Monday, December 26, 2011

How To Give Your Dog Home-Made Enema

!±8± How To Give Your Dog Home-Made Enema

Sometimes, you may need to do more than just giving solid or liquid medication to your sick dog. Depending on his condition and symptoms, you may also have to provide other kinds of nursing care, such as giving enemas. Below is an effective way to use this procedure:

The use of enemas can be beneficial for dogs that has the following conditions; constipation, during fasting, dehydration, excessive vomiting, bowel irritation caused by bone fragments or the presence of spoiled food or garbage in the digestive tract.

Before administering this procedure, make sure that you only use pure water that is warm but not hot (test it on your wrist to make sure). Use about two tablespoons for a small dog and up to a pint for a large dog. Add a few drops of freshly squeezed lemon juice to the water and administer the mixture with a plastic or rubber syringe for about 2 to 3 minutes. For large dogs, you can use and enema bag and a nozzle.

Here is how to do it: You must lubricate the end of the syringe with vegetable oil. Have someone help you hold the dog gently while he stands in a tub or on the ground. Insert the nozzle carefully into the rectum. Using gentle and consistent pressure against the anus (to prevent the fluid from leaking out), slowly fill the colon. If the solution does not flow in easily, pull back on the nozzle or syringe and slightly adjust the angle. Expect a bowel movement to begin within a few minutes. You may administer the enema once or twice a day for a couple of days.

In many cases, dogs that are dehydrated are simply retaining the fluid. This occurs when the colon absorbs the fluid which the body needs. Therefore, enemas are an excellent way to administer fluid therapy. Under these circumstances, administer the enema about every four hours or until fluid is no longer retained.

If a dog is having difficulty keeping water in his stomach due to heavy vomiting, an enema can help introduce the fluid and salts that are needed to replace those lost through vomiting. Using the solution as described earlier, add a pinch of sea salt plus a pinch of potassium chloride. The same solution can also be used to help a dog suffering from prolonged diarrhea. In this case, administer the enema every four hours or until fluid is no longer retained.


How To Give Your Dog Home-Made Enema

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Tuesday, December 20, 2011

The Accidental Natural-KeraCare Natural Textures Review

A Review of the KeraCare Naturals Textures Products. See Ingredients and purchase information below. ***All products were purchased by me and not supplied to me by the manufacturer or any retailer. I am not being paid in any way to promote or review these products. This is an honest, independent review. Ingredients List KeraCare Natural Textures: CLEANSING CREAM Aqueous (Water, Aqua Purificato, Purified) Extracts: Azadirachta Indica (Neem)1, Phyllanthus Emblica (Amla)1, Acacia Concinna (Shikakai)1, Cetrimonium Chloride, Cetearyl Alcohol2, Cetyl Alcohol2, C12-15 Alkyl Lactate, Polyquaternium-37, Propylene Glycol Dicaprylate/Dicaprate, PPG-1 Trideceth-6, Glycerin1, Argania Spinosa Kernel Oil1, Crambe Abyssinica Seed Oil1, Ricinus Communis (Castor) Seed Oil1, Poyquaternium-10, Piroctone Olamine, Potassium Sorbate, Diazolidinyl Urea, Iodopropynyl Butylcarbamate, Fragrance/Parfum, Benzyl Benzoate. LEAVE IN CONDITIONER Aqueous (Water, Aqua Purificato, Purified) Extracts: Phyllanthus Emblica (Amla)1 and Acacia Concinna (Shikakai)1, Cetyl Alcohol2, Argania Spinosa Kernel Oil1, Crambe Abyssinica Seed Oil1, Phytosterols, Betaine1, Citric Acid1, Behentrimonium Methosulfate, Serenoa Serrulata Fruit Extract1, Camellia Sinensis Leaf Extract1, Propylene Glycol, Pyrus Malus (Apple) Fruit Extract1, Citrus Medica Limonum (Lemon) Peel Extract1, Saccharum Officinarum (Sugar Cane) Stalk Extract1, Potassium Sorbate, Diazolidinyl Urea, Iodopropynyl Butylcarbamate, Dimethyl Stearamine, Fragrance ...

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Friday, December 9, 2011

Choosing a Water Softening System : Water Softeners: Salt

Salt for water softeners is manufactured on a bed. Learn about different salts for water systems from a water softening expert in this free home improvement video. Expert: Markus Anderson Bio: Markus Anderson has over eight years experience in designing, installing, maintaining and upgrading water softeners. Filmmaker: Paul Kersey

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Friday, December 2, 2011

Chemistry and Technology

!±8± Chemistry and Technology

Chemistry can and does find widespread use in technology. Most of the time, the materials employed are used on a day-to-day basis and have been perfected through myriad chemical techniques.

There are over 100 chemical elements known to date, and almost all of them can form multiple compounds. Chemistry is the science of combining these elements in order to form new materials that have an ever wider use.

One of the most far-reaching chemical discoveries was the invention of plastics and other synthetic materials. There are a number of different types of plastics and other synthetic materials, each with its own different properties. Many react as temperature changes. Some, however, are able to withstand changes in temperature.

