iron, these metals are widely used for the manufacture of tanks, pumps and pipelines intended for its storage and transportation to the mixer. Similar materials are used to supply superheated iodine to the mixer. To protect the walls of the mixer from corrosion, phosphor bronze, graphite or plastic mass - fluoroplastic 4 are used. The last two are used for the internal lining of mixers and give the best results.
The finished hydrolysate from the hydrolysate enters the evaporator 6 high pressure. This is a steel vessel that operates under pressure and is lined inside with ceramic tiles, just like a hydrolysis apparatus. There is a lid at the top of the evaporator with a capacity of 6-8 l3. The pressure in the evaporator is maintained at 4-5 atm lower than in the hydrolysis apparatus. Thanks to this, the hydrolyzate entering it instantly boils, partially evaporating, and cools to 130-140°. The resulting steam is separated from the hydrolyzate drops and through the pipe 10 enters the reshofer (heat exchanger) 11, where it condenses. Partially cooled hydrolyzate from evaporator 6 pipe 7 enters the evaporator 8 low pressure, where it cools to 105-110° as a result of boiling at a lower pressure, usually not exceeding one atmosphere. The steam generated in this evaporator through the pipe 14 fed to the second driver 13, where it also condenses. Condensates from reshuffers 11 and 13 contain 0.2-0.3% furfural and are used for its isolation in special installations, which will be discussed below.
The heat contained in the steam that leaves the evaporators 6 And 8, used to heat the water entering the mixer 17. For this purpose from the tank 16 circulating water pump 1b Warm water obtained from the distillation department of the hydrolysis plant is supplied to the low pressure reseller 13, where it heats up from 60-80° to 100-110°. Then along the pipe 12 heated water passes through a high-pressure reseller 11, where steam at a temperature of 130-140° is heated to 120-130°. Then the water temperature is increased to 180-200° in the water heating column 27. The latter is a vertical steel cylinder with a bottom and top cover designed for a working pressure of 13-15 atm.
Steam is supplied to the hot water column through a vertical pipe 26, at the end of which 30 horizontal disks are fixed 2b. Steam from the pipe 26 passes through the cracks between the individual disks into a column filled with water. The latter is continuously fed into the column through the lower fitting, mixed with steam, heated to a given temperature and through the pipe 28 enters the mixer 17.
Hydrolysis devices are installed on a special foundation in a row of 5-8 pieces. In large factories, their number is doubled and they are installed in two rows. Pipelines for hydrolyzate are made of red copper or brass. The fittings, consisting of gates and valves, are made of phosphorus or passport bronze.
The hydrolysis method described above is batchwise. Currently, new designs of hydrolps are being tested—continuous devices into which, using special feeders, crushed wood is continuously fed and lignin and hydrolyzate are continuously removed.
Work is also underway to automate batch hydrolysers. This event allows you to more accurately follow the specified cooking regime and at the same time makes the work of the cooks easier.
Acid hydrolyzate from low pressure evaporator 8 (Fig. 76) through the pipe 9 fed into equipment for its subsequent processing. The temperature of such hydrolyzate is 95-98°. It contains (in%):
Sulfuric acid. . . ………………………………………………………………………………………………………….. 0.5 -0.7:
Hexoses (glucose, mannose, galactose)……………………………………………………….. 2.5 -2.8;
Pentose (xylose, arabinose)…………………………………………………………………………………………. 0.8 -1.0;
Volatile organic acids (formic, acetic) …………………………….. 0.24-0.30;
Non-volatile organic acids (levulinic acid). . 0.2 -0.3;
Furfural…………………………………………………………………………………………………………………. 0.03-0.05;
Oxymethylfurfural…………………………………………………………………………………. 0.13-0.16;
Methanol. ………………………………………………………………………………………………………………….. 0.02-0.03
Hydrolysates also contain colloidal substances (lignin, dextrins), ash substances, terpenes, resins, etc. The content of monosaccharides in plant hydrolysates during precise chemical studies is determined by quantitative paper chromatography.
In factory laboratories, for mass rapid determinations of sugars, their ability in an alkaline environment to reduce complex compounds of copper oxide with the formation of cuprous oxide is used:
2 Cu (OH) 2 Cu5 O + 2 H2 O + 02.
Based on the amount of cuprous oxide formed, the co-i-fission of monosaccharides in solution is calculated.
