


Hydrocarbons
It is an organic compound consisting of two elements, hydrogen and carbon. Most of the petroleum composition consists of hydrocarbons of varying lengths.
The smallest hydrocarbon methane consists of a single carbon atom and four hydrogen atoms. However, hydrocarbons can consist of hundreds or thousands of individual atoms linked together in many ways, including chains, circles, and other complex shapes.
In order to classify the properties of hydrocarbons, they are divided into several basic types.
Alkanes: These are called saturated hydrocarbons. That is, they only contain single bonds between all carbon atoms. Alkanes are the basis of petroleum fuels and exist in linear and branched forms.
Unsaturated Hydrocarbons: Hydrocarbons that have one or more double bonds between carbon atoms are called alkenes.
Cycloalkanes: Any hydrocarbon containing one or more ring structures.
Aromatic Hydrocarbons: Aromatic hydrocarbons , also called arenes, are a unique class of carbon molecules in which carbon atoms are bonded by successive double and single bonds. This class of molecules has special ring structures in which the bonds between carbon atoms are an intermediate bond between single and double bonds.
Molecules in this class contain the industrial solvent "benzene".
Benzene (C6H6): Like other hydrocarbons, benzene is a natural component of petroleum. It is a colorless, flammable, sweet-smelling liquid at room temperature and is a component of most gasoline blends because of its high octane number.
Benzene is also highly carcinogenic and is well known to cause bone marrow failure and bone cancer. Of course, its carcinogenicity is not well known when used as an additive in aftershave and other cosmetics due to its "pleasant aroma".
The largest use of benzene (50%) is the product of styrene and polystyrene plastics. It is also converted into a molecule known as cyclohexane, which is important in Nylon production. About 15% of benzene is used to produce cyclohexane. Smaller amounts are used in everything from pesticides to rubber.
The benzene structure can be drawn in two ways. In the first, the double bond character is drawn explicitly. In the short handed version, a circle is drawn inside the ring to show the structure. There is only one hydrogen bonded to each carbon atom in benzene.
I. and II below. drawings are identical. III in practice. drawing is used.
Benzene is a colorless, flammable liquid with a boiling point of 80.1 ° C and a melting point of 5.5 ° C.
Binuclear Aromatic Hydrocarbons: They are compounds that contain two benzene rings in their molecules.
Hydrocarbons
It is an organic compound consisting of two elements, hydrogen and carbon. Most of the petroleum composition consists of hydrocarbons of varying lengths.
The smallest hydrocarbon methane consists of a single carbon atom and four hydrogen atoms. However, hydrocarbons can consist of hundreds or thousands of individual atoms linked together in many ways, including chains, circles, and other complex shapes.
In order to classify the properties of hydrocarbons, they are divided into several basic types.
Alkanes: These are called saturated hydrocarbons. That is, they only contain single bonds between all carbon atoms. Alkanes are the basis of petroleum fuels and exist in linear and branched forms.
Unsaturated Hydrocarbons: Hydrocarbons that have one or more double bonds between carbon atoms are called alkenes.
Cycloalkanes: Any hydrocarbon containing one or more ring structures.
Aromatic Hydrocarbons: Aromatic hydrocarbons , also called arenes, are a unique class of carbon molecules in which carbon atoms are bonded by successive double and single bonds. This class of molecules has special ring structures in which the bonds between carbon atoms are an intermediate bond between single and double bonds.
Molecules in this class contain the industrial solvent "benzene".
Benzene (C6H6): Like other hydrocarbons, benzene is a natural component of petroleum. It is a colorless, flammable, sweet-smelling liquid at room temperature and is a component of most gasoline blends because of its high octane number.
Benzene is also highly carcinogenic and is well known to cause bone marrow failure and bone cancer. Of course, its carcinogenicity is not well known when used as an additive in aftershave and other cosmetics due to its "pleasant aroma".
The largest use of benzene (50%) is the product of styrene and polystyrene plastics. It is also converted into a molecule known as cyclohexane, which is important in Nylon production. About 15% of benzene is used to produce cyclohexane. Smaller amounts are used in everything from pesticides to rubber.
The benzene structure can be drawn in two ways. In the first, the double bond character is drawn explicitly. In the short handed version, a circle is drawn inside the ring to show the structure. There is only one hydrogen bonded to each carbon atom in benzene.
I. and II below. drawings are identical. III in practice. drawing is used.
Benzene is a colorless, flammable liquid with a boiling point of 80.1 ° C and a melting point of 5.5 ° C.
Binuclear Aromatic Hydrocarbons: They are compounds that contain two benzene rings in their molecules.
