Methyl Trichlorosilane Prepared Methyl Sodium Silicate

2012 ◽  
Vol 184-185 ◽  
pp. 1064-1067
Author(s):  
Guang Xia Zhang ◽  
Qiao Yun Zhang ◽  
Ze Min Chen

This paper studied how to prepare Methyl Sodium Silicate from Methyl Trichlorosilane. Methyl trichlorosilane hydrolyzed on the interface of cyclohexane and water, then hydrolysate and sodium hydroxide prepared methyl sodium silicate at molten state. Manufactrue was characterised by XRD, IR, and differential thermal analysis. The experimental results indicate that the best hydrolyze condition was the proportion of methyl trichlorosilane and water was 10~12:100 , at 5°C, lasting for 45min; the best condition of prepared methyl sodium silicate was the proportion of sodium hydroxide and hydrolysate was 2.1~2.3:1, at 300 ~450°C, lasting for 50min. The manufacture was white powder, water-solubility and well stabilization bellow 450°C.

1993 ◽  
Vol 71 (9) ◽  
pp. 1378-1383 ◽  
Author(s):  
Raphaël Sabbah ◽  
Thi Huy Duc Le

A thermodynamic study of the three hydroxybenzoic acids was carried out by combustion and sublimation calorimetry, heat capacity measurements, and differential thermal analysis. The experimental results (in kJ mol−1) are summarized as:[Formula: see text]From these experimental results, it was possible to determine for the three isomers (i) the resonance energies. From their comparison, the ortho isomer seems to be the most stable. This result is discussed using a structural consideration; (ii) the enthalpies of atomization. These values are in good agreement with that calculated using a contribution method.


2014 ◽  
Vol 556-562 ◽  
pp. 326-329 ◽  
Author(s):  
Xu Zhang ◽  
Dan Li ◽  
Hua Xie ◽  
Wen Jie Xu

Magnesium salt flame retardant is an additive flame retardant with environmental protection performance, which has been successfully applied in various industries because of its many advantages. In this paper, the chemical precipitation method is used to prepare magnesium salt flame retardants with different alkali sources (sodium hydroxide and ammonia) and reaction temperatures. And then, study on the thermal properties of all samples is systematically carried out on the basis of differential thermal analysis. These investigations could build up a link between the thermal property and growth behaviors of magnesium salt, which may offer us theoretical help.


Author(s):  
Dominika Jendrzejczyk-Handzlik ◽  
Piotr Handzlik

In this work, the ternary Ag-Au-Ga system was studied experimentally by differential thermal analysis (DTA). Measurements were carried out along two chosen cross-sections determined by the ratio of mole fractions XAg/XGa=1:1 and XAu/XGa=1:1 by applying Pegasus 404 apparatus form Netzsch. Experiments were performed at three rates: 1 K min-1, 5 K min-1 and 10 K min-1. Next, the obtained experimental results were used to estimate the temperatures of liquidus by applying extrapolation to zero rate. Moreover, the temperatures of invariant reactions and other phase transformations were investigated from DTA measurements which were carried out with the rate 1 K min-1. Finally, the experimental results were compared with the isopleths obtained from prediction and calculation of the phase diagram which were done by using CALPHAD method. Experimental data obtained in this work are in good agreement with the results of calculation.


Author(s):  
Detlef Klimm ◽  
Bartosz Szczefanowicz ◽  
Nora Wolff ◽  
Matthias Bickermann

AbstractBy differential thermal analysis, a concentration field suitable for the growth of Zr, Mg co-doped strontium hexagallate crystals was observed that corresponds well with known experimental results. It was shown that the melting point of doped crystal is ca. 60 K higher than that of undoped crystals. This higher melting points indicate hexagallate phase stabilization by Zr, Mg co-doping and increase the growth window of (Mg,Zr):SrGa12O19, compared to undoped SrGa12O19 that grows from SrO–Ga2O3 melts.


TAPPI Journal ◽  
2010 ◽  
Vol 9 (2) ◽  
pp. 23-29 ◽  
Author(s):  
Wei-ming Wang ◽  
Zai-sheng Cai ◽  
Jian-yong Yu

Degumming of pre-chlorite treated jute fiber was studied in this paper. The effects of sodium hydroxide concentration, treatment time, temperature, sodium silicate concentration, fiber-to-liquor ratio, penetrating agent TF-107B concentration, and degumming agent TF-125A concentration were the process conditions examined. With respect to gum decomposition, fineness and mechanical properties, sodium hydroxide concentration, sodium silicate concentration, and treatment time were found to be the most important parameters. An orthogonal L9(34) experiment designed to optimize the conditions for degumming resulted in the selection of the following procedure: sodium hydroxide of 12g/L, sodium silicate of 3g/L, TF-107B of 2g/L, TF-125A of 2g/L, treatment time of 105 min, temperature of 100°C and fiber to liquor ratio of 1:20. The effect of the above degumming process on the removal of impurities was also examined and the results showed that degumming was an effective method for removing impurities, especially hemicellulose.


2018 ◽  
Author(s):  
Asel Sartbaeva ◽  
Paul R. Raithby ◽  
Remi Castaing ◽  
Antony Nearchou

Through a combination of thermogravimetry, mass spectrometry and differential thermal analysis, we demonstrate for the first time that all four zeolites show experimental differences in their host-guest interactions with 18C6. In addition, we have estimated the kinetics of 18C6 decomposition, which is a technique that has not been applied to zeolites previously. Using these findings as a toolkit, a more rational use of OSDAs can be utilised to prepare designer zeolites. Furthermore, the new methodologies presented herein can be applied to current zeolites, such as MFI-type zeolites used in the petrochemical industry.


Author(s):  
A. Z. Mohd Ali ◽  
◽  
N. A. Jalaluddin ◽  
N. Zulkiflee ◽  
◽  
...  

The production of ordinary Portland cement (OPC) consumes considerable amount of natural resources, energy and at the same time contribute in high emission of CO2 to the atmosphere. A new material replacing cement as binder called geopolymer is alkali-activated concrete which are made from fly ash, sodium silicate and sodium hydroxide (NaOH). The alkaline solution mixed with fly ash producing alternative binder to OPC binder in concrete named geopolymer paste. In the process, NaOH was fully dissolved in water and cooled to room temperature. This study aims to eliminate this process by using NaOH in solid form together with fly ash before sodium silicate liquid and water poured into the mixture. The amount of NaOH solids were based on 10M concentration. The workability test is in accordance to ASTM C230. Fifty cubic mm of the geopolymer paste were prepared which consists of fly ash to alkaline solution ratio of 1: 0.5 and the curing regime of 80℃ for 24 hours with 100% humidity were implemented. From laboratory test, the workability of dry method geopolymer paste were decreased. The compressive strength of the dry mix of NaOH showed 55% and the workability has dropped to 58.4%, it showed strength reduction compared to the wet mix method.


2020 ◽  
Vol 5 (8(77)) ◽  
pp. 65-68
Author(s):  
Teymur Mammad Ilyasly ◽  
Rahman Hasanaga Fatullazade ◽  
Zakir Islam Ismailov ◽  
Nigar Nadir Jafarova

The synthesis of alloys of the system was carried out stepwise in rotary furnaces. The synthesis mode was selected based on the physicochemical properties of the elementary components. For homogenization, the alloys were subjected to isothermal annealing at 750 and 1275 K, depending on the Tm2Te3 concentration, for 250 h after homogenization of the alloys, they were subjected to physicochemical analysis. The results of differential thermal analysis showed that reversible thermal effects are observed in the alloys of the system. In alloys in a 1: 1 ratio, a new intermediate phase is formed with a composition corresponding to the TmAsTe3 compound. The homogeneity area is observed in the concentration range 52.5-47.5. It was found that in the concentration range 98.5-52.5 Tm2Te3 there are two phases - a mixture of β and of the solid solution, and in the concentration range of 47.51 mol% Tm2Te3 phases and α are in equilibrium. ) 66 The eutectic has coordinates of 11.5 mol Tm2Te3 at a temperature of 575 K.


2016 ◽  
Vol 5 (1) ◽  
pp. 6
Author(s):  
Budi Setiawan ◽  
Erizal Zaini ◽  
Salman Umar

Sebuah penelitian tentang sistem dispersi padat dari asiklovir dengan poloxamer 188 telah dilakukan formulasi dengan pencampuran secara fisika dengan rasio 1 : 1, 1 : 3, 1 : 5 dan dispersi padat 1 : 1, 1 : 3, 1 : 5 dan penggilingan 1:1 sebagai pembanding. Dispersi padat dibuat menggunakan metode pencairan (fusi), yang digabung dengan poloxamer 188 pada hotplate kemudian asiklovir dimasukkan ke dalam hasil poloxamer 188 lalu di kocok hingga membentuk masa homogen. Semua formula yang terbentuk termasuk asiklovir poloxamer 188 murni dianalisis karakterisasinya dengan Differential Thermal Analysis (DTA), X-ray Diffraction, Scanning Electron Microscopy (SEM), dan Fourier Transform Infrared (FTIR), kemudian pengambilan dilakukan  (penentuan kadar) mengunakan spektrofotometer UV pada panjang gelombang 257,08 nm dan uji laju disolusi dengan aquadest bebas CO2 menggunakan metode dayung. Hasil pengambilan  (penentuan kadar) menunjukkan bahwa semua formula memenuhi persyaratan farmakope Amerika edisi 30 dan farmakope Indonesia edisi 4 yaitu 95-110%. Sedangkan hasil uji laju disolusi untuk campuran fisik 1: 1, dan dispersi padat 1: 1, dan penggilingan 1: 1 menunjukkan peningkatan yang nyata dibandingkan asiklovir murni. Hal ini juga dapat dilihat dari hasil perhitungan statistik  menggunakan analisis varian satu arah  SPSS 17.


1983 ◽  
Vol 48 (12) ◽  
pp. 3340-3355 ◽  
Author(s):  
Pavel Fott ◽  
Pavel Šebesta

The kinetic parameters of reactivation of a carbonized hydrodesulphurization (HDS) catalyst by air were evaluated from combined thermogravimetric (TG) and differential thermal analysis (DTA) data. In addition, the gaseous products leaving a temperature-programmed reactor with a thin layer of catalyst were analyzed chromatographically. Two exothermic processes were found to take part in the reactivation, and their kinetics were described by 1st order equations. In the first process (180-400 °C), sulphur in Co and Mo sulphides is oxidized to sulphur dioxide; in the second process (300-540 °C), in which the essential portion of heat is produced, the deposited carbon is oxidized to give predominantly carbon dioxide. If the reaction heat is not removed efficiently enough, ignition of the catalyst takes place, which is associated with a transition to the diffusion region. The application of the obtained kinetic parameters to modelling a temperature-programmed reactivation is illustrated on the case of a single particle.


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