These find use in situations when a material must be exposed to very high or very low temperature, for example in a heat insulator.

Nature has also been a reliable supplier of the basic materials that we human beings take for granted. In nature, calcium is one of the basic raw materials. From it, lime and limestones in their various forms can be produced, these often being used in the construction industry. Lime is also an ingredient in cements and cement mortar.

With the addition of certain molecules, the colour of numerous materials can be changed. Glass, for example, can be turned brown if a certain concentration of barium carbonate is added to it. It can be turned green if an iron oxide is mixed in.

The colour of foods and foodstuffs is also the domain of chemistry. At the same time, this area of the natural sciences is living proof of the numerous uses and many-sided nature of many of the compounds that make up certain materials.

And who would have thought that our bodies, the coal and other fuels we use to heat our homes, and the bubbles in many of our drinks, are all composed of one and the same element, carbon?

Today's wide variety of cleaning products were without exception tested in laboratories around the world. This is how we keep things clean: by using chemicals which can quickly and effectively remove stains, and make our world a brighter place to live in.

And what about transportation? Flying, either by airplane or by the precursors of what will one day be spaceships, is the result of long years of chemistry (and physics) research. This brings up a scientific truth: Chemistry, including the chemical industry, is closely related to other natural science branches, such as physics, biology and even mathematics. In many cases, these sciences are so closely related that it is impossible to separate them. That is why, together, they are called the natural sciences.

It is beyond the scope of this document to name all of the things that chemistry has done to improve our world. We can, of course, try to show some of the advances that have been made in the wonderful world of chemistry with the help of a few examples. It is, however, like the view through a narrow keyhole into a large room. It is possible to see a few of the larger features, such as where some of the furniture is placed. But the real content of the room, down to its intricate details - that is impossible to see without much closer examination. So are many of the discoveries made, thanks to chemistry, that we tend to take for granted.

Sulphur, sulphuric acid and its salts

Sulphur is a member of the sixth main group of the periodic table, Group VIA. It is a yellow solid which is not soluble in water. It is not a metal. In nature, it occurs in two crystalline structures:

monoclinic and hexagonal.

Sulphur burns in air as a blue flame, producing sulphur oxide (SO2). It forms sulphides with a number of metals. It is used in the production of some medicines, rubbers and fungicidal products.

Sulphur is found on Earth in what are called sulphur beds, or deposits. Besides being found in its pure form, sulphur-containing compounds are found in oil, natural gas and in some rock formations which contain carbon and other materials (for example in iron sulphides chemical formula FeS).

Sulphur oxide (SO2)

Sulphur oxide is a colourless, suffocatingly toxic and poisonous gas. When it is dissolved in water, it forms sulphuric acid. Sulphur oxide is used in the production of sulphuric acid, as a bleach and as a preservative in some foods.

Sulphurous acid (H2SO3)

Sulphurous acid is a weak acid which is found in solution only. It is a product of the dissolving of sulphur oxide in water.

Sulphuric acid (H2SO4)

Sulphuric acid is a viscous, colourless, very corrosive acid. Concentrated sulphuric acid contains 2% water. It is a very strong oxidising agent and is often used to rid a system of water (it is very hygroscopic). Sulphuric acid is a strong acid. More negative metals than hydrogen dissolve in it, forming a salt and water. A dilute solution will not dissolve copper. A more concentrated solution, however, will dissolve copper, oxidising it at the same time.

Chemists come across two terms which are oft-used in the field: sulphates and sulphides. As one might guess, both terms have something to do with sulphur. Sulphates and sulphides are the salts of sulphuric acid, derived from sulphur hydrides. Sulphates are salts which arise from the reaction between a metal and sulphuric acid. Sulphides are compounds which are the product of the reaction of a metal with sulphurous acid. Sulphates have one sulphur atom bonded to four atoms of oxygen. Sulphides have sulphur atoms which are not attached to any oxygen atoms.

Sulphates are solid materials composed of sulphur and metal atoms which contain the sulphate ion, chemical formula (SO4- ) and one metal cation. These types of compounds are widespread in nature (for example CaSO4 - calcium sulphate, also known as gypsum).

Sulphides contain a sulphur anion and the cation of a metal (for example iron sulphide, FeS).

Sulphuric acid is produced through a process known as contact oxidation. The reaction mechanism has pure SO2 oxidising at 500° C under the influence of a vanadium catalyst. The cooled gas is led through a 98% solution of sulphur acid. The compound SO3 is absorbed, to create H2S2O7. By diluting with water, sulphuric acid of the desired concentration is produced.

Sulphuric acid is used in the production of some fertilisers and nitrogen-containing compounds, as well as some phosphoric compounds and the salts of acids. It is also used in the production of storage and other batteries.

Phosphorus, phosporic acid and its salts

Besides nitrogen, phosphorus is the most important element found in the fifth main group of the period table (Group VA). It has five electrons in its outermost shell. Phosphorus is a solid at room temperature. It is found in a number of what are called alotropic modifications: For example, there is red phosphorous and white phosphorous. It is also found in the bodies of both animal and human hosts, in the compound calcium phosphate.

