Atmospheric observation and emission estimation of HFC-125 and HFC-32 in China from four representative cities.

HFC-125 and HFC-32 are fluorinated greenhouse gases of great concern due to their high GWPs and increasing background atmospheric concentrations. Long-term atmospheric observations of HFC-125 and HFC-32 were carried out in four representative cities of China (Beijing, Guangzhou, Hangzhou, and Lanzhou) from January 2012 to October 2019. Overall, the annual mean atmospheric concentrations of HFC-125 and HFC-32 both showed increasing trends, with average rates of 4.8 ppt yr-1 and 7.9 ppt yr-1. The average concentrations of HFC-125 and HFC-32 in urban areas were significantly higher than those in suburban areas. Significant differences in atmospheric concentrations of the two HFCs were observed among the four cities. HFC-125 and HFC-32 emissions were estimated accordingly, averaging 6.2 Gg yr-1 (23.6 Mt. CO2-eq) and 5.7 Gg yr-1 (4.3 Mt. CO2-eq) during 2012 and 2019 and growing at rates of 0.8 Gg yr-1 (3.1 Mt. CO2-eq) and 0.8 Gg yr-1 (0.6 Mt. CO2-eq), respectively, with an increasing contribution to global radiative forcing. The bottom-up inventories of HFC-125 and HFC-32 in the four cities increased annually from 2012 to 2019, with the highest emissions in Beijing, while the top-down emissions fluctuated during the research period. SYNOPSIS: The atmospheric concentrations of HFC-125 and HFC-32 were measured from 2012 to 2019 in four representative cities of China. Both HFC emissions at national and city levels were estimated using observation-based and inventory methods.

Initiation and Carbene Induced Radical Chain Reactions in CH2F2 Pyrolysis.

High temperature dissociations of organic molecules typically involve a competition between radical and molecular processes. In this work, we use a modeling, experiment, theory (MET) framework to characterize the high temperature thermal dissociation of CH2F2, a flammable hydrofluorocarbon (HFC) that finds widespread use as a refrigerant. Initiation in CH2F2 proceeds via a molecular elimination channel; CH2F2→CHF+HF. Here we show that the subsequent self-reactions of the singlet carbene, CHF, are fast multichannel processes and a facile source of radicals that initiate rapid chain propagation reactions. These have a marked influence on the decomposition kinetics of CH2F2. The inclusion of these reactions brings the simulations into better agreement with the present and literature experiments. Additionally, flame simulations indicate that inclusion of the CHF+CHF multichannel reaction leads to a noticeable enhancement in predictions of laminar flame speeds, a key parameter that is used to determine the flammability of a refrigerant.

Air Humidity Influence on Combustion of R-1234yf (CF3CFCH2), R-1234ze(E) (trans-CF3CHCHF) and R-134a (CH2FCF3) Refrigerants.

The influence of air humidity on flame propagation in mixtures of hydrofluorocarbons (HFCs) with air was studied through numerical simulations and comparison with measurements from the literature. Water vapor added to the air in mixtures of fluorine rich hydrofluorocarbons (F/H≥1) can be considered as a fuel additive that increases the production of radicals (H, O, OH) and increases the overall reaction rate. The hydrofluorocarbon flame is typically a two-stage reaction proceeding with a relatively fast reaction in the first stage transitioning to a very slow reaction in the second stage which leads to the combustion equilibrium products. The transition to the second stage is determined by the consumption of hydrogen-containing species and formation of HF. Despite a relatively small effect of water on the adiabatic combustion temperature, its influence is significant on the reaction rate and on the temperature increase in the first stage of the combustion leading to the increase in burning velocity. The main reaction for converting H2O to hydrogen-containing radicals and promoting combustion is H2O+F=HF+OH, as demonstrated by reaction path analyses for the fluorine rich hydrofluorocarbons R-1234yf, R-1234ze(E), and R-134a (F/H = 2). The calculated burning velocity dependence on the equivalence ratio ϕ agrees reasonably well with available experimental measurements for R1234yf and R-1234ze(E) with and without the addition of water vapor. In agreement with experimental data, with water vapor, the maximum of burning velocity over ϕ is shifted to the lean mixtures (near ϕ = 0.8).

