Development and evaluation of a palm-sized optical PM2.5 sensor

A new palm-sized optical PM_2.5 sensor has been developed and its performance evaluated. The PM_2.5 mass concentration was calculated from the distribution of light scattering intensity by considering the relationship between scattering intensity and particle size. The results of laboratory tests suggested that the sensor can detect particles with diameters as small as ～0.3 µm and can measure PM_2.5mass concentrations as high as ～600 µg/m³. Year-round ambient observations were conducted at four urban and suburban sites in Fukuoka, Kadoma, Kasugai, and Tokyo, Japan. Daily averaged PM_2.5 mass concentration data from our sensors were in good agreement with corresponding data from the collocated standard instrument at the Kadoma site, with slopes of 1.07–1.16 and correlation coefficients (R) of 0.90–0.91, and with those of the nearest observatories of the Ministry of the Environment of Japan, at 1.7–4.1 km away from our observation sites, with slopes of 0.97–1.23 and R of 0.89–0.95. Slightly greater slopes were observed in winter than in summer, except at Tokyo, which was possibly due to the photochemical formation of relatively small secondary particles. Under high relative humidity conditions (>70%), the sensor has a tendency to overestimate the PM_2.5 mass concentrations compared to those measured by the standard instruments, except at Fukuoka, which is probably due to the hygroscopic growth of particles. This study demonstrates that the sensor can provide reasonable PM_2.5 mass concentration data in urban and suburban environments and is applicable to studies on the environmental and health effects of PM_2.5.

Copyright © 2018 American Association for Aerosol Research     

Chemical Characteristics of Fine Particles (PM1) from Xi'an,China

Daily mass concentrations of water-soluble inorganic (WS-i) ions, organic carbon (OC), and elemental carbon (EC) were determined for fine particulate matter (PM₁, particles < 1.0 μm in diameter) collected at Xi'an, China. The annual mean PM₁ mass concentration was 127.3 ± 62.1 μg m^–3: WS-i ions accounted for ～38% of the PM₁ mass; carbonaceous aerosol was ～30%; and an unidentified fraction, probably mostly mineral dust, was ～32%. WS-i ions and carbonaceous aerosol were the dominant species in winter and autumn, whereas the unidentified fraction had stronger influences in spring and summer. Ion balance calculations indicate that PM₁ was more acidic than PM_2.5 from the same site. PM₁ mass, sulfate and nitrate concentrations followed the order winter > spring > autumn > summer, but OC and EC levels were higher in autumn than spring. Annual mean OC and EC concentrations were 21.0 ± 12.0 μg m^?3 and 5.1 ± 2.7 μg m^–3 with high OC/EC ratios, presumably reflecting emissions from coal combustion and biomass burning. Secondary organic carbon, estimated from the minimum OC/EC ratios, comprised 28.9% of the OC. Positive matrix factorization (PMF) analysis indicates that secondary aerosol and combustion emissions were the major sources for PM₁.     

Fine particles sampled at an urban background site and an industrialized coastal site in Northern France—Part 2: Comparison of offline and online analyses for carbonaceous aerosols

Particulate matter was sampled in Northern France during two summer and winter periods at both an urban background site (Douai, DO) and an industrialized coastal site (Grande-Synthe, GS). Ambient levels of particulate carbonaceous species and Polycyclic Aromatic Hydrocarbons (PAH) were measured by real-time measurements and via collection and analysis of offline filters (F). The comparison between online organic matter (OM) measured by an Aerosol Mass Spectrometer (AMS) and organic carbon (OC) determined by an offline thermal-optical method showed good linear trends in wintertime GS (r² = 0.82 while only 0.50 in summer), and DO (r² = 0.86 in summer and 0.92 in winter). However, significant differences were observed between analytical methods and sites with OC_AMS/OC_F ratios decreasing from 0.80 in DO during winter to ≈0.20 for GS in summer, suggesting that a large part of OM could be in the PM₁–PM_2.5 fraction. The simultaneous measurements of Black Carbon (BC) and Elemental Carbon (EC) concentrations in PM_2.5 were also well correlated at both sites with r² = 0.61–0.97 and slopes between 0.6 and 0.8. PAHs were analyzed in PM_2.5 and also measured online by AMS in PM₁. Their wintertime concentrations were highly correlated in DO (r² = 0.98) and to a lesser degree in GS (r² = 0.67). r² values determined for comparison between online and offline parameters (OC and PAHs) in GS were lower than in DO, probably due to a more complex aerosol composition and a higher variability of the physical and chemical properties resulting from the coastal situation and diversity of emission sources in the vicinity of GS.