White phosphate is an oily, poisonous substance which has a characteristic odour. It burns in air, so it has to be stored under water. When heated in the presence of oxygen, it changes into the less reactive red phosphorous. Red phosphorous forms 4-atom molecules and is soluble in fats and oils.

When heated, it reacts slowly to form phosphorous oxide. In so doing, energy is released which radiates in the presence of light. This is the characteristic gleam of white phosphorous in the dark, which has led to glowing materials being called phosphorous. The name phosphorous, then, derives its original meaning from the Latin root which means 'carrier of light'.

Red phosphorous is a red, soft crystal. It is not poisonous. It does not burn in air. It is composed of an unending chain of phosphorus atoms. It is completely and totally insoluble. Red phosphorus is used in the production of matches.

When red or white phosphorous is burned, a white solid material is formed. This is phosphoric oxide, a strongly hygroscopic reagent which reacts strongly with water and can produce phosphoric acid, which is used to protect some materials from corrosion.

Phosphoric acids are those which come from phosphorus derived from oxygen-containing acids. Phosporic acids are relatively strong and non-volatile. They have a pleasant-smelling odour and are non-toxic. When added to some drinks, they are taste boosters, making these drinks have more intensive tastes. They are produced by dissolving phosphoric oxide in water.

Phosphoric acid (H3PO4) is the most important of all of the phosphorous-containing acids. It is found in numerous physiologically important compounds (for example in DNS). Besides the better-known H3PO4, there are other phosphorous-containing acids such as H3PO3 which is produced as an intermediate in the dissociation reaction with water at a temperature of over 200° C.

Phosphates

Phosphates are salts of the phosphoric acid family, especially those of the ortho phosphorous acids. Because these have three hydrogens included, they can be replaced. There are, therefore, three degrees of phosphates which can be derived from this group of phosphoric acid.

Primary phosphates have just one atom of hydrogen replaced by a metal, giving the chemical formula

MH2PO4. Secondary phosphates have two atoms of hydrogen replaced by two atoms of metal, giving the chemical formula M2HPO4. Tertiary phosphates have all three of their hydrogens replaced, resulting in the chemical formula M3PO4.

Heating results in primary and secondary phosphates being transformed into metaphosphates (with rings in the molecules) or to high molecular polyphosphates. These phosphates are most often used in the production of wash powders or as water softeners.

There are relatively large beds of phosphates found in nature. These are often transformed into fertilisers.

The esters of acidic orthophosphates are also called phosphates. These are often used to repel pests. They can also, however, be used as intermediates in the material transport of some organisms.

Ammonia and ammonium-containing compounds

Ammonia (NH3) is one of the most important and most fundamental chemical compounds. There are three atoms of hydrogen bonded to one atom of nitrogen in a molecule of ammonia. The three bonds are all polar in nature, thanks to the differing electronegativities of N and H. The ammonia molecule has a pyramidal structure.

Ammonia, a colourless gas, has a repellent stench. It can be dissolved in water to a great degree. At room temperature, one litre of water can dissolve 700 litres of ammonia. Ammonia corrodes and is poisonous. Ammonia can be liquified rather easily. Liquid ammonia is colourless and behaves similarly to water, because molecules of ammonia create dipoles thanks to their polar bonds. With acids, ammonia forms ammonium salts.

In the laboratory, ammonia can be produced by the reaction of a concentrated solution of sodium hydroxide and ammonium chloride.

NH4 + CL + Na + OH ® NH3 + H2O + Na + Cl

Ammonia is easy to recognise in its gaseous state because of its distinctive odour. An indicator can be used to determine whether ammonia is present in an aqueous solution. If so, the paper indicates base. We get the same alkaline reaction when indicator paper is subjected to the effects of an ammonia pair. When reacted with hydrogen chloride, ammonium chloride is formed. This reaction can be recognised because of the formation of white smoke.

NH3 + HCl ® NH4Cl

Synthesis of ammonia

Ammonia can be synthesised from the elements nitrogen and hydrogen in what is known as the Haber-Bosch reaction. After years of experimentation, the technology finally developed, and in 1909, F. Haber and C. Bosch started getting close to their dream. A few years later, the synthesis had been performed successfully (F. Haber won the Nobel Prize in 1918 for the feat). An equilibrium reaction, in the presence of a catalyst, resulted in the formation of ammonia. In order to make the reaction work effectively, high temperature and high pressure are needed.

3H2 + N2 ® 2NH3

The opposite reaction is highly exothermic. When it is carried out, there is a significant loss of volume as a result. According to Le Chatelier's principle, when a force or outside variable in introduced into a system in equilibrium, that system will act to create a new equilibrium under the new conditions. The least boost to the above reaction, therefore, leads to an increase in the product side of a synthetic reaction. With the help of a catalyst, the activation energy of the reaction is greatly reduced. Still, the hydrogen present only begins to react with nitrogen at any significant rate at temperatures of 450 - 500° C. And in the end, the mixture of products formed contains only up to 20% ammonia. This is separated out from the rest of the liquids, and the unused gases can be reused. Iron, and some of its various oxides, are used as a catalyst.

