Composites of carbon quantum dots (CQDs) are important materials to utilize the optical properties of CQDs in diverse applications including photoluminescence-based sensing and LED phosphors. Combining pre-prepared CQDs with a polymeric matrix usually causes changes in the optical properties of CQDs due to unavoidable aggregation. Recently, the preparation of composites based on in-situ formed CQDs has been debated to overcome the aggregation limits of the conventional mixing methods. Herein, we have demonstrated the synthesis of homogeneous CQDs composites by simple thermal annealing blends of aluminum hydroxide (AlOH), citric acid (CA), and urea (URA). Transmission electron microscopy (TEM), X-ray diffraction, and Raman spectroscopy studies revealed the formation of individual CQDs with a diameter of about 2–9 nm dispersed homogeneously over the AlOH matrix. The composites have a broad excitation band centered at about 360 nm and exhibit excitation-dependent photoluminescence which was similar to that of hydrothermally synthesized CQDs from CA and URA. The photoluminescent intensity of the composite was stable to UV irradiation and responded selectively to Cu(II) ion demonstrating its potential application in Cu(II) sensing.

The carbon-based nanostructures are in limelight due to their widespread applications in nano-to-micro-scale technologies. The carbon dots are known for their unique physical, electrical, optical, chemical and biological properties. The carbon dots (CDs) are being produced through several well-developed synthesis methods, one of which is the green sonochemical. This method is preferred over others because it is a green source of energy, facile, fast, low-temperature process, non-toxic and less expensive. Despite the fact of using 90% less energy than other methods, this method has been overlooked in the published literature. It is possible to prepare pure and doped CDs of low toxicity and controlled physicochemical properties through sonochemical method. In recent years, sonochemically produced CDs have been tuned and characterized for a variety of applications. This review has explored the merits and demerits of sonochemical method in comparison to the other methods for the synthesis of pure CDs and their nanocomposites. The role of multiple factors in tailoring the specific parameters of CDs for their application in antibacterial, polymerization, tissue engineering, catalysis, bio-imagining, supercapacitors, drug delivery and electric devices is also elaborated in this review. This review also concludes on future directions in the applications of sonochemically produced CDs.

A facile one-pot wet chemical process to prepare pure anatase TiO2 hollow structures using ammonium hexafluorotitanate as a precursor is developed. By defining the formic acid ratio, we fabricate TiO2 hollow structures containing fluorine on the surface. The TiO2 hollow sphere is composed of an anatase phase containing fluorine by various analytical techniques. A possible formation mechanism for the obtained hollow samples by self-transformation and Ostwald ripening is proposed. The TiO2 hollow structures containing fluorine exhibits 1.2 - 2.7 times higher performance than their counterparts in photocatalytic activity. The enhanced photocatalytic activity of the TiO2 hollow structures is attributed to the combined effects of high crystallinity, specific surface area (62 m2g-1), and the advantage of surface fluorine ions (at 8%) having strong electron-withdrawing ability of the surface ≡ Ti-F groups reduces the recombination of photogenerated electrons and holes.

Graphene and Fe3O4 were bound by electrostatic attraction and prepared by effective reduction through microwave treatments. As a result of fabricating graphene with Fe3O4 as a composite material, it has been confirmed that it contributes to the structural improvement in graphene stabilization and at the same time, it shows improved electrochemical performance through improved charge transfer. It was also confirmed that the crystalline Fe3O4 was uniformly dispersed in the rGO sheet, effectively blocking the reaggregation due to the van der Waals interaction between the neighboring rGO sheets. The structural analysis of prepared composites was confirmed by transmission electron microscopy, and X-ray diffractometer. Electrochemical properties of composites were studied by cyclic voltammetry, galvanostatic charge–discharge curves, and electrochemical impedance spectroscopy. The Fe3O4 (0.4 M)/rGO composite showed a high specific capacitance of 972 F g−1 at the current density of 1 A g−1 in 6 M KOH electrolyte, which is higher than that of the pristine materials rGO (251 F g−1) and Fe3O4 (183 F g−1). Also, the prepared composites showed a very stable cyclic behavior at high current density, as well as an improvement in comparison with pristine materials in terms of resistance.

The CO2 separation membranes based on a graft copolymer consisting of hydrophobic poly(ethylene-alt-maleic anhydride) (PEMA) backbone and hydrophilic poly(propylene glycol) PPG side chains were fabricated by a facile one-pot process. The reaction between O-(2-aminopropyl)-O’-(2-methoxyethyl) polypropylene glycol (AMPPG) and PEMA was conducted in butanol at room-temperature. Without any post-treatment, the as-synthesized PEMA-g-PPG solution could be directly coated onto a microporous polysulfone support to fabricate thin-film composite membranes. The PEMA-g-PPG membrane exhibited high selectivity (82.6 for CO2/N2 and 26.8 for CO2/CH4) and good CO2 permeability (99.1 Barrer), which is a close value to the upper boundary limit (2008). The PEMA-g-PPG membrane could be commercially feasible owing to simple, inexpensive and scalable process.

In this study, simple chemical synthesis of green emitting Cd-free InP/ZnS QDs is accomplished by reacting In, P, Zn, and S precursors by one-pot process. The particle size and the optical properties were tailored, by controlling various experimental conditions, including [In]/[MA] (MA: myristic acid) mole ratio, reaction temperature and reaction time. The results of ultraviolet–visible spectroscopy (UV-vis), and of photoluminescence (PL), reveal that the exciton emission of InP was improved by surface coating, with a layer of ZnS. We report the correlation between each experimental condition and the luminescent properties of InP/ZnS core/shell QDs. Transmission electron microscopy (TEM), and X-ray powder diffraction (XRD) techniques were used to characterize the as-synthesized QDs. In contrast to core nanoparticles, InP/ZnS core/shell treated with surface coating shows a clear ultraviolet peak. Besides this work, we need to study what clearly determines the shell kinetic growth mechanism of InP/ZnS core shell QDs.