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About
Kyäni, nutritional supplement products consisting of beneficial ingredients; It delivers to more than 50 countries around the world with unique business opportunities. We use Kyäni products daily to maintain our ideal health, share these products with others, devote a certain amount of time to work almost every day to build and maintain our business, and share our success with others by involving others in the Kyäni opportunity or contributing to the Potato Pak and Caring Hands programs.
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Training / Knowledge / Solution Platform
Oil Formation
The First Carbon in the Universe:
The common belief among physicists today is that the carbon in the universe is largely formed by nuclear reactions that take place at the centers of stars. In summary, this process takes place as follows: Three alpha particles (helium atom nuclei), each consisting of two protons and two neutrons, fuse together, resulting in carbon atom nuclei consisting of six protons and six neutrons. This process is very rare. Because first of all, it is unlikely that three alpha particles will come together and fuse together. Second, even if three alpha particles fuse, the resulting high-energy carbon nuclei are unstable. The vast majority of them disintegrate in a short time, and the nuclei, which lose energy by emitting only gamma, manage to transform into stable carbon atoms. According to estimates, only four of every 10,000 carbon atom nuclei formed by the triple alpha process turn into stable carbon atoms.
The characteristics of the crude oil are determined by the geological history of the beds in which they are found. Louisiana and Nigerian crude oils are similar; both are made up of similar marine remains. Far Eastern oils are usually waxy, black or brown in color, low sulfur, and similar to Central African oils; these are based on terrestrial deposits. Middle Eastern oils are low in wax, but high in sulfur. Western Australian oil is light and honey-colored, North Sea oil is waxed, green-black in color. The characteristics of the oils in the USA are very diverse due to the very different geological histories of the regions. The oldest oil-bed rocks are more than 600 million years old, while the youngest ones are around 1 million years old. Most of the oil deposits discovered and found are 10-270 million years old.
The most critical factor in the formation of oil and gas deposits is the subsurface temperature that increases with depth. While the formation of petroleum hydrocarbons can rarely occur at temperatures lower than 150 ° F, hydrocarbons formed at temperatures above 500 ° F decompose and carbonize; the ideal temperature range is between 225-350 degrees.
Anterior cambrium layer; They are layers from the formation of the earth (~ 4 billion years ago) to the time when the first known multicellular organisms began (550 million years ago). Since the oil is considered to be of organic origin, drilling is not made up to these layers.
In Paleozoic and Mesozoic times (550-65 million years ago) dense forests and seas were filled with plants and animals. Over time, some of those who died or lived were protected from degradation by covering with sand or mud, and the process of oil formation began. The process sometimes took place with the sliding of mud, displacement of sand dunes, sometimes volcanic explosions, sometimes with meteorites colliding with the earth and throwing massive clouds and dust. These collapsed layers were subjected to increasing pressures and therefore rising temperatures with the new layers added on them.
As the earth crust slid, these layers that had begun to form were pushed deeper and deeper. The center of the earth, as is known, is very hot and the rocks are in a liquefied state. The chemical reactions that took place for thousands of years with the bacteria that were active in all these conditions created the components of natural gas and crude oil.
In Paleozoic and Mesozoic times (550-65 million years ago) dense forests and seas were filled with plants and animals. Over time, some of those who died or lived were protected from degradation by covering with sand or mud, and the process of oil formation began. The process sometimes took place with the sliding of mud, displacement of sand dunes, sometimes volcanic explosions, sometimes with meteorites colliding with the earth and throwing massive clouds and dust. These collapsed layers were subjected to increasing pressures and therefore rising temperatures with the new layers added on them.
As the earth crust slid, these layers that had begun to form were pushed deeper and deeper. The center of the earth, as is known, is very hot and the rocks are in a liquefied state. The chemical reactions that took place for thousands of years with the bacteria that were active in all these conditions created the components of natural gas and crude oil.
The organic matter was buried under sand and mud, as the pressure increased, the oil flowed into the rocks near it. Although rocks look like solid masses, they contain many pores (pore) and some rocks have larger and larger pores than others. There are three basic rock types; volcanic, metamorphic (metamorphic) and sedimentary (or sedimentary) rocks. Oil is mostly found around sedimentary rocks, but not all sediment rocks contain oil. Only 2% of the organic matter turns into oil, and only about 0.5% can be handled. Hydrocarbons are lighter than water and migrate upward from porous rocks until they are captured by non-porous layers (traps).
Conventional oil and gas deposits do not show a regular distribution both in terms of location and time. Large oil and gas deposits are located in a small number of basins or classical oil regions less than 20000 ft (6.1 km) deep. This uneven distribution is related to the forming or breaking properties of the layers.
There are more than 600 basins and sub-basins in the world and most of them are concentrated in several geological regions; possible calculations show that up to 80% of the original oil reserves are concentrated in 10 regions. The Arabian Platform and the Zagros Belt (Saudi Arabia-Iran-Iraq) have the largest known and discovered reserves.
