Chemical Warfare Agent Degradation Research Articles

Degradation of chemical warfare agents over cotton fabric functionalized with UiO-66-NH2.

Herein, cotton fabric was treated with an alkaline solution to increase the content of surface hydroxyl groups and then functionalized with UiO-66-NH2, a nanoporous metal–organic framework. Instrumental analysis of the thus treated fabric revealed that its surface was covered with UiO-66-NH2 crystals in a uniform manner. The ability of the functionalized fabric to degrade two chemical warfare agents (soman and sulfur mustard) was probed by testing its permeability to these two agents (swatch testing), and the excellent degradation performance was concluded to be well suited for a broad range of filtration and decontamination applications.

Nucleophilic Degradation of Chemical Warfare Agents Using Nonaqueous Decontamination Formula

The degradation or removal of chemical, biological, and radioactive contaminants is a supporting technique for homeland defense and countering terrorism. A highly efficient, noncorrosive, nonaqueous formula based on alkali, alcohol, and amine was developed for degradation of chemical warfare agents (CWAs). The optimized formula consisted of 50% ethanolamine, 9% benzyl alcohol, 2% KOH, 28% dimethyl sulfoxide, and 11% 18-crown-6-ether, based on the decontamination efficiency against mustard (HD). The experimental results suggested that the volume ratio of the nonaqueous decontaminant formula to CWA should be no less than 30, 2, and 10 for HD, soman (GD), and VX to achieve >99% in 30 min. The nonaqueous decontaminant can be used to decontaminate CWAs over a wide range of ambient temperature, especially low temperature. It was shown that the main degradation pathway of HD was hydrochloric acid (HCl) elimination to give chloroethyl vinyl sulfide. GD and VX degradation pathway involved P–F and P–S bond cleavage...

Chemical Warfare Agents Detoxification Properties of Zirconium Metal-Organic Frameworks by Synergistic Incorporation of Nucleophilic and Basic Sites.

The development of protective self-detoxifying materials is an important societal challenge to counteract risk of attacks employing highly toxic chemical warfare agents (CWAs). In this work, we have developed bifunctional zirconium metal-organic frameworks (MOFs) incorporating variable amounts of nucleophilic amino residues by means of formation of the mixed ligand [Zr6O4(OH)4(bdc)6(1-x)(bdc-NH2)6x] (UiO-66-xNH2) and [Zr6O4(OH)4(bpdc)6(1-x)(bpdc-(NH2)2)6x] (UiO-67-x(NH2)2) systems where bdc = benzene-1,4-dicarboxylate; bdc-NH2= benzene-2-amino-1,4-dicarboxylate; bpdc = 4,4'-biphenyldicarboxylate; bpdc-(NH2)2 = 2,2'-diamino-4,4'-biphenyldicarboxylate and x = 0, 0.25, 0.5, 0.75, 1. In a second step, the UiO-66-xNH2 and UiO-67-x(NH2)2 systems have been postsynthetically modified by introduction of highly basic lithium tert-butoxide (LiOtBu) on the oxohydroxometallic clusters of the mixed ligand MOFs to yield UiO-66-xNH2@LiOtBu and UiO-67-x(NH2)2@LiOtBu materials. The results show that the combination of pre and postsynthetic modifications on these MOF series gives rise to fine-tuning of the catalytic activity toward the hydrolytic degradation of both simulants and real CWAs in unbuffered aqueous solutions. Indeed, UiO-66-0.25NH2@LiOtBu is able to hydrolyze both CWAs simulants (diisopropylfluorophosphate (DIFP), 2-chloroethylethylsulfide (CEES), and real CWAs (soman (GD), sulfur mustard (HD)) quickly in aqueous solution. These results are related to a suitable combination of robustness, nucleophilicity, basicity, and accessibility to the porous framework.

