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SashulF [63]
3 years ago
13

Is cross flow more efficient or counter flow

Engineering
1 answer:
pochemuha3 years ago
7 0

Answer:

Cross flow

Explanation:

Preferred for several reasons that include overall efficiency and serviceability.

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How much does 5 acres of land cost in the US?
Dvinal [7]

Answer:

Larson, an economist, who placed the total value of $23 trillion for the entire 1.9 billion acres of land in the United States. This means that the average cost for an acre of land is $12,000 or $60,000 for 5 acres of land. Almost half of the land in the US is used for agricultural purposes.

Explanation:

6 0
3 years ago
Water flows through a pipe at an average temperature of T[infinity] = 70°C. The inner and outer radii of the pipe are r1 = 6 cm
Paul [167]

Answer:

The differential equation and the boundary conditions are;

A) -kdT(r1)/dr = h[T∞ - T(r1)]

B) -kdT(r2)/dr = q'_s = 734.56 W/m²

Explanation:

We are given;

T∞ = 70°C.

Inner radii pipe; r1 = 6cm = 0.06 m

Outer radii of pipe;r2 = 6.5cm=0.065 m

Electrical heat power; Q'_s = 300 W

Since power is 300 W per metre length, then; L = 1 m

Now, to the heat flux at the surface of the wire is given by the formula;

q'_s = Q'_s/A

Where A is area = 2πrL

We'll use r2 = 0.065 m

A = 2π(0.065) × 1 = 0.13π

Thus;

q'_s = 300/0.13π

q'_s = 734.56 W/m²

The differential equation and the boundary conditions are;

A) -kdT(r1)/dr = h[T∞ - T(r1)]

B) -kdT(r2)/dr = q'_s = 734.56 W/m²

6 0
2 years ago
PLEASE ANSWEAR FAST!!! <br> What does it mean if E˂1
Citrus2011 [14]
Scientific notation is another way to write a number. In scientific notation, the letter E is used to mean "10 to the power of." For example, 1.314E+1 means 1.314 * 101 which is 13.14 . Scientific notation is merely a format used for input and output.
5 0
2 years ago
How would you describe what would happen to methane if the primary bonds were to break?
erastova [34]

Answer:

All the bonds in methane (CH4CH4) are equivalent, and all have the same dissociation energy.

The product of the dissociation is methyl radical (CH3CH3). All the bonds in methyl radical are equivalent, and all have the same dissociation energy.

The product of that dissociation is methylene (CH2CH2). All the bonds in methylene are equivalent, and all have the same dissociation energy.

The product of that dissociation is methyne (CHCH) .

The C-H bonds in methane do not have the same dissociation energy as C-H bonds in methyl radical, which in turn do not have the same dissociation energy as the C-H bonds in methylene, which are again different from the C-H bond in methyne.

If (by some miracle) you were able to get all four bonds in methane to dissociate absolutely simultaneously, they would all show the same dissociation energy… but that energy, per bond broken, would be different than the energy required to break just one C-H bond in methane, because the products are different.

(In this case, it’s CH4→C+4HCH4→C+4H versus CH4→CH3+HCH4→CH3+H.)

To alter hydrocarbons you add enough energy to break a C-H bond. Why does only one bond break? What concentrates the energy on one C-H bond?

the weakest CH bond is the one that breaks. in plain alkanes it has to do with the molecular orbital interactions between neighboring carbon atoms. look at propane for example. the middle carbon has two C-C bonds, and each of those C-C bonds is strengthened by slight electron delocalization from the C-H bonds overlapping with the antibonding orbitals of the adjacent carbons.

since the C-H bonds on the middle carbon donate electron density to both of its neighbors, those two are weakest.

one of them will break preferentially.

which one actually breaks depends on the reaction conditions (kinetics). frankly it's whichever one ramdomly approaches a nucleophile first. when the nucleophile pulls of one of the H's, the other C-H bonds start to share (delocalize) the negative charge across the whole molecule. so while the middle C feels the majority of the negative charge character, the other two C's take on a fair amount as well...

by the way, alkanes don't really like to break and form anions like that.

a better example would be something like isopropyl iodide, where the C-I bond breaks and the I carries away the electron pair, forming a carbocation (also not particularly stable, but more so than the carbanion).

7 0
2 years ago
Write an ALP to separate odd and even numbers from an array of N numbers; arrange odd
Marta_Voda [28]

Below is the program to separate odd and even numbers                                  

<u>Explanation</u>:

<u>L1:</u>

         mov ah,00

         mov al,[BX]

         mov dl,al

         div dh

         cmp ah,00

         je EVEN1

         mov [DI],dl

         add OddAdd,dl

         INC DI

         INC BX

         Loop L1

         jmp CAL

    <u>EVEN1:</u>

         mov [SI],dl

         add Even Add,dl

         INC SI

         INC BX

         Loop L1

    <u>CAL:   </u>  

         mov ax,0000

         mov bx,0000

         mov al,OddAdd

         mov bl,EvenAdd

         MOV  ax,4C00h

         int 21h

end

The above program separates odd and even numbers from the array using 8086 microprocessor. It has odd numbers in 2000h and even numbers in 3000h.

6 0
3 years ago
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