Although it occurs in all geological periods, 95% of all reservoirs in the world have been formed in six geological time intervals according to known hydrocarbon deposits.
Source rocks (layers rich in organic substances that produce hydrocarbons) are the first key to any important petroleum system. Source rocks are deposited and preserved in various marine and terrestrial geological deposits.
When the distribution of these sediments formed from the Precambrian time in the world is examined, it is seen that 90% of them belong to six geological stages. The two Mesozoic phases (Upper Jurassic and Middle Cretaceous) are estimated to contain more than half of all defined hydrocarbon reserves. Source rocks of this age are found in the Middle East, Siberia, United States, North Sea, Venezuela and Mexico, where the world's important oil deposits are located.
Origin of Oil:
Since the 1800s, various opinions have been put forward, researches and experiments have been made, and theories have been produced regarding whether the oil is inorganic or organic based, and what kind of substances or compounds its origin is based on. These debates from the past to the present have ended with the acceptance of the organic origin theory, although there are still a few opposing views. Below is a brief summary of these theories.
According to a theory first put forward by Berthelot (1866) and supported by Mendeleev (1877 and 1902) oil is of inorganic origin. Chemists, who obtained materials such as methane, acetylene and benzol in the laboratory, claimed that the petroleum in nature was formed by chemical reactions and volcanic events underground.
At the beginning of the 20th century, some scientists suggested that oil was of igneous origin. According to Mendeleev's theory, the iron carbide in the mantle interacts with water leaking underground to form methane and hydrocarbons.
Peyve (1956) and Subbottin (1966) suggested that based on the hydrocarbon gases emanating from large and deep faults, these gases exit the mantle and are stored in the crust and converted into liquid petroleum. In this case, it will be possible to reach endless oil resources by opening extremely deep drillings; however, oil is mostly found in sedimentary basins. However, some scientific data invalidate the inorganic origin theory; For example, substances in petroleum such as porphyrin, pyridine and chlorophyll cannot be obtained by inorganic means,
Large molecular weight hydrocarbons cannot be formed by inorganic reactions. The polarized light deflection feature of petroleum compounds does not exist in any inorganic material other than quartz and cinnabar.
Most of the oil deposits are far from magmatic activity areas and sedimentary rocks
are in. Oil does not increase towards the depths of the earth's crust,
on the contrary, oil is more commonly found in young cover rocks:
As a result, it cannot be said that the oil is of inorganic origin.
Some researchers admit that oil is of both animal and vegetable origin (biomass origin); For example, by the distillation of fish and other animal meats, substances similar to petroleum components are obtained. It has been suggested that the oil may be of terrestrial plant origin due to the extraction of oil from coal and methane gas in the marshes. However, the absence of coal in oil fields, the absence of petroleum derived from terrestrial plants in limestones, and the chemical differences between pitch derived from lignite and petroleum show that terrestrial plants do not have a significant effect on oil formation. An original relationship can be established between marine plants and marine sediments. The most important of these are algae and diatoms. Diatoms float on the surface (several meters in depth) of oceans and lakes and over time produce some types of hydrocarbons. During this time, they also become the food of various sea creatures whose skeletal structures resemble sand (containing silicon compounds). Both formations store chemical energy through photosynthesis and increase their swimming ability.
These raw materials, which are collected in mixed form with sediments or deposits in the underground layers, undergo transformation with various and complex physical, biochemical and chemical reactions depending on the parameters of pressure, temperature and time.
Oil Formation Parameters:
Temperature: As the burial depth increases, the most important event that occurs is the increase in temperature. Increasing temperature with depth is defined as "geothermal gradient".
The world geothermal gradient average is 23.5 ° C per 1 kilometer. This value varies regionally depending on factors such as the thermal conductivity of the substances in the lithology and the amount of groundwater.
The temperature at any depth can be found in the equation below.
Tf = Ts + (D x G)
Tf = formation temperature, ° C, Ts = average annual surface temperature, ° C ("surface", 3 meters
defines the depth), G = geothermal gradient, D = depth, meter
Pressure: Pressure is very important in the migration of the oil that is formed, but pressure is also an important parameter in the formation of oil. As the depth increases, the pressure increases; for example, the pressure at a depth of 580 meters is 40.4 kg / cm² (or 575 psi).
Time: Hydrocarbons are partially stable at depths close to Earth, whereas high enough temperatures and time were required to trigger molecular transformations. For roughly 100 million years, the conversion in organic matter remains very low. When the temperature reaches 50 ° C and the atomic bonds in the kerogen begin to break at depths of about 2200 meters, oxygen outputs, CO2 and H2O are formed and the first petroleum products containing sulfur, nitrogen and oxygen, especially asphaltenes and resins, and gas products depending on the structure of organic substances. begins to occur.