Novel analytical approaches to determination of chemical warfare agents and related compounds for verification of nonproliferation of chemical weapons

Abstract In this paper a summary of the author’s approaches for investigation of the mass spectral behavior of some chemical warfare agents (CWAs), their degradation products and metabolites, as well as the results of development of analytical methods for confirmation of nerve and blister agents application are presented. Hydrolysis and oxidation metabolites of nerve agents, sulfur mustard and lewisite were used as biomarkers of the exposure. Sensitive analytical methods have been developed for their detection, based mainly on tandem mass spectrometry coupled with liquid chromatography. Several techniques for fast screening of CWAs degradation products based on capillary electrophoresis were also proposed. Some of developed approaches were successfully applied in the frame of the proficiency testing system of the Organization for the Prohibition of Chemical Weapons.

Physico-chemical Properties, Biological and Environmental Impact of Nb-saponites Catalysts for the Oxidative Degradation of Chemical Warfare Agents

Niobium-containing saponite clays are active catalysts, under mild ambient conditions and in the presence of aqueous hydrogen peroxide, in the oxidative abatement of sulfur-containing blister chemical warfare agent simulants, such as (2-chloroethyl)ethyl sulfide. Over a Nb-saponite solid, a complete, selective and safe abatement of the chemical agent was attained within 8 h. The biological and environmental impact of the Nb-containing nanostructured clays used as decontamination solids was assessed by specific rapid biotoxicity tests on bioluminescent bacteria and vegetable plants. No negative impact on the strain of luminescent bacteria was evidenced in terms of acute and chronic toxicity. No adverse effects have been observed on vegetable plants in terms of germination, vigour and induction of chlorophyll fluorescence either.

Computational enzymology for degradation of chemical warfare agents: promising technologies for remediation processes

Computational enzymology for degradation of chemical warfare agents: promising technologies for remediation processes

Computational enzymology for degradation of chemical warfare agents: promising technologies for remediation processes.

Chemical weapons are a major worldwide problem, since they are inexpensive, easy to produce on a large scale and difficult to detect and control. Among the chemical warfare agents, we can highlight the organophosphorus compounds (OP), which contain the phosphorus element and that have a large number of applications. They affect the central nervous system and can lead to death, so there are a lot of works in order to design new effective antidotes for the intoxication caused by them. The standard treatment includes the use of an anticholinergic combined to a central nervous system depressor and an oxime. Oximes are compounds that reactivate Acetylcholinesterase (AChE), a regulatory enzyme responsible for the transmission of nerve impulses, which is one of the molecular targets most vulnerable to neurotoxic agents. Increasingly, enzymatic treatment becomes a promising alternative; therefore, other enzymes have been studied for the OP degradation function, such as phosphotriesterase (PTE) from bacteria, human serum paraoxonase 1 (HssPON1) and diisopropyl fluorophosphatase (DFPase) that showed significant performances in OP detoxification. The understanding of mechanisms by which enzymes act is of extreme importance for the projection of antidotes for warfare agents, and computational chemistry comes to aid and reduce the time and costs of the process. Molecular Docking, Molecular Dynamics and QM/MM (quantum-mechanics/molecular-mechanics) are techniques used to investigate the molecular interactions between ligands and proteins.

Ultra-Fast Degradation of Chemical Warfare Agents Using MOF-Nanofiber Kebabs.

The threat associated with chemical warfare agents (CWAs) motivates the development of new materials to provide enhanced protection with a reduced burden. Metal-organic frame-works (MOFs) have recently been shown as highly effective catalysts for detoxifying CWAs, but challenges still remain for integrating MOFs into functional filter media and/or protective garments. Herein, we report a series of MOF-nanofiber kebab structures for fast degradation of CWAs. We found TiO2 coatings deposited via atomic layer deposition (ALD) onto polyamide-6 nanofibers enable the formation of conformal Zr-based MOF thin films including UiO-66, UiO-66-NH2 , and UiO-67. Cross-sectional TEM images show that these MOF crystals nucleate and grow directly on and around the nanofibers, with strong attachment to the substrates. These MOF-functionalized nanofibers exhibit excellent reactivity for detoxifying CWAs. The half-lives of a CWA simulant compound and nerve agent soman (GD) are as short as 7.3 min and 2.3 min, respectively. These results therefore provide the earliest report of MOF-nanofiber textile composites capable of ultra-fast degradation of CWAs.

