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Aluminium oxide electrolysis
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Câu 15: Sục khí SO2 vào dung dịch KMnO4 (thuốc tím), màu tím nhạt dần rồi mất màu (biết sản phẩm tạo thành là K2SO4, MnSO4, H2SO4 và H2O). Nguyên nhân là do A. SO2 đã oxi hóa KMnO4 thành MnO2. B. SO2 đã khử KMnO4 thành Mn+2. C. KMnO4 đã khử SO2 thành S+6. D. H2O đã oxi hóa KMnO4 thành Mn+2. Câu 17: Hỗn hợp tecmit dùng hàn gắn đường ray có thành phần chính là aluminium (Al) và iron (III) oxide (Fe2O3). Phản ứng xảy ra khi đung nóng hỗn hợp tecmit như sau: Fe2O3 + 2Al 2Fe + Al2O3. Phát biểu nào dưới đây là đúng? A. Al là chất bị oxi hoá. B. Fe2O3 là chất nhường electron. C. Fe2O3 là chất bị oxi hóa. D. Al2O3 là chất nhận electron. Câu 18: Phản ứng thu nhiệt là phản ứng A. giải phóng năng lượng dưới dạng nhiệt. B. hấp thu năng lượng dưới dạng nhiệt. C. cung cấp năng lượng dưới dạng nhiệt. D. hấp thu năng lượng dưới dạng hóa năng. Câu 19: Phản ứng nhiệt nhôm là phản ứng giữa bột nhôm và iron (III) oxide sinh ra một lượng nhiệt rất lớn và được ứng dụng dùng để hàn đường ray. Phản ứng nhiệt nhôm là phản ứng A. thu nhiệt. B. chưa xác định được. C. tỏa nhiệt. D. vừa thu nhiệt, vừa tỏa nhiệt. Câu 20: Phản ứng nào trong các phản ứng dưới đây là phản ứng thu nhiệt? A. Vôi sống tác dụng với nước: CaO + H2O → Ca(OH)2. B. Đốt cháy than: C + O2 CO2. C. Đốt cháy cồn: C2H5OH + 3O2 2CO2 + 3H2O. D. Nung đá vôi: CaCO3 CO2 + CaO. Câu 21: Điều kiện nào sau đây không phải là điều kiện chuẩn? A. Áp suất 1 bar và nhiệt độ 25 0C. B. Áp suất 1 bar và nhiệt độ 298 K. C. Áp suất 1 bar và nhiệt độ 25 0C hay 298 K. D. Áp suất 1 bar và nhiệt độ 25K. Câu 22: Điều kiện nào sau đây là điều kiện chuẩn? A. Áp suất 1 bar và nhiệt độ 25 K. B. Áp suất 1 bar và nhiệt độ 298 0C. C. Áp suất 1 bar và nhiệt độ 298 K. D. Áp suất 1 bar và nhiệt độ 25K. Câu 23: Nồng độ đối với chất tan trong dung dịch ở điều kiện chuẩn là? A. 0,01 mol/L. B. 0,1 mol/L. C. 1 mol/L. D. 0,5 mol/L. Câu 24: 1 mol chất khí ở điều kiện chuẩn chiếm thể tích bằng bao nhiêu? A. 24,79 lít. B. 2,479 lít. C. 22,4 lít. D. 2,24 lít. Câu 25: Kí hiệu nhiệt tạo thành chuẩn của một chất là A. . B. . C. H298.. D. . Câu 26: Số oxi hóa của một nguyên tử trong phân tử là A. điện tích quy ước của nguyên tử trong phân tử khi coi tất cả các electron liên kết đều chuyển hoàn toàn về nguyên tử của nguyên tố có độ âm điện lớn hơn. B. hóa trị của nguyên tử nguyên tố đó. C. điện tích thực của nguyên tử nguyên tố đó. D. độ âm điện của nguyên tử nguyên tố đó. Câu 27: Fe2O3 là thành phần chính của quặng hematite đỏ, dùng để luyện gang. Số oxi hoá của iron (Fe) trong Fe2O3 là A. +3. B. 3+. C. 3-. D. -3. Câu 28: Trong phản ứng oxi hóa – khử, chất nhận electron được gọi là A. chất khử. B. chất oxi hoá. C. acid. D. base. Câu 29: Các phản ứng quan trọng gắn liền với cuộc sống như sự cháy của than, củi; sự cháy của xăng, dầu trong các động cơ đốt trong,…thường thuộc loại phản ứng nào? A. Phản ứng thế. B. Phản ứng cộng. C. Phản ứng phân hủy. D. Phản ứng oxi hóa - khử. Câu 30: Enthalpy phản ứng chuẩn có kí hiệu là A. . B. . C. . D. .