Trifluoroiodomethane as a Precursor to High Global Warming Potential Climate Pollutants: Could the Transformation of Climatically Benign CF3I into Potent Greenhouse Gases Significantly Increase Refrigerant-Related Greenhouse Gas Emissions?

The transition away from the production and consumption of high global warming potential (GWP) hydrofluorocarbons (HFCs) under the 2016 Kigali Amendment to the Montreal Protocol on Substances that Deplete the Ozone Layer (Montreal Protocol) has prompted air conditioning, refrigeration, and heat pump equipment manufacturers to seek alternative refrigerants with lower direct climate impacts. Additional factors affecting alternative refrigerant choice include safety (i.e., flammability and toxicity), environmental, and thermodynamic constraints. At the same time, manufacturers are incentivized to seek refrigerants with higher energy efficiency, which saves on electricity costs and reduces indirect greenhouse gas emissions from electricity generation. The life cycle climate performance (LCCP) metric is commonly used to assess the combined direct and indirect climate impacts of refrigerant-use equipment. Here, we consider an additional impact on climate performance: the degradation of refrigerant in equipment, i.e., the direct climate impacts of high-GWP byproducts that can form as the result of adding trifluoroiodomethane (CF3I) to refrigerant blends to reduce flammability. Such a production of high-GWP gases could change the acceptability of CF3I-containing refrigerants. Further, it highlights the need to understand refrigerant degradation within equipment in calculations of the environmental acceptability of new cooling technology.

Pathway and Cost-Benefit Analysis to Achieve China's Zero Hydrofluorocarbon Emissions.

Global hydrofluorocarbon (HFC) cumulative emissions will be more than 20 Gt CO2-equiv during 2020-2060 and have a non-negligible impact on global warming even in full compliance with the Kigali Amendment (KA). Fluorochemical manufacturers (including multinationals) in China have accounted for about 70% of global HFC production since 2015, of which about 60% is emitted outside China. This study built an integrated model (i.e., DECAF) to estimate both territorial and exported emissions of China under three scenarios and assess the corresponding climate effects as well as abatement costs. Achieving near-zero territorial emissions by 2060 could avoid 23 ± 4 Gt CO2-equiv of cumulative territorial emissions (compared to the 2019 Baseline scenario) during 2020-2060 at an average abatement cost of 9 ± 6 USD/t CO2-equiv. Under the near-zero emission (including territorial and abroad) pathway, radiative forcing from HFCs will peak in 2037 (60 ± 6 mW/m2) with a 33% peak reduction and 8 years in advance compared to the path regulated by the KA, and the radiative forcing by 2060 will be lower than that in 2019. Accelerated phase-out of HFC production in China could provide a possibility for rapid global HFC abatement and achieve greater climate benefits.

Levels and distribution profiles of Per- and Polyfluoroalkyl Substances (PFAS) in a high Arctic Svalbard ice core.

