Development of a needle trap device packed with titanium-based metal-organic framework sorbent for extraction of phenolic derivatives in air.

We developed a novel method of needle trap device packed with titanium-based metal-organic framework for the extraction of phenolic derivatives in air followed by gas chromatography-flame ionization detector analysis. The synthetized adsorbent was packed inside a 22-gauge spinal needle. This method was first tested at laboratory scale, and then was used for field sampling of phenolic derivatives in air. A glass chamber placed on a heater at 60°C was used to provide different concentrations of phenolic derivatives. The desorption conditions and breakthrough volume were optimized using response surface methodology. The limit of detection and limit of quantitation of the proposed method were estimated to be in the range of 0.001-0.12 and 0.003-0.62 ng/mL, respectively, indicating a high sensitivity for the suggested sampler. Storing the packed needle trap device in a refrigerator at 4˚C for 60 days did not dramatically affect the storage stability. Our findings indicated that there was a high correlation coefficient (R2  = 0.99) between the measurement results of this method and the NIOSH recommended method (XAD-7 sorbent tube). Therefore, it can be concluded that the needle trap device packed with titanium-based metal-organic framework can be used as a efficient method for extraction of phenolic derivatives in air.

Determination of urinary methylhippuric acids using MIL-53-NH2 (Al) metal-organic framework in microextraction by packed sorbent followed by HPLC-UV analysis.

For the analysis of methylhippuric acids (MHAs) in human urine samples, in this study, a new method based on the metal-organic framework (MOF) of MIL-53-NH2 (Al) in microextraction by packed sorbent (MEPS) was developed. The synthesis of MIL-53-NH2 (Al) was characterized by Fourier transform infrared spectra, field emission-scanning electron microscopy and X-ray diffraction. Response surface methodology was used to investigate the influences of several parameters including type and volume of elution, type of conditional solvent, sample volume and extraction cycle on MEPS efficiency. The results showed good recoveries (>94%) and excellent extraction efficiencies (>96%) at three different concentrations of 50, 500 and 1500 µg ml-1 (as low, mid and high concentrations, respectively) of MHA isomers. Calibration curves of MHAs were linear over the concentration range of 1-1500 µg ml-1 , with high correlation coefficients (r ≥ 0.998). The reproducibility of the proposed MIL-53-MEPS for determination of three isomers of MHA was found to be in the range of 3.5-11.1%. After optimization of the proposed technique, it was used to analyze MHAs in urine samples of workers exposed to xylenes in a petrochemical plant in Asalouyah, Iran. The results indicated that the MOF-MEPS method was selective, sensitive, rapid and efficient for the extraction of urinary MHAs. The technique is also environmentally friendly and inexpensive, and the MOF sorbent is reusable.

A needle trap device packed with MIL-100(Fe) metal organic frameworks for efficient headspace sampling and analysis of urinary BTEXs.

The aim of this study was to develop a new method for the determination of benzene, toluene, ethylbenzene and xylene isomers (BTEXs) in urine samples. In this method, MIL-100(Fe)@Fe3 O4 @SiO2 metal-organic framework was synthesized, characterized and packed inside a needle trap device (NTD) as a sorbent for headspace extraction of unmetabolized BTEXs from urine samples followed by gas chromatography (GC) analysis. The GC device was equipped with a flame ionization detector (FID). The results showed that the optimal extraction time, extraction temperature and salt content were 60 min, 30°C and 5%, respectively. Also, the optimal desorption time and temperature were determined to be 1 min and 250°C, respectively. The limits of detection and quantification of the analytes of interest were in the ranges 0.0001-0.0005 and 0.0003-0.0014 µg ml-1 , respectively. The intra- and inter-day repeatability were <7.6%. The accuracy of the measurements in urine samples was in the range 7.1-11.4%. The results also demonstrated that the proposed NTD offered various advantages such as having high sensitivity and being inexpensive, reusable, user friendly, environmentally friendly and compatible for use with the GC device. Therefore, it can be efficiently used as a MIL-NTD for the extraction and analysis of unmetabolized BTEXs from urine samples.

Ion-pair-based hollow-fiber liquid-phase microextraction combined with high-performance liquid chromatography for the simultaneous determination of urinary benzene, toluene, and styrene metabolites.