This method for determining sugars is conditional, so Along with monosaccharides, copper oxide is also reduced into oxide by furfural, hydroxymethylfurfural, dextrins, and colloidal lignin. These impurities interfere with the determination of the true sugar content of hydrolysates. The overall error here reaches 5-8%. Since correction for these impurities requires a lot of labor, it is usually not done, and the resulting sugars, unlike monosaccharides, are called reducing substances or abbreviated as RS. In factory conditions, the amount of sugar produced in the hydrolyzate is taken into account in tons of radioactive substances.
To produce ethyl alcohol, hexoses (glucose, mannose and galactose) are fermented with alcohol-producing yeasts - Saccharomyces or Schizosaccharomycetes.
Summary equation for alcoholic fermentation of hexoses
C(i Hf, 06 - 2 C2 NG) OH + 2 C02 Hexose ethanol
Shows that with this process, theoretically for every 100 kg sugar should be 51.14 kg, or about 64 l 100% ethyl alcohol and about 49 kg carbon dioxide.
Thus, during alcoholic fermentation of hexoses, two main products are obtained in almost equal quantities: ethanol and carbon dioxide. To carry out this process, the hot acid hydrolyzate must be subjected to the following processing:
1) neutralization; 2) release from suspended solids; 3) cooling to 30°; 4) enrichment of the hydrolyzate with nutrients necessary for the life of yeast.
The acid hydrolyzate has a pH=1 -1.2. A medium suitable for fermentation must have a pH = 4.6-5.2. To impart the necessary acidity to the hydrolysate, the free sulfuric acid contained in it and a significant part of the organic acids must be neutralized. If all the acids contained in the hydrolyzate are conventionally expressed in sulfuric acid, then its concentration will be about 1%. The residual acidity of the hydrolyzate at pH = 4.6-5.2 is about 0.15%.
Therefore, to obtain the required concentration of hydrogen ions in the hydrolyzate, 0.85% of the acids must be neutralized. In this case, free sulfur, formic and part of the acetic acid are completely neutralized. Levulinic acid and a small part of acetic acid remain free.
The hydrolyzate is neutralized with lime milk, i.e., a suspension of calcium oxide hydrate in water with a concentration of 150-200 g of CaO per liter.
The scheme for preparing lime milk is shown in Fig. 77.
Quicklime CaO is continuously fed into the feed hopper of a rotating lime extinguishing drum 34.
At the same time, the required amount of water is supplied to the drum. When the drum rotates, the quicklime binds water and turns into calcium oxide hydrate. The latter is dispersed in water, forming a suspension. Unreacted pieces of lime are separated from the milk of lime at the end of the drum and dumped into a trolley. Lime milk together with sand flows through the pipe into the sand separator 35.
The latter is a horizontally located iron trough with transverse partitions and a longitudinal shaft with blades.
Lime milk in this apparatus flows slowly from right to left and further along the pipe 36 merges into a collection 2.
The sand slowly settles between the partitions of the sand separator and is removed from the apparatus using slowly rotating blades. Before lime milk enters the neutralizer, it is mixed with a given amount of ammonium sulfate, the solution of which comes from the tank 37. When lime milk is mixed with ammonium sulfate, the reaction occurs
Ca (OH)3 + (NH4)2 S04-> CaS04 + 2 NH, OH, as a result of which part of the lime is bound by sulfuric acid of ammonium sulfate and crystals of poorly soluble calcium sulfate dihydrate CaS04-2H20 are formed. At the same time, ammonia is formed, remaining in the lime milk in a dissolved state.
The small crystals of gypsum present in lime milk during subsequent neutralization are centers of crystallization of the resulting gypsum and protect against the formation of supersaturated solutions of it in the neutralized hydrolyzate. This event is important during the subsequent distillation of alcohol from the mash, since supersaturated gypsum solutions in the mash cause gypsum of the mash columns and quickly disable them. This method of work is called neutralization with directional crystallization of gypsum.
Simultaneously with lime milk into the neutralizer 5 A slightly acidic aqueous extract of superphosphate is served from a measuring jug. 38.
Salts are added to the neutralizer at the rate of 0.3 kg ammonium sulfate and 0.3 kg superphosphate per 1 m3 hydrolyzate.
