Filtration filter cake

Suspension Hydraulic Fluid Filtrate Filter Cake Vacuum... 

In situations where a low concentration of suspended solids needs to be separated from a liquid, then cross-flow filtration can be used. The most common design uses a porous tube. The suspension is passed through the tube at high velocity and is concentrated as the liquid flows through the porous medium. The turbulent flow prevents the formation of a filter cake, and the solids are removed as a more concentrated slurry. 

To filter a solution one attaches a vacuum and pours the solution into the Buchner funnel. All the solution will go whoosh into the flask leaving what is called a filter cake in the funnel. The liquid that has collected in the flask is now called the filtrate. Usually, the filter cake is then washed with a little bit of clean what-... 

The soiution is aliowed to cool and the crystals of the P2P-bisulfite addition compound are then separated by vacuum filtration, washed with a little clean dH20 then washed with a couple hundred mLs of ether, DCM or benzene. The filter cake of MD-P2P-bisulfate is processed by scraping the crystals into a flask and then 300mL of either 20% sodium carbonate solution or 10% HCi soiution are added (HCI works best). The soiution is stirred for another 30 minutes during which time the MD-P2P-bisulfite complex will be busted up and the P2P will return to its happy oil form. The P2P is then taken up with ether, dried and removed of the solvent to give pure MD-P2P. Whaddya think of that ... 

After 3 hours the stirring is stopped and the solution allowed to settle. By this time just about all the foil will have turned to dust, which is going to make the next step of vacuum filtration very difficult because it will plug up the filter paper in a second. So the chemist lets it settle, then pours off the liquid through the vacuum filtration setup (see methodology section). The flask is rinsed with lOOmL methanol, the methanol poured through the grey filter cake and the filter cake discarded. All of the filtrate is placed in a flask and vacuum distilled to remove all the methanol, isopropyl alcohol and water which will leave the chemist with oil and junk in the bottom of the flask. 

In a flask the chemist mixes 50g piperonal into 200mL glacial acetic acid, then adds 45mL nitroethane and 17g ammonium acetate. The solution is then refluxed 4 hours and takes on the color of yellow to yellow-orange. After 4 hours and cooling, yellowish crystals of p-nitropropene will spontaneously form. If not, the solution can be diluted with 50ml of dHjO and chilled in an ice bath for an hour to form the crystals with some slushy glacial acetic acid and water intermixed. The mass of crystals is broken up and plopped into a Buchner funnel to be vacuum filtered. The filter cake is washed with a little extra acetic acid or water. All of the filtrate is saved. 

The way the chemist knows that she has methylamine and not ammonium chloride is that she compares the look of the two types of crystals. Ammonium chloride crystals that come from this reaction are white, tiny and fuzzy. The methylamine hydrochloride crystals are longer, more crystalline in nature and are a lot more sparkly. The chemist leaves the methylamine crystals in the Buchner funnel of the vacuum filtration apparatus and returns the filtrate to the distillation set up so it can be reduced one last time to afford a second crop. The combined methylamine hydrochloride filter cake is washed with a little chloroform, scraped into a beaker of hot ethanol and chilled. The methylamine hydrochloride that recrystallizes in the cold ethanol is vacuum filtered to afford clean, happy product (yield=50%). 

The polymer can easily be recovered by simple vacuum filtration or centrifugation of the polymer slurry. This can be followed by direct conversion of the filter cake to dope by slurrying the filter cake in chilled solvent and then passing the slurry through a heat exchanger to form the spinning solution and a thin-film evaporator to remove residual monomer. 

Cake Dewatering. Dewatering (qv), identified as a separate entity in filtration, is used to reduce the moisture content of filter cakes either by mechanical compression or by air displacement under vacuum pressure or drainage in a gravitational or centrifugal system. Dewatering of cakes is enhanced by addition of dewatering aids to the suspensions in the form of surfactants that reduce surface tension. 

In general, pan filters are selected for freely filtering soHds and thick filter cakes. Cake washing can be introduced easily. Most appHcations are in the mining and metallurgical industries for small-scale batch filtration. 

Since 1980, a number of new filters have appeared on the market, utilising some form of mechanical compression of the filter cake, either after a conventional pressure filtration process or as a substitute for it. In most designs the compression is achieved by inflating a diaphragm which presses the slurry or the freshly formed filter cake toward the medium, thus squee2ing an additional amount of Hquid out of the cake. 

The KDF filter was first tested in prototype on a coal mine in northern Germany. It was installed in parallel with existing vacuum filters and it produced filter cakes consistendy lower in moisture content by 5 to 7% than the vacuum filters. Two production models have been installed and operated on a coal mine in Belgium. The filter is controlled by a specially developed computer system this consists of two computers, one monitoring the function of the filter and all of the detection devices installed, and the other controlling the filtration process. The system allows optimization of the performance, automatic start-up or shut-down, and can be integrated into the control system of the whole coal washing plant. 