In the current study, a novel technique for extraction and determination of trans,trans-muconic acid, hippuric acid, and mandelic acid was developed by means of ion-pair-based hollow fiber liquid-phase microextraction in the three-phase mode. Important factors affecting the extraction efficiency of the method were investigated and optimized. These metabolites were extracted from 10 mL of the source phase into a supported liquid membrane containing 1-octanol and 10% w/v of Aliquat 336 as the ionic carrier followed by high-performance liquid chromatography analysis. The organic phase immobilized in the pores of a hollow fiber was back-extracted into 24 µL of a solution containing 3.0 mol/L sodium chloride placed inside the lumen of the fiber. A very high preconcentration of 212- to 440-fold, limit of detection of 0.1-7 µg/L, and relative recovery of 87-95% were obtained under the optimized conditions of this method. The relative standard deviation values for within-day and between-day precisions were calculated at 2.9-8.5 and 4.3-11.2%, respectively. The method was successfully applied to urine samples from volunteers at different work environments. The results demonstrated that the method can be used as a sensitive and effective technique for the determination of the metabolites in urine.

Development of a needle trap device packed with modified PAF-6-MNPs for sampling and analysis of polycyclic aromatic compounds in air.

The aim of this study was to develop a new method for sampling and analyzing polycyclic aromatic hydrocarbons in the air. This was achieved by utilizing a needle trap device packed with a modified porous aromatic framework coated with magnetic nanoparticles (PAF-6-MNPs). The modified adsorbent underwent qualitative evaluation using Fourier-transform infrared spectroscopy and X-ray diffraction, as well as scanning and transmission electron microscopy. The optimal conditions for sampling polycyclic aromatic hydrocarbons compounds were determined using a dynamic atmosphere chamber. The method was validated by taking various samples from the standard chamber, and then analyzed under different environmental sampling conditions using a gas chromatography device. The limit of detection (LOD) and limit of quantification (LOQ) values for the analytes of interest, including naphthalene, anthracene, and pyrene, ranged from 0.0034-0.0051 and 0.010-0.015 µg L-1, respectively. Also, the repeatability and reproducibility of the method expressed as relative standard deviation, for the mentioned analyses were found to be in the range of 17.8-20.5% and 20-22.9%. The results indicated that over a 20 day storage period (with the needle trap device containing the analytes of interest kept in the refrigerator), there was no significant decrease in the amount of analytes compared to the initial amount. These findings suggest that, the needle trap packed with the proposed adsorbent offers a reliable, highly-sensitive, easy-to-use, and cost-effective method for sampling polycyclic aromatic hydrocarbons in the air compared to the conventional method recommended by the National Institute of Occupational Safety and Health (NIOSH), method 5515.

Correction: Development of a needle trap device packed with modified PAF-6-MNPs for sampling and analysis of polycyclic aromatic compounds in air.

[This corrects the article DOI: 10.1039/D4RA01651C.].

Degradation of 2,4-dinitrotoluene in aqueous solution by dielectric barrier discharge plasma combined with Fe-RGO-BiVO4 nanocomposite.

2,4-Dinitrotoluene (2,4-DNT) as a priority and hazardous pollutant, is widely used in industrial and military activities. In this study the synergistic effect of Fe-RGO-BiVO4 nanocomposite in a non-thermal dielectric barrier discharge plasma reactor (NTP-DBD) for degrading 2,4-DNT was evaluated. Preparation of the Fe-RGO-BiVO4 nanocomposite was done by a stepwise chemical method depositing Fe and reduced graphene oxide (RGO) on BiVO4. Field emission scanning electron microscopy (FESEM), X-ray diffraction analysis (XRD), UV-vis diffuse reflectance spectra (DRS), and energy-dispersive X-ray spectroscopy mapping (EDS-mapping) validated the satisfactory synthesis of Fe-RGO-BiVO4. To find the optimal conditions and to determine the interaction of model parameters, a central composite design (RSM-CCD) had been employed. 2,4 DNT can be completely degraded at: initial 2,4-DNT concentration of 40 mg L-1, Fe-RGO-BiVO4 dosage of 0.75 g L-1, applied voltage of 21kV, reaction time of 30 min and pH equal to 7, while the single plasma process reached a degradation efficiency of 67%. The removal efficiency of chemical oxygen demand (COD) and total organic carbon (TOC) were 90.62% and 88.02% at 30 min contact time, respectively. Results also indicated that average oxidation state (AOS) and carbon oxidation state (COS) were enhanced in the catalytic NTP-DBD process, which demonstrate the effectiveness of proposed process for facilitating biodegradability of 2,4-DNT.