Per- and polyfluoroalkyl substances (PFAS) are a group of persistent organic contaminants of which some are toxic and bioaccumulative. Several PFAS can be formed from the atmospheric degradation of precursors such as fluorotelomer alcohols (FTOHs) as well as hydrochlorofluorocarbons (HFCs) and other ozone-depleting chlorofluorocarbon (CFC) replacement compounds. Svalbard ice cores have been shown to provide a valuable record of long-range atmospheric transport of contaminants to the Arctic. This study uses a 12.3 m ice core from the remote Lomonosovfonna ice cap on Svalbard to understand the atmospheric deposition of PFAS in the Arctic. A total of 45 PFAS were targeted, of which 26 were detected, using supercritical fluid chromatography (SFC) tandem mass spectrometry (MS/MS) and ultra-performance liquid chromatography (UPLC) MS/MS. C2 to C11 perfluoroalkyl carboxylic acids (PFCAs) were detected continuously in the ice core and their fluxes ranged from 2.5 to 8200 ng m-2 yr-1 (9.51-16,500 pg L-1). Trifluoroacetic acid (TFA) represented 71 % of the total mass of C2 - C11 PFCAs in the ice core and had increasing temporal trends in deposition. The distribution profile of PFCAs suggested that FTOHs were likely the atmospheric precursor to C8 - C11 PFCAs, whereas C2 - C6 PFCAs had alternative sources, such as HFCs and other CFC replacement compounds. Perfluorooctanesulfonic acid (PFOS) was also widely detected in 82 % of ice core subsections, and its isomer profile (81 % linear) indicated an electrochemical fluorination manufacturing source. Comparisons of PFAS concentrations with a marine aerosol proxy showed that marine aerosols were insignificant for the deposition of PFAS on Lomonosovfonna. Comparisons with a melt proxy showed that TFA and PFOS were mobile during meltwater percolation. This indicates that seasonal snowmelt and runoff from post-industrial accumulation on glaciers could be a significant seasonal source of PFAS to ecosystems in Arctic fjords.

Transitioning to low-GWP alternatives with enhanced energy efficiency in cooling non-residential buildings of China.

The electricity demand for space cooling in the non-residential building (NRB) sector of China is growing significantly and is becoming increasingly critical with rapid economic development and mounting impacts of climate change. The growing demand for space cooling will increase global warming due to emissions of hydrofluorocarbons used in cooling equipment and carbon dioxide emissions from the mostly fossil fuel-based electricity currently powering space cooling. This study uses the Greenhouse Gas and Air Pollution Interaction and Synergies (GAINS) model framework to estimate current and future emissions of hydrofluorocarbons and their abatement potentials for space cooling in the NRB sector of China and assess the co-benefits in the form of savings in electricity and associated reductions in greenhouse gas (GHG), air pollution, and short-lived climate pollutant emissions. Co-benefits of space cooling are assessed by taking into account (a) regional and urban/rural heterogeneities and climatic zones among different provinces; (b) technical/economic energy efficiency improvements of the cooling technologies; and (c) transition towards lower global warming potential (GWP) refrigerants under the Kigali Amendment. Under the business-as-usual (BAU) scenario, the total energy consumption for space cooling in the NRB sector will increase from 166 TWh in 2015 to 564 TWh in 2050, primarily due to the rapid increase in the floor space area of non-residential buildings. The total GHG mitigation potential due to the transition towards low-GWP refrigerants and technical energy efficiency improvement of cooling technologies will approximately be equal to 10% of the total carbon emissions from the building sector of China in 2050. Supplementary Information: The online version contains supplementary material available at 10.1007/s11027-022-10021-w.

Hydrofluorocarbons pneumonitis as a complication of inhalation injury following air-conditioning repairs.

Hydrofluorocarbon (HFC) pneumonitis is an uncommon cause of inhalation injury. HFCs are a group of chemicals predominantly used for refrigeration and cooling. A 19-year-old air-conditioning technician developed acute onset of dyspnoea and chest tightness while servicing an air conditioner in a confined space. We diagnosed him with HFC pneumonitis based on the history of exposure and the high-resolution computed tomography (HRCT) thorax findings. He was treated with steroids and supportive oxygen therapy. He recovered fully after 5 days of hospitalization and was discharged. Review at 2 weeks in the outpatient setting showed significant radiological improvement on HRCT thorax.

Flammability and performance studies of eco-friendly ternary refrigerant mixtures used in vapour compression systems.

