Kinetic Study of Adsorption Active Carbon Cassava Skin for Removal of Acetic Acid from Aqueous Solution

The amount of liquid wastes containing acetic acid found from food industry such as tofu home industry released is relatively high and pollutes water quality and also environment nearby. Several methods reducing pollutant in liquid wastes are available, one of which is adsorption using carbon as an adsorbent. The production of cassava in Indonesia was about 23.936 tons in year 2013 which produced cassava’s skin wastes about 2.393 tons. Mostly these cassava’s skin wastes containing around 59.31% carbon is disposed as garbage. This research is to develop more on reducing acetic acid containing in liquid waste by carbon active from cassava’s skin with variation of particle sizes, reaction times and acetic acid liquid waste concentrations, and also to study the kinetic reaction of cassava skin active carbon adsorbing acetic acid between Freundlich and Langmuir isotherm equations. The result shows the kinetic adsorption follows Freundlich isotherm equation with maximum capacity of Cassava skin active carbon 0.7 mg/g at particle size of adsorbent of 0.3375 mm and reaction time of 105 minutes.

Solvent effect and Activation Parameters: A Kinetic Reaction of Ethyl Caprylate in Water-Acetone Media

The kinetic result of hydrolysis of Ethyl Caprlyate has been investigated at different composition of aqueous-organic solvent with Acetone (30-70% v/v) over the temperature range of 20 to 400c. The calculated result follows second order kinetics and is observed that the rate decreases with increasing proportion of Acetone. This behavior is attributed electrostatic nature that various solvent-solute interaction in reaction media. Linear plots of Logk against water concentration shows that equilibrium shifted from dense form to bulky form. Iso-kinetic temperature has been determined with the help of slopes of (ΔH*) versus (ΔS*). Thermodynamic parameter has been calculated with the help of Wynne-Jones and Eyring equation.

Hetero-Diels-Alder Reactions of In Situ-Generated Azoalkenes with Thioketones; Experimental and Theoretical Studies

The hetero-Diels-Alder reactions of in situ-generated azoalkenes with thioketones were shown to offer a straightforward method for an efficient and regioselective synthesis of scarcely known N-substituted 1,3,4-thiadiazine derivatives. The scope of the method was fairly broad, allowing the use of a series of aryl-, ferrocenyl-, and alkyl-substituted thioketones. However, in the case of N-tosyl-substituted cycloadducts derived from 1-thioxo-2,2,4,4-tetramethylcyclobutan-3-one and the structurally analogous 1,3-dithione, a more complicated pathway was observed. By elimination of toluene sulfinic acid, the initially formed cycloadducts afforded 2H-1,3,4-thiadiazines as final products. Advanced DFT calculations revealed that the observed high regioselectivity was due to kinetic reaction control and that the (4 + 2)-cycloadditions of sterically less unhindered thiones occurred via highly unsymmetric transition states with shorter C..S-distances (2.27–2.58 Å) and longer N..C-distances (3.02–3.57 Å). In the extreme case of the sterically very hindered 2,2,4,4-tetramethylcyclobutan-1,3-dione-derived thioketones, a zwitterionic intermediate with a fully formed C‒S bond was detected, which underwent ring closure to the 1,3,4-thiadiazine derivative in a second step. For the hypothetical formation of the regioisomeric 1,2,3-thiadiazine derivatives, the DFT calculations proposed more symmetric transition states with considerably higher energies.

Hydration Model and Evaluation of the Properties of Calcined Hwangtoh Binary Blends

Calcined hwangtoh is a pozzolanic material that is increasingly being used as a mineral admixture in the concrete industry. This study shows a hydration model for cement–hwangtoh blends and evaluates the various properties of hwangtoh-blended concrete using reaction degrees of binders. First, a kinetic reaction model is proposed for analyzing the pozzolanic reaction of hwangtoh. The reaction of hwangtoh includes three processes: the initial dormant period, boundary reaction process, and diffusion process. The mutual interactions between the binary reactions of cement and hwangtoh are thought to be in line with the items in capillary water and calcium hydroxide. Second, the reaction degrees of cement and hwangtoh are determined based on a blended hydration model. Furthermore, the chemical (chemically combined water and calcium hydroxide contents), mechanical (compressive strength), thermal (hydration heat), and durability aspects (carbonation depth) of hwangtoh-blended concrete are systematically predicted. The results show good agreement with experimental results.

Study on Hydrolysis Reaction Rate of Several Chemical Warfare Agents

According to the first-order kinetic reaction equation, the hydrolysis rate constants of homogeneous and heterogeneous phase of eight poisons under different conditions were calculated, and the relationship between hydrolysis rate constants and temperature was obtained according to the arrhenius formula, and the activation energy of hydrolysis reaction of some poisons was calculated. The evolution curve of homogeneous hydrolysis rate of 0.5 g/L HD with time was collected by T-135 method, and the hydrolysis rate was 0.1 min-1 and the half-life was 7 min. Poison concentration, pH of system, environmental temperature and structural composition of soil all affect the hydrolysis rate of Chemical Warfare Agents.

Benzofuran–stilbene hybrid compounds: an antioxidant assessment – a DFT study

The kinetic reaction of the benzofuran–stilbene hybrid compound 5-(2-(2-(4-hydroxyphenyl)benzofuran-5-yl)vinyl)benzene-1,3-diol captures the HOO˙ free radical.