Copyright © 2018 American Association for Aerosol Research     

Characterization of size-resolved aerosol components using proton induced X-ray emission, inductively coupled plasma optical emission spectrometry and ion chromatography

Size-resolved aerosol monitoring for PM₁₀, PM_2.5, and PM_1.0 was performed to qualify and quantify the elements and ions by using proton induced X-ray emission (PIXE), inductively coupled plasma optical emission spectrometry (ICP-OES), and ion chromatography (IC) analysis. Time-resolved aerosol samplings based on 2-hour and 14-hour intervals were carried out during daytime and nighttime, respectively. Physical and chemical properties of size-resolved aerosols were investigated to characterize air quality in the national park area of Gyeongju, Korea. The PIXE and ICPOES methods made elemental mass of Al, Si, S, K, Ca, Ti, Cr, Fe, Sr, and Pb. And ions of Na⁺, NH₄ ⁺, Ca²⁺, Cl^?, NO ₃ ^? , and SO ₄ ^2? were analyzed by the IC method. The mass concentrations of Si, S, Ti, and Pb determined by PIXE showed relatively good correlation with those determined by ICP-OES. But Fe and Sr had worse correlations with an average R² of 0.4703 and 0.4825, respectively. The PIXE method was a good alternative to measure chemical species of Al, Si, S, K, Ca, Ti, Cr, and Pb for size-resolved aerosols except Fe and Sr in this study. The average relative errors of sizeresolved elements for 2-hour and 14-hour interval collections were 10.1±5.7% (0.1–28.3%) and 9.9±7.7% (1.3–38.4%). Ammonium sulfates (AS), mineral dust (MD), and sea salt (SS) aerosols were reconstructed from the elements determined by PIXE and ICP-OES and ions obtained by IC. The mass concentration of MD was calculated with crustal elements of Al, Si, Ca, Ti, and Fe, which are associated with soil erosion. The average relative error of MD was the lowest value of 0.8% in the PM₁₀ regime and the highest value of 10.0% in the PM_1.0 regime. The average relative errors of AS for PM₁₀, PM_2.5, and PM_1.0 determined by PIXE, ICP-OES, and IC showed relatively lower values of 0.8–5.7%, 1.7–5.9%, and 3.3–8.3%, respectively. The average mass concentrations of AS, MD, and SS of PM₁₀, PM_2.5, and PM_1.0 except submicron SS determined by PIXE were comparable to those determined by ICP-OES and IC within the acceptable relative errors.     

EXPERIMENTAL INVESTIGATION AND MODELING OF THE INFLUENCE OF INDIRECT HEATING ON FLUIDIZED BED DRYING

Experimental results of fluidized bed drying with additional energy input by indirect heating are presented. A clear influence of moisture on wall-to-bed heat transfer coefficients is observed for particle diameters of 250 μm and 50 μm. Two different reasons for this influence may be distinguished in both, the measurements and theoretical considerations: 1 The change of bed and particle properties and 2 the increase of the local wall-to-particle heat transfer.     

Investigation of the Efficiencies of Bioaerosol Samplers for Collecting Aerosolized Bacteria Using a Fluorescent Tracer. I: Effects of Non-sampling Processes on Bacterial Culturability

By sampling aerosolized microorganisms, the efficiency of a bioaerosol sampler can be calculated depending on its ability both to collect microorganisms and to preserve their culturability during a sampling process. However, those culturability losses in the non-sampling processes should not be counted toward the sampling efficiency. Prior to the efficiency assessment, this study was designed to investigate the culturability losses in three non-sampling processes: (1) the tracer uranine induced loss; (2) the loss during aerosolization (pre-sampling process); and (3) the bacteria and uranine recovery in air sample handling procedures for the samples of the Andersen 6-stage impactor and the Airport MD8 (post-sampling process). The results indicated that uranine had no significant effect on the culturability of Enterococcus faecalis, Escherichia coli, and Mycoplasma synoviae in suspensions (P > 0.05), but negatively affected the culturability of Campylobacter jejuni (P = 0.01). The culturability of E. faecalis, E. coli, and M. synoviae was not affected by stresses caused by aerosolization (P > 0.05). Only 29% of C. jejuni were still culturable during aerosolization (P = 0.02). In the air sample handling procedures, the four species of bacteria were recovered without significant losses from the samples of the Andersen impactor, but only 33–60% uranine was recovered. E. faecalis, E. coli, and M. synoviae were recovered without significant losses from the samples of the Airport MD8. More C. jejuni was recovered (172%), probably due to multiplication or counting variation. It is suggested that tracer and bacteria should be aerosolized separately when the tracer negatively affects the bacterial culturability. In both pre- and post-sampling processes, losses of bacterial culturability (or multiplication) may occur, which should be taken into account when assessing the efficiencies of bioaerosol samplers.     