Production of the ammonium ion

Ammonia reacts with water to produce the ammonium ion and a hydroxide ion. In this reaction, one atom of hydrogen bonds to the lone electron pair of the original ammonia compound NH3. A proton, then, is transferred.

NH3 + H2O ® NH4 + OH

Because this is also an equilibrium reaction, besides molecules of water and ammonia which were in the solution to begin with, there are ammonium ions and hydroxide ions present, too. The solution behaves in an acidic manner. It is called a solution of ammonium water.

Ammonium salts

The reaction of ammonia or a solution containing ammonium ions with an acid results in the formation of a salt, which can be called an ammonium salt. These have an ionic lattice.

Ammonia plus hydrogen chloride ® ammonium chloride

NH3 + HCl ® NH4Cl

Ammonia plus sulfuric acid ® ammonium sulphide

2NH3 + H2SO4 ® (NH4)2SO4

Ammonia plus nitric acid ® ammonium nitride

NH3 + HNO3 ® NH4NO3

Ammonia and hydrogen chloride are dissociated from ammonium chloride, the reverse of the first reaction above, which is the synthesis of ammonium chloride. The hydroxide compounds of alkaline metals and alkaline earth metals and ammonium salts break down, or dissociate, into free ammonia.

Ammonium salts are used in nitrogen and other mineral fertilisers.

Nitric acid

Nitric acid is a an oxygen-containing acid composed of nitrogen. Pure nitric acid is a colourless liquid. It forms an azeotropic mixture with water. This type of azeotropic mixture should have the same boiling point if it is mixed in the same relative mixture in both mixed fractions. For this reason, the mixture cannot be separated by distillation. In the presence of light, the compound breaks down into oxygen and nitric oxide. Nitric acid was earlier called aqua regia, something similar to the king of the solvents, because all of the metals besides gold dissolve in it. Nitric acid is produced using the Oswald process: Ammonia reduces in air at a temperature of 780-940° C with the help of a platinum catalyst to produce nitric oxide. This compound gradually breaks down to NO2. When water is allowed to react with this compound, nitric acid (HNO3) is the result.

Nitric acid is used in the production of nitric fertilisers and as a nitric and oxidation agent in the chemical industry.

In nature, the nitric group is found exclusively in the form of salts, or nitrates. Nitrates are salts of nitric acid which contain the NO3 group. They are found most often in the form of ionic crystals which are water soluble. As a matter of fact, all nitric salts are water soluble - without exception. Besides fertiliser, they are used for their explosive character in fireworks.

Nitrogen and its compounds

Nitrogen (Latin nitrogenium) is the first element of Group V main group elements, a group that is called the nitrogen group. The nitrogen atom has five electrons in its outermost electron shell. Nitrogen is a colourless, odourless gas which is found as a two-atom molecule in nature (N2). The two nitrogen atoms are joined by a triple bond. Each nitrogen atom has one unbonded electron pair.

Nitrogen was recognised as one component of air in 1777 by C.W. Scheele. At the time, it was found not to be essential for either combustion processes or organism respiratory functions. It is almost completely insoluble in water. It does make up around 78.1% of the Earth's atmosphere. Besides being part of the air that we breathe, nitrogen is found in various other compounds, as nitrates bonded with, among others, sodium and potassium, as in the molecule potassium nitrate (KNO). Nitrogen, however, is generally not very reactive.

Pure nitrogen is produced by the liquification of air (Lindeo process). Air is compressed and the heat which results is removed from the system. If the air is to expand again, the gas molecules present need to be supplied with energy, to get them moving again. Instead, the heat of the system is removed. The gas cools down gradually, finally changing into a liquid. Nitrogen can be separated from the liquid air mixture using fractional distillation. Nitrogen can also be won when the oxygen component of air is removed through reaction with some other material.

Because nitrogen is not very reactive, it is often used as a protective, non-interfering gas in industry. In its liquid form, it is used as a cooling agent in the freezing of some dried, processed foods, often when those foods are canned. As a gas, nitrogen is a raw material in the production of nitrogen-based compounds like ammonia and nitric acid. Nitrogen is one of the most important components of both

plants and animals, because it is included in all protein molecules. Molecular nitrogen which is found in the atmosphere cannot, however, be used as a foodstuff. Plants, then, must take nitrogen in through its salts, through plants' roots. For this reason, the production of nitrogen-based fertilisers is extremely important for a plant's health and well-being.

Nitrogen-containing compounds which appear in nature

In the Earth's atmospheric system, 90% of the nitrogen present is in the gaseous state. Just one percent is found in bonded, compound form on the Earth's surface, or in the bodies of living organisms. When it is found on the Earth's surface, nitrogen is mostly in the form of the ammonium and nitrate ions. Living organisms contain nitrogen mostly in the form of amino acids, peptides and proteins. There is also nitrogen to be found in the form of sodium nitrate, so-called Chile saltpetre, or in potassium nitrate, also called Indian saltpetre, the latter in large quantity.