It is formed by various hydrocarbons that combine certain minerals such as sulfur under high pressure. It was formed by the transformation of dead plants and animals millions of years ago into a jelly-like mass by being trapped under the pressure of the earth's crust and ocean over millions of years, covered with a layer of sand and mud.
As the depth of this gel-like sediment accumulation increased with the movements of the earth's crust over millions of years, the pressure on the mass increased and caused it to be compressed into a much thinner layer than the beginning.
In addition, the natural heat of the earth had an effect that would cause a reaction on this mass under intense pressure, and in time caused the gel to transform into today's known oil form.
Today, the difference between the quality of all the oil extracted in the world is due to the differences between this pressure and temperature and the formation processes.
Oil is also called "fossil energy", "fossil fuel" because of this formation, and it is definitely not "renewable energy" due to the long formation process.
Originally the primary use of petroleum was as a lighting fuel, once distilled and made into kerosene.
After a short while, the demand for gasoline started to increase rapidly as Ford triggered the automobile industry and the range of what could be done with internal combustion engines expanded.
Today, oil is seen as a precious mineral that is traded like gold and diamond around the world.
Most people believe that oil is mostly used in the form of gasoline or gasoline equivalents to power internal combustion engines.
However, apart from this area of use, it is also used as asphalt and water-repellent insulation material even in its most waste form.
Oil is also an essential part of the chemical makeup of many plastics and synthetics. The most surprising possible use of oil for many people is that it also occurs in foodstuffs like beer and medicines like aspirin.
It is a fact that there is limited oil reserves in the world that will eventually be depleted. Although cheap, renewable fuel options are being created and developed instead, it is obvious that humanity will face a serious problem in the end.
The basic definition of petroleum includes only crude oil, but the common usage of the term is generally to include all liquid, gaseous and solid hydrocarbons found in a given mixture.
The basic basis is on hydrocarbons and all hydrocarbons are the same as they contain hydrogen and carbon atoms. Differences; It is due to details such as the number of carbon they have, their saturation level, and their aromaticity.
Petroleum System Basic Processes
1st Generation:
The process of burial of source rocks into a regime of temperature and pressure sufficient to transform organic materials into hydrocarbons. It contains sub-phases within itself.
The diagenesis (creation) phase is nearly normal at depths close to the earth's surface.
temperatures and pressures. In this phase, organic substances are formed by bacteria.
undergoes biogenic degradation and non-biogenic reactions;
methane, carbon dioxide and water come out of the organic substances, leaving a complex hydrocarbon structure called "kerogen". Temperature plays an important role in the process; As the burial increases, rising temperatures reduce the effects of biogenic reactions as they cause bacteria to die, whereas at high temperatures, organic reactions will accelerate and oil formation increases.
The catagenesis phase includes the processes of 'decomposition' in which organic kerogens turn into hydrocarbons in an environment of increased temperature (60-177 ° C) and pressure, as the kerogen formed is buried deeper (1000-6000 m). The higher the temperature (which is proportional to the increase in time and depth), the more the bonds between the atoms break.
As can be understood from the explanations of diagenesis and catagenesis phases, oil and gas are formed as a result of successive chemical reactions from the kerogen in the source rock. Reactions are driven by the kinetics of chemical reactions, so this transformation is directly dependent on temperature and time. Pressure is necessary to reach the required temperature, but is effective in migrating oil from one place to another rather than the formation of it.
The metagenesis phase is a metamorphism phase that occurs at high temperatures and pressures. Metamorphism can be defined as the mineralogical, chemical and crystallographic changes in a solid state rock; For example, the change of rock without melting according to new conditions (pressure, temperature, fluid entry).
2. Migration / Immigration:
Oil and gas formed by maturation begin to migrate towards the ground surface. Two major causes of migration are pressure and density. The pressure of the maturation zone is high, as the pressure decreases as it goes upwards, hydrocarbons flow into the lower pressure layers if they do not encounter obstacles; Since the density of oil and natural gas is lower compared to rocks and water, it facilitates migration.
Hydrocarbons are porous and permeable source rock (bedrock) reservoir
they migrate to rock (reservoir rock); this is called 'primary immigration'. Hopper from the rock
oil continues to migrate here as well; In this phase called 'secondary migration', the mobility of hydrocarbons begins through the pores and fractures in the reservoir rock and the fluids become stratified due to the differences in density.
Secondary migration can be directed in different ways according to various physical and chemical parameters. Physical parameters include buoyancy due to pressure difference, petrophysical properties of the reservoir, and permeability. In addition, the slope of the carrier layer, its continuity, faults and cracks are the main factors affecting migration. Chemical parameters cause the oil to undergo structural change; its composition deviates from the state in which it reaches the carrier layer, for example, it changes the migration path by enriching with heavier or lighter components.
