A stretching unit for transversely stretching elastic films, including first and second stretching devices each having respective gripping zones and respective release zones, and wherein the release zones of the first and second stretching devices are aligned to each other along a common transverse release line.

A heat-shrinkable polyester film includes at least one polyester material made of at least one polyester forming composition which includes a dibasic carboxylic mixture and a diol mixture. The heat-shrinkable polyester film has a heat shrinkage rate of not lower than 25% in a shrinkage direction, which is measured by immersing the heat-shrinkable polyester film in hot water at 65° C. for 10 seconds. A method for producing the heat-shrinkable polyester film is also disclosed.

Preparing MAX phase structures includes forming a gel including a transition metal M, a Group 3A or Group 4A metal or semimetal A, and an acidic chelating agent or gelling agent X. X includes one or both of carbon and nitrogen. Preparing the MAX phase structures further includes shaping the gel to yield a shaped gel and heating the shaped gel to yield carbonaceous MAX phase structures with a composition represented by M.sub.n+1AX.sub.n, wherein n is 1, 2, 3, or 4. The MAX phase structures can be thick films, microspheres, or microwires.

There is provided a multilayer film comprising a starch layer and at least one other layer. The multilayer film has excellent barrier properties. The starch layer comprises a modified starch having a degree of substitution less than 1.5. Suitable other layers include polyolefins. The multilayer film finds use in packaging, particularly in packaging foodstuffs.

The present invention relates to a process for the preparation of films of conductive polymers, by the technique so-called roll-to-roll, which allows to obtain freestanding films having advantageous features such as toughness, flexibility, ability to adhere to different substrates, a submicron thickness and a very high ratio surface area/thickness; the present films are suitable for use in several technological applications, in particular for the development of biosensors, and in the production of flexible electronic components with large surface, suitable for wearable devices and also intended for contacting skin.

An optically anisotropic polymer thin film includes a crystallizable polymer and an additive configured to interact with the polymer (e.g., via π-π interactions) to facilitate chain alignment and, in some examples, create a higher crystalline content within the polymer thin film. The polymer thin film may be characterized by a bimodal molecular weight distribution where the molecular weight of the additive may be less than approximately 50% of the molecular weight of the crystallizable polymer. Example crystallizable polymers include polyethylene naphthalate, polyethylene terephthalate, polybutylene naphthalate, polybutylene terephthalate, as well as derivatives thereof. Example additives, which may occupy up to approximately 10 wt. % of the polymer thin film, include aromatic ester oligomers, aromatic amide oligomers, and polycyclic aromatic hydrocarbons, for example. The optically anisotropic polymer thin film may be characterized by a refractive index greater than approximately 1.7 and an in-plane birefringence greater than approximately 0.2.

A liquid crystal polymer film that includes a liquid crystal polymer having an endothermic peak temperature that exceeds 330° C., the endothermic peak temperature being a temperature resulting from when the liquid crystal polymer is heated to 400° C. in an inert atmosphere, then cooled to room temperature at a temperature decreasing rate of 40° C./min or more, and measured using a differential scanning calorimeter while being heated again at a temperature increasing rate of 40° C./min.

This invention relates to an oriented polyethylene film comprising polyethylene having: (A) a melt flow index of 1.0 g/10 min or more, (B) a density of 0.90 g/cm.sup.3 to less than 0.940 g/cm.sup.3, (C) a g′.sub.LCB of greater than 0.8, (D) ratio of comonomer content at Mz to comonomer content at Mw is greater than 1.0, (E) ratio of comonomer content at Mn to comonomer content at Mw is greater than 1.0, and (F) a ratio of the g′.sub.LCB to the g′.sub.Zave is greater than 1.0, where the film has a 1% secant in the transverse direction of 70,000 psi or more and Dart Drop of 350 g/mil or more.

The present invention discloses a film pasting device, comprising a main board body, the main board body is provided with a film fixed area for fixing a protective film, and a pressing hole is formed in the film fixed area on the main board body; and the film fixed area is configured to be bonded with one side, deviating from a pull-up film, of a film body of the protective film, such that the protective film is connected to the main board body as a whole; the film body is disconnected from the film fixed area when pushing the side of the protective film deviating from the pull-up film after penetrating through the pressing hole.

Provided is a method for producing recycled pellets, capable of using loss films that have been inapplicable so far including a thick loss film, a wide loss film, and a loss film made of a material that has high hardness and therefore is less likely to be bent, and also capable of producing recycled pellets similar to virgin pellets. A method for producing recycled pellets includes the steps of: twisting one or more loss films (R) continuously supplied in one direction while applying a stretch to the loss film; pressurizing a twisted part to pressure-bond contact parts of the loss film (R), thereby forming a twisted string (R); and cutting the twisted string (R) to produce recycled pellets (P). The loss film (R) is preheated at a softening temperature of the loss film (R) prior to twisting the loss film (R) while stretching it.