Studies on the Combined Use of Some Different Organic Accelerators. IV. Diphenylguanidine and Dibenzothiazole Disulfide

1934 ◽  
Vol 7 (4) ◽  
pp. 648-656 ◽  
Author(s):  
Itiro Aoe ◽  
Hirosi Yokosima

Abstract 1. Diphenylguanidine and dibenzothiazole disulfide do not form a molecular compound or eutectic mixture, as judged by their melting and softening point curve. 2. The effects of scorching were studied by the use of various proportions of diphenylguanidine and dibenzothiazole disulfide; the maximum scorching was found with the mixture which had the lowest melting point in the curve. 3. These proportions were also studied for their vulcanizing power. 4. Diphenylguanidine and dibenzothiazole disulfide form a molecular compound through the medium of hydrogen sulfide. 5. This molecular compound was prepared and tested for its vulcanizing properties.

1936 ◽  
Vol 9 (1) ◽  
pp. 21-34 ◽  
Author(s):  
Ichiro Aoe ◽  
Hiroshi Kitayama

Abstract 1. Equal weights of a mixture of hexamethylenetetramine and mercaptobenzothiazole give the optimum accelerating activity and minimized scorching. 2. Scorching tests indicate that there should be no danger of scorching in practice; a comparison of the scorching tendencies of various proportions showed that a ratio of mercaptobenzothiazole 70 and hexamethylenetetramine 30 gives noticeable scorching. 3. The melting point curves, indicate some relation between the above proportion and the scorching phenomenon. 4. The heating curves of two sets of mixtures containing hexamethylenetetramine and sulfur, and hexamethylenetetramine, mercaptobenzothiazole and sulfur, respectively, in an oil bath at 150°, indicate that hexamethylenetetramine and sulfur react exothermically and that this reaction is accelerated by the presence of mercaptobenzothiazole. 5. The products of the reaction between hexamethylenetetramine and sulfur are carbon disulfide, ammonium thiocyanate, hydrogen sulfide, and ammonia. 6. The products of the reaction of two sets of samples heated in an oil bath at 150°, as indicated in 4, were determined quantitatively, and it was found that there was an increase of these products with an increase of time; which was also indicated by the loss of weight during the heating. 7. All of these reaction products had low accelerating power. Thiuram disulfide and ammonium thiocarbamate derived from carbon disulfide and ammonia and ammonium polysulfide derived from hydrogen sulfide, ammonium, and sulfur were tested, since they might have been formed during vulcanization, but they were found to be poor accelerators. 8. A preliminary test of combinations of mercaptobenzothiazole with ammonia, ammonium polysulfide, ammonium thiocyanate, and ammonium dithiocarbamate indicated that ammonia and ammonium polysulfide have some accelerating power, whereas all others are ineffective. 9. The combined use of ammonia and mercaptobenzothiazole forms a molecular compound which is effective as an accelerator, and this is true in an analogous way of the combined use of hexamethylenetetramine and mercaptobenzothiazole. 10. In order to prove experimentally the above theory, an attempt was made to treat a mixture of rubber, mercaptobenzothiazole, zinc oxide and sulfur with ammonia until the latter penetrated throughly the sample, after which the latter was vulcanized. Such treatment gives far better acceleration than does mercaptobenzothiazole without treatment with ammonia. 11. The accelerating power of ammonium polysulfide and mercaptobenzothiazole is attributed to the formation of ammonia from ammonium polysulfide and the reaction of ammonia and mercaptobenzothiazole.


1932 ◽  
Vol 5 (4) ◽  
pp. 657-670 ◽  
Author(s):  
Shukusaburo Minatoya ◽  
Kitaro Kojima ◽  
Izumi Nagai

Abstract 1. The study of the effect of the combined use of mercaptobenzothiazole and methylene-aniline is based on its eutectic curve. 2. These two accelerators do not form a molecular compound on mixing, and they have only one eutectic point. The eutectic mixture gave a stronger accelerating action than did either of the ingredients alone, vulcanization proceeded smoothly, and the products were superior. 3. The scorching effect increased with increase in the proportion of mercaptobenzothiazole, but there was no evidence that the eutectic mixture gave any increased scorching. In general, the scorching effect was less when these two accelerators were used in combined form.


