Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Cork powder

Cork Powder Explosives (Brit Amer). See Vol 3, p C541-R... [Pg.632]

Cork Powder Explosives. Aubert Nauckhoff (Ref) patented the addn of cork powder to gelatinized expls, such as mixts of NC NG. The cork permanently retains a certain quantity of occluded air and thereby ensures rapid transmission of deton thruout the expl. One example of such a blasting expl consists of NG 56, NC 2.3, NB (nitrobenzene) 1.7, AN 35 cork pdr 5%... [Pg.324]

From Cork A A 1 1 mixture of cork powder and K2CO3 calcined for 1 h at 700°C in nitrogen, and then washed with water. [Pg.803]

Cork powder (50—100 g L ) and sodium silicate (10—15 g L ) are generally used for the mould coat, although oflier components are sometimes included, too, e.g., carboxy methyl cellulose (CMC). The cork suspension is sprayed onto the mould surface and heated to 80—90 °C. During casting, the cork powder gradually bums away, and a new coating is usually applied once or twice a shift. [Pg.208]

Cork powder was oxypropylated undo- these conditions [34,35] and the ensuing polyols fully characterized in terms of structure, homopolymer content, solubility, OH index and viscosity. The latter two parameters proved to be entirely comparable with those of commo-cial counterparts used in the manufacture of polyurethane materials. A study was therefore conducted [36] on the reactivity of the polyol mixtures, as obtained from the oxypropylation process, towards various diisocyanates and on the structure and properties of the ensuing polyurethanes. [Pg.307]

The correlation between microbial growth and formation of volatile components in the cork was the object of a further investigation by the same authors [44]. The spores of 10 micro organism strains were cultivated on malt extract (Oxoid) and in sterile water containing sterilized cork powder. The behaviors of the following 10 strains were studied Penicillium (three strains), Trichoderma... [Pg.430]

Now transfer the cold distillate to a separating-funnel, and shake vigorously with about 50-60 ml. of ether run oflF the lower aqueous layer and then decantf the ethereal solution through the mouth of the funnel into a 200 ml. conical flask. Replace the aqueous layer in the funnel, and extract similarly twice more with ether, combining the ethereal extracts in the conical flask. Add 3-4 g. of dry powdered potassium carbonate to the ethereal solution, securely cork the flask and shake the contents gently. The ethereal solution of the phenol... [Pg.196]

Place 20 g. of dry powdered benzoic acid in C, add 15 ml. (25 g., i.e., a 30% excess) of thionyl chloride and some fragments of porcelain, and then clamp the apparatus on a boiling water-bath as shown so that no liquid can collect in the side-arm of C. Heat for one hour (with occasional gentle shaking), by which time the evolution of gas will be complete. Cool the flask C, detach the condenser and fit it to the side-arm for distillation, using a 360° thermometer for the neck of C. To the lower end of the condenser fit a small conical flask G (Fig. 67(B)) by a cork carrying also a calcium chloride tube. [Pg.241]

Place I ml. of benzyl alcohol in a boiling-tube and add 6 ml. of 10% sodium hydroxide solution add also 6 ml. of water to moderate the subsequent reaction, otherwise the rise in temperature may cause hydrolysis of some of the ester produced. Now add r-q g. of finely powdered />-nitrobenzoyl chloride, and shake the well-corked tube vigorously. The mixture becomes warm, and the solid ester rapidly... [Pg.246]

Fit a 250 ml. three-necked flask with a stirrer, a reflux condenser and a dropping-funnel. (Alternatively, use a two-necked flask, with the dropping-funnel fitted by a grooved cork into the condenser.) Place 15 g. of powdered thiourea and 40 ml. of water in the flask and stir the mixture whilst 18 5 g. (16 ml.) of chloroacetone are added dropwise over a period of 20 minutes the thiourea will dissolve and the temperature of the mixture... [Pg.305]

Method 1 (with acetyl chloride). Equip a dry 500 ml. round-bottomed or bolt-head flask with a reflux condenser, and fit the top of the condenser with a two hole cork, one opening for a separatory funnel and the other for a delivery tube connected to an inverted funnel which dips just below the surface of about 200 ml. of water in a beaker (compare Fig. II, 13, 8). Place 40 g. of anhydrous, finely-powdered aluminium chloride (see Section IV,2) and 88 g. (100 ml.) of dry A.R. benzene in the flask and cool the latter in a bath of cold water (not ice water since benzene may crystallise). Through the separatory funnel at the top of the condenser add 29 g. (27 ml.) of redistilled acetyl chloride slowly during half an hour and shake the flask frequently to ensure thorough mixing of the... [Pg.729]

Method 2. Into a 500 ml. round-bottomed flask place 120 ml. of dry A.R. benzene, and 35 g. (29 ml.) of redistilled benzoyl chloride. Weigh out 30 g. of finely-powdered, anhydrous aluminium chloride into a dry corked test-tube, and add the solid, with frequent shaking, during 10 minutes to the contents of the flask. Fit a reflux condenser to the flask, and heat on a water bath for 3 hours or until hydrogen chloride is no longer evolved. Pour the contents of the flask wliile still warm into a mixture of 200 g. of crushed ice and 100 ml. of concentrated hydrochloric acid. Separate the upper benzene layer (filter first, if necessary), wash it with 50 ml. of 5 per cent, sodium hydroxide solution, then with water, and dry with anhydrous magnesium sulphate. Isolate the benzophenone as in Method 1. The yield is 30 g. [Pg.734]

Preparation of benzyl cyanide. Place 100 g. of powdered, technical sodium cyanide (97-98 per cent. NaCN) (CAUTION) and 90 ml. of water in a 1 litre round-bottomed flask provided with a reflux condenser. Warm on a water bath until the sodium cyanide dissolves. Add, by means of a separatory funnel fitted into the top of the condenser with a grooved cork, a solution of 200 g. (181-5 ml.) of benzyl chloride (Section IV.22) in 200 g. of rectified spirit during 30-45 minutes. Heat the mixture in a water bath for 4 hours, cool, and filter off the precipitated sodium chloride with suction wash with a little alcohol. Distil off as much as possible of the alcohol on a water bath (wrap the flask in a cloth) (Fig. II, 13, 3). Cool the residual liquid, filter if necessary, and separate the layer of crude benzyl cyanide. (Sometimes it is advantageous to extract the nitrile with ether or benzene.) Dry over a little anhydrous magnesium sulphate, and distil under diminished pressure from a Claisen flask, preferably with a fractionating side arm (Figs. II, 24, 2-5). Collect the benzyl cyanide at 102-103°/10 mm. The yield is 160 g. [Pg.761]


See other pages where Cork powder is mentioned: [Pg.256]    [Pg.256]    [Pg.528]    [Pg.864]    [Pg.25]    [Pg.280]    [Pg.306]    [Pg.319]    [Pg.478]    [Pg.1160]    [Pg.256]    [Pg.256]    [Pg.528]    [Pg.864]    [Pg.25]    [Pg.280]    [Pg.306]    [Pg.319]    [Pg.478]    [Pg.1160]    [Pg.106]    [Pg.116]    [Pg.119]    [Pg.144]    [Pg.163]    [Pg.213]    [Pg.221]    [Pg.234]    [Pg.250]    [Pg.253]    [Pg.255]    [Pg.260]    [Pg.486]    [Pg.141]    [Pg.193]    [Pg.372]    [Pg.587]    [Pg.733]    [Pg.740]    [Pg.792]    [Pg.1037]    [Pg.1038]    [Pg.1039]   
See also in sourсe #XX -- [ Pg.208 ]




SEARCH



Corks

© 2024 chempedia.info