scholarly journals Perbandingan porselen kedokteran gigi swa-sintesis berbahan baku pasir felspar Pangaribuan dan Sukabumi

2017 ◽  
Vol 3 (3) ◽  
pp. 49
Author(s):  
Joseph Gunawan ◽  
Dede Taufik ◽  
Veni Takarini ◽  
Zulia Hasratiningsih

Comparison self-synthesized dental porcelain between feldspar from Pangaribuan and Sukabumi. Dental porcelain material as one of the esthetic indirect restorations in Indonesia is mostly imported. In fact, Indonesia is really rich of natural raw materials, including feldspar, silica, and kaolinite. The aim of this study is to synthesize the dental porcelain made from Indonesia’s two different originates, which are Pangaribuan and Sukabumi. This study was prepared by fritting and sintering the mixture of 65% wt feldspar (from Sukabumi and Pangaribuan), 25% wt silica, 5% wt kaolinite, and 5% wt potassium salt. The porcelains obtained were evaluated using X-Ray Diffraction (XRD). The results revealed that quartz and leucite were found in the composition of Pangaribuan sand that successfully showed more translucencies compared to Sukabumi sand which only imparted quartz on its component. This study shows that dental porcelain from Pangaribuan sand is successfully self-synthesized, on the other hand Sukabumi sand has not been successfully synthesized. These findings develop on a good prospect of esthetic dental porcelain made from Indonesian natural sand. ABSTRAKBahan porselen kedokteran gigi sebagai salah satu restorasi indirek estetik di Indonesia kebanyakan didatangkan dari luar negeri. Indonesia sebenarnya sangat kaya dengan bahan baku porselen kedokteran gigi seperti felspar, silika, dan kaolin. Tujuan penelitian ini adalah melakukan sintesis porselen kedokteran gigi dari 2 jenis pasir alam Indonesia yaitu Pangaribuan dan Sukabumi. Komposisi yang digunakan yaitu 65% wt felspar, 25% wt silika, 5% wt kaolin, dan 5% wt garam kalium, dicampur kemudian dilakukan fritting serta sintering. Dua komposisi porselen dibuat dengan bahan dasar berbeda yaitu felspar dari Pangaribuan dan Sukabumi. Kedua porselen yang telah disintering kemudian dievaluasi menggunakan X-Ray Diffraction (XRD). Hasilnya adalah kuarsa dan leusit ditemukan pada porselen dengan komposisi pasir Pangaribuan yang juga memberikan hasil lebih translusen secara visual dibandingkan dengan porselen dengan komposisi pasir Sukabumi yang hanya memperlihatkan hasil kuarsa. Hal ini menunjukkan bahwa porselen dengan komposisi bahan dasar pasir Pangaribuan berhasil disintesis dibandingkan komposisi bahan dasar pasir Sukabumi.Penemuan ini dapat memberikan peluang yang baik dalam pembuatan porselen kedokteran gigi yang berasal dari pasir alam Indonesia. 

2017 ◽  
Vol 262 ◽  
pp. 545-548 ◽  
Author(s):  
Yvonne M. Mos ◽  
Arnold C. Vermeulen ◽  
Cees N.J. Buisman ◽  
Jan Weijma

X-ray diffraction (XRD) is a commonly used technology to identify crystalline phases. However, care must be taken with the combination of XRD configuration and sample. Copper (most commonly used radiation source) is a poor match with iron containing materials due to induced fluorescence. Magnetite and maghemite are analysed in different configurations using copper or cobalt radiation. Results show the effects of fluorescence repressing measures and the superiority of diffractograms obtained with cobalt radiation. Diffractograms obtained with copper radiation make incontestable phase identification often impossible. Cobalt radiation on the other hand yields high quality diffractograms, making phase identification straightforward.


MRS Advances ◽  
2018 ◽  
Vol 3 (64) ◽  
pp. 3971-3978 ◽  
Author(s):  
O.E. Villanueva-Perez ◽  
I. Mejía ◽  
V. García-García ◽  
A. Bedolla-Jacuinde