Risks from accidental exposures to engineered nanoparticles and neurological health effects: A critical review

Background and Objective

Exposure to fine airborne particles (PM_2.5) has been shown to be responsible for cardiovascular and hematological effects, especially in older people with cardiovascular disease. Some epidemiological studies suggest that individuals with diabetes may be a particularly susceptible population. This study examined effects of short-term exposures to ambient PM_2.5 on markers of systemic inflammation, coagulation, autonomic control of heart rate, and repolarization in 22 adults (mean age: 61 years) with type 2 diabetes.

Methods

Each individual was studied for four consecutive days with daily assessments of plasma levels of blood markers. Cardiac rhythm and electrocardiographic parameters were examined at rest and with 24-hour ambulatory ECG monitors. PM_2.5 and meteorological data were measured daily on the rooftop of the patient exam site. Data were analyzed with models adjusting for season, weekday, meteorology, and a random intercept. To identify susceptible subgroups, effect modification was analyzed by clinical characteristics associated with insulin resistance as well as with oxidative stress and by medication intake.

Results

Interleukin (IL)-6 and tumor necrosis factor alpha showed a significant increase with a lag of two days (percent change of mean level: 20.2% with 95%-confidence interval [6.4; 34.1] and 13.1% [1.9; 24.4], respectively) in association with an increase of 10 μg/m³ in PM_2.5. Obese participants as well as individuals with elevated glycosylated hemoglobin, lower adiponectin, higher ferritin or with glutathione S-transferase M1 null genotype showed higher IL-6 effects. Changes in repolarization were found immediately as well as up to four days after exposure in individuals without treatment with a beta-adrenergic receptor blocker.

Conclusions

Exposure to elevated levels of PM_2.5 alters ventricular repolarization and thus may increase myocardial vulnerability to arrhythmias. Exposure to PM_2.5 also increases systemic inflammation. Characteristics associated with insulin resistance or with oxidative stress were shown to enhance the association.     

Composition and pH dependence on aggregation of SiO2–PVA suspension for the synthesis of porous SiO2–PVA nanocomposite

Porous monolithic SiO₂–poly(vinyl alcohol) (PVA) nanocomposites were fabricated by drying an SiO₂–PVA suspension. Depending on the amount of added PVA and pH value of the suspension, the Brunauer–Emmett–Teller surface areas, total pore volumes, and mean pore radii of the (100 ? x)SiO₂–xPVA (x = 0, 10, 20, 30 wt%) nanocomposites were 102–313 m² g^?1, 0.61–1.42 cm³ g^?1, and 8.1–14.7 nm, respectively. Some cracks were observed in the monolithic SiO₂–PVA nanocomposite, affected by the pore size. To elucidate crack generation, the correlation between the dispersion/aggregation in the SiO₂–PVA suspension and the pore size distribution of the nanocomposite was evaluated in terms of the added PVA amount and pH value. At x = 20 and pH 3, the SiO₂ particles and PVA aggregated in the suspension. The preparation of crack-free monolithic SiO₂–PVA nanocomposites was possible using the aggregated suspension owing to the low capillary force during drying because of the relatively large pores.     

CsHSO4 as proton conductor for high-temperature polymer electrolyte membrane fuel cells

The influence of CsHSO₄ inorganic solid acid was evaluated as a possible proton conductor in the catalyst layer of ABPBI (poly(2,5-benzimidazole))-based high-temperature polymer electrolyte membrane fuel cells (HT-PEMFCs). Gas diffusion electrodes (GDEs) were prepared with fixed polytetrafluoroethylene (PTFE) and polyvinylidene diflouride (PVDF) binder content, while the CsHSO₄ loading was varied. Porosimetry data showed that the addition of 10 % CsHSO₄ to the PVDF GDE increased the porosity across all the pore regions, whereas the addition of 10 % CsHSO₄ to the PTFE GDE decreased the GDEs porosity. The CsHSO₄ MEAs showed good proton transfer dynamics and low resistance for fuel cell operation. An optimum loading of 10 % CsHSO₄ in conjunction with either of the binders was observed, with CsHSO₄–PVDF GDE achieving peak power of 498.2 mW cm^?2 at a cell voltage of +352 mV. Higher CsHSO₄ loadings increased the charge transfer resistance and lowered the cell performance of these GDEs.     

