Solid–Solid Phase Transformations Induced through Cation Exchange and Strain in 2D Heterostructured Copper Sulfide Nanocrystals

Nano Letters ◽  
2014 ◽  
Vol 14 (12) ◽  
pp. 7090-7099 ◽  
Author(s):  
Don-Hyung Ha ◽  
Andrew H. Caldwell ◽  
Matthew J. Ward ◽  
Shreyas Honrao ◽  
Kiran Mathew ◽  
...  
ChemPhysChem ◽  
2015 ◽  
Vol 17 (5) ◽  
pp. 771-776 ◽  
Author(s):  
Lige Liu ◽  
Chang Liu ◽  
Wenping Fu ◽  
Luogen Deng ◽  
Haizheng Zhong

1988 ◽  
Vol 53 (12) ◽  
pp. 3072-3079
Author(s):  
Mojmír Skokánek ◽  
Ivo Sláma

Molar heat capacities and molar enthalpies of fusion of the solvates Zn(NO3)2 . 2·24 DMSO, Zn(NO3)2 . 8·11 DMSO, Zn(NO3)2 . 6 DMSO, NaNO3 . 2·85 DMSO, and AgNO3 . DMF, where DMSO is dimethyl sulfoxide and DMF is dimethylformamide, have been determined over the temperature range 240 to 400 K. Endothermic peaks found for the zinc nitrate solvates below the liquidus temperature have been ascribed to solid phase transformations. The molar enthalpies of the solid phase transformations are close to 5 kJ mol-1 for all zinc nitrate solvates investigated. The dependence of the molar heat capacity on the temperature outside the phase transformation region can be described by a linear equation for both the solid and liquid phases.


2006 ◽  
Vol 18 (6) ◽  
pp. 781-784 ◽  
Author(s):  
C. R. Lubeck ◽  
T. Y.-J. Han ◽  
A. E. Gash ◽  
J. H. Satcher ◽  
F. M. Doyle

1996 ◽  
Vol 45 (6) ◽  
pp. 1428-1432
Author(s):  
V. B. Vol'eva ◽  
I. S. Belostotskaya ◽  
A. Yu. Karmilov ◽  
N. L. Komissaroya ◽  
V. V. Ershov

ACS Nano ◽  
2015 ◽  
Vol 9 (2) ◽  
pp. 1788-1800 ◽  
Author(s):  
Shunhao Wang ◽  
Andreas Riedinger ◽  
Hongbo Li ◽  
Changhui Fu ◽  
Huiyu Liu ◽  
...  

2018 ◽  
Vol 31 (2) ◽  
pp. 541-552 ◽  
Author(s):  
Christina H. M. van Oversteeg ◽  
Freddy E. Oropeza ◽  
Jan P. Hofmann ◽  
Emiel J. M. Hensen ◽  
Petra E. de Jongh ◽  
...  

Author(s):  
Aslina Br. Ginting ◽  
Yanlinastuti Yanlinastuti ◽  
Noviarty Noviarty ◽  
Boybul Boybul ◽  
Arif Nogroho ◽  
...  