The present article analyses the refrigerant safety parameters flammability, global warming potential (GWP) and coefficient of performance (COP) for twenty-seven combinations that contain two flammable and one non-flammable (dilutant) component. The flammability of the flammable refrigerants R290, R600, R600a, R152a and R161 were investigated with different dilutants such as R245fa, R13I1 and R134a. To determine the minimum inerting concentration (which decides the flammable zone), two methods were used: thermal balance method (TBM) and the modified thermal balanced method (MTBM). The MICs estimated with both the methods are compared against the 50 experimental data points available in the literature (for different ternary mixtures). It was found that for all the ternary mixtures, majority of the MIC values estimated with MTBM are within ± 8% while with TBM are within ± 30%. Fifty-five ternary mixture compositions were identified (from the proposed twenty-seven mixture combinations) using the MICs predicted by MTBM. The COPs of the identified mixtures M1-M6, M8-M12, M14-M24, M26-M30, M34-M39 and M53-M54 are estimated to be less than 10% of the COP of R134a (at the same operating conditions). It is also estimated that the corresponding GWP value of the mixtures (M1 to M6, M8 to M12, M14 to M24, M26 to M30, M34 to M39, M53 and M54) are reduced by 91 to 99% when compared to R134a (GWP = 1300).

Speed of Sound Measurements of Binary Mixtures of Difluoromethane (R-32) with 2,3,3,3-Tetrafluoropropene (R-1234yf) or trans-1,3,3,3-Tetrafluoropropene (R-1234ze(E)) Refrigerants.

Sound speed data measured using a dual-path pulse-echo instrument are reported for binary mixtures of difluoromethane (R-32) with 2,3,3,3-tetrafluoropropene (R-1234yf) or trans-1,3,3,3-tetrafluoropropene (R-1234ze(E)). The sound speed is reported at two compositions for each binary mixture of approximately (0.33/67) and (0.67/0.33) mole fraction at temperatures between 230 K and 345 K. Data are reported from pressures slightly above the bubble point to 12 MPa for R-32/1234yf mixtures to avoid potential polymerization reactions and to 53 MPa for the R-32/1234ze(E) mixtures. The mean uncertainty of the sound speed data are less than 0.1% of the measured value where uncertainties at individual state points range from 0.04% to 0.5% of the measured value as the conditions approach the mixture critical region. The reported data are compared to available Helmholtz-energy-explicit EOS included in REFPROP and all systems studied have average absolute deviations greater than 2%. The comparisons show that further adjustments to the mixture models are needed to provide a reasonable representation of the data within its experimental uncertainty.

Spectroscopy and radiation-induced chemistry of an atmospherically relevant CH2F2 H2O complex: Evidence for the formation of CF2 H2O complex as revealed by FTIR matrix isolation and ab initio study.

Difluoromethane is considered among the environment friendly alternatives to the ozone depleting chlorofluorocarbons. Due to its chemical inertness and lack of UV absorption above 200 nm, this compound can easily come to the upper layers forming complexes with widely abundant atmospheric components, such as water. The radiation-induced degradation of this compound and its complexes may be significant for reliable prediction of its long-term evolution in the environment as well as for development of new ways for its removal. In this work we have studied the vibrational spectroscopic properties and mechanisms of the radiation-induced decay of the CH2F2⋯H2O under the action of X-rays using matrix isolation FTIR spectroscopy and ab initio calculations. The IR spectrum of the complex in an argon matrix was characterized for the first time and assigned to a hydrogen-bonded structure with a binding energy of 11.1 kJ/mol (2.65 kcal/mol) (CCSD(T)/CBS level of theory). Complexation with water leads to a certain suppression of the efficiency of the radiation-induced decomposition of difluoromethane. The obtained results provide evidence for the radiation-induced formation of previously unreported CF2⋯H2O complex (in addition to other oxygen containing molecules, such as COF2 and CO). As demonstrated by calculations, the new difluorocarbene complex reveals a hydrogen bond and it is characterized by a binding energy of 5.73 kJ/mol (1.37 kcal/mol) (CCSD(T)/CBS level of theory).

