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Sergio [31]
3 years ago
11

What kind or kinds of engineers does take to design a drone and why?

Engineering
1 answer:
storchak [24]3 years ago
4 0
Basic robots are entirely mechanical. However, when the need arises for automation the 'mechanical' way of solving the design is not adequate for other areas of technology, particularly electronics, optoelectronics, materials engineering, especially computer science.
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A round bar of chromium steel, (ρ= 7833 kg/m, k =48.9 W/m-K, c =0.115 KJ/kg-K, α=3.91 ×10^-6 m^2/s) emerges from a heat treatmen
Lerok [7]

Answer:

Q = 424523.22 kw

Explanation:

\rho =7833 kg/m

k = 48.9 W/m - K

c = 0.115 KJ/kg- K

\alpha = 3.91*10^{-6} m^2/s

T_s = 285 degree celcius

T_∞ = 35 degree celcius

velocity of air stream = 15 m/s

D = 40 cm

L = 200 cm

mass flow rate\dot m = \rho AV = 7833 *\frac{\pi}{4} 0.4^2*15

\dot m = 14764.85 kg/s

A_s = \pi DL = \pi 0.4*2 = 2.513 m^2

Q = \dot m C \Delta T = h A_s \Delta T

\dot m C \Delta T = h A_s \Delta T

solving for h

h = \frac{14764.85*0.115*(285-35)}{2.513*(285-35)}

h = 675.6 kw/m^2K

Q = h A_s\Delta T

Q = 675.6*2.513*(285-35)

Q = 424523.22 kw

7 0
2 years ago
A 2 in. diameter pipe supplying steam at 300°F is enclosed in a 1 ft square duct at 70°F. The outside of the duct is perfectly i
Shkiper50 [21]

Answer:

The value of heat transferred watt per foot length Q = 54.78 Watt per foot length.

Explanation:

Diameter of pipe = 2 in = 0.0508 m

Steam temperature T_{1} = 300 F  = 422.04 K

Duct temperature T_{2} = 70 F = 294.26 K

Emmisivity of surface 1 = 0.79

Emmisivity of surface 2 = 0.276

Net emmisivity of both surfaces ∈ = 0.25

Stefan volazman constant \sigma = 5.67 × 10^{-8} \frac{W}{m^{2} K^{4}  }

Heat transfer  per foot length is given by

Q = ∈ \sigma A ( T_{1}^{4} - T_{2} ^{4} ) ------ (1)

Put all the values in equation (1) , we get

Q = 0.25 × 5.67 × 10^{-8} × 3.14 × 0.0508 × 1 × ( 422.04^{4} - 294.26^{4} )

Q = 54.78 Watt per foot.

This is the value of heat transferred watt per foot length.

4 0
3 years ago
How to make a police car ​
S_A_V [24]

search it and you will get on internet

3 0
2 years ago
A shunt regulator utilizing a zener diode with an incremental resistance of 8 ohm is fed through an 82-Ohm resistor. If the raw
spayn [35]

Answer:

\triangle V_0=0.08V

Explanation:

From the question we are told that:

Incremental resistance  R=8ohms

Resistor Feed R_f=82ohms

Supply Change \triangle V=1

Generally the equation for  voltage rate of change is mathematically given by

 \frac{dV_0}{dV}=\frca{R}{R_1r_3}

Therefore

 \triangle V_0=\triangle V*\frac{R}{R_fR}

 \triangle V_0=1*\frac{8}{8*82}

 \triangle V_0=0.08V

7 0
3 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
3 years ago
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