Materials ◽  
2021 ◽  
Vol 14 (15) ◽  
pp. 4210
Author(s):  
Kai Jin ◽  
Shanyong Xuan ◽  
Jie Tao ◽  
Yujie Chen

The glass fiber reinforced polypropylene/AA2024 hybrid laminates (short for Al/Gf/PP laminates) as structural materials were prepared and formed by hot pressing. The synergistic effects of temperature and loading speed on the laminate deformation under tensile and bending conditions were investigated and analyzed in this study. In tension, stress–strain curves presented bimodal types effected by tensile rates and temperatures. The state of PP resin determines the mechanical behavior of the FMLs. The tensile rate has no effect on FML deformation without heating or over the melting point of PP resin (about 170 °C). The softening point of PP resin (about 100 °C) is characteristic temperature. When the temperature exceeds the softening point but does not reach the melting point, the tensile strength and elongation will demonstrate coordinated growth at a relatively high tensile speed. The efficiency of fiber bridging is affected significantly since the resin is the medium that transfers load from the metal to the fiber. Under bending, the curves presented a waterfall decrement with temperature increment. The softening point of resin matrix is the key in a bending process. When the temperature is near the softening point, deformation is sensitive to both the temperature and the loading speed to a certain extent. If temperature is lower than softening point, deformation is mainly guided by temperature. If the temperature is beyond the softening point, loading speed is in a leading position of deformation. The bending strength gradually increases with loading rate. By using these deformation characteristics, the deformation of the thermoplastic laminates can be controlled in stamping or other plastic forming processes for thermoplastic fiber metal laminates.


2017 ◽  
Vol 53 (86) ◽  
pp. 11830-11833 ◽  
Author(s):  
Seung Yeon Yi ◽  
Yu Kyung Moon ◽  
Sinheui Kim ◽  
Sonam Kim ◽  
Gyurim Park ◽  
...  

The combined use of a singlet oxygen photosensitizer and 1,3-diarylisobenzothiophene enables efficient generation of hydrogen sulfide at tunable photoirradiation wavelengths.


Cryobiology ◽  
1975 ◽  
Vol 12 (6) ◽  
pp. 583
Author(s):  
A.P. MacKenzie ◽  
D.H. Rasmussen

The object for which the present investigation was undertaken was to study the spontaneous crystallisation of mixtures of two substances which form mixed crystals and possess a minimum, or eutectic, freezing point. According to Cady, naphthalene and monochloracetic acid are such a pair of substances, and possess a minimum melting point of 53°·5 for the eutectic mixture of 29·4 per cent, naphthalene, 70·6 per cent, monochloracetic acid. We have attempted to verify Cady’s freezing and melting point curves, but, although our experiments confirm the former, we were quite unable to verify the latter. Pickering mentions four modifications of monochloracetic acid, and traces the freezing point curves for three of them. Our study of mixtures of monochloracetic acid and naphthalene has not given us the information we expected concerning the composition of the “mixed crystals” which separate spontaneously from a solution, but it has led to interesting results concerning the spontaneous crystallisation of the different modifications of a substance dissolved in another substance which is not polymorphous. The Different Modifications of Monochloracetic Acid and their Mutual Transformations . Microscopic examination of crystals of monochloracetic acid obtained from fusion or solution show clearly that three different modifications α, β , and γ of the acid exist. These modifications have melting points 61˚˙5, 55°, and 50°; they are formed on the microscope slide under different circumstances, each modification yielding rhombs quite distinct from those of the two other modifications. If fused monochloracetic acid be cooled suddenly it crystallises as the γ -modification in rhombs having a plane angle of about 59°. If these rhombs be touched they at once transform into the β -modification and give rhombs having a plane angle of about 72°; or occasionally the γ -rhombs are transformed at once into the stable a-modification of the acid, which exists as broad needles having an acute angle of 43˚. The transformation from γ to α takes place much more rapidly than the transformation from γ to β . Similarly, if rhombs of β are formed on a microscope slide they may be at once transformed into the α -modification by inoculating with a fragment of α . Each transformation is accompanied by a rise of temperature. A remarkable feature of the change is that the more stable modification crystallises with sharp edges in the solid mass of the less stable substance, as though it were growing in a liquid.