Quantitative evaluation of chemical fume hoods performance by CO2 tracer gas.

BACKGROUND: Various chemical substances and carcinogens have been presented in medical sciences universities' educational and research laboratories. For this purpose a suitable ventilation system had to be implemented to ensure the correct operation of the hoods. OBJECTIVE: To evaluate the performance of laboratory chemical fume hoods of the University of Medical Sciences using a novel quantitative method. METHODS: In this study, 43 chemical fume hoods were investigated in the laboratories of the University of Medical Sciences. The technical specifications of the hoods and their compliance with the standard have been investigated. The hoods face velocity was measured using a thermal anemometer. Quantitative evaluation was performed using the new method of CO2 tracer gas and the results were analyzed using SPSS software version 19. FINDINGS: The hoods presented both favorable and unfavorable results in terms of technical specifications and location. The results showed 50.2% of the hoods have visible leakage. Hood face velocity was not suitable for any of the hoods in the case fully open.when half open only 16.3% of the hoods and in the case of 25% open face, 34.9% of the hoods had a good velocity. Most hoods have CO2 leakage even at small amounts. CONCLUSIONS: the unsuitable performance of the hoods is mainly due to the unsuitability of the fans, furthermore investigation and correction of technical problems are required. The new quantitative method is a suitable method for routine evaluating chemical fume hoods and can replace the SF6 gas tracer method.

Evaluation of SARS-CoV-2 in Indoor Air of Sina and Shahid Beheshti Hospitals and Patients' Houses.

Side by side air sampling was conducted using a PTFE filter membrane as dry sampler and an impinger containing a suitable culture medium as a wet sampler. Most of the samples were collected from two hospitals and few air samples were collected from private houses of non-hospitalized confirmed COVID-19 patients. The collected air samples were analyzed using RT-PCR. The results indicated that all air samples collected from the hospitals were PCR negative for SARS-CoV-2. While two of four air samples collected from the house of non-hospitalized patients were PCR positive. In this study, most of the hospitalized patients had oxygen mask and face mask, and hence this may be a reason for our negative results regarding the presence of SARS-CoV-2 in indoor air of the hospitals, while non-hospitalized patients did not wear oxygen and protective face masks in their houses. Moreover, a very high concentration of particles in the size range of droplet nuclei (< 5 µm) was identified compared to particles in the size range of respiratory droplets (> 5-10 µm) in the areas where patients were hospitalized. It can be concluded that using face mask by patients can prevent the release of viruses into the indoor air, even in hospitals with a high density of patients.

Design, Implementation, and Evaluation of Industrial Ventilation Systems and Filtration for Silica Dust Emissions from a Mineral Processing Company.

OBJECTIVE: Silicosis as an incurable occupational disease is common in industries and processes that contain silica dust. Since engineering controls can reduce the risk of silicosis, the goal of this study was to design, implement and evaluate industrial ventilation systems and filtration for silica dust, which is emitted from hydrocone crusher and screener units in a mineral processing company. METHODS: In this project, local exhaust ventilation (LEV) system was designed and installed using the standard and valid guidelines. The dust concentration was measured in two stages before and after installation of the ventilation system in the workplace, silica emission sources and also in the workers' inhalation area. Finally, the efficiency of the system was determined. RESULTS: The efficiency of LEV system in reducing workplace dust concentration and dust emission sources was 79.8% and 84.92% respectively. Furthermore, the efficiency of system in reducing the Respirable Crystalline Silica (RCS) at the worker's inhalation area was 92.13%. The collection efficiency of filtration system for total particles was 99.67 %. CONCLUSION: The results indicate that with designation and installation of the local exhaust ventilation (LEV) system and also installation of bag filter to collect dust, the concentration of dust in the workplace and in the inhalation area of workers has decreased significantly. As a result, this system can be used to control dust in similar industries.

A bioactive foamed emulsion reactor for the treatment of benzene-contaminated air stream.

