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The objectives The work was carried out for extraction of natural anthrasesamones from roots of Sesamum Indicum using different organic solvents and utilization of extracts as catalyst in pulping with sodium hydroxide for a by-product of sugar industry (Sudanese bagasse). Results Sesamum Indicum roots when extracted with ethanol, it gave the highest extracts yield % (0.964), followed by ethyl acetate, chloroform, dichloromethane and petroleum ether extracts. The chemical pulping of Bagasse was done by using of sodium hydroxide, sodium hydroxide with anthraquinone, and sodium hydroxide with extract instead of anthraquinone keeping constant conditions at temperature 160 °C and applied sodium oxide 10.9% and time was 120 min, gave promising screened yield between 49.84 and 53.68%, bleachable kappa number between 15.57 and 8.26 for sodium hydroxide only and cooking with sodium hydroxide with anthraquinone. Cooking with sodium hydroxide of bagasse with anthrasesamones gave good pulping yields and kappa number. Electronic supplementary material The online version of this article (10.1186/s13104-019-4075-9) contains supplementary material, which is available to authorized users.

As a result of the recent lowering of the Occupational Safety and Health Administration's (OSHA's) permissible exposure limit (PEL) for chloroform from 50 ppm to 2 ppm, interest has increased in measuring chloroform in pulp and paper industry workplace atmospheres. OSHA suggested that its Method 5 should be used for measuring chloroform concentrations in the range of the new PEL. There are some potential problems with using Method 5 for this purpose. Pulp and paper industry atmospheres may interfere with the measurement because of high temperature, high humidity, and the presence of chlorine. The charcoal sorbent tubes specified in OSHA Method 5 were challenged in the laboratory with a test gas containing 0.1, 0.5, 1, and 2 times the PEL of chloroform at 38 degrees C with 80% to 93% relative humidity and ca. 0.5 ppm chlorine. Application of the National Institute for Occupational Safety and Health (NIOSH) validation protocol to the results indicated a bias of -8.2% and a pooled coefficient of variation (CV) of 0.0274. The method CV is less than the critical CV; thus, the method is acceptable by the NIOSH validation protocol under these conditions. Field testing of OSHA Method 5 was successful and did not reveal any unexpected problems. Additional tests showed that with some modification, OSHA Method 5 can be used to measure chloroform concentrations in ambient atmospheres down to 0.1 ppb.

Oil mist can be efficiently collected on filter paper or by an electrostatic precipitator. Samples containing 0.05 mg of oil can be accurately determined by ultraviolet spectrophotometry. Gross amounts of sample contaminants, such as soil, water, and pipe scale, can be tolerated without appreciable loss in accuracy. Petroleum distillate vapor is efficiently collected on silica gel or in a midget bubbler containing chloroform. Maximum collection efficiency is achieved at sampling rates not exceeding 100 cc/min. Samples containing as little as 0.5 mg in 10 ml of chloroform or ethanol may be determined by spectrophotometry. With both oil and petroleum distillate determinations, it is necessary to obtain a sample of the particular product in question in order to construct a standard spectrophotometric curve.

The separation of a mixture of quinine, strychnine and nicotine when added to blood is described. The procedure involves protein precipitation by hot tungstic acid and extraction of the alkaloids with ether. Ascending chromatography, which takes only 14 minutes, on cellulose citrate ion-exchange paper at pH 4.5 is used to separate the alkaloids from a chloroform solution of the dried ether extract. The alkaloids, which are clearly separated from each other and from basic compounds present in normal blood are detected by examination in ultraviolet light.

The nucleotide pools of certain mucoid, colanic acid-synthesizing strains of Escherichia coli, Salmonella typhimurium , and Aerobacter cloacae were examined, and in all cases the nucleotide sugars uridine-5′-diphosphate glucose (UDPG), uridine-5′-diphosphate galactose (UDPGal), guanosine-5′-diphosphate fucose (GDPF), and uridine-5′-diphosphate glucuronic acid (UDPGA) were detected. It is postulated that these nucleotide sugars are precursors in the synthesis of colanic acid. The levels of these nucleotide sugars and of the enzymes involved in their synthesis were examined in a number of mucoid strains and compared with the levels found in certain strains which were repressed in the synthesis of colanic acid, only becoming mucoid when grown in the presence of p -fluorophenylalanine (PFA). The levels of UDPG and UDPGal and the enzymes involved in their synthesis were substantially the same in both mucoid and repressed types, but the levels of UDPGA and GDPF and of some of the enzymes involved in their synthesis were much higher in mucoid strains. When repressed strains were grown in the presence of PFA, the levels of UDPGA and GDPF approached those found in mucoid strains. The existence of an operon, containing genes coding for certain key enzymes involved in colanic acid synthesis has been suggested.