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Click to edit Master title style,Click to edit Master text styles,Second level,Third level,Fourth level,Fifth level,*,Gravimetric Analysis,a. simple, very little equipment or training is requiredb. fast c. can be fairly specific,Example: A solution contains Hg,2+,. We can determine the amount of Hg,2+,by precipitating it with a solution of Cl,-,. Assume there are no other insoluble chloride salts present. A 25.00mL solution containing Hg,2+,was treated with excess NaCl and precipitated 0.4511g HgCl,2,. What was the molarity of the Hg,2+,originally?,1,Limitations of Gravimetric Analysis,Any interferents must be removed prior to precipitation,Method is not very sensitive,2,3,Example:,I have a solution of 100.0mL of a solution containing Li,+, Pb,2+, Na,+, and K,+,. I want to determine the amount of Pb,2+,is in the solution gravimetrically. The suggested procedure calls for precipitation with SO,4,2,. Would I be able to use CO,3,2-,instead? What potential disadvantages are associated with using Na,2,CO,3,instead of Na,2,SO,4,?,4,Part 2 of example,The lowest reliable measurement possible with the electronic balance is 0.0010g. What is the detection limit for Pb,2+,using SO,4,2-,as the precipitating agent? CO,3,2-,as the precipitating agent?,5,Characteristics of Good Gravimetric Techniques,Ideally Precipitates in a gravimetric analysis should be:,Insoluble, Ksp should be way below the amount expected in solution. Limiting factor for detection is usually the balance, not Ksp. (For larger samples, this may not be true.),Easily filterable, make large crystals which separate from solution easily,Pure with known composition, that is, they do not make a whole bunch of insoluble complexes.,6,Tips for good Gravimetric Analyses,Things which can be done for best gravimetric results:,Cool solution after precipitation has started.,Add precipitating reagent slowly so crystals are larger,Keep the volume of solution large so concentration of analyte and precipitant is low.,7,Laboratory procedures,Transfer of solids,Single chunk handle with tweezers,Powdered transfer washings with at least 3 times with solvent,Weighing bottles: tight fitting ground glass joints prevents contamination or loss of sample. When handling ground glass joints use either paper or tongs,Handling precipitates Solution is precipitated,8,Laboratory Technique Considerations,1. Filters,Paper is very hydroscopic, hard to get reliable tare weight,GFF made from glass fibers less hydroscopic but should still be kept in desicator. Very fine pores, different pore sizes available.,Sintered glass fibers cannot be heated to high temperatures,2. Transferring,decant: Pour majority of supernatant through without disturbing precipitate.,Wash precipitate: decant wash solution.,3. Control of moisture,Moisture is ubiquitous in the laboratory, in order to control for this a dry atmosphere will have to be maintained in a reproducibly dry atmosphere by storage in a desicator or evaporation or ignition,9,Laboratory Considerations continued,4. Drying: Occurs by putting an open weighing bottle (may be covered with a watch glass) at a temperature slightly above 100oC to get rid of water or waters of hydration.,5. Weighing to constant weight means with,+,0.1mg,Requires more than one weighing!,6. Desicators,Objects cannot be weighed when hot or warm. But if you were to take a sample out and wait for it to cool it would pick up moisture like that so put it in a desicator. Dont seal descicator, creates a vacuum Desicant blue dry pink wet,10,Common Desiccants,11,Silica gel goes from blue to pink as it absorbs moisture Can be regenerated in oven,Anhydrous sodium sulfate gets clumpy as it absorbs water,More Information about desiccants including common interferents and regeneration temperature can be found at:,12,Further laboratory considerations,7. Evaporating: Evaporating dishes allow rapid evaporation but also are easy to tip otherwise cause loss of analyte. Glass beads may be added to avoid bumping and loss of analyte.,8) Ignition: Hotter temperature for elimination of water or other reactant,Muffle furnaces that go up to 1100,o,C are used primarily for this Need to use porcelain crucible.,13,Example,A raw sewage sample was brought in for total suspended solids and volatile solids analysis. A portion of the sample was poured into a tared evaporating dish and weighed. The sample was then heated at 105,o,C for 4 hours, weighed, heated at 550,o,C overnight, and weighed again. The data are as follows:,Tare wt.42.9073g,Wet sample104.4680g,105 wt.45.4140g,550 wt. 43.3236g,What is the TSS in g/L? What percent of the solids are volatile?,14,Why are we concerned about solubility considerations when doing gravimetric analysis?,Precipitate must be insoluble so that greater than 99.99% of analyte present in solution precipitates in order for gravimetric analysis to be considered quantitative,Solubility losses (to solution) can be minimized by carefully controlling the composition of the solution in which the precipitate forms. This requires understanding the relevant equilibrium reactions affecting the precipitates solubility.,15,Solubility can be affected by pH,Where is the solubility of CaCO3 expected to be the least?,Be quantitative,16,Example,For what pH range will PbCrO4 have its least solubility?,17,Application of Gravimetric Analysis,A 0.3516g sample of a commercial phosphate detergent was ignited at red heat to destroy the organic matter. The residue was then taken up in hot HCl, which converts the P to H,3,PO,4,. The PO,4,was precipitated out as MgNH,4,PO,4,.,6H,2,O by addition of Mg,2+,followed by aqueous NH,3,. After being filtered and washed, the ppt. was converted to MgP,2,O,7,(MW = 222.57g/mol) by ignition at 1000,o,C. The residue weighed 0.2161g. Calculate the % P in the sample.,18,Another example,Long ago a workman at a dye factory fell into a vat containing hot concentrated H,2,SO,4,and HNO,3,. He dissolved completely. Because no one witnessed the accident, it was necessary to prove that he fell in so his wife could collect the insurance money. The man weighed 70kg. A human body contains 6.3ppt(housand) P. The acid vat was analyzed for P to see if it contained a dissolved human.,A. The vat had 8.00 x 10,3,L of liquid and 100.0mL was analyzed. If the man fell into the vat, what is the expected quantity of P in the vat?,B. The 100.0mL was treated with a molybdate reagent that caused (NH,4,),2,P(Mo,12,O,40,),.,12H,2,O to precipitate. This substance was dried at 110,o,C to remove water of hydration and heated to 400,o,C until it reached a constant composition corresponding to the formula P,2,O,5,.,24MoO,3,which weighed 0.3718g. The same acid without a person dissolved in it and treated in an identical manner had a weight of 0.00331g. How much P was present in the 100.0mL sample? Is this consistent with a dissolved man?,19,
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