ABSTRACT
Conductive metal-organic frameworks (c-MOFs) hold promise for highly sensitive sensing systems due to their conductivity and porosity. However, the fabrication of c-MOF thin films with controllable morphology, thickness, and preferential orientation remains a formidable yet ubiquitous challenge. Herein, we propose an innovative template-assisted strategy for constructing MOF-on-MOF (Ni3(HITP)2/NUS-8 (HITP: 2,3,6,7,10,11-hexamino-tri(p-phenylene))) systems with good electrical conductivity, porosity, and solution processability. Leveraging the 2D nature and solution processability of NUS-8, we achieve the controllable self-assembly of Ni3(HITP)2 on NUS-8 nanosheets, producing solution-processable Ni3(HITP)2/NUS-8 nanosheets with a film conductivity of 1.55 × 10-3 S·cm-1 at room temperature. Notably, the excellent solution processability facilitates the fabrication of large-area thin films and printing of intricate patterns with good uniformity, and the Ni3(HITP)2/NUS-8-based system can monitor finger bending. Gas sensors based on Ni3(HITP)2/NUS-8 exhibit high sensitivity (LOD ~ 6 ppb) and selectivity towards ultratrace H2S at room temperature, attributed to the coupling between Ni3(HITP)2 and NUS-8 and the redox reaction with H2S. This approach not only unlocks the potential of stacking different MOF layers in a sequence to generate functionalities that cannot be achieved by a single MOF, but also provides novel avenues for the scalable integration of MOFs in miniaturized devices with salient sensing performance.
ABSTRACT
Nitrous oxide (N2O) decomposition is increasingly acknowledged as a viable strategy for mitigating greenhouse gas emissions and addressing ozone depletion, aligning significantly with the UN's sustainable development goals (SDGs) and carbon neutrality objectives. To enhance efficiency in treatment and explore potential valorization, recent developments have introduced novel N2O reduction catalysts and pathways. Despite these advancements, a comprehensive and comparative review is absent. In this review, we undertake a thorough evaluation of N2O treatment technologies from a holistic perspective. First, we summarize and update the recent progress in thermal decomposition, direct catalytic decomposition (deN2O), and selective catalytic reduction of N2O. The scope extends to the catalytic activity of emerging catalysts, including nanostructured materials and single-atom catalysts. Furthermore, we present a detailed account of the mechanisms and applications of room-temperature techniques characterized by low energy consumption and sustainable merits, including photocatalytic and electrocatalytic N2O reduction. This article also underscores the extensive and effective utilization of N2O resources in chemical synthesis scenarios, providing potential avenues for future resource reuse. This review provides an accessible theoretical foundation and a panoramic vision for practical N2O emission controls.
ABSTRACT
Nitrate, a prevalent water pollutant, poses substantial public health concerns and environmental risks. Electrochemical reduction of nitrate (eNO3RR) has emerged as an effective alternative to conventional biological treatments. While extensive lab work has focused on designing efficient electrocatalysts, implementation of eNO3RR in practical wastewater settings requires careful consideration of the effects of various constituents in real wastewater. In this critical review, we examine the interference of ionic species commonly encountered in electrocatalytic systems and universally present in wastewater, such as halogen ions, alkali metal cations, and other divalent/trivalent ions (Ca2+, Mg2+, HCO3-/CO32-, SO42-, and PO43-). Notably, we categorize and discuss the interfering mechanisms into four groups: (1) loss of active catalytic sites caused by competitive adsorption and precipitation, (2) electrostatic interactions in the electric double layer (EDL), including ion pairs and the shielding effect, (3) effects on the selectivity of N intermediates and final products (N2 or NH3), and (4) complications by the hydrogen evolution reaction (HER) and localized pH on the cathode surface. Finally, we summarize the competition among different mechanisms and propose future directions for a deeper mechanistic understanding of ionic impacts on eNO3RR.