Eor vacuum filters, both the rate of filtration and the dryness of the cake may be important. The filter cake can be modeled as a porous soHd, and the best flocculants are the ones that can keep the pores open. The large, low density floes produced by high molecular weight polymers often coUapse and cause blinding of the filter. Low molecular weight synthetic polymers and natural products that give small but rigid floes are often found to be the best. 

Reaction times can be as short as 10 minutes in a continuous flow reactor (1). In a typical batch cycle, the slurry is heated to the reaction temperature and held for up to 24 hours, although hold times can be less than an hour for many processes. After reaction is complete, the material is cooled, either by batch cooling or by pumping the product slurry through a double-pipe heat exchanger. Once the temperature is reduced below approximately 100°C, the slurry can be released through a pressure letdown system to ambient pressure. The product is then recovered by filtration (qv). A series of wash steps may be required to remove any salts that are formed as by-products. The clean filter cake is then dried in a tray or tunnel dryer or reslurried with water and spray dried. 

The products of reaction are pumped to a filter press for separation into a sodium sulfate solution and a filter cake having a low moisture content. The filter cake is then ready to be processed for the recovery of lead. The filtrate from the process contains an excess of sodium carbonate, and can be neutralized using the sulfuric acid drained from the batteries. 

In the double-neutralization process, Na2SiFg is precipitated and removed by filtration at a pH of 3—4 (9). Upon raising the pH to 7—9, insoluble phosphates of Fe, Al, Ca, and Mg form and separate. Iron can be precipitated as hydrous ferric oxide, reducing the phosphate loss at the second filter cake. Both the fluorosihcate and metal phosphate filter residues tend to be voluminous cakes that shrink when dewatered recovery of soluble phosphates trapped within the cakes is difficult. 

Manufacture. Hemibasic calcium hypochlorite is manufactured by chlorination of lime slurry followed by filtration and dryiag of the filter cake. 

Lime-Sulfuric. Recovery of citric acid by calcium salt precipitation is shown in Figure 3. Although the chemistry is straightforward, the engineering principles, separation techniques, and unit operations employed result in a complex commercial process. The fermentation broth, which has been separated from the insoluble biomass, is treated with a calcium hydroxide (lime) slurry to precipitate calcium citrate. After sufficient reaction time, the calcium citrate slurry is filtered and the filter cake washed free of soluble impurities. The clean calcium citrate cake is reslurried and acidified with sulfuric acid, converting the calcium citrate to soluble citric acid and insoluble calcium sulfate. Both the calcium citrate and calcium sulfate reactions are generally performed in agitated reaction vessels made of 316 stainless steel and filtered on commercially available filtration equipment. 

Filtration. Diatomite is used as a filter aid for appHcations with difficult-to-filter soflds to improve permeabiUty of the filter cake, to prevent the blinding of filter elements, and where high clarity is required such as in the poHsh filtration of wine (qv) or beer (qv) before bottling. It is also used in sugar (qv) refining, water treatment, and in the production of fmit juices (qv) and industrial chemicals. 

Typically, a filter cake or precoat is built up on the filter septa to prevent blinding, short filter cycle times, and cosdy cleaning of the septa. Then diatomite is added as body feed to the Hquid to be filtered so that the permeabiHty of the filter cake may be maintained. Filler aid permeabiHty of diatomite ranges from 0.06 to 30 lnF. At the end of the filter cycle the filtrate is clear and the soHds are retained in the soHd or semisoHd diatomite filter cake. The type and amount of diatomite for precoat and body feed are normally deterrnined by pilot studies (18,19). 

In cake or surface filtration, there are two primary areas of consideration continuous filtration, in which the resistance of the filter cake (deposited process solids) is veiy large with respec t to that of the filter media and filtrate drainage, and batch pressure filtration, in which the resistance of the filter cake is not veiy Targe with respect to that of the filter media and filtrate drainage. Batch pressure filters are generally fitted with heavy, tight filter cloths plus a layer of precoat and these represent a significant resistance that must be taken into account. Continuous filters, except for precoats, use relatively open cloths that offer little resistance compared to that of the filter cake. 

It is both convenient and reasonable in continuous filtration, except for precoat filters, to assume that the resistance of the filter cloth plus filtrate drainage is neghgible compared to the resistance of the filter cake and to assume that both pressure drop and specific cake resistance remain constant throughout the filter cycle. Equation (18-51), integrated under these conditions, may then be manipulated to give the following relationships ... 

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