Dual-output kilohertz pump laser for high-energy picosecond OPCPA.

A dual-output thin-disk picosecond laser operating at 100 W with 1 kHz repetition rate is reported in this Letter. By electronically adjusting the amplitude of the optical seed pulses that are injected into the laser cavity, the energy extracted from the gain medium can be shared between two pulses. Amplified double pulses are subsequently spatially separated into two independent beams by a fast Pockels cell, compressed in one common compressor, and frequency-doubled with ∼70% efficiency. This approach significantly decreases strain on the optics, as well as nonlinear effects, and is advantageous for power scaling.

120 mJ, 1 kHz, picosecond laser at 515 nm.

We report on a 1 kHz, 515 nm laser system, based on a commercially available 230 W average power Yb:YAG thin-disk regenerative amplifier, developed for pumping one of the last optical parametric chirped pulse amplification (OPCPA) stages of the Allegra laser system at ELI Beamlines. To avoid problems with self-focusing of picosecond pulses, the 1030 nm output pulses are compressed and frequency doubled with an LBO crystal in vacuum. Additionally, development of a thermal management system was needed to ensure stable phase matching conditions at high average power. The resulting 515 nm pulses have an energy of more than 120 mJ with SHG efficiency of 60% and an average RMS stability of 1.1% for more than 8 h.

Degradation of N-Nitrosodiethylamine in aqueous solution by gamma-irradiation.

N-Nitrosodiethylamine (NNDEA) is a toxic compound which is affranchised into the medium mostly via industrial wastewater. For the investigation of degradation mechanism of NNDEA, the aqueous solutions of NNDEA were exposed to Advanced Oxidation processes (AOP's) such as gamma-irradiation, ozonation, UV irradiation and UV/Ozone (ozone effect) and UV/H2O2 (hydrogen peroxide effect). Since the structure of NNDEA is small, it is rapidly degraded in all processes except UV-irradiation process but forming acetic acid and formic acid just was seen in gamma and UV/H2O2processes. In the other processes, NNDEA is transformed directly to nitrite and nitrate which they can form NNDEA again in the medium. The concentration of NNDEA was decreased from 50 to 21 mg L-1 after 2.20 kGy gamma-irradiation. After 2.85 kGy gamma irradiation, NNDEA was completely removed from the medium. The results showed that the concentration of NNDEA decreased with UV-irradiation time, the concentration of 50 mg L-1 NNDEA was 42, 30, 24 and 19 mg L-1 after 10, 20, 40 and 60 min UV-irradiation, respectively. It has been investigated that the UV-irradiation does not have much effect on the degradation of 50 mg L-1 NNDEA solution and requires long-term irradiation. In this study, gamma-irradiation was chosen as the best method because of the complete degradation effect and the prevention of the reformation of the NNDEA.

The effect of ozonation on the degradation of carbaryl in aqueous solution.

The aim of this study is to investigate the synergetic effect of ozonation on ultraviolet irradiation on the degradation of carbaryl (CBL) (1-naphthyl-N-methylcarbamate) in aqueous solutions (40 mg L-1). The degradation of CBL and the intermediates formed during ozonation were determined by gas chromatography-mass spectrometer. The change in formaldehyde, dissolved oxygen, pH, and total acidity were determined as a function of ozonation time. It was found that the dissolved oxygen and total acidity were increased with the increasing ozonation time but the pH was decreased with the increasing ozonation time. The aliphatic acids formed during ozonation were followed by ion chromatography as a function of ozonation time. It was found that the effect of ozonation is highly effective on the degradation of CBL. The complete degradation of CBL has occurred at 75-second ozonation time. As a consequence of the obtained results the possible degradation pathway was proposed. The results confirmed that ozonation is an effective method for the degradation of CBL.

Extraction, characterization and comparison of chitins from large bodied four Coleoptera and Orthoptera species.