Subject(s)
Nitrates , Nitrates/chemistry , Catalysis , Ions , Wastewater/chemistry , Oxidation-Reduction , Water Pollutants, Chemical/chemistryABSTRACT
Nitrous oxide (N2O) is a potent greenhouse gas with a high global warming potential, emphasizing the critical need to develop efficient elimination methods. Electrocatalytic N2O reduction reaction (N2ORR) stands out as a promising approach, offering room temperature conversion of N2O to N2 without the production of NOx byproducts. In this study, we present the synthesis of a copper-based single-atom catalyst featuring atomic Cu on nitrogen-doped carbon black (Cu1-NCB). Attributed to the highly dispersed single-atom Cu sites and the effective suppression of the hydrogen evolution reaction, Cu1-NCB demonstrated an optimal N2 faradaic efficiency (82.1%) and yield rate (3.53 mmol h-1 mgmetal-1) at -0.2 and -0.5 V vs RHE, respectively, outperforming previously reported N2ORR electrocatalysts. Further, a gas diffusion electrode cell was employed to improve mass transfer and achieved a 28.6% conversion rate of 30% N2O with only a 14 s residence time, demonstrating the potential for practical application. Density functional theory calculations identified Cu-N4 as the crucial active site for N2ORR, highlighting the significance of the unsaturated coordination and metal-support electronic structure. O-terminal adsorption of N2O was favored, and the dissociative adsorption (*ON2 â *O + N2) was the rate-determining step. These findings reveal the broad prospects of N2O decomposition via electrocatalysis.
Subject(s)
Carbon , Copper , Nitrogen , Nitrous Oxide , Nitrogen/chemistry , Catalysis , Nitrous Oxide/chemistry , Carbon/chemistry , Copper/chemistry , Oxidation-ReductionABSTRACT
Wet flue gas denitrification offers a new route to convert industrial nitrogen oxides (NOx) into highly concentrated nitrate wastewater, from which the nitrogen resource can be recovered to ammonia (NH3) via electrochemical nitrate reduction reactions (NITRRs). Low-cost, scalable, and efficient cathodic materials need to be developed to enhance the NH3 production rate. Here, in situ electrodeposition was adopted to fabricate a foamy Cu-based heterojunction electrode containing both Cu-defects and oxygen vacancy loaded Cu2O (OVs-Cu2O), which achieved an NH3 yield rate of 3.59 mmol h-1 cm-2, NH3 Faradaic efficiency of 99.5%, and NH3 selectivity of 100%. Characterizations and theoretical calculations unveiled that the Cu-defects and OVs-Cu2O heterojunction boosted the H* yield, suppressed the hydrogen evolution reaction (HER), and served as dual reaction sites to coherently match the tandem reactions kinetics of NO3-to-NO2 and NO2-to-NH3. An integrated system was further built to combine wet flue gas denitrification and desulfurization, simultaneously converting NO and SO2 to produce the (NH4)2SO4 fertilizer. This study offers new insights into the application of low-cost Cu-based cathode for electrochemically driven wet denitrification wastewater valorization.
Subject(s)
Ammonia , Wastewater , Nitrates/chemistry , Nitrogen Dioxide , Denitrification , ElectrodesABSTRACT
Peroxymonosulfate (PMS)-based electrochemical advanced oxidation processes (EAOPs) have received widespread attention in recent years, but the precise nature of PMS activation and its impact on the overall process performance remain poorly understood. This study presents the first demonstration of the critical role played by the oxygen reduction reaction in the effective utilization of PMS and the subsequent enhancement of overall pollutant remediation. We observed the concurrent generation of H2O2 via oxygen reduction during the cathodic PMS activation by a model nitrogen-doped carbon nanotube catalyst. A complex interplay between H2O2 generation and PMS activation, as well as a locally increased pH near the electrode due to the oxygen reduction reaction, resulted in a SO4â¢-/â¢OH-mixed oxidation environment that facilitated pollutant degradation. The findings of this study highlight a unique dependency between PMS-driven and H2O2-driven EAOPs and a new perspective on a previously unexplored route for further enhancing PMS-based treatment processes.
Subject(s)
Environmental Pollutants , Hydrogen Peroxide , Peroxides , Oxidation-Reduction , OxygenABSTRACT
The facial nerve, also known as the seventh cranial nerve, is critical in controlling the movement of the facial muscles. It is responsible for all facial expressions, such as smiling, frowning, and moving the eyebrows. However, damage to this nerve can occur for a variety of reasons, including maxillofacial surgery, trauma, tumors, and infections. Facial nerve injuries can cause severe functional impairment and can lead to different degrees of facial paralysis, significantly affecting the quality of life of patients. Over the past ten years, significant progress has been made in the field of facial nerve repair. Different approaches, including direct suture, autologous nerve grafts, and tissue engineering, have been utilized for the repair of facial nerve injury. This article mainly summarizes the clinical methods and basic research progress of facial nerve repair in the past ten years.