An adapted bioactive foamed emulsion bioreactor for the treatment of benzene vapor has been developed. In this reactor, bed clogging was resolved by bioactive foam as a substitute of packing bed for interfacial contact of liquid to gaseous phase. The pollutant solubility has been increased using biocompatible organic phase in liquid phase and this reactor can be applied for higher inlet benzene concentration. Experimental results showed a benzene elimination capacity (EC) of 220 g m(-3) h(-1) with removal efficiency (RE) of 85% for benzene inlet concentration of 1-1.2 g m(-3) at 15 s gas residence time in bioreactor. Assessment of benzene concentration in liquid phase showed that a significant amount of transferred benzene mass has been biodegraded. By optimizing the operational parameters of bioreactor, continuous operation of bioreactor with high EC and RE was demonstrated. With respect to the results, this reactor has the potential to be applied instead of biofilter and biotrickling filters.

Application of a needle trap device packed with XAD-2 polyaniline composite for sampling naphthalene and phenanthrene in air.

The purpose of this study was to develop a new method for the sampling and analysis of naphthalene (Nap) and phenanthrene (Phe) in air. XAD-2 sorbent was prepared with polyaniline (PANI) to increase its adsorption area. Thus, 22-gauge needles were packed with XAD-2/PANI sorbent for the extraction of Nap and Phe, and sampling of the analytes of interest. The compounds were dynamically sampled from the headspace of the flask in laboratory and then analyzed using a gas chromatography (GC) device equipped with flame ionization detector (FID). The needle trap device (NTD) with the proposed sorbent was more sensitive and accurate than the NIOSH 5515 method. The results showed that the optimal temperature and time for the desorption of the analytes were 350 °C and 8 min, respectively. The analytical parameters such as carryover effect, breakthrough volume, and storage time were examined. The repeatability of the method was determined to be 9.4-13.5% for Nap and 7.1-15.7% for Phe. The limits of detection (LOD) for the analytes were in the range 0.002 - 0.09 ng L-1, and the limits of quantitation (LOQ) were in the range 0.01- 0.23 ng L-1. It was also found that the NTD packed with XAD-2/PANI sorbent was a sensitive and cost-effective method, and offered a high accuracy for the sampling and analysis of PAHs in air.

Development of Membrane Hollow Fiber for Determination of Maleic Anhydride in Ambient Air as a Field Sampler.

This research develops a rapid method for sampling and analysis of maleic anhydride (MA) in air using a one-step hollow fiber (HF) membrane in the liquid phase followed by high-performance liquid chromatography. A sampling chamber was prepared for sampling of MA with HF-supported de-ionized water absorbency. Several important parameters, such as sampling flow rate, sampling time, and breakthrough volume (BTV), were optimized at different concentrations using a central composite design. The results showed that sampling could be performed at the maximum period of 4 h with a flow rate of 1 mL min-1 for different concentrations (in the range of 0.05-2 mg m-3). The BTV was 240 mL. The relative standard deviations for the repeatability of interday and intraday were 7-10%, 10%, respectively, and the pooled standard deviation was 0.088. The limit of detection and limit of quantitation values were 0.033 and 0.060 mg m-3, respectively. Moreover, our findings revealed that the samples could be stored in sealed HF flexible plastic tubes in a cover at refrigerator temperature (4°C) for up to 7 days. The HF method was compared with method number 3512 National Institute Occupational Safety and Health for determination of MA. There was a good correlation (R2 = 0.99) between the two methods at a concentration of 0.05 to 2 mg m-3 in the laboratory and the average concentration of MA for both methods was 0.11 mg m-3 in the ambient air at an adhesive manufacturer. Our findings indicated that the proposed HF can act as a reliable, rapid, and effective approach for sampling of MA in workplaces.

Effect of TiO2/GAC and water vapor on chloroform decomposition in a hybrid plasma-catalytic system.

This paper presents the combination of TiO2/GAC catalyst and NTP for the decomposition of chloroform using a DBD reactor. The experiments were performed using an AC transformer as the power supply system to determine the optimal conditions of the chloroform conversion in the presence of a hydrogen-rich substance, that is, water vapor. TiO2/GAC enhanced the removal efficiency and also CO2 selectivity significantly, leading to an acceptable conversion rate at SIEs higher than 400 J L-1. The adsorption property of GAC was noticed to be an effective factor for catalytic activity by increasing the residence time, although the higher retention time prevented the accurate determination of chlorine and carbon balance. Selectivity toward HCl was improved considerably from 24.3% to 64.3% over catalyst when water was fed as a hydrogen-rich compound. At the same time, the harmful chlorinated by-products such as TCBA and TCE declined significantly. A noticeable enhancement in the selectivity toward CO2 was observed when both catalyst and water were introduced, regardless of the inlet concentration. Our findings suggest that the hybrid of NTP with TiO2/GAC will highly be effective in the abatement of chloroform, and the addition of H2O will successfully decline harmful chlorinated by-products.