Ultra‐Fast Degradation of Chemical Warfare Agents Using MOF–Nanofiber Kebabs

AbstractThe threat associated with chemical warfare agents (CWAs) motivates the development of new materials to provide enhanced protection with a reduced burden. Metal–organic frame‐works (MOFs) have recently been shown as highly effective catalysts for detoxifying CWAs, but challenges still remain for integrating MOFs into functional filter media and/or protective garments. Herein, we report a series of MOF–nanofiber kebab structures for fast degradation of CWAs. We found TiO2 coatings deposited via atomic layer deposition (ALD) onto polyamide‐6 nanofibers enable the formation of conformal Zr‐based MOF thin films including UiO‐66, UiO‐66‐NH2, and UiO‐67. Cross‐sectional TEM images show that these MOF crystals nucleate and grow directly on and around the nanofibers, with strong attachment to the substrates. These MOF‐functionalized nanofibers exhibit excellent reactivity for detoxifying CWAs. The half‐lives of a CWA simulant compound and nerve agent soman (GD) are as short as 7.3 min and 2.3 min, respectively. These results therefore provide the earliest report of MOF–nanofiber textile composites capable of ultra‐fast degradation of CWAs.

Decontamination of Chemical Warfare Agents on sensitive equipment materials using Zr4+ and Ge4+ co-doped TiO2 and hydrofluoroether suspension

Novel Zr4+ and Ge4+ co-doped titanium dioxide (Zr–Ge–TiO2) nanoparticles for photocatalytic degradation of Chemical Warfare Agents (CWAs) were prepared via a homogeneous precipitation method. Considering the volatilization of solvents, solubility to CWAs, and compatibility with sensitive equipments, hydrofluoroether (HFE) was first used as the dispersion solvent of suspension decontaminants. Here, Zr (5.02wt%)–Ge (0.94wt%)–TiO2 with the specific surface area of 447.9m2g−1 exhibited the best photocatalytic performance. This was dispersed in HFE-458 (HCF2CF2CH2OCF2CF2H) and HFE-6512 (HCF2CF2CF2CF2CH2OCF2CF2H) respectively. A new gas collection system was designed to study volatilization in the reaction process. As a result, HFE-6512 is more suitable as the dispersion solvent than HFE-458. The suspension prepared with HFE-6512 not only has higher degradation efficiency of HD, GD, VX, 2-CEES and DMMP, but also has fewer volatile agents. Under simulated sunlight irradiation, both the surface removal and the degradation efficiency of HD, GD, VX, 2-CEES and DMMP were over 99.95% after 37min. The results show that this suspension has potential applications in decontamination of CWAs on sensitive equipment materials. With high absorbing efficiency of CWAs and their simulants, the designed gas collection system is reliable for the selection of solvents and improvement of disinfection effect.

Nanosized inorganic metal oxides as heterogeneous catalysts for the degradation of chemical warfare agents

Nanosized inorganic metal oxides, such as TiO2, ZnO, γ-Al2O3, are proposed as heterogeneous catalysts for the oxidative degradation of chemical warfare agents (CWA), particularly of organosulfur toxic agents, into oxidised products with reduced toxicity. The morphology, structural and textural properties of the catalysts were investigated. Furthermore, their catalytic properties were evaluated in the oxidative abatement of (2-chloroethyl)ethylsulfide, CEES, a simulant of sulfur mustard (blistering CWA). Their performance was also compared to a conventional decontamination powder and a commercial Nb2O5 sample. The metal oxides powders were then employed in the active oxidative decontamination of CEES from a cotton textile substrate, mimicking a real contamination occurrence. Remarkable results in terms of abatement and degradation into desired products were recorded, achieving good conversions and decontamination efficiency with Nb2O5, TiO2 and γ-Al2O3, under very mild conditions, with hydrogen peroxide (as aqueous solution or as urea-hydrogen peroxide adduct), at room temperature and ambient pressure. In the aim of a real on-field use, the potential environmental impact of these solids was also evaluated by bioluminescence toxicity tests on reference bacteria (Photobacterium leiognathi Sh1), showing a negligible negative impact for TiO2, γ-Al2O3, and Nb2O5. A major biotoxic effect was only found for ZnO.