Câu 1: Chất khử là A. chất nhường electron. B. chất nhận electron. C. chất nhường proton. D. chất nhận proton. Câu 2: Phản ứng oxi hóa - khử là A. phản ứng hóa học trong đó có sự chuyển proton. B. phản ứng hóa học trong đó có sự thay đổi số oxi hóa. C. phản ứng hóa học trong đó phải có sự biến đổi hợp chất thành đơn chất. D. phản ứng hóa học trong đó sự chuyển electron từ đơn chất sang hợp chất. Câu 3: Sự oxi hóa một chất là quá trình A. nhận electron của chất đó. B. làm giảm số oxi hóa của chất đó. C. nhường electron của chất đó. D. làm thay đổi số oxi hóa của chất đó. Câu 4: Phát biểu nào dưới đây không đúng? A. Sự khử là sự mất hay cho electron. B. Sự oxi hoá là sự mất electron. C. Chất khử là chất nhường electron. D. Chất oxi hoá là chất nhận electron. Câu 5: Trong các phản ứng sau, phản ứng nào là phản ứng oxi hóa - khử? A. CaCO3 CaO + CO2. B. 2KClO3 2KCl + 3O2. C. 2NaHCO3 Na2CO3 + H2O + SO2. D. 2Fe(OH)3 Fe2O3 + 3H2O. Câu 6: Cho phương trình phản ứng: Fe + CuSO4 Cu + FeSO4. Vai trò của Fe trong phản ứng là A. chất oxi hóa. B. chất bị khử. C. chất khử. D. vừa là chất khử, là chất oxi hóa. Câu 7: Cho phương trình phản ứng: Cl2 + 2H2O 2HCl + 2HClO. Vai trò của Cl2 trong phản ứng là A. chất oxi hóa. B. chất bị khử. C. chất khử. D. vừa là chất khử, là chất oxi hóa. Câu 8: Cho phương trình phản ứng: AgNO3 + HCl AgCl + HNO3. Vai trò của AgNO3 trong phản ứng là A. chất oxi hóa. B. chất bị khử. C. không là chất khử, không là chất oxi hóa. D. vừa là chất khử, là chất oxi hóa. Câu 9: Trong các phản ứng sau, phản ứng nào không phải là phản ứng oxi hóa khử? A. Fe + 2HCl FeCl2 + H2. B. Zn + CuSO4 ZnSO4 + Cu. C. CH4 + Cl2 CH3Cl + HCl. D. BaCl2 + H2SO4 BaSO4 + 2HCl. Câu 10: Trong các phản ứng sau phản ứng nào là phản ứng oxi hóa - khử? A. NaOH + HCl NaCl + H2O. B. 2Fe(OH)3 + 3H2SO4 Fe2(SO4)3 + 6H2O. C. CaCO3 + 2HCl CaCl2 + H2O + CO2. D. 2CH3COOH + Mg (CH3COO)2Mg + H2. Câu 11: Số oxi hóa của S trong SO2 bằng A. +4 B. -4 C. +2 D. -2 Câu 12: Số oxi hóa của C trong CH4 bằng A. +4 B. -4 C. +1 D. -1 Câu 13: Sơ đồ: Cu → Cu+2 + 2e biểu thị quá trình A. oxi hóa. B. nhận electron. C. phân hủy. D. khử Câu 14: Sơ đồ: N+5 + 3e → N+2 biểu thị quá trình A. oxi hóa B. khử C. nhận proton D. hóa hợp Câu 15: Sục khí SO2 vào dung dịch KMnO4 (thuốc tím), màu tím nhạt dần rồi mất màu (biết sản phẩm tạo thành là K2SO4, MnSO4, H2SO4 và H2O). Nguyên nhân là do A. SO2 đã oxi hóa KMnO4 thành MnO2. B. SO2 đã khử KMnO4 thành Mn+2. C. KMnO4 đã khử SO2 thành S+6. D. H2O đã oxi hóa KMnO4 thành Mn+2. Câu 17: Hỗn hợp tecmit dùng hàn gắn đường ray có thành phần chính là aluminium (Al) và iron (III) oxide (Fe2O3). Phản ứng xảy ra khi đung nóng hỗn hợp tecmit như sau: Fe2O3 + 2Al 2Fe + Al2O3. Phát biểu nào dưới đây là đúng? A. Al là chất bị oxi hoá. B. Fe2O3 là chất nhường electron. C. Fe2O3 là chất bị oxi hóa. D. Al2O3 là chất nhận electron. Câu 18: Phản ứng thu nhiệt là phản ứng A. giải phóng năng lượng dưới dạng nhiệt. B. hấp thu năng lượng dưới dạng nhiệt. C. cung cấp năng lượng dưới dạng nhiệt. D. hấp thu năng lượng dưới dạng hóa năng. Câu 19: Phản ứng nhiệt nhôm là phản ứng giữa bột nhôm và iron (III) oxide sinh ra một lượng nhiệt rất lớn và được ứng dụng dùng để hàn đường ray. Phản ứng nhiệt nhôm là phản ứng A. thu nhiệt. B. chưa xác định được. C. tỏa nhiệt. D. vừa thu nhiệt, vừa tỏa nhiệt. Câu 20: Phản ứng nào trong các phản ứng dưới đây là phản ứng thu nhiệt? A. Vôi sống tác dụng với nước: CaO + H2O → Ca(OH)2. B. Đốt cháy than: C + O2 CO2. C. Đốt cháy cồn: C2H5OH + 3O2 2CO2 + 3H2O. D. Nung đá vôi: CaCO3 CO2 + CaO. Câu 21: Điều kiện nào sau đây không phải là điều kiện chuẩn? A. Áp suất 1 bar và nhiệt độ 25 0C. B. Áp suất 1 bar và nhiệt độ 298 K. C. Áp suất 1 bar và nhiệt độ 25 0C hay 298 K. D. Áp suất 1 bar và nhiệt độ 25K. Câu 22: Điều kiện nào sau đây là điều kiện chuẩn? A. Áp suất 1 bar và nhiệt độ 25 K. B. Áp suất 1 bar và nhiệt độ 298 0C. C. Áp suất 1 bar và nhiệt độ 298 K. D. Áp suất 1 bar và nhiệt độ 25K. Câu 23: Nồng độ đối với chất tan trong dung dịch ở điều kiện chuẩn là? A. 0,01 mol/L. B. 0,1 mol/L. C. 1 mol/L. D. 0,5 mol/L. Câu 24: 1 mol chất khí ở điều kiện chuẩn chiếm thể tích bằng bao nhiêu? A. 24,79 lít. B. 2,479 lít. C. 22,4 lít. D. 2,24 lít. Câu 25: Kí hiệu nhiệt tạo thành chuẩn của một chất là A. . B. . C. H298.. D. . Câu 26: Số oxi hóa của một nguyên tử trong phân tử là A. điện tích quy ước của nguyên tử trong phân tử khi coi tất cả các electron liên kết đều chuyển hoàn toàn về nguyên tử của nguyên tố có độ âm điện lớn hơn. B. hóa trị của nguyên tử nguyên tố đó. C. điện tích thực của nguyên tử nguyên tố đó. D. độ âm điện của nguyên tử nguyên tố đó. Câu 27: Fe2O3 là thành phần chính của quặng hematite đỏ, dùng để luyện gang. Số oxi hoá của iron (Fe) trong Fe2O3 là A. +3. B. 3+. C. 3-. D. -3. Câu 28: Trong phản ứng oxi hóa – khử, chất nhận electron được gọi là A. chất khử. B. chất oxi hoá. C. acid. D. base. Câu 29: Các phản ứng quan trọng gắn liền với cuộc sống như sự cháy của than, củi; sự cháy của xăng, dầu trong các động cơ đốt trong,…thường thuộc loại phản ứng nào? A. Phản ứng thế. B. Phản ứng cộng. C. Phản ứng phân hủy. D. Phản ứng oxi hóa - khử. Câu 30: Enthalpy phản ứng chuẩn có kí hiệu là A. . B. . C. . D. .