Neutralizer 5 (capacity 35-40 m 3) is a steel tank lined with acid-resistant ceramic tiles and equipped with vertical mixers and brake blades fixedly mounted on the walls of the tank. Neutralization at hydrolysis plants was previously carried out periodically. Currently, it is being replaced by more advanced continuous neutralization. In Fig. 77 shows the last diagram. The process is carried out in two series-connected neutralizers 5 and 6, which have the same device. The acid hydrolyzate is continuously fed through pipe 1 into the first neutralizer, where lime milk and nutrient salts are simultaneously supplied. The completeness of neutralization is monitored by measuring the concentration of hydrogen ions using potentiometer 3 with an antimony or glass electrode 4. The potentiometer continuously records the pH of the hydrolyzate and automatically adjusts it within specified limits by sending electrical impulses to a reversible motor connected to a shut-off valve on the pipe supplying lime milk to the first neutralizer. In neutralizers, the neutralization reaction occurs relatively quickly and the process of crystallization of gypsum from a supersaturated solution occurs relatively slowly.
Therefore, the rate of liquid flow through the neutralization installation is determined by the second process, which requires 30-40 min.
After this time, the neutralized hydrolyzate, called “neutralizate”, enters the semi-continuous or continuous settling tank 7.
The semi-continuous process consists of the fact that the neutralizer flows through the settling tank continuously, and the gypsum that settles to the bottom is removed periodically as it accumulates.
During continuous operation of the settling tank, all operations are carried out continuously. Before draining the sludge into the sewer 8 in the receiver it is additionally washed with water. The latter method has not yet become widespread due to some production difficulties.
Gypsum sludge from a settling tank usually consists of half calcium sulfate dihydrate and half lignin and humic substances settled from the hydrolyzate. In some hydrolysis plants, gypsum sludge is dewatered, dried and fired into building alabaster. They are dehydrated on drum vacuum filters, and dried and fired in rotating drum kilns heated by flue gases.
The neutralized product, freed from suspended particles, is cooled in the refrigerator before fermentation 10 (Fig. 77) from 85 to 30°. For this purpose, spiral or plate heat exchangers are usually used, characterized by a high heat transfer coefficient and small dimensions. During cooling, tar-like substances are released from the neutralizer, which settle on the walls of the heat exchangers and gradually contaminate them. For cleaning, the heat exchangers are periodically turned off and washed with a 2-4% hot aqueous solution of caustic soda, which dissolves resinous and humic substances.
Neutralized, purified and cooled hydrolysate.
The wood wort is fermented with special spnrt-forming yeasts acclimatized in this environment. Fermentation takes place according to a continuous method in a battery of fermentation tanks connected in series 11 And 12.
Yeast suspension, containing about 80-100 g of compressed yeast per liter, is supplied in a continuous stream through a pipe 15 into yeast 44 and then into the upper part of the first, or head, fermentation tank 11. Chilled wood wort is fed into the yeast simultaneously with the yeast suspension. For every cubic meter of yeast suspension, 8-10 m3 of wort enters the fermentation tank.
Yeasts contained in a hexose medium Sakharov, Using a system of enzymes, they break down sugars, forming ethyl alcohol and carbon dioxide. Ethyl alcohol passes into the surrounding liquid, and carbon dioxide is released on the surface of the yeast in the form of small bubbles, which gradually increase in volume, then gradually float to the surface of the vat, carrying away the yeast that has adhered to them.
When they come into contact with the surface, the carbon dioxide bubbles burst, and the yeast, having a specific gravity of 1.1, i.e., greater than that of the wort (1.025), sinks down until they are again raised to the surface by carbon dioxide. The continuous up and down movement of the yeast promotes movement of liquid currents in the fermentation tank, creating agitation or "fermentation" of the liquid. Carbon dioxide released on the surface of the liquid from fermentation tanks through a pipe 13 is supplied to a plant for the production of liquid or solid carbon dioxide, used to produce chemical products (for example, urea) or released into the atmosphere.
Partially fermented wood wort along with yeast is transferred from the head fermentation tank to the tail tank 12, Where fermentation ends. Since the concentration of sugars in the tail vat is small, fermentation in it is less intense, and some of the yeast, without having time to form carbon dioxide bubbles, settles to the bottom of the vat. To prevent this, forced mixing of the liquid with stirrers or centrifugal pumps is often arranged in the tailing tank.
The fermented or fermented liquid is called mash. At the end of fermentation, the mash is transferred to the separator 14, working on the principle of a centrifuge. The mash that gets into it, along with the yeast suspended in it, begins to rotate at a speed of 4500-6000 rpm. Centrifugal force due to the difference in the specific gravities of the mash and yeast separates them. The separator divides the liquid into two streams: the larger one, which does not contain yeast, enters the funnel 16 and the smaller one, containing the yeast, flows through the funnel into the pipe 15. Typically the first flow is 8-10 times larger than the second. Through the pipe 15 the yeast suspension is returned to the head fermentation tank 11 Through yeast 44. The wort, discarded and freed from yeast, is collected in an intermediate mash collection 17.