ABSTRACT
Wet denitrification is a promising approach to control nitrogen oxides (NOx) produced in fossil fuel combustion. Yet, the highly concentrated nitrite (NO2-) wastewater generated poses a major threat to the aqueous environment. Here, iridium nanoclusters (d = 1.63 nm) deposited on TiO2 were applied for NO2- reduction to ammonia (NRA), showing an exceptional NH4+ selectivity of 95% and a production rate of 20.51 mgN·L-1·h-1, which held significant potential for NO2- wastewater purification and ammonia resource recovery. Notably, an interesting non-first-order NO2- hydrogenation kinetics was observed, which was further confirmed to result from the competitive adsorption mechanism between H2 and NO2- over iridium. The NRA pathways on the Ir(111) surface were explored via density functional theory calculations with the NO2-* â NO* â HNO* â HNOH* â H2NOH* â NH2* â NH3* identified as the most energetically favorable pathway and the NO* â HNO* confirmed as the rate-determining step. In situ DRIFTS further experimentally verified the generation of HNO* intermediate during NO* hydrogenation on Ir(111). To verify NRA kinetics at varied NO2- concentrations or H2 pressures, a kinetic model was derived based on the Langmuir-Hinshelwood competitive adsorption mechanism. These findings provide mechanistic insights into the NRA pathways on Ir nanocatalysts, which will be beneficial for wet denitrification waste stream decontamination and valorization.
Subject(s)
Ammonia , Nitrites , Hydrogenation , Adsorption , Iridium , Nitrogen DioxideABSTRACT
The demand for monitoring chemical and physical information surrounding, air quality, and disease diagnosis has propelled the development of devices for gas sensing that are capable of translating external stimuli into detectable signals. Metal-organic frameworks (MOFs), possessing particular physiochemical properties with designability in topology, specific surface area, pore size and/or geometry, potential functionalization, and host-guest interactions, reveal excellent development promises for manufacturing a variety of MOF-coated sensing devices for multitudinous applications including gas sensing. The past years have witnessed tremendous progress on the preparation of MOF-coated gas sensors with superior sensing performance, especially high sensitivity and selectivity. Although limited reviews have summarized different transduction mechanisms and applications of MOF-coated sensors, reviews summarizing the latest progress of MOF-coated devices under different working principles would be a good complement. Herein, we summarize the latest advances of several classes of MOF-based devices for gas sensing, i.e., chemiresistive sensors, capacitors, field-effect transistors (FETs) or Kelvin probes (KPs), electrochemical, and quartz crystal microbalance (QCM)-based sensors. The surface chemistry and structural characteristics were carefully associated with the sensing behaviors of relevant MOF-coated sensors. Finally, challenges and future prospects for long-term development and potentially practical application of MOF-coated sensing devices are pointed out.
Subject(s)
Metal-Organic Frameworks , CommerceABSTRACT
Dichloromethane (DCM), a typical representative of chlorinated volatile organic compounds (CVOCs), is usually exhausted along with other volatile organic compounds (VOCs), such as toluene and ethyl acetate, in industrial factories. To address the complexity of the components, the large variation in concentration of each component and the water content of the exhaust gases emitted from the pharmaceutical and chemical industries, the adsorption characteristics of DCM, toluene (MB), and ethyl acetate (EAC) vapors on hypercrosslinked polymeric resins (NDA-88) were studied by dynamic adsorption experiments. Furthermore, the adsorption characteristics of NDA-88 for binary vapor systems of DCM-MB and DCM-EAC at different concentration ratios and the nature of the interaction force with the three VOCs were explored. NDA-88 was found to be suitable for treating binary vapor systems of DCM mixed with low concentrations of MB/EAC, and a small quantity of adsorbed MB or EAC would promote the adsorption of DCM by NDA-88, which is attributed to the microporous filling phenomenon. Finally, the influence of humidity on the adsorption performance of binary vapor systems for NDA-88 and the regeneration adsorption performance of NDA-88 were investigated. The presence of water steam shortened the penetration times of DCM, EAC, and MB, regardless of whether it was in the DCM-EAC or DCM-MB two-component systems. This study has identified a commercially available hypercrosslinked polymeric resin NDA-88, which has excellent adsorption performance and regeneration capacity for both single-component DCM gas and a binary mixture of DCM-low-concentration MB/EAC, providing experimental guidance for the treatment of emissions from pharmaceutical and chemical industries by adsorption.