The migration types of hydrocarbons can be briefly described as follows.
Horizontal Migration (Lateral Migration): Horizontal migration at continuous and permeable levels
It occurs along the contact rock with the carrier rock and occurs at a distance of 10 to 100 km.
Vertical Migration: Vertical migration occurs when the pressure of hydrocarbon in the pore is greater than the pressure created in the cover layer and the pressure that wants to keep it in the pore.
Downward Migration: This migration is seen especially in transgressive successions.
qualified reservoir rocks and stratigraphic traps are filled.
Upward Migration: The upward migration of oil through cracks and gaps in the cover
is collapse.
Oil Spill: If the leak is seen in the well, it indicates that there is migration and an oil passing through. If the leak is seen on the surface, in that area
indicates that the conditions for capping are not good.
Trap Migration: Trapping new oil causes a second migration. Deformation of the oil traps causes a new migration. If the layer pressure decreases as a result of rise and wear, the gas cap volume increases and oil may escape as a result.
3. Accumulation / Accumulation:
Three elements must come together for hydrocarbons to accumulate; these are reservoir rock (high porosity and permeability, usually sand-
(e.g., limestone and marble), seal rock preventing upper, lower and lateral leakage
(low porosity and permeability, generally shale layers, limestone, gibs, salt) and overburden rock.
4. Closure:
Traps occur when permeable reservoir rocks (carbonates, sandstones) are surrounded by less permeable rocks (cover rocks) that prevent hydrocarbons from collapsing. Typical seal (cap) rocks are tight textured shales, evaporites, concreted hard sandstones and carbonate rocks.
Traps are stratigraphic and structural formations. The earth creates sudden or gradual geological movements; such as earthquakes, volcanic eruptions, erosions caused by wind and water. Some structural formations arise as a result of these movements. For example, rocks that are pushed upward take the form of a dome or curl like an arch; this is called an anticline formation (trap). These are often the formations that capture hydrocarbons, and if they are located near a source rock, the possibility of finding oil and gas in that area increases.
The traps are where the oil has collapsed and finally settled and cannot move.
are the places where it is stuck. It is the most anticline. A closed system accumulates oil. Lower part
A clay cover easily creates a barrier and does not allow the oil to travel further downstream.
prevents it from breaking. Thus, oil accumulates at the top of the system and creates a pool. The lower part of the trap is generally planar and bounded by the oil-water contact. Most of the hydrocarbons in the sediments cannot find a suitable trap and flow towards the surface, moving along water-containing formations.
Historical Process and Timeline

1656 : John Tredescant introduces gutta percha from the Far Eastern Palaquium ree bark. This produced a hard material that could be heat molded to soften and soften products that proved to have unique properties.
1730 : Charles Marie de la Condamine begins manufacturing rubber bottles in the Amazon basin.
1830 : Thomas Hancock began researching rubber molding and its many uses.
1838 : Charles Goodyear (USA) discovered the vulcanization of rubber with sulfur, allowing formulation variants to provide a wide range of flexibility in molds.
1839 : German pharmacist Eduard Simon discovered polystyrene (PS).
1843 : Dr William Montgomerie introduces GP (Gutta Percha, a natural rubber obtained from the sap of certain trees growing in the Far East) to the Royal Society of Arts. It formed the basis of materials with excellent electrical and chemical resistance, imitation wooden moldings began to be used in the manufacture of artistic items, golf balls. Hancock refined and patented vulcanization (a hard rubber or ebonitization process), building the UK rubber industry with products such as boats, springs, hoses and bands.
1844 : Thomas Hancock patented the "vulcanization" of rubber in England.
1845 : Gutta Percha Co. (C. Hancock, H. Bewley) was founded in London and developed an extrusion process for rods and tubing.
1846 : Designed the first extruder to apply GP and rubber insulation to copper cables used in submarine telegraph connections. Belt production started from GP. Charles Macintosh purchased Alexander Parkes' "cold cure" vulcanization process, which allowed the production of brightly colored fabrics using organic dyes. Alexander Parkes began detailed studies on nitrocellulose as a thermoplastic base material. With the product he developed called Parkesina, he started to make various dough molds similar to ivory and horn.
1849 : First temporary dental filling compound used GP.
1851 : Nelson Goodyear (USA) invented patented ebonite primary thermosetting material for demanding applications such as battery cases, pumps, telephones, dental plates and fountain pens.
1850 : Shellac mixed with wood flour was patented in the USA (S.Peck, J. Critchlow) and used for safes, picture frames, etc. used in coatings.
1855 : Bois durci, wood flour resistant to heat and pressure, capable of reproducing finely, and albumen patented by Francois Lepage.