Ions Ions are charged substances that have formed through the gain or loss of electrons. Cations form from the loss of electrons and have a positive charge while anions form through the gain of electrons and have a negative charge. Cation Formation Cations are the positive ions formed by the loss of one or more electrons. The most commonly formed cations of the representative elements are those that involve the loss of all of the valence electrons. Consider the alkali metal sodium (Na) . It has one valence electron in the n=3 energy level. Upon losing that electron, the sodiu ion now has an octet of electrons from the second energy level and a charge of 1+ . The electron arrangement of the sodium ion is now the same as that of the noble gas neon. Consider a similar process with magnesium and aluminum. In this case, the magnesium atom loses its two valence electrons in order to achieve the same arrangement as the noble gas neon and a charge of 2+ . The aluminum atom loses its three valence electrons to have the same electron arrangement as neon and a charge of 3+ . For representative elements under typical conditions, three electrons is usually the maximum number that will be los. Representative elements will not lose electrons beyond their valence because they would have to "break" the octet of the previous energy level which provides stability to the ion. Anions Anions are the negative ions formed from the gain of one or more electrons. When nonmetal atoms gain elections, they often do so until their outermost principal energy level achieves an octet. For fluorine, which has an electron arrangement of (2, 7), it only needs to gain one electron to have the same electron arrangement as neon. Forming an octet (eight electrons in the outer shell) provides stability to the atom. Fluorine will gain one electron and have a charge of 1− . The electron arrangement of the fluoride ion (2, 8) will also change to reflect the gain of an electron. Oxygen has an electron arrangement of (2, 6) and needs to gain two electrons to fill the n=2 energy level and achieve an octet of electrons in the outermost shell. The oxide ion will have a charge of 2− as a result of gaining two electrons. Under typical conditions, three electrons is the maximum that will be gained in the formation of anions. Subatomic Particles in an Ion Since ions form from the gain or loss of electrons, we can also look at the number of subatomic particles (protons, neutrons, and electrons) found in an ion. Remember that the number of protons determines the identity of the element and will not change in a chemical process. Example 2.5.1 How many protons, neutrons, and electrons in a single oxide (O2−) ion? Solution Oxygen has the atomic number 8 so both the atom and the ion will have 8 protons. The average atomic mass of oxygen is 16. Therefore, there will be 8 neutrons (atomic mass−atomic number=neutrons) . A neutral oxygen atom would have 8 electrons. However, the anion has gained two electrons so O2− has 10 electrons. We can also use information about the subatomic particles to determine the identity of an ion. Example 2.5.2 An ion with a 2+ charge has 18 electrons. Determine the identity of the ion. Solution If an ion has a 2+ charge then it must have lost electrons to form the cation. If the ion has 18 electrons and the atom lost 2 to form the ion, then the neutral atom contained 20 electrons. Since it was neutral, it must also have had 20 protons. Therefore the element is calcium. Polyatomic Ions A polyatomic ion is an ion composed of two or more atoms that have a charge as a group (poly = many). The ammonium ion (see figure below) consists of one nitrogen atom and four hydrogen atoms. Together, they comprise a single ion with a 1+ charge and a formula of NH+4 . The hydroxide ion (see figure below) contains one hydrogen atom and one oxygen atom with an overall charge of 1− . The carbonate ion (see figure below) consists of one carbon atom and three oxygen atoms and carries an overall charge of 2− . The formula of the carbonate ion is CO2−3 . The atoms of a polyatomic ion are tightly bonded together and so the entire ion behaves as a single unit. The figures below show several examples. Soult Screenshot 2-2-1.png Figure 2.5.1 : The ammonium ion (NH+4) is a nitrogen atom (blue) bonded to four hydrogen atoms (white). Soult Screenshot 2-2-2.png Figure 2.5.2 : The hydroxide ion (OH−) is an oxygen atom (red) bonded to a hydrogen atom. Soult Screenshot 2-2-3.png Figure 2.5.3 : The carbonate ion (CO2−3) is a carbon atom (black) bonded to three oxygen atoms. The table below lists a number of polyatomic ions by name and by structure. The heading for each column indicates the charge on the polyatomic ions in that group. Note that the vast majority of the ions listed are anions - there are very few polyatomic cations. 