The nitrogen-containing salts found in the Earth's crust are taken in by plants through their roots and are later used in the production of amino acids, proteins and other compounds. Plants are primary producers of organic nitrogen compounds. All animals, including the human animal, must meet their nutritional needs, in a direct or indirect way, by ingesting some form of plant material. Once used, nitrogen is freed from the compound it was included in, often when that organism's organic material begins to decay, in the form of ammonia. Nitrifying bacteria then change ammonia to nitrates which can be reingested by plants.

The nitrogen cycle

Nitrogen is a vital raw material in the lives of all living organisms, if only in small doses. Animals and human beings get their nitrogen from plants, not being capable of taking it in directly from the atmosphere. Most plants take in nitrogen in the form of the ammonium ion or in nitrate ions from the ground. The nitrogen which occurs in the atmosphere is bonded by several symbiotic microorganisms (nitrogenous bacteria of legumes, fungi in the root systems of alders) and transferred into the host plant. The nitrogen dioxide which is formed in thunderstorms also makes its way into the ground. This is how nitrogen, in the form of ammonium and nitrate ions, makes its way into the food chain: through the root systems of plants. After the microorganisms that brought it into those root systems die, and nitrogen is freed from the proteins which contained it in the form of ammonia, again by the actions of microorganisms. Part of this is then once again changed by bacteria to ammonium and nitrate ions... These are once again taken in by plants... Other ammonium is used by the denitrifying bacteria, changing it to molecular nitrogen, which is then returned to the atmosphere.

The compounds of nitrogen which do reach humans and other animals are later broken back down and released as decomposed matter which returns to the Earth. There, plants and microorganisms take over once again.

The effect of human beings on the natural nitrogen cycle

The necessity of feeding the world's growing population has led to more intensive agricultural practices in recent years, and the depletion of a great amount of farmland. The harvests of some plants have shown them to be low in nitrogen, as well as other phosphorous and potassium-containing compounds. In order to produce enough high-quality food for the world, the foods that are grown need to be supplied with enough fertiliser. In the past, manure, compost and even peat were used. Now, artificial fertilisers have come into fashion, because of the fact that they do contain the nutrients that crops need - and in sufficient concentration.

Yet plants cannot take in too much of this artificial fertiliser. A significant amount of it, therefore, gets into underground water supplies, which increases the amount of ions, or the hardness, in our drinking water. The materials contained in fertilisers are dangerous for human health. Unused fertiliser gets into our seas and rivers, causing the eutrophisation of the water (water plants grow too quickly and use all of the oxygen available in the water, leading to water animals and plants dying for a lack of oxygen). With more and more traffic on the freeways, more and more carbon dioxide is being pumped into the atmosphere. This makes breathing more difficult and is causing the extinction of the rain forests, as well as increased pollution and the harming of trees. In addition, nitrogen concentration in the atmosphere is decreasing, thanks to the synthesis of ammonia.


Chemistry and Technology

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Wednesday, November 30, 2011

From Inorganic Carbon Compounds To Synthetic Macromolecules

!±8± From Inorganic Carbon Compounds To Synthetic Macromolecules

Inorganic Carbon Compounds

Inorganic macromolecule carbon-containing compounds are either found in nature or made synthetically. In the production of inorganic macromolecules, elements such as carbon or the compounds of silicon oxide and silicon-containing acids are bonded together to form polymers. Diamond, graphite and quartz are among the inorganic micromolecules found in nature which contain carbon. Diamond and graphite are composed of carbon atoms which are bonded together by interatomic forces.

Diamond

The carbon in diamond takes a crystal lattice formation in which the carbon atoms are arranged in the shape of a tetrahedron. The spatial arrangement of a material determines its hardness and the firmness of its crystals. Diamond is the hardest mineral in nature, and is valued thanks to its strange and beautiful optical effects, the result of its glimmer, shape and cut, not to mention the fact that diamonds are quite rare. Diamonds are found in the shape of octahedrons or skewed 12-sided crystals, also with contorted sides. The most valuable diamonds are the ones that are completely translucent, colourless and strongly light reflective. Besides colourless diamonds, there are diamonds that are brownish, grey, greenish, and with a slightly blue or red tinge. The value of one unit of weight of a diamond is one carat (= 200g). Diamonds are used in the production of jewelry, among other things, but they must be polished. The most well-known shape of a polished diamond is called brilliant. Around 95% of all diamonds found on Earth are not used in jewelry at all, however, instead finding use as drill bits or cutting devices, due to their hardness.

Diamonds can also be made synthetically, but natural diamonds remain more prevalent, thanks to their rough surfaces which are used for cutting and drilling. It is possible to manufacture diamonds which are used in jewelry, but it is a very long, drawn-out process which costs more than it is actually worth.

Graphite

In graphite, the carbon atoms are arranged in layers. Compared to diamond, graphite's hardness is negligible. It is an opaque, black, very soft substance with good electrical and heat conductivity. Graphite does not burn well.

