Sodium carbonate naming

On standing, gelatinous aluminium hydroxide, which may initially have even more water occluded than indicated above, is converted into a form insoluble in both acids and alkalis, which is probably a hydrated form of the oxide AI2O3. Both forms, however, have strong adsorptive power and will adsorb dyes, a property long used by the textile trade to dye rayon. The cloth is first impregnated with an aluminium salt (for example sulphate or acetate) when addition of a little alkali, such as sodium carbonate, causes aluminium hydroxide to deposit in the pores of the material. The presence of this aluminium hydroxide in the cloth helps the dye to bite by ad sorbing it—hence the name mordant (Latin mordere = to bite) dye process. 

Seaweeds. The eadiest successful manufacture of iodine started in 1817 using certain varieties of seaweeds. The seaweed was dried, burned, and the ash lixiviated to obtain iodine and potassium and sodium salts. The first process used was known as the kelp, or native, process. The name kelp, initially apphed to the ash of the seaweed, has been extended to include the seaweed itself. About 20 t of fresh seaweed was used to produce 5 t of air-dried product containing a mean of 0.38 wt % iodine in the form of iodides of alkah metals. The ash obtained after burning the dried seaweed contains about 1.5 wt % iodine. Chemical separation of the iodine was performed by lixiviation of the burned kelp, followed by soHd-Hquid separation and water evaporation. After separating sodium and potassium chloride, and sodium carbonate, the mother Hquor containing iodine as iodide was treated with sulfuric acid and manganese dioxide to oxidize the iodide to free iodine, which was sublimed and condensed in earthenware pipes (57). 

Natron, n. soda, in the following senses (1) sodium carbonate, Na2COa ( kohlensaurea Natron ) (2) sodium hydrogen carbonate, NaHCOa ( doppcltkohlensaures Natron ) (3) sodium hydroxide or caustic soda, NaOH, usually called Atznatron (4) in older names, sodium oxide, NajO (as in schwefel-saures Natron, sodium sulfate), -aiaun,... 

Similar to the pH meter, gas meters employ specific ion electrodes. The electrodes generate a potential proportional to the activity of a specific ion in solution. The calibration is achieved in standard solution and results read in mV or concentration in mg/L or ppm on the meter. The water can be adapted to monitor the concentration of carbon dioxide, hydrogen sulfide, ammonia, chloride, calcium, potassium and sodium to name a few. 

Ionic compounds are named using the same guidelines used for naming binary molecules, except that the cation name aiways precedes the anion name. Thus, NH4 NO3 is ammonium nitrate, Na2 CO3 is sodium carbonate, and Ca3 (P04)2 is caicium phosphate. The subscripts are not specified in these names because the fixed ionic charges determine the cation-anion ratios unambiguously. Example 3-6 reinforces these guidelines by showing how to construct chemicai formulas from chemical names. 

Not all bases contain hydroxide, however. For example, Na2C03 is a base, but its name is sodium carbonate. Baking soda, which has a chemical formula of NaHC03, is also a base. The scientific name for baking soda is sodium hydrogen carbonate (hydrogen carbonate is the name of the polyatomic ion). 

Namely, the reaction of 2-thioxothiazolidin-4-one N-hexanoic acid (116) with 2,5-dimethyl-l-phenylpyrrol-3-carboxaldehyde (117) in methanol under the catalytic action of ethylenediamine diacetate (EDDA) yields 5-[(2,5-dimethyl-l-phenylpyrrol-3-yl)methylidene]-2-thioxothiazolidin-4-one N-hexanoic acid (118) in 79% yield. The hydroxamate derivative of 118 is prepared by reacting this compound with 0-(tetrahydro-2H-pyran-2-yl)hydroxylamine followed by treatment with p-toluenesulfonic acid in methanol to afford compound 121 in 60% yield. Esterification of compound 118 is carried out by using methyl iodide in acetonitrile in the presence of sodium carbonate to give compound 120. The 5-(cyclohexyl)methylidene analogue (119) is obtained in 42% yield by direct reaction of compound 116 with cyclohexanecar-boxaldehyde in methanol under the catalytic action of EDDA. 

Porter-Clark The original name for the cold lime-soda process. A water-softening process using sodium carbonate and calcium hydroxide. It removes the non-carbonate, as well as the bicarbonate, hardness. Developed by J. H. Porter. See Clark. 

Salt-cake One of the two processes comprising the Leblanc process for making sodium carbonate. Salt-cake was the colloquial name for sodium sulfate. 

Soda is an old fashioned name for sodium carbonate, Na2C03 10H2O. 

Sodium (Na, [Ne s1), name from the English word soda, perhaps from the Latin word sodanum (glasswort), symbol from the Latin natrium (sodium carbonate). Identified and isolated (1807) by Sir Humphry Davy. 

Mixing sodium percarbonate with acetic anhydride led to explosive shattering of the flask [1], undoubtedly caused by the formation of acetyl peroxide. The name sodium percarbonate has been used indiscriminately to describe 3 different compounds, all of which would react with acetic anhydride to give extremely explosive acetyl peroxide [2], These are sodium monoperoxycarbonate, NaOCO.OONa, [4452-58-8] sodium peroxydicarbonate, NaOCO.OOCO.ONa, [3313-92-6] and sodium carbonate sesqui hydrogen peroxidate, Na0C0.0Na.l,5H202, [15630-89-4],... 

Ammonia is used to produce soda ash (see Sodium Carbonate, Na Oj). In the 1860s, the Belgian chemist Ernest Solvay (1838—1922) developed the process that bears his name. The Solvay process, sometimes called the ammonia method of soda production, uses ammonia, NH3, carbon dioxide, and salt to produce sodium bicarbonate (baking soda), NaHCOj. Sodium bicarbonate is then heated to give soda ash. 

Cone. soln. of sodium hypochlorite with up to 42 per cent, of available chlorine have been made under the trade name chloros, by passing chlorine into a soln. of caustic soda of such a strength that the sodium chloride which is formed separates out. The temp, is kept below 27°. The crystals of sodium chloride are removed, and more chlorine is introduced, but the sodium hydroxide is always kept in excess or the soln. will be unstable. A. J. Balard prepared potassium, sodium, and lithium hypochlorites by neutralizing a well-cooled soln. of the base with the acid. E. Soubeiian evaporated in vacuo the liquid obtained by treating a soln. of calcium hypochlorite with sodium carbonate, and obtained, before the liquid had all evaporated, crystals of sodium chloride and of sodium hypochlorite. P. Mayer and R. Schindler obtained solid potassium hypochlorite mixed with potassium hydrocarbonate by the action of chlorine—developed from 10 parts of sodium chloride—on a soln. of 24 parts of potassium hydrocarbonate and one of water. 

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