COVID 19 vaccine distribution solution to the last mile challenge: Experimental and simulation studies of ultra-low temperature refrigeration system.

Most COVID-19 vaccines require ambient temperature control for transportation and storage. Both Pfizer and Moderna vaccines are based on mRNA and lipid nanoparticles requiring low temperature storage. The Pfizer vaccine requires ultra-low temperature storage (between -80 °C and -60 °C), while the Moderna vaccine requires -30 °C storage. Pfizer has designed a reusable package for transportation and storage that can keep the vaccine at the target temperature for 10 days. However, the last stage of distribution is quite challenging, especially for rural or suburban areas, where local towns, pharmacy chains and hospitals may not have the infrastructure required to store the vaccine. Also, the need for a large amount of ultra-low temperature refrigeration equipment in a short time period creates tremendous pressure on the equipment suppliers. In addition, there is limited data available to address ancillary challenges of the distribution framework for both transportation and storage stages. As such, there is a need for a quick, effective, secure, and safe solution to mitigate the challenges faced by vaccine distribution logistics. The study proposes an effective, secure, and safe ultra-low temperature refrigeration solution to resolve the vaccine distribution last mile challenge. The approach is to utilize commercially available products, such as refrigeration container units, and retrofit them to meet the vaccine storage temperature requirement. Both experimental and simulation studies are conducted to evaluate the technical merits of this solution with the ability to control temperature at -30 °C or -70 °C as part of the last mile supply chain for vaccine candidates.

A review of bottom-up and top-down emission estimates of hydrofluorocarbons (HFCs) in different parts of the world.

Hydrofluorocarbons (HFCs) are widespread alternatives for the ozone-depleting substances chlorofluorocarbons and hydrochlorofluorocarbons. They are used mainly as refrigerants or as foam-blowing agents. HFCs do not deplete the ozone layer, but they are very potent greenhouse gases, already contributing to global warming. Since 2019 HFCs are regulated under the Kigali Amendment to the Montreal Protocol, which demands reliable emission estimates to monitor the phase-down. Quantification of emissions is performed with two methods: bottom-up from product inventories or data on chemical sales; or top-down, inferred from atmospheric measurements by inverse modelling or interspecies correlation. Here, we review and compare the two methods and give an overview of HFC emissions from different parts of the world. Emission estimates reported by the different methods vary considerably. HFC emissions of developed countries (Annex I) are reported to the United Nations Framework Convention on Climate Change. These bottom-up estimates add up to only half of global emissions estimated from atmospheric data. Several studies with regional top-down estimates have shown that this gap is not owed to large-scale underreporting of emissions from developed countries, but mostly due to emissions from developing countries (non-Annex I). China accounts for a large fraction of the emissions causing the gap, but not entirely. Bottom-up and top-down estimations of emissions from other developing countries that could identify other large emitters are largely unavailable. Especially South America, West-, Central- and East-Africa, India, the Arabian Peninsula and Northern Australia are not well covered by measurement stations that could provide atmospheric data for top-down estimates.

Minimum ignition energies and laminar burning velocities of ammonia, HFO-1234yf, HFC-32 and their mixtures with carbon dioxide, HFC-125 and HFC-134a.

Given the safety issues associated with flammability characteristics of alternative environmentally-friendly refrigerants, it is vital to establish measurement systems to accurately analyse the flammability of these mildly flammable refrigerants. In this study, we used a customised Hartmann bomb analogue to measure the minimum ignition energy (MIE) and laminar burning velocity (BV) for refrigerant/air mixtures of pure ammonia (R717), R32, R1234yf and mixtures of R32 and R1234yf with non-flammable refrigerants of R134a, R125 and carbon dioxide (R744). The MIEs of R717, R32, and R1234yf were measured at an ambient temperature of 24 °C to be (18.0 ± 1.4), (8.0 ± 1.5) and (510 ± 130) mJ at equivalence ratios of 0.9, 1.27 and 1.33, respectively. Adding the non-flammable refrigerants R134a, R125 and R744 along with R32 at volumetric concentrations of 5% each to R1234yf reduced the latter compound's flammability and increased its MIE by one order of magnitude. The laminar burning velocities of pure R717 and R32 were measured at an equivalence ratio of 1.1 using the flat flame method and found to be 8.4 and 7.4 cm/s, respectively. Adding 5% R1234yf to R32 decreased the laminar burning velocity by 11%, while a further 5% addition of R1234yf resulted in a decrease of over 30% in the laminar burning velocity.