Man-made graphite is made using the Acheson process, which is the reaction between the fuel coke and silicon are temperatures above 2000° C. It is also used as a blackening substance and a material in the production of electrodes and collectors, and as a moderating substance in nuclear reactors. Thanks to its layered structure, it is found in layers in the quarries where it is mined.

In diamond, the hydrogen atoms present are bonded with strong covalent bonds to the carbon atoms in the compound. Each carbon atom is bonded with four other carbon atoms. This explains diamond's hardness and high boiling point.

Graphite is composed of carbon atoms in layers, flat. The carbon atoms in graphite are bonded together with three covalent bonds. Between the individual layers, however, the van der Waals forces holding the material together are very weak. For this reason, individual layers of graphite can separate from one another, which reduces the hardness of the whole material.

Carbonic Acid and Carbonates

Carbonic acid (H2CO3) is a weak acid which occurs only in aqueous solution. It is sometimes mistakenly considered to be carbon dioxide (CO2) in solution, because of the reaction which produces it: Carbonic acid is formed by the dissolving in water of carbon dioxide according to the reaction

CO2 + H2O ® H2CO3.

The salts of carbonates and hydrogen carbonates are found in the Earth's crust.

Generally, hydrogen carbonates are formed by the union of a metal and the HCO3 - group in a reaction which releases one atom of hydrogen (a proton). This means that one atom of hydrogen is replaced by one atom of a metal.

Carbonates are also the salts of carbonic acid, with the only difference that the original hydrogens in the carbon acid are replaced by two metal atoms. When this occurs, the general formula of the salt formed is M2CO3 . Two atoms of hydrogen are released when this type of molecule is formed.

Carbonates are most often found in non-living matter, usually in the Earth's layers as rock-forming materials.

Calcium carbonate (CaCO3) is one of the main minerals which is able to form other compounds. It is slow to dissolve in water, forming a more easily soluble hydrogen carbonate, which reverts to its former state, an insoluble, precipitated CaCO3, when the water is evaporated out of the system.

This is the natural process which forms the beautiful stalactites that we see in caves all around the world.

Calcium carbonate is often called calcite. It is present in nature in numerous forms. It can be white or yellow, reddish, greenish or brownish, translucent or opaque. Clear calcite is an optically strong magnifier, so it was often used as an optical instrument in the past.

Another rock-forming compound is calcite. Most of the time, the products that it forms are called lime or limestones. Raw lime is transformed into quick lime at temperatures of over 1000° C. Any water mixed into the original substance forms hydrate of lime, or slack lime, which is used in the construction industry as an ingredient in cement and mortar.

Of course, many other carbonate compounds exist, most of which are found in the Earth's crust. Many of their titles have been eternalised because of the fact that they are common geological materials, or because place names have been named after them: For example, dolomite in the southern Carpatian Mountains, which now belongs to Italy.

The Compounds of Silicon

Silica sol, an acid containing silicon, glass, porcelain, bricks and mortar are some of the most important compounds which the element silicon forms.

Silicon is found in nature bonded in the form of silicon oxides which contain many complex
compounds. Many minerals are composed of silicon-containing compounds, among other materials.

Silicon is the second most common element in the Earth's crust, at 25.8% . Silicon is not very reactive. Even its oxide, silicon oxide, can only be formed at high temperature.

Silica sol, which is the common name for the oxygenated silicon-containing acid, is found in nature in the form of its salts. The silica sol compound with the simplest formula is the short-lived mono silicon, also known as orthosilicon acid (H4SiO4). As water is drawn from the molecule (condensation), the hydrogen atoms once present are replaced by atoms of silicon. This new compound is called a polysilicon or metasilicon acid. When a certain degree of condensation is reached, the dissolved siliconic acids can transform into strongly hydrated colloidal silicon gels.

The building block of silicon rock is silicon oxide, which is arranged in a polymeric atomic lattice. Silicon is found in its pure form as a so-called mineral crystal, but it often contains impurities such as sand. When melted, the bonds between its atoms are broken, leading to the breakdown of the molecule. When cooled, an amorphic structure remains: This is glass. As glass forms, the fractures consolidate with the help of oxide ions. Glass is a fairly hard, mostly non-crystalline structure which is breakable. It is inorganic material which does not have one definite melting point, because with rising temperature it gradually softens until the point when it liquifies completely. From a structural point of view, glass is a spatially irregular web composed of certain elements. It has low heat conductivity and a high resistance to electricity. Glass can be formed at high temperature in a process that uses casting, blowing, pressing and rolling.

Glass can be used in a number of areas. Thanks to its characteristics, it is most often used as a vessel for various liquids and other materials (because it is not very reactive). It can be used in electronics as an insulating material for electrical current. If other foreign materials are added to glass, it will colour, or change hues (for example iron oxide will give glass a greenish hue). This often gives glass a decorative type of feeling.

The salts and esters of silica acid are known as silicates. Silicates contain, besides silicon and acid, metal ions including potassium ions, sodium ions as well as aluminum ions. These molecules can be spatially oriented in either one, two or three dimensional structures. For this reason, there are numerous silicates.