1− 2− 3− 1+ Table 2.5.1 : Common Polyatomic Ions acetate, CH3COO− carbonate, CO2−3 arsenate, AsO3−3 ammonium, NH+4 bromate, BrO−3 chromate, CrO2−4 phosphite, PO3−3 chlorate, ClO−3 dichromate, Cr2O2−7 phosphate, PO3−4 chlorite, ClO−2 hydrogen phosphate, HPO2−4 cyanide, CN− oxalate, C2O2−4 dihydrogen phosphate, H2PO−4 peroxide, O2−2 hydrogen carbonate, HCO−3 silicate, SiO2−3 hydrogen sulfate, HSO−4 sulfate, SO2−4 hydrogen sulfide, HS− sulfite, SO2−3 hydroxide, OH− hypochlorite, ClO− nitrate, NO−3 nitrite, NO−2 perchlorate, ClO−4 permanganate, MnO−4 The vast majority of polyatomic ions are anions, many of which end in -ate or -ite. Notice that in some cases such as nitrate (NO−3) and nitrite (NO−2) , there are multiple anions that consist of the same two elements. In these cases, the difference between the ions is the number of oxygen atoms present, while the overall charge is the same. As a class, these are called oxyanions. When there are two oxyanions for a particular element, the one with the greater number of oxygen atoms gets the -ate suffix, while the one with the fewer number of oxygen atoms gets the -ite suffix. The four oxyanions of chlorine are shown below, which also includes the use of the prefixes hypo- and per-. ClO− , hypochlorite ClO−2 , chlorite ClO−3 , chlorate ClO−4 , perchlorate Not your usual ion Soult Screenshot 2-2-4.png "Drink you milk. It's good for your bones." We're told this from early childhood, and with good reason. Milk contains a good supply of calcium, part of the structure of bone. However, there are two other ionic components of hydroxyapatite, the mineral component. Phosphate ion and hydroxide ion make up the remainder of the inorganic material in bone. News You Can Use Bone is a very complex structure. It is composed of protein (mainly collagen), hydroxyapatite (a calcium-phosphate-hydroxide mixture), some other minerals, and contains 10 - 20% water. The calcium/phosphate ratios are not stoichiometric, but vary somewhat from one portion of bone to the next. Bones are very strong but will break under enough stress. Regular exercise and proper nutrition help to increase bone strength. Watch a video about bone structure at http://www.youtube.com/watch?v=d9owEvYdouk Nitrate is an anion with a complex bonding structure. Major sources for this ion in drinking water are runoff from fertilizer, septic tank leakage, sewage, and natural deposits. High concentrations of nitrates represent a significant health hazard, especially to infants. The nitrate in the body is converted to nitrite, which then binds to hemoglobin. This binding decreases the ability of hemoglobin to transport oxygen, thus depriving the cells of the O2 needed for proper functioning. Cyanide production is widespread throughout nature. Forest fires will produce significant amounts of cyanide. Many plants contain cyanide, and it is produced by a number of bacteria, algae, and fungi. Cyanide is used industrially in metal finishing, iron and steel mills, and in organic synthesis processes. This material is also an important component for the refining of precious metals. Formation of a complex between cyanide and gold allows extraction of this metal from a mixture.
A solution is a mixture in which one or more substances are uniformly distributed in another substance. Solutions can be mixtures of liquids, solids, or gases. For example, plasma, the liquid part of blood, is a very complex solution. It is composed of many types of ions and large molecules, as well as gases, that are dissolved in water. A solute (SAHL-YOOT) is a substance dissolved in the solvent. The particles that compose a solute may be ions, atoms, or molecules. The solvent is the substance in which the solute is dissolved. For example, when sugar, a solute, and water, a solvent, are mixed, a solution of sugar water results. Though the sugar dissolves in the water, neither the sugar molecules nor the water molecules are altered chemically. If the water is boiled away, the sugar molecules remain and are unchanged. Solutions can be composed of various proportions of a given solute in a given solvent. Thus, solutions can vary in concentra- tion. The concentration of a solution is the amount of solute dis- solved in a fixed amount of the solution. For example, a 2 percent saltwater solution contains 2 g of salt dissolved in enough water to make 100 mL of solution. The more solute dissolved, the greater is the concentration of the solution. A saturated solution is one in which no more solute can dissolve. Aqueous (AY-kwee-uhs) solutions—solutions in which water is the solvent—are universally important to living things. Marine microorganisms spend their lives immersed in the sea, an aqueous solution. Most nutrients that plants need are in aqueous solutions in moist soil. Body cells exist in an aqueous solution of intercellu- lar fluid and are themselves filled with fluid; in fact, most chemical reactions that occur in the body occur in aqueous solutions. Copyright © by Holt, Rinehart and Winston. All rights reserved. Liquid water Solid water Ice (solid water) is less dense than liquid water because of the structure of ice crystals. The water molecules in ice are bonded to each other in a way that creates large amounts of open space between the molecules, relative to liquid water. FIGURE 2-12 solvent from the Latin solvere, meaning “to loosen” Word Roots and Origins CHEMISTRY OF LIFE 43 ACIDS AND BASES One of the most important aspects of a living system is the degree of its acidity or alkalinity. What do we mean when we use the terms acid and base? Ionization of Water As water molecules move about, they bump into one another. Some of these collisions are strong enough to result in a chemical change: one water molecule loses a proton (a hydrogen nucleus), and the other gains this proton. This reaction really occurs in two