Abstract: The present invention relates to a modular storage system for barrels. The modular storage system includes a base rick module, an aisle rick module, and an end rick module, whereby a plurality of each module type may be assembled to construct a rickhouse.

Abstract: Methods for constructing multi-walled carbon nanotube (MWCNT) antenna arrays, may include: variable doping of the MWCNTs, forming light pipes with layers of variable dielectric glass, forming geometric diodes on full-wave rectified devices that propagate both electrons and holes, using clear conductive ground plans to form windows that can control a building's internal temperature, and generating multiple lithographic patterns with a single mask.

Abstract: A toggle fastener as a hasp lever 22 pivoted on a first axis on mounting plate 10, and pivotally mounting bail 24 28 on a second axis 30. The bail is to engage in jaw 26 in keeper 14 and when the plate 10, bail 24 and lever 22 are all substantially parallel, which is the secured position of the fastener and lugs 32 provided on the hasp 22 lie closely adjacent to the bail between axis 30 and the axis of the keeper engaged end, and serve to prevent or limit pivotal movement of the bail about either end. This enables the fastener to be used to secure panels in place.

Abstract: An improved process for controlling and reducing the concentration of free carboxyl end groups in condensation polyester melt spun fiber is provided. By selection of a multifunctional compound, it is possible to increase the intrinsic viscosity of the fiber. The process comprises admixing and reacting with molten polyester polymer an effective amount of a lactim compound of the formula ##STR1## wherein n is an integer of 2 to 15;m is an integer of 1 to 4;R.sub.1 and R.sub.2 are independently hydrogen, halogen, nitro, amine, C.sub.1 -C.sub.10 alkyl, C.sub.5 -C.sub.12 cycloalkyl, C.sub.7 -C.sub.9 alkyl aromatic, or C.sub.6 -C.sub.10 aromatic; andR.sub.3 is a mono- to tetravalent organic radical selected from the group consisting of C.sub.1 -C.sub.32 alkyl, C.sub.5 -C.sub.14 cycloalkyl, C.sub.7 -C.sub.16 alkyl aromatic, and C.sub.6 -C.sub.14 aromatic.The lactim reacted polymer is then melt spun to form a fiber.

Abstract: Permselective membranes are disclosed which comprise a layer comprising polystyrene, at least a portion of which is sulfonated, and between about 10 wt. % and about 35 wt. % monovinyl arene-hydrogentated diene block copolymer, at least a portion of which is sulfonated. The membranes exhibit a resistance of less than about 8 .OMEGA.-cm.sup.2 in 7 wt. % Na.sub.2 SO.sub.4 and an ion exchange capacity of between about 1.0 meq/g and about 1.6 meq/g. Monopolar and bipolar membranes comprising the layer are disclosed. A preferred process for forming the membranes comprises the steps of sulfonating polystryene and monovinyl arene-hydrogenated diene block copolymer, forming a mixture of the materials in a solvent, forming a layer of the mixture and drying the layer to form at least a portion of the membrane.

Abstract: Ultra-high molecular weight poly(N-propionylethylenimines) are disclosed that are useful as water purification agents. The polymers of this invention include partially deacylated poly(N-propionylethylenimines) derived from poly(N-propionylethylenimines) having a weight average molecular weight, M.sub.w, between about 1 million and about 20 million. The polymers have a degree of deacylation that ranges from about 10% to about 90%.

Abstract: A toggle fastener comprises first and second parts in which the first is a keeper having a cavity. The second part has a bolt slidable therein having a nose adapted to be received in said cavity, and also having hinged thereto a lever on which is pivoted a hasp. The nose of the bolt is adapted to protrude through an opening in the keeper. A cam surface on the nose of the bolt is inclined to the axis of the bolt, and a cam surface on the keeper adjacent to said opening and is opposed to and is inclined oppositely to the cam surface on the nose of the bolt. Said hasp is engageable with both of said cam surfaces in order to cam the keeper and the bolt in opposite directions to prevent rattling.

Abstract: A process for producing poly(ester carbonates) and polyesters by reacting an aromatic or cycloaliphatic dicarboxylate salt such as sodium terephthalate with phosgene in an organic solvent in the presence of a catalytic amount of a tertiary nitrogen compound such as pyridine, optionally separating the suspended by-product inorganic salt and then interfacially reacting with a bisphenol such as bisphenol A. Excess phosgene in the diacid chloride synthesis can be carried over to the polymerization if a poly(ester carbonate) is to be produced or removed if a polyester is to be produced. Certain low levels of a tertiary nitrogen compound with a pyridine nucleus in the organic solution do not interfere with the interfacial polymerization.

Abstract: High molecular weight linear condensation polyesters are stabilized against deterioration by heat with a stabilizer comprising 2-(phenoxy methyl)-3-phenyl oxirane.

Abstract: Poly(ester/carbonates) are produced by adding phosgene to a reaction mixture of bisphenol A and terephthalic acid as ester-forming reactants, at mole ratios in the range between 2.0:0.8 and 2.0:1.3, in which the reaction medium consists essentially of pyridine, the concentration of bisphenol A plus terephthalic acid is in the range between 5 and 50 grams per 100 ml of pyridine; and the phosgene is added under agitation at a rate of at least 0.07 gm-mmole/liter.sec. The process is carried out at temperature in the range between 50.degree. C. and 115.degree. C. and not below the temperature given by the Arrhenius equation:1nU=10-12/0.001987 Twhere U is phosgene feed rate in gram-moles/liter.second and T is absolute temperature of the reaction mixture (degrees Kelvin). Preferred phosgene feed rates are at least 0.13 gram-millimoles/liter.second; and preferred temperatures of the reaction mixture are between 60.degree. C. and 80.degree. C.

Abstract: A process for poly(ester-carbonates) from dihydric phenols, especially bisphenol A; aromatic or cycloaliphatic dicarboxylic acids, especially terephthalic acid; and phosgene as carbonate precursor wherein a reaction of the acid and phosgene is carried out in a first stage forming dicarboxylic acid chloride; and then phosgene and bisphenol A are added in separate streams, simultaneously during most of the second or condensation stage. Thereby only one kettle is required for carrying out the complete polymer production.