Cryogenic Refrigerant Burns: A Rare Occupational Hazard.

BACKGROUND: Cryogenic burns induced by coolant gases used in refrigerators and air conditioners are rarely encountered, despite the wide use of these gases. To date, only a few cases have been reported in the literature. This study examined the occupational circumstances leading to such injuries, relevant injury sites, types of chemicals involved, and treatment measures. METHODS: This study was conducted in a tertiary burn center in India between March 2015 and March 2019. The demographic details, chemicals involved, and burn regions and characteristics were analyzed. FINDINGS: There were 15 burn cases all involving injury to the hand. All injuries were managed initially with dressings and nonoperative management. One patient required anti-edema therapy with limb elevation and fingertip debridement, while another patient required skin grafting. All patients had satisfactory hand function after treatment. CONCLUSIONS/APPLICATION TO PRACTICE: Cryogenic burn injuries caused by refrigerants are rare, and their etiology varies considerably. Exposure time is the primary factor that determines burn depth and severity; hence, reducing exposure time is important in first aid. Our findings suggest that after exposure, the patient should be treated in a specialized burn center. Adequate knowledge regarding the pathophysiology of these types of burn injuries and their management is necessary; otherwise, misjudgments in the treatment plan can lead to adverse consequences.

Thermodynamic Analysis of Working Fluids for a New "Heat from Cold" Cycle.

Adsorptive Heat Transformation systems are at the interface between thermal and chemical engineering. Their study and development need a thorough thermodynamic analysis aimed at the smart choice of adsorbent-adsorptive pair and its fitting with a particular heat transformation cycle. This paper addresses such an analysis for a new "Heat from Cold" cycle proposed for amplification of the ambient heat in cold countries. A comparison of four working fluids is made in terms of the useful heat per cycle and the temperature lift. The useful heat increases in the row water > ammonia ≥ methanol > hydrofluorocarbon R32. A threshold mass of exchanged adsorbate, below which the useful heat equals zero, raises in the same sequence. The most promising adsorbents for this cycle are activated carbons Maxsorb III and SRD 1352/2. For all the adsorptives studied, a linear relationship F = A·ΔT is found between the Dubinin adsorption potential and the driving temperature difference ΔT between the two natural thermal baths. It allows the maximum temperature lift during the heat generation stage to be assessed. Thus, a larger ΔT-value promotes the removal of the more strongly bound adsorbate.

Activation of pentafluoropropane isomers at a nanoscopic aluminum chlorofluoride: hydrodefluorination versus dehydrofluorination.

The hydrofluorocarbon 245 isomers, 1,1,1,3,3-pentafluoropropane, 1,1,1,2,2- pentafluoropropane, and 1,1,1,2,3-pentafluoropropane (HFC-245fa, HFC-245cb, and HFC-245eb) were activated through C-F bond activations using aluminium chlorofluoride (ACF) as a catalyst. The addition of the hydrogen source Et3SiH is necessary for the activation of the secondary and tertiary C-F bonds. Multiple C-F bond activations such as hydrodefluorinations and dehydrofluorinations were observed, followed by hydroarylation and Friedel-Crafts-type reactions under mild conditions.

Breakthrough analysis of continuous fixed-bed adsorption of sevoflurane using activated carbons.

