Abstract:
A method for preparing a highly porous, high surface area non-degradable material includes the steps of mixing a non-degradable polymer with a solvent or mixture of solvents; gelling the mixture; and treating the gel under conditions whereby a substantially solvent free porous structure is created having a porosity greater than about 80%. The resultant material is mechanically strong and has an architecture including at least one of nano fibrous, micro fibrous, non fibrous, complex porous structure with nano fibrous architecture, and mixtures thereof.
Abstract:
Porous polymers having a plurality of openings or chambers that are highly convoluted, with each chamber being defined by multiple, thin, flat partitions are produced by a new gel enhanced phase separation technique. In a preferred embodiment, a second solvent is added to a polymer solution, the second solvent causing the solution to gel. The gel can then be shaped as needed. Subsequent solvent extraction leaves the porous polymeric body of defined shape. The porous polymers have utility as medical prostheses, the porosity permitting ingrowth of neighboring tissue. The present technique also enhances shape-making capability, for example, of bifurcated vascular grafts, which feature a common entrance region but two or more exit regions.
Abstract:
Porous membranes having a micro phase separation structure and showing a light transmittance at the wavelength of 400 nm of not less than 30% are obtained by the dry phase conversion method comprising drying a coating layer of a dope containing a polymer, a good solvent for the polymer and a poor solvent for the polymer which solvent has a higher boiling point than the good solvent. The polymer includes cellulose derivatives, vinyl-series polymers such as acrylonitrile-series polymers and (meth)acrylic acid ester-series polymers, polysulfone-series polymers, and the like. The porous polymer membranes have a porosity of 10 to 60%, a mean pore size of about 0.002 to 0.35 &mgr;m and a maximum pore size of not greater than 0.4 &mgr;m. These porous membranes shows not only excellent transparency but also high productivity.
Abstract:
Biofoam is a rigid, opaque microcellular organic foam made from organic materials derived from natural products and biological organisms. Typical organic materials are agar, agarose, gelatin, algin, alginates, gellan gum, and microcrystalline cellulose. The organic material is dissolved in a polar solvent, typically water, and the solution can be gelled immediately. The gel is frozen and freeze-dried to form the biofoam. Alternatively, a nonpolar solvent is added to the solution and emulsified. The resulting emulsion is then gelled, frozen, and freeze-dried. A variety of crystalline, fibrous, or metallic additives may be added to produce lightweight composite materials with enhanced strength and insulating properties. The amount of dilution of the organic material in the solvent(s) determines the density of the resulting biofoams, which ranges from about 1.0 mg/cm.sup.3 to about 500 mg/cm.sup.3.
Abstract translation:生物泡沫塑料是由天然产物和生物有机体衍生的有机材料制成的刚性,不透明的微孔有机泡沫。 典型的有机材料是琼脂,琼脂糖,明胶,藻酸盐,藻酸盐,结冷胶和微晶纤维素。 将有机材料溶解在极性溶剂中,通常为水,并且溶液可以立即凝胶化。 将凝胶冷冻并冷冻干燥以形成生物泡沫。 或者,将非极性溶剂加入到溶液中并乳化。 然后将所得乳液凝胶化,冷冻并冷冻干燥。 可以加入各种结晶,纤维或金属添加剂以产生具有增强的强度和绝缘性能的轻质复合材料。 有机材料在溶剂中的稀释量决定所得生物泡沫的密度,其范围为约1.0mg / cm 3至约500mg / cm 3。
Abstract:
A spongy material is produced by the steps of suspending a suitable quantity of finely divided particles of a thermoreversible gel in an aqueous solution of glucomannan-rich flour, adding an alkali to the suspension, allowing the suspension to gel, freezing the gelled suspension, thawing and leaching the same with hot water to leave a skeleton of a water-insoluble, thermally irreversible gel matrix. After drying, a spongy material having a relatively uniform cellular texture and a pleasant feel to the skin is obtained.
Abstract:
Low-density microcellular foam having a cell size of not greater than 2 .mu.m and method of making by dissolving cellulose acetate in an acetone-based solvent, gelling the solution in a water bath maintained at 0-10.degree. C for a selected period of time to allow impurities to diffuse out, freezing the gel, and then freeze-drying wherein water and solvents sublime and the gel structure solidifies into low-density microcellular foam. The foam has a density of 0.065 to 0.6.times.10.sup.3 kg/m.sup.3 and cell size of about 0.3 to 2 .mu.m. The small cell size foam is particularly adaptable for encapsulation of laser targets.
Abstract translation:细胞尺寸不大于2μm的低密度微孔泡沫体和通过将乙酸纤维素溶解在丙酮溶剂中制备的方法,将溶液凝胶保持在0-10℃的水浴中一段选定时间 时间允许杂质扩散出来,冷冻凝胶,然后冷冻干燥,其中水和溶剂升华,凝胶结构固化成低密度微孔泡沫。 泡沫体的密度为0.065〜0.6×10 3 kg / m 3,电池尺寸为0.3〜2μm左右。 小泡沫泡沫特别适用于激光靶的封装。
Abstract:
Foam encapsulated laser fusion targets are made by positioning a fusion fuel-filled sphere within a mold cavity of suitable configuration and dimensions, and then filling the cavity with a material capable of producing a low density, microcellular foam, such as cellulose acetate dissolved in an acetone-based solvent. The mold assembly is dipped into an ice water bath to gel the material and thereafter soaked in the water bath to leach out undesired components, after which the gel is frozen, then freeze-dried wherein water and solvents sublime and the gel structure solidifies into a low-density microcellular foam, thereafter the resulting foam encapsulated target is removed from the mold cavity. The fuel-filled sphere is surrounded by foam having a thickness of about 10 to 100 .mu.m, a cell size of less than 2 .mu.m, and density of 0.065 to 0.6 .times. 10.sup.3 kg/m.sup.3. Various configured foam-encapsulated targets capable of being made by this encapsulation method are illustrated.
Abstract translation:泡沫包封的激光熔化靶是通过将熔融填充的填充球定位在合适的构造和尺寸的模腔内,然后用能够产生低密度微孔泡沫的材料(例如溶解在 丙酮类溶剂。 将模具组件浸入冰水浴中以凝胶化材料,然后在水浴中浸泡以浸出不需要的组分,然后将凝胶冷冻,然后冷冻干燥,其中水和溶剂升华,凝胶结构固化成 低密度微孔泡沫,然后将所得的泡沫包封的目标物从模腔中除去。 充满燃料的球体由具有约10至100μm厚度的泡沫,细胞尺寸小于2μm,密度为0.065至0.6×10 3 kg / m 3的泡沫包围。 示出了能够通过该封装方法制造的各种配置的泡沫封装的靶。