With the help of separators, the yeast constantly circulates in a closed system of the fermentation plant. Separator productivity 10- 35 m3/hour.
During fermentation and especially during separation, part of the humic colloids contained in the wood wort coagulates, forming heavy flakes that slowly settle to the bottom of the fermentation tanks. There are fittings in the bottoms of the vats through which the sediment is periodically discharged into the sewer.
As mentioned above, the theoretical yield of alcohol per 100 kg fermented hexoses is 64 l. However, practically due to education due to Sakharov by-products (glycerin, acetaldehyde, succinic acid, etc.), as well as due to the presence of impurities harmful to yeast in the wort, the alcohol yield is 54-56 l.
To obtain good alcohol yields, it is necessary to keep the yeast active at all times. To do this, you should carefully maintain the given fermentation temperature, the concentration of hydrogen ions, the required purity of the wort, and leave a small amount of hexoses, the so-called “low-grade” (usually no more than 0.1% sugar in solution), in the mash before entering it into the separator. Due to the presence of unfermented yeast, the yeast remains in an active form all the time.
Periodically, the hydrolysis plant is shut down for scheduled maintenance or major repairs. During this time, the yeast should be kept alive. To do this, the yeast suspension is thickened using separators and poured with cold wood wort. At low temperatures, fermentation slows down sharply and the yeast consumes significantly less sugar.
Fermentation tanks with a capacity of 100-200 m3 are usually made of sheet steel or, less commonly, reinforced concrete. The duration of fermentation depends on the concentration of yeast and ranges from 6 to 10 hours. It is necessary to monitor the purity of the production yeast culture and protect it from infection by foreign harmful microorganisms. For this purpose, all equipment must be kept clean and periodically sterilized. The simplest method of sterilization is steaming all equipment and especially pipelines and pumps with live steam.
At the end of fermentation and separation of yeast, the alcohol mash contains from 1.2 to 1.6% ethyl alcohol and about 1% pentose Sakharov.
Alcohol is isolated from the mash, purified and strengthened in a three-column mash rectification apparatus consisting of mash 18, rectification 22 and methanol 28 columns (Fig. 77).
Mash from the collection 17 pumped through a heat exchanger 41 onto the feeding plate of the mash column 18. Flowing down the plates of the exhaustive part of the mash column, the mash encounters rising steam on its way. The latter, gradually enriched with alcohol, passes into the upper, strengthening part of the column. The mash flowing down is gradually freed from alcohol, and then from the still side of the column 18 through the pipe 21 goes to the heat exchanger 41, where it heats the mash entering the column to 60-70C. Next, the mash is heated to 105° in the column with live steam coming through a pipe 20. The mash freed from alcohol is called stillage. Through the pipe 42 Stillage leaves the stillage heat exchanger 41 and is sent to the yeast workshop to obtain feed yeast from pentoses. This process will be discussed in detail later.
The mash column in the upper reinforcing part ends with a reflux condenser 19, in which the vapors of the iodine-alcohol mixture coming from the upper plate of the column are condensed.
In 1 m3 of mash at a temperature of 30°, about 1 m3 of carbon dioxide formed during fermentation dissolves. When heating the brew in a heat exchanger 41 and with live steam in the lower part of the mash column, dissolved carbon dioxide is released and, together with alcohol vapor, rises into the strengthening part of the column and further into the reflux condenser 19. Non-condensable gases are separated through air vents installed on the alcohol condensate pipelines after the refrigerators. Low-boiling fractions consisting of alcohol, aldehydes and ethers pass through a reflux condenser 19 and finally condense in the refrigerator 39u From where they flow back into the column in the form of reflux through a water seal 40. Non-condensable gases consisting of carbon dioxide before leaving the refrigerator 39 pass through an additional condenser or are washed in a scrubber with water to capture the last remnants of alcohol vapor.
On the upper plates of the mash column, the liquid phase contains 20-40% alcohol.
Condensate through the pipe 25 enters the feed plate of the distillation column 22. This column works similarly to the mash column, but at higher alcohol concentrations. To the bottom of this column through a pipe 24 Live steam is supplied, which gradually boils the alcohol from the alcohol condensate flowing to the bottom of the column. Liquid freed from alcohol, called luther, through a pipe 23 goes down the drain. The alcohol content in stillage and luther is no more than 0.02%.