Chitins were extracted from large insect species of order Coleoptera (Lucanus cervus (Linnaeus, 1758) (Lucanidae) and Polyphylla fullo (Linnaeus, 1758) (Scarabaeidae) and order Orthoptera (Bradyporus (Callimenus) sureyai Ünal, 2011) (Tettigonidae) and Gryllotalpa gryllotalpa (Linnaeus, 1758) (Gryllotalpidae)) for the first time. Fourier Transform Infrared Spectrometry (FT-IR) confirms that isolation of chitin is successful. Yields of chitins on dry basis from P. fullo, L. cervus, G. gryllotalpa and B. (C.) sureyai are 11.3%, 10.9%, 10.1% and 9.8% respectively. Thermogravimetric Analysis (TGA) showed a variety of thermal stability of chitin samples from 614 °C to 748 °C with a small percent of ash. X-ray diffraction (XRD) data showed a crystallinity index percent from 80.6% to 85.2%. Scanning Electron Microscope (SEM) was examined for surface characterization determining as fibrous and porous for all species and changes from nm scales to µm scales. Elemental analysis has been applied to determine the elemental composition of chitin and nitrogen percent was relatively low for all specimens than expected. It is detected that examined insects have α-chitin form from XRD and FT-IR data. If these species can be grown in the laboratory, adults of them could be accepted as promising alternative chitin sources without negative effects on biodiversity.

Analytical studies on degradation mechanism of herbicide 4-chlorophenoxyacetic acid in water by gamma/H2O2 and gamma/ozone processes.

Radiolytic degradation of 4-chlorophenoxyacetic acid was followed in the presence of hydrogen peroxide and ozone. The synergic effect of ozone is found to be relatively high since the amounts of detected aromatic intermediates are lower as well as the amounts of small aliphatic acids are higher. Chloride ions are one of the most important mineralization products and splitted with a yield of more than 80%. The amounts of small aliphatic acids formed in the last step before mineralization (oxalic, acetic and formic acid) were followed and their formation from 4-chlorophenoxyacetic acid was confirmed. Dissolved oxygen was consumed to form reactive radicals during irradiation. Product analysis and confirmation are followed by gas chromatography/mass spectrometry and ion chromatography. The degradation path of 4-chlorophenoxyacetic acid was suggested with determined intermediates.

Mineralization of paracetamol in aqueous solution with advanced oxidation processes.

Paracetamol is a common analgesic drug widely used in all regions of the world more than hundred tonnes per year and it poses a great problem for the aquatic environment. Its phenolic intermediates are classified as persistent organic pollutants and toxic for the environment as well as human beings. In the present study, the irradiation of aqueous solutions of paracetamol with 60Co gamma-rays was examined on a laboratory scale and its degradation path was suggested with detected radiolysis products. The synergic effect of ozone on gamma-irradiation was investigated by preliminary ozonation before irradiation which reduced the irradiation dose from 5 to 3 kGy to completely remove paracetamol and its toxic intermediate hydroquinone from 6 to 4 kGy as well as increasing the radiation chemical yield (Gi values 1.36 and 1.66 in the absence and presence of ozone, respectively). The observed amount of formed hydroquinone was also decreased in the presence of ozone. There is a decrease in pH from 6.4 to 5.2 and dissolved oxygen consumed, which is up to 0.8 mg l(-1), to form some peroxyl radicals used for oxidation. Analytical measurements were carried out with gas chromatography/mass spectrometry and ion chromatography (IC) both qualitatively and quantitatively. Amounts of paracetamol and hydroquinone were measured with gas chromatography after trimethylsilane derivatization. Small aliphatic acids, such as acetic acid, formic acid and oxalic acid, were measured quantitatively with IC as well as inorganic ions (nitrite and nitrate) in which their yields increase with irradiation.

Analytical and toxicological studies of decomposition of insecticide parathion after gamma-irradiation and ozonation.

The decomposition of the widely used organophosphorus pesticide parathion was carried out in aqueous solutions by the use of gamma-irradiation from a 60Co source or ozonation by means of an ozone generator, and by combined processes of ozonation and radiolysis. Factors affecting the parathion decomposition as well formation and decomposition of the main by-products, including irradiation dose, length of ozonation time, and presence of common scavengers, were investigated. The most efficient was found to be the gamma-irradiation process combined with a short ozonation period; about 1 kGy irradiation dose was sufficient to decompose the pesticide in 15 mg/L solutions. Chemical studies of the decomposition of parathion were accompanied by monitoring of toxicity changes of irradiated solutions with the Microtox test.