Toxicity of tobacco combustion products in different phases
For answering your question I think is better split it in two. First thing you need to understand that toxicity depends on the method of administation of the toxic agent. Tobacco smoke is a physical state of the tobacco combustion products. It is an aerosol originating from combustion where its particles are liquid, gas and solid (tar). Quoting Chemistry Central Journal 2012, 6:98
Cigarette smoke is a complex and dynamic aerosol consisting of at least 5,600 chemicals and toxicants found across two phases, the particulate (tar) and vapour phase.
(I would like to add the gas phase...) so when the product of the combustion of the tobacco are in this physical state you have to look at a different method of administration in this case vapour inhalation, Dust and Mist Inhalation and gas inhalation these are the most potentially dangerous method of administration. It seems that after about 40 minutes the liquid and solid part of the aerosol deposit (of course this depends on the condition, T, wind etc. etc.) so is probable that after this period of time the toxicity of tobacco combustion products decrease considerably. However this is not true for all the combustion products. For example: carbon monoxide is recognize tobacco combustion product and it is a gas so it wont deposit after this time and it will be "removed by reactions with OH radicals (85%), by soils (10%), and by diffusion into the stratosphere" very slowly.
Benzene is a good example of how the toxicity depends on the method of administration. LC50 inhalation value of benzene is 10000 ppm TFLo Dermal is 0.92 mL/kg so it is a big difference if you wait that the areosol deposit or if you inhale it.
If you are interested in rate of decomposition of benzene it seems that biodegradation of benzene can reach 0.95% at day according to Chiang.
Regarding 1-3 butadiene according to William A. McClenny and Donald Whitaker:
i.e., a 10-6 lifetime risk level for cancer due to inhalation exposure
of 0.03 $g/m^{3}$ (12.4 pptv at 20 °C and 1 atm pressure).1 This compound
is very reactive in the ambient atmosphere with a short
atmosphericlifetime, estimated to be 2–3 hr.
The half-life of acrolein is 14.4 hr.
You can also find a very complete EPA report EPA/600/P-98/001F
October 2002.
However determine the half-life of all the compounds is a very complex task because is related to how the ecosystem respond to these compounds so to the actual capability to decompose them through different mechanism is strictly related with thousands of factors.