Nanostructured Metal Oxides for Stoichiometric Degradation of Chemical Warfare Agents.

Metal oxides have very important applications in many areas of chemistry, physics and materials science; their properties are dependent on the method of preparation, the morphology and texture. Nanostructured metal oxides can exhibit unique characteristics unlike those of the bulk form depending on their morphology, with a high density of edges, corners and defect surfaces. In recent years, methods have been developed for the preparation of metal oxide powders with tunable control of the primary particle size as well as of a secondary particle size: the size of agglomerates of crystallites. One of the many ways to take advantage of unique properties of nanostructured oxide materials is stoichiometric degradation of chemical warfare agents (CWAs) and volatile organic compounds (VOC) pollutants on their surfaces.

Nucleophilic Polymers and Gels in Hydrolytic Degradation of Chemical Warfare Agents.

Water- and solvent-soluble polymeric materials based on polyalkylamines modified with nucleophilic groups are introduced as catalysts of chemical warfare agent (CWA) hydrolysis. A comparative study conducted at constant pH and based on the criteria of the synthetic route simplicity, aqueous solubility, and rate of hydrolysis of CWA mimic, diisopropylfluorophosphate (DFP), indicated that 4-aminopyridine-substituted polyallylamine (PAAm-APy) and polyvinylamine substituted with 4-aminopyridine (PVAm-APy) were advantageous over 4-pyridinealdoxime-modified PVAm and PAAm, poly(butadiene-co-pyrrolidinopyridine), and PAAm modified with bipyridine and its complex with Cu(II). The synthesis of PVAm-APy and PAAm-APy involved generation of a betaine derivative of acrylamide and its covalent attachment onto the polyalkylamine chain followed by basic hydrolysis. Hydrogel particles of PAAm-APy and PVAm-APy cross-linked by epichlorohydrin exhibited pH-dependent swelling and ionization patterns that affected the rate constants of DFP nucleophilic hydrolysis. Deprotonation of the aminopyridine and amine groups increased the rates of the nucleophilic hydrolysis. The second-order rate of nucleophilic hydrolysis was 5.5- to 10-fold higher with the nucleophile-modified gels compared to those obtained by cross-linking of unmodified PAAm, throughout the pH range. Testing of VX and soman (GD) was conducted in 2.5-3.7 wt % PVAm-APy suspensions or gels swollen in water or DMSO/water mixtures. The half-lives of GD in aqueous PVAm-APy were 12 and 770 min at pH 8.5 and 5, respectively. Addition of VX into 3.5-3.7 wt % suspensions of PVAm-APy in DMSO-d6 and D2O at initial VX concentration of 0.2 vol % resulted in 100% VX degradation in less than 20 min. The unmodified PVAm and PAAm were 2 orders of magnitude less active than PVAm-APy and PAAm-APy, with VX half-lives in the range of 24 h. Furthermore, the PVAm-APy and PAAm-APy gels facilitated the dehydrochlorination reaction of sulfur mustard (HD) and its analogue 2-chloroethyl ethylsulfide (CEES). The ability of the reported aminopyridine-modified polyalkylamine materials to degrade the most persistent of CWAs, coupled with aqueous solubility, and the presence of numerous amino groups that provide convenient "handles" for covalent attachment on polymeric and inorganic supports yields promise for applications such as protective fabric and textile treatment and components of decontaminating materials.

