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An ore containing \(90 \mathrm{wt} \% \mathrm{MgSO}_{4} \cdot \mathrm{H}_{2} \mathrm{O}\) and the balance insoluble minerals is fed to a dissolution tank at a rate of \(60,000 \mathrm{lb}_{\mathrm{m}} / \mathrm{h}\) along with fresh water and a recycle stream. The tank contents are heated to \(120^{\circ} \mathrm{F}\), causing all of the magnesium sulfate monohydrate in the ore to dissolve, forming a solution 10^0 F above saturation. The resulting slurry of the insoluble minerals in MgSO_solution is pumped to a heated filter, where a wet filter cake is separated from a solids-free filtrate. The filter cake retains \(5 \mathrm{lb}_{\mathrm{m}}\) of solution per \(100 \mathrm{lb}_{\mathrm{m}}\) of solids. The filtrate is sent to a crystallizer in which the temperature is reduced to \(50^{\circ} \mathrm{F},\) producing a slurry of \(\mathrm{MgSO}_{4} \cdot 7 \mathrm{H}_{2} \mathrm{O}\) crystals in a saturated solution that is sent to another filler. The product filter cake contains all of the prea entrained solution in a ratio of \(5 \mathrm{Ib}_{\mathrm{m}}\) solution per \(100 \mathrm{lb}_{\mathrm{m}}\) crystals. The filtrate from this filter is returned to the dissolution tank as the recycle stream.Solubility data: Saturated magnesium sulfate solutions at \(110^{\circ} \mathrm{F}\) and \(50^{\circ} \mathrm{F}\) contain \(32 \mathrm{wt} \%\) \(\mathrm{MgSO}_{4}\) and \(23 \mathrm{wt} \% \mathrm{MgSO}_{4},\) respectively.(a) Explain why the solution is first heated (in the dissolution tank) and filtered and then cooled (in the crystallizer) and filtered. (b) Calculate the production rate of crystals and the required feed rate of fresh water to the dissolution tank. (Note: Don't forget to include water of hydration when you write a mass balance on water.)(c) Calculate the ratio \(\mathrm{lb}_{\mathrm{m}}\) recycle/lb \(_{\mathrm{m}}\) makeup water.

Short Answer

Expert verified
The production rate of MgSO4.7H2O crystals is 54000 lbm/h. The required feed rate of fresh water to the dissolution tank is 114750 lbm/h. The ratio of recycle to makeup water is 1.

Step by step solution

01

Understanding the Process

The first part of our production process is the dissolution tank, where the ore (containing 90 wt% of MgSO4.H2O) is mixed with fresh water. During this phase, all the MgSO4.H2O in the ore dissolves, forming a supersaturated solution as all the dissolved MgSO4.H2O is above saturation. This solution is then filtered to separate the insoluble solids. The filtrate is fed into a crystallizer, where the temperature is reduced to form MgSO4.7H2O crystals in a saturated solution. The slurry, in which the MgSO4.7H2O is suspended, is filtered to separate the crystals from the solution, and the remaining solution is recycled back to the dissolution tank.
02

Calculate mass of MgSO4.H2O and Insoluble Mass

From the problem, it's given that the feed rate to the dissolution tank is 60,000 lbm/h, of which 90% is MgSO4.H2O. Therefore, the mass of MgSO4.H2O = \(0.90 \times 60000 = 54000 lbm/h\). The remaining 10% of the feed is insoluble minerals, therefore, the insoluble mass in the feed = \(0.10 \times 60000 = 6000 lbm/h\).
03

Calculate production rate of crystals

Since the MgSO4.H2O is converted into MgSO4.7H2O in the crystallizer, and based on the principle of mass balance, the mass of MgSO4.H2O should be equal to the mass of MgSO4.7H20. Hence, in this case the production rate of MgSO4.7H20 crystals is the same as the mass of MgSO4.H2O = 54000 lbm/h.
04

Calculate mass of fresh water needed

From the solubility data, it's known that at \(110^{\circ} F\), the concentration of a saturated solution of magnesium sulfate is 32 wt%. Therefore, in the filtrate leaving the dissolution tank, the mass of MgSO4 (from MgSO4.H2O) is 32% of the total mass. So the total mass = \( Mass of MgSO4 /0.32 = 54000 lb_m /0.32 = 168750 lb_m/h \). Since the filtrate contains only the MgSO4 from the MgSO4.H2O and the fresh water, the mass of fresh water needed = \( total mass - mass of MgSO4.H2O = 168750 - 54000= 114750 lb_m/h\).
05

Calculate ratio of recycle to makeup water

In addition to fresh water, the dissolution tank also receives the recycle stream from the crystallizer filter. To calculate the mass of the recycle stream, since all of the magnesium sulfate monohydrate in the filtrate crystallizes in the crystallizer, the mass of the remaining solution in the slurry after filtration is \( total mass from step 4 – mass of crystals = 168750 - 54000 = 114750 lb_m/h \). Therefore, the ratio lb_m recycle/lb_m makeup water becomes \( 114750 / 114750 = 1 \)

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Understanding Mass Balance Calculations
Mass balance calculations are a fundamental aspect of chemical engineering processes, critical for designing efficient and cost-effective systems. They are based on the principle of conservation of mass, which dictates that mass cannot be created or destroyed in a chemical process, only transformed. In the process described in our textbook exercise, mass balance is applied to assess the movement and transformation of materials through the chemical process, which involves dissolving magnesium sulfate from ore in a dissolution tank and subsequently crystallizing it.