Evaluation of a particle trap laser desorption mass spectrometer (PT-LDMS) for the quantification of sulfate aerosols

A particle trap laser desorption mass spectrometer (PT-LDMS) has been developed for the online measurements of the chemical composition of submicron aerosol particles. The PT-LDMS was evaluated by both laboratory and ambient measurements, with the focus being the quantification of sulfate aerosols. Ammonium sulfate ((NH₄)₂SO₄) is generally the predominant form of sulfate aerosols in urban air; hence, it is used as a material for laboratory experiments and calibration. Major fragments of (NH₄)₂SO₄ were observed at mass-to-charge ratios (m/z) of 48 (SO⁺) and 64 (SO₂⁺). The dependence of sensitivity (expressed as the ratio of m/z 48 signal to sulfate mass) on laser power and cell temperature was investigated. An intercomparison of PT-LDMS with a commercial sulfate particle analyzer (SPA) and filter sampling was performed in Tokyo. Good agreement was observed between SPA and filter analysis (slope = 0.98, r² = 0.99). Although the mass concentration of sulfate measured by PT-LDMS exhibited a tight correlation with that measured by SPA, the mass concentration measured by PT-LDMS tended to underestimate that measured by SPA (slope = 0.70, r² = 0.96). While the discrepancy can be mainly attributed to the difference in size cut between PT-LDMS (approximately PM₁) and SPA (PM_2.5), differences in vaporization efficiency were also found to be important.

Copyright © 2016 American Association for Aerosol Research     

Combining sensor-based measurement and modeling of PM2.5 and black carbon in assessing exposure to indoor aerosols

Accurate, cost-effective methods are needed for rapid assessment of traffic-related air pollution (TRAP). Typically, real-time data of particulate matter (PM) from portable sensors have been adjusted using data from reference methods such as gravimetric measurement to improve accuracy. The objective of this study was to create a correction factor or linear regression model for the real-time measurements of the RTI’s Micro Personal Exposure Monitor (MicroPEM?) and AethLab’s microAeth^® black carbon (AE51) sensor to generate accurate real-time data for PM_2.5 (PM_2.5RT) and black carbon (BC_RT) in Cincinnati metropolitan homes. The two sensors and an SKC PM_2.5 Personal Modular impactor were collocated in 44 indoor sampling events for 2?days in residences near major roadways. The reference filter-based analyses conducted by a laboratory included particle mass (SKC PM_2.5 and MicroPEM? PM_2.5) and black carbon (SKC BC); these methods are more accurate than real-time sensors but are also more cumbersome and costly. For PM_2.5, the average correction factor, a ratio of gravimetric to real time, for the MicroPEM? PM_2.5 and SKC PM_2.5 utilizing the PM_2.5RT and was 0.94 and 0.83, respectively, with a coefficient of variation (CV) of 84% and 52%, respectively; the corresponding linear regression model had a CV of 54% and 25%. For BC, the average correction factor utilizing the BC_RT and SKC BC was 0.74 with a CV of 36% with the associated linear regression model producing a CV of 56%. The results from this study will help ensure that the real-time exposure monitors are capable of detecting an estimated PM_2.5 after an appropriate statistical model is applied.

Copyright © 2019 American Association for Aerosol Research     

Purification of Recombinant Human Serum Albumin (rHSA) Produced by Genetically Modified Pichia Pastoris

Abstract

Recombinant human serum albumin (rHSA) was produced by genetically transformed Pichia pastoris yeast. The cell-culture supernatant (CCS) contained 8–12 g/l rHSA that was purified in a three-step procedure involving (1 Andersson , L.O. ; Lundén , R. ( 1976 ) In: Plasma Proteins , Blombäck , B. ; Hanson , L.Å. , eds.; AB KABI, AWE/GEBERS , Bohuslänningen AB : Uddevalla , 31 – 34 . [Google Scholar]) a capture step using the newly developed cation exchanger Capto^TM MMC; (2 The Green Cross Corp. (Japan) : ( 1993 ) Recombinant human serum albumin, process for producing the same and pharmaceutical preparation containing the same . European Patent Application, Publication number: 0 570 916 A2 . [Google Scholar]) an intermediate step using Phenyl Sepharose^TM and, (3 The Green Cross Corp. (Japan) : ( 1995 ) Recombinant human serum albumin, process for producing the same and pharmaceutical preparation containing the same . U S Patent 5, 440, 018 . [Google Scholar]) a polishing step using Aminobutyl Sepharose^TM 6 FF. The total recovery was 25–35% and the product fulfils the purity criteria of the European Pharmacopeia.