ABSTRACT
The occurrence of high concentrations of nitrate in various water resources is a significant environmental and human health threat, demanding effective removal technologies. Single atom alloys (SAAs) have emerged as a promising bimetallic material architecture in various thermocatalytic and electrocatalytic schemes including nitrate reduction reaction (NRR). This study suggests that there exists a stark contrast between thermocatalytic (T-NRR) and electrocatalytic (E-NRR) pathways that resulted in dramatic differences in SAA performances. Among Pd/Cu nanoalloys with varying Pd-Cu ratios from 1:100 to 100:1, Pd/Cu(1:100) SAA exhibited the greatest activity (TOFPd = 2 min-1) and highest N2 selectivity (94%) for E-NRR, while the same SAA performed poorly for T-NRR as compared to other nanoalloy counterparts. DFT calculations demonstrate that the improved performance and N2 selectivity of Pd/Cu(1:100) in E-NRR compared to T-NRR originate from the higher stability of NO3* in electrocatalysis and a lower N2 formation barrier than NH due to localized pH effects and the ability to extract protons from water. This study establishes the performance and mechanistic differences of SAA and nanoalloys for T-NRR versus E-NRR.
ABSTRACT
Recently, single-atom catalysts (SACs) have attracted wide attention in the field of environmental engineering. Compared with their nanoparticle counterparts, SACs possess high atomic efficiency, unique catalytic activity, and selectivity. This review summarizes recent studies on the environmental remediation applications of SACs in (1) gaseous: volatile organic compounds (VOCs) treatment, NOx reduction, CO2 reduction, and CO oxidation; (2) aqueous: Fenton-like advanced oxidation processes (AOPs), hydrodehalogenation, and nitrate/nitrite reduction. We present the treatment activities and reaction mechanisms of various SACs and propose challenges and future opportunities. We believe that this review will provide constructive inspiration and direction for future SAC research in environmental engineering.
ABSTRACT
The release of wastewaters containing relatively low levels of nitrate (NO3-) results in sufficient contamination to induce harmful algal blooms and to elevate drinking water NO3- concentrations to potentially hazardous levels. In particular, the facile triggering of algal blooms by ultra-low concentrations of NO3- necessitates the development of efficient methods for NO3- destruction. However, promising electrochemical methods suffer from weak mass transport under low reactant concentrations, resulting in long treatment times (on the order of hours) for complete NO3- destruction. In this study, we present flow-through electrofiltration via an electrified membrane incorporating nonprecious metal single-atom catalysts for NO3- reduction activity enhancement and selectivity modification, achieving near-complete removal of ultra-low concentration NO3- (10 mg-N L-1) with a residence time of only a few seconds (10 s). By anchoring Cu single atoms supported on N-doped carbon in a carbon nanotube interwoven framework, we fabricate a free-standing carbonaceous membrane featuring high conductivity, permeability, and flexibility. The membrane achieves over 97% NO3- removal with high N2 selectivity of 86% in a single-pass electrofiltration, which is a significant improvement over flow-by operation (30% NO3- removal with 7% N2 selectivity). This high NO3- reduction performance is attributed to the greater adsorption and transport of nitric oxide under high molecular collision frequency coupled with a balanced supply of atomic hydrogen through H2 dissociation during electrofiltration. Overall, our findings provide a paradigm of applying a flow-through electrified membrane incorporating single-atom catalysts to improve the rate and selectivity of NO3- reduction for efficient water purification.