1954 ◽  
Vol 32 (5) ◽  
pp. 550-556 ◽  
Author(s):  
Paul A. Giguère ◽  
E. A. Secco

The cooling curves of a number of solutions of deuterium peroxide in heavy water in the concentration range 11% to 95% were measured in order to determine the solid-liquid phase diagram for that binary system. The apparatus of Herington and Handley, which uses a pulsing pressure for stirring the solutions, and a thermistor, was found to be particularly suitable for that purpose. As could be expected the freezing-point curve of the deuterated compounds is closely similar to that of the hydrogen compounds, being shifted up only by about 4° for water-rich solutions and by 2° for peroxide-rich solutions. The melting point of the addition compound, D2O.2D2O very nearly coincides with one of the eutectic points at 46.2% D2O2 and −51.5 °C.; the other eutectic point is at 60.5% D2O2 and −55.1 °C. By extrapolation the melting point of pure deuterium peroxide is found to be 1.5 °C. as compared with −0.43 °C. for hydrogen peroxide. Concentrated solutions of deuterium peroxide exhibit an extreme tendency to supercool, resulting sometimes in formation of glasses even at liquid-air temperature. The previous results of Foley and Giguère for the system H2O–H2O2 were confirmed, specially as regards the melting point of the addition compound H2O2•2H2O.


2016 ◽  
Vol 13 (4) ◽  
pp. 782-792
Author(s):  
Baghdad Science Journal

In the present study, new five polymers of acryloyl chloride have been synthesized by reaction 4-aminoantipyrine with many substituted acid chloride (A-E). Then condensation of polyacryloyl chloride with the product in one step (A-E), in a suitable solvent in the presence amount of (Et3N) to obtain new polyimides(A1-E5). The prepared compounds were characterized by UV. FT-IR, 1H-NMR and 13C-NMR spectroscopy and measuring of other physical properties such as softening point, melting point and solublities.


INDIAN DRUGS ◽  
2019 ◽  
Vol 56 (04) ◽  
pp. 61-64
Author(s):  
S Agarwal ◽  
Vandana ◽  
Himani Bajaj ◽  
M Yadav ◽  
R. Singh ◽  
...  

Colouring the skin particularly skin of face or lips, is an ancient practice going back to prehistoric times. The use of such coloring products has increased and the choice of shades of colour, texture and luster have changed and become wider. The present study was aimed at formulation and evaluation of a lipstick using herbal colouring agent. Herbal word is a symbol of safety in contrast to synthetic one which can have adverse effects on human health. Various physicochemical properties such as visual inspection, pH, melting point, breaking point, softening point, surface anomalies and solubility were assessed using established techniques. All the parameters were found to be within acceptable limits.


2012 ◽  
Vol 191 ◽  
pp. 159-168 ◽  
Author(s):  
Roman Przeliorz ◽  
Jaroslaw Piątkowski

The aim of the studies was to determine the oxidation kinetics of two magnesium alloys, i.e. WE43 and MSR-B, in CO2 atmosphere with and without the addition of 2 vol.% H2O. The rate of oxidation was measured by thermogravimetry in the temperature range of 530-580°C, i.e. below and above the eutectic melting point. The melting point of the eutectic mixture was determined by differential scanning calorimetry (DSC). The corrosion products were analysed by scanning electron microscopy (SEM) and X-ray microanalysis combined with EDS. Studies showed that on the WE43 alloy, a two-layer scale was formed, in which the outer part was composed of yttrium and magnesium oxides, while the inner part contained only yttrium oxide. The scale was found to preserve its good protective properties even above the eutectic temperature. Analysis of the results showed that on the MSR-B alloy, under a thin, uneven layer of scale, the process of internal oxidation occurred, and at a temperature of 580°C, the alloy underwent partial melting


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