steps. First, one molecule of water pulls apart another water molecule, or dissociates, into two ions of opposite charge: H2O ∏ H OH The OH ion is known as the hydroxide ion. The free H ion can react with another water molecule, as shown in the equation below. H H2O ∏ H3O The H3O ion is known as the hydronium ion. Acidity or alkalin- ity is a measure of the relative amounts of hydronium ions and hydroxide ions dissolved in a solution. If the number of hydronium ions in a solution equals the number of hydroxide ions, the solution is said to be neutral. Pure water contains equal numbers of hydro- nium ions and hydroxide ions and is therefore a neutral solution. Acids If the number of hydronium ions in a solution is greater than the number of hydroxide ions, the solution is an acid. For example, when hydrogen chloride gas, HCl, is dissolved in water, its mol- ecules dissociate to form hydrogen ions, H, and chloride ions, Cl, as is shown in the equation below. HCl ∏ H Cl These free hydrogen ions combine with water molecules to form hydronium ions, H3O. This aqueous solution contains many more hydronium ions than it does hydroxide ions, making it an acidic solution. Acids tend to have a sour taste; how- ever, never taste a substance to test it for acidity. In concentrated forms, they are highly corrosive to some materials, as you can see in Figure 2-13. Bases If sodium hydroxide, NaOH, a solid, is dissolved in water, it dissociates to form sodium ions, Na, and hydroxide ions, OH, as shown in the equation below. NaOH ∏ Na OH Copyright © by Holt, Rinehart and Winston. All rights reserved. Eco Connection onnection Acid Precipitation Acid precipitation, more commonly called acid rain, describes rain, snow, sleet, or fog that contains high levels of sulfuric and nitric acids. These acids form when sulfur dioxide gas, SO2, and nitrogen oxide gas, NO, react with water in the atmosphere to produce sulfuric acid, H2SO4, and nitric acid, HNO3. Acid precipitation makes soil and bodies of water, such as lakes, more acidic than normal. These high acid levels can harm plant and animal life directly. A high level of acid in a lake may kill mollusks, fish, and amphibians. Even in a lake that does not have a very elevated level of acid, acid precipitation may leach aluminum and magnesium from soils, poisoning water- dwelling species. Reducing fossil-fuel consump- tion, such as occurs in gasoline engines and coal-burning power plants, should reduce high acid levels in precipitation. Sulfur dioxide, SO2, which is produced when fossil fuels are burned, reacts with water in the atmosphere to produce acid precipitation. Acid precipitation, or acid rain, can make lakes and rivers too acidic to support life and can even corrode stone, such as the face of this statue. FIGURE 2-13 44 CHAPTER 2 This solution then contains more hydroxide ions than hydronium ions and is therefore defined as a base. The adjective alkaline refers to bases. Bases have a bitter taste; however, never taste a substance to test for alkalinity. They tend to feel slippery because the OH ions react with the oil on our skin to form a soap. In fact, commercial soap is the product of a reaction between a base and a fat. pH Scientists have developed a scale for comparing the relative con- centrations of hydronium ions and hydroxide ions in a solution. This scale is called the pH scale, and it ranges from 0 to 14, as shown in Figure 2-14. A solution with a pH of 0 is very acidic, a solution with a pH of 7 is neutral, and a solution with a pH of 14 is very basic. A solution’s pH is measured on a logarithmic scale. That is, the change of one pH unit reflects a 10-fold change in the acidity or alkalinity. For example, urine has 10 times the H3O ions at a pH of 6 than water does at a pH of 7. Vinegar, has 1,000 times more H3O ions at a pH of 3 than urine at a pH of 6, and 10,000 times more H3O ions than water at a pH of 7. The pH of a solution can be measured with litmus paper or with some other chemical indicator that changes color at various pH levels. Buffers The control of pH is important for living systems. Enzymes can function only within a very narrow pH range. The control of pH in organisms is often accomplished with buffers. Buffers are chemi- cal substances that neutralize small amounts of either an acid or a base added to a solution. As Figure 2-14 shows, the composition of your internal environment—in terms of acidity and alkalinity— varies greatly. Some of your body fluids, such as stomach acid and urine, are acidic. Others, such as intestinal fluid and blood, are