ABSTRACTLow density (LD) steels have shown particular characteristics in terms of mechanical properties and microstructure, since they have high strength, high ductility and density reduction up to 18%. On the other hand, the addition of microalloying elements such as Ti and B generate hardening by solid solution and precipitation, as well as grain refinement effect. LD steels generate nano-sized kappa phase precipitated from the austenite matrix, and these advanced steels can reach strength and elongation up to 780 MPa and 60%, respectively. The main objective of this research work is the metallographic, structural and mechanical characterization of a LD steel microalloyed with Ti/B in as-cast and -homogenized conditions. For this purpose a Fe-27Mn-7Al-1.2C (%wt) LD steel microalloyed with Ti/B was melted in a vacuum-induction furnace and cast in metallic mold. LD-Ti/B steel samples were homogenized at 1100 °C during 20, 50, 100, 150 and 200 minutes followed by water quenching. Metallographic, structural and mechanical characterization was carried out by optical (LOM) and scanning electron (SEM) microscopy, X-ray diffraction (XRD) and microhardness Vickers testing (HV10), respectively. In general, results showed a typical dendritic microstructure with average grain size of 1256 μm in the as-cast condition. On the other hand, the as-homogenized condition showed an austenitic equiaxial microstructure with average grain size from 164 to 940 μm. Austenite, ferrite and kappa phases were detected by X-ray diffraction (XRD). Also, second-phase particles such as AlN, TiC and MnS were detected by LOM and SEM-EDS analysis. LD steel microalloyed with Ti/B exhibited the highest microhardness Vickers value (235 HV10) in the as-cast condition, whilst in the as-homogenized condition microhardness gradually decreases from 223 to 198 HV10 as holding time increases.


2006 ◽  
Vol 61 (11) ◽  
pp. 1413-1420 ◽  
Author(s):  
Mohamed I. Hegab ◽  
A. M. Moustafa

The very reactive α-oxo-thioketone derivatives 2a - d, generated via thermolysis of spirobenzopyran- 3’,2-[1,3,4]oxadithiino[5,6-c]benzopyran-4’-ones 1a - d, reacted with 2,3-dimethyl-1,3-butadiene and 1,3-cyclohexadiene under [4+2]-cycloaddition to afford spirobenzopyran-3’,6-thiapyran-4’-one adducts 3a - d and spirobenzopyran-3’,3-thiabicyclo[2.2.2]oct-5-en-4’-one adducts 4a - d, respectively. On the other hand, the reaction of α-oxo-thioketones 2a - d with isoprene afforded regioselectively only 3-methyl-thiapyran derivatives 5a - d. Single crystal X-ray diffraction studies of 4b, 4c, and 5a give a good support for the established structure.


2012 ◽  
Vol 727-728 ◽  
pp. 629-633
Author(s):  
Rubens Lincoln Santana Blazutti Marçal ◽  
Marcelo Henrique Prado da Silva ◽  
Eduardo de Sousa Lima ◽  
Luis Henrique Leme Louro

In this work, glasses with compositions, close to commercial borosilicate glasses, were developed. The main raw materials were residues of ornamental rock industries ( marbles and granites ). Beach sand was used in order to enrich the compositions with silica. Also, boron oxide was added to reach borosilicate glasses compositions. The obtained glasses were characterized by X-ray diffraction (XRD), infrared spectroscopy (FTIR), and hydrolytic resistance. The measured properties were compared to those of commercial glasses, available in the market, from two different brands. XRD results confirmed amorphous patterns of the produced glasses. The other tests revealed an excellent agreement between the obtained values and those from commercial glasses. Therefore, this study showed the possibility of using ornamental rocks residues as primary sources to produce borosilicate glasses. In addition, it became clear that an economic value could be aggregated to the residues, which otherwise would be discharged into nature causing pollution.


1989 ◽  
Vol 03 (05) ◽  
pp. 447-451
Author(s):  
M.A.K.L. DISSANAYAKE ◽  
K. TENNEKONE ◽  
O.A. ILEPERUMA ◽  
S.H.S.P. SAMARAPPULI

A new superconducting phase has been found in a mixed system prepared from the YBa 2 Cu 3 O 7−δ and Bi 2 CaSr 2 Cu 2 O 9−δ high-T c materials. The new compound shows an onset of resistivity transition at ~100 K and zero resistivity below ~50 K. Powder X-ray diffraction pattern of the new compound differs completely from those of YBa 2 Cu 3 O 7−δ and Bi 2 CaSr 2 Cu 2 O 9−δ. The materials prepared using a mixture of the oxides and carbonates with identical cation stoichiometric ratios, on the other hand, does not exhibit superconductivity.