When solving mass balance problems, the first step is to create a basis of calculation. In the exercise, the known feed rate of ore is the starting point. With the given feed rate of 60,000 lbm/h and the concentration of MgSOâ‚„.Hâ‚‚O in the ore, we calculated the mass of MgSOâ‚„.Hâ‚‚O entering the dissolution tank. Understanding these relationships and the movement of mass through the system is critical for the next steps, such as determining the amount of fresh water needed and the rate of production of crystals. The mass of materials at each stage must account for all inputs, transformations, and outputs, ensuring the 'mass in equals mass out' rule is satisfied.

To make the concept more digestible, consider the following points to guide you through typical mass balance problems:
Designing Chemical Processes
The design of a chemical process, like the operation described in the exercise, involves meticulously planning each step to ensure that the desired transformation of materials is achieved efficiently and safely. Key steps in chemical process design include identifying the sequence of chemical and physical operations, selecting the appropriate equipment, and controlling process conditions such as temperature and pressure.

In this exercise, the ore dissolution and crystallization stages are carefully designed to optimize the yield of magnesium sulfate crystals. The temperature of the process is controlled to enhance solubility in the dissolution tank, and later, reduced in the crystallizer to facilitate crystallization. Additionally, filtration steps are included to separate insoluble minerals and to recover the desired product.

The design also cleverly incorporates a recycle stream, which minimizes waste and improves the sustainability of the overall process. This stream is analyzed as part of the mass balance, showing how the same principles apply whether in the initial design phase or during a problem-solving exercise.
Solubility and Crystallization
Solubility and crystallization are key concepts in many chemical engineering processes, including the exercise's purification of magnesium sulfate. Solubility refers to the maximum amount of solute that can be dissolved in a solvent at a given temperature and pressure. In our exercise, the solubility of magnesium sulfate is different at the two temperatures provided, which directly influences the design and operation of the dissolution tank and crystallizer.

During the dissolution phase, the solution is heated to a temperature where the solubility of magnesium sulfate increases, allowing for more of the compound to dissolve. This is indicated by the solution being 10°F above saturation. In contrast, the crystallization phase involves cooling the solution, decreasing solubility and encouraging the formation of magnesium sulfate heptahydrate crystals. The process steps of heating and cooling are thus critical to achieve the desired solubility before filtration.

It is important for students to grasp that temperature manipulation is a powerful tool in controlling solubility and crystallization. This understanding is not only vital to tackling exercises but also to the practical application in real-world scenarios where precise predictions of solubility behavior influence process outcomes.

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Most popular questions from this chapter

When fermentation units are operated with high aeration rates, significant amounts of water can be evaporated into the air passing through the fermentation broth. since fermentation can be adversely affected if water loss is significant, the air is humidified before being fed to the fermenter. Sterilized ambient air is combined with steam to form a saturated air-water mixture at 1 atm and \(90^{\circ} \mathrm{C}\). The mixture is cooled to the temperature of the fermenter \(\left(35^{\circ} \mathrm{C}\right),\) condensing some of the water, and the saturated air is fed to the bottom of the fermenter. For an air flow rate to the fermenter of \(10 \mathrm{L} / \mathrm{min}\) at \(35^{\circ} \mathrm{C}\) and \(1 \mathrm{atm},\) estimate the rate at which steam must be added to the sterilized air and the rate (kg/min) at which condensate is collected upon cooling the air-steam mixture.

A fuel gas containing methane and ethane is burned with air in a furnace, producing a stack gas at \(300^{\circ} \mathrm{C}\) and \(105 \mathrm{kPa}\) (absolute). You analyze the stack gas and find that it contains no unburned hydrocarbons, oxygen, or carbon monoxide. You also determine the dew-point temperature.(a) Estimate the range of possible dew-point temperatures by determining the dew points when the feed is either pure methane or pure ethane. (b) Estimate the fraction of the feed that is methane if the measured dew- point temperature is \(59.5^{\circ} \mathrm{C}\). (c) What range of measured dew point temperatures would lead to calculated methane mole fractions within 5\% of the value determined in Part (b)?