The inhalational anaesthetic agent - sevoflurane is widely employed for the induction and maintenance of surgical anaesthesia. Sevoflurane possesses a high global warming potential that imposes negative impact to the environment. The only way to resolve the issue is to remove sevoflurane from the medical waste gas before it reaches the atmosphere. A continuous adsorption study with a fixed-bed column was conducted using two commercial granular activated carbons (E-GAC and H-GAC), to selectively remove sevoflurane. The effect of bed depth (Z, 5-15 cm), gas flow rate (Q, 0.5-6.0 L/min) and inlet sevoflurane concentration (C0, ∼55-700 mg/L) was investigated. E-GAC demonstrated ∼60% higher adsorption capacity than H-GAC under the same operating conditions. Varying the levels of Z, Q and C0 showed significant differences in the adsorption capacities of E-GAC, whereas only changing the C0 level had significant differences for H-GAC. Three breakthrough models (Adams-Bohart, Thomas, and Yoon-Nelson) and Bed-depth/service time (BDST) analysis were applied to predict the breakthrough characteristics of the adsorption tests and determine the characteristic parameters of the column. The Yoon-Nelson and Thomas model-predicted breakthrough curves were in good agreement with the experimental values. In the case of the Adams-Bohart model, a low correlation was observed. The predicted breakthrough time (tb) based on kinetic constant (kBDST) in BDST analysis showed satisfactory agreement with the measured values. The results suggest the possibility of designing, scaling up and optimising an adsorption system for removing sevoflurane with the aid of the models and BDST analysis.

[Current importance of heavy fluids as intraoperative aids in vitreoretinal surgery]. / Aktueller Stellenwert von schweren Flüssigkeiten als intraoperative Hilfsmittel bei vitreoretinalen Eingriffen.

A major milestone in the treatment of complex retinal detachment was the development of heavy fluids as intraoperative short-term tamponades. Since the introduction liquid perfluorocarbons and hydrofluorocarbons are particularly noteworthy. Irrespective of the suitability of the substances in principle, the purity during the manufacturing process is a decisive factor that determines possible side effects. Also, the direct exchange with silicone oil can lead to mixing with disadvantageous results. Retinal surgeons should be informed about the properties of the tamponades used. Despite all expectations, the heavy liquids could not become established compared to silicone oil as a long-term tamponade, which is why their domain is the short-term intraoperative use.

Rising environmental degradation and impact of foreign direct investment: An empirical evidence from SAARC region.

The Pollution Haven Hypothesis is amongst the latest discussion in economics that investigates the contribution of Foreign Direct Investment in raising environmental degradation in the host countries. Whereas, the concept of the Environmental Kuznets Curve hypothesis had been in economics since 1991 and is extensively studied under the umbrella of environmental degradation. Our present study is focused upon the role of economic growth, Foreign Direct Investment and energy consumption in increasing concentration of Carbon Dioxide in the South Asian region by using panel data from 1986 to 2014. The nascent techniques, panel ARDL, and FMOLS have been applied. The results thus obtained confirmed the existence of Pollution Heaven Hypotheses and Environmental Kuznets Curve in the short run. However, long-run analysis of the panel data confirms the absence of Pollution Heaven Hypotheses and existence of Environment Kuznets Curve. Furthermore, energy consumption in the region significantly contributing to environmental degradation. Since a major portion of the energy in South Asian countries is being generated from non-renewable energy resources. In the future, these countries are planning to meet their energy requirements through non-renewable energy resources that will inject more Carbon Dioxide to the atmosphere. The pattern of Study further refers to South Asian nations for extended co-operation in environmental R&D to mitigate future challenges. The governments in the region need to initiate environment-friendly regulations to suppress environmental degradation. Keen efforts are required by the statistical/environmental institutions in the region to set up a data collection/distribution forum so that real-time analysis be complied with, in order to accelerate the progress towards projected goals and sustainability.