PEMBUATAN SUMBER RADIASI GAMMA ISOTOP 137Cs DENGAN AKTIVITAS 20 mCi DARI PEB U3Si2-Al PASCA IRADIASI DALAM CONTAINER STAINLESS STEEL. Kegiatan uji pasca iradiasi pelat elemen bakar (PEB) U3Si2-Al banyak menghasilkan larutan dengan keaktifan yang sangat tinggi. Larutan tersebut mengandung isotop 137Cs, uranium serta transuranium yang mempunyai waktu paroh panjang dan berbahaya bagi lingkungan. Namun larutan tersebut memiliki nilai ekonomis tinggi karena dapat dimanfaatkan sebagai bahan baku untuk pembuatan sumber radiasi sinar gamma isotop 137Cs. Hal ini dapat membantu bidang industri dalam memenuhi kebutuhan sumber radioaktif dalam negeri karena selama ini kebutuhan isotop 137Cs di Indonesia masih tergantung dari industri luar negeri. Selain itu, pengadaan dan transportasi isotop 137Cs dari luar negeri serta dalam penggunaannya memerlukan persyaratan yang cukup ketat dari Badan Pengawas Tenaga Nuklir Nasional (BAPETEN), sehingga menyebabkan harga isotop 137Cs menjadi mahal sampai di Indonesia. Dengan alasan tersebut, BATAN sebagai lembaga litbang nuklir di Indonesia perlu mempelajari pembuatan sumber radiasi gamma isotop 137Cs dari larutan hasil pengujian bahan bakar nuklir U3Si2-Al pasca iradiasi. Manfaat isotop 137Cs sangat luas antara lain digunakan dalam menganalisis sampel lingkungan, industri migas, konstruksi, radiografi, perikanan, rumah sakit dan pertambangan. Pembuatan sumber radiasi gamma isotop 137Cs dimulai dari pengumpulan larutan hasil pengujian PEB U3Si2-Al. Larutan larutan hasil pengujian mengandung isotop 137Cs dan isotop lainnya dikumpulkan menjadi satu dalam botol dengan volume 65 mL. Pemisahan isotop 137Cs dari hasil fisi lainnya dilakukan dengan metode penukar kation menggunakan zeolit Lampung dengan berat 45 gr. Hasil pemisahan diperoleh 137Cs-zeolit dalam fasa padat dan isotop lainnya berada dalam fasa cair. Padatan137Cs-zeolit kering kemudian kemudian ditimbang dan diukur aktivitasnya menggunakan spektrometer-g. Hasil analisis dengan spektrometer-g diperoleh aktivitas padatan 137Cs-zeolit sebesar 20 mCi. Untuk menjadi sumber radiasi gamma 137Cs, padatan 137Cs-zeolit dengan aktivitas 20 mCi dikemas dengan cara memasukkan ke dalam inner-outer capsule terbuat dari stainless steel yang telah dirancang sebelumnya. Container stainless steel diproses menjadi sumber radiasi gamma tertutup (shield source) untuk selanjutnya disertifikasi oleh PTKMR-BATAN sebagai lembaga kalibtrator bahan radioaktif di BATAN.Kata kunci: Larutan proses PEB U3Si2-Al, radioaktif gamma, isotop 137Cs, penukar kation, zeolit Lampung dan container. MANUCFACTURING OF 137Cs GAMMA RAY SOURCE WITH ACTIVITY 20 mCi FROM PEB U3Si2-Al POST IRRADIATION IN STAINLESS STEEL CONTAINER. In the post-irradiation examination of fuel element plate (PEB) U3Si2-Al), a solution of high activity as a result of testing nuclear fuel stored in hotcell with enough volume. The solution can not be discarded as waste because it still contains fission isotop such as137Cs, uranium and transuranium, which has a long half life and dangerous for the environment. This can help the industry in order to fulfill the needs of a radioactive source in Indonesia, because until now 137Cs isotope is derived from foreign industries. In addition, the procurement and transportation of isotopes 137Cs require stringent requirements, because they have toget permission from the National Nuclear Energy Agency (BAPETEN), thus causing the price of high activity 137Cs isotopes becomes expensive to Indonesia. For these reasons, BATAN as nuclear R&D institutions in Indonesia need to study make isotopes 137Cs gamma radiation source, which is contained in the waste from spent fuel test results U3Si2-Al. Isotope 137Cs can be used very widely, such as in the analysis of environmental samples, the oil and gas industry, construction, radiography, fisheries, hospitals, and mining. Making isotope 137Cs gamma radiation source starting from the collection of waste from the test results PEB U3Si2- Al. Waste solution was collected in a bottle with volume 65 mL. Collection of 137Cs isotopes of other fission carried out using the method of cation exchange with weight 45 gr of zeolite Lampung. The results of separation are 137Cs-zeolite in the solid phase and the other isotopes are in the liquid phase. 137Cs-zeolite solid is then dried and then weighed and measured its activity using a spectrometer-g. Result of analisys by spectrometer-g was obtained acitivity of 137Cs-zeolite solids was 20 mCi.137Cs-zeolite solids then packed in sealed containers (shield source) capsule-shaped stainless steel and than certificate by PTKMR-BATAN.Keywords: Process wastle of PEB U3Si2-Al, gamma radioactive, isotope 137Cs, cation exchange, zeolite Lampung and container.


The problem of step motion during lateral growth in solid-solid phase transformations is re-examined. Results are obtained for the steady motion of an individual ledge when volume diffusion in the parent phase is the predominant contribution to the growth rate. A comparison is made between our results and the earlier work of Jones & Trivedi (1971). There are significant differences between the two sets of results particularly in the limit of small perturbations to the Laplacian diffusion field. To confirm the accuracy of the results presented here the calculations have been made by two different methods.


2013 ◽  
Vol 1537 ◽  
Author(s):  
Priscilla V. Quintana-Ramírez ◽  
M. C. Arenas

ABSTRACTPoly(3-hexylthiophene)/Titania (P3HT/TiO2) heterojunction has been widely studied in the field of hybrid solar cells. Usually, organic dyes shift the neat TiO2 absorption edge toward the visible range improving the conversion efficiency or/and the TiO2 surface is modified with ligands in order to increase the electron transport. On the other hand, copper sulfide, non-toxic semiconductor, has been included in bulk organic P3HT based solar cell, increasing the photocurrent density of devices. Therefore, we propose the use of copper sulfide in the hybrid TiO2/P3HT heterojunction to determine its effect in the performance of TiO2/P3HT solar cell. Copper sulfide nanocrystals (CuxS) were synthesized at 230 °C, 240 °C and 260 °C and, they were mixed with P3HT in order to form P3HT:CuxS bulk heterojunctions. Scattered grains and irregular morphology in the final topography of the reference device (P3HT/TiO2 heterojunction) were observed by AFM, while a granular morphology and a few pores like craters were observed in the devices containing P3HT:CuxS bulk heterojunctions. Chalcocite phase (Cu2S) was obtained at 230 and 240°C and, digenite (Cu1.8S) phase at 260°C, both copper sulfide phases are very promising for solar cells. Despite this, poor rectifications in the devices were found in the current-voltage curves of the devices containing copper sulfide nanocrystals in contrast to the P3HT/TiO2 cell (device without nanocrystals), it could be due to the current leakage or recombination process in the copper sulfide/TiO2 interface. It suggests future work in order to improve the devices.


Sign in / Sign up

Export Citation Format

Share Document