Hollow Fiber Supported Liquid Membrane Extraction Combined with HPLC-UV for Simultaneous Preconcentration and Determination of Urinary Hippuric Acid and Mandelic Acid.

This work describes a new extraction method with hollow-fiber liquid-phase microextraction based on facilitated pH gradient transport for analyzing hippuric acid and mandelic acid in aqueous samples. The factors affecting the metabolites extraction were optimized as follows: the volume of sample solution was 10 mL with pH 2 containing 0.5 mol·L-1 sodium chloride, liquid membrane containing 1-octanol with 20% (w/v) tributyl phosphate as the carrier, the time of extraction was 150 min, and stirring rate was 500 rpm. The organic phase immobilized in the pores of a hollow fiber was back-extracted into 24 µL of a solution containing sodium carbonate with pH 11, which was placed inside the lumen of the fiber. Under optimized conditions, the high enrichment factors of 172 and 195 folds, detection limit of 0.007 and 0.009 µg·mL-1 were obtained. The relative standard deviation (RSD) (%) values for intra- and inter-day precisions were calculated at 2.5%-8.2% and 4.1%-10.7%, respectively. The proposed method was successfully applied to the analysis of these metabolites in real urine samples. The results indicated that hollow-fiber liquid-phase microextraction (HF-LPME) based on facilitated pH gradient transport can be used as a sensitive and effective method for the determination of mandelic acid and hippuric acid in urine specimens.

Development of Carbotrap B-packed needle trap device for determination of volatile organic compounds in air.

Carbotrap B as a highly pure surface sorbent with excellent adsorption/desorption properties was packed into a stainless steel needle to develop a new needle trap device (NTD). The performance of the prepared NTD was investigated for sampling, pre-concentration and injection of benzene, toluene, ethyl benzene, o-xylene, and p-xylene (BTEX) into the column of gas chromatography-mass spectrometry (GC-MS) device. Response surface methodology (RSM) with central composite design (CCD) was also employed in two separate consecutive steps to optimize the sampling and device parameters. First, the sampling parameters such as sampling temperature and relative humidity were optimized. Afterwards, the RSM was used for optimizing the desorption parameters including desorption temperature and time. The results indicated that the peak area responses of the analytes of interest decreased with increasing sampling temperature and relative humidity. The optimum values of desorption temperature were in the range 265-273°C, and desorption time were in the range 3.4-3.8min. The limits of detection (LODs) and limits of quantitation (LOQs) of the studied analytes were found over the range of 0.03-0.04ng/mL, and 0.1-0.13ng/mL, respectively. These results demonstrated that the NTD packed with Carbotrap B offers a high sensitive procedure for sampling and analysis of BTEX in concentration range of 0.03-25ng/mL in air.

Chlorobenzene degeradation by non-thermal plasma combined with EG-TiO2/ZnO as a photocatalyst: Effect of photocatalyst on CO2 selectivity and byproducts reduction.

The non-thermal plasma (NTP) technique, which suffers from low selectivity in complete oxidation of volatile organic compounds to CO2 and H2O, creates unwanted and harmful byproducts. NTP in concert with photocatalyst can resolve this limitation due to additional oxidation. TiO2 and ZnO nanoparticles were coated on the surface of the expanded graphite and placed downstream of the NTP reactor under UV light. In this study, to compare the performance of NTP and the combined system, chlorobenzene removal, selectivity of CO2 and byproducts formation were investigated. The results showed that the combined system enhanced both the removal efficiency and CO2 selectivity. The output gas of the NTP reactor contained chlorobenzene, phosgene, O3, NO, NO2, CO, CO2, HCL and CL. The bulk of these byproducts was oxidized on the surface of the nanocomposite; as a result, the content of the byproducts in the output gas of the combined system decreased dramatically. The removal efficiency and CO2 selectivity increased by rising the applied voltage and residence time because the collision between active species and pollutant molecules increases. Based on these results, the combined system is preferred due to a higher performance and lower formation of harmful byproducts.