Natural silicates are reactants used in the production of artificial silicates, as in for example cement and porcelain. Clay is produced by the weathering of mica. Clay and lime are used to make cement, which hardens after mixing with water.

China clay, or kaolin, a colourless clay, is used in the production of porcelain. Kaolin is mixed with a silicon sand and feldspar. Either it is formed as needed in the beginning, then heated, which is the general process of pottery, or it is made into some other shape or form using some other industrial method. Ceramic products are often used in construction, as clay bricks or brick dust of one sort or another. Sand and ash matter are used to make bricks, formable or otherwise, shingles and even canalisation pipes. Fire resistant material is usually used. The processes that individual ceramics are made from differ only according to those products' shaping. The desired shape can be attained by casting, pressing, smothering or in other various ways.

Synthetic Macromolecules

Synthetics are synthetic macromolecular compounds which are used in a variety of different ways. They replace materials such as natural fibres, wood, metals and glass. Some synthetic materials are the result of directed research, as in the production of plastics, with some desired combination of properties which might have some specific uses. Synthetics can be divided into three major categories, according to the way they behave when they are heated. We distinguish between thermoplastics, duroplastics and elastomers.

Thermoplastics soften when heated, liquifying in a certain temperature range. There is no chemical change in their structure. These macromolecules are composed of long, slightly branched chains which are held together with the help of van der Waals forces and hydrogen bonds. When heated, these forces between molecules are weakened, allowing the molecules to be able to push on each other and shift and move.

Duroplastics do not soften when heated. Their molecules are mutually strengthened with the help of paired electrons and the help of other bonds. At high temperature, these bonds do break, and the plastic begins to decompose.

Elastomers are synthetics which are easily formed mechanically. Once the stress is relieved, however, they return to their original shape. Their elasticity is caused by a web of arranged molecules with large spaces in between them. When heated, elastomers begin to shrivel, because their molecules begin to oscillate, and the network between them contracts. At high temperatures, elastomers break down.

Synthetics are used in almost every part of our daily lives. The reason is that they are materials which can be made to suit most any need. And this property of theirs is truly used to its utmost, as the various uses of the three types of developed plastics can attest to.

Colouring of Materials

Electromagnetic waves of between 400 nanometers and 750 nanometers are in the visible spectrum of light, so they can be seen by the human eye. With a prism, these wavelengths can be broken down into the colours of the spectrum, with certain ranges of wavelengths corresponding to certain colours. Colours are seen when a certain spectrum absorbs a certain length of wave. This absorption leads to electrons being excited, or even a whole molecule being excited. Unabsorbed light is reflected and is seen as complementary colour. Organic dyes have functional groups with a number of bond types. Electrons p absorb light of visible wavelengths, so that material appears as a complementary colour. Colour given off by a group of atoms with multiple bonds is therefore called chromatic (chroma = Greek colour). The colour of a substance depends on the number and size of its chromophores.

Coloured Indicators of pH

Some coloured substances change their colour according to pH. We call these acid and base indicators. They can be used to determine the pH of a solution, if not precisely. Colour change of an indicator is based on the transfer of protons between solution and indicator, which can cause a structural change in the indicator molecule. In most cases, colour changes because electrons p have been influenced by the presence of multiple bonds. Indictors exist in two forms - as an acid-base pair.

Acid-base indicator pair

Acidic form + H2O ® basic form + H3O+

According to the acidity or alkalinity of the solution, the equilibrium goes in one direction or the other. A visible change in the colour of the indicator only occurs when the concentration of the appropriate form of the indicator is increased a minimum of tenfold. For this reason, there are indicators for transition ranges, which indicate over a range of pH, not a specific one.

Laboratory indicators

phenolthalein range at pH 8.0-9.8 colourless to reddish purple

bromothymol blue range at pH 6.0-7.6 yellow to blue

methylorange range at pH 3.1-4.4 red to yellow-orange

Coloured molecules are called dyes. These can be divided into paints and pigments.

Paints are soluble molecules. Natural dyes can be produced from plant or animal matter. One well known example is saphran, which comes from the crocus flower. This dye is used as a yellow dye and as a spice. Natural colours are being replaced more and more often with synthetic colours. These colours are used first and foremost in the dyeing of textiles. Azure (blues) and anthracites are some of the most well-known examples. Azure-coloured dyes are characterised by the presence of a N=N double bond. Aniline is used to produce azure dyes, which are produced in two steps. In diazotaion are formed ions of phenyldiazone, which bonds in the following step with phenol or another aromatic amine. This combination of an aromatic amine produces an azure dye such as aniline yellow or chryzoid (yellow-brown).

Pigments do not dissolve in the basic ingredients of paints, instead forming suspensions. Pigments such as umbra? and ochre have been used for ages. Both are aluminum silicates which differ in the content of their oxides. Ochre contains iron oxide, and umbra? contains an additional manganese oxide. One of the most important synthetic pigments is a white pigment made from titanium oxide. Pigments are often used as colours employed in printing presses and printers.

