speaxng date and time of analysis, and any Control and Chemical Analysis additions made for replenishment sho uld be maintained, preferabl y of Plating Solutions using commercial software programs suc h as True Logic or Lab Wizard Adequate testing resources and consistent analytical Software . Small job shops are urged methods are essential to proper troubleshooting of to maintain paper copies for each plating baths and chemistries. sh ift, as well as any notes from trou- bleshooting ope rations. Bulk ingredi- ents in the baths are easily deter-
T h e quality of plated dep osits pri-
marily dep ends on fac to rs such as current density, solution composi- increase or decrease metal con- tent due to cu rrent efficienci es. The current effi cien cy issues may mined mostly using titrimetric meth - ods, which require simple laboratory equipment. Trace impurities in solu- tion, temperature, effecti ve bath pH, be ascribed to side reactions tions may be dete rm ined by a certi- additives concentration, speed (rpm occurring at the anode and cath - fied laboratory equ ipped with the for barrel plating or lin e sp eed for ode. For insoluble anodes, me tal desir ed instrume n tation for mic ro- reel to reel), and solution agitation in replenishments are frequently determinations the tank. Apart from mechanical fac- required. tors, tight control of main ingred ient 4. Depletion of additives due to co- SAMPLING and additive concentrations in a deposition in electrodeposits and Sampling is an extrem ely important plating bath is extremely important breakdown products. step, an d the sam ple sh ould be repre- to achieve successful plating opera- 5. D rastic pH changes in th e bath, sentative of a given tank. Tanks tions. Plating solu tions must be which may cause precipitat ion or should be identified and their levels maintain ed at the recommended turbid ity. recorded to chec k the decrease in limits, as suggested by the manufac- 6. Impurities introduced due to tank volu m e due to evaporation, turers. Sometimes, the limits may tech-grade che m ical additions drag-out, or spillage. Ideally, sa m- not be so rigid, and bath parameters and leachin g of impuri ties from pling should be done at 10 different need to be optim ized by a given job extraneous ob jects that have fall- locations in larger tanks, and a com- shop based on the type and layout of en into the tanks. pos ite sample should be pr epared. the plating line. The log sheet should have entries The status of a given bath is Wet chemical methods have been such as : dependent on th e rate of its deple- routinely employed in mo ni toring tion due to plating operations and major bath components. Advanced 1. Tank ID proper repl en ishment. The operator automatic ins tru mentation is also 2. Date and time of analysis shou ld monitor bath components available for analysis of inorganic and 3. Analytical method used frequently in order to maintain organic speci es. Plating baths are usu- 4. Results chemistries within a controlled win- ally analyzed offline after harvesting 5. Recommended high and low dow. The depletion of primar y bath samples from various tanks. Metal lim its components mainly depends on the ions are monitored using ato m ic 6. Analyst signature following factors: absorption spectrophotometry (AA), inductively coupled plasma (Iep), wet After additions to the tank and 1. Drag-out into rinse tanks causing titrations, colorimetry, polarography, adequate mixing, an analysis sh ould lo ss of useful chemicals depend- an d ion selective electrodes, depend- be performed aga in to check desired ing on mode of drain in g. ing on laboratory facilities. parameters. Normall y, well-e stab - 2. Evaporation rate of plating baths The analytical m ethods for analysis lish ed plating sh ops have reasonably depending on temperature, air ofplating solutions should be simple, good laboratories and ar e well flow, and mechanical agitation in d irect, and operato r friendl y. In o rde r eq uipped to keep track of th eir the tank. to facilitate th is, a stan dard op erating chemistries. Some job shops dep end 3. Imbalance in anode and cathode procedure should be documented, on analytical support from ch em ica] efficiencies. Soluble anodes may and adequate records with tank ID, bath suppliers, which are usually
14 Imetalfinishing I October 2009 www.metalfinishing.com