Chemical Munitions Search & Assessment—An evaluation of the dumped munitions problem in the Baltic Sea

Chemical Munitions Search & Assessment (CHEMSEA) project has performed studies on chemical weapon (CW) detection, sediment pollution and spreading as well as biological effects of chemical warfare agents (CWAs) dumped in the Baltic Sea. Results suggest that munitions containing CWAs are more scattered on the seafloor than suspected, and previously undocumented dumpsite was discovered in Gdansk Deep. Pollution of sediments with CWA degradation products was local and close to the detected objects; however the pollution range was larger than predicted with theoretical models. Bottom currents observed in the dumpsites were strong enough for sediment re-suspension, and contributed to the transport of polluted sediments. Diversity and density of the faunal communities were poor at the dumping sites in comparison to the reference area, although the direct effects of CWA on benthos organisms were difficult to determine due to hypoxic or even anoxic conditions near the bottom. Equally, the low oxygen might have affected the biological effects assessed in cod and caged blue mussels. Nonetheless, both species showed significantly elevated molecular and cellular level responses at contaminated sites compared to reference sites.

Review of environmental exposure concentrations of chemical warfare agent residues and associated the fish community risk following the construction and completion of the Nord Stream gas pipeline between Russia and Germany

This paper compiles all the measured chemical warfare agent (CWA) concentrations found in relation to the Nord Stream pipeline work in Danish waters for the past 5 years. Sediment and biota sampling were performed along the pipeline route in four campaigns, prior to (in 2008 and 2010), during (in 2011) and after (in 2012) the construction work. No parent CWAs were detected in the sediments. Patchy residues of CWA degradation products of Adamsite, Clark I, phenyldichloroarsine, trichloroarsine and Lewisite II, were detected in a total of 29 of the 391 sediment samples collected and analyzed the past 5 years. The cumulative fish community risk quotient for the different locations, calculated as a sum of background and added risk, ranged between 0 and 0.017 suggesting a negligible acute CWA risk toward the fish community. The added risk from sediment disturbance in relation to construction of the pipelines represents less than 2% of the total risk in the areas with the highest calculated risk. The analyses of benthic infauna corroborate the finding of CWA related low risk across the years. There was no significant difference in CWA risk before (2008) and after the pipeline construction (2012).

Surface-immobilization of molecules for detection of chemical warfare agents

Fabrication of nanoscale molecular assemblies with advanced functionalities is an emerging field. These systems provide new perspectives for the detection and degradation of chemical warfare agents (CWAs). The main concern in this context is the design and fabrication of "smart surfaces" able to immobilize functional molecules which can perform a certain function or under the input of external stimuli. This review addresses the above points dealing with immobilization of various molecules on different substrates and describes their adequacy as sensors for the detection of CWAs.

Application of a High Surface Area Solid-Phase Microextraction Air Sampling Device: Collection and Analysis of Chemical Warfare Agent Surrogate and Degradation Compounds

This work examines a recently improved, dynamic air sampling technique, high surface area solid-phase microextraction (HSA-SPME), developed for time-critical, high-volume sampling and analysis scenarios. The previously reported HSA-SPME sampling device, which provides 10-fold greater surface area compared to commercially available SPME fibers, allowed for an increased analyte uptake per unit time relative to exhaustive sampling through a standard sorbent tube. This sampling device has been improved with the addition of a type-K thermocouple and a custom heater control circuit for direct heating, providing precise (relative standard deviation ∼1%) temperature control of the desorption process for trapped analytes. Power requirements for the HSA-SPME desorption process were 30-fold lower than those for conventional sorbent-bed-based desorption devices, an important quality for a device that could be used for field analysis. Comparisons of the HSA-SPME device when using fixed sampling times for the chemical warfare agent (CWA) surrogate compound, diisopropyl methylphosphonate (DIMP), demonstrated that the HSA-SPME device yielded a greater chromatographic response (up to 50%) relative to a sorbent-bed method. Another HSA-SPME air sampling approach, in which two devices are joined in tandem, was also evaluated for very rapid, low-level, and representative analysis when using discrete sampling times for the compounds of interest. The results indicated that subparts per billion by volume concentration levels of DIMP were detectable with short sampling times (∼15 s). Finally, the tandem HSA-SPME device was employed for the headspace sampling of a CWA degradation compound, 2-(diisopropylaminoethyl) ethyl sulfide, present on cloth material, which demonstrated the capability to detect trace amounts of a CWA degradation product that is estimated to be less volatile than sarin. The rapid and highly sensitive detection features of this device may be beneficial in decision making for law enforcement, military, and civilian emergency organizations and responders, providing critical information in a contaminated environment scenario when time is of the essence.