ABSTRACT
Atomic dispersion of metal catalysts on a substrate accounts for the increased atomic efficiency of single-atom catalysts (SACs) in various catalytic schemes compared to the nanoparticle counterparts. However, lacking neighboring metal sites has been shown to deteriorate the catalytic performance of SACs in a few industrially important reactions, such as dehalogenation, CO oxidation, and hydrogenation. Metal ensemble catalysts (Mn), an extended concept to SACs, have emerged as a promising alternative to overcome such limitation. Inspired by the fact that the performance of fully isolated SACs can be enhanced by tailoring their coordination environment (CE), we here evaluate whether the CE of Mn can also be manipulated in order to enhance their catalytic activity. We synthesized a set of Pd ensembles (Pdn) on doped graphene supports (Pdn/X-graphene where X = O, S, B, and N). We found that introducing S and N onto oxidized graphene modifies the first shell of Pdn converting Pd-O to Pd-S and Pd-N, respectively. We further found that the B dopant significantly affected the electronic structure of Pdn by serving as an electron donor in the second shell. We examined the performance of Pdn/X-graphene toward selective reductive catalysis, such as bromate reduction, brominated organic hydrogenation, and aqueous-phase CO2 reduction. We observed that Pdn/N-graphene exhibited superior performance by lowering the activation energy of the rate-limiting step, i.e., H2 dissociation into atomic hydrogen. The results collectively suggest controlling the CE of SACs in an ensemble configuration is a viable strategy to optimize and enhance their catalytic performance.
ABSTRACT
Power conversion efficiency and long-term stability are two critical metrics for evaluating the commercial potential of organic photovoltaics. Although the field has witnessed a rapid progress of efficiency towards 19%, the intrinsic trade-off between efficiency and stability is still a challenging issue for bulk-heterojunction cells due to the very delicate crystallization dynamics of organic species. Herein, we developed a class of non-fullerene acceptors with varied side groups as an alternative to aliphatic chains. Among them, the acceptors with conjugated side groups show larger side-group torsion and more twisted backbone, however, they can deliver an efficiency as high as 18.3% in xylene-processed cells, which is among the highest values reported for non-halogenated solvent processed cells. Meanwhile, decent thermal/photo stability is realized for these acceptors containing conjugated side groups. Through the investigation of the geometry-performance-stability relationship, we highlight the importance of side-group steric hinderance of acceptors in achieving combined high-performance, stable, and eco-friendly organic photovoltaics.
ABSTRACT
All solid materials are created via nucleation. In this evolutionary process, nuclei form in solution or at interfaces, expand by monomeric growth and oriented attachment, and undergo phase transformation. Nucleation determines the location and size of nuclei, whereas growth controls the size, shape, and aggregation of newly formed nanoparticles. These physical properties of nanoparticles can affect their functionalities, reactivities, and porosities, as well as their fate and transport. Recent advances in nanoscale analytical technologies allow in situ real-time observations, enabling us to uncover the molecular nature of nuclei and the critical controlling factors for nucleation and growth. Although a single theory cannot yet fully explain such evolving processes, we have started to better understand how both classical andnonclassical theories can work together, and we have begun to recognize the importance of connecting these theories. This review discusses the recent convergence of knowledge about the nucleation and growth of nanoparticles.
Subject(s)
NanoparticlesABSTRACT
We introduce a new graphene oxide (GO)-based membrane architecture that hosts cobalt catalysts within its nanoscale pore walls. Such an architecture would not be possible with catalysts in nanoscale, the current benchmark, since they would block the pores or alter the pore structure. Therefore, we developed a new synthesis procedure to load cobalt in an atomically dispersed fashion, the theoretical limit in material downsizing. The use of vitamin C as a mild reducing agent was critical to load Co as dispersed atoms (Co1), preserving the well-stacked 2D structure of GO layers. With the addition of peroxymonosulfate (PMS), the Co1-GO membrane efficiently degraded 1,4-dioxane, a small, neutral pollutant that passes through nanopores in single-pass treatment. The observed 1,4-dioxane degradation kinetics were much faster (>640 times) than the kinetics in suspension and the highest among reported persulfate-based 1,4-dioxane destruction. The capability of the membrane to reject large organic molecules alleviated their effects on radical scavenging. Furthermore, the advanced oxidation also mitigated membrane fouling. The findings of this study present a critical advance toward developing catalytic membranes with which two distinctive and complementary processes, membrane filtration and advanced oxidation, can be combined into a single-step treatment.