Pigments used as printing press colours:

iron oxide red

chromium oxide green

Iron chromate yellow

cadmium sulfide yellow

Tensides, or Surfactants

Tensides are those materials which show surface activity. These are used in a wide variety of ways, as cleaning products or as counter or other surface finishers. The oldest, most well known cleaning product is soap. It is made from fats and active sodium bases and water. It is able to breakdown the ester bonds between glycerine and carboxylic acids, which leads to water joining in. Reactive products such as glycerine and alkaline salts are oily acids. These are actually soaps. For this reason, we call this process saponification. The effects of soaps depend on the ion content in water. Calcium ions replace the other ions present and bond with carboxylic acids to form a not very soluble calcium soap (see Fig. 1), whose cleaning power is limited, because it sediments.

Because soaps have a variety of disadvantages, they were replaced early on by synthetic tensides. We can distinguish between anionic, cationic, non-ionic and amphoteric tensides.

Anionic tensides are produced from two greasy alcohols of esterified sulphuric acids. These esters are then neutralised with sodium hydroxide, so that a sodium salt of monoalkylsulphuric acid is produced.

Cation tensides are ammonium salts with long alkyline rests. These tend to bond on to negatively charged surfaces. They are produced in the reaction of carboxylic acid with ammonia, which results in the production of alkylamines which are then substituted in a reaction with methyl chloride, resulting in ammonia as a product. Cation tensides are used mostly as softeners.

Non-ionic tensides see a charged portion of their molecule replaced by an uncharged group. With alkylpolyglycolethers it is a polyester rest which creates a polar part of the molecule of the tenside.

Non-ionic tensides have good moistening effect even at low temperatures.

Amphoteric tensides have one cation group and one anion group at their polar end. These are called amphotensides as well. Because they do not cause a reaction in human beings, they are often used in cosmetic products.

Other Cleaning Agents

In order to dissolve surface impurities, the effects of lipophilic alkyl rests are used on dirt on the surface of a given object (Figure 2). These are negatively charged and therefore repel each other. Parts of the stain are removed by the lipophile end of the tenside molecule. These are simply surrounded and carted off by the cleaning molecule. In our modern lives, we place great emphasis on cleanliness and the products which clean up after us. These products, besides cleaning agents, contain a wide variety of additives. The quality of these is improving constantly. Think of all the wonderful uses: perfumes, enzymes, inhibitors, whiteners, softeners - all of which increase the performance of water.


From Inorganic Carbon Compounds To Synthetic Macromolecules

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Friday, November 25, 2011

40# POTASSIUM CHLORIDE PELLETS

!±8± 40# POTASSIUM CHLORIDE PELLETS

Brand : North American Salt | Rate : | Price :
Post Date : Nov 26, 2011 00:34:05 | Usually ships in 1-2 business days


Provides an alternative choice to sodium chloride. Can be utilized effectively in all types of water softening units. Under normal use, it resists mushing, bridging and channeling to provide excellent percolation and brine formation. High water solubilityminimizes tank cleaning, providing efficient operation of the water-softening unit. Packaged in polyethylene bags for added moisture protection.

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Tuesday, November 22, 2011

FM-SF-01 Water Softener Resin Media in bag 1 cu.ft.

!±8±FM-SF-01 Water Softener Resin Media in bag 1 cu.ft.

Brand : Other
Rate :
Price :
Post Date : Nov 22, 2011 21:38:21
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Water Softener Resin Media is used by residential and commercial water softeners to soften water. It can be regenerated with either potassium chloride, or sodium chloride salt. Certified to NSF/ANSI 61 standard. How Water Softener Resin Media works: Water Softener Media is an Acid Cation Exchange Resin media which is commonly used by domestic water softeners. Media has to be regenerated by salt to perform at specified parameters. Either potassium chloride or sodium chloride is used for regeneration, with potassium chloride requiring about 10% more salt for regeneration. Advantage of potassium chloried regeneration is that it does not contribute to a high sodium content in water, and the backwash can be safely discharged into a drain or into environment. If sodium chloride is used for regeneration, backwash must be discharged into a sewer system. Also removes iron up to 4 ppm. Can be regenerated at 8, 12 and 15 lbs per ft3 salt dosages. Type: Gel Type Strong Acid Cation Exchange Resin Quantity: 1 cu.ft. bags Weight: 30 lb. per cubic foot Color: Red 1 cubic foot

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Monday, November 21, 2011

Water Softening with Potassium Chloride: Process, Health, and Environmental Benefits

!±8± Water Softening with Potassium Chloride: Process, Health, and Environmental Benefits

Brand : | Rate : | Price : $99.95
Post Date : Nov 21, 2011 04:05:40 | Usually ships in 24 hours


Potassium chloride is a logical alternative to sodium chloride in water softening. Water Softening with Potassium Chloride provides a thorough overview of the process, the equipment, and the techniques used. Then it compiles diverse trade and technical data on water softening with potassium chloride so readers can make informed decisions. It documents the health and environmental consequences and benefits of using potassium chloride and includes a chapter with summaries of recent research projects and FAQs. This is a key reference for professional water treatment specialists, environmental science researchers, and others.

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Friday, November 4, 2011

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