Enhanced performance of non-thermal plasma coupled with TiO2/GAC for decomposition of chlorinated organic compounds: influence of a hydrogen-rich substance.

BACKGROUND: No study was found in the literature on the combination of TiO2/GAC catalyst and non-thermal plasma for chlorinated volatile organic compounds abatement in air. This paper presents this hybrid process for the decomposition of chloroform (as a target compound) using a multi-pin to plate discharge reactor. The experiments were performed using a high frequency pulsed transformer as the power supply system to examine the effect of SIE, frequency, as well as initial concentration on the chloroform removal efficiency (RE). Toluene was added as a hydrogen-rich source to shift the reactions into the formation of environmentally desirable products. RESULTS: RE of around 60% was observed with the NTP-alone process at the highest possible SIE (3000 J L(-1)), while it rocketed up to 100% (total oxidation) in the presence of TiO2/GAC at SIE of 1000 J L(-1). About 100% O3 destruction over TiO2/GAC and both adsorption and catalytic activities of GAC may be considered as the reasons for better performance of the hybrid process. Toluene feeding diminished the chlorinated by-products such as Cl2 and TCE significantly. The selectivity towards CO2 was noticed to enhance noticeably, when both catalyst and toluene were introduced, regardless of the input concentration. CONCLUSIONS: Our findings suggest that the hybrid of NTP with TiO2/GAC will highly be effective in the abatement of chloroform, and the addition of toluene will successfully decline harmful chlorinated by-products.

Performance catalytic ozonation over the carbosieve in the removal of toluene from waste air stream.

BACKGROUND: Toluene is a volatile organic compound, one of 189 hazardous air pollutants (HAPs) and the most important pollutant found in most industries and indoor environments; owing to its adverse health, toluene must be treated before being released into the environment. METHODS: In this research study, a continuous-flow system (including an air compressor, silica gel filters and activated charcoal, impinger, an ozone generation and a fixed bed reactor packed with the carbosieve in size 1.8-2.3 mm, specific surface: 972 m2/g,) was used. This glass reactor was 0.7 m in height; at a distance of 0.2 m from its bottom, a mesh plane was installed so as to hold the adsorbent. Moreover, 3 l/min oxygen passed through this system, 0.43 g/h ozone was prepared. The flow rate of waste airstream was 300 ml/min. The efficiency of this system for removal of toluene was compared under the same experimental conditions. RESULTS: Under similar conditions, performance of catalytic ozonation was better in toluene removal than that of ozonation and carbosieve alone. On average, increasing the removal efficiency was 45% at all concentrations. When carbosieve and ozone come together, their synergistic effects increased on toluene degradation. CONCLUSIONS: Catalytic ozonation is a suitable, high-efficient and available method for removing toluene from various concentrations of waste air stream. This process due to the short contact time, low energy consuming and making use of cheap catalysts can be used as a novel process for removing various concentrations of volatile organic compounds.

Study on the performance of wet electroscrubber in purifying airborne particles.

BACKGROUND: In this study, an electroscrubber was designed and experimented for evaluation of integrating particle and droplet charging effects separately and jointly on collection efficiency of a spray tower and also to discover the optimal condition. METHODS: A homogenous concentration of relatively fine particles was introduced to influent air stream and electroscrubber efficiency in purifying them was determined through the measurement of input and output particles concentration. The effect of various conditions such as particles and droplets charging alone and together (bipolar) for several applied voltages has been studied. RESULTS: In all of experiments, the applied charging voltage has a key role in promotion of electroscrubber efficiency. Maximum collection efficiency has achieved for 15 Kilovolt (Kv). The effectiveness of bipolar charging of particles and droplets with 15 Kv was higher than that of no-charging and singly charging. In other words, efficiency can be increased from 84.43% to 93.22 for total particles and from 50.8% to 75.16% for submicron particles. The maximum improvement of collection efficiency (42.2%) relates to bipolar charging of the initial size group with diameter smaller than 0.3 micrometer (µm) and the minimum (0.5%) to sizing group of 11 with diameter 4-5 µm. CONCLUSIONS: This approach can be an appropriate option for the purpose of purifying submicron particles in spray tower scrubbers.