Subject(s)
Environmental Pollutants , Graphite , Catalysis , Cobalt/chemistryABSTRACT
Electrocatalysis has been proposed as a versatile technology for wastewater treatment and reuse. While enormous attention has been centered on material synthesis and design, the practicality of such catalyst materials remains clouded by a lack of both stability assessment protocols and understanding of deactivation mechanisms. In this study, we develop a protocol to identify the wastewater constituents most detrimental to electrocatalyst performance in a timely manner and elucidate the underlying phenomena behind these losses. Synthesized catalysts are electrochemically investigated in various electrolytes based on real industrial effluent characteristics and methodically subjected to a sequence of chronopotentiometric stability tests, in which each stage presents harsher operating conditions. To showcase, oxidized carbon black is chosen as a model catalyst for the electrosynthesis of H2O2, a precursor for advanced oxidation processes. Results illustrate severe losses in catalyst activity and/or selectivity upon the introduction of metal pollutants, namely magnesium and zinc. The insights garnered from this protocol serve to translate lab-scale electrocatalyst developments into practical technologies for industrial water treatment purposes.
Subject(s)
Water Pollutants, Chemical , Water Purification , Catalysis , Hydrogen Peroxide , Oxidation-Reduction , Wastewater , Water Pollutants, Chemical/analysis , Water Purification/methodsABSTRACT
In this study, we loaded Pd catalysts onto a reduced graphene oxide (rGO) support in an atomically dispersed fashion [i.e., Pd single-atom catalysts (SACs) on rGO or Pd1/rGO] via a facile and scalable synthesis based on anchor-site and photoreduction techniques. The as-synthesized Pd1/rGO significantly outperformed the Pd nanoparticle (Pdnano) counterparts in the electrocatalytic hydrodechlorination of chlorinated phenols. Downsizing Pdnano to Pd1 leads to a substantially higher Pd atomic efficiency (14 times that of Pdnano), remarkably reducing the cost for practical applications. The unique single-atom architecture of Pd1 additionally affects the desorption energy of the intermediate, suppressing the catalyst poisoning by Cl-, which is a prevalent challenge with Pdnano. Characterization and experimental results demonstrate that the superior performance of Pd1/rGO originates from (1) enhanced interfacial electron transfer through Pd-O bonds due to the electronic metal-support interaction and (2) increased atomic H (H*) utilization efficiency by inhibiting H2 evolution on Pd1. This work presents an important example of how the unique geometric and electronic structure of SACs can tune their catalytic performance toward beneficial use in environmental remediation applications.
Subject(s)
Environmental Restoration and Remediation , Palladium , CatalysisABSTRACT
Since doenjang quality depends on the bacterial composition, which ambient bacteria in the environment and production conditions influence, a complete understanding of the bacteria community in traditionally madetraditionally made doenjang (TMD) from different regions is needed. We aimed to investigate the bacteria composition and quality of TMD in the following areas: Chonbuk (CB), Chonnam (CN), Kyungsang (KS), Kangwon (KW), Chungchung (CC) provinces, and Jeju island (JJ) of Korea. Twenty-nine TMD samples from different regions were used to assess biogenic amine contents, bacteria composition using next-generation methods, and metabolic functions of the bacteria using Picrust2. Bacillus spp. were isolated, and their antioxidant and fibrinolytic activities were determined. Most TMD contained high amounts of beneficial bacteria (Bacillus, Lactobacillus, Pediococcus and Weissella). However, some KS samples contained harmful bacteria (Cronobacter, Proteus and Acinetobacter) and less beneficial B. velezensis bacteria. There was no similarity among the regional groups, and each TMD showed a different bacteria composition. Shannon index, α-diversity index, was lower in TMD from JJ and CB than the other areas, but there was no ß-diversity among TMD from the six area groups. Picrust2 analysis revealed that the functional potential for arachidonic acid metabolism was lowest in JJ and CN, that for supporting insulin action was highest in KS and JJ, and that for carbohydrate digestion and absorption was lowest in CB and JJ among all groups (p < 0.05) according to the Kyoto Encyclopedia of Genes and Genomes Orthology. Histamine contents were lower in CN and CC, and tyramine contents did not differ significantly. B. velezensis, B. subtilis, B. licheniformis, B. siamensis, and B. amyloliquefaciens were isolated from TMD. None of the isolated Bacillus spp. contained the B. cereus gene. B. subtilis from CN had the highest fibrinolytic activity, and B. velezensis from CB had the highest antioxidant activity. In conclusion, TMD mainly contained various Bacillus spp., and the predominant one was B. velezensis, which had antioxidant and fibrinolytic activity regardless of the regional origin.