Make mcq quiz with 4 option in which one is correct -'10 Basis of Material Science • .....;;;";;;"~~;;,,;;,,,,;.;.,,;;,,,;,,;.;,.,------------ 6. Temporary materials: Some materials are meant to be placed in the oral cavity for a short period of time for different reasons. • Temporary crowns: While a permanent crown is prepared in the dental laboratory, the patient must wait for few days before it can be fabricated and cemented into place. Does patient experience any problems during this time period? If the tooth is vital (the pulp is alive), the patient is likely to experience pain and sensitivity while eating and drinking, also it looks unesthetic. What can be done to solve this problem? A temporary crown is placed before the patient leaves the clinic. It is constructed and luted in the same appointment in which the crown preparation is done. Temporary crowns are not very strong or esthetic but they serve adequately till the permanent crown is ready to be cemented. • Temporary restorations: Sometimes it is difficult to decide immediately the best line of treatment for a particular tooth. The exact condition of the pulp may not be obvious to the dentist from the patient's symptoms. A dentist removes all or part of the decay and then places a temporary restoration to have time to observe the behaviour of the pulp or to give the pilip time to heal before deciding the further treatment required. Classification based on Location of Fabrication 4,9 Materials can be classified based on the location of fabrication into: • Direct restorative materials. • Indirect restorative materials Direct restorative materials: They include those materials which are used to restore cavity preparations directly in the oral cavity (Box 1.5). Box 1.5: Examples of direct restorative materials Amalgam, composites, glass ionomer and other materials, which set by chemical reactions in the mouth. Indirect restorative materials: It includes those restorations which must be fabricated outside the mouth, indirectly on a cast/ model/ die, because their processing condition would harm oral tissues. Materials used in the construction of such prosthesis are called indirect restorative materials (Box 1.6). Box 1.6: Examples of indirect restorative materials Gold inlays, crowns of metal, ceramic and polymers, which are processed at elevated temperatures. Some indirect composite restorations can be processed under specific wavelength of light, e.g. Ceramage. Classification based on Longevity of Use 1. Permanent restorations: These restorations are not planned to be replaced for a particular time period. Though they are referred to as permanent, actually they are not, e.g. fillings, crowns, bridges and dentures do not last forever (Fig. 1.5). 2. Temporary restorations: These restorations are planned to be replaced in a short period of time, such as few days to weeks. For ~ Permanent C/) c c -.2 0 c- :;::; Cll co Interim ~ Q; 0 .8ll::1iJ C/) o~ Cll a:: c:=:J Temporary Time period Fig. 1.5: Diagram depicting the time period of use of a restoration. (Arrow in permanent restoration depicts that such restorations are not planned to be replaced for a long period of time.) Introducton to Dental Materials Dental materials Box 1.7: Characteristics of metals 1. High thermal and electrical conductivity 2. Ductility (pure metals are very soft and they can be bent without breaking) 3. Opacity (they do not transmit light) 4. Luster (they have a surface that strongly reflects light and appears bright and shiny) 5. They tend to dissolve to some extent in water or other aqueous solutions, producing cations. 6. All metals are white (actually gray) except for gold, which is yellow, and copper, which is reddish. 7. All metals are solid at room temperature except mercury, which is liquid at room temperature and is used with silver alloys as amalgam. 8. All metals have high melting temperatures because of high strength of the metallic bond that holds the atoms together. 3. Polymers 4. Composites Composites are mixtures of two or more of the first three classes in which the different components remain distinct from one another in the final structure. A common example is composite resin. Fig. 1.7a: Three-dimensional structure of iron (metal) Metals Metals are the oldest of the three classes of materials that have been used as dental materials. Metals are characterized by metallic bonds (Box 1.7) which will be discussed in the next chapter. Metals solidify with their atoms in a regular or crystalline arrangement (see Chapter 2), often in the form of a cube (Fig. 1.7a). example, temporary fillings done in a tooth during root canal treatment, which have to be replaced within 2-4 days during subsequent visits. They are used to protect the tooth and provide function till the final restoration is done. 3. Interim restoration: At times, dental treatment requires "long-term" definite temporary restorations or "interim" restorations. For examle, a 7-year-old child, met with trauma and fractured one of his central incisors. A large composite build- up may serve his immediate requirement until the root formation is completed and a permanent crown is placed. 5 Classification based on the Chemical Nature of the Material These are the atoms that make up a material and the way they are bonded together determine the properties of that materiaLS Weak bonds make for weak materials and vice versa (Table 1.4). Materials can be classified into different categories based on their primary atomic bonds (Fig. 1.6): 1. Metals 2. Ceramics Fig. 1.6: Classification of dental materials based on chemical nature 12 Basis of Material Science Box 1.9: Benefits of ceramics in dentistry 1. Many ceramic oxides are used as pigmenting agents. These oxides produce good range of colors. Due to this characteristic, we are able to match almost any tooth color with good esthetic results. 2. They are inert, i.e. not chemically reactive. This quality provides ceramics with good bio- compatibility. 