Solar Power, Microbial fuel cell. These two and I am sure other ways as well Solar power as you guess use the sun as a power energy source with non-waste and long lasting use. Microbial fuel uses the bacteria aka decomposers turn the sugars, nutrients into rich soil while also releasing electrons back into the soil and can be used as a energy source.
The first dissociation for H2X:
H2X +H2O ↔ HX + H3O
initial 0.15 0 0
change -X +X +X
at equlibrium 0.15-X X X
because Ka1 is small we can assume neglect x in H2X concentration
Ka1 = [HX][H3O]/[H2X]
4.5x10^-6 =( X )(X) / (0.15)
X = √(4.5x10^-6*0.15)
∴X = 8.2 x 10-4 m
∴[HX] & [H3O] = 8.2x10^-4
the second dissociation of H2X
HX + H2O↔ X^2 + H3O
8.2x10^-4 Y 8.2x10^-4
Ka2 for Hx = 1.2x10^-11
Ka2 = [X2][H3O]/[HX]
1.2x10^-11= y (8.2x10^-4)*(8.2x10^-4)
∴y = 1.78x10^-5
∴[X^2] = 1.78x10^-5 m
Answer: The transition metals make up the middle block of he periodic table
Lower flammable limit means the lowest concentration of a material that will propagate a flame.
What is hazardous atmosphere?
It is an atmosphere that may expose employees to risk of death, incapacitation, impairment of ability to self-rescue, injury, or acute illness from one or more of following causes
- Flammable gas, vapor, or mist in excess of 10 percent of lower flammable limit (LFL)
- Airborne combustible dust at concentration that meets or exceeds its LFL
What is lower flammable limit?
- It means the lowest concentration of a material that will propagate a flame.
- The LFL is usually expressed as percent by volume of material in air (or other oxidant)
- Atmospheres with concentration of flammable vapors at or above 10 percent of lower explosive limit (LEL) are considered hazardous when located in confined spaces.
- However, atmospheres with flammable vapors below 10 percent of LEL are not necessarily safe. Such atmospheres are too lean to burn
Learn more about lower flammable limit at brainly.com/question/2456135
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Answer:
The ΔG° is 29 kJ and the reaction is favored towards reactant.
Explanation:
Based on the given information, the ΔH°rxn or enthalpy change is 41.2 kJ, the ΔS°rxn or change in entropy is 42.1 J/K or 42.1 * 10⁻³ kJ/K. The temperature given is 289 K. Now the Gibbs Free energy change can be calculated by using the formula,
ΔG° = ΔH°rxn - TΔS°rxn
= 41.2 kJ - 289 K × 42.1 × 10⁻³ kJ/K
= 41.2 kJ - 12.2 kJ
= 29 kJ
As ΔG° of the reaction is positive, therefore, the reaction is favored towards reactant.