1955 ◽  
Vol 38 (5) ◽  
pp. 575-580 ◽  
Author(s):  
Eric Ponder

The investigation of two thermal properties of red cells throws some light on whether sickling is a process involving the crystallization of a relatively insoluble hemoglobin. These properties are the specific heat and the heat of compression, both of which would be expected to become numerically less if the hemoglobin of the red cell were to crystallize. In the case of paracrystalline rat red cells, which give spacings at 45 A and 58 A by x-ray diffraction, the specific heat is reduced to 85 per cent of that of the normal red cells, and the heat of compression is only about 75 per cent of that found for the normal red cell. In the case of the red cell sickled by a reduction of the O2 tension, the specific heat and the heat of compression are substantially the same as found for the normal red cell. This is an argument against sickling being the result of a crystallization process, and supports the observation that sickled cells do not give x-ray spacings. The result is compatible, on the other hand, with sickling being the result of the formation of an oriented and birefringent gel.


1996 ◽  
Vol 61 (9) ◽  
pp. 1321-1334 ◽  
Author(s):  
Pavel Vojtíšek ◽  
Ivana Císařová

A number of compounds which can by their stoichiometry be classified into several groups have been prepared by reaction of tris(N-piperidinomethyl)phosphine oxide (tppo) with Zn(II) and Cd(II) salts. The structure of two Zn(II) complexes differing by their Zn : tppo ratio and of one Cd(II) complex has been determined by the X-ray diffraction technique. The results show that in all the cases tppo is bound as divalent chelate N,O-donor, but the geometry of coordination sphere of M(II) decisively affects the steric arrangement of the five-membered chelate ring. Structures of the compounds studied are entirely different from those of Zn(II) complexes of sterically less demanding P,P-dimethyl-P-aminomethylphosphine oxide (dmao). On the other hand, the way of coordination of tppo is the same as that found in the case of the Co(II) complex of tris(N,N-dimethylaminomethyl)phosphine oxide.


1990 ◽  
Vol 45 (3-4) ◽  
pp. 307-312 ◽  
Author(s):  
Koji Yamada ◽  
Takashi Matsui ◽  
Tomoko Tsuritani ◽  
Tsutomu Okuda ◽  
Sumio Ichiba

Abstract In a series of MSnI3 compounds (M = K, NH4 , Rb, Cs, CH3NH3) two types of coordination around the central Sn(II) were found by 127I-NQR and powder X-ray diffraction techniques. They are square pyramidal (for M = NH4 , Rb) and octahedral (for M = CH3NH3). CsSnI3 , on the other hand, showed a drastic structural change of the anion at 425 K from a square pyramid to a regular octahedron. Associated with this phase transition, the electrical conductivity increased from 4 x 10-3 S cm-1 to about 102 S cm-1 . This metallic modification was characterized by 127I-NQR and 119Sn Mössbauer spectroscopy.


2020 ◽  
Vol 24 (10) ◽  
pp. 1139-1147
Author(s):  
Yang Mingyan ◽  
Wang Daoquan ◽  
Wang Mingan

2-Phenylcyclododecanone and 2-cyclohexylcyclododecanone derivatives were synthesized and characterized by 1H NMR, 13C NMR, HR-ESI-MS and X-ray diffraction. Their preferred conformations were analyzed by the coupling constants in the 1H NMR spectra and X-ray diffraction, which showed the skeleton ring of these derivatives containing [3333]-2-one conformation, and the phenyl groups were located at the side-exo position of [3333]-2-one conformation due to the strong π-π repulsive interaction between the π- electron of benzene ring and π-electron of carbonyl group. The cyclohexyl groups were located at the corner-syn or the side-exo position of [3333]-2-one conformation depending on the hindrance of the other substituted groups. The π-π electron effect played a crucial role in efficiently controlling the preferred conformation of 2-aromatic cyclododecanone and the other 2-aromatic macrocyclic derivatives with the similar preferred square and rectangular conformations.


2021 ◽  
Vol 5 (2) ◽  
pp. 16
Author(s):  
Isabel Padilla ◽  
Maximina Romero ◽  
José I. Robla ◽  
Aurora López-Delgado

In this work, concentrated solar energy (CSE) was applied to an energy-intensive process such as the vitrification of waste with the aim of manufacturing glasses. Different types of waste were used as raw materials: a hazardous waste from the aluminum industry as aluminum source; two residues from the food industry (eggshell and mussel shell) and dolomite ore as calcium source; quartz sand was also employed as glass network former. The use of CSE allowed obtaining glasses in the SiO2-Al2O3-CaO system at exposure time as short as 15 min. The raw materials, their mixtures, and the resulting glasses were characterized by means of X-ray fluorescence, X-ray diffraction, and differential thermal analysis. The feasibility of combining a renewable energy, as solar energy and different waste for the manufacture of glasses, would highly contribute to circular economy and environmental sustainability.


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