Sodium bicarbonate is synthesized by reacting sodium carbonate with carbon dioxide and water at \(70^{\circ} \mathrm{C}\) and \(2.0 \mathrm{atm}\) gauge pressure: $$\mathrm{Na}_{2} \mathrm{CO}_{3}+\mathrm{CO}_{2}+\mathrm{H}_{2} \mathrm{O} \rightarrow 2 \mathrm{NaHCO}_{3}$$ An aqueous solution containing 7.00 wt\% sodium carbonate and a gas stream containing 70.0 mole\% \(\mathrm{CO}_{2}\) and the balance air are fed to the reactor. All of the sodium carbonate and some of the carbon dioxide in the feed react. The gas leaving the reactor, which contains the air and unreacted \(\mathrm{CO}_{2},\) is saturated with water vapor at the reactor conditions. A liquid-solid slurry of sodium bicarbonate crystals in a saturated aqueous solution containing \(2.4 \mathrm{wt} \%\) dissolved sodium bicarbonate and a negligible amount of dissolved \(\mathrm{CO}_{2}\) leaves the reactor and is pumped to a filter. The wet filter cake contains 86 wt\% sodium bicarbonate crystals and the balance saturated solution, and the filtrate also is saturated solution. The production rate of solid crystals is \(500 \mathrm{kg} / \mathrm{h}\).Suggestion: Although the problems to be given can be solved in terms of the product flow rate of \(500 \mathrm{kg} \mathrm{NaHCO}_{3}(\mathrm{s}) / \mathrm{h},\) it might be easier to assume a different basis and then scale the process to the desired production rate of crystals.(a) Calculate the composition (component mole fractions) and volumetric flow rate \(\left(\mathrm{m}^{3} / \mathrm{min}\right)\) of the gas stream leaving the reactor. (b) Calculate the feed rate of gas to the process in standard cubic meters/min \(\left[\mathrm{m}^{3}(\mathrm{STP}) / \mathrm{min}\right]\) (c) Calculate the flow rate \((\mathrm{kg} / \mathrm{h})\) of the liquid feed to the process. What more would you need to know to calculate the volumetric flow rate of this stream? (d) The filtrate was assumed to leave the filter as a saturated solution at \(70^{\circ} \mathrm{C}\). What would be the effect on your calculations if the temperature of the filtrate actually dropped to \(50^{\circ} \mathrm{C}\) as it passed through the filter? (e) The reactor pressure of 2 atm gauge was arrived at in an optimization study. What benefit do you suppose would result from increasing the pressure? What penalty would be associated with this increase? The term "Henry's law" should appear in your explanation. (Hint: The reaction occurs in the liquid phase and the \(\mathrm{CO}_{2}\) enters the reactor as a gas. What step must precede the reaction?)

A \(50.0-\mathrm{L}\) tank contains an air-carbon tetrachloride gas mixture at an absolute pressure of \(1 \mathrm{atm}, \mathrm{a}\) temperature of \(34^{\circ} \mathrm{C},\) and a relative saturation of \(30 \% .\) Activated carbon is added to the tank to remove the \(\mathrm{CCl}_{4}\) from the gas by adsorption and the tank is then sealed. The volume of added activated carbon may be assumed negligible in comparison to the tank volume.(a) Calculate \(p_{\mathrm{CCl}_{4}}\) at the moment the tank is sealed, assuming ideal-gas behavior and neglecting adsorption that occurs prior to sealing. (b) Calculate the total pressure in the tank and the partial pressure of carbon tetrachloride at a point when half of the CCl_ initially in the tank has been adsorbed. Note: It was shown in Example \(6.7-1\) that at \(34^{\circ} \mathrm{C}\).$$X^{*}\left(\frac{\mathrm{g} \mathrm{CCl}_{4} \text { adsorbed }}{\mathrm{g} \text { carbon }}\right)=\frac{0.0762 p_{\mathrm{CCl}_{4}}}{1+0.096 p_{\mathrm{CCl}_{4}}}$$ where \(p_{\mathrm{CCl}_{4}}\) is the partial pressure (in \(\mathrm{mm} \mathrm{Hg}\) ) of carbon tetrachloride in the gas contacting the carbon.(c) How much activated carbon must be added to the tank to reduce the mole fraction of \(\mathrm{CCl}_{4}\) in the gas to 0.001?

The solubility coefficient of a gas may be defined as the number of cubic centimeters (STP) of the gas that dissolves in \(1 \mathrm{cm}^{3}\) of a solvent under a partial pressure of 1 atm. The solubility coefficient of \(\mathrm{CO}_{2}\) in water at \(20^{\circ} \mathrm{C}\) is \(0.0901 \mathrm{cm}^{3} \mathrm{CO}_{2}(\mathrm{STP}) / \mathrm{cm}^{3} \mathrm{H}_{2} \mathrm{O}(\mathrm{l})\). (a) Calculate the Henry's law constant in atm/mole fraction for \(\mathrm{CO}_{2}\) in \(\mathrm{H}_{2} \mathrm{O}\) at \(20^{\circ} \mathrm{C}\) from the given solubility coefficient. (b) How many grams of \(\mathrm{CO}_{2}\) can be dissolved in a \(12-\mathrm{oz}\) bottle of soda at \(20^{\circ} \mathrm{C}\) if the gas above the soda is pure \(\mathrm{CO}_{2}\) at a gauge pressure of 2.5 atm ( 1 liter \(=33.8\) fluid ounces)? Assume the liquid properties are those of water. (c) What volume would the dissolved \(C O_{2}\) occupy if it were released from solution at body temperature and pressure \(-37^{\circ} \mathrm{C}\) and 1 atm?

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