1880 Phonograph records (Berliner) based on Shellac compounds were introduced and their application continued until PVC was used in the 1950s.
Shellac: Coccus Lacca , which is used in products such as chocolate-coated hazelnuts, grapes, almonds, peanuts, chewing gum, bonbons, fruits such as apples and tangerines, and in various medicines, especially in chocolate-coated products such as dragees, and which is fed on Palas trees in South Asia. It is the insect's lac secretion substance. This hardened gum, encased in a protective cover, is collected, crushed, washed and dried. It is widely used as a brightener in the food and pharmaceutical industry with the code E904.
1856 : Alexander Parkes patented celluloid compounds and plastics.
Plastic: The word itself is derived from the Greek plasticos meaning "to be shaped or molded" and refers to the formability of plastic, which allows it to be cast, pressed or extruded into a variety of shapes such as films, fibers, plates, tubes.
Plastic; It is an organic substance obtained by processing petroleum, which can harden after being shaped while in molten state.
1861: Francis Shaw introduces the first screw extruder for rubber production.
1862: Parkesine was introduced in England. Naphtha started to be produced as a by-product by atmospheric distillation for kerosene production.
1868 : John Wesley Hyatt (USA) patented Celluloid (camphor-modified cellulose nitrate) for billiard balls, eyeglass frames, photographic film, etc. developed an easily moldable material.
1869 : John Wesley Hyatt discovered a method that would simplify the production of celluloid and enable industrial production.
1870 : Vacuum distillation began to be applied, in which the by-product asphalt is obtained for fractionation of crude oil.
The first use of synthetic plastic: The history of the billiard ball is closely related to the history of celluloid, which is known as the world's first artificial polymer. The origin of celluloid lies in the economic embargo imposed by the northern states on the southern states during the American Civil War (1861-1864).
Young inventor John Wesley Hyatt set out to research an alternative to ivory billiard balls on cellulose nitrate. However, as a result of an accident, he accidentally dropped the collodion substance into the mixture he prepared and saw that the mixture hardened. It would take another seven years for him to find the solution by adding camphor to the mix. With the patent received on July 12, 1870, celluloid was born and the way for future plastics was opened. (Celluloid, which was used in the production of billiard balls for a while, was replaced by materials such as bakelite (Bakelite) in the 20th century, as it was not very resistant to the balls hitting each other. Today, billiard balls are mostly produced from phenolic resin, and this material behaves very much like ivory, but is more difficult to get dirty, it is a perfect sphere. It can take its shape and is used for a longer time.)
(The first plastics in our country are beads produced by hand presses in the 1950s and used to decorate animals.)
1872 : PVC was accidentally synthesized by Eugen Baumann.
1878 : JW Hyatt obtained a US Patent for injection molding thermoplastics.
1880 : Cellulose nitrate is mass-produced by BXL.
1889: Eastman Kodak applied for a patent for celluloid film.
1890 : Casein, a type of plastic, by Wilhelm Krische and Adolph Spitteler , Auguste Trillat discovered to render casein insoluble by dipping it in formaldehyde.
1892 : Cross, Bevan and Beadle patented cellulose acetate regenerated from chemically treated wood pulp for fibers and yarns.
1894: Shellac phonograph records were developed and soon became an industry standard.
1897 : Casein plastics from milk were discovered, patented by Adolph Spitteler (Bavaria). This important material began to be developed by Erinoid (1909) for a series of pastel and colored products.
1898 : Polyethylene (PE) was synthesized while Hansvon Pechmann was investigating diazomethane.
1899 : Arthur Smith patented phenol-formaldehyde resins to replace ebonite for electrical insulation.
1900 : J. Kondakov (Germany) synthesized methyl rubber poly(dimethylbutadiene).
1904 : The Fireproof Celluloid Syndicate (later Damask Lake Co. Ltd. - Sir James Swinburne) developed phenol-formaldehyde varnishes for metal.
1905 : J. Edwin Brandenberger (USA) invented cellophane used in thin films for fabrics and packaging and provided important applications for many years.
1907: Bakelite , the first fully synthetic thermoset, is reported by Leo Baekeland using phenol and formaldehyde.
1908 : Leo Baekeland (USA) created phenol-formaldehyde resins (p/f) and generated over 100 patents.
1909 : Leo Baekeland, wood, ivory, ebonite, etc. He patented Bakelite, the first major thermoset material used instead.
1910 : Formica electrical insulation laminate is manufactured by H. Faber and D O'Conor (USA) using p/f resin-impregnated paper plies. SV Lebedev (USSR) produced rubber from poly1-3butadiene.
1912 : After more than 10 years of research, Jacques E. Brandenberger develops a method for producing cellophane and receives a patent. Ostromislensky (Russ.) patented the polymerization of vinyl chloride to yield an unstable PVC polymer (unstable when not modified).