Purified rHSA and plasma-derived HSA were essentially identical judging by SDS- or native-PAGE, and the pigment level (expressed as A₃₅₀/A₂₈₀) in the rHSA was 0.03 or less and was strongly dependent on the quality of the CCS. Dimers and polymers in the final product were less than that found in purified plasma-derived HSA. The molar mass of the purified rHSA, as well as of its natural counterpart, is 67 000 Daltons by MALDI-ToF mass spectrometry, while the iso-electric points of both recombinant and natural HSA ranged between pH 5.42–5.55 when determined in 8 M urea. The stability profiles of both proteins after heat treatment were identical as determined by differential scanning calorimetry (DSC). The results obtained here suggest the purified rHSA to be a homogeneous protein identical to its natural counterpart.     

Short-term effects of fine particulate matter and ozone on the cardiac conduction system in patients undergoing cardiac catheterization

Background

Air pollution-induced changes in cardiac electrophysiological properties could be a pathway linking air pollution and cardiovascular events. The evidence of air pollution effects on the cardiac conduction system is incomplete yet. We investigated short-term effects of particulate matter ≤ 2.5 μm in aerodynamic diameter (PM_2.5) and ozone (O₃) on cardiac electrical impulse propagation and repolarization as recorded in surface electrocardiograms (ECG).

Methods

We analyzed repeated 12-lead ECG measurements performed on 5,332 patients between 2001 and 2012. The participants came from the Duke CATHGEN Study who underwent cardiac catheterization and resided in North Carolina, United States (NC, U.S.). Daily concentrations of PM_2.5 and O₃ at each participant’s home address were predicted with a hybrid air quality exposure model. We used generalized additive mixed models to investigate the associations of PM_2.5 and O₃ with the PR interval, QRS interval, heart rate-corrected QT interval (QTc), and heart rate (HR). The temporal lag structures of the associations were examined using distributed-lag models.

Results

Elevated PM_2.5 and O₃ were associated with four-day lagged lengthening of the PR and QRS intervals, and with one-day lagged increases in HR. We observed immediate effects on the lengthening of the QTc interval for both PM_2.5 and O₃, as well as delayed effects for PM_2.5 (lagged by 3 – 4 days). The associations of PM_2.5 and O₃ with the PR interval and the association of O₃ with the QRS interval persisted until up to seven days after exposure.

Conclusions

In patients undergoing cardiac catheterization, short-term exposure to air pollution was associated with increased HR and delays in atrioventricular conduction, ventricular depolarization and repolarization.

     

Study on the Preparation and Characterization of Biodegradable Polylactide/SiO2–TiO2 Hybrids

In this study, the silicic acid produced from sodium metasilicate hydrate and titanium tetraisopropylate were chosen as the ceramic precursors for the modification of biodegradable polylactide (PLA) through an in situ sol-gel process and the melt blending method. In addition, acrylic acid grafted polylactide (PLA-g-AA) was studied as an alternative to PLA. Hybrids were characterized by Fourier transform infrared spectroscopy, ²⁹ Kumar , P. ; Badrinarayanan , M.S. ; Sastry , M. Nanocrystalline TiO₂ studied by optical, FTIR and X-ray photoelectron spectroscopy: correlation to presence of surface states . Thin Solid Films 2000 , 358 , 122 – 130 .[Crossref], [Web of Science ®] , [Google Scholar]Si solid-state nuclear magnetic resonance (NMR), thermogravimetry analysis (TGA), scanning electron microscope (SEM), and Instron mechanical tester. The result was that properties of the PLA-g-AA/SiO₂–TiO₂ hybrid were superior to those of the PLA/SiO₂–TiO₂ hybrid. This was because the carboxylic acid groups of acrylic acid acted as coordination sites for the silica-titania phase to allow the formation of stronger chemical bonds. The ²⁹ Kumar , P. ; Badrinarayanan , M.S. ; Sastry , M. Nanocrystalline TiO₂ studied by optical, FTIR and X-ray photoelectron spectroscopy: correlation to presence of surface states . Thin Solid Films 2000 , 358 , 122 – 130 .[Crossref], [Web of Science ®] , [Google Scholar]Si solid-state NMR showed that Si atoms coordinated around SiO₄ units were predominantly Q₃ and Q₄. The 10 wt.% SiO₂–TiO₂ content gave the maximum values of tensile strength and glass transition temperature in PLA/SiO₂–TiO₂ and PLA-g-AA/SiO₂–TiO₂ both because excess SiO₂–TiO₂ particles caused separation between the organic and inorganic phases.     

Reversible addition-fragmentation chain transfer polymerization of vinyl acetate and vinyl pivalate in supercritical carbon dioxide

Two highly supercritical CO₂-soluble, poly(vinyl acetate) (PVAc)-based macro-reversible addition-fragmentation chain transfer (RAFT) agents were synthesized. The RAFT agents were used for the first time in RAFT/macromolecular design via the interchange of xanthates (MADIX) and polymerization of vinyl acetate (VAc) and vinyl pivalate (VPi) in supercritical carbon dioxide (scCO₂). A homopolymer PVAc and a block copolymer PVAc-b-PVPi made by RAFT/MADIX polymerization were characterized, and the effects of time and RAFT agents on polymerization were examined. For the 8.4 wt% RAFT agent in VAc, the molecular mass (M _n ) of homopolymer PVAc was 26,000 g mol^?1 and PDI was 1.35. For the copolymerization of VPi using 9.8 wt% PVAc-RAFT agent in VPi for 24 h, the M _n and PDI of PVAc-b-PVPi reached 32,400 g mol^?1 and 1.42, respectively. These results suggest that the polydispersity can be controlled during the clean production of PVAc and PVPi by RAFT/MADIX polymerization in scCO₂.     

Characteristics of secondhand electronic cigarette aerosols from active human use

The electronic cigarette (EC) is a new source of indoor airborne particles. To better understand the impacts of secondhand vaping (SHV) emissions on indoor air quality, real-time measurements of particle size distribution, particle number concentration (PNC), fine particulate matter (PM_2.5), CO₂, CO, and formaldehyde were conducted before, during, and after 10 min EC-use among 13 experienced users in an 80 m³ room. To assess particle transport in the room, multiple sampling locations were set up at 0.8, 1.5, 2.0, and 2.5 m away from the subjects. The arithmetic mean (standard deviation) of background PNC and PM_2.5 concentrations in the room were 6.39 × 10³ (1.58 × 10²) particles/cm³ and 8 (1) μg/m³, respectively. At 0.8 m away from EC users, right after initiation of puffing, the PNC and PM_2.5 concentrations can reach a peak of ～10⁵ particles/cm³ and ～3 × 10³ µg/m³, respectively, and then dropped quickly to background levels within 20 s due to dilution and evaporation. At the 0.8 m sampling location, the mean PNC and PM_2.5 concentrations during puffing were 2.48 × 10⁴ (2.14 × 10⁴) particles/cm³ and 188 (433) µg/m³, respectively. In addition, two modes of SHV particles were observed at about 15 and 85 nm. Moreover, concentrations of SHV particles were negatively correlated with the distances to EC users. At the 1.5 m location, PNC and PM_2.5 levels were 9.91 × 10³ (1.76 × 10³) particles/cm³ and 19 (14) µg/m³, respectively. Large variations of mean PNC levels exhaled per puff were observed both within and between EC users. Data presented in this study can be used for SHV particle exposure assessment.

Copyright © 2017 American Association for Aerosol Research     

Gold Nanoparticles-Decorated Dithiocarbamate Nanocomposite: An Efficient Heterogeneous Catalyst for the Green A<Superscript>3</Superscript>-Coupling Synthesis of Propargylamines

Gold nanoparticles decorated magnetic dithiocarbamate nanocomposite (Au@CS₂–AP@Fe₃O₄) led to a suitable catalyst for the propargylamines synthesis via A³-coupling reaction in water. The prepared catalyst was characterized by Fourier-transform infrared spectroscopy, thermogravimetric analysis, X-ray diffraction, atomic absorption spectroscopy, scanning electron microscopy, and energy-dispersive X-ray spectroscopy measurements.

Graphical Abstract

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