Oxidative degradation of chemical warfare agents in water by bleaching powder

Degradation of sulfur mustard (HD), S-2-(di-isopropylamino)ethyl O-ethyl methylphosphonothioate (VX) and Soman (GD) in water by bleaching powder was investigated. The degradation products were comprehensively analyzed by gas chromatography/mass spectrometry (GC/MS), liquid chromatography/mass spectrometry (LC/MS) and ion chromatography. Degradation pathways were deduced based on the identified products. The product analysis results indicated that HD could be degraded through oxidation and chlorination reactions, and a small portion of sulfur atoms could be mineralized into SO(4)(2-) ion. Oxidative degradation of VX could finally generate O-ethyl methylphosphonate acid (EMPA), sulfonic acids, SO(4)(2-) and NO(3)(-) ions. GD would be converted into non-toxic pinacolyl methylphosphonate via nucleophilic substitution.

Treatment of chemical warfare agents by zero-valent iron nanoparticles and ferrate(VI)/(III) composite

Nanoscale zero-valent iron (nZVI) particles and a composite containing a mixture of ferrate(VI) and ferrate(III) were prepared by thermal procedures. The phase compositions, valence states of iron, and particle sizes of iron-bearing compounds were determined by combination of X-ray powder diffraction, Mössbauer spectroscopy and scanning electron microscopy. The applicability of these environmentally friendly iron based materials in treatment of chemical warfare agents (CWAs) has been tested with three representative compounds, sulfur mustard (bis(2-chlorethyl) sulfide, HD), soman ((3,3′-imethylbutan-2-yl)-methylphosphonofluoridate, GD), and O-ethyl S-[2-(diisopropylamino)ethyl] methylphosphonothiolate (VX). Zero-valent iron, even in the nanodimensional state, had a sluggish reactivity with CWAs, which was also observed in low degrees of CWAs degradation. On the contrary, ferrate(VI)/(III) composite exhibited a high reactivity and complete degradations of CWAs were accomplished. Under the studied conditions, the estimated first-order rate constants (∼10−2s−1) with the ferrate(VI)/(III) composite were several orders of magnitude higher than those of spontaneous hydrolysis of CWAs (10−8–10−6s−1). The results demonstrated that the oxidative technology based on application of ferrate(VI) is very promising to decontaminate CWAs.

Alkyl methylphosphonic acids, the degradation products of organophosphorous CWA — preparation and direct quantitative GC-FID analysis

Abstract Seven alkyl methylphosphonic acids, products of hydrolytic degradation of organophosphorus chemical warfare agents, were obtained with a high purity (mostly above 98%), with the aim of being applyed as future certified reference materials. Ethyl (EMPA), isopropyl (IMPA), pinacolyl (PMPA), butyl (BUMPA), isobutyl (IBUMPA), cyclohexyl (CHMPA) and 2-ethylhexyl (EHMPA) monoesters of MPA were synthesized and characterized by MS EI, FTIR and NMR (1H, 13C, 31P), TLC, as well as GC and GC-MS after derivatization. The conditions for a direct quantitative GC FID analysis on CP-FFAP CB column of non-derivatized alkyl methylphosphonic acids were developed. This is the first successful attempt of a directed GC analysis of free alkyl phosphonic acids. Their chemical purity was determined and limit of quantification (LOQ) values for some of them were evaluated for the GC-FID method.