1913 : Klatte produces polyvinyl acetate. Thermal cracking started to be applied to increase gasoline efficiency.
1915 : Production of synthetic methyl rubber started in Leverkusen.
1916 : The sweetening process was introduced in order to produce sulfur and make the production process more odorless.
1918 : Hans Johns patented urea formaldehyde resins.
1920 : Peter Schidrowitz prepared prevulcanized latex, which gave rise to the "dipped rubber products" industry.
1922 : Herman Staudinger (Germany) proposed long-chain molecular structures for polymers and synthesized rubber.
1924 : Edmund Rossiter develops water-white transparent molds from thiourea-formaldehyde resins
1926 : The first truly successful commercial injection molding machine is produced by Eckert and Ziegler (German Patent 495362).
1927 : Waldo Semon and BF Goodrich Company developed a plasticization method by blending PVC with various additives. Otto Rohm (Germany) developed poly (methyl methacrylate) transparent plastic.
1928 : Wallace Carothers led the great Du Pont team to 'engineered' macromolecules. Thiourea-formaldehyde resins began to be marketed as Beetle resins.
1930 : Neoprene was produced for the first time by DuPont and polystyrene (PS) was produced by BASF. E. Tschunker developed nitrile rubbers (BUNA). The thermal reforming process, which increases the octane number, has begun to be applied.
1931 : W. Carothers et al. (Du Pont ) produced polychloroprene rubber (Neoprene). Neoprene rubber was introduced. Heidrich (Germany) produced the first screw extruder specifically for thermoplastic processing.
1932 : RCA Victor introduces vinyl -based Victrolac compound for records. J. Crawford, R. Hill, ICI, PMMA - promoted Perspex. hydrogenation to remove sulfur from petroleum and coking processes to increase gasoline base stocks.
1933: The first industrially practical synthesis of polyethylene, discovered by Eric Fawcett and Reginald Gibson at Imperial Chemical Industries (ICI). Henkel begins production of patented melamine for melamine formaldehyde resins. Ciba has mainly developed for molding powders (Melaware) and laminates with MF surface (Formica) by American Cyanamid. W. Semon produced a stable PVC polymer (Goodrich). R. Whiley (Dow) discovered polyvinylidene chloride (Saran). The solvent extraction process, in which aromatics are obtained as a by-product, has begun to be applied.
1934 : Nylon fiber (Nylon 66; Hill) is introduced.
1935: Nylon was invented and patented by DuPont. Solvent devaksing process, which regulates the pour point in the refining process, started to be applied. Floor polymerization process started to be applied to increase gasoline efficiency and octane value.
Nylon: Invented by Wallace Carothers at DuPont in 1935 as a synthetic silk, nylon is actually a trademark, and is a polyamide polymer. It was used during the war for parachutes, ropes, body armor, helmet linings and more. Plexiglass provided an alternative to glass for aircraft windows. An article published in Time magazine stated that because of the war, "plastics are turning to new uses and the adaptability of plastics has been proven once again". During the Second World War, plastic production in the USA increased by 300%.
1936 : O. Bayer (Germany) developed urethane rubbers, which were introduced to the market by RM Thomas (USA) the same year.
1937 : Polytetrafluoroethylene (teflon) was discovered by Roy Plunkett at DuPont. Following the work of BASF and Dow Chemical, it started to produce the first injection molded polystyrene products. Hans Kellerer (Austria) has launched a fully automatic injection molding machine with continuous operation. R. Colombo and C. Pasquetti (Italy) produced the first twin screw extruders. For higher octane gasoline, the catalytic cracking process, in which high octane aviation gasoline is also obtained as a by-product, has begun to be applied.
1938 : R. Plunkett (Du Pont) discovered PTFE. Nylon toothbrushes began to be used around the world. Nylon 6 fibers (Schlack, IG Farben) were produced as commercial Perlon.
1939 : Waldo Semon (Goodrich) develops suitable polybutadiene and styrene-butadiene rubbers that contributed greatly to World War II. Bayer introduced IG Farben polyurethane systems. Castan produced basic epoxy resins in Ciba (Switzerland). Visbreaking method, the process of reducing the viscosity obtained by distillate and tar by-products, has begun to be applied.
1940 : Nylon stockings began to be used in human life. Du Pont introduced Polyacrylonitrile (PAN) polymer, an early engineered product. Found polyethylene-terephthalate PET synthesized by JR Whitfield and JT Dickson at the Calico Printers Association. The isomerization process, in which alkylation raw materials and naphtha are obtained, came to life.
1941 : Polyethylene terephthalate (PET) was discovered at the Calico Printers' Association in Britain.
1942 : Fluid catalytic cracking, another process that will increase gasoline efficiency and octane value, is started.
