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3 years ago

Is it acceptable to mix used absorbents.

2 answers:

7 0

In order to comply with the used oil rule,a facility must properly manage its oil-contaminated sorbents (I.e. , don’t mix other wastes with these sorbets) and it must either recycle sorbets or send them for disposal at a permitted facility that burn them for energy recovery.

Rasek [7]3 years ago

7 0

Answer:

false

Explanation:

it is not acceptable to mix used absorbents

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Problem 1: A catchment has the following Horton’s infiltration parameters: f0=280 mm/hr, fc=25 mm/hr and k = 2.5 hr-1 . For the

harkovskaia [24]

Answer:

Ponding will occur in 40mins

Explanation:

We say that the infiltration rate is the velocity or speed at which water enters into the soil. This often times is measured by the depth (in mm) of the water layer that can enter the soil in one hour. An infiltration rate of 15 mm/hour means that a water layer of 15 mm on the soil surface, will take one hour to infiltrate.

Consider checking attachment for the step by step solution.

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4 years ago

Instead of running blood through a single straight vessel for a distance of 2 mm, one mammalian species uses an array of 100 tin

Marina CMI [18]

Solution:

Given that :

Volume flow is, $Q_1 = 1000 \ mm^3/s$

So, $Q_2= \frac{1000}{100}=10 \ mm^3/s$

Therefore, the equation of a single straight vessel is given by

$F_{f_1}=\frac{8flQ_1^2}{\pi^2gd_1^5}$ ......................(i)

So there are 100 similar parallel pipes of the same cross section. Therefore, the equation for the area is

$\frac{\pi d_1^2}{4}=1000 \times\frac{\pi d_2^2}{4}$

or $d_1=10 \ d_2$

Now for parallel pipes

$H_{f_2}= (H_{f_2})_1= (H_{f_2})_2= .... = = (H_{f_2})_{10}=\frac{8flQ_2^2}{\pi^2 gd_2^5}$ ...........(ii)

Solving the equations (i) and (ii),

$\frac{H_{f_1}}{H_{f_2}}=\frac{\frac{8flQ_1^2}{\pi^2 gd_1^5}}{\frac{8flQ_2^2}{\pi^2 gd_2^5}}$

$=\frac{Q_1^2}{Q_2^2}\times \frac{d_2^5}{d_1^5}$

$=\frac{(1000)^2}{(10)^2}\times \frac{d_2^5}{(10d_2)^5}$

$=\frac{10^6}{10^7}$

Therefore,

$\frac{H_{f_1}}{H_{f_2}}=\frac{1}{10}$

or $H_{f_2}=10 \ H_{f_1}$

Thus the answer is option A). 10

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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).

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3 years ago

La extensión de un resumen debe estar en un rango de _________ del texto inicial. a)25 a 35 % b)10 a 20 % c)15 a 20 % d)20 a 25

mestny [16]

Answer:

Explanation:

because it is correct

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3 years ago

An asbestos pad is square in cross section, measuring 5 cm on a side at its small end increasing linearly to 10 cm on a side at

polet [3.4K]

Answer: