One-Step Synthesis of CuxOy/TiO2 Photocatalysts by Laser Pyrolysis for Selective Ethylene Production from Propionic Acid Degradation.

In an effort to produce alkenes in an energy-saving way, this study presents for the first time a photocatalytic process that allows for the obtention of ethylene with high selectivity from propionic acid (PA) degradation. To this end, TiO2 nanoparticles (NPs) modified with copper oxides (CuxOy/TiO2) were synthetised via laser pyrolysis. The atmosphere of synthesis (He or Ar) strongly affects the morphology of photocatalysts and therefore their selectivity towards hydrocarbons (C2H4, C2H6, C4H10) and H2 products. Specifically, CuxOy/TiO2 elaborated under He environment presents highly dispersed copper species and favours the production of C2H6 and H2. On the contrary, CuxOy/TiO2 synthetised under Ar involves copper oxides organised into distinct NPs of ~2 nm diameter and promotes C2H4 as the major hydrocarbon product, with selectivity, i.e., C2H4/CO2 as high as 85% versus 1% obtained with pure TiO2.

TiO2 Catalyzed Dihydroxyacetone (DHA) Conversion in Water: Evidence That This Model Reaction Probes Basicity in Addition to Acidity.

In this paper, evidence is provided that the model reaction of aqueous dihydroxyacetone (DHA) conversion is as sensitive to the TiO2 catalysts' basicity as to their acidity. Two parallel pathways transformed DHA: while the pathway catalyzed by Lewis acid sites gave pyruvaldehyde (PA) and lactic acid (LA), the base-catalyzed route afforded fructose. This is demonstrated on a series of six commercial TiO2 samples and further confirmed by using two reference catalysts: niobic acid (NbOH), an acid catalyst, and a hydrotalcite (MgAlO), a basic catalyst. The original acid-base properties of the six commercial TiO2 with variable structure and texture were investigated first by conventional methods in gas phase (FTIR or microcalorimetry of pyridine, NH3 and CO2 adsorption). A linear relationship between the initial rates of DHA condensation into hexoses and the total basic sites densities is highlighted accounting for the water tolerance of the TiO2 basic sites whatever their strength. Rutile TiO2 samples were the most basic ones. Besides, only the strongest TiO2 Lewis acid sites were shown to be water tolerant and efficient for PA and LA formation.

Influence of the Micro-Nanostructuring of Titanium Dioxide Films on the Photocatalytic Degradation of Formic Acid under UV Illumination.

Surface micro-nanostructuring can provide new functionalities and properties to coatings. For example, it can improve the absorption efficiency, hydrophobicity and/or tribology properties. In this context, we studied the influence of micro-nanostructuring on the photocatalytic efficiency of sol-gel TiO2 coatings during formic acid degradation under UV illumination. The micro-nanostructuring was performed using the UV illumination of microspheres deposited on a photopatternable sol-gel layer, leading to a hexagonal arrangement of micropillars after development. The structures and coatings were characterized using Raman spectroscopy, ellipsometry, atomic force microscopy and scanning electron microscopy. When the sol-gel TiO2 films were unstructured and untreated at 500 °C, their effect on formic acid's degradation under UV light was negligible. However, when the films were annealed at 500 °C, they crystallized in the anatase phase and affected the degradation of formic acid under UV light, also depending on the thickness of the layer. Finally, we demonstrated that surface micro-nanostructuring in the form of nanopillars can significantly increase the photocatalytic efficiency of a coating during the degradation of formic acid under UV light.

Pickering Emulsions of Fluorinated TiO2: A New Route for Intensification of Photocatalytic Degradation of Nitrobenzene.

Fluorination of the TiO2 surface has been often reported as a tool to increase the photocatalytic efficiency due to the beneficial effects in terms of production of oxidizing radicals. Moreover, it is shown that the unique amphiphilic properties of the fluorinated TiO2 (TiO2-F) surface allow one to use this material as a stabilizer for the formulation of Pickering emulsions of poorly soluble pollutants such as nitrobenzene (NB) in water. The emulsions have been characterized in terms of size of the droplets, type of emulsion, possibility of phase inversion, contact angle measurements, and optical microscopy. The emulsified system presents micrometer-sized droplets of pollutant surrounded by the TiO2-F photocatalyst. Consequently, the system can be considered to be composed of microreactors for the degradation of the pollutant, which maximize the contact area between the photocatalyst and substrate. The enhanced photocatalytic activity of TiO2-F was confirmed in the present paper as the apparent rate constants of NB photodegradation were 16 × 10-3 and 12 × 10-3 min-1 for fluorinated and bare TiO2, respectively. At NB concentrations largely exceeding its solubility, the rate constant was 0.04 × 10-3 min-1 in the presence of both TiO2 and TiO2-F. However, unlike TiO2, TiO2-F stabilized NB/water emulsions and, under these conditions, the efficiency of NB photocatalytic degradation in the emulsified system was ca. 18 times higher than in the nonemulsified one. This result is relevant also in terms of practical applications because it opens the route to one-pot treatments of biphasic polluted streams without the need of preliminary physical separation treatments.

Room-temperature conversion of Cu2-xSe to CuAgSe nanoparticles to enhance the photocatalytic performance of their composites with TiO2.

Rational design and precise engineering are needed to optimize the structural and chemical parameters of functional materials. In this work, we demonstrate how pre-formed binary metal selenides can be an excellent synthetic choice for the synthesis of ternary coinage metal selenide nanoparticles (NPs) with controlled composition. The mild conditions required to obtain these ternary coinage metal selenide NPs offered an easy synthesis of n% CuAgSe-TiO2 (n = 0.01, 0.1, 0.3 and 1.0 mol%) nanocomposites for photocatalytic applications without compromising the structural and morphological characteristics of TiO2 and without having any organic ligands around the NPs. The use of ternary metal selenide nanocomposites CuAgSe-TiO2 results in a clear improvement in their photocatalytic activity for the photodegradation of formic acid as compared to the well-known benchmark for photocatalysis, TiO2 (P25), and its binary metal selenide nanocomposites Cu2-xSe-TiO2. DFT calculations establish semi-metallic behavior of CuAgSe NPs and show that CuAgSe-TiO2 forms a semimetallic-semiconductor heterojunction allowing a better charge separation to enhance its photocatalytic activity.

Photocatalytic Degradation Enhancement in Pickering Emulsions Stabilized by Solid Particles of Bare TiO2.

Pickering emulsions provide a new way to enhance the efficiency of photocatalytic degradation of water-insoluble pollutants. Indeed, the semiconductor solid particles dually act as the photocatalyst and stabilizer of the emulsion droplets whose size dramatically affects the photocatalytic reaction. The present work aims at the validation of this concept by using bare TiO2 without any surface modification. Nanostructured TiO2 has been prepared by a simple sol-gel process and characterized by X-ray diffraction, specific surface area analysis, scanning electron microscopy, and diffuse reflectance spectroscopy. The emulsions were prepared by using 1-methylnaphthalene (1-MN) as a model organic contaminant scarcely soluble in water and bare TiO2 as the photocatalyst/stabilizer. The emulsions have been characterized by electrical conductivity, optical microscopy, and light-scattering analyses. The photocatalytic degradation of 1-MN was 50 times faster in stable Pickering emulsions with respect to the case of biphasic liquid systems containing TiO2. This finding allows us to propose Pickering emulsions stabilized by TiO2 nanoparticles as an effective and novel way to intensify the photocatalytic degradation of water-insoluble organic pollutants.

Precursor-mediated synthesis of Cu2-xSe nanoparticles and their composites with TiO2 for improved photocatalysis.

The direct synthesis of copper selenide nanoparticles from the reaction of ditertiarybutyl selenide tBu2Se with copper(ii) trifluoroacetate Cu(TFA)2 under mild conditions is reported. The isolation of a molecular species during the course of this reaction, established as [Cu2(TFA)2(tBu2Se)3], by spectroscopic studies and single crystal X-ray structure analysis, confirmed that metal selenide NPs are formed via this intermediate species containing a reduced copper center. Extending this reaction in the presence of commercial TiO2 (P25) offered an easy synthesis of copper selenide-titania nanocomposites with different Cu/Ti ratios. These nanocomposites, well-characterized by powder XRD, STEM, TEM, BET, XPS, EDX and UV-Vis studies, were examined as photocatalysts for the degradation of formic acid (FA). The nCu2-xSe-TiO2 nanocomposites with low mol% of copper selenide, i.e. n = 0.1 and 0.3 mol%, displayed a superior catalytic activity over P25, which is an established benchmark for photocatalysis under UV light.

Influenza viruses production: Evaluation of a novel avian cell line DuckCelt®-T17.

The influenza vaccine manufacturing industry is looking for production cell lines that are easily scalable, highly permissive to multiple viruses, and more effective in term of viral productivity. One critical characteristic of such cell lines is their ability to grow in suspension, in serum free conditions and at high cell densities. Influenza virus causing severe epidemics both in human and animals is an important threat to world healthcare. The repetitive apparition of influenza pandemic outbreaks in the last 20years explains that manufacturing sector is still looking for more effective production processes to replace/supplement embryonated egg-based process. Cell-based production strategy, with a focus on avian cell lines, is one of the promising solutions. Three avian cell lines, namely duck EB66®cells (Valneva), duck AGE.CR® cells (Probiogen) and quail QOR/2E11 cells (Baxter), are now competing with traditional mammalian cell platforms (Vero and MDCK cells) used for influenza vaccine productions and are currently at advance stage of commercial development for the manufacture of influenza vaccines. The DuckCelt®-T17 cell line presented in this work is a novel avian cell line developed by Transgene. This cell line was generated from primary embryo duck cells with the constitutive expression of the duck telomerase reverse transcriptase (dTERT). The DuckCelt®-T17 cells were able to grow in batch suspension cultures and serum-free conditions up to 6.5×106cell/ml and were easily scaled from 10ml up to 3l bioreactor. In the present study, DuckCelt®-T17 cell line was tested for its abilities to produce various human, avian and porcine influenza strains. Most of the viral strains were produced at significant infectious titers (>5.8 log TCID50/ml) with optimization of the infection conditions. Human strains H1N1 and H3N2, as well as all the avian strains tested (H5N2, H7N1, H3N8, H11N9, H12N5) were the most efficiently produced with highest titre reached of 9.05 log TCID50/ml for A/Panama/2007/99 influenza H3N2. Porcine strains were also greatly rescued with titres from 4 to 7 log TCID50/ml depending of the subtypes. Interestingly, viral kinetics showed maximal titers reached at 24h post-infection for most of the strains, allowing early harvest time (Time Of Harvest: TOH). The B strains present specific production kinetics with a delay of 24h before reaching the maximal viral particle release. Process optimization on H1N1 2009 human pandemic strain allowed identifying best operating conditions for production (MOI, trypsin concentration, cell density at infection) allowing improving the production level by 2 log. Our results suggest that the DuckCelt®-T17 cell line is a very promising platform for industrial production of influenza viruses and particularly for avian viral strains.

Laser synthesized TiO2-based nanoparticles and their efficiency in the photocatalytic degradation of linear carboxylic acids.

Titanium dioxide nanoparticles were synthesized by laser pyrolysis, their surface and electronic properties were modified by gold and/or nitrogen. These materials were characterized by different techniques like X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and electron paramagnetic resonance (EPR). Time resolved conductivity (TRMC) was used to study the charge separation of electron/hole pairs. Altogether (XPS, EPR, TRMC), the physicochemical characterizations are well correlated with chemical photoactivity of the different samples. Their photocatalytic activity was evaluated for the degradation of linear carboxylic acids (C2-C3) under UV and visible illumination. The decomposition rate of acids was measured, it shows that the modification with gold increases the photoactivity while the presence of nitrogen slows down the process. Such observations are in good agreement with evolution of TRMC signals. A degradation pathway has been determined by identification of intermediate products by chromatography and EPR, results show different intermediate species. In particular EPR confirms the presence of NO2- paramagnetic centers and shows two novel N centered paramagnetic centers. A decrease of the degradation rate is observed with increase of carboxylic acid chain length.

A Facile Molecular Precursor-based Synthesis of Ag2 Se Nanoparticles and Its Composites with TiO2 for Enhanced Photocatalytic Activity.

The reactions of different silver(I) reagents AgX (X(-) =iodide, trifluoroacetate, triflate) with selenoethers R2 Se (R=Me, tBu) in a variety of solvents were investigated in relation with their use as precursors for Ag2 Se nanomaterials. Different reaction conditions led to different reactivities and afforded either molecular complexes or metal selenide nanoparticles. The reactions leading to in situ formation of the metal selenide nanoparticles were then extended in the presence of commercial TiO2 (P25) to prepare silver selenide-titania nanocomposites with different Ag/Ti ratios. These nanocomposites, well characterized by elemental analysis (Ag, Se), PXRD, TEM, BET, XPS and UV/Vis studies, were investigated as photocatalysts for the degradation of formic acid (FA) solution. The xAg2 Se-TiO2 nanocomposites (x=0.01, 0.13 and 0.25 mol %) exhibited a much higher catalytic activity as compared to P25, which is an established benchmark for the photocatalysis under UV light, and retained a good photocatalytic stability after recycling for several times.

Impact of photocatalysis on fungal cells: depiction of cellular and molecular effects on Saccharomyces cerevisiae.

We have investigated the antimicrobial effects of photocatalysis on the yeast model Saccharomyces cerevisiae. To accurately study the antimicrobial mechanisms of the photocatalytic process, we focused our investigations on two questions: the entry of the nanoparticles in treated cells and the fate of the intracellular environment. Transmission electronic microscopy did not reveal any entry of nanoparticles within the cells, even for long exposure times, despite degradation of the cell wall space and deconstruction of cellular compartments. In contrast to proteins located at the periphery of the cells, intracellular proteins did not disappear uniformly. Disappearance or persistence of proteins from the pool of oxidized intracellular isoforms was not correlated to their functions. Altogether, our data suggested that photocatalysis induces the establishment of an intracellular oxidative environment. This hypothesis was sustained by the detection of an increased level of superoxide ions (O2°(-)) in treated cells and by greater cell cultivability for cells expressing oxidant stress response genes during photocatalytic exposure. The increase in intracellular ROS, which was not connected to the entry of nanoparticles within the cells or to a direct contact with the plasma membrane, could be the result of an imbalance in redox status amplified by chain reactions. Moreover, we expanded our study to other yeast and filamentous fungi and pointed out that, in contrast to the laboratory model S. cerevisiae, some environmental strains are very resistant to photocatalysis. This could be related to the cell wall composition and structure.

Cognitive therapy versus Rogerian supportive therapy in borderline personality disorder. Two-year follow-up of a controlled pilot study.

BACKGROUND: To date, there have been no studies comparing cognitive therapy (CT) with Rogerian supportive therapy (RST) in borderline personality disorder. METHOD: Sixty-five DSM-IV borderline personality disorder outpatients were recruited at 2 centres: Lyon and Marseille. Thirty-three patients were randomly allocated to CT and 32 to RST. The therapists were the same in both groups. Both treatments shared the same duration (1 year) and amount of therapy. Assessment by independent evaluators utilised the Clinical Global Impression (CGI) Scale, the Hamilton Depression Scale, Beck Depression Inventory, Beck Anxiety Inventory, Hopelessness Scale, Young Schema Questionnaire II, Eysenck Impulsivity Venturesomeness Empathy (IVE) Inventory, a self-harming behaviours checklist and scales measuring quality of life and the therapeutic relationship. The response criterion was a score of 3 or less on the CGI, associated with a Hopelessness Scale score of <8. RESULTS: No patient committed suicide during the trial. Fifty-one patients were evaluated at week 24, 38 at week 52 and 21 at week 104. Cognitive therapy retained the patients in therapy for a longer time. The response criterion found no significant between-group differences at any measurement point in the completers. However, at week 24, CT was better than RST on the Hopelessness Scale, IVE scale and regarding the therapeutic relationship. At week 104, the CGI improvement (patient and evaluator) was significantly better in CT than in RST. High baseline depression and impulsivity predicted dropouts. CONCLUSIONS: CT retained the patients in therapy longer, showed earlier positive effects on hopelessness and impulsivity, and demonstrated better long-term outcomes on global measures of improvement.

Photocatalytic degradation of diuron: experimental analyses and simulation of HO degrees radical attacks by density functional theory calculations.

The photocatalytic oxidation of diuron has been performed in presence of TiO(2) suspensions. To better understand the mechanistic details of the hydroxyl radical attack on diuron, computational methods were carried out. The combination of experimental and computational methods has been employed to establish the main degradation pathways of diuron. After identification of the majority of first byproduct, the experimental study underlined that substitution of chlorines and hydroxylation by hydroxyl radicals are the main diuron degradation pathways, in agreement with MOPAC and DFT simulations carried out in the gas phase. In addition, these calculations revealed that the aromatic ring attack is led by a HO degrees addition and not a hydrogen abstraction and the main first byproduct, monochlorohydroxylated compounds, are obtained by concerted reactions.

Randomized controlled comparison of cognitive behavior therapy with Rogerian supportive therapy in chronic post-traumatic stress disorder: a 2-year follow-up.

BACKGROUND: To date, there have been no studies comparing cognitive behavior therapy (CBT) with Rogerian therapy in post-traumatic stress disorder. METHOD: Sixty outpatients with DSM-IV chronic post-traumatic stress disorder were randomized into two groups for 16 weekly individual sessions of CBT or Rogerian supportive therapy (ST) at two centers. No medication was prescribed. Measures included the Post-Traumatic Stress Disorder Checklist Scale (PCLS), the Hamilton Anxiety Scale, Beck Depression Inventory, and Quality of Life. The general criterion of improvement (GCI) was a score of less than 44 on the PCLS. RESULTS: Forty-two patients were evaluated at post-test, 38 at week 52 and 25 at week 104. At post-test, the rate of patients leaving the trial due to worsening or lack of effectiveness was significantly higher in the ST group (p = 0.004). At this point, no between-group difference was found on the GCI and any of the rating scales. Intent-to-treat analysis found no difference for the GCI, but patients in the CBT group showed greater improvement on the PCLS and Hamilton Anxiety Scale. Naturalistic follow-up showed sustained improvement without between-group differences at weeks 52 and 104. CONCLUSIONS: CBT retained significantly more patients in treatment than ST, but its effects were equivalent to those of ST in the completers. CBT was better in the dimensional intent-to-treat analysis at post-test.

Microbiological disinfection of water and air by photocatalysis.

This article is aimed at presenting (i) a fundamental research on the efficiency of photocatalysis in water disinfection and (ii) the efficiency of a photocatalytic prototype, developed by Buxair firm, to remove avian influenza virus in air. In water disinfection, two model strains of Escherichia coli (K12 PHL849 and K12 PHL1273) were selected and a comparison of the efficiencies of TiO2 Degussa P-25 versus TiO2 Millennium PC500 were estimated. A more important inactivation of E. coli PHL1273 was obtained on TiO2 Millennium PC500, in line with its better adherence on this solid. An experimental study was performed using a dialysis membrane to investigate the impact of the contact between the microorganisms and the photocatalyst and to determine the role of H2O2 generated in situ. In air disinfection, a total inactivation of virus A/H5N2, close to avian influenza virus A/H5N2, was obtained in a single pass in the Buxair® gas phase dynamic photoreactor using a contaminated air flow rate of 40 m3/h.

Dans cette publication, nous rapportons une étude fondamentale sur l'efficacité du procédé photocatalytique pour éliminer les bactéries présentes en solution aqueuse ainsi qu'une étude préliminaire concernant l'efficacité d'un prototype photocatalytique, développé par la société Buxair, pour éliminer le virus de la grippe aviaire présent dans l'air. En phase aqueuse, deux souches de E. coli ont été sélectionnées (la souche K12 PHL849 et la souche K12 PHL1273) et inactivées en présence de deux photocatalyseurs. Une inactivation beaucoup plus importante de la souche adhérente (PHL1273) se produit en présence du photocatalyseur TiO2 PC500. L'importance du contact entre photocatalyseur et bactérie et le rôle du peroxyde d'hydrogène susceptible d'être produit lors du procédé photocatalytique sont étudiés en utilisant une membrane de dialyse.

Photocatalytic degradation of p-halophenols in TiO2 aqueous suspensions: halogen effect on removal rate, aromatic intermediates and toxicity variations.

The influence of the halogen upon the TiO(2) photocatalytic degradation of p-halophenols in water has been investigated. Phenol was used as the reference compound. Compared with its value for phenol, the apparent first-order rate constant of removal, k, was slightly but significantly higher for p-fluorophenol and p-chlorophenol, and slightly but significantly lower for p-bromophenol. For p-iodophenol, k was about half that of phenol. The relative values confirm that k is roughly correlated to the Hammett constant; this constant reflects the electron density on the aromatic ring and, accordingly, the reactivity towards electrophilic species generated by UV-irradiation of TiO(2). All compounds were found to be poorly adsorbed on TiO(2). Accordingly, k was not related to the differences observed in the very low adsorbed amounts. The detected aromatic intermediate products included hydroquinone (HQ), benzoquinone (BQ) and various halodihydroxybenzenes. HQ, BQ, 4-chloro-1,2 (and 1,3)-dihydroxybenzenes and 4-bromo-1,3-dihydroxybenzene were quantified. Mechanisms are tentatively suggested to interpret the differences in the degradation pathways of the p-halophenols. The organic intermediate products accounted for only a few percents of the total carbon during the degradation. The toxicity (1/EC50) measured by the Microtox test almost did not vary in the course of the degradation of phenol, p-chlorophenol and p-bromophenol until complete removal of these compounds. By contrast, the value of 1/EC50 was multiplied by ca. 2.5 when ca. 45% of p-iodophenol had been removed; concentrations of BQ higher than with the other p-halophenols are tentatively suggested to be at the origin of this increase. Interpretation of a surprising substantial increase in the 1/EC50 value when the removal of p-fluorophenol increased from 80 to 95% requires further investigation.

Degradation mechanism of t-butyl methyl ether (MTBE) in atmospheric droplets.

The aim of this study was to obtain information about the degradation of t-butyl methyl ether (MTBE; (CH(3))(3)C-O-CH(3)) in atmospheric water droplets (rain, clouds, fog). These water droplets contain hydrogen peroxide and iron ions, which are a source of the powerful oxidising radical OH degrees, particularly under solar irradiation (photo-Fenton reaction). MTBE was chosen for this work because of its current use as an oxygenated additive in gasoline. In this study we found that MTBE is not stable in the atmosphere. More than 15 intermediate products were identified, five of which were quantified (t-butyl formate (TBF), methyl acetate (MA), t-butyl alcohol (TBA), acetone (AC), formaldehyde). The evaluation of the disappearance kinetic of the main intermediate compounds shows the following activity pattern k((TBA))>k((MTBE))>k((TBF)),k>((AC)). Acetone was found to be about 15 times more stable than MTBE in atmospheric conditions. The degradation pathways are discussed on the basis of these identifications and on the degradation of the main intermediate products in similar conditions to MTBE.

Degradation pathway of dicyclanil in water in the presence of titanium dioxide. Comparison with photolysis.

The solar photolytic behavior of the pesticide 4,6-diamino-2-cyclopropyl-pyrimidine-5-carbonitrile, currently known as dicyclanil, has been mimicked in a photoreactor operating with an artificial light flux. The rate and pathway of degradation were performed. An additional study, using TiO(2) photocatalysis, has been achieved in order to determine the efficiency of photocatalysis to degrade the molecule. The catalyst was titania Degussa P-25. The aim of this article was the identification of the intermediate products formed during the irradiation, to establish the degradation pathway of dicyclanil. The kinetics of the reactions were followed by liquid chromatography with a diode array detector (LC-DAD). Most of the organic compounds occurring during the photodegradation have been identified by means of liquid chromatography and mass spectrometry coupled techniques (HPLC-MS). Additional analyses were carried out to evaluate the mineralization rates into nitrate and ammonium ions.

The validation of the Posttraumatic Stress Disorder Checklist Scale in posttraumatic stress disorder and nonclinical subjects.

BACKGROUND: The Posttraumatic Stress Disorder Checklist Scale (PCLS) is a short self-report inventory for assessing the 3 main syndromes of Posttraumatic Stress Disorder (PTSD). The aim of this study was the validation of the French version of the PCLS in PTSD subjects and nonclinical subjects. METHODS: One-hundred and thirteen outpatients suffering from PTSD according to DSM-IV were administered the PCLS. The patients' scores on the PCLS were then compared to those of 31 nonclinical control subjects. Thirty-five of the patients were administered the PCLS twice over an interval of 1-2 weeks and also completed questionnaires measuring depression, phobia and anxiety. RESULTS: The patients' total score and subscores on the PCLS were found to be significantly higher than those of control subjects. The cutoff score of 44 on the French version PCLS distinguishes well between the PTSD group and control group with a high diagnostic efficacy (0.94). Factor analysis revealed 3 main factors corresponding to the reexperiencing, numbing and hyperarousal syndromes. The PCLS showed satisfactory test-retest reliability and internal consistency. CONCLUSIONS: The PCLS is therefore a valid and effective measurement of PTSD. It may be a useful tool for screening and assessing PTSD in psychiatric as well as in primary-care settings.