1943 : Silicone polymers are introduced by the Dow Corning Corporation, following Frederick Kipping's much earlier work on organo-silicone compounds.
Many rubber and elastomer variants were subsequently developed using controlled molecular (block) structures.
1945 : Ciba produced epoxy resins after preliminary cursor work using bisphenol A / glycidyl ethers by Schlack (Germany).
1946 : Cold cured styrene polyesters for fiber-reinforced plastics are introduced.
1947: Formica melamine faced decorative p/f laminates are introduced in the UK.
1950 : DuPont begins producing polyester . The deasphalting process was developed for increasing the cracking raw material and producing asphalt.
1951 : J.Paul Hogan and Robert L. Banks of Phillips polymerized propylene for the first time to produce polypropylene (PP).
1952 : The catalytic reforming process, the naphtha conversion process, in which aromatics are also obtained, was developed.
1953 : Polycarbonate (PC) was developed by Hermann Schnell ( Bayer) and Daniel Fox ( General Electric) in the USA. Patented polycarbonate resin Lexan (also known as Merlon, Makrolon in Europe and Asia) thermoplastics, which would be used to make airplane windows and later CDs, DVDs and iPods. Karl Ziegler, with E. Holzkamp, produced high molecular weight, low pressure polyethylene using organo-metallic catalysts. Drs H. Schnell (Bayer) and D. Fox (General Electric) independently produced polycarbonate, a precursor engineering polymer. Isotactic polypropylene was discovered by Guilo Natta, Montecatini using Ziegler type catalysts. ICI has produced 'propathene' used in high volumes for demanding domestic and engineering applications.
1954 : Polypropylene (PP), by Giulio Natta Polystyrene (PS) was invented by Dow Chemical. Extruded polystyrene foam (also known as "blue board" and trademarked as Styrofoam) is introduced. A variation colloquially known as "styrofoam," expanded polystyrene foam was later used for disposable cups and fast food packaging. A desulfurization process, hydrosulphurization, with sulfur as a by-product, was developed.
1955 : Du Pont patented the Elvax series.
1956 : Inhibitory sweetening process is developed for disulfide production and removal of mercaptans.
1957 : Italian Montecatini company started to produce Polypropylene. A catalytic isomerization process was developed for refining high-octane molecules.
1959: Du Pont launches Delrin - polyformaldehyde polymer, based on work under the direction of Robert McDonald since 1947. This proved to be a valuable lightweight engineering polymer.
1960 : Du Pont introduced EVA (ethylene-vinyl acetate copolymer) with the Elvax series. The hydrocracking process process has been developed to improve refining quality, reduce sulfur release and produce alkylation raw materials.
1961 : High-density polyethylene (HDPE) bottles are introduced, replacing glass bottles in most applications.
1962 : Du Pont introduced polyimide films (Kapton), varnishes and later foams with high insulation resins, fire resistance and mechanical properties for composite structures.
1964 : Polyphenylene oxide (PPO) polymers are patented by General Electric (USA).
1965 : Kevlar (a heat resistant and strong synthetic fiber related to aramids ) is developed by Stephanie Kwolek (DuPont). Union Carbide, 3M, and ICI produced the polysulfone thermoplastic engineering polymer.
1966 : Polyether, ketone resistant chemistry and engineering polymer PEEK started to be produced by ICI.
1967 : The PPO Norly series of General Electric high performance engineering thermoplastics is launched.
1974 : The catalytic devaksing process was developed to regulate the pour point in the refining process.
1975 : Residual hydrocracking process was developed to increase gasoline yield in refining.
1977 : Plastic bags were introduced at checkout counters in American grocery stores and eventually replaced brown paper bags.
1978 : Introduced oriented blow molded beverage containers based on PET polymers and other types such as PBT - polybutyl-terephthalate.
1980 : Polyester began to replace cellulose acetate.
1988 : Polymer banknotes (money) are introduced in Australia.
2002 : Real steps started to be taken for the control of plastic waste. In Ireland, it imposed a tax on plastic safe bags. An estimated 90 percent of consumers have switched from plastic bags to reusable bags within a year.
2009 : China introduced a nationwide ban on plastic bags, preventing the use of approximately 3 billion plastic bags per day.
2009: The District of Columbia introduces a 5-cent fee for carry-on bags from businesses that sell food or alcohol.
2011: Distribution of non-biodegradable bags is banned in Hawaii grocery checkouts.
2012 : San Francisco becomes the first American city to ban plastic bags.
2014 : California becomes the first state to impose a statewide ban on single-use plastic bags in supermarkets, liquor stores, and pharmacies.
2017 : In some states in America, decisions were made to phase out Styrofoam products in schools and school districts, cafeterias.
2019 : Bags started to be taxed in market checkouts in Turkey.