3. Ceramic materials are translucent, like natural teeth. This translucency gives the ceramic crown a more natural appearance than any other dental material. Fig. 1.7b: Internal arrangement of tetrahedral structure of ceramic (silica) four large oxygen atoms surround smaller silicon atom Ceramics A ceramic is a compound formed by the union of a metallic and a non-metallic element (Box 1.8). Most of these materials are oxides, formed by the union of oxygen with metals such as silicon, aluminum, calcium and magnesium (Fig.1.7b). Ceramics may be simple or complex. Examples of simple ceramics are alumina and silica. Examples of complex ceramics are feldspar (potassium aluminum silicate) and kaolin (hydrated aluminum silicate). Ceramics may be crystalline or non- crystalline (i.e. amorphous). Porcelain is a specific type of ceramic used extensively in dentistry (Box 1.9). Box 1.8: Characteristics of ceramics 1. High melting points. 2. Brittleness, which means they cannot be bent or deformed (no sliding) to any extent without actually cracking and breaking. 3. They are poor conductor of heat and electricity. 4. They are chemically inert. 5. They have excellent esthetic result in terms of matching natural teeth. Fig. 1.8: Stucture of synthetic polymer Polymers They are the latest addition (early to mid- 1900s) to dental materials. Most of the polymers are nowadays synthesized by humans. Polymers are giant, long-chain organic molecules (Fig. 1.8). Polymers are characterized by covalent bonds within each molecule, giving them tremendous strength in a single direction. Try to break a nylon rope by pulling it! They are poor conductors of heat and electri- city. Most polymers have a structure containing thousands of carbon atoms linked together like beads on a string. Others, such as silicone polymers are formed with silicon-oxygen bonds. Introducton to Dental Materials Table 1.4: Characteristics of different materials 13 Characteristics Bond Properties Crystal structure Metals Metallic bonding High strength and hardness, high electrical and thermal conductivity BCC, FCC, or HCP unit cells Ceramics Ionic or covalent bonding, or both High hardness and stiffness, electrically insulating, refractory, and chemically inert Crystalline or amorphous Polymers Covalent bonding Low sensitivity, high electrical resistivity, and low thermal conductivity, strength and stiffness vary widely Amorphous and crystalline Composites Composites are combinations of any of the basic ceramic, metallic and polymeric materials (Box 1.10). Each material that makes up composites is called a phase. Their properties tend to be somewhere between those of their basic constituents and are used to enhance their performance, longevity and handling chracterstics. Box 1.10: Types of composites in dentistry 1. Ceramic - metallic composite: Tungsten carbide bur. 2. Metal - polymer composite: Die materials in dental laboratory. 3. Ceramic - polymer composite: Enamel, dentin, bone and restorative composites. A composite is a kind of "combination" of materials, which compliment each other. The properties lacking in one material are compensated by those of the other material. For example, restorative composite has two phases, namely resin and fillers. Teeth and bones are examples of natural composites. Enamel is a composite of hydroxyapatite (which is a ceramic material) and protein (which is a polymer). EVALUATION OF DENTAL MATERIALS Most manufacturers of dental materials maintain a quality assurance programme (As per international standard like ADA specifications) and materials are thoroughly tested before being released into the market for dental practitioner (Fig. 1.9). Laboratory Evaluations Most ADA/ ANSI specifications involve laboratory tests. The tests performed as per these specifications are useful but they all are performed in vitro, (carried out in the laboratory away from the clinical conditions) which have a lot of limitations in clinical practice.lO Clinical Notes 1. For example, most of the direct restorative materials are tested for their compressive strength but ultimately the material is subjected to a combination of compressive, tensile and shear stresses, which may decide the final success or failure of the material under masticatory load. 2. Similarly upper dentures mostly fracture along the midline because of bending. Hence a bending or transverse strength ~B-a-s-is-o-f-M-a-t-e-ria-I-S~c-ie-n-c-e-------------- ---------. test is far more meaningful for denture base materials than a compression test. Clinical Trials The majority of new materials are subjected to extensive clinical trials normally in co-operation with a dental college or hospital departments prior to their release. CONCLUSION As the number of available materials is going up, it is important that the dentist remains more aware about new products so that their judgement about the selection of material remains successful. Materials which have not been thoroughly evaluated should be avoided, specially with clinical dentistry falling under Consumer Protection Act (CPA). I Research and development I iI Manufacturer/analysis Ideal requirements for clinical use: Thermal, optical, mechanical, chemical, biological Available materials and their properties are evaluated Launch of new I product Choice and selection of material by the dentist Critical assessment based on clinical performance I I H feedback to I
Electrolysis: extracting aluminium
110.31.b.17.C
Topic: Reading/Vocabulary Development