A reflux condenser is installed above the upper plate of the distillation column 26. The vapors that have not condensed in it are finally condensed in the condenser 26a and flow back into the column. Part of the low-boiling fractions is taken through a pipe 43 in the form of an ether-aldehyde fraction, which is returned to the fermentation tanks if it is not used.
To free ethyl alcohol from volatile organic acids, it is fed into the column from the tank. 45 10% sodium hydroxide solution, which neutralizes acids on the middle plates of the strengthening part of the column. In the middle part of the distillation column, where the alcohol strength is 45-50%, fusel oils accumulate and are taken through a pipe 46. Fusel oils are a mixture of higher alcohols (butyl, propyl, amyl) formed from amino acids.
Ethyl alcohol, freed from esters and aldehydes, as well as fusel oils, is selected using a comb from the upper plates of the strengthening part of the distillation column and through a pipe 27 enters the feed plate of the methanol column 28. The raw alcohol coming from the distillation column contains about 0.7% methyl alcohol, which was formed during the hydrolysis of plant materials and, together with monosaccharides, ended up in the wood wort.
During the fermentation of hexoses, methyl alcohol is not formed. According to the technical specifications for ethyl alcohol produced by hydrolysis plants, it should contain no more than 0.1% methyl alcohol. Studies have shown that methyl alcohol is most easily separated from raw alcohol when its water content is minimal. For this reason, raw alcohol with maximum strength (94-96% ethanol) is fed into the methanol column. It is impossible to obtain ethyl alcohol above 96% in conventional distillation columns, since this concentration corresponds to the composition of the non-separately boiling water-alcohol mixture.
In a methanol column, the low-boiling fraction is methanol, which rises to the top of the column and is strengthened in the reflux condenser 29 and through the pipe 30 is discharged into collections of the methanol fraction containing about 80% methanol. To produce commercial 100% methanol, a second methanol column is installed, not shown in Fig. 77.
Ethyl alcohol, flowing down plates, falls into the lower part of the methanol column 28 and through the pipe 33 discharged into finished product receivers. The methanol column is heated with silent steam in a remote heater 31, which is installed in such a way that, according to the principle of communicating vessels, its inter-tube space is filled with alcohol. The water vapor entering the heater heats the alcohol to a boil and the resulting alcohol vapors are used to heat the column. Steam entering the heater 31, condenses in it and in the form of condensate is supplied to clean water collections or drained into the sewer.
The quantity and strength of the resulting ethyl alcohol is measured in special equipment (flashlight, control projectile, alcohol meter). From the measuring tank, ethyl alcohol is supplied by a steam pump outside the main building - into stationary tanks located in the alcohol warehouse. From these tanks, as needed, commercial ethyl alcohol is poured into railway tanks, in which it is transported to places of consumption.
The technological process described above makes it possible to obtain from 1 T absolutely dry coniferous wood 150-180 l 100% ethyl alcohol. At the same time, by 1 dkl alcohol consumption
Absolutely dry wood in kg. . . . . 55-66;
TOC o "1-3" h z sulfuric acid - moaoidrate in kg … . 4,5;
Quicklime, 85% in kg…………………………………………………. 4,3;
Pair of technological 3- and 16-atmospheric
In megacalories. …………………………………………………………………………………….. 0.17-0.26;
Water in m3…………………………………………………………………………………………. 3.6;
Elekgrozner in kWh…………………………………………………………………….. 4,18
The annual capacity of a hydrolysis-alcohol plant with an average capacity for alcohol is 1 -1.5 million. gave. At these factories, the main product is ethyl alcohol. As already indicated, at the same time, solid or liquid carbon dioxide, furfural, feed yeast, and lignin processing products are produced from the main production waste at the hydrolysis-alcohol plant. These productions will be discussed further.
In some hydrolysis plants that produce furfural or xylitol as the main product, after hydrolysis of pentose-rich hemicelluloses, a difficult-to-hydrolyze residue remains, consisting of cellulose and lignin and called cellolignin.
Cellolignin can be hydrolyzed by the percolation method as described above, and the resulting hexose hydrolyzate, usually containing 2-2.5% Sugars, can be processed according to the method described above into technical ethyl alcohol or feed yeast. According to this scheme, cotton husks, corn cobs, oak husks, sunflower husks, etc. are processed. This production process is economically profitable only with cheap raw materials and fuel.
Hydrolysis-alcohol plants usually produce technical ethyl alcohol, which is used for subsequent chemical processing. However, if necessary, this alcohol
It is relatively easily purified by additional rectification and oxidation with an alkaline permanganate solution. After such purification, ethyl alcohol is quite suitable for food purposes.
.jpg)