비모란 선인장 2개와 다육식물인 월토이, 미니염좌, 청솔 중 1개를 혼합 식재한 상품을 소비자가 이용할 장소를 감안하여 온실, 창가 및 실내에 LED 적+청색 혼합광을 조사한 것과 안 한 것을 구분하여 위치시킨 후 6개월 동안 고사율 및 생육조사를 하였다. 창가의 식물 고사율은 처리 후 4개월만에 비모란(적)은 13.3%, 비모란(황)은 16.7%, 월토이는 39.3%, 미니 염좌는 5.7%, 청솔은 50.0%이었다. 이보다 광량이 적 은 실내의 식물 고사율은 2개월만에 비모란(적)은 13.3%, 비모란(황)은 6.7%, 월토이는 40.0%, 미니 염 좌는 10.0%, 청솔은 43.3%로서 창가의 4개월과 유사 하였다. 하지만 광도가 현저히 낮은 실내와 창가 조건 에서도 LED 적+청색 혼합광에서는 비모란 및 다육식 물은 고사된 것이 거의 없었다. 한편 LED 적+청색 혼합광에서 다육식물의 초장 및 엽수의 생장은 재배온 실의 것이 실내 것보다 양호한 경향을 보였고, 청솔은 모든 위치에서 다른 식물보다 초장이 길게 자라서 4개 월 후에는 비모란과 미관적으로 어울리지 않았다. 따라 서 접목선인장과 다육식물을 합식한 것을 실내에 들여 놓을 경우, 고사율을 감소시키기 위해서는 광이 가장 잘 비치는 곳에 놓거나 가능하다면 LED 적+청색 혼 합광 밑에 두는 것이 관상기간을 연장시킬 수 있다.

예이츠의 가장 초기 희곡 중의 하나인 『치킨 국물 뚝배기』는 어느 배고픈 부랑자가 인색하기로 소문난 노파로 하여금 국물을 끊이는 데 동참하게 만드는 희극이다. 유럽에서 널리 알려진 구전 설화로서, 예이츠는 여기서 가장 중요한 요소를 사용한다. 이 극에서 예이츠가 어떤 기법과 생각을 하는지 알 수 있다. 이 논문은 그가 평범한 구전 설화를 어떻게 재구성하여, 독백, 대화, 노래, 무대지시, 등의 서정적 형식을 통해 극화시키는지 연구한다.

사과 ‘후지’/M.9 포트묘목 개발을 위해 질소시비농도에 따른 생장특성을 조사하고, 포트 우량묘목 생산에 적합한 질소시비 농도와 잎의 무기영양성분 함량 및 토양 화학성의 안정성을 확인하였다. 질소시비농도가 높아질수록 묘목의 생장은 증가되 었고, 특히 16 mM 처리가 수체 생장에 가장 좋았으며, 우량묘목 판단기준에 부합하였다. 32 mM 이상의 고농도는 오히려 생장 을 감소시켰다. 잎의 무기영양성분 함량은 8, 16 mM 처리구에서 기존 사과과원의 적정수준보다 높았고, 이러한 무기영양성분은 정식 후 수체 생장에 도움이 될 것으로 생각되었다. 토양 화학성 또한 8, 16 mM 처리구에서 안정적이었다. 따라서 수체 생육, 잎의 무기영양성분, 포트 내 토양화학성을 고려한 결과, 사과 ‘후지’/M.9 우량 포트묘목 생산을 위한 적정 질소시비량은 16 mM로 판단되었다.

Background : Codonopsis lanceolata is a perennial herb called as ‘Deodeok’ (더덕) in Korea. The roots of C. lanceolate has been reported to have some antioxidant and antimicrobial properties. The chemically reactive saponins of C. lanceolata might be used as a capping agent for the surface of ZnO nanoparticle, ultimately making it a highly efficient photocatalyst. Methods and Results : In this paper, we report the one-pot green synthesis of ZnO nanoparticles via precipitation method using root extract of C. lanceolata. The structure of green synthesized Cl-ZnO NPs was characterized using XRD, EDX, DLS and morphology using TEM. The FT-IR exhibited the information about the functional groups that capped the metal nanoparticle and the formation of metal NPs was confirmed by UV–vis spectra at 356nm. The Cl-ZnO NPs were evaluated for their catalytic activity by measuring the degradation of methylene blue (MB) dye in aqueous solution under UV light (365 ㎚). The result showed efficient degradation of MB, which was degraded 70% within 30 min by Cl-ZnO NPs. Conclusion : This study proves that the green route synthesized ZnO NPs from the root extract of C. lanceolata are low cost, time efficient, bio-degradable and non- toxic. The UVvis spectra confirmed the synthesis of ZnO NPs from C. lanceolata root extract. The Cl- ZnO NPs mediated catalysis exhibited high photocatalysis rate in short time. Ultimately, the green rapid synthesized Cl-ZnO NPs from root extract can be used as an efficient

본 연구는 3,7-diarylpyrazolo [1,5-α]pyrimidines의 효과적인 one-pot regioselective 합성을 보여준다. 더욱이, 그 유도체는 뛰어난 CB1R 저해 활성을 나타냈다. 3,7-position에 diaryl group이 치환된 pyrazolo [1,5-α]pyrimidine은 CB1R 후보로서 가능성 있는 pharmacophore이다.